GB975733A - Process for preventing haze formation in fermented beverages - Google Patents
Process for preventing haze formation in fermented beveragesInfo
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12H—PASTEURISATION, STERILISATION, PRESERVATION, PURIFICATION, CLARIFICATION OR AGEING OF ALCOHOLIC BEVERAGES; METHODS FOR ALTERING THE ALCOHOL CONTENT OF FERMENTED SOLUTIONS OR ALCOHOLIC BEVERAGES
- C12H1/00—Pasteurisation, sterilisation, preservation, purification, clarification, or ageing of alcoholic beverages
- C12H1/02—Pasteurisation, sterilisation, preservation, purification, clarification, or ageing of alcoholic beverages combined with removal of precipitate or added materials, e.g. adsorption material
- C12H1/04—Pasteurisation, 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
- C12H1/0416—Pasteurisation, 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
- C12H1/0424—Pasteurisation, 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.
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)
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 |
-
1961
- 1961-12-18 GB GB4522861A patent/GB975733A/en not_active Expired
Cited By (51)
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 |
US10604601B2 (en) | 2011-10-19 | 2020-03-31 | 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 |
US9969822B2 (en) | 2011-10-19 | 2018-05-15 | Sirrus, Inc. | Multifunctional monomers, methods for making multifunctional 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 |
US10611861B2 (en) | 2011-10-19 | 2020-04-07 | Sirrus, Inc. | Multifunctional monomers, methods for making multifunctional monomers, polymerizable compositions and products formed thereform |
US9181365B2 (en) | 2012-03-30 | 2015-11-10 | Sirrus, Inc. | Methods for activating polymerizable compositions, polymerizable systems, and products formed thereby |
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 |
US9234107B2 (en) | 2012-03-30 | 2016-01-12 | Sirrus, Inc. | Ink coating formulations and polymerizable systems for producing the same |
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 |
US9108914B1 (en) | 2013-01-11 | 2015-08-18 | Sirrus, Inc. | Method to obtain methylene malonate via bis(hydroxymethyl) malonate pathway |
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 |
US11021617B2 (en) | 2014-09-08 | 2021-06-01 | Sirrus, Inc. | Polymers including one or more 1,1-disubstituted alkene compounds and polymer compositions thereof |
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 |
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 |
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 |
US10308802B2 (en) | 2014-09-08 | 2019-06-04 | Sirrus, Inc. | Polymers including one or more 1,1-disubstituted alkene compounds and polymer compositions thereof |
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 |
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 |
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 |
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 |
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 |
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 |
US9969819B2 (en) | 2014-09-08 | 2018-05-15 | Sirrus, Inc. | Pressure sensitive adhesive including a 1,1-disubstituted alkene compound |
US10167348B2 (en) | 2014-09-08 | 2019-01-01 | Sirrus, Inc. | Solution polymers formed from methylene malonate monomers, polymerization, and solution polymer products |
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 |
US9938223B2 (en) | 2015-02-04 | 2018-04-10 | Sirrus, Inc. | Catalytic transesterification of ester compounds with groups reactive under transesterification conditions |
US9416091B1 (en) | 2015-02-04 | 2016-08-16 | 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 |
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 |
US9334430B1 (en) | 2015-05-29 | 2016-05-10 | Sirrus, Inc. | Encapsulated polymerization initiators, polymerization systems and methods using the same |
US9217098B1 (en) | 2015-06-01 | 2015-12-22 | Sirrus, Inc. | Electroinitiated polymerization of compositions having a 1,1-disubstituted alkene compound |
US9617354B2 (en) | 2015-06-01 | 2017-04-11 | 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 |
US9745413B1 (en) | 2016-06-03 | 2017-08-29 | Sirrus, Inc. | 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 |
US9617377B1 (en) | 2016-06-03 | 2017-04-11 | Sirrus, Inc. | Polyester macromers containing 1,1-dicarbonyl-substituted 1 alkenes |
US9718989B1 (en) | 2016-06-03 | 2017-08-01 | Sirrus, Inc. | Coatings containing 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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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 |
US10087283B2 (en) | 2016-06-03 | 2018-10-02 | Sirrus, Inc. | Polyester macromers containing 1,1-dicarbonyl-substituted 1 alkenes |
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