This disclosure relates to ethylene interpolymer product having intermediate branching. Intermediate branching was defined as branching that was longer than the branch length due to comonomer and shorter than the entanglement molecular weight (M.sub.e). Intermediately branched ethylene interpolymer products were produced in a continuous solution polymerization process employing an intermediate branching catalyst formulation. Intermediately branched ethylene interpolymer products were characterized by a Non-Comonomer Index Distribution (NCID.sub.i), a melt index from 0.3 to 500 dg/minute, a density from 0.858 to 0.965 g/cm.sup.3, a polydispersity (M.sub.w/M.sub.n) from about 2 to about 25 and a CDBI.sub.50 from about 10% to about 98%. A method based on triple detection cross fractionation chromatography (3D-CFC) was disclosed to measure NCID.sub.i.

This disclosure relates to ethylene interpolymer product having intermediate branching. Intermediate branching was defined as branching that was longer than the branch length due to comonomer and shorter than the entanglement molecular weight (M.sub.e). Intermediately branched ethylene interpolymer products were produced in a continuous solution polymerization process employing an intermediate branching catalyst formulation. Intermediately branched ethylene interpolymer products were characterized by a Non-Comonomer Index Distribution (NCID.sub.i), a melt index from 0.3 to 500 dg/minute, a density from 0.858 to 0.965 g/cm.sup.3, a polydispersity (M.sub.w/M.sub.n) from about 2 to about 25 and a CDBI.sub.50 from about 10% to about 98%. A method based on triple detection cross fractionation chromatography (3D-CFC) was disclosed to measure NCID.sub.i.

A propylene copolymer, a preparation method therefor, and an application thereof are provided. The copolymer forms a cross-linked network by means of a reaction between a furan-containing propylene copolymer and a small molecule of a coupling agent, thereby achieving a chemical bond connection between a polypropylene resin phase and an ethylene-propylene copolymer elastomer phase, fundamentally strengthening the force between the two phases, and improving the mechanical properties of a material. Meanwhile, the copolymer can achieve the decrosslinking of a material during melt processing such that the material has thermoplasticity, and after cooling, it can be crosslinked again to produce network structure.

Provided is a propylene homopolymer or a copolymer of propylene and a 30 wt % or less α-olefin having 2 or 4 to 8 carbon atoms, having a intrinsic viscosity of more than 20 dl/g, as measured in a tetralin solvent at 135° C.

The present disclosure relates to a catalyst composition and a process for preparation thereof. The catalyst composition of the present disclosure is stable, and produces polyolefin having narrow molecular weight distribution during the polymerization. The process of the present disclosure is simple, cost-effective, and rapid.

A solid catalyst component for the polymerization of olefins made from or containing Mg, Ti and an electron donor of formula (I)

##STR00001##

where the R.sup.1 and R.sup.5 groups, equal to or different from each other, are selected from C.sub.1-C.sub.15 hydrocarbon groups, R.sup.2 group is selected from C.sub.2-C.sub.10 hydrocarbon groups, R.sup.3 to R.sup.4 groups, independently, are selected from hydrogen or C.sub.1-C.sub.20 hydrocarbon groups, optionally fused together to form one or more cycles, with the proviso that at least one of R.sup.3 to R.sup.4 groups is a C.sub.1-C.sub.20 alkyl group.

Disclosed are catalyst compositions having an internal electron donor which includes a 3,6-di-substituted-1,2-phenylene aromatic diester. Ziegler-Natta catalyst compositions containing the present catalyst compositions exhibit very high hydrogen response, high activity, high selectivity and produce propylene-based olefins with high melt flow rate.

The invention relates to the technical field of heterogeneous catalytic olefin polymerization, and discloses a polyolefin catalyst, its preparation and its us. A method for preparing the polyolefin catalyst comprises: (i) providing a thermally activated mesoporous material, with the thermal activation treatment being performed at a temperature of 300 to 900° C. for a period of time of 3 to 48 hours; (ii) under an inert atmosphere, (iia) conducting impregnation treatment of the thermally activated mesoporous material with a solution containing a magnesium component and then with a solution containing a titanium component, (iib) conducting impregnation treatment of the thermally activated mesoporous material with a solution containing a titanium component and then with a solution containing a magnesium component, or (iic) conducting co-impregnation treatment of the thermally activated mesoporous material with a solution containing both a titanium component and a magnesium component, to obtain a slurry to be sprayed; and (iii) spray drying the slurry to be sprayed from step (ii), to obtain a solid polyolefin catalyst component. When used in olefin polymerization, the polyolefin catalysts prepared by using the method provided by the invention have high catalytic activities, and polyolefin products having a narrow molecular weight distribution and an excellent melt index can be obtained.

Disclosed are a Z-N catalyst for α-olefin polymerization and an application thereof, specifically, an industrial production catalyst consisting of (A) a solid catalyst component, (B) a cocatalyst organoaluminum compound and (C) an external electron donor compound and used for α-olefin polymerization or copolymerization processes. The catalyst component is prepared from a transition metal such as titanium and magnesium and a composite aromatic diacid diester/1,3-diether as an internal electron donor. One or more organoaluminum compounds or a mixture thereof serve as the cocatalyst. One or more structure control agent hydrocarbyl alkoxysilicons are compounded with one or more activity regulator organic acid esters as the external electron donor capable of automatically adjusting the polymerization rate. The Z-N catalyst is used for α-olefin polymerization/copolymerization, and can automatically adjust the polymerization rate at a higher polymerization temperature so as to maintain stable operation of a reactor.

Disclosed are catalyst compositions having an internal electron donor which includes a 3,6-di-substituted-1,2-phenylene aromatic diester. Ziegler-Natta catalyst compositions containing the present catalyst compositions exhibit very high hydrogen response, high activity, high selectivity and produce propylene-based olefins with high melt flow rate.