KR20170097754A - 이중 경화 폴리티오에테르 - Google Patents
이중 경화 폴리티오에테르 Download PDFInfo
- Publication number
- KR20170097754A KR20170097754A KR1020177020355A KR20177020355A KR20170097754A KR 20170097754 A KR20170097754 A KR 20170097754A KR 1020177020355 A KR1020177020355 A KR 1020177020355A KR 20177020355 A KR20177020355 A KR 20177020355A KR 20170097754 A KR20170097754 A KR 20170097754A
- Authority
- KR
- South Korea
- Prior art keywords
- amine
- peroxide
- composition
- curable
- composition according
- Prior art date
- Legal status (The legal status 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 status listed.)
- Withdrawn
Links
- 229920006295 polythiol Polymers 0.000 title claims abstract description 23
- 239000000203 mixture Substances 0.000 claims abstract description 62
- 150000001412 amines Chemical class 0.000 claims abstract description 17
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 claims abstract description 14
- 239000000178 monomer Substances 0.000 claims abstract description 14
- 150000002978 peroxides Chemical class 0.000 claims abstract description 13
- 229920000642 polymer Polymers 0.000 claims abstract description 13
- 239000004342 Benzoyl peroxide Substances 0.000 claims abstract description 8
- 235000019400 benzoyl peroxide Nutrition 0.000 claims abstract description 8
- WFUGQJXVXHBTEM-UHFFFAOYSA-N 2-hydroperoxy-2-(2-hydroperoxybutan-2-ylperoxy)butane Chemical compound CCC(C)(OO)OOC(C)(CC)OO WFUGQJXVXHBTEM-UHFFFAOYSA-N 0.000 claims abstract description 6
- VDMLVOIDGSOUTA-UHFFFAOYSA-N 2-(4-methylanilino)ethane-1,1-diol Chemical compound CC1=CC=C(NCC(O)O)C=C1 VDMLVOIDGSOUTA-UHFFFAOYSA-N 0.000 claims abstract description 5
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 claims abstract description 5
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 claims abstract description 5
- 239000012966 redox initiator Substances 0.000 claims abstract description 5
- 150000001993 dienes Chemical class 0.000 claims abstract description 4
- 150000004662 dithiols Chemical class 0.000 claims abstract description 4
- 150000003512 tertiary amines Chemical class 0.000 claims abstract description 4
- 125000003396 thiol group Chemical group [H]S* 0.000 claims abstract description 4
- 239000000565 sealant Substances 0.000 claims description 15
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 13
- 229910052757 nitrogen Inorganic materials 0.000 claims description 11
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 7
- 239000000945 filler Substances 0.000 claims description 6
- 239000002105 nanoparticle Substances 0.000 claims description 4
- UKODFQOELJFMII-UHFFFAOYSA-N pentamethyldiethylenetriamine Chemical compound CN(C)CCN(C)CCN(C)C UKODFQOELJFMII-UHFFFAOYSA-N 0.000 abstract description 2
- 238000001723 curing Methods 0.000 description 11
- GUCYFKSBFREPBC-UHFFFAOYSA-N [phenyl-(2,4,6-trimethylbenzoyl)phosphoryl]-(2,4,6-trimethylphenyl)methanone Chemical compound CC1=CC(C)=CC(C)=C1C(=O)P(=O)(C=1C=CC=CC=1)C(=O)C1=C(C)C=C(C)C=C1C GUCYFKSBFREPBC-UHFFFAOYSA-N 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- 229920002379 silicone rubber Polymers 0.000 description 8
- 239000004945 silicone rubber Substances 0.000 description 8
- 239000008240 homogeneous mixture Substances 0.000 description 7
