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Transcript of Strengthening the Bond: SCIENCE 6 TEXTILES PREPRINTS Compiled
Strengthening the Bond:
SCIENCE 6 TEXTILESPREPRINTS
Compiled by Virginia J.Whelan
North American Textile Conservation Confere nce 2002
April 5 and 6,2002
- HELD AT -
Philadelphia Museum of Art rsr- philsflslphia, pennsylvania
Winterthur Museum, Garden and Library cr\, Wintspthur, Delaware
The Preprints of the North American Textile Conservation Conference 2002:
Strengthening the Bond: Science and Textiles
is published by the North American Textile Conservation Conference 2002.
Responsibiliry for the methods and/or materials described herein rests solely
with the conrriburors and should not be considered official statement of the NATCC organizing body.
preprints are distributed ro attendees of the NAICC 2002. Additional copies may be purchased.
Please contact the Philadelphia Museum of Art, Textile conservation,
P.O. Box 7546,Phlladelphia, PA 19101-7646 USA for details'
Volume 3. CoPYright 2002
The North American Textile Conservation Conference.
All rights reserved by individual authors.
Cover art: Detail from bedcover
John Hewson (7744-t821)
Philadelphia, PA, c. 1800
105" x 1.03' (266.7 x261,.6 cm)
Cofton plain weave with block printing
Owned by the Philadelphia Museum of ArtGift of John P. Hodgson, .fr., 1930-100-1
Photo by Joe Mikuliak
John Hewson (1744-1821.) is one of the very few eighteenth-century American
textile printers whose work can be identified. Before emigrating to the colonies, he
is known to have worked at Bromley Hall, near London. Hewson was persuaded
by Benjamin Franklin, sraresman, diplomat, and signer of the Declaration of
Independence, to settle in Philadelphi a in I773 where Hewson established himself
as one of the first textile printers in North America'
The printed bedcover in the Philadelphia Museum of Art was bequeathed to one
of Hewson's daughters and given to the museum by a descendent. Two additional
bedcovers are known to exist; one is in a private collection while the other is owned
by Winterthur Museum, Garden 8c Library.'lTinterthur's bedcover
(1963.0048) is stamped "FM" for Frances lWardale Lieber McAliister' who rnarried
John McAllister in Philadelphia in 1783. \Tinterthur also owns a fragment (below)
donated bv a descendent of .fohn Hewson'
Textile fragment
John Hewson (1,744-182f)
Philadelphia, PA, c. 1800
10.5" x 8" (26.7 cm x 20.3 cm)
Cotton plain weave with block printing
Courtesy'Winterthur Museum, Garden & Library
Gift of Claire Herbert Hogan 1982'01'00
A, BENEATH THE SURFACE:SALT MOVEMENT INARCHAE OLOGICAT TEXTI tE S
Glennda Susan Marsh-Letts and Samuel B. Adelojw
ABSTRACT-An understanding of the physical and chem-
ical nature of ancient Egyptian linen, while interesting for
its own sake, is also important as a prerequisite for the suc-
cessful conservation treatment, display and storage of
archaeological linen. Treatments for archaeological textiles
that contain salts were tested. A combination of optical
microscopy, environmental scanning electron microscopy
(ESEM), ion chromatography (IC) and energy dispersive
X-ray analysis (EDXA) has been successfully used to distin-
guish between the natural fiber of an ancient Egyptian linen
and salts or other foreign matter absorbed into the linen. In
particular, the use of ESEM enabled the observation and
recording of the movement of salts within the fibers, in real
time, during cycles of hydration and dehydration. Results
indicated that a long water washing to remove salts, soils
and organic deposits, followed immediately by carefully
controlled freeze drying, was effective in preserving the
integrity of the linen, but also suggest that some salts
remain within the fibers. This study can be interpreted as
demonstrating the effectiveness of carbonates as buffering
agents for organic materials by showing that these materials
have aided in the preservation of Egyptian linen (a 4,000+
years natural ageing test!). However, this study also raises
questions about the advisabiliry of deliberately introducing
crystalline materials-salts-into fiber structures withinfluctuating environments. This has implications for the care
of archaeological textiles and the care of linen painting sup-
ports that have been sized with carbonate materials.
