The ultrahigh-molecular-weight polyethylene powder of the present invention is an ultrahigh-molecular-weight polyethylene powder having a viscosity-average molecular weight Mv of 10×10.sup.4 or higher and 1000×10.sup.4 or lower, wherein viscosity-average molecular weight Mv(A) of a kneaded product obtained by kneading under specific kneading conditions, and the Mv satisfy the following relationship: “{Mv−Mv(A)}/Mv is 0.20 or less”, and the ultrahigh-molecular-weight polyethylene powder contains an ultrahigh-molecular-weight polyethylene powder having a particle size of 212 μm or larger, wherein the powder having a particle size of 212 μm or larger has an average pore volume of 0.6 ml/g or larger and an average pore size of 0.3 μm or larger.

The ultrahigh-molecular-weight polyethylene powder of the present invention is an ultrahigh-molecular-weight polyethylene powder having a viscosity-average molecular weight Mv of 10×10.sup.4 or higher and 1000×10.sup.4 or lower, wherein viscosity-average molecular weight Mv(A) of a kneaded product obtained by kneading under specific kneading conditions, and the Mv satisfy the following relationship: “{Mv−Mv(A)}/Mv is 0.20 or less”, and the ultrahigh-molecular-weight polyethylene powder contains an ultrahigh-molecular-weight polyethylene powder having a particle size of 212 μm or larger, wherein the powder having a particle size of 212 μm or larger has an average pore volume of 0.6 ml/g or larger and an average pore size of 0.3 μm or larger.

The present invention relates to a compound according to formula 1: wherein: •each of R.sub.1 to R.sub.12 may individually be a moiety selected from hydrogen, an aryl moiety, an aryl moiety, a halogen, an alkyl or aryl moiety with halogen substituent(s), an alkoxy moiety, a siloxy moiety, or a nitrogen-containing moiety, wherein each R moiety may optionally form a ring structure with an adjacent R moiety; •each of A.sub.1 and A.sub.2 may individually be a moiety selected from: o an element of Group 16 of the periodic system; and o a moiety containing an element of Group 15 of the periodic system; preferably wherein A.sub.1 and A.sub.2 are selected from O or NR.sub.13, wherein R.sub.13 is an alkyl, aryl or aralkyl moiety, preferably a substituted or unsubstituted phenyl moiety, preferably a p-tolyl moiety; •T is a divalent hydrocarbyl moiety; •D is a substituted element of Group 15 or Group 16 of the periodic system, preferably an N(R.sub.14).sub.2 or OR.sub.14 moiety, in which R.sub.14 is selected to be an alkyl moiety, an aryl moiety, or an aralkyl moiety, preferably R.sub.14 is a methyl moiety; •Y is an element selected from Group 15 of the periodic system, preferably N; •Mt is a transition metal, preferably selected from Group 3 or 4 of the periodic system, more preferably selected from Ti, Hf and Zr; •X is a sigma-bonded ligand, preferably selected from a halogen, an alkyl moiety, an aralkyl moiety, an alkoxy moiety, an aryloxy moiety, and a dialkylamine moiety; and Classification: General Business Use •n is the amount of X ligands bonded to X. Such compound allow for use in catalysts that result in high molecular weight polymers, display high catalyst activities and give excellent comonomer incorporation.

The present invention relates to a compound according to formula 1: wherein: •each of R.sub.1 to R.sub.12 may individually be a moiety selected from hydrogen, an aryl moiety, an aryl moiety, a halogen, an alkyl or aryl moiety with halogen substituent(s), an alkoxy moiety, a siloxy moiety, or a nitrogen-containing moiety, wherein each R moiety may optionally form a ring structure with an adjacent R moiety; •each of A.sub.1 and A.sub.2 may individually be a moiety selected from: o an element of Group 16 of the periodic system; and o a moiety containing an element of Group 15 of the periodic system; preferably wherein A.sub.1 and A.sub.2 are selected from O or NR.sub.13, wherein R.sub.13 is an alkyl, aryl or aralkyl moiety, preferably a substituted or unsubstituted phenyl moiety, preferably a p-tolyl moiety; •T is a divalent hydrocarbyl moiety; •D is a substituted element of Group 15 or Group 16 of the periodic system, preferably an N(R.sub.14).sub.2 or OR.sub.14 moiety, in which R.sub.14 is selected to be an alkyl moiety, an aryl moiety, or an aralkyl moiety, preferably R.sub.14 is a methyl moiety; •Y is an element selected from Group 15 of the periodic system, preferably N; •Mt is a transition metal, preferably selected from Group 3 or 4 of the periodic system, more preferably selected from Ti, Hf and Zr; •X is a sigma-bonded ligand, preferably selected from a halogen, an alkyl moiety, an aralkyl moiety, an alkoxy moiety, an aryloxy moiety, and a dialkylamine moiety; and Classification: General Business Use •n is the amount of X ligands bonded to X. Such compound allow for use in catalysts that result in high molecular weight polymers, display high catalyst activities and give excellent comonomer incorporation.

