JP2022539516A - 結合樹脂を調製する方法 - Google Patents
結合樹脂を調製する方法 Download PDFInfo
- Publication number
- JP2022539516A JP2022539516A JP2021576569A JP2021576569A JP2022539516A JP 2022539516 A JP2022539516 A JP 2022539516A JP 2021576569 A JP2021576569 A JP 2021576569A JP 2021576569 A JP2021576569 A JP 2021576569A JP 2022539516 A JP2022539516 A JP 2022539516A
- Authority
- JP
- Japan
- Prior art keywords
- ether
- diglycidyl
- triglycidyl
- polyglycidyl
- diglycidyl ether
- 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
- 229920005989 resin Polymers 0.000 title claims abstract description 47
- 239000011347 resin Substances 0.000 title claims abstract description 47
- 238000000034 method Methods 0.000 title claims description 29
- 229920005610 lignin Polymers 0.000 claims abstract description 49
- 239000011120 plywood Substances 0.000 claims abstract description 18
- 239000003637 basic solution Substances 0.000 claims abstract description 15
- 239000011094 fiberboard Substances 0.000 claims abstract description 15
- 238000009413 insulation Methods 0.000 claims abstract description 15
- 239000011490 mineral wool Substances 0.000 claims abstract description 15
- 239000002023 wood Substances 0.000 claims abstract description 14
- 238000004519 manufacturing process Methods 0.000 claims abstract description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000007787 solid Substances 0.000 claims abstract description 10
- 239000000654 additive Substances 0.000 claims abstract description 8
- 239000006185 dispersion Substances 0.000 claims abstract description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 64
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical group C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 claims description 31
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 27
- 150000002148 esters Chemical class 0.000 claims description 20
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical class OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 17
- 150000001540 azides Chemical class 0.000 claims description 15
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical group CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 14
- 150000002009 diols Chemical group 0.000 claims description 14
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 claims description 13
- 150000001720 carbohydrates Chemical class 0.000 claims description 10
- 235000014633 carbohydrates Nutrition 0.000 claims description 10
- KVVSCMOUFCNCGX-UHFFFAOYSA-N cardol Chemical compound CCCCCCCCCCCCCCCC1=CC(O)=CC(O)=C1 KVVSCMOUFCNCGX-UHFFFAOYSA-N 0.000 claims description 10
- 229920001451 polypropylene glycol Polymers 0.000 claims description 10
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 claims description 10
- IVIDDMGBRCPGLJ-UHFFFAOYSA-N 2,3-bis(oxiran-2-ylmethoxy)propan-1-ol Chemical compound C1OC1COC(CO)COCC1CO1 IVIDDMGBRCPGLJ-UHFFFAOYSA-N 0.000 claims description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 9
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims description 9
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 claims description 9
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims description 9
- -1 polyoxy Propylene glycol diglycidyl ether Polymers 0.000 claims description 9
- 239000000600 sorbitol Substances 0.000 claims description 9
- 239000004971 Cross linker Substances 0.000 claims description 8
- 239000000853 adhesive Substances 0.000 claims description 8
- 230000001070 adhesive effect Effects 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 238000002156 mixing Methods 0.000 claims description 8
- 229920000223 polyglycerol Polymers 0.000 claims description 8
