IP Library › Granted Patent US 10,975,180
Granted Patent B2
US 10,975,180 · App. 16/074,229 · Granted Apr 13, 2021

Process for preparing high-reactivity isobutene homo- or copolymers

Inventors: Rosa Corberan Roc (Ludwigshafen, DE); Klaus Muehlbach (Ludwigshafen, DE); Thomas Wettling (Ludwigshafen, DE); Sergei V. Kostjuk (Minsk, BY); Irina Vasilenko (Minsk, BY); Dmitryi Shiman (Minsk, BY)
Assignee: BASF SE
C08F110/10C08F2410/04C08F2500/01
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Quick Facts
Patent No.
US 10,975,180
App. No.
16/074,229
Granted
Apr 13, 2021
Kind
B2
Abstract

The present invention relates to a process for preparing high-reactivity isobutene homo- or copolymers with a content of terminal vinylidene double bonds per polyisobutene chain end of at least 70 mol %, which comprises polymerizing isobutene or an isobutene-comprising monomer mixture in the presence of an aluminum trihalide-donor complex effective as a polymerization catalyst or an alkylaluminum halide-donor complex effective as a polymerization catalyst, wherein the aluminum trihalide or alkylaluminum halide is treated with at least one inorganic hydrate.

Claims (25)

1. A process for preparing high-reactivity isobutene homo- or copolymers having a number-average molecular weight Mn (determined by gel permeation chromatography) of 500 to 25 000 g/mol and a content of terminal vinylidene double bonds per polyisobutene chain end of at least 70 mol % based on a total amount of chain ends, the process comprising:

polymerizing isobutene or an isobutene-comprising monomer mixture in the presence of an aluminum trihalide-donor complex or an alkylaluminum halide-donor complex,

wherein the aluminum trihalide of the aluminum trihalide-donor complex and the alkylaluminum halide of the alkylaluminum halide-donor complex are each treated with at least one inorganic hydrate, wherein a molar ratio of total water bound as water of crystallization in the at least one inorganic hydrate to the aluminum trihalide or alkylaluminum halide is 0.001:1 to 0.4:1,

wherein the at least one inorganic hydrate is an ionic compound of formula:

[M m+ x A a− y ]× z H 2 O,

wherein:

a, m, x, and y are positive natural numbers, with the proviso that x×m=y×a;

z is a positive rational number;

wherein M m+ is an m-fold positively charged cation;

wherein A a− is an a-fold negatively charged anion; and

wherein M is selected from the main groups 1, 2, and 3, and the transition groups 6, 7, 8, and 1 of the Periodic Table of the Elements.

2. The process according to claim 1 , wherein the at least one inorganic hydrate is a solid ionic compound which comprises fixed stoichiometric amounts of water of crystallization, wherein at least one water molecule is located at a fixed position of a crystal lattice.

3. The process according to claim 1 , wherein the aluminum trihalide-donor complex is an aluminum trichloride-donor complex, and

wherein the alkylaluminum halide-donor complex is an alkyl aluminum chloride-donor complex or the alkylaluminum halide-donor complex is a dialkyl aluminum chloride-donor complex.

4. The process according to claim 1 , wherein the aluminum trihalide-donor complex is an aluminum trichloride-donor complex, and

wherein the alkylaluminum halide-donor complex is a methylaluminum dichloride-donor complex, an ethylaluminum dichloride-donor complex, or an iso-butylaluminum dichloride-donor complex.

5. The process according to claim 1 , wherein a, m, x, and y are each independently 1, 2, 3, or 4.

6. The process according to claim 1 , wherein z is greater than 0 and less than or equal to 18.

7. The process according to claim 1 , wherein cations M m+ are selected from the group consisting of Cs + , Rb + , K + , NH 4+ , Na + , Li + , Ba 2+ , Sr 2+ , Ca 2+ , Mg 2+ , Zn 2+ , Ni 2+ , Cu 2+ , Al 3+ , Mn 2+ , Fe 2+ , Fe 3+ , and Cr 3+ .

8. The process according to claim 1 , wherein anions A a− are selected from the group consisting of NO 3− , CN − , I − , Br − , Cl − , F − , SO 4 2− , and CO 3 2− .

9. The process according to claim 1 , wherein the at least one inorganic hydrate is selected from the group consisting of Na 2 CO 3 ×10H 2 O, Na 2 CO 3 ×1H 2 O, Na 2 SO 4 ×10H 2 O, NiSO 4 ×7H 2 O, ZnSO 4 ×7H 2 O, ZnCl 2 ×2H 2 O, FeSO 4 ×7H 2 O, MnSO 4 ×1H 2 O, MnSO 4 ×4H 2 O, MgCl 2 ×6H 2 O, Mg(OH) 2 ×4H 2 O, MgCO 3 ×4H 2 O, MgSO 4 ×7H 2 O, MgSO 4 ×1H 2 O, K 2 Mg(SO 4 ) 2 ×6H 2 O, (NH 4 ) 2 Mg(SO 4 ) 2 ×6H 2 O, CaCl 2 ×6H 2 O, CaSO 4 ×2H 2 O, CuCl 2 ×2H 2 O, CuSO 4 ×5H 2 O, IOCuSO 4 ×3H 2 O, CuSO 4 ×1H 2 O, CoCl 2 ×6H 2 O, CoCl×4H 2 O, CoCl 2 ×2H 2 O, CoCl 2 ×1.5H 2 O, CoCl 2 ×1H 2 O, CoSO 4 ×7H 2 O, Al 2 (SO 4 ) 3 ×18H 2 O, Al 2 (SO 4 ) 3 ×16H 2 O, Al 2 (SO 4 ) 3 ×10H 2 O, Al 2 (SO 4 ) 3 ×6H 2 O, and KAl(SO 4 ) 2 ×12H 2 O.

10. The process according to claim 1 , wherein the donor of the aluminum trihalide-donor complex and the donor of the alkylaluminum halide-donor complex are each independently selected from the group consisting of compounds with at least one ether function, compounds with at least one carboxylic ester function, alcohols, aldehydes, ketones, phenols, acetals, and hemiacetals.

11. The process according to claim 1 , wherein the donor of the aluminum trihalide-donor complex and the donor of the alkylaluminum halide-donor complex are each independently dihydrocarbyl ethers of formula R 1 —O—R 2 , in which the variables R 1 and R 2 are each independently selected from the group consisting of C 1 - to C 4 -alkyl radicals, C 6 - to C 12 -aryl radicals, and C 7 - to C 12 -arylalkyl radicals.

12. The process according to claim 1 , wherein the polymerization is performed at a temperature from −90° C. to +30° C.

13. The process according to claim 1 , wherein the aluminum trihalide-donor complex and the alkylaluminum halide-donor complex are prepared separately from the polymerization.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 31, 2018
From: KOSTJUK, SERGEI V.; VASILENKO, IRINA; SHIMAN, DMITRYI
To: RESEARCH INSTITUTE FOR PHYSICAL CHEMICAL PROBLEMS OF THE BELARUSIAN STATE UNIVERSITY
Reel/Frame 046511/0865 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 31, 2018
From: CORBERAN ROC, ROSA; MUEHLBACH, KLAUS; WETTLING, THOMAS
To: BASF SE
Reel/Frame 046512/0089 →
Priority Claims (1)
EP 16155937 · Feb 16, 2016 · regional
Continuity (1)
Related Publication 20200317832A1 · Oct 8, 2020
Cited By (1)
US 12,723,113