KR102158665B1 - 카르복시-관능성 폴리에테르-기재 반응 생성물 및 상기 반응 생성물을 함유하는 수성 베이스코트 - Google Patents
카르복시-관능성 폴리에테르-기재 반응 생성물 및 상기 반응 생성물을 함유하는 수성 베이스코트 Download PDFInfo
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- KR102158665B1 KR102158665B1 KR1020187019096A KR20187019096A KR102158665B1 KR 102158665 B1 KR102158665 B1 KR 102158665B1 KR 1020187019096 A KR1020187019096 A KR 1020187019096A KR 20187019096 A KR20187019096 A KR 20187019096A KR 102158665 B1 KR102158665 B1 KR 102158665B1
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- polyether
- aqueous basecoat
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Classifications
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- B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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- C—CHEMISTRY; METALLURGY
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
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- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
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- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
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- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/04—Coating
- C08J7/046—Forming abrasion-resistant coatings; Forming surface-hardening coatings
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
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- C08L51/08—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to macromolecular compounds obtained otherwise than by reactions only involving unsaturated carbon-to-carbon bonds
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
- C08L61/20—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
- C08L61/26—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds
- C08L61/28—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds with melamine
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D151/00—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers
- C09D151/08—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers grafted on to macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
- C09D175/04—Polyurethanes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D179/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen, with or without oxygen, or carbon only, not provided for in groups C09D161/00 - C09D177/00
- C09D179/04—Polycondensates having nitrogen-containing heterocyclic rings in the main chain; Polyhydrazides; Polyamide acids or similar polyimide precursors
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/08—Anti-corrosive paints
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2351/00—Characterised by the use of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Derivatives of such polymers
- C08J2351/08—Characterised by the use of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Derivatives of such polymers grafted on to macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Materials Engineering (AREA)
- Paints Or Removers (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Polyethers (AREA)
- Inorganic Chemistry (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP15198679.1A EP3178864B1 (de) | 2015-12-09 | 2015-12-09 | Carboxyfunktionelle polyether-basierte reaktionsprodukte und wässrige basislacke enthaltend die reaktionsprodukte |
| EP15198679.1 | 2015-12-09 | ||
| PCT/EP2016/079192 WO2017097642A1 (de) | 2015-12-09 | 2016-11-30 | Carboxyfunktionelle polyether-basierte reaktionsprodukte und wässrige basislacke enthaltend die reaktionsprodukte |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20180090345A KR20180090345A (ko) | 2018-08-10 |
| KR102158665B1 true KR102158665B1 (ko) | 2020-09-22 |
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| EP (2) | EP3178864B1 (enExample) |
| JP (1) | JP6710760B2 (enExample) |
| KR (1) | KR102158665B1 (enExample) |
| CN (1) | CN108368245B (enExample) |
| BR (1) | BR112018011608B1 (enExample) |
| CA (1) | CA3006340C (enExample) |
| ES (1) | ES2701844T3 (enExample) |
| MX (1) | MX390990B (enExample) |
| PL (1) | PL3178864T3 (enExample) |
| RU (1) | RU2707886C1 (enExample) |
