Increased throughput in the manufacture of anionic polymers by reduction in polymers by reduction in polymer cement viscosity through the addition of metal alkyls

• US 6,492,469 B2
• Filed: 03/26/2002
• Issued: 12/10/2002
• Est. Priority Date: 04/23/1999
• Status: Expired due to Term

• Current Assignee: Kraton Polymers Usllc
• Original Assignee: Kraton Polymers US LLC (DL Holdings Co., Ltd.)
• Inventors: Willis, Carl Lesley, Handlin, Dale Lee Jr., Murany, Peter Taylor, Bening, Robert Charles, Weddle, Steven Jon
• Primary Examiner(s): Henderson, Christopher
• Application Number:
  US10/106,265
• Publication Number:
  US 20020151658A1
• Time in Patent Office: 259 Days
• Field of Search: 525/360, 525/366, 525/370, 526/78, 526/173, 526/177, 526/178
• US Class Current: 525/366
• CPC Class Codes: C08F 12/08 Styrene
• CPC Class Codes: C08F 297/04 polymerising vinyl aromatic monomers and conjugated dienes
• CPC Class Codes: C08F 297/042 using a polyfunctional initiator
• CPC Class Codes: C08F 36/04 conjugated
• CPC Class Codes: C08F 4/46 selected from alkali metals
• CPC Class Codes: C08F 4/48 selected from lithium, rubidium, caesium or francium C08F4/461 takes precedence
• CPC Class Codes: C08F 4/50 selected from alkaline earth metals, zinc, cadmium, mercury, copper or silver
• CPC Class Codes: C08F 4/52 selected from boron, aluminium, gallium, indium, thallium or rare earths C08F4/14 takes precedence

Abstract

The present invention is an improvement upon the known method of anionically polymerizing monomers by contacting the monomers with an anionic polymerization initiator which is an organo-substituted alkali metal compound. The improvement comprises decreasing the viscosity of the polymer cement by adding at least 0.01 equivalent of a metal alkyl compound per equivalent of alkali metal initiator if the metal alkyl is added before or at the beginning of polymerization. If the metal alkyl is added during the polymerization or after but before the living polymer is terminated, then at least 0.01 equivalent of the metal alkyl compound per equivalent of living polymer chain ends is should be used. The alkyl groups of the metal alkyl are chosen such that they do not exchange with the organo substituents of the alkali metal, which can be the living polymer chain ends or the organo substituents of the initiator. To avoid this undesired exchange reaction, the alkyl groups of the metal alkyl compound are selected to be more basic and/or less bulky or both than the organo substituents of the alkali metal compound.

Claims

1. A method for anionically polymerizing monomers, comprising:

a) forming a reaction mixture by contacting monomers with a mono- or multi-functional anionic polymerization initiator, wherein the polymerization initiator is an organo-substituted alkali metal compound in a suitable solvent;

b) adding to (a) before, or at the beginning of polymerization, at least 0.01 equivalents of a metal alkyl compound per equivalent of alkali metal to reduce the viscosity of the reaction mixture, wherein the alkyl groups of the metal alkyl compound are chosen so that they will not exchange with the alkali metal.

2. The method of claim 1, wherein from 0.01 to 1.5 equivalents of the metal alkyl compound per equivalent of the alkali metal.

3. The method of claim 1, wherein from 0.01 to 1.0 equivalents of the metal alkyl compound per equivalent of the alkali metal.

4. The method of claim 1, wherein the metal alkyl compound is selected from the group consisting of aluminum, zinc, boron, and magnesium alkyls having from 1 to 20 carbon atoms per alkyl substituent.

5. The process of claim 4, wherein the metal alkyl compound is selected from the group consisting of triethylaluminum, trimethylaluminum, tri-n-propylaluminum, tri-n-butylaluminum, triisobutylaluminum, tri-n-hexylaluminum, trioctylaluminum, butylethyl-magnesium, di-n-butylmagnesium, di-n-hexylmagnesium, dimthylzinc, diethylzinc, di-n-propylzinc, diisobutylzinc, and di-n-butylzinc.

6. The process of claim 5, wherein the metal alkyl compound is triethyl aluminum.

7. The method of claim 1, wherein the organo substituent of the alkali metal compound is aliphatic, cycloaliphatic, aromatic, or alkyl-substituted aromatic.

8. The method of claim 7, wherein the alkali metal compound is sec-butyllithium.

9. The method of claim 7, wherein the initiator is a diinitiator.

10. The method of claim 9, wherein the alkali metal compound is the sec-butyl lithium adduct of diisopropenyl benzene.