KR20130131402A - 경화성 접착제 조성물 - Google Patents
경화성 접착제 조성물 Download PDFInfo
- Publication number
- KR20130131402A KR20130131402A KR1020137018858A KR20137018858A KR20130131402A KR 20130131402 A KR20130131402 A KR 20130131402A KR 1020137018858 A KR1020137018858 A KR 1020137018858A KR 20137018858 A KR20137018858 A KR 20137018858A KR 20130131402 A KR20130131402 A KR 20130131402A
- Authority
- KR
- South Korea
- Prior art keywords
- adhesive composition
- curable adhesive
- epoxy
- carbon atoms
- weight percent
- 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.)
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- 239000000853 adhesive Substances 0.000 title claims abstract description 210
- 230000001070 adhesive effect Effects 0.000 title claims abstract description 210
- 239000000203 mixture Substances 0.000 title claims abstract description 204
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 108
- 239000003822 epoxy resin Substances 0.000 claims abstract description 87
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 87
- -1 polyol compound Chemical class 0.000 claims abstract description 61
- 229920005862 polyol Polymers 0.000 claims abstract description 35
- 150000003141 primary amines Chemical class 0.000 claims abstract description 12
- 150000003335 secondary amines Chemical class 0.000 claims abstract description 12
- 150000003573 thiols Chemical class 0.000 claims abstract description 12
- 125000003700 epoxy group Chemical group 0.000 claims abstract description 8
- 239000003921 oil Substances 0.000 claims description 67
- 239000000463 material Substances 0.000 claims description 43
- 239000000758 substrate Substances 0.000 claims description 40
- 239000003607 modifier Substances 0.000 claims description 35
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- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 18
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 15
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- 125000001931 aliphatic group Chemical group 0.000 claims description 9
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- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 7
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- 230000007797 corrosion Effects 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 3
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- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 2
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- RREANTFLPGEWEN-MBLPBCRHSA-N 7-[4-[[(3z)-3-[4-amino-5-[(3,4,5-trimethoxyphenyl)methyl]pyrimidin-2-yl]imino-5-fluoro-2-oxoindol-1-yl]methyl]piperazin-1-yl]-1-cyclopropyl-6-fluoro-4-oxoquinoline-3-carboxylic acid Chemical compound COC1=C(OC)C(OC)=CC(CC=2C(=NC(\N=C/3C4=CC(F)=CC=C4N(CN4CCN(CC4)C=4C(=CC=5C(=O)C(C(O)=O)=CN(C=5C=4)C4CC4)F)C\3=O)=NC=2)N)=C1 RREANTFLPGEWEN-MBLPBCRHSA-N 0.000 claims 1
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- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 17
- 125000000466 oxiranyl group Chemical group 0.000 description 17
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- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 12
- 125000003277 amino group Chemical group 0.000 description 12
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 12
- 238000012360 testing method Methods 0.000 description 11
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- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 7
- 238000003466 welding Methods 0.000 description 7
- 229920000049 Carbon (fiber) Polymers 0.000 description 6
- 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 6
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 6
