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SynchrotronSynchrotronSynchrotron RadiationRadiationRadiation andandandARCHAEOMETRYARCHAEOMETRYARCHAEOMETRY

Simona Quartieri Dipartimento di Scienze della Terra

Università di Messina

Quartieri - SILS 2006 Napoli

SynchrotronSynchrotronSynchrotron radiationradiationradiation and and and archaeometryarchaeometryarchaeometryHighly intense X-ray beams as produced at synchrotronradiation facilities, that are also highly monochromatic and have a low divergence, are highly suitable tools forexamining fragile, valuable and/or unique artefacts withminimal or no damage. We can achieve information about the major- and trace-level composition of the objects, about the chemical state of one or more atomic species that are present and/or about crystallographic phases on the materials.

Since the materials and objects encountered in the field of art-analysis, archaeology and conservation are oftencomplex in shape, covered with alteration layers and/or maybe highly heterogeneous, the use of X-ray micro beams isvery often required to allow for the measurement of localrather than bulk properties.

Quartieri - SILS 2006 Napoli

The questions that archaeologists ask more often regarding an object are:

what material is it made of (composition)

when was it made (dating)

where was it made (provenance)

how was it made (art technology)

how can we avoid its destruction (conservation)

Quartieri - SILS 2006 Napoli

AppliedAppliedApplied techniquestechniquestechniquesElemental microanalysis down to the sub-ppm level is possible bymeans of µ-XRF (X-ray fluorescence analysis).

Local chemical state determinations of selected (trace) constituentsare possible by applying XAFS and µ-XAFS (X-ray absorptionspectroscopy)

Information on the presence and nature of crystalline phases can beobtained via XRD (X-ray diffraction), which usually employ X-rayphotons with energies in the 0.5 to 30 keV range.

Alternatively, entire objects may be bathed in highly-energeticsynchrotron beams to allow high quality radiographic or tomographicimaging measurements, revealing the internal structure of theseartefacts.

Quartieri - SILS 2006 Napoli

XRD applicationsat SRA2005

Manufacturing Manufacturing cosmeticscosmetics in in ancientancient EgyptEgypt

Manufacturing Manufacturing cosmeticscosmetics in in ancientancient EgyptEgypt

Manufacturing Manufacturing cosmeticscosmetics in in ancientancient EgyptEgypt

Quartieri - SILS 2006 Napoli

Manufacturing Manufacturing cosmeticscosmetics in in ancientancient EgyptEgypt

Quartieri - SILS 2006 Napoli

artificially synthesized !

Quartieri - SILS 2006 Napoli

Quartieri - SILS 2006 Napoli

Quartieri - SILS 2006 Napoli

Mural painting representing an eagle-knight, probably a religious symbol (Cacaxtla, Tlaxcala, Mexico)

Pottery vase representing Tlàloc, the Mayan god of rain (Templo Mayor museum , Mexico).

MAYA BLUE PIGMENT[G. Chiari, R. Giustetto, G. Ricchiardi (2003) Eur. J. Mineral. 15:21-33]

G. Chiari (2005) IUCr, Firenze

Quartieri - SILS 2006 Napoli

In Mexico it was used until the end of ‘600. In Cuba it is found on walls dating 1830. It was “re-discovered” in 1849, together with the remains of the Maya civilisation.

Maya BlueMaya Blue is a synthetic pigment, produced by the Mayas probably around the VIII century AD

A bright turquoise, it was used in mural paintings, statues, ceramics, codices, and even to tint prisoners to be sacrificed.

Quartieri - SILS 2006 Napoli

Maya BlueMaya Blue is extremely stable: it can resist the attack of boiling, concentrated nitric acid, alkali and any sort of organic solvents.

Its composition and structure was a mystery for a long time. Kleber (1967) proposed a mixture of the colourless clay palygorskite and the blue organic dye indigo:

HE WAS RIGHTHE WAS RIGHT

Quartieri - SILS 2006 Napoli

PALYGORSKITE PALYGORSKITE [(Mg, Al)4 (Si)8 (O, OH, H2O)24 nH2O]

Micro-channels filled with weakly bound zeolitic H2OThe cations complete their coordination with tightly bound structural H2O

Fibrous clay (SEM image, 3520X)

Quartieri - SILS 2006 NapoliIndigo molecule

INDIGOINDIGO

The Mayas extracted it from the leaves of Indigofera suffruticosa

Quartieri - SILS 2006 Napoli

Orthorombic Palygorskite projected on (001) face

MAYA BLUE PIGMENT ?

