Acrylic emulsion paints have been widely used by artists since their development in the late 1950s. This paper reviews the conservation information that currently exists about them. Brief descriptions are given of their development and how they are analysed, but the focus of this review is on current conservation concerns about their physical properties, how they will age and the effects of cleaning.
Acrylic emulsion artists’ paints were received with much fanfare and excitement in the 1950s and 1960s. They embodied the characteristics that many artists had been searching for at that time, affording a means of expression that was distinct from oil painting and its associated history and traditions. As Kenneth Noland described it, ‘there was an urge to loosen painting. [These colours] released new kinds of tactile qualities’.1These synthetic paints produced films of great clarity and phenomenal elasticity, were easy to manipulate, could be painted directly onto supports, dried quickly, were thinned with water and exhibited high resistance to ultraviolet degradation. John Hoyland recalled, ‘I remember reading articles in magazines. They talked about the radiance of [acrylic paint] and the fluidity of it and that it would never yellow. It seemed exciting in the way people got excited about the use of plastics, aluminium and other industrial materials’.2 Helen Frankenthaler, who switched from using oil paints to acrylic emulsions in the early 1960s, said:
I changed to acrylics for a number of reasons. Once, I was told that they dry faster, which they do, and that they retain their original colour, which they do. I would say durability and light and the fact that one can use water instead of turpentine: all that makes it easier given the abstract image. As painting needed less and less drying time, depth, and so forth, the materials came along that made that more obvious.3
In spite of their outstanding mechanical and aging properties, acrylic emulsion paintings do suffer damage, often through external influences. Within the conservation profession, concerns were soon raised as some of these newly painted works began to require cleaning and repair.45 Similar themes were discussed in the following decades.678
Essentially, three fundamental problems were identified. The first was that most conservation treatments had been designed for traditional paintings in oil and were found unsuitable for acrylic emulsion paintings, due in particular to the high sensitivity of these synthetic paints to the majority of organic solvents and heat. The second was the complete lack of knowledge about acrylic emulsion systems, especially the complexity and constant changes to the formulas, with insufficient information coming from the manufacturers of both raw materials and artists’ paints. The third was that damage may be especially noticeable in colour field or monochromatic paintings, disrupting the delicate surface texture, colour or gloss,1910 all of which are often integral to the artists’ intent and can be altered by even the slightest contact. Even small damages can therefore soon become ‘unacceptable’. Since remedial treatment is so difficult with acrylic paintings, preventive conservation is crucial.11
In general, very few studies of the conservation of acrylic emulsion paintings have been published. Instead, concerns tend to be communicated through informal discussion. The intent in this paper is to review the majority of available information from the conservation literature and to encourage further discussion and research by conservators, conservation scientists, paint manufacturers and artists. It should be stressed that this review only takes into account publications in the English language. Naturally, a broader understanding of the subject would be possible from surveying material written in other languages, in particular German texts by Röhm, who first reported the production of a solid acrylic polymer in 1901 and developed a commercial synthesis of acrylate esters in 1927.1213 The authors also do not review the incredible developments that have taken place with organic and inorganic pigments, although good accounts by de Keijzer and Marontate, for instance, already exist.1415
The conservation concerns with acrylic paint media tend to fall into four categories and will be presented as such, beginning with the development of water-borne acrylic artists’ paints, and followed by paint properties, aging properties and issues associated with cleaning.
The development of water-borne acrylic artists paints
Henry Levison, a chemist-turned-paint maker, founded the company Permanent Pigments in 1933, which produced the first line of waterborne acrylic emulsion paints called Liquitex® in 1954.16 He often supplied artists in exchange for soliciting their advice, occasionally hiring them as consultants or staff. The development of Liquitex® came not long after the introduction of the first artists’ acrylic paint, Magna®, by the paint makers Leonard Bocour and Samuel Golden in 1947. Magna® acrylic paints were solution paints and quite distinct from waterborne emulsion paints. In practical terms, Magna® dried quickly by evaporation of an organic solvent; it remained resoluble in many hydrocarbon solvents as well as further layers of paint and could be blended with oil paint.171819 In contrast, the drying process of emulsion paints involves a complicated coalescence of emulsified polymer spheres after an initial evaporation of water. These paints become insoluble in water – and further layers of emulsion paint – after they have dried.
Confusingly, many terms are used to refer to waterborne acrylic paints, such as acrylic emulsions, latex, and polymer colours. In fact, technically, they are dispersions rather than ‘emulsions’, because they are composed of tiny beads of solid, amorphous polymer suspended in water. The fact that these paints could be diluted and thinned with water, instead of mineral spirits, made them – and continues to make them – very appealing to artists. The raw polymer emulsions used by artists’ colourmen and paint makers were frequently those from Rohm and Haas’ Rhoplex® series of products (known as PrimalTM in Europe), such as AC-22, AC-33, AC-234 and AC-634. Rhoplex® AC-33 first became available in 1953. All of these emulsions were copolymers, utilising the harder methyl methacrylate (MMA) and softer ethyl acrylate (EA) to create the required working properties, such as flexibility as well as durability for house paints, satisfying their primary market. Since the end of the 1980s many of the resin formulations have changed to a poly (n-butyl acrylate/methyl methacrylate) copolymer, such as Rhoplex® (or PrimalTM) AC 235. In the form of a paint film these tend to be slightly tougher and more hydrophobic than the poly(EA/MMA) resins, making them more durable to outdoor exposure. Styrene has sometimes replaced, either partly or entirely, the MMA component to save on manufacturing costs.202122
Acrylic emulsions contain a multitude of additives that determine the performance properties of the paint, from shelf life, application and longevity, to properties affecting health and safety.23242526 Additives are introduced at two distinct stages of production: during the manufacture of the emulsion polymer and during the formulation of the paint itself. With the exception of a few volatile additives (see below), all additives remain in the dry paint film. Research into their interaction with the binder is therefore necessary for a complete understanding of the aging properties and effects of treatment on acrylic emulsion paints. However, almost nothing has been achieved towards this, either analytically or from manufacturer’s information, on their precise identity. While the paint formulator knows the basics of these materials, the additives themselves contain proprietary materials and are constantly changed to meet the needs of the large coatings industry.2427
Additives in the emulsion binder
- Initiators are used as a source of free radicals to initiate the polymerisation process, in which monomers condense to form the polymers. These are most often persulfates, eg. potassium persulfate,28 which thermally decompose to form free radicals. The polymer manufacturer may also use a redox system, adding ferrous and thiosulfate along with the persulfate salts, to allow for room temperature reaction.29
- Chain transfer agents are incorporated to aid in controlling/limiting molecular weight (MW) during polymerisation, eg. dodecyl mercaptan.30
- Buffers, typically ammonia, are added to maintain a pH between 8 and 10, for maximum dispersion stability of the acrylic polymer.