- 239000002904 solvent Substances 0.000 claims description 8
- 239000001648 tannin Substances 0.000 claims description 8
- 235000018553 tannin Nutrition 0.000 claims description 8
- 229920001864 tannin Polymers 0.000 claims description 8
- UWFRVQVNYNPBEF-UHFFFAOYSA-N 1-(2,4-dimethylphenyl)propan-1-one Chemical compound CCC(=O)C1=CC=C(C)C=C1C UWFRVQVNYNPBEF-UHFFFAOYSA-N 0.000 claims description 7
- SYEWHONLFGZGLK-UHFFFAOYSA-N 2-[1,3-bis(oxiran-2-ylmethoxy)propan-2-yloxymethyl]oxirane Chemical compound C1OC1COCC(OCC1OC1)COCC1CO1 SYEWHONLFGZGLK-UHFFFAOYSA-N 0.000 claims description 7
- JEBWAOITKHXCBF-BEAPMJEYSA-N (3s,3ar,6r,6ar)-3,6-bis(oxiran-2-ylmethoxy)-2,3,3a,5,6,6a-hexahydrofuro[3,2-b]furan Chemical compound O([C@@H]1[C@H]2OC[C@H]([C@H]2OC1)OCC1OC1)CC1CO1 JEBWAOITKHXCBF-BEAPMJEYSA-N 0.000 claims description 6
- JTINZFQXZLCHNS-UHFFFAOYSA-N 2,2-bis(oxiran-2-ylmethoxymethyl)butan-1-ol Chemical compound C1OC1COCC(CO)(CC)COCC1CO1 JTINZFQXZLCHNS-UHFFFAOYSA-N 0.000 claims description 6
- HDPLHDGYGLENEI-UHFFFAOYSA-N 2-[1-(oxiran-2-ylmethoxy)propan-2-yloxymethyl]oxirane Chemical compound C1OC1COC(C)COCC1CO1 HDPLHDGYGLENEI-UHFFFAOYSA-N 0.000 claims description 6
- PLDLPVSQYMQDBL-UHFFFAOYSA-N 2-[[3-(oxiran-2-ylmethoxy)-2,2-bis(oxiran-2-ylmethoxymethyl)propoxy]methyl]oxirane Chemical compound C1OC1COCC(COCC1OC1)(COCC1OC1)COCC1CO1 PLDLPVSQYMQDBL-UHFFFAOYSA-N 0.000 claims description 6
- UUODQIKUTGWMPT-UHFFFAOYSA-N 2-fluoro-5-(trifluoromethyl)pyridine Chemical compound FC1=CC=C(C(F)(F)F)C=N1 UUODQIKUTGWMPT-UHFFFAOYSA-N 0.000 claims description 6
- MECNWXGGNCJFQJ-UHFFFAOYSA-N 3-piperidin-1-ylpropane-1,2-diol Chemical compound OCC(O)CN1CCCCC1 MECNWXGGNCJFQJ-UHFFFAOYSA-N 0.000 claims description 6
- 241000196324 Embryophyta Species 0.000 claims description 6
- 239000002202 Polyethylene glycol Substances 0.000 claims description 6
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 claims description 6
- 150000002989 phenols Chemical class 0.000 claims description 6
- 229920001223 polyethylene glycol Polymers 0.000 claims description 6
- HYYJOCXNESGFSB-UHFFFAOYSA-N 1-(oxiran-2-yl)-n-(oxiran-2-ylmethyl)methanamine Chemical class C1OC1CNCC1CO1 HYYJOCXNESGFSB-UHFFFAOYSA-N 0.000 claims description 5
- JOLVYUIAMRUBRK-UHFFFAOYSA-N 11',12',14',15'-Tetradehydro(Z,Z-)-3-(8-Pentadecenyl)phenol Natural products OC1=CC=CC(CCCCCCCC=CCC=CCC=C)=C1 JOLVYUIAMRUBRK-UHFFFAOYSA-N 0.000 claims description 5
- IGZBSJAMZHNHKE-UHFFFAOYSA-N 2-[[4-[bis[4-(oxiran-2-ylmethoxy)phenyl]methyl]phenoxy]methyl]oxirane Chemical compound C1OC1COC(C=C1)=CC=C1C(C=1C=CC(OCC2OC2)=CC=1)C(C=C1)=CC=C1OCC1CO1 IGZBSJAMZHNHKE-UHFFFAOYSA-N 0.000 claims description 5
- YLKVIMNNMLKUGJ-UHFFFAOYSA-N 3-Delta8-pentadecenylphenol Natural products CCCCCCC=CCCCCCCCC1=CC=CC(O)=C1 YLKVIMNNMLKUGJ-UHFFFAOYSA-N 0.000 claims description 5
- 229940090248 4-hydroxybenzoic acid Drugs 0.000 claims description 5
- JOLVYUIAMRUBRK-UTOQUPLUSA-N Cardanol Chemical compound OC1=CC=CC(CCCCCCC\C=C/C\C=C/CC=C)=C1 JOLVYUIAMRUBRK-UTOQUPLUSA-N 0.000 claims description 5
- FAYVLNWNMNHXGA-UHFFFAOYSA-N Cardanoldiene Natural products CCCC=CCC=CCCCCCCCC1=CC=CC(O)=C1 FAYVLNWNMNHXGA-UHFFFAOYSA-N 0.000 claims description 5
- 235000019484 Rapeseed oil Nutrition 0.000 claims description 5
- ORLQHILJRHBSAY-UHFFFAOYSA-N [1-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1(CO)CCCCC1 ORLQHILJRHBSAY-UHFFFAOYSA-N 0.000 claims description 5
- KAOMOVYHGLSFHQ-UTOQUPLUSA-N anacardic acid Chemical compound CCC\C=C/C\C=C/CCCCCCCC1=CC=CC(O)=C1C(O)=O KAOMOVYHGLSFHQ-UTOQUPLUSA-N 0.000 claims description 5
- 235000014398 anacardic acid Nutrition 0.000 claims description 5
- ADFWQBGTDJIESE-UHFFFAOYSA-N anacardic acid 15:0 Natural products CCCCCCCCCCCCCCCC1=CC=CC(O)=C1C(O)=O ADFWQBGTDJIESE-UHFFFAOYSA-N 0.000 claims description 5
