Abstract:
The present invention relates to a non-cryogenic process for the large scale synthesis of disentangled ultra high molecular weight polyethylene (DUHMWPE) polymers. The process comprises of the following steps: a. mixing FI catalyst of formula I with a hydrocarbon solvent containing poly-methyl aluminoxane (P-MAO) co-catalyst in a vessel under stirring before polymerization or directly in the polymerization vessel at a temperature ranging between 25° C. and 29° C. under a dry Nitrogen atmosphere; and lower concentration of co-catalyst resulting in the associated benefits as described earlier in the claims and descriptions. b. pressurizing ethylene in the polymerization vessel and polymerizing ethylene in a solution or a suspension, continuously or batch wise, in one or more stages at a temperature is in the range of 30° C. to 50° C.
Abstract:
The present disclosure provides a process for separating oxygenates present in an aromatic hydrocarbon stream to obtain an oxygenates-free aromatic hydrocarbon stream. The process involves selectively removing oxygenates from the aromatic hydrocarbon stream by passing said stream through at least one zeolite based adsorbing material.
Abstract:
The present disclosure relates to a thermo-reversible and self-healing blend comprising polybutadiene compounded with at least one ring opening agent and at least one ring compound containing at least one hetero-cyclic compound and at least one grafting enabling moiety, wherein the ring opening agent is capable of opening the ring compound to provide at least one open functional group to which the ring opening agent is capable of bonding, and wherein the ring compound is capable of grafting on the backbone of a polymer through the grafting enabling moiety. The present disclosure also relates to a process for preparing a thermo-reversible and self-healing blend and its use in preparing molded articles.
Abstract:
The present disclosure provides a process for separating oxygenates present in an aromatic hydrocarbon stream to obtain an oxygenates-free aromatic hydrocarbon stream. The process involves selectively removing oxygenates from the aromatic hydrocarbon stream by passing said stream through at least one zeolite based adsorbing material.
Abstract:
There is provided a chemically immobilized heterogeneous single site polymerization catalyst represented by Formula I. wherein, M is a Group IV transition metal; R1 is or a functionalized inorganic oxide support selected from the group consisting of such that R8 is a molecule having a carboxylic or sulphonic acid group; R2-R5, are independently, H or a hydrocarbon; R6 is t-butyl; R7 is a functionalized inorganic oxide support selected from the group consisting of such that R8 is a molecule having a carboxylic or sulphonic acid group; and X1 and X2 are independently F, Cl, Br or I. There is also provided a method for the preparation of the chemically immobilized heterogeneous single site polymerization catalyst as represented by Formula I.
Abstract:
The present disclosure provides an effective and efficient process for the preparation of a dry chlorinated polyvinyl chloride (CPVC), comprising introducing chlorine gas into slurry of polyvinyl chloride in water to obtain a reaction mixture; irradiating the reaction mixture to obtain a product mixture comprising CPVC and water solution including unreacted chlorine gas and hydrogen chloride; filtering the product mixture to obtain a first mass; adding water to the first mass for extracting unreacted chlorine gas and hydrogen chloride to obtain an aqueous suspension, and filtering the aqueous suspension to obtain a second mass; passing nitrogen through the second mass to extract residual water solution to leave behind a third mass; and agitating the third mass in a high-speed mixer together with a neutralizing agent, and optionally with a stabilizer and a processing additive to obtain dry thermally stable CPVC with thermal stability in the range of 1000 seconds to 1500 seconds.
Abstract:
The present disclosure relates to a process for the halogenation of hydrocarbon. In accordance with the process of the present disclosure a hydrocarbon and a halogen is introduced in a reaction vessel. Light having wavelength in the range of 390 to 780 nm is then passed into the reaction vessel for a time period of 2 to 12 hrs. to obtain a halogenated hydrocarbon. The hydrocarbon is agitated before or after the introduction of the halogen in to the reaction vessel.
Abstract:
In accordance with the present disclosure there is provided a process for preparing a hydrogenated olefin polymer by hydrogenation of a polyoctene; said polyoctene being prepared by reacting a C8-olefin feed comprising an isomeric mixture of an alpha-olefin and a non-alpha olefin monomer in a controlled manner with the help of an ionic catalyst, while controlling at least one condition of the reaction selected from the group of condition consisting of exotherm, contact time of the olefin feed with ionic catalyst and molar ratio of the ionic catalyst to the olefin feed within predetermined ranges to obtain an oligomerized mixture comprising at least one polyoctene and unreacted ionic catalyst.
Abstract:
There is provided a chemically immobilized heterogeneous single site polymerization catalyst represented by Formula I. wherein, M is a Group IV transition metal; R1 is or a functionalized inorganic oxide support selected from the group consisting of such that R8 is a molecule having a carboxylic or sulphonic acid group; R2-R5, are independently, H or a hydrocarbon; R6 is t-butyl; R7 is a functionalized inorganic oxide support selected from the group consisting of such that R8 is a molecule having a carboxylic or sulphonic acid group; and X1 and X2 are independently F, Cl, Br or I. There is also provided a method for the preparation of the chemically immobilized heterogeneous single site polymerization catalyst as represented by Formula I.
Abstract:
In accordance with the present disclosure there is provided a process for preparing a hydrogenated olefin polymer by hydrogenation of a polyoctene; said polyoctene being prepared by reacting a C8-olefin feed comprising an isomeric mixture of an alpha-olefin and a non-alpha olefin monomer in a controlled manner with the help of an ionic catalyst, while controlling at least one condition of the reaction selected from the group of condition consisting of exotherm, contact time of the olefin feed with ionic catalyst and molar ratio of the ionic catalyst to the olefin feed within predetermined ranges to obtain an oligomerized mixture comprising at least one polyoctene and unreacted ionic catalyst.