Treatment of coupled polymers prior to hydrogenation

Claim 2

The process of hydrogenation of a silicon-coupled or germanium-coupled conjugated diene polymer which comprises: treating said coupled conjugated diene polymer as said solution in hydrocarbon diluent with a minor effective amount of an organometal treating agent which is hydrocarbonlithium, -sodium, -potassium, -magnesium, -calcium, -zinc, or -aluminum compound, wherein said minor effective amount of said organometal treating agent is effective to reduce the residual olefinic unsaturation of said coupled polymer on subsequent hydrogenation of said coupled polymer, and thereafter hydrogenating said organometal-treated coupled polymer under hydrogenation conditions to substantially reduce at least the olefinic unsaturation,

Claim 3

wherein said organometal treating agent is represented by R a H b M wherein b is 0 for all metals except aluminum, and is 0, 1, 2, or 3 where M is aluminum, and a + b = valence of M.

Claim 4

wherein said organometal treating agent is represented by R a H b M wherein b is 0 for all metals except aluminum, and is 0, 1, 2, or 3 where M is aluminum, and a + b = valence of M.

Claim 5

The process according to claim 1 wherein said organometal treating agent is represented by R a H b M wherein M is said lithium, sodium, potassium, calcium, magnesium, zinc, or aluminum; R represents a hydrocarbon radical of 1 to 12 carbon atoms, such that said organometal treating agent contains up to 20 carbon atoms per molecule; a = 1 and b = 0 when M is lithium, sodium, or potassium; a = 2 and b = 0 when M is zinc, magnesium or calcium; and a is 1, 2 or 3, and b is 0, 1, or 2, such that a + b = 3, when M is aluminum.

Claim 6

The process according to claim 2 wherein said organometal treating agent is n-butyllithium, sec-butyllithium, tert-butyllithium, n-amylsodium, n-hexylpotassium, di-n-amylmagnesium, dimethylmagnesium, diethylmagnesium, diisopropylcalcium, di-n-butylmagnesium, di(2-ethylhexyl)magnesium, diethylzinc, phenyllithium, diphenylmagnesium, benzyllithium, di-p-tolylmagnesium, p-tolyllithium, cyclohexyllithium, cyclohexyl-2-ethylpentylmagnesium, bis(3-phenylpropyl)magnesium, trimethylaluminum, triethylaluminum, di-n-butylaluminum hydride, 2-ethylhexylaluminum dihydride, triphenylaluminum, cyclohexylbis(2-ethylpentyl)aluminum, or mixtures thereof.

Claim 7

The process according to claim 1 wherein said minor effective amount of said organometal treating agent is in the range of about 0.1 to 25 gram millimoles per 100 grams of coupled polymer, and wherein said treating is conducted at a temperature in the range of about 10° C to 110° C.

Claim 8

The process according to claim 4 wherein said minor effective amount of said organometal treating agent is in the range of about 1 to 10 gram millimoles per 100 grams of coupled polymer, said treating temperature is in the range of about 20° C to 90° C, and wherein said hydrocarbon diluent is cyclohexane, methylcyclohexane, hexane, benzene, isooctane, or n-heptane.

Claim 9

The process according to claim 4 wherein said coupled polymer in said hydrocarbon diluent represents a concentration of said polymer of about 1 to 50 weight percent, and said organometal treating agent is employed as a solution in a hydrocarbon diluent of about 0.1 to 2 molar.

Claim 10

The process according to claim 6 wherein said hydrogenation is conducted at a temperature in the range of about 25° C to 175° C, under pressure of about 10 to 5000 psig for a time of about 30 minutes to 4 hours, employing a catalyst comprising (B) a cobalt or nickel carboxylate or alkoxide, and (A) an aluminum alkyl in amounts effective for hydrogenation.

Claim 11

The process according to claim 7 wherein said (B) nickel or cobalt carboxylate or alkoxide is the acetate, propionate, benzoate, octanoate, butoxide, ethoxide, or isopropoxide, and wherein said (A) aluminum alkyl compound is triisobutylaluminum, triethylaluminum, triisopropylaluminum, tripropylaluminum, or trioctyaluminum.

