JP2007514858A - ポリウレタン系感圧接着剤および製造方法 - Google Patents
ポリウレタン系感圧接着剤および製造方法 Download PDFInfo
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- JP2007514858A JP2007514858A JP2006545707A JP2006545707A JP2007514858A JP 2007514858 A JP2007514858 A JP 2007514858A JP 2006545707 A JP2006545707 A JP 2006545707A JP 2006545707 A JP2006545707 A JP 2006545707A JP 2007514858 A JP2007514858 A JP 2007514858A
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- Prior art keywords
- isocyanate
- weight
- reactive
- parts
- polyurethane
- Prior art date
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- 239000004745 nonwoven fabric Substances 0.000 description 1
- OGJPXUAPXNRGGI-UHFFFAOYSA-N norfloxacin Chemical compound C1=C2N(CC)C=C(C(O)=O)C(=O)C2=CC(F)=C1N1CCNCC1 OGJPXUAPXNRGGI-UHFFFAOYSA-N 0.000 description 1
- 229960001180 norfloxacin Drugs 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 239000011146 organic particle Substances 0.000 description 1
- 125000003544 oxime group Chemical group 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- RUVINXPYWBROJD-UHFFFAOYSA-N para-methoxyphenyl Natural products COC1=CC=C(C=CC)C=C1 RUVINXPYWBROJD-UHFFFAOYSA-N 0.000 description 1
- 230000001717 pathogenic effect Effects 0.000 description 1
- 231100000255 pathogenic effect Toxicity 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 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
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920005547 polycyclic aromatic hydrocarbon Chemical group 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920006254 polymer film Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920006295 polythiol Polymers 0.000 description 1
- 229920003226 polyurethane urea Polymers 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- MCSINKKTEDDPNK-UHFFFAOYSA-N propyl propionate Chemical compound CCCOC(=O)CC MCSINKKTEDDPNK-UHFFFAOYSA-N 0.000 description 1
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 1
- VHNQIURBCCNWDN-UHFFFAOYSA-N pyridine-2,6-diamine Chemical compound NC1=CC=CC(N)=N1 VHNQIURBCCNWDN-UHFFFAOYSA-N 0.000 description 1
- FGVVTMRZYROCTH-UHFFFAOYSA-N pyridine-2-thiol N-oxide Chemical compound [O-][N+]1=CC=CC=C1S FGVVTMRZYROCTH-UHFFFAOYSA-N 0.000 description 1
- 229960002026 pyrithione Drugs 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 230000003252 repetitive effect Effects 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 230000008313 sensitization Effects 0.000 description 1
- 229940100890 silver compound Drugs 0.000 description 1
- 150000003379 silver compounds Chemical class 0.000 description 1
- 229910001923 silver oxide Inorganic materials 0.000 description 1
- 230000003381 solubilizing effect Effects 0.000 description 1
- 239000012258 stirred mixture Substances 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L sulfate group Chemical group S(=O)(=O)([O-])[O-] QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229940116411 terpineol Drugs 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 229960002180 tetracycline Drugs 0.000 description 1
- 229930101283 tetracycline Natural products 0.000 description 1
- 235000019364 tetracycline Nutrition 0.000 description 1
- 150000003522 tetracyclines Chemical class 0.000 description 1
- 239000002470 thermal conductor Substances 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 229960000790 thymol Drugs 0.000 description 1
- 239000001585 thymus vulgaris Substances 0.000 description 1
- KJAMZCVTJDTESW-UHFFFAOYSA-N tiracizine Chemical compound C1CC2=CC=CC=C2N(C(=O)CN(C)C)C2=CC(NC(=O)OCC)=CC=C21 KJAMZCVTJDTESW-UHFFFAOYSA-N 0.000 description 1
- 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 1
- RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 description 1
- VOZKAJLKRJDJLL-UHFFFAOYSA-N tolylenediamine group Chemical group CC1=C(C=C(C=C1)N)N VOZKAJLKRJDJLL-UHFFFAOYSA-N 0.000 description 1
- CRDAMVZIKSXKFV-UHFFFAOYSA-N trans-Farnesol Natural products CC(C)=CCCC(C)=CCCC(C)=CCO CRDAMVZIKSXKFV-UHFFFAOYSA-N 0.000 description 1
- GTZCVFVGUGFEME-UHFFFAOYSA-N trans-aconitic acid Natural products OC(=O)CC(C(O)=O)=CC(O)=O GTZCVFVGUGFEME-UHFFFAOYSA-N 0.000 description 1
- QURCVMIEKCOAJU-UHFFFAOYSA-N trans-isoferulic acid Natural products COC1=CC=C(C=CC(O)=O)C=C1O QURCVMIEKCOAJU-UHFFFAOYSA-N 0.000 description 1
- 230000008733 trauma Effects 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- MBYLVOKEDDQJDY-UHFFFAOYSA-N tris(2-aminoethyl)amine Chemical compound NCCN(CCN)CCN MBYLVOKEDDQJDY-UHFFFAOYSA-N 0.000 description 1
- 239000010681 turmeric oil Substances 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 229940043810 zinc pyrithione Drugs 0.000 description 1
- PICXIOQBANWBIZ-UHFFFAOYSA-N zinc;1-oxidopyridine-2-thione Chemical compound [Zn+2].[O-]N1C=CC=CC1=S.[O-]N1C=CC=CC1=S PICXIOQBANWBIZ-UHFFFAOYSA-N 0.000 description 1
- 229930007845 β-thujaplicin Natural products 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
- C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
- C09J175/04—Polyurethanes
-
- 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
- C08G18/0804—Manufacture of polymers containing ionic or ionogenic groups
- C08G18/0819—Manufacture of polymers containing ionic or ionogenic groups containing anionic or anionogenic groups
- C08G18/0823—Manufacture of polymers containing ionic or ionogenic groups containing anionic or anionogenic groups containing carboxylate salt groups or groups forming them
-
- 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
- C08G18/12—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step using two or more compounds having active hydrogen in the first polymerisation step
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Polyurethanes Or Polyureas (AREA)
- Adhesive Tapes (AREA)
- Adhesives Or Adhesive Processes (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/742,420 US20050137375A1 (en) | 2003-12-19 | 2003-12-19 | Polyurethane-based pressure sensitive adhesives and methods of manufacture |
| PCT/US2004/040391 WO2005066234A1 (en) | 2003-12-19 | 2004-12-03 | Polyurethane-based pressure sensitive adhesives and methods of manufacture |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2007514858A true JP2007514858A (ja) | 2007-06-07 |
| JP2007514858A5 JP2007514858A5 (https=) | 2008-01-31 |
Family
ID=34678441
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006545707A Withdrawn JP2007514858A (ja) | 2003-12-19 | 2004-12-03 | ポリウレタン系感圧接着剤および製造方法 |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US20050137375A1 (https=) |
| EP (1) | EP1694734A1 (https=) |
| JP (1) | JP2007514858A (https=) |
| WO (1) | WO2005066234A1 (https=) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2014502297A (ja) * | 2010-11-15 | 2014-01-30 | コヘラ メディカル インコーポレイテッド | 感圧性接着特性を有する生分解性組成物 |
| JP2014028877A (ja) * | 2012-07-31 | 2014-02-13 | Nitto Denko Corp | 表面保護フィルム |
| JP2018002954A (ja) * | 2016-07-07 | 2018-01-11 | 東ソー株式会社 | ウレタン形成性組成物、及びそれを用いたウレタン粘着剤 |
Families Citing this family (40)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101061352B1 (ko) * | 2002-12-20 | 2011-08-31 | 케모센트릭스 | 인간 종양-발현된 ｃｃｘｃｋｒ2의 저해물질 |
| US7371511B2 (en) | 2004-08-19 | 2008-05-13 | 3M Innovative Properties Company | Polydiacetylene polymer blends |
| US7816472B2 (en) * | 2004-08-19 | 2010-10-19 | 3M Innovative Properties Company | Polydiacetylene polymer compositions and methods of manufacture |
| JP5008046B2 (ja) * | 2005-06-14 | 2012-08-22 | ローム株式会社 | 半導体デバイス |
