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Page 1: Modern Vapor Degreasing - InfoHouseinfohouse.p2ric.org/ref/28/27368.pdf · Modern Vapor Degreasing and Chlorinated Solvents ... answer any customer or user ques- ... A straight vapor
Page 2: Modern Vapor Degreasing - InfoHouseinfohouse.p2ric.org/ref/28/27368.pdf · Modern Vapor Degreasing and Chlorinated Solvents ... answer any customer or user ques- ... A straight vapor

Modern Vapor Degreasing and Chlorinated Solvents '"CONTENTS

MODERN VAPOR DEGREASING USES OF DEGREASING . . . . . . . . . . . . . . . . . . . 1 DEGREASING METHODS . . . . . . . . . . . . . . . . . . 1

Vapor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 Vapor Plus Distillate Flush or Spray . . . . . . . . 1 Vapor Plus Immersion - Single Dip . . . . . . . 2 Vapor Plus Immersion . Multiple Dip . . . . . . 3 Missile and Large Tank Cleaning . . . . . . . . . . 3 Ultrasonic Cleaning ...................... 3

ECONOMICS OF DEGREASING . . . . . . . . . . . . 4 Selection of Heat Source . . . . . . . . . . . . . . . . . 4 Selection of Water Source . . . . . . . . . . . . . . . . 4

DEGREASING EQUIPMENT . . . . . . . . . . . . . . . . 4 Design Assistance .. . . . . . . . . . . . . . . . . . . . . . 4 Design Factors . . . . . . . . . . . . . . . . . . . . . . . . . . 5 Work Opening . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 Heat Requirements ...................... 5 Heat Sources ........................... 6 Heat Safety Controls ..................... 7 Vapor Control ........................... 7 Freeboard Cooler or Water Jacket . . . . . . . . . 7 Freeboard . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 Water Separator ......................... 7

Provisions for Cleanout . . . . . . . . . . . . . . . . . . . 9 Materials of Construction . . . . . . . . . . . . . . . . . 9

MATERIALS HANDLING . . . . . . . . . . . . . . . . . . . 9 Manual or Open-Top Units . . . . . . . . . . . . . . . . 9 Conveyorized Units ...................... 10

DEGREASER INSTALLATION . . . . . . . . . . . . . . . 11 Location . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11 Space Requirements ..................... 11 Room Size . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11

'3 StorageTank . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9

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TOXICITY. HANDLING PRECAUTIONS. FIRST AID . . . . . . . . . . . . . . . . . . . . . . . . . . . . . i s . . . ._ TOXICITY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15 HANDLING . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15 SAFETY RULES . . . . . . . . . . . . . . : . . . . . . . . . . . . 16 SELECTION OF OPERATORS . . . . . . . . . . . . . . 17 SAFETY EQUIPMENT ..................... 17

Operators' Garments and Equipment . . . . . . . 17 Maintenance Personnel Equipment . . . . . . . . 17

DECOMPOSITION HAZARDS . . . . . . . . . . . . . . 17

DEGREASER OPERATION . . . . . . . . . . . . . . i g DO'S AND DON'TS FOR THE OPERATOR . . 19 STARTING PROCEDURE . . . . . . . . . . . . . . . . . . 19 CONCERN FOR THE ENVIRONMENT . . . . . . . 20 DISPOSAL ................................ 20 SAFETY RESEARCH AND COUNSEL . . . . . . . 20 CLEANING THE WORK .................... 21

Size of Work Load ....................... 21 Proper Positioning of Work . . . . . . . . . . . . . . . . 21 Rate of Entry and Removal . . . . . . . . . . . . . . . 21 Vapor Contact Time ...................... 21 Transfer of Work ......................... 21 Spraying ................................ 21 Solvent Level in Heating Chamber . . . . . . . . . 21 Solvent Contamination . . . . . . . . . . . . . . . . . . . 21

SHUT-DOWN PROCEDURE . . . . . . . . . . . . . . . . 21 OPERATION OF EXTERNAL STILL . . . . . . . . . 22 COMMON DEGREASER PROBLEMS ....... 22

Pronounced Vapor Odors . . . . . . . . . . . . . . . . . 22 Excessive Solvent Consumption . . . . . . . . . . . 23 Corrosion ............................... 23 Stained Work ............................ 24

.................................... Pits DEGREASER MAINTENANCE 25 12 Location of Gas-Heated Degreasers 12 Avoidance of Heat and Flames 12 Avoidance of Drafts ...................... 12

. . . . . . . . . . . . . . . . . CLEANING PROCEDURE 25 RESTORATION OF ACID DEGREASERS 26

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .... Heat Information ......................... 12 PROPERTIES OF VAPOR Water Piping Requirements . . . . . . . . . . . . . . . 13 DEGREASING SOLVENTS . . . . . . . . . 27

SOLVENT RECLAMATION . . . . . . . . . . . . . . . . . 13 GENERAL PROPERTIES . . . . . . . . . . . . . . . . . . . 27 Internal Distillation ....................... 13 CHLOROTHENE VG SOLVENT . . . . . . . . . . . . . 28 External Distillation ....................... 13 NEU-TRI SOLVENT ........................ 30 Solvent Recovery with Activated Carbon . . . . 14 DOW PERCHLOROETHYLENE SVG . . . . . . . . 32 Refrigerated Freeboard Chiller . . . . . . . . . . . . 14 DOW METHYLENE CHLORIDE.

VAPOR DEGREASING GRADE ........... 36

SOLVENT CONDITION MONITORING . . 38

TECHNICAL ASSISTANCE . . . . . . . . . . . . . . . . . . . 39

EQUIPMENT SUPPLIERS .................... 40

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Modern Vapor Degreasing

3 Uses of Degreasing Degreasing is an essential part of the modern production process, partic- ularly in industries fabricating or assembling metal parts - aircraft, appliance, automotive, electronics, railroad. It is widely used to remove oils and oil-borne soils such as chips, metal fines, and fluxes from objects that have been stamped, machined, welded, soldered, molded, diecast, etc. Tiny transistor parts, printed-circuit assemblies, precision surgical equip- ment, diesel motors, aircraft compo- nents, automotive parts, spacecraft assemblies - all can be safely, com- pletely and quickly cleaned with mod- ern vapor degreasing techniques, in most cases more effectively than with aqueous or fluorocarbon solvent clean- ing, particularly if oil or grease is an element of the soil. The Dow Chemical Company, the world’s largest producer of chlori- nated solvents, has a metal-cleaning technical service staff at its Midland, Michigan, headquarters prepared to answer any customer or user ques- tions not covered in this publication. Dow offers the most complete line of chlorinated solvents for modern vapor degreasing. These include: CHLOROTHENE* VG* Inhib- ited l,l,l-Trichloroethane for Vapor Degreasing DOW Methylene Chloride, Vapor Degreasing Grade NEU-TRI* Brand Trichloro- ethylene DOW Perchloroethylene SVG

g r ]

Degreasing Methods This section serves as a guide to help select the right degreasing method for the size, mass, gauge, shape, specific heat, and design intricacy of the work to be cleaned and the type and amount of soil to be removed. Conduct small-scale experiments to determine the method best suited to the job. The shortest cleaning cycle that gives the required standard of cleanliness is best.

VAPOR Vapor degreasing is an effective and economical process for cleaning pro- duction or service parts prior to as- sembly, packaging or other usages requiring grease- and dirt-free parts. Sufficient heat is applied to a powerful cleaning solvent to vaporize it. The vapor is heavier than air and thus con- tainable in an open-top tank into which the dirty parts are lowered. On contact with the cold parts (called “the work”), the vapor condenses into pure liquid solvent which dissolves the grease and carries off the soil as it drains off the parts into the heating sump or reservoir below. The cleaning process continues until the work reaches the temperature of the vapor. At that point, condensation will cease. The work can then be lifted out of the vapor, clean and dry.

Unit - The basic principle of vapor degreasing is illustrated in a simple unit (see Figure 1, page 2). A relatively small amount of solvent in the bottom of the tank is heated and vaporized. The dense vapors rise and fill a zone above the boiling liquid solvent and constitute the work area. The solvent vapors are confined in the machine by condensing coils and a water jacket.

Cleaning Cycle - The work is sus- pended in pure condensing solvent vapor which dissolves and washes away contaminants. When the tem- perature of the work reaches that of the vapor, condensation and cleaning cease, and upon removal the part is dry and clean. This cleaning method may be used with any work of simple shape with a light film of highly soluble oil or grease.

VAPOR PLUS DISTILLATE FLUSH O W R A Y This degreasinglcleaning method is especially recommended for removing insoluble abrasives and metal fines held on the work by oils remaining after completion of buffing or polishing op- erations. A straight vapor cycle may remove the lubricants and leave be- hind the insolubles. This method is also recommended for small parts which can be stacked in baskets. Nozzles can be arranged to break air pockets and to spray into enclosed areas. This method is used frequently for large castings and sheet stock as well as for high-volume production cleaning of small objects.

Unit - This unit is similar to the one previously described but with the addi- tion of a spray lance (see Figure 2) or fixed nozzles, a pump, and a storage tank for continuously collecting clean solvent.

‘Trademark of The Dow Chemical Company

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3 FIGURE 1 Typical Open-Top Vapor Degreaser

Condensing Coils7 /Safety Thermostat

Heating Elements ’ -[Work Rest and Protective Grate Solvent Level

Sight Glass

FIGURE 2 Vapor Degreaser with Spray Attachment

Condensing Coils

Water Jacket

Steam coils

Heating Elements

Grate

Cleaning Cycle - The part is sus- pended in the vapor zone for initial cleaning. To dislodge remaining oils and insoluble contaminants from re- cesses and crevices, the work is flushed with clean, cool solvent. This lowers its surface temperature and permits further vapor condensation. The nozzle of the spray lance or fixed nozzles should be kept as low as possible in the vapor zone to minimize vapor disturbance. This cleaning method, adaptable to both hand-operated and conveyorized equipment, is preferred for heavily contaminated parts that cannot be cleaned by straight vapor condensation.

VAPOR PLUS IMMERSION - SINGLE DIP (Vapor I Warm Liquid Wash I Vapor Rinse) This method is used when the amount of soil is heavy, the contour of the work is intricate, or bulk quantities of small parts are covered with a light film of oil or grease. Both tumbling and agitation are practical means of minimizing sol- vent dragout but should be used only when the parts will not be damaged.

Unit - Generally, a two-compartment unit is used, one being a boiling-solvent sump and the other, a warm-liquid chamber.

Cleaning Cycle - Work is lowered through the vapor zone, rotated or agi- tated in the warm liquid, then raised into the vapor zone for final rinsing.

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VAPOR PLUS IMMERSION - MULT I PLEP (Vapor-Boiling Liquid Wash I Warm Liquid Rinse I Vapor) This is one of the most efficient clean- ing methods for removal of stubborn soils such as heavy oil deposits and insoluble particles.

Unit -This unit may be either a two- or three-compartment design with one or two boiling-liquid chambers and a warm-liquid rinse compartment (see Figure 3).

Cleaning Cycle - Vapor contacts the work as it is lowered into the boiling- liquid compartment, where boiling sol- vent adds mechanical agitation to sol- vent action to remove heavy oils and insoluble contaminants. The work is transferred to the warm-liquid rinse compartment, where clean solvent continues the cleaning action and cools the work to permit further va- por condensation. The warm-liquid compartment is continuously replen- ished with clean, condensing solvent and overflows into the boiling compartment.

MISSILE AND LARGE TANK CLEANING The interiors of enclosed vessels or tanks such as tank transports, storage tanks, and processing tanks can be cleaned and dried by spraying with sol- vent distillate and vapor degreasing with vapors produced in a separate generator. Recycling of solvent be- tween generator and tank is continued until the cleaning is complete.

FIGURE 3 Diagram of Typical Immersion Multiple Dip Vapor Degreaser

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Water Jacket

Condensing 1 Coils

43- f & P’

aqJar u1u Heating Coil

ULTRASONIC CLEANING Motion of either the cleaning solution or the part to be cleaned improves and speeds cleaning. Ultrasonic cleaning is industry’s most advanced application of this simple principle. When ultrasonic energy is transmitted to a solution, it produces cavitation - the rapid buildup and collapse of thousands of tiny bubbles. Cavitation imparts a scrubbing action to the sur- face of soiled parts, and, when teamed with the action of a solvent, results in highly effective cleaning.

Ultrasonic cleaning helps remove heavy oil deposits and solids that adhere to metal surfaces and are in- soluble in solvents. It is also very effec- tive for removing fluxes on printed circuit boards as well as micro-sized contaminants on precision elec- tronic components. Soils that are slowly soluble in a given solvent respond well to an ultrasonic bath. Ultrasonic cleaning can be espe- cially effective in loosening contam- inants from parts with hard-to-reach recesses.

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cycles - To limit solvent contam- ination and reduce cleaning time, pre-cleaning cycles often precede ul- trasonic immersion, and a distillate rinse and a vapor rinse often follow the ultrasonic bath. A typical cycle employ- ing ultrasonic would be: (1) vapor cleaning, (2) immersion in an ultrasonic-activated liquid chamber, (3) spraying, and (4) vapor cleaning.

Equipment - New degreasing equipment is not necessary for ul- trasonic cleaning if present equipment is made of stainless steel. Transducers can be installed on the bottom or sides of most degreasers. Completely sealed transducers should be specified if the immersible type is to be used. Transducers, particularly the piezo- electric type, are rated for a maximum temperature exposure and may be ad- versely affected if used at tempera- tures higher than rated. Generally, the optimum frequency range for effective chlorinated solvent cavitation is 20-50 kHz (kilo Hertz). Ultrasonic vibration should take place in the clean-solvent immersion chamber, not in the boiling compartment of the degreaser. Operat- ing temperatures of 2540°F below the boiling point of the solvent are op- timum. These lower temperatures will cool hot parts, permitting a final rinse with pure condensing vapors.

