WO2002027071A1 - Verfahren zur elektrochemischen herstellung von wasserstoffperoxid - Google Patents
Verfahren zur elektrochemischen herstellung von wasserstoffperoxid Download PDFInfo
- Publication number
- WO2002027071A1 WO2002027071A1 PCT/EP2001/010267 EP0110267W WO0227071A1 WO 2002027071 A1 WO2002027071 A1 WO 2002027071A1 EP 0110267 W EP0110267 W EP 0110267W WO 0227071 A1 WO0227071 A1 WO 0227071A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- hydrogen peroxide
- membrane
- fuel cell
- range
- microns
- Prior art date
Links
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 title claims abstract description 69
- 238000000034 method Methods 0.000 title claims abstract description 34
- 239000012528 membrane Substances 0.000 claims abstract description 33
- 239000000446 fuel Substances 0.000 claims abstract description 15
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 14
- 239000001257 hydrogen Substances 0.000 claims abstract description 14
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 14
- 239000001301 oxygen Substances 0.000 claims abstract description 14
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 14
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- 229920001577 copolymer Polymers 0.000 claims description 11
- 229920000642 polymer Polymers 0.000 claims description 11
- 238000004519 manufacturing process Methods 0.000 claims description 8
- 125000000542 sulfonic acid group Chemical group 0.000 claims description 8
- 239000011230 binding agent Substances 0.000 claims description 7
- 239000006229 carbon black Substances 0.000 claims description 7
- 229910044991 metal oxide Inorganic materials 0.000 claims description 7
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 6
- 150000004706 metal oxides Chemical class 0.000 claims description 6
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 4
- 239000007795 chemical reaction product Substances 0.000 claims description 3
- 239000011787 zinc oxide Substances 0.000 claims description 3
- 229920002313 fluoropolymer Polymers 0.000 claims description 2
- 239000007789 gas Substances 0.000 claims description 2
- 230000003647 oxidation Effects 0.000 claims description 2
- 238000007254 oxidation reaction Methods 0.000 claims description 2
- 229910052697 platinum Inorganic materials 0.000 claims description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 8
- 238000005868 electrolysis reaction Methods 0.000 description 8
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- -1 polytetrafluoroethylene Polymers 0.000 description 5
- 229920000557 Nafion® Polymers 0.000 description 4
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 229910052731 fluorine Inorganic materials 0.000 description 3
- 239000011737 fluorine Substances 0.000 description 3
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 3
- 229910002804 graphite Inorganic materials 0.000 description 3
- 239000010439 graphite Substances 0.000 description 3
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 3
- 239000004810 polytetrafluoroethylene Substances 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- 239000003513 alkali Substances 0.000 description 2
- 238000005341 cation exchange Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- YADSGOSSYOOKMP-UHFFFAOYSA-N dioxolead Chemical compound O=[Pb]=O YADSGOSSYOOKMP-UHFFFAOYSA-N 0.000 description 2
- 239000003792 electrolyte Substances 0.000 description 2
- 239000010931 gold Substances 0.000 description 2
- 239000006199 nebulizer Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- ZQOMKIOQTCAGCM-UHFFFAOYSA-L [Na+].[Na+].OS(O)(=O)=O.[O-]S([O-])(=O)=O Chemical compound [Na+].[Na+].OS(O)(=O)=O.[O-]S([O-])(=O)=O ZQOMKIOQTCAGCM-UHFFFAOYSA-L 0.000 description 1
- PIYVNGWKHNMMAU-UHFFFAOYSA-N [O].O Chemical compound [O].O PIYVNGWKHNMMAU-UHFFFAOYSA-N 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
- 229910001854 alkali hydroxide Inorganic materials 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 239000003575 carbonaceous material Substances 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002848 electrochemical method Methods 0.000 description 1
- 230000005518 electrochemistry Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 229910001922 gold oxide Inorganic materials 0.000 description 1
- 238000010559 graft polymerization reaction Methods 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 239000003014 ion exchange membrane Substances 0.000 description 1
- 229910052747 lanthanoid Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229910000510 noble metal Inorganic materials 0.000 description 1
- 229920005548 perfluoropolymer Polymers 0.000 description 1
- 239000005518 polymer electrolyte Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B1/00—Electrolytic production of inorganic compounds or non-metals
- C25B1/01—Products
- C25B1/28—Per-compounds
- C25B1/30—Peroxides
Definitions
- the invention relates to a method for the electrochemical production of hydrogen oxide in an electrolysis cell, the structure of which is essentially analogous to that of a fuel cell.