| US7956123B2 (en) * | 2005-10-24 | 2011-06-07 | Momentive Performance Materials Inc. | Solvent resistant polyurethane adhesive compositions |
| US8247514B2 (en) * | 2006-09-01 | 2012-08-21 | Momentive Performance Materials Inc. | Silylated polyurethane compositions and adhesives therefrom |
| US20080268983A1 (en) * | 2006-09-01 | 2008-10-30 | Callaway Golf Company | Golf balls with polyurethane covers formed from low-monol content polyols |
| US8247079B2 (en) * | 2006-09-01 | 2012-08-21 | Momentive Performance Materials Inc. | Laminate containing a silylated polyurethane adhesive composition |
| US20080114145A1 (en) * | 2006-11-09 | 2008-05-15 | Richard Czarnecki | Self catalyzing polyurethanes |
| EP2193024A4 (en) | 2007-09-25 | 2013-11-06 | Entrotech Inc | PAINT SHEET FILMS, COMPOUNDS THEREOF AND RELATED METHODS |
| US20130022746A9 (en) * | 2007-12-10 | 2013-01-24 | Harry Joseph Spinelli | Aqueous inkjet inks with ionically stabilized dispersions and polyurethane ink additives |
| US9410010B2 (en) | 2007-12-10 | 2016-08-09 | E I Du Pont De Nemours And Company | Urea-terminated polyurethane dispersants |
| US20090259012A1 (en) * | 2007-12-10 | 2009-10-15 | Roberts C Chad | Urea-terminated ether polyurethanes and aqueous dispersions thereof |
| US10981371B2 (en) | 2008-01-19 | 2021-04-20 | Entrotech, Inc. | Protected graphics and related methods |
| WO2009143441A1 (en) * | 2008-05-23 | 2009-11-26 | E. I. Du Pont De Nemours And Company | Urea-terminated polyurethane dispersants |
| US20110060102A1 (en) * | 2008-05-23 | 2011-03-10 | E.I. Du Pont De Nemours And Company | Urea-terminated polyurethane dispersants |
| JP2011523964A (ja) * | 2008-05-23 | 2011-08-25 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 自己分散顔料とポリウレタンインク添加剤とを有するインクジェットインク |
| WO2009149036A1 (en) * | 2008-06-03 | 2009-12-10 | Dow Global Technologies Inc. | Pressure sensitive adhesive compositions and method of making the same |
| US9790318B2 (en) | 2008-09-26 | 2017-10-17 | entrotech, inc | Methods for polymerizing films in-situ |
| EP2373270B8 (en) | 2009-01-07 | 2023-04-12 | entrotech life sciences, inc. | Chlorhexidine-containing antimicrobial laminates |
| US9732252B2 (en) | 2012-05-15 | 2017-08-15 | 3M Innovative Properties Company | Polyurethane-based protective coatings for rotor blades |
| KR102117890B1 (ko) * | 2012-12-28 | 2020-06-02 | 엘지디스플레이 주식회사 | 플렉서블 표시 장치 및 플렉서블 표시 장치 제조 방법 |
| WO2015161302A1 (en) * | 2014-04-18 | 2015-10-22 | Entrotech Life Sciences, Inc. | Methods of processing chlorhexidine-containing polymerizable compositions and antimicrobial articles formed thereby |
| US10611873B2 (en) | 2014-12-16 | 2020-04-07 | 3M Innovative Properties Company | Polyurethane pressure-sensitive adhesives |
| EP3353258B1 (en) * | 2015-09-21 | 2020-10-28 | 3M Innovative Properties Company | Chemical resistant polyurethane adhesive |
| JP6657921B2 (ja) * | 2015-12-21 | 2020-03-04 | Dic株式会社 | ウレタン樹脂組成物、及び、合成皮革 |
| ES2852199T3 (es) | 2016-03-23 | 2021-09-13 | Fuller H B Co | Composición adhesiva termofusible reactiva |
| SI3419826T1 (sl) | 2016-09-20 | 2026-01-30 | Ppg Advanced Surface Technologies, Llc | Metoda oblikovanja aplikacij barvne folije, aplikacije barvne folije, izdelki in uporaba |
| EP3589713A4 (en) | 2017-02-28 | 2020-12-30 | 3M Innovative Properties Company | POLYURETHANE ADHESIVE WITH CHEMICAL RESISTANCE |
| JP6891701B2 (ja) * | 2017-07-26 | 2021-06-18 | 日油株式会社 | ウレタン塗料組成物、硬化塗膜、および樹脂部材 |
| JP6931741B2 (ja) | 2017-08-25 | 2021-09-08 | スリーエム イノベイティブ プロパティズ カンパニー | 損傷のない取り外しを可能にする接着性物品 |
| JP7237063B2 (ja) | 2017-08-25 | 2023-03-10 | スリーエム イノベイティブ プロパティズ カンパニー | 損傷のない取り外しを可能にする接着性物品 |
