ES2542981T3 - Procedimiento para convertir polisacáridos en un hidrato de sal fundida inorgánica - Google Patents
Procedimiento para convertir polisacáridos en un hidrato de sal fundida inorgánica Download PDFInfo
- Publication number
- ES2542981T3 ES2542981T3 ES09720250.1T ES09720250T ES2542981T3 ES 2542981 T3 ES2542981 T3 ES 2542981T3 ES 09720250 T ES09720250 T ES 09720250T ES 2542981 T3 ES2542981 T3 ES 2542981T3
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- Prior art keywords
- molten salt
- inorganic molten
- salt hydrate
- dehydration
- hydrogenation
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- 238000006243 chemical reaction Methods 0.000 claims abstract description 43
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- WBJZTOZJJYAKHQ-UHFFFAOYSA-K iron(3+) phosphate Chemical compound [Fe+3].[O-]P([O-])([O-])=O WBJZTOZJJYAKHQ-UHFFFAOYSA-K 0.000 claims description 2
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- 229910052772 Samarium Inorganic materials 0.000 description 1
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- 229910021627 Tin(IV) chloride Inorganic materials 0.000 description 1
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- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 239000003929 acidic solution Substances 0.000 description 1
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- QQINRWTZWGJFDB-UHFFFAOYSA-N actinium atom Chemical compound [Ac] QQINRWTZWGJFDB-UHFFFAOYSA-N 0.000 description 1
- WQZGKKKJIJFFOK-PHYPRBDBSA-N alpha-D-galactose Chemical compound OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-PHYPRBDBSA-N 0.000 description 1
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- PYMYPHUHKUWMLA-WDCZJNDASA-N arabinose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)C=O PYMYPHUHKUWMLA-WDCZJNDASA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
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- 238000004517 catalytic hydrocracking Methods 0.000 description 1
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- ZMIGMASIKSOYAM-UHFFFAOYSA-N cerium Chemical compound [Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce] ZMIGMASIKSOYAM-UHFFFAOYSA-N 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
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- 239000007857 degradation product Substances 0.000 description 1
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- 238000007865 diluting Methods 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- KBQHZAAAGSGFKK-UHFFFAOYSA-N dysprosium atom Chemical compound [Dy] KBQHZAAAGSGFKK-UHFFFAOYSA-N 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000000909 electrodialysis Methods 0.000 description 1
- 238000005868 electrolysis reaction Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- UYAHIZSMUZPPFV-UHFFFAOYSA-N erbium Chemical compound [Er] UYAHIZSMUZPPFV-UHFFFAOYSA-N 0.000 description 1
- OGPBJKLSAFTDLK-UHFFFAOYSA-N europium atom Chemical compound [Eu] OGPBJKLSAFTDLK-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000007701 flash-distillation Methods 0.000 description 1
- 239000008396 flotation agent Substances 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- UIWYJDYFSGRHKR-UHFFFAOYSA-N gadolinium atom Chemical compound [Gd] UIWYJDYFSGRHKR-UHFFFAOYSA-N 0.000 description 1
- 229930182830 galactose Natural products 0.000 description 1
- 125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 235000008216 herbs Nutrition 0.000 description 1
- 150000002402 hexoses Chemical class 0.000 description 1
