Abstract:
Random copolymers may be prepared using a process that includes polymerizing a mixture of monomers including at least propylene and ethylene monomer, in the presence of a catalyst system including a metallocene catalyst having the general structure: racemic-X(2-R1-4-R2-Ind)2MCl2 wherein M is a Group 4, 5 or 6 transition metal, or a lanthanide or actinide series metal; X is a structural bridge imparting stereorigidity; R1 is hydrogen or an alkyl, aryl or a substitution moiety; R2 is hydrogen, or a C1-C4 alkyl; and Ind is an indenyl group. The copolymers are prepared under reaction conditions suitable to form a copolymer, wherein the copolymer has a higher level of ethylene incorporation than a corresponding polymer formed under otherwise identical reaction conditions except that a different bisindeny metallocene catalyst having a 4-indenyl substitution larger than 4 carbons is used. The copolymers may have a lower melt temperature than the corresponding polymers. The resulting copolymers may be used to prepare articles of manufacture including, but not limited to films, fibers and injection molded articles.
Abstract:
Disclosed are blends of polystyrene and at least one of syndiotactic polypropylene, ethylene propylene copolymers, and styrene-butadiene-styrene triblock copolymers. These blends are prepared using solution polymerization and have unique morphologies and desirable physical properties. The blends can also be prepared with graft-promoting or crosslinking agents and rubbers to prepare modified high impact polystyrene.
Abstract:
A process for the reduction of a phenylacetylene contaminant in the presence of a styrene monomer. A styrene monomer stream containing a minor amount of phenylacetylene is supplied to a hydrogenation reactor. A hydrogenation gas comprising hydrogen is also supplied to the hydrogenation reactor. The styrene monomer stream and the hydrogen are brought into contact with a catalyst bed containing a catalyst comprising a reduced copper compound on a theta alumina support. The hydrogenation reactor is operated at a temperature of at least 60° C. and a pressure of at least 30 psig to hydrogenate phenylacetylene to styrene. A product is recovered from the hydrogenation reactor having a substantially reduced phenylacetylene content and an enhanced styrene content. The hydrogenation gas comprises a mixture of nitrogen and hydrogen.
Abstract:
Methods and processes for reducing alkylation catalyst poisoning are described herein. Such methods generally include contacting ethylbenzene with a dehydrogenation catalyst to form a dehydrogenation output stream within a dehydrogenation system and passing at least a portion of the dehydrogenation output stream to an alkylation system, wherein the at least a portion of the dehydrogenation output stream contacts an alkylation catalyst. The at least a portion of the dehydrogenation output stream includes a level of impurities resulting from offtest and wherein the level of impurities is sufficiently low to result in essentially no observed effect on the alkylation catalyst life in comparison with an alkylation system feed absent offtest.
Abstract:
Alkylation processes are described herein. The alkylation process generally includes contacting an input stream including benzene with an alkylation catalyst and an alkylating agent to form an alkylation output stream including ethylbenzene. The alkylation process further includes contacting at least a portion of the alkylation output stream with a transalkylation catalyst and a benzene source to form a transalkylation output stream, wherein the benzene source is selected to minimize the amount of alkylation catalyst poisons contacting the alkylation catalyst.
Abstract:
Methods for the preparation of fluorenyl-type ligand structures and substituted fluorenyl groups which may be employed in metallocene-type olefin polymerization catalysts. There is provided a 2,2′-dihalogen-diphenylmethylene having a methylene bridge connecting a pair of phenyl groups. Each phenyl group has a halogen on a proximal carbon atom relative to the methylene bridge. The halogenated diphenylmethylene is reacted with a coupling agent comprising a Group 2 or 12 transition metal in the presence of a nickel or palladium-based catalyst to remove the halogen atoms from the phenyl groups and couple the phenyl groups at the proximal carbon atoms to produce a fluorene ligand structure. The coupling agent may be zinc, cadmium or magnesium and the catalyst may be a monophosphene nickel complex. The halogenated diphenylmethylene may be an unsubstituted ligand structure or a monosubstituted or disubstituted ligand structure. The halogenated diphenylmethylene may be monosubstituted with a tertiary butyl group or may be a dialkyl diphenylmethylene having alkyl substituents at the directly distal positions of the phenyl groups relative to the methylene bridge.