- Surfactants are a critical group of components, necessary to create the micelles for particle formation and long-term particle stabilisation. Common surfactants are non-ionic (eg. alkyl phenol ethoxylates) and anionic (eg. sodium lauryl sulfate or dodecylbenzene sulfonate) that are typically added at 2 to 6% by weight (%/wt).25 These provide stability through electrostatic and steric hindrance mechanisms.
- Protective colloids also contribute to steric stabilisation and are water-soluble natural or synthetic polymeric emulsifiers such as hydroxyethylcellulose and polyvinyl alcohol, added in 1 to 10%/wt.
- Preservatives are generally added in low doses (less than 1%/wt) to protect against the growth of microorganisms, commonly methyl benzisothiazolinones, chloromethylisothiazolinones, barium metaborate and formaldehyde donors, such as 1-(3-chloroallyl)-3,5,7-triaza-1-azoniaadamantane chloride.
- Residual acrylic monomers are also present at 50 to 1000 parts per million or so, resulting from incomplete polymerisation.
Additives utilised by paint formulators to achieve the intended performance properties
- Wetting and dispersing agents are added to wet pigment surfaces, allowing pigment agglomerates to break apart – a critical process in developing colour strength – and providing steric and/or electrostatic stabilisation of the pigments. Typical wetting agents include alkyl phenol ethoxylates, acetylenic diols, alkylaryl sulfonates and sulfosuccinates.31These are similar to the surfactants used during polymerisation. Dispersing agents are typically polyphosphates (generally calcium or potassium salts of oligophosphates with two to six phosphate units) or polycarboxylates (sodium and ammonium salts of polyacrylic acids, 2,000 to 20,000 MW).32
- Coalescing solvents are added to ensure film formation under varying atmospheric conditions. They are slow evaporating solvents with some solubility in the polymer phase. They act as a temporary plasticiser, allowing film formation at temperatures below the system’s glass transition temperature (Tg) for the system,33 after which they slowly diffuse to the surface and evaporate, increasing the hardness and block resistance of the film. Typical coalescents are ester alcohols, e.g., Texanol® (Eastman Chemical Co.), benzoate esters such as Velate® (Velsicol Chemical Co), glycol ethers, glycol ether esters and n-methyl-2-pyrrolidone.
- Defoamers are necessary to reduce the inherent tendency of emulsions to foam, a consequence of incorporating surfactants. Typically these are mineral oils or silicone oils, the latter (polydimethylsiloxanes) are much more efficient and active, but more likely to produce film defects (craters, fisheyes, etc.). The mechanism by which defoamers function is not fully understood, but these very hydrophobic materials are thought to move to the air/liquid interface, allowing the air to release.3429
- Preservatives, although typically included in acrylic emulsions, are supplied in additional quantities and are introduced to avoid dilution as water and other components are added.
- Thickeners and rheology modifiers are required to achieve the desired viscosity and flow properties. Thickeners function through multiple hydrogen bonds to the acrylic polymer, thereby causing chain entanglement, looping and/or swelling which results in volume restriction. The most common group is that of cellulose derivatives, including hydroxyethylcellulose, methylcellulose and carboxymethylcellulose. Also important are alkali-swellable polyacrylate emulsions, which add considerable viscosity upon neutralisation with an appropriate base (such as ammonia). Polysaccharides such as xanthan and guar gums are also used. A relatively new group of organic rheology modifiers – altering rheological properties more than building viscosity – is that of hydrophobically-modified ethoxylate urethanes (HEURs). Inorganic thickening agents can also be used, such as forms of bentone clays, including the bentonites, smectites and attapulgites, and fumed silicas.
- Freeze/thaw stabilisers are added to prevent the freezing of a waterborne paint, avoiding the formation of ice crystals that would disrupt the dispersion stability and causing permanent damage through polymer coagulation. The incorporation of 2 to 10% ethylene or propylene glycol ensures that water, surfactants and protective colloids will return to the acrylic emulsion surface in an orderly way.30
Identification and analysis
There is a need for conservation-driven research, publications and interviews with artists about their chosen materials, reasons for using them and thoughts on the conservation of their work. Several papers have presented the history of the manufacture of artists’ acrylic paints and their commercial introduction to artists.311635 Marontate presented in-depth interviews with paint manufacturers and examined their early concerns for the durability of the materials, and participation in groups such as the American Society for Testing and Materials.14 Lodge and Barclay presented concise reviews of the history of synthetic paints in the hands of artists.1735 In addition to charting the manufacturing history of synthetic paint media, Crook and Learner conducted detailed studies of several artists, their materials and the construction of their paintings.36
Several museums have established programs of artists’ interviews either on audiotape or video, or through written questionnaires about specific artworks, typically upon their acquisition. Many issues can complicate the gathering of such information, for instance, the artist may not recall the exact materials or may provide contradictory information.373839404142All of these issues were extensively considered and a methodology of interviewing artists proposed in the symposium and publication, Modern Art-Who Cares?434244 The importance of using scientific analysis to confirm an artist’s recollections has been stressed.36
Several papers have now appeared on methods of scientific analysis and chemical characterisation of acrylic emulsion paints. Essentially, it is now possible to identify the major components in an acrylic paint, e.g. binder, pigment and extenders. The three main techniques have been Fourier transform infrared (FTIR) spectroscopy,13212645464748495051 pyrolysis – gas chromatography (Py-GC)265253 and pyrolysis – gas chromatography – mass spectrometry (Py-GC-MS).13214547 In addition, direct thermally-resolved mass spectroscopy (DTMS) has been shown to be effective at identification of acrylic binders and the majority of pigments.1354 However, the use of ultraviolet (UV) fluorescence microscopy staining gave inconsistent results for layers of acrylic in cross-sections,26 perhaps an inevitable consequence for such complex formulations. The analysis of additives, however, is very scarce; with the exception of recent FTIR studies, which have identified polyethylene glycol (PEG)-type surfactants.5556 This may support the presence of alkyl phenol ethoxylate surfactants, which are common in the coatings industry.
Other characteristics of acrylic emulsions have also been studied. The relative proportion of each monomer in copolymer emulsions was measured by nuclear magnetic resonance (NMR)57 and thermomechanical analysis (TMA).12 Molecular-weight distributions of the soluble component and an estimate of the degree of cross-linking in dried films were made by size exclusion chromatography (SEC) and thermogravimetric analysis (TMA).5556 Scanning electron microscopy (SEM) has also been used to document film coalescence and topography.585960
The basic process of film coalescence has been described frequently in the conservation and paint industry literature, though authors acknowledge the over-simplification of this model and the need for further research6162636465666768Acrylic emulsions are composed of particles of amorphous polymer suspended in water. The two-phased system is held in suspension by surfactants and/or other surface stabilisers. During drying, water evaporates to draw the spherical polymer particles closer, which then meld together to form a ‘honeycomb’ network. A coalescing-solvent additive ensures that the polymer particles remain malleable during – and after– this process, to produce more complete compaction, even after the water has evaporated. Eventually, the boundaries between particles become barely detectable and the film is considered continuous. However, it has been shown that pores or micro-voids are often left within the film, readily seen with light microscopy and SEM.2661697071727374minimum film formation temperature (MFT), modulus of elasticity and viscosity of the resin, as well as the function of additives such as coalescing agents.66467 Paints left to dry slightly below their Tg and MFT will result in films of higher porosity. A paint drying significantly below its Tg will form a loose, powdery layer.
