BR112015009055B1 - método para purificar 1,4-diaminobutano, e 1,4-diaminobutano - Google Patents
método para purificar 1,4-diaminobutano, e 1,4-diaminobutano Download PDFInfo
- Publication number
- BR112015009055B1 BR112015009055B1 BR112015009055-9A BR112015009055A BR112015009055B1 BR 112015009055 B1 BR112015009055 B1 BR 112015009055B1 BR 112015009055 A BR112015009055 A BR 112015009055A BR 112015009055 B1 BR112015009055 B1 BR 112015009055B1
- Authority
- BR
- Brazil
- Prior art keywords
- diaminobutane
- fermentation solution
- mpa
- mmhg
- concentration
- Prior art date
Links
- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 title claims abstract description 300
- 239000005700 Putrescine Substances 0.000 title claims abstract description 146
- 238000000034 method Methods 0.000 title claims abstract description 67
- 238000000855 fermentation Methods 0.000 claims abstract description 84
- 230000004151 fermentation Effects 0.000 claims abstract description 84
- 239000000203 mixture Substances 0.000 claims abstract description 61
- 239000012141 concentrate Substances 0.000 claims abstract description 34
- 150000003839 salts Chemical class 0.000 claims abstract description 10
- 238000004821 distillation Methods 0.000 claims description 46
- 230000001580 bacterial effect Effects 0.000 claims description 35
- 238000011084 recovery Methods 0.000 claims description 31
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 18
- 239000002904 solvent Substances 0.000 claims description 16
- 239000006227 byproduct Substances 0.000 claims description 12
- 238000004508 fractional distillation Methods 0.000 claims description 12
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 9
- 238000000926 separation method Methods 0.000 claims description 7
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 claims description 6
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 claims description 6
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 claims description 6
- INHCSSUBVCNVSK-UHFFFAOYSA-L lithium sulfate Chemical compound [Li+].[Li+].[O-]S([O-])(=O)=O INHCSSUBVCNVSK-UHFFFAOYSA-L 0.000 claims description 6
- 239000007788 liquid Substances 0.000 claims description 5
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 claims description 4
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 claims description 4
- 229910052939 potassium sulfate Inorganic materials 0.000 claims description 4
- 239000001120 potassium sulphate Substances 0.000 claims description 4
- 235000011151 potassium sulphates Nutrition 0.000 claims description 4
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims description 3
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 claims description 3
- 229910052921 ammonium sulfate Inorganic materials 0.000 claims description 3
- 235000011130 ammonium sulphate Nutrition 0.000 claims description 3
- RQPZNWPYLFFXCP-UHFFFAOYSA-L barium dihydroxide Chemical compound [OH-].[OH-].[Ba+2] RQPZNWPYLFFXCP-UHFFFAOYSA-L 0.000 claims description 3
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 claims description 3
- 239000000920 calcium hydroxide Substances 0.000 claims description 3
- 229910001861 calcium hydroxide Inorganic materials 0.000 claims description 3
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 claims description 3
- 239000000347 magnesium hydroxide Substances 0.000 claims description 3
- 229910001862 magnesium hydroxide Inorganic materials 0.000 claims description 3
- 229910052943 magnesium sulfate Inorganic materials 0.000 claims description 3
- 235000019341 magnesium sulphate Nutrition 0.000 claims description 3
- 229910052938 sodium sulfate Inorganic materials 0.000 claims description 3
- 235000011152 sodium sulphate Nutrition 0.000 claims description 3
- 239000000908 ammonium hydroxide Substances 0.000 claims description 2
- 229910001863 barium hydroxide Inorganic materials 0.000 claims description 2
- 239000001175 calcium sulphate Substances 0.000 claims description 2
- 235000011132 calcium sulphate Nutrition 0.000 claims description 2
- 238000000746 purification Methods 0.000 abstract description 26
- 239000004952 Polyamide Substances 0.000 abstract description 10
- 229920002647 polyamide Polymers 0.000 abstract description 10
- 239000000243 solution Substances 0.000 description 71
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 24
- 239000012528 membrane Substances 0.000 description 18
- 239000002585 base Substances 0.000 description 11
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 10
- 239000000706 filtrate Substances 0.000 description 10
- 230000007935 neutral effect Effects 0.000 description 8
