JP2003524042A - ポリウレタン系接着剤、かかる接着剤系、それらによる物品、および製造方法 - Google Patents
ポリウレタン系接着剤、かかる接着剤系、それらによる物品、および製造方法Info
- Publication number
- JP2003524042A JP2003524042A JP2001562597A JP2001562597A JP2003524042A JP 2003524042 A JP2003524042 A JP 2003524042A JP 2001562597 A JP2001562597 A JP 2001562597A JP 2001562597 A JP2001562597 A JP 2001562597A JP 2003524042 A JP2003524042 A JP 2003524042A
- Authority
- JP
- Japan
- Prior art keywords
- isocyanate
- weight
- reactive
- polyurethane
- sensitive adhesive
- 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
- 239000000853 adhesive Substances 0.000 title claims abstract description 91
- 230000001070 adhesive effect Effects 0.000 title claims abstract description 91
- 229920002635 polyurethane Polymers 0.000 title claims abstract description 91
- 239000004814 polyurethane Substances 0.000 title claims abstract description 91
- 238000004519 manufacturing process Methods 0.000 title claims description 4
- 239000000463 material Substances 0.000 claims abstract description 136
- 239000004820 Pressure-sensitive adhesive Substances 0.000 claims abstract description 73
- 150000001875 compounds Chemical class 0.000 claims abstract description 43
- 230000001804 emulsifying effect Effects 0.000 claims abstract description 39
- 239000004970 Chain extender Substances 0.000 claims abstract description 18
- 239000007795 chemical reaction product Substances 0.000 claims abstract description 18
- 229920005862 polyol Polymers 0.000 claims description 135
- 150000003077 polyols Chemical class 0.000 claims description 134
- 239000006185 dispersion Substances 0.000 claims description 84
- 238000000034 method Methods 0.000 claims description 46
- 229920001730 Moisture cure polyurethane Polymers 0.000 claims description 32
- 150000002009 diols Chemical class 0.000 claims description 25
- 239000000758 substrate Substances 0.000 claims description 17
- 239000002612 dispersion medium Substances 0.000 claims description 15
- 238000000576 coating method Methods 0.000 claims description 12
- 239000011248 coating agent Substances 0.000 claims description 11
- 125000005442 diisocyanate group Chemical group 0.000 claims description 11
- 239000012948 isocyanate Substances 0.000 claims description 11
- 150000002513 isocyanates Chemical class 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 8
- 238000001035 drying Methods 0.000 claims description 7
- 239000002609 medium Substances 0.000 claims description 7
- 239000000376 reactant Substances 0.000 claims description 6
- 238000007614 solvation Methods 0.000 claims description 4
- OYQYHJRSHHYEIG-UHFFFAOYSA-N ethyl carbamate;urea Chemical compound NC(N)=O.CCOC(N)=O OYQYHJRSHHYEIG-UHFFFAOYSA-N 0.000 claims description 3
- -1 aqueous Substances 0.000 abstract description 38
- 239000002904 solvent Substances 0.000 abstract description 15
- 239000007787 solid Substances 0.000 abstract description 11
- 238000002360 preparation method Methods 0.000 description 90
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- 238000006243 chemical reaction Methods 0.000 description 37
- 229920000642 polymer Polymers 0.000 description 31
- PTBDIHRZYDMNKB-UHFFFAOYSA-N 2,2-Bis(hydroxymethyl)propionic acid Chemical compound OCC(C)(CO)C(O)=O PTBDIHRZYDMNKB-UHFFFAOYSA-N 0.000 description 29
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 27
- 239000011521 glass Substances 0.000 description 26
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 24
