NO136466B - - Google Patents
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- Publication number
- NO136466B NO136466B NO723473A NO347372A NO136466B NO 136466 B NO136466 B NO 136466B NO 723473 A NO723473 A NO 723473A NO 347372 A NO347372 A NO 347372A NO 136466 B NO136466 B NO 136466B
- Authority
- NO
- Norway
- Prior art keywords
- parts
- weight
- percent
- fabric
- textile fabric
- Prior art date
Links
- 239000004744 fabric Substances 0.000 claims description 59
- 239000004753 textile Substances 0.000 claims description 45
- 239000000835 fiber Substances 0.000 claims description 28
- 239000000463 material Substances 0.000 claims description 28
- 229920000058 polyacrylate Polymers 0.000 claims description 28
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 21
- 238000000034 method Methods 0.000 claims description 21
- SWLVFNYSXGMGBS-UHFFFAOYSA-N ammonium bromide Chemical compound [NH4+].[Br-] SWLVFNYSXGMGBS-UHFFFAOYSA-N 0.000 claims description 19
- 239000000126 substance Substances 0.000 claims description 18
- 239000000203 mixture Substances 0.000 claims description 17
- 229920000642 polymer Polymers 0.000 claims description 17
- 238000005470 impregnation Methods 0.000 claims description 14
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 13
- 239000004202 carbamide Substances 0.000 claims description 13
- 229920001577 copolymer Polymers 0.000 claims description 10
- LWFBRHSTNWMMGN-UHFFFAOYSA-N 4-phenylpyrrolidin-1-ium-2-carboxylic acid;chloride Chemical compound Cl.C1NC(C(=O)O)CC1C1=CC=CC=C1 LWFBRHSTNWMMGN-UHFFFAOYSA-N 0.000 claims description 8
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 claims description 8
- SMTDFMMXJHYDDE-UHFFFAOYSA-N 2-prop-1-enylpyridine Chemical compound CC=CC1=CC=CC=N1 SMTDFMMXJHYDDE-UHFFFAOYSA-N 0.000 claims description 7
- 238000010438 heat treatment Methods 0.000 claims description 7
- 239000007864 aqueous solution Substances 0.000 claims description 6
- 238000001035 drying Methods 0.000 claims description 6
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 4
- 239000012467 final product Substances 0.000 claims description 3
- 230000000694 effects Effects 0.000 claims description 2
- 230000008569 process Effects 0.000 claims description 2
- 238000011282 treatment Methods 0.000 description 29
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 26
- 230000003068 static effect Effects 0.000 description 12
- 239000000178 monomer Substances 0.000 description 11
- 230000005611 electricity Effects 0.000 description 10
- 239000007787 solid Substances 0.000 description 9
- 239000003795 chemical substances by application Substances 0.000 description 8
- 150000005673 monoalkenes Chemical class 0.000 description 6
- 239000000523 sample Substances 0.000 description 6
- 230000002411 adverse Effects 0.000 description 5
- 239000013068 control sample Substances 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 210000002268 wool Anatomy 0.000 description 5
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 4
- 238000009825 accumulation Methods 0.000 description 4
- 230000003750 conditioning effect Effects 0.000 description 4
- 239000003063 flame retardant Substances 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 229920002239 polyacrylonitrile Polymers 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 229920002678 cellulose Polymers 0.000 description 3
- 239000001913 cellulose Substances 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000006482 condensation reaction Methods 0.000 description 3