- the molar ratio of, for example, NaOH to hydrogen peroxide is in the range from 2.3 to 1 to approximately 1 to 1.
- the company Dow Chemical Co. operates, for example, a trickle bed cell with a cathodically arranged trickle bed, the particles of the trickle bed consisting of graphite particles with a coating of polytetrafluoroethylene and carbon black. This process works at room temperature and normal pressure, and the catholyte flow is controlled by the anolyte through a diaphragm. Platinized titanium serves as the anode.
- a molar sodium hydroxide solution is used as the electrolyte.
- the electrolysis takes place in an electrolysis cell, the cathode being designed as an oxygen diffusion electrode and the anode as an oxygen-developing metal electrode or as a hydrogen diffusion electrode.
- the catholyte is water
- the anolyte is a sulfuric acid sodium sulfate solution
- the reaction product is an alkaline hydrogen peroxide solution - see DE 195 16 304.
- a fuel cell as the electrolysis cell.
- a fuel cell contains a membrane electrode assembly (MEA) which contains a membrane based on a perfluorinated polymer or copolymer containing sulfonic acid groups, one side of which is in direct contact with an anode layer and the other side of which is in contact with a cathode layer.
- MEA membrane electrode assembly
- the electrocatalytically active anode layer contains a binder based on a perfluorinated polymer or copolymer and a catalytically active component, which in this case is preferably a noble metal, such as in particular gold, or a metal oxide, such as in particular zinc oxide or a lanthanide metal oxide, on a carbon-containing carrier material.
- a catalytically active component which in this case is preferably a noble metal, such as in particular gold, or a metal oxide, such as in particular zinc oxide or a lanthanide metal oxide, on a carbon-containing carrier material.
- hydrogen is supplied to the anode compartment and oxygen to the cathode compartment.
- the oxygen is humidified. This process can be used to obtain alkali-free aqueous hydrogen peroxide solutions with a content of more than 1% with a selectivity in the range from 20 to 70%.
- the electrolysis is expediently carried out at high pressure and low temperature.
- the object of the invention is to provide an improved process for the production of hydrogen peroxide by electrochemical conversion of oxygen and hydrogen in a fuel cell.
- a way should be shown by which the concentration of the aqueous hydrogen peroxide solution obtained at the cathode can be controlled or increased.
- aqueous hydrogen peroxide solution comprising cathodic reduction of oxygen and anodic oxidation of hydrogen in a membrane electrode assembly (MEA), the membrane of which consists essentially of a fluorinated polymer containing sulfonic acid groups or Copolymer consists of equipped fuel cell and stripping of the reaction products and unreacted gases, which is characterized in that a membrane with a thickness in the range of greater 50 ⁇ to 300 ⁇ m.
- MEA membrane electrode assembly
- the membrane has a thickness in the range from 100 to 250 ⁇ , in particular 150 to 250 ⁇ .
- the extraordinary effect is illustrated in Figure 2.
- the basic structure of the fuel cell which is designed as a flow-through cell, and where a large number of cells can be combined in a sandwich-like manner, is known per se - an example is given in the previously acknowledged document by S. P. Webb et al. and referenced the documents cited therein.
- the cell thus comprises, in a symmetrical arrangement on both sides of a membrane electrode unit, a diffuser made of a carbon-containing porous material and an end plate made of usually graphite. The elements mentioned are in close electrical contact with one another.
- the diffuser In addition to the function of good contacting, the diffuser also has the function of an even distribution of the starting materials.
- the electrode end plates have parallel, meandering or other shaped channels - obtainable, for example, from a stud profile of the end plate. These channels are useful with regard to a trouble-free, i.e. without flooding, the removal of the water and hydrogen peroxide formed in the electrochemical process and the water introduced by humidifying the oxygen and / or hydrogen.
- the cation-exchanging polymer electrolyte membrane is a fluorinated ion exchange membrane of the cation type, preferably fluorine or perfluoropolymers, in particular copolymers of two or more fluorine or perfluoro monomers, of which at least one of the polymers has sulfonic acid groups.