| WO2019121388A1 (de) | 2017-12-21 | 2019-06-27 | Covestro Deutschland Ag | Frostbeständige klebstoffe auf basis von polyisocyanaten |
| TWI785203B (zh) | 2018-02-05 | 2022-12-01 | 美商3M新設資產公司 | 可調整大小的傢俱墊 |
| WO2020068999A1 (en) | 2018-09-26 | 2020-04-02 | 3M Innovative Properties Company | Fiber tows with a heat-activated sizing |
| EP3897304B1 (en) | 2018-12-19 | 2024-10-30 | 3M Innovative Properties Company | Flexible hardgoods with enhanced peel removability |
| PL3990510T3 (pl) | 2019-06-25 | 2025-02-10 | H.B. Fuller Company | Utwardzalna wilgocią kompozycja poliuretanowego kleju topliwego o niskim poziomie monomeru diizocyjanianu |
| CA3198869A1 (en) | 2020-10-15 | 2022-04-21 | 3M Innovative Properties Company | Adhesive assemblies permitting enhanced weight bearing performance with damage free removal |
| USD996195S1 (en) | 2022-02-28 | 2023-08-22 | 3M Innovative Properties Company | Mounting hook |
| EP4530329A1 (en) * | 2023-09-27 | 2025-04-02 | Bostik SA | Label comprising polyether-based wash-off adhesives |
Family Cites Families (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3246049A (en) * | 1963-08-30 | 1966-04-12 | Norton Co | Pressure sensitive adhesive comprising an isocyanate cross-linked polyester of castor oil and diglycolic acid, and tape coated with said adhesive |
| US3360599A (en) * | 1963-11-06 | 1967-12-26 | Shell Oil Co | Preparation of coherent block copolymer films of high tensile strength and extensibility |
| US3437622A (en) * | 1965-12-06 | 1969-04-08 | Anchor Continental Inc | Polyurethane-based pressure-sensitive adhesives |
| US3503917A (en) * | 1967-03-09 | 1970-03-31 | Burke Oliver W Jun | Aqueous latices of high polymer compositions and processes for producing same |
| US3925283A (en) * | 1970-06-29 | 1975-12-09 | Continental Tapes Inc | Polyurethane pressure-sensitive adhesive products and processes |
| US3796678A (en) * | 1970-08-17 | 1974-03-12 | Minnesota Mining & Mfg | Highly branched,capped polyurethanes for pressure sensitive adhesives |
| US3718712A (en) * | 1971-03-01 | 1973-02-27 | Minnesota Mining & Mfg | Pressure-sensitive adhesives based on cyclic terpene urethane resin |
| US3767040A (en) * | 1971-03-01 | 1973-10-23 | Minnesota Mining & Mfg | Pressure-sensitive polyurethane adhesives |
| US3743617A (en) * | 1971-05-17 | 1973-07-03 | D Kest | Urethane base pressure sensitive adhesive |
| US3769071A (en) * | 1971-06-04 | 1973-10-30 | Minnesota Mining & Mfg | Pressure sensitive adhesive tape comprising 5-fluorouracil |
| DE2436873A1 (de) * | 1974-07-31 | 1976-02-19 | Basf Ag | Verfahren zur herstellung von haftklebern |
| US4123403A (en) * | 1977-06-27 | 1978-10-31 | The Dow Chemical Company | Continuous process for preparing aqueous polymer microsuspensions |
| US5102714A (en) * | 1988-12-20 | 1992-04-07 | The Dow Chemical Company | Removable polyurethane adhesive |
| US5045601A (en) * | 1989-06-13 | 1991-09-03 | Biointerface Technologies, Inc. | Pressure-sensitive adhesive compositions suitable for medical uses |
| US5037864A (en) * | 1989-07-11 | 1991-08-06 | The Dow Chemical Company | Semi-continuous process for the preparation of polyurethane-urea aqueous dispersions |
| US4985491A (en) * | 1989-10-05 | 1991-01-15 | Olin Corporation | Polyurethane sealants made using high molecular weight polyols prepared with double metal cyanide catalysts |
| US5532058A (en) * | 1990-12-10 | 1996-07-02 | H. B. Fuller Licensing & Financing, Inc. | Dry-bonded film laminate employing polyurethane dispersion adhesives with improved crosslinkers |
| EP0552420A3 (en) * | 1992-01-24 | 1993-09-15 | H.B. Fuller Licensing & Financing, Inc. | Water dispersed polyurethane polymer for improved coatings and adhesives |
