JP2010500362A - 唯一の原料としての空気の中の二酸化炭素と水(水蒸気)からメタノール、ジメチルエーテル、合成炭化水素及びそれらの生成物を生産する方法 - Google Patents
唯一の原料としての空気の中の二酸化炭素と水(水蒸気)からメタノール、ジメチルエーテル、合成炭化水素及びそれらの生成物を生産する方法 Download PDFInfo
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- JP2010500362A JP2010500362A JP2009523894A JP2009523894A JP2010500362A JP 2010500362 A JP2010500362 A JP 2010500362A JP 2009523894 A JP2009523894 A JP 2009523894A JP 2009523894 A JP2009523894 A JP 2009523894A JP 2010500362 A JP2010500362 A JP 2010500362A
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- Prior art keywords
- carbon dioxide
- air
- methanol
- water
- dimethyl ether
- Prior art date
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- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 title claims abstract description 156
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 title claims abstract description 110
- 239000001569 carbon dioxide Substances 0.000 title claims abstract description 55
- 229910002092 carbon dioxide Inorganic materials 0.000 title claims abstract description 55
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims abstract description 43
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 title claims abstract description 42
- 238000000034 method Methods 0.000 title claims abstract description 33
- 229930195733 hydrocarbon Natural products 0.000 title claims abstract description 18
- 150000002430 hydrocarbons Chemical class 0.000 title claims abstract description 18
- 230000008569 process Effects 0.000 title claims abstract description 14
- 239000002994 raw material Substances 0.000 title claims description 11
- VUZPPFZMUPKLLV-UHFFFAOYSA-N methane;hydrate Chemical compound C.O VUZPPFZMUPKLLV-UHFFFAOYSA-N 0.000 title claims description 8
- 239000001257 hydrogen Substances 0.000 claims abstract description 17
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 17
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 15
- 238000005868 electrolysis reaction Methods 0.000 claims abstract description 5
- 238000005984 hydrogenation reaction Methods 0.000 claims abstract description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 4
- 239000002250 absorbent Substances 0.000 claims abstract description 4
- 230000002745 absorbent Effects 0.000 claims abstract description 4
- TZIHFWKZFHZASV-UHFFFAOYSA-N methyl formate Chemical compound COC=O TZIHFWKZFHZASV-UHFFFAOYSA-N 0.000 claims description 14
- 238000004519 manufacturing process Methods 0.000 claims description 12
- 239000003054 catalyst Substances 0.000 claims description 9
- 238000006243 chemical reaction Methods 0.000 claims description 9
- 239000003463 adsorbent Substances 0.000 claims description 7
- 239000000126 substance Substances 0.000 claims description 7
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims description 6
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 6
- 239000005977 Ethylene Substances 0.000 claims description 6
- 238000010521 absorption reaction Methods 0.000 claims description 6
- 229910002091 carbon monoxide Inorganic materials 0.000 claims description 6
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 6
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 6
- 229920000642 polymer Polymers 0.000 claims description 5
- 238000007791 dehumidification Methods 0.000 claims description 4
- 230000000694 effects Effects 0.000 claims description 4
- 238000001179 sorption measurement Methods 0.000 claims description 4
- 239000000758 substrate Substances 0.000 claims description 3
- 230000002378 acidificating effect Effects 0.000 claims description 2