- XFUOBHWPTSIEOV-UHFFFAOYSA-N bis(oxiran-2-ylmethyl) cyclohexane-1,2-dicarboxylate Chemical class C1CCCC(C(=O)OCC2OC2)C1C(=O)OCC1CO1 XFUOBHWPTSIEOV-UHFFFAOYSA-N 0.000 claims description 5
- 239000004202 carbamide Substances 0.000 claims description 5
- PTFIPECGHSYQNR-UHFFFAOYSA-N cardanol Natural products CCCCCCCCCCCCCCCC1=CC=CC(O)=C1 PTFIPECGHSYQNR-UHFFFAOYSA-N 0.000 claims description 5
- UFMJCOLGRWKUKO-UHFFFAOYSA-N cardol diene Natural products CCCC=CCC=CCCCCCCCC1=CC(O)=CC(O)=C1 UFMJCOLGRWKUKO-UHFFFAOYSA-N 0.000 claims description 5
- 239000000945 filler Substances 0.000 claims description 5
- 125000000524 functional group Chemical group 0.000 claims description 5
- 235000021388 linseed oil Nutrition 0.000 claims description 5
- 239000000944 linseed oil Substances 0.000 claims description 5
- JAYXSROKFZAHRQ-UHFFFAOYSA-N n,n-bis(oxiran-2-ylmethyl)aniline Chemical compound C1OC1CN(C=1C=CC=CC=1)CC1CO1 JAYXSROKFZAHRQ-UHFFFAOYSA-N 0.000 claims description 5
- 229920002454 poly(glycidyl methacrylate) polymer Polymers 0.000 claims description 5
- YQUVCSBJEUQKSH-UHFFFAOYSA-N protochatechuic acid Natural products OC(=O)C1=CC=C(O)C(O)=C1 YQUVCSBJEUQKSH-UHFFFAOYSA-N 0.000 claims description 5
- 229960004889 salicylic acid Drugs 0.000 claims description 5
- 235000012424 soybean oil Nutrition 0.000 claims description 5
- 239000003549 soybean oil Substances 0.000 claims description 5
- XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 5
- WKOLLVMJNQIZCI-UHFFFAOYSA-N vanillic acid Chemical compound COC1=CC(C(O)=O)=CC=C1O WKOLLVMJNQIZCI-UHFFFAOYSA-N 0.000 claims description 5
- TUUBOHWZSQXCSW-UHFFFAOYSA-N vanillic acid Natural products COC1=CC(O)=CC(C(O)=O)=C1 TUUBOHWZSQXCSW-UHFFFAOYSA-N 0.000 claims description 5
- 235000015112 vegetable and seed oil Nutrition 0.000 claims description 5
- 239000008158 vegetable oil Substances 0.000 claims description 5
- VQKFNUFAXTZWDK-UHFFFAOYSA-N 2-Methylfuran Chemical compound CC1=CC=CO1 VQKFNUFAXTZWDK-UHFFFAOYSA-N 0.000 claims description 4
- 239000004593 Epoxy Substances 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- 150000001412 amines Chemical class 0.000 claims description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- 239000002270 dispersing agent Substances 0.000 claims description 2
- 230000032050 esterification Effects 0.000 claims description 2
- 238000005886 esterification reaction Methods 0.000 claims description 2
- 238000006266 etherification reaction Methods 0.000 claims description 2
- 239000004094 surface-active agent Substances 0.000 claims description 2
- 150000003573 thiols Chemical class 0.000 claims description 2
- 230000000996 additive effect Effects 0.000 claims 2
- 239000003431 cross linking reagent Substances 0.000 abstract description 8
- 238000009408 flooring Methods 0.000 abstract description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 18
- 239000002245 particle Substances 0.000 description 11
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- AOBIOSPNXBMOAT-UHFFFAOYSA-N 2-[2-(oxiran-2-ylmethoxy)ethoxymethyl]oxirane Chemical compound C1OC1COCCOCC1CO1 AOBIOSPNXBMOAT-UHFFFAOYSA-N 0.000 description 6
- 150000001408 amides Chemical class 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 150000002118 epoxides Chemical group 0.000 description 5
- 125000003118 aryl group Chemical group 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 238000003825 pressing Methods 0.000 description 4
- 230000009257 reactivity Effects 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- SOGYZZRPOIMNHO-UHFFFAOYSA-N [2-(hydroxymethyl)furan-3-yl]methanol Chemical compound OCC=1C=COC=1CO SOGYZZRPOIMNHO-UHFFFAOYSA-N 0.000 description 3
