DE2056080A1 - Hartbare Epoxyharzzubereitungen - Google Patents
Hartbare EpoxyharzzubereitungenInfo
- Publication number
- DE2056080A1 DE2056080A1 DE19702056080 DE2056080A DE2056080A1 DE 2056080 A1 DE2056080 A1 DE 2056080A1 DE 19702056080 DE19702056080 DE 19702056080 DE 2056080 A DE2056080 A DE 2056080A DE 2056080 A1 DE2056080 A1 DE 2056080A1
- Authority
- DE
- Germany
- Prior art keywords
- epoxy resin
- groups
- molecular weight
- polymeric
- epoxy resins
- 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.)
- Pending
Links
- 239000003822 epoxy resin Substances 0.000 title claims description 45
- 229920000647 polyepoxide Polymers 0.000 title claims description 45
- 238000002360 preparation method Methods 0.000 title claims description 11
- 239000012948 isocyanate Substances 0.000 claims description 16
- 239000003607 modifier Substances 0.000 claims description 16
- 150000002513 isocyanates Chemical class 0.000 claims description 15
- 239000000463 material Substances 0.000 claims description 11
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 7
- 229920000642 polymer Polymers 0.000 claims description 7
- 125000001931 aliphatic group Chemical group 0.000 claims description 6
- 239000002981 blocking agent Substances 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 239000001257 hydrogen Substances 0.000 claims description 5
- 125000003118 aryl group Chemical group 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 150000005846 sugar alcohols Polymers 0.000 claims description 3
- 239000007795 chemical reaction product Substances 0.000 claims description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims 1
- 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 21
- 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 16
- 239000000047 product Substances 0.000 description 14
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 12
- 239000000203 mixture Substances 0.000 description 12
- 230000001070 adhesive effect Effects 0.000 description 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 10
- 239000000853 adhesive Substances 0.000 description 9
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 9
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 8
- NEJMTSWXTZREOC-UHFFFAOYSA-N 4-sulfanylbutan-1-ol Chemical compound OCCCCS NEJMTSWXTZREOC-UHFFFAOYSA-N 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 5
- 235000011187 glycerol Nutrition 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 150000002739 metals Chemical class 0.000 description 5
- 229920000728 polyester Polymers 0.000 description 5
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical group SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 4
- 235000011037 adipic acid Nutrition 0.000 description 4
- 239000001361 adipic acid Substances 0.000 description 4
- -1 aliphatic isocyanates Chemical class 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- 229920002857 polybutadiene Polymers 0.000 description 4
- 239000004848 polyfunctional curative Substances 0.000 description 4
- 150000003077 polyols Chemical class 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- LCZVSXRMYJUNFX-UHFFFAOYSA-N 2-[2-(2-hydroxypropoxy)propoxy]propan-1-ol Chemical compound CC(O)COC(C)COC(C)CO LCZVSXRMYJUNFX-UHFFFAOYSA-N 0.000 description 3
- 239000004593 Epoxy Substances 0.000 description 3
- 239000004952 Polyamide Substances 0.000 description 3
- 239000004721 Polyphenylene oxide Substances 0.000 description 3
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 3
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical class C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 3
- 229910052736 halogen Chemical group 0.000 description 3
- 150000002367 halogens Chemical group 0.000 description 3
- 229920002647 polyamide Polymers 0.000 description 3
- 229920000570 polyether Polymers 0.000 description 3
- 229920005862 polyol Polymers 0.000 description 3
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- 229920000459 Nitrile rubber Polymers 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- 229920003006 Polybutadiene acrylonitrile Polymers 0.000 description 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- NTXGQCSETZTARF-UHFFFAOYSA-N buta-1,3-diene;prop-2-enenitrile Chemical compound C=CC=C.C=CC#N NTXGQCSETZTARF-UHFFFAOYSA-N 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- DGTNSSLYPYDJGL-UHFFFAOYSA-N phenyl isocyanate Chemical compound O=C=NC1=CC=CC=C1 DGTNSSLYPYDJGL-UHFFFAOYSA-N 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- 229920001451 polypropylene glycol Polymers 0.000 description 2
