JP5984776B2 - 複合アミン吸収液、co2又はh2s又はその双方の除去装置及び方法 - Google Patents
複合アミン吸収液、co2又はh2s又はその双方の除去装置及び方法 Download PDFInfo
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- JP5984776B2 JP5984776B2 JP2013215064A JP2013215064A JP5984776B2 JP 5984776 B2 JP5984776 B2 JP 5984776B2 JP 2013215064 A JP2013215064 A JP 2013215064A JP 2013215064 A JP2013215064 A JP 2013215064A JP 5984776 B2 JP5984776 B2 JP 5984776B2
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- compound
- amine compound
- amine
- disulfide
- absorbent
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- 239000007788 liquid Substances 0.000 title claims description 59
- 150000001412 amines Chemical class 0.000 title claims description 56
- 238000000034 method Methods 0.000 title claims description 19
- -1 amine compound Chemical class 0.000 claims description 167
- 238000010521 absorption reaction Methods 0.000 claims description 52
- 230000002745 absorbent Effects 0.000 claims description 39
- 239000002250 absorbent Substances 0.000 claims description 39
- 239000003112 inhibitor Substances 0.000 claims description 35
- NQRYJNQNLNOLGT-UHFFFAOYSA-N tetrahydropyridine hydrochloride Natural products C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims description 33
- 239000002131 composite material Substances 0.000 claims description 28
- 238000010525 oxidative degradation reaction Methods 0.000 claims description 24
- 125000000217 alkyl group Chemical group 0.000 claims description 23
- 125000004432 carbon atom Chemical group C* 0.000 claims description 23
- 239000000203 mixture Substances 0.000 claims description 23
- 230000008929 regeneration Effects 0.000 claims description 21
- 238000011069 regeneration method Methods 0.000 claims description 21
- 239000000126 substance Substances 0.000 claims description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 18
- 150000001875 compounds Chemical class 0.000 claims description 16
- DBSDZVMWEMKFCH-UHFFFAOYSA-N 2-(2-methylpiperidin-1-yl)ethanamine Chemical compound CC1CCCCN1CCN DBSDZVMWEMKFCH-UHFFFAOYSA-N 0.000 claims description 4
- NNWUEBIEOFQMSS-UHFFFAOYSA-N 2-Methylpiperidine Chemical compound CC1CCCCN1 NNWUEBIEOFQMSS-UHFFFAOYSA-N 0.000 claims description 4
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 claims description 4
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 3
- 229910052717 sulfur Inorganic materials 0.000 claims description 3
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical group CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 claims description 2
- 230000001172 regenerating effect Effects 0.000 claims description 2
- 239000007789 gas Substances 0.000 description 50
- 238000007254 oxidation reaction Methods 0.000 description 33
- 230000003647 oxidation Effects 0.000 description 31
- 230000006866 deterioration Effects 0.000 description 22
- 238000011084 recovery Methods 0.000 description 14
- 238000010586 diagram Methods 0.000 description 12
- 238000002485 combustion reaction Methods 0.000 description 10
- 230000000052 comparative effect Effects 0.000 description 10
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 8
- 229910052760 oxygen Inorganic materials 0.000 description 8
- 239000001301 oxygen Substances 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 7
