Abstract: A vehicle kill switch assembly includes a switch that is coupled to a vehicle. The switch is positioned beneath a driver's seat of the vehicle and the switch is electrically coupled to the ignition system of the vehicle. The ignition system is turned off when the switch is disengaged. A biasing unit is coupled to the vehicle and the driver's seat is coupled to the biasing unit. The biasing unit biases the driver's seat upwardly in the vehicle and the biasing unit is compressed when the driver sits in the driver's seat. The switch is engaged when the biasing unit is compressed to facilitate the vehicle to be driven. Conversely, the switch is disengaged when the biasing unit biases the driver's seat upwardly to inhibit the vehicle from being driven.

Abstract: The present disclosure provides borate or aluminate activators comprising cations having linear alkyl groups, catalyst systems comprising, and methods for polymerizing olefins using such activators. Specifically, the present disclosure provides activator compounds represented by Formula: [R1R2R3EH]d+[Mk+Qn]d?, wherein: E is nitrogen or phosphorous; d is 1, 2 or 3; k is 1, 2, or 3; n is 1, 2, 3, 4, 5, or 6; n?k=d; R1 is C1-C20 linear alkyl group; each of R2 and R3 is a C1-C40 linear alkyl group, a meta- and/or para-substituted phenyl group, an alkoxy group, a silyl group, a halogen, or a halogen containing group, wherein R1+R2+R3?15 carbon atoms; M is an element selected from group 13, typically B or Al; and each Q is independently a hydride, bridged or unbridged dialkylamido, halide, alkoxide, aryloxide, hydrocarbyl, substituted hydrocarbyl, halocarbyl, substituted halocarbyl, or halosubstituted-hydrocarbyl radical, provided that when Q is a fluorophenyl group, then R2 is not a C1-C40 linear alkyl group.

Abstract: A method for making a polymer, having the steps of (a) polymerizing one or more monomers in the presence of a solvent and a catalyst to form a reaction product; (b) removing an effluent from the reaction product, where the effluent comprises an active catalyst and one or more unreacted monomers; (c) combining a quench, comprising carbon dioxide, with the effluent to form a quenched polymer stream, having a carboxyl metal complex; and (d) recovering a polymer from the quenched polymer stream.

Abstract: Methods for forming polyolefin films using a model including a multivariate adaptive regression splines (MARS)-derived algorithm are provided. Related computing devices are also provided.

Abstract: A vehicle kill switch assembly includes a switch that is coupled to a vehicle. The switch is positioned beneath a driver's seat of the vehicle and the switch is electrically coupled to the ignition system of the vehicle. The ignition system is turned off when the switch is disengaged. A biasing unit is coupled to the vehicle and the driver's seat is coupled to the biasing unit. The biasing unit biases the driver's seat upwardly in the vehicle and the biasing unit is compressed when the driver sits in the driver's seat. The switch is engaged when the biasing unit is compressed to facilitate the vehicle to be driven. Conversely, the switch is disengaged when the biasing unit biases the driver's seat upwardly to inhibit the vehicle from being driven.

Abstract: This disclosure relates to syndiotactic polymers containing units derived from propylene and units derived from C4 to C20 alpha olefins. The polymers can be prepared is slurry or solution polymerization processes using a zirconium-containing metallocene catalyst system. The polymers have a melt flow rate as determined by ASTM D-1238 (230° C., 2.16 kg) of from about 0.1 to about 20 g/10 min. The syndiotactic polymers are useful as viscosity index improvers.

Abstract: A method for making a polymer, having the steps of (a) polymerizing one or more monomers in the presence of a solvent and a catalyst to form a reaction product; (b) removing an effluent from the reaction product, where the effluent comprises an active catalyst and one or more unreacted monomers; (c) combining a quench, comprising carbon dioxide, with the effluent to form a quenched polymer stream, having a carboxyl metal complex; and (d) recovering a polymer from the quenched polymer stream.

