JP2012522873A5 - - Google Patents
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- Publication number
- JP2012522873A5 JP2012522873A5 JP2012503643A JP2012503643A JP2012522873A5 JP 2012522873 A5 JP2012522873 A5 JP 2012522873A5 JP 2012503643 A JP2012503643 A JP 2012503643A JP 2012503643 A JP2012503643 A JP 2012503643A JP 2012522873 A5 JP2012522873 A5 JP 2012522873A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- methylimidazolium
- butyl
- independently selected
- branched
- 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.)
- Abandoned
Links
- 229910052757 nitrogen Inorganic materials 0.000 claims 20
- 150000001336 alkenes Chemical class 0.000 claims 16
- 125000001072 heteroaryl group Chemical group 0.000 claims 15
- 125000005842 heteroatom Chemical group 0.000 claims 15
- 229910052760 oxygen Inorganic materials 0.000 claims 15
- 229910052710 silicon Inorganic materials 0.000 claims 15
- 229910052717 sulfur Inorganic materials 0.000 claims 15
- 239000000203 mixture Substances 0.000 claims 13
- 238000010521 absorption reaction Methods 0.000 claims 12
- AMXOYNBUYSYVKV-UHFFFAOYSA-M lithium bromide Chemical compound [Li+].[Br-] AMXOYNBUYSYVKV-UHFFFAOYSA-M 0.000 claims 12
- 125000003107 substituted aryl group Chemical group 0.000 claims 10
- 150000001924 cycloalkanes Chemical class 0.000 claims 9
- 239000012530 fluid Substances 0.000 claims 9
- 150000008040 ionic compounds Chemical class 0.000 claims 8
- JOOXCMJARBKPKM-UHFFFAOYSA-M 4-oxopentanoate Chemical compound CC(=O)CCC([O-])=O JOOXCMJARBKPKM-UHFFFAOYSA-M 0.000 claims 7
- 229940058352 levulinate Drugs 0.000 claims 7
- 229910019142 PO4 Inorganic materials 0.000 claims 6
- 239000006096 absorbing agent Substances 0.000 claims 6
- 150000001335 aliphatic alkanes Chemical class 0.000 claims 6
- 235000021317 phosphate Nutrition 0.000 claims 6
- 239000003507 refrigerant Substances 0.000 claims 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 6
- 125000003118 aryl group Chemical group 0.000 claims 5
- 229910052794 bromium Inorganic materials 0.000 claims 5
- 150000001768 cations Chemical class 0.000 claims 5
- 125000001424 substituent group Chemical group 0.000 claims 5
- NJMWOUFKYKNWDW-UHFFFAOYSA-N 1-ethyl-3-methylimidazolium Chemical compound CCN1C=C[N+](C)=C1 NJMWOUFKYKNWDW-UHFFFAOYSA-N 0.000 claims 4
- 239000002253 acid Substances 0.000 claims 4
- 229910052801 chlorine Inorganic materials 0.000 claims 4
- 229910052731 fluorine Inorganic materials 0.000 claims 4
- 229910052740 iodine Inorganic materials 0.000 claims 4
- 238000000034 method Methods 0.000 claims 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims 4
- 239000010452 phosphate Substances 0.000 claims 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 3
- 229910052783 alkali metal Inorganic materials 0.000 claims 3
- 150000001340 alkali metals Chemical class 0.000 claims 3
- 150000001450 anions Chemical class 0.000 claims 3
- SXDBWCPKPHAZSM-UHFFFAOYSA-M bromate Chemical class [O-]Br(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-M 0.000 claims 3
