BR122016015199B1 - processo para isomerização de corrente de alimentação de hidrocarboneto aromático esgotada de para-xileno - Google Patents
processo para isomerização de corrente de alimentação de hidrocarboneto aromático esgotada de para-xileno Download PDFInfo
- Publication number
- BR122016015199B1 BR122016015199B1 BR122016015199A BR122016015199A BR122016015199B1 BR 122016015199 B1 BR122016015199 B1 BR 122016015199B1 BR 122016015199 A BR122016015199 A BR 122016015199A BR 122016015199 A BR122016015199 A BR 122016015199A BR 122016015199 B1 BR122016015199 B1 BR 122016015199B1
- Authority
- BR
- Brazil
- Prior art keywords
- feed stream
- xylene
- ppm
- para
- styrene
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 75
- 230000008569 process Effects 0.000 title claims abstract description 62
- 238000006317 isomerization reaction Methods 0.000 title claims abstract description 51
- URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical group CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 title claims description 112
- 150000004945 aromatic hydrocarbons Chemical class 0.000 title claims description 19
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims abstract description 96
- 239000008096 xylene Substances 0.000 claims abstract description 51
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims abstract description 35
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims abstract description 35
- 150000003738 xylenes Chemical class 0.000 claims abstract description 24
- 239000003054 catalyst Substances 0.000 claims description 62
- 239000007791 liquid phase Substances 0.000 claims description 25
- 239000013078 crystal Substances 0.000 claims description 17
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 17
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 11
- 239000000203 mixture Substances 0.000 claims description 8
- 238000005804 alkylation reaction Methods 0.000 claims description 6
- 125000004122 cyclic group Chemical group 0.000 claims description 6
- 239000000463 material Substances 0.000 claims description 6
- 238000011144 upstream manufacturing Methods 0.000 claims description 6
- 229910052593 corundum Inorganic materials 0.000 claims description 4
- 229910001845 yogo sapphire Inorganic materials 0.000 claims description 4
- 230000009467 reduction Effects 0.000 claims description 3
- 230000003247 decreasing effect Effects 0.000 claims 2
- 238000002407 reforming Methods 0.000 claims 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 21
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 20
- IVSZLXZYQVIEFR-UHFFFAOYSA-N m-xylene Chemical group CC1=CC=CC(C)=C1 IVSZLXZYQVIEFR-UHFFFAOYSA-N 0.000 description 18
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 11
- 229910052739 hydrogen Inorganic materials 0.000 description 11
- 239000001257 hydrogen Substances 0.000 description 11
- 230000008929 regeneration Effects 0.000 description 11
- 238000011069 regeneration method Methods 0.000 description 11
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 10
- 238000012360 testing method Methods 0.000 description 10
- 239000000047 product Substances 0.000 description 9
- 238000005516 engineering process Methods 0.000 description 8
- 239000010457 zeolite Substances 0.000 description 8
- 229910021536 Zeolite Inorganic materials 0.000 description 7
- 239000011230 binding agent Substances 0.000 description 7
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 230000008901 benefit Effects 0.000 description 6
- 239000006227 byproduct Substances 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 239000000377 silicon dioxide Substances 0.000 description 6
- 230000032683 aging Effects 0.000 description 5
- 230000007423 decrease Effects 0.000 description 5
- 239000012535 impurity Substances 0.000 description 5
- 239000002808 molecular sieve Substances 0.000 description 5