- 229920001021 polysulfide Polymers 0.000 description 2
- 239000005077 polysulfide Substances 0.000 description 2
- 150000008117 polysulfides Polymers 0.000 description 2
- 229920006295 polythiol Polymers 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- SMTQKQLZBRJCLI-UHFFFAOYSA-N (2-cyanatophenyl) cyanate Chemical compound N#COC1=CC=CC=C1OC#N SMTQKQLZBRJCLI-UHFFFAOYSA-N 0.000 description 1
- ALQLPWJFHRMHIU-UHFFFAOYSA-N 1,4-diisocyanatobenzene Chemical compound O=C=NC1=CC=C(N=C=O)C=C1 ALQLPWJFHRMHIU-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- ROHTVIURAJBDES-UHFFFAOYSA-N 2-n,2-n-bis(prop-2-enyl)-1,3,5-triazine-2,4,6-triamine Chemical compound NC1=NC(N)=NC(N(CC=C)CC=C)=N1 ROHTVIURAJBDES-UHFFFAOYSA-N 0.000 description 1
- PHRRYVOQWOVNLF-UHFFFAOYSA-N 3-sulfanylbutan-1-ol Chemical compound CC(S)CCO PHRRYVOQWOVNLF-UHFFFAOYSA-N 0.000 description 1
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 1
- OKUJJVAASUSBCG-UHFFFAOYSA-N 5-sulfanylpentan-1-ol Chemical compound OCCCCCS OKUJJVAASUSBCG-UHFFFAOYSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- 229910014033 C-OH Inorganic materials 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 229910014570 C—OH Inorganic materials 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- 229920002396 Polyurea Polymers 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910001854 alkali hydroxide Inorganic materials 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- HDFRDWFLWVCOGP-UHFFFAOYSA-N carbonothioic O,S-acid Chemical class OC(S)=O HDFRDWFLWVCOGP-UHFFFAOYSA-N 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000007872 degassing Methods 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 150000004662 dithiols Chemical class 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- QOHMWDJIBGVPIF-UHFFFAOYSA-N n',n'-diethylpropane-1,3-diamine Chemical compound CCN(CC)CCCN QOHMWDJIBGVPIF-UHFFFAOYSA-N 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920001289 polyvinyl ether Polymers 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000001730 thiiranyl group Chemical group 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
-
- 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
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/67—Unsaturated compounds having active hydrogen
- C08G18/69—Polymers of conjugated dienes
-
- 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
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/67—Unsaturated compounds having active hydrogen
- C08G18/69—Polymers of conjugated dienes
- C08G18/696—Polymers of conjugated dienes containing heteroatoms other than oxygen and other than the heteroatoms of copolymerised vinyl monomers
-
- 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
- C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
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)
- Polyurethanes Or Polyureas (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US87744669A | 1969-11-17 | 1969-11-17 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2056080A1 true DE2056080A1 (de) | 1971-05-27 |
Family
ID=25369979
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19702056080 Pending DE2056080A1 (de) | 1969-11-17 | 1970-11-14 | Hartbare Epoxyharzzubereitungen |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US3636133A (enExample) |
| JP (1) | JPS4949199B1 (enExample) |
| BE (1) | BE758976A (enExample) |
| DE (1) | DE2056080A1 (enExample) |
| FR (1) | FR2069357A5 (enExample) |
| GB (1) | GB1329112A (enExample) |
| NL (1) | NL7016563A (enExample) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3134496A1 (de) * | 1980-09-02 | 1982-06-24 | Texaco Development Corp., 10650 White Plains, N.Y. | "polyole, verfahren zu ihrer herstellung und zur herstellung von polyurethanschaeumen" |
| DE3134493A1 (de) * | 1980-09-02 | 1982-06-24 | Texaco Development Corp., 10650 White Plains, N.Y. | Polyole, verfahren zu ihrer herstellung und zur herstellung von polyisocyanuratschaeumen |
