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US4191815A Expired / Lapsed US ⏱️ 0.0 years remaining

Hydrophile polyurethane foam, process for preparing said foam and hydrophile product based on said foam

Assignee: GECHEM
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Filing: 1977-03-11
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Granted: 1980-03-04
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Expires: 1997-03-11
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Abstract

Abstract A hydrophile polyurethane foam prepared from a hydrophile polyol, a polyisocyanate in which NCO groups are not directly bonded to an aromatic ring, a surface active agent, a swelling agent and a catalyst comprising: (A) at least one compound selected from the group consisting of: (1) diazabicyclo-alkenes of formula: ##STR1## (2) substituted guanidines and salts of formula: ##STR2## (3) substituted biguanidines of formula: ##STR3## (4) substituted biguanidines of formula: ##STR4## wherein the substituents can have different meanings, and (B) at least an alkali metal or alkaline earth metal salt of organic acids having a dissociation constant Ka<10 -1 .

Inventors

  • 👤 Lucien Jourquin
  • 👤 Eddie Du Prez

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-24 20:21
CPC Classifications
A; A61; A61L; A61L15/00; A61L15/16; A61L15/42; A61L15/425; C; C08; C08G; C08G18/00; C08G18/06; C08G18/08; C08G18/16; C08G18/161; C08G18/163; C08G18/28; C08G18/40; C08G18/48; C08G18/4833; C08G18/70; C08G18/72; C08G18/73; C08G18/74; C08G18/75; C08G18/751; C08G18/752; C08G18/753; C08G18/755; C08G18/758; C08G18/76; C08G18/7614; C08G18/7628; C08G18/7642; C08G2110/00; C08G2110/0008; C08G2110/0041; C08G2110/005; C08G2110/0083; Y; Y10; Y10S; Y10S521/00; Y10S521/905; Y10T; Y10T428/00; Y10T428/249921; Y10T428/249953; Y10T428/249987; Y10T428/249988; Y10T428/249989