Quartieri - SILS 2006 Napoli

SR X-ray powder diffraction at GILDA beamline

Quartieri - SILS 2006 Napoli

Electron Density map at the level of indigo

Indigo

Quartieri - SILS 2006 Napoli

Quartieri - SILS 2006 Napoli

MODEL OF ENCAPSULATION OF INDIGO IN THE PALYGORSKITE FRAMEWORK

Quartieri - SILS 2006 Napoli

Indigo can go into the channels only if the zeolitic water is removed (130 < T < 220°C).

MAYA BLUEMAYA BLUE forms at about T = 100°C.

Even if indigo could displace water, the molecule has to break strong H bonds (≈ 1.8 Å between

indigo -C=O and structural water) to move inside the channels.

The formation of Maya Blue depends upon a very long series of highly unlikely events.

Quartieri - SILS 2006 Napoli

ThermalThermal AnalysisAnalysis of of paligorskitepaligorskite (black) (black) and Maya Blue (and Maya Blue (redred))

The water loss at 120<T<300°C (ZEOLITIC ZEOLITIC water) is the sameis the same for both palygorskite and Maya Blue.

Quartieri - SILS 2006 Napoli

The water loss at 120<T<300°C (ZEOLITIC ZEOLITIC water) is the same for both materials. It makes sense if indigo does not enterdoes not enterthe channels.

The ADSORBEDADSORBED water loss at low temperature (<120°C) is much higher for palygorskite than for MB. It makes sense if indigo occupies the grooves instead of water.

Quartieri - SILS 2006 Napoli

A new theory is needed:A new theory is needed:Indigo does not go inside the channels but Indigo does not go inside the channels but only fills the grooves all around the crystalonly fills the grooves all around the crystal

Water

Indigo

H2O

Indigo

Quartieri - SILS 2006 Napoli

The indigo molecule is imbedded into the channel. Water does not have access to the groove because the hydrophobic part of indigo repels it.

Nitric acid cannot attack the indigo double bond because of steric hindrance.

Quartieri - SILS 2006 Napoli

XAFS spectroscopy is a potentially very useful technique tobe applied in archaeological studies.

It is a non-destructive method which can be applied in air; itvirtually does not require any restriction on the type and size of the sample, which can be metal, ceramic, glass, cloth etc. and, finally, it is applicable to most of the elements of interest, even in very low concentration.

All these characteristics are particularly important in archaeological applications, in which samples are preciouscultural heritage made of very different materials.

Archaeometrical applications of X-ray Absorption Spectroscopy

Quartieri - SILS 2006 Napoli

Quartieri - SILS 2006 Napoli

The The originorigin of color in of color in ancientancient glassglass

Quartieri - SILS 2006 Napoli

Various colors in glass can be causedby metal ions in them.

They are usually transition elementswhich absorb characteristic frequencies

of visible region.

This mechanism is also influenced bythe oxidation state of the metal cation.

Quartieri - SILS 2006 Napoli

Since the characterization of colorant and decolorant componentsis important in understanding the

manufacturing technique, XAFS has been applied to the study of the oxidation state of transition metals

in a number of glass samplescharacterized by different color

Quartieri - SILS 2006 Napoli

Application of X-ray Absorption Spectroscopy with synchrotron radiation to the study of glasses of archaeological interest

(Quartieri et al. Eur. J. Mineral. 2002)

Synchrotron X-ray absorption spectroscopy has been applied to the study of the oxidation state of iron and manganese in a number of glass samples of the 2nd century AD, characterized by different color (from pale green to pale brown) found in the Roman villa of Patti, near Messina.

Quartieri - SILS 2006 Napoli

AIMS

-to test the influence of iron oxidation state on the color of the studied samples

- to identify the possible decolorant role of manganese oxide in the almost uncoloredsamples

Quartieri - SILS 2006 Napoli

The Fe and Mn K-edge XANES spectra were collected directlyon the glass fragments in the fluorescence mode on the GILDA-CRG beamline (ESRF).

A dynamically sagittally-focussing monochromator withSi(311) crystals and a 13-element high-purity Ge detector were used.

SiO2 TiO2 Al2O3 FeO MnO MgO CaO Na2O K2O NiO Cu2O CoO Cr2O3 ClA 70.70 0.10 3.31 0.40 0.02 0.63 8.02 16.45 0.59 0.02 0.06 0.02 — 0.99

B 65.89 0.18 3.39 1.00 1.20 1.11 8.98 14.31 1.15 0.06 0.03 — 0.02 0.91

C 65.51 0.20 2.83 0.97 1.40 1.24 8.72 17.45 0.69 — 0.06 0.02 0.01 0.88

ExperimentalChemical analyses of the glass samples.

