SK287690B6 - Spôsob prípravy alkylesterov mastných kyselín - Google Patents

Spôsob prípravy alkylesterov mastných kyselín Download PDF

Info

Publication number: SK287690B6
Authority: SK; Slovakia
Prior art keywords: phase; fatty acid; fatty acids; mixture; transesterification
Prior art date: 2000-10-05

Application number

SK774-2002A

Other languages

English (en)

Slovak (sk)

Other versions

SK7742002A3 (en

Inventor

Michael Koncar

Martin Mittelbach

Helmut G�Ssler

Wilhelm Hammer

Original Assignee

Michael Koncar

Martin Mittelbach

Bdi-Bio Diesel International Ag

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2000-10-05

Filing date

2001-10-05

Publication date

2011-06-06

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=3688690&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SK287690(B6) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

2001-10-05 Application filed by Michael Koncar, Martin Mittelbach, Bdi-Bio Diesel International Ag filed Critical Michael Koncar

2003-09-11 Publication of SK7742002A3 publication Critical patent/SK7742002A3/sk

2011-06-06 Publication of SK287690B6 publication Critical patent/SK287690B6/sk

Links

235000014113 dietary fatty acids Nutrition 0.000 title claims abstract description 77
229930195729 fatty acid Natural products 0.000 title claims abstract description 77
239000000194 fatty acid Substances 0.000 title claims abstract description 77
238000004519 manufacturing process Methods 0.000 title abstract description 3
150000004665 fatty acids Chemical class 0.000 claims abstract description 63
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims abstract description 47
239000000203 mixture Substances 0.000 claims abstract description 29
238000005809 transesterification reaction Methods 0.000 claims abstract description 29
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 25
238000000034 method Methods 0.000 claims abstract description 21
150000003626 triacylglycerols Chemical class 0.000 claims abstract description 18
230000032050 esterification Effects 0.000 claims abstract description 15
238000005886 esterification reaction Methods 0.000 claims abstract description 15
150000002148 esters Chemical class 0.000 claims abstract description 11
239000011541 reaction mixture Substances 0.000 claims abstract description 5
239000012071 phase Substances 0.000 claims description 54
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 24
235000011187 glycerol Nutrition 0.000 claims description 18
125000005907 alkyl ester group Chemical group 0.000 claims description 8
239000002253 acid Substances 0.000 claims description 6
150000007513 acids Chemical class 0.000 claims description 4
238000007171 acid catalysis Methods 0.000 claims description 3
239000008346 aqueous phase Substances 0.000 claims description 3
238000006555 catalytic reaction Methods 0.000 claims description 3
238000002360 preparation method Methods 0.000 claims description 3
230000003197 catalytic effect Effects 0.000 abstract description 2
235000021588 free fatty acids Nutrition 0.000 description 14
239000003921 oil Substances 0.000 description 14
235000019198 oils Nutrition 0.000 description 14
239000003925 fat Substances 0.000 description 11
-1 Fatty acid esters Chemical class 0.000 description 7
238000006243 chemical reaction Methods 0.000 description 7
239000003054 catalyst Substances 0.000 description 5
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
230000015572 biosynthetic process Effects 0.000 description 4
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical class [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
150000004702 methyl esters Chemical class 0.000 description 3
235000011118 potassium hydroxide Nutrition 0.000 description 3
UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 3
WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
238000006136 alcoholysis reaction Methods 0.000 description 2
WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 2
OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
239000008157 edible vegetable oil Substances 0.000 description 2
125000004494 ethyl ester group Chemical group 0.000 description 2
238000000605 extraction Methods 0.000 description 2
235000019387 fatty acid methyl ester Nutrition 0.000 description 2
239000000706 filtrate Substances 0.000 description 2
238000005191 phase separation Methods 0.000 description 2
239000002994 raw material Substances 0.000 description 2
239000002904 solvent Substances 0.000 description 2
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
235000015112 vegetable and seed oil Nutrition 0.000 description 2
239000008158 vegetable oil Substances 0.000 description 2
229910015900 BF3 Inorganic materials 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
102000004190 Enzymes Human genes 0.000 description 1
108090000790 Enzymes Proteins 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
239000004367 Lipase Substances 0.000 description 1
102000004882 Lipase Human genes 0.000 description 1
108090001060 Lipase Proteins 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
239000003377 acid catalyst Substances 0.000 description 1
229910001854 alkali hydroxide Inorganic materials 0.000 description 1
150000008044 alkali metal hydroxides Chemical class 0.000 description 1
150000001450 anions Chemical class 0.000 description 1
OGBUMNBNEWYMNJ-UHFFFAOYSA-N batilol Chemical class CCCCCCCCCCCCCCCCCCOCC(O)CO OGBUMNBNEWYMNJ-UHFFFAOYSA-N 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000008162 cooking oil Substances 0.000 description 1
239000002283 diesel fuel Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000002815 homogeneous catalyst Substances 0.000 description 1
239000008240 homogeneous mixture Substances 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
239000000543 intermediate Substances 0.000 description 1
239000013067 intermediate product Substances 0.000 description 1
235000019421 lipase Nutrition 0.000 description 1
239000011707 mineral Substances 0.000 description 1
235000010755 mineral Nutrition 0.000 description 1
238000002156 mixing Methods 0.000 description 1
230000020477 pH reduction Effects 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
238000000746 purification Methods 0.000 description 1
238000010992 reflux Methods 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
239000013049 sediment Substances 0.000 description 1
238000000926 separation method Methods 0.000 description 1
238000004904 shortening Methods 0.000 description 1
239000000344 soap Substances 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
235000011121 sodium hydroxide Nutrition 0.000 description 1
239000007790 solid phase Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
230000009466 transformation Effects 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
239000002699 waste material Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11C—FATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
- C11C3/00—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom
- C11C3/04—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom by esterification of fats or fatty oils
- C11C3/10—Ester interchange
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/03—Preparation of carboxylic acid esters by reacting an ester group with a hydroxy group

