AU2011276362B2 - Novel catalyst mixtures - Google Patents
Novel catalyst mixtures Download PDFInfo
- Publication number
- AU2011276362B2 AU2011276362B2 AU2011276362A AU2011276362A AU2011276362B2 AU 2011276362 B2 AU2011276362 B2 AU 2011276362B2 AU 2011276362 A AU2011276362 A AU 2011276362A AU 2011276362 A AU2011276362 A AU 2011276362A AU 2011276362 B2 AU2011276362 B2 AU 2011276362B2
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- AU
- Australia
- Prior art keywords
- group
- electrochemical cell
- reaction
- hydrogen
- catalyst
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 239000003054 catalyst Substances 0.000 title abstract description 186
- 239000000203 mixture Substances 0.000 title description 58
- 238000006243 chemical reaction Methods 0.000 claims abstract description 187
- 229910002091 carbon monoxide Inorganic materials 0.000 claims description 143
- 239000001257 hydrogen Substances 0.000 claims description 115
- 229910052739 hydrogen Inorganic materials 0.000 claims description 115
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 108
- 238000000034 method Methods 0.000 claims description 53
- 229910052737 gold Inorganic materials 0.000 claims description 35
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 33
- 229910052763 palladium Inorganic materials 0.000 claims description 33
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 33
- 229910052697 platinum Inorganic materials 0.000 claims description 31
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 30
- 239000000446 fuel Substances 0.000 claims description 22
- 150000001768 cations Chemical class 0.000 claims description 19
- 229910052718 tin Inorganic materials 0.000 claims description 17
- 229910052759 nickel Inorganic materials 0.000 claims description 16
- 239000001569 carbon dioxide Substances 0.000 claims description 15
- 239000012530 fluid Substances 0.000 claims description 15
- OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical compound C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 claims description 13
- 229960001231 choline Drugs 0.000 claims description 13
- 150000004820 halides Chemical group 0.000 claims description 13
- 239000000376 reactant Substances 0.000 claims description 13
- 125000001931 aliphatic group Chemical group 0.000 claims description 12
- 239000000463 material Substances 0.000 claims description 12
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- 229910052709 silver Inorganic materials 0.000 claims description 11
- 229910052793 cadmium Inorganic materials 0.000 claims description 10
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 10
- 229910052802 copper Inorganic materials 0.000 claims description 10
- 125000004122 cyclic group Chemical group 0.000 claims description 10
- 229910052707 ruthenium Inorganic materials 0.000 claims description 10
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- 229910052745 lead Inorganic materials 0.000 claims description 9
- 230000002441 reversible effect Effects 0.000 claims description 9
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- 229910052772 Samarium Inorganic materials 0.000 claims description 8
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- 229910052782 aluminium Inorganic materials 0.000 claims description 8
- 125000003277 amino group Chemical group 0.000 claims description 8
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- 125000005496 phosphonium group Chemical group 0.000 claims description 8
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- 229910052703 rhodium Inorganic materials 0.000 claims description 8
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- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 140
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- 239000010931 gold Substances 0.000 description 35
- 239000003792 electrolyte Substances 0.000 description 31
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 27
- 239000000243 solution Substances 0.000 description 27
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 26
- 230000008569 process Effects 0.000 description 25
- 238000002474 experimental method Methods 0.000 description 23
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 22
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- 239000000126 substance Substances 0.000 description 18
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- -1 acetic acid Chemical class 0.000 description 15
- 150000002431 hydrogen Chemical class 0.000 description 15
- 150000003839 salts Chemical class 0.000 description 14
- 238000006722 reduction reaction Methods 0.000 description 13
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 12
- 150000001412 amines Chemical group 0.000 description 12
- 238000006056 electrooxidation reaction Methods 0.000 description 12
- 238000005516 engineering process Methods 0.000 description 12
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 12
- 239000002904 solvent Substances 0.000 description 12
- 238000001179 sorption measurement Methods 0.000 description 12