Film porosity and pin-holes
The porosity of acrylic emulsions was exploited early on in the coatings industry. Acrylics were ideal as coatings for wood because they allowed water vapour to pass through them, reducing the risk of delamination.6467 However, porosity in an artwork coating has obvious conservation implications: dirt and air pollution may become trapped, making removal difficult and providing a haven for biological growth.757677
Similar concerns have been raised about pin-holes, or craters.24266469717879 These defects are often produced in emulsion paints as a result of the foam created during both manufacturing and application,2426 although this phenomenon can occur in other types of paint, even oil-based media. It has also been suggested that voids may trap conservation cleaning agents through capillary action, possibly causing long-term damage.79 In the case of outdoor murals, efflorescence of the substrate or the formation of ice crystals can occur, causing a build-up of material on the surface or between the coating and substrate.64697180
A phenomenon sometimes observed in clear acrylic emulsion films is haziness. Under natural and accelerated aging conditions, haziness was observed in young films of Liquitex® Acrylic Gloss Medium.56 The haziness was composed of microscopic spherulitic crystals on the surface of the acrylic film, as characterised by light microscopy. These water-soluble crystals formed as the temperature and relative humidity (RH) to which the films were exposed increased. FTIR revealed that the crystals contained compounds similar to those found in PEG of about 1500 MW. It was predicted that crystals might develop if the temperature was between the melting point of the crystalline material and the Tg, of the polymer. At that point, the PEG-type material would be free to migrate through the film and crystallise. Proposed temporary solutions were either to raise the temperature of the film, melting the crystals once formed, or to keep the film temperature below its Tg, eg. to prevent crystal formation. The risks associated with both techniques were mentioned.
A different type of haziness or cloudiness has also been reported, which can occur during the drying process before all the water has evaporated or when coalescence is incomplete, leaving pores or micro-voids within the film.616981717282
The temperature sensitivity of acrylics can be problematic, especially while paintings are in storage or transit. Their low Tg makes them rubbery at room temperature, attracting dirt and airborne pollution. High temperatures and RH can cause packing materials to stick to the surface. In one reported instance,83 an acrylic painting on paper became adhered to its PerspexTM glazing, although separation was possible through localised applications of a heated spatula to the front of the PerspexTM.
Low temperatures and RH are particularly damaging, as they can cause a significant decrease in elasticity of the paint film and consequent cracking of the paint upon flexing, as demonstrated by Erlebacher et al.8485 Emulsion films were exposed to various temperature and RH combinations and their strength, modulus and elongation at break were measured. In general, the strength and stiffness of the films increased as the temperature and RH decreased, particularly under conditions of 40 to 50% RH at 15 °C and below. However, at very cool temperatures, such as -3°C, the strength actually began to decrease, as well. At 40% RH, brittleness occurred in some colours at 5 °C, but at 5% RH this figure could rise to as high as 11°C. The warning was clear: cold temperatures and low RH, conditions that are feasible in winter, make acrylic emulsion paintings brittle and susceptible to cracking.
Conversely, a warm, humid environment, even if only experienced during shipment, can encourage mould growth, as reported by Gatenby.86 In this case, loose mould and dirt were removed by dry brushing and vacuuming and then with distilled water and non-ionic surfactant. However, this treatment was complicated further by the matte and powdery nature of the paint; the mould left black stains in some areas of the paint.
Properties of additives
Although most additives remain to be studied in-depth, recent attention has been focused on the effect of the surfactants. These have been located in dried films, especially within the subtle boundaries among the coalesced polymer beads.636667698788 It has also been suggested that surfactants (and other additives) migrate to both the surface of the film and the film/substrate interface.896590918892939495969798 The migration occurs at several stages: first, during application of the paint to the substrate, as a way of breaking the surface tension and allowing the paint to wet-out the substrate.9596 because porous substrates can absorb surfactant;99100second, during drying of the paint film when capillary action forces water and water-miscible additives to the film surface;71101 and third, after drying upon elongation of the film.96 Surfactants on the film surface may change its gloss, both in degree and uniformity, may cause adhesion failure of varnish25 and may harbour dirt and biological growth.102 Surfactants are also likely to foam and be susceptible to removal during surface cleaning.259293 The effect of a surfactant on the mechanical properties of the dried film has only recently been investigated.103
Clear acrylic paint media were observed to yellow or discolour slightly in three studies. In the first, an artist had observed yellowing of Golden® clear acrylic medium in one of his paintings, prompting a joint research project between Golden Artist Colors, Inc. and the Buffalo State College Art Conservation Program.104 A variety of non-pigmented artists’ acrylic media were subjected to both natural and accelerated aging. Discoloration was noticed in the samples applied to cotton and linen supports, more so than in those applied to glass. The discoloration appeared shortly after the samples had dried naturally; accelerated aging did not significantly increase yellowing. The discolouration was attributed to the migration of components from the support into the medium during drying. The water in the media dampened the support and components within, such as size, dirt and degradation products, and, upon evaporation through the film surface, pulled the decolourants into the media. This support-induced discoloration (SID) can be avoided by thoroughly washing the canvas or linen with water before use.
Yellowing of clear acrylic emulsion media was also noticed during another study.105 The samples of clear acrylic media, supported on glass plates, exhibited slight yellowing (and an increase in UV fluorescence) after natural aging in the dark, after light aging and after oven-ageing. The yellowing was more intense in the thickest areas of the film and not confined to the surface. During the aging process, the films were submitted to periodic solvent extraction to monitor changes in MW through viscosity. The increase in yellowing coincided with a decrease in solubility. Naturally aged films became increasingly insoluble in benzene two weeks after application, exhibiting partial swelling instead, and after 60 days the samples became so insoluble that elevated temperatures were necessary for dissolution. The yellowing was attributed to slight cross-linking of the film. It was proposed that even though chromophores are not present in the initial formulation of the acrylic, their development may be catalysed by other reactions within the film.
Finally, in an additional study by Whitmore et al,106 the yellowing of clear acrylic films in the dark was explored, providing evidence that they can be bleached in the light, to varying degrees, as can oil paint; films with SID are less susceptible to light-bleaching.
Cross-linking and oxidation
Cross-linking in waterborne acrylic emulsions can occur at three stages: during the polymerisation/production of the raw polymer resin; during drying/coalescence of the paint film; and during aging (both natural and accelerated) of the dried film. Acrylic emulsions can be formulated to undergo varying degrees of cross-linking during drying, depending on the end use of the product, using additives called cross-linkers. However, these are not thought to be present in artists’ emulsion paints.5866107 Instead, the high MW of the polymer is enough to provide high film strength from chain entanglement.10866 It has been reported that during aging, a film can cross-link and oxidise as a result of photo-degradation and from the effect of residual surfactant.99 However, while Chiantore detected cross-linking in sample films, both before and after aging, oxidation products were not found.92 The principal consequences of cross-linking are an increase in brittleness and hardness,99109 which may actually improve the film’s resistance to dirt pick-up and abrasion.