- 238000000354 decomposition reaction Methods 0.000 claims description 2
- 239000007789 gas Substances 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
- 230000009467 reduction Effects 0.000 claims description 2
- 229910021536 Zeolite Inorganic materials 0.000 claims 1
- 238000005336 cracking Methods 0.000 claims 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims 1
- 239000005350 fused silica glass Substances 0.000 claims 1
- 238000010926 purge Methods 0.000 claims 1
- 239000010457 zeolite Substances 0.000 claims 1
- 239000000446 fuel Substances 0.000 abstract description 15
- 150000001875 compounds Chemical class 0.000 abstract description 4
- 239000000463 material Substances 0.000 abstract description 4
- 229910021485 fumed silica Inorganic materials 0.000 abstract description 3
- 229920002873 Polyethylenimine Polymers 0.000 abstract description 2
- 239000002816 fuel additive Substances 0.000 abstract description 2
- 239000000047 product Substances 0.000 description 17
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 15
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 10
- 239000002803 fossil fuel Substances 0.000 description 7
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 5
- 235000019253 formic acid Nutrition 0.000 description 5
- 102000004169 proteins and genes Human genes 0.000 description 5
- 108090000623 proteins and genes Proteins 0.000 description 5
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
- 238000000926 separation method Methods 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 3
- 235000015097 nutrients Nutrition 0.000 description 3
- 230000002411 adverse Effects 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 238000006356 dehydrogenation reaction Methods 0.000 description 2
- IEJIGPNLZYLLBP-UHFFFAOYSA-N dimethyl carbonate Chemical compound COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 description 2
- -1 for example Chemical compound 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- 244000005700 microbiome Species 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000003345 natural gas Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 235000019728 animal nutrition Nutrition 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000003763 carbonization Methods 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000000567 combustion gas Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000010612 desalination reaction Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000004146 energy storage Methods 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 230000000116 mitigating effect Effects 0.000 description 1
- 239000002086 nanomaterial Substances 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 238000005832 oxidative carbonylation reaction Methods 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000001172 regenerating effect Effects 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 230000009919 sequestration Effects 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
- C07C41/01—Preparation of ethers
- C07C41/09—Preparation of ethers by dehydration of compounds containing hydroxy groups
-
- 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
- C07C29/15—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 oxides of carbon exclusively
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B61/00—Other general methods
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C1/00—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon
- C07C1/20—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only oxygen atoms as heteroatoms
-
- 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
