Shape controlled pro-catalyst and a single pot process for preparing the same

Patent metadata

Field	Value
Publication number	US-10259896-B2
Application number	US-201515312303-A
Country	US
Kind code	B2
Filing date	May 22, 2015
Priority date	May 22, 2014
Publication date	Apr 16, 2019
Grant date	Apr 16, 2019

Abstract

The present disclosure relates to a single-pot multi step process for the preparation of a shape controlled pro-catalyst. The process comprises the steps of: i. reacting magnesium metal and at least one alkanol to obtain spheroidal magnesium alkoxide; ii. treating the spheroidal magnesium alkoxide with at least one transition metal tetrahalide, at least one organic modifier, and optionally, at least one in-organic modifier in the presence of at least one solvent to obtain a reaction mixture; iii. cooling, settling the reaction mixture and decanting the supernatant; iv. adding at least one transition metal tetrahalide, at least one solvent and optionally, at least one organic or inorganic modifier; and v. iterating steps (iii) and (iv) to obtain the shape controlled pro-catalyst.

First claim

The invention claimed is:

1. A single-pot multi step process for the preparation of a shape controlled iodine free pro-catalyst; said process comprising the following steps:
i. reacting magnesium metal and at least one alkanol at a temperature in the range of 20° C. to the boiling point of the alkanol used for 0.5 to 8 hrs to obtain spheroidal magnesium alkoxide in the presence of at least one solvent;
ii. treating the spheroidal magnesium alkoxide with at least one transition metal tetrahalide, at least one organic modifier, and optionally, at least one in-organic modifier in the presence of at least one solvent to obtain a reaction mixture;
iii. cooling, settling the reaction mixture and decanting the supernatant;
iv. adding at least one transition metal tetrachloride, at least one solvent and optionally, at least one organic or inorganic modifier; and
v. iterating steps (iii) and (iv) to obtain the shape controlled pro-catalyst.

2. The process as claimed in claim 1 , wherein steps (ii) and (iv) are carried out at a temperature in the range of 30 to 150° C. for 0.5 to 2 hrs.

3. The process as claimed in claim 1 , wherein the reaction mixture is cooled to a temperature of 30 to 60° C.

4. The process as claimed in claim 1 , wherein the alkanol is selected from the group consisting of methanol, ethanol, propanol, isopropanol, butanol, isobutanol and t-butanol.

5. The process as claimed in claim 1 , wherein the particle size of the spheroidal magnesium alkoxide ranges between 10 and 25μ.

6. The process as claimed in claim 1 , wherein the particle size of the procatalyst ranges between 10 and 35μ.

7. The process as claimed in claim 1 , wherein the organic modifier of step (ii), of step (iv) or of both steps (ii) and (iv) is selected from the group consisting of ethyl benzoate, di-isobutyl phthalate and 9, 9-bis (methoxymethyl) fluorene.

8. The process as claimed in claim 1 , wherein the inorganic modifier of step (ii), of step (iv) or of both steps (ii) and (iv) is selected from the group consisting of tetra ethoxy silane, cyclohexylmethyl dimethoxysilane, dicyclopentyl dimethoxysilane, isobutylisopropyl dimethoxy silane, n-propyltriethoxy silane, isobutyltriethoxy silane, phenyltriethoxy silane, diisopropyldimethoxy silane, diethyldimethoxy silane, diisobutyldimethoxy silane, aminopropyltriethoxy silane, diphenyldimethoxy silane and methyltrimethoxy silane.

9. The process as claimed in claim 1 , wherein the transition metal tetrachloride is selected from the group consisting of titanium tetrachloride (TiCl 4 ), vanadium tetrachloride (VCl 4 ), silicon tetrachloride (SiCl 4 ), zirconium tetrachloride (ZrCl 4 ) and hafnium tetrachloride (HfCl 4 ).

10. The process as claimed in claim 1 , wherein the solvent of step (ii), of step (iv) or of both steps (ii) and (iv) is selected from the group consisting of aliphatic and aromatic solvent.

11. The process as claimed in claim 1 , further comprises a method step of mixing at least one aluminum based co-catalyst to obtain a catalyst system, said co-catalyst being tri-ethyl aluminum.

12. The process as claimed in claim 11 , further comprises a method step of mixing at least one external donor; said external donor being selected from the group consisting of p-isopropoxy ethyl benzoate and cyclohexyl methyl di-methoxy silane, wherein the molar ratio of said elemental aluminum present in said co-catalyst and said external donor ranges from 1:1 to 1:50.

13. A pro-catalyst obtained by the process as claimed in claim 1 ; said pro-catalyst comprising spheroidal magnesium alkoxide having particle size in the range of 10 to 25μ, complexed with said transition metal tetrahalide and at least one said modifier, wherein, said pro-catalyst is devoid of elemental iodine and the particle size of said pro-catalyst ranges between 10 and 35μ.

14. A catalyst system comprising:
i. the pro-catalyst of claim 13 ,
ii. at least one aluminum based co-catalyst, and
iii. optionally, at least one external donor.

15. A catalyst system comprising: i. a pro-catalyst comprising spheroidal magnesium alkoxide having particle size in the range of 10 to 25μ, complexed with said transition metal tetrahalide, at least one organic and optionally at least one inorganic modifier, and ii. at least one aluminum based co-catalyst,
wherein, said pro-catalyst is devoid of elemental iodine and the particle size of said pro-catalyst ranges between 10 and 35μ.

16. A process for the preparation of polyethylene, said process comprising the following steps:
i. mixing the pro-catalyst as claimed in claim 13 , at least one aluminum based co-catalyst and optionally, at least one external donor selected from the group consisting of an organo-silane compound and aromatic ester to obtain a catalyst system, wherein the molar ratio of the elemental aluminum, present in said co-catalyst to the external donor ranges from 1:1 to 1:50, and
ii. polymerizing an ethylene monomer in the presence of the catalyst system to obtain polyethylene having a molecular weight in the range of 1 to 60 lac and the particle size in a range of 200 to 300μ.

Assignees

• Reliance Industries Ltd

Inventors

• Gupta Virendrakumar
• Chauhan Sanjay Govindbhai
• Bhajiwala Hiren Manojkumar
• Sayyed Shakil Shabbir
• Vakil Suketu

Classifications

• C08F10/02

  Ethene · CPC title

• C08F2500/01

  High molecular weight, e.g. >800,000 Da. · CPC title

• C08F110/02 Primary

  Ethene · CPC title

• C08F2500/18

  Bulk density · CPC title

• C08F2500/24

  Polymer with special particle form or size · CPC title