TW201004655A - Hair setting composition - Google Patents
Hair setting composition Download PDFInfo
- Publication number
- TW201004655A TW201004655A TW098109646A TW98109646A TW201004655A TW 201004655 A TW201004655 A TW 201004655A TW 098109646 A TW098109646 A TW 098109646A TW 98109646 A TW98109646 A TW 98109646A TW 201004655 A TW201004655 A TW 201004655A
- Authority
- TW
- Taiwan
- Prior art keywords
- group
- acid
- amine
- hair
- functional
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 114
- 210000004209 hair Anatomy 0.000 title claims abstract description 64
- 229920002635 polyurethane Polymers 0.000 claims abstract description 48
- 239000004814 polyurethane Substances 0.000 claims abstract description 48
- 238000002360 preparation method Methods 0.000 claims abstract description 12
- -1 polyols Polyols Chemical class 0.000 claims description 65
- 239000002253 acid Substances 0.000 claims description 60
- 229920000768 polyamine Polymers 0.000 claims description 60
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 50
- 150000001875 compounds Chemical class 0.000 claims description 45
- 229920005862 polyol Polymers 0.000 claims description 45
- 150000003077 polyols Chemical class 0.000 claims description 40
- 150000001412 amines Chemical class 0.000 claims description 36
- 229920000515 polycarbonate Polymers 0.000 claims description 24
- 235000021419 vinegar Nutrition 0.000 claims description 24
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 claims description 23
- 239000004417 polycarbonate Substances 0.000 claims description 23
- 239000000834 fixative Substances 0.000 claims description 21
- 229920000570 polyether Polymers 0.000 claims description 21
- 125000003010 ionic group Chemical group 0.000 claims description 20
- 239000000052 vinegar Substances 0.000 claims description 20
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 19
- 150000003839 salts Chemical class 0.000 claims description 15
- 150000004985 diamines Chemical class 0.000 claims description 14
- 125000003277 amino group Chemical group 0.000 claims description 13
- 238000006243 chemical reaction Methods 0.000 claims description 13
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 11
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- 239000005056 polyisocyanate Substances 0.000 claims description 10
- 229920001228 polyisocyanate Polymers 0.000 claims description 10
- 239000012855 volatile organic compound Substances 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 9
- 150000003335 secondary amines Chemical class 0.000 claims description 9
- 239000002537 cosmetic Substances 0.000 claims description 8
- 238000007493 shaping process Methods 0.000 claims description 8
- 229920001730 Moisture cure polyurethane Polymers 0.000 claims description 7
- 239000012948 isocyanate Substances 0.000 claims description 7
- 150000002513 isocyanates Chemical class 0.000 claims description 7
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- 229910052708 sodium Inorganic materials 0.000 claims description 3
- 239000011734 sodium Substances 0.000 claims description 3
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 claims description 3
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- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
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- IVGRSQBDVIJNDA-UHFFFAOYSA-N 2-(2-aminoethylamino)ethanesulfonic acid Chemical group NCCNCCS(O)(=O)=O IVGRSQBDVIJNDA-UHFFFAOYSA-N 0.000 claims 1