- 150000001875 compounds Chemical class 0.000 claims 3
- 150000003983 crown ethers Chemical class 0.000 claims 3
- 238000002425 crystallisation Methods 0.000 claims 3
- 230000008025 crystallization Effects 0.000 claims 3
- 229920000137 polyphosphoric acid Polymers 0.000 claims 3
- HVVRUQBMAZRKPJ-UHFFFAOYSA-N 1,3-dimethylimidazolium Chemical compound CN1C=C[N+](C)=C1 HVVRUQBMAZRKPJ-UHFFFAOYSA-N 0.000 claims 2
- ARSMIBSHEYKMJT-UHFFFAOYSA-M 1,3-dimethylimidazolium iodide Chemical compound [I-].CN1C=C[N+](C)=C1 ARSMIBSHEYKMJT-UHFFFAOYSA-M 0.000 claims 2
- QPDGLRRWSBZCHP-UHFFFAOYSA-M 1-butyl-3-methylimidazol-3-ium;2,2,2-trifluoroacetate Chemical compound [O-]C(=O)C(F)(F)F.CCCC[N+]=1C=CN(C)C=1 QPDGLRRWSBZCHP-UHFFFAOYSA-M 0.000 claims 2
- MXBRPRXKTHPJRI-UHFFFAOYSA-M 1-butyl-3-methylimidazol-3-ium;2-methylpropanoate Chemical compound CC(C)C([O-])=O.CCCCN1C=C[N+](C)=C1 MXBRPRXKTHPJRI-UHFFFAOYSA-M 0.000 claims 2
- BJMHXLGHJQKGNI-UHFFFAOYSA-M 1-butyl-3-methylimidazol-3-ium;propanoate Chemical compound CCC([O-])=O.CCCC[N+]=1C=CN(C)C=1 BJMHXLGHJQKGNI-UHFFFAOYSA-M 0.000 claims 2
- JOKVYNJKBRLDAT-UHFFFAOYSA-M 1-ethyl-3-methylimidazol-3-ium;2,2,2-trifluoroacetate Chemical compound [O-]C(=O)C(F)(F)F.CC[N+]=1C=CN(C)C=1 JOKVYNJKBRLDAT-UHFFFAOYSA-M 0.000 claims 2
- XIYUIMLQTKODPS-UHFFFAOYSA-M 1-ethyl-3-methylimidazol-3-ium;acetate Chemical compound CC([O-])=O.CC[N+]=1C=CN(C)C=1 XIYUIMLQTKODPS-UHFFFAOYSA-M 0.000 claims 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 2
- AEMRFAOFKBGASW-UHFFFAOYSA-M Glycolate Chemical compound OCC([O-])=O AEMRFAOFKBGASW-UHFFFAOYSA-M 0.000 claims 2
- DTQVDTLACAAQTR-UHFFFAOYSA-M Trifluoroacetate Chemical compound [O-]C(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-M 0.000 claims 2
- 150000007513 acids Chemical class 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- SXDBWCPKPHAZSM-UHFFFAOYSA-N bromic acid Chemical compound OBr(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-N 0.000 claims 2
- 150000003841 chloride salts Chemical class 0.000 claims 2
- 150000001805 chlorine compounds Chemical class 0.000 claims 2
- OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical compound C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 claims 2
- 229960001231 choline Drugs 0.000 claims 2
- 125000004122 cyclic group Chemical group 0.000 claims 2
- XQRLCLUYWUNEEH-UHFFFAOYSA-N diphosphonic acid Chemical compound OP(=O)OP(O)=O XQRLCLUYWUNEEH-UHFFFAOYSA-N 0.000 claims 2
- 229910052736 halogen Inorganic materials 0.000 claims 2
- 150000002367 halogens Chemical class 0.000 claims 2
- OEDJAKMCWJUAHH-UHFFFAOYSA-M methyl(trioctyl)azanium;2,2,2-trifluoroacetate Chemical compound [O-]C(=O)C(F)(F)F.CCCCCCCC[N+](C)(CCCCCCCC)CCCCCCCC OEDJAKMCWJUAHH-UHFFFAOYSA-M 0.000 claims 2
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 claims 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims 2
- 125000000547 substituted alkyl group Chemical group 0.000 claims 2
- QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical compound C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 0.000 claims 2
