Styrene isobutylene copolymer

Butyl rubber was and is enormously successful both technolc cally and in the business sense. But other Sparks inventions and coinventions also were commercially successful. Examples are styrene-isobutylene copolymers as coating for paper and paper milk bottles, styrene-isoprene copolymers as artificial leather, colored asphalt paving materials, oxo alcohols, and oxo ester plasticizers. During his brief period of employment as a research supervisor at USDA s Northern Regional Research Center, Peoria, Illinois, Dr. Sparks initiated work on dimer acids... 

Particular studies of the IR spectra of polymers include isotactic poly(l-pentane), poly(4-methyl-l-pentene), and atactic poly(4-methyl-pentene) [18], chlorinated PE [19], aromatic polymers including styrene, terephthalic acid, isophthalic acid [20], PS [21, 22], styrene-glycidyl-p-isopropenylphenyl ether copolymers [23], styrene-isobutylene copolymers [24], vinyl chloride-vinyl acetate-vinyl fluoride terpolymers [25], vinyl chloride-vinyl acetate copolymers [26], styrene copolymers [27], ethylene-vinyl acetate copolymers, graft copolymers, and butadiene-styrene [28] and acrylonitrile-styrene copolymers [29]. 

Emulsifying agents Styrene-isobutylene copolymer United States 2,871,137 1958 Esso Research... 

Other applications of IR spectroscopy in copolymer characterisation include styrene-glycidyl-p-isopropenylphenyl ether copolymers [4], styrene-isobutylene copolymers [5], vinyl chloride - vinyl acetate - vinyl fluoride terpolymers [6], vinylchloride - vinyl acetate copolymers [7], styrene copolymers [8], ethylene-vinyl acetate copolymers [9], graft copolymers, and butadiene-styrene [10] and acrylonitrile - styrene copolymers [11], polyurethane - polyacrylate [12], polymethylmethacrylate grafted high alpha cellulose [13], bisphenol-polycarbonate (PC) [14], bromobutyl isoprene [15], styrene - methacrylonitrile (SMAN) [16, 17] and styrene - acrylonitrile [18]. 

Neagu, C., Puskas, J.E., Singh, M.A., and Natansohn, A. Domain sizes and interface thickness determination for styrene-isobutylene block copolymer systems using solid-state NMR spectroscopy. Macromolecules, 33, 5976-5981, 2000. 

Elabd, Y. A. and Napadensky E. 2004. Sulfonation and characterization of poly(styrene-isobutylene-styrene) triblock copolymers at high ion-exchange capacities. Polymer 45 3037-3043. 

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. 

Treatment of polyisobutylene (which contains terminal double bonds) with ozone followed by thermolysis produces polymeric radicals. Isobutylene-styrene block copolymer is formed when thermolysis is performed in the presence of styrene, but the process is not efficient because polystyrene and polyisobutylene homopolymers constitute more than half of the product [Cunliffe et al., 2001]. 

R.F. Storey, B.J. Chisholm, and M.A. Masse, Morphology and physical properties of poly(styrene-b-isobutylene-b-styrene) block copolymers, Polymer, 37(14) 2925-2938, July 1996. 

Poly(St-b-IB) Poly(pClceMeSt-b-IB) Poly(styrene- block-isobutylene) copolymer Poly(p-chloro-a-methylstyrene-Z Zock-isobutylene) copolymer... 

Biostable polymers have been chosen for use in the majority of DES that are marketed or in clinical development. The main attractiveness of biostable polymers is their physical stability, inertness toward the drug, and predictable drug kinetics. In Cypher, a blend of poly(ethylene-co-butyl methacrylate) (PEVAc/PBMA) is used as the drug carrier. This hydrophobic polymer, along with additional polymer process steps, effectively controls the release of sirolimus, eluting 80% of the drug over 30 days after implantation. In the case of Taxus, atri-block copolymer of styrene-isobutylene-styrene (SIBS) is used as the hydrophobic polymer matrix that releases 10% of incorporated paclitaxel in the first 30 days (20). 

Fonagy, T., Ivan, B., and Szesztay, M. (1998). Poly(isobutylene-g-styrene) graft copolymers by quasiliving atom transfer radical grafting of styrene. Polym. Mater. Sci. Eng., 79 3-4. 