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims 1
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- 229920001002 functional polymer Polymers 0.000 claims 1
- STIABRLGDKHASC-UHFFFAOYSA-N phthalic acid;prop-2-enoic acid Chemical compound OC(=O)C=C.OC(=O)C1=CC=CC=C1C(O)=O STIABRLGDKHASC-UHFFFAOYSA-N 0.000 claims 1
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- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical class OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 13
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- 239000000443 aerosol Substances 0.000 description 8
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 8
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 8
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- 239000000047 product Substances 0.000 description 8
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- 229920002554 vinyl polymer Polymers 0.000 description 8
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 7
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 7
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Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/87—Polyurethanes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
- Polyurethanes Or Polyureas (AREA)
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|---|---|---|---|
| EP08153274A EP2105127A1 (de) | 2008-03-26 | 2008-03-26 | Haarfestiger-Zusammensetzung |
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| TW201004655A true TW201004655A (en) | 2010-02-01 |
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| TW098109646A TW201004655A (en) | 2008-03-26 | 2009-03-25 | Hair setting composition |
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|---|---|
| EP (2) | EP2105127A1 (enExample) |
| JP (1) | JP2011515425A (enExample) |
| KR (1) | KR20100127792A (enExample) |
| CN (1) | CN101980691B (enExample) |
| BR (1) | BRPI0910035B1 (enExample) |
| CA (1) | CA2719451A1 (enExample) |
| ES (1) | ES2755404T3 (enExample) |
| RU (1) | RU2508088C9 (enExample) |
| TW (1) | TW201004655A (enExample) |
| WO (1) | WO2009118105A1 (enExample) |
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|---|---|---|---|---|
| WO2011126978A1 (en) * | 2010-04-07 | 2011-10-13 | Isp Investments Inc. | Sprayable composition comprising high molecular weight charged polymer |
| EP2407145A1 (en) | 2010-07-13 | 2012-01-18 | The Procter & Gamble Company | Aerosol hairspray product for styling and/or shaping hair |
| EP2407144A1 (en) | 2010-07-13 | 2012-01-18 | The Procter & Gamble Company | Aerosol hairspray product for styling and/or shaping hair |
| DE102010063927A1 (de) * | 2010-12-22 | 2012-06-21 | Henkel Ag & Co. Kgaa | Haarbehandlungsmittel |
| DE102010063923A1 (de) * | 2010-12-22 | 2012-06-28 | Henkel Ag & Co. Kgaa | Haarbehandlungsmittel |
| WO2012130683A1 (de) | 2011-03-25 | 2012-10-04 | Bayer Materialscience Ag | Polyurethanharnstoff-mischung für die haarkosmetik |
| EP2688550A2 (de) | 2011-03-25 | 2014-01-29 | Bayer Intellectual Property GmbH | Kosmetische polyurethanharnstoff-copolymer-zusammensetzung |
| MX2014013685A (es) | 2012-05-11 | 2015-02-05 | Procter & Gamble | Tratamiento para el cabello que comprende almidon con injerto de silicona. |
| DE102012224298A1 (de) * | 2012-12-21 | 2014-06-26 | Henkel Ag & Co. Kgaa | Spray für elastischen und dauerhaften Halt |
| CN106572964B (zh) * | 2014-08-05 | 2020-05-19 | 科思创德国股份有限公司 | 用于化妆品组合物的聚氨酯脲溶液 |