Claim 12

The process according to claim 7 wherein said conjugated diene polymer is a polymer of a conjugated diene of 4 to 12 carbon atoms per molecule, or a copolymer of at least one thereof with a copolymerizable vinylidine group-containing monomer of up to 18 carbon atoms per molecule selected from the group consisting of monovinyl arenes, substituted styrenes, monopropenylbenzenes, vinylnaphthalenes, vinylquinolines, vinylisoquinolines, and vinylpyridines.

Claim 13

The process according to claim 9 wherein said coupled polymer is a silicon coupled polymer and said organometal treating agent is hydrocarbyl lithium or hydrocarbyl aluminum compound.

Claim 14

The process according to claim 10 wherein said conjugated diene polymer is a copolymer of a said conjugated diene with a said monovinylarene.

Claim 15

The process according to claim 11 wherein said copolymer is a rubbery butadiene/styrene copolymer coupled with silicon tetrachloride, and wherein said organometal treating agent is n-butyllithium.

Claim 16

A process for preparing a hydrogenated polymer which comprises the steps of: polymerizing, under anionic solution polymerization conditions in a hydrocarbon diluent at polymerization temperatures employing an organoalkali metal or organoalkaline earth metal initiator, at least one conjugated diene or at least one conjugated diene with a copolymerizable vinylidine group-containing comonomer selected from the group consisting of monovinylarenes, hydrocarbyl substituted styrenes, monopropenylbenzenes, vinylnaphthalenes, vinylquinolines, vinylisoquinolines, and vinylpyridines, thereby preparing a conjugated diene polymer, treating said conjugated diene polymer with a silicon- or germanium-based coupling agent in a minor effective amount and under conditions effective to couple said conjugated diene polymer, thereby preparing a coupled conjugated diene polymer, treating said coupled conjugated diene polymer with a minor effective amount of an organometal treating agent which is a hydrocarbyl lithium, hydrocarbyl sodium, hydrocarbyl potassium, hydrocarbyl magnesium, hydrocarbyl calcium, hydrocarbyl zinc, hydrocarbyl aluminum, or hydrocarbyl aluminum hydride compound, wherein said minor effective amount of said organometal treating agent is effective to reduce the residual olefinic unsaturation of said coupled polymer on subsequent hydrogenation of said coupled polymer, and hydrogenating said organometal treated coupled conjugated diene polymer under hydrogenation conditions of a catalyst, time, temperature, and pressure, effective to substantially saturate at least the olefinically derived double bonds of said treated polymer, thereby producing a hydrogenated polymer.

Claim 17

A process for preparing a hydrogenated polymer which comprises the steps of: polymerizing, under anionic solution polymerization conditions in a hydrocarbon diluent at polymerization temperatures employing an organoalkali metal or organoalkaline earth metal initiator, at least one conjugated diene or at least one conjugated diene with a copolymerizable vinylidine group-containing comonomer selected from the group consisting of monovinylarenes, hydrocarbyl substituted styrenes, monopropenylbenzenes, vinylnaphthalenes, vinylquinolines, vinylisoquinolines, and vinylpyridines, thereby preparing a conjugated diene polymer, treating said conjugated diene polymer with a silicon- or germanium-based coupling agent in a minor effective amount and under conditions effective to couple said conjugated diene polymer, thereby preparing a coupled conjugated diene polymer, treating said coupled conjugated diene polymer with a minor effective amount of an organometal treating agent which is a hydrocarbyl lithium, hydrocarbyl sodium, hydrocarbyl potassium, hydrocarbyl magnesium, hydrocarbyl calcium, hydrocarbyl zinc, hydrocarbyl aluminum, or hydrocarbyl aluminum hydride compound, wherein said minor effective amount of said organometal treating agent is effective to reduce the residual olefinic unsaturation of said coupled polymer on subsequent hydrogenation of said coupled polymer, and hydrogenating said organometal treated coupled conjugated diene polymer under hydrogenation conditions of a catalyst, time, temperature, and pressure, effective to substantially saturate at least the olefinically derived double bonds of said treated polymer, thereby producing a hydrogenated polymer.

