749results about How to "High polymerization activity" patented technology

The invention discloses an equivoluminal dipping loading method of non-metallocene olefin polymeric catalyst as well as application of copolymerizing course within two or more different olefins, which comprises the following steps: dissolving non-metallocene olefin polymeric catalyst in the solvent; mixing solution and carrier; stirring wet solid material evenly; drying; obtaining the load-typed non-metallocene olefin polymeric catalyst; making the solvent and carrier satisfy specific relationship.

The invention relates to a magnesium compound supported non-metallocene catalyst, which is obtained by directly contacting a compound of catalytic active metal and a magnesium compound containing a non-metallocene ligand through an in-situ supporting method. The preparation method for the magnesium compound supported non-metallocene catalyst has simple, feasible and flexible process, and has more adjustable parameters to the polymerization activity of the catalyst. When the supported non-metallocene catalyst and a catalyst promoter are adopted to form a catalytic system for the homopolymerization/copolymerization of olefins, the obtained polymer has high bulk density and low ash, and the molecular weight distribution of the polymer has wide adjustable range.

The invention relates to a supported non-metallocene catalyst and its preparation method. The supported non-metallocene catalyst is characterized by simple preparation method, flexible polymerization activity etc. In addition, non-metallocene complexes in the catalyst cooperate with the chemical disposal agent to enhance the activity. The invention also relates to the application of the supportednon-metallocene catalyst in alkene homopolymerization/copolymerization. Less amount of co-catalyst is required in use compared with the prior art.

The invention relates to a load type non-metallocene catalyst and a preparation method thereof. The load type non-metallocene catalyst has the characteristics of simple preparation method, flexible and adjustable polymerization activity and the like, and synergistic reaction which is beneficial to activity development is formed between non-metallocene complexes and chemical conditioning agents inthe catalyst. The invention also relates to the application of the load type non-metallocene catalyst in olefin homopolymerization/copolymerization. Compared with the prior art, the application has the characteristic of less cocatalyst amount.

The invention relates to a loaded non-metallocene catalyst and a preparation method and application thereof. The loaded non-metallocene catalyst has the characteristics of simple and practicable preparation method, flexible and adjustable polymerization activity and the like. The invention also relates to the application of the loaded non-metallocene catalyst to the homopolymerisation/copolymerization of olefin. Compared with the prior art, the application has the characteristic of small using amount of a cocatalyst.

The invention relates to a loaded non-metallocene catalyst and a preparation method and application thereof. The loaded non-metallocene catalyst has the characteristics of simple and practicable preparation method, flexible and adjustable polymerization activity and the like. The invention also relates to the application of the loaded non-metallocene catalyst to the homopolymerisation/copolymerization of olefin. Compared with the prior art, the application has the characteristic of small using amount of a cocatalyst.

According to the present invention, there are disclosed a radical polymerization catalyst comprising an aryl borate compound, an acidic compound and a +tetravalent and/or +pentavalent vanadium compound; and a curable composition, a dental composition, a dental adhesive, a dental pretreatment agent, a dental adhesive kit, etc. all containing the radical polymerization catalyst.

The invention relates to a supported non-metallocene catalyst. The supported non-metallocene catalyst is obtained by a non-metallocene ligand and a transition metal compound which directly react on a carrier through an in-situ supporting method. The preparation method for the supported non-metallocene catalyst has simple and feasible process, and the supporting capacity and the polymerization activity of the catalyst have wide adjustable range. When the supported non-metallocene catalyst is combined with a catalyst promoter to catalyze the homopolymerization/copolymerization of olefins, high polymerization activities of the olefins can be obtained only by using small amount of the catalyst promoter.

PCT No. PCT/JP97/01387 Sec. 371 Date Dec. 11, 1997 Sec. 102(e) Date Dec. 11, 1997 PCT Filed Apr. 22, 1997 PCT Pub. No. WO97/40075 PCT Pub. Date Oct. 30, 1997A catalyst component for polyolefin production catalysts comprising a metallocene compound represented by general formula (1) (symbols have the meanings as described in the specification), polyolefin production catalyst containing the component, and method for producing polyolefin with the catalyst are provided. Use of a catalyst containing the novel metallocene compound as a catalyst component of the invention in polymerization of alpha -olefin, particularly propylene, enables one to prepare high rigid, high melting point isotactic polypropylene useful as an industrial material for automobiles and the like, more specifically isotactic polypropylene having highly controlled stereoregulartity and regioregularity, particularly the one having a high regioregularity that has been difficult to achieve with conventional metallocene catalysts.

