JP2004162068A - バインダ−および金属製容器の被覆材料としてそれを用いる方法 - Google Patents
バインダ−および金属製容器の被覆材料としてそれを用いる方法 Download PDFInfo
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- JP2004162068A JP2004162068A JP2003380046A JP2003380046A JP2004162068A JP 2004162068 A JP2004162068 A JP 2004162068A JP 2003380046 A JP2003380046 A JP 2003380046A JP 2003380046 A JP2003380046 A JP 2003380046A JP 2004162068 A JP2004162068 A JP 2004162068A
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- CAYJDIDYXCENIR-UHFFFAOYSA-N 2-[5-(oxiran-2-ylmethoxy)pentoxymethyl]oxirane Chemical compound C1OC1COCCCCCOCC1CO1 CAYJDIDYXCENIR-UHFFFAOYSA-N 0.000 description 1
- WTYYGFLRBWMFRY-UHFFFAOYSA-N 2-[6-(oxiran-2-ylmethoxy)hexoxymethyl]oxirane Chemical compound C1OC1COCCCCCCOCC1CO1 WTYYGFLRBWMFRY-UHFFFAOYSA-N 0.000 description 1
- KUAUJXBLDYVELT-UHFFFAOYSA-N 2-[[2,2-dimethyl-3-(oxiran-2-ylmethoxy)propoxy]methyl]oxirane Chemical compound C1OC1COCC(C)(C)COCC1CO1 KUAUJXBLDYVELT-UHFFFAOYSA-N 0.000 description 1
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- WXQZLPFNTPKVJM-UHFFFAOYSA-N 4-[(4-hydroxycyclohexyl)methyl]cyclohexan-1-ol Chemical compound C1CC(O)CCC1CC1CCC(O)CC1 WXQZLPFNTPKVJM-UHFFFAOYSA-N 0.000 description 1
- KJMVGAOYRRKQPY-UHFFFAOYSA-N 4-[2,4,6-tri(propan-2-yl)phenyl]phenol Chemical compound CC(C)C1=CC(C(C)C)=CC(C(C)C)=C1C1=CC=C(O)C=C1 KJMVGAOYRRKQPY-UHFFFAOYSA-N 0.000 description 1
- QHPQWRBYOIRBIT-UHFFFAOYSA-N 4-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C=C1 QHPQWRBYOIRBIT-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 244000226021 Anacardium occidentale Species 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 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 description 1
- 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 description 1
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical class CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 1
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- FQYUMYWMJTYZTK-UHFFFAOYSA-N Phenyl glycidyl ether Chemical compound C1OC1COC1=CC=CC=C1 FQYUMYWMJTYZTK-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004146 Propane-1,2-diol Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 235000019486 Sunflower oil Nutrition 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- FDLQZKYLHJJBHD-UHFFFAOYSA-N [3-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=CC(CN)=C1 FDLQZKYLHJJBHD-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 1
- 235000020661 alpha-linolenic acid Nutrition 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- UYQMSQMCIYSXOW-UHFFFAOYSA-N benzene-1,2,4,5-tetrol Chemical compound OC1=CC(O)=C(O)C=C1O UYQMSQMCIYSXOW-UHFFFAOYSA-N 0.000 description 1
- 235000013361 beverage Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- VCCBEIPGXKNHFW-UHFFFAOYSA-N biphenyl-4,4'-diol Chemical group C1=CC(O)=CC=C1C1=CC=C(O)C=C1 VCCBEIPGXKNHFW-UHFFFAOYSA-N 0.000 description 1
- YXVFYQXJAXKLAK-UHFFFAOYSA-N biphenyl-4-ol Chemical compound C1=CC(O)=CC=C1C1=CC=CC=C1 YXVFYQXJAXKLAK-UHFFFAOYSA-N 0.000 description 1
- JRPRCOLKIYRSNH-UHFFFAOYSA-N bis(oxiran-2-ylmethyl) benzene-1,2-dicarboxylate Chemical compound C=1C=CC=C(C(=O)OCC2OC2)C=1C(=O)OCC1CO1 JRPRCOLKIYRSNH-UHFFFAOYSA-N 0.000 description 1
