KR20170116114A - 내한성 실란트 및 그의 성분 - Google Patents
내한성 실란트 및 그의 성분 Download PDFInfo
- Publication number
- KR20170116114A KR20170116114A KR1020177025323A KR20177025323A KR20170116114A KR 20170116114 A KR20170116114 A KR 20170116114A KR 1020177025323 A KR1020177025323 A KR 1020177025323A KR 20177025323 A KR20177025323 A KR 20177025323A KR 20170116114 A KR20170116114 A KR 20170116114A
- Authority
- KR
- South Korea
- Prior art keywords
- polymer
- polythioether
- polythioether polymer
- formula
- chr
- 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- Withdrawn
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- 239000000565 sealant Substances 0.000 title claims abstract description 56
- 229920000642 polymer Polymers 0.000 claims abstract description 210
- 229920006295 polythiol Polymers 0.000 claims abstract description 200
- 150000001875 compounds Chemical class 0.000 claims abstract description 35
- 230000000087 stabilizing effect Effects 0.000 claims abstract description 34
- 239000000178 monomer Substances 0.000 claims abstract description 28
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 23
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 9
- 239000000203 mixture Substances 0.000 claims description 32
- 229920000647 polyepoxide Polymers 0.000 claims description 27
- 125000004122 cyclic group Chemical group 0.000 claims description 22
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 22
- 239000004593 Epoxy Substances 0.000 claims description 16
- 229910052760 oxygen Inorganic materials 0.000 claims description 16
- 229910052717 sulfur Inorganic materials 0.000 claims description 16
- 239000003795 chemical substances by application Substances 0.000 claims description 15
- 239000000463 material Substances 0.000 claims description 14
- 229920001577 copolymer Polymers 0.000 claims description 11
- 150000004662 dithiols Chemical class 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 9
- 239000011541 reaction mixture Substances 0.000 claims description 6
- 229910052799 carbon Inorganic materials 0.000 claims description 5
- 239000004848 polyfunctional curative Substances 0.000 claims description 2
- 150000003568 thioethers Chemical class 0.000 claims 1
- 238000003860 storage Methods 0.000 abstract description 11
- 239000004568 cement Substances 0.000 abstract description 2
- 238000002360 preparation method Methods 0.000 abstract description 2
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 description 24
- 150000001993 dienes Chemical class 0.000 description 20
- 239000007787 solid Substances 0.000 description 19
- 238000003756 stirring Methods 0.000 description 17
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 14
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 238000000034 method Methods 0.000 description 11
- 125000003118 aryl group Chemical group 0.000 description 9
- FFHWGQQFANVOHV-UHFFFAOYSA-N dimethyldioxirane Chemical compound CC1(C)OO1 FFHWGQQFANVOHV-UHFFFAOYSA-N 0.000 description 9
- 238000003786 synthesis reaction Methods 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 7
- 229910052757 nitrogen Inorganic materials 0.000 description 7
- 239000012973 diazabicyclooctane Substances 0.000 description 6
- -1 thiol epoxide Chemical class 0.000 description 6
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 3
- 239000003431 cross linking reagent Substances 0.000 description 3
- 238000002425 crystallisation Methods 0.000 description 3
- 230000008025 crystallization Effects 0.000 description 3
- 125000003396 thiol group Chemical group [H]S* 0.000 description 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 2
- 239000002318 adhesion promoter Substances 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- 125000005842 heteroatom Chemical group 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 230000004584 weight gain Effects 0.000 description 2
- 235000019786 weight gain Nutrition 0.000 description 2
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 description 1
- KUBDPQJOLOUJRM-UHFFFAOYSA-N 2-(chloromethyl)oxirane;4-[2-(4-hydroxyphenyl)propan-2-yl]phenol Chemical compound ClCC1CO1.C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 KUBDPQJOLOUJRM-UHFFFAOYSA-N 0.000 description 1