- 230000008021 deposition Effects 0.000 description 3
- 230000002209 hydrophobic effect Effects 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Substances C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 3
- -1 vinylidene halides Chemical class 0.000 description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical class C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 2
- 239000004677 Nylon Substances 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 229920001807 Urea-formaldehyde Polymers 0.000 description 2
- 150000001253 acrylic acids Chemical class 0.000 description 2
- 239000003125 aqueous solvent Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- FUSUHKVFWTUUBE-UHFFFAOYSA-N buten-2-one Chemical compound CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 2
- 239000002964 rayon Substances 0.000 description 2
- 229920001897 terpolymer Polymers 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- KYPOHTVBFVELTG-OWOJBTEDSA-N (e)-but-2-enedinitrile Chemical compound N#C\C=C\C#N KYPOHTVBFVELTG-OWOJBTEDSA-N 0.000 description 1
- BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical group C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 description 1
- FPBWSPZHCJXUBL-UHFFFAOYSA-N 1-chloro-1-fluoroethene Chemical group FC(Cl)=C FPBWSPZHCJXUBL-UHFFFAOYSA-N 0.000 description 1
- JWYVGKFDLWWQJX-UHFFFAOYSA-N 1-ethenylazepan-2-one Chemical compound C=CN1CCCCCC1=O JWYVGKFDLWWQJX-UHFFFAOYSA-N 0.000 description 1
- VOCDJQSAMZARGX-UHFFFAOYSA-N 1-ethenylpyrrolidine-2,5-dione Chemical compound C=CN1C(=O)CCC1=O VOCDJQSAMZARGX-UHFFFAOYSA-N 0.000 description 1
- WUIJTQZXUURFQU-UHFFFAOYSA-N 1-methylsulfonylethene Chemical compound CS(=O)(=O)C=C WUIJTQZXUURFQU-UHFFFAOYSA-N 0.000 description 1
- IGGDKDTUCAWDAN-UHFFFAOYSA-N 1-vinylnaphthalene Chemical compound C1=CC=C2C(C=C)=CC=CC2=C1 IGGDKDTUCAWDAN-UHFFFAOYSA-N 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- GPOGMJLHWQHEGF-UHFFFAOYSA-N 2-chloroethyl 2-methylprop-2-enoate Chemical class CC(=C)C(=O)OCCCl GPOGMJLHWQHEGF-UHFFFAOYSA-N 0.000 description 1
- MLMGJTAJUDSUKA-UHFFFAOYSA-N 2-ethenyl-1h-imidazole Chemical class C=CC1=NC=CN1 MLMGJTAJUDSUKA-UHFFFAOYSA-N 0.000 description 1
- OHAHNWHDCLIFSX-UHFFFAOYSA-N 2-ethenyl-4-ethylpyridine Chemical compound CCC1=CC=NC(C=C)=C1 OHAHNWHDCLIFSX-UHFFFAOYSA-N 0.000 description 1
- YQUDMNIUBTXLSX-UHFFFAOYSA-N 2-ethenyl-5-ethylpyridine Chemical compound CCC1=CC=C(C=C)N=C1 YQUDMNIUBTXLSX-UHFFFAOYSA-N 0.000 description 1
- IGDLZDCWMRPMGL-UHFFFAOYSA-N 2-ethenylisoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(C=C)C(=O)C2=C1 IGDLZDCWMRPMGL-UHFFFAOYSA-N 0.000 description 1
- KANZWHBYRHQMKZ-UHFFFAOYSA-N 2-ethenylpyrazine Chemical class C=CC1=CN=CC=N1 KANZWHBYRHQMKZ-UHFFFAOYSA-N 0.000 description 1
- XUGNJOCQALIQFG-UHFFFAOYSA-N 2-ethenylquinoline Chemical class C1=CC=CC2=NC(C=C)=CC=C21 XUGNJOCQALIQFG-UHFFFAOYSA-N 0.000 description 1
- KFDVPJUYSDEJTH-UHFFFAOYSA-N 4-ethenylpyridine Chemical compound C=CC1=CC=NC=C1 KFDVPJUYSDEJTH-UHFFFAOYSA-N 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 239000008365 aqueous carrier Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 239000007844 bleaching agent Substances 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000012459 cleaning agent Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000005536 corrosion prevention Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 229960004419 dimethyl fumarate Drugs 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- XJELOQYISYPGDX-UHFFFAOYSA-N ethenyl 2-chloroacetate Chemical compound ClCC(=O)OC=C XJELOQYISYPGDX-UHFFFAOYSA-N 0.000 description 1
