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© Effects Of Increased Solar Ultraviolet Radiation On Materials Andrady, AL; Hamid, SH; Hu, X; Torikai, A ELSEVIER SCIENCE SA, JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY; pp: 96-103; Vol: 46 King Fahd University of Petroleum & Minerals http://www.kfupm.edu.sa Summary etic polymers such as plastics, as well as naturally occurring polymer materi as wood, are extensively used in building construction and other o cations where they are routinely exposed to sunlight. The W-B conte ght is well known to affect adversely the mechanical properties of ials, limiting their useful life. Presently their outdoor Lifetimes depend on f photostabilizers in the case of plastics and on protective surface coatings of wood. Any increase in the solar UV-B content due to a partial ozone deplet therefore tend to decrease the outdoor service life of these materials. It i gistic effect of increased UV radiation with other factors such as the temper would determine the extent of such reduction in service Life. The increased c iated with such a change would be felt unevenly across the globe. oping countries that depend on plastics as a prime material of construction a ience high ambient temperatures are likely to be particularly affected in spi elatively small fractional decrease in ozone at those locations. Assessment o e to materials, associated with ozone depletion, requires a knowledge of the ength dependence as well as the dose-response characteristics of the polymer dation processes of interest. While the recent literature includes some relia ral sensitivity data, little dose-response information has been reported, so cult to make such assessments reliably at the present time. This is particula he naturally occurring materials popularly used in construction applications. ain polymers at the same useful Lifetime in spite of increased sol nt, the amount of photostabilizers used in the formulations might be increase strategy assumes that conventional stabilizers will continue to be effective Copyright: King Fahd University of Petroleum & Minerals; http://www.kfupm.edu.sa

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Page 1: © Effects Of Increased Solar Ultraviolet Radiation On Materials Andrady, AL; Hamid, SH; Hu, X; Torikai, A ELSEVIER SCIENCE SA, JOURNAL OF PHOTOCHEMISTRY

©

Effects Of Increased Solar Ultraviolet Radiation On Materials

Andrady, AL; Hamid, SH; Hu, X; Torikai, A

ELSEVIER SCIENCE SA, JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY

B-BIOLOGY; pp: 96-103; Vol: 46

King Fahd University of Petroleum & Minerals

http://www.kfupm.edu.sa

Summary

Synthetic polymers such as plastics, as well as naturally occurring polymer materials

such as wood, are extensively used in building construction and other outdoor

applications where they are routinely exposed to sunlight. The W-B content in

sunlight is well known to affect adversely the mechanical properties of these

materials, limiting their useful life. Presently their outdoor Lifetimes depend on the

use of photostabilizers in the case of plastics and on protective surface coatings in the

case of wood. Any increase in the solar UV-B content due to a partial ozone depletion

would therefore tend to decrease the outdoor service life of these materials. It is the

synergistic effect of increased UV radiation with other factors such as the temperature

that would determine the extent of such reduction in service Life. The increased cost

associated with such a change would be felt unevenly across the globe. Those

developing countries that depend on plastics as a prime material of construction and

experience high ambient temperatures are likely to be particularly affected in spite of

the relatively small fractional decrease in ozone at those locations. Assessment of the

damage to materials, associated with ozone depletion, requires a knowledge of the

wavelength dependence as well as the dose-response characteristics of the polymer

degradation processes of interest. While the recent literature includes some reliable

spectral sensitivity data, little dose-response information has been reported, so it is

difficult to make such assessments reliably at the present time. This is particularly true

for the naturally occurring materials popularly used in construction applications. To

maintain polymers at the same useful Lifetime in spite of increased solar W-B

content, the amount of photostabilizers used in the formulations might be increased.

This strategy assumes that conventional stabilizers will continue to be effective with

Copyright: King Fahd University of Petroleum & Minerals;http://www.kfupm.edu.sa

Page 2: © Effects Of Increased Solar Ultraviolet Radiation On Materials Andrady, AL; Hamid, SH; Hu, X; Torikai, A ELSEVIER SCIENCE SA, JOURNAL OF PHOTOCHEMISTRY

1.2.3.4.5.6.7.8.9.10.11.12.13.14.15.16.17.18.19.20.21.22.23.24.25.26.27.28.29.30.31.32.33.

©

the spectrally altered W-B-enhanced solar radiation. While the present understanding

of the degradation chemistry suggests the strategy to have merit, its effectiveness, in

an altered solar radiation environment, has not been demonstrated for common

polymers. The availability of these data is crucial for reliably estimating the cost of

mitigating the increased damage to materials as a result of a possible partial depletion

of the ozone layer using this approach. (C) 1998 UNEP. Published by Elsevier

Science S.A. All rights reserved.

