GB1487766A - Aromatic diisocyanates and polymers thereof - Google Patents

Aromatic diisocyanates and polymers thereof

Info

Publication number
GB1487766A
GB1487766A GB5025574A GB5025574A GB1487766A GB 1487766 A GB1487766 A GB 1487766A GB 5025574 A GB5025574 A GB 5025574A GB 5025574 A GB5025574 A GB 5025574A GB 1487766 A GB1487766 A GB 1487766A
Authority
GB
United Kingdom
Prior art keywords
radical
weight
polymerized units
polymers
hydrogen
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB5025574A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Goodrich Corp
Original Assignee
Goodrich Corp
BF Goodrich Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Goodrich Corp, BF Goodrich Corp filed Critical Goodrich Corp
Priority to GB5025574A priority Critical patent/GB1487766A/en
Publication of GB1487766A publication Critical patent/GB1487766A/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/16—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms condensed with carbocyclic rings or ring systems
    • C07D249/18—Benzotriazoles
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F20/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
    • C08F20/02—Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
    • C08F20/10—Esters
    • C08F20/34—Esters containing nitrogen, e.g. N,N-dimethylaminoethyl (meth)acrylate
    • C08F20/36—Esters containing nitrogen, e.g. N,N-dimethylaminoethyl (meth)acrylate containing oxygen in addition to the carboxy oxygen, e.g. 2-N-morpholinoethyl (meth)acrylate or 2-isocyanatoethyl (meth)acrylate
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72—Polyisocyanates or polyisothiocyanates
    • C08G18/728—Polymerisation products of compounds having carbon-to-carbon unsaturated bonds and having isocyanate or isothiocyanate groups or groups forming isocyanate or isothiocyanate groups
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/20—Macromolecular organic compounds
    • D21H17/33—Synthetic macromolecular compounds
    • D21H17/34—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

1487766 Polymers containing blocked isocyanate groups B F GOODRICH CO 20 Nov 1974 50255/74 Heading C3P [Also in Division C2] A polymer comprises from about 0À1 to 100% by weight of polymerized units of an ethylenically unsaturated blocked aromatic diisocyanate of the formula wherein R is hydrogen or a methyl or ethyl radical; A is a carbonyloxyalkylene radical containing 2 to 8 carbon atoms or an aralkylene radical; B is a bivalent aromatic radical selected from arylene, naphthalene, and the structure where R is defined as above; Y is O, S, or -(-CH 2 -)- n ; n=0 to 3; X is the radical fragment remaining after a hydrogen atom is removed from the nitrogen atom of an oxime, benzimidazole, pyrazole, benzotriazole, caprolactam, thiocaprolactam, or p-nitroaniline, and up to 99À9% by weight of polymerized units of a copolymerizable vinylidene monomer.
GB5025574A 1974-11-20 1974-11-20 Aromatic diisocyanates and polymers thereof Expired GB1487766A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB5025574A GB1487766A (en) 1974-11-20 1974-11-20 Aromatic diisocyanates and polymers thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB5025574A GB1487766A (en) 1974-11-20 1974-11-20 Aromatic diisocyanates and polymers thereof

Publications (1)

Publication Number Publication Date
GB1487766A true GB1487766A (en) 1977-10-05

Family

ID=10455245

Family Applications (1)

Application Number Title Priority Date Filing Date
GB5025574A Expired GB1487766A (en) 1974-11-20 1974-11-20 Aromatic diisocyanates and polymers thereof

Country Status (1)

Country Link
GB (1) GB1487766A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5159011A (en) * 1990-07-16 1992-10-27 Basf Aktiengesellschaft Aqueous formulations of copolymer latices and polyisocyanate dispersions
FR2699182A1 (en) * 1992-12-15 1994-06-17 Rhone Poulenc Chimie Monomer having at least one isocyanate function and an insuturation its synthetic process and (co) polymers derived therefrom.

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5159011A (en) * 1990-07-16 1992-10-27 Basf Aktiengesellschaft Aqueous formulations of copolymer latices and polyisocyanate dispersions
FR2699182A1 (en) * 1992-12-15 1994-06-17 Rhone Poulenc Chimie Monomer having at least one isocyanate function and an insuturation its synthetic process and (co) polymers derived therefrom.
WO1994013712A1 (en) * 1992-12-15 1994-06-23 Rhone-Poulenc Chimie Monomer presenting at least one isocyanate function and an insaturation, synthesis process and (co)polymers derived therefrom

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Legal Events

Date Code Title Description
PS Patent sealed
PCNP Patent ceased through non-payment of renewal fee