- 239000004917 carbon fiber Substances 0.000 description 6
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 6
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- 239000002904 solvent Substances 0.000 description 6
- 239000003981 vehicle Substances 0.000 description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 5
- 125000000732 arylene group Chemical group 0.000 description 5
- 238000011109 contamination Methods 0.000 description 5
- 239000012784 inorganic fiber Substances 0.000 description 5
- 239000000314 lubricant Substances 0.000 description 5
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 5
- 239000004848 polyfunctional curative Substances 0.000 description 5
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 4
- UMILHIMHKXVDGH-UHFFFAOYSA-N Triethylene glycol diglycidyl ether Chemical group C1OC1COCCOCCOCCOCC1CO1 UMILHIMHKXVDGH-UHFFFAOYSA-N 0.000 description 4
- 239000002318 adhesion promoter Substances 0.000 description 4
- 150000008064 anhydrides Chemical class 0.000 description 4
- ZCCIPPOKBCJFDN-UHFFFAOYSA-N calcium nitrate Chemical compound [Ca+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ZCCIPPOKBCJFDN-UHFFFAOYSA-N 0.000 description 4
- 125000005708 carbonyloxy group Chemical group [*:2]OC([*:1])=O 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- 229960005237 etoglucid Drugs 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
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- 125000002560 nitrile group Chemical group 0.000 description 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 4
- 125000001476 phosphono group Chemical group [H]OP(*)(=O)O[H] 0.000 description 4
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- CYFLXLSBHQBMFT-UHFFFAOYSA-N sulfamoxole Chemical group O1C(C)=C(C)N=C1NS(=O)(=O)C1=CC=C(N)C=C1 CYFLXLSBHQBMFT-UHFFFAOYSA-N 0.000 description 4
- 235000007586 terpenes Nutrition 0.000 description 4
- 125000004149 thio group Chemical group *S* 0.000 description 4
- 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 3
- FVCSARBUZVPSQF-UHFFFAOYSA-N 5-(2,4-dioxooxolan-3-yl)-7-methyl-3a,4,5,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound C1C(C(OC2=O)=O)C2C(C)=CC1C1C(=O)COC1=O FVCSARBUZVPSQF-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
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- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
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- QLBRROYTTDFLDX-UHFFFAOYSA-N [3-(aminomethyl)cyclohexyl]methanamine Chemical compound NCC1CCCC(CN)C1 QLBRROYTTDFLDX-UHFFFAOYSA-N 0.000 description 3
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- 239000011159 matrix material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000010297 mechanical methods and process Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- RTWNYYOXLSILQN-UHFFFAOYSA-N methanediamine Chemical group NCN RTWNYYOXLSILQN-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- QYDYPVFESGNLHU-KHPPLWFESA-N methyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC QYDYPVFESGNLHU-KHPPLWFESA-N 0.000 description 1
- 229940073769 methyl oleate Drugs 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
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- 239000002480 mineral oil Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- 229940094933 n-dodecane Drugs 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 229960002446 octanoic acid Drugs 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- NDLPOXTZKUMGOV-UHFFFAOYSA-N oxo(oxoferriooxy)iron hydrate Chemical compound O.O=[Fe]O[Fe]=O NDLPOXTZKUMGOV-UHFFFAOYSA-N 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920002587 poly(1,3-butadiene) polymer Polymers 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920005594 polymer fiber Polymers 0.000 description 1
