KR980009220A - 분산매체 치환장치를 사용한 고순도 테레프탈산의 제조방법 - Google Patents
분산매체 치환장치를 사용한 고순도 테레프탈산의 제조방법 Download PDFInfo
- Publication number
- KR980009220A KR980009220A KR1019970035012A KR19970035012A KR980009220A KR 980009220 A KR980009220 A KR 980009220A KR 1019970035012 A KR1019970035012 A KR 1019970035012A KR 19970035012 A KR19970035012 A KR 19970035012A KR 980009220 A KR980009220 A KR 980009220A
- Authority
- KR
- South Korea
- Prior art keywords
- dispersion medium
- slurry
- terephthalic acid
- replacement
- temperature
- Prior art date
Links
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 title claims abstract description 138
- 239000002612 dispersion medium Substances 0.000 title claims abstract description 126
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 14
- 239000002002 slurry Substances 0.000 claims abstract description 104
- 239000013078 crystal Substances 0.000 claims abstract description 40
- 238000000034 method Methods 0.000 claims abstract description 23
- 238000009826 distribution Methods 0.000 claims abstract description 14
- 238000003756 stirring Methods 0.000 claims abstract description 13
- 239000006185 dispersion Substances 0.000 claims abstract description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 23
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- 238000006467 substitution reaction Methods 0.000 abstract description 22
- 239000002609 medium Substances 0.000 abstract description 11
- 238000007254 oxidation reaction Methods 0.000 description 13
- 239000002904 solvent Substances 0.000 description 12
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 10
- 230000003647 oxidation Effects 0.000 description 9
- 238000000926 separation method Methods 0.000 description 9
- 239000007788 liquid Substances 0.000 description 7
- 239000007791 liquid phase Substances 0.000 description 7
- URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical group CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 description 6
- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 6
- LPNBBFKOUUSUDB-UHFFFAOYSA-N p-toluic acid Chemical compound CC1=CC=C(C(O)=O)C=C1 LPNBBFKOUUSUDB-UHFFFAOYSA-N 0.000 description 6
- 238000000746 purification Methods 0.000 description 6
- 239000005711 Benzoic acid Substances 0.000 description 5
- 235000010233 benzoic acid Nutrition 0.000 description 5
- 238000002425 crystallisation Methods 0.000 description 5
- 230000008025 crystallization Effects 0.000 description 5
- 239000012535 impurity Substances 0.000 description 5
- GOUHYARYYWKXHS-UHFFFAOYSA-N 4-formylbenzoic acid Chemical compound OC(=O)C1=CC=C(C=O)C=C1 GOUHYARYYWKXHS-UHFFFAOYSA-N 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 230000005484 gravity Effects 0.000 description 4
- 238000001953 recrystallisation Methods 0.000 description 4
- 230000000630 rising effect Effects 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 3
- 238000000605 extraction Methods 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000006073 displacement reaction Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000001747 exhibiting effect Effects 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 238000005070 sampling Methods 0.000 description 2
- 238000004062 sedimentation Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 description 1
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical class [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 1
- 230000001174 ascending effect Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 230000005465 channeling Effects 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- 229940011182 cobalt acetate Drugs 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- QAHREYKOYSIQPH-UHFFFAOYSA-L cobalt(II) acetate Chemical compound [Co+2].CC([O-])=O.CC([O-])=O QAHREYKOYSIQPH-UHFFFAOYSA-L 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000006606 decarbonylation reaction Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 239000013505 freshwater Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 229940071125 manganese acetate Drugs 0.000 description 1
- UOGMEBQRZBEZQT-UHFFFAOYSA-L manganese(2+);diacetate Chemical compound [Mn+2].CC([O-])=O.CC([O-])=O UOGMEBQRZBEZQT-UHFFFAOYSA-L 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000012264 purified product Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C63/00—Compounds having carboxyl groups bound to a carbon atoms of six-membered aromatic rings
- C07C63/14—Monocyclic dicarboxylic acids
- C07C63/15—Monocyclic dicarboxylic acids all carboxyl groups bound to carbon atoms of the six-membered aromatic ring
- C07C63/26—1,4 - Benzenedicarboxylic acid
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/42—Separation; Purification; Stabilisation; Use of additives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/42—Separation; Purification; Stabilisation; Use of additives
- C07C51/43—Separation; Purification; Stabilisation; Use of additives by change of the physical state, e.g. crystallisation
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Crystallography & Structural Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)
Abstract
Description
Claims (4)
- 제1의 분산매체와 테레프탈산결정으로된 본래의 슬러리를 상부로부터 제2분산매체를 하부로부터 도입하고 하부로부터 주로 테레프탈산결정과 제2분산매체로된 치환슬러리를 빼내고 정상부로부터 주로 제1분산매체를 빼내고 하부에 균일 분산을 위한 교반장치를 갖는 분산매체 치환장치를 사용한 고순도 테레프탈산의 제조방법으로서, 하부의 균일분산된 슬러리농도를 장치중간부의 슬러리농도보다도 고농도로하고 장치내의 세로방향의 온도분포를 상부가 고온이 되도록해서 그 온도변화영역의 위치에 의해 제2분산매체의 도입량 및 치환슬러리의 빼내는 양을 한가지 이상 제어하는 것을 특징으로 하는 고순도 테레프탈산의 제조방법.