Claim 18

The process according to claim 13 wherein said organometal treating agent is represented by R a H b M c wherein M is said lithium, sodium, potassium, magnesium, calcium, zinc, or aluminum; a is 1 and b is 0 where M is lithium, sodium, or potassium; a is 2 and b is 0 where M is zinc, magnesium or calcium; and a is 1, 2, or 3 and b is 0, 1, or 2, such that a + b = 3, where M is aluminum; and each R is a hydrocarbyl radical of 1 to 12 carbon atoms.

Claim 19

The process according to claim 14 wherein said organometal treating agent is n-butyllithium, sec-butyllithium, tert-butyllithium, n-amylsodium, n-hexylpotassium, di-n-amylmagnesium, dimethylmagnesium, diethylmagnesium, di-isopropylcalcium, di-n-butylmagnesium, di(2-ethylhexyl)magnesium, diethylzinc, phenyllithium, diphenylmagnesium, benzyllithium, di-p-tolylmagnesium, p-tolyllithium, cyclohexyllithium, cyclohexyl-2-ethylpentylmagnesium, bis(3-phenylpropyl)magnesium, trimethylaluminum, triethylaluminum, di-n-butylaluminum hydride, 2-ethylhexylaluminum dihydride, triphenylaluminum, cyclohexylbis(2-ethylpentyl)aluminum, or mixtures thereof.

Claim 20

The process according to claim 15 wherein said minor effective amount of said organometal treating agent is in the range of about 0.1 to 25 gram millimoles per 100 grams of coupled polymer, and wherein said treating is conducted at a temperature in the range of about 10° C to 110° C.

Claim 21

The process according to claim 16 wherein said minor effective amount of said organometal treating agent is in the range of about 1 to 10 gram millimoles per 100 grams of coupled polymer, said treating temperature is in the range of about 20° C to 90° C, and wherein said hydrocarbon diluent is cyclohexane, methylcyclohexane, hexane, benzene, isooctane, or n-heptane.

Claim 22

The process according to claim 16 wherein said coupled polymer in said hydrocarbon diluent represents a concentration of said polymer of about 1 to 50 weight percent, and said organometal treating agent is employed as a solution in a hydrocarbon diluent of about 0.1 to 2 molar.

Claim 23

The process according to claim 18 wherein said hydrogenation is conducted at a temperature in the range of about 25° C to 175° C, under pressure of about 10 to 5000 psig, for a time of about 30 minutes to 4 hours, employing a catalyst comprising (B) a cobalt or nickel carboxylate or alkoxide, and (A) an aluminum alkyl in amounts effective for hydrogenation.

Claim 24

The process according to claim 11 wherein said conjugated diene polymer is a copolymer of a conjugated diene and a said monovinylarene.

Claim 25

The process according to claim 20 wherein said conjugated diene is selected from the group consisting of 1,3-butadiene, 2-methyl-1,3-butadiene, 2,3-dimethyl-1,2-butadiene, 1,3-pentadiene, 1,3-octadiene, 2-phenyl-1,3-butadiene, and 3-n-butyl-1,3-octadiene.

Claim 26

The process according to claim 21 wherein said initiator is selected from the group consisting of n-butyllithium, sec-butyllithium, tertbutyllithium, n-amylsodium, n-hexylpotassium, calcium anthracene, and n-phenylsodium, employing said initiator in amounts sufficient to provide about 0.05 to 100 gram milliequivalents of metal in the initiator per 100 grams monomer polymerized, and employing polymerization temperatures in the range of about 50° to 200° C under a pressure sufficient to maintain monomer and diluent substantially in the liquid phase.

Claim 27

The process according to claim 22 employing said silicon or germanium treating agent in an amount sufficient to provide about 0.5 to 2.0 equivalents of treating agent per equivalent of polymer-alkali metal or polymeralkaline earth metal.

Claim 28

The process according to claim 23 wherein said treating agent is a silicon treating agent, and is a silicon polyhalide, silane, or siloxane.

Claim 29

The process according to claim 23 wherein said treating agent is a germanium polyhalide or germane.

Claim 30

The process according to claim 24 wherein said treating agent is a silicon polyhalide and is silicon tetrachloride, the coupled polymer is a rubbery block copolymer of styrene and butadiene, and said organometal treating agent is n-butyllithium or triethylaluminum.