| EP3177266A1 (de) | 2014-08-05 | 2017-06-14 | Covestro Deutschland AG | Polyurethanharnstofflösungen für haarstyling-zusammensetzungen |
| US10668007B2 (en) | 2015-02-17 | 2020-06-02 | Noxell Corporation | Method for providing a film comprising pigment on keratin fibres |
| WO2016133806A1 (en) | 2015-02-17 | 2016-08-25 | The Procter & Gamble Company | Composition for providing a film on keratin fibres |
| MX368181B (es) | 2015-02-17 | 2019-09-23 | Noxell Corp | Composición para formar una película sobre fibras de queratina. |
| MX364078B (es) | 2015-02-17 | 2019-04-11 | Noxell Corp | Composicion para formar una pelicula sobre fibras de queratina. |
| JP6832860B2 (ja) | 2015-02-17 | 2021-02-24 | ノクセル・コーポレーション | ケラチン繊維上にフィルムを提供するための組成物 |
| CN107771191B (zh) | 2015-06-17 | 2020-08-28 | 科莱恩国际有限公司 | 作为水泥浆中的降失水剂的水溶性或水溶胀性聚合物 |
| AU2017229125B2 (en) * | 2016-03-08 | 2021-07-29 | Living Proof, Inc. | Long lasting cosmetic compositions |
| CN109563030B (zh) | 2016-06-20 | 2022-06-10 | 科莱恩国际有限公司 | 包含一定水平的生物基碳的化合物 |
| BR112018077158B1 (pt) | 2016-06-29 | 2022-12-13 | Clariant International Ltd | Composição para inibição de microrganismos, processo para sintetizar a dita composição e seus usos |
| WO2018046977A1 (en) * | 2016-09-08 | 2018-03-15 | Sc Adv Communication S.R.L. | Product for perfuming and shaping the hair |
| JP7050784B2 (ja) | 2016-12-12 | 2022-04-08 | クラリアント・インターナシヨナル・リミテツド | 化粧料組成物、皮膚科学的組成物または医薬組成物におけるバイオベースのポリマーの使用 |
| JP7032402B2 (ja) | 2016-12-12 | 2022-03-08 | クラリアント・インターナシヨナル・リミテツド | ある特定のレベルのバイオベース炭素を含むポリマー |
| WO2018108665A1 (en) | 2016-12-15 | 2018-06-21 | Clariant International Ltd | Water-soluble and/or water-swellable hybrid polymer |
| EP3554646B1 (en) | 2016-12-15 | 2025-03-19 | Clariant International Ltd | Water-soluble and/or water-swellable hybrid polymer |
| ES3033231T3 (en) | 2016-12-15 | 2025-07-31 | Clariant Int Ltd | Water-soluble and/or water-swellable hybrid polymer |
| ES3017507T3 (en) | 2016-12-15 | 2025-05-13 | Clariant Int Ltd | Water-soluble and/or water-swellable hybrid polymer |
| US10821067B2 (en) | 2017-04-28 | 2020-11-03 | L'oreal | Hair-treatment compositions comprising a polyurethane latex polymer and thickening agent |
| JP6885783B2 (ja) * | 2017-05-16 | 2021-06-16 | 株式会社ダイゾー | ウェーブヘア復元用発泡性エアゾール組成物 |
| CN109419643B (zh) * | 2017-09-04 | 2022-01-07 | 万华化学（宁波）有限公司 | 含水性聚氨酯分散体的洗发剂组合物及该分散体的用途 |
| CA3074843A1 (en) | 2017-09-13 | 2019-03-21 | Living Proof, Inc. | Long lasting cosmetic compositions |
| EP3681921A2 (en) | 2017-09-13 | 2020-07-22 | Living Proof, Inc. | Color protectant compositions |
| EP3495024A1 (en) * | 2017-12-07 | 2019-06-12 | Covestro Deutschland AG | A cosmetic composition and a cleaning and caring product comprising the same |
| CN109662908A (zh) * | 2017-10-13 | 2019-04-23 | 科思创德国股份有限公司 | 一种化妆品组合物及包含其的洗护剂 |
| US11234923B2 (en) | 2017-10-13 | 2022-02-01 | Covestro Deutschland Ag | Cosmetic composition and a cleaning and caring product comprising the same |
| CN111356501A (zh) | 2017-11-20 | 2020-06-30 | 生活实验公司 | 实现持久化妆品性能的属性 |
| WO2019115478A1 (en) | 2017-12-11 | 2019-06-20 | Clariant International Ltd | Composition for inhibiting micro-organisms |
| EP3498338A1 (de) | 2017-12-18 | 2019-06-19 | Covestro Deutschland AG | Spezieller polyurethanharnstoff zur erhöhung der wasserbeständigkeit einer geformten frisur |
| EP3530322A1 (de) | 2018-02-27 | 2019-08-28 | Covestro Deutschland AG | Kosmetische zusammensetzung zur verbesserung der beständigkeit einer frisur |