- 제1항에 있어서, 정치내에 미약한 상승류를 생기게 하는 것을 특징으로 하는 고순도 테레프탈산의 제조방법.
- 제1항에 있어서, 제2분산매체의 온도를 공급슬러리의 온도보다 낮게 하는 것을 특징으로 하는 고순도 테레프탈산의 제조방법.
- 제1항에 있어서, 제1분산매체가 물 또는 아세트산이며 제2분산매체가 물인 것을 특징으로 하는 고순도 테레프탈산의 제조방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP199142 | 1996-07-29 | ||
JP8199142A JPH1045667A (ja) | 1996-07-29 | 1996-07-29 | 分散媒置換装置を用いた高純度テレフタル酸の製造方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR980009220A true KR980009220A (ko) | 1998-04-30 |
KR100518258B1 KR100518258B1 (ko) | 2005-12-26 |
Family
ID=16402854
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019970035012A KR100518258B1 (ko) | 1996-07-29 | 1997-07-25 | 분산매체치환장치를사용한고순도테레프탈산의제조방법 |
Country Status (7)
Country | Link |
---|---|
US (1) | US5777161A (ko) |
EP (1) | EP0822176B1 (ko) |
JP (1) | JPH1045667A (ko) |
KR (1) | KR100518258B1 (ko) |
ES (1) | ES2167651T3 (ko) |
ID (1) | ID17599A (ko) |
TW (1) | TW363962B (ko) |
Families Citing this family (52)
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---|---|---|---|---|
US7276625B2 (en) * | 2002-10-15 | 2007-10-02 | Eastman Chemical Company | Process for production of a carboxylic acid/diol mixture suitable for use in polyester production |
US7074954B2 (en) * | 2002-12-09 | 2006-07-11 | Eastman Chemical Company | Process for the oxidative purification of terephthalic acid |
US7161027B2 (en) | 2002-12-09 | 2007-01-09 | Eastman Chemical Company | Process for the oxidative purification of terephthalic acid |
US7132566B2 (en) * | 2003-09-22 | 2006-11-07 | Eastman Chemical Company | Process for the purification of a crude carboxylic acid slurry |
EP1569888A1 (en) * | 2002-12-09 | 2005-09-07 | Eastman Chemical Company | Process for the oxidative purification of terephthalic acid |
US7193109B2 (en) * | 2003-03-06 | 2007-03-20 | Eastman Chemical Company | Process for production of a carboxylic acid/diol mixture suitable for use in polyester production |
US7547803B2 (en) * | 2003-06-20 | 2009-06-16 | Mitsubishi Gas Chemical Company, Inc. | Process for producing a high purity aromatic polycarboxylic acid |
KR101107927B1 (ko) * | 2003-10-02 | 2012-01-25 | 미츠비시 가스 가가쿠 가부시키가이샤 | 고순도 테레프탈산의 제조 방법 |
CN1842378B (zh) * | 2003-10-03 | 2012-06-06 | 三菱瓦斯化学株式会社 | 固体颗粒的清洗方法 |
US7214760B2 (en) * | 2004-01-15 | 2007-05-08 | Eastman Chemical Company | Process for production of a carboxylic acid/diol mixture suitable for use in polyester production |
US7546747B2 (en) * | 2004-01-15 | 2009-06-16 | Eastman Chemical Company | Process for production of a dried carboxylic acid cake suitable for use in polyester production |
US7692036B2 (en) * | 2004-11-29 | 2010-04-06 | Eastman Chemical Company | Optimized liquid-phase oxidation |
US7589231B2 (en) * | 2004-09-02 | 2009-09-15 | Eastman Chemical Company | Optimized liquid-phase oxidation |
US7504535B2 (en) * | 2004-09-02 | 2009-03-17 | Eastman Chemical Company | Optimized liquid-phase oxidation |
US20060047153A1 (en) * | 2004-09-02 | 2006-03-02 | Wonders Alan G | Optimized liquid-phase oxidation |