- KJZYNXUDTRRSPN-UHFFFAOYSA-N holmium atom Chemical compound [Ho] KJZYNXUDTRRSPN-UHFFFAOYSA-N 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000003456 ion exchange resin Substances 0.000 description 1
- 229920003303 ion-exchange polymer Polymers 0.000 description 1
- 229910052741 iridium Inorganic materials 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- 238000006317 isomerization reaction Methods 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- OHSVLFRHMCKCQY-UHFFFAOYSA-N lutetium atom Chemical compound [Lu] OHSVLFRHMCKCQY-UHFFFAOYSA-N 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 235000011147 magnesium chloride Nutrition 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000011565 manganese chloride Substances 0.000 description 1
- 235000002867 manganese chloride Nutrition 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 229910001510 metal chloride Inorganic materials 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- QEFYFXOXNSNQGX-UHFFFAOYSA-N neodymium atom Chemical compound [Nd] QEFYFXOXNSNQGX-UHFFFAOYSA-N 0.000 description 1
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- 150000002815 nickel Chemical class 0.000 description 1
- 238000010534 nucleophilic substitution reaction Methods 0.000 description 1
- 238000006384 oligomerization reaction Methods 0.000 description 1
- 238000000399 optical microscopy Methods 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- YHBDIEWMOMLKOO-UHFFFAOYSA-I pentachloroniobium Chemical compound Cl[Nb](Cl)(Cl)(Cl)Cl YHBDIEWMOMLKOO-UHFFFAOYSA-I 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- PUDIUYLPXJFUGB-UHFFFAOYSA-N praseodymium atom Chemical compound [Pr] PUDIUYLPXJFUGB-UHFFFAOYSA-N 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000003586 protic polar solvent Substances 0.000 description 1
- 230000005588 protonation Effects 0.000 description 1
- AOJFQRQNPXYVLM-UHFFFAOYSA-N pyridin-1-ium;chloride Chemical compound [Cl-].C1=CC=[NH+]C=C1 AOJFQRQNPXYVLM-UHFFFAOYSA-N 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 229910052702 rhenium Inorganic materials 0.000 description 1
- KZUNJOHGWZRPMI-UHFFFAOYSA-N samarium atom Chemical compound [Sm] KZUNJOHGWZRPMI-UHFFFAOYSA-N 0.000 description 1
- 238000007790 scraping Methods 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 230000007928 solubilization Effects 0.000 description 1
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- 239000007858 starting material Substances 0.000 description 1
- 238000000629 steam reforming Methods 0.000 description 1
- 239000010902 straw Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- GZCRRIHWUXGPOV-UHFFFAOYSA-N terbium atom Chemical compound [Tb] GZCRRIHWUXGPOV-UHFFFAOYSA-N 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- FRNOGLGSGLTDKL-UHFFFAOYSA-N thulium atom Chemical compound [Tm] FRNOGLGSGLTDKL-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 238000005199 ultracentrifugation Methods 0.000 description 1
- 238000011144 upstream manufacturing Methods 0.000 description 1
- DNYWZCXLKNTFFI-UHFFFAOYSA-N uranium Chemical compound [U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U] DNYWZCXLKNTFFI-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000003809 water extraction Methods 0.000 description 1
- 230000003313 weakening effect Effects 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- NAWDYIZEMPQZHO-UHFFFAOYSA-N ytterbium Chemical compound [Yb] NAWDYIZEMPQZHO-UHFFFAOYSA-N 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/04—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D307/18—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D307/20—Oxygen atoms