- XFUOBHWPTSIEOV-UHFFFAOYSA-N bis(oxiran-2-ylmethyl) cyclohexane-1,2-dicarboxylate Chemical compound C1CCCC(C(=O)OCC2OC2)C1C(=O)OCC1CO1 XFUOBHWPTSIEOV-UHFFFAOYSA-N 0.000 description 1
- KBWLNCUTNDKMPN-UHFFFAOYSA-N bis(oxiran-2-ylmethyl) hexanedioate Chemical compound C1OC1COC(=O)CCCCC(=O)OCC1CO1 KBWLNCUTNDKMPN-UHFFFAOYSA-N 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical class CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 235000020226 cashew nut Nutrition 0.000 description 1
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- 239000000919 ceramic Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000004567 concrete Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- IFDVQVHZEKPUSC-UHFFFAOYSA-N cyclohex-3-ene-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCC=CC1C(O)=O IFDVQVHZEKPUSC-UHFFFAOYSA-N 0.000 description 1
- MIHINWMALJZIBX-UHFFFAOYSA-N cyclohexa-2,4-dien-1-ol Chemical class OC1CC=CC=C1 MIHINWMALJZIBX-UHFFFAOYSA-N 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- IMHDGJOMLMDPJN-UHFFFAOYSA-N dihydroxybiphenyl Natural products OC1=CC=CC=C1C1=CC=CC=C1O IMHDGJOMLMDPJN-UHFFFAOYSA-N 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 238000003618 dip coating Methods 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 125000005908 glyceryl ester group Chemical group 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 239000004312 hexamethylene tetramine Substances 0.000 description 1
- 235000010299 hexamethylene tetramine Nutrition 0.000 description 1
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical class CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 1
- 150000001469 hydantoins Chemical class 0.000 description 1
- 239000012433 hydrogen halide Substances 0.000 description 1
- 229910000039 hydrogen halide Inorganic materials 0.000 description 1
- ARZLUCYKIWYSHR-UHFFFAOYSA-N hydroxymethoxymethanol Chemical class OCOCO ARZLUCYKIWYSHR-UHFFFAOYSA-N 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 239000006115 industrial coating Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 229960004488 linolenic acid Drugs 0.000 description 1
- KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 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
- 229910021645 metal ion Inorganic materials 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
- ZMVMYBGDGJLCHV-UHFFFAOYSA-N n-methyl-4-[[4-(methylamino)phenyl]methyl]aniline Chemical compound C1=CC(NC)=CC=C1CC1=CC=C(NC)C=C1 ZMVMYBGDGJLCHV-UHFFFAOYSA-N 0.000 description 1
- NXPPAOGUKPJVDI-UHFFFAOYSA-N naphthalene-1,2-diol Chemical class C1=CC=CC2=C(O)C(O)=CC=C21 NXPPAOGUKPJVDI-UHFFFAOYSA-N 0.000 description 1
- RXOHFPCZGPKIRD-UHFFFAOYSA-N naphthalene-2,6-dicarboxylic acid Chemical compound C1=C(C(O)=O)C=CC2=CC(C(=O)O)=CC=C21 RXOHFPCZGPKIRD-UHFFFAOYSA-N 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 125000005429 oxyalkyl group Chemical group 0.000 description 1
- 150000003003 phosphines Chemical class 0.000 description 1
