IL32277A - Process of clarifying and improving vegetable beverages - Google Patents

Process of clarifying and improving vegetable beverages

Info

Publication number: IL32277A
Authority: IL; Israel
Prior art keywords: beads; beer; water; beverage; beverages
Prior art date: 1968-06-12

Application number

IL32277A

Other languages

English (en)

Other versions

IL32277A0 (en

Original Assignee

Gaf Corp

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.)

1968-06-12

Filing date

1969-05-22

Publication date

1973-01-30

1969-05-22 Application filed by Gaf Corp filed Critical Gaf Corp

1969-07-30 Publication of IL32277A0 publication Critical patent/IL32277A0/xx

1973-01-30 Publication of IL32277A publication Critical patent/IL32277A/en

Links

235000013361 beverage Nutrition 0.000 title claims description 31
238000000034 method Methods 0.000 title claims description 29
230000008569 process Effects 0.000 title claims description 26
235000013311 vegetables Nutrition 0.000 title claims description 7
239000011324 bead Substances 0.000 claims description 42
235000013405 beer Nutrition 0.000 claims description 28
WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 26
229920000642 polymer Polymers 0.000 claims description 22
239000008187 granular material Substances 0.000 claims description 12
235000014101 wine Nutrition 0.000 claims description 12
238000001035 drying Methods 0.000 claims description 2
229920001577 copolymer Polymers 0.000 claims 1
238000010828 elution Methods 0.000 claims 1
230000001172 regenerating effect Effects 0.000 claims 1
238000000926 separation method Methods 0.000 claims 1
YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 16
239000000178 monomer Substances 0.000 description 12
229920000036 polyvinylpyrrolidone Polymers 0.000 description 11
235000013855 polyvinylpyrrolidone Nutrition 0.000 description 11
239000001267 polyvinylpyrrolidone Substances 0.000 description 11
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
238000006116 polymerization reaction Methods 0.000 description 10
238000001914 filtration Methods 0.000 description 9
229920001864 tannin Polymers 0.000 description 9
235000018553 tannin Nutrition 0.000 description 9
239000001648 tannin Substances 0.000 description 9
239000003431 cross linking reagent Substances 0.000 description 8
239000003792 electrolyte Substances 0.000 description 8
239000000463 material Substances 0.000 description 8
FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 8
229960004889 salicylic acid Drugs 0.000 description 8
238000005352 clarification Methods 0.000 description 7
238000012360 testing method Methods 0.000 description 7
MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 6
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
239000003054 catalyst Substances 0.000 description 6
HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 5
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
239000002585 base Substances 0.000 description 5
238000000605 extraction Methods 0.000 description 5
239000011521 glass Substances 0.000 description 5
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239000000047 product Substances 0.000 description 5
230000001476 alcoholic effect Effects 0.000 description 4
239000007864 aqueous solution Substances 0.000 description 4
230000000694 effects Effects 0.000 description 4
239000012530 fluid Substances 0.000 description 4
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235000013824 polyphenols Nutrition 0.000 description 4
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UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
125000000217 alkyl group Chemical group 0.000 description 3
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
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238000007254 oxidation reaction Methods 0.000 description 3
150000002989 phenols Chemical class 0.000 description 3
150000008442 polyphenolic compounds Chemical class 0.000 description 3
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
239000011734 sodium Substances 0.000 description 3
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TUSDEZXZIZRFGC-UHFFFAOYSA-N 1-O-galloyl-3,6-(R)-HHDP-beta-D-glucose Natural products OC1C(O2)COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC1C(O)C2OC(=O)C1=CC(O)=C(O)C(O)=C1 TUSDEZXZIZRFGC-UHFFFAOYSA-N 0.000 description 2
OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
XFCMNSHQOZQILR-UHFFFAOYSA-N 2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOC(=O)C(C)=C XFCMNSHQOZQILR-UHFFFAOYSA-N 0.000 description 2
239000001263 FEMA 3042 Substances 0.000 description 2
WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
LRBQNJMCXXYXIU-PPKXGCFTSA-N Penta-digallate-beta-D-glucose Natural products OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-PPKXGCFTSA-N 0.000 description 2
102000035195 Peptidases Human genes 0.000 description 2
108091005804 Peptidases Proteins 0.000 description 2
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 2
150000001252 acrylic acid derivatives Chemical class 0.000 description 2
238000013019 agitation Methods 0.000 description 2
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XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
230000008901 benefit Effects 0.000 description 2
FUSUHKVFWTUUBE-UHFFFAOYSA-N buten-2-one Chemical compound CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 description 2
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
230000008859 change Effects 0.000 description 2
