SE463923B - Latexbindemedel med isocyanatreaktiv funktionalitet, foerfarande foer dess framstaellning samt med bindemedlet sammanfogad traekomposit - Google Patents

Latexbindemedel med isocyanatreaktiv funktionalitet, foerfarande foer dess framstaellning samt med bindemedlet sammanfogad traekomposit

Info

Publication number: SE463923B
Authority: SE; Sweden
Prior art keywords: latex; binder composition; latex polymer; multiisocyanate; isocyanate
Prior art date: 1983-09-29

Application number

SE8404842A

Other languages

English (en)

Swedish (sv)

Other versions

SE8404842L (sv

SE8404842D0 (sv

Inventor

N J Gruber

C E Powell

Original Assignee

Ashland Oil Inc

Priority date (The priority date 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 date listed.)

1983-09-29

Filing date

1984-09-27

Publication date

1991-02-11

1984-09-27 Application filed by Ashland Oil Inc filed Critical Ashland Oil Inc

1984-09-27 Publication of SE8404842D0 publication Critical patent/SE8404842D0/xx

1985-03-30 Publication of SE8404842L publication Critical patent/SE8404842L/xx

1991-02-11 Publication of SE463923B publication Critical patent/SE463923B/sv

Links

239000004816 latex Substances 0.000 title claims description 114
239000000203 mixture Substances 0.000 title claims description 72
238000000034 method Methods 0.000 title claims description 13
238000002360 preparation method Methods 0.000 title claims description 4
229920000126 latex Polymers 0.000 claims description 113
239000011230 binding agent Substances 0.000 claims description 78
239000000945 filler Substances 0.000 claims description 35
229920000642 polymer Polymers 0.000 claims description 30
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 25
239000000178 monomer Substances 0.000 claims description 22
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 18
239000002562 thickening agent Substances 0.000 claims description 18
239000002245 particle Substances 0.000 claims description 17
239000004971 Cross linker Substances 0.000 claims description 15
239000002023 wood Substances 0.000 claims description 11
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 10
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 9
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 8
239000002131 composite material Substances 0.000 claims description 8
239000002904 solvent Substances 0.000 claims description 8
239000000853 adhesive Substances 0.000 claims description 7
230000001070 adhesive effect Effects 0.000 claims description 7
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 claims description 6
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 6
230000008569 process Effects 0.000 claims description 6
OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 claims description 5
238000006243 chemical reaction Methods 0.000 claims description 4
230000009477 glass transition Effects 0.000 claims description 4
239000011256 inorganic filler Substances 0.000 claims description 3
229910003475 inorganic filler Inorganic materials 0.000 claims description 3
229920001897 terpolymer Polymers 0.000 claims 3
239000012071 phase Substances 0.000 description 28
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 25
239000012948 isocyanate Substances 0.000 description 19
150000002513 isocyanates Chemical class 0.000 description 18
238000001035 drying Methods 0.000 description 16
238000009835 boiling Methods 0.000 description 15
239000003795 chemical substances by application Substances 0.000 description 10
239000007787 solid Substances 0.000 description 10
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
239000004094 surface-active agent Substances 0.000 description 9
238000012360 testing method Methods 0.000 description 8
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 6
230000008901 benefit Effects 0.000 description 6
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 6
210000001145 finger joint Anatomy 0.000 description 6
-1 for example Substances 0.000 description 6
239000000126 substance Substances 0.000 description 6
238000010276 construction Methods 0.000 description 5
238000001723 curing Methods 0.000 description 5
