Difference between revisions of "Cyanoacrylate resin"

From CAMEO
Jump to navigation Jump to search
 
(8 intermediate revisions by the same user not shown)
Line 16: Line 16:
  
 
== Environmental Risks ==
 
== Environmental Risks ==
Formaldehyde degradation product (more so in ethyl type).<ref>Jane L. Down and Elzbieta Kaminska, "A Preliminary Study of the Degradation of Cyanoacrylate Adhesives in the Presence and Absence of Fossil Material", ''Journal of Vertebrate Paleontology'', Vol. 26, No. 3 (Sep. 11, 2006), pp. 519-525</ref>
+
Formaldehyde degradation product (more so in ethyl type).<ref name=Jane>Jane L. Down and Elzbieta Kaminska, "A Preliminary Study of the Degradation of Cyanoacrylate Adhesives in the Presence and Absence of Fossil Material", ''Journal of Vertebrate Paleontology'', Vol. 26, No. 3 (Sep. 11, 2006), pp. 519-525</ref>
  
 
== Collection Risks ==
 
== Collection Risks ==
*Hydrolysis degradation can occur in alkaline conditions (glass surfaces).<sup>1,2</sup>
+
* Hydrolysis degradation can occur in alkaline conditions (glass surfaces).<ref name=Jane/>, <ref name=IIC>A literature review of cyanoacrylate adhesives. Reviews in conservation no. 2 (2001), pp. 35-38 International Institute for Conservation of Historic and Artistic Works, London, United Kingdom</ref>
*Cyanoacrylates undergo ultraviolet degradation.<ref>Jane L. Down and Elzbieta Kaminska, "A Preliminary Study of the Degradation of Cyanoacrylate Adhesives in the Presence and Absence of Fossil Material", ''Journal of Vertebrate Paleontology'', Vol. 26, No. 3 (Sep. 11, 2006), pp. 519-525</ref>, <ref>A literature review of cyanoacrylate adhesives. ''Reviews in conservation'' no. 2 (2001), pp. 35-38 International Institute for Conservation of Historic and Artistic Works, London, United Kingdom.</ref>
+
* Cyanoacrylates undergo ultraviolet degradation.<ref name=Jane/>, <ref name=IIC/>
 +
 
 
== Physical and Chemical Properties ==
 
== Physical and Chemical Properties ==
  
Line 41: Line 42:
 
[[media:download_file_336.pdf|General Characteristics of Polymers]]
 
[[media:download_file_336.pdf|General Characteristics of Polymers]]
  
== References ==
+
== Resources and Citations ==
 
+
<references />
 
 
 
 
 
 
  
* Contributions: Kate Wight Tyler, Polymer Group, AIC 2020.
+
* Contributions: Kate Wight Tyler, AIC Plastics Panel, 2020.
  
 
* H.W.Coover, J.M.McIntire, "Cyanoacrylate Adhesives" in ''Handbook of Adhesives'', I.Skeist (ed.), Van Nostrand Reinhold, New York, 1977, p.569-580.  
 
* H.W.Coover, J.M.McIntire, "Cyanoacrylate Adhesives" in ''Handbook of Adhesives'', I.Skeist (ed.), Van Nostrand Reinhold, New York, 1977, p.569-580.  

Latest revision as of 08:20, 7 July 2020

Description

A thermoplastic polymer commonly used as a fast-setting, strong adhesive. The first cyanoacrylate adhesive was made in 1941, but not marketed till 1958 as Eastman 910® [Eastman Kodak]. Cyanoacrylate adhesives are based on ethyl-2-cyanoacrylate polymers. Most commercial formulations also contain stabilizers, thickeners and catalysts. The glues set rapidly (5 seconds - 3 minutes) upon exposure to ultraviolet radiation or moisture. When cured, they form an extremely strong bond that is fairly insoluble. Cyanoacrylate glues has been used for gluing glass, ceramics and other hard materials. They also have medical and dental applications to suture skin and weld crowns. Some cyanoacrylate glues may lose adhesive strength with time. Ultraviolet light and contact with alkaline materials (glass and some stones) will accelerate the degradation process.

Synonyms and Related Terms

CA; super glue; instant adhesive; Super Glue Gel [Loctite]; Krazy® glue [Borden]; Super Attack [Loctite]; Zap; Eastman 910® [Eastman Chemical]; ELFY® super glue; ethyl cyanoacrylate; Dermabond; Traumaseal; cianoacrilati (It.); cyanoacrylaat (Ned.); resina de cianoacrilato (Esp.)

Applications

FTIR

AaiCYANOacrylate.jpg

  • Adhesive

Personal Risks

May cause irritation to skin and eyes. Will adhere objects on contact, including skin. Flash points range from 75-80°C.

Environmental Risks

Formaldehyde degradation product (more so in ethyl type).[1]

Collection Risks

  • Hydrolysis degradation can occur in alkaline conditions (glass surfaces).[1], [2]
  • Cyanoacrylates undergo ultraviolet degradation.[1], [2]

Physical and Chemical Properties

  • Uncured glue soluble in acetone, methanol, toluene, MEK.
  • Cured glue is slightly soluble in DMF or nitromethane.
  • Soaking in acetone may decrease adhesion and cause the join to separate.
  • CAS = 7085-85-0
  • Density = 1.05-1.10

Working Properties

Cures quickly

Forms/Sizes

Often sold in small container with application device

Comparisons

Physical Properties for Selected Thermoplastic Resins

General Characteristics of Polymers

Resources and Citations

  1. 1.0 1.1 1.2 Jane L. Down and Elzbieta Kaminska, "A Preliminary Study of the Degradation of Cyanoacrylate Adhesives in the Presence and Absence of Fossil Material", Journal of Vertebrate Paleontology, Vol. 26, No. 3 (Sep. 11, 2006), pp. 519-525
  2. 2.0 2.1 A literature review of cyanoacrylate adhesives. Reviews in conservation no. 2 (2001), pp. 35-38 International Institute for Conservation of Historic and Artistic Works, London, United Kingdom
  • Contributions: Kate Wight Tyler, AIC Plastics Panel, 2020.
  • H.W.Coover, J.M.McIntire, "Cyanoacrylate Adhesives" in Handbook of Adhesives, I.Skeist (ed.), Van Nostrand Reinhold, New York, 1977, p.569-580.
  • Theodore J. Reinhart, 'Glossary of Terms', Engineered Plastics, ASM International, 1988
  • Richard S. Lewis, Hawley's Condensed Chemical Dictionary, Van Nostrand Reinhold, New York, 10th ed., 1993
  • Michael McCann, Artist Beware, Watson-Guptill Publications, New York City, 1979
  • Irving Skeist, Handbook of Adhesives, Van Nostrand Reinhold Company, New York, 1977

Retrieved from "https://cameo.mfa.org/index.php?title=Cyanoacrylate_resin&oldid=73330"