Abstract: The present disclosure provides borate or aluminate activators comprising cations having linear alkyl groups, catalyst systems comprising, and methods for polymerizing olefins using such activators. Specifically, the present disclosure provides activator compounds represented by Formula: [R1R2R3EH]d+[Mk+Qn]d-, wherein: E is nitrogen or phosphorous; d is 1, 2 or 3; k is 1, 2, or 3; n is 1, 2, 3, 4, 5, or 6; n?k=d; R1 is C1-C20 linear alkyl group; each of R2 and R3 is a C1-C40 linear alkyl group, a meta- and/or para-substituted phenyl group, an alkoxy group, a silyl group, a halogen, or a halogen containing group, wherein R1+R2+R3?15 carbon atoms; M is an element selected from group 13, typically B or Al; and each Q is independently a hydride, bridged or unbridged dialkylamido, halide, alkoxide, aryloxide, hydrocarbyl, substituted hydrocarbyl, halocarbyl, substituted halocarbyl, or halosubstituted-hydrocarbyl radical, provided that when Q is a fluorophenyl group, then R2 is not a C1-C40 linear alkyl group.

Abstract: Systems and methods are provided for pairing an electronic wallet for a consumer with a service provider. One exemplary method includes receiving, by a computing device, a request to pair the electronic wallet with the service provider where the electronic wallet is associated with an account and where the account is associated with a user, and requesting, by the computing device, consent from the user to pair the electronic wallet with the service provider. The method also includes generating, by the computing device, a pairing token for the wallet application and the service provider upon consent from the user, and storing the pairing token in association with the wallet application, whereby the service provider is permitted to use the pairing token in a subsequent network transaction involving an entity associated with the service provider and the wallet application, regardless of whether the wallet application is separately paired with the entity.

Abstract: Described is a silane functionalized polyolefin and a method of forming the composition, the composition comprising compounds having the following structure: wherein R2, R3, and R4 are independently selected from hydrogen, C1 to C10 linear alkyls, C6 to C14 aryls, C7 to C20 alkylaryls, and substituted versions thereof; n has a value within the range from 20 to 2000; m has a value within the range from 1 to 10 or 20; R is selected from hydrogen or C1 to C10 alkyls; and fa and fb are residual functional moieties selected from carbon, oxygen, nitrogen, sulfur, phosphorous, silicon, and boron, where any remaining valences are bound to a group selected from hydrogen, C1 to C10 linear alkyls, C6 to C14 aryls, C7 to C20 alkylaryls, and substituted versions thereof.

Abstract: An atactic polypropylene comb-block polyolefin comprising two blocks including a polyolefin backbone and atactic polypropylene combs pendant to the backbone having a weight average molecular weight of at least 8000 g/mole and a crystallinity of less than 20%, where the atactic polypropylene comb-block polyolefin has comb number of at least 2. The atactic polypropylene comb-block polyolefin is made by contacting at a temperature within a range from 20 to 70° C. propylene with a first metallocene precursor to form vinyl-terminated atactic polypropylene to form vinyl-terminated atactic polypropylene, then contacting at a temperature within a range from 40 to 150° C. the vinyl-terminated atactic polypropylene with ethylene, propylene, or both and a second metallocene precursor to form the backbone.

Abstract: This disclosure relates to syndiotactic polymers containing units derived from propylene and units derived from C4 to C20 alpha olefins. The polymers can be prepared is slurry or solution polymerization processes using a zirconium-containing metallocene catalyst system. The polymers have a melt flow rate as determined by ASTM D-1238 (230° C., 2.16 kg) of from about 0.1 to about 20 g/10 min. The syndiotactic polymers are useful as viscosity index improvers.

Abstract: An atactic polypropylene comb-block polyolefin comprising two blocks including a polyolefin backbone and atactic polypropylene combs pendant to the backbone having a weight average molecular weight of at least 8000 g/mole and a crystallinity of less than 20%, where the atactic polypropylene comb-block polyolefin has comb number of at least 2. The atactic polypropylene comb-block polyolefin is made by contacting at a temperature within a range from 20 to 70° C. propylene with a first metallocene precursor to form vinyl-terminated atactic polypropylene to form vinyl-terminated atactic polypropylene, then contacting at a temperature within a range from 40 to 150° C. the vinyl-terminated atactic polypropylene with ethylene, propylene, or both and a second metallocene precursor to form the backbone.

