AU732525B2 - Curable resin compositions - Google Patents
Curable resin compositions Download PDFInfo
- Publication number
- AU732525B2 AU732525B2 AU40955/97A AU4095597A AU732525B2 AU 732525 B2 AU732525 B2 AU 732525B2 AU 40955/97 A AU40955/97 A AU 40955/97A AU 4095597 A AU4095597 A AU 4095597A AU 732525 B2 AU732525 B2 AU 732525B2
- Authority
- AU
- Australia
- Prior art keywords
- epoxy resin
- slump
- composition
- composition according
- hardener
- 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.)
- Ceased
Links
- 239000011342 resin composition Substances 0.000 title description 9
- 239000000203 mixture Substances 0.000 claims abstract description 161
- 239000004848 polyfunctional curative Substances 0.000 claims abstract description 68
- 239000003822 epoxy resin Substances 0.000 claims abstract description 61
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 61
- 229920002873 Polyethylenimine Polymers 0.000 claims abstract description 48
- 150000001412 amines Chemical class 0.000 claims abstract description 26
- 239000013008 thixotropic agent Substances 0.000 claims abstract description 14
- 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 claims abstract description 11
- 230000000694 effects Effects 0.000 claims abstract description 7
- 230000009974 thixotropic effect Effects 0.000 claims abstract description 7
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 6
- 229920001281 polyalkylene Polymers 0.000 claims abstract description 5
- 229920000768 polyamine Polymers 0.000 claims abstract description 5
- 125000004103 aminoalkyl group Chemical group 0.000 claims abstract description 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims abstract description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 14
- 239000000853 adhesive Substances 0.000 claims description 12
- 230000001070 adhesive effect Effects 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 12
- 229910002011 hydrophilic fumed silica Inorganic materials 0.000 claims description 9
- 238000001879 gelation Methods 0.000 claims description 7
- 239000013521 mastic Substances 0.000 claims description 5
- 239000000463 material Substances 0.000 claims description 5
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 4
- 239000000565 sealant Substances 0.000 claims description 4
- 230000015572 biosynthetic process Effects 0.000 claims description 3
- 238000000576 coating method Methods 0.000 claims description 3
- 230000000052 comparative effect Effects 0.000 claims description 3
- 239000008393 encapsulating agent Substances 0.000 claims description 3
- 239000011248 coating agent Substances 0.000 claims description 2
- 150000005846 sugar alcohols Polymers 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims 1
- 125000005263 alkylenediamine group Chemical group 0.000 abstract description 2
- 150000004982 aromatic amines Chemical class 0.000 abstract 1
- 238000002156 mixing Methods 0.000 description 35
- 229920005989 resin Polymers 0.000 description 35
- 239000011347 resin Substances 0.000 description 35
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 27
- 230000035882 stress Effects 0.000 description 16
- 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 15
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 13
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 11
- 235000019445 benzyl alcohol Nutrition 0.000 description 9
- 239000007788 liquid Substances 0.000 description 9
- 239000004593 Epoxy Substances 0.000 description 8
- 239000003085 diluting agent Substances 0.000 description 8
- 238000012360 testing method Methods 0.000 description 8
- -1 2 amino hydrogen Chemical class 0.000 description 7
- 238000010008 shearing Methods 0.000 description 7
- 229960001124 trientine Drugs 0.000 description 7
- 240000005428 Pistacia lentiscus Species 0.000 description 6
- 150000002118 epoxides Chemical class 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 230000014759 maintenance of location Effects 0.000 description 5
