Patent classifications
C08F10/14
Hybrid supported metallocene catalyst and polyolefin preparation method using same
The present invention relates to a hybrid supported metallocene catalyst and a polyolefin preparation method using the same. Using the hybrid supported metallocene catalyst can not only significantly reduce the amount of wax produced when polymerizing olefin monomers, but can also enhance the stress cracking resistance of the polyolefin that is prepared.
Processes to produce poly alpha-olefin trimers
The present disclosure generally relates to processes to produce alpha-olefin oligomers and poly alpha-olefins. In an embodiment, a process to produce a poly alpha-olefin (PAO) includes introducing a first alpha-olefin and a first catalyst system comprising a metallocene compound into a continuous stirred tank reactor or a continuous tubular reactor under first reactor conditions to form a first reactor effluent. The alpha-olefin is introduced to the reactor at a flow rate of about 100 g/hr or more. The first reactor effluent includes PAO dimer comprising at least 96 mol % of vinylidene and 4 mol % or less of trisubstituted vinylene and disubstituted vinylene, based on total moles of vinylidene, trisubstituted vinylene, and disubstituted vinylene. The method includes introducing the first reactor effluent, a second alpha-olefin and a second catalyst composition comprising an acid catalyst into a second reactor under second reactor conditions to form a second reactor effluent comprising PAO trimer.
Processes to produce poly alpha-olefin trimers
The present disclosure generally relates to processes to produce alpha-olefin oligomers and poly alpha-olefins. In an embodiment, a process to produce a poly alpha-olefin (PAO) includes introducing a first alpha-olefin and a first catalyst system comprising a metallocene compound into a continuous stirred tank reactor or a continuous tubular reactor under first reactor conditions to form a first reactor effluent. The alpha-olefin is introduced to the reactor at a flow rate of about 100 g/hr or more. The first reactor effluent includes PAO dimer comprising at least 96 mol % of vinylidene and 4 mol % or less of trisubstituted vinylene and disubstituted vinylene, based on total moles of vinylidene, trisubstituted vinylene, and disubstituted vinylene. The method includes introducing the first reactor effluent, a second alpha-olefin and a second catalyst composition comprising an acid catalyst into a second reactor under second reactor conditions to form a second reactor effluent comprising PAO trimer.
Method for fabricating pattern of cured product and methods for manufacturing optical component, circuit board and quartz mold replica as well as coating material for imprint pretreatment and cured product thereof
The method for fabricating pattern of a cured product includes a first step (arranging step) of arranging a layer formed of a liquid film of a curable composition (α1) containing at least a component (A1) serving as a polymerizable compound on a substrate and a second step (dispensing step) of dispensing liquid droplets of a curable composition (α2) containing at least a component (A2) serving as a polymerizable compound discretely onto a layer formed of a composition (α1′) of components of the curable composition (α1) except a component (D1) serving as a solvent, in which: the mixing of the composition (α1′) and the curable composition (α2) is exothermic.
4-methyl-1-pentene polymer, resin composition and molded article
A 4-methyl-1-pentene polymer (X) wherein a content of a constitutional unit derived from 4-methyl-1-pentene is 90 to 100% by mol; a content of a constitutional unit derived from at least one olefin selected from ethylene and an α-olefin, other than 4-methyl-1-pentene, having 3 to 20 carbon atoms is 0 to 10% by mol; and the 4-methyl-1-pentene polymer satisfies certain requirements (a) to (f): (a) a meso diad fraction (m) measured by .sup.13C-NMR falling within a certain range; (b) a ratio of weight-average molecular weight Mw within a certain range; (c) a melt flow rate (MFR) within a certain range; (d) a cumulative weight fraction within a certain range; (e) a proportion of a polymer having a molecular weight of a certain range; and (f) a heat of fusion and a melting point of the 4-methyl-1-pentene polymer within certain ranges.
