Abstract:
Processes are provided which include copolymerization using two different metallocene catalysts, one capable of producing high Mooney-viscosity polymers and one suitable for producing lower Mooney-viscosity polymers having at least a portion of vinyl terminations. The two catalysts may be used together in polymerization to produce copolymer compositions of particularly well-tuned properties. For instance, polymerizations are contemplated to produce high-Mooney metallocene polymers that exhibit excellent processability and elasticity, notwithstanding their high Mooney viscosity. Other polymerizations are also contemplated in which lower-Mooney metallocene polymers are produced, which also exhibit excellent processability and elasticity, while furthermore having excellent cure properties suitable in curable elastomer compound applications. Many of the contemplated polymerizations include controlling the ratio of the two metallocene catalysts used in the polymerization so as to obtain the desired Mooney viscosity and desired rheology (indicated by Mooney Relaxation Area) of the copolymer compositions.
Abstract:
Processes are provided which include copolymerization using one or both of a metallocene catalyst capable of producing high molecular weight polymers and a metallocene catalyst capable of producing polymers having 60% or more vinyl terminations. Polymerization processes include dual catalyst polymerization in a single polymerization zone comprising both metallocene catalysts. Other processes include serial or parallel polymerizations in multiple polymerization zones, using either or both catalysts in each polymerization zone. Such polymerization processes produce reactor blends, and are particularly suited for producing copolymer compositions (such as EP or EPDM copolymer compositions) exhibiting improved melt elasticity and rheological properties.
Abstract:
Provided herein are ethylene copolymers, methods for making such copolymers, and compositions made from such copolymers. The ethylene copolymers have 70 wt. % to 85 wt. % of units derived from ethylene and at least 12 wt. % of units derived from at least one α-olefin having 3 to 20 carbon atoms. The copolymers preferably further have a weight-average molecular weight (Mw) ranging from about 50,000 to about 200,000 g/mol, melting point of at least 100° C., ratio of Mw/Mn of about 1.5 to about 3.5, a content of group 4 metals of no more than 25 ppm, and a ratio of wt ppm Group 4 metals/wt ppm Group 5 metals of at least 3. Such copolymers may be particularly useful as viscosity modifiers for lubricating oil compositions.
Abstract:
Provided is an ethylene copolymer having 40 wt. % to 70 wt. % of units derived from ethylene and at least 30 wt. % of units derived from at least one α-olefin having 3 to 20 carbon atoms and has the following properties: (a) a weight-average molecular weight (Mw), as measured by GPC, in the range of about 50,000 to about 200,000 g/mol; (b) a melting point (Tm) in ° C., as measured by DSC, that satisfies the relation: Tm>3.4×E−180 where E is the weight % of units derived from ethylene in the copolymer; (c) a ratio of Mw/Mn of about 1.8 to about 2.5; (d) a content of Group 4 metals of no more than 5 ppm; and (e) a ratio of wt ppm Group 4 metals/wt ppm Group 5 metals of at least 3. Also provided are methods for making an ethylene copolymer and compositions comprising an ethylene copolymer.
Abstract:
Lubricant compositions, as well as processes for their formulation, are provided. The lubricant compositions comprise an oil basestock and one or more blocky ethylene propylene copolymers. The copolymers are preferably prepared using metallocene catalyst systems but without using a chain shuttling agent.
Abstract:
A method, including: contacting a carbene or carbyne precatalyst with a first co-catalyst, under reaction conditions sufficient to cause the first-co-catalyst to activate the carbene or carbyne precatalyst, wherein the first co-catalyst is selected from the group consisting of an aluminum activator, a Br2-1,4-dioxane complex, I2, PhICl2, and PCl5.
Abstract:
A multilayer structure can include at least one layer that comprises an ethylene propylene diene copolymer compound that comprises: 60 parts per hundred rubber (phr) to 95 phr of a first ethylene propylene diene copolymer (EP(D)M) having an ethylene content of 62 wt % to 90 wt % based on the first EP(D)M and a heat of fusion (Hf) of 15 J/g or greater; 5 phr to 40 phr of an second EP(D)M having an ethylene content of 40 wt % to 60 wt % based on the second EP(D)M and a Hf of 0 J/g to 14 J/g, wherein the Hf of the first EP(D)M minus the Hf of the second EP(D)M is 5 J/g or greater; wherein the first EP(D)M and second EP(D)M combined are 100 parts; a filler at 40 phr to 500 phr; and a curing agent at 0.5 phr to 20 phr.
Abstract:
Systems and methods are provided for integration of polymeric waste co-processing in cokers to produce circular chemical products from coker naphtha, including a method of producing circular chemical products comprising: providing a coker naphtha that is at least partially derived from polymeric waste, wherein the coker naphtha has a total halide content of about 1 wppm to about 0.5 wt %, a 2-3 ring aromatic content of about 0 wt % to about 5 wt %, and a sulfur content of about 750 ppm to about 2 wt %; and converting the coker naphtha into at least a polymer.
Abstract:
A propylene-α-olefin-diene (PEDM) terpolymer may comprise 75 to 95 wt % propylene, 5 to 20 wt % α-olefin, and 0.5 to 5 wt % diene, said wt % based on the weight of the PEDM terpolymer. The propylene-α-olefin-diene terpolymer may be blended with an ethylene-based copolymer and optionally a variety of additives to form an elastomeric composition. An exemplary elastomeric composition includes 5 to 40 parts by weight per hundred parts by weight rubber (phr) of the PEDM terpolymer, 60 to 95 phr of the ethylene-based copolymer, and optionally additives like carbon black, zinc dimethacrylate, paraffinic oil, zinc oxide, and/or zinc stearate.
Abstract:
Processes are provided which include copolymerization using two different metallocene catalysts, one capable of producing high Mooney-viscosity polymers and one suitable for producing lower Mooney-viscosity polymers having at least a portion of vinyl terminations. The two catalysts may be used together in polymerization to produce copolymer compositions of particularly well-tuned properties. For instance, polymerizations are contemplated to produce high-Mooney metallocene polymers that exhibit excellent processability and elasticity, notwithstanding their high Mooney viscosity. Other polymerizations are also contemplated in which lower-Mooney metallocene polymers are produced, which also exhibit excellent processability and elasticity, while furthermore having excellent cure properties suitable in curable elastomer compound applications. Many of the contemplated polymerizations include controlling the ratio of the two metallocene catalysts used in the polymerization so as to obtain the desired Mooney viscosity and desired rheology (indicated by Mooney Relaxation Area) of the copolymer compositions.