- AFSIMBWBBOJPJG-UHFFFAOYSA-N ethenyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC=C AFSIMBWBBOJPJG-UHFFFAOYSA-N 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000004079 fireproofing Methods 0.000 description 1
- XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical compound FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 description 1
- 229940015043 glyoxal Drugs 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000002198 insoluble material Substances 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- HNEGQIOMVPPMNR-NSCUHMNNSA-L mesaconate(2-) Chemical compound [O-]C(=O)C(/C)=C/C([O-])=O HNEGQIOMVPPMNR-NSCUHMNNSA-L 0.000 description 1
- 125000005395 methacrylic acid group Chemical class 0.000 description 1
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
Classifications
-
- 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
- C12P19/10—Pullulan
-
- 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
- C08B37/0006—Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid
- C08B37/0009—Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid alpha-D-Glucans, e.g. polydextrose, alternan, glycogen; (alpha-1,4)(alpha-1,6)-D-Glucans; (alpha-1,3)(alpha-1,4)-D-Glucans, e.g. isolichenan or nigeran; (alpha-1,4)-D-Glucans; (alpha-1,3)-D-Glucans, e.g. pseudonigeran; Derivatives thereof
- C08B37/0018—Pullulan, i.e. (alpha-1,4)(alpha-1,6)-D-glucan; Derivatives thereof
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S435/00—Chemistry: molecular biology and microbiology
- Y10S435/8215—Microorganisms
- Y10S435/911—Microorganisms using fungi
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biochemistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Materials Engineering (AREA)
- General Chemical & Material Sciences (AREA)
- General Engineering & Computer Science (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Microbiology (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP46079413A JPS5136360B2 (pt) | 1971-10-11 | 1971-10-11 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NO136466B true NO136466B (pt) | 1977-05-31 |
| NO136466C NO136466C (no) | 1977-09-07 |
Family
ID=13689166
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO723473A NO136466C (no) | 1971-10-11 | 1972-09-28 | Fremgangsm}te til fremstilling av pullulan. |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US3827937A (pt) |
| JP (1) | JPS5136360B2 (pt) |
| AR (1) | AR194508A1 (pt) |
| AU (1) | AU468633B2 (pt) |
| BE (1) | BE789940A (pt) |
| CA (1) | CA994269A (pt) |
| CH (1) | CH540975A (pt) |
| DE (1) | DE2249836C3 (pt) |
| DK (1) | DK131873C (pt) |
| ES (1) | ES407544A1 (pt) |
| FI (1) | FI50138C (pt) |
| FR (1) | FR2156220B1 (pt) |
| GB (1) | GB1368903A (pt) |
| IT (1) | IT968463B (pt) |
| NL (1) | NL162137C (pt) |
| NO (1) | NO136466C (pt) |
| PH (1) | PH9462A (pt) |
| SE (1) | SE383358B (pt) |
| SU (1) | SU735177A3 (pt) |
| ZA (1) | ZA726693B (pt) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5060530A (pt) * | 1973-09-29 | 1975-05-24 | ||
| JPS5231019B2 (pt) * | 1973-10-16 | 1977-08-12 | ||
| JPS5633696B2 (pt) * | 1973-11-12 | 1981-08-05 | ||
| JPS5542635B2 (pt) * | 1974-01-31 | 1980-10-31 | ||
| JPS5414678B2 (pt) * | 1974-02-23 | 1979-06-08 | ||
| JPS5385163U (pt) * | 1976-12-16 | 1978-07-13 | ||
| JPS5733387Y2 (pt) * | 1977-03-17 | 1982-07-23 | ||
| US4258132A (en) * | 1977-10-11 | 1981-03-24 | Satoru Shinohara | Process for producing an agglutinating substance utilizing dematium ATCC 20524 |