XLJMAIOERFSOGZ-UHFFFAOYSA-M cyanate Chemical compound [O-]C#N XLJMAIOERFSOGZ-UHFFFAOYSA-M 0.000 description 5
239000000839 emulsion Substances 0.000 description 5
BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 5
229920003048 styrene butadiene rubber 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
235000010319 Acer grandidentatum Nutrition 0.000 description 4
235000010328 Acer nigrum Nutrition 0.000 description 4
235000002629 Acer saccharinum Nutrition 0.000 description 4
244000046139 Acer saccharum Species 0.000 description 4
235000010157 Acer saccharum subsp saccharum Nutrition 0.000 description 4
239000002174 Styrene-butadiene Substances 0.000 description 4
RUHVTDYVRPZQAZ-UHFFFAOYSA-L [O-]C#N.[Mn+2].[O-]C#N Chemical compound [O-]C#N.[Mn+2].[O-]C#N RUHVTDYVRPZQAZ-UHFFFAOYSA-L 0.000 description 4
238000005516 engineering process Methods 0.000 description 4
150000002148 esters Chemical class 0.000 description 4
230000006872 improvement Effects 0.000 description 4
239000007788 liquid Substances 0.000 description 4
238000004519 manufacturing process Methods 0.000 description 4
235000012069 sugar maple Nutrition 0.000 description 4
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
FEWFXBUNENSNBQ-UHFFFAOYSA-N 2-hydroxyacrylic acid Chemical compound OC(=C)C(O)=O FEWFXBUNENSNBQ-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
235000014466 Douglas bleu Nutrition 0.000 description 3
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 3
240000001416 Pseudotsuga menziesii Species 0.000 description 3
235000005386 Pseudotsuga menziesii var menziesii Nutrition 0.000 description 3
LDLCEGCJYSDJLX-OWOJBTEDSA-N ac1q3hc4 Chemical compound C1N(C2)CN3CN2C[N+]1(C/C=C/Cl)C3 LDLCEGCJYSDJLX-OWOJBTEDSA-N 0.000 description 3
239000002253 acid Substances 0.000 description 3
239000000654 additive Substances 0.000 description 3
125000001931 aliphatic group Chemical group 0.000 description 3
239000002518 antifoaming agent Substances 0.000 description 3
235000010216 calcium carbonate Nutrition 0.000 description 3
229910000019 calcium carbonate Inorganic materials 0.000 description 3
238000010411 cooking Methods 0.000 description 3
235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 description 3
YHAIUSTWZPMYGG-UHFFFAOYSA-L disodium;2,2-dioctyl-3-sulfobutanedioate Chemical compound [Na+].[Na+].CCCCCCCCC(C([O-])=O)(C(C([O-])=O)S(O)(=O)=O)CCCCCCCC YHAIUSTWZPMYGG-UHFFFAOYSA-L 0.000 description 3
239000006185 dispersion Substances 0.000 description 3
230000008030 elimination Effects 0.000 description 3
238000003379 elimination reaction Methods 0.000 description 3
239000005038 ethylene vinyl acetate Substances 0.000 description 3
XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 3
238000002156 mixing Methods 0.000 description 3
239000000049 pigment Substances 0.000 description 3
229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 3
229920005862 polyol Polymers 0.000 description 3
150000003077 polyols Chemical class 0.000 description 3
CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-heptanol Chemical compound CCCCCCCO BBMCTIGTTCKYKF-UHFFFAOYSA-N 0.000 description 2
WNWHHMBRJJOGFJ-UHFFFAOYSA-N 16-methylheptadecan-1-ol Chemical compound CC(C)CCCCCCCCCCCCCCCO WNWHHMBRJJOGFJ-UHFFFAOYSA-N 0.000 description 2
YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 2
HCFAJYNVAYBARA-UHFFFAOYSA-N 4-heptanone Chemical compound CCCC(=O)CCC HCFAJYNVAYBARA-UHFFFAOYSA-N 0.000 description 2
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
QORUGOXNWQUALA-UHFFFAOYSA-N N=C=O.N=C=O.N=C=O.C1=CC=C(C(C2=CC=CC=C2)C2=CC=CC=C2)C=C1 Chemical compound N=C=O.N=C=O.N=C=O.C1=CC=C(C(C2=CC=CC=C2)C2=CC=CC=C2)C=C1 QORUGOXNWQUALA-UHFFFAOYSA-N 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
239000000783 alginic acid Substances 0.000 description 2
125000005907 alkyl ester group Chemical group 0.000 description 2
ZOJBYZNEUISWFT-UHFFFAOYSA-N allyl isothiocyanate Chemical compound C=CCN=C=S ZOJBYZNEUISWFT-UHFFFAOYSA-N 0.000 description 2
RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 2
MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 2
DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
