GB1247802A - Linear, segmented polyurethane elastomers - Google Patents

Linear, segmented polyurethane elastomers

Info

Publication number
GB1247802A
GB1247802A GB27412/69A GB2741269A GB1247802A GB 1247802 A GB1247802 A GB 1247802A GB 27412/69 A GB27412/69 A GB 27412/69A GB 2741269 A GB2741269 A GB 2741269A GB 1247802 A GB1247802 A GB 1247802A
Authority
GB
United Kingdom
Prior art keywords
diol
nco
semicarbazide
hydrazide
solution
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
GB27412/69A
Inventor
Wilhelm Thoma
Harald Oertel
Heinrich Rinke
Ulrich Bahr
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 GB1247802A publication Critical patent/GB1247802A/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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic System
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6515Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having three nitrogen atoms as the only ring hetero atoms
    • C07F9/6521Six-membered rings
    • 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
    • C08G18/12Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step using two or more compounds having active hydrogen in the first polymerisation step

Abstract

1,247,802. Linear segmented polyurethane elastomers. FARBENFABRIKEN BAYER A.G. 30 May, 1969 [7 June, 1968], No. 27412/69. Heading C3R. [Also in Division C2] Linear segmentedpolyurethane elastomers containing a chain extending segment of the formula wherein X is 1 or 2 may be prepared by reacting an NCO-terminated prepolymer suitably derived from a dihydroxy compound having a M.W. of 600 to 5000 and excess of an organic diisocyanate with a substantially equivalent quantity of an aliphatic semicarbazide hydrazide of the formula wherein x is 1 or 2 in the presence of a highly polar solvent. The prepolymer may suitably be prepared in the further presence of a diol having a M.W. of 62 to 300, which diol preferably contains tertiary amino groups in the molecule. Up to 45 mol. per cent of the aliphatic semicarbazide hydrazide may be replaced by a conventional bifunctional chain extender. Preferred solvents are those containing amide, urea or sulphoxide groups. The elastomer containing solutions may be spun into filaments. In a typical example (1) a polyester derived from adipic acid, 1,6-hexane diol and 2.2-dimethyl propane diol is heated with N,N-bis-(#-hydroxy propyl)- methylamine and diphenylmethane-4,41-diisocyanate in chlorobenzene to form an NCO- terminated prepolymer which is then reacted with a solution of #-semicarbazide propionic acid hydrazide in dimethyl formamide. The viscosity of the elastomer solution is increased by the addition of a further quantity of the NCO- terminated prepolymer, and after pigmenting with TiO 2 the solution is spun to form filaments.
GB27412/69A 1968-06-07 1969-05-30 Linear, segmented polyurethane elastomers Expired GB1247802A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE19681770591 DE1770591A1 (en) 1968-06-07 1968-06-07 Linear, segmented polyurethane elastomers

Publications (1)

Publication Number Publication Date
GB1247802A true GB1247802A (en) 1971-09-29

Family

ID=5700565

Family Applications (2)

Application Number Title Priority Date Filing Date
GB38781/70A Expired GB1247803A (en) 1968-06-07 1969-05-30 beta-SEMICARBAZIDO-PROPIONIC ACID HYDRAZIDE
GB27412/69A Expired GB1247802A (en) 1968-06-07 1969-05-30 Linear, segmented polyurethane elastomers

Family Applications Before (1)

Application Number Title Priority Date Filing Date
GB38781/70A Expired GB1247803A (en) 1968-06-07 1969-05-30 beta-SEMICARBAZIDO-PROPIONIC ACID HYDRAZIDE

Country Status (10)

Country Link
US (1) US3640937A (en)
AT (2) AT310928B (en)
BE (1) BE734194A (en)
CH (1) CH534191A (en)
DE (1) DE1770591A1 (en)
ES (1) ES368123A1 (en)
FR (1) FR2010399A1 (en)
GB (2) GB1247803A (en)
NL (1) NL6908673A (en)
SE (1) SE363838B (en)