- 150000007519 polyprotic acids Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 229920000909 polytetrahydrofuran Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 150000003839 salts Chemical group 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229960001866 silicon dioxide Drugs 0.000 description 1
- 239000002210 silicon-based material Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 238000005476 soldering Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 229910002029 synthetic silica gel Inorganic materials 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 229960001124 trientine Drugs 0.000 description 1
- DQWPFSLDHJDLRL-UHFFFAOYSA-N triethyl phosphate Chemical compound CCOP(=O)(OCC)OCC DQWPFSLDHJDLRL-UHFFFAOYSA-N 0.000 description 1
- RXPQRKFMDQNODS-UHFFFAOYSA-N tripropyl phosphate Chemical compound CCCOP(=O)(OCCC)OCCC RXPQRKFMDQNODS-UHFFFAOYSA-N 0.000 description 1
- DSROZUMNVRXZNO-UHFFFAOYSA-K tris[(1-naphthalen-1-yl-3-phenylnaphthalen-2-yl)oxy]alumane Chemical compound C=1C=CC=CC=1C=1C=C2C=CC=CC2=C(C=2C3=CC=CC=C3C=CC=2)C=1O[Al](OC=1C(=C2C=CC=CC2=CC=1C=1C=CC=CC=1)C=1C2=CC=CC=C2C=CC=1)OC(C(=C1C=CC=CC1=C1)C=2C3=CC=CC=C3C=CC=2)=C1C1=CC=CC=C1 DSROZUMNVRXZNO-UHFFFAOYSA-K 0.000 description 1
- 239000004762 twaron Substances 0.000 description 1
- RSJKGSCJYJTIGS-UHFFFAOYSA-N undecane Chemical compound CCCCCCCCCCC RSJKGSCJYJTIGS-UHFFFAOYSA-N 0.000 description 1
- 229940005605 valeric acid Drugs 0.000 description 1
- DJXRIQMCROIRCZ-XOEOCAAJSA-N vibegron Chemical compound C1([C@H]([C@@H]2N[C@H](CC=3C=CC(NC(=O)[C@H]4N5C(=O)C=CN=C5CC4)=CC=3)CC2)O)=CC=CC=C1 DJXRIQMCROIRCZ-XOEOCAAJSA-N 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000010456 wollastonite Substances 0.000 description 1
- 229910052882 wollastonite Inorganic materials 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
Classifications
-
- 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
- C09J163/00—Adhesives based on epoxy resins; Adhesives based on derivatives of epoxy resins
-
- 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
-
- 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/182—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing using pre-adducts of epoxy compounds with curing agents
-
- 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/182—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing using pre-adducts of epoxy compounds with curing agents
- C08G59/186—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing using pre-adducts of epoxy compounds with curing agents with acids
-
- 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
- C09J5/00—Adhesive processes in general; Adhesive processes not provided for elsewhere, e.g. relating to primers
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Epoxy Resins (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP10196904.6 | 2010-12-23 | ||
| EP10196904A EP2468792A1 (en) | 2010-12-23 | 2010-12-23 | Curable adhesive composition |
| PCT/US2011/063254 WO2012087546A1 (en) | 2010-12-23 | 2011-12-05 | Curable adhesive composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20130131402A true KR20130131402A (ko) | 2013-12-03 |
Family
ID=44232849
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020137018858A Withdrawn KR20130131402A (ko) | 2010-12-23 | 2011-12-05 | 경화성 접착제 조성물 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20130255879A1 (enExample) |
| EP (2) | EP2468792A1 (enExample) |
| JP (1) | JP2014501303A (enExample) |
| KR (1) | KR20130131402A (enExample) |
| CN (1) | CN103270073A (enExample) |