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
General Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Chemical Kinetics & Catalysis (AREA)
Oil, Petroleum & Natural Gas (AREA)
Wood Science & Technology (AREA)
Fats And Perfumes (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Storage Device Security (AREA)

SK774-2002A 2000-10-05 2001-10-05 Spôsob prípravy alkylesterov mastných kyselín SK287690B6 (sk)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
AT0169900A ATA16992000A (de)	2000-10-05	2000-10-05	Verfahren zur herstellung von fettsäurealkylestern
PCT/AT2001/000320 WO2002028811A1 (fr)	2000-10-05	2001-10-05	Procede de production d'esters alkyliques d'acides gras

Publications (2)

Publication Number	Publication Date
SK7742002A3 SK7742002A3 (en)	2003-09-11
SK287690B6 true SK287690B6 (sk)	2011-06-06

Family

ID=3688690

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK774-2002A SK287690B6 (sk)	2000-10-05	2001-10-05	Spôsob prípravy alkylesterov mastných kyselín

Country Status (20)

Country	Link
US (1)	US6696583B2 (fr)
EP (1)	EP1322588B1 (fr)
JP (1)	JP2004510044A (fr)
CN (2)	CN101792388A (fr)
AT (1)	ATA16992000A (fr)
AU (1)	AU9146601A (fr)
BR (1)	BR0107288A (fr)
CA (1)	CA2392723C (fr)
CZ (1)	CZ298652B6 (fr)
DK (1)	DK1322588T3 (fr)
EE (1)	EE200200289A (fr)
ES (1)	ES2593283T3 (fr)
HU (1)	HUP0204190A3 (fr)
LT (1)	LT1322588T (fr)
NZ (1)	NZ519001A (fr)
PL (1)	PL206658B1 (fr)
RU (1)	RU2287519C2 (fr)
SK (1)	SK287690B6 (fr)
WO (1)	WO2002028811A1 (fr)
ZA (1)	ZA200203786B (fr)