Families Citing this family (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4125693A (en) * 1973-11-03 1978-11-14 Chemie-Anlagenbau Bischofsheim Gmbh Process for the production of polyurethanes dissolved in a solvent and also their use for the production of fabricated shapes, especially of microporous structures
US3978156A (en) * 1975-05-14 1976-08-31 The B. F. Goodrich Company Color stabilized polyurethanes
DE2542449A1 (en) * 1975-09-24 1977-04-07 Bayer Ag MONO METHYLOL ETHER DIOL
US4286014A (en) * 1978-01-31 1981-08-25 Toray Industries, Incorporated Composite sheet material
JPS61218659A (en) * 1985-03-26 1986-09-29 Asahi Chem Ind Co Ltd Polyurethane composition
US5055545A (en) * 1989-05-18 1991-10-08 Bridgestone/Firestone, Inc. Urethane-rubber adhesives based on azoester prepolymers and derivatives thereof
US5059647A (en) * 1989-09-29 1991-10-22 E. I. Du Pont De Nemours And Company Oligomeric semicarbazide additives for spandex
JP3001358B2 (en) * 1992-11-06 2000-01-24 サカタインクス株式会社 Aqueous printing ink composition for plastic film, adhesive for aqueous lamination, and method for producing a laminated product using the same
US5518764A (en) * 1994-03-22 1996-05-21 Bayer Aktiengesellschaft Process for coating textiles
DE4433437A1 (en) 1994-09-20 1996-03-21 Bayer Ag Crosslinker for textile printing binders
DE19548030A1 (en) 1995-12-21 1997-06-26 Bayer Ag Use of aqueous dispersions of postcrosslinkable coating compositions for textile and leather coating
DE10260270A1 (en) 2002-12-20 2004-07-01 Bayer Ag Hydrophilic polyurethane-polyurea dispersion
DE10306243A1 (en) * 2003-02-14 2004-08-26 Bayer Ag One-component coating systems
EP1664225A1 (en) * 2003-09-18 2006-06-07 Bayer MaterialScience AG Aqueous adhesive dispersions
DE102004002525A1 (en) * 2004-01-16 2005-08-04 Bayer Materialscience Ag Coating composition
DE102004002527A1 (en) * 2004-01-16 2005-08-04 Bayer Materialscience Ag size composition
DE102004017436A1 (en) * 2004-04-08 2005-10-27 Bayer Materialscience Ag Process for the continuous preparation of an aqueous polyurethane dispersion
WO2011144530A1 (en) 2010-05-17 2011-11-24 Bayer Materialscience Ag Process for joining together components, in particular in the production of shoes
EP2387900A1 (en) 2010-05-17 2011-11-23 Bayer MaterialScience AG Method for joining components together, in particular in the production of shoes
TWI485187B (en) 2010-08-17 2015-05-21 Stahl Internat Bv Stable aqueous wax dispersions
EP2441791A1 (en) 2010-10-14 2012-04-18 Clariant International Ltd. Stable aqueous wax dispersions
US8846174B2 (en) 2011-02-25 2014-09-30 Schott Corporation Transparent laminate structures
AU2011360911B2 (en) 2011-03-01 2015-08-27 Roidec India Chemicals (P) Ltd. Natural oil based poly-urethane dispersion
WO2012117416A1 (en) 2011-03-01 2012-09-07 Roidec India Chemicals (P) Ltd. A non-plastic and biodegradable aqueous natural oil based lacquer for food grade flexible packaging
WO2012117414A1 (en) 2011-03-01 2012-09-07 Roidec India Chemicals (P) Ltd. Process for the preparation of a natural oil based poly-urethane dispersion
PE20141014A1 (en) 2011-08-09 2014-08-17 Bayer Ip Gmbh PROCEDURE FOR THE REINFORCEMENT OF A CONSTRUCTION UNIT
WO2016162394A1 (en) 2015-04-07 2016-10-13 Covestro Deutschland Ag Method for adhesively bonding substrates using adhesives
WO2016170060A1 (en) 2015-04-21 2016-10-27 Covestro Deutschland Ag Process for producing polyisocvanurate plastics having functionalized surfaces
CN107438635B (en) 2015-04-21 2021-01-19 科思创德国股份有限公司 Process for making polyisocyanurate plastics
US10590226B2 (en) 2015-04-21 2020-03-17 Covestro Deutschland Ag Solids based on polyisocyanurate polymers produced under adiabatic conditions
EP3286244B1 (en) 2015-04-21 2023-11-01 Covestro Intellectual Property GmbH & Co. KG Polyisocyanurate polymers and process for the production of polyisocyanurate polymers
US10597484B2 (en) 2015-04-21 2020-03-24 Covestro Deutschland Ag Polyisocyanurate plastics having high thermal stability
WO2017174303A1 (en) 2016-04-04 2017-10-12 Tesa Se Radiation-activatable pressure-sensitive adhesive tape having a dark reaction and use thereof
DE102022105185A1 (en) 2022-03-04 2023-09-07 Tesa Se Releasable laminate and method for breaking permanent structural bonds

Also Published As

Publication number Publication date
BE734194A (en) 1969-11-17
NL6908673A (en) 1969-12-09
US3640937A (en) 1972-02-08
AT310928B (en) 1973-10-25
GB1247803A (en) 1971-09-29
FR2010399A1 (en) 1970-02-13
DE1770591A1 (en) 1971-11-04
ES368123A1 (en) 1971-05-01
SE363838B (en) 1974-02-04
AT292310B (en) 1971-08-25
CH534191A (en) 1973-02-28

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