4-methyl-1-pentene polymer, resin composition and molded article
A 4-methyl-1-pentene polymer (X) wherein a content of a constitutional unit derived from 4-methyl-1-pentene is 90 to 100% by mol; a content of a constitutional unit derived from at least one olefin selected from ethylene and an α-olefin, other than 4-methyl-1-pentene, having 3 to 20 carbon atoms is 0 to 10% by mol; and the 4-methyl-1-pentene polymer satisfies certain requirements (a) to (f): (a) a meso diad fraction (m) measured by .sup.13C-NMR falling within a certain range; (b) a ratio of weight-average molecular weight Mw within a certain range; (c) a melt flow rate (MFR) within a certain range; (d) a cumulative weight fraction within a certain range; (e) a proportion of a polymer having a molecular weight of a certain range; and (f) a heat of fusion and a melting point of the 4-methyl-1-pentene polymer within certain ranges.
4-methyl-1-pentene polymer, resin composition and molded article
A 4-methyl-1-pentene polymer (X) wherein a content of a constitutional unit derived from 4-methyl-1-pentene is 90 to 100% by mol; a content of a constitutional unit derived from at least one olefin selected from ethylene and an α-olefin, other than 4-methyl-1-pentene, having 3 to 20 carbon atoms is 0 to 10% by mol; and the 4-methyl-1-pentene polymer satisfies certain requirements (a) to (f): (a) a meso diad fraction (m) measured by .sup.13C-NMR falling within a certain range; (b) a ratio of weight-average molecular weight Mw within a certain range; (c) a melt flow rate (MFR) within a certain range; (d) a cumulative weight fraction within a certain range; (e) a proportion of a polymer having a molecular weight of a certain range; and (f) a heat of fusion and a melting point of the 4-methyl-1-pentene polymer within certain ranges.
Non-coordinating anion type activators containing cation having branched alkyl groups
The present disclosure provides borate or aluminate activators comprising cations having branched alkyl groups, catalyst systems comprising, and methods for polymerizing olefins using such activators. Specifically, the present disclosure provides activator compounds represented by Formula: [R.sup.1R.sup.2R.sup.3EH].sub.d.sup.+[M.sup.k+Q.sub.n].sup.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; each of R.sup.1, R.sup.2, and R.sup.3 is independently C.sub.1-C.sub.40 branched or linear alkyl or C.sub.5-C.sub.50-aryl, wherein each of R.sup.1, R.sup.2, and R.sup.3 is independently unsubstituted or substituted with at least one of halide, C.sub.5-C.sub.50 aryl, C.sub.6-C.sub.35 arylalkyl, C.sub.6-C.sub.35 alkylaryl and, in the case of the C.sub.5-C.sub.50-aryl, C.sub.1-C.sub.50 alkyl; wherein R.sup.1, R.sup.2, and R.sup.3 together comprise 15 or more carbon atoms; M is an element selected from group 13 of the Periodic Table of the Elements; 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 at least one of R.sup.1, R.sup.2, and R.sup.3 is a branched alkyl.
Non-coordinating anion type activators containing cation having branched alkyl groups
The present disclosure provides borate or aluminate activators comprising cations having branched alkyl groups, catalyst systems comprising, and methods for polymerizing olefins using such activators. Specifically, the present disclosure provides activator compounds represented by Formula: [R.sup.1R.sup.2R.sup.3EH].sub.d.sup.+[M.sup.k+Q.sub.n].sup.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; each of R.sup.1, R.sup.2, and R.sup.3 is independently C.sub.1-C.sub.40 branched or linear alkyl or C.sub.5-C.sub.50-aryl, wherein each of R.sup.1, R.sup.2, and R.sup.3 is independently unsubstituted or substituted with at least one of halide, C.sub.5-C.sub.50 aryl, C.sub.6-C.sub.35 arylalkyl, C.sub.6-C.sub.35 alkylaryl and, in the case of the C.sub.5-C.sub.50-aryl, C.sub.1-C.sub.50 alkyl; wherein R.sup.1, R.sup.2, and R.sup.3 together comprise 15 or more carbon atoms; M is an element selected from group 13 of the Periodic Table of the Elements; 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 at least one of R.sup.1, R.sup.2, and R.sup.3 is a branched alkyl.
Process to make non-coordinating anion type activators in aliphatic and alicyclic hydrocarbon solvents
The present disclosure provides borate activators comprising cations having linear alkyl groups, catalyst systems comprising, and processes for polymerizing olefins using such activators. Specifically, the present disclosure provides polymerization activator compounds which may be prepared in, and which are soluble in aliphatic hydrocarbon and alicyclic hydrocarbon solvents.