| DE3134492A1 (de) * | 1980-09-02 | 1982-07-01 | Texaco Development Corp., 10650 White Plains, N.Y. | "aminopolyole, verfahren zu ihrer herstellung und zur herstellung von polyurethanschaeumen" |
| EP0630929A1 (en) * | 1993-05-17 | 1994-12-28 | Nippon Paint Co., Ltd. | Soft segment-containing modified epoxy resin and cathodic electrodeposition paints containing same |
Families Citing this family (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA997495A (en) * | 1972-08-14 | 1976-09-21 | Witco Chemical Corporation | Amine terminated polyurethane urea polymers cured with epoxides |
| US3931116A (en) * | 1972-08-14 | 1976-01-06 | Witco Chemical Corporation | Curable amine-terminated polyurethane-urea-epoxide lacquers |
| JPS4959839A (enExample) * | 1972-10-11 | 1974-06-11 | ||
| US4000214A (en) * | 1973-05-29 | 1976-12-28 | Reichhold Chemicals, Inc. | Urethane additive to a standard epoxy resin to improve adhesion to vinyl materials |
| DE2418041C3 (de) * | 1974-04-13 | 1982-04-29 | Schering Ag, 1000 Berlin Und 4619 Bergkamen | Verfahren zur Herstellung von elastifizierten Formteilen nach Flächengebilden |
| US3886228A (en) * | 1974-06-03 | 1975-05-27 | Amicon Corp | Polyurethane composition curable with polyamine/acid anhydride adduct |
| US4073776A (en) * | 1975-01-28 | 1978-02-14 | Schenectady Chemicals, Inc. | Tackifiers for elastomers |
| US4111917A (en) * | 1976-05-11 | 1978-09-05 | W. R. Grace & Co. | Use of latent amines to cure epoxy resins |
| US4130546A (en) * | 1976-10-19 | 1978-12-19 | Hitachi Chemical Company, Ltd. | Thermosetting resin composition |
| JPS5356294A (en) * | 1976-10-30 | 1978-05-22 | Hitachi Chem Co Ltd | Thermosetting resin composition |
| DE2735047A1 (de) * | 1977-08-03 | 1979-02-15 | Bayer Ag | Arylsulfonsaeurealkylestergruppen aufweisende polyurethane |
| US4137276A (en) * | 1977-08-19 | 1979-01-30 | National Starch And Chemical Corporation | Flexible film laminating adhesives |
| US4482671A (en) * | 1980-03-21 | 1984-11-13 | Scm Corporation | Base for a graft polymer, novel graft polymer compositions, solvent and water-reducible coatings incorporating the novel graft polymers, and processes for making them |
| US4399241A (en) * | 1980-03-21 | 1983-08-16 | Scm Corporation | Base for a graft polymer, novel graft polymer compositions, solvents and water-reducible coatings incorporating the novel graft polymers, and processes for making them |
| US4423201A (en) * | 1982-10-29 | 1983-12-27 | Celanese Corporation | Co-reactive urethane surfactants and stable aqueous epoxy dispersions |
| US4520144A (en) * | 1984-02-06 | 1985-05-28 | Desoto, Inc. | Polydimethylsiloxane-modified polyepoxides |
| JPS60260620A (ja) * | 1984-06-08 | 1985-12-23 | Yokohama Rubber Co Ltd:The | 防食材組成物 |
| US4613660A (en) * | 1985-02-19 | 1986-09-23 | Ashland Oil, Inc. | Polyol/polyepoxide/polyurethane adhesive |
| US4726868A (en) * | 1985-02-19 | 1988-02-23 | Ashland Oil, Inc. | Polyol/polyepoxide/polyurethane adhesive |
| GB2176197B (en) * | 1985-05-31 | 1989-10-25 | Ashland Oil Inc | Vapour permeation curable coatings comprising polymercapto compounds and polyisocyanate curing agents |
| US4786693A (en) * | 1985-10-18 | 1988-11-22 | The Dow Chemical Company | Vinyl ester resins prepared from urethane modified epoxy resin compositions containing oxazolidinone or thiazolidinone groups |
| US4742146A (en) * | 1985-10-18 | 1988-05-03 | The Dow Chemical Company | Urethane modified epoxy resin compositions containing oxazolidinone or thiazolidinone groups |
| US4766183A (en) * | 1986-01-27 | 1988-08-23 | Essex Specialty Products, Inc. | Thermosetting composition for an interpenetrating polymer network system |
| US5686541A (en) * | 1995-11-14 | 1997-11-11 | National Science Council | Modification of epoxy resins with urethane prepolymer for electronic encapsulation |
| DE602005020260D1 (de) * | 2005-06-02 | 2010-05-12 | Dow Global Technologies Inc | Schlagzähmodifizierter Strukturklebstoff auf Epoxid Basis |
| CN101517029B (zh) * | 2006-07-31 | 2013-10-16 | 汉高股份及两合公司 | 可固化的环氧树脂-基粘合剂组合物 |
| KR20090080956A (ko) * | 2006-10-06 | 2009-07-27 | 헨켈 아게 운트 코. 카게아아 | 발수성의 펌핑가능한 에폭시 페이스트 접착제 |
| CN101821333A (zh) * | 2007-07-26 | 2010-09-01 | 汉高公司 | 可固化的环氧树脂基粘合剂组合物 |