Economics of Degreasing Vapor degreasing is a process low in cost compared to other production cleaning operations.. Investment and utility costs are low, and floor-space needs are small. Work of excellent quality is achieved with a minimum of operator control. Factors to be considered in comparing the costs of various types of degreas- ing operations include the following:

Cost of chemicals or solvents Services available with the chemi- cals/ solvents Cost of utilities Labor cost Cost of waste disposal Maintenance costs Initial capital investment Building space Depreciation

SELECTION OF HEAT SOURCE Heat-source costs vary from one locale to another and within individual plants. Although steam is the safest and pre- ferred heat source, economic or other factors may preclude its use and necessitate using alternate methods.

SELECTION OF WATER SOURCE City water passed once through a sys- tem is expensive. However, process water, or city water cooled in water towers and recycled, is more eco- nomical. To conserve water and lower costs, water can be routed from the degreasers to other industrial/ plant processes.

Degreasing Equipment Vapor degreasing equipment is de- signed not only to vaporize solvent for cleansing and drying parts, but also to confine and recycle the solvent and solvent vapor 'to maintain a healthful environment and keep cleaning costs low. Vapor degreasing equipment must provide for - 1. Cleaning to remove soluble and

2. Recovery of solvent by distillation

3. Concentration of soils. These requirements are met by the basic degreasing unit shown in Figure 1, which is an open rectangular tank with a pool of solvent in the bottom. The solvent is heated in the boiling sump and vaporized into a dense, heavier- than-air vapor layer that lies above the liquid and constitutes the vapor cleaning zone. The condensing coils, installed high on the inside periphery of the tank, condense the vapor reaching that level. The solvent condensate is returned to the solvent boiling sump via the condensate trough and water separator. The freeboard, a very important verti- cal extension of the degreaser wall, provides a stationary air zone above the vapor level. The freeboard shields the normal vapor zone from moderate drafts which could carry the vapors into the work environment. In addition, a very thin solvent film evaporates from the work as it is slowly withdrawn from the vapor zone, and the freeboard area confines these vapors.

DESIGN ASSISTANCE Dow's metal cleaning technical service staff can assist in the selection of the right equipment for the job. Standard units for a variety of work capacities as well as custom-built units for specific needs or processes are available.

particulate soil.

for repeated use.

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DESIGN FACTORS Factors influencing design are:

Size, shape, mass, specific heat, composition and gauge of part to be cleaned 8

Volume of work per unit of time Amount and nature of contaminants Cleaning cycle Method of work suspension and

Space allotted for installation Government regulations Available utilities at degreaser site

WORK OPENING The degreaser work opening must be adequate to handle the work dimen- sions and cleaning cycle, but should be kept to a minimum to maintain econom- ical operation and acceptable working conditions. Even when vapor loss is controlled and no work is passing through, every square foot of exposed surface permits loss of a given amount of solvent related to the equipment de- sign and the solvent used. Table l shows the relative loss ratio of the vari- ous degreasing solvents in a typical open top (58 x 24 in) degreaser. In designing a unit, the equipment manufacturer should provide for minimum solvent loss by cutting down vapor disturbance. Since vapor in the center of the tank passes to the walls for condensation, extending the tank width increases tur- bulence which causes entrainment of air resulting in vapor loss. As narrow a tank as feasible is recommended.

materials handling

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TABLE I. Solvent Consumption Comparison - Idling Vapor Degreaser

- CWLOROTHENE VG

NEU-TRI trichloroethylene . . . . . . 47 0.201 42 DOW Methylene Chloride,

Vapor Degreasing Grade . . . . . 59 0.255 80 DOW Perchloroethylene SVG . . . 68 0.293 106

1 ,l ,1-trichloroethane . . . . . . . . 33 0.142

Of typical 58 x 24-in open-top degreaser

*Hourly average (Ib/hr/flz of degreaser opening) Daily average for 7 days (Iblday)

HEAT REQUIREMENTS vapor layer collapse than light, thin The amount of heat required to operate a vapor degreaser can be computed on an hourly basis and includes:

Heat to raise the temperature of the work and work-carrier to the solvent boiling point Radiation losses from tank walls in contact with vapors or boiling solvent Solvent distillation for replenishment of spray pump reservoirs or dilution of immersion baths.

The heat requirement for the work and carrier depends on their weight, spe- cific heat, and surface area. Since a constant vapor level is required for minimum vapor losses, sufficient heat (in the form of vapors) must be availa- ble to bring the work bad surface temperature up to the vapor tempera- ture in a minimum practical time. Heavy parts with a small surface area often cause less condensation and thus less

parts with a large surface. The de- greaser walls should be insulated if radiation losses are high or if the de- greaser requires a significant amount of heat. The radiation heat losses of a degreaser vary directly with the boiling points of the solvents employed. The amount of heating surface re- quired is determined by a heat transfer coefficient from this surface to the sol- vent when contaminated with approxi- mately 25 percent oil or similar soluble soil. Heat densities that are too high will result in premature fouling of the sur- face as well as possible decomposition of the solvent. Inadequate vapor gen- eration results in poor cleaning, col- lapse of the vapor zone, and excessive solvent losses. Immersion heating elements are fre- quently protected by a metal grating above the element. These grates may also serve as work rests.

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3 HEAT SOURCES

Steam - Steam is the preferred heat source if it is available or can be gen- erated economically. When steam pressure is controlled, the risk of excessively high temperatures and the resultant problems and recovery costs are eliminated. Usually pipe coils are the preferred type of heating sur- face. Occasionally, steam-jacketed tank bottoms or steam panels are used. Use of Pressure Regulators - When a plant steam supply provides pressures higher than recommended (see Table 11), a pressure regulator is required. Possible superheating can be avoided by placing a pressure reducing valve at least 15 feet from the degreaser for 75 psig steam and at least 35 feet away for 1s psig steam. Care should be taken -30 ensure that the steam supply line and reducer are of the proper capacity for the required steam volume and

pressure. A pressure gauge and pop- off or relief valve should be installed on the low-pressure side. Use of Steam Traps - A steam trap drains steam condensate from the equipment and vents air from the sys- tem while preventing the escape of live steam. For efficient operation, each steam outlet should be trapped indi- vidually to insure proper circulation and air elimination. The trap capacity must be adequate. This capacity is based on the differential pressure, not the operat- ing pressure. Also, the height to which a trap can elevate condensate de- pends on the differential pressure - approximately two feet of height per pound (psig) of differential pressure is required. The more common types of traps are inverted-bucket, thermo- static, and ball-float. Traps should be selected to operate in the range of the solvent employed (see Table 11). The steam coil must drain down into the trap.

TABLE II. Recommended Steam Pressures for Steam-Heated Solvent Systems

Grade ................................. <2

richloroethane ..................................... 1-6 trichloroethylene .................................. 10-1 5

rchloroethylene SVG .............................. 45-60

Electricity - Electricity is another heat source for degreasers. Immer- sion-coil-type heaters with a heat den- sity less than 22 watts per square inch are recommended. Strip or contact heaters clamped to the bottom of the boiling sump are used to heat small degreasers. Soil accumulation on the heating elements can cause “hot spots” and result in solvent decomposi- tion and element burnout. Immersion heating coils are preferred. More fre- quent cleanouts and lower soil con- centrations will increase heater life. When operating this equipment, the solvent liquid level should be main- tained above the heating elements. If the heating elements become exposed, the heating surfaces will sharply increase in temperature and degrade the solvent causing an “acid” condition. Dow recommends install- ing a “low-liquid-level’’ switch which shuts off the heating element before this condition can occur.

Gas - Gas also is used to heat de- greasers. The burners are generally atmospheric types. Immersion coils are preferable to line burners under the liquid sump. Direct heating of the de- greaser bottom has the disadvantage of poor heat exchange caused by the settling of metal fines on this surface. Again, as in the electrically-heated equipment, soil accumulation on the heating surfaces can cause “hot spots” and degrade the solvent. As with elec- tric heaters, this problem can be avoided by maintaining the solvent level above the heating elements. The stack should vent to the outside atmosphere, should be of an acid-resistant material or have an acid-resistant lining, and should be equipped with a back-draft eliminator.

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Gas burners should have safety pilot protection that shuts off the gas flow within 45 seconds after pilot failure. Continuous pilot systems are inadvis- able since they may be left on when solvent is low or when the degreaser is being cleaned. Pilots should be turned off during cleanout to avoid contact of solvent vapor with open flame. It is recommended that the burners be enclosed in a housing designed to pro- vide inlet combustion air that is free from solvent vapors. This is more sig- nificant when a degreaser is installed in a pit. If it is installed in a room with a negative pressure, air should be supplied from the outside.

HEAT SAFETY CONTROLS No matter what type of heat is used, it is recommended that shut-off safety con- trols be installed in the supply line, such as valves in the steam or gas supply lines and a switch in the electrical power supply. These controls may be operated by:

Vapor safety thermostats, located above the condenser coils, to inter- rupt the heat supply when the condensation is inadequate and the vapor rises to contact the thermostats.

* Bottom safety thermostats which in- terrupt the heat supply when the solvent-oil temperature exceeds the limit set in the thermostat. Float switches to turn off the heat when the solvent level is danger-

Flow switches in the water supply line to assure that condenser water is flowing before the heat can be turned on.

All shut-off controls should require manual resetting so the cause may be investigated and remedied before

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ously low.

-\ restarting.

VAPOR CONTROL The basis of effective vapor degreaser design is control of the vapor level. This control is best done by use of condens- ing coils. Condensing coils are located within the degreaser tank at a height above the boiling solvent equal to the work height plus allowances for clear- ance below the work and a 3-9 inch vapor layer above the work. The usual design of a degreaser provides for the normal vapor level to be at the midpoint of the vertical span of these coils. Thus the positioning of the condensing coils also establishes the freeboard height in a given tank. To prevent excessive condensation of atmospheric moisture on the coil sur- faces above the vapor line, the tem- perature of the water leaving the coils should be above the dew-point of the ambient air. To help accomplish this, the water should flow into the lowest coil and out the top coil.

FREEBOARD COOLER OR WATER JACKET

FREEBOARD Freeboard is the area formed by the uppermost sections of the sides of a degreaser from the vapor level to the top of the tank. This freeboard zone permits drainage of the work being re- moved, evaporation of residual solvent and drying of the part with a minimum of solvent loss as well as reduced sol- vent emissions into the air. Addition- ally, the freeboard zone reduces vapor disturbance caused by air motion in the work area. The height of the freeboard is generally YZ to 3/4 of the open width of the tank, or a minimum of 12 inches. In degreas- ers of extreme length, the height of the freeboard is increased. Generally speaking, the higher the freeboard the lower the solvent consumption. NOTE: Minimum freeboard height may be stipulated by existing or proposed federal, state and local air pollution regulations.

WATER SEPARATOR Water enters a degreaser from several -

This is a small-channelled perimeter sources: cooler around the outside of the tank at Condensation of atmosPheric mois-

~~

the vapor level. Its primary function is to prevent the conduction of heat from the walls in contact with the vapor and boil- ing solvent to the freeboard area.

ture on the condenser Coils. Moisture on work being cleaned.

* Steam or cooling-water leaks.

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In water separation, the condensed solvent-water mixture drops into a trough below the condenser coils and flows by gravity to the separator (see Figure 4). The mixture enters the separator below the solvent level. The water, because of its lower specific gravity and insolubility, rises to the top and is discharged through a water drain. Relatively moisture-free solvent is then discharged through the sol- vent return line to the degreaser or storage tank. This separation requires time. Since five minutes is a practical minimum, the separation chamber should have a capacity of at least 1/12 the hourly sol- vent condensing rate. A deep separator is more efficient to operate than a shallow one of equal volume, the reason being that the Tv%ii%waferTferface area is less in

The cooler the solvent, the less water it will carry. Cooling can be accom- plished by:

Locating the water separator away from the degreaser sidewall to es- tablish an air insulating space of 3 to 5 inches. Installing cooling coils within the separation chamber of the water separator. Utilizing a heat exchanger through which the hot solvent-water mixture flows before entering the water separator.

3$ he deeper design.

FIGURE 4 Water Separator

Cooling Cooling Water Inlet, Removable Lid Water Vent to 7 ,-Outlet

u

Drain Valve

Since the temperature of the water should be colder than that used in the condensing coils, it is recommended the heat exchanger or solvent cooling coils have a water source independent of the condenser coils. Typically, cool- ing water is piped through the water separator before entering the condens- ing coils. The flooding valve reduces corrosion by periodically purging the free water layer from the separator. When this valve is c!osed, the solvent level in the separator rises and allows the free water to overflow through the drain trap. The overflow should con- tinue until solvent flows from this drain,

at which time the flooding valve is opened and normal levels are established. The flooding valve should be of the ball, gate, or butterfly type. Ideally, the open- ing mechanism should be spring- loaded so it will close only when held by the operator and will return to the open position when released. Periodic cleaning and maintenance of the water separator should be scheduled to prolong the life of the sol- vent and minimize corrosion of the equipment.

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STORAGE TANK Storage tanks, usually vented, may be built in as a part of the degreaser or provided as auxiliary units. These tanks are receptacles for clean solvent when the degreaser is used as a self- distilling unit before cleanout. They may also be used as spray pump reservoirs.

PROVISIONS FOR CLEANOUT Danger to life may exist in any de- greaser with any solvent. Safety precautions must be observed! See page 16. Degreaser units should have openings of sufficient size to be convenient for cleanout procedures. If possible, they should be designed so that cleaning

7- J

Materials Handling

J

MANUAL OR OPEN-TOP UNITS In manually operated units, the work is usually processed through various cleaning cycles in metal baskets or on racks or hooks and is transferred either manually or by electric or air-driven hoists.

Use of Hoists - The handling of heavy, bulky work is done by electric or air-driven hoists. A maximum vertical travel speed of 11 feet per minute (1 ft per 5Y.2 sec) is recommended for entry and removal of work. Metal chains should be used for suspending the work. Link type hoist chains require the least maintenance, although roller chains are acceptable.

does not require human entry. Very large units should have access doors in major compartments to minimize es- cape travel distance in case of emergency. Drain lines from all compartments should start from a recessed portion of each compartment bottom. This facil- itates complete drainage of solvent, reduces ventilation time required for removal of residual solvent, and lowers the hazard to entering personnel. NOTE: However, completely draining the solvent does not eliminate the va- pors, which are heavier than air and thus remain in the tank, constituting a hazard to life if inhaled in excessive concentrations. See page 16 for safety precautions and page 17 for protective clothing and equipment to be used in cleaning a vapor degreaser.

