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US4918148A Expired / Lapsed US ⏱️ 0.0 years remaining

Polyamide modified with monoisocyanates

Assignee: Bayer AG
•
Filing: 1988-10-03
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Granted: 1990-04-17
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Expires: 2008-10-03
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Abstract

Abstract The reaction of--preferably partially crystalline--polyamides with monoisocyanate or monoisocyanate precursors gives products having improved flowability, mould release and/or notched impact strength.

Inventors

  • 👤 Rolf-Volker Meyer
  • 👤 Josef Merten
  • 👤 Rolf Dhein
  • 👤 Harald Selbeck

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-04 23:18
CPC Classifications
C; C08; C08G; C08G69/00; C08G69/48; C08G18/00; C08G18/06; C08G18/28; C08G18/40; C08G18/60; C08G18/603; C08G18/70; C08G18/71; C08K; C08K5/00; C08K5/16; C08K5/29; C08G2250/00

Claims Analysis

Total Claims: 16
Claim 1
Independent Claim 127 words
A thermoplastically processable polyamide molding coposition obtained by melt blending 95.5 to 97% by weight of a polyamide with 0.5 to 3% by weight of at least one organic monoisocyanate of the formula where R is (i) a hydrocarbon radical containing at least six carbon atoms selected form an aliphatic radical, a cycloaliphatic radical, an araliphatic radical or an aromatic radical, (ii) a substituted hydrocarbon radical containing at least six carbon atoms selected from a substituted aliphatic radical, a substituted cycloaliphatic radical, a substituted araliphatic radical or a substituted aromatic radical or (iii) an organic radical comprised of a hydrocarbon radical (i), (ii) or a mixture thereof and bridging members selected from sulfur, oxygen or amide groups where the R does not include any additional NCO groups.
Claim 2
Dependent Claim 127 words
A thermoplastically processable polyamide molding coposition obtained by melt blending 95.5 to 97% by weight of a polyamide with 0.5 to 3% by weight of at least one organic monoisocyanate of the formula where R is (i) a hydrocarbon radical containing at least six carbon atoms selected form an aliphatic radical, a cycloaliphatic radical, an araliphatic radical or an aromatic radical, (ii) a substituted hydrocarbon radical containing at least six carbon atoms selected from a substituted aliphatic radical, a substituted cycloaliphatic radical, a substituted araliphatic radical or a substituted aromatic radical or (iii) an organic radical comprised of a hydrocarbon radical (i), (ii) or a mixture thereof and bridging members selected from sulfur, oxygen or amide groups where the R does not include any additional NCO groups.
Claim 3
Dependent Claim 125 words
A thermoplastically processable polyamide molding composition obtained by melt blending 95.5 to 97% by weight of a polyamide with 0.5 to 3% by weight of at least one organic monoisocyanate of the formula R--NCO formed by reacting 1 mole of (i) a monocarboxylic acid containing six carbon atoms selected from an aliphatic carboxylic acid, a cycloaliphatic carboxylic acid, an araliphatic carboxylic acid or an aromatic carboxylic acid or (ii) a substituted monocarboxylic acid containing at least six carbon atoms substituted with halogen in one or more positions selected from a substituted aliphatic carboxylic acid, a substituted cycloaliphatic carboxylic acid, a substituted araliphatic carboxylic acid or a substituted aromatic carboxylic acid with 1 mole of an isocyanate selected from toluylene diisocyanates, diphenylmethane diisocyanates or hexamethylene diisocyanates.
Claim 4
Dependent Claim 125 words
A thermoplastically processable polyamide molding composition obtained by melt blending 95.5 to 97% by weight of a polyamide with 0.5 to 3% by weight of at least one organic monoisocyanate of the formula R--NCO formed by reacting 1 mole of (i) a monocarboxylic acid containing six carbon atoms selected from an aliphatic carboxylic acid, a cycloaliphatic carboxylic acid, an araliphatic carboxylic acid or an aromatic carboxylic acid or (ii) a substituted monocarboxylic acid containing at least six carbon atoms substituted with halogen in one or more positions selected from a substituted aliphatic carboxylic acid, a substituted cycloaliphatic carboxylic acid, a substituted araliphatic carboxylic acid or a substituted aromatic carboxylic acid with 1 mole of an isocyanate selected from toluylene diisocyanates, diphenylmethane diisocyanates or hexamethylene diisocyanates.
