Diene rubbers stereoregular

Historically, the most important application of the electron transfer initiation involved the production of stereoregular diene rubbers by lithium metal initiation. The lithium was used as a fine dispersion with a large surface area to speed up the initiation reaction and the process was carried out in hydrocarbon solvents because polar solvents increase the generally undesired vinyl side chain content of the product polymer.)... 

Formation of a strong interfacial layer is the key factor of the mechanism describing retardation of ozone degradation of a diene rubber by elastomer additives with a low degree of unsaturation [1-4]. The effect of comonomer ratio in ethylene-propylene-diene terpolymers (EPDMs) and stereoregularity of propylene units on the interfacial interaction and the amount of crosslinks in ihe interfacial layer was considered for heterophase crosslinked blends with butadiene-acrylonitrile mbbers (BNRs) of different polarities. 

During the last two decades, a number of diene homopolymers and copolymers have been developed to fill the diverse elastomer needs in the production of tires. The earliest developments were mainly concerned with the preparation of stereoregular cis-1,4-polyisoprene, as a substitute for natural rubber, using... 

Stereospecific polymerization has particular significance for the preparation of stereoregular polymeric dienes. In the radical polymerization of butadiene or isoprene the molecular chains always consist of varying proportions of adjacent cis- and trans-1,4-units as well as 1,2- and 3,4- linked units, depending on the polymerization conditions but it is now possible, using particular ionic initiation systems to make a synthetic natural rubber that contains more than 90% cfs-l,4-isoprene repeating units (see Example 3-21). 

Recently, several lanthanide complexes, based on Nd, Ln, Sm, or Yb, have been smdied for controlling stereoregularity and activity of diene polymerizations and copolymerizations. Specifically, Nd-based catalysts have shown very good stereoregularity control over the production of high CM-polybutadiene rubber [36]. 

The polyallomers constitute the class of block copolymers where both components are capable of crystallizing independently (Coover et al, 1966 Hagenmeyer and Edwards, 1966, 1970 Eastman Chemical Products, n.d.). The most important member of this family contains crystalline, stereoregular polypropylene as the major component and polyethylene as the minor component. As expected for a block copolymer, these products differ greatly in behavior from mechanical blends of polyethylene and polypropylene, and also from their random copolymers, poly(propylene-co-ethylene). When crosslinked with a diene monomer, the latter copolymers are known as EPDM rubbers (Lee et a/., 1966 Rodriguez, 1970, Chapter 13), while the former blends are of apparently little interest. In Figure 6.28 and 6.29 the... 

Classification of Polymers Free-Radical Chain-Growth Polymerization Cationic Chain-Growth Polymerization Anionic Chain-Growth Polymerization Stereoregular Polymers Ziegler-Natta Polymerization A WORD ABOUT... Polyacetylene and Conducting Polymers Diene Polymers Natural and Synthetic Rubber Copolymers... 

Ziegler-Natta catalysts can also be used for preparation of stereoregular polymers from 1,3-dienes. For example, polyisoprene with 96-97 per cent cw-1,4 content (i.e. synthetic natural rubber ) can be prepared using catalysts obtained from TiCU-f Ai Bu3. 

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