Work Baskets and Racks - Baskets and racks should be constructed of open-mesh, non-porous material as light in weight as possible (see Figure 5) since basket and rack weights in- crease the heat requirement of the de- greaser and add to process costs. Oversized baskets act as pistons, dis- turbing the vapor level and forcing va- pors out of the unit. Generally, basket or work size should have a minimum of four inches of clearance on each side. However, applicable governmental regulations should be checked to as- sure compliance of your system, since some states prescribe basket size in their implementing regulations of the Clean Air Act.

MATERIALS OF CONSTRUCTION Stainless steel is the recommended construction material for degreaser units since it exhibits superior corro- sion resistance to all solvents. Mild steel is satisfactory if suitably protected against corrosion by an organic coating such as Heresite (Heresite i3 Chemical Co.) or Plasite (Wisconsin Protective Coating Gorp.) brands. Hot-dip gal- vanized or sprayed-zinc metallized are not preferred materials but offer economy. Zinc plating of accessory parts is satisfactory. NOTE: Aluminum alloys are nor rec- ommended as durable materials of construction with degreasing units, pumps, valves, lines, tanks, nozzles or associated equipment.

FIGURE 5 Work Basket

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CONVEYORIZED UNITS FIGURE 6 Monorail Conveyorized Degreaser Conveyorized degreasers generally are large, automatic units designed to handle a large volume of work in either a straight-through process or a return- type of process where work enters and leaves from the same end. Con- veyorized equipment, when it can be used economically, has the advantage of minimizing the human element and producing consistently good cleaning with a minimum of solvent loss.

Monorail Conveyorized Type - This type of conveyor (see Figure 6) is ideal when production rates are high. It facili- tates the cleaning of such parts as cabinets, panels, and castings which can be suspended on hooks or hang- ers. Horizontal conveyor speeds de- wnd u w n the size of the work face

_the solvent vapors. hould be limited to 11 he monorail trolleys

should travel above the vapor level; if this is not possible, the trolleys should be automatically regreased as soon as they emerge from the unit.

Cross-Rod Conveyorized Type - This type (see Figure 7) is generally used for processing small parts placed either in baskets or drum-shaped mesh cylinders. The cylinders are used when rotation is required to drain solvent from parts of irregular shape. If there is any danger that the surface finish of the work may be damaged during rotation with other parts, the work can be im- mobilized within the cylinder.

Gyro or Ferris Wheel Type - This wheel-type conveyor permits the oper- ator to load and unload a basket at the same station. Between loading and un- loading, the freely suspended baskets pass through solvent vapor and liquid.

FIGURE 7 Cross-Rod Conveyorized Degreaser

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Vibra Type - In this patented proc- ess, the work is dipped into solvent, rises on a vibrating spiral elevator trough through a counter-flowing rinse of clean solvent distillate and vapor and, finally, a drying section (see Figure 8). Cleaning is done by the combination of vibration and solvent action. Controlled feeding and unload- ing permit removal of excess chips and contaminants such as oil and cutting solutions. A vibratory drive draws up and releases a spiral track. These pul- sations move the work at uniform speeds upward along the track. As the

FIGURE 8 Vibra Degreaser

work is vibrated up the spiral, it passes through and is cleaned by solvent con- densate flowing down the track. Usually hard-to-remove particles are dislodged and washed away. Vibra de- greasers are especially effective for cleaning small objects such as nails, nuts, bolts, rivets, fasteners, small stampings, screw machine parts and small die castings. Hourly cleaning capacity ranges in the thousands of pounds, depending on the size of the unit. This equipment has proven prac- tical in cleaning metal chips in prepara- tion for remelting.

L

~~ ~~~~~ - ~~

Distillate Return for Counterflow Wash

Degreaser Installation Equipment manufacturers provide qualified representatives to supervise the installation of vapor degreasers. The representative should check the location, wiiing, piping, service con- nections, regulators, thermostats and setting of controls. Additional help with installation and initial operation can be obtained by contacting the nearest Dow sales off ice.

LOCAT I ON Vapor degreasing equipment should be integrated into the production flow in a manufacturing process, a factor which usually predetermines location.

SPACE REQUIREMENTS Since the cleaning and drying process ordinarily takes only one to three min- utes, space requirements for equip- ment are minimal. When a low ceiling imposes restrictions, equipment can be installed in a pit. Length restrictions are often overcome by utilizing wider units that route workloads through a U-shaped path. Adequate space should be provided to service and maintain all parts of the equipment.

ROOM SIZE In a large room, dragout vapors are readily dissipated. Many factors should be considered when selecting proper room size, such as room ventilation, vapor degreaser size, workload, etc., to assure maintenance of a healthful environment. Exhaust ventilation is commonly used in situations where solvent vapor concentrations need to be lowered.

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PITS

Safety Rail - A railing around any uncovered portion of the degreaser pit at a height of 42 inches above the work-floor level is recommended for protection of the operator.

Clearance - Sufficient clearance should be provided around the tank in the pit area to permit easy access to all degreaser doors, controls and connec- tions and for the removal of clean-out ports. Access and clearance for the removal and maintenance of heating elements must be provided. Subway gratings or other flooring material should be installed as a safety meas- ure over the open area of the pit sur- rounding the degreaser.

exhaust - Provision should be made , f w n exhaust system capable of clear-

eavys.svmrvapors e at least twice the

volume of air in the pit. Intake of the exhaust system should be at the bot- tom of the pit and near the cleanout door. Pit exhausts are primarily to eliminate vapors that would result if solvent accumulates in the pit. Addi- tional exhaust intake at the top of the degreaser may be required to handle vapor losses.

Drainage - The pit should be pro- vided with a drain to a holding tank or with a sump pump to avoid accumula- tion of solvent, rinse water or sludge in the bottom of the pit.

LOCATION OF GAS-HEATED DEGREASERS These must not be located in a room where mechanical exhaust produces a negative pressure unless complete exhaust of combustion products is pro- vided by an exhaust fan.

AVOIDANCE OF HEAT AND FLAMES Degreasers should not be installed in areas where the solvent vapors can come in contact with open flames, ex- cessively hot metal surfaces, or weld- ing operations. See Decomposition Hazards on p. 7 7. If plant layout neces- sitates placement of the degreaser near such heat sources, exhaust in- takes must be provided near the equipment to minimize contact of sol- vent vapor with flames or excessively hot surfaces and to remove the de- composition products that result from such exposure.

AVOIDANCE OF DRAFTS To minimize solvent loss induced by air turbulence over the vapor zone, de- greasers should be placed away from excessive air currents, open windows or doors, heating and ventilating equipment, or any device causing rapid, uncontrolled air displacement. Normal air circulation is sufficient to di- lute small quantities of vapor that nor- mally escape from the degreaser. When the degreaser must be placed in an unfavorable location, two- to three- foot baffles on the windward side will divert drafts and protect the vapor level.

HEAT INFORMATION

Steam - Locate unions so as to minimize the length of external piping which must be removed when servic- ing steam coils and plates. Leave suffi- cient room for easy removal of the door. The steam condensate outlet should be located lower than the inlet to insure complete drainage of the coil.

Gas Hookup - Local codes or Article 2, Chimneys and Flues, National Board of Fire Underwriters, should be ob- served to insure proper installation of the stack venting the combustion chamber or heating tube. The follow- ing construction practices should be followed:

Flues must exhaust combustion products outside the building to pre- vent corrosion and toxicity hazards. Flue gas should not be exhausted near fresh-air intakes. Flues must be insulated to a height above the top of the tank sufficient to provide protection to the operator. There must not be a back draft down the stack; this would release flue gases into the room. The flue should be constructed of acid-resistant material such as asbestos-cement since acid de- composition products may mix with condensing moisture, resulting in a corrosive mixture. To avoid severe corrosion, a means should be provided to minimize entry of rain or other atmospheric mois- ture into the flue.

Electrical Grounding - Electrical degreasers must be properly grounded and provided with fuses.

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WATER PIPING Solvent Reclamation

REQUIREMENTS One water valve should open and shut off the cooling water supply. A control valve on each water inlet to the de- greaser is used for regulation of flow rate. Water outlets from condenser jackets or from cooling coils should not flow directly into sewer lines but should drain into an open sight funnel where water flow and temperature can be checked. Water flow should be con- trolled to maintain a water outlet tem- perature of 100" to 120°F (38" to 49°C). Because of its low boiling point, methylene chloride may require refrig- eration coils. Where direct piping to sewers is preferred, flow meters and thermometers can be installed in the water lines for control purposes. A

statically controlled valve is pre- = 4atdfoavCrid the need for operator

Warning: Nothing should be welded on the body of the degreaser or storage tank when solvent or solvent vapors are present, since thermal decomposi- tion will occur and form toxic products. Many degreasers are internally coated with organic or inorganic protective films which can be damaged by the high temperatures involved in welding. Consequently, welding on such units should be avoided.

= ~~~ ~

INTERNAL DISTILLATION Solvent can be reclaimed and soil con- centrated in the degreaser itself by tak- ing the degreaser out of production and boiling down the residues and diverting the distillate to a storage tank or other container. The minimum operational level of liquid in the boiling sump of 11/2 inches above the heating element must also be maintained during this process. The degreaser should therefore be turned off when the solvent reaches this level. The solvent-soil mixture should then be removed from the sump and stored until the next boiling- down operation when it may be added

FIGURE 9 Solvent Recovery Still

back into the degreaser for further distillation. I t is important that metal fines (aluminum, brass, iron, zinc, etc.) be removed from the solvent-soil mixture before storing to avoid potentially dangerous chemical reactions.

EXTERNAL DISTILLATION This operation becomes necessary under the following conditions: produc- tion volume is high; contaminants are heavy; a minimum of interruption to production cleaning is desired; or addi- tional solvent distillate is required.

Water Outlet, - Condensate 7

Steam Inlets-

Freeboard \Water

Jacket

'Water Inlet

Automatic Level Control

7 Steam Outlets-

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3 Continuous - Solvent is pumped di- rectly from the boiling sump, which is the most contaminated compartment of the degreaser, to the still for purifica- tion. There it is boiled to produce pure solvent vapor which is then con- densed. Distillate, after passing through a water-cooled separator, is returned directly to the degreaser or to a storage reservoir common to the still and the degreaser. Solvent level in the still is maintained by an automatic level- ing device actuating a transfer pump. Use of a remote still affords maximum cleaning efficiency in the degreaser and enables continuous production with infrequent shutdowns for cleaning the degreaser. Periodic concentration and removal of ~esidues in a continuous still is re- q@red,theincrease - in boiling point of

requerrcy. Depending on the nature of ' 3 a r y to

remove heating coils or cleanout ports for eliminating solids from the still. Residues should be handled in ac- cordance with plant and municipal reg- ulations and should not be dumped into city sewage systems. Ventilation should be provided at cleanout ports

. . - ~~

~ g-the-

Batch - Batch reclaiming stills are operated in a manner similar to con- tinuous stills except that the solvent supplied to the unit is generally concen- trated to some extent in the degreaser and then transferred to a reclaiming still for final solvent recovery.

SOLVENT RECOVERY WITH ACTIVATED CARBON This solvent recovery/ air cleansing system takes vapor-laden air from de- greasing or cleaning operations and passes it through a specially prepared activated carbon bed to remove the solvent which would otherwise be lost. At predetermined intervals, steam is passed through the carbon bed to carry the vapors to a condenser. A water separator removes the water from the solvent which is then recovered and returned to storage tanks. The carbon adsorption vapor-recovery system is designed to permit high air flows for better ventilation. Carbon adsorption tends to remove significant portions of the solvent stabilizers while adding water con- tamination. Your nearest Dow sales office should be contacted for informa- tion to assure trouble-free operation.

when residues are being removed. The activated carbon system can re- cover some chlorinated or fluorinated hydrocarbons, including trichloroethyl- ene and perchloroethylene. Recovery of CHLOROTHENE brand solvents re- quires special considerations. Before attempting this recovery technique with the CHLOROTHENE solvents, your nearest Dow sales office should be contacted for information.

REFRIGERATED FREEBOARD CHILLER This system is designed to reduce sol- vent emissions at. the solvent vapor-air interface by placing a cool, dry layer of air above the vapor zone. This cool air blanket assists in confining the solvent vapors. The refrigerated freeboard chiller con- sists of a coil which is placed on the inside perimeter of the unit, immedi- ately above the primary condensing coils. An external refrigeration unit supplies the coils with the necessary cooling. The chiller unit will condense, and in some cases freeze, atmospheric mois- ture onto the coils. The additional water from these coils should be handled by placing a separate trough under the coils, with the trough draining to its own waterseparatoror a hsMingbnk.-lf %R additional trough is not placed on the equipment, the coils should drip into the solvent condensate trough; but a larger water separator should then be considered for effectively separating the water from the solvent. Additional water in the solvent may cause corro- sion and shorten equipment life.

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Toxicity, Handling Precautions, First Aid

Toxicity Trichloroethylene, perchloroethylene, 1,l ,l-trichloroethane and methylene chloride - the four basic chlorinated solvents used in vapor degreasers - all present minimal hazard from acci- dental oral ingestion of small amounts of solvent. When splashed into the human eye, the solvents will all produce transient irritation but no serious injury. They all can defat the skin, may pro- duce dermatitis from frequent daily contact, and may produce a burn if con- fined against the skin. Occasional brief contact with the skin is not likely to pro- duce adverse effects.

Dow Perchloroethylene SVG has been specifically developed as an outstand- ing vapor degreasing solvent for cleaning metals, and it is intended for

tion, it should not be used in operations where skin contact will normally occur, such as dry-cleaning or cold cleaning. Of the various routes of exposure, inha- lation presents the greatest potential for hazard. Although all four solvents may produce an anesthetic effect upon inhalation, the concentration and dura- tion of exposure required to bring on lightheadedness or dizziness will vary from solvent to solvent. Repeated and prolonged exposure to organic sol- vents at or above levels producing be- ginning anesthetic effects, such as dizziness or lightheadedness, should be considered a potential health hazard and should be avoided. Ex- posure to extremely high vapor con- centrations can cause death.

