Cyanoacrylate is the generic name for a family of strong fast-acting adhesives with industrial, medical and household uses. Cyanoacrylate adhesives have a short shelf life if not used, about one year from manufacture if unopened, one month once opened. They have some minor toxicity.
Cyanoacrylates include methyl 2-cyanoacrylate, ethyl-2-cyanoacrylate (commonly sold under trade names such as "Super Glue" and "Krazy Glue"), n-butyl cyanoacrylate and 2-octyl cyanoacrylate (used in medical, veterinary and first aid applications). Octyl cyanoacrylate was developed to address toxicity concerns and to reduce skin irritation and allergic response. Cyanoacrylate adhesives are sometimes known generically as instant glues or superglues (although "Super Glue" is a trade name). The abbreviation "CA" is commonly used for industrial grades.
- 1 Development
- 2 Properties
- 3 Uses
- 4 Safety issues
- 5 Solvents and debonders
- 6 Shelf life
- 7 See also
- 8 References
- 9 Further reading
- 10 External links
The original cyanoacrylates (the chemical name for the glue) were discovered in 1942 in a search for materials to make clear plastic gun sights during World War II, when a team of scientists headed by Harry Coover Jr. stumbled upon a formulation that stuck to everything that it came in contact with; it was rejected for the application. In 1951 cyanoacrylates were rediscovered by Eastman Kodak researchers Harry Coover Jr. and Fred Joyner, who recognized their true commercial potential; "Eastman #910" (later "Eastman 910") was the first cyanoacrylate adhesive to be sold, in 1958.
During the 1960s Eastman Kodak sold cyanoacrylate to Loctite, which in turn repackaged and distributed it under a different brand name "Loctite Quick Set 404". In 1971 Loctite developed its own manufacturing technology and introduced its own line of cyanoacrylate, called "Super Bonder". Loctite quickly gained market share, and by the late 1970s it was believed to have exceeded Eastman Kodak's share in the North American industrial cyanoacrylate market. National Starch and Chemical Company purchased Eastman Kodak’s cyanoacrylate business and combined it with several acquisitions made throughout the 1970s forming Permabond. Other manufacturers of cyanoacrylate include LePage (a Canadian company acquired by Henkel in 1996), the Permabond Division of National Starch and Chemical, Inc., which was a subsidiary of Unilever. Together, Loctite, Eastman and Permabond accounted for approximately 75% of the industrial cyanoacrylate market. As of 2013[update] Permabond continued to manufacture the original 910 formula.
In its liquid form, cyanoacrylate consists of monomers of cyanoacrylate molecules. Methyl-2-cyanoacrylate (CH2=C(CN)COOCH3 or C5H5NO2) has a molecular weight equal to 111.1, a flashpoint of 79 °C, and a density of 1.1 g/ml. Ethyl 2-cyanoacrylate (C6H7NO2) has a molecular weight equal to 125 and a flashpoint of >75 °C. To facilitate easy handling, a cyanoacrylate adhesive is frequently formulated with an ingredient such as fumed silica to make it more viscous or gel-like. More recently, formulations are available with additives to increase shear strength, creating a more impact resistant bond. Such additives may include rubber, as in Loctite's Ultra Gel, or others which are not specified.
In general, cyanoacrylate is an acrylic resin that rapidly polymerises in the presence of water (specifically hydroxide ions), forming long, strong chains, joining the bonded surfaces together. Because the presence of moisture causes the glue to set, exposure to normal levels of humidity in the air causes a thin skin to start to form within seconds, which very greatly slows the reaction. Because of this cyanoacrylate is applied thinly, to ensure that the reaction proceeds rapidly and a strong bond is formed within a reasonable time.
The reaction with moisture can cause a container of glue which has been opened and resealed to become unusable more quickly than if never opened. To minimise this reduction in shelf life cyanoacrylate, once opened, can be stored in an airtight container with a package of silica gel desiccant. Another technique is to insert a hypodermic needle into the opening of a tube. After using the glue, residual glue soon clogs the needle, keeping moisture out. The clog is removed by heating the needle (e.g., by a lighter) before use.
Cyanoacrylates are mainly used as adhesives. They require some care and knowledge for effective use: they do not bond some materials; their shelf life at room temperature is about 12 months unopened and one month once opened; they do not fill spaces, unlike epoxies, and a very thin layer bonds more effectively than a thicker one that does not cure properly; they bond many substances, including human skin and tissues, almost instantly and can cause harm to people. They have an exothermic reaction to natural fibres: cotton, wool, leather, see reaction with cotton below.
Cyanoacrylate glue has a low shearing strength, which has led to its use as a temporary adhesive in cases where the piece needs to be sheared off later. Common examples include mounting a workpiece to a sacrificial glue block on a lathe, and tightening pins and bolts.