- 229910052786 argon Inorganic materials 0.000 description 11
- 238000006555 catalytic reaction Methods 0.000 description 11
- 239000002608 ionic liquid Substances 0.000 description 11
- 230000009467 reduction Effects 0.000 description 11
- 239000011651 chromium Substances 0.000 description 10
- 239000010949 copper Substances 0.000 description 10
- 230000005518 electrochemistry Effects 0.000 description 10
- 150000002500 ions Chemical class 0.000 description 10
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- 229910052757 nitrogen Inorganic materials 0.000 description 9
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- 230000001629 suppression Effects 0.000 description 9
- FNPBHXSBDADRBT-UHFFFAOYSA-M 2-hydroxyethyl(trimethyl)azanium;iodide Chemical compound [I-].C[N+](C)(C)CCO FNPBHXSBDADRBT-UHFFFAOYSA-M 0.000 description 8
- SHFJWMWCIHQNCP-UHFFFAOYSA-M hydron;tetrabutylazanium;sulfate Chemical compound OS([O-])(=O)=O.CCCC[N+](CCCC)(CCCC)CCCC SHFJWMWCIHQNCP-UHFFFAOYSA-M 0.000 description 8
- 239000002253 acid Substances 0.000 description 7
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- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 6
- 239000007853 buffer solution Substances 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 239000002574 poison Substances 0.000 description 6
- 235000017557 sodium bicarbonate Nutrition 0.000 description 6
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 6
- 239000004381 Choline salt Substances 0.000 description 5
- 229910021607 Silver chloride Inorganic materials 0.000 description 5
- OIPILFWXSMYKGL-UHFFFAOYSA-N acetylcholine Chemical class CC(=O)OCC[N+](C)(C)C OIPILFWXSMYKGL-UHFFFAOYSA-N 0.000 description 5
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- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 5
- WHBHBVVOGNECLV-OBQKJFGGSA-N 11-deoxycortisol Chemical compound O=C1CC[C@]2(C)[C@H]3CC[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 WHBHBVVOGNECLV-OBQKJFGGSA-N 0.000 description 4
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 4
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- KYCQOKLOSUBEJK-UHFFFAOYSA-M 1-butyl-3-methylimidazol-3-ium;bromide Chemical compound [Br-].CCCCN1C=C[N+](C)=C1 KYCQOKLOSUBEJK-UHFFFAOYSA-M 0.000 description 3
- IQQRAVYLUAZUGX-UHFFFAOYSA-N 1-butyl-3-methylimidazolium Chemical compound CCCCN1C=C[N+](C)=C1 IQQRAVYLUAZUGX-UHFFFAOYSA-N 0.000 description 3
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- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
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- VCOBYGVZILHVOO-UHFFFAOYSA-M 2-butanoyloxyethyl(trimethyl)azanium;chloride Chemical compound [Cl-].CCCC(=O)OCC[N+](C)(C)C VCOBYGVZILHVOO-UHFFFAOYSA-M 0.000 description 2
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Applications Claiming Priority (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12/830,338 | 2010-07-04 | ||
| US12/830,338 US20110237830A1 (en) | 2010-03-26 | 2010-07-04 | Novel catalyst mixtures |
| AUPCT/US2011/030098 | 2011-03-25 | ||
| PCT/US2011/030098 WO2011120021A1 (en) | 2010-03-26 | 2011-03-25 | Novel catalyst mixtures |
| US201161484072P | 2011-05-09 | 2011-05-09 | |
| US61/484,072 | 2011-05-09 | ||
| US13/174,365 US9566574B2 (en) | 2010-07-04 | 2011-06-30 | Catalyst mixtures |
| US13/174,365 | 2011-06-30 | ||
| PCT/US2011/042809 WO2012006240A1 (en) | 2010-07-04 | 2011-07-01 | Novel catalyst mixtures |
Publications (2)
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| AU2011276362A1 AU2011276362A1 (en) | 2013-02-21 |
| AU2011276362B2 true AU2011276362B2 (en) | 2016-03-17 |
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| JP5591606B2 (ja) | 2010-07-08 | 2014-09-17 | 三井造船株式会社 | 二酸化炭素の還元,固定方法 |
| US8524066B2 (en) | 2010-07-29 | 2013-09-03 | Liquid Light, Inc. | Electrochemical production of urea from NOx and carbon dioxide |
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| BR112014000052A2 (pt) | 2011-07-06 | 2017-02-07 | Liquid Light Inc | redução de dióxido de carbono em ácidos carboxílicos, glicóis e carboxilatos |
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| US4968393A (en) * | 1988-04-18 | 1990-11-06 | A. L. Sandpiper Corporation | Membrane divided aqueous-nonaqueous system for electrochemical cells |
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Also Published As
| Publication number | Publication date |
|---|---|
| JP6059140B2 (ja) | 2017-01-11 |
| US20120308903A1 (en) | 2012-12-06 |
| US9566574B2 (en) | 2017-02-14 |
| CA2802893A1 (en) | 2012-01-12 |
| CA2802893C (en) | 2018-08-28 |
| WO2012006240A4 (en) | 2012-02-02 |
| WO2012006240A1 (en) | 2012-01-12 |
| JP2017082334A (ja) | 2017-05-18 |
| CN102971451A (zh) | 2013-03-13 |
| KR20130043178A (ko) | 2013-04-29 |
| BR112013000261A2 (pt) | 2017-05-16 |
| JP6449839B2 (ja) | 2019-01-09 |
| KR101801659B1 (ko) | 2017-11-27 |
| CN102971451B (zh) | 2016-09-14 |
| AU2011276362A1 (en) | 2013-02-21 |
| JP2013538285A (ja) | 2013-10-10 |
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