| WO (1) | WO2017097642A1 (enExample) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP6441388B2 (ja) * | 2014-07-01 | 2018-12-19 | ビーエーエスエフ コーティングス ゲゼルシャフト ミット ベシュレンクテル ハフツングＢＡＳＦ Ｃｏａｔｉｎｇｓ ＧｍｂＨ | ポリエーテルを基礎とするカルボキシ官能性反応生成物、および前記反応生成物を含む水性ベースコート材料 |
| CN108368244B (zh) | 2015-12-09 | 2020-12-29 | 巴斯夫涂料有限公司 | 羧基官能的聚醚基反应产物和包含所述反应产物的水性底涂料 |
| EP3178864B1 (de) * | 2015-12-09 | 2018-09-12 | BASF Coatings GmbH | Carboxyfunktionelle polyether-basierte reaktionsprodukte und wässrige basislacke enthaltend die reaktionsprodukte |
| US10975264B2 (en) | 2016-03-14 | 2021-04-13 | Basf Coatings Gmbh | Hydroxy-functional polyether-based reaction products and aqueous base paint which contains the reaction products |
| EP3526268B1 (de) | 2016-10-13 | 2023-09-20 | BASF Coatings GmbH | Beschichtungsmittelsystem basierend auf salzen einer aliphatischen monocarbonsäure |
| US12071561B2 (en) | 2018-06-11 | 2024-08-27 | Ppg Industries Ohio, Inc. | Coating compositions curable at low temperatures and coatings formed therefrom |
| US11104759B2 (en) * | 2018-06-15 | 2021-08-31 | Hodogaya Chemical Co., Ltd. | Polyol for crosslinkable polyurethane resin composition, and crosslinkable polyurethane resin |
| WO2022073986A1 (en) | 2020-10-05 | 2022-04-14 | Basf Coatings Gmbh | Screening method using cured coating film properties |
| CN116507681A (zh) | 2020-10-05 | 2023-07-28 | 巴斯夫涂料有限公司 | 使用涂料组合物性能或湿膜性能的筛选方法 |
| US20240018384A1 (en) * | 2020-12-10 | 2024-01-18 | Ppg Industries Ohio, Inc. | High acid value polyester |
| MX2023010767A (es) | 2021-03-19 | 2023-11-28 | Basf Coatings Gmbh | Sistemas de recubrimiento multicapa obtenidos a partir de composiciones del recubrimiento superior que contienen copolimeros en bloque. |
| CA3211750A1 (en) | 2021-03-19 | 2022-09-22 | Rosalva Castrejon BOKHART | Multilayer coating systems obtained from block copolymer containing basecoat compositions |
| US20240318008A1 (en) | 2021-08-30 | 2024-09-26 | Basf Coatings Gmbh | Lidar reflective multilayer coatings with high flop index |
| US20240352258A1 (en) | 2021-08-30 | 2024-10-24 | Basf Coatings Gmbh | Dark primer coatings with high lidar reflectivity |
| CN120051537A (zh) | 2022-10-07 | 2025-05-27 | 巴斯夫涂料有限公司 | 由含有嵌段共聚物的底涂层组合物获得的多层涂层体系 |
| EP4353786A1 (en) | 2022-10-13 | 2024-04-17 | BASF Coatings GmbH | Sustainably producible pigments and dyes for automotive coatings |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20060188738A1 (en) * | 2005-02-24 | 2006-08-24 | Jennings Robert E | Coating compositions that include a polyester polyol, related coated substrates, multi-layer coating and methods |
| US20090269577A1 (en) | 2008-04-24 | 2009-10-29 | Ppg Industries Ohio, Inc. | Waterborne anti-chip primer coating composition |
| WO2015028197A1 (de) * | 2013-08-27 | 2015-03-05 | Basf Coatings Gmbh | Dimerfettsäure-polyether-reaktionsprodukt und beschichtungsmittel enthaltend das reaktionsprodukt |
Family Cites Families (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5146560B2 (enExample) * | 1973-08-28 | 1976-12-09 | ||
| JPS5392897A (en) * | 1977-01-25 | 1978-08-15 | Nippon Soda Co Ltd | Preparation of solid urethane elastomer for injection use |
| DE3545618A1 (de) | 1985-12-21 | 1987-06-25 | Basf Lacke & Farben | Wasserverduennbares ueberzugsmittel zur herstellung der basisschicht eines mehrschichtueberzuges |
| DE4009858C2 (de) | 1990-03-28 | 1998-02-05 | Basf Lacke & Farben | Wäßriger pigmentierter Basislack enthaltend als Bindemittel ein wasserverdünnbares Polyacrylatharz und Verwendung eines solchen Basislacks |
| DE4010176A1 (de) | 1990-03-30 | 1991-10-02 | Basf Lacke & Farben | Verfahren zur herstellung einer mehrschichtigen lackierung und waessriger lack |
| JP2948639B2 (ja) * | 1990-09-06 | 1999-09-13 | 関西ペイント株式会社 | 鋼板への塗装方法 |
| DE4107136A1 (de) | 1991-03-06 | 1992-09-10 | Basf Lacke & Farben | Verfahren zur herstellung einer mehrschichtigen, schuetzenden und/oder dekorativen lackierung |
| CA2127761C (en) | 1993-07-16 | 2005-10-18 | Armin Gobel | An aqueous dispersion of polyurethane resins, a method of manufacturing them, coating agents containing them and use thereof |
| US5436314A (en) * | 1994-04-18 | 1995-07-25 | Arco Chemical Technology, L.P. | Process for making a polyetherester by insertion of a carboxylic acid into a polyether |
| DE4437535A1 (de) | 1994-10-20 | 1996-04-25 | Basf Lacke & Farben | Polyurethanmodifziertes Polyacrylat |
