← Back to Patent Explorer
US4987207A Expired / Lapsed US ⏱️ 0.0 years remaining

Thermosetting resin compositions

Assignee: Mitsui Chemicals Inc
•
Filing: 1989-05-15
•
Granted: 1991-01-22
•
Expires: 2009-05-15
📄 Original PDF 🌐 Google Patents 🔄 Sync Now

Abstract

Abstract The present invention relates to a thermosetting resin composition comprising about 100 parts by weight of a polyimide and from 5 to about 100 parts by weight of a bismaleimide having a similar structure and processes for preparing the same.

Inventors

  • 👤 Norimasa Yamaya
  • 👤 Masahiro Ohta
  • 👤 Akihiro Yamaguchi

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-06 19:58
CPC Classifications
C; C08; C08L; C08L79/00; C08L79/04; C08L79/08; C08K; C08K5/00; C08K5/36; C08K5/37; C08K5/375; C08K5/16; C08K5/34; C08K5/3412; C08K5/3415; C08K5/41

Claims Analysis

Total Claims: 13
Claim 1
Independent Claim 218 words
A thermosetting resin composition comprising: (i) about 100 parts by weight of a polymer having recurring units represented by the formula (I): ##STR12## wherein R 1 represents a divalent group selected from the group consisting of ##STR13## X is selected from the group consisting of a direct bond, divalent hydrocarbon groups containing from about 1 to about 10 carbon atoms, hexafluorinated isopropylidene groups, carbonyl groups, thio groups, sulfinyl groups, sulfonyl groups and oxo groups, and Z represents at least one compound selected from the group consisting of ##STR14## wherein Y represents a tetravalent group selected from the group consisting of aliphatic groups having at least two carbon atoms, cycloaliphatic groups, monocyclic aromatic groups, fused polycyclic aromatic groups, and non-fused cyclic aromatic groups composed of aromatic groups bonded together directly or via a crosslink; and (ii) from about 5 to about 100 parts by weight of a bismaleimide compound selected from the group consisting of compounds of the formula (II): ##STR15## and compounds of the formula (III): ##STR16## wherein R 2 represents a divalent group selected from the group consisting of ##STR17## X is selected from the group consisting of a direct bond, divalent hydrocarbon groups having from about 1 to about 10 carbon atoms, hexafluorinated isopropylidene groups, carbonyl groups, thio groups, sulfinyl groups, sulfonyl groups and oxo groups.
Claim 2
Dependent Claim 218 words
A thermosetting resin composition comprising: (i) about 100 parts by weight of a polymer having recurring units represented by the formula (I): ##STR12## wherein R 1 represents a divalent group selected from the group consisting of ##STR13## X is selected from the group consisting of a direct bond, divalent hydrocarbon groups containing from about 1 to about 10 carbon atoms, hexafluorinated isopropylidene groups, carbonyl groups, thio groups, sulfinyl groups, sulfonyl groups and oxo groups, and Z represents at least one compound selected from the group consisting of ##STR14## wherein Y represents a tetravalent group selected from the group consisting of aliphatic groups having at least two carbon atoms, cycloaliphatic groups, monocyclic aromatic groups, fused polycyclic aromatic groups, and non-fused cyclic aromatic groups composed of aromatic groups bonded together directly or via a crosslink; and (ii) from about 5 to about 100 parts by weight of a bismaleimide compound selected from the group consisting of compounds of the formula (II): ##STR15## and compounds of the formula (III): ##STR16## wherein R 2 represents a divalent group selected from the group consisting of ##STR17## X is selected from the group consisting of a direct bond, divalent hydrocarbon groups having from about 1 to about 10 carbon atoms, hexafluorinated isopropylidene groups, carbonyl groups, thio groups, sulfinyl groups, sulfonyl groups and oxo groups.
Claim 3
Dependent Claim 95 words
The thermosetting resin composition of claim 1, wherein said polymer is a polyamic acid prepared by reacting (a) a diamine compound of the formula (IV): ##STR18## wherein R 3 represents a divalent group selected from the group consisting of ##STR19## X is selected from the group consisting of a direct bond, divalent hydrocarbon groups having from about 1 to about 10 carbon atoms, hexafluorinated isopropylidene groups, carbonyl groups, thio groups, sulfinyl groups, sulfonyl groups and oxo groups, with (b) a compound selected from the group consisting of at least one tetracarboxylic dianhydride and a polyimide.
Claim 4
Dependent Claim 25 words
The resin composition of claim 2 wherein in said diamine compound of the formula (IV), R 3 is selected from the group consisting of ##STR20##
Claim 5
Dependent Claim 49 words
The resin composition of claim 2, wherein said tetracarboxylic dianhydride has the formula (V): ##STR21## wherein Y is a tetravalent group selected from the group consisting of aliphatic groups having at least two carbon atoms, cycloaliphatic groups, monocyclic aromatic groups, fused polycyclic aromatic groups, and non-fused cyclic aromatic groups.
Claim 6
Dependent Claim 78 words