| WO (1) | WO2012087546A1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20200058438A (ko) * | 2017-09-12 | 2020-05-27 | 디디피 스페셜티 일렉트로닉 머티리얼즈 유에스, 인크. | 1액형 강화 에폭시 접착제 |
Families Citing this family (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103184022B (zh) * | 2011-12-30 | 2017-09-19 | 汉高股份有限及两合公司 | 用于硅片制备中的暂时性粘合用粘合剂组合物 |
| AR098268A1 (es) | 2013-11-18 | 2016-05-18 | Rohm & Haas | Composición adhesiva |
| AR098267A1 (es) | 2013-11-18 | 2016-05-18 | Rohm & Haas | Poliéster terminado en epoxi |
| AR098269A1 (es) * | 2013-11-18 | 2016-05-18 | Rohm & Haas | Poliéster terminado en epoxi |
| AR098270A1 (es) | 2013-11-18 | 2016-05-18 | Rohm & Haas | Poliéster terminado en epoxi |
| CN106471421B (zh) * | 2014-07-03 | 2019-07-09 | 3M创新有限公司 | 具有减小的边缘侵入和改善的颜色稳定性的量子点制品 |
| WO2016130455A1 (en) * | 2015-02-11 | 2016-08-18 | Dow Global Technologies Llc | Low temperature curable adhesives and use thereof |
| EP3262092B1 (en) * | 2015-02-27 | 2019-01-02 | 3M Innovative Properties Company | Two-part adhesive including toughened curative |
| US20170096577A1 (en) * | 2015-10-01 | 2017-04-06 | PRC-DeSoto International. Inc. | Primer-less coated substrates |
| EP3170657B1 (en) | 2015-11-19 | 2020-09-09 | 3M Innovative Properties Company | Multilayer structural adhesive film |
| EP3170860B1 (en) | 2015-11-19 | 2020-07-29 | 3M Innovative Properties Company | Structural adhesive with improved corrosion resistance |
| ES2887114T5 (en) | 2016-05-12 | 2025-03-05 | 3M Innovative Properties Company | Structural adhesive film |
| EP3385297A1 (en) | 2017-04-04 | 2018-10-10 | 3M Innovative Properties Company | Epoxy-silicone hybrid sealant composition with low shrinkage and lower postcuring properties with chemical resistance for aerospace applications |
| MX2020008332A (es) | 2018-02-09 | 2020-09-21 | Ppg Ind Ohio Inc | Composiciones de recubrimiento. |
| CN111770947A (zh) * | 2018-02-12 | 2020-10-13 | 3M创新有限公司 | 可固化组合物、由其制得的制品，及其制造和使用方法 |
| CN112424300A (zh) * | 2018-06-14 | 2021-02-26 | 3M创新有限公司 | 用于可固化组合物的增粘剂 |
| US20210340311A1 (en) * | 2018-11-19 | 2021-11-04 | 3M Innovative Properties Company | Polymer comprising hydroxy groups and tertiary amine groups suitable for use as a catalyst |
| EP3677560A1 (en) | 2019-01-03 | 2020-07-08 | Sika Technology Ag | Modified oxyalkilamines as shrinkage reducing agents in cementitious compositions |
| JP7256642B2 (ja) * | 2019-01-07 | 2023-04-12 | 日東電工株式会社 | 粘接着シート |
| KR102273807B1 (ko) * | 2019-03-14 | 2021-07-06 | 주식회사 케이씨씨 | 아민-아마이드 수지 조성물 및 이의 제조 방법 |
| WO2020191579A1 (en) * | 2019-03-25 | 2020-10-01 | 3M Innovative Properties Company | Curable compositions, articles therefrom, and methods of making and using same |
| CN114127151A (zh) * | 2019-04-03 | 2022-03-01 | 汉高股份有限及两合公司 | 基于改性环氧树脂的双组分(2k)组合物 |
| US20220185949A1 (en) * | 2019-04-25 | 2022-06-16 | 3M Innovative Properties Company | Adhesion promoters for structural adhesive applications |
| US20220177753A1 (en) * | 2019-05-15 | 2022-06-09 | Dow Global Technologies Llc | Two-component adhesive compositions, articles prepared with same and preparation methods thereof |
| EP4017897A1 (en) * | 2019-08-23 | 2022-06-29 | PRC-Desoto International, Inc. | Coating compositions |
| EP3798246B1 (en) * | 2019-09-27 | 2024-01-31 | Henkel AG & Co. KGaA | One component (1k) composition based on modified epoxy resin |
| CN110728078B (zh) * | 2019-11-14 | 2022-11-25 | 吉林大学 | 一种基于胶粘剂化学特性的粘接结构在全服役温度区间下的力学性能的预测方法 |
| US20240124754A1 (en) * | 2019-11-15 | 2024-04-18 | Zephyros, Inc. | Methods and Compositions for Adhering to Low Surface Energy Materials |
| WO2021124051A1 (en) * | 2019-12-16 | 2021-06-24 | 3M Innovative Properties Company | Two-part curable adhesive |