- ROJODBUHUVCAJX-UHFFFAOYSA-M 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate;trihexyl(tetradecyl)phosphanium Chemical compound [O-]S(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F.CCCCCCCCCCCCCC[P+](CCCCCC)(CCCCCC)CCCCCC ROJODBUHUVCAJX-UHFFFAOYSA-M 0.000 claims 1
- KZWJWYFPLXRYIL-UHFFFAOYSA-M 1,1,2,2-tetrafluoroethanesulfonate Chemical compound [O-]S(=O)(=O)C(F)(F)C(F)F KZWJWYFPLXRYIL-UHFFFAOYSA-M 0.000 claims 1
- IEOTWKMBQULPKX-UHFFFAOYSA-M 1,1,2,2-tetrafluoroethanesulfonate;tetrakis(2-hydroxyethyl)azanium Chemical compound [O-]S(=O)(=O)C(F)(F)C(F)F.OCC[N+](CCO)(CCO)CCO IEOTWKMBQULPKX-UHFFFAOYSA-M 0.000 claims 1
- BCAMEJSXAFAOHI-UHFFFAOYSA-M 1,1,2,2-tetrafluoroethanesulfonate;tributyl(tetradecyl)phosphanium Chemical compound [O-]S(=O)(=O)C(F)(F)C(F)F.CCCCCCCCCCCCCC[P+](CCCC)(CCCC)CCCC BCAMEJSXAFAOHI-UHFFFAOYSA-M 0.000 claims 1
- BGGUZIZLOYTWFU-UHFFFAOYSA-M 1,1,2,3,3,3-hexafluoropropane-1-sulfonate;tributyl(tetradecyl)phosphanium Chemical compound [O-]S(=O)(=O)C(F)(F)C(F)C(F)(F)F.CCCCCCCCCCCCCC[P+](CCCC)(CCCC)CCCC BGGUZIZLOYTWFU-UHFFFAOYSA-M 0.000 claims 1
- XHCDOFZBVYGCFK-UHFFFAOYSA-M 1-butyl-1-methylpyrrolidin-1-ium;2,2,2-trifluoroacetate Chemical compound [O-]C(=O)C(F)(F)F.CCCC[N+]1(C)CCCC1 XHCDOFZBVYGCFK-UHFFFAOYSA-M 0.000 claims 1
- VFKJFIDWVGPBDV-UHFFFAOYSA-M 1-butyl-2,3-dimethylimidazol-3-ium;1,1,2,2-tetrafluoroethanesulfonate Chemical compound [O-]S(=O)(=O)C(F)(F)C(F)F.CCCC[N+]=1C=CN(C)C=1C VFKJFIDWVGPBDV-UHFFFAOYSA-M 0.000 claims 1
- KUWPEQAOGNPMOP-UHFFFAOYSA-M 1-butyl-3-methylimidazol-3-ium;1,1,2,2-tetrafluoroethanesulfonate Chemical compound CCCC[N+]=1C=CN(C)C=1.[O-]S(=O)(=O)C(F)(F)C(F)F KUWPEQAOGNPMOP-UHFFFAOYSA-M 0.000 claims 1
- MXDXOYOYMBHGQD-UHFFFAOYSA-M 1-butyl-3-methylimidazol-3-ium;1,1,2,3,3,3-hexafluoropropane-1-sulfonate Chemical compound CCCC[N+]=1C=CN(C)C=1.[O-]S(=O)(=O)C(F)(F)C(F)C(F)(F)F MXDXOYOYMBHGQD-UHFFFAOYSA-M 0.000 claims 1
- ZIPFNZZMKGEBFU-UHFFFAOYSA-M 1-butyl-3-methylimidazol-3-ium;1,1,2-trifluoro-2-(1,1,2,2,2-pentafluoroethoxy)ethanesulfonate Chemical compound CCCC[N+]=1C=CN(C)C=1.[O-]S(=O)(=O)C(F)(F)C(F)OC(F)(F)C(F)(F)F ZIPFNZZMKGEBFU-UHFFFAOYSA-M 0.000 claims 1
- MIQNTLMZSDFZQY-UHFFFAOYSA-M 1-butyl-3-methylimidazol-3-ium;1,1,2-trifluoro-2-(trifluoromethoxy)ethanesulfonate Chemical compound CCCC[N+]=1C=CN(C)C=1.[O-]S(=O)(=O)C(F)(F)C(F)OC(F)(F)F MIQNTLMZSDFZQY-UHFFFAOYSA-M 0.000 claims 1
- BSKSXTBYXTZWFI-UHFFFAOYSA-M 1-butyl-3-methylimidazol-3-ium;acetate Chemical compound CC([O-])=O.CCCC[N+]=1C=CN(C)C=1 BSKSXTBYXTZWFI-UHFFFAOYSA-M 0.000 claims 1
- DBEDBKKZBBRGDK-UHFFFAOYSA-N 1-butyl-3-methylimidazol-3-ium;dihydrogen phosphite Chemical compound OP(O)[O-].CCCCN1C=C[N+](C)=C1 DBEDBKKZBBRGDK-UHFFFAOYSA-N 0.000 claims 1
- MEMNKNZDROKJHP-UHFFFAOYSA-M 1-butyl-3-methylimidazol-3-ium;methyl sulfate Chemical compound COS([O-])(=O)=O.CCCCN1C=C[N+](C)=C1 MEMNKNZDROKJHP-UHFFFAOYSA-M 0.000 claims 1
- IQQRAVYLUAZUGX-UHFFFAOYSA-N 1-butyl-3-methylimidazolium Chemical compound CCCCN1C=C[N+](C)=C1 IQQRAVYLUAZUGX-UHFFFAOYSA-N 0.000 claims 1
