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510 results about "Aluminum alkyl" patented technology

Industrially, simple aluminium alkyls of the type Al2R6 (R = Me, Et) are prepared in a two-step process beginning with the alkylation of aluminium powder: The reaction resembles the synthesis Grignard reagents. The product, (CH3CH2)3Al2Cl3, is called ethylaluminium sesquichloride.

Metallocene domino catalytic system for preparing branched polyethylene using ethylene as only monomer and use thereof

InactiveCN101392036ALower synthesis costAchieve the effect of molecular tailoringTriisobutylaluminiumStructural formula
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.
Owner:HEBEI UNIV OF TECH

Olefin polymerization catalyst system and application thereof

The invention relates to the field of olefin polymerization, and discloses a catalyst system. The catalyst system comprises a titaniferous solid catalyst component, an aluminum alkyl compound and an external electron donor compound, wherein the titaniferous solid catalyst component contains at least two internal electron donor compounds of a polytrimethylene terephthalate type compound and a diether type compound, and the external electron donor compound is an ether base ester compound or a combination of the ether base ester compound and hydroxyl silane dialkyl oxygen radicals. The invention further provides application of the catalyst in olefin polymerization reaction. According to the catalyst system and the application of the catalyst in the olefin polymerization reaction, by adding the ether base ester compound or the combination of the ether base ester compound and the hydroxyl silane dialkyl oxygen radicals as the external electron donors to be used in the olefin polymerization reaction when the solid catalyst component with the polytrimethylene terephthalate type compound and the diether type compound being the internal electron donors is subjected to the olefin polymerization reaction, not only can the catalyst maintain high activity, but also sensibility of hydrogen regulation of the catalyst can be improved.
Owner:CHINA PETROLEUM & CHEM CORP +1

Aza cyclic carbine rear earth catalyst for crystallinity 3,4-polyisoprene

The present invention relates to a nitrogen heterocyclic carbene rare earth complex, a catalyst system which consists of the present invention, aluminum alkyl and an organoboron salt can catalyse the isoprene to carry out the solution polymerization, so as to prepare the polyisoprene with the crystallization property, high 3, 4-structure and high glass transition temperature (Tg). The molar ratio of aluminum alkyl and the rare earth complex is within the scope of 1 to 100, the molar ratio of the organoboron salt and the rare earth complex is within the scope of 0.5 to 2.0; the solvent which is used for polymerization can be toluene, bromobenzene, n-hexane, dichloromethane or chlorobenzene; the polymerization temperature range is -20 DEG C to 80 DEG C, the reaction time of polymerization at minus 20 DEG C is 36 hours, the reaction time of polymerization at 80 DEG C is 1 hour, and the monomer conversion rate can be up to 100 percent. The reaction is characterized by active polymerization, the molecular weight of the product can be controlled by the molar ratio of the monomer and the catalyst, the molecular weight of the polyisoprene can achieve 360,000 at most, and the glass transition temperature Tg is equal to 5 DEG C to 50 DEG C. The content of the 3, 4 structure of the polyisoprene is affected by the spatial effect and the electronic effect of the rare earth complex, the solvent type for polymerization reaction and the polymerization reaction temperature and so on, which is changed between 76 percent and 99 percent.
Owner:CHANGCHUN INST OF APPLIED CHEMISTRY - CHINESE ACAD OF SCI

HBPE (hyperbranched polyethylene) functionalized with terminal hydroxyl groups and preparation method thereof

The invention relates to HBPE (hyperbranched polyethylene), and aims to provide HBPE functionalized with terminal hydroxyl groups and a preparation method thereof. According to the preparation of the HBPE functionalized with terminal hydroxyl groups, ethylidene acenaphthene (alpha-diimine) nickel catalyst is adopted as a main catalyst, aluminum alkyl is adopted as a cocatalyst, and diethyl zinc is adopted as a chain transfer agent; ethylene is catalyzed to be homopolymerized; the homopolymerized ethylene is subjected to ligand chain transfer polymerization to obtain diethyl zinc-terminated HBPE. The catalysts in the preparation require no precious metal, so that the synthesis cost of the HBPE is greatly reduced; diethyl zinc is adopted as the chain transfer agent, and the HBPE is prepared from the method of ligand chain transfer polymerization, so that the HBPE is high in polymerization activity and simple in technology; the method of obtaining terminal hydroxyl groups is simple and low in cost, and has good practical value; the hydroxyl in terminal hydroxyl groups HBPE is high in reaction activity, and a plurality of polymer chains with different properties can be introduced into the HBPE through condensation reaction, coupling reaction, click chemistry reaction, and the like, to prepare polymers with various properties and different functions.
Owner:ZHEJIANG UNIV
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