Daeeyo DE LA SUIERFICIE: MovruIcNto DE sALES
EN TEXTTLES ARQUEOL6GTCOS.
RESUMEN-La comprensi6n de la naturaleza fisica y
quimica del lino del antiguo Egipto, interesante de por si,
es tambi6n importante como prerrequisito para el exitoso
tratamiento de conservaci5n, exhibici6n y dep6sito del lino
arqueol6gico. Se hicieron pruebas de los tratamientos en
textiles arqueol6gicos que conten(an sales. Los resultados
indicaron que un lavado prolongado con agua para
remover sales, suciedades y dep6sitos orgdnicos; seguido en
forma inmediata por un secado por congelaci6n cuidadosa-
mente controlado, puede proporcionar excelentes resulta-
dos; sin embargo algunas sales permanecerin dentro de las
fibras.
Utilizando una combinaci6n de microscopia 6ptica
ESEM (Microscopio de Barrido Electr6nico Ambiental), IC
(Cromatografia Ionica) y XRDA (Andlisis de rayos-X de
Dispersia de Energia) para el an6lisis de muestras de fibras
individuales, de lino del antiguo Egipto, fue posible distin-
guir entre la fibra natural de lino y cualquier sal o materia
extrafla que el lino hubiera absorbido. Un avance exitoso y
productivo es indudablemente el uso de ESEM para la
observaci6n y el registro del movimiento de las sales dentro
de las fibras, en tiempo real, durante los ciclos de
hidrataci6n y deshidrataci6n.
Este estudio puede interpretarse como la demostraci6n
de la efectividad de los carbonatos como una barrera
neutralizadora para materiales org6nicos, demostrando que
estos materiales han ayudado en la preservaci6n de linos
egipcios (prueba de envejecimiento natural de mis de 4,000
aflos). Sin embargo, este estudio tambi6n genera inqui-
etudes acerca de la conveniencia de introducir deliberada-
mente materiales cristalinos-sales- dentro de la estructura de
las fibras en ambientes fluctuantes. Esto tiene implicaciones
para el cuidado de textiles arqueol6gicos y de soportes de
pintura en lino a los cuales se les ha colocado apresto con
materiales carbonatados.
l.INTRODUCTION
In order to understand the chemical and biological rea-
sons behind the survival of archaeological textiles it has
been necessary to look below the surface and to identify
what is present within the archaeological textiles. This
knowledge may help reveal how the fibers have interacted
with the archaeological deposit, and yield clues to the fac-
North American Textile Conseruation Conference 2002 ig\, 69
tors that have aided the preservation of the textiles. The
need for such investigation has been clearly highlighted by
\fild (1990) who stated that, "We talk glibly about tex-
tiles preserved in damp anaerobic peat-bogs or the dry
desert conditions of the Near East; but we still do not
understand fully the reasons why textiles survive in
archaeological contexts and therefore the treatment which
they require for that survival to continue." Once some of
the reasons why textiles survive in certain archaeological
contexts are understood, then it would be possible to
begin to determine the best methods of treatment for
archaeological textiles.
Most of the linen archaeologically recovered in Egypt has
come from burial or tomb environments. In the tombs of
the wealthy the deceased were supplied with all they would
need for their future lives, including the mummy wrap-
pings, clothing, andlor shrouds placed on the bodies as well
as supplies of linen clothing (often in large quantities)
stored in chests, boxes, or woven baskets (Hall 1985).
Another interesting observation here is that ancient
Egyptian tomb linen, both garments and mummy wrap-
pings, was often "used" prior to burial. Evidence for this
comes from laundry marks on the garments and also from
crease marks created by normal wear (Hall 1986). If the
garment or household linen had been used it has also been
probably washed, as Egyptians placed great emphasis on
the cleanliness of a person. This view is further supported
by Herodotus' (trans. '1,972) claim that linen cloth was kept
clean by constant washing.