- CTEAXVWYCINNCA-UHFFFAOYSA-M 1-ethyl-3-methylimidazol-3-ium;1,1,2,2-tetrafluoroethanesulfonate Chemical compound CC[N+]=1C=CN(C)C=1.[O-]S(=O)(=O)C(F)(F)C(F)F CTEAXVWYCINNCA-UHFFFAOYSA-M 0.000 claims 1
- KPTIHKIMIVDQEG-UHFFFAOYSA-M 1-methyl-3-octylimidazol-1-ium;1,1,2,2-tetrafluoroethanesulfonate Chemical compound [O-]S(=O)(=O)C(F)(F)C(F)F.CCCCCCCCN1C=C[N+](C)=C1 KPTIHKIMIVDQEG-UHFFFAOYSA-M 0.000 claims 1
- FURUVJOXOXSHDX-UHFFFAOYSA-M 2,2-dichloroacetate;tetramethylazanium Chemical compound C[N+](C)(C)C.[O-]C(=O)C(Cl)Cl FURUVJOXOXSHDX-UHFFFAOYSA-M 0.000 claims 1
- JSGREAVPDCFWAB-UHFFFAOYSA-M 2-oxopropanoate;tetramethylazanium Chemical compound C[N+](C)(C)C.CC(=O)C([O-])=O JSGREAVPDCFWAB-UHFFFAOYSA-M 0.000 claims 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims 1
- 229910016467 AlCl 4 Inorganic materials 0.000 claims 1
- 229910021591 Copper(I) chloride Inorganic materials 0.000 claims 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Chemical compound CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims 1
- 229910018286 SbF 6 Inorganic materials 0.000 claims 1
- VHRRKJWPRRTKLZ-UHFFFAOYSA-N acetic acid;2-methoxy-n-(2-methoxyethyl)ethanamine Chemical compound CC([O-])=O.COCC[NH2+]CCOC VHRRKJWPRRTKLZ-UHFFFAOYSA-N 0.000 claims 1
- 150000003973 alkyl amines Chemical class 0.000 claims 1
- 125000003282 alkyl amino group Chemical group 0.000 claims 1
- 229940072107 ascorbate Drugs 0.000 claims 1
- 235000010323 ascorbic acid Nutrition 0.000 claims 1
- 239000011668 ascorbic acid Substances 0.000 claims 1
- HXQJXUWXAOFEQT-UHFFFAOYSA-M benzyl(trimethyl)azanium;2-phosphonoacetate Chemical compound OP(O)(=O)CC([O-])=O.C[N+](C)(C)CC1=CC=CC=C1 HXQJXUWXAOFEQT-UHFFFAOYSA-M 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- BKMGMIWOLYYOCK-UHFFFAOYSA-L butanedioate;tetrabutylphosphanium Chemical compound [O-]C(=O)CCC([O-])=O.CCCC[P+](CCCC)(CCCC)CCCC.CCCC[P+](CCCC)(CCCC)CCCC BKMGMIWOLYYOCK-UHFFFAOYSA-L 0.000 claims 1
- 229910052792 caesium Inorganic materials 0.000 claims 1
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical compound [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 claims 1
- OXBLHERUFWYNTN-UHFFFAOYSA-M copper(I) chloride Chemical compound [Cu]Cl OXBLHERUFWYNTN-UHFFFAOYSA-M 0.000 claims 1
- OUTUSTULKLPJNX-UHFFFAOYSA-N dihydrogen phosphite;1-ethyl-3-methylimidazol-3-ium Chemical compound OP(O)[O-].CCN1C=C[N+](C)=C1 OUTUSTULKLPJNX-UHFFFAOYSA-N 0.000 claims 1
- XIXADJRWDQXREU-UHFFFAOYSA-M lithium acetate Chemical compound [Li+].CC([O-])=O XIXADJRWDQXREU-UHFFFAOYSA-M 0.000 claims 1
- CBKJDTFDVVXSJR-UHFFFAOYSA-M methyl sulfate;1,2,4-trimethylpyrazol-2-ium Chemical compound COS([O-])(=O)=O.CC1=CN(C)[N+](C)=C1 CBKJDTFDVVXSJR-UHFFFAOYSA-M 0.000 claims 1
- WLTHPEHYBIKNHR-UHFFFAOYSA-M methyl sulfate;tris(2-hydroxyethyl)-methylazanium Chemical compound COS([O-])(=O)=O.OCC[N+](C)(CCO)CCO WLTHPEHYBIKNHR-UHFFFAOYSA-M 0.000 claims 1
- 150000002763 monocarboxylic acids Chemical class 0.000 claims 1
