BR112018012849B1 - Composição de silicone, utilização da composição, elastômero de silicone, método de preparação de filmes de silicone com propriedades antiaderentes, método de preparação de um revestimento em um substrato, substrato revestido, compostos e utilização dos compostos - Google Patents
Composição de silicone, utilização da composição, elastômero de silicone, método de preparação de filmes de silicone com propriedades antiaderentes, método de preparação de um revestimento em um substrato, substrato revestido, compostos e utilização dos compostos Download PDFInfo
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- BR112018012849B1 BR112018012849B1 BR112018012849-0A BR112018012849A BR112018012849B1 BR 112018012849 B1 BR112018012849 B1 BR 112018012849B1 BR 112018012849 A BR112018012849 A BR 112018012849A BR 112018012849 B1 BR112018012849 B1 BR 112018012849B1
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- Prior art keywords
- composition
- silicone
- radical
- compounds
- photoinitiator
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 123
- 229920001296 polysiloxane Polymers 0.000 title claims abstract description 85
- 150000001875 compounds Chemical class 0.000 title claims abstract description 49
- 238000000034 method Methods 0.000 title claims abstract description 19
- 239000000758 substrate Substances 0.000 title claims abstract description 17
- 238000000576 coating method Methods 0.000 title claims abstract description 12
- 239000011248 coating agent Substances 0.000 title claims abstract description 8
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- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 19
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- 206010073306 Exposure to radiation Diseases 0.000 claims abstract description 10
- 239000012965 benzophenone Substances 0.000 claims description 26
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 claims description 21
- 238000004132 cross linking Methods 0.000 claims description 21
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
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- 125000000217 alkyl group Chemical group 0.000 claims description 7
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- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 claims description 5
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- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 claims description 3
- 229930006711 bornane-2,3-dione Natural products 0.000 claims description 3
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- 229930195733 hydrocarbon Natural products 0.000 claims description 3
- 125000005702 oxyalkylene group Chemical group 0.000 claims description 3
- FAQJJMHZNSSFSM-UHFFFAOYSA-N phenylglyoxylic acid Chemical compound OC(=O)C(=O)C1=CC=CC=C1 FAQJJMHZNSSFSM-UHFFFAOYSA-N 0.000 claims description 3
- CDSULTPOCMWJCM-UHFFFAOYSA-N 4h-chromene-2,3-dione Chemical class C1=CC=C2OC(=O)C(=O)CC2=C1 CDSULTPOCMWJCM-UHFFFAOYSA-N 0.000 claims description 2
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N benzo-alpha-pyrone Natural products C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 claims description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
- 235000001671 coumarin Nutrition 0.000 claims description 2
- 150000004775 coumarins Chemical class 0.000 claims description 2
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- NPFYZDNDJHZQKY-UHFFFAOYSA-N 4-Hydroxybenzophenone Chemical compound C1=CC(O)=CC=C1C(=O)C1=CC=CC=C1 NPFYZDNDJHZQKY-UHFFFAOYSA-N 0.000 description 22
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 21
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- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 16
