ZA200301754B - Process for the production of chemically or enzymatically modified polysaccharides, and products made thereby. - Google Patents
Process for the production of chemically or enzymatically modified polysaccharides, and products made thereby. Download PDFInfo
- Publication number
- ZA200301754B ZA200301754B ZA200301754A ZA200301754A ZA200301754B ZA 200301754 B ZA200301754 B ZA 200301754B ZA 200301754 A ZA200301754 A ZA 200301754A ZA 200301754 A ZA200301754 A ZA 200301754A ZA 200301754 B ZA200301754 B ZA 200301754B
- Authority
- ZA
- South Africa
- Prior art keywords
- composition
- viscosity
- reducing agent
- gum
- polysaccharide
- Prior art date
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- 238000000034 method Methods 0.000 title claims description 163
- 229920001282 polysaccharide Polymers 0.000 title claims description 132
- 239000005017 polysaccharide Substances 0.000 title claims description 130
- 150000004676 glycans Chemical class 0.000 title claims description 50
- 230000008569 process Effects 0.000 title description 54
- 238000004519 manufacturing process Methods 0.000 title description 3
- 239000000203 mixture Substances 0.000 claims description 382
- 150000001720 carbohydrates Chemical class 0.000 claims description 182
- 239000003638 chemical reducing agent Substances 0.000 claims description 156
- 229920001223 polyethylene glycol Polymers 0.000 claims description 126
- 239000002202 Polyethylene glycol Substances 0.000 claims description 93
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 82
- 229920002907 Guar gum Polymers 0.000 claims description 55
- 239000000665 guar gum Substances 0.000 claims description 55
- 235000010417 guar gum Nutrition 0.000 claims description 55
- 229960002154 guar gum Drugs 0.000 claims description 55
- 230000002829 reductive effect Effects 0.000 claims description 43
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims description 41
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 35
- 108010015133 Galactose oxidase Proteins 0.000 claims description 30
- 239000007787 solid Substances 0.000 claims description 25
- 230000001590 oxidative effect Effects 0.000 claims description 19
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 15
- 244000215068 Acacia senegal Species 0.000 claims description 14
- 102000016938 Catalase Human genes 0.000 claims description 14
- 108010053835 Catalase Proteins 0.000 claims description 14
- 229920000084 Gum arabic Polymers 0.000 claims description 14
- 235000010489 acacia gum Nutrition 0.000 claims description 14
- 239000000205 acacia gum Substances 0.000 claims description 14
- 239000001814 pectin Substances 0.000 claims description 14
- 229920001277 pectin Polymers 0.000 claims description 14
- 235000010987 pectin Nutrition 0.000 claims description 14
- 229920001817 Agar Polymers 0.000 claims description 12
- 229920002134 Carboxymethyl cellulose Polymers 0.000 claims description 12
- 239000001856 Ethyl cellulose Substances 0.000 claims description 12
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 claims description 12
- 239000008272 agar Substances 0.000 claims description 12
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- 239000003125 aqueous solvent Substances 0.000 claims description 12
- 239000001768 carboxy methyl cellulose Substances 0.000 claims description 12
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- 239000008112 carboxymethyl-cellulose Substances 0.000 claims description 12
- 235000019325 ethyl cellulose Nutrition 0.000 claims description 12
- 229920001249 ethyl cellulose Polymers 0.000 claims description 12
- 238000010438 heat treatment Methods 0.000 claims description 12
- 229920000609 methyl cellulose Polymers 0.000 claims description 12
- 239000001923 methylcellulose Substances 0.000 claims description 12
- 235000010981 methylcellulose Nutrition 0.000 claims description 12
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- 239000001863 hydroxypropyl cellulose Substances 0.000 claims description 11