- 229910052700 potassium Inorganic materials 0.000 claims 1
- 239000011591 potassium Substances 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 229910052708 sodium Inorganic materials 0.000 claims 1
- 239000011734 sodium Substances 0.000 claims 1
- 229940023144 sodium glycolate Drugs 0.000 claims 1
- BJQWBACJIAKDTJ-UHFFFAOYSA-N tetrabutylphosphanium Chemical compound CCCC[P+](CCCC)(CCCC)CCCC BJQWBACJIAKDTJ-UHFFFAOYSA-N 0.000 claims 1
- WWIYWFVQZQOECA-UHFFFAOYSA-M tetramethylazanium;formate Chemical compound [O-]C=O.C[N+](C)(C)C WWIYWFVQZQOECA-UHFFFAOYSA-M 0.000 claims 1
- DBMLHBBWANTBLN-UHFFFAOYSA-N trimethyl-[2-(4-oxopentanoyloxy)ethyl]azanium Chemical compound CC(=O)CCC(=O)OCC[N+](C)(C)C DBMLHBBWANTBLN-UHFFFAOYSA-N 0.000 claims 1
- JEJAMASKDTUEBZ-UHFFFAOYSA-N tris(1,1,3-tribromo-2,2-dimethylpropyl) phosphate Chemical compound BrCC(C)(C)C(Br)(Br)OP(=O)(OC(Br)(Br)C(C)(C)CBr)OC(Br)(Br)C(C)(C)CBr JEJAMASKDTUEBZ-UHFFFAOYSA-N 0.000 claims 1
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US16516609P | 2009-03-31 | 2009-03-31 | |
| US16517309P | 2009-03-31 | 2009-03-31 | |
| US16516009P | 2009-03-31 | 2009-03-31 | |
| US61/165,160 | 2009-03-31 | ||
| US61/165,173 | 2009-03-31 | ||
| US61/165,166 | 2009-03-31 | ||
| PCT/US2010/029322 WO2010117836A1 (en) | 2009-03-31 | 2010-03-31 | Ionic compounds in lithium bromide/water absorption cycle systems |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2012522873A JP2012522873A (ja) | 2012-09-27 |
| JP2012522873A5 true JP2012522873A5 (enExample) | 2013-05-09 |
Family
ID=42236734
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012503643A Abandoned JP2012522873A (ja) | 2009-03-31 | 2010-03-31 | 臭化リチウム／水中のイオン性化合物、吸収サイクルシステム |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US20120011886A1 (enExample) |
| EP (1) | EP2414476A1 (enExample) |
| JP (1) | JP2012522873A (enExample) |
| KR (1) | KR20120003471A (enExample) |
| CN (1) | CN102449101A (enExample) |
| AU (1) | AU2010234813A1 (enExample) |
| BR (1) | BRPI1006734A2 (enExample) |
| CA (1) | CA2754599A1 (enExample) |
| WO (1) | WO2010117836A1 (enExample) |
Families Citing this family (40)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2087930A1 (de) * | 2008-02-05 | 2009-08-12 | Evonik Degussa GmbH | Verfahren zur Absorption eines flüchtigen Stoffes in einem flüssigen Absorptionsmittel |
| EP2088389B1 (de) * | 2008-02-05 | 2017-05-10 | Evonik Degussa GmbH | Absorptionskältemaschine |
| WO2010054230A2 (en) * | 2008-11-07 | 2010-05-14 | E. I. Du Pont De Nemours And Company | Absorption cycle utilizing ionic compounds and/or non-ionic absorbents as working fluids |
| DE102009047564A1 (de) * | 2009-12-07 | 2011-06-09 | Evonik Degussa Gmbh | Arbeitsmedium für eine Absorptionskältemaschine |
| CA2817264C (en) * | 2010-11-08 | 2016-12-13 | Evonik Degussa Gmbh | Working medium for absorption heat pumps |
| DE102011077377A1 (de) | 2010-11-12 | 2012-05-16 | Evonik Degussa Gmbh | Verfahren zur Absorption von sauren Gasen aus Gasmischungen |
| JP5937303B2 (ja) * | 2011-05-13 | 2016-06-22 | ミヨシ油脂株式会社 | 耐腐食性イオン液体を熱媒体に用いた冷却液、不凍液、凍結防止剤、融雪剤 |