- OXBLVCZKDOZZOJ-UHFFFAOYSA-N 2,3-Dihydrothiophene Chemical compound C1CC=CS1 OXBLVCZKDOZZOJ-UHFFFAOYSA-N 0.000 description 6
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 6
- 238000009472 formulation Methods 0.000 description 6
- 206010028980 Neoplasm Diseases 0.000 description 5
- 201000011510 cancer Diseases 0.000 description 5
- FFHWGQQFANVOHV-UHFFFAOYSA-N dimethyldioxirane Chemical compound CC1(C)OO1 FFHWGQQFANVOHV-UHFFFAOYSA-N 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 239000012973 diazabicyclooctane Substances 0.000 description 4
- 230000009977 dual effect Effects 0.000 description 4
- 239000000446 fuel Substances 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 230000009477 glass transition Effects 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- CYIGRWUIQAVBFG-UHFFFAOYSA-N 1,2-bis(2-ethenoxyethoxy)ethane Chemical compound C=COCCOCCOCCOC=C CYIGRWUIQAVBFG-UHFFFAOYSA-N 0.000 description 2
- 102100025848 Acyl-coenzyme A thioesterase 8 Human genes 0.000 description 2
- 101710175468 Acyl-coenzyme A thioesterase 8 Proteins 0.000 description 2
- -1 CMP dienes Chemical class 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 239000004809 Teflon Substances 0.000 description 2
- 229920006362 Teflon® Polymers 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 2
- 239000013500 performance material Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 230000004584 weight gain Effects 0.000 description 2
- 235000019786 weight gain Nutrition 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- MNZAKDODWSQONA-UHFFFAOYSA-N 1-dibutylphosphorylbutane Chemical compound CCCCP(=O)(CCCC)CCCC MNZAKDODWSQONA-UHFFFAOYSA-N 0.000 description 1
- IMQFZQVZKBIPCQ-UHFFFAOYSA-N 2,2-bis(3-sulfanylpropanoyloxymethyl)butyl 3-sulfanylpropanoate Chemical compound SCCC(=O)OCC(CC)(COC(=O)CCS)COC(=O)CCS IMQFZQVZKBIPCQ-UHFFFAOYSA-N 0.000 description 1
- BJELTSYBAHKXRW-UHFFFAOYSA-N 2,4,6-triallyloxy-1,3,5-triazine Chemical compound C=CCOC1=NC(OCC=C)=NC(OCC=C)=N1 BJELTSYBAHKXRW-UHFFFAOYSA-N 0.000 description 1
- WYGWHHGCAGTUCH-UHFFFAOYSA-N 2-[(2-cyano-4-methylpentan-2-yl)diazenyl]-2,4-dimethylpentanenitrile Chemical compound CC(C)CC(C)(C#N)N=NC(C)(C#N)CC(C)C WYGWHHGCAGTUCH-UHFFFAOYSA-N 0.000 description 1
- HCZMHWVFVZAHCR-UHFFFAOYSA-N 2-[2-(2-sulfanylethoxy)ethoxy]ethanethiol Chemical compound SCCOCCOCCS HCZMHWVFVZAHCR-UHFFFAOYSA-N 0.000 description 1
- RCEJCSULJQNRQQ-UHFFFAOYSA-N 2-methylbutanenitrile Chemical compound CCC(C)C#N RCEJCSULJQNRQQ-UHFFFAOYSA-N 0.000 description 1
- OHXAOPZTJOUYKM-UHFFFAOYSA-N 3-Chloro-2-methylpropene Chemical compound CC(=C)CCl OHXAOPZTJOUYKM-UHFFFAOYSA-N 0.000 description 1
- 229910002016 Aerosil® 200 Inorganic materials 0.000 description 1
- 241000579895 Chlorostilbon Species 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- QYTDEUPAUMOIOP-UHFFFAOYSA-N TEMPO Chemical group CC1(C)CCCC(C)(C)N1[O] QYTDEUPAUMOIOP-UHFFFAOYSA-N 0.000 description 1
- 229910000323 aluminium silicate Inorganic materials 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 229910052876 emerald Inorganic materials 0.000 description 1
- 239000010976 emerald Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- GDOPTJXRTPNYNR-UHFFFAOYSA-N methyl-cyclopentane Natural products CC1CCCC1 GDOPTJXRTPNYNR-UHFFFAOYSA-N 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000000016 photochemical curing Methods 0.000 description 1