Effect of pigments
Inclusion of pigments tends to stabilise the binder, as they are often effective UV absorbers. Inorganic pigments tend to offer improved durability in comparison to the organics. Titanium dioxide is probably the most studied pigment. Of the two different crystalline forms, rutile, rather than anatase is appropriate for exterior paints because it is far less reactive to ultraviolet radiation. Anatase, which is highly reactive to ultraviolet radiation, can form radicals and degrade the polymer.32
Recently, Klein conducted a census to ‘determine the most commonly used methods and materials used by painting conservators in their treatment of acrylic paintings’.110 Out of 190 surveys sent to paintings conservators in North America, only 31 were completed. In addition, 41 letters of refusal were returned, citing reasons such as insufficient experience in treating acrylics and lack of time or staff to fill out the survey. It was confirmed that many conservators treat acrylic artwork with products and techniques developed for traditional paintings and more conservators considered themselves ‘self-taught’ in the treatment of acrylic paintings as opposed to being trained through their university program. By far the most common treatment problem encountered on both unvarnished and varnished paintings was some form of cleaning, typically requiring the removal of dirt or marks from vandalism. A wide range of cleaning materials and methods were identified, principally dry methods, such as brushes and erasers, and aqueous methods, e.g. saliva or water, often with small additions of ammonia, surfactants or triammonium citrate, or even baby wipes. However, a range of organic solvents and solvent gels were also cited. Some of the major concerns of the participants were the difficulty of grime removal, the sensitivity of the paint, leaching during aqueous cleaning, identifying the specific components of the media, the application and future removal of varnishes and the protection of unvarnished paintings from deterioration.
Affinity for dirt pick-up
Frequently mentioned in the literature, yet rarely analysed, is the tendency of an acrylic emulsion paint film to imbibe surface dirt. Dirt can come into contact with the painting through airborne pollutants,111 handling (eg. fingerprints) and accidents or vandalism. It has been suggested that indoor air pollution, accumulating gradually on a painting surface, may take approximately 50 years to become perceptible to the human eye.93112 The principal factors thought to affect the attraction of dirt to acrylic paintings mentioned in the literature include:
- Tg, MW, MFT and softening point of the acrylic resin. If all are low, then the resulting film exhibits a low hardness at room temperature, forming a tacky ‘trap’ for incidental dirt.617113114
- static charge. Acrylic paint films are non-conductors and therefore can accumulate a static charge, attracting dust from the air.115
- pigment concentration. It has been suggested that high pigment load can block dirt pick-up.116 However, it is likely that the uneven surface resulting from a paint of high pigment load would trap dirt mechanically and therefore significantly increase the difficulty of dirt removal.
- hydrophilic additives, such as surfactants. Such additives located at the film surface can attract and imbed dirt particles.117
Sensitivity to solvents
The sensitivity of acrylic emulsion paint films to organic solvents clearly limits a conservator’s choice of cleaning techniques, consolidants, inpainting materials and options for varnishing and varnish removal. There is difficulty in removing imbedded grime without disturbing the surface texture, colour and gloss. Mechanical cleaning, such as with eraser crumbs or a molecular trap like Groomstick!TM are sometimes used before testing wet-cleaning techniques,86118and have been investigated by Saulnier.119
Solubility tests have been proposed as a simple form of analysis/identification preliminary to more complex instrumental techniques.47120Nielsen discussed such solubility tests during forensic investigations.120 Small quantities of unknown samples to be identified were exposed to solvents to view the following phenomena: bleeding of organic pigments, swelling, dissolution of the film, and effervescence from carbonate extenders and other additives. The reactions were compared with the reactions of control samples for initial characterisation before further tests were conducted. The necessity of building a library of identified standards is often stressed.2647121
Sensitivity to water
Even water or water-based cleaning methods can impact the paint surface. Acrylic emulsion films can remain soluble in water up to a week and beyond after application. Upon drying, they become less soluble in water.61646787101 However, it is widely known among conservators of modern paintings that acrylic emulsion films remain sensitive to swelling by water. A recent study by Murray et al tested the effect of several water-based cleaning agents on the dimensions and mechanical properties of acrylic emulsion paint films.118Sample films of cobalt blue paint were submersed in water-based cleaning agents for either one minute or one hour and then left to dry. One percent solutions of Orvus® WA Paste and Aerosol® OT (both anionic surfactants), TritonTM X-100 (a non-ionic surfactant) and triammonium citrate (a chelating agent with a pH of 7.2) were tested, all commonly used and visually effective cleaning agents. Immersion, though not a conservation cleaning technique, is a repeatable test that may indicate the effect of multiple cleanings on a painting and/or any residual cleaning agent left in the film, as well as results from disaster conditions.
An interesting conclusion was that samples immersed for one minute showed weakened mechanical properties compared to those immersed for an hour. It was concluded that in one minute, only limited penetration of the cleaning solution into the paint sample was possible, causing expansion of the outer surface, but not the core, stressing the sample prior to mechanical testing. However, an hour’s immersion allowed the solution to reach and react with all parts of the sample, leaving the sample uniform in condition and in reaction to mechanical testing. After the minute-long immersions and subsequent drying, the sample volumes had increased, mostly due to an increase in thickness, however, after the hour-long immersions the samples returned to the original volume; indications were that after longer immersion times the thickness and volume would decrease further.
Although discussion about the conservation of these paintings has taken place almost since the introduction of artists’ acrylic paint, there is clearly a lack of information on these materials and works of art that is relevant to conservation. It is important to continue research and to share the information among conservators, conservation scientists, artists’ materials manufacturers and artists. In terms of future research, a fuller understanding in two broad areas is needed: 1) the structure and components of acrylic paints, in and of themselves, including the individual properties of additives and their interactions, and 2), the effect of outside influences on the film, such as ageing, abrasions, dirt pick-up and dirt location within the film strata, wet and dry conservation cleaning techniques, as well as the paint film’s interaction with other materials such as priming and varnish.
- 1. a. b. Kenneth Noland, personal communication, 2003.
- 2. Jo Crook and Tom Learner, The Impact of Modern Paints, London 2000, p.101.
- 3. Emile de Antonio and Mitch Tuchman, Painters Painting: A Candid History of the Modern Art Scene, 1940–1970, New York 1984, p.82.
- 4. Caroline Keck, ‘Conservation of Contemporary Art’, Museum News, January, 1960, pp.34–7.
- 5. Louis Pomerantz, Is Your Contemporary Painting More Temporary Than You Think?, A Chicago Chapter Artists Equity Publication, Chicago 1964.
