Ziegler-natta catalyst synthesis and process thereof

Patent metadata

Field	Value
Publication number	US-2016376384-A1
Application number	US-201615185019-A
Country	US
Kind code	A1
Filing date	Jun 17, 2016
Priority date	Jun 26, 2015
Publication date	Dec 29, 2016
Grant date	—

Abstract

The present invention describes a process of preparing a catalyst for olefin polymerization comprising: (i) treating a magnesium metal with an organohalide along with an internal donor to obtain a reaction mixture having solid component (A); (ii) treating the reaction mixture having solid component (A) with an acyl halide to obtain a reaction mixture having solid component (B); and (iii) treating the reaction mixture having solid component (B) of step (ii) with a transition metal compound to obtain the catalyst. The present invention also relates to a process for preparation of a catalyst system from said catalyst and preparation of a polyolefins from the catalyst system.

First claim

1 . A process of preparing a catalyst for olefin polymerization comprising:
treating a magnesium metal with an organohalide along with an internal donor to obtain a reaction mixture having solid component (A); (ii) treating the reaction mixture having solid component (A) with an acyl halide to obtain a reaction mixture having solid component (B); and (iii) treating the reaction mixture having solid component (B) of step (ii) with a transition metal compound to obtain the catalyst.

2 . The process as claimed in claim 1 , wherein the organohalide is selected from a group comprising of alkyl halides, benzylic halides, halogenated alkyl benzene and mixture thereof; wherein:
alkyl halide is selected from a group comprising of methyl chloride, ethyl chloride, propyl chloride, isopropyl chloride, 1,1-dichloropropane, 1,2-dichloropropane, 1,3-dichloropropane, 2,3-dichloropropane, butyl chloride, 1,4-dichlorobutane, tert-butylchloride, amylchloride, tert-amylchloride, 2-chloropentane, 3-chloropentane, 1,5-dichloropentane, 1-chloro-8-iodoctane, 1-chloro-6-cyanohexane, cyclopentylchloride, cyclohexylchloride, chlorinated dodecane, chlorinated tetradecane, chlorinated eicosane, chlorinated pentacosane, chlorinated triacontane, iso-octylchloride, 5-chloro-5-methyl decane, and 9-chloro-9-ethyl-6-methyl eiscosane; (ii) benzylic halide is selected from a group comprising of benzyl chloride and α,α′ dichloro xylene; and (iii) halogenated alkyl benzene comprises alkyl radical containing from about 10 to 15 carbon atoms, and the halogen is selected from the group comprising of chlorine, bromine, fluorine and iodine.

3 . The process as claimed in claim 1 , wherein the magnesium metal is reacted with the organohalide in a molar ratio of between 1:30 to 1:1.

4 . The process as claimed in claim 1 , wherein the internal electron donor is selected from a group comprising of phthalates, benzoates, diethers, succinates, malonates, carbonates/carboxylate, silyl esters, amide esters, ether esters, amide ethers, silyl ethers, silyl ether esters, 1,2-phenylene dioates and combinations thereof; wherein:
(i) phthalates is selected from a group comprising of di-n-butyl phthalate, di-i-butyl phthalate, di-2-ethylhexyl phthalate, di-n-octyl phthalate, di-i octyl phthalate, di-n-nonyl phthalate; (ii) benzoates is selected from a group comprising of methyl benzoate, ethyl benzoate, propyl benzoate, phenyl benzoate, cyclohexyl benzoate, methyl toluate, ethyl toluate, p-ethoxy ethyl benzoate, p-isopropoxy ethyl benzoate, methyl anisate, and ethyl anisate; (iii) succinate is selected from a group comprising of diethyl succinate, di-propyl succinate, diisopropyl succinate, dibutyl succinate, and diisobutyl succinate; (iv) malonates is selected from a group comprising of diethyl malonate, diethyl ethylmalonate, diethyl propyl malonate, diethyl isopropylmalonate, and diethyl butylmalonate; (v) carbonates/carboxylate is selected from a group comprising of diethyl 1,2-cyclohexanedicarboxylate, di-2-ethylhexyl 1,2-cyclohexanedicarboxylate, di-2- isononyl 1,2-cyclohexanedicarboxylate, 1,2-phenylene diisopentanoate, 4-t-butyl- 1,2-phenylene diisopentanoate, 4-t-butyl-1,2-phenylene bis(2-ethylhexanoate), and diisobutyl 2,2′-((4-tert-butyl)-1,2-pheylene)bis(oxy)diacetate; and (vi) diether/ether is selected from a group comprising of 9,9-bis(methoxymethyl)fluorene, 2-isopropyl-2-isopentyl-1,3-dimethoxypropane, 2,2-diisobutyl-1,3-dimethoxypropane, 2,2-diisopentyl-1,3-dimethoxypropane, 2-isopropyl-2-cyclohexyl-1,3-dimethoxypropane, and tetrahydrofuran or mixture thereof.

