IP Library Granted Patent US 8,344,079
Granted Patent B2
US 8,344,079 · App. 11/967,815 · Granted Jan 1, 2013

Molar ratio modifications to larger polyolefin catalysts

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Quick Facts
Patent No.
US 8,344,079
App. No.
11/967,815
Granted
Jan 1, 2013
Kind
B2
Abstract

Disclosed are catalyst systems and methods of making the catalyst systems/supports for the polymerization of an olefin containing a solid titanium catalyst component having a substantially spherical shape and containing an internal electron donor, a support made by contacting substantially equal molar amounts of a magnesium compound and an epoxy compound in the presence of an aprotic solvent and subsequent treatment with a halogenating agent to provide a magnesium based catalyst support. The catalyst system can further contain an organoaluminum compound and an organosilicon compound. Also disclosed are methods of polymerizing or copolymerizing an alpha-olefin. The methods involve contacting an olefin with a catalyst system containing the solid titanium catalyst component.

Claims (22)

1. A catalyst system for use in olefinic polymerization to form a resultant polymer product, comprising:

a solid titanium catalyst component having a substantially spherical shape and a diameter from about 5 microns to about 90 microns on a 50% by volume basis and a degree of sphericalness of 0.9 or more, the solid titanium catalyst component comprising a titanium compound and a support made by contacting substantially equal molar amounts of a magnesium compound and an epoxy compound with an aprotic solvent and a surfactant selected from one or more of the group consisting of polymer surfactants, non-ionic surfactants and anionic surfactants, the magnesium compound and the epoxy compound contacted in an organic medium to form an intermediate, the organic medium comprising an organic solvent capable of forming an emulsion with the intermediate, followed by contacting the intermediate with a halogenating agent

an organoaluminum compound having at least one aluminum-carbon bond; and

an organosilicon compound,

wherein the support has a size span from about 0.7 to about 1.1, and the resultant polymer product produced by the catalyst system has an average diameter of about 500 microns or more on a 50% by volume basis.

2. The catalyst system of claim 1 , wherein a molar ratio of magnesium compound to epoxy compound is from about 1:0.75 to about 1:1.25.

3. The catalyst system of claim 1 , wherein a molar ratio of magnesium compound to epoxy compound is from about 1:0.8 to about 1:1.2.

4. The catalyst system of claim 1 , wherein a molar ratio of magnesium compound to epoxy compound is from about 1:0.9 to about 1:1.1.

5. The catalyst system of claim 1 , wherein a molar ratio of magnesium compound to epoxy compound is from about 1:0.95 to about 1:1.05 and a molar ratio of magnesium compound to aprotic solvent is from about 1:0.85 to about 1:1.

6. The catalyst system of claim 1 , wherein the magnesium compound and the epoxy compound are contacted in the presence of a titanium compound and/or an internal electron donor.

7. The catalyst system of claim 1 , wherein the solid titanium catalyst component does not substantially contain the epoxy compound.

8. The catalyst system of claim 1 , wherein the magnesium compound comprises at least one selected from the group consisting of magnesium chloride, magnesium bromide, magnesium iodide, magnesium fluoride, methoxy magnesium chloride, ethoxy magnesium chloride, isopropoxy magnesium chloride, butoxy magnesium chloride, octoxy magnesium chloride, phenoxy magnesium chloride, methylphenoxy magnesium chloride, ethoxy magnesium, isopropoxy magnesium, butoxy magnesium, n-octoxy magnesium, 2-ethylhexoxy magnesium, phenoxy magnesium, dimethylphenoxy magnesium, magnesium laurate, and magnesium stearate; and wherein the halogenating agent comprises at least one selected from the group consisting of titanium tetrahalides, alkoxytitanium trihalides, dialkoxytitanium dihalides, trialkoxytitanium monohalides, and tetraalkoxytitaniums.

9. The catalyst system of claim 1 , wherein the epoxy compound comprises at least one selected from the group consisting of aliphatic epoxy compounds, alicyclic epoxy compounds, and aromatic epoxy compounds.