-
- 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
- A23L29/00—Foods or foodstuffs containing additives; Preparation or treatment thereof
- A23L29/30—Foods or foodstuffs containing additives; Preparation or treatment thereof containing carbohydrate syrups; containing sugars; containing sugar alcohols, e.g. xylitol; containing starch hydrolysates, e.g. dextrin
- A23L29/37—Sugar alcohols
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/132—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
- C07C29/136—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH
- C07C29/143—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of ketones
-
- 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
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08H—DERIVATIVES OF NATURAL MACROMOLECULAR COMPOUNDS
- C08H8/00—Macromolecular compounds derived from lignocellulosic materials
-
- C—CHEMISTRY; METALLURGY
- C13—SUGAR INDUSTRY
- C13K—SACCHARIDES OBTAINED FROM NATURAL SOURCES OR BY HYDROLYSIS OF NATURALLY OCCURRING DISACCHARIDES, OLIGOSACCHARIDES OR POLYSACCHARIDES
- C13K1/00—Glucose; Glucose-containing syrups
- C13K1/02—Glucose; Glucose-containing syrups obtained by saccharification of cellulosic materials
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Polymers & Plastics (AREA)
- Biochemistry (AREA)
- Medicinal Chemistry (AREA)
- Molecular Biology (AREA)
- General Health & Medical Sciences (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nutrition Science (AREA)
- Emergency Medicine (AREA)
- Food Science & Technology (AREA)
- Catalysts (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP08152706 | 2008-03-13 | ||
| EP08152706A EP2100972A1 (en) | 2008-03-13 | 2008-03-13 | Process for converting polysaccharides in a molten salt hydrate |
| PCT/EP2009/053027 WO2009112588A1 (en) | 2008-03-13 | 2009-03-13 | Process for converting polysaccharides in an inorganic molten salt hydrate |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2542981T3 true ES2542981T3 (es) | 2015-08-13 |
Family
ID=39645536
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES09720250.1T Active ES2542981T3 (es) | 2008-03-13 | 2009-03-13 | Procedimiento para convertir polisacáridos en un hidrato de sal fundida inorgánica |
Country Status (10)
| Country | Link |
|---|---|
| US (2) | US8445704B2 (enExample) |
| EP (2) | EP2100972A1 (enExample) |
| JP (1) | JP5757739B2 (enExample) |
| CN (1) | CN102027138B (enExample) |
| BR (1) | BRPI0909325A2 (enExample) |
| CA (1) | CA2718145A1 (enExample) |
| ES (1) | ES2542981T3 (enExample) |
| MY (1) | MY156012A (enExample) |
| RU (1) | RU2503722C2 (enExample) |
| WO (1) | WO2009112588A1 (enExample) |
Families Citing this family (43)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2408782A1 (en) * | 2009-03-17 | 2012-01-25 | BIOeCON International Holding N.V. | Process for converting polysaccharides in an inorganic molten salt hydrate |
| WO2010106052A1 (en) * | 2009-03-17 | 2010-09-23 | Bioecon International Holding N.V. | Process for converting polysaccharides in an inorganic molten salt hydrate |
| EP2408937A1 (en) * | 2009-03-17 | 2012-01-25 | BIOeCON International Holding N.V. | Process for converting polysaccharides in an inorganic molten salt hydrate |
| ES2438180T3 (es) * | 2009-03-17 | 2014-01-16 | Bioecon International Holding N.V. | Procedimiento para convertir polisacáridos en una sal fundida inorgánica hidratada |