Claim 5
Dependent Claim 17 words
A thermoplastically processable polyamide molding composition in accordance with claim 1, wherein the substitution is halogen substitution.
Claim 6
Dependent Claim 17 words
A thermoplastically processable polyamide molding composition in accordance withh claim 2, wherein the substitution is halogen substitution.
Claim 7
Dependent Claim 19 words
A thermoplastically processable polyamide molding composition in accordance with claim 1, wherein R contains at least ten carbon atoms.
Claim 8
Dependent Claim 24 words
A thermoplastically processable polyamide molding composition in accordance with claim 2, wherein the substituted or unsubstituted hydrocarbon radical contains at least ten carbon atoms.
Claim 9
Dependent Claim 29 words
A thermoplastically processable polyamide molding composition in accordance with claim 1, wherein R is a substituted or unsubstituted aliphatic or cycloaliphatic radical containing from 6 to 50 carbon atoms.
Claim 10
Dependent Claim 29 words
A thermoplastically processable polyamide molding composition in accordance with claim 2, wherein R is a substituted or unsubstituted aliphatic or cycloaliphatic radical containing from 6 to 50 carbon atoms.
Claim 11
Dependent Claim 27 words
A thermoplastically processable polyamide molding composition in accordance with claim 1, wherein R is a substituted or unsubstituted araliphaic radical containing from 7 to 50 carbon atoms.
Claim 12
Dependent Claim 27 words
A thermoplastically processable polyamide molding composition in accordance with claim 2, wherein R is a substituted or unsubstituted araliphatic radical containing from 7 to 50 carbon atoms.
Claim 13
Dependent Claim 98 words
A thermoplastically processable polyamide molding composition in accordance with claim 2, wherein the monoisocyanate is selected from hexylisocyanate, 6-chlorohexyl isocyanate, n-octyl isocyanate, cyclohexyl isocyanate, 2-ethylhexyl isocyanate, 2,3,4-methylcyclohexyl isocyanate, 3,3,5-trimethylcyclohexyl isocyanate, 2-norbornyl-methyl isocyanate, decyl isocyanate, dodecyl isocyanate, tetradecyl isocyanate, hexadecyl isocyanate, octadecyl isocyanate, technical stearyl isocyanate (mixture of C 12 -C 18 -alkyl isocyanates), 3-butoxypropyl isocyanate, 3-(2-ethylhexyloxy)-propyl isocyanate, phenyl isocyanate, tolyl isocyanates, chlorophenyl isocyanates (2,3,5-isomers), dichlorophenyl isocyanates, 4-nitrophenyl isocyanate, 3-trifluoromethylphenyl isocyanate, benzyl isocyanate, dimethylphenyl isocyanates (technical mixture and individual isomers), nonyl-phenylisocyanate, dodecyl-phenyl isocyanates, 4-cyclohexylphenyl isocyanate, 1-naphthyl isocyanate, (6-isocyanatohexyl)-stearic acid amide, (3-isocyanatotolyl)-stearic acid amide, (6-isocyanatohexyl)-benzamide, (3-isocyanatophenyl) stearic amide or 4-monoisocyanate-4'(stearylamido)-diphenyl-methane.
Claim 14
Dependent Claim 43 words
A thermoplastically processable polyamide molding composition in accordance with claim 11 wherein the monoisocyanate is selected from dodecyl isocyanate, tetradecyl isocyanate, octadecyl isocyanate, technical stearyl isocyanate (mixture of C 12-18 -alkyl isocyanates), (3-isocyanatotolyl)-stearylamide, chlorophenyl isocyanate, nonyl phenyl isocyanate, dodecylphenyl isocyanate or 4-isocyanate-4'-(stearyl amido)-diphenylmethane.
Claim 15
Dependent Claim 29 words
A thermoplastically processable polyamide molding composition in accordance with claim 1, wherein the polyamide is polyamide -6, -6,6, -6,9, -6,10, -6,12, -11 or -12, corresponding copolyamides or mixtures thereof.
Claim 16
Dependent Claim 29 words
A pharmaceutically processable polyamide molding composition in accordance with claim 2, wherein the polyamide is polyamide -6, -6,6, -6,9, -6,10, -6,12, -11 or -12, corresponding copolyamides or mixtures thereof.

References Cited (Backward Citations)

US2333914A Cited
US3545911A Cited
US3668171A Cited
US3867352A Cited
JPS5013697A Cited
US4600752A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1993-04-16 1993-10-16 1994-04-17 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1997-04-16 1997-10-16 1998-04-17 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2001-04-16 2001-10-16 2002-04-17 $7700.00 Window Closed / Lapsed

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