BR112012028981B1 - Método para inibir a polimerização de monômero aromático de vinila e composição antipolimerização de monômero aromático de vinila - Google Patents
Método para inibir a polimerização de monômero aromático de vinila e composição antipolimerização de monômero aromático de vinila Download PDFInfo
- Publication number
- BR112012028981B1 BR112012028981B1 BR112012028981-0A BR112012028981A BR112012028981B1 BR 112012028981 B1 BR112012028981 B1 BR 112012028981B1 BR 112012028981 A BR112012028981 A BR 112012028981A BR 112012028981 B1 BR112012028981 B1 BR 112012028981B1
- Authority
- BR
- Brazil
- Prior art keywords
- monomer
- alkyl
- polymerization
- vinyl aromatic
- aromatic monomer
- Prior art date
Links
- 239000000178 monomer Substances 0.000 title claims abstract description 43
- 238000006116 polymerization reaction Methods 0.000 title claims abstract description 30
- 229920002554 vinyl polymer Polymers 0.000 title claims abstract description 26
- 238000000034 method Methods 0.000 title claims abstract description 25
- ORGHESHFQPYLAO-UHFFFAOYSA-N vinyl radical Chemical class C=[CH] ORGHESHFQPYLAO-UHFFFAOYSA-N 0.000 title claims abstract 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical group C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims abstract description 39
- 239000000203 mixture Substances 0.000 claims abstract description 24
- -1 phenol compound Chemical class 0.000 claims abstract description 22
- 230000002401 inhibitory effect Effects 0.000 claims abstract description 12
- 150000004059 quinone derivatives Chemical class 0.000 claims abstract description 9
- 125000003118 aryl group Chemical group 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- 239000007788 liquid Substances 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 5
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 claims description 4
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 claims description 4
- DKCPKDPYUFEZCP-UHFFFAOYSA-N 2,6-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=CC(C(C)(C)C)=C1O DKCPKDPYUFEZCP-UHFFFAOYSA-N 0.000 claims description 4
- HCUWXYBKPSKTAB-UHFFFAOYSA-N 4-benzylidene-2,6-ditert-butylcyclohexa-2,5-dien-1-one Chemical compound C1=C(C(C)(C)C)C(=O)C(C(C)(C)C)=CC1=CC1=CC=CC=C1 HCUWXYBKPSKTAB-UHFFFAOYSA-N 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 4
- 239000012535 impurity Substances 0.000 claims description 4
- 239000003495 polar organic solvent Substances 0.000 claims description 4
- 239000002904 solvent Substances 0.000 claims description 4
- 125000003884 phenylalkyl group Chemical group 0.000 claims description 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 2
- JPUUAYFQHNNDBM-UHFFFAOYSA-N bicyclo[4.1.0]hepta-1(6),3-diene-2,5-dione Chemical class O=C1C=CC(=O)C2=C1C2 JPUUAYFQHNNDBM-UHFFFAOYSA-N 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
- 239000008096 xylene Substances 0.000 claims description 2
- 229920000642 polymer Polymers 0.000 abstract description 7
- 238000012545 processing Methods 0.000 abstract description 7
- 238000003860 storage Methods 0.000 abstract description 4
- 239000003112 inhibitor Substances 0.000 description 6
- RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical compound SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 description 6
- 239000004793 Polystyrene Substances 0.000 description 5
- 229920002223 polystyrene Polymers 0.000 description 5
- 125000000923 (C1-C30) alkyl group Chemical group 0.000 description 4