- 6. a. b. c. Carolyn Lamb, ‘Acrylics: New Material, New Problems’ in The Conservation of Modern Paintings: Introductory Notes on Papers to be Presented, United Kingdom Institute for Conservation (UKIC) and Tate Gallery, London 1982, pp.4–6.
- 7. Robert Lodge, ‘A History of Synthetic Painting Media with Special Reference to Commercial Materials’, in S. Rosenberg (ed.), Preprints of Papers Presented at Sixteenth Annual Meeting, New Orleans, June 1–5 1988, American Institute for Conservation, Washington, DC, 1988, pp.118–27.
- 8. Margaret Watherston, ‘The Cleaning of Color Field Paintings’, in E. Carmean (ed.), The Great Decade of American Abstraction: Modernist Art 1960 to 1970, Museum of Fine Arts, Houston 1974, pp.119–29.
- 9. Margaret Watherston, ‘The Cleaning of Color Field Paintings’, in E. Carmean (ed.), The Great Decade of American Abstraction: Modernist Art 1960 to 1970, Museum of Fine Arts, Houston 1974, pp.119–29.
- 10. Louise Wijinberg, ‘Problems of Perfection’, in Ysbrand Hummelen and Dionne Sillé (eds), Modern Art: Who Cares?, Foundation for the Conservation of Modern Art and the Netherlands Institute for Cultural Heritage, Amsterdam 1999, pp.362–3.
- 11. Liesbeth Abraham, ‘Treatment is Almost Impossible’, in Ysbrand Hummelen and Dionne Sillé (eds.), Modern Art, Who Cares?, Foundation for the Conservation of Modern Art and the Netherlands Institute for Cultural Heritage, Amsterdam 1999, pp.364–6.
- 12. Sheldon Hochheiser, Rohm and Haas: History of a Chemical Company, Philadelphia 1986.
- 13. a. b. c. d. Tom Learner, ‘The Characterisation of Acrylic Painting Materials and Implications for their Use, Conservation and Stability’, PhD thesis, University of London 1997.
- 14. Mattheis de Keizjer, ‘The History of Modern Synthetic Inorganic and Organic Artists’ Pigments’ in J. A. Mosk and Norman Tennant (eds.), Contributions to Conservation: Research in Conservation at the Netherlands Institute for Cultural Heritage (ICN), London 2001, pp.42–54.
- 15. Jan Marontate, ‘Synthetic Media and Modern Painting: A Case Study in the Sociology of Innovation’, PhD thesis, University of Montreal, Montreal 1996.
- 16. a. b. Jan Marontate, ‘Synthetic Media and Modern Painting: A Case Study in the Sociology of Innovation’, PhD thesis, University of Montreal, Montreal 1996.
- 17. a. b. c. Robert Lodge, ‘A History of Synthetic Painting Media with Special Reference to Commercial Materials’, in S. Rosenberg (ed.), Preprints of Papers Presented at Sixteenth Annual Meeting, New Orleans, June 1–5 1988, American Institute for Conservation, Washington, DC, 1988, pp.118–27.
- 18. Jose Gutierrez, ‘From Fresco to Plastics: New Materials for Mural and Easel Paintings’, Ottawa 1956.
- 19. Jose Gutierrez, Painting with Acrylics, London 1969.
- 20. Tom Learner, ‘The Characterisation of Acrylic Painting Materials and Implications for their Use, Conservation and Stability’, PhD thesis, University of London 1997.
- 21. a. b. c. Tom Learner, ‘The Analysis of Synthetic Resins Found in Twentieth-Century Paint Media’ in Pre-prints, Resins: Ancient and Modern, Scottish Society for Conservation and Restoration, Edinburgh 1995, pp.76–84.
- 22. Tom Learner, ‘A Review of Synthetic Binding Media in Twentieth-century Paints’, The Conservator, no.24, 2000, pp.96–103.
- 23. Tom Learner, ‘A Review of Synthetic Binding Media in Twentieth-century Paints’, The Conservator, no.24, 2000, pp.96–103.[/fn
Peter Eastman, ‘Characterization of Acrylics at Rohm and Haas’, in Extended Abstracts, The Fifth Annual Infrared and Raman Users Group Conference, The Getty Center, Los Angeles 2002, pp.88–9.
- 24. a. b. c. d. Mark Golden, ‘Basic Paint Research and Development’, in Extended Abstracts: The Fifth Annual Infrared and Raman Users Group Conference, The Getty Center, Los Angeles 2002, pp.84–6.
- 25. a. b. c. Mark Golden, James Hayes and Elizabeth Jablonski, ‘The Conservation of Acrylic Dispersion Paintings: An Overview’, in Paintings Specialty Group Postprints, American Institute for Conservation 2001, pp.47–51.
- 26. a. b. c. d. e. f. g. h. Carol Stringari and Ellen Pratt, ‘The Identification and Characterization of Acrylic Emulsion Paint Media’ in David Grattan (ed.) Saving the Twentieth Century: The Conservation of Modern Materials, Canadian Conservation Institute, Ottawa 1993, pp.411–40.
- 27. Carol Mancusi-Ungaro, ‘William C. Agee and Daniel Cytron Discuss the Sam Francis Exhibition’, camera, L. McDonald, video interview, Mellon Artists Interviews Program, The Menil Collection, Houston 1999.
- 28. [Ulrich Zorll (ed.), Waterbased Acrylates for Decorative Coatings, Hannover 2001.
- 29. a. b. Zeno Wicks, Frank Jones and Peter Pappas, Organic Coatings – Science and Technology, Volume 1: Film Formation, Components and Appearance, New York 1992.
- 30. a. b. Oil and Colour Chemist’s Association, Surface Coatings Volume 1 – Raw Materials and their Usage, New York 1983.
- 31. a. b. Ernest Flick, Handbook of Paint Raw Materials, Park Ridge 1982.
- 32. a. b. Ulrich Zorll (ed.), Waterbased Acrylates for Decorative Coatings, Hannover 2001.
- 33. Zeno Wicks, Frank Jones and Peter Pappas, Organic Coatings – Science and Technology, Volume 1: Film Formation, Components and Appearance, New York 1992.
- 34. Ulrich Zorll (ed.), Waterbased Acrylates for Decorative Coatings, Hannover 2001.
- 35. a. b. Marion Barclay, ‘Materials Used in Certain Canadian Abstract Paintings of the 1950s’ in D. Leclerc (ed.), The Crisis of Abstraction in Canada: The 1950s, National Gallery of Canada, Ottawa 1992, pp.205–32.
- 36. a. b. Jo Crook and Tom Learner, The Impact of Modern Paints, London 2000, p.101.
- 37. Jim Coddington, Carol Mancusi-Ungaro and Kirk Varnedoe, ‘Time and Change: A Discussion about the Conservation of Modern and Contemporary Art’, Conservation: The Getty Conservation Institute Newsletter, 17, 2002, pp.11–17.
- 38. Camilla Gray, ‘Conservation of Contemporary Paintings: The Interaction Between the Living Artist and Conservator’, unpublished thesis, Diploma in the Conservation of Easel Paintings, Courtauld Institute of Art, London 2000.