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- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 8
- 150000008366 benzophenones Chemical class 0.000 description 8
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- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 239000000654 additive Substances 0.000 description 6
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 6
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 6
- 239000011541 reaction mixture Substances 0.000 description 6
- 150000004756 silanes Chemical class 0.000 description 6
- 125000004469 siloxy group Chemical group [SiH3]O* 0.000 description 6
- YIKSHDNOAYSSPX-UHFFFAOYSA-N 1-propan-2-ylthioxanthen-9-one Chemical compound S1C2=CC=CC=C2C(=O)C2=C1C=CC=C2C(C)C YIKSHDNOAYSSPX-UHFFFAOYSA-N 0.000 description 5
- VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 description 5
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 5
- 230000000996 additive effect Effects 0.000 description 5
- 239000003480 eluent Substances 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- 229920001684 low density polyethylene Polymers 0.000 description 5
- 239000004702 low-density polyethylene Substances 0.000 description 5
- 239000000123 paper Substances 0.000 description 5
- 229920000139 polyethylene terephthalate Polymers 0.000 description 5
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- 239000000377 silicon dioxide Substances 0.000 description 5
- 239000004447 silicone coating Substances 0.000 description 5
- NJWGQARXZDRHCD-UHFFFAOYSA-N 2-methylanthraquinone Chemical compound C1=CC=C2C(=O)C3=CC(C)=CC=C3C(=O)C2=C1 NJWGQARXZDRHCD-UHFFFAOYSA-N 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
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- XMLYCEVDHLAQEL-UHFFFAOYSA-N 2-hydroxy-2-methyl-1-phenylpropan-1-one Chemical compound CC(C)(O)C(=O)C1=CC=CC=C1 XMLYCEVDHLAQEL-UHFFFAOYSA-N 0.000 description 3
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- 230000000052 comparative effect Effects 0.000 description 3
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- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
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- SCHZCUMIENIQMY-UHFFFAOYSA-N tris(trimethylsilyl)silicon Chemical compound C[Si](C)(C)[Si]([Si](C)(C)C)[Si](C)(C)C SCHZCUMIENIQMY-UHFFFAOYSA-N 0.000 description 3
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- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 2
- ATZDXNDVDOQLRW-UHFFFAOYSA-N C(C)OP(=O)(C1=CC=CC=C1)C(C1(CC=C(C=C1CC)CC)CC)=O Chemical compound C(C)OP(=O)(C1=CC=CC=C1)C(C1(CC=C(C=C1CC)CC)CC)=O ATZDXNDVDOQLRW-UHFFFAOYSA-N 0.000 description 2
- 125000000041 C6-C10 aryl group Chemical group 0.000 description 2
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- KKZJGLLVHKMTCM-UHFFFAOYSA-N mitoxantrone Chemical compound O=C1C2=C(O)C=CC(O)=C2C(=O)C2=C1C(NCCNCCO)=CC=C2NCCNCCO KKZJGLLVHKMTCM-UHFFFAOYSA-N 0.000 description 1
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- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
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- 238000012306 spectroscopic technique Methods 0.000 description 1
- 239000010421 standard material Substances 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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Classifications
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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
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/06—Preparatory processes
- C08G77/08—Preparatory processes characterised by the catalysts used
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/42—Block-or graft-polymers containing polysiloxane sequences
- C08G77/44—Block-or graft-polymers containing polysiloxane sequences containing only polysiloxane sequences