- YYAYTNPNFKPFNG-UHFFFAOYSA-N 3-(2-methylpiperidin-1-yl)propan-1-amine Chemical compound CC1CCCCN1CCCN YYAYTNPNFKPFNG-UHFFFAOYSA-N 0.000 description 6
- CETBSQOFQKLHHZ-UHFFFAOYSA-N Diethyl disulfide Chemical compound CCSSCC CETBSQOFQKLHHZ-UHFFFAOYSA-N 0.000 description 6
- CUDSBWGCGSUXDB-UHFFFAOYSA-N Dibutyl disulfide Chemical compound CCCCSSCCCC CUDSBWGCGSUXDB-UHFFFAOYSA-N 0.000 description 5
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 5
- 150000004985 diamines Chemical group 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- NDNUANOUGZGEPO-UHFFFAOYSA-N (s)-2-propylpiperidine Chemical compound CCCC1CCCCN1 NDNUANOUGZGEPO-UHFFFAOYSA-N 0.000 description 4
- AXWLKJWVMMAXBD-UHFFFAOYSA-N 1-butylpiperidine Chemical compound CCCCN1CCCCC1 AXWLKJWVMMAXBD-UHFFFAOYSA-N 0.000 description 4
- PAMIQIKDUOTOBW-UHFFFAOYSA-N 1-methylpiperidine Chemical compound CN1CCCCC1 PAMIQIKDUOTOBW-UHFFFAOYSA-N 0.000 description 4
- VTDIWMPYBAVEDY-UHFFFAOYSA-N 1-propylpiperidine Chemical compound CCCN1CCCCC1 VTDIWMPYBAVEDY-UHFFFAOYSA-N 0.000 description 4
- OPKOKAMJFNKNAS-UHFFFAOYSA-N N-methylethanolamine Chemical compound CNCCO OPKOKAMJFNKNAS-UHFFFAOYSA-N 0.000 description 4
- 230000015556 catabolic process Effects 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 238000006731 degradation reaction Methods 0.000 description 4
- ALVPFGSHPUPROW-UHFFFAOYSA-N dipropyl disulfide Chemical compound CCCSSCCC ALVPFGSHPUPROW-UHFFFAOYSA-N 0.000 description 4
- CRVGTESFCCXCTH-UHFFFAOYSA-N methyl diethanolamine Chemical compound OCCN(C)CCO CRVGTESFCCXCTH-UHFFFAOYSA-N 0.000 description 4
- 150000003335 secondary amines Chemical class 0.000 description 4
- KYNFOMQIXZUKRK-UHFFFAOYSA-N 2,2'-dithiodiethanol Chemical compound OCCSSCCO KYNFOMQIXZUKRK-UHFFFAOYSA-N 0.000 description 3
- AKNUHUCEWALCOI-UHFFFAOYSA-N N-ethyldiethanolamine Chemical compound OCCN(CC)CCO AKNUHUCEWALCOI-UHFFFAOYSA-N 0.000 description 3
- 239000006096 absorbing agent Substances 0.000 description 3
- 150000003141 primary amines Chemical class 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 150000003512 tertiary amines Chemical class 0.000 description 3
- KODLUXHSIZOKTG-UHFFFAOYSA-N 1-aminobutan-2-ol Chemical compound CCC(O)CN KODLUXHSIZOKTG-UHFFFAOYSA-N 0.000 description 2
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 description 2
- IWSZDQRGNFLMJS-UHFFFAOYSA-N 2-(dibutylamino)ethanol Chemical compound CCCCN(CCO)CCCC IWSZDQRGNFLMJS-UHFFFAOYSA-N 0.000 description 2
- BKCNDTDWDGQHSD-UHFFFAOYSA-N 2-(tert-butyldisulfanyl)-2-methylpropane Chemical compound CC(C)(C)SSC(C)(C)C BKCNDTDWDGQHSD-UHFFFAOYSA-N 0.000 description 2
- NWYYWIJOWOLJNR-UHFFFAOYSA-N 2-Amino-3-methyl-1-butanol Chemical compound CC(C)C(N)CO NWYYWIJOWOLJNR-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- GVNHOISKXMSMPX-UHFFFAOYSA-N 2-[butyl(2-hydroxyethyl)amino]ethanol Chemical compound CCCCN(CCO)CCO GVNHOISKXMSMPX-UHFFFAOYSA-N 0.000 description 2
- 229940058020 2-amino-2-methyl-1-propanol Drugs 0.000 description 2
- JCBPETKZIGVZRE-UHFFFAOYSA-N 2-aminobutan-1-ol Chemical compound CCC(N)CO JCBPETKZIGVZRE-UHFFFAOYSA-N 0.000 description 2
- BKMMTJMQCTUHRP-UHFFFAOYSA-N 2-aminopropan-1-ol Chemical compound CC(N)CO BKMMTJMQCTUHRP-UHFFFAOYSA-N 0.000 description 2