- 229920000123 polythiophene Polymers 0.000 description 1
- 230000000644 propagated effect Effects 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- XOTMHFNWERTCLG-UHFFFAOYSA-N tris(4-ethenoxybutyl) benzene-1,2,4-tricarboxylate Chemical compound C=COCCCCOC(=O)C1=CC=C(C(=O)OCCCCOC=C)C(C(=O)OCCCCOC=C)=C1 XOTMHFNWERTCLG-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Images
Classifications
-
- 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
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/02—Polythioethers
- C08G75/04—Polythioethers from mercapto compounds or metallic derivatives thereof
- C08G75/045—Polythioethers from mercapto compounds or metallic derivatives thereof from mercapto compounds and unsaturated compounds
-
- 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
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/02—Polythioethers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D3/00—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials
- B05D3/02—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by baking
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B64—AIRCRAFT; AVIATION; COSMONAUTICS
- B64D—EQUIPMENT FOR FITTING IN OR TO AIRCRAFT; FLIGHT SUITS; PARACHUTES; ARRANGEMENT OR MOUNTING OF POWER PLANTS OR PROPULSION TRANSMISSIONS IN AIRCRAFT
- B64D45/00—Aircraft indicators or protectors not otherwise provided for
- B64D45/02—Lightning protectors; Static dischargers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/34—Introducing sulfur atoms or sulfur-containing groups
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/04—Polymeric products of isocyanates or isothiocyanates with vinyl compounds
-
- 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
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
-
- 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
- C08G8/00—Condensation polymers of aldehydes or ketones with phenols only
- C08G8/28—Chemically modified polycondensates
- C08G8/34—Chemically modified polycondensates by natural resins or resin acids, e.g. rosin
-
- 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/24—Acids; Salts thereof
- C08K3/26—Carbonates; Bicarbonates
-
- 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
- C08K5/14—Peroxides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L81/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing sulfur with or without nitrogen, oxygen or carbon only; Compositions of polysulfones; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L81/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing sulfur with or without nitrogen, oxygen or carbon only; Compositions of polysulfones; Compositions of derivatives of such polymers
- C08L81/02—Polythioethers; Polythioether-ethers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J181/00—Adhesives based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing sulfur, with or without nitrogen, oxygen, or carbon only; Adhesives based on polysulfones; Adhesives based on derivatives of such polymers
- C09J181/02—Polythioethers; Polythioether-ethers
-
- 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/24—Acids; Salts thereof
- C08K3/26—Carbonates; Bicarbonates