- 229940045720 antineoplastic alkylating drug epoxides Drugs 0.000 description 3
- 239000011230 binding agent Substances 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000002131 composite material Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 239000000123 paper Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 240000000731 Fagus sylvatica Species 0.000 description 2
- 235000010099 Fagus sylvatica Nutrition 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 230000003750 conditioning effect Effects 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 239000011121 hardwood Substances 0.000 description 2
- 238000007731 hot pressing Methods 0.000 description 2
- 229920005611 kraft lignin Polymers 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- 239000004848 polyfunctional curative Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 2
- BXGYYDRIMBPOMN-UHFFFAOYSA-N 2-(hydroxymethoxy)ethoxymethanol Chemical compound OCOCCOCO BXGYYDRIMBPOMN-UHFFFAOYSA-N 0.000 description 1
- RQZUWSJHFBOFPI-UHFFFAOYSA-N 2-[1-[1-(oxiran-2-ylmethoxy)propan-2-yloxy]propan-2-yloxymethyl]oxirane Chemical group C1OC1COC(C)COC(C)COCC1CO1 RQZUWSJHFBOFPI-UHFFFAOYSA-N 0.000 description 1
- SEFYJVFBMNOLBK-UHFFFAOYSA-N 2-[2-[2-(oxiran-2-ylmethoxy)ethoxy]ethoxymethyl]oxirane Chemical group C1OC1COCCOCCOCC1CO1 SEFYJVFBMNOLBK-UHFFFAOYSA-N 0.000 description 1
- 241000218631 Coniferophyta Species 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- UMILHIMHKXVDGH-UHFFFAOYSA-N Triethylene glycol diglycidyl ether Chemical group C1OC1COCCOCCOCCOCC1CO1 UMILHIMHKXVDGH-UHFFFAOYSA-N 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- JRPRCOLKIYRSNH-UHFFFAOYSA-N bis(oxiran-2-ylmethyl) benzene-1,2-dicarboxylate Chemical class C=1C=CC=C(C(=O)OCC2OC2)C=1C(=O)OCC1CO1 JRPRCOLKIYRSNH-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 235000010980 cellulose Nutrition 0.000 description 1
- 239000012707 chemical precursor Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000004925 denaturation Methods 0.000 description 1
- 230000036425 denaturation Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000006735 epoxidation reaction Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 229960005237 etoglucid Drugs 0.000 description 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 1
- 125000003827 glycol group Chemical group 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000002655 kraft paper Substances 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 238000004537 pulping Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 229940079877 pyrogallol Drugs 0.000 description 1
- 229920003987 resole Polymers 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 229940080313 sodium starch Drugs 0.000 description 1
- 239000011122 softwood Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 239000012855 volatile organic compound 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
- C09J171/00—Adhesives based on polyethers obtained by reactions forming an ether link in the main chain; Adhesives based on derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/62—Alcohols or phenols
- C08G59/621—Phenols
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
- C08G59/32—Epoxy compounds containing three or more epoxy groups
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
- B27N—MANUFACTURE BY DRY PROCESSES OF ARTICLES, WITH OR WITHOUT ORGANIC BINDING AGENTS, MADE FROM PARTICLES OR FIBRES CONSISTING OF WOOD OR OTHER LIGNOCELLULOSIC OR LIKE ORGANIC MATERIAL
- B27N1/00—Pretreatment of moulding material
- B27N1/003—Pretreatment of moulding material for reducing formaldehyde gas emission
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
