GB975733A - Process for preventing haze formation in fermented beverages - Google Patents

Process for preventing haze formation in fermented beverages

Info

Publication number
GB975733A
GB975733A GB4522861A GB4522861A GB975733A GB 975733 A GB975733 A GB 975733A GB 4522861 A GB4522861 A GB 4522861A GB 4522861 A GB4522861 A GB 4522861A GB 975733 A GB975733 A GB 975733A
Authority
GB
United Kingdom
Prior art keywords
diisocyanate
reaction
mixture
tolylene
hexamethylene
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
GB4522861A
Inventor
Herbert Gudgeon
Gordon Albert Thomas
Harry James Twitchett
Dennis John Cecil Wood
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
Priority to GB4522861A priority Critical patent/GB975733A/en
Publication of GB975733A publication Critical patent/GB975733A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12HPASTEURISATION, STERILISATION, PRESERVATION, PURIFICATION, CLARIFICATION OR AGEING OF ALCOHOLIC BEVERAGES; METHODS FOR ALTERING THE ALCOHOL CONTENT OF FERMENTED SOLUTIONS OR ALCOHOLIC BEVERAGES
    • C12H1/00Pasteurisation, sterilisation, preservation, purification, clarification, or ageing of alcoholic beverages
    • C12H1/02Pasteurisation, sterilisation, preservation, purification, clarification, or ageing of alcoholic beverages combined with removal of precipitate or added materials, e.g. adsorption material
    • C12H1/04Pasteurisation, sterilisation, preservation, purification, clarification, or ageing of alcoholic beverages combined with removal of precipitate or added materials, e.g. adsorption material with the aid of ion-exchange material or inert clarification material, e.g. adsorption material
    • C12H1/0416Pasteurisation, sterilisation, preservation, purification, clarification, or ageing of alcoholic beverages combined with removal of precipitate or added materials, e.g. adsorption material with the aid of ion-exchange material or inert clarification material, e.g. adsorption material with the aid of organic added material
    • C12H1/0424Pasteurisation, sterilisation, preservation, purification, clarification, or ageing of alcoholic beverages combined with removal of precipitate or added materials, e.g. adsorption material with the aid of ion-exchange material or inert clarification material, e.g. adsorption material with the aid of organic added material with the aid of a polymer

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biochemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Food Science & Technology (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Polyurethanes Or Polyureas (AREA)