| DE102009023458A1 (de) * | 2009-06-02 | 2010-12-30 | Carl Freudenberg Kg | Lösung, umfassend Cellulose, Verfahren zu deren Herstellung sowie deren Verwendung |
| US8628623B2 (en) * | 2009-12-21 | 2014-01-14 | Andritz Technology And Asset Management Gmbh | Method and process for dry discharge in a pressurized pretreatment reactor |
| JP5823756B2 (ja) * | 2010-07-21 | 2015-11-25 | 国立大学法人北海道大学 | 糖アルコールの製造方法 |
| FR2963008B1 (fr) * | 2010-07-23 | 2013-01-04 | IFP Energies Nouvelles | Procede de production de sucres a partir de biomasse lignocellulosique pretraitee avec un melange de sels inorganiques hydrates et de sels metalliques |
| FR2963009B1 (fr) * | 2010-07-23 | 2013-01-04 | IFP Energies Nouvelles | Procede de production de sucres a partir de biomasse lignocellulosique pretraitee avec des sels inorganiques hydrates |
| EP2431394A1 (en) | 2010-09-17 | 2012-03-21 | BIOeCON International Holding N.V. | Simultaneous hydrolysis and hydrogenation of cellulose |
| CN102600640B (zh) * | 2012-01-09 | 2015-05-13 | 中德瑞生物炼制实验室(厦门)有限公司 | 一种木质纤维素水解物的糖、酸、盐分离方法 |
| EP2620442A1 (en) * | 2012-01-27 | 2013-07-31 | BIOeCON International Holding N.V. | Process for recovering saccharides from cellulose hydrolysis reaction mixture |
| JPWO2014007295A1 (ja) * | 2012-07-03 | 2016-06-02 | 昭和電工株式会社 | 植物性バイオマスの分解方法及びグルコースの製造方法 |
| EP2882755B1 (en) * | 2012-08-08 | 2019-02-06 | Roquette Freres | Method of synthesis of a composition containing at least one internal dehydration product of a hydrogenated sugar by heterogeneous catalysis |
| FR2999604B1 (fr) * | 2012-12-14 | 2017-01-13 | Ifp Energies Now | Procede de production de solutions de sucres et d'alcools a partir de biomasse lignocellulosique avec traitement complementaire du residu solide par un sel inorganique hydrate |
| CN103012065B (zh) * | 2012-12-27 | 2015-03-18 | 中国科学院广州能源研究所 | 一种生物质循环水解氢化制取高浓度多元醇的方法 |
| DE102014208368A1 (de) * | 2014-05-05 | 2015-11-05 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Verfahren zur Gewinnung von aromatischen Verbindungen |
| WO2015198267A1 (en) * | 2014-06-27 | 2015-12-30 | Eni S.P.A. | Process for obtaining compounds useful for the production of biofuels starting from cellulose |
| CN104226131A (zh) * | 2014-09-16 | 2014-12-24 | 广州大学 | 一种溶解淀粉方法 |
| EP3230480B1 (en) | 2014-12-09 | 2018-10-03 | BIOeCON International Holding N.V. | Process for the isolation of monosaccharides |
| JP6521659B2 (ja) * | 2015-02-16 | 2019-05-29 | 株式会社日本触媒 | ポリオール類またはアルコール類の製造方法 |
| JP6725994B2 (ja) * | 2015-03-03 | 2020-07-22 | 株式会社豊田中央研究所 | 水蒸気改質触媒、それを用いた水蒸気改質方法、及び水蒸気改質反応装置 |
| WO2016139936A1 (ja) * | 2015-03-03 | 2016-09-09 | 株式会社デンソー | 水蒸気改質触媒、それを用いた水蒸気改質方法、及び水蒸気改質反応装置 |
| CN106938196A (zh) | 2015-12-10 | 2017-07-11 | 财团法人工业技术研究院 | 固体催化剂及应用该催化剂的醣类的制备方法 |
| EP3416740B1 (en) | 2016-02-19 | 2021-01-06 | Intercontinental Great Brands LLC | Processes to create multiple value streams from biomass sources |
| EP3213814A1 (en) * | 2016-03-01 | 2017-09-06 | Antecy B.V. | Novel sorbent and/or catalyst composition |
| US20190060820A1 (en) | 2016-03-01 | 2019-02-28 | Antecy B.V. | Shaped attrition resistant particles for co2 capturing and conversion |
| TWI653085B (zh) * | 2016-06-13 | 2019-03-11 | 鼎唐能源科技股份有限公司 | 從水解纖維素製程產物水溶液中分離醣類的方法 |
| US10781196B2 (en) | 2016-08-17 | 2020-09-22 | University Of Delaware | Integrated process for direct saccharification and dehydration of intact biomass to furfurals |
| CN108690039A (zh) * | 2018-06-26 | 2018-10-23 | 大连理工大学 | 一种山梨醇脱水制备异山梨醇的方法 |
| CN109569591A (zh) * | 2018-12-19 | 2019-04-05 | 武汉轻工大学 | 一种纤维素基Ru/C催化剂及其制备方法 |
