GB1005047A - Improvements in and relating to segmented polyurethane copolymers - Google Patents

Improvements in and relating to segmented polyurethane copolymers

Info

Publication number
GB1005047A
GB1005047A GB1608864A GB1608864A GB1005047A GB 1005047 A GB1005047 A GB 1005047A GB 1608864 A GB1608864 A GB 1608864A GB 1608864 A GB1608864 A GB 1608864A GB 1005047 A GB1005047 A GB 1005047A
Authority
GB
United Kingdom
Prior art keywords
diphenyl
xylylenediamine
reacted
methylene
relating
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
GB1608864A
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.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
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 EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Publication of GB1005047A publication Critical patent/GB1005047A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08Processes
    • C08G18/10Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/58Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products
    • D01F6/70Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyurethanes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Artificial Filaments (AREA)

Abstract

A segmented polymer consisting essentially of a plurality of intralinear structural units of the formula <FORM:1005047/C3/1> wherein m and n are positive integers; G is a long chain polymeric radical free from substituents reactive with an isocyanate and having a M.W. above 950; and R is p,p1-methylene - diphenyl, p,p1 - isopropylidene-diphenyl, p,p1 - oxydiphenyl, p,p1 - thiodiphenyl, or the foregoing radicals having methyl or ethyl as ring substituents. The above polymer may be prepared by reacting a hydroxyl terminated polyether or polyester of M.W. above 1000 with an organic diisocyanate in a molar ratio of between 1.7 and 2.2 : 1 to provide a prepolymer of M.W. above 1500 which is then reacted with m-xylylenediamine. In a typical Example (1) the reaction product of excess p,p1-methylene diphenyl diisocyanate and polytetramethylene ether glycol is diisolved in N,N-dimethylacetamide and reacted with m-xylylenediamine and diethylamine and the solution dry-spun to produce elastic filaments. Specification 849,154 is referred to.
GB1608864A 1963-04-17 1964-04-17 Improvements in and relating to segmented polyurethane copolymers Expired GB1005047A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US27355863A 1963-04-17 1963-04-17

Publications (1)

Publication Number Publication Date
GB1005047A true GB1005047A (en) 1965-09-22

Family

ID=23044437

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1608864A Expired GB1005047A (en) 1963-04-17 1964-04-17 Improvements in and relating to segmented polyurethane copolymers

Country Status (6)

Country Link
BE (1) BE646637A (en)
CH (1) CH434557A (en)
DE (2) DE1494714C3 (en)
GB (1) GB1005047A (en)
LU (1) LU45896A1 (en)
NL (1) NL139048B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3483167A (en) * 1966-12-02 1969-12-09 Glanzstoff Ag Viscosity control in the chain extension of linear polyurethanes using a combination of chain extenders and a chain-stopper

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3483167A (en) * 1966-12-02 1969-12-09 Glanzstoff Ag Viscosity control in the chain extension of linear polyurethanes using a combination of chain extenders and a chain-stopper

Also Published As

Publication number Publication date
CH434557A (en) 1967-04-30
BE646637A (en) 1964-10-16
DE1904123U (en) 1964-11-12
LU45896A1 (en) 1964-06-17
DE1494714A1 (en) 1969-12-04
NL6404154A (en) 1964-10-19
DE1494714B2 (en) 1973-05-24
NL139048B (en) 1973-06-15
DE1494714C3 (en) 1973-12-13

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