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Rubber vulcanization crosslinking

Rubber vulcanization crosslinking was an early chemical modification method. Block and graft methods are also widely used in polymer modification. One of the successful examples of a block copolymer is a thermoplastic elastomer. It is a new material that can be processed like plastic and has elasticity like rubber. Among graft copolymers, the most widely used one is the acrylonitrile butadiene and styrene copolymer... [Pg.24]

Sulfur chemistry [29] has also been used to crosslink rubber/resin PSAs, although the use of elemental sulfur itself yields tapes that can stain substrates. Other patents exemplify the use of typical rubber vulcanizing chemistry such as Tetrone A , dipentamethylenethiuramtetrasulfide, and Tuads , tetramethylthiu-ram disulfide [30], or zinc butyl xanthate [31] for this purpose. Early art [32] also claimed electron beam curing of both natural rubber and other adhesives that were solvent coated on tape backings. Later references to electron beam curing... [Pg.475]

The vulcanization of polychloroprene (Neoprene) is carried out in different ways. Vulcanization by sulfur, even with an accelerator, is not practiced to a large extent. Vulcanizations by metal oxides (without diamine), either alone or in combination with sulfur (sometimes together with an accelerator), give the best physical properties for the crosslinked product. Halogenated butyl rubber is crosslinked in a similar manner. The mechanism for crosslinking by metal oxide alone is not established [Stewart et al., 1985 Vukov, 1984]. [Pg.745]

M 4. Meltzer, T. H., W. J. Dermody, and A. V. Tobolsky The fraction of effective sulfur crosslinking in high sulfur-natural rubber vulcanizers. J. Appl. Polymer Sci. 7, 1493 (1963). [Pg.233]

Zinc oxide is a reactive filler commonly used in rubber vulcanization. The crosslink density of rubber can be doubled by reaction of ZnO with HCl. Only a few specific fillers have the catalytic activity to promote crosslinking but fillers can take part directly in crosslinking processes initiated by an external source such as y-radialion. Generally, fillers reduce the effect of radiation. But y-rays are not screened by the filler so the protection given by fillers comes from reduction in chain mobility which lessens the probability of photoconversion. [Pg.339]

A growing volume of waste materials, especially vulcanized rubbers and crosslinked polymers are proving difficult to recycle. As an alternative to their disposal in landfills, there have been many attempts to grind these materials and use the products as a substitute for fillers in composite materials. Other non-plastic materials such as glass, paper, natural fibrous materials, and fly ash are also used for filler replacement. There is extensive literature on the use of ground tires as filler replacements. This is a specialized topic with only a minor relationship to fillers. [Pg.531]

BQDI 53 may induce undesirable reduction of the processing safety and efficiency of crosslinking in rubber vulcanization [3]. [Pg.112]

S/Ac in a natural rubber-like fashion. A difference here is that evidence for model monosulfidic crosslinks was lacking while model disulfldic crosslinks were more apparent than in the case of natural rubber vulcanization. [Pg.364]

Rubbers and resins normally vulcanize/crosslink in heated molds at 150-220 °C. The cycle times are normally much longer than for uncrosslinked plastics [7, 63]. [Pg.220]

Uses Crosslinking agent for rubber vulcanization, moisture barrier films and coatings, photopolymer printing plates and letterpress inks, conversion coatings and adhesives crosslinked actylic/vinyl resin comonomer syn. resin modifier plastisols photosensitive resins textile modifier... [Pg.1074]

This figure also illustrates the three main regions of rubber vulcanization. The first regime is the induction period, or scorch delay, during which accelerator complex formation occurs. The second time period is the cure period, in which the network or sulfurization structures are formed. The network structures can include crosslinks, cyclics, main chain modification, isomerization, etc. The third regime is the overcure, or reversion regime. [Pg.78]


See other pages where Rubber vulcanization crosslinking is mentioned: [Pg.351]    [Pg.95]    [Pg.31]    [Pg.411]    [Pg.343]    [Pg.37]    [Pg.128]    [Pg.66]    [Pg.85]    [Pg.153]    [Pg.633]    [Pg.15]    [Pg.583]    [Pg.110]    [Pg.21]    [Pg.31]    [Pg.211]    [Pg.242]    [Pg.411]    [Pg.154]    [Pg.697]    [Pg.117]    [Pg.340]    [Pg.1485]    [Pg.461]    [Pg.534]    [Pg.5043]    [Pg.7150]    [Pg.581]    [Pg.337]    [Pg.324]    [Pg.349]    [Pg.24]    [Pg.291]    [Pg.351]    [Pg.531]    [Pg.1]   
See also in sourсe #XX -- [ Pg.24 ]




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Crosslinked rubber

Crosslinks vulcanization

Rubber vulcanization

Rubber, vulcanized

Vulcan

Vulcanization

Vulcanization plastics/crosslinked rubbers

Vulcanize

Vulcanized

Vulcanizing

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