Epoxy is the cured end product of epoxy resins, as well as a colloquial name for the epoxide functional group.
Epoxy resins, also known as polyepoxides are a class of reactive prepolymers and polymers which contain epoxide groups. Epoxy resins may be reacted (cross-linked) either with themselves through catalytic homopolymerisation, or with a wide range of co-reactants including polyfunctional amines, acids (and acid anhydrides), phenols, alcohols, and thiols. These co-reactants are often referred to as hardeners or curatives, and the cross-linking reaction is commonly referred to as curing. Reaction of polyepoxides with themselves or with polyfunctional hardeners forms a thermosetting polymer, often with strong mechanical properties as well as high temperature and chemical resistance. Epoxy has a wide range of applications, including metal coatings, use in electronic and electrical components, high tension electrical insulators, fibre-reinforced plastic materials, and structural adhesives. Epoxy resin is employed to bind gutta percha in some root canal procedures. 1
- 1 Epoxy chemistry
- 2 Curing epoxy resins
- 3 History
- 4 Applications
- 5 Industry
- 6 Health risks
- 7 Accidents
- 8 References
- 9 External links
Epoxy resins are low molecular weight pre-polymers or higher molecular weight polymers which normally contain at least two epoxide groups. The epoxide group is also sometimes referred to as a glycidyl or oxirane group.
A wide range of epoxy resins are produced industrially. The raw materials for epoxy resin production are today largely petroleum derived, although some plant derived sources are now becoming commercially available (e.g. plant derived glycerol used to make epichlorohydrin).
Epoxy resins are polymeric or semi-polymeric materials, and as such rarely exist as pure substances, since variable chain length results from the polymerisation reaction used to produce them. High purity grades can be produced for certain applications, e.g. using a distillation purification process. One disadvantage of high purity liquid grades is their tendency to form crystalline solids due to their highly regular structure, which require melting to enable processing.
An important characteristic of epoxy resins is the epoxide content. This is commonly expressed as the epoxide number, which is the number of epoxide equivalents in 1 kg of resin (Eq./kg), or as the equivalent weight, which is the weight in grams of resin containing 1 mole equivalent of epoxide (g/mol). One measure may be simply converted to another:
Equivalent weight (g/mol) = 1000 / epoxide number (Eq./kg)
The equivalent weight or epoxide number is used to calculate the amount of co-reactant (hardener) required when curing epoxy resins. Epoxies are typically cured with stoichiometric or near-stoichiometric quantities of curative to achieve the best physical properties.
As with other classes of thermosetting polymer materials, blending different grades of epoxy resin, as well as use of additives, plasticizers or fillers is common to achieve the desired processing and/or final properties, or to reduce cost. Use of blending, additives, and fillers is often referred to as formulating.
The most common and important class of epoxy resins is formed from reacting epichlorohydrin with bisphenol A to form diglycidyl ethers of bisphenol A. The simplest resin of this class is formed from reacting two moles of epichlorohydrin with one mole of bisphenol A to form the bisphenol A diglycidyl ether (commonly abbreviated to DGEBA or BADGE). DGEBA resins are transparent colourless-to-pale-yellow liquids at room temperature, with viscosity typically in the range of 5-15 Pa.s at 25°C. Industrial grades normally contain some distribution of molecular weight, since pure DGEBA shows a strong tendency to form a crystalline solid upon storage at ambient temperature.
Increasing the ratio of bisphenol A to epichlorohydrin during manufacture produces higher molecular weight linear polyethers with glycidyl end groups, which are semi-solid to hard crystalline materials at room temperature depending on the molecular weight achieved. As the molecular weight of the resin increases, the epoxide content reduces and the material behaves more and more like a thermoplastic. Very high molecular weight polycondensates (ca. 30 000 – 70 000 g/mol) form a class known as phenoxy resins and contain virtually no epoxide groups (since the terminal epoxy groups are insignificant compared to the total size of the molecule). These resins do however contain hydroxyl groups throughout the backbone, which may also undergo other cross-linking reactions, e.g. with aminoplasts, phenoplasts and isocyanates.