239000003086 colorant Substances 0.000 description 2
230000000536 complexating effect Effects 0.000 description 2
239000012153 distilled water Substances 0.000 description 2
STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 2
239000000706 filtrate Substances 0.000 description 2
239000011491 glass wool Substances 0.000 description 2
239000007788 liquid Substances 0.000 description 2
KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 2
239000002245 particle Substances 0.000 description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
239000011591 potassium Substances 0.000 description 2
239000002244 precipitate Substances 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
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239000000377 silicon dioxide Substances 0.000 description 2
235000012239 silicon dioxide Nutrition 0.000 description 2
229910052938 sodium sulfate Inorganic materials 0.000 description 2
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LRBQNJMCXXYXIU-NRMVVENXSA-N tannic acid Chemical compound OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-NRMVVENXSA-N 0.000 description 2
229940033123 tannic acid Drugs 0.000 description 2
235000015523 tannic acid Nutrition 0.000 description 2
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BSSNZUFKXJJCBG-OWOJBTEDSA-N (e)-but-2-enediamide Chemical compound NC(=O)\C=C\C(N)=O BSSNZUFKXJJCBG-OWOJBTEDSA-N 0.000 description 1
QLLUAUADIMPKIH-UHFFFAOYSA-N 1,2-bis(ethenyl)naphthalene Chemical compound C1=CC=CC2=C(C=C)C(C=C)=CC=C21 QLLUAUADIMPKIH-UHFFFAOYSA-N 0.000 description 1
MWZJGRDWJVHRDV-UHFFFAOYSA-N 1,4-bis(ethenoxy)butane Chemical compound C=COCCCCOC=C MWZJGRDWJVHRDV-UHFFFAOYSA-N 0.000 description 1
FYBFGAFWCBMEDG-UHFFFAOYSA-N 1-[3,5-di(prop-2-enoyl)-1,3,5-triazinan-1-yl]prop-2-en-1-one Chemical compound C=CC(=O)N1CN(C(=O)C=C)CN(C(=O)C=C)C1 FYBFGAFWCBMEDG-UHFFFAOYSA-N 0.000 description 1
IROFMMHLTOVXFS-UHFFFAOYSA-N 1-chloro-2,3-bis(ethenyl)benzene Chemical compound ClC1=CC=CC(C=C)=C1C=C IROFMMHLTOVXFS-UHFFFAOYSA-N 0.000 description 1
UBPXWZDJZFZKGH-UHFFFAOYSA-N 1-ethenyl-3-methylpyrrolidin-2-one Chemical compound CC1CCN(C=C)C1=O UBPXWZDJZFZKGH-UHFFFAOYSA-N 0.000 description 1
OSSNTDFYBPYIEC-UHFFFAOYSA-N 1-ethenylimidazole Chemical compound C=CN1C=CN=C1 OSSNTDFYBPYIEC-UHFFFAOYSA-N 0.000 description 1
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 1
JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
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XHJRWVTZUOPCBI-UHFFFAOYSA-N 2-ethenoxyethylurea Chemical compound NC(=O)NCCOC=C XHJRWVTZUOPCBI-UHFFFAOYSA-N 0.000 description 1
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ZXABMDQSAABDMG-UHFFFAOYSA-N 3-ethenoxyprop-1-ene Chemical compound C=CCOC=C ZXABMDQSAABDMG-UHFFFAOYSA-N 0.000 description 1
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KWARHWWINPVBFR-UHFFFAOYSA-N 3-penta-1,4-dien-3-yloxypropane-1,2-diol Chemical compound C(C(O)CO)OC(C=C)C=C KWARHWWINPVBFR-UHFFFAOYSA-N 0.000 description 1
DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 1
YKXAYLPDMSGWEV-UHFFFAOYSA-N 4-hydroxybutyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCO YKXAYLPDMSGWEV-UHFFFAOYSA-N 0.000 description 1
JHWGFJBTMHEZME-UHFFFAOYSA-N 4-prop-2-enoyloxybutyl prop-2-enoate Chemical class C=CC(=O)OCCCCOC(=O)C=C JHWGFJBTMHEZME-UHFFFAOYSA-N 0.000 description 1
VJOWMORERYNYON-UHFFFAOYSA-N 5-ethenyl-2-methylpyridine Chemical compound CC1=CC=C(C=C)C=N1 VJOWMORERYNYON-UHFFFAOYSA-N 0.000 description 1
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
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KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
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230000007935 neutral effect Effects 0.000 description 1
HVAMZGADVCBITI-UHFFFAOYSA-M pent-4-enoate Chemical compound [O-]C(=O)CCC=C HVAMZGADVCBITI-UHFFFAOYSA-M 0.000 description 1
DBSDMAPJGHBWAL-UHFFFAOYSA-N penta-1,4-dien-3-ylbenzene Chemical compound C=CC(C=C)C1=CC=CC=C1 DBSDMAPJGHBWAL-UHFFFAOYSA-N 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
238000005191 phase separation Methods 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
229920006216 polyvinyl aromatic Polymers 0.000 description 1
229910052573 porcelain Inorganic materials 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
WCUXLLCKKVVCTQ-UHFFFAOYSA-M potassium chloride Inorganic materials [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 1
OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 description 1
229910052939 potassium sulfate Inorganic materials 0.000 description 1
235000011151 potassium sulphates Nutrition 0.000 description 1
239000012254 powdered material Substances 0.000 description 1
QTECDUFMBMSHKR-UHFFFAOYSA-N prop-2-enyl prop-2-enoate Chemical compound C=CCOC(=O)C=C QTECDUFMBMSHKR-UHFFFAOYSA-N 0.000 description 1
239000000376 reactant Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
238000005070 sampling Methods 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Inorganic materials [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
230000003381 solubilizing effect Effects 0.000 description 1
238000004448 titration Methods 0.000 description 1
LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 1
239000002966 varnish Substances 0.000 description 1
229960000834 vinyl ether Drugs 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
238000005406 washing Methods 0.000 description 1
235000020097 white wine Nutrition 0.000 description 1

