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US4456685A Expired / Lapsed US ⏱️ 0.0 years remaining

Microorganisms immobilized with hydrolysis resistant polyurethane foam

Assignee: Hampshire Chemical Corp
•
Filing: 1982-08-23
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Granted: 1984-06-26
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Expires: 2002-08-23
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Abstract

Abstract Foams having aspartase-producing microorganisms bound to the foam are made from polyurethane prepolymers which are capped with polyisocyanates, including diisocyanates, derived from methylene-bis (phenyl isocyanate) which is commonly known as MDI. These MDI based foams are hydrolysis resistant as compared to the previously used TDI based foams. The foams can be used to produce L-aspartic acid under high pH conditions.

Inventors

  • 👤 James L. Guthrie

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-24 19:52
CPC Classifications
C; C08; C08J; C08J9/00; C08J9/0004; C12; C12N; C12N11/00; C12N11/02; C12N11/08; C12N11/089; C12N11/093; C12N11/098; C12P; C12P13/00; C12P13/04; C12P13/20; C08J2375/00; C08J2375/04

Claims Analysis

Total Claims: 20
Claim 1
Independent Claim 168 words
A water insoluble, hydrolysis resistant, hydrophilic polyether polyurea polyurethane foam having aspartase-producing microorganisms bound to the foam prepared by reacting under foaming conditions an aqueous mixture containing a culture of aspartase-producing microorganisms and a hydrophilic polyether polyurethane prepolymer, said foam having a weight ratio of polyurea polyurethane polymer to microorganisms in the foam ranging from about 2 to about 4, a weight ratio of prepolymer to water is from about 2 to about 0.5, and said prepolymer having an isocyanate functionality in excess of 2 but not greater than 8 with at least 50 mole % of the alkylene oxide units in the polyether segments of the polyurethane being ethylene oxide, and obtained by reacting a poly(oxy-C 2-4 alkylene) diol having at least about 50% by weight of oxyethylene groups. a diphenylmethane diisocyanate-containing isocyanate product with a functionality of greater than 2.0 comprising a mixture of diphenylmethane diisocyanate and isocyanate containing derivatives of diphenylmethane diisocyanate, and a polyol cross-linking agent having 3 or 4 hydroxyl equivalents per mole.
Claim 2
Dependent Claim 168 words
A water insoluble, hydrolysis resistant, hydrophilic polyether polyurea polyurethane foam having aspartase-producing microorganisms bound to the foam prepared by reacting under foaming conditions an aqueous mixture containing a culture of aspartase-producing microorganisms and a hydrophilic polyether polyurethane prepolymer, said foam having a weight ratio of polyurea polyurethane polymer to microorganisms in the foam ranging from about 2 to about 4, a weight ratio of prepolymer to water is from about 2 to about 0.5, and said prepolymer having an isocyanate functionality in excess of 2 but not greater than 8 with at least 50 mole % of the alkylene oxide units in the polyether segments of the polyurethane being ethylene oxide, and obtained by reacting a poly(oxy-C 2-4 alkylene) diol having at least about 50% by weight of oxyethylene groups. a diphenylmethane diisocyanate-containing isocyanate product with a functionality of greater than 2.0 comprising a mixture of diphenylmethane diisocyanate and isocyanate containing derivatives of diphenylmethane diisocyanate, and a polyol cross-linking agent having 3 or 4 hydroxyl equivalents per mole.
Claim 3
Dependent Claim 32 words
A foam according to claim 1, wherein said isocyanate product comprises a mixture of a major amount of pure diphenylmethane diisocyanate and minor amounts of carbodiimides and trifunctional cycloadducts of diphenylmethane diisocyanate.
Claim 4
Dependent Claim 444 words
A foam according to claim 1, wherein said prepolymer is either (A) a prepolymer derived from (a) a poly(oxy C 2-4 alkylene) diol having at least about 50% by weight of oxyethylene groups and a nominal number average molecular weight of about at least 1100, said diol having nominally two hydroxyl equivalents per mole, (b) a diphenylmethane diisocyanate-containing isocyanate product with a functionality of greater than 2.0 comprising a mixture of diphenylmethane diisocyanate and isocyanate containing derivatives of diphenylmethane diisocyanate, and (c) a monomeric polyol crosslinking agent having 3 or 4 hydroxyl equivalents per mole, said isocyanate containing product comprising less than 50% by weight of the prepolymer, said diol and polyol crosslinking agent being present in a mole ratio in the range of about 4:1 to 8:1, and the ratio of the isocyanate equivalents to the total hydroxyl equivalents being in the range of about 2.5:1 to 3.5:1; (B) a prepolymer derived from (a) a poly(oxy C 2-4 alkylene) diol having at least about 50% by weight of oxyethylene groups and a nominal number average molecular weight of about less than 2000, said diol having nominally two hydroxyl equivalents per mole, (b) a diphenylmethane diisocyanate-containing isocyanate product with a functionality of greater than 2.0 comprising a mixture of diphenylmethane diisocyanate and isocyanate containing derivatives of diphenylmethane diisocyanate, and (c) a polymeric poly(oxy C 2-4 alkylene) polyol crosslinking agent having 3 or 4 hydroxyl equivalents per mole, and having a number average molecular weight of at least 500 said isocyanate containing product comprising less than 50% weight of the prepolymer, said polymeric polyol crosslinking agent being present so that the hydroxy equivalents constitute 5 to 35 mole % of the total hydroxy equivalents in the diol and polyol, the ratio of the isocyanate equivalents to the total hydroxyl equivalents being in the range of about 2.5:1 to 3.5:1; or (C) a prepolymer derived from (a) a poly(oxy C 2-4 alkylene) diol having at least about 50% by weight of oxyethylene groups and a nominal number average molecular weight of about at most 1100, said diol having nominally two hydroxyl equivalents per mole, (b) a diphenylmethane diisocyanate-containing isocyanate product with a functionality of greater than 2.0 comprising a mixture of diphenylmethane diisocyanate and isocyanate containing derivatives of diphenylmethane diisocyanate, and (c) a monomeric polyol cross-linking agent having 3 or 4 hydroxyl equivalents per mole, said isocyanate product comprising more than 50% by weight of the prepolymer, said diol and polyol crosslinking agent being present in a mole ratio in the range of 4:1 to 8:1, and the ratio of the isocyanate equivalents to the total hydroxyl equivalents being in the range of 3:1 to 4:1.
Claim 5
Dependent Claim 73 words
A foam according to claim 3, wherein the nominal number average molecular weight of the poly(oxy C 2-4 alkylene) diol in part A is between 1100 and 2000 and the diol has at least 80% by weight of oxyethylene groups and wherein the nominal number average molecular weight of the poly(oxy C 2-4 alkylene) diol in part B is 600-2000 and the diol has preferably at least 80% by weight of oxyethylene groups.
Claim 6
Dependent Claim 51 words
A foam according to claim 4, wherein the nominal number average molecular weight of the poly(oxy C 2-4 alkylene) diol in part A is between 1200 and 1500 and wherein the nominal number average molecular weight of the poly(oxy C 2-4 alkylene) diol in part B is between 950 and 1500.
Claim 7
Dependent Claim 33 words
A foam according to claim 3, wherein the poly(oxy C 2-4 alkylene) diol in part A comprises a mixture of at least 2 diols each having a different nominal number average molecular weight.
Claim 8
Dependent Claim 39 words
A foam according to claim 6, wherein the poly(oxy C 2-4 alkylene) diol in part A comprises a mixture of a diol with a molecular weight of about 1000 and a diol of a molecular weight of about 1450.
Claim 9
Dependent Claim 74 words
A foam according to claim 3, wherein the polyol crosslinking agent in part A and part C is selected from the group consisting of trimethylolpropane, trimethylolethane, glycerol, triethanolamine, pentaerythritol, and mixtures thereof and wherein the polymeric polyol crosslinking agent in part B is selected from the group consisting of a poly(oxyethylene) triol having a molecular weight of about 900, and an oxyethylene-capped poly(oxypropylene) triol having a molecular weight of about 1400 and mixtures thereof.
Claim 10
Dependent Claim 40 words
A foam according to claim 3, wherein the nominal number average molecular weight of the poly(oxy C 2-4 alkylene) diol in part C is between 600 and 1100 and the diol has at least 80% by weight of oxyethylene groups.
Claim 11
Dependent Claim 32 words
A foam according to claim 3, wherein said isocyanate product comprises a mixture of a major amount of pure diphenylmethane diisocyanate and minor amounts of carbodiimides and trifunctional cycloadducts of diphenylmethane diisocyanate.
Claim 12
Dependent Claim 21 words
A process for preparing L-aspartic acid wherein a substrate comprising fumarate ion is contacted with the foam according to claim 1.
Claim 13
Dependent Claim 17 words
A process as in claim 11, wherein the substrate has a pH of from 8 to 10.
Claim 14
Dependent Claim 19 words
A process as in claim 11, wherein the temperature of the substrate is from 15° C. to 60° C.
Claim 15
Dependent Claim 12 words
A process as in claim 11, wherein the substrate comprises ammonium fumarate.
Claim 16
Dependent Claim 12 words
A process as in claim 11, wherein the substrate comprises magnesium ion.
Claim 17
Dependent Claim 14 words
A process as in claim 11, said process carried out on a continuous basis.
Claim 18
Dependent Claim 14 words
A process as in claim 11, said process carried out on a batch basis.
Claim 19
Dependent Claim 21 words
A process for preparing L-aspartic acid wherein a substrate comprising fumarate ion is contacted with the foam according to claim 2.
Claim 20
Dependent Claim 21 words
A process for preparing L-aspartic acid wherein a substrate comprising fumarate ion is contacted with the foam according to claim 3.

References Cited (Backward Citations)

US3929574A Cited
US4312946A Cited
US4342834A Cited
US4160076A Cited
US4377645A Cited
US4384050A Cited
US4384051A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1987-06-26 1987-12-26 1988-06-26 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1991-06-26 1991-12-26 1992-06-26 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1995-06-26 1995-12-26 1996-06-26 $7700.00 Window Closed / Lapsed

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