Bisphenol F may also undergo epoxidation in a similar fashion to bisphenol A. Compared to DGEBA, bisphenol F epoxy resins have lower viscosity and a higher mean epoxy content per gram, which (once cured) gives them increased chemical resistance.
Reaction of phenols with formaldehyde and subsequent glycidylation with epichlorohydrin produces epoxidised novolacs, such as epoxy phenol novolacs (EPN) and epoxy cresol novolacs (ECN). These are highly viscous to solid resins with typical mean epoxide functionality of around 2 to 6. The high epoxide functionality of these resins forms a highly crosslinked polymer network displaying high temperature and chemical resistance, but low flexibility. 100% solids hybrid novolac epoxy resin systems have been developed that contain no solvents and no volatile or organic compounds. These hybrid novolac epoxies have been documented to withstand up to 98% sulfuric acid and can be engineered to service temperatures exceeding 400 degrees Fahrenheit.
There are two types of aliphatic epoxy resins: glycidyl epoxy resins and cycloaliphatic epoxides.
Glycidyl epoxy resins are typically formed by the reaction of epichlorohydrin with aliphatic alcohols or polyols to give glycidyl ethers or aliphatic carboxylic acids to give glycidyl esters.2 This reaction is normally done in the presence of an alkali, such as sodium hydroxide, to facilitate the dehydrochlorination of the intermediate chlorohydrin. The resulting resins may be monofunctional (e.g. dodecanol glycidyl ether), difunctional (diglycidyl ester of hexahydrophthalic acid), or higher functionality (e.g. trimethylolpropane triglycidyl ether). These resins typically display low viscosity at room temperature (10-200 mPa.s) and are often used as reactive diluents. As such, they are employed to modify (reduce) the viscosity of other epoxy resins. This has led to the term ‘modified epoxy resin’ to denote those containing viscosity-lowering reactive diluents. However, they are also used without other epoxide ingredients along with anhydride curing agents such as hexahydrophthalic anhydride to make molded objects such as high voltage insulators. This is in fact the main use of the diglycidyl esters.
The cycloaliphatic epoxides contain one or more cycloaliphatic rings in the molecule to which the oxirane ring is fused (e.g. 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexane carboxylate). They are formed by the reaction of cyclo-olefins with a peracid, such as peracetic acid.3 This class also displays low viscosity at room temperature, but offers significantly higher temperature resistance and correspondingly better electrical properties at high temperatures to cured resins than the glycidyl aliphatic epoxy resins. Another advantage is the complete absence of chlorine, since no epichlorohydrin is used in the manufacturing process. This is particularly useful for electronic applications such as the encapsulation of light emitting diodes. However, room temperature reactivity is rather low compared to other classes of epoxy resin, and high temperature curing using suitable accelerators is normally required.
Glycidylamine epoxy resins are higher functionality epoxies which are formed when aromatic amines are reacted with epichlorohydrin. Important industrial grades are triglycidyl-p-aminophenol (functionality 3) and N,N,N,N-tetraglycidyl-4,4-methylenebis benzylamine (functionality 4). The resins are low to medium viscosity at room temperature, which makes them easier to process than EPN or ECN resins. This coupled with high reactivity, plus high temperature resistance and mechanical properties of the resulting cured network make them important materials for aerospace composite applications.
In general, uncured epoxy resins have only poor mechanical, chemical and heat resistance properties. However, good properties are obtained by reacting the linear epoxy resin with suitable curatives to form three-dimensional cross-linked thermoset structures. This process is commonly referred to as curing. Curing of epoxy resins is an exothermic reaction and in some cases produces sufficient heat to cause thermal degradation if not controlled.