Maleic anhydride grafting (cont.) poly(styrene-co-divinylbenzene), 694 poly(styrene-co-isobutylene), 675, 689 poly(styrene-co-nfialeic anhydride), 676, 679 poly(vinyl acetate), 676, 694 poly(vinyl acetate-co-vinyl fluoride), 678 poly(vinyl alkyl ethers), 675, 679, 692, 701 poly(vinyl chloride), 683, 692, 693, 695, 702 poly(vinylidene chloride), 691 poly(vinyl toluene-co-butadiene), 689 radical—initiated, 459-462, 464-466, 471, 475, 476 radiation—initiated, 459, 461, 466, 471, 474 redox-initiated, 476 rubber, 678, 686, 687, 691, 694 to saturated polymers, 459-466, 475, 476 solvents used 460-463, 465, 466, 469, 474-476 styrene block copolymers, 679 tall oil pitch, 678, 697 terpene polymers, 679, 700 thermally-initiated, 462, 464-467, 469, 476 to unsaturated polymers, 459, 466-474 vapor-phase techniques, 464, 474, 475 to wool fibers, 476 Maleic anhydride monomer acceptor for complex formation, 207-210 acetal copolymerization, 316 acetone CTC thermodynamic constants, 211 acetone photo-adduct pyrolysis, 195, 196 acetylacetone reaction, 235 acetylenic photochemical reactions, 193-196 acrylamide eutectic mixtures, 285 acylation of aromatic acids, 97 acylation of aromatics, 91, 92 acylation of fused aromatics, 92, 95, 97, 98 acylation of olefins, 99 acylation of phenols, 94-96 acylic diene Diels-Alder reactions, 104-111, 139 addition polymer condensations, 503-505 adduct with 2-cyclohexylimino-cyclopentanedi-thiocarboxylic acid, 51 adducts for epoxy resins curing, 507-510 adduct with 2-iminocyclopentanedithiocarboxylic acid, 51... 

The corresponding block copolymers are referred to as S-B-S, S-I-S and S-EB-S. Later, polymers with poly(ethylene-propylene) midsegments (S-EP-S) were introduced. A more recent development, now commercialized, is styrenic block copolymers with an isobutylene midsegment (S-iB-S) [9,10]. These can also be produced with substituted polystyrene end segments. 

PEVA poly(ethylene-co-vinyl acetate), PBMA poly(n-butyl methacrylate), SIBS poly(styrene-b-isobutylene-b-styrene) block copolymer, PC phosphorylcholine pol5rmer, PVDF-HFP poly(vinyUdene fluoride)-hexafluoropropylene, BioLinx hydrophobic Cio-polymer/hydrophilic Ci9-polymer/poly(vinylpyrrolidone) (PVP), PLA polylactide... 

C150H186 hexabenzocoronene derivative polymantanes acenaphthofluoranthenes c/s-polyisoprene -[CH2C(CH3)=CHCH2].-isoprene—isobutylene copolymer styrene—butadiene copolymer ethylene—propylene copolymer liquid crystal (component for photovoltaic films) new material hydrocarbons built from fused adamantine units conductive ladder polymer natural rubber synthetic rubber... 

New copolymers based on a copolymerization of isobutylene and p-methyl-styrene with improved heat resistance have been reported [64]. Once copolymerization was accomplished, the polymer was selectively brominated in the p-methyl position to yield a terpolymer called EXXPO. In contrast to butyl and halobutyl, the new terpolymer has no unsaturation in the backbone and therefore shows enhanced thermal stability and resistance to oxidation. Useful solvent-based adhesives can be formulated using the new terpolymer in combination with block copolymers [65]. The hydrocarbon nature of the new terpolymer results in excellent compatibility with hydrocarbon resins and oils. 

Table IV shows the data on rigidity changes of the end-sealing compounds at two dose levels. Rigidity was determined by torsional braid analysis (5). These data indicate that the blend of cured and uncured isobutylene-isoprene copolymer was softened most by the irradiation treatment, the blend of polychloroprene and butadiene-styrene copolymer softened the least, and the blend of polychloroprene and the uncured isobutylene-isoprene copolymer was intermediate. Increasing the irradiation dose from 3-4 Mrad to 6-7.5 Mrad decreased the rigidity of the three end-sealing compounds. The irradiation temperature did not significantly influence rigidity.

Poly(styrene-/7-isobutylene-/ -styrene) (PS-PIB-PS), triblock copolymers can be prepared via coupling of living PS-PIB diblock copolymers in a one-pot procedure [12]. 

Cao X. and Faust R., Polyisobutylene based thermoplastic elastomer 5. Poly(styrene-b-isobutylene-b-styrene) tri-block copolymers by coupling of living poly(styrene-b-isobutylene) di-block copolymers. Macromolecules, 32, 5487, 1999. 

---