- 230000000052 comparative effect Effects 0.000 description 21
- 229920000768 polyamine Polymers 0.000 description 20
- 239000000243 solution Substances 0.000 description 20
- 238000012360 testing method Methods 0.000 description 19
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 17
- 239000012153 distilled water Substances 0.000 description 16
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 15
- 239000005056 polyisocyanate Substances 0.000 description 15
- 229920001228 polyisocyanate Polymers 0.000 description 15
- 239000005058 Isophorone diisocyanate Substances 0.000 description 14
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- 125000000524 functional group Chemical group 0.000 description 9
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- 125000001183 hydrocarbyl group Chemical group 0.000 description 8
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 8
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- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 6
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- 125000000129 anionic group Chemical group 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
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- 239000003995 emulsifying agent Substances 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 125000003277 amino group Chemical group 0.000 description 3
- 125000000732 arylene group Chemical group 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
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- 229920003009 polyurethane dispersion Polymers 0.000 description 3
- 229920003226 polyurethane urea Polymers 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 229910001220 stainless steel Inorganic materials 0.000 description 3
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- 150000003512 tertiary amines Chemical class 0.000 description 3
- PLFFHJWXOGYWPR-HEDMGYOXSA-N (4r)-4-[(3r,3as,5ar,5br,7as,11as,11br,13ar,13bs)-5a,5b,8,8,11a,13b-hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-3-yl]pentan-1-ol Chemical compound C([C@]1(C)[C@H]2CC[C@H]34)CCC(C)(C)[C@@H]1CC[C@@]2(C)[C@]4(C)CC[C@@H]1[C@]3(C)CC[C@@H]1[C@@H](CCCO)C PLFFHJWXOGYWPR-HEDMGYOXSA-N 0.000 description 2
- AZYRZNIYJDKRHO-UHFFFAOYSA-N 1,3-bis(2-isocyanatopropan-2-yl)benzene Chemical compound O=C=NC(C)(C)C1=CC=CC(C(C)(C)N=C=O)=C1 AZYRZNIYJDKRHO-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 239000009261 D 400 Substances 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 238000005481 NMR spectroscopy Methods 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000008064 anhydrides Chemical class 0.000 description 2
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- KXDHJXZQYSOELW-UHFFFAOYSA-N carbonic acid monoamide Natural products NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 150000004985 diamines Chemical class 0.000 description 2
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- 229920006158 high molecular weight polymer Polymers 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000004816 latex Substances 0.000 description 2
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- 230000014759 maintenance of location Effects 0.000 description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
- 125000004430 oxygen atom Chemical group O* 0.000 description 2
- 229920001281 polyalkylene Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 150000003141 primary amines Chemical class 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 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 2