| CN115427477B (zh) | 2020-04-28 | 2024-09-24 | 3M创新有限公司 | 可固化组合物 |
| CN114867787B (zh) * | 2020-07-22 | 2022-12-06 | 株式会社有泽制作所 | 热固性树脂组合物、覆盖膜、粘接片材及柔性印刷布线板 |
| WO2022053954A2 (en) * | 2020-09-11 | 2022-03-17 | 3M Innovative Properties Company | Color stable epoxy compositions |
| CN112812721B (zh) * | 2021-02-08 | 2022-12-06 | Sika技术股份公司 | 可固化的环氧树脂组合物 |
| CN113150700B (zh) * | 2021-03-25 | 2022-03-04 | 湖南神力铃胶粘剂制造有限公司 | 一种耐黄变、低粘度、可亲水固化的环氧石材修补面胶及其制备方法 |
| CN113831062A (zh) * | 2021-11-12 | 2021-12-24 | 深圳市华厦环境科技有限公司 | 无机固废固化剂专用粘合剂及其制备方法 |
| CN114316807B (zh) * | 2021-12-15 | 2023-06-02 | 武汉市科达云石护理材料有限公司 | 一种低粘度耐黄变快固石材面胶及其制备方法与应用 |
| EP4245786B1 (en) * | 2022-03-15 | 2024-08-28 | Basf Se | New epoxy resin composition for use as structural adhesive |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4197389A (en) * | 1977-07-18 | 1980-04-08 | Hoechst Aktiengesellschaft | Hardening agent for aqueous epoxy resin compositions |
| JPS5657820A (en) * | 1979-10-18 | 1981-05-20 | Semedain Kk | Curable epoxy resin composition |
| DE3674902D1 (de) | 1985-06-26 | 1990-11-15 | Dow Chemical Co | Mit rubber modifizierte epoxyzusammensetzungen. |
| CN1033283A (zh) * | 1987-11-21 | 1989-06-07 | 青岛港务局环境工程研究所 | 油面胶粘剂 |
| DE19525826C1 (de) * | 1995-07-15 | 1996-10-24 | Herberts Gmbh | Wäßriges zweikomponentiges Überzugsmittel und dessen Verwendung bei Verfahren zur Herstellung von Mehrschichtlackierungen |
| EA000908B1 (ru) | 1995-08-29 | 2000-06-26 | Эксон Кемикэл Пейтентс Инк. | Стойкий к излучению полипропилен и изделия из него |
| CN1096479C (zh) * | 1996-03-11 | 2002-12-18 | 万迪科股份公司 | 含有可水处理的多胺硬化剂的可固化环氧树脂组合物 |
| DE19630277A1 (de) * | 1996-07-26 | 1998-01-29 | Hoechst Ag | Härter für wasserverdünnbare Epoxidharzsysteme mit Topfzeit-Anzeige |
| JP4358505B2 (ja) * | 2000-06-21 | 2009-11-04 | 三井化学株式会社 | プラスチック製液晶表示セル用シール剤組成物 |
| US6632872B1 (en) | 2000-09-19 | 2003-10-14 | 3M Innovative Properties Company | Adhesive compositions including self-assembling molecules, adhesives, articles, and methods |
| EP1328567A1 (en) * | 2000-10-26 | 2003-07-23 | Vantico AG | High functional polymers |
| US6916505B2 (en) * | 2003-03-04 | 2005-07-12 | Air Products And Chemicals, Inc. | Mannich based adducts as water based epoxy curing agents with fast cure capabilities for green concrete application |
| KR101719019B1 (ko) * | 2009-09-11 | 2017-03-22 | 쓰리엠 이노베이티브 프로퍼티즈 컴파니 | 경화성 및 경화된 접착제 조성물 |
-
2010
- 2010-12-23 EP EP10196904A patent/EP2468792A1/en not_active Withdrawn
-
2011
- 2011-12-05 JP JP2013546179A patent/JP2014501303A/ja active Pending
- 2011-12-05 EP EP11794609.5A patent/EP2655469A1/en not_active Withdrawn
- 2011-12-05 WO PCT/US2011/063254 patent/WO2012087546A1/en not_active Ceased
- 2011-12-05 CN CN2011800617148A patent/CN103270073A/zh active Pending
- 2011-12-05 KR KR1020137018858A patent/KR20130131402A/ko not_active Withdrawn
- 2011-12-05 US US13/993,201 patent/US20130255879A1/en not_active Abandoned
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20200058438A (ko) * | 2017-09-12 | 2020-05-27 | 디디피 스페셜티 일렉트로닉 머티리얼즈 유에스, 인크. | 1액형 강화 에폭시 접착제 |
Also Published As
| Publication number | Publication date |
|---|---|
| CN103270073A (zh) | 2013-08-28 |
| EP2468792A1 (en) | 2012-06-27 |
| JP2014501303A (ja) | 2014-01-20 |
| EP2655469A1 (en) | 2013-10-30 |
| WO2012087546A1 (en) | 2012-06-28 |
| US20130255879A1 (en) | 2013-10-03 |
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Patent event date: 20130718 Patent event code: PA01051R01D Comment text: International Patent Application |
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| WITN | Application deemed withdrawn, e.g. because no request for examination was filed or no examination fee was paid |