- 238000010979 pH adjustment Methods 0.000 description 8
- 238000004128 high performance liquid chromatography Methods 0.000 description 7
- 244000005700 microbiome Species 0.000 description 7
- 239000002002 slurry Substances 0.000 description 7
- 238000001704 evaporation Methods 0.000 description 6
- 230000008020 evaporation Effects 0.000 description 6
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 5
- 239000008103 glucose Substances 0.000 description 5
- 239000001301 oxygen Substances 0.000 description 5
- 229910052760 oxygen Inorganic materials 0.000 description 5
- 239000010802 sludge Substances 0.000 description 5
- 238000001159 Fisher's combined probability test Methods 0.000 description 4
- 150000001413 amino acids Chemical class 0.000 description 4
- 229910021529 ammonia Inorganic materials 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 4
- 238000001914 filtration Methods 0.000 description 4
- LELOWRISYMNNSU-UHFFFAOYSA-N hydrogen cyanide Chemical compound N#C LELOWRISYMNNSU-UHFFFAOYSA-N 0.000 description 4
- 150000002500 ions Chemical class 0.000 description 4
- 239000002609 medium Substances 0.000 description 4
- 150000007524 organic acids Chemical class 0.000 description 4
- 239000003637 basic solution Substances 0.000 description 3
- LWWAWNHGTUALAU-UHFFFAOYSA-N butane-1,4-diamine carbonic acid Chemical compound C(O)(O)=O.NCCCCN LWWAWNHGTUALAU-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- 229920006153 PA4T Polymers 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- GHWVXCQZPNWFRO-UHFFFAOYSA-N butane-2,3-diamine Chemical compound CC(N)C(C)N GHWVXCQZPNWFRO-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000005119 centrifugation Methods 0.000 description 2
- 238000005345 coagulation Methods 0.000 description 2
- 230000015271 coagulation Effects 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 239000012527 feed solution Substances 0.000 description 2
- 238000005188 flotation Methods 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 238000005374 membrane filtration Methods 0.000 description 2
- 230000002028 premature Effects 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 238000004326 stimulated echo acquisition mode for imaging Methods 0.000 description 2
- 231100000167 toxic agent Toxicity 0.000 description 2
- 238000003828 vacuum filtration Methods 0.000 description 2
- ULTHEAFYOOPTTB-UHFFFAOYSA-N 1,4-dibromobutane Chemical compound BrCCCCBr ULTHEAFYOOPTTB-UHFFFAOYSA-N 0.000 description 1
- KJDRSWPQXHESDQ-UHFFFAOYSA-N 1,4-dichlorobutane Chemical compound ClCCCCCl KJDRSWPQXHESDQ-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 241000186216 Corynebacterium Species 0.000 description 1
- 241000588724 Escherichia coli Species 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 239000001166 ammonium sulphate Substances 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007809 chemical reaction catalyst Substances 0.000 description 1
- 238000012258 culturing Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- -1 for example Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000001963 growth medium Substances 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 238000005192 partition Methods 0.000 description 1
- XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical compound C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 description 1
- 239000012264 purified product Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- IAHFWCOBPZCAEA-UHFFFAOYSA-N succinonitrile Chemical compound N#CCCC#N IAHFWCOBPZCAEA-UHFFFAOYSA-N 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
- 238000007738 vacuum evaporation Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
- C07C209/82—Purification; Separation; Stabilisation; Use of additives
- C07C209/84—Purification
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
- C07C211/01—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms
- C07C211/02—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C211/09—Diamines
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
- C08G69/04—Preparatory processes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
- C08G69/26—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from polyamines and polycarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P13/00—Preparation of nitrogen-containing organic compounds
- C12P13/001—Amines; Imines
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P13/00—Preparation of nitrogen-containing organic compounds
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Zoology (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- General Chemical & Material Sciences (AREA)