125000005442 diisocyanate group Chemical group 0.000 description 2
239000000539 dimer Substances 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
NOPFSRXAKWQILS-UHFFFAOYSA-N docosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCO NOPFSRXAKWQILS-UHFFFAOYSA-N 0.000 description 2
230000000694 effects Effects 0.000 description 2
230000001804 emulsifying effect Effects 0.000 description 2
238000011156 evaluation Methods 0.000 description 2
239000006260 foam Substances 0.000 description 2
238000005187 foaming Methods 0.000 description 2
230000005484 gravity Effects 0.000 description 2
CATSNJVOTSVZJV-UHFFFAOYSA-N heptan-2-one Chemical compound CCCCCC(C)=O CATSNJVOTSVZJV-UHFFFAOYSA-N 0.000 description 2
NGAZZOYFWWSOGK-UHFFFAOYSA-N heptan-3-one Chemical compound CCCCC(=O)CC NGAZZOYFWWSOGK-UHFFFAOYSA-N 0.000 description 2
ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
BTFJIXJJCSYFAL-UHFFFAOYSA-N icosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCO BTFJIXJJCSYFAL-UHFFFAOYSA-N 0.000 description 2
ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Chemical compound CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 description 2
GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
239000003921 oil Substances 0.000 description 2
239000011120 plywood Substances 0.000 description 2
229920006389 polyphenyl polymer Polymers 0.000 description 2
239000000843 powder Substances 0.000 description 2
APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 2
238000003860 storage Methods 0.000 description 2
239000000758 substrate Substances 0.000 description 2
HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 2
239000008096 xylene Substances 0.000 description 2
ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
QXRRAZIZHCWBQY-UHFFFAOYSA-N 1,1-bis(isocyanatomethyl)cyclohexane Chemical compound O=C=NCC1(CN=C=O)CCCCC1 QXRRAZIZHCWBQY-UHFFFAOYSA-N 0.000 description 1
125000001989 1,3-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([H])C([*:2])=C1[H] 0.000 description 1
ALQLPWJFHRMHIU-UHFFFAOYSA-N 1,4-diisocyanatobenzene Chemical class O=C=NC1=CC=C(N=C=O)C=C1 ALQLPWJFHRMHIU-UHFFFAOYSA-N 0.000 description 1
SBJCUZQNHOLYMD-UHFFFAOYSA-N 1,5-Naphthalene diisocyanate Chemical compound C1=CC=C2C(N=C=O)=CC=CC2=C1N=C=O SBJCUZQNHOLYMD-UHFFFAOYSA-N 0.000 description 1
VZXPHDGHQXLXJC-UHFFFAOYSA-N 1,6-diisocyanato-5,6-dimethylheptane Chemical compound O=C=NC(C)(C)C(C)CCCCN=C=O VZXPHDGHQXLXJC-UHFFFAOYSA-N 0.000 description 1
ICLCCFKUSALICQ-UHFFFAOYSA-N 1-isocyanato-4-(4-isocyanato-3-methylphenyl)-2-methylbenzene Chemical compound C1=C(N=C=O)C(C)=CC(C=2C=C(C)C(N=C=O)=CC=2)=C1 ICLCCFKUSALICQ-UHFFFAOYSA-N 0.000 description 1
XUJLWPFSUCHPQL-UHFFFAOYSA-N 11-methyldodecan-1-ol Chemical compound CC(C)CCCCCCCCCCO XUJLWPFSUCHPQL-UHFFFAOYSA-N 0.000 description 1
QVVSQLONZBANPD-UHFFFAOYSA-N 2-(trioxidanylcarbonyl)benzoic acid Chemical compound OOOC(=O)C1=CC=CC=C1C(O)=O QVVSQLONZBANPD-UHFFFAOYSA-N 0.000 description 1
QCHSJPKDWOFACC-UHFFFAOYSA-N 2-Ethyl-4-methyl-1-pentanol Chemical compound CCC(CO)CC(C)C QCHSJPKDWOFACC-UHFFFAOYSA-N 0.000 description 1
GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
TZYRSLHNPKPEFV-UHFFFAOYSA-N 2-ethyl-1-butanol Chemical compound CCC(CC)CO TZYRSLHNPKPEFV-UHFFFAOYSA-N 0.000 description 1
ZPVFWPFBNIEHGJ-UHFFFAOYSA-N 2-octanone Chemical compound CCCCCCC(C)=O ZPVFWPFBNIEHGJ-UHFFFAOYSA-N 0.000 description 1
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BWDBEAQIHAEVLV-UHFFFAOYSA-N 6-methylheptan-1-ol Chemical compound CC(C)CCCCCO BWDBEAQIHAEVLV-UHFFFAOYSA-N 0.000 description 1
PLLBRTOLHQQAQQ-UHFFFAOYSA-N 8-methylnonan-1-ol Chemical compound CC(C)CCCCCCCO PLLBRTOLHQQAQQ-UHFFFAOYSA-N 0.000 description 1
KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 1
AXPZDYVDTMMLNB-UHFFFAOYSA-N Benzyl ethyl ether Chemical compound CCOCC1=CC=CC=C1 AXPZDYVDTMMLNB-UHFFFAOYSA-N 0.000 description 1
IRIAEXORFWYRCZ-UHFFFAOYSA-N Butylbenzyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCC1=CC=CC=C1 IRIAEXORFWYRCZ-UHFFFAOYSA-N 0.000 description 1
SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical class CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