US7741515B2 (en) | 2004-09-02 | 2010-06-22 | Eastman Chemical Company | Optimized liquid-phase oxidation |
US7507857B2 (en) * | 2004-09-02 | 2009-03-24 | Eastman Chemical Company | Optimized liquid-phase oxidation |
US7608732B2 (en) * | 2005-03-08 | 2009-10-27 | Eastman Chemical Company | Optimized liquid-phase oxidation |
US7390921B2 (en) * | 2004-09-02 | 2008-06-24 | Eastman Chemical Company | Optimized liquid-phase oxidation |
US7572936B2 (en) * | 2004-09-02 | 2009-08-11 | Eastman Chemical Company | Optimized liquid-phase oxidation |
US7572932B2 (en) * | 2004-09-02 | 2009-08-11 | Eastman Chemical Company | Optimized liquid-phase oxidation |
US7381836B2 (en) | 2004-09-02 | 2008-06-03 | Eastman Chemical Company | Optimized liquid-phase oxidation |
US7361784B2 (en) * | 2004-09-02 | 2008-04-22 | Eastman Chemical Company | Optimized liquid-phase oxidation |
US7399882B2 (en) * | 2004-09-02 | 2008-07-15 | Eastman Chemical Company | Optimized liquid-phase oxidation |
US7615663B2 (en) * | 2004-09-02 | 2009-11-10 | Eastman Chemical Company | Optimized production of aromatic dicarboxylic acids |
US7910769B2 (en) * | 2004-09-02 | 2011-03-22 | Eastman Chemical Company | Optimized liquid-phase oxidation |
US7608733B2 (en) * | 2004-09-02 | 2009-10-27 | Eastman Chemical Company | Optimized liquid-phase oxidation |
US7495125B2 (en) * | 2004-09-02 | 2009-02-24 | Eastman Chemical Company | Optimized liquid-phase oxidation |
US7683210B2 (en) | 2004-09-02 | 2010-03-23 | Eastman Chemical Company | Optimized liquid-phase oxidation |
US7692037B2 (en) | 2004-09-02 | 2010-04-06 | Eastman Chemical Company | Optimized liquid-phase oxidation |
US7582793B2 (en) | 2004-09-02 | 2009-09-01 | Eastman Chemical Company | Optimized liquid-phase oxidation |
US7586000B2 (en) * | 2004-09-02 | 2009-09-08 | Eastman Chemical Company | Optimized liquid-phase oxidation |
US7371894B2 (en) * | 2004-09-02 | 2008-05-13 | Eastman Chemical Company | Optimized liquid-phase oxidation |
US7482482B2 (en) * | 2004-09-02 | 2009-01-27 | Eastman Chemical Company | Optimized liquid-phase oxidation |
US7568361B2 (en) | 2004-09-02 | 2009-08-04 | Eastman Chemical Company | Optimized liquid-phase oxidation |
US7884232B2 (en) * | 2005-06-16 | 2011-02-08 | Eastman Chemical Company | Optimized liquid-phase oxidation |
US7355068B2 (en) * | 2006-01-04 | 2008-04-08 | Eastman Chemical Company | Oxidation system with internal secondary reactor |
US7358389B2 (en) * | 2006-01-04 | 2008-04-15 | Eastman Chemical Company | Oxidation system employing internal structure for enhanced hydrodynamics |
US20070179312A1 (en) * | 2006-02-02 | 2007-08-02 | O'meadhra Ruairi Seosamh | Process for the purification of a crude carboxylic axid slurry |
US20070208199A1 (en) * | 2006-03-01 | 2007-09-06 | Kenny Randolph Parker | Methods and apparatus for isolating carboxylic acid |
US7863483B2 (en) * | 2006-03-01 | 2011-01-04 | Eastman Chemical Company | Carboxylic acid production process |
US7847121B2 (en) * | 2006-03-01 | 2010-12-07 | Eastman Chemical Company | Carboxylic acid production process |
