Cyanoacrylate

Cyanoacrylates are a family of strong fast-acting adhesives with industrial, medical, and household uses. They are derived from ethyl cyanoacrylate and related esters. The cyanoacrylate group in the monomer rapidly polymerizes in the presence of water to form long, strong chains. They have some minor toxicity.

Specific cyanoacrylates include methyl 2-cyanoacrylate (MCA), ethyl 2-cyanoacrylate (ECA, commonly sold under trade names such as "Super Glue" and "Krazy Glue", or Toagosei), ''n''-butyl cyanoacrylate (n-BCA), octyl 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, power glues or superglues. The abbreviation "CA" is commonly used for industrial grade cyanoacrylate.

Development

The original patent for cyanoacrylate was filed in 1947 by the B.F. Goodrich Company as an outgrowth of a search for materials suitable for clear plastic gun sights for the war effort. In 1942, a team of scientists headed by Harry Coover Jr. stumbled upon a formulation that stuck to everything with which it came in contact. The team quickly rejected the substance for the wartime application, but in 1951, while working as researchers for Eastman Kodak, Coover and a colleague, Fred Joyner, rediscovered cyanoacrylates. The two realized the true commercial potential, and a form of the adhesive was first sold in 1958 under the title "Eastman #910" (later "Eastman 910").

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, which was a subsidiary of Unilever. Together, Loctite, Eastman, and Permabond accounted for approximately 75% of the industrial cyanoacrylate market. Permabond continued to manufacture the original 910 formula.

Monomers

In its liquid form, cyanoacrylate consists of monomers of cyanoacrylate ester molecules. Methyl 2-cyanoacrylate (CH₂=C(C≡N)COOCH₃) has a molecular weight of 111.1 g/mol, a flashpoint of , and a density of 1.1 g/mL. Ethyl 2-cyanoacrylate ((CH₂=C(C≡N)COOCH₂CH₃)) has a molecular weight of 125 g/mol and a flashpoint of more than . 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, the acryl groups rapidly undergo chain-growth polymerisation 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; hence, cyanoacrylates are applied as thin coats to ensure that the reaction proceeds rapidly for bonding.

Cyanoacrylate adhesives have a short shelf life—about one year from manufacture if unopened, and one month once opened.

Uses

General properties

Cyanoacrylates are mainly used as adhesives. Thin layers bond effectively, thick layers much less so. They bond many substances, including human skin and tissues, natural fibres, cotton, wool, and leather.

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. It is also used in conjunction with another slower, but more resilient, adhesive as a way of rapidly forming a joint, which then holds the pieces in the appropriate configuration until the second adhesive has set.

Cyanoacrylate-based glue has a weak bond with smooth surfaces and as such easily gives to friction; a good example of this is the fact that cyanoacrylates may be removed from human skin by means of abrasives (e.g. sugar or sandpaper).

Electronics

Cyanoacrylates are used to assemble prototype electronics (used in 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.

Aquaria

Cyanoacrylate glue's ability to resist water has made it popular with marine aquarium hobbyists for fragmenting 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 fragment to grow out. It is 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. Cyanoacrylate glue is also used frequently in aquascaping both freshwater and marine aquariums for the purpose of securing the rhizomes of live plants to pieces of wood or stone.

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.

Filler

When added to baking soda ( sodium bicarbonate), cyanoacrylate glue forms a hard, lightweight adhesive filler. This works well with porous materials that do not work well with the adhesive alone. This method is sometimes used by aircraft modelers to assemble or repair polystyrene parts. It is also used to repair small nicks in the leading edge of wood propeller blades on light aircraft, although this technique is limited to use on aircraft registered in the "experimental" category (composite propellers can be repaired in a similar way using two-part epoxies). This technique can also be used to fill in the slots in the nut of a guitar so that new ones can be cut. The reaction between cyanoacrylate and baking soda is very exothermic (heat-producing) and also produces noxious vapors.

One brand of cyanoacrylate, "SupaFix", uses calcium oxide as a filler giving an even harder (mortar-like in texture) result that can be used to join hard materials and even repair cracked castings.

Forensics

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.

Woodworking

Thin cyanoacrylate glue has application in woodworking. It can be used as a fast-drying, glossy finish. An oil, such as boiled linseed oil, may be used to control the rate at which the cyanoacrylate cures. Cyanoacrylate 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. Cyanoacrylate glue is also used in the finishing of pen blanks (wooden blanks for turning pens) that have been turned on a lathe by applying multiple thin layers to build up a hard, clear finish that can then be sanded and polished to a glossy finish.

Medical and veterinary

Cyanoacrylate 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 cyanoacrylate spray was used in the Vietnam War to reduce bleeding in wounded soldiers until they could be taken to a hospital. ''n''-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 (FDA) did not approve its use as a medical adhesive until 1998 with Dermabond (2-octyl cyanoacrylate). A 1986 independent study suggests that cyanoacrylate can be safer and more functional for wound closure than traditional suturing (stitches). The adhesive is superior in terms of time required to close wounds, the incidence of infection (suture canals through the skin's epidermal, dermal, and subcutaneous fat layers introduce additional routes of contamination), and finally cosmetic appearance.

