[go: up one dir, main page]

GB885234A - Polyurethane compositions - Google Patents

Polyurethane compositions

Info

Publication number
GB885234A
GB885234A GB2057757A GB2057757A GB885234A GB 885234 A GB885234 A GB 885234A GB 2057757 A GB2057757 A GB 2057757A GB 2057757 A GB2057757 A GB 2057757A GB 885234 A GB885234 A GB 885234A
Authority
GB
United Kingdom
Prior art keywords
catalyst
polyisocyanate
piperazine
reactants
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
GB2057757A
Inventor
Kurt Charles Frisch
Walter Franz Schulz
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.)
Wyandotte Chemicals Corp
Original Assignee
Wyandotte Chemicals 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 Wyandotte Chemicals Corp filed Critical Wyandotte Chemicals Corp
Priority to GB2057757A priority Critical patent/GB885234A/en
Priority to DEW23489A priority patent/DE1089164B/en
Priority to FR1208564D priority patent/FR1208564A/en
Publication of GB885234A publication Critical patent/GB885234A/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
    • C08G18/16Catalysts
    • C08G18/18Catalysts containing secondary or tertiary amines or salts thereof
    • C08G18/20Heterocyclic amines; Salts thereof
    • C08G18/2009Heterocyclic amines; Salts thereof containing one heterocyclic ring
    • C08G18/2027Heterocyclic amines; Salts thereof containing one heterocyclic ring having two nitrogen atoms in the ring

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polyurethanes Or Polyureas (AREA)

Abstract

Odourless polyurethane compositions comprise the reaction product of a polyisocyanate, an active hydrogen-containing compound, and an amount, preferably 0,25 to 5,0 parts per 100 parts of the other two reactants, of an N,N1-bis (2-hydroxyalkyl) piperazine as catalyst. By including water among the reactants foamed products are obtained. The catalyst conforms to the structural formula <FORM:0885234/IV (a)/1> wherein R1 and R2, and R3, R4, R5 and R6 are hydrogen, alkyl, aryl or alkylaryl; R1 and R2 are preferably ethyl or propyl groups, and 2-methyl-and 2,5-dimethyl piperazine compounds are preferred. Specified reactive hydrogen-containing compounds include polyesters, polyesteramides, polyalcohols, and polyether alcohols. Suitable polyisocyanates are listed in the Specification and include ethylene-, propylene 1,2-, butylene 1,3-, cyclohexylane 1,2- 2,4- toluene-, triphenylmethane-, 3,31-dimethyl-, and 4,4-biphenylenediisocyanate. The polyurethane reaction may be effected by conventional technique, e.g. all the reactants may be simultaneously mixed together or the catalyst may be dissolved in water and the reactive hydrogen-containing organic compound added, followed by polyisocyanate; alternatively excess polyisocyanate may be reacted with reactive hydrogen-containing compound and aqueous piperazine catalyst solution added to the "prepolymer" formed in amount stoichiometrically equivalent to the "free" isocyanate content thereof. Reference has been directed by the Comptroller to Specifications 754,502 and 795,276.ALSO:Odourless foamed polyurethane products comprise the reaction product of water, a polyisocyanate, an active hydrogen-containing compound, and an amount, preferably 0,25 to 5,0 parts per 100 parts of the former two reactants, of an N-N1 bis (2-hydroxyalkyl) piperazine as catalyst which conforms to the structural formula:- <FORM:0885234/V/1> wherein R1 and R2, and R3, R4, R5 and R6 are hydrogen, alkyl, aryl, or alkylaryl; R1 and R2 are preferably ethyl or propyl groups; 2-methyl-and 25-dimethyl substituted piperazine compounds are preferred. Specified reactive hydrogen-containing compounds include polyesters, polyesteramides, polyalcohols, and polyether alcohols. Suitable polyisocyanates are listed in the Specification and include ethylenepropylene 1,2-; butylene 1,3-; cyclohexene 1,2-; 2,4-toluene-; triphenylmethane-, 3,31-dimethyl-; and 4,4 biphenylene-, diisocyanates. The polyurethane reaction may be effected by conventional techniques, e.g. all the reactants may be simultaneously mixed together or the catalyst may be dissolved in water and the reactive hydrogen-containing organic compound added, followed by polyisocyanate; alternatively excess polyisocyanate may be reacted with reactive hydrogen-containing compound and aqueous piperazine catalyst solution added to the "prepolymer" formed, in amount stocchiometrically equivalent to the "free" isocyanate content thereof. Reference has been directed by the Comptroller to Specifications 754,502 and 795,276.
GB2057757A 1957-06-28 1957-06-28 Polyurethane compositions Expired GB885234A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
GB2057757A GB885234A (en) 1957-06-28 1957-06-28 Polyurethane compositions
DEW23489A DE1089164B (en) 1957-06-28 1958-06-12 Process for the production of odorless, crosslinked, optionally foam-shaped polyurethanes
FR1208564D FR1208564A (en) 1957-06-28 1958-06-21 Improvements to polyurethane-based compositions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2057757A GB885234A (en) 1957-06-28 1957-06-28 Polyurethane compositions

