Polypropylene composition comprising a polypropylene base material, a carbon fibre and an adhesion promoter with an excellent impact/stiffness balance, its preparation, articles comprising the composition and the use of the composition.

A heterophasic propylene ethylene copolymer composition having an MFR.sub.2 in the range from 1.0 to 55.0 g/10 min and a melting temperature in the range from 155 to 162° C., comprising: i) from 60 to 88 wt.-% of a xylene cold insoluble fraction (XCI) having an intrinsic viscosity iV(XCI) in the range from 1.40 to 2.50 dl/g, an isotactic pentad concentration [mmmm] of more than 97.0% and a content of 2,1-regiodefects in the range from 0.1 to 0.4 mol %, ii) from 12 to 40 wt.-% of a xylene cold soluble fraction (XCS) having an intrinsic viscosity iV(XCS) in the range from 1.80 to 3.20 dl/g and an ethylene content C2(XCS) in the range from 25 to 80 wt.-%, wherein the ratio of the intrinsic viscosities of the two fractions, iV(XCS)/iV(XCI), is in the range from 1.0 to 2.0.

The present invention relates to heterophasic polypropylene compositions comprising a propylene homo- or copolymer forming a crystalline fraction as a matrix and an amorphous propylene ethylene elastomer as a soluble fraction dispersed in said matrix. The heterophasic polypropylene compositions further comprise an elastomeric ethylene/alpha-olefin random copolymer. The heterophasic polypropylene compositions have a well-balanced relation between stiffness and impact strength, low volatile and semi-volatile emissions and good processability.

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.

A thermoplastic vulcanizate composition, comprising a first phase bi-continuously intertwined with from about 10 wt % to 80 wt % of a second phase throughout the composition, and from about 0.1 wt % to about 10 wt % of a curative system, the first phase comprising polypropylene and the second phase comprising an at least partially cured elastomeric rubber composition, comprising from about 10 wt % to about 40 wt % ethylene, from about 5 wt % to about 10 wt % of a conjugated diene having from 4 to 12 carbon atoms, and from about 50 wt % to about 85 wt % of a C.sub.4-C.sub.8 alpha olefin, based on the total weight of the elastomeric rubber composition present. A process for making is also disclosed.

A degradable elastomeric material that is formed from a composite blend of elastomeric particles in a continuous degradable binder. The degradable binder is generally a water-soluble binder which has a temperature dependent solubility in water and brine systems. Such degradable elastomers are particularly useful in the fabrication of degradable oil tools, among other applications.

A polypropylene composition made from or containing

a first polymer consisting of component (1) made from or containing a propylene homopolymer having an MFR of 80 to 300 and containing 97.5% by weight or more of xylene insolubles (XI), wherein XI of the propylene homopolymer has a Mw/Mn of 4 to 10; and component (2) made from or containing an ethylene/propylene copolymer containing 35 to 50% by weight of an ethylene-derived unit;
wherein the polypropylene composition has the following characteristics: 1) the relative proportions of component (2)/[component (1) and component (2)] is more than 30% by weight and not more than 50% by weight, 2) the intrinsic viscosity of xylene solubles (XSIV) of the first polymer is in the range of 1.5 to 4.0 dl/g, and 3) the MFR of the first polymer is in the range of 20 to 100 g/10 min.

Provided is a solid catalyst component for olefin polymerization which is capable of exerting favorable ethylene responsiveness while forming a propylene homopolymer having high stereoregularity, when subjected to ethylene-propylene copolymerization reaction. The present invention provides a solid catalyst component for olefin polymerization, comprising titanium, magnesium, halogen, and an internal electron-donating compound, wherein the internal electron-donating compound comprises an electron-donating compound (i) having a phthalic acid ester structure, and an electron-donating compound (ii) having two or more kinds of groups selected from an ether group, an ester group and a carbonate group and having no phthalic acid ester structure, wherein a content ratio of the electron-donating compound (ii) having two or more kinds of groups selected from an ether group, an ester group and a carbonate group and having no phthalic acid ester structure is 0.5 to 1.5% by mass.

New polypropylene composition which combines low sealing initiation temperature (SIT), high hot-tack and good mechanical properties, like high dart drop strength (DDI), and its use especially for film applications.

Disclosed is a polypropylene with an MFR of at least 20 g/10 min comprising a homopolypropylene and within a range from 2 wt % to 20 wt % of a propylene-α-olefin copolymer by weight of the polypropylene, where the homopolypropylene has a MFR within a range from 30 g/10 min to 200 g/10 min, where the propylene-α-olefin copolymer comprises within a range from 30 wt % to 50 wt % α-olefin derived units by weight of the propylene-α-olefin copolymer, and has an IV within a range from 4 to 9 dL/g. The polypropylene may be obtained by combining a Ziegler-Natta catalyst having two transition metals with propylene in reactors in series to produce the homopolypropylene followed by a gas phase reactor to produce a propylene-α-olefin copolymer blended with the homopolypropylene.