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 230000029936 alkylation Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 230000000737 periodic effect Effects 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 229910000323 aluminium silicate Inorganic materials 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 239000004927 clay Substances 0.000 description 3
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000012808 vapor phase Substances 0.000 description 3
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000000356 contaminant Substances 0.000 description 2
- 230000009849 deactivation Effects 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 238000001179 sorption measurement Methods 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- BTOVVHWKPVSLBI-UHFFFAOYSA-N 2-methylprop-1-enylbenzene Chemical compound CC(C)=CC1=CC=CC=C1 BTOVVHWKPVSLBI-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 1
- 230000000274 adsorptive effect Effects 0.000 description 1
- IXWIAFSBWGYQOE-UHFFFAOYSA-M aluminum;magnesium;oxygen(2-);silicon(4+);hydroxide;tetrahydrate Chemical compound O.O.O.O.[OH-].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[Mg+2].[Al+3].[Si+4].[Si+4].[Si+4].[Si+4] IXWIAFSBWGYQOE-UHFFFAOYSA-M 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000011143 downstream manufacturing Methods 0.000 description 1
- 238000001493 electron microscopy Methods 0.000 description 1
- 230000008451 emotion Effects 0.000 description 1
- 238000013213 extrapolation Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 229910052733 gallium Inorganic materials 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 210000002741 palatine tonsil Anatomy 0.000 description 1
- 238000005453 pelletization Methods 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/22—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by isomerisation
- C07C5/27—Rearrangement of carbon atoms in the hydrocarbon skeleton
- C07C5/2729—Changing the branching point of an open chain or the point of substitution on a ring
- C07C5/2732—Catalytic processes
- C07C5/2737—Catalytic processes with crystalline alumino-silicates, e.g. molecular sieves
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J29/00—Catalysts comprising molecular sieves
- B01J29/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
- B01J29/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
- B01J29/70—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of types characterised by their specific structure not provided for in groups B01J29/08 - B01J29/65
- B01J29/7038—MWW-type, e.g. MCM-22, ERB-1, ITQ-1, PSH-3 or SSZ-25
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2529/00—Catalysts comprising molecular sieves
- C07C2529/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites, pillared clays
- C07C2529/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
- C07C2529/40—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the pentasil type, e.g. types ZSM-5, ZSM-8 or ZSM-11
-
- 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
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261695493P | 2012-08-31 | 2012-08-31 | |
| PCT/US2013/054070 WO2014035626A1 (en) | 2012-08-31 | 2013-08-08 | Xylene isomerization process and catalyst therefor |
| BR112014033014A BR112014033014B1 (pt) | 2012-08-31 | 2013-08-08 | processo para isomerização de corrente de alimentação de hidrocarboneto aromático esgotada de para-xileno compreendendo fenol e catalisador para o mesmo |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| BR122016015199A2 BR122016015199A2 (pt) | 2016-10-11 |
| BR122016015199B1 true BR122016015199B1 (pt) | 2016-12-20 |
Family
ID=50184127
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BR122016015199A BR122016015199B1 (pt) | 2012-08-31 | 2013-08-08 | processo para isomerização de corrente de alimentação de hidrocarboneto aromático esgotada de para-xileno |
