Phenol formaldehyde nitrile

MC MDI MEKP MF MMA MPEG MPF NBR NDI NR OPET OPP OSA PA PAEK PAI PAN PB PBAN PBI PBN PBS PBT PC PCD PCT PCTFE PE PEC PEG PEI PEK PEN PES PET PF PFA PI PIBI PMDI PMMA PMP PO PP PPA PPC PPO PPS PPSU Methyl cellulose Methylene diphenylene diisocyanate Methyl ethyl ketone peroxide Melamine formaldehyde Methyl methacrylate Polyethylene glycol monomethyl ether Melamine-phenol-formaldehyde Nitrile butyl rubber Naphthalene diisocyanate Natural rubber Oriented polyethylene terephthalate Oriented polypropylene Olefin-modified styrene-acrylonitrile Polyamide Poly(aryl ether-ketone) Poly(amide-imide) Polyacrylonitrile Polybutylene Poly(butadiene-acrylonitrile) Polybenzimidazole Polybutylene naphthalate Poly(butadiene-styrene) Poly(butylene terephthalate) Polycarbonate Polycarbodiimide Poly(cyclohexylene-dimethylene terephthalate) Polychlorotrifluoroethylene Polyethylene Chlorinated polyethylene Poly(ethylene glycol) Poly(ether-imide) Poly(ether-ketone) Polyethylene naphthalate Polyether sulfone Polyethylene terephthalate Phenol-formaldehyde copolymer Perfluoroalkoxy resin Polyimide Poly(isobutylene), Butyl rubber Polymeric methylene diphenylene diisocyanate Poly(methyl methacrylate) Poly(methylpentene) Polyolefins Polypropylene Polyphthalamide Chlorinated polypropylene Poly(phenylene oxide) Poly(phenylene sulfide) Poly(phenylene sulfone)... 

Structural adhesives Polyvinyl formal-phenol formaldehyde Polyvinyl butyral-phenol formaldehyde Nitrile-phenolic Epoxy-polyamine Epoxy-anhydride Epoxy-nylon Epoxy-phenolic Epoxy-polyamide Epoxy-polyurethane... 

Other modifications of the polyamines include limited addition of alkylene oxide to yield the corresponding hydroxyalkyl derivatives (225) and cyanoethylation of DETA or TETA, usuaHy by reaction with acrylonitrile [107-13-1/, to give derivatives providing longer pot Hfe and better wetting of glass (226). Also included are ketimines, made by the reaction of EDA with acetone for example. These derivatives can also be hydrogenated, as in the case of the equimolar adducts of DETA and methyl isobutyl ketone [108-10-1] or methyl isoamyl ketone [110-12-3] (221 or used as is to provide moisture cure performance. Mannich bases prepared from a phenol, formaldehyde and a polyamine are also used, such as the hardener prepared from cresol, DETA, and formaldehyde (228). Other modifications of polyamines for use as epoxy hardeners include reaction with aldehydes (229), epoxidized fatty nitriles (230), aromatic monoisocyanates (231), or propylene sulfide [1072-43-1] (232). 

Nitrile rubber is compatible with phenol-formaldehyde resins, resorcinol-formaldehyde resins, vinyl chloride resins, alkyd resins, coumarone-indene resins, chlorinated rubber, epoxies and other resins, forming compositions which can be cured providing excellent adhesives of high strength, high oil resistance and high resilience. On the other hand, NBR adhesives are compatible with polar adherends such as fibres, textiles, paper and wood. Specific formulations of NBR adhesives can be found in [12]. 

Chlorinated rubber is also an effective bonding agent. It can be used for bonding neoprene, nitrile and natural rubbers to metals. Phenol formaldehyde resins have been used alone or in conjunction with chlorinated rubbers, but curing time is lengthy. 

The mechanical degradation and production of macroradicals can also be performed by mastication of polymers brought into a rubbery state by admixture with monomer several monomer-polymer systems were examined (10, 11). This technique was for instance studied for the cold mastication of natural rubber or butadiene copolymers in the presence of a vinyl monomer (13, 31, 52). The polymerization of methyl methacrylate or styrene during the mastication of natural rubber has yielded copolymers which remain soluble up to complete polymerization vinyl acetate, which could not produce graft copolymers by the chain transfer technique, failed also in this mastication procedure. Block and graft copolymers were also prepared by cross-addition of the macroradicals generated by the cold milling and mastication of mixtures of various elastomers and polymers, such as natural rubber/polymethyl methacrylate (74), natural rubber/butadiene-styrene rubbers (76) and even phenol-formaldehyde resin/nitrile rubber (125). 

Kargin, V. A., B. Kovarsxaya, L. I. Golubenkova, M. S. Akutin and S. L. Slonimskii Block copolymer from phenol-formaldehyde resin and nitrile rubber. Doklady Akad. Nauk SSSR112,485 (1957) Chem. Abstr. 52, 15122 (1958). 

Cellular Cellulose Acetate Conventional adhesives recommended include polyurethanes, synthetic resins, thermoplastics, resorcinol-formaldehyde, nitrile-phenolic, and rubber-based materials (8). 

Urea-Formaldehyde Adhesives used are epoxies, nitrile-phenolics, phenol-formaldehyde, resorcinol-formaldehyde, furan, polyesters, butadiene-nitrile rubber, neoprene, cyanoacrylate, and phenolic-polyvinyl butyral (1). 