| US20090104448A1 (en) * | 2007-10-17 | 2009-04-23 | Henkel Ag & Co. Kgaa | Preformed adhesive bodies useful for joining substrates |
| EP2205692B1 (en) * | 2007-10-30 | 2020-02-19 | Henkel AG & Co. KGaA | Epoxy paste adhesives resistant to wash-off |
| US7847034B2 (en) * | 2008-03-20 | 2010-12-07 | Loctite (R&D) Limited | Adducts and curable compositions using same |
| CN112266753A (zh) * | 2020-10-09 | 2021-01-26 | 合肥精特仪表有限公司 | 一种含水测量装置用密封胶 |
| KR20240162504A (ko) * | 2022-03-25 | 2024-11-15 | 듀퐁 테크놀로지 (상하이) 컴퍼니 리미티드 | 2-성분 폴리우레탄 접착제 |
-
0
- BE BE758976D patent/BE758976A/xx unknown
-
1969
- 1969-11-17 US US877446A patent/US3636133A/en not_active Expired - Lifetime
-
1970
- 1970-11-12 NL NL7016563A patent/NL7016563A/xx unknown
- 1970-11-13 FR FR7040690A patent/FR2069357A5/fr not_active Expired
- 1970-11-14 DE DE19702056080 patent/DE2056080A1/de active Pending
- 1970-11-17 GB GB5469270A patent/GB1329112A/en not_active Expired
- 1970-11-17 JP JP45101423A patent/JPS4949199B1/ja active Pending
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3134496A1 (de) * | 1980-09-02 | 1982-06-24 | Texaco Development Corp., 10650 White Plains, N.Y. | "polyole, verfahren zu ihrer herstellung und zur herstellung von polyurethanschaeumen" |
| DE3134493A1 (de) * | 1980-09-02 | 1982-06-24 | Texaco Development Corp., 10650 White Plains, N.Y. | Polyole, verfahren zu ihrer herstellung und zur herstellung von polyisocyanuratschaeumen |
| DE3134492A1 (de) * | 1980-09-02 | 1982-07-01 | Texaco Development Corp., 10650 White Plains, N.Y. | "aminopolyole, verfahren zu ihrer herstellung und zur herstellung von polyurethanschaeumen" |
| EP0630929A1 (en) * | 1993-05-17 | 1994-12-28 | Nippon Paint Co., Ltd. | Soft segment-containing modified epoxy resin and cathodic electrodeposition paints containing same |
Also Published As
| Publication number | Publication date |
|---|---|
| FR2069357A5 (enExample) | 1971-09-03 |
| JPS4949199B1 (enExample) | 1974-12-25 |
| NL7016563A (enExample) | 1971-05-19 |
| US3636133A (en) | 1972-01-18 |
| GB1329112A (en) | 1973-09-05 |
| BE758976A (fr) | 1971-05-17 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2056080A1 (de) | Hartbare Epoxyharzzubereitungen | |
| EP0675143B1 (de) | Amin-modifizierte Epoxidharz-Zusammensetzung | |
| EP0338985B1 (de) | Modifizierte Epoxidharze | |
| EP2060592B1 (de) | Hitzehärtende Epoxidharzzusammensetzung enthaltend nichtaromatische Harnstoffe als Beschleuniger | |
| EP1648950B1 (de) | Hitzehärtende zusammensetzungen mit tieftemperatur-schlagzähigkeitsmodifikatoren | |
| EP1957554B1 (de) | Tieftemperatur-schlagzähe hitze-härtbare epoxidharzzusammensetzung mit epoxidfestharzen | |
| DE2152606C3 (de) | Härtbare Kunststoffmischungen | |
| DE3877231T2 (de) | Zusammensetzung aus polyurethanharz. | |
| EP0308664A1 (de) | Modifizierte Epoxidharze | |
| EP0307666A1 (de) | Phenol-terminierte Polyurethane oder Polyharnstoffe und Epoxidharze enthaltend diese Verbindungen | |
| DE2346404A1 (de) | Verfahren, um oberflaechen miteinander zu verbinden | |
| DE69025025T2 (de) | Polysulfid-Polyether und härtbare Zusammensetzungen | |
| DE3303387A1 (de) | Hitzehaertbare, epoxygruppen enthaltende zusammensetzungen | |
| EP0066167B1 (de) | Verfahren zur Herstellung von Mercaptogruppen aufweisenden Oligourethanen, sowie ihre Verwendung als Bindemittel für oxidativ härtbare Beschichtungs- und Dichtungsmassen bzw. als Zusatzmittel für Epoxidharze | |
| DE69108056T2 (de) | Polyoxazolidone. | |
| EP0819733A2 (de) | Amin-modifizierte Epoxidharz-Zusammensetzung | |
| WO2007020266A1 (de) | Aminogruppen-terminierte zähigkeitsverbesserer und deren folgeprodukte und verwendungen | |
| DE3624314A1 (de) | Verwendung von epoxidharz/haerter-mischungen zur herstellung von beschichtungen mit erhoehter zwischenschichthaftung | |
| DE2847102A1 (de) | Epoxidharzgemisch zur herstellung flexibler formstoffe | |
| EP0358603A2 (de) | Mit blockpolymeren modifizierte Epoxidharze | |
| DE10210625A1 (de) | Härtbare Harzmasse und neues latentes Härtungsmittel | |
| CH494257A (de) | Klebmittel, Kitte, Überzugsmittel oder Vergussmassen | |
| EP0566822B1 (de) | Flexible Härter | |
| DE19755031B4 (de) | Bei Raumtemperatur härtbare Epoxidharzmischungen und ihre Verwendung | |
| DE4141858A1 (de) | Mit mercaptoverbindungen vorverlaengerte bisphenol a-diglycidylether |