| BR112014033014A BR112014033014B1 (pt) | 2012-08-31 | 2013-08-08 | processo para isomerização de corrente de alimentação de hidrocarboneto aromático esgotada de para-xileno compreendendo fenol e catalisador para o mesmo |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BR112014033014A BR112014033014B1 (pt) | 2012-08-31 | 2013-08-08 | processo para isomerização de corrente de alimentação de hidrocarboneto aromático esgotada de para-xileno compreendendo fenol e catalisador para o mesmo |
Country Status (9)
| Country | Link |
|---|---|
| US (2) | US9193645B2 (cg-RX-API-DMAC7.html) |
| JP (1) | JP5933127B2 (cg-RX-API-DMAC7.html) |
| KR (1) | KR101659203B1 (cg-RX-API-DMAC7.html) |
| CN (1) | CN104395266B (cg-RX-API-DMAC7.html) |
| BR (2) | BR122016015199B1 (cg-RX-API-DMAC7.html) |
| IN (1) | IN2014DN10781A (cg-RX-API-DMAC7.html) |
| MY (1) | MY178398A (cg-RX-API-DMAC7.html) |
| SG (2) | SG11201408189SA (cg-RX-API-DMAC7.html) |
| WO (1) | WO2014035626A1 (cg-RX-API-DMAC7.html) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10010878B2 (en) | 2015-03-03 | 2018-07-03 | Uop Llc | High meso-surface area, low Si/Al ratio pentasil zeolite |
| US9643897B2 (en) | 2015-03-03 | 2017-05-09 | Uop Llc | Enhanced propylene production in OTO process with modified zeolites |
| EP3442933B1 (en) | 2016-04-14 | 2022-11-30 | Uop Llc | Liquid phase xylene isomerization in the absence of hydrogen |
| CN107029783B (zh) * | 2017-05-08 | 2019-05-03 | 宁夏大学 | 一种lpg直接转化为乙烯、丙烯的催化剂及其制备方法 |
| WO2021041021A1 (en) * | 2019-08-23 | 2021-03-04 | Exxonmobil Chemical Patents Inc. | Processes for isomerizing c8 aromatic hydrocarbons |
| WO2021041022A1 (en) * | 2019-08-23 | 2021-03-04 | Exxonmobil Chemical Patents Inc. | Processes for isomerizing c8 aromatic hydrocarbons using serial reactors |
| CN116390900A (zh) * | 2020-09-30 | 2023-07-04 | 埃克森美孚化学专利公司 | C8芳族烃的转化方法 |
Family Cites Families (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5043502A (en) | 1990-03-16 | 1991-08-27 | Uop | Production of xylenes from light aliphatic hydrocarbons via dehydrocyclodimerization and methylation |
| US6376733B1 (en) | 1996-01-25 | 2002-04-23 | Exxonmobil Chemical Patents Inc. | Process for production of paraxylene |
| US6207871B1 (en) | 1997-12-19 | 2001-03-27 | Mobil Oil Corporation | High-purity meta-xylene production process |
| US6180550B1 (en) | 1998-12-22 | 2001-01-30 | Mobile Oil Corporation | Small crystal ZSM-5, its synthesis and use |
| FR2792632B1 (fr) | 1999-04-22 | 2004-02-13 | Inst Francais Du Petrole | Procede de production de paraxylene comprenant une etape d'adsorption, une etape d'isomerisation en phase liquide et une etape d'isomerisation en phase gazeuse avec une zeolithe de type eu0 |
| DE19951781A1 (de) | 1999-10-27 | 2001-05-03 | Sued Chemie Ag | Verfahren zur Herstellung von synthetischen Zeolithen mit MFI-Struktur |
| FR2844790B1 (fr) | 2002-09-20 | 2004-10-22 | Inst Francais Du Petrole | Procede de coproduction de paraxylene et de styrene |
| US6872866B1 (en) | 2003-12-15 | 2005-03-29 | Uop Llc | Liquid phase process for C8 alkylaromatic isomerization |
| US7368620B2 (en) | 2005-06-30 | 2008-05-06 | Uop Llc | Two-stage aromatics isomerization process |
| US7371913B2 (en) | 2005-06-30 | 2008-05-13 | Uop Llc | Selective aromatics isomerization process |
| CN101466655B (zh) | 2006-04-25 | 2013-01-23 | 埃克森美孚化学专利公司 | 对二甲苯的制备方法 |
| US7932426B2 (en) | 2007-12-12 | 2011-04-26 | Uop Llc | Process for isomerizing a non-equilibrium alkylaromatic feed mixture and an aromatic production facility |
| US8273934B2 (en) | 2008-12-15 | 2012-09-25 | Exxonmobil Chemical Patents Inc. | Process for producing para-xylene |
| US8252967B2 (en) | 2009-04-14 | 2012-08-28 | Exxonmobil Chemical Patents Inc. | Process for the purification of paraxylene |
| US8344197B2 (en) | 2009-10-21 | 2013-01-01 | Exxonmobil Chemical Patents Inc. | Production of para-xylene by the methylation of benzene and/or toluene |