Publications (1)

Publication Number Publication Date
GB885234A true GB885234A (en) 1961-12-20

Family

ID=10148208

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2057757A Expired GB885234A (en) 1957-06-28 1957-06-28 Polyurethane compositions

Country Status (3)

Country Link
DE (1) DE1089164B (en)
FR (1) FR1208564A (en)
GB (1) GB885234A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2231878A (en) * 1989-05-22 1990-11-28 Basf Corp Molded flexible polyurethane compositions of polycarbonate compatibility

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4500654A (en) * 1983-11-01 1985-02-19 Abbott Laboratories Catalyst system and process for the production of polyurethanes

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE926880C (en) * 1952-01-30 1955-04-25 Bayer Ag Process for the production of foams with a very low specific weight
DE954376C (en) * 1953-05-23 1956-12-13 Bayer Ag Process for the production of crosslinked plastics

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2231878A (en) * 1989-05-22 1990-11-28 Basf Corp Molded flexible polyurethane compositions of polycarbonate compatibility

Also Published As

Publication number Publication date
DE1089164B (en) 1960-09-15
FR1208564A (en) 1960-02-24

Similar Documents

Publication Publication Date Title
JPS57112363A (en) Manufacture of n,o-disubstituted urethane suitable for manufacturing isocyanate as starting substance
GB1018320A (en) Polyurethanes
ES444780A1 (en) Polyisocyanates which contain carbodiimide groups and which are stable in storage
ATE6938T1 (en) MODIFIED DIISOCYANATE COMPOSITIONS AND POLYURETHANES THEREOF.
GB754502A (en) Foamed products based on polyurethanes
GB874430A (en) Improvements in or relating to the manufacture of polymeric materials
GB1165877A (en) Production of Polyurethanes
ES261632A1 (en) Method of making polyurethane foam using an organic silane
GB1258600A (en)
JPS56103152A (en) Manufacture of n*oodisubstituted urethane useful for manufacture of isocyanate
ES416044A1 (en) Flexible cellular polyurethane foam compositions having increased flame retardance
GB885234A (en) Polyurethane compositions
ES459062A1 (en) Process for the solvent-free production of solid plastic moldings sealing compounds and insulations using a polyisocyanate mixture containing 2,4{40 -diisocyanatodiphenylmethane
GB901396A (en) Process for the production of polyurethane plastics
GB879167A (en) Improvements in or relating to the manufacture of cellular polyurethanes
GB1420059A (en) Rigid foams of a polymer containing carbodiimide linkages and process for preparing them
ES487339A1 (en) Polyisocyanates, process for their preparation and their use.
GB852988A (en) Alkylbenzene diisocyanates
GB967443A (en) Improvements in or relating to the production of urethanes
GB1221534A (en) Improvements relating to poromeric materials
GB1339931A (en) Process for preparing polyurethanes
GB1057428A (en) Polyurethane articles
GB908949A (en) Improvements in or relating to the manufacture of polymers
GB794403A (en) Improvements in manufacture of cellular foams derived from polyisocyanates and polyalkylene ether glycols
ATE65517T1 (en) LIQUID ORGANIC POLYISOCYANAE COMPOSITIONS CONTAINING UREA AND/OR BIURETIE GROUPS.