CN106471087B - 用于反渗透组件的聚氨酯粘合剂 - Google Patents
用于反渗透组件的聚氨酯粘合剂 Download PDFInfo
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- CN106471087B CN106471087B CN201580025242.9A CN201580025242A CN106471087B CN 106471087 B CN106471087 B CN 106471087B CN 201580025242 A CN201580025242 A CN 201580025242A CN 106471087 B CN106471087 B CN 106471087B
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- acid esters
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- 239000000853 adhesive Substances 0.000 title claims abstract description 231
- 230000001070 adhesive effect Effects 0.000 title claims abstract description 231
- 239000004814 polyurethane Substances 0.000 title claims abstract description 66
- 229920002635 polyurethane Polymers 0.000 title claims abstract description 66
- 238000001223 reverse osmosis Methods 0.000 title claims abstract description 37
- 239000000203 mixture Substances 0.000 claims abstract description 298
- 229920005862 polyol Polymers 0.000 claims abstract description 80
- 150000003077 polyols Chemical class 0.000 claims abstract description 80
- 239000004014 plasticizer Substances 0.000 claims abstract description 49
- 239000003054 catalyst Substances 0.000 claims abstract description 16
- 239000005056 polyisocyanate Substances 0.000 claims abstract description 14
- 229920001228 polyisocyanate Polymers 0.000 claims abstract description 14
- 239000004359 castor oil Substances 0.000 claims abstract description 13
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- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 claims abstract description 13
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims abstract description 12
- 239000002904 solvent Substances 0.000 claims abstract description 12
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims abstract description 11
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- 239000003085 diluting agent Substances 0.000 claims abstract description 9
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- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 6
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- PZTAGFCBNDBBFZ-UHFFFAOYSA-N tert-butyl 2-(hydroxymethyl)piperidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCCCC1CO PZTAGFCBNDBBFZ-UHFFFAOYSA-N 0.000 claims description 5
- ZFMQKOWCDKKBIF-UHFFFAOYSA-N bis(3,5-difluorophenyl)phosphane Chemical compound FC1=CC(F)=CC(PC=2C=C(F)C=C(F)C=2)=C1 ZFMQKOWCDKKBIF-UHFFFAOYSA-N 0.000 claims description 4
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- JCTXKRPTIMZBJT-UHFFFAOYSA-N 2,2,4-trimethylpentane-1,3-diol Chemical compound CC(C)C(O)C(C)(C)CO JCTXKRPTIMZBJT-UHFFFAOYSA-N 0.000 claims description 3
- RWLALWYNXFYRGW-UHFFFAOYSA-N 2-Ethyl-1,3-hexanediol Chemical compound CCCC(O)C(CC)CO RWLALWYNXFYRGW-UHFFFAOYSA-N 0.000 claims description 3
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- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 3
- YSRSBDQINUMTIF-UHFFFAOYSA-N decane-1,2-diol Chemical compound CCCCCCCCC(O)CO YSRSBDQINUMTIF-UHFFFAOYSA-N 0.000 claims description 3
- SITULKFUBJXOJH-UHFFFAOYSA-N diheptyl hexanedioate Chemical compound CCCCCCCOC(=O)CCCCC(=O)OCCCCCCC SITULKFUBJXOJH-UHFFFAOYSA-N 0.000 claims description 3
- WIYAGHSNPUBKDT-UHFFFAOYSA-N dinonyl hexanedioate Chemical compound CCCCCCCCCOC(=O)CCCCC(=O)OCCCCCCCCC WIYAGHSNPUBKDT-UHFFFAOYSA-N 0.000 claims description 3
- 229910021485 fumed silica Inorganic materials 0.000 claims description 3
- FHKSXSQHXQEMOK-UHFFFAOYSA-N hexane-1,2-diol Chemical compound CCCCC(O)CO FHKSXSQHXQEMOK-UHFFFAOYSA-N 0.000 claims description 3
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 claims description 3