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
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Preparation or treatment thereof
- A23L2/70—Clarifying or fining of non-alcoholic beverages; Removing unwanted matter
- A23L2/80—Clarifying or fining of non-alcoholic beverages; Removing unwanted matter by adsorption

Landscapes

Engineering & Computer Science (AREA)
Chemical & Material Sciences (AREA)
Food Science & Technology (AREA)
Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Organic Chemistry (AREA)
General Health & Medical Sciences (AREA)
General Engineering & Computer Science (AREA)
Bioinformatics & Cheminformatics (AREA)
Genetics & Genomics (AREA)
Biochemistry (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Nutrition Science (AREA)
Polymers & Plastics (AREA)
Distillation Of Fermentation Liquor, Processing Of Alcohols, Vinegar And Beer (AREA)
Solid-Sorbent Or Filter-Aiding Compositions (AREA)

IL32277A 1968-06-12 1969-05-22 Process of clarifying and improving vegetable beverages IL32277A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US73629768A	1968-06-12	1968-06-12

Publications (2)

Publication Number	Publication Date
IL32277A0 IL32277A0 (en)	1969-07-30
IL32277A true IL32277A (en)	1973-01-30

Family

ID=24959322

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL32277A IL32277A (en)	1968-06-12	1969-05-22	Process of clarifying and improving vegetable beverages

Country Status (9)

Country	Link
BE (1)	BE733399A (de)
CH (1)	CH515329A (de)
DE (1)	DE1929500A1 (de)
FR (1)	FR2010745A1 (de)
GB (1)	GB1268875A (de)
IL (1)	IL32277A (de)
IT (1)	IT998013B (de)
NL (1)	NL151738B (de)
SE (1)	SE380828B (de)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0080298A3 (de) *	1981-11-21	1983-10-05	Canadian Patents and Development Limited Société Canadienne des Brevets et d'Exploitation Limitée	Behandlung von Obst, Gemüse- und Fleischprodukten
DE4000978A1 (de) *	1990-01-16	1991-07-18	Basf Ag	Verfahren zur entfernung von schwermetallionen aus wein und weinaehnlichen getraenken
DE9012026U1 (de) *	1990-08-21	1992-01-02	Emil Lux Gmbh & Co Kg, 5632 Wermelskirchen	Handwerkzeug aus Stahl
US5882521A (en) *	1996-04-18	1999-03-16	Waters Investment Ltd.	Water-wettable chromatographic media for solid phase extraction
US5866660A (en) *	1997-03-13	1999-02-02	Isp Investments Inc.	Polyvinyl prolidone and crosslinker with divinyl and chelation group
US6548076B2 (en) *	1999-08-17	2003-04-15	Shanbrom Technologies, Llc	Antimicrobial lees
US7119145B2 (en)	2002-01-25	2006-10-10	Phenomenex, Inc.	Surface graft modified resins and formation thereof
DE102024139221A1 (de) *	2024-12-20	2026-06-25	Albert Handtmann Armaturenfabrik Gmbh & Co. Kg	Verfahren zur Herstellung von sphärischen PVP Beads als Bierstabilisierungsmittel