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 claims description 11
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 claims description 11
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 claims description 11
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 claims description 11
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 claims description 11
- LNAZSHAWQACDHT-XIYTZBAFSA-N (2r,3r,4s,5r,6s)-4,5-dimethoxy-2-(methoxymethyl)-3-[(2s,3r,4s,5r,6r)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6r)-4,5,6-trimethoxy-2-(methoxymethyl)oxan-3-yl]oxyoxane Chemical compound CO[C@@H]1[C@@H](OC)[C@H](OC)[C@@H](COC)O[C@H]1O[C@H]1[C@H](OC)[C@@H](OC)[C@H](O[C@H]2[C@@H]([C@@H](OC)[C@H](OC)O[C@@H]2COC)OC)O[C@@H]1COC LNAZSHAWQACDHT-XIYTZBAFSA-N 0.000 claims description 10
- -1 polyethylene Polymers 0.000 claims description 6
- KMUONIBRACKNSN-UHFFFAOYSA-N potassium dichromate Chemical compound [K+].[K+].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O KMUONIBRACKNSN-UHFFFAOYSA-N 0.000 claims description 6
- 239000003054 catalyst Substances 0.000 claims description 4
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- 244000007835 Cyamopsis tetragonoloba Species 0.000 claims 4
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- 244000303965 Cyamopsis psoralioides Species 0.000 description 145
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- 150000004804 polysaccharides Chemical class 0.000 description 82
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- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 24
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- 238000005119 centrifugation Methods 0.000 description 1
- YARKTHNUMGKMGS-LQGKIZFRSA-N chembl3193980 Chemical compound COC1=C(O)C(OC)=CC(\C=N\N=C\C=2C=C(OC)C(O)=C(OC)C=2)=C1 YARKTHNUMGKMGS-LQGKIZFRSA-N 0.000 description 1
- GVPFVAHMJGGAJG-UHFFFAOYSA-L cobalt dichloride Chemical compound [Cl-].[Cl-].[Co+2] GVPFVAHMJGGAJG-UHFFFAOYSA-L 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 229960003280 cupric chloride Drugs 0.000 description 1
- 238000013480 data collection Methods 0.000 description 1
- 238000010511 deprotection reaction Methods 0.000 description 1
- 238000000502 dialysis Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 230000003028 elevating effect Effects 0.000 description 1
- 208000027386 essential tremor 1 Diseases 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 108010093305 exopolygalacturonase Proteins 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 238000013467 fragmentation Methods 0.000 description 1
- 238000006062 fragmentation reaction Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 238000002290 gas chromatography-mass spectrometry Methods 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 239000008131 herbal destillate Substances 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000002356 laser light scattering Methods 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000006140 methanolysis reaction Methods 0.000 description 1
- XLSZMDLNRCVEIJ-UHFFFAOYSA-N methylimidazole Natural products CC1=CNC=N1 XLSZMDLNRCVEIJ-UHFFFAOYSA-N 0.000 description 1
- 150000002772 monosaccharides Chemical class 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000006395 oxidase reaction Methods 0.000 description 1
- 239000003415 peat Substances 0.000 description 1
- 108010087558 pectate lyase Proteins 0.000 description 1
- 108020004410 pectinesterase Proteins 0.000 description 1
- 239000008363 phosphate buffer Substances 0.000 description 1
- 229920002523 polyethylene Glycol 1000 Polymers 0.000 description 1
- 239000004293 potassium hydrogen sulphite Substances 0.000 description 1
- 229910000160 potassium phosphate Inorganic materials 0.000 description 1
- 235000011009 potassium phosphates Nutrition 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
- 239000003755 preservative agent Substances 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 229940079877 pyrogallol Drugs 0.000 description 1