- 125000005628 tolylene group Chemical group 0.000 description 2
- 150000004072 triols Chemical class 0.000 description 2
- BZCOSCNPHJNQBP-UPHRSURJSA-N (z)-2,3-dihydroxybut-2-enedioic acid Chemical compound OC(=O)C(\O)=C(\O)C(O)=O BZCOSCNPHJNQBP-UPHRSURJSA-N 0.000 description 1
- NCYNKWQXFADUOZ-UHFFFAOYSA-N 1,1-dioxo-2,1$l^{6}-benzoxathiol-3-one Chemical compound C1=CC=C2C(=O)OS(=O)(=O)C2=C1 NCYNKWQXFADUOZ-UHFFFAOYSA-N 0.000 description 1
- GFNDFCFPJQPVQL-UHFFFAOYSA-N 1,12-diisocyanatododecane Chemical compound O=C=NCCCCCCCCCCCCN=C=O GFNDFCFPJQPVQL-UHFFFAOYSA-N 0.000 description 1
- RBACIKXCRWGCBB-UHFFFAOYSA-N 1,2-Epoxybutane Chemical compound CCC1CO1 RBACIKXCRWGCBB-UHFFFAOYSA-N 0.000 description 1
- GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 description 1
- RTTZISZSHSCFRH-UHFFFAOYSA-N 1,3-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC(CN=C=O)=C1 RTTZISZSHSCFRH-UHFFFAOYSA-N 0.000 description 1
- VGHSXKTVMPXHNG-UHFFFAOYSA-N 1,3-diisocyanatobenzene Chemical compound O=C=NC1=CC=CC(N=C=O)=C1 VGHSXKTVMPXHNG-UHFFFAOYSA-N 0.000 description 1
- 125000004955 1,4-cyclohexylene group Chemical group [H]C1([H])C([H])([H])C([H])([*:1])C([H])([H])C([H])([H])C1([H])[*:2] 0.000 description 1
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- LCJLEYPRGLFMGM-UHFFFAOYSA-N 1-(chloromethyl)-2,4-diisocyanatobenzene Chemical compound ClCC1=CC=C(N=C=O)C=C1N=C=O LCJLEYPRGLFMGM-UHFFFAOYSA-N 0.000 description 1
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- 239000012530 fluid Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 229910021485 fumed silica Inorganic materials 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- VANNPISTIUFMLH-UHFFFAOYSA-N glutaric anhydride Chemical compound O=C1CCCC(=O)O1 VANNPISTIUFMLH-UHFFFAOYSA-N 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 150000002483 hydrogen compounds Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 208000014674 injury Diseases 0.000 description 1
- 239000012784 inorganic fiber Substances 0.000 description 1
- 239000010954 inorganic particle Substances 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 239000004761 kevlar Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000008204 material by function Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000002923 metal particle Substances 0.000 description 1
- RTWNYYOXLSILQN-UHFFFAOYSA-N methanediamine Chemical compound NCN RTWNYYOXLSILQN-UHFFFAOYSA-N 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- PJUIMOJAAPLTRJ-UHFFFAOYSA-N monothioglycerol Chemical compound OCC(O)CS PJUIMOJAAPLTRJ-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 125000000962 organic group Chemical group 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
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- WTSXICLFTPPDTL-UHFFFAOYSA-N pentane-1,3-diamine Chemical compound CCC(N)CCN WTSXICLFTPPDTL-UHFFFAOYSA-N 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
- 229920000435 poly(dimethylsiloxane) 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
- 230000008569 process Effects 0.000 description 1
- 230000001737 promoting effect Effects 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
- ZZYXNRREDYWPLN-UHFFFAOYSA-N pyridine-2,3-diamine Chemical compound NC1=CC=CN=C1N ZZYXNRREDYWPLN-UHFFFAOYSA-N 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 230000008313 sensitization Effects 0.000 description 1
- 238000000926 separation method Methods 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