- 39. Ysbrannd Hummelen and Dionne Sillé (eds.), Modern Art, Who Cares?, Foundation for the Conservation of Modern Art and the Netherlands Institute for Cultural Heritage, Amsterdam 1999.
- 40. Carol Mancusi-Ungaro, Shelley Sturman and Erich Gantzert-Castrillo, ‘Working With Artists In Order to Preserve Original Intent: Seminar 15’, ibid., pp.391–9.
- 41. M. Skopek, personal communication 2002.
- 42. a. b. Netherlands Institute for Cultural Heritage/Foundation for the Conservation of Modern Art, ‘Concept Scenario: Artists’ Interviews’, http://www.incca.org, 1999, accessed 4 May 2003.
- 43. Ysbrannd Hummelen and Dionne Sillé (eds.), Modern Art, Who Cares?, Foundation for the Conservation of Modern Art and the Netherlands Institute for Cultural Heritage, Amsterdam 1999
- 44. Carol Mancusi-Ungaro, ‘Original Intent: The Artist and Conservator in Dialogue’, video recording of lecture, The Menil Collection, Houston 2000.
- 45. a. b. David Bauer, ‘Predicting Coating Durability Using Chemical Methods’, Progress in Organic Coatings 23, 1993, pp.105–14.
- 46. Michele Derrick, Dusan Stulik and James Landry, Infrared Spectroscopy in Conservation Science, Getty Center for Education in the Arts, Los Angeles 2000.
- 47. a. b. c. d. Elyse Klein, Jai-sun Tsang and Mary Baker, ‘Non-instrumental Methods for the Identification and Characterization of Artists’ Acrylic Paint’, Smithsonian Materials Centre for Research and Education, 1995, unpublished typescript.
- 48. Tom Learner, ‘The Use of FTIR in the Conservation of Twentieth-Century Paintings’, Spectroscopy Europe 8 (4), 1996, pp.14–19.
- 49. Tom Learner, ‘The Use of a Diamond Cell for the FTIR Characterisation of Paints and Varnishes available to Twentieth-Century Artists’, in Boris Pretzel (ed.), Postprints: Infrared and Raman User’s Group Conference, Victoria and Albert Museum, London 1998, pp.7–20.
- 50. Graham Martin, ‘The Identification of Modern Polymer Systems Using FTIR’, in Preprints, Modern Organic Materials Meeting, Scottish Society for Conservation, Edinburgh 1988, pp.47–56.
- 51. Richard Newman, ‘Some Applications of Infrared Spectroscopy in the Examination of Painting Materials’, Journal of the American Institute for Conservation, 19, 1980, pp.42–62.
- 52. Naoko Sonoda and Jean-Paul Rioux, ‘Identification des Matériaux Synthétiques dans les Peintures Modernes. I. Vernis et Liants Polymères’, Studies in Conservation, 35, 1990, pp.189–204.
- 53. Naoko Sonoda, Jean-Paul Rioux and Alain Duval, ‘Identification des matériaux synthétiques dans les peintures modernes. II. Pigments organiques et matière picturale’, Studies in Conservation, 38, 1993, pp.99–127.
- 54. Jaap Boon and Tom Learner,‘Analytical Mass Spectrometry of Artists’ Acrylic Emulsion Paints by Direct Temperature Resolved Mass Spectrometry and Laser Desorption Ionisation Mass Spectrometry’, Journal of Analytical and Applied Pyrolysis, 64, 2002, pp.327–44.
- 55. a. b. Tom Learner, Oscar Chiantore and Dominique Scalarone,‘Ageing Studies of Acrylic Emulsion Paints’, in Preprints of the 13th Triennial Meeting of the ICOM Committee for Conservation, London 2002, pp.911–19.
- 56. a. b. c. Paul Whitmore, Val Colaluca and Eugene Farrell, ‘A Note on the Origin of Turbidity in films of an Artists’ Acrylic Paint Medium’, Studies in Conservation, 41, 1996, pp.250–5.
- 57. Oscar Chiantore, Dominique Scalarone and Tom Learner, ‘Characterisation of Artists’ Acrylic Emulsion Paints’, Journal of Polymer Analysis and Characterisation, 8, 2003, pp.67–82.
- 58. a. b. Peter Eastman, ‘Characterization of Acrylics at Rohm and Haas’, in Extended Abstracts, The Fifth Annual Infrared and Raman Users Group Conference, The Getty Center, Los Angeles 2002, pp.88–9.
- 59. Alexander du Chesne, ‘Film Formation of Latex Dispersions’, Max Planck Institute, Ackermannweg 10, 55128 Mainz, Germany, www.mpip-mainz.mpg.de/documents/projects98/C5.htm 1998, accessed 8 November 2000.
- 60. H.W. Talen, ‘Some Considerations on the Formation of Films’, Journal of Oil & Colour Chemists’ Association, 45 (6), 1962, pp.387–415.
- 61. a. b. c. d. H.W. Talen, ‘Some Considerations on the Formation of Films’, Journal of Oil & Colour Chemists’ Association, 45 (6), 1962, pp.387–415.
- 62. T. Bartley, ‘The Effect of Moisture on Dimensional Changes in Selected Recent Unsupported Acrylic Paint Films’, Master’s project, Queen’s University, Kingston 1995.
- 63. a. b. C. Bondy and M.M. Coleman, ‘Film Formation and Film Properties Obtained with Acrylic, Styrene/Acrylic and Vinyl Acetate/VeoVa Copolymer Emulsions’, Journal of Oil & Colour Chemists’ Association, 53, 1970, pp.555–77.
- 64. a. b. c. d. e. f. Robert Feller, ‘Polymer Emulsions’, in Robert Feller, Nathan Stolow and Elizabeth Jones (eds.), On Picture Varnishes and Their Solvents, Washington 1985, pp.218–25.
- 65. a. b. B. Niu and Marek Urban, ‘Recent Advances in Stratification and Film formation of Latex Films: Attenuated total Reflection and Step-Scan Photoacoustic FTIR Spectroscopic Studies’, Journal of Applied Polymer Science, 70, (7), 1998, pp.1321–48.
- 66. a. b. c. d. J.C. Padget, ‘Additives for Water-based Coatings: A Polymer Chemist’s Point of View’, in D.R Karsa (ed.), Additives for Water-based Coatings, Cambridge 1990, pp.1–29.
- 67. a. b. c. d. e. Scott Williams, ‘Workshop: The Conservation of Plastics in Museums’, Queen’s University, Kingston 1999.
- 68. Mitchell Winnik, ‘The Formation and Properties of Latex Films’, in P.A. Lovell and M.S. El-Aasser (eds.), Emulsion Polymerization and Emulsion Polymers, New York 1997, pp.468–518.
- 69. a. b. c. d. e. C. Bondy, ‘Binder Design and Performance in Emulsion Paints’, Journal of Oil and Colour Chemists Association, 51, 1968, pp.409–27.
