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Temperature cation

These results confirm that cobalt oxides particles (C03O4 and CoOx) have a very important role in the direct oxidation of methane to C02. On the other hand, at high temperature, cationic cobalt (Co2+) appears to be able to reduce NO to N2, even in the presence of an excess of oxygen. [Pg.283]

Therefore, when the reaction is carried out under conditions which facilitate the stabilization of the cationic intermediate, electrophilic attack on the cyclobutene double bond of A gives intermediate C, which on lactonization affords the cage compound. At higher temperature, cation B might be trapped by the counterion before the formation of C (equation 48). The attack of the bromide ion on this intermediate occurs from the... [Pg.580]

Over 5.5 billion pounds of synthetic rubber is produced annually in the United States. The principle elastomer is the copolymer of butadiene (75%) and styrene (25) (SBR) produced at an annual rate of over 1 million tons by the emulsion polymerization of butadiene and styrene. The copolymer of butadiene and acrylonitrile (Buna-H, NBR) is also produced by the emulsion process at an annual rate of about 200 million pounds. Likewise, neoprene is produced by the emulsion polymerization of chloroprene at an annual rate of over 125,000 t. Butyl rubber is produced by the low-temperature cationic copolymerization of isobutylene (90%) and isoprene (10%) at an annual rate of about 150,000 t. Polybutadiene, polyisoprene, and EPDM are produced by the anionic polymerization of about 600,000, 100,000, and 350,000 t, respectively. Many other elastomers are also produced. [Pg.554]

POLYVINYL ALKYL ETHERS. These products have properties which range from sticky resins to elastic solids. They are obtained by the low-temperature cationic polymerization of alkyl vinyl ethers having the general formula ROCH=CH-. These monomers are prepared by the addition of die selected alkanol to acetylene in the presence of sodium alkoxide or mercury(ll) catalyst, As shown by the following equations, the latter yields an acetal which must be thermally decomposed to produce the alkyl vinyl ether. [Pg.1356]

Cationic photoinitiators are frequently found in classes of compounds such as the triaryl sulfonium, tetraaryl phosphonium, and diaryliodonium salts of large protected anions (hexafluorophosphates or antimonates). These compounds are soluble in most epoxy resins, do not activate epoxy cure until exposed to uv light, are insensitive to room lighting, and have long storage life at room temperature. Cationic photoinitiators form an acid catalyst when exposed to uv light and consequently start the cationic chemical reaction. [Pg.264]

Methylbutene-l, 4-methylpentene-1 and 5-methylhexene-l represent a homologous series. Thus, it is conceivable that intramolecular hydride shift polymerization will also occur with the latter two monomers. Indeed NMR spectra seem to suggest that a predominantly 1,4 and 1,5 type isomerization polymerization occurs when 4-methylpentene-1 and 5-methylhexene-l are reacted with catalysts of the Lewis acid type at low temperatures (—73° C.) (163). According to the NMR evidence, low temperature cationic poly(4-methylpentene-l) shows only 2 sharp peaks, characteristic for the CH3 and CH2 groups. This is in agreement with a gem. dimethyl structure of the a,a-dimethylbutane type ... [Pg.534]

Termination involving intramolecular proton shift or intermolecular proton transfer, both followed by elimination of a molecule of water has been reported for the high temperature cationic polymerization of lactams a) intramolecular ... [Pg.124]

This method can be successfully used for polymers of the methacrylic series (the macroradicals of which do not react Iwmolytically with the anthryl group). It can also be applied to introduce LM into the chains of such polymers as polystyrene. However, in this case the copolymerization can be complicated by homolytic reactions between the growing macroradicals and the anthracene groups (see Scheme 1). Presumably, it is possible to avoid side reactions by low-temperature cationic poly-merization ... [Pg.26]

Attempts to conduct kinetic experiments at varying temperatures are equally frustrating. Temperature effects are not limited to sorption kinetics, but the sorbent surfaces themselves can be affected by temperature. Cation exchange capacity, particularly of amorphous and organic surfaces (Wada and Harada, 1971) is temperature dependent, as is the stability of soil minerals (Mattigod and Kittrick, 1980). In turn, specific sorption will be affected by mineral stability due to associated surface changes. [Pg.138]

Lysozyme Melting temperature Cation effect (Cl as common anion) ... [Pg.239]

Process E is a room-temperature cation exchange using a 0.4 molar nickel acetate solution. It leads to a low nickel loading, smaller than the theoretical exchange capacity of the zeolite. [Pg.580]

NMR analysis of the product from the low-temperature cationic polymerization of 4-methyl-1-pentene showed that both isobutyl and methyl side groups were present. Explain this finding. [Pg.116]

Consider the low-temperature cationic polymerization of vinyl ethers and discuss the effect of solvent on polymer stereochemistry. [Pg.173]

Polystyrene Polyisoprene (cis) Polyisobutylene CH2=CHPh CH, CH2=CH-C=CH2 CHj / CH2=C CHa peroxide-catalyzed radical-chain polymerization coordination or butyllithium-catalyzed anionic polymerization low-temperature cationic polymerization, BF3 and AIQ3 catalysis... [Pg.470]

Jalani NH, Datta R (2005) The effect of equivalent weight, temperature, cationic forms, sorbates and nanoinorganic additives on the sorption behaviour of Nafion. J Membr Sci... [Pg.219]

If the leaving group X = OCH2CF3 or OPh, polymerization can be achieved by heating the monomers between 190-220 °C. The thermolysis reaction leads to the elimination of the silyl ether MesSiX. If X = F, Cl or Br, thermolysis reaction does not lead to polymerization. However, if X = Cl, by the use of PCI5 as the initiator, ambient temperature cationic polymerization can be achieved. [Pg.136]

Allcock HR (2004) Ambient temperature cationic condensation synthesis of polyphosphazenes In Gleria M, De Jaeger R (eds) Phosphazenes - a worldwide insight. Nova Science, New York, pp 49-68... [Pg.154]

An early example of isomerization polymerization, now quite well understood, is the low temperature cationic polymerization of 3-methyl-1-butene to yield a crystalline polymer containing rearranged 1,3-repeating units (Eqn 2). [Pg.15]


See other pages where Temperature cation is mentioned: [Pg.109]    [Pg.538]    [Pg.629]    [Pg.191]    [Pg.21]    [Pg.473]    [Pg.2788]    [Pg.120]    [Pg.977]    [Pg.111]    [Pg.473]    [Pg.510]    [Pg.425]    [Pg.439]    [Pg.154]    [Pg.244]    [Pg.355]    [Pg.405]    [Pg.405]    [Pg.81]    [Pg.218]    [Pg.482]    [Pg.155]    [Pg.70]    [Pg.152]    [Pg.145]    [Pg.229]    [Pg.243]    [Pg.868]    [Pg.75]    [Pg.10]   
See also in sourсe #XX -- [ Pg.4 , Pg.7 ]




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