Glass A: green; glass B: uncolored; glass C: pale brown.A

Quartieri - SILS 2006 Napoli

Fe K-edge

7100 7125 7150 7175

Nor

m. A

bsor

ptio

n

Energy (eV)

C

Olivine

Hematite

Magnetite

B

A

abcd

Quartieri - SILS 2006 Napoli

Glass A

7112.4 7113.9

7114.6

7110 7112 7114 7116 7118Energy (eV)

0

0.1

0.2

0.3

0.4

Nor

m. A

bsor

banc

e

Glass B

7112.3

7114

7110 7112 7114 7116 7118Energy (eV)

-0.5

0

0.5

1

1.5

2

Nor

m. A

bsor

banc

e

Glass C

7112.3

7114

7110 7112 7114 7116 7118Energy (eV)

0

0.2

0.4

0.6

0.8

1

Nor

m. A

bsor

banc

e

Olivine

7112.4

7113.6

7114.4

7110 7112 7114 7116 7118Energy (eV)

0

0.01

0.02

Nor

m. A

bsor

banc

e

Magnetite

7112.3

7114

7115.4

7110 7112 7114 7116 7118Energy (eV)

0

0.02

0.04

0.06

0.08

Nor

m. A

bsor

ptio

n

Hematite

7113.2

7114.5

7115.7

7110 7112 7114 7116 7118Energy (eV)

-0.005

0.005

0.015

0.025

0.035

Nor

m. A

bsor

ptio

n

Roman glass samples

Reference compounds

Fe K-edge:

Quartieri - SILS 2006 Napoli

6530 6540 6550 6560 6570

Nor

m. A

bsor

ptio

n

Energy (eV)

MnO

Glass B

Glass C

MnO2

Mn2O

3ab

c d

6540 6550 6560

Nor

m. A

bsor

ptio

n

Energy (eV)

Glass B

Glass C

Rhodonite

Tephroite

Mn K-edge

In glass B and C Mn is in the reduced form

Quartieri - SILS 2006 Napoli

In the ancient glass B and C Mn4+ has oxidized Fe2+ to Fe3+ and, as a consequence, is present in the reduced form.

This confirms the hypothesis of a redoxinteraction between iron and manganese, as a result of a deliberate addition of pyrolusite − reported in literature as one of the main decolorants in the Roman period − during the melting procedure of the almost uncoloredglasses.

Results

Quartieri - SILS 2006 Napoli

The glasswork of Val GargassaTHE ARCHAEOLOGICAL SITE

Quartieri et al. 2005

Quartieri - SILS 2006 Napoli

Quartieri - SILS 2006 Napoli

Production indicators: those remains which testify specific operationscarried out during the productive cycle (like melting, flashing, boiling, working) and which can be useful to reconstruct the technologicalprocesses and expedients used in the past to produce glass.

Glassartifact

cruciblesdrops

drippings

Vitreous massfragments

collarscuttings

Building materialsconcotti

THE ARCHAEOLOGICAL FINDINGS

Quartieri - SILS 2006 Napoli

worked glassdrippings

fluidity test

collars of blowing pipe

cuttings

Vitreous masses

Quartieri - SILS 2006 Napoli

US1-2

US1-3

US3-2

US5-1

US5-3

US5-1

US5-3

Glass artifacts

Fe K-edge

Sample Total area pre-edge Centroid (eV) Sample Total area pre-edge Centroid (eV)

US1-2 0.1356 7114.17 US5-3 0.1178 7113.26

US1-3 0.1838 7113.95 VGRH-US2-29 0.2080 7114.19

US3-2 0.1420 7113.52 VGRH-US2-27 0.1793 7114.23

US5-1 0.1465 7113.90 F-VGR34 0.1289 7113.36

ST1 0.1515 7113.68 ST2 0.1768 7113.70

Olivine 0.0521 7112.95 Hematite 0.0750 7114.56

Magnetite 0.2182 7114.06

Quartieri - SILS 2006 NapoliFeO = 0.4, MnO = 0.6

Addition of decolorant

FeO = 0.8, MnO = 0.0

F-VGR34

7112.7

7114.1

7114.7

7110 7112 7114 7116-0.01

0

0.01

0.02

0.03

0.04

0.05

-0.01

0

0.01

0.02

0.03

0.04

0.05

Pre-edge centroid7113.36 eV

VGRH-US2-27-

7112.8

7114.1

7114.6

7111 7113 7115 7117-0.05

0

0.05

0.1

0.15

-0.05

0

0.05

0.1

0.15

Pre-edge centroid7114.23 eV

St1

7111.8

7112.6

7114.1

7110 7112.3 7114.7 7117

0

0.02

0.04

0.06

0

0.02

0.04

0.06

Reference glass (Fe2+=40%)