- 239000000347 magnesium hydroxide Substances 0.000 claims description 3
- 229910001862 magnesium hydroxide Inorganic materials 0.000 claims description 3
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- KHLCTMQBMINUNT-UHFFFAOYSA-N octadecane-1,12-diol Chemical compound CCCCCCC(O)CCCCCCCCCCCO KHLCTMQBMINUNT-UHFFFAOYSA-N 0.000 claims description 3
- AEIJTFQOBWATKX-UHFFFAOYSA-N octane-1,2-diol Chemical compound CCCCCCC(O)CO AEIJTFQOBWATKX-UHFFFAOYSA-N 0.000 claims description 3
- 150000003014 phosphoric acid esters Chemical class 0.000 claims description 3
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- 150000001278 adipic acid derivatives Chemical class 0.000 claims description 2
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- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical class OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 2
- 150000003021 phthalic acid derivatives Chemical class 0.000 claims description 2
- 150000003329 sebacic acid derivatives Chemical class 0.000 claims description 2
- 150000003900 succinic acid esters Chemical class 0.000 claims description 2
- 125000005590 trimellitic acid group Chemical class 0.000 claims description 2
- -1 salt ions Chemical class 0.000 description 18
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- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 8
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 7
- 125000005442 diisocyanate group Chemical group 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 230000003204 osmotic effect Effects 0.000 description 6
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 5
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- 229920000570 polyether Polymers 0.000 description 5
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 4
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Chemical compound CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 4
- ZFOZVQLOBQUTQQ-UHFFFAOYSA-N Tributyl citrate Chemical compound CCCCOC(=O)CC(O)(C(=O)OCCCC)CC(=O)OCCCC ZFOZVQLOBQUTQQ-UHFFFAOYSA-N 0.000 description 4
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- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- YCZJVRCZIPDYHH-UHFFFAOYSA-N ditridecyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCCCCCC YCZJVRCZIPDYHH-UHFFFAOYSA-N 0.000 description 3
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- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/34—Silicon-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/34—Silicon-containing compounds
- C08K3/36—Silica
-
- 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
- C09J11/00—Features of adhesives not provided for in group C09J9/00, e.g. additives
- C09J11/02—Non-macromolecular additives
- C09J11/04—Non-macromolecular additives inorganic
-
- 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
- C09J175/04—Polyurethanes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2313/00—Details relating to membrane modules or apparatus
- B01D2313/04—Specific sealing means
- B01D2313/042—Adhesives or glues
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Water Supply & Treatment (AREA)
- Nanotechnology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Inorganic Chemistry (AREA)
- Wood Science & Technology (AREA)
- Materials Engineering (AREA)
- Adhesives Or Adhesive Processes (AREA)
Abstract
Description
Claims (36)
Applications Claiming Priority (3)
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US201461951714P | 2014-03-12 | 2014-03-12 | |
US61/951714 | 2014-03-12 | ||
PCT/US2015/019882 WO2015138561A1 (en) | 2014-03-12 | 2015-03-11 | Polyurethane adhesives for reverse osmosis modules |