- B27N—MANUFACTURE BY DRY PROCESSES OF ARTICLES, WITH OR WITHOUT ORGANIC BINDING AGENTS, MADE FROM PARTICLES OR FIBRES CONSISTING OF WOOD OR OTHER LIGNOCELLULOSIC OR LIKE ORGANIC MATERIAL
- B27N1/00—Pretreatment of moulding material
- B27N1/02—Mixing the material with binding agent
- B27N1/0209—Methods, e.g. characterised by the composition of the agent
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
- B27N—MANUFACTURE BY DRY PROCESSES OF ARTICLES, WITH OR WITHOUT ORGANIC BINDING AGENTS, MADE FROM PARTICLES OR FIBRES CONSISTING OF WOOD OR OTHER LIGNOCELLULOSIC OR LIKE ORGANIC MATERIAL
- B27N3/00—Manufacture of substantially flat articles, e.g. boards, from particles or fibres
- B27N3/002—Manufacture of substantially flat articles, e.g. boards, from particles or fibres characterised by the type of binder
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
- B27N—MANUFACTURE BY DRY PROCESSES OF ARTICLES, WITH OR WITHOUT ORGANIC BINDING AGENTS, MADE FROM PARTICLES OR FIBRES CONSISTING OF WOOD OR OTHER LIGNOCELLULOSIC OR LIKE ORGANIC MATERIAL
- B27N3/00—Manufacture of substantially flat articles, e.g. boards, from particles or fibres
- B27N3/04—Manufacture of substantially flat articles, e.g. boards, from particles or fibres from fibres
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B19/00—Layered products comprising a layer of natural mineral fibres or particles, e.g. asbestos, mica
- B32B19/06—Layered products comprising a layer of natural mineral fibres or particles, e.g. asbestos, mica next to a fibrous or filamentary layer
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B21/00—Layered products comprising a layer of wood, e.g. wood board, veneer, wood particle board
- B32B21/02—Layered products comprising a layer of wood, e.g. wood board, veneer, wood particle board the layer being formed of fibres, chips, or particles, e.g. MDF, HDF, OSB, chipboard, particle board, hardboard
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B21/00—Layered products comprising a layer of wood, e.g. wood board, veneer, wood particle board
- B32B21/04—Layered products comprising a layer of wood, e.g. wood board, veneer, wood particle board comprising wood as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B21/042—Layered products comprising a layer of wood, e.g. wood board, veneer, wood particle board comprising wood as the main or only constituent of a layer, which is next to another layer of the same or of a different material of wood
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B21/00—Layered products comprising a layer of wood, e.g. wood board, veneer, wood particle board
- B32B21/12—Layered products comprising a layer of wood, e.g. wood board, veneer, wood particle board next to a particulate layer
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B21/00—Layered products comprising a layer of wood, e.g. wood board, veneer, wood particle board
- B32B21/13—Layered products comprising a layer of wood, e.g. wood board, veneer, wood particle board all layers being exclusively wood
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B21/00—Layered products comprising a layer of wood, e.g. wood board, veneer, wood particle board
- B32B21/14—Layered products comprising a layer of wood, e.g. wood board, veneer, wood particle board comprising wood board or veneer
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
- B32B7/04—Interconnection of layers
- B32B7/12—Interconnection of layers using interposed adhesives or interposed materials with bonding properties
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08H—DERIVATIVES OF NATURAL MACROMOLECULAR COMPOUNDS
- C08H6/00—Macromolecular compounds derived from lignin, e.g. tannins, humic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L97/00—Compositions of lignin-containing materials