Ancient Egyptian linens were usually washed in water,
either directly in the Nile or in pots alongside the river, with
natron, potash, or a vegetable derived soap called soapwort
(Saponaria officinalis) or some combination of these sub-
stances (Lutz 1923). However, in the Pharonic period
natron was the washing agent of choice. Soap, as we know
it, was not in common use until the Roman period. A letter
from the reign of Ramses II found at the workman's village
of Deir el-Medina, from a Scribe of the Tomb to the Scribe
Amenemope, succinctly describes the distribution system
for natron at that time:
As for Nakht-Sobki, I found no natron (i.e.,
'soap') in his possession- you (shall) give him
[... some...] ...When you know the [amount] that's
short, they can seek out natron for the cloths, and
you shall not (further) [allow] this failure to sup-
ply natron. For Pharaoh has assigned natron to
you-it just cannot be that he has not allotted it!(Kitchen 1982,197).
0.00 1.80 5.50
FrcunE, 1. AN EDXA spEcrRUM sHorvrNc THE pRocREsstvE
LovERING oF sALT LEVELs IN A sAMpLE oF ANCIENT EcvptlaNLrNEN DURTNG A 16-HouR vASHTNG rEsr. 1e.Tsp coNTRoL,
BEFORE ANY TREATMENT.
Natron is a natural soda, ideally a compound of sodium
carbonate and sodium bicarbonate in the proportion of one
molecule of each, (Na2 CO3- NaHCO3- z}{zo), but gener-
ally found in its natural state with a large proportion of
"impurities," including sodium chloride and sodium sulfate
(Lucas 1932). Also present are magnesium and various
metals and (other) salts. As natron or other materials were
used in the washing and bleaching process in ancient Egypt,
it is possible that residues from these cleaning agents may
have remained in the cloth.
$7hile conducting ageing studies of cellulose on archaeo-
logically recovered Egyptian linen obtained from museum
collections, Stoll and Fengel (1988) found evidence of salts
on the surface of linen fibers, which could have been
residues from natron washing. In that study they used energy
dispersive X-ray analysis (EDXA) to identify the compo-
sition of extraneous materials found in the linen fibers, and
were successful in using scanning electron microscopy
(SEM) to photograph salt crystals on the surface of fibers.
However, they were not able to demonstrate the presence
or otherwise of the crystals within the fibers. As the role of
natron in the preservation of linen was not the primary
focus of their work, they did not pursue the subject further.
From a review of the literature (Marsh-Letts 2002), itwas postulated that:
(a) linen textiles from ancient Egypt had often undergone
a form of mineralisation through washing treatments
involving natron and other soluble inorganic salts, as well
as through deposit in environments which contained alka-
line inorganic salts; and (b) this mineralization had con-
tributed to their survival by buffering them against acidiry.
This is consistent with Hardman's (1994) definition of min-
eralization as "the combination andlor replacement of the
7.20
70 .t?^' North American Textile Conseruation Conference 2002
t.2n6.402.101.60 6.'10 7.20 1.50 2.10 3.20
Frcunr, 1s. AN EDXA SPECTRUM oF
wes soexro rN Mrr-lr-Q IvATER FoR
THE SAME SAMPLE AFTER IT
1 Horrn.
organic matrix with an inorganic one." In order to test the
above propositions, samples of ancient Egyptian linen and a
number of control samples were examined before, during,
and after washing and drying trials by optical microscopy,
environmental scanning electron microscopy (ESEM), ion
chromatography (IC) and EDXA. Of main interest here
was the identification of both the presence and movement
of salts within the fibers.
2. EXPERIMENTAL2.1 LINEN AND NATRON SAMPLES
Control samples consisted of (a) new linen, (b) new linen
washed in natural natron, to replicate as closely as possible
the pre-deposit state of ancient Egyptian linen, and (c) sam-
ples of archaeological textiles from different archaeological
environments, for comparative purposes.