Cyanoacrylates are used to assemble prototype electronics (see wire wrap), flying model aircraft, and as retention dressings for nuts and bolts. Their effectiveness in bonding metal and general versatility have made them popular among modeling and miniatures hobbyists. They are used to re-harden the boxes and shanks of ballerinas' pointe shoes.
Cyanoacrylate glue's ability to resist water has made it popular with marine aquarium hobbyists for fragging corals. The cut branches of hard corals such as Acropora can be glued to a piece of live rock (harvested reef coral) or Milliput (epoxy putty) to allow the new frag to grow out. It is actually safe to use directly in the tank, unlike silicone, which must be cured to be safe. However, as a class of adhesives, traditional cyanoacrylates are classified as having "weak" resistance to both moisture and heat although the inclusion of phthalic anhydride reportedly counteracts both of these characteristics.
Bonding smooth surfaces
Most standard cyanoacrylate adhesives do not bond well with smooth glass, although they can be used as a quick, temporary bond prior to application of an epoxy or cyanoacrylate specifically formulated for use on glass. A mechanical adhesive bond may be formed around glass fibre mat or tissue to reinforce joints or to fabricate small parts.
When added to baking soda (sodium bicarbonate), cyanoacrylate glue forms a hard, lightweight adhesive filler (baking soda is first used to fill a gap then the adhesive is dropped onto the baking soda). This works well with porous materials that the glue does not work well with alone. This method is sometimes used by aircraft modelers to assemble or repair polystyrene foam parts. It is also used to repair small nicks in the leading edge of composite propeller blades on light aircraft. The reaction between cyanoacrylate and baking soda is very exothermic (heat-producing) and also produces noxious vapors. See Reaction with cotton below.
Cyanoacrylate is used as a forensic tool to capture latent fingerprints on non-porous surfaces like glass, plastic, etc. Cyanoacrylate is warmed to produce fumes that react with the invisible fingerprint residues and atmospheric moisture to form a white polymer (polycyanoacrylate) on the fingerprint ridges. The ridges can then be recorded. The developed fingerprints are, on most surfaces (except on white plastic or similar), visible to the naked eye. Invisible or poorly visible prints can be further enhanced by applying a luminescent or non-luminescent stain.
Thin CA glue has application in woodworking. It can be used as a fast-drying, glossy finish. The use of oil (such as boiled linseed oil) may be used to control the rate at which the CA cures. CA glue is also used in combination with sawdust (from a saw or sanding) to fill voids and cracks. These repair methods are used on piano soundboards, wood instruments, and wood furniture.
Some rock climbers use cyanoacrylate to repair damage to the skin on their fingertips. Similarly, stringed-instrument players can form protective finger caps (in addition to calluses) with cyanoacrylates.
CA glue was in veterinary use for mending bone, hide, and tortoise shell by the early 1970s or before. Harry Coover said in 1966 that a CA spray was used in the Vietnam war to retard bleeding in wounded soldiers until they could be brought to a hospital. Butyl cyanoacrylate has been used medically since the 1970s. In the US, due to its potential to irritate the skin, the U.S. Food and Drug Administration did not approve its use as a medical adhesive until 1998 with Dermabond. Research has demonstrated the use of cyanoacrylate in wound closure as being safer and more functional than traditional suturing (stitches). The adhesive has demonstrated superior performance in the time required to close a wound, incidence of infection (suture canals through the skin's epidermal, dermal, and subcutaneous fat layers introduce extra routes of contamination), and final cosmetic appearance.
While standard "superglue" is 100% ethyl cyanoacrylate, many custom formulations (e.g.,, 91% ECA, 9% poly(methyl methacrylate), <0.5% hydroquinone, and a small amount of organic sulfonic acid and variations on the compound N-butyl-cyanoacrylate's for medical applications) have come to be used for specific applications.
Cyanoacrylate is used in archery to glue fletching to arrow shafts. Some special fletching glues are really cyanoacrylate repackaged in special fletching glue kits. Often these tubes have a long thin metal nozzle to aid in better accuracy in the application of the glue to the base of the feather or plastic fletching to ensure a good bond to the arrow shaft.
Cyanoacrylate is used in the cosmetology/beauty industry as a "nail glue" for some artificial nail enhancements such as nail tips and nail wraps, and is sometimes mistaken for eye drops causing accidental injury.
CA adhesives may glue skin and eyelids together within seconds. In the course of separating the glued body parts, injuries may occur by ripping off parts of the skin. However, when left alone, the glue will separate from the skin over the course of time (up to four days). The separation process can be accelerated by applying vegetable oil near on and around the glue. In the case of glued eyelids, a doctor should be consulted.