| CN109879723B (zh) * | 2019-01-23 | 2020-10-20 | 厦门大学 | 从半纤维素直接制备木糖醇的方法 |
| CN109879721B (zh) * | 2019-01-23 | 2021-10-01 | 厦门大学 | 一种从半纤维素直接制备木糖醇的方法 |
| CN110183538A (zh) * | 2019-06-21 | 2019-08-30 | 大连工业大学 | 一种无机熔盐-微酸共促进体系制备纤维素纳米晶体的方法 |
| CN110894097B (zh) * | 2019-12-12 | 2022-04-12 | 山东理工大学 | 含叔丁醇废水的深度氧化处理方法 |
| CN111876454B (zh) * | 2020-08-14 | 2022-09-13 | 中国科学院青岛生物能源与过程研究所 | 采用熔盐水合物体系预处理木质纤维原料的方法 |
| US12163288B2 (en) | 2021-01-19 | 2024-12-10 | Solenis Technologies, L.P. | Treated substrates and methods of producing the same |
| WO2023104635A1 (en) | 2021-12-06 | 2023-06-15 | Heiq Materials Ag | Process for fabrication of regenerated cellulose yarns derived from recycled waste feedstocks |
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| WO2025162806A1 (en) | 2024-01-31 | 2025-08-07 | HeiQ AeoniQ Holding AG | Process for fabrication of cellulose yarns derived from cellulose feedstocks |
| CN118308684B (zh) * | 2024-04-01 | 2025-11-04 | 福州大学 | 一种热喷涂预处理木质素制氢催化剂的方法及其处理装置 |
| CN119016104B (zh) * | 2024-08-14 | 2025-05-13 | 北京石油化工学院 | 一种用于山梨醇脱水制异山梨醇反应的改性分子筛催化剂及其制备方法和应用 |
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| US607091A (en) | 1898-07-12 | einar simonsen | ||
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| SU114200A1 (ru) * | 1957-09-26 | 1957-11-30 | А.М. Малков | Способ кислотного гидролиза целлюлозосодержащего сырь |
| US3538019A (en) * | 1968-03-07 | 1970-11-03 | Atlas Chem Ind | Nickel phosphate-promoted supported nickel catalyst |
| US3471580A (en) * | 1968-04-19 | 1969-10-07 | Hydrocarbon Research Inc | Production of glycerol from saccharides |
| US4018620A (en) | 1975-05-19 | 1977-04-19 | Biocel Corporation | Method of hydrolyzing cellulose to monosaccharides |
| US4313884A (en) | 1980-01-21 | 1982-02-02 | Uop Inc. | Use of metal ions in preparation of anhydropolyols |
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| JPH01202300A (ja) * | 1988-02-05 | 1989-08-15 | Agency Of Ind Science & Technol | セルロース類の糖化方法 |
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| JP2005341924A (ja) * | 2004-06-07 | 2005-12-15 | Electric Power Dev Co Ltd | 植物性資源から糖類を製造する方法 |
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| NZ571184A (en) * | 2006-03-24 | 2011-06-30 | Wisconsin Alumni Res Found | Method for producing bio-fuel that integrates heat from carbon-carbon bond-forming reactions to drive biomass gasification reactions |
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- 2009-03-13 EP EP09720250.1A patent/EP2283164B1/en not_active Not-in-force
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- 2009-03-13 BR BRPI0909325-7A patent/BRPI0909325A2/pt not_active IP Right Cessation
- 2009-03-13 JP JP2010550217A patent/JP5757739B2/ja not_active Expired - Fee Related
- 2009-03-13 CA CA2718145A patent/CA2718145A1/en not_active Abandoned
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|---|---|
| MY156012A (en) | 2015-12-31 |
| JP2011517552A (ja) | 2011-06-16 |
| JP5757739B2 (ja) | 2015-07-29 |
| EP2100972A1 (en) | 2009-09-16 |
| US20110060148A1 (en) | 2011-03-10 |
| RU2010141854A (ru) | 2012-04-20 |
| US20140039208A1 (en) | 2014-02-06 |
| WO2009112588A1 (en) | 2009-09-17 |
| EP2283164B1 (en) | 2015-05-06 |
| US8445704B2 (en) | 2013-05-21 |
| CN102027138A (zh) | 2011-04-20 |
| BRPI0909325A2 (pt) | 2015-08-04 |
| EP2283164A1 (en) | 2011-02-16 |
| CA2718145A1 (en) | 2009-09-17 |
| RU2503722C2 (ru) | 2014-01-10 |
| CN102027138B (zh) | 2015-06-10 |
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