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000002470 thermal conductor Substances 0.000 description 1
- 229940035024 thioglycerol Drugs 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 239000012974 tin catalyst Substances 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
- 238000012546 transfer Methods 0.000 description 1
- 230000008733 trauma Effects 0.000 description 1
- SRPWOOOHEPICQU-UHFFFAOYSA-N trimellitic anhydride Chemical compound OC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 SRPWOOOHEPICQU-UHFFFAOYSA-N 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
- 239000008096 xylene Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-UHFFFAOYSA-N 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
- C09J175/08—Polyurethanes from polyethers
-
- 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
-
- 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
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/4804—Two or more polyethers of different physical or chemical nature
- C08G18/4808—Mixtures of two or more polyetherdiols
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
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)
- Polyurethanes Or Polyureas (AREA)
- Lining Or Joining Of Plastics Or The Like (AREA)
- Adhesive Tapes (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/514,122 | 2000-02-25 | ||
| US09/514,122 US6642304B1 (en) | 2000-02-25 | 2000-02-25 | Polyurethane-based adhesives, systems for such adhesives, articles therefrom, and methods of making |
| PCT/US2000/018317 WO2001062818A1 (en) | 2000-02-25 | 2000-06-30 | Polyurethane-based adhesives, systems for such adhesives, articles therefrom, and methods of making |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2003524042A true JP2003524042A (ja) | 2003-08-12 |
| JP2003524042A5 JP2003524042A5 (https=) | 2007-08-02 |
Family
ID=24045887
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001562597A Pending JP2003524042A (ja) | 2000-02-25 | 2000-06-30 | ポリウレタン系接着剤、かかる接着剤系、それらによる物品、および製造方法 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US6642304B1 (https=) |
| EP (1) | EP1263830B1 (https=) |
| JP (1) | JP2003524042A (https=) |
| AT (1) | ATE327268T1 (https=) |
| AU (1) | AU2000262048A1 (https=) |
| DE (1) | DE60028255T2 (https=) |
| WO (1) | WO2001062818A1 (https=) |
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| JP2006124693A (ja) * | 2004-09-30 | 2006-05-18 | Asahi Glass Co Ltd | ウレタン樹脂の製造方法および粘着剤 |
| 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 |
| JP2018532011A (ja) * | 2015-09-21 | 2018-11-01 | スリーエム イノベイティブ プロパティズ カンパニー | 耐薬品性ポリウレタン接着剤 |
| JP2018532867A (ja) * | 2015-09-08 | 2018-11-08 | ヘンケル・アクチェンゲゼルシャフト・ウント・コムパニー・コマンディットゲゼルシャフト・アウフ・アクチェンＨｅｎｋｅｌ ＡＧ ＆ Ｃｏ． ＫＧａＡ | ポリウレタン水性分散体に基づくコールドシール接着剤 |
| KR20190025642A (ko) * | 2016-06-30 | 2019-03-11 | 코베스트로 도이칠란트 아게 | 폴리우레탄 수지를 기재로 하는 접촉 접착제 제품, 그의 제조법, 및 상응하는 접촉 접착제 |
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| US20060058438A1 (en) * | 2004-09-16 | 2006-03-16 | Williams Thomas H | Fluid sulfopolyester formulations and products made therefrom |
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| DE102006020482A1 (de) | 2006-04-28 | 2007-10-31 | Tesa Ag | Wieder ablösbarer Haftklebstoff aus Polyurethan |
| DE102006033796A1 (de) | 2006-07-19 | 2008-01-31 | Tesa Ag | Haftklebestoffe aus einem harzmodifizierten Polyurethan |
| US20080268983A1 (en) * | 2006-09-01 | 2008-10-30 | Callaway Golf Company | Golf balls with polyurethane covers formed from low-monol content polyols |