Pre-edge centroid= 7113.68

US1-2

7112.5

7114.2

7115.4

7111 7113 7115 7117

0

0.02

0.04

0.06

0

0.02

0.04

0.06

US1-3

7112.7

7114.2

7115.2

7110 7112 7114 7116

0

0.02

0.04

0.06

0.08

0

0.02

0.04

0.06

0.08

US3-2

7111.9

7112.8

7114.2

7110 7112 7114 71160

0.01

0.02

0.03

0.04

0.05

0.06

0

0.01

0.02

0.03

0.04

0.05

0.06

US5-1

7112.7

7114.2

7115

7110.5 7112 7113.5 7115 7116.5

0

0.02

0.04

0.06

0.08

0

0.02

0.04

0.06

0.08

US5-3

7111.7

7112.6 7114.1

7114.7

7110 7112 7114 7116

0

0.01

0.02

0.03

0.04

0

0.01

0.02

0.03

0.04

St1

7111.8

7112.6

7114.1

7110 7112.3 7114.7 7117

0

0.02

0.04

0.06

0

0.02

0.04

0.06

Normalized Fe-K pre-edge spectra and the bestmodel for the glass artifacts

Quartieri - SILS 2006 Napoli

Quartieri - SILS 2006 Napoli

Luster decoration, typical of the Medieval and Renaissance pottery of the Mediterranean basin, consists of a metal-glass nanocomposite thin layer.

TEM measurements showed that luster consists of a thin film composed of a heterogenous distribution of silver and copper nanoparticles of sizes rangingfrom 5 to 100 nm.

These decorations show peculiar optical properties, producing brilliant reflections of different colors, cangiant effects and iridescences.

Quartieri - SILS 2006 Napoli

Quartieri - SILS 2006 Napoli

Red mosaic tesserae from Pompeii

(Arletti et al. APA 2006)

Red mosaic tesserae from Pompeii

(Arletti et al. APA 2006)1.5 mm 2 mm

Quartieri - SILS 2006 Napoli

Red mosaic tesserae from Pompeii(Arletti et al. APA 2006)

Red mosaic tesserae from Pompeii(Arletti et al. APA 2006)

-1

0

1

2

3

4

8950 9000 9050 9100

Cu K-Edge

Nor

m. A

bs. (

arbi

trar

y un

it)

Energy eV

CuO

Cu2O

Cu

Red Sample

0.5

1

1.5

2

2.5

3

Cu2O

C u

R ed Sam ple

8995.5

8994.5

8995.3

9011.1

9003.1

9003.0

Cu-XANES region

Quartieri - SILS 2006 Napoli

Red samples: Cu K-edgeRedRed samplessamples: Cu K: Cu K--edgeedge

0

0.5

1

1.5

2

0 1 2 3 4 5

FITEXP

R (Å1)

χ ׀(R

׀( (Å

-3)

a)

-1

-0,5

0

0,5

1

1,5

0 4 8 12 16

EXPFIT

Re

[ χ(q

)] (

Å-2

)

b)

k (Å-1) Cu - O Cu - Cu R (Å) N σ2(10-4 Å2) R (Å) N σ2(10-4 Å2)

Lipari 6 1.83±0.02 2.78±1.3 29±11 2.55±0.02 4.91±0.81 23±49 CuO 1.95±0.02 4 41±14 2.91±0.02 4 83±29 3.09±0.02 4 43±10 Cu2O 1.84±0.02 2 26±6 3.03±0.02 12 171±9 Cu met - - - 2.55±0.02 12 40±10

• Prevalent phase: Cu metallic clusters• Presence of Cu1+ in the glass matrix

• Absence of cuprite crystals

EXAFS region

ChalminChalmin etet al.al. APA (2006)APA (2006)

Quartieri - SILS 2006 Napoli

Quartieri - SILS 2006 Napoli

Quartieri - SILS 2006 Napoli

Quartieri - SILS 2006 Napoli

Natural deposit

A majority of charcoal pigment for horses

But also manganese oxide in two particular figures:

Non crystalline manganese oxide

?

?

Question of provenance

The case of The case of EkainEkain (Basque Country, Spain)

Upper Paleolithic (16500-12500 BP)

6520 6600 6680

Nor

mal

ized

abs

orba

nce

Energy (eV)

Point 1

Point 2

Groutite

deposit sampledeposit sample

Manganese localization

ESRF, ID21Point 1

Point 2

Head horse sample

GROUTITE

GROUTITEα-MnOOH

Mineral never identified before

The case of The case of EkainEkain (Basque Country, Spain)

Quartieri - SILS 2006 Napoli

Quartieri - SILS 2006 Napoli

Quartieri - SILS 2006 Napoli

CONCLUSIONS

- Various manganese oxides were identified as black prehistoricpigments, such as pyrolusite, romanechite, hollandite, cryptomelane, todorokite, manganite and groutite

- For the first time, manganite and groutite were identified aspigments. These minerals are very rare where the paintings wererealized unsuspected trade routes ?

- These Paleolithic people produced their own painting matter withoutapplying extensive heat treatments, but grounding together black pigments from different ores.

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