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- 229940079877 pyrogallol Drugs 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 238000010345 tape casting Methods 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- UFDHBDMSHIXOKF-UHFFFAOYSA-N tetrahydrophthalic acid Natural products OC(=O)C1=C(C(O)=O)CCCC1 UFDHBDMSHIXOKF-UHFFFAOYSA-N 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000002562 thickening agent 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
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- 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
- C08G8/00—Condensation polymers of aldehydes or ketones with phenols only
- C08G8/38—Block or graft polymers prepared by polycondensation of aldehydes or ketones onto macromolecular compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D163/00—Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Paints Or Removers (AREA)
- Epoxy Resins (AREA)
- Phenolic Resins Or Amino Resins (AREA)
- Details Of Rigid Or Semi-Rigid Containers (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Adhesives Or Adhesive Processes (AREA)
Abstract
【選択図】 なし
Description
p−クレゾール、3,5−ジメチルフェノール、1,3,5−キシレノール、p−フェニルフェノールおよびアルキルフェノール類、例えばp−第三ブチルフェノール、オクチルフェノールおよびノニルフェノールがある。アルデヒド類Dのうちではホルムアルデヒドを用いるのが有利である。その他には、アセトアルデヒド、プロピオンアルデヒド、ブチルアルデヒド、イソブチルアルデヒド、バレルアルデヒド、ヘキシル−、ヘプチル−、オクチル−、ノニル−およびデシルアルデヒドおよびそれらの異性体も適する。
I:バインダーの製造
1:バインダー1の製造
ビスフェノールAのジグリシジルエーテル215部(5.26mol/kgの比エポキシ基含有量;“エポキシ当量”=190g/mol)およびビスフェノールA168部を、100部のキシレンに溶解し、この溶液を130℃に加熱する。0.5部のトリフェニルホスフィンの添加後に、比エポキシ基含有量が0.1mol/kgより小さく(即ち10000g/molより大きいエポキシ当量に)なるまで攪拌する。次いでこの溶液を100部のブタノールで希釈しそして22部の水酸化ナトリウム水溶液(33%濃度)と混合する。次に70℃で55部のホルムアルデヒド水溶液(37%濃度)を添加しそして攪拌を5時間継続する。480部のブタノールを添加しそして50%濃度の硫酸で3.5のpHを達成した後に、蒸留を水分離器を通して循環して15時間実施する。その後に溶剤を、60%の乾燥残留物(135℃で1時間乾燥)に達するまで留去する。残留溶液を次に濾過する。
ビスフェノールAのジグリシジルエーテル215部(5.26mol/kgの比エポキシ基含有量;“エポキシ当量”=190g/mol)、o−クレゾール20部およびビスフェノールA168部を、100部のキシレンに溶解し、この溶液を130℃に加熱する。0.5部のトリフェニルホスフィンの添加後に、比エポキシ基含有量が0.1mol/kgより小さく(即ち10000g/molより大きいエポキシ当量に)なるまで攪拌する。次いでこの溶液を100部のブタノールで希釈しそして22部の水酸化ナトリウム水溶液(33%濃度)と混合する。次に70℃で55部のホルムアルデヒド水溶液(37%濃度)を添加しそして攪拌を5時間継続する。480部のブタノールを添加しそして50%濃度の硫酸で3.5のpHを達成した後に、蒸留を水分離器を通して循環して15時間実施する。その後に溶剤を、60%の乾燥残留物(135℃で1時間乾燥)に達するまで留去する。残留溶液を次に濾過する。
ビスフェノールAのジグリシジルエーテル215部(5.26mol/kgの比エポキシ基含有量;“エポキシ当量”=190g/mol)およびビスフェノールA168部を、100部のキシレンに溶解し、この溶液を130℃に加熱する。0.5部のトリフェニルホスフィンの添加後に、比エポキシ基含有量が0.1mol/kgより小さく(即ち10000g/molより大きいエポキシ当量に)なるまで攪拌する。次いでこの溶液を100部のブタノールで希釈し、30部の60%濃度フェノールノボラック溶液(重量平均分子量Mw=750g/mol)と混合しそして22部の水酸化ナトリウム水溶液(33%濃度)と混合する。次に70℃で55部のホルムアルデヒド水溶液(37%濃度)を添加しそして攪拌を5時間継続する。480部のブタノールを添加しそして50%濃度の硫酸で3.5のpHを達成した後に、蒸留を水分離器を通して循環して15時間実施する。その後に溶剤を、60%の乾燥残留物(135℃で1時間乾燥)に達するまで留去する。残留溶液を次に濾過する。
ビスフェノールAのジグリシジルエーテル215部(5.26mol/kgの比エポキシ基含有量;“エポキシ当量”=190g/mol)およびビスフェノールA148部を、100部のキシレンに溶解し、この溶液を30部の60%濃度フェノールノボラック溶液(重量平均分子量Mw=750g/mol)と混合しそして130℃に加熱する。1部のトリフェニルホスフィンの添加後に、比エポキシ基含有量が0.1mol/kgより小さく(即ち10000g/molより大きいエポキシ当量に)なるまで攪拌する。次いでこの溶液を100部のブタノールで希釈し、22部の水酸化ナトリウム水溶液(33%濃度)と混合する。次に70℃で55部のホルムアルデヒド水溶液(37%濃度)を添加しそして攪拌を5時間継続する。480部のブタノールを添加しそして50%濃度の硫酸で3.5のpHを達成した後に、蒸留を水分離器を通して循環して15時間実施する。その後に溶剤を、60%の乾燥残留物(135℃で1時間乾燥)に達するまで留去する。残留溶液を次に濾過する。
ll 被覆試験
被覆剤の製造および試験:
試験するバインダーをメトキシプロパノールで調製して、40〜60秒のDIN53211(4mmの流出口;23℃)の流出時間に調整する。このものは40〜45%の固形分重量割合である。この希釈工程は別として樹脂を動かないままにする。