Small samples were collected from museum collection ofwell provenanced ancient Egyptian linen, as excavated and
without any treatment. These samples were taken from
linen fragments recovered from a variety of locations in
Egypt, and from as large a range of environments as possi-
ble. Other samples, of unknown provenance, were also
studied for comparative purposes.
Natron was collected from the Wadi Natrun (also called
the Wadi Natron), a depression in the Libyan Desert,
approximately northwest of modern Cairo that was an
ancient source of natron. The samples were collected from
one of the lakes in January 1.999.
2.2 -STASHING TRIALS
Linen samples were soaked ultra pure (Milli-Q) deionized
water. At intervals of 1.,2, 4, and 'J.6 hours the deionized
Frcunt 1c. EDXA SPEcTRUM oF
rNG rN cHANcEs or Mrllr-Q ronTHE SAME SAMPLE AFTER SOAK-
4 Houns.
water was drained off and the pH of the water was tested
with Merck pH test strips. Samples of the water were col-
lected for analysis by IC while small samples of the fabric
were cut from each linen sample; one to be air-dried and
the other freeze dried. These small textile samples were
examined, dr5 using ESEM and EDXA. Therefore at the
end of the trials samples were available which could show
when certain salts had been released into the wash water,
and exactly what salts remained in the fabrics at each stage
of the washing trials.
The pH of solutions was kept in the safe zone for linen
fibers, between 5.0 and 10.0. The presence of chloride
and/or bromide salts in solution may have played a part in
the tendency for some samples to swell and to disintegrate
during washing, however those sulfates present would have
retarded swelling (Florian 1987).
2.3 FP.EEZE DRYING AFTER THE \TASHINGTESTS
The object of freeze-drying samples was to see whether
there was any difference in the physical condition of the
freeze-dried fibers and the air-dried fibers of samples whose
original condition and subsequent treatment were otherwise
the same. The freeze-dried samples were examined using
optical microscopy and the results were recorded photo-
graphically.
2.4 INSTRUMENTAL ANALYSIS
A Phillips ESEM XL 30 equipped with an EDXA light
element energy dispersive X-ray detector and DX4 X-ray
analyzer was used for the ESEM and EDXA studies. APeltier cold stage was used for the dynamic hydration and
Nortb American Textile Conseruation Conference 2002 rSl- 71
FTGURE 2. ESEM TMAGES FRoM THE 16-soun TflASHING TEsr.
2a. ANcrEur EcvptreN LrNEN SoAKED rN cHANGES Eon MIllr-QDEIoNIZED vATER FoR 1 Houn, sHowtNc A cRUsr oF sALTS oNTHE FIBERS AND DAMAGE TO THE T'ISER.S. MECNIPICETION 8OOX.
Frcunl 2e. ANcrrNr EcvprraN LrNEN SoAKED rN cHANGES oF
Mrrlr-Q DEroNrzED VATER FoR 4 HouRS, sHowrNG suRFAcEs oF
THE FIBERS ro BE RELATIVELy UNDAMAGEI. MecNrptcertoN800x.
dehydration experiments. The computer software used was
eDX-ZAF. A video recorder was also attached to the system.
This integrated system was used at the Microanalysis Unit
of the Department of Science, University of Technology
Sydney (Australia). Analysis was undertaken with the assis-
tance of Miss Katie McBean and under the supervision ofthe head of the Microanalysis Unit, Dr. Matthew Phillips.
A description of the experimental procedure and results has
been previously published in Archaeological Textiles
I,Jetusletter (Marsh-Letts et al. 2001).
Ion chromatography uses ion-exchange resins to separate
atomic or molecular ions and detect these individually at a
detector, usually a conductivity detector. In this study IC
analysis was carried out using a DIONEX DX 120 withDIONEX Automatic Sampler AS40. For anions the eluent
used was 3.5 mM Na2CO3/ 1.0 mM NaHCO3. Flow rate
was 1..2 ml/min. Detection: Suppressed conductivity at 1.0
pL. The storage solution was the eluent. For cations the
eluent used was 20.0 mN methanesulfonic acid. The flowrate was 1.0 mVmin. Auto suppressed conductiviry was
used.
