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ES404932A1 - Process for the manufacture of polyurethanes - Google Patents

Process for the manufacture of polyurethanes

Info

Publication number
ES404932A1
ES404932A1 ES404932A ES404932A ES404932A1 ES 404932 A1 ES404932 A1 ES 404932A1 ES 404932 A ES404932 A ES 404932A ES 404932 A ES404932 A ES 404932A ES 404932 A1 ES404932 A1 ES 404932A1
Authority
ES
Spain
Prior art keywords
isocyanate
polyester
excess
solution
amount
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
ES404932A
Other languages
Spanish (es)
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Publication of ES404932A1 publication Critical patent/ES404932A1/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J175/00Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
    • C09J175/04Polyurethanes
    • 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
    • C08G18/0838Manufacture of polymers in the presence of non-reactive compounds
    • C08G18/0842Manufacture of polymers in the presence of non-reactive compounds in the presence of liquid diluents
    • C08G18/0847Manufacture of polymers in the presence of non-reactive compounds in the presence of liquid diluents in the presence of solvents for the polymers
    • C08G18/0852Manufacture of polymers in the presence of non-reactive compounds in the presence of liquid diluents in the presence of solvents for the polymers the solvents being organic
    • 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
    • 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
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/65Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
    • C08G18/6505Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen the low-molecular compounds being compounds of group C08G18/32 or polyamines of C08G18/38
    • 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
    • C08G18/70Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72Polyisocyanates or polyisothiocyanates
    • C08G18/74Polyisocyanates or polyisothiocyanates cyclic
    • C08G18/75Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic
    • 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
    • C08G18/70Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72Polyisocyanates or polyisothiocyanates
    • C08G18/74Polyisocyanates or polyisothiocyanates cyclic
    • C08G18/75Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic
    • C08G18/751Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring
    • C08G18/752Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group
    • C08G18/753Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group containing one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group having a primary carbon atom next to the isocyanate or isothiocyanate group
    • C08G18/755Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group containing one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group having a primary carbon atom next to the isocyanate or isothiocyanate group and at least one isocyanate or isothiocyanate group linked to a secondary carbon atom of the cycloaliphatic ring, e.g. isophorone diisocyanate

Landscapes

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

Abstract

Process for obtaining a solution of a polyurethane containing isocyanate-reactive groups, characterized in that it comprises reacting together, in a solvent inert with respect to the isocyanate groups, a mixture of (a) a molar proportion of a polyester, polyester esteramide or substantially linear polyether, (b) from 1.15 to 8.0 molar ratios of 3-isocyanatomethyl-3,5,5-trimethylcyclohexyl-isocyanate and (c) simultaneously or subsequently an amount of a chain extender, practically equivalent to the amount of diisocyanate in excess of that necessary for the reaction with the polyester, polyesteramide or polyether, until the solution has a viscosity of 1 to 1,500 poises at 25ºC; and then add an excess of isocyanate-reactive organic compound. (Machine-translation by Google Translate, not legally binding)
ES404932A 1971-07-16 1972-07-15 Process for the manufacture of polyurethanes Expired ES404932A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3345671 1971-07-16

Publications (1)

Publication Number Publication Date
ES404932A1 true ES404932A1 (en) 1975-06-16

Family

ID=10353198

Family Applications (1)

Application Number Title Priority Date Filing Date
ES404932A Expired ES404932A1 (en) 1971-07-16 1972-07-15 Process for the manufacture of polyurethanes

Country Status (9)

Country Link
AU (1) AU472166B2 (en)
BE (1) BE786329A (en)
DE (1) DE2235025A1 (en)
ES (1) ES404932A1 (en)
FR (1) FR2146296B1 (en)
GB (1) GB1351773A (en)
IT (1) IT962750B (en)
NL (1) NL7209768A (en)
ZA (1) ZA724550B (en)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2515766C3 (en) * 1975-04-10 1980-12-11 Bayer Ag, 5090 Leverkusen Improved process for the production of high molecular weight, isocyanate group-free polyurethanes which are soluble in organic solvents
NL176864C (en) * 1976-11-25 1985-06-17 Akzo Nv PROCESS FOR THE PREPARATION OF A THIXOTROPE COATING COMPOSITION
US4424335A (en) 1981-02-27 1984-01-03 Thermo Electron Corporation Keratoprosthetic polyurethane
FR2511014B1 (en) * 1981-08-10 1987-02-06 Ethicon Inc PROCESS FOR THE PREPARATION OF A POLYURETHANE RESIN SUITABLE FOR ELECTROSTATIC SPINNING
US4523005A (en) * 1981-10-30 1985-06-11 Thermedics, Inc. Extrudable polyurethane for prosthetic devices prepared from a diisocyanate, a polytetramethylene ether polyol, and 1,4-butane diol
US4447590A (en) * 1981-10-30 1984-05-08 Thermo Electron Corporation Extrudable polyurethane for prosthetic devices prepared from a diisocyanate, a polytetramethylene ether polyol and 1,4 butane diol
DE3401753A1 (en) * 1984-01-19 1985-08-01 Bayer Ag, 5090 Leverkusen METHOD FOR THE PRODUCTION OF POLYURETHANES, POLYURETHANES WITH AROMATIC AMINO END GROUPS AND THE USE THEREOF
US4925732A (en) * 1988-07-27 1990-05-15 W. L. Gore & Associates, Inc. Breathable flexible laminates adhered by a breathable adhesive
WO2009053307A1 (en) * 2007-10-22 2009-04-30 Basf Se Polyisocyanate containing urethane groups

Also Published As

Publication number Publication date
ZA724550B (en) 1973-03-28
BE786329A (en) 1973-01-15
FR2146296B1 (en) 1976-10-29
DE2235025A1 (en) 1973-02-01
AU472166B2 (en) 1976-05-20
AU4423272A (en) 1974-01-10
IT962750B (en) 1973-12-31
FR2146296A1 (en) 1973-03-02
NL7209768A (en) 1973-01-18
GB1351773A (en) 1974-05-01

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