JP5210858B2 (ja) | 2006-03-17 | 2013-06-12 | 株式会社きもと | ポリエステル系フィルム用バインダー組成物及びこれを用いた光学フィルム |
JP5291459B2 (ja) * | 2006-06-12 | 2013-09-18 | 三菱瓦斯化学株式会社 | 分散媒置換方法 |
US9144750B2 (en) | 2006-06-12 | 2015-09-29 | Mitsubishi Gas Chemical Company, Ltd. | Method of replacing dispersion medium and apparatus therefor |
KR101419071B1 (ko) * | 2006-07-24 | 2014-07-11 | 미츠비시 가스 가가쿠 가부시키가이샤 | 분산매 치환 방법 |
JP5173474B2 (ja) * | 2007-02-28 | 2013-04-03 | 三菱瓦斯化学株式会社 | テレフタル酸の製造方法 |
JP5162960B2 (ja) * | 2007-05-22 | 2013-03-13 | 三菱瓦斯化学株式会社 | イソフタル酸原スラリーの分散媒置換方法 |
US8455680B2 (en) | 2008-01-15 | 2013-06-04 | Eastman Chemical Company | Carboxylic acid production process employing solvent from esterification of lignocellulosic material |
US8614350B2 (en) | 2008-01-15 | 2013-12-24 | Eastman Chemical Company | Carboxylic acid production process employing solvent from esterification of lignocellulosic material |
JP6848866B2 (ja) * | 2015-07-22 | 2021-03-24 | 三菱瓦斯化学株式会社 | 高純度テレフタル酸の製造方法 |
EP3438086B1 (en) | 2016-03-31 | 2020-10-21 | Mitsubishi Gas Chemical Company, Inc. | Method of producing terephthalic acid |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4201871A (en) * | 1978-02-23 | 1980-05-06 | Asahi Kasei Kogyo Kabushiki Kaisha | Process for recovering terephthalic acid |
JPS5587744A (en) * | 1978-12-26 | 1980-07-02 | Asahi Chem Ind Co Ltd | Recovery of terephthalic acid |
JP3939367B2 (ja) * | 1993-11-30 | 2007-07-04 | 三菱瓦斯化学株式会社 | 高純度テレフタル酸を製造する方法 |
US5712412A (en) * | 1994-12-26 | 1998-01-27 | Mitsubishi Gas Chemical Co., Inc. | Process for producing highly pure terephthalic acid |
JP3979505B2 (ja) * | 1995-05-17 | 2007-09-19 | 三菱瓦斯化学株式会社 | 高純度テレフタル酸の製造方法 |
JPH08325197A (ja) * | 1995-05-30 | 1996-12-10 | Mitsubishi Gas Chem Co Inc | テレフタル酸の製造方法 |
JP3729284B2 (ja) * | 1995-09-22 | 2005-12-21 | 三菱瓦斯化学株式会社 | 高純度テレフタル酸の製造方法 |
-
1996
- 1996-07-29 JP JP8199142A patent/JPH1045667A/ja active Pending
-
1997
- 1997-07-07 US US08/888,419 patent/US5777161A/en not_active Expired - Lifetime
- 1997-07-16 EP EP97112164A patent/EP0822176B1/en not_active Expired - Lifetime
- 1997-07-16 ES ES97112164T patent/ES2167651T3/es not_active Expired - Lifetime
- 1997-07-16 TW TW086110065A patent/TW363962B/zh not_active IP Right Cessation
- 1997-07-25 KR KR1019970035012A patent/KR100518258B1/ko not_active IP Right Cessation
- 1997-07-29 ID IDP972626A patent/ID17599A/id unknown
Also Published As
Publication number | Publication date |
---|---|
KR100518258B1 (ko) | 2005-12-26 |
TW363962B (en) | 1999-07-11 |
EP0822176A2 (en) | 1998-02-04 |
ID17599A (id) | 1998-01-15 |
ES2167651T3 (es) | 2002-05-16 |
EP0822176A3 (en) | 1998-11-04 |
EP0822176B1 (en) | 2001-11-14 |
US5777161A (en) | 1998-07-07 |
JPH1045667A (ja) | 1998-02-17 |
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Patent event code: PA02012R01D Patent event date: 20020521 Comment text: Request for Examination of Application Patent event code: PA02011R01I Patent event date: 19970725 Comment text: Patent Application |
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