Concentrations of chlorinated solvents that produce “drunkenness” or un- consciousness may sensitize the heart to epinephrine and similar drugs (see note, “To the Physician,” extreme bottom right of summary table on page 18.) Although all four solvents show some similar toxic effects - anesthetic ef- fects, for example - other toxic effects such as metabolism of methylene chloride to carbon monoxide are unique to a specific solvent. When methylene chloride is inhaled, it may be converted by the body into car- bon monoxide, which combines with the protein pigment of red blood cells to form carboxyhemoglobin. The levels of carboxyhemoglobin generally experi- enced from exposure to methylene chloride are comparable to those caused by breathing tobacco smoke, fumes from charcoal grilling or the exhaust of cars in city traff ic. Any defini- tive relationship between carboxy- hemoglobin levels and coronary heart disease has not been established. Be- cause of this uncertainty, persons with a history of angina or other cardiac problems should consult a physician before working in an environment where they could be exposed to sig- nificant levels of methylene chloride vapor. The Dow Material Safety Data Sheet (MSDS) for each of these solvents pro- vides up-to-date information and de- tails on special areas of concern, such as toxicity, handling and storage, and first aid. It is recommended that you consult the current MSDS if you use these solvents. If you need further as- sistance, please contact your Dow sol- vent representative.

Handling It is essential that all persons who are responsible for operating or maintain- ing vapor degreasers and all others who may be exposed to chlorinated solvents be thoroughly trained in the proper handling of solvents and the equipment in which they are used. Such persons should be aware of the hazards, the first aid treatment pre- scribed in case of accident, and the proper use of protective equipment to safeguard worker health and promote maximum safety. Potential problems with chlorinated solvents arise most often during maintenance operations and spills. Refer any problems or questions con- cerning solvent handling or equipment maintenance to your Dow solvent represen fa five.

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Jkty Rules 1.

2.

3.

4.

~~

~~

Always wear protective garments and use safety equipment when excessive exposure to chlorinated solvents cannot be avoided. Do not use solvents in open containers unless ventilation is adequate to draw the vapors away from the breathing zone of employees. Avoid using solvents near open flames or any welding operations. Do not tolerate a continuing strong or objectionable solvent odor, since that is an indication of ex- cessive vapor in the air. However, the odor of chlorinated solvents alone cannot be relied on as the only necessary indicator of over- exposure. Employers should mon- itor solvent concentrations in the air in order to assure the safety of

~~

5.

6.

7. a.

9.

~

employees and compliance with governmental regulations, such as the Federal Occupational Safety and Health Act (OSHA) of 1970. An individual who becomes light- headed or dizzy near solvents should leave the work area immediately. Avoid prolonged or repeated con- tact of solvents with the skin. Do not take solvents internally. To avoid respiratory irritation, do not smoke while handling chlori- nated solvents. Contaminated solvent should be stored away from inhabited build- ings and water supplies in sealed, leak-proof containers and then disposed of through a licensed re-

1 o.

11.

claimer, by approved incineration or by burial in an approved landfill in compliance with all local, state and federal disposal regulations. See “Disposal” on page 20. Clean up small spills and leaks immediately, placing solvent- laden rags in a closed container or outdoors until they are thoroughly dry. Major spills will require the use of respiratory protection as de- scribed on page 17 under “Main- tenance Personnel Equipment.” Label all containers of chlorinated solvents to identify them and in- dicate the hazards involved in their use, as shown on the original Dow labels.

J Summary of OSHA Exposure Limits and Warning Guide Lines VAPOR INHALATION SUBJECTIVE

RESPONSE‘*’ CHEMICAL OSHA EXPOSURE LIMITS SOLVENT ODOR‘#*

8-Hour Acceptable Acceptable Slight, Strong, Anesthetic Timeweighted Ceiling Maximum Barely Not Un- Un- Eye Respiratory (Light-Headed

Average’ Concentrationa Peaka Detectable pleasant pleasant None Irritation Irritation Dizzy) Perchloto- 100 200 300, 5 min 50 1 50 400 100, 400 600 200, 8 hrs; ethylene In any 3 hrs 8 hrs 400, 2 hrs;

600, 10 min Trichloro- 100 200 300, 5min 100 200 600 100, 400 1000 400, 20 min; ethylene In any 2 hrs 8 hrs slight; 1000, 6 min;

daily, 1000, 1500, <5 min 5 days; definite 200, 3 hrs

4 4 l,l,l- 350 100 350 1500 500, 1000 2000 1000, Trichloro- 7 hrs 30-70 min; ethane daily, 1500,

5 days 1560 min; 2000, 5 min

Methylene 500’ 1000B 2000, 5 min 310 200- 1500 500, 2300 2300 900-1200, Chloride In any 2 hrs‘ 800 8 hrs 20 min;

daily 2300, 5 min

‘All values in the table are in parts per million, by volume, in air. Wow’s Medical Research Laboratory is the source for odor data for the listed solvents except methylene chloride, for which the source is Lehman, K. B.. and Flury, F.. Toxicology and ‘9 ‘i 8-Hour Time-Weighted Average is an employee’s permissible average exposure in any 8-hour work shift of a 40-hour work week. The Acceptable Ceiling Concentration is the maximum

‘No limits established by OSHA. Dow recommends a Ceiling Concentration of 500 ppm and a Maximum Peak of 800 ppm for 5 minutes in any 2 hours based on 237.26-1970 of the American

‘The American Conference of Governmental Industrial Hygienists has as its 1981 recommended TLV (threshold limit value - an &hour time-weighted average exposure) for methylene

giene of Industrial Solvents.

concentration to which the worker may be exposed during the shift, except that brief excursions to a higher level (the Acceptable Maximum Peak) are permissible.

National Standards Institute, Inc.

chloride, perchloroethylene and trichloroethylene. 100 ppm; and 1 ,l.t-trichloroethane. 350 ppm.

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12. Never allow anyone to enter a de- greaser, storage tank or other vessel who is not equipped with pressure-demand, self-contained breathing apparatus and a rescue harness with a lifeline. A second person should be stationed out- side to observe and be prepared to perform a rescue. Even when per- sonnel are wearing the proper pro- tective equipment, they should not enter a degreaser or other vessel that has contained a chlorinated solvent until it has been com- pletely aerated.

Selection of Operators There are no special or specific physi- cal requirements or restrictions for per- sawel operating vapor degreasers or handling chlorinated solvents, except

guneth-

No one except properly equipped per- sonnel should be permitted to remain in areas that are contaminated by leaking or otherwise malfunctioning degreas- ers, regardless of the individual’s phys- ical fitness. Improperly operating equipment can be a potential health hazard for everybody.

Protective Equipment should be pro- vided to safeguard the health and as- sure the safety of degreaser operators, maintenance men and all other per- sons who work with solvents. Such equipment is not intended as a substi- tute for proper operating and mainte- nance practices. Be sure to follow the equipment manufacturer’s instructions at all times.

Safety Equipment

OPERATORS’ GARMENTS AND EQUIPMENT Gloves: Butyl, neoprene, nitrile, polyvinyl alcohol (PVA) or Viton@ Fluoroelastomer Apron: Butyl, neoprene, nitrile, PVA or Viton. Eye Protection: Safety glasses or their equivalent. NOTE: PVA, though solvent resistant, is soluble in water.