10. The catalyst system of claim 1 , wherein the epoxy compound comprises at least one selected from the group consisting of halogenated aliphatic epoxy compounds, aliphatic epoxy compounds having a keto group, aliphatic epoxy compounds having an ether bond, aliphatic epoxy compounds having an ester bond, aliphatic epoxy compounds having a tertiary amino group, aliphatic epoxy compounds having a cyano group, halogenated alicyclic epoxy compounds, alicyclic epoxy compounds having a keto group, alicyclic epoxy compounds having an ether bond, alicyclic epoxy compounds having an ester bond, alicyclic epoxy compounds having a tertiary amino group, alicyclic epoxy compounds having a cyano group, halogenated aromatic epoxy compounds, aromatic epoxy compounds having a keto group, aromatic epoxy compounds having an ether bond, aromatic epoxy compounds having an ester bond, aromatic epoxy compounds having a tertiary amino group, and aromatic epoxy compounds having a cyano group.

11. The catalyst system of claim 1 , wherein the epoxy compound comprises at least one selected from the group consisting of ethylene oxide, propylene oxide, 1,2-epoxybutane, 2,3-epoxybutane, 1,2-epoxyhexane, 1,2-epoxyoctane, 1,2-epoxydecane, 1,2-epoxydodecane, 1,2-epoxytetradecane, 1,2-epoxyhexadecane, 1,2-epoxyoctadecane, 7,8-epoxy-2-methyloctadecane, 2-vinyl oxirane, 2-methyl-2-vinyloxirane, 1,2-epoxy-5-hexene, 1,2-epoxy-7-octene, 1-phenyl-2,3-epoxypropane, 1-(1-naphthyl)-2,3-epoxypropane, 1-cyclohexyl-3,4-epoxybutane, 1,3-butadiene dioxide, 1,2,7,8-diepoxyoctane, cyclopentene oxide, 3-methyl-1,2-cyclopentene oxide, cyclohexene oxide, cyclooctene oxide, alpha-pinene oxide, 2,3-epoxynorbornane, limonene oxide, cyclododecane epoxide, 2,3,5,6-diepoxynorbornane, styrene oxide, 3-methylstyrene oxide, 1,2-epoxybutylbenzene, 1,2-epoxyoctylbenzene, stilbene oxide, 3-vinyistyrene oxide, 1-(1-methyl-1,2-epoxyethyl)-3-(1-methylvinyl)benzene, 1,4-bis(1,2-epoxypropyl)benzene, 1,3-bis(1,2-epoxy-1-methylethyl)benzene, 1,4-bis(1,2-epoxy-1-methylethyl)benzene, epifluorohydrin, epichlorohydrin, epibromohydrin, hexafluoropropylene oxide, 1,2-epoxy-4-fluorobutane, 1-(2,3-epoxypropyl)-4-fluorobenzene, 1-(3,4-epoxybutyl)-2-fluorobenzene, 1-(2,3-epoxypropyl)-4-chlorobenzene, 1-(3,4-epoxybutyl)-3-chlorobenzene, 4-fluoro-1,2-cyclohexene oxide, 6-chloro-2,3-epoxybicyclo[2.2.1]heptane, 4-fluorostyrene oxide, 1-(1,2-epoxypropyl)-3-trifluorobenzene, 3-acetyl-1,2-epoxypropane, 4-benzoyl-1,2-epoxybutane, 4-(4-benzoyl)phenyl-1,2-epoxybutane, 4,4′-bis(3,4-epoxybutyl)benzophenone, 3,4-epoxy-1-cyclohexanone, 2,3-epoxy-5-oxobicyclo[2.2.1]heptane, 3-acetylstyrene oxide, 4-(1,2-epoxypropyl)benzophenone, glycidyl methyl ether, butyl glycidyl ether, 2-ethylhexyl glycidyl ether, allyl glycidyl ether, ethyl 3,4-epoxybutyl ether, glycidyl phenyl ether, glycidyl 4-tert-butylphenyl ether, glycidyl 4-chlorophenyl ether, glycidyl 4-methoxyphenyl ether, glycidyl 2-phenylphenyl ether, glycidyl 1-naphthyl ether, glycidyl 4-indolyl ether, glycidyl N-methyl-alpha-quinolon-4-yl ether, ethyleneglycol diglycidyl ether, 1,4-butanediol diglycidyl ether, 1,2-diglycidyloxybenzene, 2,2-bis(4-glycidyloxyphenyl)propane, tris(4-glycidyloxyphenyl)methane, poly(oxypropylene)triol triglycidyl ether, a glycidyl ether of phenol novolac, 1,2-epoxy-4-methoxycyclohexane, 2,3-epoxy-5,6-dimethoxybicyclo[2.2.1]heptane, 4-methoxystyrepe oxide, 1-(1,2-epoxybutyl)-2-phenoxybenzene, glycidyl formate, glycidyl acetate, 2,3-epoxybutyl acetate, glycidyl butyrate, glycidyl benzoate, diglycidyl terephthalate, poly(glycidyl acrylate), poly(glycidyl methacrylate), 1,2-epoxy-4-methoxycarbonylcyclohexane, 2,3-epoxy-5-butoxycarbonylbicyclo[2.2.1]heptane, ethyl 4-(1,2-epoxyethy)benzoate, methyl 3-(1,2-epoxybutyl)benzoate, methyl 3(1,2-epoxybutyl)-5-phenylbenzoate, N,N-glycidylmethylacetamide, N,N -ethylglycidylpropionamide, N,N-glycidylmethylbenzamide, N-(4,5-epoxypentyl)-N -methylbenzamide, N,N-diglycidylaniline, bis(4-diglycidylaminophenyl)methane, poly(N,N-glycidylmethylacrylamide), 1,2-epoxy-3-(diphenylcarbamoyl)cyclohexane, 2,3-epoxy-6-(dimethylcarbamoy)bicyclo[2.2.1]heptane, 2-(dimethylcarbamoyl)styrene oxide, 4-(1,2-epoxybutyl)-4′-(dimethylcarbamoyl)biphenyl, 4-cyano-1,2-epoxybutane, 1-(3-cyanophenyl)-2,3-epoxybutane, 2-cyanostyrene oxide, and 6-cyano-1-(1,2-epoxy-2-phenylethyl)naphthalene.