- 70. Edgar Gutoff, ‘The Drying of Waterborne Coatings’ in J.E. Glass (ed.), Technology for Waterborne Coatings, American Chemical Society, Washington 1997, pp.245–64.
- 71. a. b. c. d. e. Manfred Hess, W.A Edwards, T.W. Wilkinson, N.A. Bennett, G.N. Hill, and W. Phillips, Paint Film Defects: Their Causes and Cure, 2nd ed., London 1965.
- 72. a. b. Paul Nylen and Edward Sutherland, Modern Surface Coatings: A Textbook of the Chemistry and Technology of Paints, Varnishes and Lacquers, New York 1965.
- 73. Richard Wolbers, ‘Varnishing Acrylic Emulsion Paintings’, in Painting Conservation Catalog, Volume 1: Varnishes and Surface Coatings, American Institute for Conservation, Paintings Specialty Group, Washington 1998, pp.273–4.[/fn
The degree of coalescence is dependent upon a variety of conditions, including the ambient conditions during drying, the Tg, which is approximately 10 C for poly(EA/MMA) emulsions,
Tom Learner, ‘The Characterisation of Acrylic Painting Materials and Implications for their Use, Conservation and Stability’, PhD thesis, University of London 1997.
- 74. Tom Learner, ‘A Review of Synthetic Binding Media in Twentieth-century Paints’, The Conservator, no.24, 2000, pp.96–103.
- 75. Rachel Becker, Moshe Puterman and J. Laks, ‘The Effect of Porosity of Emulsion Paints on Mould Growth’, Durability of Building Materia, 3 (4), 1986, pp.369–80.
- 76. John Boxall and W. Worley, ‘The Efflorescence Resistance of Certain Emulsion Coatings’, The Journal of Oil and Colour Chemists Association, 62 (5), 1979, pp.173–6.
- 77. Susan Gatenby, ‘An Investigation into Cleaning Procedures for Mould Stained Australian Aboriginal Objects Painted with Modern Media’, in Preprints, 9th Triennial Meeting, Dresden, German Democratic Republic, ICOM Committee for Conservation, London 1990, pp.157–62.
- 78. D.L. Cassons and W.C. Feist, Finishing Wood Exteriors: Selection, Application, and Maintenance, Agriculture Handbook, no.647, Forest Service, United States Department of Agriculture 1986.
- 79. a. b. Mary Baker, The Degradation of Plastics: Workshop, Annual Meeting of the American Institute for Conservation, Philadelphia 2000.
- 80. Rachel Becker, Moshe Puterman and J. Laks, ‘The Effect of Porosity of Emulsion Paints on Mould Growth’, Durability of Building Materia, 3 (4), 1986, pp.369–80.
- 81. Edgar Gutoff, ‘The Drying of Waterborne Coatings’ in J.E. Glass (ed.), Technology for Waterborne Coatings, American Chemical Society, Washington 1997, pp.245–64.
- 82. Richard Wolbers, ‘Varnishing Acrylic Emulsion Paintings’, in Painting Conservation Catalog, Volume 1: Varnishes and Surface Coatings, American Institute for Conservation, Paintings Specialty Group, Washington 1998, pp.273–4.
- 83. Sophia Fairclough, ‘Acrylic and Poster Paint: Two Case Studies of Works by Sam Francis and Roger Hilton’, in Conference Papers, Modern Works-Modern Problems, Institute of Paper Conservation, London 1994, pp.150–6.
- 84. Jonah Erlebacher, E. Brown, Marion Mecklenburg and Charles Tumosa, ‘The Effects of Temperature and Relative Humidity on the Mechanical Properties of Modern Painting Materials’ in Proceedings of the Materials Research Society Symposium, 267, 1992, pp.359–70.
- 85. Jonah Erlebacher, E. Brown, Marion Mecklenburg and Charles Tumosa, ‘The Mechanical Behavior of Artists’ Acrylic Paints with Changing Temperature and Relative Humidity’, in Postprints, American Institute for Conservation Paintings Specialty Group, Washington 1992, pp.35–40.
- 86. a. b. Susan Gatenby, ‘An Investigation into Cleaning Procedures for Mould Stained Australian Aboriginal Objects Painted with Modern Media’, in Preprints, 9th Triennial Meeting, Dresden, German Democratic Republic, ICOM Committee for Conservation, London 1990, pp.157–62.
- 87. a. b. C. Bogstadt, personal communication, Tri-art Manufacturing, Kingston 1998.
- 88. a. b. Rohm and Haas Company, Philadelphia, personal communication 1999 and 2000.
- 89. aul Whitmore, Val Colaluca and Eugene Farrell, ‘A Note on the Origin of Turbidity in films of an Artists’ Acrylic Paint Medium’, Studies in Conservation, 41, 1996, pp.250–5.
- 90. Scott Williams, ‘Workshop: The Conservation of Plastics in Museums’, Queen’s University, Kingston 1999.
- 91. Richard Wolbers, ‘Varnishing Acrylic Emulsion Paintings’, in Painting Conservation Catalog, Volume 1: Varnishes and Surface Coatings, American Institute for Conservation, Paintings Specialty Group, Washington 1998, pp.273–4.
- 92. a. b. c. Oscar Chiantore, ‘Characterization and Aging of Commercial Acrylic Resins’, in Extended Abstracts, Infrared and Raman Users Group Meeting, The Getty Center, Los Angeles 2002, pp.75–7.
- 93. a. b. c. James Druzik, Tom Learner and Michael Schilling, ‘Recent Investigations in Contemporary Artist Paints’, in Extended Abstracts, TheFifth Annual Infrared and Raman Users’ Group Conference, The Getty Center, Los Angeles 2002, pp.92–5.
- 94. K.W. Evanson, T.A. Thorstenson and Marek Urban, ‘Surface and Interfacial FTIR Studies of Latexes II: Surfactant-copolymer Compatibility and Mobility of Surfactants’, Journal of Applied Polymer Science, 42, 1991, pp.2297–2307.
- 95. a. b. K.W. Evanson and Marek Urban, ‘Surface and Interfacial FTIR Spectroscopic Studies of Latexes. I. Surfactant—Copolymer Interactions’, Journal of Applied Polymer Science 42, 1991, pp.2287–96.
- 96. a. b. c. K.W. Evanson and Marek Urban, ‘Surface and Interfacial FTIR Spectroscopic Studies of Latexes. III. The Effects of Substrate Surface Tension and Elongation on Exudation of Surfactants’, Journal of Applied Polymer Science, 42, 1991, pp.2309–20.
- 97. B. Niu and Marek Urban, ‘Surface and Interfacial Fourier Transform Infrared Spectroscopic Studies of Latexes. XVI. Quantitative Analysis of Surfactant in Multilayered Films’, Journal of Applied Polymer Science, 62 (11), 1996, pp.1903–11.