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 150000002989 phenols Chemical class 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- NXXYKOUNUYWIHA-UHFFFAOYSA-N 2,6-Dimethylphenol Chemical compound CC1=CC=CC(C)=C1O NXXYKOUNUYWIHA-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 238000005054 agglomeration Methods 0.000 description 2
- 230000002776 aggregation Effects 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 239000000806 elastomer Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- 238000012719 thermal polymerization Methods 0.000 description 2
- METWAQRCMRWDAW-UHFFFAOYSA-N 2,6-diethylphenol Chemical compound CCC1=CC=CC(CC)=C1O METWAQRCMRWDAW-UHFFFAOYSA-N 0.000 description 1
- NAILKKRDWBJCNH-UHFFFAOYSA-N 2,6-dipropylphenol Chemical compound CCCC1=CC=CC(CCC)=C1O NAILKKRDWBJCNH-UHFFFAOYSA-N 0.000 description 1
- AKNMPWVTPUHKCG-UHFFFAOYSA-N 2-cyclohexyl-6-[(3-cyclohexyl-2-hydroxy-5-methylphenyl)methyl]-4-methylphenol Chemical compound OC=1C(C2CCCCC2)=CC(C)=CC=1CC(C=1O)=CC(C)=CC=1C1CCCCC1 AKNMPWVTPUHKCG-UHFFFAOYSA-N 0.000 description 1
- FKDNZARQQHSYAM-UHFFFAOYSA-N 2-tert-butyl-4-(3-tert-butyl-4-hydroxy-5-methylphenyl)sulfanyl-6-methylphenol 2,6-ditert-butyl-4-methylphenol Chemical compound S(C1=CC(=C(C(=C1)C(C)(C)C)O)C)C1=CC(=C(C(=C1)C(C)(C)C)O)C.C(C)(C)(C)C1=C(C(=CC(=C1)C)C(C)(C)C)O FKDNZARQQHSYAM-UHFFFAOYSA-N 0.000 description 1
- MQVDCVRWVSDQNN-UHFFFAOYSA-N 4-methyl-2-(1-methylcyclohexyl)phenol Chemical compound CC1=CC=C(O)C(C2(C)CCCCC2)=C1 MQVDCVRWVSDQNN-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 241001136616 Methone Species 0.000 description 1
- LOUPRKONTZGTKE-LHHVKLHASA-N Quinidine Natural products C([C@H]([C@H](C1)C=C)C2)C[N@@]1[C@H]2[C@@H](O)C1=CC=NC2=CC=C(OC)C=C21 LOUPRKONTZGTKE-LHHVKLHASA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- YMOONIIMQBGTDU-VOTSOKGWSA-N [(e)-2-bromoethenyl]benzene Chemical compound Br\C=C\C1=CC=CC=C1 YMOONIIMQBGTDU-VOTSOKGWSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000003282 alkyl amino group Chemical group 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- FQUNFJULCYSSOP-UHFFFAOYSA-N bisoctrizole Chemical compound N1=C2C=CC=CC2=NN1C1=CC(C(C)(C)CC(C)(C)C)=CC(CC=2C(=C(C=C(C=2)C(C)(C)CC(C)(C)C)N2N=C3C=CC=CC3=N2)O)=C1O FQUNFJULCYSSOP-UHFFFAOYSA-N 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- LOUPRKONTZGTKE-UHFFFAOYSA-N cinchonine Natural products C1C(C(C2)C=C)CCN2C1C(O)C1=CC=NC2=CC=C(OC)C=C21 LOUPRKONTZGTKE-UHFFFAOYSA-N 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- 239000012969 di-tertiary-butyl peroxide Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- SSDSCDGVMJFTEQ-UHFFFAOYSA-N octadecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SSDSCDGVMJFTEQ-UHFFFAOYSA-N 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000011403 purification operation Methods 0.000 description 1
- 229960001404 quinidine Drugs 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C7/00—Purification; Separation; Use of additives
- C07C7/20—Use of additives, e.g. for stabilisation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F12/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
- C08F12/02—Monomers containing only one unsaturated aliphatic radical
- C08F12/04—Monomers containing only one unsaturated aliphatic radical containing one ring
- C08F12/06—Hydrocarbons
- C08F12/08—Styrene
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Analytical Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Water Supply & Treatment (AREA)
- Polymerisation Methods In General (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12/793,226 | 2010-06-03 | ||
