GB820266A - Process for the manufacture of porous or homogeneous polyurethane plastics - Google Patents

Process for the manufacture of porous or homogeneous polyurethane plastics

Info

Publication number
GB820266A
GB820266A GB4952/59A GB495259A GB820266A GB 820266 A GB820266 A GB 820266A GB 4952/59 A GB4952/59 A GB 4952/59A GB 495259 A GB495259 A GB 495259A GB 820266 A GB820266 A GB 820266A
Authority
GB
United Kingdom
Prior art keywords
mixture
hydrogen atoms
reactive hydrogen
cross
polyisocyanate
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
GB4952/59A
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.)
Bayer AG
Original Assignee
Bayer AG
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 Bayer AG filed Critical Bayer AG
Publication of GB820266A publication Critical patent/GB820266A/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
    • C08G18/0895Manufacture of polymers by continuous processes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)

Abstract

A process for the production of polyurethane plastics by the reaction of an organic compound containing at least two reactive hydrogen atoms with a polyisocyanate and a cross-linking agent and/or an accelerator, comprises injecting at least one but less than all of the three last-mentioned reactants into a stream of the organic compound containing at least two reactive hydrogen atoms in a first mixing zone, and injecting the remaining component or components into the mixture thus obtained in a second mixing zone. The process is suitably carried out in the apparatus described in Specification 820,265. The injection pressure may be 300 to 15,000 lbs./sq. inch. Preferably the polyisocyanate or the cross-linking agent and/or accelerator is or are injected into a stream of the organic compound having at least two reactive hydrogen atoms or of a prepolymer prepared from such a compound. This is followed by the injection in a second step of the cross-linking agent and/or accelerator or polyisocyanate, and if desired, of an additional amount of the compound having two reactive hydrogen atoms. The process is applicable to the production both of homogeneous and porous polyurethanes. The compound having reactive hydrogen atoms may be a polyester, polyalkylene ether glycol or a hydrogenation product of olefine-carbon monoxide copolymers. Water, glycols and diamines are suitable cross-linking agents and tertiary amines and heavy metal compounds are suitable accelerators. Emulsifiers may be added to the mixture. In a typical example, using the apparatus of Specification 820,265 an activator mixture consisting of N-diethyl-b -phenoxyethylamine and the sodium salt of sulphonated castor oil in water is injected into a mixture of an adipic acid/phthalic anhydride/hexanetriol polyester, an adipic acid/hexanetriol/butanediol polyester and ethoxylated trimethylol propane in a mixing zone. The mixture obtained is then passed to a mixing head in which toluylene diisocyanate is injected and the mixture is then passed out through a nozzle.ALSO:A process for the production of polyurethane plastics (which may be porous) by the reaction of an organic compound containing at least two reactive hydrogen atoms with a polyisocyanate and a cross-linking agent and/or an accelerator, comprises injecting at least one but less than all of the three least-mntioned reactants into a stream of the organic compound containing at least two reactive hydrogen atoms in a first mixing zone, and injecting the remaining component or components into the mixture thus obtained in a second mixing zone. The process is suitably carried out in the apparatus described in Specification 820,265. The injection pressure may be 300 to 15,000 lbs./sq. inch. Preferably the polyisocyanate or the cross-linking agent and/or accelerator is or are injected into a stream of the organic compound having at least two reactive hydrogen atoms or of a prepolymer prepared from such a compound. This is followed by the injection in a second step of the cross-linking agent or/and accelerator or polyisocyanate, and if desired, of an additional amount of the compound having two reactive hydrogen atoms. The process is applicable to the production both of homogeneous and porous polyurethanes. The compound having reactive hydrogen atoms may be a polyester, polyalkylene ether glycol or a hydrogenation product of olefine-carbon monoxide copolymers. Water, glycols and diamines are suitable cross-linking agents and tertiary amines and heavy metals compound are suitable accelerators. Emulsifiers may be added to the mixture. In a typical example, using the apparatus of Specification 820,265 an activator mixture consisting of N-diethyl-b -phenoxyethylamine and the sodium salt of sulphonated castor oil in water is injected into a mixture of an adipic acid/phthalic anhydride/hexanetriol polyester, an adipic acid/hexanetriol/butanediol polyester and ethoxylated trimethylol propane in a mixing zone. The mixture obtained is then passed to a mixing head in which toluylene diisocyanate is injected and the mixture is then passed out through a nozzle.
GB4952/59A 1956-05-11 1957-05-10 Process for the manufacture of porous or homogeneous polyurethane plastics Expired GB820266A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE820266X 1956-05-11

Publications (1)

Publication Number Publication Date
GB820266A true GB820266A (en) 1959-09-16

Family

ID=6736609

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4952/59A Expired GB820266A (en) 1956-05-11 1957-05-10 Process for the manufacture of porous or homogeneous polyurethane plastics

Country Status (1)

Country Link
GB (1) GB820266A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2257150A (en) * 1991-07-04 1993-01-06 Hennecke Gmbh Maschf A process for the production of elastomeric polyurethanes, particularly in the form of shoe soles
WO2000031161A1 (en) * 1997-09-26 2000-06-02 Bayer Aktiengesellschaft Polyurea-containing polyurethane elastomers rapidly removable from the mould

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2257150A (en) * 1991-07-04 1993-01-06 Hennecke Gmbh Maschf A process for the production of elastomeric polyurethanes, particularly in the form of shoe soles
GB2257150B (en) * 1991-07-04 1995-02-08 Hennecke Gmbh Maschf A process for the production of elastomeric polyurethanes, more particularly in the form of shoe soles
WO2000031161A1 (en) * 1997-09-26 2000-06-02 Bayer Aktiengesellschaft Polyurea-containing polyurethane elastomers rapidly removable from the mould

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