- C07C29/147—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 carboxylic acids or derivatives thereof
- C07C29/149—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 carboxylic acids or derivatives thereof with hydrogen or hydrogen-containing gases
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C31/00—Saturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
- C07C31/02—Monohydroxylic acyclic alcohols
- C07C31/04—Methanol
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/36—Preparation of carboxylic acid esters by reaction with carbon monoxide or formates
-
- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P30/00—Technologies relating to oil refining and petrochemical industry
- Y02P30/20—Technologies relating to oil refining and petrochemical industry using bio-feedstock
-
- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P30/00—Technologies relating to oil refining and petrochemical industry
- Y02P30/40—Ethylene production
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Carbon And Carbon Compounds (AREA)
- Gas Separation By Absorption (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Description
空気の水分は、適切な冷却及び吸収技術を用いて、適切に利用可能ないかなる除湿の方法によっても除去される。多量に大気中の水分を除去した後、処理された空気は、二酸化炭素を効率よく吸収することが知られている適切な化学的な吸収剤からなる吸収システムに通される。
空気の除湿により取り除かれたきれいな水は、電気分解による水素の生成に用いられる。
例1にしたがって吸収または吸着された二酸化炭素は、次に、加熱又は/及び減圧化により放出され、化学的にメタノールに転換される。
除湿された空気から二酸化炭素を取り除く吸収システムは、好ましくはポリエチレンイミンや他のポリマーからなるポリアミノからなる。
例4で用いる吸収剤は、フュームドシリカ、アルミナ、その他の高表面活性を有するナノ構造性質を有する適切な単体に、有意に活性が増大された状態で担持される。
Claims (13)
- 大気圏の空気からメタノールを生産する方法であって、
大気圏の空気から水蒸気を除湿して水を除去し、
触媒又は他の分解手段により除去された水から水素を取得し、
除湿された大気圏の空気から吸収又は吸着により二酸化炭素を取得し、
このように取得された前記二酸化炭素を、メタノールを生産するのに充分な条件下で適切な還元や水素化の方法により、変換し、
前記二酸化炭素、前記水及び生成された前記水素は、任意の必要なエネルギー形態を用いて原料としての大気圏の空気からだけから取得される方法。 - 反応に用いられる全ての水は、空気を除湿して得られる請求項1に記載の方法。
- 二酸化炭素は、除湿の後得られる空気から分離される請求項2に記載の方法。
- 吸収剤は、高表面活性を有するナノ構造性質を有する担体に堆積したポリマーを含むポリアミノである請求項1に記載の方法。
- ポリマーを含むポリアミノは、ポリエチルイミンであり、担体は、フューズドシリカである請求項4に記載の方法。
- 前記二酸化炭素は、大気圏中の二酸化炭素を吸着剤で捕捉した後、前記吸着剤を処理して捕捉した二酸化炭素を放出して取得される請求項3に記載の方法。
- 前記吸着剤は、捕捉した二酸化炭素を、充分な加熱下、減圧下、真空下若しくはガスパージ下又はこれらの組み合わせにより、放出する処理が行われる請求項6に記載の方法。
- 前記水素は、大気圏中の空気から除去された水の電気分解又は触媒若しくは熱による分解で取得される請求項7に記載の方法。
- 前記空気から取得される前記二酸化炭素と水とからメチルアルコール又はジメチルエーテルが生産される請求項8に記載の方法。
- 前記二酸化炭素を、一酸化炭素を生成するのに十分な条件下で還元し、ギ酸メチルを取得するのに充分な条件下で前記一酸化炭素にメタノールを反応させ、メタノールだけを生産するのに充分な条件下で前記ギ酸メチルを触媒により水素化する請求項1に記載の方法。
- ジメチルエーテルを生産するのに充分な条件下でメタノールを転換する請求項1に記載の方法。
- 前記ジメチルエーテルを、酸性基材あるはゼオライト触媒の存在下でエチレン及び/又はプロピレンを生成するのに充分な条件下にて反応させる請求項11に記載の方法。
- エチレン又はプロピレンを、種々の合成炭化水素、生成された化学物質、ポリマー、これらより生産される生産物を生産するのに充分な条件下で転換する請求項12に記載の方法。
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US83727306P | 2006-08-10 | 2006-08-10 | |
| US11/780,171 US7378561B2 (en) | 2006-08-10 | 2007-07-19 | Method for producing methanol, dimethyl ether, derived synthetic hydrocarbons and their products from carbon dioxide and water (moisture) of the air as sole source material |
| PCT/US2007/074601 WO2008021698A2 (en) | 2006-08-10 | 2007-07-27 | Method for producing methanol, dimethyl ether, derived synthetic hydrocarbons and their products from carbon dioxide and water (moisture) of the air as sole source material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2010500362A true JP2010500362A (ja) | 2010-01-07 |
| JP2010500362A5 JP2010500362A5 (ja) | 2010-07-15 |
Family
ID=38956389
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009523894A Pending JP2010500362A (ja) | 2006-08-10 | 2007-07-27 | 唯一の原料としての空気の中の二酸化炭素と水(水蒸気)からメタノール、ジメチルエーテル、合成炭化水素及びそれらの生成物を生産する方法 |
Country Status (8)
| Country | Link |
|---|---|
| US (2) | US7378561B2 (ja) |