| US12/793,226 US8298440B2 (en) | 2010-06-03 | 2010-06-03 | Methods and compositions for inhibiting vinyl aromatic monomer polymerization |
| PCT/US2011/035934 WO2011152961A2 (en) | 2010-06-03 | 2011-05-10 | Methods and compositions for inhibiting vinyl aromatic monomer polymerization |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| BR112012028981A2 BR112012028981A2 (pt) | 2016-07-26 |
| BR112012028981B1 true BR112012028981B1 (pt) | 2020-10-20 |
Family
ID=44626629
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BR112012028981-0A BR112012028981B1 (pt) | 2010-06-03 | 2011-05-10 | Método para inibir a polimerização de monômero aromático de vinila e composição antipolimerização de monômero aromático de vinila |
Country Status (14)
| Country | Link |
|---|---|
| US (2) | US8298440B2 (https=) |
| EP (1) | EP2576718B1 (https=) |
| JP (1) | JP5683692B2 (https=) |
| KR (1) | KR101877069B1 (https=) |
| AR (1) | AR081555A1 (https=) |
| BR (1) | BR112012028981B1 (https=) |
| CA (1) | CA2800495C (https=) |
| ES (1) | ES2621605T3 (https=) |
| MX (1) | MX2012014075A (https=) |
| MY (1) | MY158328A (https=) |
| PL (1) | PL2576718T3 (https=) |
| SG (1) | SG185758A1 (https=) |
| TW (1) | TWI501947B (https=) |
| WO (1) | WO2011152961A2 (https=) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8901362B2 (en) * | 2012-02-02 | 2014-12-02 | General Electric Company | Methods and compositions for styrene inhibition via in situ generation of quinone methides |
| US9234057B2 (en) | 2012-08-24 | 2016-01-12 | Dorf Ketal Chemicals (India) Private Limited | Composition of quinone methide derivatives and amines for control and inhibition of polymerization of monomers, and method of preparation and use thereof |
| EP2958949A1 (en) * | 2013-02-19 | 2015-12-30 | General Electric Company | Use of aliphatic nitroso compounds as inhibitors of radical polymerization of activated vinyl monomers |
| CN108884004B (zh) * | 2016-02-13 | 2020-02-25 | 多尔夫凯塔尔化学制品（I）私人有限公司 | 用于控制和抑制乙烯基芳族单体聚合的组合物，及其使用方法 |
| CN109651040A (zh) * | 2017-10-12 | 2019-04-19 | 中国石油化工股份有限公司 | 高级炔烃复配阻聚剂 |
| CN110878209A (zh) * | 2018-09-05 | 2020-03-13 | 中国石油化工股份有限公司 | 用于苯乙烯精馏系统的环保阻聚剂及其应用 |
| CN116553996A (zh) * | 2023-07-07 | 2023-08-08 | 吉林金海化工新材料有限公司 | 一种阻聚剂及其应用 |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3741906A (en) * | 1971-12-17 | 1973-06-26 | Exxon Research Engineering Co | Hindered phenoxy radicals |
| US4040911A (en) * | 1976-01-02 | 1977-08-09 | Gulf Research & Development Company | Process for inhibiting the polymerization of styrene |
| US4032547A (en) | 1976-02-23 | 1977-06-28 | Gulf Research & Development Company | Quinone alkide synthesis system |
| US4929778A (en) | 1989-06-05 | 1990-05-29 | Betz Laboratories, Inc. | Methods and compositions for inhibiting styrene polymerization |
| US5470440A (en) | 1994-04-19 | 1995-11-28 | Betz Laboratories, Inc. | Method for inhibiting vinyl aromatic monomer polymerization |
| US5616774A (en) * | 1995-04-14 | 1997-04-01 | Ciba-Geigy Corporation | Inhibition of unsaturated monomers with 7-aryl quinone methides |
| EP0744392A1 (en) * | 1995-05-26 | 1996-11-27 | Ciba-Geigy Ag | A new one-pot process for the preparation of 7-aryl-2,6-disubstituted quinone methides |
| JPH09227608A (ja) * | 1996-02-22 | 1997-09-02 | Asahi Chem Ind Co Ltd | スチレンーアクリロニトリル系樹脂の製造方法 |
| CN1232472A (zh) * | 1996-09-04 | 1999-10-20 | 陶氏化学公司 | 在聚烯烃中加入自由基抑制剂 |
| US6024894A (en) | 1998-03-25 | 2000-02-15 | Betzdearborn Inc. | Compositions and methods for inhibiting vinyl aromatic monomer polymerization |