The ion chromatography was used to identify and quan-
tify the levels of salts present in "wash water" from the
ancient textiles. This enabled the determination of exactly
what salts were removed by various textile conservation
treatments. From this it was possible to chart the relative
amounts of salts released from the textile fibers. Any partic-
ulate materials that had not been removed by conservation
treatments from the fibers were subsequently examined by
transmitted light microscopy, scanning electron microscopy
or environmental scanning electron microscopy and also
identified by environmental scanning electron microscopy
coupled with energy dispersive X-ray analysis.
3. RESULTS AND DISCUSSION3.1 \TASHING TESTS
A wide review of the conservation literature (Marsh-Letts
2002) showed that ancient linens have been washed for
varying times, some as little as t hour and some as long as
16 hours, or even longer. Therefore it was decided to sam-
ple at varying intervals to determine the effects of stopping
the washing process at these times.
The results obtained from the 16-hour washing tests
showed that the washing of the ancient linen textiles
reduced the levels of some of the salts present, and the
reduction of the salt contents followed a paffern similar to
that known for the solubiliry of salts. Hence, the level ofsodium chloride, which was the most soluble salt present in
the samples, was reduced first. In general, the levels of salts
were reduced with the washing, but were not completely
eliminated from any sample.
The experience gained from the washing tests gives a
clear indication that sodium chloride is released very quick-
ly at the beginning of a washing treatment, as can be seen
in Figure 1 (a-c). The results clearly show that the levels ofsalt in the linen decreased progressively with further wash-
ings. While much of the salt content of an archaeologicaily
recovered textile may be washed out in the first one or rwo
hours of soaking, not all of the salts are washed out as
quickly. Hence, caution must be taken not to stop the
72 .t?1 North American Textile Conseruation Conference 2002
washing process early as the residual salt may still result
in considerable damage to the fibers upon drying. ESEM
observations of linen samples, one of which is recorded as
Figure 2 (a-b), indicates that salt laden ancient linen textiles
that were washed longer tended to show less fiber damage
upon drying.
Progressive washing had no visible effect upon new linen,
but was potentially detrimental to ancient fabrics, particu-
larly to those that were previously known to have had a
high salt content. This was because the fibers often became
very soft and fragile, and could not be safely moved or
manipulated while wet. This may be due to the removal of
salts that had entered the fibers, leaving gaps in the physical
structure. This is in contrast to historic fabrics without a
high salt content, which are generally amenable to manipu-
lation while in a damp or wet condition, in order to
reshape the textile and realign the warp and weft threads.
Therefore fabric samples had to be either carefully handled
when wet or not moved at all during the washing and
drying procedures.
3.2 FP*EEZE DRYING AFTER THE \TASHINGTESTS
The results of the freeze-drying of the linen samples showed
that rapid drying of samples appeared to have adverse
effects on the fabrics. At a normal rate of air drying the
textile disintegrated badly during drying and became like
paper pulp, even resembling paper pulp to the extent that
it retained the imprint of the drying screen after it had
hardened into shape.
In contrast the results obtained for slow freeze-drying
and vacuum freeze-drying of the linen samples appeared
to be successful to the naked eye. Freeze-drying (either
vacuum or slow) did not leave left any crust of dirt or debris
or crystals of salts on the surface of the fabric. However,
samples that were vacuum freeze-dried appeared to have a
greater tendency to powdering when moved or flexed.