| NZ248977A (en) * | 1992-11-09 | 1995-06-27 | Squibb & Sons Inc | Pressure-sensitive adhesive comprising a polyurethane having excess hydroxyl functionality; medical articles comprising a layer of such adhesive |
| US5354808A (en) * | 1992-12-08 | 1994-10-11 | Minnesota Mining And Manufacturing Company | Polyurethanes including pendant hindered amines and compositions incorporating same |
| US5554686A (en) * | 1993-08-20 | 1996-09-10 | Minnesota Mining And Manufacturing Company | Room temperature curable silane-terminated polyurethane dispersions |
| US5442028A (en) * | 1993-08-20 | 1995-08-15 | Morton International, Inc. | Curatives for aqueous adhesives |
| US5608000A (en) * | 1993-09-24 | 1997-03-04 | H. B. Fuller Licensing & Financing, Inc. | Aqueous polyurethane dispersion adhesive compositions with improved heat resistance |
| US5703158A (en) * | 1993-09-24 | 1997-12-30 | H.B. Fuller Licensing & Financing, Inc. | Aqueous anionic poly (urethane/urea) dispersions |
| US5714543A (en) * | 1994-01-13 | 1998-02-03 | Bristol-Myers Squibb Company | Water soluble polymer additives for polyurethane-based pressure sensitive adhesives |
| US5486570A (en) * | 1994-09-29 | 1996-01-23 | Shell Oil Company | Polyurethane sealants and adhesives containing saturated hydrocarbon polyols |
| US5505958A (en) * | 1994-10-31 | 1996-04-09 | Algos Pharmaceutical Corporation | Transdermal drug delivery device and method for its manufacture |
| WO1997022632A1 (en) * | 1995-12-19 | 1997-06-26 | Bristol Myers Squibb Company | Polyurethane pressure-sensitive adhesives |
| KR0173522B1 (ko) * | 1995-12-20 | 1999-04-01 | 최근배 | 폴리우레탄 프리폴리머의 제조방법, 상기 프리폴리머로부터 제조되는 수용성 폴리우레탄 분산체의 제조방법 및 그의 용도 |
| US5807919A (en) * | 1996-08-13 | 1998-09-15 | H.B. Fuller Licensing & Financing, Inc. | Water-based sulfonated polymer compositions |
| US5880250A (en) * | 1996-08-16 | 1999-03-09 | Inolex Investment Corporation | Polymeric acid functional polyols, polyurethanes and methods for making same |
| US5985317A (en) * | 1996-09-06 | 1999-11-16 | Theratech, Inc. | Pressure sensitive adhesive matrix patches for transdermal delivery of salts of pharmaceutical agents |
| US6518359B1 (en) * | 2000-02-25 | 2003-02-11 | 3M Innovative Properties Co. | Polyurethane-based pressure-sensitive adhesives, systems for such adhesives, articles therefrom, and methods of making |
| US6642304B1 (en) * | 2000-02-25 | 2003-11-04 | 3M Innovative Properties Company | Polyurethane-based adhesives, systems for such adhesives, articles therefrom, and methods of making |
| US6605666B1 (en) * | 2000-07-27 | 2003-08-12 | 3M Innovative Properties Company | Polyurethane film-forming dispersions in alcohol-water system |
| EP1319032B1 (en) * | 2000-09-21 | 2005-11-30 | Cytec Technology Corp. | Low-temperature, heat-activated adhesives with high heat resistance properties |
-
2003
- 2003-12-19 US US10/742,420 patent/US20050137375A1/en not_active Abandoned
-
2004
- 2004-12-03 EP EP04812827A patent/EP1694734A1/en not_active Withdrawn
- 2004-12-03 WO PCT/US2004/040391 patent/WO2005066234A1/en not_active Ceased
- 2004-12-03 JP JP2006545707A patent/JP2007514858A/ja not_active Withdrawn
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2014502297A (ja) * | 2010-11-15 | 2014-01-30 | コヘラ メディカル インコーポレイテッド | 感圧性接着特性を有する生分解性組成物 |
| JP2014028877A (ja) * | 2012-07-31 | 2014-02-13 | Nitto Denko Corp | 表面保護フィルム |
| JP2018002954A (ja) * | 2016-07-07 | 2018-01-11 | 東ソー株式会社 | ウレタン形成性組成物、及びそれを用いたウレタン粘着剤 |
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| Publication number | Publication date |
|---|---|
| US20050137375A1 (en) | 2005-06-23 |
| EP1694734A1 (en) | 2006-08-30 |
| WO2005066234A1 (en) | 2005-07-21 |
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