- 239000000377 silicon dioxide Substances 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 230000032683 aging Effects 0.000 description 4
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 4
- 239000007795 chemical reaction product Substances 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 239000011324 bead Substances 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000004850 liquid epoxy resins (LERs) Substances 0.000 description 3
- 235000015112 vegetable and seed oil Nutrition 0.000 description 3
- 239000008158 vegetable oil Substances 0.000 description 3
- RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 230000003068 static effect Effects 0.000 description 2
- 230000000007 visual effect Effects 0.000 description 2
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 description 1
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 1
- HVOBSBRYQIYZNY-UHFFFAOYSA-N 2-[2-(2-aminoethylamino)ethylamino]ethanol Chemical compound NCCNCCNCCO HVOBSBRYQIYZNY-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- ZAXCZCOUDLENMH-UHFFFAOYSA-N 3,3,3-tetramine Chemical compound NCCCNCCCNCCCN ZAXCZCOUDLENMH-UHFFFAOYSA-N 0.000 description 1
- UVLSCMIEPPWCHZ-UHFFFAOYSA-N 3-piperazin-1-ylpropan-1-amine Chemical compound NCCCN1CCNCC1 UVLSCMIEPPWCHZ-UHFFFAOYSA-N 0.000 description 1
- YBRVSVVVWCFQMG-UHFFFAOYSA-N 4,4'-diaminodiphenylmethane Chemical compound C1=CC(N)=CC=C1CC1=CC=C(N)C=C1 YBRVSVVVWCFQMG-UHFFFAOYSA-N 0.000 description 1
- 229910002012 Aerosil® Inorganic materials 0.000 description 1
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- MQJKPEGWNLWLTK-UHFFFAOYSA-N Dapsone Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=C1 MQJKPEGWNLWLTK-UHFFFAOYSA-N 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000003679 aging effect Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- IMUDHTPIFIBORV-UHFFFAOYSA-N aminoethylpiperazine Chemical compound NCCN1CCNCC1 IMUDHTPIFIBORV-UHFFFAOYSA-N 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- IUNMPGNGSSIWFP-UHFFFAOYSA-N dimethylaminopropylamine Chemical compound CN(C)CCCN IUNMPGNGSSIWFP-UHFFFAOYSA-N 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- KYBYPDUGGWLXNO-GRVYQHKQSA-N ethane-1,2-diamine;(9z,12z)-octadeca-9,12-dienoic acid Chemical compound NCCN.CCCCC\C=C/C\C=C/CCCCCCCC(O)=O.CCCCC\C=C/C\C=C/CCCCCCCC(O)=O KYBYPDUGGWLXNO-GRVYQHKQSA-N 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000010881 fly ash Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- GKQPCPXONLDCMU-CCEZHUSRSA-N lacidipine Chemical compound CCOC(=O)C1=C(C)NC(C)=C(C(=O)OCC)C1C1=CC=CC=C1\C=C\C(=O)OC(C)(C)C GKQPCPXONLDCMU-CCEZHUSRSA-N 0.000 description 1
- 239000003550 marker Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 1
- 238000007665 sagging Methods 0.000 description 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
- 239000012745 toughening agent Substances 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 239000000080 wetting agent Substances 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
- 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
- C08G59/40—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 characterised by the curing agents used
- C08G59/50—Amines
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Epoxy Resins (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Laminated Bodies (AREA)
- Paper (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB9621196.6A GB9621196D0 (en) | 1996-10-11 | 1996-10-11 | Curable resin compositions |
| GB9621196 | 1996-10-11 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU4095597A AU4095597A (en) | 1998-04-23 |
| AU732525B2 true AU732525B2 (en) | 2001-04-26 |
Family
ID=10801246
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU40955/97A Ceased AU732525B2 (en) | 1996-10-11 | 1997-10-10 | Curable resin compositions |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US6077886A (enExample) |
| EP (2) | EP0835910B1 (enExample) |
| JP (1) | JP3826334B2 (enExample) |
| AT (1) | ATE243727T1 (enExample) |