Curing may be achieved by reacting an epoxy with itself (homopolymerisation) or by forming a copolymer with polyfunctional curatives or hardeners. In principle, any molecule containing a reactive hydrogen may react with the epoxide groups of the epoxy resin. Common classes of hardeners for epoxy resins include amines, acids, acid anhydrides, phenols, alcohols and thiols. Relative reactivity (lowest first) is approximately in the order: phenol < anhydride < aromatic amine < cycloaliphatic amine < aliphatic amine < thiol.
Whilst some epoxy resin/ hardener combinations will cure at ambient temperature, many require heat, with temperatures up to 150°C being common, and up to 200°C for some specialist systems. Insufficient heat during cure will result in a network with incomplete polymerisation, and thus reduced mechanical, chemical and heat resistance. Cure temperature should typically attain the glass transition temperature (Tg) of the fully cured network in order to achieve maximum properties. Temperature is sometimes increased in a step-wise fashion to control the rate of curing and prevent excessive heat build-up from the exothermic reaction.
Hardeners which show only low or limited reactivity at ambient temperature, but which react with epoxy resins at elevated temperature are referred to as latent hardeners. When using latent hardeners, the epoxy resin and hardener may be mixed and stored for some time prior to use, which is advantageous for many industrial processes. Very latent hardeners enable one-component (1K) products to be produced, whereby the resin and hardener are supplied pre-mixed to the end user and only require heat to initiate curing. One-component products generally have shorter shelf-lives than standard 2-component systems, and products may require cooled storage and transport.
The epoxy curing reaction may be accelerated by addition of small quantities of accelerators. Tertiary amines, carboxylic acids and alcohols (especially phenols) are effective accelerators. Bisphenol A is a highly effective and widely used accelerator, but is now increasingly replaced due to health concerns with this substance.
Epoxy resin may be reacted with itself in the presence of an anionic catalyst (a Lewis base such as tertiary amines or imidazoles) or a cationic catalyst (a Lewis acid such as a boron trifluoride complex) to form a cured network. This process is known as catalytic homopolymerisation. The resulting network contains only ether bridges, and exhibits high thermal and chemical resistance, but is brittle and often requires elevated temperature to effect curing, so finds only niche applications industrially. Epoxy homopolymerisation is often used when there is a requirement for UV curing, since cationic UV catalysts may be employed (e.g. for UV coatings).
Polyfunctional primary amines form an important class of epoxy hardeners. Primary amines undergo an addition reaction with the epoxide group to form a hydroxyl group and a secondary amine. The secondary amine can further react with an epoxide to form a tertiary amine and an additional hydroxyl group. Kinetic studies have shown the reactivity of the primary amine to be approximately double that of the secondary amine. Use of a difunctional or polyfunctional amine forms a three-dimensional cross-linked network. Aliphatic, cycloaliphatic and aromatic amines are all employed as epoxy hardeners. Amine type will alter both the processing properties (viscosity, reactivity) and the final properties (mechanical, temperature and chemical resistance) of the cured copolymer network. Thus amine structure is normally selected according to the application. Reactivity is broadly in the order aliphatic amines > cycloaliphatic amines > aromatic amines. Temperature resistance generally increases in the same order, since aromatic amines form much more rigid structures than aliphatic amines. Whilst aromatic amines were once widely used as epoxy resin hardeners due to the excellent end properties they imparted, health concerns with handling these materials means that they have now largely been replaced by safer aliphatic or cycloaliphatic alternatives.
Epoxy resins may be cured with cyclic anhydrides at elevated temperatures. Reaction occurs only after opening of the anhydride ring, e.g. by secondary hydroxyl groups in the epoxy resin. A possible side reaction may also occur between the epoxide and hydroxyl groups, but this may be suppressed by addition of tertiary amines. The low viscosity and high latency of anhydride hardeners makes them suitable for processing systems which require addition of mineral fillers prior to curing, e.g. for high voltage electrical insulators.