Abstract

A polymer for preventing the formation of haze in a fermented beverage by the adsorption of haze-forming non-protein substances on the polymer, contains urea and/or urethane groups and may be obtained by the reaction of a polyisocyanate with water or with a polyhydric alcohol, or by reaction of the polyisocyanate with a polyamine, an amino alcohol, an amino carboxylic acid or a mixture of these, the reaction being carried out optionally in the presence of water and/or a polyhydric alcohol. Basic or metallic compounds capable of accelerating the reaction and a dispersing agent are included in the reaction mixture. Preferred polymers are obtained by the reaction of either a mixture of the 2:4 and 2:6 isomers of tolylene diisocyanate or hexamethylene diisocyanate with ammonia or ethylene diamine in aqueous solution. Polyisocyanates mentioned: hexamethylene diisocyanate, dicyclohexylmethane diisocyanate, tolylene-2:4-diisocyanate or a mixture of the 2:4 and 2:6 isomers, p-xylylene diisocyanate, 3-(a -isocyanate-ethyl) phenyl isocyanate, and the reaction products of an excess of a diisocyanate with polyhydric alcohols such as trimethylol propane. Polyamines: ethylene diamine, hexamethylene-diamine, bis-hexamethylene triamine, pentaethylene tetramine and p-phenylenediamine. Amino alcohols: ethanolamine, triiso-propanolamine and 4-aminobenzyl alcohol. Amino carboxylic acids: glycine, amino caproic acid and anthranilic acid. Polyhydric alcohols: ethylene glycol, glycerol, trimethylol propane, pentaerythritol, mannitol, glucose, sucrose, polypropylene glycols and polypropylene triols. Accelerators; potassium acetate, sodium carbonate, sodium and potassium hydroxide, tertiary amines such as triethylamine, and metallic compounds such as stannous octoate and ferric acetylacetonate. Dispersing agents: long chain quaternary ammonium halide, an oxyalkylated phenol or an alkali metal salt of an alkyl or aryl sulphonic acid. The polyureas may be used either as powder or paste alone or in admixture with other non-toxic adsorbents. The powder may be ground and the paste dispersed by milling with gravel in the presence of surface-active agents and the absorptive properties may be regenerated after use by treatment with dilute aqueous sodium carbonate or caustic soda. The Specification discloses the preparations of five polymers which were employed to adsorb anthocyanogens from pale ale by shaking 0.2g (dry weight) of the polymer with 300 ml. of degassed ale for 10 minutes; the anthocyanogen removal amounted to 12, 28, 22, 23 and 21% respectively. (1) Tolylene-2:4-diisocyanate and tolylene-2:6-diisocyanate are added to a solution of the condensation product of octyl phenol with ethylene oxide in water at 20 DEG C. and caustic soda dissolved in water is added to the mixture. The suspension of polyurea obtained is stirred, filtered and thoroughly washed with water. In Examples 2, 3 and 4, the reaction mixture includes ammonia, ethylene diamine and hexamethylene diamine, respectively. In Example 5, hexamethylene diisocyanate replaces the mixture of tolylene diisocyanates.ALSO:The formation of haze in a fermented beverage is prevented or lessened by the adsorption of haze-forming non-protein substances on a finely divided insoluble polymer containing urea and/or urethane groups. The polymer may be obtained by the reaction of a polyisocyanate with water or with a polyhydric alcohol, or by reaction of the polyisocyanate with a polyamine, an amino alcohol, an amino carboxylic acid or a mixture of these, the reaction being carried out optionally in the presence of water and/or a polyhydric alcohol. Basic or metallic compounds capable of accelerating the reaction and a dispersing agent are included in the reaction mixture. Preferred polymers are obtained by the reaction of either a mixture of the 2:4 and 2:6 isomers of tolylene diisocyanate or hexamethylene diisocyanate with ammonia or ethylene diamine in aqueous solution. Polyisocyanates mentioned: hexamethylene diisocyanate, dicyclohexylmethane diisocyanate, tolylene-2:4-diisocyanate or a mixture of the 2:4 and 2:6 isomers, p-xylylene diisocyanate, 3-(a -isocyanatoethyl) phenyl isocyanate, and the reaction products of an excess of a diisocyanate with polyhydric alcohols such as trimethylol propane. Polyamines: ethylene diamine, hexamethylene-diamine, bis-hexamethylene triamine, pentaethylene tetramine and p-phenylenediamine. Amino alcohols: ethanolamine, tri-iso-propanolamine and 4-aminobenzyl alcohol. Amino carboxylic acids: glycine, amino caproic acid and anthranilic acid. Polyhydric alcohols: ethylene glycol, glycerol, trimethylol propane, pentaerythritol, mannitol, glucose, sucrose, polypropylene glycols and polypropylene triols. Accelerators: potassium acetate, sodium carbonate, sodium and potassium hydroxide, tertiary amines such as triethylamine, and metallic compounds such as stannous octoate and ferric acetylacetonate. Dispersing agents: long chain quaternary ammonium halide, an oxylalkylated phenol or an alkali metal salt of an alkyl or aryl sulphonic acid. The polyureas may be used either as powder or paste alone or in admixture with other non-toxic adsorbents. The powder may be ground and the paste dispersed by milling with gravel in the presence of surface-active agents and the absorptive properties may be regenerated after use by treatment with dilute aqueous sodium carbonate or caustic soda. The Specification discloses the preparations of five polymers which were employed to adsorb anthocyanogens from pale ale by shaking 0.2 g. (dry weight) of the polymer with 300 ml. of degassed ale for 10 minutes; the anthocyanogen removal amounted to 12, 28, 22, 23 and 21% respectively. (1) 174 parts of an 80:20 mixture of tolylene-2:4-diisocyanate and tolylene-2:6-diisocyanate are added during 6 hours to a vigorously agitated solution of 10 parts of the condensation product of octyl phenol with 10 molecular proportions of ethylene oxide in 750 parts of water at 20 DEG C. Eight parts of caustic soda dissolved in 30 parts of water are added to the agitated mixture at such a rate during the addition of the diisocyanate that an alkaline reaction to red-litmus test paper is maintained. The suspension of polyurea obtained is stirred for 16 hours at 20 DEG C., filtered and thoroughly washed with water. There is obtained 650 parts of a white paste, the solid content of which is 53.5%. In Examples 2, 3 and 4, the reaction mixture includes ammonia, ethylene diamine and hexamethylene diamine, respectively. In Example 5, hexamethylene diisocyanate replaces the mixture of tolylene diisocyanates. The Specification acknowledges the prior use of the following materials in preventing the formation of haze in beverages: carbon, polyvinyl-pyrrolidone, polyvinylimidazole, poly(N-vinyl-5-ethyl-2-oxazolidinone), polyamides and polyacrylamides.
GB4522861A 1961-12-18 1961-12-18 Process for preventing haze formation in fermented beverages Expired GB975733A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB4522861A GB975733A (en) 1961-12-18 1961-12-18 Process for preventing haze formation in fermented beverages