Families Citing this family (54)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US9725397B2 (en)	2003-01-27	2017-08-08	REG Seneca, LLC	Production of biodiesel and glycerin from high free fatty acid feedstocks
US8088183B2 (en)	2003-01-27	2012-01-03	Seneca Landlord, Llc	Production of biodiesel and glycerin from high free fatty acid feedstocks
US7806945B2 (en)	2003-01-27	2010-10-05	Seneca Landlord, Llc	Production of biodiesel and glycerin from high free fatty acid feedstocks
US7871448B2 (en)	2003-01-27	2011-01-18	Seneca Landlord, Llc	Production of biodiesel and glycerin from high free fatty acid feedstocks
US20050027137A1 (en) *	2003-07-29	2005-02-03	Hooker Jeffrey D.	Apparatus and method for the production of fatty acid alkyl ester
US6822105B1 (en) *	2003-08-12	2004-11-23	Stepan Company	Method of making alkyl esters using glycerin
US8313667B2 (en) *	2003-09-23	2012-11-20	Mli Associates, L.L.C.	Environmentally benign anti-icing or deicing fluids employing triglyceride processing by-products
US6890451B2 (en) *	2003-09-23	2005-05-10	Richard Sapienza	Environmentally benign anti-icing or deicing fluids employing triglyceride processing by-products
US7473539B2 (en) *	2004-09-20	2009-01-06	Sunho Biodiesel Corporation	Methods for producing alkyl esters
US9000040B2 (en)	2004-09-28	2015-04-07	Atrium Medical Corporation	Cross-linked fatty acid-based biomaterials
US8263102B2 (en)	2004-09-28	2012-09-11	Atrium Medical Corporation	Drug delivery coating for use with a stent
US9801982B2 (en)	2004-09-28	2017-10-31	Atrium Medical Corporation	Implantable barrier device
US9012506B2 (en)	2004-09-28	2015-04-21	Atrium Medical Corporation	Cross-linked fatty acid-based biomaterials
WO2006036984A2 (fr)	2004-09-28	2006-04-06	Atrium Medical Corporation	Film autonome et procedes de fabrication d'un tel film
RU2379332C1 (ru) *	2004-10-20	2010-01-20	Каунсил Оф Сайентифик Энд Индастриал Рисерч	Усовершенствованный способ получения метилового эфира жирной кислоты (биодизеля) путем переэтерификации триглицеридов масла
US7842653B2 (en) *	2005-06-16	2010-11-30	Council Of Scientific & Industrial Research	Process for the preparation of lubricants
US8119824B2 (en)	2005-06-27	2012-02-21	Tokyo Institute Of Technology	Processes for producing higher fatty acid esters
JP2007022988A (ja) *	2005-07-20	2007-02-01	Rebo International:Kk	脂肪酸アルキルエステルの製造方法
ES2245270B1 (es) *	2005-07-22	2006-09-16	Fundacion Cidaut	Procedimiento para la obtencion de comustible para motores de ciclo diesel a partir de aceites vegetales usados.
JP4219349B2 (ja) *	2005-09-16	2009-02-04	富士フイルム株式会社	脂肪酸アルキルエステルの製造方法及び燃料
FR2890962B1 (fr) *	2005-09-21	2007-11-23	Inst Francais Du Petrole	Procede ameliore de fabrication d'esters ethyliques a partir de corps gras d'origine naturelle
FR2890961B1 (fr)	2005-09-21	2007-11-23	Inst Francais Du Petrole	Procede perfectionne de fabrication d'esters ethyliques a partir de corps gras d'origine naturelle
US9278161B2 (en)	2005-09-28	2016-03-08	Atrium Medical Corporation	Tissue-separating fatty acid adhesion barrier
US9427423B2 (en)	2009-03-10	2016-08-30	Atrium Medical Corporation	Fatty-acid based particles
US7754643B2 (en) *	2005-10-07	2010-07-13	Council Of Scientific & Industrial Research	Transesterification catalyst and a process for the preparation thereof
ATE440815T1 (de) *	2005-10-10	2009-09-15	Council Scient Ind Res	Verfahren zur herstellung von dialkylcarbonaten
US7482480B2 (en) *	2005-10-10	2009-01-27	Council Of Scientific & Industrial Research	Process for the preparation of hydrocarbon fuel
US20070155859A1 (en) *	2006-01-04	2007-07-05	Zhengzhe Song	Reactive polyurethane hot melt adhesive
US7622600B1 (en) *	2006-01-06	2009-11-24	Redland Industries, Inc.	System and method for the continuous production of bio-diesel
US7828978B2 (en) *	2006-01-11	2010-11-09	Doug Geier	Simultaneous synthesis and purification of a fatty acid monoester biodiesel fuel
US20070261294A1 (en) *	2006-05-10	2007-11-15	Aiken John E	Process for production of biodiesel from high acid feed
US7901469B2 (en) *	2006-07-26	2011-03-08	Alternative Fuels Group Inc.	Alternative organic fuel formulations including vegetable oil
CA2663692A1 (fr) *	2006-09-19	2008-03-27	Best Energies, Inc.	Procedes de production de biocarburant en presence d'acides gras libres et compositions destinees a la production de biocarburant
WO2008057328A2 (fr)	2006-11-06	2008-05-15	Atrium Medical Corporation	Dispositif de séparation de tissu avec support renforcé pour mécanismes d'ancrage
US9492596B2 (en)	2006-11-06	2016-11-15	Atrium Medical Corporation	Barrier layer with underlying medical device and one or more reinforcing support structures
HU0700128D0 (en) *	2007-02-06	2007-03-28	Thesz Janos	Method for fabrication of modifided structured triglyceride as biodisel fuel
WO2008123925A2 (fr) *	2007-03-22	2008-10-16	Cps Biofuels, Inc.	Procédé de production de biodiesel
US20100242346A1 (en) *	2007-09-19	2010-09-30	Best Energies, Inc	Processes for the esterification of free fatty acids and the production of biodiesel
WO2009158379A2 (fr)	2008-06-25	2009-12-30	Benefuel Inc.	Procédé de fabrication d’alkylesters d’acides gras
EP2303827B1 (fr)	2008-06-25	2019-10-16	Benefuel Inc.	Procédé de fabrication d' alkylesters d' acides gras
US20110038910A1 (en)	2009-08-11	2011-02-17	Atrium Medical Corporation	Anti-infective antimicrobial-containing biomaterials
RU2426770C1 (ru) *	2009-11-24	2011-08-20	Государственное унитарное предприятие "Институт нефтехимпереработки Республики Башкортостан" (ГУП "ИНХП РБ")	Способ получения экологически чистого дизельного топлива
CN103119094B (zh)	2010-01-22	2014-07-16	阿彻丹尼尔斯米德兰德公司	制备高纯度可更新来源基增塑剂的方法和由其制备的产品
WO2012009707A2 (fr)	2010-07-16	2012-01-19	Atrium Medical Corporation	Composition et procédés destinés à modifier la vitesse d'hydrolyse de substances vulcanisées à base d'huile
AT510636B1 (de)	2010-10-28	2016-11-15	Wimmer Theodor	Verfahren zur herstellung von fettsäureestern niederer alkohole
CN103619856A (zh)	2011-02-15	2014-03-05	德克萨斯大学系统董事会	一种用于在室温下高甲烷存储的具有优化的开放金属位点以及孔空间的金属-有机构架
WO2012122197A2 (fr)	2011-03-09	2012-09-13	Benefuel Inc.	Systèmes et procédés de fabrication de bioproduits
US8304566B2 (en) *	2012-03-09	2012-11-06	Antonio Cantizani	Processes and apparatus for small-scale in situ biodiesel production
US9867880B2 (en)	2012-06-13	2018-01-16	Atrium Medical Corporation	Cured oil-hydrogel biomaterial compositions for controlled drug delivery
EP3008200B1 (fr)	2013-06-11	2020-01-08	Renewable Energy Group, Inc.	Production de biodiésel et produits obtenus à partir de celui-ci
UY35649A (es)	2013-07-09	2015-02-27	Reg Seneca Llc	?producción de productos a partir de materias primas que contienen ácidos grasos libres?.
US9328054B1 (en)	2013-09-27	2016-05-03	Travis Danner	Method of alcoholisis of fatty acids and fatty acid gyicerides
CZ308339B6 (cs) *	2016-02-17	2020-06-03	Stanislav Nikl	Způsob přípravy esterů mastných kyselin esterifikací olejů a tuků s vyšším obsahem volných mastných kyselin methanolem nebo ethanolem
CN111574363B (zh) *	2020-05-26	2023-09-26	杭州潜阳科技有限公司	一种邻苯二甲酸二甲酯的生产工艺

