Hydrogenation alcohol comonomer

The hydrogenation reaction is also sensitive to the structure of the alcohol comonomer, with the primary alcohols of the hydroxyethyl methacrylate polymer interacting with the catalyst to give results more closely resembling those found when ethanol is used as the solvent. Similar results were found with DIOP-type ligands (Figure 4). 

In commercial polyethylene operations, poisons may enter the process as trace (ppm) contaminants in ethylene, comonomer, hydrogen (CTA), nitrogen (used as inert gas), solvents and other raw materials. These poisons reduce catalyst activity. Most damaging are oxygen and water. However, CO, CO, alcohols, acetylenics, dienes, sulfur-containing compounds and other protic and polar contaminants can also lower catalyst performance. With the exception of CO, aluminum alkyls react with contaminants converting them to alkylaluminum derivatives that are less harmful to catalyst performance. Illustrative reactions of contaminants with triethylaluminum are provided in eq 4.9-4.11 ... 

Vinyl Acetate, Homo- and Copolymer Latexes Vinyl Acetate Comonomer (butyl acrylate, ethylene, vinyl ester of versatic add) Partially Hydrolyzed Polyvinyl Alcohol Sodium Bicarbonate Hydrogen Peroxide (35%) Sodium Formaldehyde Sulfoxylate Water 70.0-100.0 0.0-30.0 6.0 0.3 0.7 0.5 80.0... 

It does not homopolymerize easily and hence can be stored as a liquid. It undergoes many addition reactions typical of an olefin. Reactions inclnde preparation of linear dimers and trimers and cyclic dimers (21,22) decomposition at 600°C with subsequent formation of octafluoro-2-butene and octafluoroisobutylene (23) oxidation with formation of an epoxide (24), an intermediate for a number of perflu-oroalkyl perfluorovinyl ethers (25,26) and homopolymerization to low molecular weight liquids (27,28) and high molecular weight solids (29,30). Hexafluoropropylene reacts with hydrogen (31), alcohols (32), ammonia (33), and the halogens and their acids, except I2 and HI (31,34-36). It is used as a comonomer to produce elastomers and other copolymers (37-41). The toxicological properties are discussed in Reference 42. 

Method of synthesis cationic polymerization of high purity Isobutylene and isoprene is used to produce butyl rubber in the presence of complex systems of catalysts polymerization is terminated by irreversible destruction of the propagating carbenium ion by the collapse of the ion pair, by hydrogen abstraction from the comonomer, by formation of stable allylic carbenium ions, or by reaction with nucleophilic species such as alcohols or amines ... 

Despite the low catalyst activity, all studied amides 19—23 formed copolymers with ethylene and propylene. The maximum amount of amide incorporated was 1.3 mol% with ethylene and 0.96 mol% with propylene. In the copolymerizations of amines with ethylene, the highest comonomer contents were on the same level (1.2 mol%), even though much higher comonomer concentrations could be used in the polymerizations. It seems that when the functional comonomers are better masked by the cocatalyst, the reactivities are at the same time decreased. Nonetheless, even the unhindered primary and secondary amines with acidic hydrogens were incorporated in the polymer chain. In this respect, the amines behave much like the alcohols and ethers, whereas amides resemble the less-shielded esters. 

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