| US7045647B2 (en) * | 2000-10-16 | 2006-05-16 | Uniroyal Chemical Company, Inc. | Blends of quinone alkide and nitroxyl compounds and polymerization inhibitors |
| US20030065177A1 (en) * | 2001-08-08 | 2003-04-03 | Crompton Corporation, A Corporation Of The State Of Delaware | High boiling inhibitors for distillable, polymerizable monomers |
| US6960279B2 (en) * | 2002-05-06 | 2005-11-01 | Fina Technology, Inc. | Method for stabilizing vinyl aromatic monomers using selected polymerization inhibitors and polymers prepared therewith |
| US6926820B2 (en) | 2002-09-20 | 2005-08-09 | G.E. Betz, Inc. | Inhibition of viscosity increase and fouling in hydrocarbon streams including unsaturation |
| WO2004083156A1 (ja) * | 2003-03-17 | 2004-09-30 | Hakuto Co., Ltd. | 芳香族ビニル化合物の重合抑制剤および重合抑制方法 |
| JP2004352735A (ja) * | 2003-05-27 | 2004-12-16 | Techno Network Shikoku Co Ltd | ラジカル重合体の製造方法 |
| US7128826B2 (en) | 2003-07-31 | 2006-10-31 | General Electric Company | Polymerization inhibitor for styrene dehydrogenation units |
| DE102007052891A1 (de) * | 2007-11-02 | 2009-05-07 | Evonik Degussa Gmbh | Verfahren zur Stabilisierung von olefinisch ungesättigten Monomeren |
| JP5139103B2 (ja) * | 2008-02-05 | 2013-02-06 | 京セラドキュメントソリューションズ株式会社 | 電子写真感光体及び画像形成装置 |
| JP5266991B2 (ja) * | 2008-09-11 | 2013-08-21 | コニカミノルタビジネステクノロジーズ株式会社 | 電子写真感光体とそれを用いた画像形成装置 |
-
2010
- 2010-06-03 US US12/793,226 patent/US8298440B2/en active Active
-
2011
- 2011-05-10 MY MYPI2012004898A patent/MY158328A/en unknown
- 2011-05-10 EP EP11721893.3A patent/EP2576718B1/en active Active
- 2011-05-10 SG SG2012086864A patent/SG185758A1/en unknown
- 2011-05-10 CA CA2800495A patent/CA2800495C/en active Active
- 2011-05-10 MX MX2012014075A patent/MX2012014075A/es not_active Application Discontinuation
- 2011-05-10 WO PCT/US2011/035934 patent/WO2011152961A2/en not_active Ceased
- 2011-05-10 JP JP2013513183A patent/JP5683692B2/ja active Active
- 2011-05-10 KR KR1020127031218A patent/KR101877069B1/ko active Active
- 2011-05-10 PL PL11721893T patent/PL2576718T3/pl unknown
- 2011-05-10 ES ES11721893.3T patent/ES2621605T3/es active Active
- 2011-05-10 BR BR112012028981-0A patent/BR112012028981B1/pt active IP Right Grant
- 2011-05-30 TW TW100118905A patent/TWI501947B/zh active
- 2011-06-01 AR ARP110101886A patent/AR081555A1/es active IP Right Grant
-
2012
- 2012-09-27 US US13/628,536 patent/US20130030225A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| KR101877069B1 (ko) | 2018-07-10 |
| BR112012028981A2 (pt) | 2016-07-26 |
| WO2011152961A3 (en) | 2013-08-22 |
| EP2576718A2 (en) | 2013-04-10 |
| ES2621605T3 (es) | 2017-07-04 |
| WO2011152961A2 (en) | 2011-12-08 |
| US20110297878A1 (en) | 2011-12-08 |
| EP2576718B1 (en) | 2017-01-11 |
| KR20130122517A (ko) | 2013-11-07 |
| MX2012014075A (es) | 2013-01-25 |
| PL2576718T3 (pl) | 2017-11-30 |
| JP5683692B2 (ja) | 2015-03-11 |
| US8298440B2 (en) | 2012-10-30 |
| AR081555A1 (es) | 2012-10-03 |
| SG185758A1 (en) | 2012-12-28 |
| US20130030225A1 (en) | 2013-01-31 |
| MY158328A (en) | 2016-09-30 |
| TW201202192A (en) | 2012-01-16 |
| TWI501947B (zh) | 2015-10-01 |
| JP2013539473A (ja) | 2013-10-24 |
| CA2800495A1 (en) | 2011-12-08 |
| CA2800495C (en) | 2019-07-09 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| B06F | Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette] | ||
| B25A | Requested transfer of rights approved |
Owner name: BL TECHNOLOGIES, INC. (US) |
|
| B06T | Formal requirements before examination [chapter 6.20 patent gazette] | ||
| B06A | Patent application procedure suspended [chapter 6.1 patent gazette] | ||
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