| JPH11207252A (ja) * | 1998-01-23 | 1999-08-03 | Kansai Paint Co Ltd | 複層塗膜形成法 |
| DE19914896A1 (de) * | 1999-04-01 | 2000-10-05 | Basf Coatings Ag | Thermisch und/oder mit aktinischer Strahlung härtbarer wäßriger Beschichtungsstoff und seine Verwendung |
| DE19930665A1 (de) | 1999-07-02 | 2001-01-11 | Basf Coatings Ag | Basislack und seine Verwendung zur Herstellung von farb- und/oder effektgebenden Basislackierungen und Mehrschichtlackierung |
| DE19948004B4 (de) | 1999-10-06 | 2006-05-11 | Basf Coatings Ag | Polyurethane und Pfropfmischpolymerisate auf Polyurethanbasis sowie ihre Verwendung zur Herstellung von Beschichtungsstoffen, Klebstoffen und Dichtungsmassen |
| DE10043405C1 (de) | 2000-09-04 | 2002-06-27 | Basf Coatings Ag | Verfahren zur Herstellung farb- und/oder effektgebender Lackierungen |
| DE10310446A1 (de) | 2003-03-07 | 2004-09-23 | Ppg Industries Lacke Gmbh | Polyester |
| RU2525391C9 (ru) * | 2008-11-06 | 2015-10-10 | Байер Матириальсайенс Аг | Способ получения полиэфирполиолов с малым количеством отходов диоксана |
| US20120082795A1 (en) * | 2010-10-01 | 2012-04-05 | Ppg Industries Ohio, Inc. | Method for using a primer comprising a self-emulsified polyester microgel |
| CA2880839A1 (en) * | 2012-08-10 | 2014-02-13 | Akzo Nobel Coatings International B.V. | Polyester polyol |
| BR112016012328B1 (pt) * | 2013-12-18 | 2021-11-23 | Basf Coatings Gmbh | Método para produzir um sistema de pintura de multirrevestimento e sistema de pintura de multirrevestimento |
| CN108368244B (zh) * | 2015-12-09 | 2020-12-29 | 巴斯夫涂料有限公司 | 羧基官能的聚醚基反应产物和包含所述反应产物的水性底涂料 |
| EP3178864B1 (de) * | 2015-12-09 | 2018-09-12 | BASF Coatings GmbH | Carboxyfunktionelle polyether-basierte reaktionsprodukte und wässrige basislacke enthaltend die reaktionsprodukte |
-
2015
- 2015-12-09 EP EP15198679.1A patent/EP3178864B1/de active Active
- 2015-12-09 ES ES15198679T patent/ES2701844T3/es active Active
- 2015-12-09 PL PL15198679T patent/PL3178864T3/pl unknown
-
2016
- 2016-11-30 WO PCT/EP2016/079192 patent/WO2017097642A1/de not_active Ceased
- 2016-11-30 US US16/060,482 patent/US10889090B2/en active Active
- 2016-11-30 BR BR112018011608-4A patent/BR112018011608B1/pt active IP Right Grant
- 2016-11-30 CN CN201680071947.9A patent/CN108368245B/zh active Active
- 2016-11-30 RU RU2018123760A patent/RU2707886C1/ru active
- 2016-11-30 EP EP16805067.2A patent/EP3387040A1/de not_active Withdrawn
- 2016-11-30 MX MX2018007028A patent/MX390990B/es unknown
- 2016-11-30 KR KR1020187019096A patent/KR102158665B1/ko active Active
- 2016-11-30 JP JP2018530619A patent/JP6710760B2/ja active Active
- 2016-11-30 CA CA3006340A patent/CA3006340C/en active Active
-
2020
- 2020-10-19 US US17/073,569 patent/US11866563B2/en active Active
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20060188738A1 (en) * | 2005-02-24 | 2006-08-24 | Jennings Robert E | Coating compositions that include a polyester polyol, related coated substrates, multi-layer coating and methods |
| US20090269577A1 (en) | 2008-04-24 | 2009-10-29 | Ppg Industries Ohio, Inc. | Waterborne anti-chip primer coating composition |
| WO2015028197A1 (de) * | 2013-08-27 | 2015-03-05 | Basf Coatings Gmbh | Dimerfettsäure-polyether-reaktionsprodukt und beschichtungsmittel enthaltend das reaktionsprodukt |
Also Published As
| Publication number | Publication date |
|---|---|
| CN108368245A (zh) | 2018-08-03 |
| BR112018011608B1 (pt) | 2022-08-09 |
| EP3387040A1 (de) | 2018-10-17 |
| CA3006340A1 (en) | 2017-06-15 |
| BR112018011608A2 (pt) | 2018-11-27 |
| MX390990B (es) | 2025-03-21 |
| RU2707886C1 (ru) | 2019-12-02 |
| EP3178864A1 (de) | 2017-06-14 |
| WO2017097642A1 (de) | 2017-06-15 |
| MX2018007028A (es) | 2018-08-01 |
| KR20180090345A (ko) | 2018-08-10 |
| US20180362799A1 (en) | 2018-12-20 |
| ES2701844T3 (es) | 2019-02-26 |
| US11866563B2 (en) | 2024-01-09 |
| CN108368245B (zh) | 2023-10-20 |
| JP6710760B2 (ja) | 2020-06-17 |
| US10889090B2 (en) | 2021-01-12 |
| CA3006340C (en) | 2020-07-14 |
| JP2019505613A (ja) | 2019-02-28 |
| US20210031496A1 (en) | 2021-02-04 |
| EP3178864B1 (de) | 2018-09-12 |
| PL3178864T3 (pl) | 2019-05-31 |
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