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AMINO RESINS AND PLASTICS

Amino resins are thermosetting polymers made by combining an aldehyde with a compound containing an amino (—NH2) group. Urea—formaldehyde (U/F) accounts for over 80% of amino resins melamine—formaldehyde accounts for most of the rest. Other aldehydes and other amino compounds are used to a very minor extent. The first commercially important amino resin appeared about 1930, or some 20 years after the introduction of phenol—formaldehyde resins and plastics (see Phenolic resins). [Pg.321]

Amino resins are manufactured throughout the industrialized world to provide a wide variety of useful products. Adhesives (qv), representing the largest single market, are used to make plywood, chipboard, and sawdust board. Other types are used to make laminated wood beams, parquet flooring, and for furniture assembly (see Wood-BASED composites and laminates). [Pg.321]

Some amino resins are used as additives to modify the properties of other materials. For example, a small amount of amino resin added to textile fabric imparts the familiar wash-and-wear quaUties to shirts and dresses. Automobile tires are strengthened by amino resins which improve the adhesion of mbber to tire cord (qv). A racing sailboat may have a better chance to win because the sails of Dacron polyester have been treated with an amino resin (1). Amino resins can improve the strength of paper even when it is wet. Molding compounds based on amino resins are used for parts of electrical devices, botde and jar caps, molded plastic dinnerware, and buttons. [Pg.321]

Amino resins are also often used for the cure of other resins such as alkyds and reactive acryUc polymers. These polymer systems may contain 5—50% of the amino resin and are commonly used in the flexible backings found on carpets and draperies, as well as in protective surface coatings, particularly the durable baked enamels of appHances, automobiles, etc. [Pg.321]

The term amino resin is usually appHed to the broad class of materials regardless of appHcation, whereas the term aminoplast or sometimes amino plastic is more commonly appHed to thermosetting molding compounds based on amino resins. Amino plastics and resins have been in use since the 1920s. Compared to other segments of the plastics industry, they are mature products, and their growth rate is only about half of that of the plastics industry as a whole. They account for about 3% of the United States plastics and resins production. [Pg.321]


Commercially, urea is produced by the direct dehydration of ammonium carbamate, NH2COONH4, at elevated temperature and pressure. Ammonium carbamate is obtained by direct reaction of ammonia and carbon dioxide. The two reactions are usually carried out simultaneously in a high pressure reactor. Recendy, urea has been used commercially as a catde-feed supplement (see Feeds and feed additives). Other important appHcations are the manufacture of resins (see Amino resins and plastics), glues, solvents, and some medicinals. Urea is classified as a nontoxic compound. [Pg.298]

Amino and Phenolic Resins. The largest use of formaldehyde is in the manufacture of urea—formaldehyde, phenol—formaldehyde, and melamine—formaldehyde resins, accounting for over one-half (51%) of the total demand (115). These resins find use as adhesives for binding wood products that comprise particle board, fiber board, and plywood. Plywood is the largest market for phenol—formaldehyde resins particle board is the largest for urea—formaldehyde resins. Under certain conditions, urea—formaldehyde resins may release formaldehyde that has been alleged to create health or environmental problems (see Amino RESINS AND PLASTICS). [Pg.497]

Formaldehyde. Worldwide, the largest amount of formaldehyde (qv) is consumed in the production of urea—formaldehyde resins, the primary end use of which is found in building products such as plywood and particle board (see Amino resins and plastics). The demand for these resins, and consequently methanol, is greatly influenced by housing demand. In the United States, the greatest market share for formaldehyde is again in the constmction industry. However, a fast-growing market for formaldehyde can be found in the production of acetylenic chemicals, which is driven by the demand for 1,4-butanediol and its subsequent downstream product, spandex fibers (see Fibers, elastomeric). [Pg.281]

Polymers. AH nitro alcohols are sources of formaldehyde for cross-linking in polymers of urea, melamine, phenols, resorcinol, etc (see Amino RESINS AND PLASTICS). Nitrodiols and 2-hydroxymethyl-2-nitro-l,3-propanediol can be used as polyols to form polyester or polyurethane products (see Polyesters Urethane polymers). 2-Methyl-2-nitro-l-propanol is used in tires to promote the adhesion of mbber to tire cord (qv). Nitro alcohols are used as hardening agents in photographic processes, and 2-hydroxymethyl-2-nitro-l,3-propanediol is a cross-linking agent for starch adhesives, polyamides, urea resins, or wool, and in tanning operations (17—25). Wrinkle-resistant fabric with reduced free formaldehyde content is obtained by treatment with... [Pg.61]

Catalysts. The alkanolamines continue to find use as blocked catalysts for textile resins, coatings resins, adhesives, etc. Of particular utifity in curing durable-press textiles is AMP-HCl. Other salts, such as those of the benzoin tosylate or A-toluenesulfonic acid, find utifity in melamine- or urea-based coatings (18) (see Amino resins and plastics). [Pg.19]

The future for amino resins and plastics seems secure because they can provide quaHties that are not easily obtained in other ways. New developments will probably be in the areas of more highly specialized materials for treating textiles, paper, etc, and for use with other resins in the formulation of surface coatings, where a small amount of an amino resin can significantly increase the value of a more basic material. Additionally, since amino resins contain a large proportion of nitrogen, a widely abundant element, they may be in a better position to compete with other plastics as raw materials based on carbon compounds become more costly. [Pg.321]

Since melamine resins are derived from urea, they are more cosdy and are therefore restricted to appHcations requiring superior performance. Essentially ad of the melamine produced is used for making amino resins and plastics. [Pg.323]

Approximately 25% of the formaldehyde produced in the United States is used in the manufacture of amino resins and plastics. [Pg.323]


See other pages where AMINO RESINS AND PLASTICS is mentioned: [Pg.30]    [Pg.266]    [Pg.417]    [Pg.419]    [Pg.420]    [Pg.485]    [Pg.641]    [Pg.721]    [Pg.819]    [Pg.953]    [Pg.979]    [Pg.979]    [Pg.1021]    [Pg.1041]    [Pg.1043]    [Pg.489]    [Pg.60]    [Pg.5]    [Pg.10]    [Pg.11]    [Pg.20]    [Pg.321]    [Pg.321]    [Pg.321]    [Pg.322]    [Pg.323]    [Pg.324]    [Pg.325]    [Pg.326]    [Pg.327]    [Pg.328]    [Pg.329]    [Pg.330]    [Pg.331]    [Pg.332]    [Pg.333]    [Pg.333]    [Pg.334]    [Pg.31]    [Pg.228]    [Pg.203]    [Pg.341]   


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