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0025—Crosslinking or vulcanising agents; including accelerators
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/07—Aldehydes; Ketones
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/45—Heterocyclic compounds having sulfur in the ring
-
- 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
- C09D183/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers
- C09D183/04—Polysiloxanes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/12—Polysiloxanes containing silicon bound to hydrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/20—Polysiloxanes containing silicon bound to unsaturated aliphatic groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2312/00—Crosslinking
- C08L2312/06—Crosslinking by radiation
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Paints Or Removers (AREA)
- Polymerisation Methods In General (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Polymerization Catalysts (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
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| FR1563147 | 2015-12-22 | ||
| FR1563147A FR3045641B1 (fr) | 2015-12-22 | 2015-12-22 | Utilisation d'un systeme photoamorceur de type ii pour la reticulation de compositions silicones |
| PCT/EP2016/082456 WO2017109116A1 (fr) | 2015-12-22 | 2016-12-22 | Utilisation d'un système photoamorceur de type ii pour la réticulation de compositions silicones |
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| BR112018012849A2 BR112018012849A2 (pt) | 2018-12-04 |
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| FR (1) | FR3045641B1 (enExample) |
| WO (1) | WO2017109116A1 (enExample) |
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| RU2696454C1 (ru) * | 2015-07-06 | 2019-08-01 | Блюстар Силикон Франс Сас | Самоклеящееся многослойное изделие и способ его производства |
| FR3045641B1 (fr) * | 2015-12-22 | 2021-04-30 | Bluestar Silicones France | Utilisation d'un systeme photoamorceur de type ii pour la reticulation de compositions silicones |
| KR102240076B1 (ko) * | 2017-11-10 | 2021-04-14 | 주식회사 엘지화학 | 이형 조성물 및 이의 경화물을 포함하는 이형층을 포함하는 이형 필름 |
| IL257535B (en) * | 2018-02-14 | 2020-01-30 | N3 Coat Ltd | Benzophenone compounds as light catalysts for polyolefins |
| KR102888120B1 (ko) * | 2018-12-28 | 2025-11-18 | 아이지엠 레진스 이탈리아 에스.알.엘. | 광개시제 |
| KR102498354B1 (ko) * | 2019-10-23 | 2023-02-08 | 주식회사 엘지화학 | 실리콘계 이형제 조성물, 이로부터 경화된 이형층을 구비하는 이형필름 및 그 제조방법 |
| US20220411642A1 (en) * | 2019-11-27 | 2022-12-29 | Threebond Co., Ltd. | Primer composition |
| WO2021225675A1 (en) * | 2020-05-07 | 2021-11-11 | Dow Silicons Corporation | Silicone hybrid pressure sensitive adhesive and methods for its preparation and use on uneven surfaces |
| JP7411500B2 (ja) * | 2020-05-11 | 2024-01-11 | 信越化学工業株式会社 | 光硬化性シリコーン組成物、接着剤、シリコーン硬化物 |
| CA3206866A1 (fr) | 2021-01-08 | 2022-07-14 | Elkem Silicones France Sas | Composition silicone reticulable par irradiation comprenant un modulateur d'adherence |
| KR20230173661A (ko) * | 2021-03-10 | 2023-12-27 | 엘켐 실리콘즈 프랑스 에스에이에스 | 실리콘 조성물 경화용 유형i 광개시제 |
| CN113173851B (zh) * | 2021-04-13 | 2023-02-14 | 华南理工大学 | 一种uv交联单体及其制备方法与在制备含氟丙烯酸酯乳液中的应用 |
| CN113651904B (zh) * | 2021-08-12 | 2023-05-12 | 管和平 | 一种可光聚合单组分硫杂蒽酮类光引发剂 |
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| US4064027A (en) * | 1973-09-28 | 1977-12-20 | Dow Corning Corporation | UV curable composition |
| FR2507608A1 (fr) | 1981-06-15 | 1982-12-17 | Rhone Poulenc Spec Chim | Compositions organopolysiloxaniques liquides photopolymerisables pour enduction de materiaux |
| US4558082A (en) * | 1984-05-10 | 1985-12-10 | General Electric Company | Acrylated polymers |