12. The catalyst system of claim 1 , wherein the aprotic solvent comprises one or more selected from the group consisting of tributyl phosphate, tetrahydrofuran, dimethyl sulfoxide, dimethylformamide, and hexamethylphosphorotriamide.

13. The catalyst system of claim 1 , wherein the epoxy compound comprises epichlorohydrin.

14. The catalyst system of claim 2 , wherein the epoxy compound comprises epichlorohydrin.

15. The catalyst system of claim 8 , wherein the epoxy compound comprises epichlorohydrin.

16. The catalyst system of claim 3 , wherein the epoxy compound comprises epichlorohydrin.

17. The catalyst system of claim 4 , wherein the epoxy compound comprises epichlorohydrin.

18. The catalyst system of claim 5 , wherein the epoxy compound comprises epichlorohydrin.

Assignments (4)
RELEASE OF SECURITY INTEREST Recorded Sep 23, 2021
From: GOLDMAN SACHS BANK USA
To: W. R. GRACE & CO.-CONN.
Reel/Frame 057594/0026 →
SECURITY INTEREST Recorded Apr 3, 2018
From: W. R. GRACE & CO.-CONN.
To: GOLDMAN SACHS BANK USA, AS COLLATERAL AGENT
Reel/Frame 045828/0683 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 22, 2016
From: BASF CORPORATION
To: W. R. GRACE & CO. - CONN.
Reel/Frame 040255/0136 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 5, 2008
From: SPENCER, MICHAEL D.
To: BASF CATALYSTS LLC
Reel/Frame 020467/0605 →