WO2007033807A3 - Verfahren zur selektiven herstellung von dihydroxyaceton aus glycerin sowie ein verfahren zur herstellung eines metallkatalysators zur selektiven oxidation von glycerin - Google Patents
Verfahren zur selektiven herstellung von dihydroxyaceton aus glycerin sowie ein verfahren zur herstellung eines metallkatalysators zur selektiven oxidation von glycerin Download PDFInfo
- Publication number
- WO2007033807A3 WO2007033807A3 PCT/EP2006/009045 EP2006009045W WO2007033807A3 WO 2007033807 A3 WO2007033807 A3 WO 2007033807A3 EP 2006009045 W EP2006009045 W EP 2006009045W WO 2007033807 A3 WO2007033807 A3 WO 2007033807A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- glycerin
- organic compound
- production
- dihydroxyacetone
- metal catalyst
- Prior art date
Links
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 title abstract 10
- RXKJFZQQPQGTFL-UHFFFAOYSA-N dihydroxyacetone Chemical compound OCC(=O)CO RXKJFZQQPQGTFL-UHFFFAOYSA-N 0.000 title abstract 8
- 238000000034 method Methods 0.000 title abstract 7
- 229910052751 metal Inorganic materials 0.000 title abstract 6
- 239000002184 metal Substances 0.000 title abstract 6
- 239000003054 catalyst Substances 0.000 title abstract 5
- 235000011187 glycerol Nutrition 0.000 title abstract 5
- 230000003647 oxidation Effects 0.000 title abstract 5
- 238000007254 oxidation reaction Methods 0.000 title abstract 5
- 229940120503 dihydroxyacetone Drugs 0.000 title abstract 4
- 150000002894 organic compounds Chemical class 0.000 abstract 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 4
- 125000000468 ketone group Chemical group 0.000 abstract 3
- 239000007787 solid Substances 0.000 abstract 3
- 239000000463 material Substances 0.000 abstract 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 1
- 125000003172 aldehyde group Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- -1 glycerin Chemical class 0.000 abstract 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 abstract 1
- 239000010931 gold Substances 0.000 abstract 1
- 229910052737 gold Inorganic materials 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 150000002739 metals Chemical class 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 229910052697 platinum Inorganic materials 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000003381 stabilizer Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/27—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
- C07C45/32—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen
- C07C45/37—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of >C—O—functional groups to >C=O groups
- C07C45/39—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of >C—O—functional groups to >C=O groups being a secondary hydroxyl group
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
- B01J23/48—Silver or gold
- B01J23/52—Gold
-
- B01J35/23—
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/02—Impregnation, coating or precipitation
- B01J37/03—Precipitation; Co-precipitation
- B01J37/031—Precipitation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/16—Reducing
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Die Erfindung betrifft ein Verfahren zur Oxidation einer sekundären Hydroxygruppe einer organischen Verbindung in Gegenwart mindestens einer primären Hydroxygruppe derselben organischen Verbindung zu einer Ketogruppe, insbesondere zur Herstellung von Dihydroxyaceton (DHA) aus Glycerin, wobei die organische Verbindung, insbesondere das Glycerin, mit Sauerstoff in Gegenwart eines geträgerten Metallkatalysators, insbesondere Multimetallkatalysators, umfassend Gold und Platin und gegebenenfalls weitere, die Oxidation dieser organischen Verbindung, insbesondere von Glycerin, katalysierende Metalle in einem alkalischen wäßrigen System unter Ausbildung einer organischen Verbindung enthaltend eine Ketogruppe und mindestens eine primäre Hydroxygruppe, insbesondere von Dihydroxyaceton, umgesetzt wird. Hierfür wird bevorzugt auf solche geträgerten Oxidationskatalysatoren zurückgegriffen, die man bei Befolgung der folgenden Verfahrensschritte erhält: a) Reduktion von mindestens einem Metallsalz und/oder mindestens einer -säure eines Metalls, das zur katalytischen Oxidation von Hydroxylgruppen zu Aldehyd- bzw. Ketogruppen befähigt ist, unter Verwendung mindestens eines reduzierend wirkenden Stabilisierungsagens nach der Sol-Methode in einem alkalischen wäßrigen System, b) Inkontaktbringen eines Trägermaterials mit dem alkalischen wäßrigen System und Trägern des Trägermaterials, c) Abtrennen des Feststoffanteils von dem flüssigen Bestandteil, d) Waschen des abgetrennten Feststoffanteils und e) Tempern des gewaschenen Feststoffanteils. Ferner betrifft die Erfindung die nach dem vorangehend geschilderten Verfahren erhältlichen geträgerten Oxidationskatalysatoren.