The present invention relates to a method for preparing a catalyst, and in particular provides a method for preparing a catalyst suitable for the polymerisation of ethylene and/or propylene, said catalyst comprising a compound of yttrium, neodymium or scandium supported on a silica support, and wherein the method comprises: a) Treating a silica support by heating at a temperature of at least 550° C., b) Contacting the treated silica support with a complex of the following formula: D.sub.mMX.sup.1X.sup.2R wherein M is selected from Y, Sc and Nd, R is a hydrocarbyl group, X.sup.1 and X.sup.2 are anionic groups, D is a neutral donor group, and m is 0 or greater.

This invention relates to a method comprising contacting C3-C32 alpha olefin with catalyst system comprising activator and catalyst of the formula wherein: M is Hf or Zr; T is a bridging group; each X is independently a leaving group; R1 and R2 are independently hydrogen, or a Ci-Gto optionally substituted hydrocarbyl group, halide, or siloxyl group; R3, R4, R5 and R6 are independently a Ci-Gto optionally substituted hydrocarbyl, halocarbyl, silylcarbyl, aminocarbyl, or siloxyl group; and A is an aliphatic, aromatic or heteroaromatic ring, optionally bearing one or more additional fused rings which may be aliphatic, aromatic or heteroaromatic; obtaining a plurality of vinyl-terminated polyalphaolefins (PAOs) having at least 30 mol % vinyl terminated PAO's.

##STR00001##

This invention relates to a method comprising contacting C3-C32 alpha olefin with catalyst system comprising activator and catalyst of the formula wherein: M is Hf or Zr; T is a bridging group; each X is independently a leaving group; R1 and R2 are independently hydrogen, or a Ci-Gto optionally substituted hydrocarbyl group, halide, or siloxyl group; R3, R4, R5 and R6 are independently a Ci-Gto optionally substituted hydrocarbyl, halocarbyl, silylcarbyl, aminocarbyl, or siloxyl group; and A is an aliphatic, aromatic or heteroaromatic ring, optionally bearing one or more additional fused rings which may be aliphatic, aromatic or heteroaromatic; obtaining a plurality of vinyl-terminated polyalphaolefins (PAOs) having at least 30 mol % vinyl terminated PAO's.

##STR00001##

A polypropylene comprising within a range from 0.1 wt % to 4 wt % ethylene and/or C4 to C12 α-olefin derived units, one or more clarifiers, or both; wherein the polypropylene has a flexural modulus of at least 200 kpsi (0.05 in/min ASTM D790(A)) and an Mz/Mw of at least 4. The polypropylenes may be made by combining propylene and a comonomer with a Ziegler-Natta catalyst and at least two external electron donors, wherein the concentration of the electron donors is within a range from 1 to 100 ppm. The concentration of electron donors may be decreased to control the haze level of the polypropylene, and/or the level of comonomer derived units may be controlled to reduce the haze level of the polypropylene.

A polypropylene comprising within a range from 0.1 wt % to 4 wt % ethylene and/or C4 to C12 α-olefin derived units, one or more clarifiers, or both; wherein the polypropylene has a flexural modulus of at least 200 kpsi (0.05 in/min ASTM D790(A)) and an Mz/Mw of at least 4. The polypropylenes may be made by combining propylene and a comonomer with a Ziegler-Natta catalyst and at least two external electron donors, wherein the concentration of the electron donors is within a range from 1 to 100 ppm. The concentration of electron donors may be decreased to control the haze level of the polypropylene, and/or the level of comonomer derived units may be controlled to reduce the haze level of the polypropylene.

The invention relates to a process for the preparation of a propylene homopolymer or a propylene α-olefin random copolymer comprising the step of a) preparing a propylene homopolymer or a propylene α-olefin random copolymer, wherein the α-olefin is chosen from the group consisting of ethylene, and α-olefins having 4 to 10 carbon atoms, for example 1-butene or 1-hexene by contacting at least the propylene and optionally α-olefin, with a catalyst in a gas-phase reactor at a temperature T1 and a pressure P1, wherein T1 is chosen in the range from 75 to 90° C., for example in the range from 77 to 85° C., for example in the range from 78 to 83° C., wherein P1 is chosen in the range from 22 to 30 bar to prepare a propylene homopolymer (A′) or a propylene α-olefin random copolymer (A′).

The invention relates to a process for the preparation of a propylene homopolymer or a propylene α-olefin random copolymer comprising the step of a) preparing a propylene homopolymer or a propylene α-olefin random copolymer, wherein the α-olefin is chosen from the group consisting of ethylene, and α-olefins having 4 to 10 carbon atoms, for example 1-butene or 1-hexene by contacting at least the propylene and optionally α-olefin, with a catalyst in a gas-phase reactor at a temperature T1 and a pressure P1, wherein T1 is chosen in the range from 75 to 90° C., for example in the range from 77 to 85° C., for example in the range from 78 to 83° C., wherein P1 is chosen in the range from 22 to 30 bar to prepare a propylene homopolymer (A′) or a propylene α-olefin random copolymer (A′).

New bisindenyl ligand complexes and catalysts comprising those complexes. The invention is directed to improving the manufacturing of specific C1-symmetric bisindenyl complexes by modifying one of the indenyl ligands in order to improve the selectivity of the complex synthesis towards the desired anti-isomer, increase the yield and simplify the purification of the complex. The invention also relates to the use of the new bisindenyl metallocene catalysts for the production of polypropylene homopolymers or propylene copolymers.

Described herein is an absorbent article. The absorbent article includes an assembly of components and an adhesive composition joining at least two of the assembly of components together. The adhesive composition includes from about 50 wt. % to about 80 wt. % of one or more copolymers and a blend of one or more heterophase copolymers. The one or more copolymers include from about 30 mole % to about 70 mole % of monomer units selected from ethylene. 1-butene, and mixtures thereof. The one or more copolymers also include from about 30 mole % to about 70 mole % of propene monomer units. The adhesive composition is free of polyisobutylene and has a viscosity of from about 2,000 mPa.Math.s to about 11,500 mPa.Math.s at 150° C.

Described herein is an absorbent article. The absorbent article includes an assembly of components and an adhesive composition joining at least two of the assembly of components together. The adhesive composition includes from about 50 wt. % to about 80 wt. % of one or more copolymers and a blend of one or more heterophase copolymers. The one or more copolymers include from about 30 mole % to about 70 mole % of monomer units selected from ethylene. 1-butene, and mixtures thereof. The one or more copolymers also include from about 30 mole % to about 70 mole % of propene monomer units. The adhesive composition is free of polyisobutylene and has a viscosity of from about 2,000 mPa.Math.s to about 11,500 mPa.Math.s at 150° C.