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239000001293 FEMA 3089 Substances 0.000 description 1
239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 1
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YZBOVSFWWNVKRJ-UHFFFAOYSA-N Monobutylphthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(O)=O YZBOVSFWWNVKRJ-UHFFFAOYSA-N 0.000 description 1
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235000005018 Pinus echinata Nutrition 0.000 description 1
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230000002378 acidificating effect Effects 0.000 description 1
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239000004599 antimicrobial Substances 0.000 description 1
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150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
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239000004566 building material Substances 0.000 description 1
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BTMVHUNTONAYDX-UHFFFAOYSA-N butyl propionate Chemical compound CCCCOC(=O)CC BTMVHUNTONAYDX-UHFFFAOYSA-N 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
150000007942 carboxylates Chemical class 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
229960000541 cetyl alcohol Drugs 0.000 description 1
238000012512 characterization method Methods 0.000 description 1
239000008199 coating composition Substances 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
238000004132 cross linking Methods 0.000 description 1
238000005115 demineralization Methods 0.000 description 1
230000002328 demineralizing effect Effects 0.000 description 1
239000002274 desiccant Substances 0.000 description 1
229910003460 diamond Inorganic materials 0.000 description 1
239000010432 diamond Substances 0.000 description 1
238000007598 dipping method Methods 0.000 description 1
229960000735 docosanol Drugs 0.000 description 1
LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
238000004945 emulsification Methods 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000012634 fragment Substances 0.000 description 1
230000000855 fungicidal effect Effects 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
UPBDXRPQPOWRKR-UHFFFAOYSA-N furan-2,5-dione;methoxyethene Chemical compound COC=C.O=C1OC(=O)C=C1 UPBDXRPQPOWRKR-UHFFFAOYSA-N 0.000 description 1
239000003502 gasoline Substances 0.000 description 1
125000005456 glyceride group Chemical group 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical class OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
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 1
JMMWKPVZQRWMSS-UHFFFAOYSA-N isopropyl acetate Chemical compound CC(C)OC(C)=O JMMWKPVZQRWMSS-UHFFFAOYSA-N 0.000 description 1
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
229910052622 kaolinite Inorganic materials 0.000 description 1
239000003350 kerosene Substances 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
238000003475 lamination Methods 0.000 description 1
235000013490 limbo Nutrition 0.000 description 1
229940057995 liquid paraffin Drugs 0.000 description 1
230000014759 maintenance of location Effects 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
239000004579 marble Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
AYLRODJJLADBOB-QMMMGPOBSA-N methyl (2s)-2,6-diisocyanatohexanoate Chemical compound COC(=O)[C@@H](N=C=O)CCCCN=C=O AYLRODJJLADBOB-QMMMGPOBSA-N 0.000 description 1
150000004702 methyl esters Chemical class 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
229940073584 methylene chloride Drugs 0.000 description 1
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
229940043348 myristyl alcohol Drugs 0.000 description 1
GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
NZIDBRBFGPQCRY-UHFFFAOYSA-N octyl 2-methylprop-2-enoate Chemical compound CCCCCCCCOC(=O)C(C)=C NZIDBRBFGPQCRY-UHFFFAOYSA-N 0.000 description 1
ANISOHQJBAQUQP-UHFFFAOYSA-N octyl prop-2-enoate Chemical compound CCCCCCCCOC(=O)C=C ANISOHQJBAQUQP-UHFFFAOYSA-N 0.000 description 1
150000002888 oleic acid derivatives Chemical class 0.000 description 1
229940055577 oleyl alcohol Drugs 0.000 description 1
XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