Claims Analysis

Total Claims: 3
Claim 1
Independent Claim 658 words
A process for preparing a hydrophile polyurethane foam absorption material for medical and hygienic use comprising reaction of hydrophile polyol, a polyisocyanate wherein NCO groups are not directly bonded to an aromatic ring, a foam stabilizer, a swelling agent and an effective amount of a catalyst, wherein the catalyst consists essentially of: (A) at least one compound selected from the group consisting of (1)diazabicycloalkenes of the formula: ##STR23## wherein m varies from 3 to 7 and n from 2 to 4, and salts thereof with organic acids the dissociation constant of which is Ka≦10 -2 ; (2) substituted guanidines and salts thereof of the formula: ##STR24## wherein R 1 , R 2 , R 3 and R 4 can independently represent a C 1 -C 4 alkyl radical, a C 1 -C 4 alkyl radical substituted by a C 1 -C 4 alkoxy radical, or a heterocyclic C 5 -C 7 radical comprising at most two atoms from the group consisting of sulfur and oxygen, R 1 and R 2 and/or R 3 and R 4 may form with the adjacent nitrogen a heterocyclic C 5 -C 7 ring containing at most one member from the group consisting of sulfur or oxygen atom, X represents a member selected from the group consisting of hydrogen, phenyl, a phenyl group substituted by one or more C 1 -C 4 alkoxy radicals, C 1 -C 12 alkyl radicals or halogens, or represents a radical of the formula: ##STR25## wherein R 5 , R 6 and R 7 can independently represent hydrogen, a C 1 -C 4 alkyl radical or a C 1 -C 4 alkyl radical substituted by a member selected from the group consisting of phenyl, substituted phenyl, C 1 -C 4 alkoxy, C 6 -C 15 aryloxy, nitrile or carbalkoxy, or R 7 may represent a member selected from the group consisting of a C 5 -C 18 alkyl radical, a substituted phenyl radical or a C 1 -C 4 alkoxy radical; or one or two of the groups R 5 -R 6 , R 5 -R 7 or R 6 -R 7 can form a cyclic ring of more than one member selected from the group consisting of nitrogen, sulfur or oxygen atom, and X may also represent a radical of the formula: ##STR26## wherein z is an integer of from 2 to 12, R' and R" represent a member selected from the group consisting of hydrogen or a C 1 -C 4 alkyl radical, R''' and R'''' represent a member selected from the group consisting of a C 1 -C 4 alkyl radical or form with the adjacent nitrogen of a C 5 -C 6 cycloalkyl radical; and addition salts of said guanidines; and addition salts of guanidines; (3) substituted biguanidines of the formula: ##STR27## wherein Q 1 to Q 6 can independently represent a member selected from the group consisting of C 1 -C 4 alkyl or a C 3 -C 4 cycloalkyl radical, and X' is hydrogen or a carbamoyl radical of the formula: ##STR28## in which Z is a monovalent radical remaining after elimination of an isocyanate group from the above mentioned polyisocyanate, Q 1 to Q 6 , X' and Z may optionally be substituted by a member selected from the group consisting of chlorine, bromine or a C 1 or C 2 alkoxy radical; and (4 ) substituted biguanidines of the formula: ##STR29## wherein M 1 to M 8 can independently represent a C 1 -C 4 alkyl radical, Y represents a group of the formula: ##STR30## wherein M 9 and M 10 represent a member selected from the group consisting of hydrogen or a C 1 -C 4 alkyl radical, and α is an integer from 3 to 12 or represents a divalent cyclohexyl or a divalent isophorene radical; and (B) at least one alkali or alkaline earth metal salt of an organic acid having a dissociation constant Ka≦10 -1 .
Claim 2
Dependent Claim 658 words
A process for preparing a hydrophile polyurethane foam absorption material for medical and hygienic use comprising reaction of hydrophile polyol, a polyisocyanate wherein NCO groups are not directly bonded to an aromatic ring, a foam stabilizer, a swelling agent and an effective amount of a catalyst, wherein the catalyst consists essentially of: (A) at least one compound selected from the group consisting of (1)diazabicycloalkenes of the formula: ##STR23## wherein m varies from 3 to 7 and n from 2 to 4, and salts thereof with organic acids the dissociation constant of which is Ka≦10 -2 ; (2) substituted guanidines and salts thereof of the formula: ##STR24## wherein R 1 , R 2 , R 3 and R 4 can independently represent a C 1 -C 4 alkyl radical, a C 1 -C 4 alkyl radical substituted by a C 1 -C 4 alkoxy radical, or a heterocyclic C 5 -C 7 radical comprising at most two atoms from the group consisting of sulfur and oxygen, R 1 and R 2 and/or R 3 and R 4 may form with the adjacent nitrogen a heterocyclic C 5 -C 7 ring containing at most one member from the group consisting of sulfur or oxygen atom, X represents a member selected from the group consisting of hydrogen, phenyl, a phenyl group substituted by one or more C 1 -C 4 alkoxy radicals, C 1 -C 12 alkyl radicals or halogens, or represents a radical of the formula: ##STR25## wherein R 5 , R 6 and R 7 can independently represent hydrogen, a C 1 -C 4 alkyl radical or a C 1 -C 4 alkyl radical substituted by a member selected from the group consisting of phenyl, substituted phenyl, C 1 -C 4 alkoxy, C 6 -C 15 aryloxy, nitrile or carbalkoxy, or R 7 may represent a member selected from the group consisting of a C 5 -C 18 alkyl radical, a substituted phenyl radical or a C 1 -C 4 alkoxy radical; or one or two of the groups R 5 -R 6 , R 5 -R 7 or R 6 -R 7 can form a cyclic ring of more than one member selected from the group consisting of nitrogen, sulfur or oxygen atom, and X may also represent a radical of the formula: ##STR26## wherein z is an integer of from 2 to 12, R' and R" represent a member selected from the group consisting of hydrogen or a C 1 -C 4 alkyl radical, R''' and R'''' represent a member selected from the group consisting of a C 1 -C 4 alkyl radical or form with the adjacent nitrogen of a C 5 -C 6 cycloalkyl radical; and addition salts of said guanidines; and addition salts of guanidines; (3) substituted biguanidines of the formula: ##STR27## wherein Q 1 to Q 6 can independently represent a member selected from the group consisting of C 1 -C 4 alkyl or a C 3 -C 4 cycloalkyl radical, and X' is hydrogen or a carbamoyl radical of the formula: ##STR28## in which Z is a monovalent radical remaining after elimination of an isocyanate group from the above mentioned polyisocyanate, Q 1 to Q 6 , X' and Z may optionally be substituted by a member selected from the group consisting of chlorine, bromine or a C 1 or C 2 alkoxy radical; and (4 ) substituted biguanidines of the formula: ##STR29## wherein M 1 to M 8 can independently represent a C 1 -C 4 alkyl radical, Y represents a group of the formula: ##STR30## wherein M 9 and M 10 represent a member selected from the group consisting of hydrogen or a C 1 -C 4 alkyl radical, and α is an integer from 3 to 12 or represents a divalent cyclohexyl or a divalent isophorene radical; and (B) at least one alkali or alkaline earth metal salt of an organic acid having a dissociation constant Ka≦10 -1 .
Claim 3
Dependent Claim 40 words
A process as claimed in claim 1, comprising reaction according to the "one-shot" technique, of a hydrophile polyol, a polyisocyanate wherein NCO groups are not directly bonded to an aromatic ring, a foam stabilizer, a swelling agent and said catalyst.

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1983-03-04 1983-09-03 1984-03-04 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1987-03-04 1987-09-03 1988-03-04 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1991-03-04 1991-09-03 1992-03-04 $7700.00 Window Closed / Lapsed

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