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB4522861A GB975733A (en) 1961-12-18 1961-12-18 Process for preventing haze formation in fermented beverages

Publications (1)

Publication Number Publication Date
GB975733A true GB975733A (en) 1964-11-18

Family

ID=10436384

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4522861A Expired GB975733A (en) 1961-12-18 1961-12-18 Process for preventing haze formation in fermented beverages

Country Status (1)

Country Link
GB (1) GB975733A (en)

Cited By (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4073954A (en) * 1976-02-03 1978-02-14 Mobius Christian Hermann Method of removing tannins and reducing clouding in drinks
US4594250A (en) * 1981-11-21 1986-06-10 Canadian Patents And Development Limited Extraction of fruit, vegetable and meat products with a polyether-based polymer
US20140248485A1 (en) * 2010-10-20 2014-09-04 Bioformix Inc. Synthesis of methylene malonates substantially free of impurities
US9108914B1 (en) 2013-01-11 2015-08-18 Sirrus, Inc. Method to obtain methylene malonate via bis(hydroxymethyl) malonate pathway
US9181365B2 (en) 2012-03-30 2015-11-10 Sirrus, Inc. Methods for activating polymerizable compositions, polymerizable systems, and products formed thereby
US9217098B1 (en) 2015-06-01 2015-12-22 Sirrus, Inc. Electroinitiated polymerization of compositions having a 1,1-disubstituted alkene compound
US9234107B2 (en) 2012-03-30 2016-01-12 Sirrus, Inc. Ink coating formulations and polymerizable systems for producing the same
US9249265B1 (en) 2014-09-08 2016-02-02 Sirrus, Inc. Emulsion polymers including one or more 1,1-disubstituted alkene compounds, emulsion methods, and polymer compositions
US9279022B1 (en) 2014-09-08 2016-03-08 Sirrus, Inc. Solution polymers including one or more 1,1-disubstituted alkene compounds, solution polymerization methods, and polymer compositions
US9315597B2 (en) 2014-09-08 2016-04-19 Sirrus, Inc. Compositions containing 1,1-disubstituted alkene compounds for preparing polymers having enhanced glass transition temperatures
US9334430B1 (en) 2015-05-29 2016-05-10 Sirrus, Inc. Encapsulated polymerization initiators, polymerization systems and methods using the same
US9416091B1 (en) 2015-02-04 2016-08-16 Sirrus, Inc. Catalytic transesterification of ester compounds with groups reactive under transesterification conditions
US9512058B2 (en) 2011-10-19 2016-12-06 Sirrus Inc. Multifunctional monomers, methods for making multifunctional monomers, polymerizable compostions and products formed thereform
US9518001B1 (en) 2016-05-13 2016-12-13 Sirrus, Inc. High purity 1,1-dicarbonyl substituted-1-alkenes and methods for their preparation
US9567475B1 (en) 2016-06-03 2017-02-14 Sirrus, Inc. Coatings containing polyester macromers containing 1,1-dicarbonyl-substituted 1 alkenes
US9617377B1 (en) 2016-06-03 2017-04-11 Sirrus, Inc. Polyester macromers containing 1,1-dicarbonyl-substituted 1 alkenes
US9752059B2 (en) 2012-11-16 2017-09-05 Sirrus, Inc. Plastics bonding systems and methods
US9828324B2 (en) 2010-10-20 2017-11-28 Sirrus, Inc. Methylene beta-diketone monomers, methods for making methylene beta-diketone monomers, polymerizable compositions and products formed therefrom
US10047192B2 (en) 2012-06-01 2018-08-14 Sirrus, Inc. Optical material and articles formed therefrom
US10196481B2 (en) 2016-06-03 2019-02-05 Sirrus, Inc. Polymer and other compounds functionalized with terminal 1,1-disubstituted alkene monomer(s) and methods thereof
US10414839B2 (en) 2010-10-20 2019-09-17 Sirrus, Inc. Polymers including a methylene beta-ketoester and products formed therefrom
US10428177B2 (en) 2016-06-03 2019-10-01 Sirrus, Inc. Water absorbing or water soluble polymers, intermediate compounds, and methods thereof
US10501400B2 (en) 2015-02-04 2019-12-10 Sirrus, Inc. Heterogeneous catalytic transesterification of ester compounds with groups reactive under transesterification conditions
US10607910B2 (en) 2012-11-30 2020-03-31 Sirrus, Inc. Composite compositions for electronics applications
US10913875B2 (en) 2012-03-30 2021-02-09 Sirrus, Inc. Composite and laminate articles and polymerizable systems for producing the same