| JPS57174583U (pt) * | 1981-04-25 | 1982-11-04 | ||
| JPS62126727U (pt) * | 1986-12-15 | 1987-08-11 | ||
| US5260214A (en) * | 1988-07-19 | 1993-11-09 | Takara Shuzo Co. | Aureobasidium pullulans which produces antibiotic R106 |
| US5057493A (en) * | 1988-07-19 | 1991-10-15 | Takara Shuzo Co., Ltd. | Novel antibiotics r106 |
| JP3350823B2 (ja) * | 1992-03-04 | 2002-11-25 | 株式会社林原生物化学研究所 | 結着剤とその用途 |
| KR20110038739A (ko) | 2002-06-25 | 2011-04-14 | 가부시키가이샤 아데카 | β글루칸 함유 유지 조성물 및 β글루칸을 생산하는 신규 미생물 |
| US20060041118A1 (en) * | 2002-11-22 | 2006-02-23 | Mitsuyuki Kanbe | High- concentration liquid pullulan and method of circulating the same |
| EP2663294B1 (en) | 2011-01-11 | 2015-09-30 | Capsugel Belgium NV | New hard capsules comprising pullulan |
| JP7222911B2 (ja) * | 2017-04-14 | 2023-02-15 | カプスゲル・ベルギウム・ナムローゼ・フェンノートシャップ | プルランを作製する方法 |
| AU2018251256B2 (en) | 2017-04-14 | 2023-10-05 | Capsugel Belgium Nv | Pullulan capsules |
| WO2018204175A1 (en) | 2017-05-03 | 2018-11-08 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Rapid detection of zika virus by reverse transcription loop-mediated isothermal amplification |
| CN115521959A (zh) * | 2022-10-12 | 2022-12-27 | 江苏力凡胶囊有限公司 | 一种普鲁兰多糖的提取方法 |
-
1971
- 1971-10-11 JP JP46079413A patent/JPS5136360B2/ja not_active Expired
-
1972
- 1972-09-28 NO NO723473A patent/NO136466C/no unknown
- 1972-09-29 IT IT29896/72A patent/IT968463B/it active
- 1972-09-29 ZA ZA726693A patent/ZA726693B/xx unknown
- 1972-10-02 US US00294167A patent/US3827937A/en not_active Expired - Lifetime
- 1972-10-04 AU AU47377/72A patent/AU468633B2/en not_active Expired
- 1972-10-05 SE SE7212899A patent/SE383358B/xx unknown
- 1972-10-09 FI FI722773A patent/FI50138C/fi active
- 1972-10-09 PH PH13995*UA patent/PH9462A/en unknown
- 1972-10-09 GB GB4650372A patent/GB1368903A/en not_active Expired
- 1972-10-09 SU SU721834802A patent/SU735177A3/ru active
- 1972-10-10 FR FR7235862A patent/FR2156220B1/fr not_active Expired
- 1972-10-10 CA CA153,619A patent/CA994269A/en not_active Expired
- 1972-10-10 DK DK499672A patent/DK131873C/da not_active IP Right Cessation
- 1972-10-10 AR AR244557A patent/AR194508A1/es active
- 1972-10-10 CH CH1477272A patent/CH540975A/fr not_active IP Right Cessation
- 1972-10-11 BE BE789940D patent/BE789940A/xx unknown
- 1972-10-11 NL NL7213743.A patent/NL162137C/xx not_active IP Right Cessation
- 1972-10-11 DE DE2249836A patent/DE2249836C3/de not_active Expired
- 1972-10-11 ES ES407544A patent/ES407544A1/es not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| FI50138C (fi) | 1975-12-10 |
| DK131873B (da) | 1975-09-15 |
| FI50138B (pt) | 1975-09-01 |
| ZA726693B (en) | 1973-06-27 |
| DE2249836B2 (de) | 1977-11-03 |
| CA994269A (en) | 1976-08-03 |
| CH540975A (fr) | 1973-08-31 |
| NL162137C (nl) | 1980-04-15 |
| NL7213743A (pt) | 1973-04-13 |
| DE2249836C3 (de) | 1978-06-15 |
| GB1368903A (en) | 1974-10-02 |
| AU4737772A (en) | 1974-04-11 |
| SE383358B (sv) | 1976-03-08 |
| FR2156220B1 (pt) | 1977-07-29 |
| JPS5136360B2 (pt) | 1976-10-07 |
| SU735177A3 (ru) | 1980-05-15 |
| DK131873C (da) | 1976-02-16 |
| BE789940A (fr) | 1973-02-01 |
| FR2156220A1 (pt) | 1973-05-25 |
| ES407544A1 (es) | 1975-11-01 |
| JPS4844492A (pt) | 1973-06-26 |
| NO136466C (no) | 1977-09-07 |
| IT968463B (it) | 1974-03-20 |
| PH9462A (en) | 1975-12-10 |
| AR194508A1 (es) | 1973-07-23 |
| DE2249836A1 (de) | 1973-04-19 |
| US3827937A (en) | 1974-08-06 |
| AU468633B2 (en) | 1976-01-15 |
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