Difference between revisions of "Melamine formaldehyde resin"

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== Description ==
 
== Description ==
  
A thermosetting [[amino%20resin|amino resin]] that is made by reacting melamine with [[formaldehyde|formaldehyde]]. First made in 1933 by CIBA, melamine formaldehyde resins were most often used for molded plastic products and were filled with [[cellulose|cellulose]], [[wood%20flour|wood flour]], or mineral powders. They produce a hard, high gloss plastic that was used for utensils, containers, dishware ([[Melmac|Melmac]]) and countertops ([[Formica%C2%AE|Formica®]]). Melamine formaldehyde resins are also used for [[plywood|plywood]], textile sizing, leather processing, and paper strengthening. They are resistant to water and biodegradation.
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A thermosetting [[amino%20resin|amino resin]] that is made by reacting melamine with [[formaldehyde|formaldehyde]]. First made in 1933 by CIBA, melamine formaldehyde resins were most often used for molded plastic products and were filled with [[cellulose|cellulose]], [[wood%20flour|wood flour]], or mineral powders. They produce a hard, high gloss plastic that was used for utensils, containers, dishware ([[Melmac|Melmac]]) and countertops ([[Formica|Formica®]]). Melamine formaldehyde resins are also used for [[plywood|plywood]], textile sizing, leather processing, and paper strengthening. They are resistant to water and biodegradation.
  
 
== Synonyms and Related Terms ==
 
== Synonyms and Related Terms ==
  
melamine; Melmac; Formica® [Formica]; amino resin; melamine-formaldehyde resin
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melamine; amino resin; melamine-formaldehyde resin
  
== Other Properties ==
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Commercial products: Melamine; Melmac; Meladur; Prolon; Formica® [Formica]; Texasware; Boontonware
  
Resistant to water, acids, bases and organic solvents.
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== Risks ==
  
{| class="wikitable"
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* volves formaldehyde and ammonia as it degrades.
|-
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== Physical and Chemical Properties ==
! scope="row"| Density
 
| 1.5
 
|}
 
  
== Hazards and Safety ==
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Resistant to water, acids, bases and organic solvents. Density = 1.5
 
 
Evolves formaldehyde and ammonia as it degrades.
 
  
 
== Comparisons ==
 
== Comparisons ==
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[[media:download_file_277.pdf|Physical Properties for Selected Thermoset Resins]]
 
[[media:download_file_277.pdf|Physical Properties for Selected Thermoset Resins]]
  
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== Resources and Citations ==
  
 
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* History of Plastics: www.nswpmith.com.au/historyofplastics.html .. commercial processes for melamine synthesis patented in 1933 (CIBA) and 1946 (DUPONT).
== Sources Checked for Data in Record ==
 
 
 
* Website address 1  Comment: www.nswpmith.com.au/historyofplastics.html .. commercial processes for melamine synthesis patented in 1933 (CIBA) and 1946 (DUPONT).
 
  
 
* Sharon Blank, An introduction to plastics and rubbers in collections, ''Studies in Conservation'', 35, 53-63, 1990  Comment: Introduced in 1934
 
* Sharon Blank, An introduction to plastics and rubbers in collections, ''Studies in Conservation'', 35, 53-63, 1990  Comment: Introduced in 1934

Revision as of 10:36, 4 December 2020

Description

A thermosetting Amino resin that is made by reacting melamine with Formaldehyde. First made in 1933 by CIBA, melamine formaldehyde resins were most often used for molded plastic products and were filled with Cellulose, Wood flour, or mineral powders. They produce a hard, high gloss plastic that was used for utensils, containers, dishware (Melmac) and countertops (Formica®). Melamine formaldehyde resins are also used for Plywood, textile sizing, leather processing, and paper strengthening. They are resistant to water and biodegradation.

Synonyms and Related Terms

melamine; amino resin; melamine-formaldehyde resin

Commercial products: Melamine; Melmac; Meladur; Prolon; Formica® [Formica]; Texasware; Boontonware

Risks

  • volves formaldehyde and ammonia as it degrades.

Physical and Chemical Properties

Resistant to water, acids, bases and organic solvents. Density = 1.5

Comparisons

General Characteristics of Polymers

Physical Properties for Selected Thermoset Resins

Resources and Citations

  • History of Plastics: www.nswpmith.com.au/historyofplastics.html .. commercial processes for melamine synthesis patented in 1933 (CIBA) and 1946 (DUPONT).
  • Sharon Blank, An introduction to plastics and rubbers in collections, Studies in Conservation, 35, 53-63, 1990 Comment: Introduced in 1934
  • G.S.Brady, Materials Handbook, McGraw-Hill Book Co., New York, 1971
  • Richard S. Lewis, Hawley's Condensed Chemical Dictionary, Van Nostrand Reinhold, New York, 10th ed., 1993
  • Pam Hatchfield, Pollutants in the Museum Environment, Archetype Press, London, 2002

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