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Citations (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62270613A (ja) * | 1986-05-19 | 1987-11-25 | Dainippon Ink & Chem Inc | 接着力のすぐれたポリウレタン水性分散液の製造方法 |
| JPS62280278A (ja) * | 1986-05-30 | 1987-12-05 | Idemitsu Petrochem Co Ltd | 接着剤組成物 |
| JPH0693244A (ja) * | 1991-10-17 | 1994-04-05 | Nippon Polyurethane Ind Co Ltd | 反応型ホットメルト接着剤 |
| JPH08225780A (ja) * | 1995-02-20 | 1996-09-03 | Sekisui Chem Co Ltd | ウレタン系水性接着剤組成物 |
| JPH10330445A (ja) * | 1997-05-28 | 1998-12-15 | Sekisui Chem Co Ltd | 水性組成物及び接着方法 |
| JPH11279518A (ja) * | 1998-03-27 | 1999-10-12 | Arakawa Chem Ind Co Ltd | 湿気硬化型接着剤組成物 |
| JP2001501233A (ja) * | 1996-09-20 | 2001-01-30 | ティンデイル プレインズ―ハンター，リミテッド | カルボン酸を含む親水性ポリエーテルポリウレタン |
| JP2001525428A (ja) * | 1997-12-04 | 2001-12-11 | ヘンケル・コマンディットゲゼルシャフト・アウフ・アクチエン | 尿素−ウレタン結合を有する水系ポリウレタン |
| JP2002501954A (ja) * | 1998-01-28 | 2002-01-22 | ブリストル−マイヤーズ スクイブ カンパニー | ポリウレタン接着剤の製造法、該方法によって製造される接着剤および該接着剤を用いる医療器具 |
| JP2003524041A (ja) * | 2000-02-25 | 2003-08-12 | スリーエム イノベイティブ プロパティズ カンパニー | ポリウレタンベースの感圧接着剤、かかる接着剤用の系、それから得られる物品、および製造方法 |
Family Cites Families (39)
| 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 |
| GB1113925A (en) | 1964-09-18 | 1968-05-15 | Dunlop Co Ltd | Polyurethane pressure-sensitive adhesives |
| 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 |
| GB1216672A (en) | 1967-05-16 | 1970-12-23 | Dunlop Co Ltd | Polyurethane pressure-sensitive adhesives |
| 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 |
| US3767040A (en) | 1971-03-01 | 1973-10-23 | Minnesota Mining & Mfg | Pressure-sensitive polyurethane adhesives |
| US3718712A (en) | 1971-03-01 | 1973-02-27 | Minnesota Mining & Mfg | Pressure-sensitive adhesives based on cyclic terpene urethane resin |
| US3743617A (en) | 1971-05-17 | 1973-07-03 | D Kest | Urethane base pressure sensitive adhesive |
| 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 |
| JPS5552369A (en) | 1978-10-13 | 1980-04-16 | Toyo Tire & Rubber Co Ltd | Water-dispersed pressure-sensitive adhesive composition |
| US5102714A (en) | 1988-12-20 | 1992-04-07 | The Dow Chemical Company | Removable polyurethane adhesive |
| 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 |
| CA2095876A1 (en) | 1992-06-05 | 1993-12-06 | Nigel Barksby | Isocyante-terminated prepolymers derived from polyether polyol mixtures having low monol content and their use in polyurethanes |
| 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 |
| DE4242687B8 (de) | 1992-12-17 | 2006-01-12 | Henkel Kgaa | Hydrophile Polyurethane |
| US5442028A (en) | 1993-08-20 | 1995-08-15 | Morton International, Inc. | Curatives for aqueous adhesives |
| US5554686A (en) | 1993-08-20 | 1996-09-10 | Minnesota Mining And Manufacturing Company | Room temperature curable silane-terminated polyurethane dispersions |
| US5703158A (en) | 1993-09-24 | 1997-12-30 | H.B. Fuller Licensing & Financing, Inc. | Aqueous anionic poly (urethane/urea) dispersions |
| US5608000A (en) | 1993-09-24 | 1997-03-04 | H. B. Fuller Licensing & Financing, Inc. | Aqueous polyurethane dispersion adhesive compositions with improved heat resistance |
| JPH07102233A (ja) | 1993-10-01 | 1995-04-18 | Sekisui Chem Co Ltd | 水性接着剤組成物 |
| 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 |
| AU722654B2 (en) | 1995-12-19 | 2000-08-10 | Bristol-Myers Squibb Company | Polyurethane pressure-sensitive adhesives |