- fluorinated ion exchange membrane of the cation type preferably fluorine or perfluoropolymers, in particular copolymers of two or more fluorine or perfluoro monomers, of which at least one of the polymers has sulfonic acid groups.
- Such membranes are commercially available with different equivalent weights and thicknesses.
- the document by S. P. Webb et al. gives no information about the thickness of the membrane.
- the electrode layers are thin film-shaped layers which contain a mixture of a metal or metal oxide and carbon black or preferably a carbon black coated with a metal or metal oxide in a fluorine-containing polymeric binder.
- each electrode layer is first applied to one side of the respective macroporous diffuser based on a carbon material and the diffuser coated in this way is then pressed onto the membrane.
- the electrode layer contains a perfluorinated polymer or copolymer containing sulfonic acid groups as a binder.
- Polymers containing sulfonic acid groups can also be used other perfluorinated polymers obtained by, for example, graft polymerization with other hydrophilic side groups.
- the cathode preferably contains carrier-bound gold or metal oxide, such as in particular zinc oxide, the carrier being carbon black.
- Suitable as an anode in the electrochemical production of hydrogen peroxide from oxygen and hydrogen in a fuel cell is a combination of essentially a platinum-coated carbon black and polytetrafluoroethylene, preferably a perfluorinated polymer or copolymer containing sulfonic acid groups, as a binder.
- FIG. 1 shows the diagram of a device for the electrochemical production of hydrogen peroxide.
- Figure 2 shows a diagram showing the dependence of the concentration of the aqueous hydrogen peroxide solution on the membrane thickness.
- FIG. 1 shows a diagram of a device for the electrochemical production of an aqueous hydrogen peroxide solution from oxygen and hydrogen.
- the electrolysis cell (1) is a typical fuel cell, the structure of which is known to those skilled in the art; K denotes the cathode compartment, A the anode compartment and MEA a membrane-electrode unit.
- the cathode and anode are connected to a current source (2).
- Oxygen is supplied to the cathode compartment via line (5) and hydrogen to the anode compartment via line (6).
- Water is introduced into the line (5) from a water storage container (9) by means of a high-pressure pump or another device, for example a nebulizer; the oxygen-water vapor mixture is brought to the desired reaction temperature in the heat exchanger (3).
- the hydrogen flow in line (6) can be moistened with water, water being introduced from a storage container (10) via a high-pressure pump or nebulizer or the like and the gas-water mixture in a further heat exchanger (4) to the desired temperature brought.
- the one from the Product streams emerging from the fuel cell contain aqueous hydrogen peroxide and unconverted oxygen on the cathode side and water and unconverted hydrogen on the anode side.
- the gas-liquid mixtures produced can be separated in a separation device (11 or 12).
- the H 2 0 2 concentration can be increased in particular by feeding water vapor at a temperature of 180 ° C. into the 0 2 stream.
- Figure 2 shows the dependence of the concentration of hydrogen peroxide in g / 1 on the membrane thickness.
- the comparative examples VB1 to VB3 are experiments in which a commercial membrane from different manufacturers was used, the thickness of which was in the range from 40 to 50 ⁇ m. In contrast, in the examples B1 and B2 according to the invention, the membrane thickness was 180 and 170 ⁇ m, respectively.
- the H 2 0 2 concentration could be increased many times over by the increase in membrane thickness shown in the figure.
- the method according to the invention can be carried out at normal or elevated temperature.
- the H 2 0 2 concentration can also be increased by increasing the pressure. At a pressure of about 30 bar, the H 2 0 2 concentration can be increased to well over 10% by weight.
- VBl Nafion® 112
- VB2 Gore 40 ⁇ m
- VB3 PallRlOlO
- Bl Nafion® 117
- B2 PallBCM4010.