239000012766 organic filler Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
150000003901 oxalic acid esters Chemical class 0.000 description 1
239000003973 paint Substances 0.000 description 1
150000003014 phosphoric acid esters Chemical class 0.000 description 1
150000003021 phthalic acid derivatives Chemical class 0.000 description 1
229920002432 poly(vinyl methyl ether) polymer Polymers 0.000 description 1
229920000867 polyelectrolyte Polymers 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
239000005056 polyisocyanate Substances 0.000 description 1
229920001228 polyisocyanate Polymers 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical class CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 description 1
PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
230000005855 radiation Effects 0.000 description 1
238000011160 research Methods 0.000 description 1
238000007761 roller coating Methods 0.000 description 1
150000003329 sebacic acid derivatives Chemical class 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
239000000779 smoke Substances 0.000 description 1
235000017557 sodium bicarbonate Nutrition 0.000 description 1
229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
239000007921 spray Substances 0.000 description 1
238000003892 spreading Methods 0.000 description 1
230000007480 spreading Effects 0.000 description 1
230000000087 stabilizing effect Effects 0.000 description 1
239000008107 starch Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
229940012831 stearyl alcohol Drugs 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
239000008399 tap water Substances 0.000 description 1
235000020679 tap water Nutrition 0.000 description 1
230000009974 thixotropic effect Effects 0.000 description 1
239000004408 titanium dioxide Substances 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
239000013638 trimer Substances 0.000 description 1
KGLSETWPYVUTQX-UHFFFAOYSA-N tris(4-isocyanatophenoxy)-sulfanylidene-$l^{5}-phosphane Chemical compound C1=CC(N=C=O)=CC=C1OP(=S)(OC=1C=CC(=CC=1)N=C=O)OC1=CC=C(N=C=O)C=C1 KGLSETWPYVUTQX-UHFFFAOYSA-N 0.000 description 1
PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
235000020234 walnut Nutrition 0.000 description 1
125000006839 xylylene group Chemical group 0.000 description 1
239000011787 zinc oxide Substances 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
- C09J133/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
- C09J133/04—Homopolymers or copolymers of esters
- C09J133/14—Homopolymers or copolymers of esters of esters containing halogen, nitrogen, sulfur or oxygen atoms in addition to the carboxy oxygen
- 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
- C08G18/62—Polymers of compounds having carbon-to-carbon double bonds
- C08G18/6216—Polymers of alpha-beta ethylenically unsaturated carboxylic acids or of derivatives thereof
- C08G18/622—Polymers of esters of alpha-beta ethylenically unsaturated carboxylic acids
- C08G18/6225—Polymers of esters of acrylic or methacrylic acid
- C08G18/6229—Polymers of hydroxy groups containing esters of acrylic or methacrylic acid with aliphatic polyalcohols
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L29/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical; Compositions of hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Compositions of derivatives of such polymers
- 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
- C08G2170/00—Compositions for adhesives
- C08G2170/80—Compositions for aqueous adhesives
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
- C08L2666/04—Macromolecular compounds according to groups C08L7/00 - C08L49/00, or C08L55/00 - C08L57/00; Derivatives thereof
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
- C08L2666/10—Homopolymers or copolymers according to C08L39/00 - C08L49/00; Derivatives thereof
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
- C08L2666/14—Macromolecular compounds according to C08L59/00 - C08L87/00; Derivatives thereof
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/04—Polyurethanes
- 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.]
- Y10T428/31591—Next to cellulosic

