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Polymers development

Solid Polymer E,kctroljte. The electrolyte in soHd polymer electrolyte (SPE) units is Nafion, a soHd polymer developed by Du Pont, which has sulfonic acid groups attached to the polymer backbone. Electrodes are deposited on each side of the polymer sheet. H" ions produced at the anode move across the polymer to the cathode, and produce hydrogen. The OH ions at the anode produce oxygen. These units have relatively low internal resistances and can operate at higher temperatures than conventional alkaline electrolysis units. SPE units are now offered commercially. [Pg.425]

ACS polymers, developed primarily in Japan, are grafts of acrylonitrile and styrene onto elastomeric chlorinated polyethylene. Although the polymer has good weathering properties it is somewhat susceptible to thermal degradation during processing and to date these polymers have been of limited interest. [Pg.449]

Since the last edition several new materials have been aimounced. Many of these are based on metallocene catalyst technology. Besides the more obvious materials such as metallocene-catalysed polyethylene and polypropylene these also include syndiotactic polystyrenes, ethylene-styrene copolymers and cycloolefin polymers. Developments also continue with condensation polymers with several new polyester-type materials of interest for bottle-blowing and/or degradable plastics. New phenolic-type resins have also been announced. As with previous editions I have tried to explain the properties of these new materials in terms of their structure and morphology involving the principles laid down in the earlier chapters. [Pg.927]

Of the many nitro polymers developed as propints by Aerojet General Corp, one polyamide polymer resulted which can be considered an expl and is presented below ... [Pg.323]

As argued above, it is not reasonable to expect that new polymer developments will easily stay away from the use of additives. In this respect e-beam processing of plastics constitutes an alternative to chemical additives, but is very limited in scope [15]. Table 10.12 gives the current status for several additive groups. [Pg.717]

No shrink-resist polymer developed so far meets all the above requirements [301]. There is clearly some similarity with easy-care finishing of cotton. Although effective crosslinking agents are readily available for application to cotton, the morphological complexity of the wool fibre is such that an equally effective polymer has yet to be identified for wool treatment [304]. [Pg.164]

Compelling evidence suggesting that the breakdown of hydroperoxyl groups is not related to polymer destruction, at least in the initial period of oxidation at temperatures below 400 K, comes from experiments on the initiated oxidation of polymers. It was found that the destruction of polymers develops in parallel with their oxidation from the very onset of the process, but not after a delay related to the accumulation of a sufficient amount of hydroperoxyl groups [129]. These experiments also demonstrated that it is free macroradicals that undergo destruction. Oxidation of polymers gives rise to alkyl, alkoxyl, and peroxyl macroradicals. Which radicals undergo destruction can be decided based on the kinetics of initiated destructive oxidation. [Pg.477]

Flexomer A gas-phase process for making ethylene-propylene co-polymers. Developed by Union Carbide Corporation and first commercialized in 1989. [Pg.108]

SDS [Sulzer Dainippon Sumitomo] A continuous process for polymerizing styrene. The reactants are mixed in a static mixer, which gives a very uniform time/temperature history for the polymer. Developed jointly by Sulzer, Dainippon Ink Chemicals, and Sumotomo Heavy Industries. Offered for license in 1990. [Pg.239]

Poly(phenylene oxide) PPO, or poly(phenylene ether) PPE, is an engineering polymer developed by General Electric. It concerns the oxidative coupling of phenols discovered in 1956 by Allan S. Hay [21], Oxidative coupling leads to the formation of carbon-oxygen bonds between carbon atoms 2,4, and 6 and the phenolic oxygen atom. To avoid coupling with carbon atoms 2 and 6, alkyl substituents at these two positions were introduced. In addition to the polymer a 4,4 dimer is formed, named diphenoquinone (DPQ). The... [Pg.332]

Brocchini S (2001) Combinatorial chemistry and biomedical polymer development. Adv Drug Delivery Rev 53 123-130... [Pg.149]

Figure 1.1 (a) Supramolecular polymers developed by Lehn using three-point hydrogen... [Pg.5]

Nobel laureate Emil Fischer elucidated the c bohydrates and proteins, and Leo Baekeland prodi synthetic polymer in the early part of the 20th cen many other synthetic polymers developed in the firs were produced without much knowledge of po ym<... [Pg.1]


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See also in sourсe #XX -- [ Pg.1031 ]




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