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Processing plasticized polyurethanes

Physical Stabilization Process. Cellular polystyrene, the outstanding example polytvinyl chloride) copolymers of styrene and acrylonitrile (SAN copolymers) and polyethylene can be manufactured by this process, Chemical Stabilization Processes. This method is more versatile and thus has been used successfully for more materials than the physical stabilization process. Chemical stabilization is more adaptable for condensation polymers than for vinyl polymers because of the fast yet controllable curing reactions and the absence of atmospheric inhibition. Foamed plastics produced by these processes include polyurethane foams, polyisocyanurates. and polyphenols. [Pg.664]

Blowing agents for plastics, polyurethane foams as Freon substitutes. For example, t.butyl methyl pyrocarbonate (R = methyl, R = t. butyl) was claimed as a foaming agent added during processing of polymers to achieve a cellular structure by liberation of carbon dioxide (Ref. 40). [Pg.26]

A further example of the new materials research being done on RIM processable polymers are the high modulus urethane -epoxy UN s, shown in Table IX (12). These materials are shown compared to a toughened plastic polyurethane 146,000 psi flexural modulus urethane naterial. The urethane-epoxy IEN s are based on two epoxies (Bisphnol A type and Novalak type). [Pg.9]

Waxes, e. g., ester waxes and ethoxylated wax alcohols, are used in water-based systems. - Metallic soaps are widely used in plastics processing (- plastics additives) and in injection molding of polyurethane foams as internal lubricants and r. - Fats and oils and some of their ester derivatives can be used also if the processing temperature is below 150 °C. They are mainly used in woodworking and in food applications (- food additives). [Pg.241]

Butanediol. 1,4-Butanediol [110-63-4] made from formaldehyde and acetylene, is a significant market for formaldehyde representing 11% of its demand (115). It is used to produce tetrahydrofuran (THF), which is used for polyurethane elastomers y-butyrolactone, which is used to make various pyrroHdinone derivatives poly(butylene terephthalate) (PBT), which is an engineering plastic and polyurethanes. Formaldehyde growth in the acetylenic chemicals market is threatened by alternative processes to produce 1,4-butanediol not requiring formaldehyde as a raw material (140) (see Acetylene-derived chemicals). [Pg.497]

Catalysts. Mercury is or has been used in the catalysis (qv) of various plastics, including polyurethane [26778-67-6] poly(vinyl chloride) [9002-86-2] and poly(vinyl acetate) [9003-20-7]. Most poly(vinyl chloride) and poly(vinyl acetate) is manufactured by processes that do not use mercury (3). [Pg.110]

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]

Ammonia is used in the fibers and plastic industry as the source of nitrogen for the production of caprolactam, the monomer for nylon 6. Oxidation of propylene with ammonia gives acrylonitrile (qv), used for the manufacture of acryHc fibers, resins, and elastomers. Hexamethylenetetramine (HMTA), produced from ammonia and formaldehyde, is used in the manufacture of phenoHc thermosetting resins (see Phenolic resins). Toluene 2,4-cHisocyanate (TDI), employed in the production of polyurethane foam, indirectly consumes ammonia because nitric acid is a raw material in the TDI manufacturing process (see Amines Isocyanates). Urea, which is produced from ammonia, is used in the manufacture of urea—formaldehyde synthetic resins (see Amino resins). Melamine is produced by polymerization of dicyanodiamine and high pressure, high temperature pyrolysis of urea, both in the presence of ammonia (see Cyanamides). [Pg.358]

The late 1950s saw the emergence of cast elastomers, which led to the development of reaction injection mol ding (RIM) at Bayer AG in Leverkusen, Germany, in 1964 (see Plastics processing). Also, thermoplastic polyurethane elastomers (TPUs) and Spandex fibers (see Fibers, elastomeric) were introduced during this time. In addition, urethane-based synthetic leather (see Leather-LIKEmaterials) was introduced by Du Pont under the trade name Corfam in 1963. [Pg.341]

Multiblock Copolymers. Replacement of conventional vulcanized mbber is the main appHcation for the polar polyurethane, polyester, and polyamide block copolymers. Like styrenic block copolymers, they can be molded or extmded using equipment designed for processing thermoplastics. Melt temperatures during processing are between 175 and 225°C, and predrying is requited scrap is reusable. They are mostiy used as essentially pure materials, although some work on blends with various thermoplastics such as plasticized and unplasticized PVC and also ABS and polycarbonate (14,18,67—69) has been reported. Plasticizers intended for use with PVC have also been blended with polyester block copolymers (67). [Pg.19]

The basic RIM process is illustrated in Fig. 4.47. A range of plastics lend themselves to the type of fast polymerisation reaction which is required in this process - polyesters, epoxies, nylons and vinyl monomers. However, by far the most commonly used material is polyurethane. The components A and B are an isocyanate and a polyol and these are kept circulating in their separate systems until an injection shot is required. At this point the two reactants are brought together in the mixing head and injected into the mould. [Pg.302]

Thermoplastic polyurethane (TPU) is a type of synthetic polymer that has properties between the characteristics of plastics and rubber. It belongs to the thermoplastic elastomer group. The typical procedure of vulcanization in rubber processing generally is not needed for TPU instead, the processing procedure for normal plastics is used. With a similar hardness to other elastomers, TPU has better elasticity, resistance to oil, and resistance to impact at low temperatures. TPU is a rapidly developing polymeric material. [Pg.137]

Most rigid polyurethane foams have a closed cell structure. Closed cells form when the plastic cell walls remain intact during the expansion process and are not ruptured by the increasing cell pressure. Depending on the blowing process a small fraction (5-10%) of the cells remain open. Closed cell structures provide rigidity and obstruct gaseous or fluid diffusional processes. [Pg.499]

This low pressure process, also known as elastic reservoir molding, consists of making basically a sandwich of plastic-impregnated open-celled flexible polyurethane foam between the face layers of fibrous reinforcements. When this plastic composite is placed in a mold and squeezed, the foam is compressed, forcing the plastic outward and into the reinforcement. The elastic foam exerts sufficient pressure to force the plastic-impregnated reinforcement into contact with the heated mold surface. Other plastics are used. [Pg.503]

SCRIMP process This Seeman Composites Resin Infusion Process (SCRIMP) is described as a gas-assist resin transfer molding process. As an example glass fiber fabrics/ thermoset vinyl ester polyester plastic and polyurethane foam panels (for insulation) are placed in a segmented tool. A vacuum is pulled with a bag so that a huge amount of plastic can be drawn into the mold (Marco process approach). Its curved roof is made separately and bonded to the box with mechanical and adhesive fastening. It is similar to various reinforced plastics molding processes. [Pg.522]

In 2002, the world production of polymers (not including synthetic libers and rubbers) was ca. 190 million metric tons. Of these, the combined production of poly(ethylene terephthalate), low- and high-density polyethyelene, polypropylene, poly(vinyl chloride), polystyrene, and polyurethane was 152.3 milhon metric tons [1]. These synthetic, petroleum-based polymers are used, inter alia, as engineering plastics, for packing, in the construction-, car-, truck- and food-industry. They are chemically very stable, and can be processed by injection molding, and by extrusion from the melt in a variety of forms. These attractive features, however, are associated with two main problems ... [Pg.104]


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See also in sourсe #XX -- [ Pg.102 ]




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