- C08K2003/265—Calcium, strontium or barium carbonate
-
- 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
- C08K2201/00—Specific properties of additives
- C08K2201/011—Nanostructured additives
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Aviation & Aerospace Engineering (AREA)
- General Chemical & Material Sciences (AREA)
- Sealing Material Composition (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201462095952P | 2014-12-23 | 2014-12-23 | |
| US62/095,952 | 2014-12-23 | ||
| PCT/US2015/067450 WO2016106352A1 (en) | 2014-12-23 | 2015-12-22 | Dual cure polythioether |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20170097754A true KR20170097754A (ko) | 2017-08-28 |
Family
ID=55221521
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020177020355A Withdrawn KR20170097754A (ko) | 2014-12-23 | 2015-12-22 | 이중 경화 폴리티오에테르 |
Country Status (8)
| Country | Link |
|---|---|
| US (2) | US10703906B2 (enExample) |
| EP (1) | EP3237494B1 (enExample) |
| JP (1) | JP7016698B2 (enExample) |
| KR (1) | KR20170097754A (enExample) |
| CN (1) | CN107108894B (enExample) |
| BR (1) | BR112017013742A2 (enExample) |
| CA (1) | CA2970960A1 (enExample) |
| WO (1) | WO2016106352A1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20200016956A (ko) * | 2017-06-09 | 2020-02-17 | 피알시-데소토 인터내쇼날, 인코포레이티드 | 이중 경화 실란트 |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN107108833B (zh) | 2014-11-24 | 2022-06-14 | Ppg工业俄亥俄公司 | 通过挤出用于反应性三维打印的方法 |
| CN107207426B (zh) * | 2015-02-13 | 2020-02-14 | 3M创新有限公司 | 耐寒性密封剂及其组分 |
| WO2016176548A1 (en) | 2015-04-29 | 2016-11-03 | 3M Innovative Properties Company | Composition including a polythiol and a polyepoxide and methods relating to the composition |
| JP2019521223A (ja) | 2016-06-30 | 2019-07-25 | スリーエム イノベイティブ プロパティズ カンパニー | ポリチオール、不飽和化合物、光開始剤、及び有機ハイドロパーオキサイドを含む、二元硬化性チオール−エン組成物、並びにそれから調製した航空宇宙産業における使用のための架橋ポリマーシーラント |
| JP2019534363A (ja) | 2016-11-03 | 2019-11-28 | スリーエム イノベイティブ プロパティズ カンパニー | シーラントを航空機用部品に適用する方法 |
| US11198757B2 (en) | 2016-11-03 | 2021-12-14 | 3M Innovative Properties Company | Compositions including a photolatent amine, camphorquinone, and coumarin and related methods |
| WO2018085190A1 (en) * | 2016-11-03 | 2018-05-11 | 3M Innovative Properties Company | Polythiol sealant compositions |
| US10434704B2 (en) | 2017-08-18 | 2019-10-08 | Ppg Industries Ohio, Inc. | Additive manufacturing using polyurea materials |
| US12384097B2 (en) | 2017-08-18 | 2025-08-12 | Ppg Industries Ohio, Inc. | Additive manufacturing using reactive compositions |
| JP2020535257A (ja) * | 2017-09-26 | 2020-12-03 | スリーエム イノベイティブ プロパティズ カンパニー | 硬化性シーラント組成物、シールキャップ、並びにその作製方法及び使用 |
| CN111492026B (zh) | 2017-12-22 | 2023-01-13 | 3M创新有限公司 | 多层聚醚酮酮制品及其方法 |
| WO2019202472A2 (en) | 2018-04-17 | 2019-10-24 | 3M Innovative Properties Company | Conductive films |
| CN112236363B (zh) | 2018-06-07 | 2024-10-01 | 3M创新有限公司 | 雷击保护膜 |
| CN112262014A (zh) | 2018-06-15 | 2021-01-22 | 3M创新有限公司 | 组件和制备垫片的方法 |
| EP3877449A1 (en) * | 2018-11-09 | 2021-09-15 | 3M Innovative Properties Company | Curable sealant compositions, seal cap, and methods of making and using the same |
| KR102763793B1 (ko) | 2019-02-11 | 2025-02-05 | 피피지 인더스트리즈 오하이오 인코포레이티드 | 엘라스토머성 조성물 및 사용 방법 |
| EP3924167B1 (en) | 2019-02-11 | 2024-07-24 | PPG Industries Ohio Inc. | 3d printing of seal caps |