The invention discloses a domino catalyzing system of a primary metallocene catalyst, which takes ethane as a sole monomer to prepare branched polyethylene, and the application thereof, which relates to vinyl copolymer. the catalyzing system is a compound catalyzing system consisting of the single primary metallocene catalyst and two different catalyst promoters, wherein, the primary catalyst is a metallocene catalyst with a structural formula of Cp<1>MR<1>R<2>R<3>, Cp<1>Cp<2>MR<1>R<2> or Cp<1>-D-Cp<2>MR<1>R<2>; alkyl aluminium acts as an oligomerization catalyst promoter; methylaluminoxane or triisobutyl aluminium or triethyl aluminum that is not used together with the oligomerization catalyst promoter acts as a copolymerization catalyst promoter; the mole ratio between the oligomerization catalyst promoter and the primary catalyst is 10-1000 to 1, and the mole ratio between the copolymerization catalyst promoter and the primary catalyst is 20-1000 to 1. The catalytic activity of the metallocene domino catalyzing system for preparing the branched polyethylene is 5 multiplied by 10<5> to 5 multiplied by 10<7>gPE/(molM per hour), the degree of branching is 10-200/1000C, the molecular weight of the branched polyethylene prepared under the effect of the catalyzing system ranges from 1 multiplied by 10<5> to 4 multiplied by 10<5> and the melting point is below 120 DEG C or even no melting point exists.

The invention relates to a supported non-metallocene catalyst. The supported non-metallocene catalyst is obtained by a non-metallocene ligand and a transition metal compound which directly react on a carrier through an in-situ supporting method. The preparation method for the supported non-metallocene catalyst has simple and feasible process, and has wide adjustable range of the supporting capacity and the polymerization activity of the catalyst. When the supported non-metallocene catalyst is combined with a catalyst promoter to catalyze the homopolymerization/copolymerization of olefins, high polymerization activities of the olefins can be obtained only by the less using amount of the catalyst promoter.

Disclosed is a solid support-polymethylaluminoxane complex exhibiting a higher polymerization activity than a conventional substance and being homogeneous. Also disclosed is a method for producing an olefin-based polymer having a favorable quality using the complex and a transition metal compound. The complex comprises a coating layer containing polymethylaluminoxane and trimethylaluminum on the surface of a solid support. The coating layer comprises a solid polymethylaluminoxane composition in which (i) the content of aluminum is in a range of 36 to 41 mass % and (ii) the molar fraction of methyl groups derived from a trimethylaluminum moiety to the total number of moles of methyl groups is 12 mol % or less. Also disclosed is an olefin polymerization catalyst comprising the complex and a transition metal compound represented by general formula (III): MR⁵R⁶R⁷R⁸ as catalyst components, and a method for producing a polyolefin comprising polymerizing an olefin using the catalyst.

The invention discloses a high oil absorbing resin, and a process for preparation comprises utilizing short-chain ester of (metyl group) acrylic acid, long-chain ester of acrylic acid and styrene monomer to be monomers, adding dispersing agent and surface active agent, and getting through suspension polymerization and random copolymerization under the condition of the existence of cross linker and initiating agent. The process for synthesizing has lithe time consumption, which can be industrialized, and high oil absorbing resin which is got has high oil absorbing efficiency, fast oil absorbing speed, and which can be recycled to be repeatedly used.

The invention discloses a bimetallic catalyst precursor for catalyzing olefin to polymerize or copolymerize and belongs to the field of olefin coordination polymerization. The catalyst precursor is based on a salicvlaldimine ligand and an IV group transition metal. Compared with a monometallic catalyst, with the synergistic effect of bimetals, a catalyst consisting of the precursor and alkyl aluminum has higher activity when used for catalyzing the olefin to homopolymerize or copolymerize; particularly, the activity of the catalyst can reach 5.2*104g/mol<-1>h<-1> at the ethylene pressure of 1atm when used for catalyzing 1,5-hexadiene to be copolymerized with the ethylene; and in addition, the catalyst has higher ratio of inducing a comonomer into a polymer.