MAINTENANCE PERSONNEL EQUIPMENT Goggles: Splash-proof. Rescue harness and a lifeline for en- tering tanks or enclosed spaces. Use air line masks with proper reduc- tion valves and filters or pressure demand, self-contained breathing

~~~ equipment with stored oxygen or air.- Approved industrial gas masks should be used only for short-duration emergency situations such as evacua- tion of a contaminated area. All re- spiratory protective programs must conform to OSHA requirements as stated in Title 29, Subpart I, section 1910.134.

Decomposition Hazards Do not use chlorinated solvents near open flames or very hot surfaces. When solvent vapors are exposed to heat, they tend to decompose, yielding hydrogen chloride, carbon dioxide, carbon monoxide and chlorine. By a secondary reaction, carbon monoxide and chlorine have the potential to

combine and form small quantities of phosgene, an extremely toxic gas. Of all the gases produced by decom- position of chlorinated solvents, hydro- gen chloride generally creates the greatest problems because it is highly corrosive to metals. It is also a strong lung irritant which gives warning that decomposition has taken place. As a result, the hazardous condition can generally be detected and corrected in time to prevent accumulation of poisonous gases.

Do not weld or torch-cut chlorinated solvent containers! Do not arc weld in any area where there may be chlorinated solvent va- pors. Radiation from the welding may decompose the solvent, creating toxic gases, Therefore, there cOUKbe the potential for hazardous concentrations of phosgene to build up before the warning odor of hydrogen chloride is detected. If hot processes, such as welding op- erations, must be performed in an area where solvent vapors may be present, the products of combustion should be vented outside the building through corrosion-resistant ducts. Also, in such areas, air for combustion in space heaters or heat-treating furnaces should be drawn from the outside atmosphere.

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3 Summary of Health Hazards, Handling and First Aid Treatment

ROUTE OF EXPOSURE RESULT HANDLING

PROCEDURE FIRST AID

Frequent daily contact with chlori- nated solvents can defat skin tissues, and may cause dermatitis. Occasional contacts of short duration are not likely to have adverse effects. If sol- vent is confined against the skin so that it cannot evaporate, a burn may result.

For frequent or prolonged contact, use neoprene or neoprene-coated gloves, and discard them when they begin to deteriorate. Poly- vinyl alcohol, butyl, nitryl or Viton gloves are satisfactory.

In case of contact, flush the skin with water. Wash clothing before reusing it.

SKIN CONTACT

Undiluted solvent spattered into the eyes will produce only slight irritation, which clears within hours. No serious injury results, but it can cause appre- ciable discomfort.

Swallowing solvents incidental to in- dustrial handling present no problem, but the swallowing of substantial quantities may cause serious injury.

EYE CONTACT

ORAL INGESTION

Under normal conditions, use Irrigate with flowing water im- safety glasses or their equiv- mediately and continuously for 15 alent. Contact lens wearing is minutes. Refer to medical personnel. not recommended.

Never store solvents in un- labeled or improperly labeled containers. emergency facility.

Do not induce vomiting. Call a physi- cian or transport the worker to an

Inhaling excessive amounts of solvent The use of gas masks, hose ce an anesthetic ef- masks or a pressure-de-

of exces- ~ mand, self-contained breath- ay cause ing apparatus may be neces-

avoid such expo- sary, depending upon the sures. Death can result if too much operation. Such protection is solvent vapor is breathed. essential where cleaning re-

INHALATION quires individuals to enter tanks and confined places, and standard safety practices must be followed. Some spraying applications may require similar precautions. See “Safety Equipment,” page 17.

Remove the worker to fresh air if effects occur. Call a physician or transport him to a medical facility. If KspTration- stops, givemoufii-fa; mouth resuscitation. TO THE PHYSICIAN: May increase myocardial irritability. At anesthetic levels avoid epinephrine or similar- acting drugs if possible.

Special Caution -Chlorinated solvent vapors are heavier than air, and will tend to concentrate in low, unventilated spaces such as degreasers, tanks and pits. Prior to entry obtain supervisory approvaland follow tank entryprocedures.

Entry into degreasers, tanks, and other confined, unventilated spaces where solvent vapors are present, without the aid of adequate protective equipment and self-contained breathing apparatus, could result in exposure to extremely high vapor concentrations which may cause dizziness, drunkenness, unconsciousness, or even death. See Figure 9 for illustration of recommended precautions to take when entering a degreaser or other confined area. Refer any problems involving solvent handling or equipment maintenance to your solvent representative.

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Deg reaser Operation

Do's and Don'ts for the Operator DO. 1. Understand the basic theory of

solvent degreasing. 2. Know your degreaser, its opera-

tion, cleaning cycles, control and maintenance.

3. Be aware of the hazards asso- ciated with the use of the specific chlorinated solvent involved.

4. Wear appropriate protective equipment.

5. Know the first-aid treatment appli- cable in case of emergency.

6. Follow the recommended proce- dure in starting up the unit.

7. Process the work as recom- mended.

8. Follow instructions in shuttinq off

"7: 1. Don't smoke within 15 feet of the

2. 3. 4.

5.

6.

f 7.

L 8.

9.

3

Starting Procedure 1. Start air exhaust equipment. 2. Turn on condensing water. Check

condenser water discharge point to insure proper flow.

3. Check to see that solvent drain valves are closed.

4. Add solvent to all compartments and water separators to recom- mended operating levels. Add sol- vent in such a way that free-fall of solvent stream and splashing are minimized. Addition of solvent by transfer pump is preferred.

5. Turn on heat supply. For steam heat, adjust to settings recom- mended for specific solvent.

6. Allow degreaser to reach operat- ing temperature as evidenced by solvent condensing on water coils.

7. Check temperature of immersion

10. If necessary, recheck and adjust solvent levels in all compartments.

11. When vapor level reaches con- densing coils, check auxiliary vapor level control by turning off water supply and allowing vapors to operate safety thermostat and cut off heat supply. Adjust setting as necessary.

12. Restore water supply to con- densers.

13. Actuate maximum solvent tem- perature control in cleaning compartments to insure proper operation.

14. Check all thermometers and gauges to insure operation in proper range for system.

15. Start work load through unit. 16. Check condenser water discharge

rinse bath or spray pump reser- ~~ temperature ~~~ ~~~~~ and ~ ~~~ adjust to 10% v s . AdjitsThKt cO8GE at these ~ 1 20°F(38-49"C) for allsolvents points if required. except methylene chloride. This

will minimize likelihood of atmo- applicable. spheric moisture condensing on

8. Start spray pump and conveyor, if . .

degreaser. Don't overload the degreaser. Don't process the work too rapidly. Don't become exposed unneces- sarily to solvent vapors. Don't use baskets, racks or hang- ers made of porous materials. Don't clean textiles, leather gloves or other absorbent materials in the degreaser. Don't use a fan blowing across the degreaser opening during normal operation of the unit. Don't permit excessive heat or open flames in the proximity of the degreaser. Don't enter a degreaser until it has been emptied and thoroughly ventilated and another person is present. A safety harness, life- line, respiratory protection and observer should always be used (see Figure 10).

9. Check to insure solvent conden- sate flow to water separator, and solvent return to proper compart- ments of degreaser.

the cooling coils. Because of methylene chloride's low boiling point (1 O4"F/4O0C), condensing water for that solvent should be held in the 60-70°F (16-21°C) range.

19

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’3 2 FIGURE 10 The “Buddy System” for Entering a Degreaser Tank

or Other Confined Area Concern for the Environment Legislation for protecting the environ- ment will have an ever-increasing effect on the choice of solvents. En- vironmental regulations have already been put into effect by cities, states and the federal government. Federal-level examples include the Clean Air Act of 1970 and Amendments of 1977, the Occupational Safety and Health Act of 1970 and the Resource Conservation and Recovery Act of 1976.

Disposal “Disposal Method: (In order of prefer- ence) send solvent to licensed re- claimer; incineration; evaporation of very small quantities; or approved land- fill burial in compliance with local, state, and federal regulations. Dumping into sewers, on the ground, or into any body of water is strongly discouraged and may be illegal.”

Safety Research and Counsel Dow has invested millions of dollars in ongoing research on toxicity, safe use, and disposal of chlorinated solvents. Industrial hygienists, toxicologists and physicians on our staff stand ready to counsel customers on the safe han- dling and usage of the solvents. We invite you to solicit their support through your Dow sales representa- tive.

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3 Cleaning the Work SIZE OF WORK LOAD Machines are designed with sufficient heat capacity to generate the solvent vapor necessary to clean specified load-pounds per hour. Vapor drop should not exceed 3 to 4 inches upon entry of work. Work loads exceeding

vaporLlevel fluctuations which cause poor cleaning and increase solvent consumption.

PROPER POSITIONING OF WORK The work should be placed in baskets or suspended from hooks so that maximum solvent or vapor contacts the work during the entire cleaning cycle and maximum solvent drains from re- cesses or pockets.

RATE OF ENTRY AND REMOVAL

and removal of work is 1 1 fpm (1 ft per 5% sec) to minimize disturbance of vapors. It may be necessary to reduce this rate when the work load approx- imates the size of the degreaser opening and produces a piston effect. After cleaning, the work remains in the freeboard zone until it is com- pletely dry.

VAPOR CONTACT TIME The work should remain in the vapor zone long enough to raise the tempera- ture of the work until all condensation on the parts ceases. Too short a time in vapor results in poor cleaning; work withdrawn when wet causes unneces- sary loss of solvent.

t

I I

the prescribed maximum result in

I

I

TRANSFER OF WORK When work is transferred from one compartment to another, the work should be kept within the vapor zone.

SPRAYING Work should be sprayed as low as pos- sible within the vapor zone to minimize vapor disturbance from the high veloc- ity of either a lance or header spray. Solvent supply should be clean or only lightly contaminated and maintained at a temperature below that of the va- porized solvent.

SOLVENT LEVEL IN HEATING CHAMBER The solvent level should be 2 to 4 in- ches above the heating coils and should never be allowed to drop below 11h inches above the uppermost part of the heating element. Failure to keep the ~- solvent ~~ level ~ above ~~ the heating coils can result in solvent decomposi- tion and acid formation. A low-level in- dicator device can be installed to shut off the heat supply prior to the heating elements' being exposed.

SOLVENT CONTAMINATION High contamination in the boiling com- partment of a unit results in decreased cleaning efficiency, poor vapor genera- tion, sludge formation and coking of the heating element. As the concentration of contaminants increases, the boiling temperature of the solvent-oil mixture gradually rises to a point where the effi- ciency of the operation is impaired. Maximum recommended boiling points are: Methylene Chloride . . .112"F (44°C) CHLOROTHENE VG Solvent . . . . . . . . . . . . .175"F (79°C) NEU-TRI Solvent . . . .195"F (91°C) Perchloroethylene . . . .260"F (1 2PC)

When the solvent boils at these higher temperatures, the soil concentration is about 30%. The solvent then must be reclaimed. This can be accomplished by draining the degreaser and using external stills, sending the solvent to a reclaimer, or utilizing the degreaser as a still. When the degreaser is used as a still, the solvent condensate should be rerouted to an external storage tank or a 55-gallon drum. Boildown should be continued until:

No more condensate is going to the

The solvent level approaches the

It is then mandatory that the remaining sludge, soils, oils, and all contaminants be removed from the degreaser. For longer solvent life, less frequent cleanouts, and better cleaning, a screen may be placed over the work res+tm"fect-excessive metat-fines and nonsolubles. The screen will re- quire occasional removal and cleaning. This is good preventive maintenance.

storage tank or drum.

top of the heating coils.

S hut-Down Procedure 1. Stop work through-put. 2. Shut off heatsupply. 3. Allow vapor level to drop below

condenser coils. 4. Shut off water. 5. Shut off exhaust fans. 6. Place cover over open-top de-

greasers, especially overnight and on weekends.

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3 Operation of External Still

1. Turn on water supply to still condenser.

2. Open solvent lines from degreaser boiling sump to still transfer pump.

3. Be sure the drain valve is closed. Start solvent transfer pump to fill still to operating level. (On stills operating continuously, pump will cut off automatically when pre- determined level is reached.)

4. Open steam inlet valve and adjust steam pressure to level prescribed for solvent involved. In the event of foaming, steam pressure should be reduced to eliminate possible entrainment of contaminants into distillate compartment.

5. Increase steam pressure gradu- ally to maintain constant distillate flow. This is necessary - as conta- minmts &n%t and rdse tne M)II--

-- - _ _ _

3 ing point of solvent-soil mixture. 6. The flow of distillate will normally

cease for the respective solvents when the oil-solvent temperatures

At the previous points, optimum solvent recovery will have been achieved for Chlorothene VG and methylene chloride. For Neu-Tri and Perchloroethylene SVG, move on to step 7.

7. (Steps 7 & 8 for NEU-TRI and Per- chloroethylene only; not for CHLOROTHEN€ VG or methylene chloride.) Close steam coil inlet valve and carefully open steam in- jector valve, taking care to prevent foaming of the concentrated solvent-oil mixture.

8. Continue steam injection until nearly all solvent is recovered; this occurs when distillate return stops, as evidenced in sight glasses or at discharge end of sol- vent line from the water separator.

- - - C M e a m injectar-ualue.--- ~

9. When distillation is complete, close cold water valve.

10. Allow residue to cool. Drain and discard in accordance with ac-

Common Degreaser Problems It is beyond the scope of this bulletin to discuss in detail all the problems that occur with inefficient, improper, and unsafe degreasing 'practices. Most of these problems can be avoided by a better understanding of the theory of solvent degreasing, and by following the equipment manufacturer's instruc- tions in the operation of the degreaser. A few of the most common problems that result in health hazards, excessive operating costs and unsatisfactorily degreased work are discussed here.

PRONOUNCED VAPOR ODORS Continuing strong or objectionable sol- vent odor can prove serious. It indi- cates high vapor concentrations that may endanger the health of the operator and others working in the vic-

TnFof Tie degreaser. Thls condT€bn must be investigated at once and im- mediate steps taken to remedy it, both as a safety precaution and as an economv measure.

reach the following ranges: ceptable disposal practices (see page 20). Causes and Remedies

Following are common causes and suggested remedies for excessive

-- - . . __ _ _ - - -

Excessive Heat Applied to the Boil- ing Solvent Chamber - Proper con- trols should be provided and periodi- cally checked to control the heat supplied to the solvent.

Excessive Rate of Immersion or Withdrawal of Work from Unit - The work should not be immersed or with- drawn from the unit faster than 11 fpm (1 ft per 51/2 sec).

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Drafts Across Open Area of Unit - Avoid open windows, fans, etc. near a degreaser, to minimize disturbance of vapor level.

Improper Racking of Parts - Rack parts to provide maximum drainage and to avoid solvent dragout.

Spraying Above Vapor Level in Sol- vent Flush Units - Spray below the vapor level to avoid excessive disturb- ance of vapor.

Excessive Moisture in Unit - Vari- ous factors may cause this undesirable condition. Excessive moisture is easily recognized by the presence of white, cloud-like (ghost) vapors that float lightly around the cooling coils. Leaks in cooling coils, atmospheric conden-

- - ' a c n i l s ~ h g @ c m s s & e ~ 1- E f cold water, and entrainment of

moisture in the degreaser by water- soluble or dispersible cutting com- pounds are the most common causes of excessive moisture. Moisture in sol- vent lowers the vapor density, causing excessive solvent loss. Water sepa- rators of efficient design will continu- ously eliminate water that gets into the system.

i

Work Baskets Too Large for Unit - The dimensions of the work basket should allow for enough clearance from the walls of the degreaser to avoid pistonlike action that expels solvent vapor during immersion or withdrawal of the work.

the unit causes excessive drop in vapor level. Air displaced and replaced in the degreaser is subsequently expelled with a mixture of solvent vapors as the vapor level recovers to operat- ing height.

, 1

f , Overloading the Unit - Overloading

i )

Cleaning Cycle Too Short - Too short a cleaning cycle may result in poorly cleaned work but, more impor- tantly, the work will probably not attain vapor temperature. Consequently the work will be wet with solvent upon re- moval from the degreaser.

Leaks in Solvent Compartments or Lines - All leaks should be repaired immediately and all solvent line con- nections, access doors, and solvent transfer pumps checked periodically.

EXCESSIVE SOLVENT CONSUMPTION The economical operation of a metal degreaser is of paramount importance to all those concerned with plant pro- duction costs. Solvent consumption varies with the volume, type, physical l3"SEm mdesigrr- - C p s t s cleaned. It is also dependent on the nature and amount of contaminants removed, as well as many other factors. No overall figure can be es- tablished for solvent consumption, although strict observance of the equipment manufacturer's operating instructions will result in more efficient degreasing at minimum cost.

Causes Pronounced vapor odors and exces- sive solvent losses are related. Any vapors that can be smelled have, of course, left the machine. The elimina- tion or reduction of vapor escape from the degreaser reduces solvent con- sumption. Other factors contributing to excessive solvent consumption are:

Fluctuating vapor level due to faulty thermostat control or to heavy work loads. Failure to cover open top of unit dur- ing shutdown periods. Dumping insufficiently distilled sludge during cleanout of unit.

Cleaning of garments, leather goods and other solvent-absorbing mate- rials in a degreaser. Use of wood or absorbent materials in basket construction or as parts separators to prevent scratching of the work. Open-top water separators. These should have covers provided with gaskets. Vapor vent lines can be in- stalled, running from separator and emptying into degreaser at the top cooling coil. Water contamination of the degreas- ing solvent.

Remedies The remedies outlined for correcting pronounced odors will substantially re- duce solvent consumption. Proper mim%TZEeani Ins~et3kon7quent cleaning, and strict observance of in- structions will result in rapid, efficient and economical metal degreasing. Use of a cold trap or carbon adsorption may be of assistance.

CORROSION Corrosion, if not immediately arrested, can result in serious damage to the equipment and may eventually cause complete deterioration. Generally, corrosion first becomes apparent at the vapor-atmosphere interface when rust appears on the walls of the unit around the cooling coils and conden- sate trough.

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Causes fhe most common cause of corrosion is water contamination. Corrosion within a metal degreaser can result from the thermal decomposition of sol- vent and the formation of acid. This decomposition results from localized over-heating caused by high surface temperatures of the heater or elevation of the solvent boiling point because of excessive oil content. Poor housekeep- ing, which allows excessive accumu- lation of contaminants that might catalyze decomposition, may be re- sponsible for acid formation. Solvent vapors that escape the de- greasing equipment can result in a cor- rosion problem as well as present a toxicity hazard. Vapor that contacts hot metal surfaces or open flame - such as uninsulated heat-treating ovens, gas vent stacks, welding arcs, or cut-

- can decompose to form - 7 r Z c acid. The acid vapors can

corrode both cleaned and uncleaned production articles as well as surrounding equipment and struc- tural metals. NOTE: Highly clean metal surfaces are more susceptible to atmospheric moisture corrosion and should be pro- tected for storage.

Remedies 0 Avoid high surface temperatures of

the heaters by frequent inspection of all temperature controls.

0 Avoid excessive accumulation of contaminants with good housekeep- ing and frequent distillation of the solvent and cleaning of the unit.

0 Make periodic additions of fresh sol- vent to maintain stabilizer concen- tration and to avoid exposing the heating coils. Be sure water separator is of adequate size. Open drain valve frequently to eliminate accumulated water. Controls can fail despite inspection; visually check and make sure heat- ing elements are properly covered with solvent. To combat corrosion of cleaned or

tural metals or surrounding equip- ment, don't locate degreasers near high-temperature equipment in welding or cutting areas. If such location is necessary, high- temperature equipment should be insulated or ventilation of vapors provided.

li"e-,- ~~~

STAINED WORK Staining generally occurs in the clean- ing of heavily contaminated light- gauge metals, which may reach vapor temperature before sufficient condens- ing action has taken place to dissolve and rinse away the soils. The tempera- ture involved may change the physical and chemical properties of these soils and possibly render them insoluble and difficult to remove by further recycling. This condition may be corrected by changing the cleaning cycle - i.e., rapidly immersing the work in warm liquid solvent or spraying to dissolve most of the contaminants before com- pleting the cleaning action in the pure vapor phase. Another corrective mea- sure is the use of a higher-boiling solvent such as perchloroethylene to prolong the vapor condensing action before the parts attain vapor temperature. ~

Staining is also caused by overloading, which produces a prolonged drop in vapor level, thereby lessening the amount of washing action normally realized by condensing vapor. Work degreased in a unit containing excess moisture may emerge with a film of surface rust. This can occur when the work is withdrawn through a solvent-moisture mixture (ghost va- pors). The solvent is readily evapo- rated, leaving minute water droplets, which accelerate corrosion, on the surface. One cause of this problem is conden- sation of moisture in the air onto the cooling coils. It can be reduced by con- trolling the rate of cooling-water flow to keep the temperature of the exhaust water above the dew point. Leaks in condensers and steam coils are other sources of moisture in solvent.

~ ~ ~~~

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Degreaser Ma i ntena nce

Cleanliness is essential for safety, operating economy and process effi- ciency. Factors determining frequency of cleaning include: 0 Volume of work 0 Nature and amount of soil 0 Boiling temperature of solvent-oil

mixtures (see temperature by sol- vent, page 21).

Cleaning Procedure ROUTINE The accumulation of metal chips, turn- ings, or fines and oils (particularly buffing compounds) invites solvent decomposition. Therefore, routine cleaning is essential. Following is the procedure: 1. Turn off heat supply to all compart-

ments except vapor generating

2. Close solvent distillate return lines to degreaser.

3. Route condensate return from water separator to a clean storage tank or a suitable, clean container.

4. Continue distillation in boiling chamber until solvent reaches the recommended minimum level of 11/2 inches above the heating sur- face, or until vapors fail to reach condenser. At no time should the heating elements be exposed. De- terioration of solvent, destruction of heater and, if low-flash oils are in- volved, a flash fire might result.

5. Turn off heat supply to boiling chamber and allow residue to cool before draining.

6. If residues must be drained prior to cooling, wear approved respiratory equipment and provide adequate ventilation.

_ _ _ ~ ~ _ _ _ _ _ ~ - ~~

~ ~~ ~

)

7. Metallic fines and chips or other in- solubles should be removed with a hoe or similar tool. Particular atten- tion should be given the area under the heating coil.

8. Replace plug in drain line or close drain valve. Open solvent return line to the degreaser and adjust liquid level in all compartments with dis- tilled solvent, using additional fresh solvent as necessary.

9. Disposal of the residue should comply with local regulations gov- erning the disposal of waste prod- ucts. Residues should not be emptied into municipal sewers.

CAUTION: Do not store solvent- sludge mixtures in tightly closed drums. Occasionally, some mixtures of metal fines (aluminum, brass, iron, zinc, etc.), oils and solvent can un- dergo reacfion,wrtnneration o fsu j - ficient gases and pressure to burst standard steel drums.

COMPREHENSIVE Comprehensive cleaning should be performed periodically. This necessi- tates the removal of all solvent from the degreaser and still. It also requires the services of competent maintenance personnel thoroughly familiar with metal degreasing and with the hazards associated with the process. The pro- cedure is as follows: 1. Transfer all solvent from the de-

greaser to storage tanks or suita- ble containers and blank off lines. It is preferable to distill all dirty sol- vent prior to cleaning. Observe minimum solvent levels as pre- scribed to prevent exposure of heating elements.

2. Turn off heat and allow unit to cool; drain residual solvent and sludge from all compartments.

3. Thoroughly aerate the unit by forced ventilation from a fan, com- pressed air or blower to expel the solvent-laden air outside the build- ing by.means of a suitable exhaust system.

4. Remove or protect indicating thermometers, controls, etc., to avoid damage.

5. Disconnect heat supply and re- move steam or gas coils or electric heaters.

6. Remove cleanout ports, taking care not to damage the gaskets.

7. Remove all dirt, sludge and metal chips from the bottom of each compartment with a scraper or hoe. It may be necessary for maintenance personnel to enter some units. Such entry should be permitted only when the de-

and maintenance personnel suit- ably protected.

8. When the degreaser is thoroughly ventilated, a maintenance worker, wearing a harness and lifeline and equipped with approved respira- tory protection, may enter the degreaser (under the constant observation of a second person in attendance outside the degreaser; see Figure 10) and clean out the condensate trough, condensing coils, and walls of each compartment. Care should be exercised to avoid damaging any corrosion-resistant finish on the interior of the unit. The unit should be checked for rusted areas and the conveyor system in- spected for defects.

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3 Restoration of Acid Degreasers A degreaser becomes acid when its solvent loses the stabilizers added to protect it against acid build-up due to the natural chemical reaction to heat, metals, water, oils, etc., encountered in the degreasing process. To deacidify: 1. Remove the solvent from the de-

greaser.

9.

10.

11.

12.

13.

14.

Scrape thoroughly the removed steam coils or electric elements to remove caked sludge that may in- terfere with heat transfer and dis- rupt the heat balance of the unit. Clean condensate line from col- lecting trough to water separator by blowing out with compressed air or cleaning with a wire brush. For proper cleaning of the water separator, remove if necessary. The various controls, indicators and regulators should be cleaned and checked before reassembly. All strainers, filters, liquid level glasses, etc., should be cleaned and checked before reassembly and replaced if necessary.

15.

16.

17.

With the cleaning operation com- pleted, the various components should be reassembled and an pints ana connections made leakproof. Before reinstalling cleanout ports,

_ _ _ I

the machined surfaces should be coated with litharge-glycerol or ethylene glycol. The gaskets should be examined for breaks or blistering and replaced if necessary. When the unit is reassembled, the various compartments should be filled to their normal operating levels with clean solvent and the unit started. All controls and regulators should be checked and reset if necessary. The degreaser is then ready for operation.

2. - If entry into the degreaser or pit is required, the unit must first be thoroughly aerated by forced venti- lation from a fan, compressed air or blower to expel all solvent vapor to the outside of the building. When degreaser is thoroughly ventilated, a maintenance person wearing harness and lifeline and euqipped with approved respiratory protec- tion may enter the degreaser under the constant observation of a sec- ond person in attendance outside

and proceed with the following stem.

3.

4.

5.

Scrape carefully or brush off res- idues on the equipment, including water separators. Do not damage coating. Flush off the equipment with a solu- tion of sodium carbonate (Na2C03), 8 ounces per gallon water. Be sure to flush solvent lines and pumps. (Replacement of piping is often more economical. Note: Sodium hydroxide (NaOH) or other strong alkalis should never be used. Remove all water and dry the equipment, lines and pumps before recharging with fresh solvent.

6. After going through normal startup procedures, run an acid acceptance test at least once daily until it is ob- vious that the system has reached safe operating equilibrium. If acid acceptance drops to 0.08 within the first day or so, draw off 25-50% of the solvent charge and replace with

11

new solvent. Dow provides a free Acid Acceptance Test Kit (see Fig- ure 23) that can be used to deter- mine the acid condition of DOW vapor degreasing solvents.

Note: Solvents do not become acid without cause. Determine the reason and eliminate it to prevent further diffi- culty. Send Dow a sample of solvent removed from the degreaser for com- plete chemical analysis and recom- mendation from our unique Solvent Analysis Service regarding its re- claimability and reuse. -

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ai3m=----

Properties of Vapor Degreasing Solvents

Methylene Chloride

Perchloroethylene

1 ,1 ,1-Trichloroethane Trichloroethylene

General Properties 3 Properties required and desirable in an industrial degreasing solvent are summarized first, followed by an indi- vidual evaluation of each of the four Dow solvents’ advantages and disad- vantages and the general specifica- tions for each. To provide thorough, safe, economical and rapid metal degreasing, the ideal solvent must have the properties described below. The industrial chlorinated solvents possess these properties and therefore are widely ac- cepted by industry for metal degreas- ing applications. However, different solvents don’t possess all of these properties to the same extent. Choice should depend on various considera- tions relative to the specific cleaning operation.

HIGH SOLVENT POWER A prime requirement is the ability to dissolve all greases, fats, oils, waxes, resins, gums and rosin fluxes generally encountered in any metalworking operation.

INERTNESS TO METALS AND PLASTICS The solvent must clean the parts with- out corroding, oxidizing, staining, etch- ing, pitting, or dulling the work or the degreaser itself.

NONFLAMMABILITY The elevated temperatures involved in vapor degreasing exclude the use of flammable solvents. The chlorinated solvents are relatively nonflammable, exhibiting no flashpoints by standard laboratory test methods. Under normal conditions the likelihood of flammability problems with these solvents is extremely remote. Figure 12 shows the flammability limits of the four solvents at 25°C. For additional information on solvent flammability, contact your nearest DOW sales office.

___ _________ ~-

->

J

LOWER LIMIT UPPER LIMIT TEMPERATURE 15 21 25°C 8 10.5 25°C 8 10.5 25°C

NONE NONE 25°C

Warning: Drums that contain or have contained chlorinated solvents must not be welded or cut with a cutting torch because of decomposition and explo- sion hazards.

The safety and health of operating per- sonnel must be assured at all times. It is essential that the solvent used be

low in tclxuty that the expo- sure likely to occur when the material is properly used will not impair the health of the operator.

LOW LATENT HEAT This property provides more pounds of vapor per unit of heat input, there- by reducing the cost of vaporizing the solvent.

HIGH DENSITY VAPOR This property assures ease of solvent vapor recovery and provides effective control of the solvent vapor level by means of condensing coils or thermo- stats. High density vapor reduces the amount of solvent lost through work transfer and air disturbance of the vapor blanket - factors which can be controlled but not entirely eliminated.

. .

CHEMICAL STABILITY The solvent should remain stable and effective in both the liquid and vapor

cleaning cycles under recommended operating practices. Degreasing sol- vents must be properly stabilized to provide adequate protection against reactive metal chips and fines, acidic salts, lubricants, buffing compounds, heat, air, moisture, and other metal- working contaminants.

BOILING POINT The boiling point should be low enough for the solvent to separate easily, by simple distillation, from the higher boil- ing cutting oils, greases, and other con- taminants. At the same time, the boiling point should be high enough that the degreaser condensation coils can function efficiently with plant water. All of the DOW solvents discussed in the followng pages meet these de- manding requirements.

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'JLOROTHENE VG sdvent cHLOROTHENE VG solvent is vapor-degreasing-grade inhibited 1,i ,1-trichloroethane (C2H3C13). It is a clear, colorless liquid with a charac- teristic odor and incorporates a special stabilizer system. It has had wide ac- ceptance as an excellent vapor de- greasing solvent.

ADVANTAGES Extra Safety - The 8-hour time- weighted average (TWA) concentra- tion accepted by the Occupational Safety and Health Administration (OSHA) for 1,1,1 -trichloroethane is 350 ppm by volume in air, compared to 100 ppm for trichloroethylene and per- chloroethylene. Many laboratory studies on animals and humans have documented the low toxicity of inhibited 1,1,1 -trichloroethane. Lower Solvent Consumption - Be-

se ot its tower boili br weight per g a l l o n , n ~ ~ ~ ~ h a ~

40% lower solvent consumption has been reported with CHLOROTHENE VG solvent than with trichloroethylene. Conversion Ease - CHLOROTHENE VG solvent can be used in existing trichloroethylene degreasers with minor modifications. These include re- ducing the heat input, readjusting the thermostats and installing a proper sized water separator. Versatility - CHLOROTHENE VG solvent is an excellent solvent com- monly used for cold cleaning as well as vapor degreasing. Plants can reduce inventory and purchasing costs by using just this one solvent. When used in wipe, dip, spray or flush operations, the solvent can also be economically reclaimed in a vapor degreasing or rec- lamation still.

__

Reduced Utilities Cost - Because of the low boiling point of CHLOROTHEN E VG solvent (24" F below that of trichloroethylene), less heat and water are required to clean a given work load and to provide for con- densation. Cleaned parts are cooler, permitting more rapid handling and processing, while reduced heat radia- tion means further heat savings. Greater Operator Comfort - The re- duced sidewall radiation loss results in a cooler working area, and the lower parts temperature adds to operator comfort. Selective Solvent Power - The spe- cial solvent characteristics of CHLOROTHENE VG solvent permit it to dissolve and clean metalworking soils without attacking certain sensitive materials such as many plastics and resins. It is the chosen solvent for de- greasing hermetic stators and printed circuit boards where other solvents may damage insulation, remove iden- tification, or cause heat warping.

Distillation Ease - The lower boiling point of CHLOROTHENE VG solvent allows it to be efficiently distilled with- out steam distillation. This source of added energy cost and water contami- nation is thus avoided.

DISADVANTAGES Not Recoverable by Carbon Adsorp- tion - This process depletes the stabilizers in CHLOROTHENE VG sol- vent below acceptable levels and is not recommended for vapor recovery of this solvent with conventional systems.

Won't Tolerate Excessive Water - Degreasing operations having gross water contamination should not employ CHLOROTHENE VG solvent. Moderate or intermittent water con- tamination is effectively handled by an adequately sized and designed water

For additional information about CHLOROTHENE VG solvent, request Brochure No. 100-5436, available from your nearest Dow sales off ice.

~~ ~

~

FIGURE 11 Boiling Point of Mixtures of CHLOROTHENE VG

# w" 5 $ d

f J

K w a

"F "C

and Oil

80

70

60

50

40

10