References:ALLEN NS, 1983, DEGRADATION STABILIZ, P373ANDRADY AL, UNPUBANDRADY AL, 1989, J APPL POLYM SCI, V37, P935ANDRADY AL, 1990, J APPL POLYM SCI, V39, P363ANDRADY AL, 1991, J APPL POLYM SCI, V42, P2105ANDRADY AL, 1992, POLYM DEGRAD STABIL, V35, P235ANDRADY AL, 1993, J ENV POLYM DEG, V1, P171ANDRADY AL, 1996, J APPL POLYM SCI, V62, P1465ANDRADY AL, 1997, ADV POLYM SCI, V128, P49BURN LS, 1994, PLAST RUB COMPOS PRO, V21, P99DECKER C, 1984, DEGRADATION STABILIZ, P81FACTOR A, 1987, ADV STABILIZATION CO, V2, P45FACTOR A, 1995, ANGEW MAKROMOL CHEM, V232, P27FORSSKAHL I, 1993, ACS SYM SER, V531, P45FUKUDA Y, 1991, POLYM DEGRAD STABIL, V34, P75GAPPERT G, 1996, VINYL 2020 PROGR CHAGARDETTE JL, 1991, POLYM DEGRAD STABIL, V34, P135GHAFFAR A, 1976, EUR POLYM J, V11, P271GUGUMUS F, 1993, POLYM DEGRAD STABIL, V39, P117HAMID H, 1998, COMMUNICATIONHAMID SH, 1991, J APPL POLYM SCI, V43, P651HAMID SH, 1995, HDB POLYM DEGRADATIOHEITNER C, 1993, ACS SYM SER, V531, P3HIRT RC, 1967, APPL POLYMER S, V4, P61HO BYK, 1984, J VINYL TECHNOL, V6, P162HON DNS, 1991, WOOD CELLULOSIC CHEM, P525HU X, 1998, IN PRESS POLYM DEGRAHU XZ, 1997, POLYM DEGRAD STABIL, V55, P131HUSSAIN I, 1995, J VINYL ADDIT TECHN, V1, P137JAHAN MS, 1987, PHOTOCHEM PHOTOBIOL, V45, P543LAUNER HF, 1965, TEXT RES J, V35, P395LENNOX FG, 1971, APPL POLYM S, V18, P353

MADER FW, 1992, MAKROMOL CHEM-M SYMP, V57, P15

Copyright: King Fahd University of Petroleum & Minerals;http://www.kfupm.edu.sa

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34.35.36.37.38.39.40.41.42.43.44.45.46.47.48.49.50.51.52.53.54.

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MATSUMOTO S, 1984, J POLYM SCI POL CHEM, V22, P869MITSUOKA T, 1993, J APPL POLYM SCI, V47, P1027MOORE S, 1994, MODERN PLASTICS APR, P46OWEN ED, 1984, DEGRADATION STABILIZ, P320PAN JQ, 1993, POLYM DEGRAD STABIL, V40, P375PYRDE CA, 1985, ACS SYM SER, V280, P329RABEK JF, 1995, POLYM PHOTODEGRADATI, P655RABONAVITCH EB, 1983, J VINYL TECHNOL, V5, P110RIVATON A, 1988, POLYM DEGRADATION ST, V23, P51SCOTT G, 1985, NEW TRNEDS PHOTOCHEMSCOTT G, 1990, POLYM DEGRADATION STSHLYAPNIKOV YA, 1996, ANTIOXIDATIVE STABILSUMMERS JW, 1983, J VINYL TECHNOL, V5, P43TITOW WV, 1984, PVC TECHNOLOGY, P1233TORIKAI A, 1993, J APPL POLYM SCI, V50, P2185TORIKAI A, 1993, J POLYM SCI POL CHEM, V31, P2785TORIKAI A, 1993, POLYM PREPR-JAPAN, V42, P2045TORIKAI A, 1998, J APPL POLYM SCI, V67, P1293WARNER WC, 1966, I EC P RES DEV, V5, P219WYPYCH J, 1990, WEATHERING HDB, P512ZHANG ZF, 1996, POLYM DEGRAD STABIL, V51, P93

For pre-prints please write to: [email protected]

Copyright: King Fahd University of Petroleum & Minerals;http://www.kfupm.edu.sa