| CN112041365A (zh) * | 2018-04-27 | 2020-12-04 | 生活实验公司 | 持久性化妆品组合物 |
| EP3636321A1 (en) | 2018-10-10 | 2020-04-15 | Covestro Deutschland AG | Polyurethane urea dispersions at least partially originated from renewable sources and their production and uses |
| EP3636686A1 (en) | 2018-10-10 | 2020-04-15 | Covestro Deutschland AG | Cosmetic formulations or compositions comprising biodegradable film formers |
| WO2021175672A1 (de) * | 2020-03-02 | 2021-09-10 | Covestro Deutschland Ag | Kosmetische zusammensetzung zur bildung eines films mit erhöhter elastizität und dehnungsfähigkeit |
| EP3888627A1 (de) * | 2020-03-31 | 2021-10-06 | Covestro Deutschland AG | Biobasierte polyurethan-dispersionen für dekorative kosmetische anwendungen |
| CN113527620A (zh) * | 2021-06-23 | 2021-10-22 | 合肥科天水性科技有限责任公司 | 一种非离子型水性聚氨酯啫喱及其制备方法 |
| CN113520916A (zh) * | 2021-07-02 | 2021-10-22 | 上海永熙信息科技有限公司 | 一种高成膜性的化妆品定妆组合物 |
| WO2025068356A1 (en) | 2023-09-27 | 2025-04-03 | Clariant International Ltd | Use of a sulf-containing polymer for improving sun protection |
Family Cites Families (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1400366A (fr) | 1963-05-15 | 1965-05-28 | Oreal | Nouveaux composés pouvant être utilisés en particulier pour le traitement des cheveux |
| US3836537A (en) | 1970-10-07 | 1974-09-17 | Minnesota Mining & Mfg | Zwitterionic polymer hairsetting compositions and method of using same |
| DE2446440C3 (de) * | 1974-09-28 | 1981-04-30 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von wäßrigen Dispersionen von Sulfonatgruppen aufweisenden Polyurethanen |
| DE4225045A1 (de) | 1992-07-29 | 1994-02-03 | Basf Ag | Verwendung von wasserlöslichen oder in Wasser dispergierbaren Polyurethanen als Hilfsmittel in kosmetischen und pharmazeutischen Zubereitungen und Polyurethane, die Polymilchsäurepolyole einpolymerisiert enthalten |
| DE4241118A1 (de) * | 1992-12-07 | 1994-06-09 | Basf Ag | Verwendung von kationischen Polyurethanen und Polyharnstoffen als Hilfsmittel in kosmetischen und pharmazeutischen Zubereitungen |
| EP0619111B2 (en) | 1993-04-06 | 2005-09-14 | National Starch and Chemical Investment Holding Corporation | Use of polyurethanes with carboxylate functionality for hair fixative applications |
| FR2708615B1 (fr) | 1993-08-04 | 1995-09-15 | Oreal | Nouveaux polyester-polyuréthannes, leur procédé de préparation, pseudo-latex réalisés à partir desdits polyester-polyuréthannes et leur utilisation dans des compositions cosmétiques. |
| DE4438849A1 (de) | 1994-11-02 | 1996-05-09 | Henkel Kgaa | Haarfestlegemittel |
| DE19517185A1 (de) * | 1995-05-11 | 1996-11-14 | Bayer Ag | Biologisch abbaubare und kompostierbare Formkörper einschließlich Flächengebilden |
| FR2736057B1 (fr) | 1995-06-27 | 1997-08-01 | Oreal | Polycondensats sequences polyurethanes et/ou polyurees a greffons silicones, compositions cosmetiques les contenant et utilisations |
| DE19541326A1 (de) | 1995-11-06 | 1997-05-07 | Basf Ag | Wasserlösliche oder wasserdispergierbare Polyurethane mit endständigen Säuregruppen, ihre Herstellung und ihre Verwendung |
| FR2743297B1 (fr) | 1996-01-05 | 1998-03-13 | Oreal | Composition cosmetiques a base de polycondensats ionisables multisequences polysiloxane/polyurethane et/ou polyuree en solution et utilisation |
| JP4165669B2 (ja) * | 1998-02-09 | 2008-10-15 | 日本エヌエスシー株式会社 | 化粧品用樹脂組成物およびその製法 |
| DE19821732A1 (de) * | 1998-05-14 | 1999-11-18 | Basf Ag | Vernetzte, wasserlösliche oder wasserdispergierbare Polyurethane |