~~~ 0 165 174 183 192 201 210 219 228

74 79 84 89 94 99 104 109 BOILING POINT

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FIGURE 72. Specific Gravity of Mixtures of CHLOROETHENE VG and Oil

1.OOO 1.050 1.100 1.150 1.200 1.250 1.300 1.350 1.400

SPECIFIC GRAVITY AT 2fi125”C.

FIGURE 73. Vapor Pressure of CHLOROETHENE VG brand of 1-1 1-Tr-e I - # * - - - ~

TEMPERATURE

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TABLE 111. Typical Properties of CHLOROETHENE VG Brand of 1 ,1 ,1-Trichloroethane

, Boiling point, 760 mm Hg ....................... 165°F (74°C) Freezing point ................................. -34.4"F (-36.9"C) Specific gravity, 251 25°C ....................... 1.320 Specific heat, Btul Ib/"F ........................ 0.25 Heat of vaporization:

cal/g ....................................... 56.7 Btul Ib ...................................... 102

Refractive index at 25°C ........................ 1.434 Viscosity at 25"C, centipoises . . . . . . . . . . . . . . . . . . . 0.79 Pounds per gallon at 25°C ...................... 10.97 Flash point (Tag open cup, ASTM Method D1310) . None Fire point (Tag open cup, ASTM Method D1310) . . None Vapor density (air = 1 .OO) ...................... 4.55 Kauri butanol value ............................. 124 Solvent-water azeotropic boiling point . . . . . . . . . . . . 149°F (65°C)

NOTE: These properties are laboratory values typical of the product but should not be confused with, or regarded as specifications.

L JU-TRI Solvent This chlorinated solvent, stabilized trichloroethylene (C2HCh), satisfies the basic requirements for a metal de- greasing solvent. It is a clear, colorless liquid with a characteristic odor.

ADVANTAGES High Solvent Power - NEU-TRI brand of trichloroethylene has a high solvency for oils, greases, waxes, tars, lubricants and coolants generally found in the metal processing indus- tries. It is effective and economical. Its aggressive solvent action is often chosen for removing difficult soils, such as, semi-cured varnish or paint films, heavy rosins, buffing compounds, etc.