Abstract:
A process for the dehydrogenation of a C2 or C3 alkyl aromatic compound to a corresponding vinyl aromatic compound in a tubular reactor incorporating a spiral flow path. Preferred embodiments of the invention provide processes for the production of styrene or divinylbenzene by the catalytic dehydrogenation of ethylbenzene or diethylbenzene, respectively. A feedstock containing a C2 or C3 alkyl aromatic and steam is supplied into the inlet of a tubular reactor containing a dehydrogenation catalyst and comprising a hydrogen permeable outer wall. The alkyl aromatic compound is dehydrogenated to a corresponding vinyl aromatic compound with the attendant production of hydrogen. The feedstock and products of the dehydrogenation reactor are flowed along a longitudinal spiral flow path providing for an outward radial flow of hydrogen to provide a pressure gradient through the hydrogen permeable outer wall of the reactor with the flow of hydrogen therethrough. Hydrogen is removed from the outer wall of the reactor. The resulting vinyl aromatic product is recovered from the tubular reactor.
Abstract:
An olefin polymerization catalyst may be prepared using a process including contacting a metal compound of the formula M(OR1)2 with a diketone to form a catalyst precursor having the general formula: wherein M is a Group IIA metal; O is oxygen; n=1 or 2; R1, R2, R3, and R4 are the same or different; and are a hydrogen or a substituted or unsubstituted alkyl or aryl moiety having from about 1 to about 20 carbons atoms.
Abstract translation:烯烃聚合催化剂可以使用包括使式M(OR 1)2 N 2的金属化合物与二酮接触以形成具有通式 :其中M是IIA族金属; O是氧; n = 1或2; R 1,R 2,R 3和R 4相同或不同; R 1,R 2,R 3和R 4相同或不同; 并且是具有约1至约20个碳原子的氢或取代或未取代的烷基或芳基部分。
Abstract:
A polymer can be prepared using a loop reactor and process including feeding a process stream through the loop reactor and maintaining the loop reactor at a steady state by controlling a flow of coolant fluid to maintain a temperature in the loop reactor at a preset point. The temperature in the loop reactor may be maintained at a preset point by using a coolant fluid flow controller and valve unit having a substantially linear response over the normal operating range of the controller and valve unit. The normal operating range of the controller and valve unit may be sufficient to provide a flow range not limiting to the throughput of the loop reactor.
Abstract:
Asphalt and elastomeric polymer compositions crosslinked with mixed polythiomorpholines or at least one alkyl polysulfide can give polymer modified asphalts (PMAs) with improved properties and/or reduced H2S evolution. When at least one alkyl polysulfide is used to completely or partially replace conventional crosslinkers such as S or MBT, mercaptobenzimidazole (MBI) may be optionally used as a co-crosslinker. The use of mixed polythiomorpholines as crosslinkers provide PMAs with better low temperature profiles (BBR m-values). The use of at least one alkyl polysulfide crosslinker gives PMAs with improved PAV-aged DSR results, and reduced H2S evolution. The use of at least one alkyl polysulfide crosslinker together with MBI may give PMAs with improved PAV DSR Fail Temperatures.
Abstract translation:用混合多硫代吗啉或至少一种烷基多硫化物交联的沥青和弹性体聚合物组合物可以得到具有改进性能和/或降低的H 2 S 2 S演化的聚合物改性沥青(PMA)。 当使用至少一种烷基多硫化物来完全或部分替代常规交联剂如S或MBT时,巯基苯并咪唑(MBI)可以任选地用作共交联剂。 使用混合的聚硫代吗啉作为交联剂为PMA提供了更好的低温谱(BBR m值)。 使用至少一种烷基多硫化物交联剂使得PMA具有改进的PAV老化的DSR结果和降低的H 2 S 2 S进化。 使用至少一种烷基多硫化物交联剂与MBI一起可以使PMA具有改进的PAV DSR失败温度。