- PCNXNSPEWIRGJO-UHFFFAOYSA-N 2-butylpiperidine Chemical compound CCCCC1CCCCN1 PCNXNSPEWIRGJO-UHFFFAOYSA-N 0.000 description 2
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 description 2
- 229940013085 2-diethylaminoethanol Drugs 0.000 description 2
- QBBKKFZGCDJDQK-UHFFFAOYSA-N 2-ethylpiperidine Chemical compound CCC1CCCCN1 QBBKKFZGCDJDQK-UHFFFAOYSA-N 0.000 description 2
- YCLSOMLVSHPPFV-UHFFFAOYSA-N 3-(2-carboxyethyldisulfanyl)propanoic acid Chemical compound OC(=O)CCSSCCC(O)=O YCLSOMLVSHPPFV-UHFFFAOYSA-N 0.000 description 2
- PYSGFFTXMUWEOT-UHFFFAOYSA-N 3-(dimethylamino)propan-1-ol Chemical compound CN(C)CCCO PYSGFFTXMUWEOT-UHFFFAOYSA-N 0.000 description 2
- QCTOLMMTYSGTDA-UHFFFAOYSA-N 4-(dimethylamino)butan-1-ol Chemical compound CN(C)CCCCO QCTOLMMTYSGTDA-UHFFFAOYSA-N 0.000 description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 2
- ODHAQPXNQDBHSH-UHFFFAOYSA-N Dicyclohexyl disulfide Chemical compound C1CCCCC1SSC1CCCCC1 ODHAQPXNQDBHSH-UHFFFAOYSA-N 0.000 description 2
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 2
- HTLZVHNRZJPSMI-UHFFFAOYSA-N N-ethylpiperidine Chemical compound CCN1CCCCC1 HTLZVHNRZJPSMI-UHFFFAOYSA-N 0.000 description 2
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 2
- 239000000498 cooling water Substances 0.000 description 2
- 239000003546 flue gas Substances 0.000 description 2
- 239000002803 fossil fuel Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000007348 radical reaction Methods 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000010792 warming Methods 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- PVXVWWANJIWJOO-UHFFFAOYSA-N 1-(1,3-benzodioxol-5-yl)-N-ethylpropan-2-amine Chemical compound CCNC(C)CC1=CC=C2OCOC2=C1 PVXVWWANJIWJOO-UHFFFAOYSA-N 0.000 description 1
- MYIBLRZZTNNKLN-UHFFFAOYSA-N 1-n,1-n'-diethylpropane-1,1-diamine Chemical compound CCNC(CC)NCC MYIBLRZZTNNKLN-UHFFFAOYSA-N 0.000 description 1
- CYXGZZFAAUDHQL-UHFFFAOYSA-N 1-n,1-n'-dimethylpropane-1,1-diamine Chemical compound CCC(NC)NC CYXGZZFAAUDHQL-UHFFFAOYSA-N 0.000 description 1
- AYHQRYOMLOEVPZ-UHFFFAOYSA-N 1-n,1-n'-ditert-butylethane-1,1-diamine Chemical compound CC(C)(C)NC(C)NC(C)(C)C AYHQRYOMLOEVPZ-UHFFFAOYSA-N 0.000 description 1
- COWPTMLRSANSMQ-UHFFFAOYSA-N 2,3-dimethylpiperazine Chemical compound CC1NCCNC1C COWPTMLRSANSMQ-UHFFFAOYSA-N 0.000 description 1
- NSMWYRLQHIXVAP-UHFFFAOYSA-N 2,5-dimethylpiperazine Chemical compound CC1CNC(C)CN1 NSMWYRLQHIXVAP-UHFFFAOYSA-N 0.000 description 1
- VJWZYGQIJWDACM-UHFFFAOYSA-N 2-(2-methylpropylamino)ethanol Chemical compound CC(C)CNCCO VJWZYGQIJWDACM-UHFFFAOYSA-N 0.000 description 1
- LJDSTRZHPWMDPG-UHFFFAOYSA-N 2-(butylamino)ethanol Chemical compound CCCCNCCO LJDSTRZHPWMDPG-UHFFFAOYSA-N 0.000 description 1
- MIJDSYMOBYNHOT-UHFFFAOYSA-N 2-(ethylamino)ethanol Chemical compound CCNCCO MIJDSYMOBYNHOT-UHFFFAOYSA-N 0.000 description 1
- SALYKAIZVOFAEJ-UHFFFAOYSA-N 2-(pentylamino)ethanol Chemical compound CCCCCNCCO SALYKAIZVOFAEJ-UHFFFAOYSA-N 0.000 description 1
- RILLZYSZSDGYGV-UHFFFAOYSA-N 2-(propan-2-ylamino)ethanol Chemical compound CC(C)NCCO RILLZYSZSDGYGV-UHFFFAOYSA-N 0.000 description 1
- BCLSJHWBDUYDTR-UHFFFAOYSA-N 2-(propylamino)ethanol Chemical compound CCCNCCO BCLSJHWBDUYDTR-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- JOMNTHCQHJPVAZ-UHFFFAOYSA-N 2-methylpiperazine Chemical compound CC1CNCCN1 JOMNTHCQHJPVAZ-UHFFFAOYSA-N 0.000 description 1
- BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 1
- QMMZSJPSPRTHGB-UHFFFAOYSA-N MDEA Natural products CC(C)CCCCC=CCC=CC(O)=O QMMZSJPSPRTHGB-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 150000002019 disulfides Chemical class 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000002309 gasification Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- MFIGJRRHGZYPDD-UHFFFAOYSA-N n,n'-di(propan-2-yl)ethane-1,2-diamine Chemical compound CC(C)NCCNC(C)C MFIGJRRHGZYPDD-UHFFFAOYSA-N 0.000 description 1
- KVKFRMCSXWQSNT-UHFFFAOYSA-N n,n'-dimethylethane-1,2-diamine Chemical compound CNCCNC KVKFRMCSXWQSNT-UHFFFAOYSA-N 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- 150000003053 piperidines Chemical class 0.000 description 1
- 238000010248 power generation Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
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- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Gas Separation By Absorption (AREA)
- Treating Waste Gases (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2013215064A JP5984776B2 (ja) | 2013-10-15 | 2013-10-15 | 複合アミン吸収液、co2又はh2s又はその双方の除去装置及び方法 |
| CA2924300A CA2924300A1 (en) | 2013-10-15 | 2014-10-10 | Composite amine absorbent, and apparatus and method for removing co2 and/or h2s |
| PCT/JP2014/077264 WO2015056657A1 (ja) | 2013-10-15 | 2014-10-10 | 複合アミン吸収液、co2又はh2s又はその双方の除去装置及び方法 |
| AU2014335384A AU2014335384B2 (en) | 2013-10-15 | 2014-10-10 | Composite amine absorption solution, and method and device for removing CO2 and/or H2S |
| EP14853761.6A EP3034152A4 (en) | 2013-10-15 | 2014-10-10 | COMPOUND AMINE ABSORPTION SOLUTION AND PROCESS AND DEVICE FOR REMOVING CO2 AND / OR H2S |
| US15/022,125 US20160220947A1 (en) | 2013-10-15 | 2014-10-10 | Composite amine absorbent, and apparatus and method for removing co2 and/or h2s |
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| Application Number | Priority Date | Filing Date | Title |
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| JP2013215064A JP5984776B2 (ja) | 2013-10-15 | 2013-10-15 | 複合アミン吸収液、co2又はh2s又はその双方の除去装置及び方法 |
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| Publication Number | Publication Date |
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| JP2015077537A JP2015077537A (ja) | 2015-04-23 |
| JP2015077537A5 JP2015077537A5 (enExample) | 2015-06-18 |
| JP5984776B2 true JP5984776B2 (ja) | 2016-09-06 |
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| JP2013215064A Expired - Fee Related JP5984776B2 (ja) | 2013-10-15 | 2013-10-15 | 複合アミン吸収液、co2又はh2s又はその双方の除去装置及び方法 |
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| US (1) | US20160220947A1 (enExample) |
| EP (1) | EP3034152A4 (enExample) |
| JP (1) | JP5984776B2 (enExample) |
| AU (1) | AU2014335384B2 (enExample) |
| CA (1) | CA2924300A1 (enExample) |
| WO (1) | WO2015056657A1 (enExample) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA3003795A1 (en) * | 2015-11-09 | 2017-05-18 | Shell Internationale Research Maatschappij B.V. | Process for removing mercaptans from a gas stream |
| US10710020B2 (en) * | 2017-06-30 | 2020-07-14 | Uop Llc | Processes for gas separation by solvent or absorbent |