Cited By (51)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4073954A (en) * 1976-02-03 1978-02-14 Mobius Christian Hermann Method of removing tannins and reducing clouding in drinks
US4594250A (en) * 1981-11-21 1986-06-10 Canadian Patents And Development Limited Extraction of fruit, vegetable and meat products with a polyether-based polymer
US10414839B2 (en) 2010-10-20 2019-09-17 Sirrus, Inc. Polymers including a methylene beta-ketoester and products formed therefrom
US20140248485A1 (en) * 2010-10-20 2014-09-04 Bioformix Inc. Synthesis of methylene malonates substantially free of impurities
US9828324B2 (en) 2010-10-20 2017-11-28 Sirrus, Inc. Methylene beta-diketone monomers, methods for making methylene beta-diketone monomers, polymerizable compositions and products formed therefrom
US9527795B2 (en) 2011-10-19 2016-12-27 Sirrus, Inc. Methylene beta-ketoester monomers, methods for making methylene beta-ketoester monomers, polymerizable compositions and products formed therefrom
US10604601B2 (en) 2011-10-19 2020-03-31 Sirrus, Inc. Multifunctional monomers, methods for making multifunctional monomers, polymerizable compositions and products formed therefrom
US9969822B2 (en) 2011-10-19 2018-05-15 Sirrus, Inc. Multifunctional monomers, methods for making multifunctional monomers, polymerizable compositions and products formed therefrom
US9512058B2 (en) 2011-10-19 2016-12-06 Sirrus Inc. Multifunctional monomers, methods for making multifunctional monomers, polymerizable compostions and products formed thereform
US10611861B2 (en) 2011-10-19 2020-04-07 Sirrus, Inc. Multifunctional monomers, methods for making multifunctional monomers, polymerizable compositions and products formed thereform
US9234107B2 (en) 2012-03-30 2016-01-12 Sirrus, Inc. Ink coating formulations and polymerizable systems for producing the same
US10913875B2 (en) 2012-03-30 2021-02-09 Sirrus, Inc. Composite and laminate articles and polymerizable systems for producing the same
US9523008B2 (en) 2012-03-30 2016-12-20 Sirrus, Inc. Ink coating formulations and polymerizable systems for producing the same
US9181365B2 (en) 2012-03-30 2015-11-10 Sirrus, Inc. Methods for activating polymerizable compositions, polymerizable systems, and products formed thereby
US10047192B2 (en) 2012-06-01 2018-08-14 Sirrus, Inc. Optical material and articles formed therefrom
US9752059B2 (en) 2012-11-16 2017-09-05 Sirrus, Inc. Plastics bonding systems and methods
US10607910B2 (en) 2012-11-30 2020-03-31 Sirrus, Inc. Composite compositions for electronics applications
US9522381B2 (en) 2013-01-11 2016-12-20 Sirrus, Inc. Method to obtain methylene malonate via bis(hydroxymethyl) malonate pathway
US10086355B2 (en) 2013-01-11 2018-10-02 Sirrus, Inc. Method to obtain methylene malonate via bis(hydroxymethyl) malonate pathway
US9108914B1 (en) 2013-01-11 2015-08-18 Sirrus, Inc. Method to obtain methylene malonate via bis(hydroxymethyl) malonate pathway
US9637564B2 (en) 2014-09-08 2017-05-02 Sirrus, Inc. Emulsion polymers including one or more 1,1-disubstituted alkene compounds, emulsion methods, and polymer compositions
US9969819B2 (en) 2014-09-08 2018-05-15 Sirrus, Inc. Pressure sensitive adhesive including a 1,1-disubstituted alkene compound
US10308802B2 (en) 2014-09-08 2019-06-04 Sirrus, Inc. Polymers including one or more 1,1-disubstituted alkene compounds and polymer compositions thereof
US10519257B2 (en) 2014-09-08 2019-12-31 Sirrus, Inc. Compositions containing 1,1-di-carbonyl-substituted alkene compounds for preparing polymers having enhanced glass transition temperatures
US10184073B2 (en) 2014-09-08 2019-01-22 Sirrus, Inc. Emulsion including polymers containing a 1,1-disubstituted alkene compound, adhesives, coatings, and methods thereof
US11021617B2 (en) 2014-09-08 2021-06-01 Sirrus, Inc. Polymers including one or more 1,1-disubstituted alkene compounds and polymer compositions thereof