| WO2013072147A1 (de) | 2011-11-14 | 2013-05-23 | Evonik Degussa Gmbh | Verfahren und vorrichtung zur abtrennung von sauren gasen aus einer gasmischung |
| DE102012200907A1 (de) | 2012-01-23 | 2013-07-25 | Evonik Industries Ag | Verfahren und Absorptionsmedium zur Absorption von CO2 aus einer Gasmischung |
| DE102012207509A1 (de) | 2012-05-07 | 2013-11-07 | Evonik Degussa Gmbh | Verfahren zur Absorption von CO2 aus einer Gasmischung |
| WO2014172042A1 (en) * | 2013-03-15 | 2014-10-23 | Sandia Corporation | Synthesis of novel ionic liquids from lignin-derived compounds |
| US8720216B1 (en) | 2013-10-01 | 2014-05-13 | King Fahd University Of Petroleum And Minerals | Hybrid aqua-ammonia and lithium bromide-water absorption chiller |
| US20160231032A1 (en) * | 2015-02-07 | 2016-08-11 | Morteza Ghassemi | Piezo Electric and High Voltage Absorption Cooling System |
| JP6224648B2 (ja) * | 2015-04-28 | 2017-11-01 | ファナック株式会社 | スポット溶接の品質診断システム |
| DE102015212749A1 (de) | 2015-07-08 | 2017-01-12 | Evonik Degussa Gmbh | Verfahren zur Entfeuchtung von feuchten Gasgemischen |
| GB201513304D0 (en) * | 2015-07-28 | 2015-09-09 | Innospec Ltd | Compositions and Methods |
| WO2017058747A1 (en) | 2015-09-28 | 2017-04-06 | University Of Florida Research Foundation, Inc. | Ionic liquid-based absorption cooling system with high coefficient of performance |
| DE102016106234B4 (de) * | 2016-04-06 | 2022-03-03 | Fahrenheit Gmbh | Adsorptionswärmepumpe und Verfahren zum Betreiben einer Adsorptionswärmepumpe |
| WO2017205807A1 (en) * | 2016-05-26 | 2017-11-30 | Yazaki Corporation | Eutectic mixtures of ionic liquids in absorption chillers |
| JP2019517654A (ja) * | 2016-05-26 | 2019-06-24 | 矢崎総業株式会社 | 吸収式冷凍機におけるグアニジニウム系イオン液体 |
| WO2017214334A1 (en) | 2016-06-07 | 2017-12-14 | National Technology & Engineering Solutions Of Sandia, Llc | Conversion of lignin to ionic liquids |
| DE102016210478A1 (de) | 2016-06-14 | 2017-12-14 | Evonik Degussa Gmbh | Verfahren zur Entfeuchtung von feuchten Gasgemischen |
| DE102016210483A1 (de) | 2016-06-14 | 2017-12-14 | Evonik Degussa Gmbh | Verfahren und Absorptionsmittel zur Entfeuchtung von feuchten Gasgemischen |
| DE102016210484A1 (de) | 2016-06-14 | 2017-12-14 | Evonik Degussa Gmbh | Verfahren zur Entfeuchtung von feuchten Gasgemischen |
| EP3257568B1 (de) | 2016-06-14 | 2019-09-18 | Evonik Degussa GmbH | Verfahren zur entfeuchtung von feuchten gasgemischen mit ionischen flüssigkeiten |
| EP3257843A1 (en) | 2016-06-14 | 2017-12-20 | Evonik Degussa GmbH | Method of preparing a high purity imidazolium salt |
| DE102016210481B3 (de) | 2016-06-14 | 2017-06-08 | Evonik Degussa Gmbh | Verfahren zum Reinigen einer ionischen Flüssigkeit |
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| US11028249B2 (en) * | 2017-08-31 | 2021-06-08 | National Technology & Engineering Solutions Of Sandia, Llc | Methods of synthesizing ionic liquids from primary alcohol-containing lignin compounds |
| CN108190916B (zh) * | 2017-12-29 | 2020-09-18 | 新奥泛能网络科技股份有限公司 | 合成氨分离的方法和系统 |