Polyphenols, such as bisphenol A or novolacs can react with epoxy resins at elevated temperatures (130-180°C), normally in the presence of a catalyst. The resulting material has ether linkages and displays higher chemical and oxidation resistance than typically obtained by curing with amines or anhydrides. Since many novolacs are solids, this class of hardeners is often employed for powder coatings.
Also known as mercaptans, thiols with the (S-H) functional group, contain an electron poor hydrogen which reacts very readily with the epoxide group, even at ambient or sub-ambient temperatures. Whilst the resulting network does not typically display high temperature or chemical resistance, the high reactivity of the thiol group makes it useful for applications where heated curing is not possible, or very fast cure is required e.g. for domestic DIY adhesives and chemical rock bolt anchors. Thiols have a characteristic odour, which can be detected in many two-component household adhesives.
The first commercial attempts to prepare resins from epichlorohydrin were made in 1927 in the United States. Credit for the first synthesis of bisphenol-A-based epoxy resins is shared by Dr. Pierre Castan of Switzerland and Dr. S.O. Greenlee of the United States in 1936. Dr. Castan's work was licensed by Ciba, Ltd. of Switzerland, which went on to become one of the three major epoxy resin producers worldwide. Ciba's epoxy business was spun off and later sold in the late 1990s and is now the Advanced Materials business unit of Huntsman Corporation of the United States. Dr. Greenlee's work was for the firm of Devoe-Reynolds of the United States. Devoe-Reynolds, which was active in the early days of the epoxy resin industry, was sold to Shell Chemical (now Momentive Specialty Chemicals, formerly Hexion, Resolution Polymers and others).
The applications for epoxy-based materials are extensive and include coatings, adhesives and resin matrices for composite materials such as those using carbon fiber and fiberglass reinforcements (although polyester, vinyl ester, and other thermosetting resins are also used for glass-reinforced plastic). The chemistry of epoxies and the range of commercially available variations allows cure polymers to be produced with a very broad range of properties. In general, epoxies are known for their excellent adhesion, chemical and heat resistance, good-to-excellent mechanical properties and very good electrical insulating properties. Many properties of epoxies can be modified (for example silver-filled epoxies with good electrical conductivity are available, although epoxies are typically electrically insulating). Variations offering high thermal insulation, or thermal conductivity combined with high electrical resistance for electronics applications, are available.5
Two part epoxy coatings were developed for heavy duty service on metal substrates and use less energy than heat-cured powder coatings. These systems generally use a 4:1 by volume mixing ratio, and dry quickly providing a tough, protective coating with excellent hardness. Their low volatility and water cleanup makes them useful for factory cast iron, cast steel, cast aluminium applications and reduces exposure and flammability issues associated with solvent-borne coatings. They are usually used in industrial and automotive applications since they are more heat resistant than latex-based and alkyd-based paints. Epoxy paints tend to deteriorate, known as chalk out, due to UV exposure.
Polyester epoxies are used as powder coatings for washers, driers and other "white goods". Fusion Bonded Epoxy Powder Coatings (FBE) are extensively used for corrosion protection of steel pipes and fittings used in the oil and gas industry, potable water transmission pipelines (steel), and concrete reinforcing rebar. Epoxy coatings are also widely used as primers to improve the adhesion of automotive and marine paints especially on metal surfaces where corrosion (rusting) resistance is important. Metal cans and containers are often coated with epoxy to prevent rusting, especially for foods like tomatoes that are acidic. Epoxy resins are also used for decorative flooring applications such as terrazzo flooring, chip flooring, and colored aggregate flooring. Epoxy flooring has been proven to be an environmentally friendly alternate to other types of flooring, reducing the facility's impact on the environment through less water consumption and less pesticides needed.6
Epoxy adhesives are a major part of the class of adhesives called "structural adhesives" or "engineering adhesives" (that includes polyurethane, acrylic, cyanoacrylate, and other chemistries.) These high-performance adhesives are used in the construction of aircraft, automobiles, bicycles, boats, golf clubs, skis, snowboards, and other applications where high strength bonds are required. Epoxy adhesives can be developed to suit almost any application. They can be used as adhesives for wood, metal, glass, stone, and some plastics. They can be made flexible or rigid, transparent or opaque/colored, fast setting or slow setting. Epoxy adhesives are better in heat and chemical resistance than other common adhesives. In general, epoxy adhesives cured with heat will be more heat- and chemical-resistant than those cured at room temperature. The strength of epoxy adhesives is degraded at temperatures above 350 °F (177 °C).7
Epoxy systems are used in industrial tooling applications to produce molds, master models, laminates, castings, fixtures, and other industrial production aids. This "plastic tooling" replaces metal, wood and other traditional materials, and generally improves the efficiency and either lowers the overall cost or shortens the lead-time for many industrial processes. Epoxies are also used in producing fiber-reinforced or composite parts. They are more expensive than polyester resins and vinyl ester resins, but usually produce stronger and more temperature-resistant composite parts.