The fumes from CA are a vaporized form of the cyanoacrylate monomer that irritate sensitive membranes in the eyes, nose, and throat. They are immediately polymerized by the moisture in the membranes and become inert. These risks can be minimized by using CA in well ventilated areas. About 5% of the population can become sensitized to CA fumes after repeated exposure, resulting in flu-like symptoms. It may also act as a skin irritant and may cause an allergic skin reaction. The ACGIH assign a Threshold Limit Value exposure limit of 200 parts per billion. On rare occasions, inhalation may trigger asthma. There is no singular measurement of toxicity for all cyanoacrylate adhesives as there is a wide variety of adhesives that contain various cyanoacrylate formulations.
The United States National Toxicology Program and the United Kingdom Health and Safety Executive have concluded that the use of ethyl cyanoacrylate is safe and that additional study is unnecessary. 2-octyl cyanoacrylate degrades much more slowly due to its longer organic backbone that slows the degradation of the adhesive enough to remain below the threshold of tissue toxicity. Due to the toxicity issues of ethyl cyanoacrylate, the use of 2-octyl cyanoacrylate for sutures is preferred.
Reaction with cotton
Applying cyanoacrylate to some natural materials such as cotton, leather or wool (cotton swabs, cotton balls, and certain yarns or fabrics) results in a powerful, rapid exothermic reaction. The heat released may cause serious burns, ignite the cotton product, or release irritating white smoke. Material Safety Data Sheets for cyanoacrylate instruct users not to wear cotton or wool clothing, especially cotton gloves, when applying or handling cyanoacrylates.
Solvents and debonders
Acetone, commonly found in nail polish remover, is a widely available solvent capable of softening cured cyanoacrylate. Other solvents include nitromethane, dimethyl sulfoxide, and methylene chloride. gamma-Butyrolactone may also be used to remove cured cyanoacrylate. Commercial debonders are also available.
Cyanoacrylate adhesives have a short shelf life. Date-stamped containers help to ensure that the adhesive is still viable. One manufacturer supplies the following information and advice: when kept unopened in a cool, dry location such as a refrigerator at a temperature of about 55 °F (13 °C), the shelf life of cyanoacrylate will be extended from about one year from manufacture to at least 15 months. If the adhesive is to be used within six months, it is not necessary to refrigerate it. Cyanoacrylates are moisture-sensitive, and moving from a cool to a hot location will create condensation; after removing from the refrigerator, it is best to let the adhesive reach room temperature before opening. After opening, it should be used within 30 days. Open containers should not be refrigerated. Another manufacturer says that the maximum shelf life of 12 months is obtained for some of their cyanoacrylates if the original containers are stored at 35 to 40 °F (2 to 4 °C). User forums and some manufacturers say that an almost unlimited shelf life is attainable by storing unopened at −20 °C (−4 °F), the typical temperature of a domestic freezer, and allowing to reach room temperature before use. (Rechilling an opened container is not advisable as it will cause moisture from the air to condense in the container, causing deterioration.)
As cyanoacrylates age they polymerize, become thicker, and cure more slowly. They can be thinned with a cyanoacrylate of the same chemical composition with lower viscosity.
- Methyl cyanoacrylate
- Ethyl cyanoacrylate
- Butyl cyanoacrylate
- Octyl cyanoacrylate
- 2-Octyl cyanoacrylate
- Oxford English Dictionary, 2nd ed. cites "Croid Super Glue can be used..." (1937); "‘Gunk’ is what workers in the Chrysler Corporation factory call their superglue named Cycleweld" (1944)
- "Inventor of the Week Archive". Lemelson-MIT Program. September 2004. Retrieved 13 February 2010.
- HBS, “Loctite Corporation: Industrial Product Group,” 15 July 1991, p.3
- Petrie, Edward M. (2000). Handbook of adhesives and sealants. New York: McGraw-Hill. p. 354. ISBN 0-07-049888-1.
- Petrie, Edward M. (2000). Handbook of adhesives and sealants. New York: McGraw-Hill. p. 389. ISBN 0-07-049888-1.
- Eric W. Brown "The Cyanoacrylate Fuming Method"
- "Bouldering". climbingaction.com. Retrieved 19 February 2011.
- Anahad O'Connor (4 December 2007). "The Claim: Super Glue Can Heal Wounds". The New York Times. Retrieved 19 February 2011.
- Singer, A. J.; McClain, S. A.; Katz, A. (2004). "A porcine epistaxis model: hemostatic effects of octylcyanoacrylate". Otolaryngology-Head and Neck Surgery 130 (5): 553–557. doi:10.1016/j.otohns.2003.09.035. PMID 15138419.