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102005044913A DE102005044913A1 (de) | 2005-09-20 | 2005-09-20 | Verfahren zur selektiven Herstellung von Dihydroxyaceton aus Glycerin sowie ein Verfahren zur Herstellung eines Metallkatalysators zur selektiven Oxidation von Glycerin |
DE102005044913.1 | 2005-09-20 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2007033807A2 WO2007033807A2 (de) | 2007-03-29 |
WO2007033807A3 true WO2007033807A3 (de) | 2007-05-18 |
Family
ID=37507597
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2006/009045 WO2007033807A2 (de) | 2005-09-20 | 2006-09-18 | Verfahren zur selektiven herstellung von dihydroxyaceton aus glycerin sowie ein verfahren zur herstellung eines metallkatalysators zur selektiven oxidation von glycerin |
Country Status (2)
Country | Link |
---|---|
DE (1) | DE102005044913A1 (de) |
WO (1) | WO2007033807A2 (de) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109499581B (zh) * | 2018-12-22 | 2021-11-30 | 江西师范大学 | 一种由甘油制备1,3-二羟基丙酮的催化剂及其制备方法 |
CN110624592A (zh) * | 2019-09-29 | 2019-12-31 | 上海纳米技术及应用国家工程研究中心有限公司 | 单原子金属-氮掺杂石墨烯聚集体的合成方法及其产品和应用 |
CN113956150B (zh) * | 2020-07-21 | 2024-03-22 | 中国石油大学(华东) | 一种甘油酸的制备方法 |
CN115155577A (zh) * | 2022-07-29 | 2022-10-11 | 华东理工大学 | 一种甘油选择性氧化制备1,3-二羟基丙酮的催化剂及制备方法 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4228487A1 (de) * | 1991-08-30 | 1993-03-04 | Kao Corp | Verfahren zur herstellung einer eine carbonyl- und/oder carboxylgruppe aufweisenden verbindung |
DE19734973A1 (de) * | 1997-08-13 | 1999-02-25 | Hoechst Ag | Edelmetallcluster enthaltende nano-poröse Aluminium-oxid-Membranen |
WO2005003072A1 (en) * | 2003-07-01 | 2005-01-13 | Universita' Degli Studi Di Milano | Process and catalyst for the preparation of aldonic acids |
-
2005
- 2005-09-20 DE DE102005044913A patent/DE102005044913A1/de not_active Withdrawn
-
2006
- 2006-09-18 WO PCT/EP2006/009045 patent/WO2007033807A2/de active Application Filing
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4228487A1 (de) * | 1991-08-30 | 1993-03-04 | Kao Corp | Verfahren zur herstellung einer eine carbonyl- und/oder carboxylgruppe aufweisenden verbindung |
DE19734973A1 (de) * | 1997-08-13 | 1999-02-25 | Hoechst Ag | Edelmetallcluster enthaltende nano-poröse Aluminium-oxid-Membranen |
WO2005003072A1 (en) * | 2003-07-01 | 2005-01-13 | Universita' Degli Studi Di Milano | Process and catalyst for the preparation of aldonic acids |
Non-Patent Citations (4)
Title |
---|
BIANCHI C L ET AL: "Selective oxidation of glycerol with oxygen using mono and bimetallic catalysts based on Au, Pd and Pt metals", CATALYSIS TODAY, ELSEVIER, vol. 102-103, 15 May 2005 (2005-05-15), pages 203 - 212, XP004898688, ISSN: 0920-5861 * |
DEMIREL-GULEN S ET AL: "Liquid phase oxidation of glycerol over carbon supported gold catalysts", CATALYSIS TODAY, ELSEVIER, vol. 102-103, 15 May 2005 (2005-05-15), pages 166 - 172, XP004898682, ISSN: 0920-5861 * |
GARCIA R ET AL.: "Chemoselective catalytic oxidation of glycerol with air on platinum metals", APPLIED CATALYSIS A: GENERAL, vol. 127, 1995, pages 165 - 176, XP002412416 * |
PORTA F ET AL: "Selective oxidation of glycerol to sodium glycerate with gold-on-carbon catalyst: an insight into reaction selectivity", JOURNAL OF CATALYSIS, ACADEMIC PRESS, DULUTH, MN, US, vol. 224, no. 2, 10 June 2004 (2004-06-10), pages 397 - 403, XP004506500, ISSN: 0021-9517 * |
Also Published As
Publication number | Publication date |
---|---|
DE102005044913A1 (de) | 2007-03-22 |
WO2007033807A2 (de) | 2007-03-29 |
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