1969
- 1969-05-21 BE BE733399D patent/BE733399A/xx unknown
- 1969-05-22 IL IL32277A patent/IL32277A/en unknown
- 1969-06-05 SE SE6907997A patent/SE380828B/xx unknown
- 1969-06-06 NL NL696908685A patent/NL151738B/xx unknown
- 1969-06-06 GB GB28859/69A patent/GB1268875A/en not_active Expired
- 1969-06-11 CH CH890969A patent/CH515329A/de not_active IP Right Cessation
- 1969-06-11 DE DE19691929500 patent/DE1929500A1/de active Pending
- 1969-06-11 FR FR6919323A patent/FR2010745A1/fr not_active Withdrawn
- 1969-06-11 IT IT18067/69A patent/IT998013B/it active

Also Published As

Publication number	Publication date
DE1929500A1 (de)	1969-12-18
GB1268875A (en)	1972-03-29
IT998013B (it)	1976-01-20
FR2010745A1 (de)	1970-02-20
SE380828B (sv)	1975-11-17
BE733399A (de)	1969-11-03
NL6908685A (de)	1969-12-16
NL151738B (nl)	1976-12-15
CH515329A (de)	1971-11-15
IL32277A0 (en)	1969-07-30

Publication	Publication Date	Title
US3878310A (en)	1975-04-15	Treatment of beverages to clarify and to prevent haze
US5094867A (en)	1992-03-10	Removal of heavy metal ions from wine and wine-like beverages
RU2204596C2 (ru)	2003-05-20	Способ стабилизации напитков
GB2487762A (en)	2012-08-08	Composite material for haze prevention in beverages
WO2005117616A9 (en)	2006-05-04	Method of preventing or reducing haze in a beverage using silane-treated silica filter media
JP2003502465A (ja)	2003-01-21	フッ素化ポリマー吸着剤粒子の製造法
RU2375436C2 (ru)	2009-12-10	Способ приготовления жидкости, содержащей белки, для последующего отделения посредством использования одного или более агента, образующего с белком комплекс
US6239206B1 (en)	2001-05-29	Complexes of heavy metal ions and a polymer, and their use for selective removal of compounds from liquids
JP2017051194A (ja)	2017-03-16	液体食品および飲料の安定化
US2947633A (en)	1960-08-02	Treatment of vegetable beverages
US3818111A (en)	1974-06-18	Fining and increasing the chill haze stability of fermented alcoholic beverages
US5505973A (en)	1996-04-09	Process for removing aluminum ions from beer or fruit juice
JP6851581B2 (ja)	2021-03-31	醸造酒の安定化
JP2013532474A (ja)	2013-08-19	酵母発酵飲料を安定化させる方法
AU2014355200A1 (en)	2016-05-12	Stabilization of fermented beverages
US20030124233A1 (en)	2003-07-03	Use of insoluble highly crosslinked popcorn polymers as filter aids and/or stabilizers
US20250215193A1 (en)	2025-07-03	Chromatography media for removal of polyphenol substances and preparation method thereof
AU610332B2 (en)	1991-05-16	Process for the reduction in size of the pores of a filter medium for beverages
US3146107A (en)	1964-08-25	Clarifying beverages
Denizli et al.	1998	New chelate-forming polymer microspheres carrying dyes as chelators for iron overload
Boulton et al.	1999	The fining and clarification of wines
GB2028340A (en)	1980-03-05	Finings for beer
JPS6323808B2 (de)	1988-05-18
RU2046630C1 (ru)	1995-10-27	Способ сорбционной очистки виноматериала и установка для его осуществления
SU1157051A1 (ru)	1985-05-23	Водорастворимые сополимеры метилвинилсульфида и @ -винилпирролидона в качестве осветлителей и стабилизаторов напитков