Epoxy resin formulations are important in the electronics industry, and are employed in motors, generators, transformers, switchgear, bushings, and insulators. Epoxy resins are excellent electrical insulators and protect electrical components from short circuiting, dust and moisture. In the electronics industry epoxy resins are the primary resin used in overmolding integrated circuits, transistors and hybrid circuits, and making printed circuit boards. The largest volume type of circuit board—an "FR-4 board"—is a sandwich of layers of glass cloth bonded into a composite by an epoxy resin. Epoxy resins are used to bond copper foil to circuit board substrates, and are a component of the solder mask on many circuit boards.
Flexible epoxy resins are used for potting transformers and inductors. By using vacuum impregnation on uncured epoxy, winding-to-winding, winding-to-core, and winding-to-insulator air voids are eliminated. The cured epoxy is an electrical insulator and a much better conductor of heat than air. Transformer and inductor hot spots are greatly reduced, giving the component a stable and longer life than unpotted product.
Epoxy resins are applied using the technology of resin dispensing.
Epoxies are sold in hardware stores, typically as a pack containing separate resin and hardener, which must be mixed immediately before use. They are also sold in boat shops as repair resins for marine applications. Epoxies typically are not used in the outer layer of a boat because they deteriorate by exposure to UV light. They are often used during boat repair and assembly, and then over-coated with conventional or two-part polyurethane paint or marine-varnishes that provide UV protection.
There are two main areas of marine use. Because of the better mechanical properties relative to the more common polyester resins, epoxies are used for commercial manufacture of components where a high strength/weight ratio is required. The second area is that their strength, gap filling properties and excellent adhesion to many materials including timber have created a boom in amateur building projects including aircraft and boats.
Normal gelcoat formulated for use with polyester resins and vinylester resins does not adhere to epoxy surfaces, though epoxy adheres very well if applied to polyester resin surfaces. "Flocoat" that is normally used to coat the interior of polyester fibreglass yachts is also compatible with epoxies.
Epoxy materials tend to harden somewhat more gradually, while polyester materials tend to harden quickly, particularly if a lot of catalyst is used. The chemical reactions in both cases are exothermic. Large quantities of mix will generate their own heat and greatly speed the reaction, so it is usual to mix small amounts which can be used quickly.
While it is common to associate polyester resins and epoxy resins, their properties are sufficiently different that they are properly treated as distinct materials. Polyester resins are typically low strength unless used with a reinforcing material like glass fibre, are relatively brittle unless reinforced, and have low adhesion. Epoxies, by contrast, are inherently strong, somewhat flexible and have excellent adhesion. However, polyester resins are much cheaper.
Epoxy resins typically require a precise mix of two components which form a third chemical. Depending on the properties required, the ratio may be anything from 1:1 or over 10:1, but in every case they must be mixed in exactly the right proportions, and thoroughly to avoid unmixed portions. The final product is then a precise thermo-setting plastic. Until they are mixed the two elements are relatively inert, although the 'hardeners' tend to be more chemically active and should be protected from the atmosphere and moisture. The rate of the reaction can be changed by using different hardeners, which may change the nature of the final product, or by controlling the temperature.