Abstract: A corrosion inhibitor composition useful in pipes, pilings and hulls comprising the reaction product of a vinyl/vinylidene-terminated polyolefin having at least 14 carbon atoms and a polyamine having a molecular weight of at least 500 g/mole.

Abstract: A multi-modal polymer blend for use in an adhesive composition comprising at least two compositionally different propylene-based polymers. The multi-modal polymer blend has a Mw of about 10,000 g/mol to about 150,000 g/mol. When subjected to Temperature Rising Elution Fractionation, the multi-modal polymer blend exhibits a first fraction that is soluble at ?15° C. in a hydrocarbon solvent, such as xylene or ortho-dichlorobenzene, the first fraction having an isotactic (mm) triad tacticity of about 70 mol % to about 90 mol %; and a second fraction that is insoluble or less soluble than the first fraction at ?15° C. in the hydrocarbon solvent, the second fraction having an isotactic (mm) triad tacticity of about 85 mol % to about 98 mol %.

Abstract: Described is a silane functionalized polyolefin and a method of forming the composition, the composition comprising compounds having the following structure: wherein R2, R3, and R4 are independently selected from hydrogen, C1 to C10 linear alkyls, C6 to C14 aryls, C7 to C20 alkylaryls, and substituted versions thereof; n has a value within the range from 20 to 2000; m has a value within the range from 1 to 10 or 20; R is selected from hydrogen or C1 to C10 alkyls; and fa and fb are residual functional moieties selected from carbon, oxygen, nitrogen, sulfur, phosphorous, silicon, and boron, where any remaining valences are bound to a group selected from hydrogen, C1 to C10 linear alkyls, C6 to C14 aryls, C7 to C20 alkylaryls, and substituted versions thereof.

Abstract: Methods and systems for pelletizing low molecular weight semi-crystalline polymers are provided herein. Polymer compositions comprising the semi-crystalline polymer and a solvent are provided to a devolatilizing device, where the solvent is at least partially evaporated under vacuum conditions, resulting in removal of heat from the polymer by evaporative cooling and crystallization of the polymer. Once the polymer has reached the desired temperature, the polymer exits the devolatilizer and is pelletized. Semi-crystalline polymers that may be used in the present invention include propylene-based copolymers, such as propylene-ethylene and propylene-hexene copolymers having a heat of fusion, Hf, from about 5 to about 75 J/g and a weight average molecular weight, Mw, from about 10,000 to about 200,000 g/mol.

Abstract: This invention relates to a reaction product obtained by contacting a polymer comprising units derived from dicyclopentadiene with a vinyl terminated macromonomer, a vinyl monomer or a vinylene monomer, in the presence of a metathesis catalyst, where the vinyl monomer or vinylene monomer is represented by the formula: wherein each X is, independently, —CO2R, —CONR1R2, CN, a C1 to a C20 alkyl group; R is a C1 to a C20 alkyl group or an aromatic group; each R1 and R2 is, independently, a hydrogen, a C1 to a C20 alkyl group, or an aromatic group; each R5 is, independently, a hydrogen atom or a C1 to a C40 alkyl group; each Ar is, independently, an aromatic group; and each n is, independently, from 0 to about 40.

Abstract: Disclosed herein are methods of preparing a catalyst system comprising a spray-dried activator and polymerization processes employing these catalyst systems.

Abstract: A multi-modal polymer blend for use in an adhesive composition comprising at least two compositionally different propylene-based polymers. The multi-modal polymer blend has a Mw of about 10,000 g/mol to about 150,000 g/mol. When subjected to Temperature Rising Elution Fractionation, the multi-modal polymer blend exhibits a first fraction that is soluble at ?15° C. in a hydrocarbon solvent, such as xylene or ortho-dichlorobenzene, the first fraction having an isotactic (mm) triad tacticity of about 70 mol % to about 90 mol %; and a second fraction that is insoluble or less soluble than the first fraction at ?15° C. in the hydrocarbon solvent, the second fraction having an isotactic (mm) triad tacticity of about 85 mol % to about 98 mol %.