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CN106471087A CN106471087A (zh) | 2017-03-01 |
CN106471087B true CN106471087B (zh) | 2020-07-07 |
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CN201580025242.9A Active CN106471087B (zh) | 2014-03-12 | 2015-03-11 | 用于反渗透组件的聚氨酯粘合剂 |
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US (1) | US9808765B2 (zh) |
KR (1) | KR102339480B1 (zh) |
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Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014194303A1 (en) | 2013-05-31 | 2014-12-04 | Cytec Industries, Inc. | Formulated polyurethane resin compositions for flood coating electronic circuit assemblies |
US10590318B2 (en) | 2014-11-26 | 2020-03-17 | Elantas Pdg, Inc. | Multi-part polyurethane compositions, articles thereof, and method of making |
BR112017021652B1 (pt) | 2015-04-09 | 2022-04-12 | Elantas Pdg, Inc | Adesivos de poliuretano para módulos de osmose reversa |
TWI698274B (zh) * | 2015-05-29 | 2020-07-11 | 日商住友化學股份有限公司 | 螺旋形酸性氣體分離膜元件、酸性氣體分離膜模組,以及酸性氣體分離裝置 |
CN107083229B (zh) * | 2017-05-12 | 2020-11-03 | 南京威邦新材料有限公司 | 一种水处理膜用双组分聚氨酯灌封胶的制备方法 |
WO2018232239A1 (en) * | 2017-06-15 | 2018-12-20 | Dow Global Technologies, Llc | Compositions containing hydrophobic modified isocyanate functional prepolymer containing adhesives |
US11046850B2 (en) * | 2017-09-27 | 2021-06-29 | Evonik Operations Gmbh | Mixed metal catalyst compositions and methods for making polyurethane foam |
CN111448236B (zh) * | 2017-12-27 | 2022-10-11 | 陶氏环球技术有限责任公司 | 用于黏附到金属和/或金属化基材的双组分无溶剂黏合剂组合物 |
CN109181621A (zh) * | 2018-09-11 | 2019-01-11 | 浙江奔富新能源股份有限公司 | 一种用于聚合物锂离子电池软包装膜的双组份聚氨酯树脂胶黏剂及其制备方法 |
WO2020069475A1 (en) * | 2018-09-28 | 2020-04-02 | Henkel IP & Holding GmbH | Polypropylene glycol-based pre-polymers for the isocyanate component of a two-component polyurethane adhesive for bonding membranes |
EP3856396A4 (en) * | 2018-09-28 | 2022-06-22 | Henkel IP & Holding GmbH | HYDROGENATED NATURAL OILS FOR THICKENING THE POLYOL COMPONENT OF A TWO-COMPONENT POLYURETHANE ADHESIVE FOR BONDING MEMBRANES |
EP3689929B1 (en) * | 2019-02-01 | 2023-06-28 | Henkel AG & Co. KGaA | Adhesive composition comprising a thixotropic agent |
CN117321167A (zh) * | 2021-05-10 | 2023-12-29 | 汉高股份有限及两合公司 | 绿色替代品聚氨酯粘合剂 |
CN114133911A (zh) * | 2021-12-23 | 2022-03-04 | 上海回天新材料有限公司 | 一种无溶剂双组分聚氨酯胶粘剂及其用途 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1558938A (zh) * | 2001-09-27 | 2004-12-29 | H��B��������ɺͽ��ڹ�˾ | 具有宽范围开模时间的热熔湿固化聚氨酯粘合剂 |
CN101842406A (zh) * | 2007-11-02 | 2010-09-22 | 日本聚氨酯工业株式会社 | 反应固化型聚氨酯树脂组合物、及使用该组合物的双组分反应固化型聚氨酯粘接剂 |
Family Cites Families (60)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3747037A (en) | 1968-01-11 | 1973-07-17 | Gen Electric | Petroleum based oil modified castor oil-urethane composition for electrical potting |
BE792621A (fr) | 1971-12-15 | 1973-03-30 | Western Electric Co | Procede et produit pour chasser l'eau infiltree dans des cablestelephoniques et analogues |
US3962094A (en) | 1973-09-18 | 1976-06-08 | The Dow Chemical Company | Hollow fiber separatory device |
US4008197A (en) | 1974-01-11 | 1977-02-15 | N L Industries, Inc. | Mineral oil extended polyurethane system containing a coupling agent for decontaminating and sealing the interior spaces of an insulated electrical device |
US4170559A (en) | 1976-11-05 | 1979-10-09 | N L Industries, Inc. | Hollow fiber separatory device |
US4224164A (en) | 1978-10-20 | 1980-09-23 | Nl Industries, Inc. | Non-wicking polyurethane casting systems |
US4168258A (en) | 1978-02-15 | 1979-09-18 | N L Industries, Inc. | Grease compatible, mineral oil extended polyurethane |