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)
Compositions Of Macromolecular Compounds (AREA)

SE8404842A 1983-09-29 1984-09-27 Latexbindemedel med isocyanatreaktiv funktionalitet, foerfarande foer dess framstaellning samt med bindemedlet sammanfogad traekomposit SE463923B (sv)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US06/537,294 US4491646A (en)	1983-09-29	1983-09-29	Aqueous hydroxyl-acrylic latex and multi-isocyanate adhesive composition

Publications (3)

Publication Number	Publication Date
SE8404842D0 SE8404842D0 (sv)	1984-09-27
SE8404842L SE8404842L (sv)	1985-03-30
SE463923B true SE463923B (sv)	1991-02-11

Family

ID=24142049

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SE8404842A SE463923B (sv)	1983-09-29	1984-09-27	Latexbindemedel med isocyanatreaktiv funktionalitet, foerfarande foer dess framstaellning samt med bindemedlet sammanfogad traekomposit

Country Status (9)

Country	Link
US (1)	US4491646A (da)
JP (1)	JPS6092376A (da)
AU (1)	AU548554B2 (da)
CA (1)	CA1267992A (da)
DE (1)	DE3435777C2 (da)
DK (1)	DK157368C (da)
FI (1)	FI79131C (da)
NO (1)	NO158947C (da)
SE (1)	SE463923B (da)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4609690A (en) *	1983-09-29	1986-09-02	Ashland Oil, Inc.	Aqueous hydroxyl-acrylic latex and water dispersible multi-isocyanate adhesive composition
JPS61225249A (ja) *	1985-03-29	1986-10-07	Toyoda Gosei Co Ltd	水膨潤性組成物
JP2540736B2 (ja) *	1986-03-17	1996-10-09	大日本インキ化学工業株式会社	塗料用樹脂組成物
US5092953A (en) *	1989-03-21	1992-03-03	Air Products And Chemicals, Inc.	Aqueous vinyl chloride-ethylene copolymer/polyisocyanate adhesive compositions for wood composites
SE465740B (sv) *	1990-03-08	1991-10-21	Gisip Innovations Ab	Saett foer torkning av limfogar
US5215783A (en) *	1991-06-24	1993-06-01	E. I. Du Pont De Nemours And Company	Low voc clear epoxy acrylic coating composition for basecoat clear finish
SE512316C2 (sv) *	1993-03-01	2000-02-28	Cirrus Ab	Sätt och anordning vid framställning av produkt av expanderad polymer
US5800658A (en) *	1993-03-01	1998-09-01	Cirrus Ab	Method and means by manufacture of a product of expanded polymer
US5807919A (en) *	1996-08-13	1998-09-15	H.B. Fuller Licensing & Financing, Inc.	Water-based sulfonated polymer compositions
US6348679B1 (en) *	1998-03-17	2002-02-19	Ameritherm, Inc.	RF active compositions for use in adhesion, bonding and coating
US6649888B2 (en) *	1999-09-23	2003-11-18	Codaco, Inc.	Radio frequency (RF) heating system
JP3524462B2 (ja) *	2000-03-03	2004-05-10	日本エヌエスシー株式会社	水系接着剤
US6489024B2 (en) *	2001-02-12	2002-12-03	Rohm And Haas Company	Pressure sensitive adhesive tape containing natural rubber latex
DE60218387T2 (de) *	2001-07-20	2007-11-08	Rohm And Haas Co.	Wässrige Hybridklebemittelzusammensetzung und Verfahren
US20040065425A1 (en) *	2002-10-07	2004-04-08	Kemira Chemicals, Inc.	Latex paper sizing composition
KR100515573B1 (ko) *	2003-03-20	2005-09-20	주식회사 엘지화학	플라즈마 디스플레이 패널용 전자파 차폐 필터 및 이의 제조방법
FR2870549B1 (fr) *	2004-05-24	2006-08-25	Financ Elysees Balzac Sa	Non-tisse recurant, outil d'entretien incorporant dans sa structure ledit non-tisse recurant, fabrication
JP4455472B2 (ja) *	2005-09-28	2010-04-21	ロームアンドハースカンパニー	二成分アクリル‐ウレタン接着剤
US20090162680A1 (en) *	2005-11-08	2009-06-25	Jun Zheng	Process for making wood laminates using fast setting adhesives at ambient temperature
US20070102108A1 (en) *	2005-11-08	2007-05-10	Jun Zheng	Process for making wood laminates using fast setting adhesives at ambient temperature
US20070155879A1 (en) *	2005-12-22	2007-07-05	Ips Corporation	Adhesive compositions for bonding metals
US8568888B2 (en)	2007-03-15	2013-10-29	Nanovere Technologies, Inc.	Dendritic polyurethane coating
US8206827B2 (en) *	2007-03-15	2012-06-26	Nanovere Technologies, Llc	Dendritic polyurethane coating
CN102115630A (zh) *	2009-12-31	2011-07-06	广东华润涂料有限公司	水性封闭剂体系、木制品以及封闭木质基材的方法
CN105593292B (zh) *	2013-10-11	2019-02-22	陶氏环球技术有限责任公司	聚合物混合物、含有其的多层物品和制造所述多层物品的方法
JP7153026B2 (ja) *	2017-03-13	2022-10-13	ダウグローバルテクノロジーズエルエルシー	水性感圧接着剤組成物およびその製造方法