| AU (1) | AU732525B2 (enExample) |
| BR (1) | BR9705016A (enExample) |
| CA (1) | CA2217834C (enExample) |
| DE (1) | DE69723020T2 (enExample) |
| ES (1) | ES2202567T3 (enExample) |
| GB (1) | GB9621196D0 (enExample) |
| ID (1) | ID18836A (enExample) |
| IN (1) | IN213824B (enExample) |
| MY (1) | MY130974A (enExample) |
| TW (1) | TW347398B (enExample) |
| ZA (1) | ZA979097B (enExample) |
Families Citing this family (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20040101643A1 (en) * | 1996-11-26 | 2004-05-27 | National Starch And Chemical Limited | Adhesives containing FDA approved materials |
| ATE280037T1 (de) * | 2000-09-11 | 2004-11-15 | Huntsman Adv Mat Switzerland | Nahtloses modell und verfahren zur herstellung eines nahtlosen modells |
| US6650044B1 (en) * | 2000-10-13 | 2003-11-18 | Lumileds Lighting U.S., Llc | Stenciling phosphor layers on light emitting diodes |
| GB2383009A (en) * | 2001-12-14 | 2003-06-18 | Vantico Ag | Method of making models |
| JP4799416B2 (ja) | 2003-11-04 | 2011-10-26 | ハンツマン・アドヴァンスト・マテリアルズ・（スイッツランド）・ゲーエムベーハー | ２成分系の硬化可能な組成物 |
| EP1616924A1 (en) * | 2004-07-13 | 2006-01-18 | Huntsman Advanced Materials (Switzerland) GmbH | Fire retardant composition |
| CN101060962A (zh) * | 2004-11-17 | 2007-10-24 | 亨斯迈先进材料（瑞士）有限公司 | 制造耐高温模型或工具的方法 |
| JP4718220B2 (ja) * | 2005-03-30 | 2011-07-06 | 三洋化成工業株式会社 | コンクリート素地調整材 |
| JP2006312747A (ja) * | 2006-06-12 | 2006-11-16 | Sumitomo Osaka Cement Co Ltd | 成形用材料 |
| US9133306B2 (en) | 2007-04-26 | 2015-09-15 | Air Products And Chemicals, Inc. | Amine composition |
| WO2009025991A1 (en) * | 2007-08-17 | 2009-02-26 | Dow Global Technologies, Inc. | Two part crash durable epoxy adhesives |
| JP2010202686A (ja) * | 2009-02-27 | 2010-09-16 | Sumitomo Bakelite Co Ltd | 液状封止樹脂組成物および半導体パッケージ |
| BRPI1015170A2 (pt) * | 2009-04-24 | 2016-04-19 | Huntsman Adv Mat Switzerland | método para produzir uma temperatura ou molde, composição curável, e, uso de uma composição |
| BR112012008587A2 (pt) * | 2009-10-14 | 2016-04-05 | Henkel Ag & Co Kgaa | processo de distribuição homogênea para uma composição epóxi com teor de carga elevado |
| RU2462488C1 (ru) * | 2011-03-30 | 2012-09-27 | Государственное образовательное учреждение высшего профессионального образования "Мордовский государственный университет им. Н.П. Огарева" | Полимерная композиция |
| JP5746939B2 (ja) * | 2011-09-15 | 2015-07-08 | 株式会社ブリヂストン | 有機繊維コード用接着剤組成物及びそれを用いた接着方法、並びにゴム補強材及びタイヤ |
| EP2592100A1 (de) * | 2011-11-10 | 2013-05-15 | Sika Technology AG | Härter für epoxidharz-beschichtungen |
| KR20150003373A (ko) * | 2012-04-26 | 2015-01-08 | 다우 글로벌 테크놀로지스 엘엘씨 | 에폭시 접착제 조성물 |
| US20140127499A1 (en) * | 2012-11-02 | 2014-05-08 | Ashland Licensing And Intellectual Property Llc | Two Part Primer Composition |
| WO2014139982A1 (de) | 2013-03-11 | 2014-09-18 | Byk-Chemie Gmbh | Thixotropie-verstärkendes additiv und dieses enthaltende zusammensetzung |
| WO2014161638A1 (de) * | 2013-04-05 | 2014-10-09 | Fischerwerke Gmbh & Co. Kg | Biogene flüssige nichtreaktive verdünner in kunstharz-verklebungsmitteln |
| CN103320071B (zh) * | 2013-06-28 | 2015-08-12 | 上海悍马建筑科技有限公司 | 改性环氧透明裂缝封口胶 |
| US20170158838A1 (en) | 2014-06-24 | 2017-06-08 | Byk-Chemie, Gmbh | Polyurethane two-component or multi-component systems having a latent thickening tendency |
| EP3161058B1 (de) | 2014-06-24 | 2017-11-22 | BYK-Chemie GmbH | Acrylat-systeme mit latenter verdickungsneigung |
| CN106459563B (zh) * | 2014-06-24 | 2019-04-05 | 比克化学股份有限公司 | 具有潜在增稠趋势的环氧树脂-环氧固化体系 |
| US10392494B2 (en) | 2014-06-24 | 2019-08-27 | Byk-Chemie Gmbh | Latent thickeners, rheology control kit and multi-component systems |
| US20170152337A1 (en) | 2014-06-24 | 2017-06-01 | Byk-Chemie, Gmbh | Unsaturated polyester resin systems with latent thickening tendencies |
| US9670339B1 (en) | 2016-06-22 | 2017-06-06 | Byk Usa Inc. | Process of manufacturing thickeners and the use of thus produced thickeners in high-viscosity epoxy resin formulations |