| CN108854459B (zh) * | 2018-09-25 | 2022-03-15 | 天津工业大学 | 一种低能耗无水co2相变吸收剂及再生方法和应用 |
| JP7178911B2 (ja) * | 2019-01-24 | 2022-11-28 | 三菱重工エンジニアリング株式会社 | 複合アミン吸収液、co2又はh2s又はその双方の除去装置及び方法 |
| JP2025086680A (ja) * | 2023-11-28 | 2025-06-09 | 川崎重工業株式会社 | 固体吸収材ならびにそれを用いた酸性ガスの吸収および脱離方法 |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4020144A (en) * | 1975-05-02 | 1977-04-26 | Exxon Research And Engineering Company | Method for removal of gaseous sulfur and nitrogen compounds from gas streams |
| US4804485A (en) * | 1987-05-08 | 1989-02-14 | Pennwalt Corporation | Polyalkyleneoxyamine catalysts for dialkyl disulfides and/or polysulfides used in dissolving sulfur |
| US4959177A (en) * | 1987-10-09 | 1990-09-25 | Shell Oil Company | Reducing stress corrosion cracking in treating gases with alkanol amines |
| JPH0751537A (ja) | 1993-06-30 | 1995-02-28 | Mitsubishi Heavy Ind Ltd | Co2 含有ガス中のco2 を除去する方法 |
| JP4690659B2 (ja) | 2004-03-15 | 2011-06-01 | 三菱重工業株式会社 | Co2回収装置 |
| FR2877858B1 (fr) * | 2004-11-12 | 2007-01-12 | Inst Francais Du Petrole | Procede de desacidification d'un gaz avec une solution absorbante a regeneration fractionnee |
| EP1872846B1 (en) * | 2005-04-04 | 2013-07-24 | Mitsubishi Heavy Industries, Ltd. | Absorbing solution and method for absorbing co2 or h2s or both |
| FR2898284B1 (fr) * | 2006-03-10 | 2009-06-05 | Inst Francais Du Petrole | Procede de desacidification d'un gaz par solution absorbante avec regeneration fractionnee par chauffage. |
| JP5215595B2 (ja) * | 2007-06-18 | 2013-06-19 | 三菱重工業株式会社 | 吸収液、吸収液を用いたco2又はh2s除去装置及び方法 |
| FR2933001B1 (fr) * | 2008-06-27 | 2010-08-20 | Inst Francais Du Petrole | Solution absorbante contenant un inhibiteur de degradation a fonction thiocarbonyle et methode pour limiter la degradation d'une solution absorbante |
| ES2443307T3 (es) * | 2009-02-02 | 2014-02-18 | Basf Se | Absorbente que comprende aminas cíclicas para la eliminación de gases ácidos |
| WO2012076378A1 (en) * | 2010-12-06 | 2012-06-14 | Shell Internationale Research Maatschappij B.V. | Process for removing mercaptans from a gas stream |
| JP5659127B2 (ja) * | 2010-12-22 | 2015-01-28 | 株式会社東芝 | 酸性ガス吸収剤、酸性ガス除去方法および酸性ガス除去装置 |
| JP5659084B2 (ja) * | 2011-05-30 | 2015-01-28 | 株式会社東芝 | 酸性ガス吸収剤、酸性ガス除去方法および酸性ガス除去装置 |
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2013
- 2013-10-15 JP JP2013215064A patent/JP5984776B2/ja not_active Expired - Fee Related
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2014
- 2014-10-10 CA CA2924300A patent/CA2924300A1/en not_active Abandoned
- 2014-10-10 US US15/022,125 patent/US20160220947A1/en not_active Abandoned
- 2014-10-10 EP EP14853761.6A patent/EP3034152A4/en not_active Withdrawn
- 2014-10-10 WO PCT/JP2014/077264 patent/WO2015056657A1/ja not_active Ceased
- 2014-10-10 AU AU2014335384A patent/AU2014335384B2/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| WO2015056657A1 (ja) | 2015-04-23 |
| EP3034152A4 (en) | 2016-12-21 |
| AU2014335384B2 (en) | 2017-03-16 |
| JP2015077537A (ja) | 2015-04-23 |
| EP3034152A1 (en) | 2016-06-22 |
| AU2014335384A1 (en) | 2016-04-07 |
| US20160220947A1 (en) | 2016-08-04 |
| CA2924300A1 (en) | 2015-04-23 |
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