- OSDWBNJEKMUWAV-UHFFFAOYSA-N Allyl chloride Chemical compound ClCC=C OSDWBNJEKMUWAV-UHFFFAOYSA-N 0.000 description 1
- 229920003319 Araldite® Polymers 0.000 description 1
- 101500000959 Bacillus anthracis Protective antigen PA-20 Proteins 0.000 description 1
- 101000836394 Homo sapiens Sestrin-1 Proteins 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- 101000701286 Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) Alkanesulfonate monooxygenase Proteins 0.000 description 1
- 102100027288 Sestrin-1 Human genes 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- 101000983349 Solanum commersonii Osmotin-like protein OSML13 Proteins 0.000 description 1
- 101000983338 Solanum commersonii Osmotin-like protein OSML15 Proteins 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XUCHXOAWJMEFLF-UHFFFAOYSA-N bisphenol F diglycidyl ether Chemical compound C1OC1COC(C=C1)=CC=C1CC(C=C1)=CC=C1OCC1CO1 XUCHXOAWJMEFLF-UHFFFAOYSA-N 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical class C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 1
- VLXBWPOEOIIREY-UHFFFAOYSA-N dimethyl diselenide Natural products C[Se][Se]C VLXBWPOEOIIREY-UHFFFAOYSA-N 0.000 description 1
- WQOXQRCZOLPYPM-UHFFFAOYSA-N dimethyl disulfide Chemical compound CSSC WQOXQRCZOLPYPM-UHFFFAOYSA-N 0.000 description 1
- 150000002118 epoxides Chemical class 0.000 description 1
- 229920006332 epoxy adhesive Polymers 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000002828 fuel tank Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000010099 solid forming Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 230000003442 weekly effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/10—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and singly-bound oxygen atoms bound to the same carbon skeleton
- C07C323/11—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and singly-bound oxygen atoms bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton
- C07C323/12—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and singly-bound oxygen atoms bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated
-
- 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
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C321/00—Thiols, sulfides, hydropolysulfides or polysulfides
- C07C321/12—Sulfides, hydropolysulfides, or polysulfides having thio groups bound to acyclic carbon atoms
- C07C321/14—Sulfides, hydropolysulfides, or polysulfides having thio groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C321/00—Thiols, sulfides, hydropolysulfides or polysulfides
- C07C321/12—Sulfides, hydropolysulfides, or polysulfides having thio groups bound to acyclic carbon atoms
- C07C321/18—Sulfides, hydropolysulfides, or polysulfides having thio groups bound to acyclic carbon atoms of an acyclic unsaturated carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/10—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and singly-bound oxygen atoms bound to the same carbon skeleton
- C07C323/11—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and singly-bound oxygen atoms bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton
- C07C323/14—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and singly-bound oxygen atoms bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and unsaturated
-
- 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
- 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
-
- 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
-
- 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
- C08G75/12—Polythioether-ethers
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Sealing Material Composition (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Epoxy Resins (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201562116019P | 2015-02-13 | 2015-02-13 | |
| US62/116,019 | 2015-02-13 | ||
| PCT/US2016/017347 WO2016130673A1 (en) | 2015-02-13 | 2016-02-10 | Cold-tolerant sealants and components thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20170116114A true KR20170116114A (ko) | 2017-10-18 |
Family
ID=55587328
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020177025323A Withdrawn KR20170116114A (ko) | 2015-02-13 | 2016-02-10 | 내한성 실란트 및 그의 성분 |