By contrast, polyester resins are usually made available in a 'promoted' form, such that the progress of previously-mixed resins from liquid to solid is already underway, albeit very slowly. The only variable available to the user is to change the rate of this process using a catalyst, often Methyl-Ethyl-Ketone-Peroxide (MEKP), which is very toxic. The presence of the catalyst in the final product actually detracts from the desirable properties; just enough catalyst to harden fast enough is preferable. The rate of cure of polyesters is controlled by the amount and type of catalyst, and the temperature.
As adhesives, epoxies bond in three ways: a) mechanically, because the bonding surfaces are roughened; b) by proximity, because the cured resins are physically so close to the bonding surfaces that they are hard to separate; c) ionically, because the epoxy resins form ionic bonds at an atomic level with the bonding surfaces. This last is substantially the strongest of the three. By contrast, polyester resins can only bond using the first two of these, which greatly reduces their utility as adhesives and in marine repair.
In the aerospace industry, epoxy is used as a structural matrix material which is then reinforced by fiber.8 Typical fiber reinforcements include glass, carbon, Kevlar, and boron. Epoxies are also used as a structural glue; wood and other 'low-tech' materials are glued with epoxy resin. In 1968, Apollo 8's capsule reentered Earth's atmosphere, protected by a heat shield of epoxy resins manufactured by Dow Chemical Company.9
As of 2006, the epoxy industry amounts to more than US$5 billion in North America and about US$15 billion worldwide. The Chinese market has been growing rapidly, and accounts for more than 30% of the total worldwide market. It is made up of approximately 50–100 manufacturers of basic or commodity epoxy resins and hardeners.
These commodity epoxy manufacturers mentioned above typically do not sell epoxy resins in a form usable to smaller end users, so there is another group of companies that purchase epoxy raw materials from the major producers and then compounds (blends, modifies, or otherwise customizes) epoxy systems from these raw materials. These companies are known as "formulators". The majority of the epoxy systems sold are produced by these formulators and they comprise over 60% of the dollar value of the epoxy market. There are hundreds of ways that these formulators can modify epoxies—by adding mineral fillers (talc, silica, alumina, etc.), by adding flexibilizers, viscosity reducers, colorants, thickeners, accelerators, adhesion promoters, etc.. These modifications are made to reduce costs, to improve performance, and to improve processing convenience. As a result a typical formulator sells dozens or even thousands of formulations—each tailored to the requirements of a particular application or market.
Impacted by the global economic slump, the epoxy market size declined to $15.8 billion in 2009, almost to the level of 2005. In some regional markets it even decreased nearly 20%. The current epoxy market is experiencing positive growth as the global economy revives. With an annual growth rate of 3.5 - 4% the epoxy market is expected to reach $17.7 billion by 2012 and $21.35 by 2015. Higher growth rate is foreseen thereafter due to stronger demands from epoxy composite market and epoxy adhesive market.14
The primary risk associated with epoxy use is often related to the hardener component and not to the epoxy resin itself. Amine hardeners in particular are generally corrosive, but may also be classed toxic and/or carcinogenic or mutagenic. Aromatic amines present a particular health hazard (most are known or suspected carcinogens), but their use is now restricted to specific industrial applications, and safer aliphatic or cycloaliphatic amines are commonly employed.