5 . The process as claimed in claim 1 , wherein the internal electron donor is used in an amount of from 0.01 to 1 moles with respect to one mole of magnesium.

6 . The process as claimed in claim 1 , wherein the contact of magnesium metal, organohalide and internal donor is either neat or in a solvent.

7 . The process as claimed in claim 6 , wherein the solvent is selected from a group comprising of chlorinated aromatic hydrocarbon, non chlorinated aromatic hydrocarbon, chlorinated aliphatic hydrocarbon, non chlorinated aliphatic hydrocarbon and combination thereof.

8 . The process as claimed in claim 6 , wherein the solvent is comprising from 40 to 60 volume percent and is selected from a group comprising of benzene, decane, kerosene, ethyl benzene, chlorobenzene, dichlorobenzene, toluene, o-chlorotoluene, xylene, dichloromethane, chloroform, hexane, heptane, isooctane, cyclohexane and combination thereof.

9 . The process as claimed in claim 6 , wherein the contact of magnesium, organohalide and internal donor either neat or in the solvent is at temperature between about 0° C. and about 150° C. and the contact time is for about 0.5 to 12 h.

10 . The process as claimed in claim 1 , wherein the solid component (A) is separated from the reaction mixture either by filtration or decantation and finally washed with a solvent to remove unreacted components and other side products before reacting with the acyl halide.

11 . The process as claimed in claim 1 , wherein the solid component (A) is washed one or more times with a solvent selected from a group comprising of pentanes, hexanes, heptanes, octanes, decanes, toluene, chlorobenzene at a temperature from about 20° C. to about 120° C.

12 . The process as claimed in claim 1 , wherein the solid component (A) is used as such after washing or is isolated and treated further with solvent to form a reaction mixture, before reacting with acyl halide.

13 . The process as claimed in claim 1 , wherein the acyl halide is represented by RCOX where R is H, C 1 -C 20 linear or branched alkyl group which optionally linked with cyclic rings, C 6 -C 14 aryl groups, C 3 -C 15 cycloalkyl groups, C 1 -C 20 alkoxy group, optionally containing heteroatom and X is selected from halides.

14 . The process as claimed in claim 1 , wherein the acyl halide is selected from a group comprising of formyl chloride, acetyl chloride, benzoyl chloride, tert-butylbenzoyl chloride, 2-ethyl hexanoyl chloride, valeryl chloride, isovaleryl chloride, phthaloyl chloride, 2,3-naphthalenedicarboxylic dichloride, endo-5-norborene-2,3-dicarboxylic acid dichloride, maleic dichloride, citraconic acid dichloride and combination thereof.

15 . The process as claimed in claim 1 , wherein a molar ratio of magnesium to acyl halide is between 1:5 to 1:0.05.

16 . The process as claimed in claim 1 , wherein the acyl halide contact with the solid component (A) results in formation of solid component (B) and the contacting time is immediate to 2 h, and a contact temperature is between about 5° C. and about 150° C.

17 . The process as claimed in claim 1 , wherein the solid component (B) is separated from the reaction mixture either by filtration or decantation and finally washed with a solvent to remove unreacted components and other side products before reacting with the transition metal compound.

18 . The process as claimed in claim 17 , wherein the solid component (B) is washed one or more times with the solvent selected from a group comprising of pentanes, hexanes, heptanes, octanes, decanes, toluene, and chlorobenzene at a temperature from about 20° C. to about 120° C.

19 . The process as claimed in claim 1 , wherein the transition metal compound is transition metal halide selected from compounds represented by M(OR′) p X 4-p , where M is a transition metal and is selected from a group comprising of Ti, V, Zr, and Hf; X is a halogen atom; R′ is a hydrocarbon group and p is an integer having value equal or le

Assignees

• Indian Oil Corp Ltd

Inventors

• Singh Gurmeet
• Kumar Naresh
• Kaur Sukhdeep
• Bantu Bhasker
• Kapur Gurpreet Singh
• Shashikant

Classifications

• C08F110/02 Primary

  Ethene · CPC title