Catalyst system, the catalyst system comprising (i) at least one metallocene complex of formula (I) wherein Mt1 is Hf, X is a sigma-donor ligand, R.sup.1, R.sup.2, R.sup.3 are the same or different from each other and can be hydrogen or a saturated linear or branched C.sub.1-C.sub.10 alkyl, whereby the alkyl group can optionally contain up to 2 heteroatoms belonging to groups 14-16 of the periodic table, or R.sup.1 and R.sup.2 or R.sup.2 and R.sup.3 can form a ring having 4 to 6 C-atoms and 1 to 3 double bonds, R.sup.4 and R.sup.5 are the same or different from each other and can be saturated linear or branched C.sub.1-C.sub.10 alkyl, C.sub.5-C.sub.10 aryl, C.sub.6-C.sub.20 alkylaryl or C.sub.6-C.sub.20 arylalkyl groups, which can optionally contain up to 2 heteroatoms belonging to groups 14-16 of the periodic table, n can be 1 to 5, Ar is a C.sub.6-C.sub.20-aryl or -heteroaryl group, which can be unsubstituted or substituted by 1 to 5 linear or branched C.sub.1-C.sub.10 alkyl group(s), and (ii) an aluminoxane cocatalyst and (iii) optionally an aluminium alkyl compound AI(R.sup.7).sub.3, with R.sup.7 being a linear or branched C.sub.2-C.sub.8-alkyl group. ##STR00001##

The present invention relates to a process for producing a propylene polymer, such as a propylene homopolymer, a propylene-ethylene random copolymer or a heterophasic propylene copolymer using a specific class of metallocene complexes in combination with a cocatalyst system comprising a boron containing cocatalyst and an aluminoxane cocatalyst, preferably in a multistage polymerization process including a gas phase polymerization step.

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.

Disclosed is a catalyst for olefin polymerization, comprising a main catalyst and a cocatalyst; the main catalyst is a bisphenol metal complex represented by formula I, and the cocatalyst comprises an organoaluminum compound; in formula I, R.sub.1, R.sub.1′, R.sub.2, R.sub.2′ are the same or different, and are each independently selected from hydrogen and a substituted or unsubstituted C.sub.1-C.sub.20 hydrocarbyl; R.sub.3-R.sub.7, R.sub.3′-R.sub.7′ are the same or different, and are each independently selected from hydrogen and a substituted or unsubstituted C.sub.1-C.sub.20 hydrocarbyl; R.sub.8 and R.sub.9 are the same or different, and are each independently selected from hydrogen or a substituted or unsubstituted C.sub.1-C.sub.20 hydrocarbyl; M and M′ are the same or different, and are selected from Group IV metals; and X is halogen;

##STR00001##

This invention relates to polyolefin. More specifically, this invention relates to polyolefin that has small copolymer content, but exhibits excellent mechanical properties.

Metallocene complexes represented by the structure below are useful for alpha olefin oligomerization in the presence of an activator to generate polyalphaolefins having a high percentage of vinylidene termination and relatively low Mn values. ##STR00001##
M is a group 4 transition metal. A is a bridging group having one bridging atom extending between a first indenyl ring and a second indenyl ring. Each X is independently an anionic ligand, or two Xs are joined and bound to M to form a metallocycle ring, or two Xs are joined to form a chelating ligand, a diene ligand, or an alkylidene ligand. R.sup.1, R.sup.1′, R.sup.3, R.sup.3′, R.sup.4, R.sup.4′, R.sup.7 and R.sup.7′ are hydrogen. R.sup.5, R.sup.5′, R.sup.6, and R.sup.6′ are independently a C.sub.1-C.sub.10, optionally substituted, hydrocarbyl group, or R.sup.5 and R.sup.6 and/or R.sup.5′ and R.sup.6′ are bonded together to form an optionally substituted hydrocarbyl ring structure.

A method of assembling and/or operating apparatus for undertaking a chemical reaction. The apparatus includes a housing in which a precursor of a receptacle is arranged. A fluid (F1) may be introduced into said precursor to cause the precursor to inflate.

The purpose of the present invention is to provide a method for efficiently producing an olefin (co)polymer containing a constituent unit derived from 1-butene, the (co)polymer having a molecular weight that is sufficiently high even for high temperature conditions that are beneficial for industrial production methods. This purpose can be achieved by means of a method for producing an olefin (co)polymer containing a constituent unit derived from 1-butene, wherein at least 1-butene and, if necessary, an α-olefin having 2 or more carbon atoms (excluding 1-butene) and other monomers are (co)polymerized in the presence of an olefin polymerization catalyst that contains (A) a crosslinked metallocene compound represented by general formula [I] and (B) at least one type of compound selected from among (b-1) an organic aluminum oxy compound, (b-2) a compound that forms an ion pair upon a reaction with the crosslinked metallocene compound (A), and (b-3) an organic aluminum compound, at a polymerization temperature of 55-200° C. and a polymerization pressure of 0.1-5.0 MPaG.

Provided are a transition metal compound for an olefin polymerization catalyst, an olefin polymerization catalyst containing the transition metal compound, and a polyolefin prepared using the olefin polymerization catalyst for polymerization thereof, wherein the transition metal compound is represented by Chemical Formula A1 or Chemical Formula B1.

The present invention provides a polyolefin polymer having a bimodal composition with a reduced higher molecular weight component prepared using a self-supported phosphinimine single site catalyst. The catalyst is prepared by precipitating an emulsion of the activated catalyst from a perfluoroalkane continuous phase resulting in spherical catalyst particles having a diameter typically from 5 to 200 μm.