- C08L97/005—Lignin
-
- 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
- C09J163/00—Adhesives based on epoxy resins; Adhesives based on derivatives of epoxy resins
-
- 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
- C09J197/00—Adhesives based on lignin-containing materials
- C09J197/005—Lignin
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
- B27N—MANUFACTURE BY DRY PROCESSES OF ARTICLES, WITH OR WITHOUT ORGANIC BINDING AGENTS, MADE FROM PARTICLES OR FIBRES CONSISTING OF WOOD OR OTHER LIGNOCELLULOSIC OR LIKE ORGANIC MATERIAL
- B27N3/00—Manufacture of substantially flat articles, e.g. boards, from particles or fibres
- B27N3/02—Manufacture of substantially flat articles, e.g. boards, from particles or fibres from particles
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2255/00—Coating on the layer surface
- B32B2255/08—Coating on the layer surface on wood layer
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2255/00—Coating on the layer surface
- B32B2255/26—Polymeric coating
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2419/00—Buildings or parts thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Wood Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Materials Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Forests & Forestry (AREA)
- Biochemistry (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Epoxy Resins (AREA)
- Dry Formation Of Fiberboard And The Like (AREA)
Abstract
Description
結合樹脂を調製する方法であって、
固形または水中分散液の形態のリグニンを、
グリセロールジグリシジルエーテル、ジグリセロールポリグリシジルエーテル、ポリグリセロールポリグリシジルエーテル、グリセロールトリグリシジルエーテル、ソルビトールポリグリシジルエーテル、アルコキシル化グリセロールポリグリシジルエーテル、トリメチロールプロパントリグリシジルエーテル、トリメチロールプロパンジグリシジルエーテル、ポリオキシプロピレングリコールジグリシジルエーテル、ポリオキシプロピレングリコールトリグリシジルエーテル、シクロヘキサンジメタノールのジグリシジルエーテル、レゾルシノールジグリシジルエーテル、イソソルビドジグリシジルエーテル、ペンタエリスリトールテトラグリシジルエーテル、エチレングリコールジグリシジルエーテル、2~9のエチレングリコール単位を有するポリエチレングリコールジグリシジルエーテル、1~5のプロピレングリコール単位を有するプロピレングリコールジグリシジルエーテル、3~6個の炭素原子の直鎖炭素鎖を有する末端ジオールのヘキサヒドロフタル酸ジグリシジルエステルおよび/もしくは当該末端ジオールのジグリシジルエーテル、または、炭水化物のジグリシジル-、トリグリシジル-もしくはポリグリシジル-エーテル、炭水化物のジグリシジル-、トリグリシジル-もしくはポリグリシジル-エステル、サリチル酸、バニリン酸、もしくは4-ヒドロキシ安息香酸のジグリシジルエーテルもしくはジグリシジルエステル、エポキシ化もしくはグリシジル置換の植物系フェノール化合物(タンニン、カルダノール、カルドール、アナカルド酸など)、エポキシ化植物油(菜種油、亜麻仁油、大豆油など)、トリス(4-ヒドロキシフェニル)メタントリグリシジルエーテル、N,N-ビス(2,3-エポキシプロピル)アニリン、p-(2,3-エポキシプロポキシ-N,N-ビス(2,3-エポキシプロピル)アニリン、ビス-ヒドロキシメチルフランのジグリシジルエーテル、ならびに、ジグリシジルアミド、トリグリシジルアミド、ポリグリシジルアミド、ジグリシジルエステル、トリグリシジルエステル、ポリグリシジルエステル、ジグリシジルアジド、トリグリシジルアジド、ポリグリシジルアジド、ジグリシジルメタクリラート、トリグリシジルメタクリラート、およびポリグリシジルメタクリラートから選択された官能基を有する架橋剤の1種または複数種と混合し、
次いで、塩基性溶液を添加することを含む、
上記方法。
40gのリグニンを60gのポリグリセロールポリグリシジルエーテルおよび30gのグリセロールに分散させることによって第1の成分を調製した。17.4gの50%水酸化ナトリウム溶液と49.8gの水とを混合することによって第2の成分を調製した。両方の成分を混合し、室温でオーバーヘッドスターラーを使用して20分間撹拌した。
40gのリグニンを60gのポリエチレングリコールジグリシジルエーテルに分散させることによって第1の成分を調製した。22.6gの50%水酸化ナトリウム溶液と80gの水とを混合することによって第2の成分を調製した。第1の成分および第2の成分を混合し、室温でオーバーヘッドスターラーを使用して20分間撹拌した。
Claims (13)
- 結合樹脂を調製する方法であって、
固形または水中分散液の形態のリグニンを、
グリセロールジグリシジルエーテル、ジグリセロールポリグリシジルエーテル、ポリグリセロールポリグリシジルエーテル、グリセロールトリグリシジルエーテル、ソルビトールポリグリシジルエーテル、アルコキシル化グリセロールポリグリシジルエーテル、トリメチロールプロパントリグリシジルエーテル、トリメチロールプロパンジグリシジルエーテル、ポリオキシプロピレングリコールジグリシジルエーテル、ポリオキシプロピレングリコールトリグリシジルエーテル、シクロヘキサンジメタノールのジグリシジルエーテル、レゾルシノールジグリシジルエーテル、イソソルビドジグリシジルエーテル、ペンタエリスリトールテトラグリシジルエーテル、エチレングリコールジグリシジルエーテル、2~9のエチレングリコール単位を有するポリエチレングリコールジグリシジルエーテル、1~5のプロピレングリコール単位を有するプロピレングリコールジグリシジルエーテル、3~6個の炭素原子の直鎖炭素鎖を有する末端ジオールのヘキサヒドロフタル酸ジグリシジルエステルおよび/もしくは当該末端ジオールのジグリシジルエーテル、または、炭水化物のジグリシジル-、トリグリシジル-もしくはポリグリシジル-エーテル、炭水化物のジグリシジル-、トリグリシジル-もしくはポリグリシジル-エステル、サリチル酸、バニリン酸、もしくは4-ヒドロキシ安息香酸のジグリシジルエーテルもしくはジグリシジルエステル、エポキシ化もしくはグリシジル置換の植物系フェノール化合物(タンニン、カルダノール、カルドール、アナカルド酸など)、エポキシ化植物油(菜種油、亜麻仁油、大豆油など)、トリス(4-ヒドロキシフェニル)メタントリグリシジルエーテル、N,N-ビス(2,3-エポキシプロピル)アニリン、p-(2,3-エポキシプロポキシ-N,N-ビス(2,3-エポキシプロピル)アニリン、ビス-ヒドロキシメチルフランのジグリシジルエーテル、ならびに、ジグリシジルアミド、トリグリシジルアミド、ポリグリシジルアミド、ジグリシジルエステル、トリグリシジルエステル、ポリグリシジルエステル、ジグリシジルアジド、トリグリシジルアジド、ポリグリシジルアジド、ジグリシジルメタクリラート、トリグリシジルメタクリラート、およびポリグリシジルメタクリラートから選択された官能基を有する架橋剤の1種または複数種と、さらに、任意選択で1種または複数種の添加剤と混合し、