No Conversion Costs - Most indus- trial degreasing equipment was origi- nally designed for trichloroethylene and can therefore be used to full advan- taqe and without modification with

I )I-TRI solvent.

Recoverable by Carbon Adsorption - Carbon adsorption recovery of NEU-TRI solvent is widely and suc- cessfully practiced. This recovery process does stress the stabilizer sys- tem, and monitoring the system when this solvent is first installed is rec- ommended to assure efficient performance.

DISADVANTAGES

Not Recommended for Cold Clean- ing - The use of NEU-TRI solvent is not generally recommended for wipe, spray, dip and flush operations. Its evaporation rate is not significantly different from 1,l ,l-trichloroethane; however, its toxicity is less favorable for these applications.

Attacks Some Plastics - In op- erations involving printed circuit boards, plastics, and electric motors, CHLOROTHENE VG is a solvent

preferable to NEU-TRI which, having strong solvent properties, will remove printed circuit board markings, swell or dissolve plastics and attack electric motor insulations.

Steam Distillation - Steam distilla- tion is commonly practiced with tri- chloroethylene to recover the solvent effectively without causing thermal degradation. This practice, however, does result in undesirable water con- tamination and requires manual control and operator attention.

Reactive with Caustic Soda (NaOH) - NEU-TRI solvent reacts with caustic soda to form the toxic and spontane- ously combustible product dichloro- acetylene. For additional information about NEU-TRI solvent, request bulletin 100-5548, available from your nearest Dow sales off ice.

30

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"C 85 90 95 100 105 110 115 120 125 BOILING POINT

~

~~

~~~ ~~~~ ~~~

-> FIGURE 15 Specific Gravity of Mixtures of NEU-TRI and Oil

0 10

20

30

40 50

60

70 80 1.OOO 1.100 1.200 1.300 1.400 1.500

SPECIFIC GRAVITY AT 251 25°C

31

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FIGURE 16 Vapor Pressure of NEU-TRl Brand of Trichloroethylene

- -

'C -20 0 20 40 60 80 100 140 180 240 TEMPERATURE

TABLE IV Typical Properties of NEU-TRI Brand of Trichloroethylene

DOW Perchloroethylene SVG This chlorinated solvent, suitably stabilized with a tough corrosion in- hibitor, fulfills the requirements for many types of metal degreasing. In cer- tain applications, it is preferred. Per- chloroethylene (C2C14) is a clear liquid with a characteristic odor.

ADVANTAGES

Effective with Wet Metals - The high boiling point of this solvent (121°C; 250°F) permits complete and thorough drying of the work by vaporizing mois- ture entrapped in porous metals, deeply recessed parts and blind holes. This property is particularly advan- tageous where the presence of mois- ture may prove detrimental to the finish of the work.

Reduced Staining - Light-gauge

Boiling point, 760 mm Hg ....................... 189°F (87°C) Freezing point (approx.) ........................ - 124°F (- 86.7%) Specific gravity, 251 25°C ....................... 1.456 Specific heat, Btul Ibl"F ........................ 0.22 Heat of vaporization:

callg ....................................... 56.4 Btul Ib ...................................... 101.6

Refractive index at 25°C ........................ 1.474 Viscosity at 25"C, centipises ................... 0.54

...................... 12.1 1 Flash point (Tag open cup, ASTM Method D1310) . None Fire point (Tag open cup, ASTM Method D1310) . . None Vapor density (air = 1 .OO) ...................... 4.53 Kauri butand value ............................. 129 Solvent-water azeotropic boiling point ............ 164°F (73.3"C)

Pounds per gallon at 25°C

temperature of the lower boiling sol- vents before sufficient condensing ac- tion takes place to dissolve all the oil and rinse away the contaminants. The higher boiling point of perchloro- ethylene permits a longer and more thorough rinsing action and may re- duce staining in cleaning operations employing vapor exposure only.

Removes Stubborn Soils - With its high boiling point, perchloroethylene is especially effective for removing high-melting pitches and waxes and for cleaning grossly contaminated parts.

Stability - Perchloroethylene is in- herently stable and shows little ten- dency to hydrolyze (degrade with water).

NOTE Thsse properties are laboratory values typical of the product but should not be confused with, or regarded as. SpecMcations.

--

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Decreased Corrosion - DOW Per- chloroethylene SVG contains an inhib- itor system that provides extra corrosion protection for cleaned parts and the degreaser.

Vapor Recoverable by Carbon Ad- sorption - Perchloroethylene has had the longest and most successful experience with carbon adsorption re- covery of all degreasing solvents.

DISADVANTAGES High Heat Required -The high boil- ing point of perchloroethylene (250°F) necessitates added heat to bring work up to the solvent vapor temperature. Thus, utility costs are higher. Steam- heated units require a pressure of 45 to 60 psig, which is not always available in small plants.

~~ ;e- Because o the high temperature of parts emergin; from the degreaser, more time must be allowed for the work to cool before it can be handled.

Higher Solvent Consumption -The higher boiling point of perchloroethyl- ene raises the temperature of the air next to the degreaser wall, causing air turbulence. This, combined with its higher liquid density, yields greater weight loss with equal volume, result- ing in higher solvent losses than with CHLOROTHENE VG or NEU-TRI solvents.

Steam Distillation - As with tri- chloroethylene, steam stripping is used to obtain good recovery of the solvent. This process results in some water contamination and requires closer

~

~

operator attention.

Heat Effects - Certain aircraft alumi- ethylene makes it useful as a cold num alloys are subject to structural cleaning solvent, the special inhibitors change at temperatures near 250°F, used in the vapor degreasing grade the boiling point of perchloroethylene. perchloroethylene SVG requires that Also, printed circuit boards and plastic special skin protectors be used to avoid materials may warp or melt. sensitization effects.

For additional information about DOW 'OLD Perchloroethylene SVG, request b u l k

CLEAN"G While the 'low evapora- tins 100-272 and 100-5645, available tion rate and low toxicity of perchloro- from your nearest sales office.

FIGURE 17. Boiling Point of Mixtures of Perchloroethylene and Oil

"F 248 257 266 275 284 293 302 311 320 "C 120 125 130 135 140 145 150 155 160

BOILING POINT

33

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FIGURE 18 Specific Gravity of Mixtures of Perchloroethylene - and Oil

TABLE V. Typical Properties of DOW Perchloroethylene SVG

Boiling point, 760" Hg ........................ 250°F (121.1"C) Freezing point (approx.) ........................ -9°F (-22.8"C) Specific gravity, 251 25°C ....................... 1.61 9 Specific heat, Btullb/"F ........................ 0.21 Heat of vaporization:

call g ....................................... 50.1 Btul Ib ...................................... 90.2

Refractive index at 25°C ........................ 1.503 Viscosity at 25"C, centipoises . . . . . . . . . . . . . . . . . . . 0.75 Pounds per gallon at 25°C ...................... 13.47 Flash point (Tag open cup, ASTM Method D1310) . None Fire point (Tag open cup, ASTM Method D1310) . . None Vapor density (air = 1.00) ...................... 5.76 Kauri butanol value ............................. 90 Solvent-water azeotropic boiling point . . . . . . . . . . . . 190°F (87.8"C)

NOTE: These properties are laboratory values lypical Of the product but should not be confused with, or regarded as, specifications

34

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FIGURE 19 Vapor Pressure of Perchloroethylene

35

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egreasing Grade Methylene Chloride (CH2C12) is an in- herently stable solvent, clear and color- less, with characteristic odor. DOW Methylene Chloride, Vapor Degreas- ing Grade, formulated with a special inhibitor, provides better corrosion pro- tection than technical-grade material.

ADVANTAGES

High Solvent Power - Methylene Chloride is the strongest of the com- mon vapor degreasing solvents. This solvent power enables it to perform ef- fectively in such diverse tasks as paint mask cleaning and removing excess impregnating resin from castings.

Good for Temperature-Sensitive Parts - Often, the boiling point (40°C; 104°F) of methylene chloride makes possible the degreasing of thermal switches, thermometers, etc., which would be damaged by high tempera- tures. This solvent is chosen when parts must be near room temperature after cleaning, such as, for immediate handling or air gaging.

Low Cost- DOW Methylene Chloride - Vapor Degreasing Grade, is low in cost compared to alternative low- temperature solvents used for similar applications.

DISADVANTAGES Low Vapor Density - This property makes methylene chloride vapors more susceptible .to losses from air movement around the equipment. Specialized equipment design, with a higher freeboard, is recommended for efficient use.

Rapid Evaporation Rate - Methyl- ene chloride evaporates more rapidly than the other vapor degreasing sol- vents. Covering the degreaser during non-operating periods is imperative to prevent excessive solvent losses. For additional information on DOW Methylene Chloride, Vapor Degreas- ing Grade, request the bulletin by that name, available from your nearest Dow sales office.

-28dmaf_ddixturr\c af Methylene Chlaride and Oil

~

~

BOILING POINT "C 38 41 43 46 49 52 54 57 60 63

38

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FIGURE 27 Specific Gravity of Mixtures of Methylene Chloride and Oil

I I I ti

d 3

I I I I 0.900 1.OOO 1.100 1.200 1.300 1.400

SPECIFIC GRAVITY AT 251 25°C

TABLE VI Typical Properties of DOW Methylene Chloride - Vapor Degreasing Grade

Boiling point, 760 mm Hg .. . . . . . . . . . . . . . . . . . . . . . 104°F (39.8"C) Freezing point (approx.) . . . . . . . . . . . . . . . . . . . . . . . . - 142.6"F (-97.0") Specific gravity, 25125°C .. . . . . . . . . . . . . . . . . . . . . . 1.320 Specific heat, Btul Ib/"F ........................ 0.28 Heat of vaporization:

caVg . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 78.7 Btu/lb . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 141.7

Refractive index at 25°C ........................ 1.421 Viscosity at 25"C, centipoises . . . . . . . . . . . . . . . . . . . 0.329 Pounds per gallon at 25°C ...................... 10.98 Flash point (Tag open cup, ASTM Method D1310) . None Fire point (Tag open cup, ASTM Method D1310) . . None Vapor density (air = 1.00) . . . . . . . . . . . . . . . . . . . . . . 2.93 Kauri butanol value . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 136 Solvent-water azeotropic boiling point . . . . . . . . . . . . 100.6"F (38.1"C)

~ ~~~

NOTE: These properties are laboratory values typical of the product but should not be confused wlth. or regarded as, specificatlons

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Solvent Condition Mon i tori n g 3

FIGURE 22 Vapor Pressure of Methylene Chloride

~

"F -4 32 68 104 140 176 212 284 356 464 "C -20 0 20 40 60 80 100 140 180 240

TEMPERATURE

Dow provides two important services to enable its customers to guard against solvent breakdown. Both services are provided without charge to the cus- tomer. They are: . 1. Acid acceptance test kits for cus-

tomer use on the customer's site. 2. Dow laboratory analysis of Dow

solvents in customer use. A description of those services and how Dow customers may avail them- selves of them is set forth in the Tech- nical Services section immediately following.

38

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Technica I Assistance -3

You get more than just a high-per- formance product when you choose a DOW vapor degreasing solvent. You also get Dow’s unmatched brand of technical expertise on solvents and their use.

Exclusive Solvent Analysis Service Periodically, you can send us a sample of the DOW solvent you’re using. We’ll give it a complete chemical analysis, and report back to you on its condition for effective vapor degreasing. If any unusual conditions are detected, we’ll then recommend methods for changes in your operation to make optimum use of our product.

Acid Acceptance Test Kit ~~~ ~

Dow provides a free Acid Acceptance Test Kit (see Figure 23) which you can use to guard against solvent breakdown. DOW vapor degreasing solvents are stabilized with neutral, acid-accepting stabilizers, and the concentration of these stabilizers at any time is an excellent indicator of solvent condition. Dow’s easy-to-use kit enables you to check stabilizer con- centration “on the spot” and keep the solvent from becoming acidic. Your nearest Dow Sales Off ice (see list on page 44) will tell you how to obtain these two valuable Dow services.

1

We’re Ready to Help Dow maintains the largest, most ex- perienced solvents technical service and development department in the industry - more than 30 trained spe- cialists capable of assisting you with any technical problems involving our products. If you have a new cleaning/degreasing application or a problem with an old one, why not place a call to Dow’s ex-

perts? The number is (517) 636-3616. Based on past experience, our special- ists most likely will have a ready an- swer; or ttiey may decide that an on- site evaluation of your operation, equipment and requirements is appro- priate. In any case, the service is at Dow’s expense because helping your operation run smoothly means busi- ness to Dow.

FIGURE 23. Dow’s Acid Acceptance Test Kit

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Equipment Suppliers

APOR DEGREASING 2 QUIPMENT Autosonics, Inc. 2574 Industry Ln. Norristown, PA 19403

Baron-Blakeslee 2001 N. Janice Ave. Melrose Park, IL 60160

Blackstone Ultrasonics, Inc. 1111 Allen St. Jamestown, NY 14701

Branson Cleaning Equipment Co. 1 Parret Dr. Shelton, CT 06484

Crest Ultrasonics Corp. P.O. Box 7266 Scotch Rd. Mercer County Airport Trenton, NJ 08628

(21 5) 539-0330

(31 2) 450-3900

(71 6) 665-2620

(203) 929-7301

~- @OQJ 883-4000 ~

etrex Chemical Industries, Inc. 2 .O. Box 501 Detroit, MI 48232

Lewis Corporation Main Street Woodbury, CT 06798

Phillips Manufacturing Co. 7334 N. Clark St. Chicago, IL 60626

Ramco Equipment Corp. 32 Montgomery St. Hillside, NJ 07205

S & W Enterprises P.O. Box 383 Savannah, GA 31402

Tally Degreaser P.O. Box 1305 Attleboro Falls, MA 02763

I)Vapo-Kleen Products Co. I- 11 544 Sheldon St. - P.O. Box 1278

Sun Valley, CA 91352

(313) 358-5800

(203) 263-2158

(312) 338-6200

(201) 687-6700

(91 2) 232-71 51

(61 7) 695-2700

(213) 875-3810

DISTILLATION EQUIPMENT Acra Electric Corp. 3801 N. 25th Ave. Schiller Park, IL 60176

Artisan Industries Inc. 73 Pond St. Waltham, MA 02154

Baron-Blakeslee 2001 N. Janice Ave. Melrose Park, IL 60160

Branson Cleaning Equipment Co. P.O. Box 786 Shelton, CT 06484

Brighton Corporation 11861 Mosteller Rd. Cincinnati, OH 45241

Crest Ultrasonic Corp.

Mercer County Airport Trenton, NJ 08628

Detrex Chemical Industries, Inc. P.O. Box 501 Detroit, MI 48232

Eaton Corp. Process Control Components Div. P.O. Box 7 Aurora, OH 44202

Phillips Manufacturing Co. 7334 N. Clark St. Chicago, IL 60626

Ramco Equipment Corp. 40-50 Montgomery St. Hillside, NJ 07205

(31 2) 678-8870

(61 7) 893-6800

(31 2) 450-3900

(203) 929-7301

(513) 771-2300