| US8399727B2 (en) | 2009-10-21 | 2013-03-19 | Exxonmobil Chemical Patents Inc. | Production of para-xylene by the methylation of benzene and/or toluene |
| KR101020998B1 (ko) | 2009-11-12 | 2011-03-09 | 엘지이노텍 주식회사 | 발광소자 및 그 제조방법 |
| SG2014014088A (en) | 2010-04-21 | 2014-04-28 | Exxonmobil Chem Patents Inc | Xylene isomerization process and catalyst therefor |
| SG10201508779UA (en) * | 2010-10-29 | 2015-11-27 | Exxonmobil Chem Patents Inc | Process for the production of paraxylene |
| US20120108868A1 (en) | 2010-10-29 | 2012-05-03 | Dana Lynn Pilliod | Process for the Production of Paraxylene |
| US9295962B2 (en) | 2011-06-10 | 2016-03-29 | Exxonmobil Chemical Patents Inc. | Production of para-xylene |
| US20130217940A1 (en) | 2011-07-11 | 2013-08-22 | Xiaobo Zheng | Alkylation of Benzene and/or Toluene with Methanol |
| TWI495511B (zh) | 2011-07-27 | 2015-08-11 | Exxonmobil Chem Patents Inc | 具有分階擋板的流體床反應器 |
| WO2013052260A2 (en) | 2011-10-07 | 2013-04-11 | Exxonmobil Chemical Patents Inc. | Alkylation process |
| US9227888B2 (en) | 2012-04-17 | 2016-01-05 | Exxonmobil Chemical Patents Inc. | Liquid phase isomerization process |
| KR101632529B1 (ko) * | 2012-05-31 | 2016-06-21 | 엑손모빌 케미칼 패턴츠 인코포레이티드 | 파라크실렌 회수 공정에서의 페놀 제거 |
| SG11201407082YA (en) * | 2012-05-31 | 2014-11-27 | Exxonmobil Chem Patents Inc | Styrene removal in paraxylene recovery process |
-
2013
- 2013-08-07 US US13/961,530 patent/US9193645B2/en active Active
- 2013-08-08 CN CN201380034969.4A patent/CN104395266B/zh active Active
- 2013-08-08 KR KR1020147036077A patent/KR101659203B1/ko not_active Expired - Fee Related
- 2013-08-08 SG SG11201408189SA patent/SG11201408189SA/en unknown
- 2013-08-08 WO PCT/US2013/054070 patent/WO2014035626A1/en not_active Ceased
- 2013-08-08 MY MYPI2014703884A patent/MY178398A/en unknown
- 2013-08-08 SG SG10201609679PA patent/SG10201609679PA/en unknown
- 2013-08-08 IN IN10781DEN2014 patent/IN2014DN10781A/en unknown
- 2013-08-08 BR BR122016015199A patent/BR122016015199B1/pt not_active IP Right Cessation
- 2013-08-08 BR BR112014033014A patent/BR112014033014B1/pt not_active IP Right Cessation
- 2013-08-08 JP JP2015520721A patent/JP5933127B2/ja not_active Expired - Fee Related
-
2015
- 2015-10-23 US US14/921,464 patent/US9266794B1/en active Active
Also Published As
| Publication number | Publication date |
|---|---|
| BR112014033014B1 (pt) | 2016-11-29 |
| CN104395266B (zh) | 2016-08-24 |
| BR122016015199A2 (pt) | 2016-10-11 |
| MY178398A (en) | 2020-10-12 |
| SG10201609679PA (en) | 2016-12-29 |
| CN104395266A (zh) | 2015-03-04 |
| BR112014033014A2 (pt) | 2016-07-26 |
| KR101659203B1 (ko) | 2016-09-22 |
| WO2014035626A1 (en) | 2014-03-06 |
| KR20150022882A (ko) | 2015-03-04 |
| SG11201408189SA (en) | 2015-01-29 |
| IN2014DN10781A (cg-RX-API-DMAC7.html) | 2015-09-04 |
| US20140066675A1 (en) | 2014-03-06 |
| JP5933127B2 (ja) | 2016-06-08 |
| JP2015527989A (ja) | 2015-09-24 |
| US9193645B2 (en) | 2015-11-24 |
| US9266794B1 (en) | 2016-02-23 |
| US20160039727A1 (en) | 2016-02-11 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| B03A | Publication of a patent application or of a certificate of addition of invention [chapter 3.1 patent gazette] | ||
| B09A | Decision: intention to grant [chapter 9.1 patent gazette] | ||
| B16A | Patent or certificate of addition of invention granted [chapter 16.1 patent gazette] |
Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 08/08/2013, OBSERVADAS AS CONDICOES LEGAIS. |
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| B21F | Lapse acc. art. 78, item iv - on non-payment of the annual fees in time |
Free format text: REFERNTE A 19A ANUIDADE |
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| B24J | Lapse because of non-payment of annual fees (definitively: art 78 iv lpi, resolution 113/2013 art. 12) |
Free format text: MANUTENCAO DA EXTINCAO - ART. 78 INCISO IV DA LPI |