- Microbiology (AREA)
- Biotechnology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polyamides (AREA)
- Vaporization, Distillation, Condensation, Sublimation, And Cold Traps (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR1020120117501A KR20140052189A (ko) | 2012-10-22 | 2012-10-22 | 1,4-디아미노부탄의 정제방법, 상기 방법으로 정제된 1,4-디아미노부탄 및 이로부터 제조되는 폴리아미드 |
| KR10-2012-0117501 | 2012-10-22 | ||
| PCT/KR2013/009399 WO2014065553A1 (ko) | 2012-10-22 | 2013-10-22 | 1,4-디아미노부탄의 정제방법, 상기 방법으로 정제된 1,4-디아미노부탄 및 이로부터 제조되는 폴리아미드 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| BR112015009055A2 BR112015009055A2 (pt) | 2017-07-04 |
| BR112015009055B1 true BR112015009055B1 (pt) | 2020-12-08 |
Family
ID=50544882
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BR112015009055-9A BR112015009055B1 (pt) | 2012-10-22 | 2013-10-22 | método para purificar 1,4-diaminobutano, e 1,4-diaminobutano |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US9376370B2 (https=) |
| EP (1) | EP2910543B1 (https=) |
| JP (1) | JP6050895B2 (https=) |
| KR (1) | KR20140052189A (https=) |
| CN (1) | CN104822652B (https=) |
| AU (1) | AU2013335491B2 (https=) |
| BR (1) | BR112015009055B1 (https=) |
| ES (1) | ES2797379T3 (https=) |
| IN (1) | IN2015DN03205A (https=) |
| MY (1) | MY175861A (https=) |
| RU (1) | RU2616002C2 (https=) |
| WO (1) | WO2014065553A1 (https=) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2615774B2 (ja) | 1988-03-09 | 1997-06-04 | 株式会社豊田自動織機製作所 | 織機における不要緯糸排出方法 |
| KR101773135B1 (ko) * | 2015-05-08 | 2017-08-30 | 씨제이제일제당 주식회사 | 1,4-디아미노부탄의 정제방법 |
| US20210252421A1 (en) * | 2018-07-10 | 2021-08-19 | Givaudan Sa | Improvements in or relating to organic compounds |
| KR102352784B1 (ko) * | 2020-03-19 | 2022-01-18 | 씨제이제일제당 주식회사 | 탄산 함유 디아미노알칸 용액의 분리막 분리 공정 |
| EP4151619A1 (en) * | 2021-09-20 | 2023-03-22 | Covestro Deutschland AG | Method for the removal of water from and transport of aliphatic diamines |
| CN117986134A (zh) * | 2022-10-28 | 2024-05-07 | 中国科学院过程工程研究所 | 一种高纯度1,5-戊二胺的提纯方法 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4836948B2 (ja) * | 2004-07-15 | 2011-12-14 | ディーエスエム アイピー アセッツ ビー．ブイ． | １，４−ブタンジアミンの生化学合成 |
| BRPI0620980A2 (pt) * | 2006-01-11 | 2011-11-29 | Dsm Ip Assets Bv | processo para isolamento de uma amina orgánica |
| WO2009092793A2 (de) * | 2008-01-23 | 2009-07-30 | Basf Se | Verfahren zur fermentativen herstellung von 1,5-diaminopentan |
| JP5782674B2 (ja) | 2008-03-12 | 2015-09-24 | 東レ株式会社 | ジアミンおよびポリアミドの製造方法 |
| KR101188432B1 (ko) | 2008-04-10 | 2012-10-08 | 한국과학기술원 | 퓨트레신 고생성능을 가지는 변이 미생물 및 이를 이용한 퓨트레신의 제조방법 |
| ES2589378T3 (es) | 2008-04-10 | 2016-11-14 | Korea Advanced Institute Of Science And Technology | Microorganismo mutante con capacidad elevada para producir putrescina, y preparación de putrescina usando el mismo |
| KR101286158B1 (ko) * | 2011-08-24 | 2013-07-15 | 씨제이제일제당 (주) | 발효액에서 1,4-디아미노부탄의 분리 및 정제하는 방법 |
| CA2851817A1 (en) * | 2011-10-14 | 2013-04-18 | Toray Industries, Inc. | Process for producing 2,3-butanediol |
-
2012
- 2012-10-22 KR KR1020120117501A patent/KR20140052189A/ko not_active Ceased
-
2013
- 2013-10-22 MY MYPI2015001008A patent/MY175861A/en unknown
- 2013-10-22 ES ES13849534T patent/ES2797379T3/es active Active
- 2013-10-22 JP JP2015536723A patent/JP6050895B2/ja active Active
- 2013-10-22 WO PCT/KR2013/009399 patent/WO2014065553A1/ko not_active Ceased
- 2013-10-22 US US14/437,172 patent/US9376370B2/en active Active
- 2013-10-22 AU AU2013335491A patent/AU2013335491B2/en active Active
- 2013-10-22 IN IN3205DEN2015 patent/IN2015DN03205A/en unknown
- 2013-10-22 EP EP13849534.6A patent/EP2910543B1/en active Active
- 2013-10-22 BR BR112015009055-9A patent/BR112015009055B1/pt active IP Right Grant
- 2013-10-22 CN CN201380062423.XA patent/CN104822652B/zh active Active
- 2013-10-22 RU RU2015114079A patent/RU2616002C2/ru active
Also Published As
| Publication number | Publication date |
|---|---|
| CN104822652B (zh) | 2017-07-14 |
| WO2014065553A1 (ko) | 2014-05-01 |
| BR112015009055A2 (pt) | 2017-07-04 |
| JP6050895B2 (ja) | 2016-12-21 |
| JP2015533830A (ja) | 2015-11-26 |
| IN2015DN03205A (https=) | 2015-10-02 |
| RU2616002C2 (ru) | 2017-04-12 |
| AU2013335491A1 (en) | 2015-04-30 |
| AU2013335491B2 (en) | 2016-04-28 |
| RU2015114079A (ru) | 2016-12-10 |
| ES2797379T3 (es) | 2020-12-02 |
| US20150284315A1 (en) | 2015-10-08 |
| KR20140052189A (ko) | 2014-05-07 |
| EP2910543B1 (en) | 2020-04-15 |
| MY175861A (en) | 2020-07-14 |
| EP2910543A4 (en) | 2016-06-08 |
| US9376370B2 (en) | 2016-06-28 |
| CN104822652A (zh) | 2015-08-05 |
| EP2910543A1 (en) | 2015-08-26 |
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