~~~ Scotch R4- - P.O. BOX-7266

(609) 883-4000

(313) 868-8600

(216) 562-51 51

(31 3) 656-7300

(201) 687-6700

STEAM CONTROLS, PRESSURE-REDUCI NG VALVES A.W. Cash Valve Mfg. Co. 666 E. Wabash Ave. Decatur, IL 62525

Fisher Controls Co. P.O. Box 190 Marshalltown, IA 501 58

Marshalltown Instruments 901 E. Nevada St. Marshalltown, IA 501 58 R-P & C Valve Div. of White Consolidated Ind. 8150 W. Ridge Rd. Fairview, PA 16415

SOLENOID VALVES Automatic Switch Co. 50-56 Hanover Rd. Florham Park, NJ 07932

Magnatrot Valve Corp. 67 Fifth Ave. P.O. Box 17 Hawthorne, NJ 07507

STEAM TRAPS Armstrong Machine Works 816 Maple St. Three Rivers, MI 49093

A.W. Cash Valve Mfg. Co. 666 E. Wabash Ave. Decatur, IL 62525

R-P & C Valve Div of White Consolidated !nd. 8150 W. Ridge Rd. Fairview, PA 16415

(21 7) 422-8574

(51 5) 754-301 1

(814) 474-1551

(201) 966-2000

(201) 427-4341

(616) 273-1415

(21 7) 422-8574

(814) 474-1551

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STEAM CONDENSATE RETURN PUMPS American-Marsh Pumps, Inc. 722 Porter Lansing, MI 48905

Aurora Pump Division General Signal Corp. 800 Airport Rd. North Aurora, IL 60542

Weinman Pumps Co. 100 Skiff St. Hamden, CT 06514

SAFETY THERMOSTATS Honeywell, Inc. 2701 Fourth Ave. S. Minneapolis, MN 55408

Penn Controls Division of Johnson Service Co.

(517) 489-1471

(31 2) 859-7000

(203) 281-8000

(612) 870-5200

-~ - ~~~ - - 222l!2aDlde_nn. ~ ~~~

-OakBrook, IL 60521

WATER FLOW CONTROL VALVES Penn Controls Division of Johnson Service Co. 2221 Camden Ct. Oak Brook, IL 60521

DEGREASER WALL PROTECTIVE COATINGS Heresite & Chemical Co. 822 S. 14th Street - P.O. Box 249

1 (312) 654-4900

(31 2) 654-4900

I Manitowoc, WI 54220 (414) 684-6646 Wisconsin Protective Coating Corp.

P.O. Box 216 Green Bay, WI 54305

1 614 Elizabeth St.

(41 4) 437-6561

WATER SEPARATORS Baron-Blakeslee, Inc. 1622 So. Laramie Chicago, IL 60650

Branson Cleaning Equipment Co. P.O. Box 786 Shelton, CT 06484

Crest Ultrasonics Corp.

Mercer County Airport Trenton, NJ 08628

Detrex Chemical Ind. P.O. Box 501 Detroit, MI 48232

Freeland Fabricating, Inc. 1100 E. Washington St. P.O. Box 280 Freeland, MI 48623 (517)495-5515 ~ ~ ~ -~

PERSONAL PROTECTIVE EQUIPMENT: Aprons, Gloves, Masks, Respirators, etc. American Optical Corp. 14 Mechanic St. Southbridge, MA 01 550

Boss Manufacturing Co. 221 West First Street Kewanee, IL 61443 Edmont-Wilson Division of Becton, Dickenson & Co. Coshocton, OH 43812

Magid Glove Mfg. Co. 2060 N. Kolmar Chicago, IL 60639

(31 2) 656-7300

(203) 929-7301

Scotch Rd. - P.O. BOX 7266

(609) 883-4000

(31 3) 868-8600

(61 7) 764-971 1

(61 4) 622-431 1

(31 2) 384-2070

Mine Safety Appliances co. 600 Penn Center Pittsburgh, PA 15235

Norton Safety Products Charleston, S. Carolina

The Surety Rubber Co. 611 N. High St. - Box 97 Carrollton, OH 4461 5

Willson Products Div. lnco Safety Products P.O. Box 622 Reading, PA 19603

HOSES: TRANSFER, SPRAY Binks Manufacturing Co. 9201 W. Belmont Ave. Franklin Park, IL 60131 (3 1 2)_671-3000 -~

Eaton Corp. Process Control Components Div. Box 7 Aurora, OH 44202

Resistoflex Corp. Woodland Rd. Roseland, NJ 07068

(412) 273-5000

(803) 554-0660

(2 1 6) 627-2 1 66

(21 5) 376-6161

(21 6) 562-51 51

(201) 226-7700

41

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, L Y EQUIPMENT American LaFrance Div.

of A-T-0, Inc. 100 E. LaFrance St. Elmira, NY 14901

Binks Manufacturing Co. 9201 W. Belmont Ave. Franklin Park, IL 60131

DeVilbiss Co. 300 Phillips Ave. - P.O. Box Toledo, OH 43692

CENTRIFUGAL PUMPS Allis Chalmers Industrial

1150 Tennessee Ave. Cincinnati, OH 45229

lngersoll Rand Co. 277 Park Ave.

(607) 734-8 1 8 1

(312) 671-3000

(419) 470-2169

Pump Div.

(51 3) 482-2500

455 Godwin Ave. Midland Park, NJ 07432

HAND PUMPS Baldwin Manufacturing Co. 6130 American Rd. Toledo, OH 43612 (419) 729-3747 Blackmer Pump Co. 1809 Century Ave. Grand Rapids, MI 49509

(201) 444-6900

(616) 241-161 1

Graco Inc. P.O. Drawer 1441 Minneapolis, MN 55440 Halprin Supply Co. 3804 S. Broadway Place Los Angeles, CA 90037

Tokheim Corp. 1602 Wabash Ave. Fort Wayne, IN 46801

GASKETS Anchor Packing Co. 3789 Main St. Philadelphia, PA 191 27

Crane Packing Co. 6400 Oakton St. Morton Grove, IL 60053

Garlock, Inc. f25€-Mi$tewt? Tower Rochester NY 14604

Federal-Mogul Corp. Rubber and Plastics Group P.O. Box 1966 Detroit, MI 48235

Johns-Manville Greenwood Plaza Denver, CO 80217

SOLVENT RESISTANT GREASE LUBRICANTS Tower Oil & Technology Co. 300 W. Washington Chicago, IL 60606

(213) 232-3131

913 (219) 423-2552

(21 5) 482-8700

(31 2) 967-2400

(71 6) 232-1 400

(31 3) 354-7700

(303) 979- 1 000

(31 2) 346-0562

AIR SAMPLING INSTRUMENTS Anatole J. Sipin Co. 505 8th Avenue New York, NY 10016

Bendix Corp. Environmental & Process

Instruments Div. 1400 Taylor Ave. Baltimore, MD 21204

En Met Corp. 2308 S. Industrial Hwy. Ann Arbor, MI 48104

Gastech, Inc. 331 Fairchild Dr. Mountain View, CA 94043

National Mine Service Co. 4900/600 Grand St. Pittsburgh, PA 15219

LEVEL GAUGES Liquidometer Corp. Subsidiary, Lewis Engineering Co. 1929 Shelden St. Norwich, NY 13815

Uehling Instrument Co. 437 Getty Ave. Paterson, NJ 07503

PORTABLE AIR BLOWERS AND VENTILATORS Copus Engineering Corp. 344 Park Ave. Worcester, MA 01613

Mine Safety Appliances Co. 600 Penn Center Pittsburgh, PA 15235

(212) 695-5706

(301) 321-5200

(31 3) 761 -1 270

(41 5) 967-6794

(41 2) 281 -0688

(607) 334-3939

(201) 742-8710

(61 7) 757-8391

(41 2) 273-5000

42

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-) VENT DRIERS FOR BULK TANKS Midland Specialties Co. Box 247 Brookfield, IL 6051 3

FILTERS AMF Cuno Div. AMF Inc. 402 Research Parkway Meriden, CT 06450

Commercial Filters Division The Carborundum Co. State Rd., 32 West Lebanon, IN 46052

Millipore Corp. Wigging Ave. Bedford, MA 01730

Serfilco

(3 12) 865-0575

(203) 237-5541

(3 17) 482-3900

(617) 275-9200

~ ~ - Div. of Service Filtration Corp. ~~~ ~~ ~ ~

7- F234 Depot St. -) Glenview, IL 60065

(312) 998-9300

EXHAUST BLOWERS Buffalo Forge Co. 490 Broadway Buffalo, NY 14240

Chicago Blower Corp. 1675 Glen Ellyn Rd. Glendale Heights, IL 60137

Garden City Fan & Blower Company 1701 Terminal Rd. - P.O. Box 760 Niles, MI 49120

(716) 847-5121

(3 12) 858-2600

(616) 683-1150

3

43

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AREA HEADQUARTERS OF THE DOW CHEMICAL COMPANY DOW CHEMICAL U.S.A. .......................... .......................................... . MIDLAND, Michigan 48640 DOW CHEMICAL LATIN AMERICA ............................................................. CORAL GABLES, Florida 33134 DOW CHEMICAL EUROPE, S.A. . . . . . . . . . . . . ................................................... .8810 HORGEN, Switzerland DOW CHEMICAL PACIFIC . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . P.O. Box 71 1, HONG KONG DOW CHEMICAL CANADA INC.. .................................................................... SARNIA, Ontario N7T 7K7 DOW QUIMICA, S.A. ..................................................................................... SA0 PAULO, Brazil

SALES OFFICES OF DOW CHEMICAL U.S.A. ATlANTA .......................................... Suite 2005, 20 Perimeter Center East, Atlanta, GA 30346 404-394-4141 BATON ROUGE . . . .. .4150 S. Shewood Forest Blvd., Suite 101, Baton Rouge, LA 70816 504-293-2222 BOSTON.. ........................................................... .20 William St., Wellesley, MA 02181 617-237-2070 CHARLOTTE ....................... . .2 Woodlawn Green, Woodlawn Road, Charlotte, NC 28210 704-525-9030 CHICAGO ..... ite 500, 1701 West Golf Rd., Rolling Meadows, IL 60008 312-228-2700 CINCINNATI . . . . . . . . . . . . . itehall Park, 8050 Hosbrook Road, Cincinnati, OH 45236 513-793-6200 CLEVELAND ............ . . . . . . . . . . . . 14955 Sprague Road, P.O. Box 8800, Strongsville, OH 44136 216-826-6000

. . . . SuifeSm 4700 S Syracuse Parkway, Denver, CO 80237 383-740-9300

GRAND RAPIDS ................................. ,611 Cascade We kway S.E., Grand Rapids, MI 49506 616-949-9000

INDIANAPOLIS .............................. P.O. Box 6851 1,9550 nsville Road, Indianapolis, IN 46268 317-873-7000 KANSAS CITY ......... ..... Suite 160, 10890 Benson Drive, Shawnee Mission, KS 66210 913-341-2500 LOS ANGELES .......................................................... P.O. Bin 48, Pasadena, CA 91 109 213-577-1515 MEMPHIS .................................. Suite 2210, 5100 Poplar Ave., Memphis, TN 38137 901-767-5000 MINNEAPOLIS . . . . . . . . . . . . . . . . . . 1 1 100 West Bren Road, Minnetonka, MN 55343 612-938-4300 NEW YORK . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Park 80 Plaza East, Saddle Brook, NJ 07662 201-845-5000 PHILADELPHIA . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .505 S. Lenola Road, Moorestown, NJ 08057 609-234-0400 PllTSBURGH .. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Four Gateway Center, Suite 1313, Pittsburgh, PA 15222 412-281-3030

. . . 400 Perinton Hills mice Park, Fairport, NY 14450 716-425-1200

. . . . . . .2800 Mitchell Drive, Walnut Creek, CA 94598 415-944-2000 SEATTLE ....... . . . . . . . . . . . . Suite 522, 600 - 108th Ave., N.E., Bellevue, WA 98004 206-455-7250 STAMFORD ........................................................ 1600 Summer St., Stamford, CT 06902 203-359-3300 TAMPA ........................................... Suite 450, 5100 W. Kennedy Boulevard, Tampa, FL 33609 813-877-8300

~~ ~ ~ . 12700 Park Central Place, Suite 600, Dallas, TX 75251 214-387-221 1

Suite 415, 26555 Evergreen Road, Southfield, MI 48076 313-358-1300

HOUSTON ....................................................... P.O. Box 4269, Houston, TX 77210 0 713-978-3700

Suite 415, 8002 Discovery Dr., Richmond, VA 23288 804-288-1601

450 University Club Tower, 1034 S. Brentwood Blvd., St. Louis, MO 63117 314-726-5000

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DOW CHEMICAL U.S.A. INORGANIC CHEMICALS DEPARTMENT MIDLAND, MICHIGAN 48640

NOTICE - This information is presented in good faith, but no warranty, express or implied, is given nor is freedom from any patent owned by The Dow Chemical Company or by others to be inferred. Inasmuch as any assistance furnished by Dow with reference to the proper use and disposal of its products is provided without charge, Dow assumes no obligation or liability therefor,

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Printed in U S A . Trademark of The Dow Chemical Company Form No. 100-5185-81