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Vinyl chloride bond strength

It has been shown that tensile shear and peel strength for several latex polymers (ethylene vinyl acetate, polyvinyl alcohol, ethylene vinyl chloride, polyvinyl chloride, and acrylic) can be significantly increased by the addition of 10 percent by weight of an epoxy emulsion cured with a tertiary amine curing agent.17 The epoxy modification improves the bond strength in all cases. The degree of improvement is dependent on the selection of the latex type and the chemistry of the latex polymer. [Pg.269]

IR, Raman and 13C NMR spectroscopic studies have been performed on various [Ir(acac)(L)2] complexes (L = ethylene, propene, vinyl chloride, vinyl acetate, methyl acrylate, styrene) for the elucidation of the bonding between Ir and the alkene ligand.142 Also, the square planar iridium(I) acetylacetonate complexes [Ir(LL)(L )2], where LL is a /J-diketonate and L is CO or ethylene, have been studied by UVPES.143 The enthalpies of reaction of the crystalline [Ir(acac)(L)2] complexes with gaseous CO (reaction 28) have been determined by differential scanning calorimetry. The enthalpies for the gaseous reaction have been derived from these results and Ir—L bond strengths estimated.143... [Pg.1116]

Copolymers of vinyl chloride and methyl vinyl ketone undergo chain scission with concomitant rapid decreases in tensile strength and elongation when exposed to near ultraviolet li t and solar radiation. Free radicals formed by the homol3rtic scission of the acyl group apparently deplete the stabilizers used and lead to rapid discoloration of the polymer, presumably by the usual radical chain reaction involving the production of HCl and conjugated double bonds. [Pg.280]

The most important industrial applications of radical reaction to date are used for the manufacture of polymers. Around 108 tonnes (or 75%) of all polymers are prepared using radical processes. These are chain reactions in which an initial radical adds to the double bond of an alkene monomer and the resulting radical adds to another alkene monomer and so on. This addition polymerisation is used to make a number of important polymers, including poly(vinyl chloride) (PVC), polystyrene, polyethylene and poly(methyl methacrylate). Copolymers can also be easily prepared starting from a mixture of two or more monomers. These polymers have found widespread use as they possess a range of chemical and mechanical properties (such as strength and toughness). [Pg.12]

Epoxidizedsoybean oil (ESO) is produced via conversion of the double bonds of soybean oil with peracids or peroxides, resulting in more reactive oxirane or epoxide moieties, promoting chemical reactions [230-232]. ESO is normally used to plasticize and/or stabilize poly(vinyl chloride) (PVC), chlorinated rubber, and PVOH emulsions [231, 232]. The effects of ESO as a PLA plasticizer were reported elsewhere [230, 233, 234]. In summary, ESO lowered Tg, cold crystallization temperature Tm. enthalpy of cold crystallization (AHcc), tensile strength, and tensile... [Pg.261]

These admixtures are used to increase the bond strength in repair applications, to decrease shrinkage, increase tensile strength, etc. The polymers used include latexes, redispersible polymer powders, water-soluble polymers, liquid resins, and monomers. In practieal applications, styrene butadiene rubber, polyacrylic ester and polyvinylidene chloride-vinyl chloride, methylcellulose, etc., have been used. [Pg.180]

Figure 3.9 Relation between measured joint strength and critical surface tension, yc, of the substrate for an epoxy bonding various polymeric substrates [107]. (a) Polytetra-fluoroethylene, (b) poly(vinyl fluoride), (c) polystyrene, (d) poly(vinyl alcohol), (e) poly(vinylidene chloride), (f) poly(vinyl chloride), (g) poly(ethylene terephthalate) and (h) poly (1,4-cyclohexylene dimethylene terephthalate). Figure 3.9 Relation between measured joint strength and critical surface tension, yc, of the substrate for an epoxy bonding various polymeric substrates [107]. (a) Polytetra-fluoroethylene, (b) poly(vinyl fluoride), (c) polystyrene, (d) poly(vinyl alcohol), (e) poly(vinylidene chloride), (f) poly(vinyl chloride), (g) poly(ethylene terephthalate) and (h) poly (1,4-cyclohexylene dimethylene terephthalate).
Body sealer is used to seal the parts with joints bonded by spot welding. In contrast, spot sealer is applied to complement the strength of parts and to modify the steps for a painted surface needed for a good finish. Vinyl chloride plastisol sealer (PVC sol) and synthetic rubber sealer are used for undercoated steel plates. [Pg.127]

Fig. 5.15. Creep strength of bonded joints of decorative steel sheet coated with vinyl chloride and galvanized steel sheet bonded by SGA A6. Fig. 5.15. Creep strength of bonded joints of decorative steel sheet coated with vinyl chloride and galvanized steel sheet bonded by SGA A6.

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See also in sourсe #XX -- [ Pg.51 ]




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Bond strength

Bonding strength

Bonds vinylic

Vinyl chloride

Vinylic chlorides

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