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB612667A (en) *	1945-05-29	1948-11-16	Unilever Ltd	Improvements in or relating to methods of alcoholysis of low grade fatty materials
US2521742A (en) *	1946-07-16	1950-09-12	Lever Brothers Ltd	Method of treating low-grade fatty materials
BR8300429A (pt)	1983-01-28	1984-09-04	Brasil Pesquisa Agropec	Processo da transesterificacao de oleos vegetais
DE3319590A1 (de)	1983-05-30	1984-12-06	Henkel KGaA, 4000 Düsseldorf	Verfahren zur herstellung von fettsaeureestern kurzkettiger aliphatischer alkohole aus freie fettsaeuren enthaltenden fetten und/oder oelen
DE3444893A1 (de)	1984-12-08	1986-06-12	Henkel KGaA, 4000 Düsseldorf	Verfahren zur herstellung von fettsaeuremethylestern
AT392977B (de)	1989-10-13	1991-07-25	Wimmer Theodor	Verfahren zur aufbereitung der bei der umesterung von fetten und oelen mit niederen alkoholen anfallenden glycerinphase
AT394374B (de) *	1990-06-29	1992-03-25	Wimmer Theodor	Verfahren zur herstellung von fettsaeureestern niederer alkohole
FR2696185B1 (fr) *	1992-09-25	1994-12-02	Inst Francais Du Petrole	Procédé amélioré de fabrication d'esters à partir de corps gras d'origine naturelle.
DE4301686C1 (de) *	1993-01-22	1994-03-31	Chem & Pharm Patent Hold Ltd	Verfahren zur Herstellung von Fettsäureestern niederer Alkohole
AT399336B (de) *	1993-07-14	1995-04-25	Martin Mag Dr Mittelbach	Verfahren zur herstellung von fettsäurealkylestern