| CN113710481A (zh) | 2019-02-11 | 2021-11-26 | Ppg工业俄亥俄公司 | 多层系统和制造多层系统的方法 |
| CN118082177A (zh) | 2019-02-11 | 2024-05-28 | Ppg工业俄亥俄公司 | 制作耐化学性密封组件的方法 |
| US11015057B2 (en) * | 2019-04-03 | 2021-05-25 | Prc-Desoto International, Inc. | Dual-cure compositions |
| CN114080448A (zh) | 2019-07-08 | 2022-02-22 | 3M创新有限公司 | 清洁和抛光流体及其使用方法 |
| EP4003708A1 (en) | 2019-07-25 | 2022-06-01 | 3M Innovative Properties Company | Methods of shimming an assembly |
| US12428559B2 (en) | 2019-11-15 | 2025-09-30 | 3M Innovative Properties Company | Curable compositions and methods of making and using the same |
| CN113929908B (zh) * | 2021-09-28 | 2023-08-04 | 武汉纺织大学 | 一种生物基抗菌胶粘剂及其制备方法 |
| KR20240153332A (ko) * | 2022-03-01 | 2024-10-22 | 나믹스 가부시끼가이샤 | 수지 조성물, 접착제, 봉지재, 경화물, 반도체 장치 및 전자 부품 |
| KR102495856B1 (ko) * | 2022-03-31 | 2023-02-06 | 김용환 | 사상 시스템 |
Family Cites Families (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3923748A (en) * | 1973-11-12 | 1975-12-02 | Prod Res & Chem Corp | Mercaptan terminated polymers and method therefor |
| JP3083307B2 (ja) * | 1990-01-12 | 2000-09-04 | 旭電化工業株式会社 | 光学的造形用樹脂組成物 |
| US5236967A (en) | 1990-01-12 | 1993-08-17 | Asahi Denka Kogyo K.K. | Optical molding resin composition comprising polythiol-polyene compounds |
| JPH05194672A (ja) | 1992-01-23 | 1993-08-03 | Mitsubishi Petrochem Co Ltd | 高屈折率光学材料 |
| JPH08143747A (ja) | 1994-11-24 | 1996-06-04 | San Medical Kk | 複合充填材、複合充填材の製造法及びそれらを用いた歯科用レジンの組成物 |
| DE69942571D1 (de) | 1998-04-23 | 2010-08-26 | Dentsply Detrey Gmbh | Lagerungsbeständige polymerisierbare Zusammensetzung |
| EP1272147B1 (en) * | 2000-04-03 | 2006-06-21 | 3M Innovative Properties Company | Dental materials with extendable work time, kits, and methods |
| US7097883B2 (en) | 2003-06-05 | 2006-08-29 | Ppg Industries Ohio, Inc. | Low temperature liquid polythioether polymers |
| US7390859B2 (en) | 2005-02-08 | 2008-06-24 | Ppg Industries Ohio, Inc. | Compositions and methods of making compositions exhibiting fuel resistance |
| DE102005010327A1 (de) | 2005-03-03 | 2006-09-07 | Basf Ag | Ratikalisch härtbare Beschichtungsmassen |
| US9243083B2 (en) | 2008-04-03 | 2016-01-26 | Henkel IP & Holding GmbH | Thiol-ene cured oil-resistant polyacrylate sealants for in-place gasketing applications |
| US8921490B2 (en) | 2009-06-30 | 2014-12-30 | Henkel US IP LLC | Ultrafast heat/room temperature adhesive composition for bonding applications |
| DE102009046251A1 (de) | 2009-10-30 | 2011-05-19 | Evonik Röhm Gmbh | Reaktive 1-Komponenten-Fahrbahnmarkierung |
| US20110319559A1 (en) | 2010-06-25 | 2011-12-29 | PRC-DeSolo International, Inc. | Polythioether polymers, methods for preparation thereof, and compositions comprising them |
| US8932685B2 (en) | 2010-08-13 | 2015-01-13 | Prc-Desoto International, Inc. | Methods for making cured sealants by actinic radiation and related compositions |
| CN102896869B (zh) | 2011-07-25 | 2016-03-02 | 汉高股份有限公司 | 利用紫外辐照固化-氧化还原固化粘合剂体系粘结基底的方法 |
| IN2014DN02047A (enExample) | 2011-10-03 | 2015-05-15 | Synthes Gmbh | |
| WO2013090988A1 (en) | 2011-12-22 | 2013-06-27 | Commonwealth Scientific And Industrial Research Organisation | Light triggered cure on demand sealants |
| KR20140146145A (ko) | 2012-04-02 | 2014-12-24 | 쓰리엠 이노베이티브 프로퍼티즈 컴파니 | 폴리티오에테르 실란트 |