次いで、塩基性溶液を添加することを含む、
上記方法。 - 固形のリグニンを、
グリセロールジグリシジルエーテル、ジグリセロールポリグリシジルエーテル、ポリグリセロールポリグリシジルエーテル、グリセロールトリグリシジルエーテル、ソルビトールポリグリシジルエーテル、アルコキシル化グリセロールポリグリシジルエーテル、トリメチロールプロパントリグリシジルエーテル、トリメチロールプロパンジグリシジルエーテル、ポリオキシプロピレングリコールジグリシジルエーテル、ポリオキシプロピレングリコールトリグリシジルエーテル、シクロヘキサンジメタノールのジグリシジルエーテル、レゾルシノールジグリシジルエーテル、イソソルビドジグリシジルエーテル、ペンタエリスリトールテトラグリシジルエーテル、エチレングリコールジグリシジルエーテル、2~9のエチレングリコール単位を有するポリエチレングリコールジグリシジルエーテル、1~5のプロピレングリコール単位を有するプロピレングリコールジグリシジルエーテル、3~6個の炭素原子の直鎖炭素鎖を有する末端ジオールのヘキサヒドロフタル酸ジグリシジルエステルおよび/もしくは当該末端ジオールのジグリシジルエーテルの1種または複数種と、さらに、任意選択で1種または複数種の添加剤と混合し、
次いで、塩基性溶液を添加する、
請求項1に記載の方法。 - 前記エーテルがポリグリセロールポリグリシジルエーテルである、請求項1または2に記載の方法。
- 1種の添加剤が溶媒である、請求項1~3のいずれか1項に記載の方法。
- 乾燥リグニンに基づいて計算されたリグニンの重量と、グリセロールジグリシジルエーテルおよび/またはエチレングリコールジグリシジルエーテルの総重量との重量比が1:10~10:1である、請求項1~4のいずれか1項に記載の方法。
- 1種の添加剤が、尿素、タンニン、界面活性剤、分散剤、充填剤および/または溶媒である、請求項1~5のいずれか1項に記載の方法。
- 前記溶媒が、グリセロール、エチレングリコール、ポリエチレングリコール、プロピレングリコール、ポリプロピレングリコール、ソルビトール、および/または3~6個の炭素原子の直鎖炭素鎖を有する任意の末端ジオールである、請求項6に記載の方法。
- 前記リグニンが、グリオキシル化、エーテル化、エステル化または他のいずれかの手段によって変性され、リグニンのヒドロキシル含有量またはカルボキシル含有量またはアミン含有量またはチオール含有量が増大されている、請求項1~7のいずれか1項に記載の方法。
- 結合樹脂を調製する方法であって、
固形のリグニンを、1種もしくは複数種の架橋剤および/または1種もしくは複数種のグリシジルエーテルと混合し、次いで塩基性溶液を添加することを含み、この架橋剤が4当量/kgを超えるエポキシ当量を有する、
上記方法。 - 請求項1~9のいずれか1項に記載の方法によって得られる結合樹脂。
- ラミネート、ミネラルウール断熱材、ならびに、合板、配向性ストランドボード(OSB)、単板積層材(LVL)、中密度繊維板(MDF)、高密度繊維板(HDF)、寄木細工の床材、湾曲した合板、ベニヤのパーティクルボード、およびベニヤのMDFなどの木材製品、ラミネートまたはミネラルウール断熱材の製造における、請求項10に記載の結合樹脂の使用。
- ラミネート、ミネラルウール断熱材、および、合板、配向性ストランドボード(OSB)、単板積層材(LVL)、中密度繊維板(MDF)、高密度繊維板(HDF)、寄木細工の床材、湾曲した合板、ベニヤのパーティクルボード、ベニヤのMDFもしくはパーティクルボードなどの木材製品、ラミネートまたはミネラルウール断熱材の製造において、前記結合樹脂が表面に提供され、そして、その表面が圧力および加熱に曝されるときに、接着剤を形成する前記結合樹脂の硬化が起こる、請求項10に記載の結合樹脂の使用。
- 請求項12に記載の結合樹脂を使用して製造された、ラミネート、ミネラルウール断熱材、および、合板、配向性ストランドボード(OSB)、単板積層材(LVL)、中密度繊維板(MDF)、高密度繊維板(HDF)、寄木細工の床材、湾曲した合板、ベニヤのパーティクルボード、ベニヤのMDFもしくはパーティクルボードなどの木材製品、ラミネートまたはミネラルウール断熱材。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE1950773-0 | 2019-06-24 | ||
SE1950773A SE543597C2 (en) | 2019-06-24 | 2019-06-24 | Process for preparing a bonding resin |
PCT/IB2020/055857 WO2020261087A1 (en) | 2019-06-24 | 2020-06-22 | Process for preparing a bonding resin |
Publications (1)
Publication Number | Publication Date |
---|---|
JP2022539516A true JP2022539516A (ja) | 2022-09-12 |
Family
ID=74061373
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2021576569A Pending JP2022539516A (ja) | 2019-06-24 | 2020-06-22 | 結合樹脂を調製する方法 |
Country Status (11)
Country | Link |
---|---|
US (1) | US20220243105A1 (ja) |
EP (1) | EP3986973A4 (ja) |
JP (1) | JP2022539516A (ja) |
KR (1) | KR20220025743A (ja) |
CN (1) | CN114008168A (ja) |
AU (1) | AU2020307468A1 (ja) |
BR (1) | BR112021025809A2 (ja) |
CA (1) | CA3141289A1 (ja) |
CL (1) | CL2021003339A1 (ja) |
SE (1) | SE543597C2 (ja) |
WO (1) | WO2020261087A1 (ja) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2021529845A (ja) * | 2018-07-02 | 2021-11-04 | ストラ エンソ オーワイジェイ | 結合用樹脂を調製するためのプロセス |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA654728A (en) * | 1962-12-25 | J. Ball Frank | Lignin resins and the manufacture thereof | |
US7252735B2 (en) * | 2002-05-13 | 2007-08-07 | State Of Oregon Acting By And Through The Oregon State Board Of Higher Education On Behalf Of Oregon State University | Formaldehyde-free lignocellulosic adhesives and composites made from the adhesives |
PL1740670T3 (pl) * | 2004-04-20 | 2012-11-30 | State Of Oregon Acting By And Through The State Board Of Higher Education On Behalf Of Oregon State | Klejące środki i kompozyty lignocelulozowe wolne od formaldehydu wykonane z klejących środków |