Landscapes
- Chemical & Material Sciences (AREA)
- Metallurgy (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Inorganic Chemistry (AREA)
- Organic Chemistry (AREA)
- Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
- Fuel Cell (AREA)
- Inert Electrodes (AREA)
- Inorganic Compounds Of Heavy Metals (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
Abstract
Description
Claims
Priority Applications (10)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2002530831A JP2004510060A (ja) | 2000-09-26 | 2001-09-06 | 過酸化水素の電気化学的な製造方法 |
IL15506001A IL155060A0 (en) | 2000-09-26 | 2001-09-06 | Method for electrochemically producing hydrogen peroxide |
BR0114165-1A BR0114165A (pt) | 2000-09-26 | 2001-09-06 | Processo para produção eletroquìmica de peróxido de hidrogênio |
AU2001289868A AU2001289868A1 (en) | 2000-09-26 | 2001-09-06 | Method for electrochemically producing hydrogen peroxide |
CA002423467A CA2423467C (en) | 2000-09-26 | 2001-09-06 | Method for electrochemically producing hydrogen peroxide |
EP01969697A EP1327011B1 (de) | 2000-09-26 | 2001-09-06 | Verfahren zur elektrochemischen herstellung von wasserstoffperoxid |
KR10-2003-7004279A KR20030043968A (ko) | 2000-09-26 | 2001-09-06 | 과산화수소의 전기화학적 제조방법 |
AT01969697T ATE265559T1 (de) | 2000-09-26 | 2001-09-06 | Verfahren zur elektrochemischen herstellung von wasserstoffperoxid |
DE50102166T DE50102166D1 (de) | 2000-09-26 | 2001-09-06 | Verfahren zur elektrochemischen herstellung von wasserstoffperoxid |
NO20031355A NO20031355L (no) | 2000-09-26 | 2003-03-25 | Fremgangsmåte for elektrokjemisk fremstilling av hydrogenperoksid |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10048030A DE10048030A1 (de) | 2000-09-26 | 2000-09-26 | Verfahren zur elektrochemischen Herstellung von Wasserstoffperoxid |
DE10048030.6 | 2000-09-26 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2002027071A1 true WO2002027071A1 (de) | 2002-04-04 |
Family
ID=7657935
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2001/010267 WO2002027071A1 (de) | 2000-09-26 | 2001-09-06 | Verfahren zur elektrochemischen herstellung von wasserstoffperoxid |
Country Status (12)
Country | Link |
---|---|
US (1) | US6685818B2 (de) |
EP (1) | EP1327011B1 (de) |
JP (1) | JP2004510060A (de) |
KR (1) | KR20030043968A (de) |
AT (1) | ATE265559T1 (de) |
AU (1) | AU2001289868A1 (de) |
BR (1) | BR0114165A (de) |
CA (1) | CA2423467C (de) |
DE (2) | DE10048030A1 (de) |
IL (1) | IL155060A0 (de) |
NO (1) | NO20031355L (de) |
WO (1) | WO2002027071A1 (de) |
Families Citing this family (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6890680B2 (en) * | 2002-02-19 | 2005-05-10 | Mti Microfuel Cells Inc. | Modified diffusion layer for use in a fuel cell system |
US20040126313A1 (en) * | 2002-06-24 | 2004-07-01 | Haase Richard A. | Methods and processes of hydrogen peroxide production |
US7241521B2 (en) | 2003-11-18 | 2007-07-10 | Npl Associates, Inc. | Hydrogen/hydrogen peroxide fuel cell |
US7939210B2 (en) * | 2004-03-31 | 2011-05-10 | Gs Yuasa Corporation | Electric automobile |
EP1736436A1 (de) * | 2004-03-31 | 2006-12-27 | GS Yuasa Corporation | Wasserstoffzufuhrsystem |
KR100699415B1 (ko) * | 2004-10-25 | 2007-03-27 | 한국기계연구원 | 정전분무 세정장치 |
US8268269B2 (en) * | 2006-01-24 | 2012-09-18 | Clearvalue Technologies, Inc. | Manufacture of water chemistries |
GB2437957A (en) * | 2006-04-11 | 2007-11-14 | Dyson Technology Ltd | An electrolytic cell for the production of hydrogen peroxide |
