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US3957913A Expired / Lapsed US ⏱️ 0.0 years remaining

Process for the preparation of thermoplastic elastomeric block copolymers

Assignee: Stamicarbon BV
•
Filing: 1974-04-12
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Granted: 1976-05-18
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Expires: 1994-04-12
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Abstract

Abstract Polyfunctional anionic initiators for the preparation of elastomeric block copolymers are prepared by reacting a monofunctional anionic initiator, such as secondary butyl lithium, with a monovinyl aromatic compound, such as styrene, or a conjugated diene, such as butadiene or isoprene or mixtures thereof to form a polyuric reaction product which in turn, is reacted with a polyvinyl aromatic compound, such as divinyl benzene. The cross-linked reaction product, prior to use, is reacted with styrene or another monovinyl aromatic compound. The resulting polyfunctional anionic initiators are useful in producing elastomeric block co-polymers of the A-B-(A)n type exhibiting good elastomeric properties.

Inventors

  • 👤 Bernard C. Roest
  • 👤 Herman A. J. Schepers

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-09 13:17
CPC Classifications
C; C08; C08F; C08F297/00; C08F297/02; C08F297/04; C08F297/046

Claims Analysis

Total Claims: 7
Claim 1
Independent Claim 313 words
Process for preparing elastomeric block copolymers having the general configuration: A -- B -- (A).sub.n wherein A is a non-elastomeric polymer block with a number average molecular weight between 200 and 100,000, and a glass transition temperature above 25°C. formed from a monovinyl aromatic compound having from 8-20 carbon atoms per molecule; B is an elastomeric polymer block with a number average molecular weight between 20,000 and 1,000,000, and a glass transition temperature below 10°C. formed from a conjugated diene having from 4-12 carbon atoms in its molecule; and n is a whole or fractional number; comprising polymerizing, in the presence of a polyfunctional anionic initiator, a monomer to form elastomeric block B and thereafter continuing said polymerization also in the presence of said polyfunctional anionic initiator to polymerize a monomer of mixture of monomers to form polymer blocks A attached to polymer block B; said polyfunctional anionic initiator prepared by reacting (a) a monofunctional anionic initiator having the formula: R -- Li wherein R is an alkyl having 1 - 12 carbon atoms or allyl or allyl substituted with a lower alkyl having 1 - 4 carbon atoms; with (b) a monovinyl aromatic compound having from 8 - 12 carbon atoms per molecule the molar ratio of component (a) being from 1 to 5000 for each mole of component (b), and reacting the polymeric reaction product of (a) and (b) with: (c) a polyvinyl aromatic compound having up to 24 carbon atoms per molecule at a temperature between 10°C. and 150°C. in molar ratio of 0.25 to 10 moles per mole of component (a), and thereafter reacting the cross-linked polymeric reaction product of components (a), (b) and (c) with: (d) a monovinyl aromatic compound having 8 - 12 carbon atoms per molecule in a molar ratio of 0.5 - 100 moles per mole of component (a), to produce said polyfunctional anionic initiator.
Claim 2
Dependent Claim 313 words
Process for preparing elastomeric block copolymers having the general configuration: A -- B -- (A).sub.n wherein A is a non-elastomeric polymer block with a number average molecular weight between 200 and 100,000, and a glass transition temperature above 25°C. formed from a monovinyl aromatic compound having from 8-20 carbon atoms per molecule; B is an elastomeric polymer block with a number average molecular weight between 20,000 and 1,000,000, and a glass transition temperature below 10°C. formed from a conjugated diene having from 4-12 carbon atoms in its molecule; and n is a whole or fractional number; comprising polymerizing, in the presence of a polyfunctional anionic initiator, a monomer to form elastomeric block B and thereafter continuing said polymerization also in the presence of said polyfunctional anionic initiator to polymerize a monomer of mixture of monomers to form polymer blocks A attached to polymer block B; said polyfunctional anionic initiator prepared by reacting (a) a monofunctional anionic initiator having the formula: R -- Li wherein R is an alkyl having 1 - 12 carbon atoms or allyl or allyl substituted with a lower alkyl having 1 - 4 carbon atoms; with (b) a monovinyl aromatic compound having from 8 - 12 carbon atoms per molecule the molar ratio of component (a) being from 1 to 5000 for each mole of component (b), and reacting the polymeric reaction product of (a) and (b) with: (c) a polyvinyl aromatic compound having up to 24 carbon atoms per molecule at a temperature between 10°C. and 150°C. in molar ratio of 0.25 to 10 moles per mole of component (a), and thereafter reacting the cross-linked polymeric reaction product of components (a), (b) and (c) with: (d) a monovinyl aromatic compound having 8 - 12 carbon atoms per molecule in a molar ratio of 0.5 - 100 moles per mole of component (a), to produce said polyfunctional anionic initiator.
Claim 3
Dependent Claim 14 words
Process as claimed in claim 1 wherein said monovinyl aromatic compound (b) is styrene.
Claim 4
Dependent Claim 27 words
Process as claimed in claim 1 wherein from 2 - 50 moles of monovinyl aromatic compound (d) are used for each mole of monofunctional anionic initiator (a).
Claim 5
Dependent Claim 27 words
Process as claimed in claim 3 wherein from 5 - 25 moles of monovinyl aromatic compound (d) are used for each mole of monofunctional anionic initiator (a).
Claim 6
Dependent Claim 17 words
Process as claimed in claim 1 wherein said polyvinyl aromatic compound of component (c) is divinyl benzene.
Claim 7
Dependent Claim 14 words
Process as claimed in claim 1 wherein said monovinyl aromatic compound (d) is styrene.

References Cited (Backward Citations)

US3562204A Cited
US3534965A Cited
US3644322A Cited
US3652516A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1979-05-18 1979-11-17 1980-05-18 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1983-05-18 1983-11-17 1984-05-18 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1987-05-18 1987-11-17 1988-05-18 $7700.00 Window Closed / Lapsed

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