**評点:1−滑らかで均一;5−凹凸があり、不規則。
***:碁盤目試験:ISO2409に従って測定した。
Claims (13)
- ジヒドロキシ芳香族化合物AとジエポキシドまたはポリエポキシドBとの縮合生成物において、該縮合生成物がアルデヒド類Dとの反応によってアルキロール化されていることを特徴とする縮合生成物。
- ジヒドロキシ芳香族化合物AおよびジエポキシドまたはポリエポキシドBの他に、出発化合物が更にモノ−および/またはポリヒドロキシ芳香族化合物Cを含有がする請求項1に記載の縮合生成物。
- アルデヒド類Dとの反応によって導入されるアルキロール基の少なくともいくつかがアルコールEでエーテル化されている請求項1または2に記載の縮合生成物。
- モノヒドロキシ芳香族化合物C1が出発化合物中に含まれている、請求項2に記載の縮合生成物。
- ポリヒドロキシ芳香族化合物C3が出発化合物中に含まれている、請求項2に記載の縮合生成物。
- 2つより多いフェノール性水酸基を有するアキリデンポリフェノールレゾール類またはノボラック類Cx が出発化合物中に含まれている、請求項2に記載の縮合生成物。
- 請求項1に記載の縮合生成物およびアルキリデンポリフェノールレゾールまたはアルキリデンポリフェノールノボラックCxよりなる混合物。
- 請求項1に記載の縮合生成物を製造する方法において、
− ジヒドロキシ芳香族化合物AをジエポキシドまたはポリエポキシドBと縮合しそして− この縮合生成物をアルデヒド類Dとの反応によってアルキロール化する
各段階を含むことを特徴とする、上記方法。 - 請求項2に記載の縮合生成物を製造する方法において、
− ジヒドロキシ芳香族化合物Aとモノ−および/またはポリヒドロキシ芳香族化合物C との混合物をジエポキシドまたはポリエポキシドBと縮合反応させ、
− この縮合生成物をアルデヒドDとの反応によってアルキロール化する
各段階を含むことを特徴とする、上記方法。 - アルキロール化の後にアリキロール基の少なくとも一部をアルコールEでエーテル化する、請求項8または9に記載の方法。
- 請求項1に記載の縮合生成物を用いる方法において、請求項1の縮合生成物を可塑性化物質と混合して被覆剤、接着剤または含浸剤を生成する、上記方法。
- エポキシ樹脂、ポリビニルアセタール、ポリビニルアルコール、アルキッド樹脂、ポリエステル、脂肪油、ポリウレタンおよびゴムよりなる群から選択される可塑性化物質を縮合生成物に混入する、請求項11に記載の使用方法。
- 食品または飲料水用缶の内側用被覆剤を製造するための請求項11または12に記載の使用方法。
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DE10252627A DE10252627A1 (de) | 2002-11-11 | 2002-11-11 | Bindemittel und ihre Anwendung als Beschichtungsmaterial für die Beschichtung von Metallbehältern |
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EP (1) | EP1418191B1 (ja) |
JP (1) | JP4500990B2 (ja) |
AT (1) | ATE500284T1 (ja) |
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EP1609200A1 (en) * | 2003-04-09 | 2005-12-28 | MURRAY, Graham Simpson | Conductive polymer, conductive polymer compositions and their use |
US8333909B2 (en) | 2003-04-09 | 2012-12-18 | Bac2 Limited | Conductive polymer, conductive polymer compositions and methods for their use |
CN101040016B (zh) | 2004-10-20 | 2011-08-03 | 威士伯采购公司 | 用于罐的涂料组合物和涂覆方法 |
MX2012011843A (es) * | 2010-04-16 | 2012-11-12 | Valspar Sourcing Inc | Composiciones de revestimiento para envasar articulos y metodos de revestimiento. |
PL3878912T3 (pl) | 2011-02-07 | 2023-06-26 | Swimc Llc | Kompozycje powłokowe do pojemników i innych wyrobów i sposoby powlekania |
CN104540744B (zh) | 2012-08-09 | 2017-08-25 | 威士伯采购公司 | 容器涂层体系 |
AU2013299578A1 (en) | 2012-08-09 | 2015-02-19 | Valspar Sourcing, Inc. | Compositions for containers and other articles and methods of using same |
CN106536624B (zh) | 2014-04-14 | 2019-11-19 | 宣伟投资管理有限公司 | 制备用于容器和其它制品的组合物的方法以及使用所述组合物的方法 |
TWI614275B (zh) | 2015-11-03 | 2018-02-11 | Valspar Sourcing Inc | 用於製備聚合物的液體環氧樹脂組合物 |
CA3056987A1 (en) | 2017-04-07 | 2018-10-11 | Akzo Nobel Coatings International B.V. | Coating compositions containing a hydroxyphenyl functional polymer and a latex polymer |
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JPS57155226A (en) * | 1981-03-19 | 1982-09-25 | Matsushita Electric Works Ltd | Preparation of modified epoxy resin |
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ES2360208T3 (es) | 2011-06-01 |
ATE500284T1 (de) | 2011-03-15 |
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DE10252627A1 (de) | 2004-05-27 |
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