US4267044A (en) | 1978-04-10 | 1981-05-12 | Nl Industries, Inc. | Thixotropic polyurethane compositions as sealants for membrane separatory devices |
US4300184A (en) | 1979-07-11 | 1981-11-10 | Johnson Controls, Inc. | Conformal coating for electrical circuit assemblies |
BR8008833A (pt) | 1979-09-14 | 1981-06-23 | Minnesota Mining & Mfg | Adesivo ativavel pelo calor com aperfeicoada resistencia a temperatura |
US4256617A (en) | 1979-11-01 | 1981-03-17 | Nl Industries, Inc. | Catalyzed non-toxic polyurethane forming compositions and separatory devices employing the same |
US4284506A (en) | 1979-12-26 | 1981-08-18 | Nl Industries, Inc. | Biomedical devices |
US4395530A (en) | 1980-10-24 | 1983-07-26 | Colamco, Inc. | Catalyst initiated prepolymer systems |
DE3046409A1 (de) | 1980-12-10 | 1982-07-15 | Bayer Ag, 5090 Leverkusen | Beschichtungsmittel und ein verfahren zur herstellung von ueberzuegen |
US4375521A (en) | 1981-06-01 | 1983-03-01 | Communications Technology Corporation | Vegetable oil extended polyurethane systems |
US4454176A (en) | 1981-10-21 | 1984-06-12 | E. I. Du Pont De Nemours And Company | Supported reverse osmosis membranes |
US4444976A (en) | 1982-12-20 | 1984-04-24 | The Goodyear Tire & Rubber Company | Sag resistant two component adhesive and sealant |
US4518631A (en) | 1983-11-14 | 1985-05-21 | Dow Corning Corporation | Thixotropic curable coating compositions |
US4879032A (en) | 1984-06-04 | 1989-11-07 | Allied Resin Corporation | Fluid separatory devices having improved potting and adhesive compositions |
US4876303A (en) | 1984-06-15 | 1989-10-24 | American Telephone And Telegraph Company, At&T Bell Laboratories | Mineral-oil-free encapsulant composition |
US4603188A (en) | 1985-07-10 | 1986-07-29 | Itoh Seiyu Kabushiki Kaisha | Curable urethane composition |
US5266145A (en) | 1986-03-05 | 1993-11-30 | Teroson Gmbh | Sealant and adhesive |
US4923756A (en) | 1987-08-20 | 1990-05-08 | Ashland Oil, Inc. | Primerless adhesive for fiberglass reinforced polyester substrates |
US4865735A (en) | 1988-02-18 | 1989-09-12 | Caschem, Inc. | Amine containing polyurethane compositions for separatory devices |
US4886600A (en) | 1988-02-18 | 1989-12-12 | Caschem, Inc. | Moisture and glycerine resistant polyurethane compositions for separatory devices |
JPH01284303A (ja) | 1988-05-10 | 1989-11-15 | Asahi Chem Ind Co Ltd | 表面親水化高選択性透過膜とその製造方法 |
US4842736A (en) | 1988-09-06 | 1989-06-27 | Desalination Systems, Inc. | Spiral wound membrane |
JPH03217473A (ja) | 1990-01-23 | 1991-09-25 | Toyobo Co Ltd | 被覆剤組成物およびそれを用いた印刷配線板 |
CA2041532C (en) | 1991-04-30 | 2002-01-01 | Hamdy Khalil | Urethane sealant having improved sag properties |
DE4134693A1 (de) | 1991-10-21 | 1993-04-22 | Basf Ag | Transparente, heissdampfsterilisierbare, nicht zytotoxische, im wesentlichen kompakte polyurethan-vergussmassen, verfahren zu ihrer herstellung und ihre verwendung, insbesondere fuer medizinisch-technische artikel |
US5360543A (en) | 1992-06-05 | 1994-11-01 | Caschem, Inc. | Polyurethane compositions |
JP3340762B2 (ja) * | 1992-08-11 | 2002-11-05 | 横浜ゴム株式会社 | ケーブル接続部密封用混和物 |
US5556934A (en) | 1993-09-03 | 1996-09-17 | H. B. Fuller Licensing & Financing Inc. | Isocyanurate embedment compound |
US5863597A (en) | 1996-01-23 | 1999-01-26 | Sundstrand Corporation | Polyurethane conformal coating process for a printed wiring board |
US5871822A (en) | 1996-09-26 | 1999-02-16 | Honeywell Inc. | Low emissions method for spray application of conformal coating to electronic assemblies |
US6130268A (en) | 1997-06-23 | 2000-10-10 | Polyfoam Products, Inc. | Two component polyurethane construction adhesive |
