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Resin content, polyurethane

Several factors were utilized in bringing formaldehyde release down. In particular, resin manufacturer executed more careful control of variables such as pH, formaldehyde content, and control of methylolation. There has also been a progressive decrease in the resin content of pad baths. The common practice of applying the same level of resin to a 50% cotton—50% polyester fabric as to a 100% cotton fabric was demonstrated to be unnecessary and counter productive (89). Smooth-dry performance can be enhanced by using additives such as polyacrylates, polyurethanes, or siUcones without affecting formaldehyde release. [Pg.446]

Combinations of bitumen with reaction-curing paint binders (e.g., epoxy resins and polyurethanes) are not usually employed in solvent-based paints due to their unsatisfactory compatibility. Only with high epoxy resin contents can a certain compatibility be achieved by addition of solubilizing phenols and aromatic oils. [Pg.93]

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]

Phenolics are consumed at roughly half the volume of PVC, and all other plastics are consumed in low volume quantities, mosdy in single apphcation niches, unlike workhorse resins such as PVC, phenoHc, urea—melamine, and polyurethane. More expensive engineering resins have a very limited role in the building materials sector except where specific value-added properties for a premium are justified. Except for the potential role of recycled engineering plastics in certain appHcations, the competitive nature of this market and the emphasis placed on end use economics indicates that commodity plastics will continue to dominate in consumption. The apphcation content of each resin type is noted in Table 2. Comparative prices can be seen in Table 5. The most dynamic growth among important sector resins has been seen with phenoHc, acryUc, polyurethane, LLDPE/LDPE, PVC, and polystyrene. [Pg.331]

Traditionally carpet tile backings have been made from bitumen, PVC or polyurethane. There are problems with the environmental impact of these materials and they are difficult to recycle. Shaw industries developed their EcoWorx carpet tile backing using a polyolefin resin. This has superior environmental profile to PVC and is easier to recycle than bitumen and the cross-linked polyurethane backings. EcoWorx has lower toxicity, better adhesion and good dimensional stability. It is easy to recycle and can be separated from any fibre type used in the carpet tile. It works particularly well with nylon-6 fibres. EcoWorx tiles contain 40% recycled content and Shaw have established a collection and return scheme to close the loop. [Pg.61]

Polyurethanes are frequently used in anticorrosion coatings. The R D drive of most coatings and resin producers is the reduction of the solvent content of the paint and resin systems. One method of achieving the environmental aims demanded by legislation in the PU coatings industry is to use oxazolidines which are suitable as latent hardeners to enable production of single-pack moisture activated PUs. The isocyanate chosen for this research is tetramethylxylene diisocyanate, which has been available commercially only since 1988. 19 refs. [Pg.101]

Figure 4. Variation of relative fracture energy, Gc/G , and tensile toughness, Uy, with rubber content for rubber-modified, highly crosslinked polyurethane resins. Gc/G (-0- polymyrcene, polybutadiene) Uy ( -A- polymyrcene). Figure 4. Variation of relative fracture energy, Gc/G , and tensile toughness, Uy, with rubber content for rubber-modified, highly crosslinked polyurethane resins. Gc/G (-0- polymyrcene, polybutadiene) Uy ( -A- polymyrcene).
Disperse colorants Resin dispersions with synthetic resin binders (e. g. alkyd resins, polyurethane resins or polyacrylates), water content 35-45 %, organic solvent mixtures 5-10 %, additional other hydrocarbons 1,2-PG, EG, DPGMM, DEGMM, EGMB, DEGMB... [Pg.120]

Polymer characterization is an important use of NIR spectrometry. Polymers can be made either from a single monomer, as is polyethylene, or from mixtures of monomers, as are styrene-butadiene rubber from styrene and butadiene and nylon 6-6, made from hexamethylenediamine and adipic acid. An important parameter of such copolymers is the relative amount of each present. This can be determined by NIR for polymers with the appropriate functional groups. Styrene content in a styrene-butadiene copolymer can be measured using the aromatic and aliphatic C—H bands. Nylon can be characterized by the NH band from the amine monomer and the C=0 band from the carboxylic acid monomer. Nitrogen-containing polymers such as nylons, polyurethanes, and urea formaldehyde resins can be measured by using the NH bands. Block copolymers, which are typically made of a soft block of polyester and a hard block containing aromatics, for example, polystyrene, have been analyzed by NIR. These analyses have utilized the... [Pg.288]

Curing with Atmospheric Moisture. Type 2 in Table 2.5. High molecular mass polyaddition products of polyols with excess diisocyanate contain reactive isocyanate groups. They are used to formulate one-pack polyurethane paints that cross-link with the formation of urea groups under the influence of atmospheric moisture to produce paint films with excellent resistance to chemical and mechanical attack. Solvent-free products and dissolved products with isocyanate contents of 5- 15% (based on the solid resin) are commercially available. [Pg.66]

Although two-pack epoxy primers and polyurethane intermediate coats have high solids contents, they still contain significant amounts (20-30 wt%) of organic solvents. In polyurethane topcoats, the VOC is even higher. Anticorrosive, waterborne primers based on aqueous dispersions of two-pack epoxy resins and one-pack acrylic resins have been developed to decrease solvent emission. Waterborne, one-pack acrylic topcoats are also used. All of these waterborne paints contain 2 - 5 % organic cosolvents that are required for film formation. [Pg.250]

Polyurethane Paints. Polyester, polyether, or acrylic resins containing hydroxyl groups are cured with isocyanate hardeners, medium to high solids contents, best overall properties in terms of mechanical and chemical resistance [11.32]. [Pg.262]

Nitrile polymers used for the manufacture of adhesives generally contain 25% or more acrylonitrile, but in the base polymer the acrylonitrile content can vary from 15% to 50%. Increasing the acrylonitrile content improves the oil and plasticizer resistance and increases the polarity of the compound. However, higher levels of acrylonitrile also increase the hardness and modulus of the polymer, reducing the elasticity of the resulting polymer. Nitrile rubber can be produced by a cold (5°C) or hot (25-50°C) process, with most adhesive polymers produced by the hot process which induces more chain branching. Nitriles can be combined with other monomers in solution polymerization which increases functionality and improves compatibility with other reactive resins like acrylics, epoxies, and polyurethanes. [Pg.520]


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See also in sourсe #XX -- [ Pg.515 ]




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