| US5952422A (en) | 1995-12-20 | 1999-09-14 | 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 |
| ES2190583T3 (es) | 1997-01-16 | 2003-08-01 | Dow Global Technologies Inc | Adhesivo de latex de poliuretano sensible a la presion y procedimiento para fabricarlo. |
| DE19725297A1 (de) | 1997-06-14 | 1998-12-17 | Basf Ag | Wässrige Polyurethandispersionen aus Polypropylenglykol mit geringem Harnstoffgehalt |
| BR9812514A (pt) | 1997-09-24 | 2000-07-25 | Henkel Kgaa | Adesivo de poliuretana |
-
2000
- 2000-02-25 US US09/514,122 patent/US6642304B1/en not_active Expired - Lifetime
- 2000-06-30 DE DE2000628255 patent/DE60028255T2/de not_active Expired - Lifetime
- 2000-06-30 EP EP20000948572 patent/EP1263830B1/en not_active Revoked
- 2000-06-30 AU AU2000262048A patent/AU2000262048A1/en not_active Abandoned
- 2000-06-30 JP JP2001562597A patent/JP2003524042A/ja active Pending
- 2000-06-30 AT AT00948572T patent/ATE327268T1/de not_active IP Right Cessation
- 2000-06-30 WO PCT/US2000/018317 patent/WO2001062818A1/en not_active Ceased
Patent Citations (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62270613A (ja) * | 1986-05-19 | 1987-11-25 | Dainippon Ink & Chem Inc | 接着力のすぐれたポリウレタン水性分散液の製造方法 |
| JPS62280278A (ja) * | 1986-05-30 | 1987-12-05 | Idemitsu Petrochem Co Ltd | 接着剤組成物 |
| JPH0693244A (ja) * | 1991-10-17 | 1994-04-05 | Nippon Polyurethane Ind Co Ltd | 反応型ホットメルト接着剤 |
| JPH08225780A (ja) * | 1995-02-20 | 1996-09-03 | Sekisui Chem Co Ltd | ウレタン系水性接着剤組成物 |
| JP2001501233A (ja) * | 1996-09-20 | 2001-01-30 | ティンデイル プレインズ―ハンター，リミテッド | カルボン酸を含む親水性ポリエーテルポリウレタン |
| JPH10330445A (ja) * | 1997-05-28 | 1998-12-15 | Sekisui Chem Co Ltd | 水性組成物及び接着方法 |
| JP2001525428A (ja) * | 1997-12-04 | 2001-12-11 | ヘンケル・コマンディットゲゼルシャフト・アウフ・アクチエン | 尿素−ウレタン結合を有する水系ポリウレタン |
| JP2002501954A (ja) * | 1998-01-28 | 2002-01-22 | ブリストル−マイヤーズ スクイブ カンパニー | ポリウレタン接着剤の製造法、該方法によって製造される接着剤および該接着剤を用いる医療器具 |
| JPH11279518A (ja) * | 1998-03-27 | 1999-10-12 | Arakawa Chem Ind Co Ltd | 湿気硬化型接着剤組成物 |
| JP2003524041A (ja) * | 2000-02-25 | 2003-08-12 | スリーエム イノベイティブ プロパティズ カンパニー | ポリウレタンベースの感圧接着剤、かかる接着剤用の系、それから得られる物品、および製造方法 |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006124693A (ja) * | 2004-09-30 | 2006-05-18 | Asahi Glass Co Ltd | ウレタン樹脂の製造方法および粘着剤 |
| JP2018532867A (ja) * | 2015-09-08 | 2018-11-08 | ヘンケル・アクチェンゲゼルシャフト・ウント・コムパニー・コマンディットゲゼルシャフト・アウフ・アクチェンＨｅｎｋｅｌ ＡＧ ＆ Ｃｏ． ＫＧａＡ | ポリウレタン水性分散体に基づくコールドシール接着剤 |
| JP2018532011A (ja) * | 2015-09-21 | 2018-11-01 | スリーエム イノベイティブ プロパティズ カンパニー | 耐薬品性ポリウレタン接着剤 |
| KR20190025642A (ko) * | 2016-06-30 | 2019-03-11 | 코베스트로 도이칠란트 아게 | 폴리우레탄 수지를 기재로 하는 접촉 접착제 제품, 그의 제조법, 및 상응하는 접촉 접착제 |
| JP2019527256A (ja) * | 2016-06-30 | 2019-09-26 | コベストロ、ドイチュラント、アクチエンゲゼルシャフトＣｏｖｅｓｔｒｏ Ｄｅｕｔｓｃｈｌａｎｄ Ａｇ | ポリウレタン樹脂に基づくコンタクト接着剤製品、その作製、および対応するコンタクト接着剤 |
| KR102358216B1 (ko) | 2016-06-30 | 2022-02-04 | 코베스트로 도이칠란트 아게 | 폴리우레탄 수지를 기재로 하는 접촉 접착제 제품, 그의 제조법, 및 상응하는 접촉 접착제 |
| JP7039496B2 (ja) | 2016-06-30 | 2022-03-22 | コベストロ、ドイチュラント、アクチエンゲゼルシャフト | ポリウレタン樹脂に基づくコンタクト接着剤製品、その作製、および対応するコンタクト接着剤 |
| 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 |
Also Published As
| Publication number | Publication date |
|---|---|
| ATE327268T1 (de) | 2006-06-15 |
| AU2000262048A1 (en) | 2001-09-03 |
| US6642304B1 (en) | 2003-11-04 |
| DE60028255T2 (de) | 2007-03-29 |
| EP1263830B1 (en) | 2006-05-24 |
| DE60028255D1 (de) | 2006-06-29 |
| EP1263830A1 (en) | 2002-12-11 |
| WO2001062818A1 (en) | 2001-08-30 |
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