Liquid epoxy resins in their uncured state are mostly classed as irritant to the eyes and skin, as well as toxic to aquatic organisms. Solid epoxy resins are generally safer than liquid epoxy resins, and many are classified non-hazardous materials. One particular risk associated with epoxy resins is sensitization. The risk has been shown to be more pronounced in epoxy resins containing low molecular weight epoxy diluents.15 Exposure to epoxy resins can, over time, induce an allergic reaction. Sensitization generally occurs due to repeated exposure (e.g. through poor working hygiene and/or lack of protective equipment) over a long period of time. Allergic reaction sometimes occurs at a time which is delayed several days from the exposure. Allergic reaction is often visible in the form of dermatitis, particularly in areas where the exposure has been highest (commonly hands and forearms). Epoxy use is a main source of occupational asthma among users of plastics.16 Bisphenol A, which is used to manufacture a common class of epoxy resins, is a known endocrine disruptor.
The Big Dig ceiling collapse, which occurred on July 10, 2006, is an accident which was caused by the use of fast-set epoxy which had a higher rate of creep than standard-set epoxy.
The accident resulted in one fatality and cost $54 million to redesign, repair, and inspect all of the tunnels in the D Street connector.
The cost of the fast-set epoxy used to secure the bolts was $1,287.60.
- M. A. Marciano, R. Ordinola-Zapata, T. V. R. N. Cunha, M. A. H. Duarte, B. C. Cavenago, R. B. Garcia, C. M. Bramante, N. Bernardineli, I. G. Moraes (April 2011). "Analysis of four gutta-percha techniques used to fill mesial root canals of mandibular molars". International Endodontic Journal 44 (4): 321–329. doi:10.1111/j.1365-2591.2010.01832.x. PMID 21219361.
- Epoxy Resins Chemistry and technology, 1988 Marcel Dekker, Chapter 2: Synthesis and Characterization of Epoxides, by Yoshio Tanaka, , pp 54 to 63
- Recent Developments in Epoxy Resins, by L. Hammerton, RAPRA Review Reports, 1997, ed. by Rebecca Dolbey, p. 8
- "WoodenBoat forum: Shelf life of epoxy". Forum.woodenboat.com. 2010-07-31. Retrieved 2014-02-23.
- May, Clayton A. (1987-12-23). Epoxy Resins: Chemistry and Technology (Second ed.). New York: Marcel Dekker Inc. p. 794. ISBN 0-8247-7690-9.
- "Environmentally Friendly Epoxy Floors". Everlastepoxy.com. Retrieved 2014-02-23.
- Morena, John J (1988). Advanced Composite Mold Making. New York: Van Nostrand Reinhold Co. Inc. pp. 124–125. ISBN 978-0-442-26414-7.
- Sikarwar, Rahul S.; Raman Velmurugan, Velmuri Madhu (December 2012). "Experimental and analytical study of high velocity impact on Kevlar/Epoxy composite plates". Central European Journal of Engineering 2 (4): 638–649. doi:10.2478/s13531-012-0029-x. Retrieved 2 April 2013.
- Cameron, Doug, Chemical giant launches makeover, Wall Street Journal, December 3, 2013, p.A4
- Stäubli, W. (1963). "A new embedding technique for electron microscopy, combining a water-soluble epoxy resin (Durcupan) with water-insoluble Araldite". The Journal of Cell Biology (Rockefeller Univ Press) 16 (1): 197. doi:10.1083/jcb.16.1.197.
- Kushida, H. (1963). "A Modification of the Water-miscible Epoxy Resin "Durcupan" Embedding Method for Ultrathin Sectioning". Journal of Electron Microscopy (Japan Society Microscopy) 12 (1): 72.
- Luft, J.H. (1961). "Improvements in epoxy resin embedding methods". The Journal of biophysical and biochemical cytology (Rockefeller Univ Press) 9 (2): 409. doi:10.1083/jcb.9.2.409.
- McCreight, Tim; Bsullak, Nicole. Color on Metal: 50 Artists Share Insights and Techniques. Madison, WI: Guild. p. 74. ISBN 1-893164-06-3.
- "Market Report: World Epoxy Resin Market". Acmite Market Intelligence.
- An assessment of skin sensitisation by the use of epoxy resin in the construction industry, 2003
- MayoClinic --> Occupational asthma May 23, 2009