3.3 ESEM STUDIES
The most exciting and productive advance in the analysis
of the linen samples was undoubtedly the use of ESEM
for the observation and recording of the movement of salts
within the fibers, in real time, during cycles of hydration
and dehydration. Figure 3 (a-c) shows this process using the
usual sample size, which was either 0.5 cm of one single
thread or a small square of representative threads taken
from the fabric. In some cases the dynamic record showed
crystals form and groq breaking through the surface of the
fiber. In other cases crystals formed in fissures in the surface
of the fibers that were already present, expanding the
fissures and causing damage to the fiber surface. This
evidence demonstrates clearly that salts in solution are car-
ried into the core of the linen fiber, through the porous sur-
face and/or breaks in the surface, and do not simply form on
the surface of the fiber. A comparison of the visual record for
the hydration and dehydration of ancient Egyptian fibers and
new fibers that were both treated with natron shows that the
relatively undamaged and flexible surface of new linen fibers
is more resistant to the penetration of salts in solution than is
the surface of ancient linen, where fissures allow an easy
pathway for the salts in solution. The presence of the fissures
in the ancient linen may have resulted from its use in ancient
times or from extreme desiccation.
Evidence from these studies would indicate that the type
and extent of damage is dependent on many factors, such
as: (a) the physical condition of the textile fibers, (b) the
amount and types of salt present in the fibers, (c) the range
and frequency of fluctuations of relative humiditS and (d)
the rate of hydration and dehydration of the fibers.
From a single cycle of hydration and dehydration the
damage for the new linen appears to be less than for the
ancient linen. Damage during cycles of hydration and dehy-
dration for ancient linen with a high salt content appears to
be higher than damage for ancient linen with a lower salt
content. Damage appears to be progressive with multiple
cycles of hydration and dehydration. This is consistent with
the behavior of salts during multiple cycles of hydration
and dehydration as Doehne (1.994), and Stambolov and van
Asperen de Boer (1,975) observed in studies of salt damage
in stone, building materials, and pottery as well as the
damage observed by $Tallert (1,996) in papyrus.
3.4 OBSERVATIONS AND RECOMMENDATIONS
This study adds further support to the findings of Barrow
and other paper conservators (Morrison 1979) on the effec-
tiveness of carbonates in buffering organic materials, partic-
ularly cellulose, against acid attacks by showing that these
materials have aided the preservation of Egyptian linen over
thousands of years. It suggests that the preservation of ancient
Egyptian linen has been a 4,000+ years natural ageing test,
as opposed to the artificial heat ageing tests that rwentieth-
century conservators used to prove the effectiveness of
deacidification solutions in the preservation of paper
(Morrison 1979). However, it raises other questions about
the advisability of deliberately introducing crystalline mate-
rials-salts-into fiber structures within fluctuating envi-
ronments. Changes in temperature and humidity may cause
the salts to move within the fibers, causing mechanical
North American Textile Conseruation Conference 2002 .gr, 73
abrasion and damage, or widening fissures within the fiber.
This study also raises questions about the introduction of
materials that will be crystalline in structure and relatively
rigid within what was created as a flexible fabric. This has
implications for care of all textiles treated with deacidifica-
tion solutions and also of linen painting supports which
have been sized with carbonate materials, where fluctua-
tions of humidity will cause movement of fibers through
swelling of the fibers (intake of moisture). This movement
may cause abrasion of the fibers as they move in relation to
hard, crystalline particulate matter. Furthermore, once solu-
ble salts are introduced into linen the evidence cited above
shows that it may be very difficult if not impossible to
remove all salts from the fabric in the future without severe
disruption of the fibers.
Therefore, the following recommendations could be
made:
r It would be advisable to store and display linen from
Ancient Egypt in stable, low humidity environments, in
order to prevent the deliquescence and recrystalization ofany salts within the fibers.
r Before any ancient linen undergoes any vapor or other
aqueous treatment the salt content of the fibers could be
checked using ESEM with EDXA to determine the level of
salts and to assess the physical condition of the linen fiber.
r The deliberate introduction of salts to linen fabrics
through deacidification procedures should receive careful
consideration, and could be the topic of further research.