- 238000011002 quantification Methods 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 102200017272 rs28931576 Human genes 0.000 description 1
- 239000012488 sample solution Substances 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- VUYXVWGKCKTUMF-UHFFFAOYSA-N tetratriacontaethylene glycol monomethyl ether Chemical compound COCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO VUYXVWGKCKTUMF-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000000108 ultra-filtration Methods 0.000 description 1
- 238000000196 viscometry Methods 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B37/00—Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P19/00—Preparation of compounds containing saccharide radicals
- C12P19/04—Polysaccharides, i.e. compounds containing more than five saccharide radicals attached to each other by glycosidic bonds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B37/00—Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
- C08B37/006—Heteroglycans, i.e. polysaccharides having more than one sugar residue in the main chain in either alternating or less regular sequence; Gellans; Succinoglycans; Arabinogalactans; Tragacanth or gum tragacanth or traganth from Astragalus; Gum Karaya from Sterculia urens; Gum Ghatti from Anogeissus latifolia; Derivatives thereof
- C08B37/0087—Glucomannans or galactomannans; Tara or tara gum, i.e. D-mannose and D-galactose units, e.g. from Cesalpinia spinosa; Tamarind gum, i.e. D-galactose, D-glucose and D-xylose units, e.g. from Tamarindus indica; Gum Arabic, i.e. L-arabinose, L-rhamnose, D-galactose and D-glucuronic acid units, e.g. from Acacia Senegal or Acacia Seyal; Derivatives thereof
- C08B37/0096—Guar, guar gum, guar flour, guaran, i.e. (beta-1,4) linked D-mannose units in the main chain branched with D-galactose units in (alpha-1,6), e.g. from Cyamopsis Tetragonolobus; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L1/00—Compositions of cellulose, modified cellulose or cellulose derivatives
- C08L1/08—Cellulose derivatives
- C08L1/26—Cellulose ethers
- C08L1/28—Alkyl ethers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L5/00—Compositions of polysaccharides or of their derivatives not provided for in groups C08L1/00 or C08L3/00
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L5/00—Compositions of polysaccharides or of their derivatives not provided for in groups C08L1/00 or C08L3/00
- C08L5/04—Alginic acid; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L5/00—Compositions of polysaccharides or of their derivatives not provided for in groups C08L1/00 or C08L3/00
- C08L5/14—Hemicellulose; Derivatives thereof
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/21—Macromolecular organic compounds of natural origin; Derivatives thereof
- D21H17/24—Polysaccharides
- D21H17/31—Gums
- D21H17/32—Guar or other polygalactomannan gum
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H21/00—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
- D21H21/14—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by function or properties in or on the paper
- D21H21/18—Reinforcing agents
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Molecular Biology (AREA)
- Materials Engineering (AREA)
- Emergency Medicine (AREA)
- Microbiology (AREA)
- General Chemical & Material Sciences (AREA)
- Biotechnology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- Genetics & Genomics (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Medicinal Preparation (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Cosmetics (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US22273000P | 2000-08-03 | 2000-08-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
ZA200301754B true ZA200301754B (en) | 2004-02-05 |
Family
ID=22833437
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ZA200301754A ZA200301754B (en) | 2000-08-03 | 2003-03-03 | Process for the production of chemically or enzymatically modified polysaccharides, and products made thereby. |
Country Status (11)
Country | Link |
---|---|