US9790295B2 (en) 2014-09-08 2017-10-17 Sirrus, Inc. Compositions containing 1,1-disubstituted alkene compounds for preparing polymers having enhanced glass transition temperatures
US10167348B2 (en) 2014-09-08 2019-01-01 Sirrus, Inc. Solution polymers formed from methylene malonate monomers, polymerization, and solution polymer products
US9890227B1 (en) 2014-09-08 2018-02-13 Sirrus, Inc. Compositions containing 1,1-di-substituted alkene compounds for preparing polymers having enhanced glass transition temperatures
US9249265B1 (en) 2014-09-08 2016-02-02 Sirrus, Inc. Emulsion polymers including one or more 1,1-disubstituted alkene compounds, emulsion methods, and polymer compositions
US9279022B1 (en) 2014-09-08 2016-03-08 Sirrus, Inc. Solution polymers including one or more 1,1-disubstituted alkene compounds, solution polymerization methods, and polymer compositions
US9676875B2 (en) 2014-09-08 2017-06-13 Sirrus, Inc. Solution polymers including one or more 1,1-disubstituted alkene compounds, solution polymerization methods, and polymer compositions
US9315597B2 (en) 2014-09-08 2016-04-19 Sirrus, Inc. Compositions containing 1,1-disubstituted alkene compounds for preparing polymers having enhanced glass transition temperatures
US10081685B2 (en) 2014-09-08 2018-09-25 Sirrus, Inc. Emulson polymers including one or more 1,1-disubstituted alkene compounds, emulson methods, and polymer compositions
US9416091B1 (en) 2015-02-04 2016-08-16 Sirrus, Inc. Catalytic transesterification of ester compounds with groups reactive under transesterification conditions
US9938223B2 (en) 2015-02-04 2018-04-10 Sirrus, Inc. Catalytic transesterification of ester compounds with groups reactive under transesterification conditions
US10501400B2 (en) 2015-02-04 2019-12-10 Sirrus, Inc. Heterogeneous catalytic transesterification of ester compounds with groups reactive under transesterification conditions
US9334430B1 (en) 2015-05-29 2016-05-10 Sirrus, Inc. Encapsulated polymerization initiators, polymerization systems and methods using the same
US10087272B2 (en) 2015-05-29 2018-10-02 Sirrus, Inc. Encapsulated polymerization initiators, polymerization systems and methods using the same
US9683147B2 (en) 2015-05-29 2017-06-20 Sirrus, Inc. Encapsulated polymerization initiators, polymerization systems and methods using the same
US9617354B2 (en) 2015-06-01 2017-04-11 Sirrus, Inc. Electroinitiated polymerization of compositions having a 1,1-disubstituted alkene compound
US9217098B1 (en) 2015-06-01 2015-12-22 Sirrus, Inc. Electroinitiated polymerization of compositions having a 1,1-disubstituted alkene compound
US9518001B1 (en) 2016-05-13 2016-12-13 Sirrus, Inc. High purity 1,1-dicarbonyl substituted-1-alkenes and methods for their preparation
US9718989B1 (en) 2016-06-03 2017-08-01 Sirrus, Inc. Coatings containing polyester macromers containing 1,1-dicarbonyl-substituted 1 alkenes
US10428177B2 (en) 2016-06-03 2019-10-01 Sirrus, Inc. Water absorbing or water soluble polymers, intermediate compounds, and methods thereof
US10196481B2 (en) 2016-06-03 2019-02-05 Sirrus, Inc. Polymer and other compounds functionalized with terminal 1,1-disubstituted alkene monomer(s) and methods thereof
US10150886B2 (en) 2016-06-03 2018-12-11 Sirrus, Inc. Coatings containing polyester macromers containing 1,1-dicarbonyl-substituted 1 alkenes
US10087283B2 (en) 2016-06-03 2018-10-02 Sirrus, Inc. Polyester macromers containing 1,1-dicarbonyl-substituted 1 alkenes
US9745413B1 (en) 2016-06-03 2017-08-29 Sirrus, Inc. Polyester macromers containing 1,1-dicarbonyl-substituted 1 alkenes
US9617377B1 (en) 2016-06-03 2017-04-11 Sirrus, Inc. Polyester macromers containing 1,1-dicarbonyl-substituted 1 alkenes
US9567475B1 (en) 2016-06-03 2017-02-14 Sirrus, Inc. Coatings containing polyester macromers containing 1,1-dicarbonyl-substituted 1 alkenes

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