The present disclosure provides catalyst compounds represented by Formula (I): ##STR00001##
where Q is OR.sup.13, SR.sup.13, NR.sup.13R.sup.14, PR.sup.13R.sup.14, or a heterocyclic ring; each R.sup.1-14 is independently hydrogen, C.sub.1-C.sub.40 hydrocarbyl, substituted C.sub.1-C.sub.40 hydrocarbyl, a heteroatom, or a heteroatom-containing group, or multiple R.sup.1-14 are joined together to form a C.sub.4-C.sub.62 cyclic, heterocyclic, or polycyclic ring structure, or combination(s) thereof; each X.sup.1 and X.sup.2 is independently C.sub.1-C.sub.20 hydrocarbyl, substituted C.sub.1-C.sub.20 hydrocarbyl, a heteroatom, or a heteroatom-containing group, or X.sup.1 and X.sup.2 join together to form a C.sub.4-C.sub.62 cyclic, heterocyclic, or polycyclic ring structure; and Y is a hydrocarbyl. The present disclosure also provides catalyst systems including an activator, a support, and a catalyst of the present disclosure. The present disclosure also provides polymerization processes including introducing olefin monomers to a catalyst system. Additionally, the present disclosure provides a polyolefin formed by a catalyst system or method of the present disclosure.

Disclosed is a method using a metallocene catalyst system so as to control the polymer structure of a diene-modified polypropylene through process simplification, thereby being capable of preparing a hyperbranched polypropylene resin having a low gel content and improved melt strength. The present invention provides a method using a catalyst so as to polymerize propylene and a diene compound, thereby preparing a diene-modified polypropylene resin having a branching index of 0.95 or less, a gel content of 3 wt % or less and an advanced rheometric expansion system (ARES) melt strength of 5 g or more.

Disclosed is a method using a metallocene catalyst system so as to control the polymer structure of a diene-modified polypropylene through process simplification, thereby being capable of preparing a hyperbranched polypropylene resin having a low gel content and improved melt strength. The present invention provides a method using a catalyst so as to polymerize propylene and a diene compound, thereby preparing a diene-modified polypropylene resin having a branching index of 0.95 or less, a gel content of 3 wt % or less and an advanced rheometric expansion system (ARES) melt strength of 5 g or more.

Embodiments of the present application are directed to procatalysts, and catalyst systems including procatalysts, including a metal-ligand complex having the structure of formula (I): [Formula I].

##STR00001##

Embodiments of the present application are directed to procatalysts, and catalyst systems including procatalysts, including a metal-ligand complex having the structure of formula (I): [Formula I].

##STR00001##

An organometallic complex, a catalyst composition employing the same, and a method for preparing polyolefin are provided. The organometallic compound has a structure represented by Formula (I)

##STR00001##

, wherein M is Ti, Zr, or Hf; X is —O—, or —NR.sup.6—; R.sup.1 and R.sup.2 are independently hydrogen, C.sub.1-6 alkyl group, C.sub.6-12 aryl group, or R.sup.1 and R.sup.2 are combined with the carbon atoms, to which they are attached, to form an C.sub.6-12 aryl moiety; R.sup.3, R.sup.4 and R.sup.5 are independently fluoride, chloride, bromide, C.sub.1-6 alkyl group, C.sub.6-12 aryl group, C.sub.3-6 hetero aryl group, C.sub.7-13 aryl alkyl group or C.sub.7-12 alkyl aryl group; and R.sup.6 is hydrogen, C.sub.6-12 aryl group or C.sub.7-12 alkyl aryl group.