Process for preparing high-reactivity isobutene homo- or copolymers

Patent metadata

Field	Value
Publication number	US-10975180-B2
Application number	US-201716074229-A
Country	US
Kind code	B2
Filing date	Feb 13, 2017
Priority date	Feb 16, 2016
Publication date	Apr 13, 2021
Grant date	Apr 13, 2021

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.

First claim

The invention claimed is:

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.

Assignees

• Basf Se

Inventors

• Corberan Roc Rosa
• Muehlbach Klaus
• Wettling Thomas
• Kostjuk Sergei V
• Vasilenko Irina
• Shiman Dmitryi

Classifications

• C08F2500/02

  Low molecular weight, e.g. <100,000 Da. · CPC title

• C08F110/10 Primary

  Isobutene · CPC title

• C08F2500/01

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

• C08F4/54

  together with other compounds thereof · CPC title

• C08F2/38

  Polymerisation using regulators, e.g. chain terminating agents {, e.g. telomerisation} · CPC title