| EP (1) | EP2054364A2 (ja) |
| JP (1) | JP2010500362A (ja) |
| KR (2) | KR20090057240A (ja) |
| CN (1) | CN101500975B (ja) |
| AU (1) | AU2007284226B2 (ja) |
| CA (1) | CA2660634C (ja) |
| WO (1) | WO2008021698A2 (ja) |
Cited By (7)
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| WO2022091524A1 (ja) * | 2020-10-30 | 2022-05-05 | 株式会社辰巳菱機 | 電力・水素供給ステーション |
| WO2022091459A1 (ja) * | 2020-10-30 | 2022-05-05 | 株式会社辰巳菱機 | 電力・水素供給ステーション、電力・水素供給システム |
| JP7141670B1 (ja) * | 2020-10-30 | 2022-09-26 | 株式会社辰巳菱機 | 電力・水素供給ステーション、電力・水素供給システム |
| JP7141671B1 (ja) * | 2020-10-30 | 2022-09-26 | 株式会社辰巳菱機 | 電力・水素供給ステーション |
| WO2023210169A1 (ja) * | 2022-04-27 | 2023-11-02 | 国立大学法人東京大学 | 空気調和システム及び空気調和方法 |
| WO2024004833A1 (ja) * | 2022-06-30 | 2024-01-04 | 住友化学株式会社 | 炭素原子数2~8の不飽和炭化水素の製造方法、炭素原子数2~8の不飽和炭化水素混合物の製造方法、オレフィン系重合体の製造方法、化合物の製造方法、重合体の製造方法、オレフィン系重合体および重合体 |
| WO2024048675A1 (ja) * | 2022-09-01 | 2024-03-07 | 日本碍子株式会社 | 液体燃料製造システムおよび液体燃料の製造方法 |
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| US7608743B2 (en) | 2005-04-15 | 2009-10-27 | University Of Southern California | Efficient and selective chemical recycling of carbon dioxide to methanol, dimethyl ether and derived products |
| AU2006236801B2 (en) * | 2005-04-15 | 2010-11-11 | University Of Southern California | Efficient and selective conversion of carbon dioxide to methanol, dimethyl ether and derived products |
| US20080234523A1 (en) * | 2006-12-01 | 2008-09-25 | Leo Ernest Manzer | Process for making isooctenes from aqueous 2-butanol |
| US9557057B2 (en) | 2007-02-09 | 2017-01-31 | Dale Robert Lutz | Reliable carbon-neutral power generation system |
| EP2115098A2 (en) * | 2007-02-09 | 2009-11-11 | Dale R. Lutz | Reliable carbon-neutral power generation system |
| GB2448685A (en) * | 2007-04-23 | 2008-10-29 | David Andrew Johnston | Carbon dioxide absorbed from air and hydrogen from electrolysis of water, for production of carbon monoxide, alcohols, Fischer-Tropsch hydrocarbons & fuels |
| KR20100031500A (ko) * | 2007-05-04 | 2010-03-22 | 프린시플 에너지 솔루션스, 인코포레이티드 | 탄소원과 수소원으로부터 탄화수소 제조 |
| US20100135894A1 (en) * | 2007-06-26 | 2010-06-03 | Taiko Pharmaceutical Co., Ltd. | Method of producing chlorine dioxide, and alkaline composition for chlorine dioxide production to be used in the method |
| CN102056652A (zh) * | 2008-05-16 | 2011-05-11 | 南加州大学 | 减轻或消除人类活动的碳足迹 |
| CA2728322A1 (en) * | 2008-06-26 | 2009-12-30 | University Of Southern California | Stockpiling methanol and/or dimethyl ether for fuel and energy reserves |
| CN102105425A (zh) * | 2008-07-24 | 2011-06-22 | 南加州大学 | 从地热源和它们的能量专门地制备甲醇及其产物 |
| EP2382174A4 (en) * | 2009-01-29 | 2013-10-30 | Trustees Of The University Of Princeton | CONVERSION OF CARBON DIOXIDE IN ORGANIC PRODUCTS |
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| WO2024004833A1 (ja) * | 2022-06-30 | 2024-01-04 | 住友化学株式会社 | 炭素原子数2~8の不飽和炭化水素の製造方法、炭素原子数2~8の不飽和炭化水素混合物の製造方法、オレフィン系重合体の製造方法、化合物の製造方法、重合体の製造方法、オレフィン系重合体および重合体 |
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| WO2008021698A2 (en) | 2008-02-21 |
| WO2008021698A3 (en) | 2008-07-10 |
| US7378561B2 (en) | 2008-05-27 |
| CN101500975B (zh) | 2013-05-29 |
| CN101500975A (zh) | 2009-08-05 |
| AU2007284226A1 (en) | 2008-02-21 |
| CA2660634A1 (en) | 2008-02-21 |
| CA2660634C (en) | 2013-07-16 |
| EP2054364A2 (en) | 2009-05-06 |
| US20080039538A1 (en) | 2008-02-14 |
| KR20130043694A (ko) | 2013-04-30 |
| US7459590B2 (en) | 2008-12-02 |
| AU2007284226B2 (en) | 2011-12-08 |
| KR20090057240A (ko) | 2009-06-04 |
| US20080220480A1 (en) | 2008-09-11 |
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