| CA1256239A (en) * | 1984-09-28 | 1989-06-20 | Richard P. Eckberg | Dual cure silicone compositions |
| US4585669A (en) * | 1984-09-28 | 1986-04-29 | General Electric Company | Novel dual cure silicone compositions |
| DE4003079A1 (de) * | 1990-02-02 | 1991-08-08 | Bayer Ag | Benzophenonderivate und polymere mit phenolischen hydroxylgruppen |
| DE4435487A1 (de) * | 1994-10-04 | 1996-04-11 | Hoechst Ag | Mit Silikonen kompatible Photoinitiatoren und diese enthaltende lichtempfindliche Gemische |
| EP0894112A2 (en) * | 1996-04-19 | 1999-02-03 | Minnesota Mining And Manufacturing Company | Process for radiation cross-linking polymers and radiation cross-linkable compositions |
| JP3950493B2 (ja) * | 1996-04-26 | 2007-08-01 | 東レ・ダウコーニング株式会社 | 導電性シリコーンゴム組成物、半導体装置の製造方法およびその半導体装置 |
| US6254802B1 (en) * | 1997-05-16 | 2001-07-03 | Cryovac, Inc. | Low migratory photoinitiators for oxygen-scavenging compositions |
| DE60005699T2 (de) * | 1999-07-27 | 2004-08-19 | Pirelli S.P.A. | Kabel, insbesondere für transport und verteilung von elektrischer energie und isolierungszusammensetzung |
| EP2444450A1 (de) | 2010-10-19 | 2012-04-25 | Hinterwaldner Consulting & Partner (Gbr) | Zusammensetzungen zur Herstellung abhäsiver Beschichtungen |
| BR112014003900A2 (pt) * | 2011-09-01 | 2017-03-14 | 3M Innovative Properties Co | métodos para produção de uma camada ao menos parcialmente curada |
| JP5735446B2 (ja) * | 2012-03-27 | 2015-06-17 | 信越化学工業株式会社 | オルガノポリシロキサン組成物、該オルガノポリシロキサン組成物の硬化方法、及び発光ダイオード |
| JP2014001342A (ja) * | 2012-06-20 | 2014-01-09 | Momentive Performance Materials Inc | 紫外線硬化型シリコーン樹脂組成物、及びそれを用いた画像表示装置 |
| FR3015508B1 (fr) * | 2013-12-20 | 2016-02-05 | Bluestar Silicones France | Nouveau systeme d'inhibition d'hydrosilylation photoactivable |
| GB2525453A (en) * | 2014-04-23 | 2015-10-28 | Uponor Innovation Ab | Polyolefin pipe |
| TWI738684B (zh) * | 2015-12-09 | 2021-09-11 | 德商漢高智慧財產控股公司 | 可脫黏組合物 |
| FR3045641B1 (fr) * | 2015-12-22 | 2021-04-30 | Bluestar Silicones France | Utilisation d'un systeme photoamorceur de type ii pour la reticulation de compositions silicones |
-
2015
- 2015-12-22 FR FR1563147A patent/FR3045641B1/fr active Active
-
2016
- 2016-12-22 CN CN201680082028.1A patent/CN109072001B/zh active Active
- 2016-12-22 BR BR112018012849-0A patent/BR112018012849B1/pt active IP Right Grant
- 2016-12-22 KR KR1020187021082A patent/KR102671096B1/ko active Active
- 2016-12-22 WO PCT/EP2016/082456 patent/WO2017109116A1/fr not_active Ceased
- 2016-12-22 CA CA3009545A patent/CA3009545C/en active Active
- 2016-12-22 EP EP16819932.1A patent/EP3408340A1/fr not_active Withdrawn
- 2016-12-22 JP JP2018533771A patent/JP6805256B2/ja active Active
- 2016-12-22 US US16/065,258 patent/US10954384B2/en active Active
-
2020
- 2020-02-20 JP JP2020027376A patent/JP2020111574A/ja not_active Abandoned
-
2021
- 2021-01-27 US US17/159,417 patent/US11603468B2/en active Active
-
2022
- 2022-04-07 JP JP2022064106A patent/JP7496579B2/ja active Active
Also Published As
| Publication number | Publication date |
|---|---|
| US20190002695A1 (en) | 2019-01-03 |
| US10954384B2 (en) | 2021-03-23 |
| KR20180127962A (ko) | 2018-11-30 |
| US20210147684A1 (en) | 2021-05-20 |
| JP2022106747A (ja) | 2022-07-20 |
| FR3045641B1 (fr) | 2021-04-30 |
| JP2019507205A (ja) | 2019-03-14 |
| JP7496579B2 (ja) | 2024-06-07 |
| FR3045641A1 (fr) | 2017-06-23 |
| JP6805256B2 (ja) | 2020-12-23 |
| KR102671096B1 (ko) | 2024-05-30 |
| CA3009545C (en) | 2023-02-28 |
| EP3408340A1 (fr) | 2018-12-05 |
| CN109072001A (zh) | 2018-12-21 |
| US11603468B2 (en) | 2023-03-14 |
| CA3009545A1 (en) | 2017-06-29 |
| CN109072001B (zh) | 2021-09-28 |
| JP2020111574A (ja) | 2020-07-27 |
| BR112018012849A2 (pt) | 2018-12-04 |
| WO2017109116A1 (fr) | 2017-06-29 |
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