2000
- 2000-10-05 AT AT0169900A patent/ATA16992000A/de unknown
2001
- 2001-10-05 ES ES01971467.4T patent/ES2593283T3/es not_active Expired - Lifetime
- 2001-10-05 CN CN200910223185A patent/CN101792388A/zh active Pending
- 2001-10-05 WO PCT/AT2001/000320 patent/WO2002028811A1/fr not_active Ceased
- 2001-10-05 JP JP2002532398A patent/JP2004510044A/ja active Pending
- 2001-10-05 AU AU91466/01A patent/AU9146601A/en not_active Abandoned
- 2001-10-05 DK DK01971467.4T patent/DK1322588T3/en active
- 2001-10-05 LT LTEP01971467.4T patent/LT1322588T/lt unknown
- 2001-10-05 HU HU0204190A patent/HUP0204190A3/hu unknown
- 2001-10-05 SK SK774-2002A patent/SK287690B6/sk not_active IP Right Cessation
- 2001-10-05 RU RU2002115817/04A patent/RU2287519C2/ru active
- 2001-10-05 PL PL355294A patent/PL206658B1/pl not_active IP Right Cessation
- 2001-10-05 NZ NZ519001A patent/NZ519001A/en not_active IP Right Cessation
- 2001-10-05 BR BR0107288-9A patent/BR0107288A/pt not_active Application Discontinuation
- 2001-10-05 CN CN01803011A patent/CN1392873A/zh active Pending
- 2001-10-05 CA CA2392723A patent/CA2392723C/fr not_active Expired - Fee Related
- 2001-10-05 EE EEP200200289A patent/EE200200289A/xx unknown
- 2001-10-05 CZ CZ20021854A patent/CZ298652B6/cs not_active IP Right Cessation
- 2001-10-05 EP EP01971467.4A patent/EP1322588B1/fr not_active Revoked
2002
- 2002-05-13 ZA ZA200203786A patent/ZA200203786B/en unknown
- 2002-06-04 US US10/161,761 patent/US6696583B2/en not_active Expired - Lifetime

Also Published As

Publication number	Publication date
EP1322588B1 (fr)	2016-06-29
ES2593283T3 (es)	2016-12-07
SK7742002A3 (en)	2003-09-11
CA2392723A1 (fr)	2002-04-11
HUP0204190A3 (en)	2011-01-28
DK1322588T3 (en)	2016-09-19
PL355294A1 (en)	2004-04-05
WO2002028811A1 (fr)	2002-04-11
BR0107288A (pt)	2002-08-27
HUP0204190A2 (hu)	2003-04-28
RU2287519C2 (ru)	2006-11-20
LT1322588T (lt)	2016-10-10
CN1392873A (zh)	2003-01-22
EP1322588A1 (fr)	2003-07-02
ZA200203786B (en)	2003-05-13
CA2392723C (fr)	2011-01-25
ATA16992000A (de)	2001-12-15
CZ298652B6 (cs)	2007-12-05
CN101792388A (zh)	2010-08-04
JP2004510044A (ja)	2004-04-02
EE200200289A (et)	2003-12-15
PL206658B1 (pl)	2010-09-30
US6696583B2 (en)	2004-02-24
CZ20021854A3 (cs)	2002-11-13
AU9146601A (en)	2002-04-15
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