Some rock climbers use cyanoacrylate to repair damage to the skin on their fingertips. Similarly, stringed-instrument players can form protective finger caps (typically, when they lose their calluses due to inactivity or accidents) with cyanoacrylates. While the glue is not very toxic and wears off quickly with shed skin, applying large quantities of glue and its fumes directly to the skin can cause chemical burns.

While standard "superglue" is 100% ethyl 2-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 for medical applications) have come to be used for specific applications. There are three cyanoacrylate compounds currently available as topical skin adhesives. 2-Octyl cyanoacrylate is marketed as Dermabond, SurgiSeal, and more recently LiquiBand Exceed. ''n''-Butyl cyanoacrylate is marketed as Histoacryl, Indermil, GluStitch, GluSeal, PeriAcryl, and LiquiBand. The compound ethyl 2-cyanoacrylate is available as Epiglu.

The ester substituent has several effects upon the biocompatibility of the adhesive. Longer side chains result in higher flexibility of the cured adhesive allowing a better match for the flexibility of skin, and can result in a slower release of formaldehyde after curing. Alkoxy-ethyl substituents have also been investigated and have shown some promise as a medical adhesive.

Archery

Cyanoacrylate is used in archery to glue fletching to arrow shafts. Some special fletching glues are primarily cyanoacrylate repackaged in special fletching glue kits. Such tubes often have a long, thin metal nozzle for improved precision in applying the glue to the base of the fletching and to ensure secure bonding to the arrow shaft.

Cosmetics

Cyanoacrylate is used in the cosmetology and beauty industry as an eyelash extension glue, or 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 (chemical eye injury).

Safety issues

Skin injuries

Cyanoacrylate adhesives may adhere to body parts, and injuries may occur when parts of the skin are torn off. Without force, however, the glue will spontaneously separate from the skin in time (up to four days). Separation can be accelerated by applying vegetable oil near, on, and around the glue. In the case of glued eyelids, especially if it has contacted the eyeball, a doctor should be consulted.

Toxicity

The fumes from cyanoacrylate are a vaporized form of the cyanoacrylate monomer that irritate the sensitive mucous membranes of the respiratory tract (nose, throat, and lungs) and the eyes. They are immediately polymerized by the moisture in the membranes and become inert. These risks can be minimized by using cyanoacrylate in well-ventilated areas. About 5% of the population can become sensitized to cyanoacrylate fumes after repeated exposure, resulting in flu-like symptoms. Cyanoacrylate may also be a skin irritant, causing an allergic skin reaction. The American Conference of Governmental Industrial Hygienists (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 because of the large number of adhesives that contain various cyanoacrylate formulations.

The United Kingdom's Health and Safety Executive and the United States National Toxicology Program have concluded that the use of ethyl cyanoacrylate is safe and that additional study is unnecessary. The compound 2-octyl cyanoacrylate degrades much more slowly due to its longer organic backbone (series of covalently bonded carbon molecules) and the adhesive does not reach 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, wool, and other fibrous materials

Applying cyanoacrylate to some natural materials such as cotton ( jeans, cotton swabs, cotton balls, and certain yarns or fabrics), or leather or wool results in a powerful, rapid, exothermic reaction. This reaction also occurs with fiberglass and carbon fiber. The heat released may cause serious burns or release irritating white smoke. Material safety data sheets for cyanoacrylate instruct users not to wear cotton (jeans) or wool clothing, especially cotton gloves, when applying or handling cyanoacrylates.

Solvents and debonders

Acetone, commonly found as a fraction of nail polish remover (or at hardware stores in pure form), is a widely available solvent capable of softening cured cyanoacrylate. Other solvents include nitromethane, dimethylformamide, dimethyl sulfoxide, and methylene chloride. Another viable solvent for removing cured cyanoacrylate is ''gamma''-butyrolactone. Commercial debonders are also available, many based on propylene carbonate.

Shelf life

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 . User forums and some manufacturers say that an almost unlimited shelf life is attainable by storing unopened at , the typical temperature of a domestic freezer, and allowing the contents to reach room temperature before use. Opening a container while chilled may cause moisture from the air to condense in the container; however, reports from hobbyists suggest that storing cyanoacrylate in a freezer can preserve opened cyanoacrylate indefinitely.

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. Storing cyanoacrylates below will nearly stop the polymerization process and prevent aging.

References

Further reading

* 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
*
*
*
*
*
*
*

External links

Was Super Glue invented to seal battle wounds in Vietnam?
(from The Straight Dope)

Cyanoacrylate Toxicity



Safety in the Home: Super Glue
- Queensland Health

Cyanoacrylate Technical Data Sheet
* ''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

{{Authority control

Adhesives
American inventions
Medical treatments
Monomers
Synthetic resins
Cyanoacrylate esters