Country Status (8)
| Country | Link |
|---|---|
| US (2) | US10287466B2 (enExample) |
| EP (1) | EP3256512B1 (enExample) |
| JP (2) | JP6715853B2 (enExample) |
| KR (1) | KR20170116114A (enExample) |
| CN (1) | CN107207426B (enExample) |
| BR (1) | BR112017017414A2 (enExample) |
| CA (1) | CA2976436A1 (enExample) |
| WO (1) | WO2016130673A1 (enExample) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2017044704A1 (en) | 2015-09-10 | 2017-03-16 | 3M Innovative Properties Company | Polymerizable compositions, polymerized compositions, and methods of making and using the same |
| JP6875519B2 (ja) * | 2016-11-04 | 2021-05-26 | ピーアールシー−デソト インターナショナル，インコーポレイティド | 硫黄含有ポリ（アルケニル）エーテル、硫黄含有ポリエーテル（アルケニル）エーテルを包含するプレポリマー及びその使用 |
| EP3822298A1 (en) | 2016-12-13 | 2021-05-19 | 3M Innovative Properties Co. | Epoxy stabilization using substituted barbituric acids |
| EP3555169A1 (en) | 2016-12-13 | 2019-10-23 | 3M Innovative Properties Company | Epoxy stabilization using acid-coated nitrogen-containing catalysts, particles, and methods |
| WO2018112130A1 (en) | 2016-12-14 | 2018-06-21 | 3M Innovative Properties Company | Sealant tape |
| US20210062858A1 (en) | 2017-09-26 | 2021-03-04 | 3M Innovative Properties Company | Curable sealant compositions, seal cap, and methods of making and using the same |
| US11396583B2 (en) | 2017-12-07 | 2022-07-26 | Nouryon Chemicals International B.V. | Process for the preparation of a polythioethersulfide |
| WO2019123260A2 (en) | 2017-12-19 | 2019-06-27 | 3M Innovative Properties Company | Multi-part composition having staged viscosity prior to hardening |
| US20210024793A1 (en) | 2018-03-16 | 2021-01-28 | 3M Innovative Properties Company | Compositions, method of bonding, and assembly |
| WO2019175709A1 (en) | 2018-03-16 | 2019-09-19 | 3M Innovative Properties Company | Compositions, method of bonding, and bonded assembly |
| EP3807043A1 (en) | 2018-06-15 | 2021-04-21 | 3M Innovative Properties Company | Assemblies and methods of making a shim |
| EP3856816A1 (en) | 2018-09-25 | 2021-08-04 | 3M Innovative Properties Company | Polymeric material including uretdione-containing material, polythiol, and acidic stabilizer, two-part compositions, and methods |
| WO2020065456A1 (en) | 2018-09-25 | 2020-04-02 | 3M Innovative Properties Company | One-part thermally curable composition |
| WO2020095153A1 (en) | 2018-11-09 | 2020-05-14 | 3M Innovative Properties Company | Curable sealant compositions, seal cap, and methods of making and using the same |
| US20220258848A1 (en) | 2019-07-25 | 2022-08-18 | 3M Innovative Properties Company | Methods of shimming an assembly |
| WO2021094887A1 (en) | 2019-11-15 | 2021-05-20 | 3M Innovative Properties Company | Curable compositions and methods of making and using the same |
| WO2021124033A1 (en) | 2019-12-19 | 2021-06-24 | 3M Innovative Properties Company | Two-part compositions including a uretdione-containing material and inorganic filler, products, and methods |
| JP7613861B2 (ja) | 2020-09-23 | 2025-01-15 | サトーホールディングス株式会社 | Ｒｆｉｄラベル及びｒｆｉｄラベルの使用方法 |
| CN113913150B (zh) * | 2021-11-18 | 2023-03-14 | 中国航发北京航空材料研究院 | 用于飞机钣金件的贴合面密封剂 |
| US20260027675A1 (en) | 2022-03-21 | 2026-01-29 | 3M Innovative Properties Company | Curable composition, treated backing, coated abrasive articles including the same, and methods of making and using the same |
| US20250196292A1 (en) | 2022-03-21 | 2025-06-19 | 3M Innovative Properties Company | Curable composition, coated abrasive article containing the same, and methods of making and using the same |
| WO2025200154A1 (en) | 2024-03-29 | 2025-10-02 | 3M Innovative Properties Company | Two-part epoxy composition comprising thiol curative, and catalyst |
Family Cites Families (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2664414A (en) | 1952-03-08 | 1953-12-29 | Shell Dev | Monomers and polymers of unsaturated thioethers |
| GB1276362A (en) | 1968-05-21 | 1972-06-01 | Aquitaine Petrole | Synthesis of halogenated thioethers |
| CH628074A5 (de) | 1977-03-10 | 1982-02-15 | Ciba Geigy Ag | Haertbare mischungen auf basis von epoxidverbindungen. |
| US4366307A (en) | 1980-12-04 | 1982-12-28 | Products Research & Chemical Corp. | Liquid polythioethers |