| US9546252B1 (en) | 2016-06-22 | 2017-01-17 | Byk-Chemie Gmbh | Process of manufacturing thickeners and use of thus produced thickeners in high-viscosity unsaturated polyester containing formulations |
| US9637614B1 (en) | 2016-06-22 | 2017-05-02 | Byk Usa Inc. | Process of manufacturing thickeners and the use of thus produced thickeners in high-viscosity unsaturated polyester containing formulations |
| US9522981B1 (en) | 2016-06-22 | 2016-12-20 | Byk-Chemie Gmbh | Process of manufacturing thickeners and use of thus produced thickeners in high-viscosity non aqueous formulations |
| EP3381961B1 (en) | 2017-04-01 | 2020-11-11 | CliQ SwissTech (Netherlands) B.V. | A casting resin composition |
| WO2019222402A1 (en) * | 2018-05-15 | 2019-11-21 | Nd Industries, Inc. | Multifunctional coatings and adhesive compositions for fasteners |
| WO2021096556A1 (en) * | 2019-11-14 | 2021-05-20 | Nd Industries, Inc. | Adhesive compositions for anchoring fasteners |
| JP6736118B1 (ja) * | 2020-03-10 | 2020-08-05 | イイダ産業株式会社 | マスチック接着剤 |
| WO2021185898A1 (en) * | 2020-03-17 | 2021-09-23 | Byk-Chemie Gmbh | Rheology control agent |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60104173A (ja) * | 1983-11-11 | 1985-06-08 | Konishi Kk | ２成分系エポキシ樹脂接着用並びに充填用組成物 |
| JPH06345942A (ja) * | 1993-06-03 | 1994-12-20 | Shikoku Chem Corp | エポキシ樹脂組成物 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3939020A (en) * | 1969-09-18 | 1976-02-17 | John A. Caramanian | Method of balancing a rotor |
| US4238387A (en) * | 1978-11-20 | 1980-12-09 | E. I. Du Pont De Nemours And Company | Rheology control additive for paints |
| JPS605052A (ja) * | 1983-06-22 | 1985-01-11 | 花王株式会社 | セメント分散剤 |
| JP2678557B2 (ja) * | 1993-06-03 | 1997-11-17 | 四国化成工業株式会社 | エポキシ樹脂系塗材及びその調製方法 |
-
1996
- 1996-10-11 GB GBGB9621196.6A patent/GB9621196D0/en active Pending
-
1997
- 1997-10-09 MY MYPI97004739A patent/MY130974A/en unknown
- 1997-10-09 CA CA002217834A patent/CA2217834C/en not_active Expired - Fee Related
- 1997-10-09 IN IN2900DE1997 patent/IN213824B/en unknown
- 1997-10-09 TW TW86114825A patent/TW347398B/zh not_active IP Right Cessation
- 1997-10-09 US US08/947,997 patent/US6077886A/en not_active Expired - Lifetime
- 1997-10-10 EP EP97810763A patent/EP0835910B1/en not_active Expired - Lifetime
- 1997-10-10 ID IDP973411A patent/ID18836A/id unknown
- 1997-10-10 DE DE69723020T patent/DE69723020T2/de not_active Expired - Lifetime
- 1997-10-10 AU AU40955/97A patent/AU732525B2/en not_active Ceased
- 1997-10-10 ZA ZA9709097A patent/ZA979097B/xx unknown
- 1997-10-10 AT AT97810763T patent/ATE243727T1/de not_active IP Right Cessation
- 1997-10-10 EP EP03001380A patent/EP1314748A3/en not_active Withdrawn
- 1997-10-10 BR BR9705016A patent/BR9705016A/pt not_active Application Discontinuation
- 1997-10-10 ES ES97810763T patent/ES2202567T3/es not_active Expired - Lifetime
- 1997-10-13 JP JP29483197A patent/JP3826334B2/ja not_active Expired - Fee Related
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60104173A (ja) * | 1983-11-11 | 1985-06-08 | Konishi Kk | ２成分系エポキシ樹脂接着用並びに充填用組成物 |
| JPH06345942A (ja) * | 1993-06-03 | 1994-12-20 | Shikoku Chem Corp | エポキシ樹脂組成物 |
Also Published As
| Publication number | Publication date |
|---|---|
| ID18836A (id) | 1998-05-14 |
| JPH10130463A (ja) | 1998-05-19 |
| EP0835910B1 (en) | 2003-06-25 |
| JP3826334B2 (ja) | 2006-09-27 |
| EP1314748A3 (en) | 2009-07-29 |
| MY130974A (en) | 2007-07-31 |
| CA2217834A1 (en) | 1998-04-11 |
| AU4095597A (en) | 1998-04-23 |
| EP1314748A2 (en) | 2003-05-28 |
| IN1997DE02900A (enExample) | 2007-02-23 |
| GB9621196D0 (en) | 1996-11-27 |
| ATE243727T1 (de) | 2003-07-15 |
| IN213824B (enExample) | 2008-01-25 |
| ES2202567T3 (es) | 2004-04-01 |
| DE69723020D1 (de) | 2003-07-31 |
| ZA979097B (en) | 1998-05-11 |
| BR9705016A (pt) | 1998-12-29 |
| US6077886A (en) | 2000-06-20 |
| CA2217834C (en) | 2009-07-14 |
| DE69723020T2 (de) | 2004-04-01 |
| TW347398B (en) | 1998-12-11 |
| EP0835910A1 (en) | 1998-04-15 |
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