Numata and Kinjo (52) have shown rubber-modified isocyanurate-oxazolidone resins may be effectively modified with carboxyl-reactive nitrile liquids. The viscoelastic behavior of models using a polyglycidyl ether of phenol-formaldehyde novolac resin and di-phenylmethane-4,4 -diisocyanate is discussed. Such resins have suggested utility in thin films as electrical varnishes. 

Elastomeric 1, Natural rubber. 2, Neoprene. 3, Nitrile. 4, Urethane. 5, Styrene-butadiene. Thermoplastic 6, Poly(vinyl acetate). 7, Polyamide. Thermosetting 8, Phenol-formaldehyde. 9, Resorcinol, Phenol-resorcinol/formaldehyde. 10, Epoxy. 11, urea-formaldehyde. Resin 12, Phenolic-poly(vinyl butyral). 13, Polyeser. Other 14, Cyanoacrylate. 15, Solvent. 

There are a number of types, based on their chemical structure, but the most important and most widely used is nylon 6,6. The best adhesives for bonding nylon to nylon are solvents. Various commercial adhesives, especially those based on phenol-formaldehyde (phenolics) and epoxy resins, are sometimes used for bonding nylon to nylon, although they are usually considered inferior to the solvent type because they result in a brittle joint. Adhesives recommended include nylon-phenoUc, nitrile-phenolic, nitriles, neoprene, modified epoxy, cyanoacrylate, modified phenolic, resorcinol-formaldehyde, and polyurethane. Bonds in the range of 1.7-6.9 MPa, depending on the thickness of the adherends, have been obtained. ... 

Suggested adhesives include modified acrylics, epoxies, polyesters, resorcinol-formaldehyde, furane, phenol-formaldehyde, polyvinyl formal-phenolic, polyvinyl butyral, nitrile rubber-phenolic, polyisobutylene rubber, polyurethane rubber, reclaimed rubber, melamine-formaldehyde, epoxy-phenolic, and cyanoacrylates. For maximum adhesion primers should be used. Nitrile-phenoUcs give excellent bonds if cured under pressure at temperatures of 149 C. Lower-strength bonds are obtained with most rubber-based adhesives. 

The first completely synthetic resin, based on phenol and formaldehyde, was invented by Baekeland and others in the first decade of this century. " While the phenol-formaldehyde resins yielded excellent adhesives then as now, blends with carboxylic rubber, epoxy resins, neoprene, nitrile rubber, and other polymers Improved adhesive properties for various purposes. 

Polyhydroxymethyl compounds phenol-formaldehyde resins, also in combination with poly(vinyl formal) resins, nitrile rubber or epoxy resins (as adhesive film), urea-fprmaldehyde resins, melamine - formaldehyde resins, resorcinol - formaldehyde resins. Uses wood (plywood manufacture), metals. 

Phenolics or phenol-formaldehyde structural adhesives are chemically reactive systems that cure to form thermosets. In one-component systems, meltable powders (resols) are used as binders for particle board or as alloys (including nitrile-phenolics, vinyl - phenolics, and epoxy-phenolics), which are used in the structural bonding of metals. In two-component systems, the resin and catalyst are mixed and then heated to initiate curing. Both systems cure by a condensation reaction that produces a byproduct. 

Miscellaneous - Polyvinyl butyral is used as a olear adhesive film to laminate two sheets of glass to form safety glass for car windshields. Phenol formaldehyde resins are used to make brake lining composites, and blends of nitrile rubber and phenolic resin are used to bond brake linings to brake shoes. 

The last two items of the earlier list involve the behaviour of primers, in part chemical, in part physical, as forms of adhesives sticking the bulk adhesive to the actual metal, wood or other adherend. When dissimilar materials are to be joined, an adhesive suitable for one may not be so for the other. In these circumstances a primer for one of the substrates is chosen to be both suitable for it and compatible with the adhesive. Phenol-formaldehyde condensation products are often thus used particularly when the adhesive itself contains such material dispersed in another polymer, e.g. Redux775 (Bonded Structures, Ltd) or various epoxy-phenolic or nitrile-phenolic adhesives. Most important members of the class of coupling agents are the reactive silanes (siloxanes) and titanates. These materials have achieved their main use in the treatment of glass fibres for the manufacture of glass reinforced plastics. 

Adhesives which incorporate phenol-formaldehyde resins are much used as structural adhesives for metals. They comprise the original polyvinyl formal/PF, and polyvinyl butyral/PF together with nitrile phenolics and epoxy phenolics. The ratio of non-phenolic polymer to the PF resin in the structural adhesives determines the morphology of the material, whether it is two-phased, and which phase is continuous and which discrete. This, in turn, influences the flexibility of the... 

The nitrile is an acrylonitrile-butadiene copolymer or nitrile rubber. It reacts chemically with the phenol formaldehyde resin which is present in its B stage. 

Water-base adhesives are made of materials that can be dissolved or dispersed in water. Both natural (cellulosic, dextrin, starch) and synthetic (phenol formaldehyde, polyvinyl acetate, styrene-butadiene rubber, nitrile rubber) polymer materials are used in manufacturing water-base adhesives. Their primary application is in packaging, with a much smaller percentage usage in construction. Their share of the market, however, has been increasing due to health concerns associated with some of the solvents used in organic-solvent adhesives. 

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