DE10108025A1 (de) | 2001-02-19 | 2002-09-05 | Henkel Kgaa | Zweikomponentiger Polyurethan-Klebstoff für Holzwerkstoffe |
WO2002086977A1 (en) | 2001-04-23 | 2002-10-31 | Carmanah Technologies Inc. | Potted domed solar panel capsule and traffic warning lamps incorporating same |
EP1519782B1 (en) | 2002-06-21 | 2009-09-23 | GE Osmonics, Inc. | Blister protection for spiral wound elements |
US20040012936A1 (en) | 2002-07-18 | 2004-01-22 | Gravelin Pascal A. | Device and method for enclosure of electronic printed circuit board based products |
US20040072953A1 (en) | 2002-10-15 | 2004-04-15 | Ju-Ming Hung | Reactive hot melt adhesive with non-polymeric aliphatic difunctionals |
US6797799B1 (en) | 2003-04-02 | 2004-09-28 | Bayer Materialscience Llc | High 2,4′-diphenylmethane diisocyanate content prepolymers |
US7121647B2 (en) | 2003-10-03 | 2006-10-17 | Lexmark International, Inc. | Method of applying an encapsulant material to an ink jet printhead |
KR100603813B1 (ko) * | 2004-03-25 | 2006-07-26 | 코오롱유화주식회사 | 충격 흡수능 및 미끄럼 방지능이 우수한 폴리우레탄 트랙및 이의 시공방법 |
JP4548072B2 (ja) * | 2004-09-30 | 2010-09-22 | 横浜ゴム株式会社 | 2液硬化型ポリウレタン樹脂組成物 |
DE602007010346D1 (de) | 2006-12-21 | 2010-12-16 | Dow Global Technologies Inc | Zusammensetzung, die zur verwendung als klebstoff beim einbau von fahrzeugfenstern brauchbar ist |
EP2176312A1 (en) | 2007-08-06 | 2010-04-21 | Dow Global Technologies Inc. | Polyol blends and their use in making polymers |
US20110098417A1 (en) | 2007-09-21 | 2011-04-28 | Dow Global Technologies Inc. | Polyurethane polymer systems |
US7781513B2 (en) | 2007-11-14 | 2010-08-24 | Momentive Performance Materials Inc. | Two-part moisture-curable resin composition and adhesive, sealant and coating compositions based thereon |
US8349123B2 (en) | 2008-04-01 | 2013-01-08 | Henkel Corporation | High heat resistant adhesive and sealant compositions |
US8360390B2 (en) | 2009-01-13 | 2013-01-29 | Enphase Energy, Inc. | Method and apparatus for potting an electronic device |
CN103052666A (zh) | 2010-07-22 | 2013-04-17 | 建筑研究和技术有限公司 | 使用绿色预聚合物的密封剂和胶粘剂 |
US8822844B1 (en) | 2010-09-27 | 2014-09-02 | Rockwell Collins, Inc. | Shielding and potting for electrical circuits |
RU2608034C2 (ru) | 2011-09-02 | 2017-01-12 | Констракшн Рисёрч Энд Текнолоджи Гмбх | Полиуретановые системы, имеющие отсутствие оседания и способность окрашиваться |
CN102850989B (zh) | 2012-09-26 | 2014-04-09 | 贵阳时代沃顿科技有限公司 | 一种双组分聚氨酯胶粘剂及其制备方法 |
CN102911636B (zh) | 2012-09-26 | 2013-12-18 | 贵阳时代沃顿科技有限公司 | 一种双组分聚氨酯胶粘剂及其制备方法和应用 |
WO2014194303A1 (en) | 2013-05-31 | 2014-12-04 | Cytec Industries, Inc. | Formulated polyurethane resin compositions for flood coating electronic circuit assemblies |
US9832902B2 (en) | 2013-05-31 | 2017-11-28 | Elantas Pdg, Inc. | Formulated resin compositions for flood coating electronic circuit assemblies |
US10590318B2 (en) | 2014-11-26 | 2020-03-17 | Elantas Pdg, Inc. | Multi-part polyurethane compositions, articles thereof, and method of making |
BR112017021652B1 (pt) | 2015-04-09 | 2022-04-12 | Elantas Pdg, Inc | Adesivos de poliuretano para módulos de osmose reversa |
-
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- 2015-03-11 CN CN201580025242.9A patent/CN106471087B/zh active Active
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Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1558938A (zh) * | 2001-09-27 | 2004-12-29 | H��B��������ɺͽ��ڹ�˾ | 具有宽范围开模时间的热熔湿固化聚氨酯粘合剂 |
CN101842406A (zh) * | 2007-11-02 | 2010-09-22 | 日本聚氨酯工业株式会社 | 反应固化型聚氨酯树脂组合物、及使用该组合物的双组分反应固化型聚氨酯粘接剂 |
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