| WO2014066315A1 (en) | 2012-10-26 | 2014-05-01 | Henkel US IP LLC | Adhesive compositions |
| CN105073837B (zh) | 2013-03-13 | 2017-11-10 | 3M创新有限公司 | 具有基于炔烃的键的可辐射固化的聚硫醚 |
| CA2906350A1 (en) * | 2013-03-13 | 2014-10-09 | 3M Innovative Properties Company | Polythioether sealants |
| MX2015013169A (es) | 2013-03-15 | 2015-12-15 | 3M Innovative Properties Co | Compuestos benzotiazol-2-ilazo-fenilo como colorante, composiciones que incluyen el colorante y metodo para determinar el grado de curado de esas composiciones. |
| WO2014172305A1 (en) | 2013-04-15 | 2014-10-23 | 3M Innovative Properties Company | Light weight seal cap |
| PL3090006T3 (pl) | 2013-12-30 | 2018-03-30 | 3M Innovative Properties Company | Kompozycje zawierające politiol, nienasycony związek chemiczny i barwnik oraz sposoby powiązane z takimi kompozycjami |
-
2015
- 2015-12-22 EP EP15828442.2A patent/EP3237494B1/en active Active
- 2015-12-22 WO PCT/US2015/067450 patent/WO2016106352A1/en not_active Ceased
- 2015-12-22 JP JP2017531873A patent/JP7016698B2/ja active Active
- 2015-12-22 BR BR112017013742A patent/BR112017013742A2/pt not_active Application Discontinuation
- 2015-12-22 US US15/533,758 patent/US10703906B2/en active Active
- 2015-12-22 KR KR1020177020355A patent/KR20170097754A/ko not_active Withdrawn
- 2015-12-22 CA CA2970960A patent/CA2970960A1/en not_active Abandoned
- 2015-12-22 CN CN201580070296.7A patent/CN107108894B/zh active Active
-
2020
- 2020-06-12 US US16/946,253 patent/US11319440B2/en active Active
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20200016956A (ko) * | 2017-06-09 | 2020-02-17 | 피알시-데소토 인터내쇼날, 인코포레이티드 | 이중 경화 실란트 |
| US12559593B2 (en) | 2017-06-09 | 2026-02-24 | Prc-Desoto International, Inc. | Dual cure sealants |
Also Published As
| Publication number | Publication date |
|---|---|
| US11319440B2 (en) | 2022-05-03 |
| BR112017013742A2 (pt) | 2018-03-13 |
| CN107108894B (zh) | 2021-04-06 |
| EP3237494A1 (en) | 2017-11-01 |
| CA2970960A1 (en) | 2016-06-30 |
| US20170362434A1 (en) | 2017-12-21 |
| US10703906B2 (en) | 2020-07-07 |
| US20200308403A1 (en) | 2020-10-01 |
| WO2016106352A1 (en) | 2016-06-30 |
| JP2018501356A (ja) | 2018-01-18 |
| JP7016698B2 (ja) | 2022-02-07 |
| EP3237494B1 (en) | 2021-06-16 |
| CN107108894A (zh) | 2017-08-29 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US11319440B2 (en) | Dual cure polythioether | |
| EP2834287B1 (en) | Polythioether sealants | |
| KR20150131076A (ko) | 폴리티오에테르 실란트 | |
| CN105073837B (zh) | 具有基于炔烃的键的可辐射固化的聚硫醚 | |
| CN104031599B (zh) | 一种液体聚硫代醚橡胶和制备方法以及聚硫代醚密封胶和密封方法 | |
| CN1480439A (zh) | 乙烯基化合物及其固化产物 | |
| CN106715477A (zh) | 光固化性树脂组合物 | |
| CN109354685B (zh) | 一种耐极低温液体聚硫代醚橡胶 | |
| CN107493684B (zh) | 光固化性组合物 | |
| JP5839934B2 (ja) | 樹脂組成物及びその硬化物 | |
| US11072687B2 (en) | pH sensitive quantum dots for use as cure indicators | |
| JP7474961B2 (ja) | ビスマレイミド化合物とポリチオール化合物による光硬化樹脂 | |
| JP2022128119A (ja) | 樹脂組成物および該樹脂組成物からなるエラストマー材料 | |
| JP6511753B2 (ja) | 硬化型組成物 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PA0105 | International application |
Patent event date: 20170720 Patent event code: PA01051R01D Comment text: International Patent Application |
|
| PG1501 | Laying open of application | ||
| PC1203 | Withdrawal of no request for examination |