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Publication number	Priority date	Publication date	Assignee	Title
DE1621822B2 (de) *	1967-12-06	1974-07-18	Basf Ag, 6700 Ludwigshafen	Verfahren zur Herstellung von Überzügen
JPS4926346A (da) *	1972-07-04	1974-03-08
JPS5130577B2 (da) *	1972-08-05	1976-09-01
US4215023A (en) *	1978-11-13	1980-07-29	E. I. Du Pont De Nemours And Company	Urethane enamel coating composition
US4268641A (en) *	1979-04-24	1981-05-19	Union Carbide Corporation	Acrylic acid-acrylate copolymer thickening agents
DE3112117A1 (de) *	1981-03-27	1982-10-07	Bayer Ag, 5090 Leverkusen	Verwendung von in wasser dispergierbaren polyisocyanat-zubereitungen als zusatzmittel fuer waessrige klebstoffe

1983
- 1983-09-29 US US06/537,294 patent/US4491646A/en not_active Expired - Fee Related
1984
- 1984-09-19 CA CA000463637A patent/CA1267992A/en not_active Expired - Lifetime
- 1984-09-27 NO NO843873A patent/NO158947C/no unknown
- 1984-09-27 FI FI843811A patent/FI79131C/fi not_active IP Right Cessation
- 1984-09-27 DK DK463784A patent/DK157368C/da not_active IP Right Cessation
- 1984-09-27 SE SE8404842A patent/SE463923B/sv not_active IP Right Cessation
- 1984-09-28 DE DE3435777A patent/DE3435777C2/de not_active Expired
- 1984-09-28 AU AU33669/84A patent/AU548554B2/en not_active Ceased
- 1984-09-28 JP JP59202104A patent/JPS6092376A/ja active Pending

Also Published As

Publication number	Publication date
DK157368B (da)	1989-12-27
DK463784A (da)	1985-03-30
FI843811A0 (fi)	1984-09-27
SE8404842L (sv)	1985-03-30
AU548554B2 (en)	1985-12-19
DE3435777A1 (de)	1985-04-11
DK463784D0 (da)	1984-09-27
CA1267992A (en)	1990-04-17
FI843811L (fi)	1985-03-30
SE8404842D0 (sv)	1984-09-27
DE3435777C2 (de)	1987-01-02
NO158947B (no)	1988-08-08
FI79131B (fi)	1989-07-31
AU3366984A (en)	1985-04-04
JPS6092376A (ja)	1985-05-23
FI79131C (fi)	1989-11-10
DK157368C (da)	1990-05-21
US4491646A (en)	1985-01-01
NO158947C (no)	1988-11-16
NO843873L (no)	1985-04-01

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Publication	Publication Date	Title
SE463923B (sv)	1991-02-11	Latexbindemedel med isocyanatreaktiv funktionalitet, foerfarande foer dess framstaellning samt med bindemedlet sammanfogad traekomposit
US4609690A (en)	1986-09-02	Aqueous hydroxyl-acrylic latex and water dispersible multi-isocyanate adhesive composition
CA2055419C (en)	1999-07-13	Nonaqueous polyisocyanate formulation
JP4684379B2 (ja)	2011-05-18	コポリマー混合物を含有する水性分散液、及び結合剤へのその使用
EP1632530B1 (en)	2010-08-18	Aqueous polyolefin resin dispersion, process for producing the same, and water-based coating material comprising the same
KR100735867B1 (ko)	2007-07-06	이-성분 아크릴릭-우레탄 결합제
CA2321692C (en)	2004-11-02	High solids water-borne surface coating containing hollow particulates
MXPA06014864A (es)	2007-03-23	Dispersante de pigmento, metodo para hacer composiciones de revestimiento, y composiciones de revestimiento.
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