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| JP6444556B1 (ja) * | 2018-05-25 | 2018-12-26 | 株式会社日立パワーソリューションズ | 吸収冷温水機、吸収冷温水機用追加液、吸収冷温水機用吸収液及びメンテナンス方法 |
| JP2020015688A (ja) * | 2018-07-25 | 2020-01-30 | 国立大学法人千葉大学 | 硫黄を含むホスホニウム型カチオン及び硫黄を含むホスホニウム型イオン液体 |
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| WO2020132467A1 (en) | 2018-12-20 | 2020-06-25 | Rebound Technologies, Inc. | Thermo-chemical recuperation systems, devices, and methods |
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| CN113025282B (zh) * | 2021-03-26 | 2022-04-08 | 苏州佳永新能源科技有限公司 | 一种化学吸收循环用复配吸附介质 |
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| US5176210A (en) * | 1990-07-06 | 1993-01-05 | Arctic Systems Limited | Thermochemical ice melting |
| GB9123794D0 (en) * | 1991-11-08 | 1992-01-02 | Atkinson Stephen | Vapour absorbent compositions |
| JP2750834B2 (ja) * | 1995-06-30 | 1998-05-13 | 川崎重工業株式会社 | 吸収冷凍機用吸収液 |
| US5653117A (en) * | 1996-04-15 | 1997-08-05 | Gas Research Institute | Absorption refrigeration compositions containing thiocyanate, and absorption refrigeration apparatus |
| US6177025B1 (en) * | 1998-11-17 | 2001-01-23 | University Of Utah | Absorption heat pumps having improved efficiency using a crystallization-inhibiting additive |
| US6155057A (en) * | 1999-03-01 | 2000-12-05 | Arizona Board Of Regents | Refrigerant fluid crystallization control and prevention |
| WO2000061698A1 (en) * | 1999-04-12 | 2000-10-19 | Arizona Board Of Regents | Two-phase refrigeration fluid for an absorption refrigeration apparatus and a method of preventing corrosion |
| JP2000319646A (ja) * | 1999-05-06 | 2000-11-21 | Yazaki Corp | 吸収冷凍機用吸収液および吸収冷凍機 |
| DE102004024967A1 (de) | 2004-05-21 | 2005-12-08 | Basf Ag | Neue Absorptionsmedien für Absorptionswärmepumpen, Absorptionskältemaschinen und Wärmetransformatoren |
| US7157588B2 (en) | 2005-04-15 | 2007-01-02 | E. I. Du Pont De Nemours And Company | Ionic liquids |
| DE102005028451B4 (de) * | 2005-06-17 | 2017-02-16 | Evonik Degussa Gmbh | Verfahren zum Transport von Wärme |
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| US8506839B2 (en) * | 2005-12-14 | 2013-08-13 | E I Du Pont De Nemours And Company | Absorption cycle utilizing ionic liquids and water as working fluids |
-
2010
- 2010-03-31 CN CN2010800241084A patent/CN102449101A/zh active Pending
- 2010-03-31 JP JP2012503643A patent/JP2012522873A/ja not_active Abandoned
- 2010-03-31 AU AU2010234813A patent/AU2010234813A1/en not_active Abandoned
- 2010-03-31 KR KR1020117025482A patent/KR20120003471A/ko not_active Withdrawn
- 2010-03-31 WO PCT/US2010/029322 patent/WO2010117836A1/en not_active Ceased
- 2010-03-31 BR BRPI1006734A patent/BRPI1006734A2/pt not_active IP Right Cessation
- 2010-03-31 EP EP10712637A patent/EP2414476A1/en not_active Withdrawn
- 2010-03-31 US US13/259,229 patent/US20120011886A1/en not_active Abandoned
- 2010-03-31 CA CA2754599A patent/CA2754599A1/en not_active Abandoned
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