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Polyvinyl acetate

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(Redirected from Poly(vinyl acetate)) Adhesive used for porous materials Not to be confused with Polyvinyl alcohol.
Polyvinyl acetate
Polyvinyl acetate
Names
IUPAC name Poly
Other names PVAc, PVA, Poly(ethenyl ethanoate), Poly(ethenyl acetate)
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
  • none
ECHA InfoCard 100.108.147 Edit this at Wikidata
KEGG
PubChem CID
UNII
CompTox Dashboard (EPA)
SMILES
  • O((C*)*)C(C)=O
Properties
Chemical formula (C4H6O2)n
Molar mass 86.09 g/mol per unit
Density 1.19 g/cm (25 °C)
Boiling point 112 °C (234 °F; 385 K)
Hazards
Safety data sheet (SDS) MSDS
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). ☒N verify (what is  ?) Infobox references
Chemical compound

Polyvinyl acetate (PVA, PVAc, poly(ethenyl ethanoate)), commonly known as wood glue (a term that may also refer to other types of glues), PVA glue, white glue, carpenter's glue, school glue, or Elmer's Glue in the US, is a widely available adhesive used for porous materials like wood, paper, and cloth. An aliphatic rubbery synthetic polymer with the formula (C4H6O2)n, it belongs to the polyvinyl ester family, with the general formula −−. It is a type of thermoplastic.

Properties

The degree of polymerization of polyvinyl acetate is typically 100 to 5000, while its ester groups are sensitive to base hydrolysis and slowly convert PVAc into polyvinyl alcohol and acetic acid.

The glass transition temperature of polyvinyl acetate is between 30 and 45 °C depending on the molecular weight.

PVAc dispersions such as Elmer's Glue-All contain polyvinyl alcohol as a protective colloid. In alkaline conditions, boron compounds such as boric acid or borax cause the polyvinyl alcohol to cross-link, forming tackifying precipitates or toys, such as Slime and Flubber.

A number of microorganisms can degrade polyvinyl acetate. Most commonly, damage is caused by filamentous fungi; however, algae, yeasts, lichens, and bacteria can also degrade polyvinyl acetate.

Discovery

Polyvinyl acetate was discovered in Germany in 1912 by Fritz Klatte.

The monomer, vinyl acetate, was first produced on an industrial scale by the addition of acetic acid to acetylene with a mercury(I) salt, but it is now primarily made by palladium-catalyzed oxidative addition of acetic acid to ethylene.

Preparation

PVA is a vinyl polymer. Polyvinyl acetate is prepared by the polymerization of vinyl acetate monomer (free-radical vinyl polymerization of the monomer vinyl acetate).

Applications

As a dispersion in water (usually an emulsion), PVAc preparations are used as adhesives for porous materials, particularly for wood, paper, and cloth, and as a consolidant for porous building stone, in particular sandstone. PVAc is considered a food-safe material, and is thus used often in such applications (e.g., in food packaging material).

Uses:

The stiff homopolymer PVAc, but mostly the softer copolymer, a combination of vinyl acetate and ethylene, vinyl acetate ethylene (VAE), is also used in paper coatings, paint and other industrial coatings, as a binder in nonwovens in glass fibers, sanitary napkins, filter paper and in textile finishing.

Polyvinyl acetate is also the raw material to make other polymers like:

See also

References

  1. Murray, G. T. (1997), Handbook of materials selection for engineering applications, CRC Press, p. 242, ISBN 978-0-8247-9910-6.
  2. Francesca Cappitelli; Claudia Sorlini (2008). "Microorganisms Attack Synthetic Polymers in Items Representing Our Cultural Heritage". Applied and Environmental Microbiology. 74 (3): 564–569. Bibcode:2008ApEnM..74..564C. doi:10.1128/AEM.01768-07. PMC 2227722. PMID 18065627.
  3. See:
    • Deutsches Reichspatent no. 281687 (4 July 1913), Journal of the Society of Chemical Industry (London), vol. 34, p. 623 (1915);
    • Deutsches Reichspatent no. 281688 (2 April 1914);
    • British patent no. 15271 (25 June 1914.);
    • Fritz Klatte and Adolf Rollett, "Plastic composition and process of producing it" Archived 2017-05-10 at the Wayback Machine, U.S. Patent 1,241,738 (filed: July 3, 1914; issued: Oct. 2, 1917), an abstract of which appears in the Journal of the Society of Chemical Industry (London), vol. 36, p. 1185 (1917).
  4. Rutherford John Gettens and George Leslie Stout, Painting Materials: A Short Encyclopaedia (Princeton, New Jersey: D. Van Nostrand, 1942), page 74.
  5. Young, M. E.; Murray, M.; Cordiner, P. (1999). "Stone consolidants and chemical treatments in Scotland". Robert Gordon University, Building Research Establishment and Historic Scotland. Archived from the original on 2016-11-17. Retrieved 2009-07-30.
  6. "CFR - Code of Federal Regulations Title 21". www.accessdata.fda.gov. DEPARTMENT OF HEALTH AND HUMAN SERVICES. Mar 22, 2024. Retrieved Sep 25, 2024.
  7. "The Conservation of the Archimedes Palimpsest". The Walters Art Museum. 2011. Retrieved February 22, 2018.
  8. Amann, Manfred; Minge, Oliver (2012). "Biodegradability of Poly(vinyl acetate) and Related Polymers". Advances in Polymer Science. 245: 137–172. doi:10.1007/12_2011_153. ISBN 978-3-642-27153-3.
  9. "Ultimate Materials Guide - Tips for 3D Printing with PVA".
  10. Coggins, Christopher R. E.; Jerome, Ann M.; Lilly, Patrick D.; McKinney, Willie J.; Oldham, Michael J. (2013). "A comprehensive toxicological evaluation of three adhesives using experimental cigarettes". Inhalation Toxicology. 25 Suppl 2: 6–18. Bibcode:2013InhTx..25S...6C. doi:10.3109/08958378.2013.854430. ISSN 1091-7691. PMID 24341843. S2CID 6414435.
  11. Van den Berg, G. (2002-01-01), "Dutch-Type Cheeses", in Roginski, Hubert (ed.), Encyclopedia of Dairy Sciences, Oxford: Elsevier, pp. 371–378, ISBN 978-0-12-227235-6, retrieved 2021-12-10
  12. H. Staudinger, K. Frey, W. Stark, Ber. Deut. Chem. Ges. 1927, 60, 1782.
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