SE0402201D0 (sv) | 2004-09-14 | 2004-09-14 | Stfi Packforsk Ab | Method for separating lignin from black liquor |
US8377853B2 (en) * | 2006-04-20 | 2013-02-19 | M-I L.L.C. | Aqueous gels for well bore strengthening |
JP5555520B2 (ja) * | 2009-10-27 | 2014-07-23 | パナソニック株式会社 | 植物由来接着剤と植物由来組成物および木質複合材料 |
DE102010008393A1 (de) * | 2010-02-10 | 2011-10-06 | Technische Universität Dresden | Substrat zur Bodenverbesserung mit Wasser speichernder Eigenschaft, Verfahren zur Herstellung und dessen Verwendung |
WO2011111664A1 (ja) * | 2010-03-08 | 2011-09-15 | 独立行政法人森林総合研究所 | リグニン系酵素安定化剤 |
CN104995236B (zh) * | 2012-12-18 | 2017-11-28 | 阿克佐诺贝尔国际涂料股份有限公司 | 木素基涂料组合物 |
US20150329753A1 (en) * | 2014-05-16 | 2015-11-19 | Board Of Trustees Of The Leland Stanford Junior University | Biobased lignin adhesives for plywood applications and manufacturing of improved wood-based products |
CN107532060B (zh) * | 2015-04-15 | 2020-06-05 | Fp创新研究中心 | 作为木材粘合剂中的成分的高残留含量(hrc)硫酸盐/碱木质素 |
CN106497149B (zh) * | 2016-10-19 | 2018-11-06 | 武汉工程大学 | 一种利用木质素规模化制备纳米碳黑的方法 |
CN108192547B (zh) * | 2017-12-29 | 2020-09-18 | 武汉市科达云石护理材料有限公司 | 高填充高韧性环氧石材胶粘剂及其制备方法 |
US20210253922A1 (en) * | 2018-07-02 | 2021-08-19 | Stora Enso Oyj | Process for preparing a bonding resin |
SE544555C2 (en) * | 2018-07-02 | 2022-07-12 | Stora Enso Oyj | An epoxy bonding resin obtainable from black liquor lignin |
-
2019
- 2019-06-24 SE SE1950773A patent/SE543597C2/en unknown
-
2020
- 2020-06-22 EP EP20831745.3A patent/EP3986973A4/en active Pending
- 2020-06-22 KR KR1020217042380A patent/KR20220025743A/ko unknown
- 2020-06-22 WO PCT/IB2020/055857 patent/WO2020261087A1/en unknown
- 2020-06-22 JP JP2021576569A patent/JP2022539516A/ja active Pending
- 2020-06-22 CA CA3141289A patent/CA3141289A1/en active Pending
- 2020-06-22 BR BR112021025809A patent/BR112021025809A2/pt unknown
- 2020-06-22 AU AU2020307468A patent/AU2020307468A1/en active Pending
- 2020-06-22 CN CN202080043811.3A patent/CN114008168A/zh active Pending
- 2020-06-22 US US17/622,368 patent/US20220243105A1/en active Pending
-
2021
- 2021-12-14 CL CL2021003339A patent/CL2021003339A1/es unknown
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2021529845A (ja) * | 2018-07-02 | 2021-11-04 | ストラ エンソ オーワイジェイ | 結合用樹脂を調製するためのプロセス |
JP7511485B2 (ja) | 2018-07-02 | 2024-07-05 | ストラ エンソ オーワイジェイ | 結合用樹脂を調製するためのプロセス |
Also Published As
Publication number | Publication date |
---|---|
CN114008168A (zh) | 2022-02-01 |
WO2020261087A1 (en) | 2020-12-30 |
SE543597C2 (en) | 2021-04-13 |
BR112021025809A2 (pt) | 2022-02-08 |
KR20220025743A (ko) | 2022-03-03 |
CL2021003339A1 (es) | 2022-08-26 |
SE1950773A1 (en) | 2020-12-25 |
US20220243105A1 (en) | 2022-08-04 |
EP3986973A4 (en) | 2023-05-03 |
EP3986973A1 (en) | 2022-04-27 |
CA3141289A1 (en) | 2020-12-30 |
AU2020307468A1 (en) | 2021-12-16 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP7511485B2 (ja) | 結合用樹脂を調製するためのプロセス | |
CN114008161B (zh) | 粘合树脂的用途 | |
CA2867391A1 (en) | Adhesive compositions having a reduced cure time and methods for making and using same | |
JP2022539516A (ja) | 結合樹脂を調製する方法 | |
SE545325C2 (en) | Process for the preparation of a bonding resin | |
EP4077579A1 (en) | Novel process for preparing a bonding resin | |
JP2023506815A (ja) | 接合用樹脂を調製するための方法 | |
SE545570C2 (en) | A bonding resin and a process for the preparation of a bonding resin |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20230522 |
|
A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20240214 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20240305 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20240531 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20240830 |