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Vulcanization studies

After the compound has been compounded by the addition of the appropriate curing agents, processed and formed, it is then vulcanized. The vulcanization process occurs in three stages 1) an [Pg.143]


Now the lone chlorine atom has found itself isolated since the zinc only extracts two adjacent chlorines. Such a result is called reactant isolation, and one wishes to predict the chlorine concentration left in the polymer as a function of time. It was shown by Flory76 that the fraction of chlorines unreacted should approach e 2, and this was used in fact by Marvel77 to determine the structure of polyvinyl chloride. Other examples are the condensation of the polymer of methyl vinyl ketone76 and the vulcanization of natural rubber.78 The vulcanization studies supply another example where a molecular structure was determined by a kinetic scheme. The complete time dependence of the process was recently derived by Cohen and Reiss24 using a novel method of multiplets, which will now be outlined. [Pg.166]

Polypropylene is also used in a number of blends, some of them with applications in rubber industry, automotive industry, home constructions, etc. Some of the copolymers and blends used in rubber industry are vulcanized. Studies on thermal properties and pyrolysis of these copolymers and blends are common in literature [97, 105,110-118]. [Pg.220]

It has been shown that the viscoelastic losses of OH-terminated poly(dimethyl-siloxane), crosslinked with tetra-functional silicates, decreases with increased crosslink density. Furthermore, identical results were obtained when the polymer was crosslinked with y-irradiation, in bulk and in solution this indicates that there is no significant change in the number of interchain entanglements, and these are responsible for the observed losses. Vulcanization studies of poly(di-methylsiloxane)s, y-irradiated up to 500 Mrad, have shown linear correlation of the crosslink density with swelling, indentation and extension behaviour up to 160 Mrad, and exponentially for higher doses. Basic principles for the thermal stabilization of silicone rubbers, filled with carbon blacks and silica, have been discussed and a tentative stabilization mechanism put forward. ... [Pg.212]

Procedure B. Excess n-heptane (4-6 vols.) was added and the heptane-insoluble polymer was collected, washed once with heptane, washed once with 0,5% HCl in CH3OH, washed neutral with CH3OH, washed with 0.1% Santonox in CH3OH, and then dried. Run 5, which was used in the vulcanization studies, was stabilized with 1% phenyl 6-naphthyl amine. [Pg.104]

The mechanisms for the reaction of sulfur with alkanes and unsaturated compounds are highly speculative, being strongly influenced by the specific stmcture of the substrate and by the conditions (particularly temperature) of reaction. Alkane (4), olefin (5), animal fat (6), and vegetable oil (7) sulfurization have been extensively studied because these reactions are models for vulcanization. Moreover, the products are used as lubricant additives. [Pg.206]

Wire and cable insulation based on vulcanizates of PZ has also been studied. Again, low fire risk was the target property, and this was achieved. The need to vulcanize the coating, somewhat modest tensile properties, tensile strength of 5.2 to 12.2 MPa (760 to 1770 psi), and high dielectric constant (4—5 at 10,000 Hz) limited interest in this appHcation (19). [Pg.529]

They have studied the properties of NR-epoxidized natural rubber (ENR) blend nanocomposites also. Vulcanization kinetics of natural mbber-based nanocomposite was also smdied. The effect of different nanoclays on the properties of NR-based nanocomposite was studied. The tensile properties of different nanocomposites are shown in Figure 2.7 [33]. [Pg.35]

When two polymers interact or react with each other, they are likely to provide a compatible, even a miscible, blend. Epoxidized natural rubber (ENR) interacts with chloro-sulfonated polyethylene (Hypalon) and polyvinyl chloride (PVC) forming partially miscible and miscible blends, respectively, due to the reaction between chlorosulfonic acid group and chlorine with epoxy group of ENR. Chiu et al. have studied the blends of chlorinated polyethylene (CR) with ENR at blend ratios of 75 25, 50 50, and 25 75, as well as pure rubbers using sulfur (Sg), 2-mercapto-benzothiazole, and 2-benzothiazole disulfide as vulcanizing agents [32]. They have studied Mooney viscosity, scorch... [Pg.316]

Fluoroelastomers Novikova et al. [32] reported unproved physico-mechanical properties of fluoro mbbers by reinforcement with chopped polyamide fibers. Other fiber reinforcements are covered by Grinblat et al. [33]. Watson and Francis [34] described the use of aramid (Kevlar) as short fiber reinforcement for vulcanized fluoroelastomer along with polychloroprene mbber and a co-polyester TPE in terms of improvement in the wear properties of the composites. Rubber diaphragms, made up of fluorosilicone mbbers, can be reinforced using aramid fiber in order to impart better mechanical properties to the composite, though surface modification of the fiber is needed to improve the adhesion between fluorosUicone mbber and the fiber [35]. Bhattacharya et al. [36] studied the crack growth resistance of fluoroelastomer vulcanizates filled with Kevlar fiber. [Pg.353]

MEAs used in this study were prepared in the following procedure [5]. The diffusion backing layers for anode and cathode were a Teflon-treated (20 wt. %) carbon paper (Toray 090, E-Tek) of 0.29 mm thickness. A thin diffusion layer was formed on top of the backing layer by spreading Vulcan XC-72 (85 wt. %) with PTFE (15 wt. %) for both anode and cathode. After the diffusion layers were sintered at a temperature of 360 C for 15 min., the catalyst layer was then formed with Pl/Ru (4 mg/cm ) and Nafion (1 mg/cm ) for anode and with Pt (4 mg/cm ) and Nafion (1 mg/cm ) for cathode. The prepared electrodes were placed either side of a pretreated Nafion 115 membrane and the assembly was hot-pressed at 85 kg/cm for 3 min. at 135 C. [Pg.594]

Paulus UA, Schmidt TJ, Gasteiger HA, Behm RJ. 2001. Oxygen reduction on a high-surface area Pt/Vulcan carbon catalyst A thin-film rotating ring-disk electrode study. J Electroanal Chem 495 134-145. [Pg.339]

Methanol Oxidation Methanol oxidation on a Pt/Vulcan catalyst was studied and discussed extensively in our previous papers [Jusys and Behm, 2001 Jusys et al., 2003]. Therefore, we will focus her on the most important features and refer to those previous studies for more detailed discussions. [Pg.433]

Zinc dithiocarbamates have been used for many years as antioxidants/antiabrasives in motor oils and as vulcanization accelerators in rubber. The crystal structure of bis[A, A-di- -propyldithio-carbamato]zinc shows identical coordination of the two zinc atoms by five sulfur donors in a trigonal-bipyramidal environment with a zinc-zinc distance of 3.786 A.5 5 The electrochemistry of a range of dialkylthiocarbamate zinc complexes was studied at platinum and mercury electrodes. An exchange reaction was observed with mercury of the electrode.556 Different structural types have been identified by variation of the nitrogen donor in the pyridine and N,N,N, N -tetra-methylenediamine adducts of bis[7V,7V-di- .vo-propyldithiocarbamato]zinc. The pyridine shows a 1 1 complex and the TMEDA gives an unusual bridging coordination mode.557 The anionic complexes of zinc tris( V, V-dialkyldithiocarbamates) can be synthesized and have been spectroscopically characterized.558... [Pg.1196]


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See also in sourсe #XX -- [ Pg.143 ]

See also in sourсe #XX -- [ Pg.105 , Pg.120 ]

See also in sourсe #XX -- [ Pg.105 , Pg.120 ]




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