- 98. Marek Urban and K.W. Evanson, ‘Factors Governing Surfactant Assembly at the Latex Film Interfaces: An FTIR Spectroscopic Study’, Polymer Communications, 31, 1990, pp.279–82.
- 99. a. b. c. Stephen Stinson, ‘Polymer Chemists Seek Solutions to Museum Restoration Problems’, Chemical & Engineering News, 72 (36), 1994, pp.28–30.
- 100. d Hofland,‘Water-borne Coatings for Decorative and Protective Coatings: A Comparative Survey’, Surface Coatings International, 77 (7), 1994, pp.270–81.
- 101. a. b. Charles Martens (ed.), Technology of Paints, Varnishes, and Lacquers, New York 1968.
- 102. John Gillatt, The Biodeterioration of Polymer Emulsions and its Prevention with Biocides, International Biodeterioration, 26, 1990, pp.205–16.
- 103. Alison Murray, Celina Contreras de Berenfeld, Sue Chang, Elizabeth Jablonski, Tracey Klein, Marion Riggs, Elizabeth Robertson, and Anthony Tse, ‘The Condition and Cleaning of Acrylic Emulsion Paintings’, in Materials Research Society Fall Meeting, Materials Issues in Art and Archaeology VI, Boston 2001, II1.4, pp.1–8.
- 104. James Hamm, Ben Gavett, Mark Golden, James Hayes, C. Kelly, John Messinger, Margaret Contompasis and Bruce Suffield, ‘The Discoloration of Acrylic Dispersion Media’ in David Grattan (ed.) Saving the Twentieth Century: The Conservation of Modern Materials, Canadian Conservation Institute, Ottawa 1993, pp.381–92.
- 105. Paul Whitmore and Val Colaluca, ‘The Natural and Accelerated Aging of an Acrylic Artists’ Medium.’, Studies in Conservation, 40, 1995, pp.51–64.
- 106. Paul Whitmore, Val Colaluca and Heather Morris, ‘The Light Bleaching of Discolored Films of an Acrylic Artists’ Medium’, Studies in Conservation, 47, 2002, pp.237–49.
- 107. P.T. Elliot, W.H. Wetzel, Lu Xing and J.E. Glass, ‘Particle Coalescence’ in J.E. Glass (ed.), Technology for Waterborne Coatings, American Chemical Society, Washington 1997, pp.57–70.
- 108. Robert Feller, ‘Polymer Emulsions’, in Robert Feller, Nathan Stolow and Elizabeth Jones (eds.), On Picture Varnishes and Their Solvents, Washington 1985, pp.218–25
- 109. W.H. Brendley, ‘Fundamentals of Acrylics: Acrylic Polymers’, Paint and Varnish Production, July 1973, pp.19–27.
- 110. Tracey Klein, Identifying Suitable Approaches Used in the Treatment of Acrylic Paintings: A Census of Art Conservators on the Conservation of Acrylic Paintings, Master’s project, Queen’s University Master of Art Conservation Program, Kingston 2000.
- 111. Helen Lloyd, Katy Lithgow, Peter Brimblecombe, Young Yoon, Kate Frame and Barry Knight, ‘The Effects of Visitor Activity on Dust in Historic Collections’, The Conservator, 26, 2002, pp.72–84.
- 112. James Druzik and Glen Cass, ‘Abstract: A New Look at Soiling of Contemporary Paintings by Soot in Art Museums’, in Conference Report, Third Indoor Air Quality Meeting, 10–12 July, Brookes University, Oxford, http://iaq.dk/iap/iaq2000/2000_10.htm 2000, accessed 27 April 2003.
- 113. Robert Feller, ‘Conservators Advise Artists’, Art Journal, 39 (1), 1977, pp.37–9.
- 114. R.E. Harren, A. Mercurio and J.D. Scott, ‘Weatherability of Acrylic Coatings’ in Australian Organization of Coatings Chemistry Proceedings and News, October 1977, pp.17–23.
- 115. Elyse Klein, Jai-sun Tsang and Mary Baker, ‘Non-instrumental Methods for the Identification and Characterization of Artists’ Acrylic Paint’, Smithsonian Materials Centre for Research and Education, 1995, unpublished typescript.
- 116. H. van de Wiel and W. Zom, ‘Waterborne Acrylics and Urethanes for the Coatings Industry’, Journal of Oil and Colour Chemists Association, 64, 1981, pp.273–8.
- 117. Roy Perry, ‘Problems of Dirt Accumulation and its Removal From Unvarnished Paintings: A Practical Review’, in Dirt and Pictures Separated, United Kingdom Institute for Conservation and the Tate Gallery, London 1990, pp.3–6.
- 118. a. b. Alison Murray, Celina Contreras de Berenfeld, Sue Chang, Elizabeth Jablonski, Tracey Klein, Marion Riggs, Elizabeth Robertson, and Anthony Tse, ‘The Condition and Cleaning of Acrylic Emulsion Paintings’, in Materials Research Society Fall Meeting, Materials Issues in Art and Archaeology VI, Boston 2001, II1.4, pp.1–8.
- 119. Geneviève Saulnier, Cleaning Acrylic Emulsion Paint Using Dry-Cleaning Methods, Master’s project, Queen’s University Master of Art Conservation Program, Kingston 2002.
- 120. a. b. H.K.R. Nielson, ‘Forensic Analysis of Coatings’, Journal of Coatings Technology, 56 (718), 1984, pp.21–32.
- 121. H.K.R. Nielson, ‘Forensic Analysis of Coatings’, Journal of Coatings Technology, 56 (718), 1984, pp.21–32.
We would like to extend great appreciation to Dr Alison Murray, Associate Professor, Queen’s University, Kingston, Ontario, for her expert guidance and encouragement at the earliest stages in this research. We would also like to thank Tracey Klein, paintings conservator, Edmonton, Alberta, Canada, for sharing her informative survey results. Thanks also to Dr Rene de la Rie, Jay Krueger, Dr Suzanne Quillen Lomax and Ross Merrill at the National Gallery of Art, Washington, DC; Benjamin Gavett, Braxton J. Tomsic and Bill Berthel at Golden Artist Colors, Inc.; Dr Frank Jones, Professor, Coatings Research Institute, Eastern Michigan University; Elizabeth Lunning, Chief Conservator, and Bradford Epley, Associate Paintings Conservator, at the Menil Collection, Houston, Texas; and Ian Loughead, Conservator, Parks Canada.
This paper is based on the article by the same authors first published in Reviews in Conservation in 2003. Reviews in Conservation is published annually by the International Institute for Conservation of Historic and Artistic Works.
Elizabeth Jablonski is an Associate Paintings Conservator at the Museum of Fine Arts, Boston. Tom Learner is a Senior Conservation Scientist at Tate. James Hayes is the Technical Director for Golden Artist Colors, Inc., New Berlin, New York. Mark Golden is CEO and co-founder of Golden Artist Colors, Inc.
Tate Papers Autumn 2004 © Elizabeth Jablonski, Tom Learner, James Hayes, Mark Golden