4. CONCLUSION
It has been demonstrated that the analytical techniques ofIC, ESEM and EDXA can be used together with optical
microscopy for the examination of linen in order to assess
its chemical and physical nature prior to any conservation
treatment, or when considering environmental conditions
for the storage or display of linen textiles. lfhile optical
microscopy and SEM were able to identify fibers, and both
ESEM and IC were able to record the chemistry of each
sample, only ESEM was able to demonstrate the processes
of salt movement (deliquescence and crystallization) withinfibers. These methods can therefore show the level of fiber
damage akeady experienced by the specimen fiber, and so
give an indication of the relative strength of the textile
fibers. The methods can also be used to monitor any con-
servation treatment of textiles for salts, enabling the wash-
ing process to be carefully monitored for effectiveness.
Frcunr, 3e. AN ESEM rMAcE oF A SAMpLE oF ANCTENT
EcvprreN r.rNEN BEFoRF- HvDRATToN. MecNrrrcntloN 400x.
ACKNOWLEDGMENTS'We would like to express our thanks to Dr. Eric Doehne
of the Getty Conservation Institute, Los Angeles, USA, forinitially demonstrating the range and possibilities of the
Environmental Scanning Electron Microscope for the
study of salts.
The assistance of Dr. Matthew Phillips of the University
of Technology, SydneS who shared the first experience ofusing ESEM and EDXA to look at mummy cloths, was
essential to this study. We would also like to thank Dr.
Andrew Hadjichari, Mr. Chris Myors, and Mr.MartinCraine of the University of \Testern Sydney, and Miss Katie
McBean of the Universiry of Technology, Sydney who have
provided very welcome, and always able, analytical support
for this project.
Most grateful thanks go to the Museum of Ancient
Cultures, Macquarie University, and the Nicholson
Museum of Antiquities, The University of Sydney,
Australia, for their permission to examine their collections
of Ancient Egyptian linen.
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74 .t?) North American Textile Conseruation Conference 2002
Frcunr 3s. AN ESEM rMAcE sHowrNc rHE SAME FTBERS As
Frcunl 3 a). Tsr IMAGE sHows rHE SvELLING oF A FTBER DUR-
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Frcunr 3c. AN ESEM rMAGE sHowrNG THE sAME FTBERS As
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rNG FoRMATToN oF cRysrAt-s. MecNrrrcerroN 643x.
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Conservator, April 1988, held by the United Kingdom
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London: UKIC. No. 10:3-4.
North American Textile Conseruation Conference 2002 .'$- 75
GLENNDA SUSAN MARSH-LETTS originally trained
as an archaeologist. She holds a M.App. Sc., Materials
Conservation, from the Universiry of Canberra and has
recently completed her Doctoral dissertation, "Ancient
Egyptian linen; the role of natron and other salts in the
preservation and conservation of archaeological textiles"
at the University of .Western
Sydney, Australia. She has
worked as a paper, textile, and archaeological conservator,
and has also lectured in materials conservation at the
University of 'Western Sydney and the University of SydneS
Australia. Address: 1 Silva Road (Corner of George and
Silva), Springwood, New South'Wales, 2777 Australia;
Telephone: +61 2 4751.3013;
email: [email protected]
SAMUEL B. ADELOJU is a Professor of Chemistry and
Environmental Science at the University of Western Sydney
(tl\fs). He holds a Ph.D in Electroanalytical Chemistry
from Deakin Universiry Australia and has been the
Director of the Center for Electrochemical and Analytical
Technology at UlfS since 1988. He is also the Program
Leader for the Research Training Concentration in
Environmental and Materials Technology at the universiry.
He was the recipient of the 1.997 Royal Australia Chemical
Institutet Citation for outstanding contributions to the pro-
fession and the institute, and the 2001 Eckart Australia
Visiting Professor at the University of Tasmania. Address:
School of Science, Food & Horticulture, University ofWestern Sydneg Building I Locked Bag 1.797 , Penrith
South DC, NS\f 1797, Australia; Telephone: +61.2 4736
0811; email: [email protected] (7
76 .t?^' Nortb American Textile Conseruation Conference 2002