GB2437079A (en) * | 2006-04-11 | 2007-10-17 | Dyson Technology Ltd | Hydrogen peroxide production apparatus |
GB2437956A (en) * | 2006-04-11 | 2007-11-14 | Dyson Technology Ltd | Production of hydrogen peroxide |
US7754064B2 (en) * | 2006-09-29 | 2010-07-13 | Eltron Research & Development | Methods and apparatus for the on-site production of hydrogen peroxide |
JP5130781B2 (ja) * | 2007-05-08 | 2013-01-30 | 三菱電機株式会社 | 過酸化水素製造装置並びにそれを用いた空調機、空気清浄機及び加湿器 |
JP5386684B2 (ja) * | 2009-03-13 | 2014-01-15 | 国立大学法人東京工業大学 | 燃料電池型反応装置及びそれを用いた化合物の製造方法 |
US8459275B2 (en) | 2009-09-23 | 2013-06-11 | Ecolab Usa Inc. | In-situ cleaning system |
KR20110109351A (ko) | 2010-03-31 | 2011-10-06 | 엘지전자 주식회사 | 산소발생기 |
US8937037B2 (en) | 2011-03-02 | 2015-01-20 | Ecolab Usa Inc. | Electrochemical enhancement of detergent alkalinity |
KR101282763B1 (ko) | 2011-08-17 | 2013-07-05 | 광주과학기술원 | 생물학적 전기화학 전지를 이용한 해수 담수화 및 과산화수소 제조 방법 |
WO2018075483A1 (en) | 2016-10-17 | 2018-04-26 | The Board Of Trustees Of The Leland Stanford Junior University | Electrochemical hydrogen peroxide generating device |
EP3620438A1 (de) | 2018-09-10 | 2020-03-11 | Covestro Deutschland AG | Vorrichtung und verfahren zur reinigung von abwasser |
KR102446703B1 (ko) * | 2020-11-24 | 2022-09-22 | 울산과학기술원 | 과산화수소를 이용한 저전압 수소 발생 시스템 |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1997013006A1 (en) * | 1995-10-06 | 1997-04-10 | The Dow Chemical Company | Composite membrane and use thereof for chemical synthesis |
-
2000
- 2000-09-26 DE DE10048030A patent/DE10048030A1/de not_active Withdrawn
-
2001
- 2001-09-06 EP EP01969697A patent/EP1327011B1/de not_active Expired - Lifetime
- 2001-09-06 AU AU2001289868A patent/AU2001289868A1/en not_active Abandoned
- 2001-09-06 BR BR0114165-1A patent/BR0114165A/pt active Search and Examination
- 2001-09-06 WO PCT/EP2001/010267 patent/WO2002027071A1/de active IP Right Grant
- 2001-09-06 KR KR10-2003-7004279A patent/KR20030043968A/ko not_active Application Discontinuation
- 2001-09-06 CA CA002423467A patent/CA2423467C/en not_active Expired - Fee Related
- 2001-09-06 JP JP2002530831A patent/JP2004510060A/ja active Pending
- 2001-09-06 AT AT01969697T patent/ATE265559T1/de not_active IP Right Cessation
- 2001-09-06 IL IL15506001A patent/IL155060A0/xx unknown
- 2001-09-06 DE DE50102166T patent/DE50102166D1/de not_active Expired - Lifetime
- 2001-09-25 US US09/961,401 patent/US6685818B2/en not_active Expired - Fee Related
-
2003
- 2003-03-25 NO NO20031355A patent/NO20031355L/no not_active Application Discontinuation
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1997013006A1 (en) * | 1995-10-06 | 1997-04-10 | The Dow Chemical Company | Composite membrane and use thereof for chemical synthesis |
Also Published As
Publication number | Publication date |
---|---|
IL155060A0 (en) | 2003-10-31 |
CA2423467A1 (en) | 2003-03-25 |
CA2423467C (en) | 2009-11-17 |
DE10048030A1 (de) | 2002-04-11 |
US6685818B2 (en) | 2004-02-03 |
AU2001289868A1 (en) | 2002-04-08 |
NO20031355L (no) | 2003-05-22 |
ATE265559T1 (de) | 2004-05-15 |
JP2004510060A (ja) | 2004-04-02 |
KR20030043968A (ko) | 2003-06-02 |
NO20031355D0 (no) | 2003-03-25 |
EP1327011A1 (de) | 2003-07-16 |
US20020036147A1 (en) | 2002-03-28 |
DE50102166D1 (de) | 2004-06-03 |
EP1327011B1 (de) | 2004-04-28 |
BR0114165A (pt) | 2003-07-29 |
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