| FR2782637B1 (fr) | 1998-08-27 | 2000-11-24 | Oreal | Composition capillaire contenant un polycondensat comprenant au moins un motif polyurethanne et/ou polyuree et un polyol |
| FR2782635B1 (fr) | 1998-08-27 | 2001-09-14 | Oreal | Dispositif aerosol contenant un polycondensat comprenant au moins un motif polyurethanne et/ou polyuree |
| CN1222268C (zh) * | 2000-04-13 | 2005-10-12 | 国家淀粉及化学投资控股公司 | 化妆树脂组合物和使用它们的化妆品 |
| DE10024624A1 (de) | 2000-05-18 | 2001-11-22 | Bayer Ag | Modifizierte Polyisocyanate |
| US6576702B2 (en) * | 2000-07-20 | 2003-06-10 | Noveon Ip Holdings Corp. | Plasticized waterborne polyurethane dispersions and manufacturing process |
| US6613314B1 (en) * | 2000-07-27 | 2003-09-02 | L'oreal | Reshapable hair styling composition comprising polyurethane dispersions |
| FR2821621B1 (fr) * | 2001-03-05 | 2004-11-05 | Oreal | Polyurethannes anioniques a caractere elastique et leur utilisation dans des compositions cosmetiques |
| FR2852239B1 (fr) | 2003-03-11 | 2006-08-11 | Oreal | Dispositif aerosol contenant une composition cosmetique comprenant un poluyrethane et un agent propulseur comprenant du dimethylether et au moins un hydrocarbure |
| FR2877214B1 (fr) | 2004-10-28 | 2006-12-29 | Oreal | Composition capillaire epaissie comprenant un polyurethane de haut poids moleculaire |
| ATE510595T1 (de) * | 2005-11-03 | 2011-06-15 | Unilever Nv | Haarbehandlungszusammensetzungen |
| JP2009523922A (ja) * | 2006-01-18 | 2009-06-25 | インビスタ テクノロジーズ エス エイ アール エル | 織物以外のポリマー組成物および方法 |
| DE102006016639A1 (de) * | 2006-04-08 | 2007-10-11 | Bayer Materialscience Ag | Verfahren zur Herstellung von Polyurethan-Schäumen |
| US20080075685A1 (en) * | 2006-09-22 | 2008-03-27 | Steven Michael Baxter | Polymer compositions containing polyurethanes |
| US20080175875A1 (en) * | 2006-09-25 | 2008-07-24 | Hari Babu Sunkara | Cosmetic compositions |
| US7445770B2 (en) * | 2007-03-14 | 2008-11-04 | Bayer Materialscience Llc | Polyurethane dispersions for use in personal care products |
-
2008
- 2008-03-26 EP EP08153274A patent/EP2105127A1/de not_active Ceased
-
2009
- 2009-03-13 CA CA2719451A patent/CA2719451A1/en not_active Abandoned
- 2009-03-13 ES ES09725213T patent/ES2755404T3/es active Active
- 2009-03-13 BR BRPI0910035A patent/BRPI0910035B1/pt not_active IP Right Cessation
- 2009-03-13 WO PCT/EP2009/001816 patent/WO2009118105A1/de not_active Ceased
- 2009-03-13 CN CN200980110774.7A patent/CN101980691B/zh not_active Expired - Fee Related
- 2009-03-13 KR KR1020107021253A patent/KR20100127792A/ko not_active Withdrawn
- 2009-03-13 EP EP09725213.4A patent/EP2271304B1/de active Active
- 2009-03-13 JP JP2011501124A patent/JP2011515425A/ja active Pending
- 2009-03-13 RU RU2010143443/15A patent/RU2508088C9/ru not_active IP Right Cessation
- 2009-03-25 TW TW098109646A patent/TW201004655A/zh unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP2105127A1 (de) | 2009-09-30 |
| KR20100127792A (ko) | 2010-12-06 |
| CN101980691B (zh) | 2014-08-20 |
| RU2010143443A (ru) | 2012-05-10 |
| ES2755404T3 (es) | 2020-04-22 |
| JP2011515425A (ja) | 2011-05-19 |
| EP2271304B1 (de) | 2019-09-04 |
| BRPI0910035A2 (pt) | 2015-12-29 |
| WO2009118105A1 (de) | 2009-10-01 |
| RU2508088C9 (ru) | 2014-09-20 |
| CN101980691A (zh) | 2011-02-23 |
| BRPI0910035B1 (pt) | 2017-03-07 |
| RU2508088C2 (ru) | 2014-02-27 |
| CA2719451A1 (en) | 2009-10-01 |
| EP2271304A1 (de) | 2011-01-12 |
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