The resin composition of claim 4 wherein Y is a tetravalent group selected from the group consisting of aliphatic hydrocarbons having from 1 to 4 carbon atoms, cycloaliphatic hydrocarbons having from 4 to 8 carbon atoms, ##STR22## wherein X is selected from the group consisting of a direct bond, aliphatic hydrocarbons having from 1 to 4 carbon atoms, aliphatic hydrocarbons having from 1 to 4 carbon atoms substituted by from 1 to 6 fluorine atoms, --O--, --CO--, ##STR23##
Claim 7
Dependent Claim 22 words
The resin composition of claim 2 wherein said diamine compound is selected from the group consisting of 4,4'-bis(3-aminophenoxy)biphenyl, 2,2-bis[4-(3-aminophenoxy)phenyl]propane, bis[4-(3aminophenoxy)phenyl]sulfite and 1,3-bis(3-aminophenoxy)benzene.
Claim 8
Dependent Claim 21 words
The resin composition of claim 2 wherein said tetracarboxylic dianhydride selected from the group consisting of pyromellitic dianhydride and 3,3',4,4'-benzophenonetetracarboxylic dianhydride.
Claim 9
Dependent Claim 23 words
The resin composition of claim 1 wherein said bismaleimide compound is selected from the group consisting of N,N'-4,4'-diphenylmethanebismaleimide, 4,4'-bis(3-maleimidophenoxy)biphenyl, 2,2-bis[4-(3maleimidophenoxy)phenyl]propane, bis[4-(3-maleimidophenoxy)phenyl]sulfide and 1,3-bis(3-maleimidophenoxy)benzene.
Claim 10
Dependent Claim 223 words
A process for preparing a thermosetting resin composition comprising mixing (i) about 100 parts by weight of a polymer having recurring units represented by the formula (I): ##STR24## wherein R 1 represents a divalent group selected from time group consisting of ##STR25## X is selected from the group consisting of a direct bond, divalent hydrocarbon groups having from about 1 to about 10 carbon atoms, hexafluorinated isopropylidene groups, carbonyl groups, thio groups, sulfinyl groups, sulfonyl groups and oxo groups, and Z represents at least one compound selected from the group consisting of ##STR26## wherein Y represents a tetravalent group selected from the group consisting of aliphatic groups having at least two carbon atoms, cycloaliphatic groups, monocyclic aromatic groups, fused polycyclic aromatic groups, and non-fused cyclic aromatic groups composed of aromatic groups bonded together directly or via a crosslink, and (ii) from about 5 to about 100 parts by weight of a bismaleimide compound selected from the group consisting of compounds of the formula (II): ##STR27## and compounds of the formula (III): ##STR28## wherein R 2 represents a divalent group selected from the group consisting of ##STR29## X is selected from the group consisting of a direct bond, divalent hydrocarbon groups having from about 1 to about 10 carbon atoms, hexafluorinated isopropylidene groups, carbonyl groups, thio groups, sulfinyl groups, sulfonyl groups and oxo groups.
Claim 11
Dependent Claim 223 words
A process for preparing a thermosetting resin composition comprising mixing (i) about 100 parts by weight of a polymer having recurring units represented by the formula (I): ##STR24## wherein R 1 represents a divalent group selected from time group consisting of ##STR25## X is selected from the group consisting of a direct bond, divalent hydrocarbon groups having from about 1 to about 10 carbon atoms, hexafluorinated isopropylidene groups, carbonyl groups, thio groups, sulfinyl groups, sulfonyl groups and oxo groups, and Z represents at least one compound selected from the group consisting of ##STR26## wherein Y represents a tetravalent group selected from the group consisting of aliphatic groups having at least two carbon atoms, cycloaliphatic groups, monocyclic aromatic groups, fused polycyclic aromatic groups, and non-fused cyclic aromatic groups composed of aromatic groups bonded together directly or via a crosslink, and (ii) from about 5 to about 100 parts by weight of a bismaleimide compound selected from the group consisting of compounds of the formula (II): ##STR27## and compounds of the formula (III): ##STR28## wherein R 2 represents a divalent group selected from the group consisting of ##STR29## X is selected from the group consisting of a direct bond, divalent hydrocarbon groups having from about 1 to about 10 carbon atoms, hexafluorinated isopropylidene groups, carbonyl groups, thio groups, sulfinyl groups, sulfonyl groups and oxo groups.
Claim 12
Dependent Claim 21 words
The process of claim 9 wherein said bismaleimide compound is dissolved in a polymer varnish prior to mixing with said polymer.
Claim 13
Dependent Claim 21 words
The process of claim 9 wherein said bismaleimide compound is dissolved in a polymer suspension prior to mixing with said polymer.

References Cited (Backward Citations)

US4255313A Cited
US4362826A Cited
EP0107897A1 Cited
US4621122A Cited
JPS63191810A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1994-01-21 1994-07-23 1995-01-22 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1998-01-21 1998-07-23 1999-01-22 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2002-01-21 2002-07-23 2003-01-22 $7700.00 Window Closed / Lapsed

Assigned Categories & Tags

No categories assigned to this patent yet.

Assign Category Tag