US (1) | US20020134281A1 (ja) |
EP (1) | EP1305344A2 (ja) |
JP (1) | JP2004506057A (ja) |
KR (1) | KR20030020955A (ja) |
CN (1) | CN1468261A (ja) |
AU (1) | AU2001283103A1 (ja) |
CA (1) | CA2417633A1 (ja) |
MX (1) | MXPA03000950A (ja) |
PL (1) | PL360411A1 (ja) |
WO (1) | WO2002012388A2 (ja) |
ZA (1) | ZA200301754B (ja) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101974131B (zh) | 2002-06-25 | 2015-05-20 | 罗狄亚公司 | 瓜尔胶和其它多糖用电子束接枝聚合的方法 |
US7259192B2 (en) | 2002-06-25 | 2007-08-21 | Rhodia, Inc. | Molecular weight reduction of polysaccharides by electron beams |
JP4933251B2 (ja) * | 2003-04-09 | 2012-05-16 | ハーキュリーズ・インコーポレーテッド | コンディショニング用途におけるカチオン性酸化多糖類 |
US20100184630A1 (en) * | 2009-01-16 | 2010-07-22 | Sullivan Philip F | Breaking the rheology of a wellbore fluid by creating phase separation |
JP4837086B2 (ja) * | 2009-12-15 | 2011-12-14 | 株式会社 資生堂 | 乳化化粧料 |
FI125713B (fi) * | 2010-10-01 | 2016-01-15 | Upm Kymmene Corp | Menetelmä märän paperirainan ajettavuuden parantamiseksi ja paperi |
CN105839443A (zh) * | 2016-03-29 | 2016-08-10 | 华南理工大学 | 一种提高高得率浆性能的方法 |
CN111454899B (zh) * | 2020-04-30 | 2021-04-20 | 青岛思拓新源细胞医学有限公司 | 角叉菜多糖在抑制间充质干细胞成脂转化中的用途 |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1047467A (en) * | 1962-09-12 | 1966-11-02 | Mo Och Domsjoe Ab | Improvements in the treatment of leather |
US3231560A (en) * | 1963-01-25 | 1966-01-25 | Gen Mills Inc | Dialdehyde polysaccharide bisulfite adducts |
US3297604A (en) * | 1963-10-28 | 1967-01-10 | American Mach & Foundry | Oxidized galactose containing reaction products |
JPS4852848A (ja) * | 1971-11-05 | 1973-07-25 | ||
DE2805907B2 (de) * | 1978-02-13 | 1980-12-18 | Hoechst Ag, 6000 Frankfurt | Verfahren zur Herstellung einer stabilen Celluloseether-Suspension und deren Verwendung |
DD158904A1 (de) * | 1980-05-22 | 1983-02-09 | Betancourt Oscar Quintela | Verfahren zur herstellung von viskose mit guter filtrierbarkeit aus bagassezellstoff |
US4425241A (en) * | 1981-02-18 | 1984-01-10 | Phillips Petroleum Company | Drilling fluids |
US4474902A (en) * | 1982-12-07 | 1984-10-02 | Richardson-Vicks Inc. | Karaya gum adhesive in a hydrophilic denture vehicle |
US4453979A (en) * | 1983-03-23 | 1984-06-12 | Lever Brothers Company | Dispersion of hydrophilic gums to form non-swelling aqueous alcoholic mixtures |
US4874854A (en) * | 1985-10-08 | 1989-10-17 | Merck & Co., Inc. | Low viscosity heteropolysaccharides |
EP0465992B1 (en) * | 1990-07-02 | 1998-06-17 | Aqualon Company | High solids low viscosity polysaccharide composition |
US6022717A (en) * | 1997-12-31 | 2000-02-08 | Hercules Incorporated | Use of oxidation promoting chemicals in the oxidation oxidizable galactose type of alcohol configuration containing polymer |
-
2001
- 2001-08-01 JP JP2002517686A patent/JP2004506057A/ja active Pending
- 2001-08-01 CN CNA018167977A patent/CN1468261A/zh active Pending
- 2001-08-01 PL PL01360411A patent/PL360411A1/xx unknown
- 2001-08-01 CA CA002417633A patent/CA2417633A1/en not_active Abandoned
- 2001-08-01 MX MXPA03000950A patent/MXPA03000950A/es unknown
- 2001-08-01 US US09/920,122 patent/US20020134281A1/en active Pending
- 2001-08-01 EP EP01961872A patent/EP1305344A2/en not_active Withdrawn
- 2001-08-01 AU AU2001283103A patent/AU2001283103A1/en not_active Abandoned
- 2001-08-01 KR KR10-2003-7001440A patent/KR20030020955A/ko not_active Application Discontinuation
- 2001-08-01 WO PCT/US2001/024329 patent/WO2002012388A2/en not_active Application Discontinuation
-
2003
- 2003-03-03 ZA ZA200301754A patent/ZA200301754B/en unknown
Also Published As
Publication number | Publication date |
---|---|
US20020134281A1 (en) | 2002-09-26 |
PL360411A1 (en) | 2004-09-06 |
CN1468261A (zh) | 2004-01-14 |
CA2417633A1 (en) | 2002-02-14 |
EP1305344A2 (en) | 2003-05-02 |
WO2002012388A2 (en) | 2002-02-14 |
MXPA03000950A (es) | 2003-06-30 |
KR20030020955A (ko) | 2003-03-10 |
JP2004506057A (ja) | 2004-02-26 |
WO2002012388A3 (en) | 2002-05-30 |
AU2001283103A1 (en) | 2002-02-18 |
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