- Fischl, R.A.: An adhesive for primary closure of skin incisions: a preliminary report. Plast. Reconstr. Surg. 30: 607-610, 1962
- Rothnie, N.G. and Taylor, G. W. Sutureless skin closure-a clinical trial. Brit. Med. J. 2: 1027–1030, 1963
- Safety data for ethyl cyanoacrylate from the Physical and Theoretical Chemistry Laboratory of Oxford University
- Needham, A. D (2001). "Similarities in the packaging of cyanoacrylate nail glue and ophthalmic preparations: an ongoing problem". British Journal of Ophthalmology 85 (4): 496a–496. doi:10.1136/bjo.85.4.496a. ISSN 0007-1161.
- First aid information (in German) by Industrieverband Klebstoffe e.V.
- CA PLUS Adhesives, Inc. FAQ
- Methyl Cyanoacrylate and Ethyl Cyanoacrylate from inchem.org
- Clarke, TFE (March 2011). "Superglue (Cyanoacrylate) in the Nose". Journal of Plastic, Reconstructive & Aesthetic Surgery 64 (7): e170–3. doi:10.1016/j.bjps.2011.03.009. PMID 21481658.
- "Material Safety Data Sheet". accumetricinc.com. Retrieved 9 June 2008.
- Moschos, M.; Droutsas, D.; Boussalis, P.; Tsioulias, G. (1997). "Clinical experience with cyanoacrylate tissue adhesive". Documenta Ophthalmologica (Soringer) 93 (3): 237–245. doi:10.1007/BF02569064. PMID 9550352. Retrieved 29 March 2011.
- Duvvi, Sham K.; Lo, Stephen; Kumar, R; Spraggs, P (2005). "Superglue (Cyanoacrylate) in the Nose". Otolaryngology-Head and Neck Surgery 133 (5): 803–804. doi:10.1016/j.otohns.2004.09.090. Retrieved 29 March 2011.
- Shantha, K.L.; Krishnamurti, N.; Krishnamurti, N. (1989). "Developments and applications of cyanoacrylate adhesives". Journal of Adhesion Science and Technology (VSP) 3 (1): 237–260. doi:10.1163/156856189X00191. Retrieved 29 March 2011.
- "Product Description". 3M. Retrieved 27 March 2011.[dead link]
- Palm Labs Adhesives: Cyanoacrylate Adhesive Shelf Life
- MASTER BOND MB SERIES CYANOACRYLATES: Technical Data Sheet
- WEICON Contact Cyanoacrylate Adhesives
- CA Plus Adhesives FAQ
- derma+flex QS 510k Letter: http://www.accessdata.fda.gov/cdrh_docs/pdf10/K101276.pdf
- LiquiBand 510k Letter: http://www.accessdata.fda.gov/cdrh_docs/pdf8/K083531.pdf
- Fernandez, Tania & Bliskovsky, Val (2 January 2003). "Cyanoacrylate Technology: Stay Glued". Pharmbiz.com.
- Hayes, Sharon Caskey (11 July 2004). "Discovery of Super Glue helped land Coover in National Inventors Hall of Fame". Kingsport Times-News.
- Jueneman, F. (August 1981). "Stick it to um". Industrial Research & Development. p. 19.
- Perry, L. C. "An evaluation of acute incisional strength with Traumaseal surgical tissue adhesive wound closure". Dimensional Analysis Systems Inc.
- Quinn, J. & Kissack, J. (1994). "Tissue Adhesives for Laceration Repair During Sporting Events". Clinical Journal of Sports Medicine 4 (4): 245. doi:10.1097/00042752-199410000-00006.
- Schwade, Nathan D. (10 April 2002). "Wound Adhesives, 2-Octyl Cyanoacrylate". eMedicine article.
- Vinters, H. V.; Galil, K. A.; Lundie, M. J.; Kaufmann, J. C. (1985). "The histotoxicity of cyanoacrylates. A selective review". Neuroradiology 27 (4): 279–291. doi:10.1007/BF00339559. PMID 3900798.
- Was Super Glue invented to seal battle wounds in Vietnam? (from The Straight Dope)
- Cyanoacrylate Toxicity
- Cyanoacrylate Adhesive / Super Glue Safety Data Sheets
- Safety in the Home: Super Glue - Queensland Health
- Cyanoacrylate Technical Data Sheet
- U.S. Patent 2,768,109 Alcohol-Catalyzed α-Cyanoacrylate Adhesive Compositions, filed June 1954, issued October 1956.
- 3M Activators, Primers and Debonder
- Application note on measuring cure kinetics of cyanoacrylate glues