| US4609762A (en) | 1984-01-30 | 1986-09-02 | Products Research & Chemical Corp. | Thioethers having a high sulfur content and method therefor |
| JPH0477576A (ja) * | 1990-07-13 | 1992-03-11 | Tatsuta Electric Wire & Cable Co Ltd | 圧電ブザー及びその電極形成用塗料 |
| US5415794A (en) * | 1990-12-28 | 1995-05-16 | Institut Francais Du Petrole | New sulfured compounds, their preparation and their use as additives for lubricating oils |
| FR2671080B1 (fr) * | 1990-12-28 | 1994-05-27 | Inst Francais Du Petrole | Nouveaux composes sulfures, leur preparation et leur utilisation comme additifs pour huile lubrifiantes. |
| US5225472A (en) | 1992-05-19 | 1993-07-06 | Courtaulds Aerospace, Inc. | Low viscosity polythiol and method therefor |
| DE69318369T2 (de) | 1992-10-22 | 1999-01-28 | Ajinomoto Co., Inc., Tokio/Tokyo | Polythiol-Epoxidharz-Mischung mit längerer Verarbeitungszeit |
| US5464910A (en) | 1993-12-22 | 1995-11-07 | Shikoku Chemicals Corporation | Epoxy resin adduct combined with a borate ester and phenolic compound |
| US5593795A (en) | 1995-05-01 | 1997-01-14 | Minnesota Mining And Manufacturing Company | Polymer electrolyte composition based upon thiol-ene chemistry |
| US5912319A (en) | 1997-02-19 | 1999-06-15 | Courtaulds Aerospace, Inc. | Compositions and method for producing fuel resistant liquid polythioether polymers with good low temperature flexibility |
| ATE243232T1 (de) * | 1997-02-19 | 2003-07-15 | Prc Desoto Int Inc | Zusammensetzung und verfahren zur herstellung von flüssiger, treibstoffbeständiger polymere mit hoher biegsamkeit bei tiefer temperatur |
| US6372849B2 (en) | 1997-02-19 | 2002-04-16 | Prc-Desoto International, Inc. | Sealants and potting formulations including polymers produced by the reaction of a polythiol and polyvinyl ether monomer |
| US6509418B1 (en) | 1997-02-19 | 2003-01-21 | Prc-Desoto International, Inc. | Sealants and potting formulations including mercapto-terminated polymers produced by the reaction of a polythiol and polyvinyl ether monomer |
| US5959071A (en) | 1998-03-31 | 1999-09-28 | Courtaulds Aerospace, Inc. | Composition and method for producing polythioethers having pendent methyl chains |
| JP4704573B2 (ja) | 1999-05-10 | 2011-06-15 | スリーエム イノベイティブ プロパティズ カンパニー | エン−チオールエラストマーを作成するための組成物 |
| ATE297429T1 (de) | 2000-03-09 | 2005-06-15 | Advanced Chemistry And Technol | Hochfeste polymere und raumfahrtversiegelungen daraus |
| MXPA02012550A (es) * | 2000-06-30 | 2004-05-05 | Prc De Soto International Inc | Formulaciones obturantes y encapsulantes que incluyen polimeros producidos por la reaccion de un politiol y monomero polivinil eter. |
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2016
- 2016-02-10 JP JP2017542145A patent/JP6715853B2/ja active Active
- 2016-02-10 CN CN201680009517.4A patent/CN107207426B/zh not_active Expired - Fee Related
- 2016-02-10 BR BR112017017414-6A patent/BR112017017414A2/pt not_active Application Discontinuation
- 2016-02-10 EP EP16711038.6A patent/EP3256512B1/en active Active
- 2016-02-10 CA CA2976436A patent/CA2976436A1/en not_active Abandoned
- 2016-02-10 US US15/545,849 patent/US10287466B2/en not_active Expired - Fee Related
- 2016-02-10 KR KR1020177025323A patent/KR20170116114A/ko not_active Withdrawn
- 2016-02-10 WO PCT/US2016/017347 patent/WO2016130673A1/en not_active Ceased
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2019
- 2019-05-01 US US16/400,092 patent/US10544339B2/en active Active
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2020
- 2020-06-10 JP JP2020100997A patent/JP6972238B2/ja active Active
Also Published As
| Publication number | Publication date |
|---|---|
| WO2016130673A1 (en) | 2016-08-18 |
| CN107207426A (zh) | 2017-09-26 |
| JP6972238B2 (ja) | 2021-11-24 |
| EP3256512A1 (en) | 2017-12-20 |
| CA2976436A1 (en) | 2016-08-18 |
| JP2018506543A (ja) | 2018-03-08 |
| US10544339B2 (en) | 2020-01-28 |
| BR112017017414A2 (pt) | 2018-04-03 |
| JP6715853B2 (ja) | 2020-07-01 |
| CN107207426B (zh) | 2020-02-14 |
| US20180016480A1 (en) | 2018-01-18 |
| US10287466B2 (en) | 2019-05-14 |
| EP3256512B1 (en) | 2022-07-20 |
| US20190256752A1 (en) | 2019-08-22 |
| JP2020158778A (ja) | 2020-10-01 |
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