Catalyst component for olefin polymerization and preparation method thereof

Patent metadata

Field	Value
Publication number	US-9353197-B2
Application number	US-201013502508-A
Country	US
Kind code	B2
Filing date	Apr 19, 2010
Priority date	Oct 20, 2009
Publication date	May 31, 2016
Grant date	May 31, 2016

Abstract

A catalyst component for olefin polymerization is disclosed, which comprises at least one diol ester type electron donor compound (a) and at least one diether type electron donor compound (b) among others, wherein the molar ratio of a to b is 0.55-50. A preparation method of the catalyst component, a catalyst comprising the catalyst component, and an olefin polymerization method using the catalyst which can especially be used for preparation of polypropylenes of low ash contents are also disclosed.

First claim

What is claimed is:

1. A catalyst component for olefin polymerization, comprising a reaction product of:
(1) an adduct represented by general formula (I): MgX 2 .m(R′OH).nE.qH 2 O;
(2) at least one titanium compound represented by general formula (II): Ti(OR) 4-k X k ; and
(3) at least one electron donor compound a and at least one electron donor compound b;
wherein,
in the general formula (I), X is Cl or Br; R′ is a C 1 -C 4 alkyl; E is at least one o-alkoxybenzoate represented by general formula (III):

wherein R 1 and R 2 are independently chosen from C 1 -C 12 linear or branched alkyl, C 3 -C 10 cycloalkyl, C 4 -C 10 cycloalkylalkyl, C 6 -C 10 aryl, C 7 -C 10 alkaryl and C 7 -C 10 aralkyl; m ranges from 1.0 to 5.0; n ranges from 0 to 0.5; and q ranges from 0 to 0.8;
in the general formula (II), R is a C 1 -C 20 alkyl, X is a halogen, and k is 0, 1, 2, 3, or 4;
the at least one electron donor compound a is chosen from esters of diol represented by general formula (IV):

wherein R 1 and R 2 are independently chosen from C 1 -C 10 linear or branched alkyl, C 3 -C 20 cycloalkyl, C 4 -C 20 cycloalkylalkyl, C 6 -C 20 aryl, and C 7 -C 20 aralkyl, the aryl ring or cycloalkyl ring of which is optionally further substituted by a substituent chosen from halogen, C 1 -C 6 alkyl and C 1 -C 6 alkoxy; R 3 -R 6 and R 1 -R 2n are independently chosen from hydrogen, halogen, substituted or unsubstituted linear or branched C 1 -C 20 alkyl, C 3 -C 20 cycloalkyl, C 4 -C 20 cycloalkylalkyl, C 6 -C 20 aryl, C 7 -C 20 alkaryl, C 7 -C 20 aralkyl, C 2 -C 10 alkenyl, C 10 -C 20 fused aryl, and ester group, each of R 3 -R 6 and R 1 -R 2n comprises optionally one or more heteroatoms as a substitution of a carbon atom or a hydrogen atom or both, said heteroatom being chosen from N, O, S, Si, P, and halogen, and one or more of R 3 -R 6 and R 1 -R 2n are optionally linked to form a ring; and n is an integer ranging from 0 to 10;
the at least one electron donor compound b is chosen from diether compounds represented by general formula (V):

wherein R I , R II , R III , R IV , R V , and R VI are independently chosen from hydrogen, halogen, linear or branched C 1 -C 20 alkyl, C 3 -C 20 cycloalkyl, C 4 -C 20 cycloalkylalkyl, C 6 -C 20 aryl, and C 7 -C 20 aralkyl, the aryl ring or cycloalkyl ring of which is optionally further substituted by a substituent chosen from halogen, C 1 -C 6 alkyl and C 1 -C 6 alkoxy; R VII and R VIII are independently chosen from linear or branched C 1 -C 20 alkyl, C 3 -C 20 cycloalkyl, C 6 -C 20 aryl, C 7 -C 20 alkaryl, and C 7 -C 20 aralkyl; and the R I to R VI groups are optionally linked to form a ring; and
the molar ratio of the electron donor compound a to the electron donor compound b ranges from 0.60 to 10.

2. The catalyst component of claim 1 , wherein in the general formula (I), m ranges from 1.5 to 3.5, and n ranges from 0 to 0.2.

3. The catalyst component of claim 1 , wherein in the general formula (I), m ranges from 1.5 to 3.5, and n is 0 or ranges from 0.005 to 0.2.

4. The catalyst component of claim 1 , wherein in the general formula (III), R 1 and R 2 are independently chosen from methyl, ethyl, n-propyl, isopropyl, n-butyl, and isobutyl.

5. The catalyst component of claim 1 , wherein the adduct represented by the general formula (I) is of spherical shape.

6. The catalyst component of claim 1 , wherein the electron donor compound a is an ester of diol represented by general formula (VI):

wherein R 1 -R 6 are independently chosen from hydrogen and linear or branched C 1 -C 20 alkyl, R is independently chosen from hydrogen, halogen, C 1 -C 6 alkyl and C 1 -C 6 alkoxy.

7. The catalyst component of claim 1 , wherein the electron donor compound b is a 1,3-diether represented by general formula (VII):
R 1 R 2 C(CH 2 OR 3 )(CH 2 OR 4 )  (VII)

wherein R 1 and R 2 are independently chosen from C 1 -C 18 alkyl, C 3 -C 18 cycloalkyl, C 4 -C 18 cycloalkylalkyl, C 6 -C 18 aryl and C 7 -C 18 aralkyl, the aryl ring or cycloalkyl ring of which is optionally further substituted by a substituent chosen from halogen, C 1 -C 6 alkyl and C 1 -C 6 alkoxy, and R 1 and R 2 are optionally linked to form a ring; R 3 and R 4 are independently a C 1 -C 10 alkyl.

8. The catalyst component of claim 1 , wherein the catalyst component is of spherical shape.

9. A process for the preparation of the catalyst component according to claim 1 , comprising the steps of
(A) suspending the adduct represented by the general formula (I) in the titanium compound represented by the general formula (II) or a mixture of the titanium compound and an inert solvent, and optionally maintaining a period of time;
(B) slowly heating the above suspension to a temperature of from 90° C. to 130° C. with stirring, and adding thereto the electron donor compound a and the electron donor compound b during the heating or after the temperature reaches the target value;
(C) continuously stirring for 0.5 to 3 hours, and then separating the liquid from the solids;
(D) treating the solids from step (C) with the titanium compound represented by the general formula (II) or a mixture of the titanium compound and an inert solvent at 90 to 130° C. for 0.5 to 3 h, and then separating the liquid from the solids;
(E) optionally, repeating the titanium compound treatment of step (D) one or more times; and
(F) washing the solids from step (D) or (E), if present, with an inert solvent and then drying, to obtain the solid catalyst component.

10. The process of claim 9 , having at least one of the following features:
step (A) is carried out by suspending the adduct of the general formula (I) in the titanium compound of the general formula (II) or a mixture of the titanium compound and an inert hydrocarbon solvent prechilled to a temperature of from −40° C. to 0° C., and then maintaining optionally at that temperature for 5 min to 2 h;
in step (A), the concentration of the adduct in the resultant suspension is lower than 200 g/L;
step (B) is carried out by heating slowly the suspension from step (A) to 90° C. to 130° C. with stirring, and adding thereto the electron donor compound a and the electron donor compound b during the heating or after the temperature reaches the target value, wherein the electron donor compounds a and b may be added together, separately, or stepwise;
in step (B), the electron donor compound a or the electron donor compound b or the both are added after the temperature of the suspension have reached above 30° C.;
step (C) is carried out by stirring the mixture from step (B) for 0.5 to 3 hours, then stopping the stirring, and separating the liquid from the solids;
step (D) is carried out by treating the solids from step (C) with the titanium compound of the general formula (II) or a mixture of the titanium compound and an inert hydrocarbon solvent at 90 to 130° C. with stirring for 0.5 to 3 h, then stopping the stirring, and separating the liquid from the solids;
the process comprises step (E), i.e., repeating the titanium compound treatment of step (D) one or more times;
the titanium compounds used in step (A), step (D), and optional step (E) are the same or different, the molar number of the total titanium compounds used in s

Assignees

• Xia Xianzhi
• Zhao Jin
• Liu Yuexiang
• Zhang Jigui
• Li Weili
• Tan Yang
• Qiao Suzhen
• Peng Renqi
• Gao Ping
• Yin Maoping
• Zhang Tianyi
• China Petroleum & Chemical
• Beijing Res Inst Chem Ind

Inventors

• Xia Xianzhi
• Zhao Jin
• Liu Yuexiang
• Zhang Jigui
• Li Weili
• Tan Yang
• Qiao Suzhen
• Peng Renqi
• Gao Ping
• Yin Maoping
• Zhang Tianyi

Classifications

• C08F110/06

  Propene · CPC title

• C08F4/651

  Pretreating with non-metals or metal-free compounds · CPC title

• C08F10/00 Primary

  Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond · CPC title

• C08F4/6543

  halides of magnesium · CPC title

• C08F4/654 Primary

  with magnesium or compounds thereof · CPC title