CN107759754B - 利用对羟基苯海因生产废渣制备海因甲醛树脂的方法 - Google Patents
利用对羟基苯海因生产废渣制备海因甲醛树脂的方法 Download PDFInfo
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- CN107759754B CN107759754B CN201711028512.9A CN201711028512A CN107759754B CN 107759754 B CN107759754 B CN 107759754B CN 201711028512 A CN201711028512 A CN 201711028512A CN 107759754 B CN107759754 B CN 107759754B
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- Prior art keywords
- formaldehyde
- hydantoin
- solution
- solid waste
- waste residue
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- WJRBRSLFGCUECM-UHFFFAOYSA-N hydantoin Chemical compound O=C1CNC(=O)N1 WJRBRSLFGCUECM-UHFFFAOYSA-N 0.000 title claims abstract description 30
- 229920005989 resin Polymers 0.000 title claims abstract description 23
- 239000011347 resin Substances 0.000 title claims abstract description 23
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 15
- 238000000034 method Methods 0.000 title claims abstract description 8
- 229940091173 hydantoin Drugs 0.000 title claims description 27
- TYNDBNTXKWNGDS-UHFFFAOYSA-N formaldehyde;imidazolidine-2,4-dione Chemical compound O=C.O=C1CNC(=O)N1 TYNDBNTXKWNGDS-UHFFFAOYSA-N 0.000 title claims description 11
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 title claims description 9
- 239000002699 waste material Substances 0.000 title abstract description 5
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims abstract description 77
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 18
- 229920000642 polymer Polymers 0.000 claims abstract description 15
- 239000007864 aqueous solution Substances 0.000 claims abstract description 14
- 238000006243 chemical reaction Methods 0.000 claims abstract description 13
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000007787 solid Substances 0.000 claims abstract description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 9
- 229920003986 novolac Polymers 0.000 claims abstract description 8
- 238000010992 reflux Methods 0.000 claims abstract description 5
- 239000002904 solvent Substances 0.000 claims abstract description 5
- 238000005292 vacuum distillation Methods 0.000 claims abstract description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 3
- 239000002910 solid waste Substances 0.000 claims description 27
- 239000000243 solution Substances 0.000 claims description 21
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 10
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 9
- 239000004202 carbamide Substances 0.000 claims description 8
- 229960003742 phenol Drugs 0.000 claims description 8
- 239000002994 raw material Substances 0.000 claims description 6
- -1 methylol groups Chemical group 0.000 claims description 5
- 238000003756 stirring Methods 0.000 claims description 5
- WOFTVESNUIDLHD-UHFFFAOYSA-N (2,4-dioxoimidazolidin-1-yl)urea Chemical compound NC(=O)NN1CC(=O)NC1=O WOFTVESNUIDLHD-UHFFFAOYSA-N 0.000 claims description 4
- 150000002989 phenols Chemical class 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 3
- 239000000725 suspension Substances 0.000 claims description 3
- YHXHKYRQLYQUIH-UHFFFAOYSA-N 4-hydroxymandelic acid Chemical compound OC(=O)C(O)C1=CC=C(O)C=C1 YHXHKYRQLYQUIH-UHFFFAOYSA-N 0.000 claims description 2
- 239000006227 byproduct Substances 0.000 claims description 2
- 230000002209 hydrophobic effect Effects 0.000 claims description 2
- 125000000879 imine group Chemical group 0.000 claims description 2
- 238000005070 sampling Methods 0.000 claims description 2
- 239000008098 formaldehyde solution Substances 0.000 claims 1
- UMTNMIARZPDSDI-UHFFFAOYSA-N 5-(4-hydroxyphenyl)imidazolidine-2,4-dione Chemical compound C1=CC(O)=CC=C1C1C(=O)NC(=O)N1 UMTNMIARZPDSDI-UHFFFAOYSA-N 0.000 abstract description 3
- 239000003431 cross linking reagent Substances 0.000 abstract description 2
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 abstract description 2
- QXJBCEOCUZMELC-UHFFFAOYSA-N C=O.C(CO)(=O)NC(=O)N Chemical compound C=O.C(CO)(=O)NC(=O)N QXJBCEOCUZMELC-UHFFFAOYSA-N 0.000 abstract 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical class OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 2
- 239000002893 slag Substances 0.000 abstract 2
- 238000004064 recycling Methods 0.000 abstract 1
- HHLFWLYXYJOTON-UHFFFAOYSA-N glyoxylic acid Chemical compound OC(=O)C=O HHLFWLYXYJOTON-UHFFFAOYSA-N 0.000 description 12
- FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 4
- 230000007613 environmental effect Effects 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- IWYDHOAUDWTVEP-UHFFFAOYSA-N R-2-phenyl-2-hydroxyacetic acid Natural products OC(=O)C(O)C1=CC=CC=C1 IWYDHOAUDWTVEP-UHFFFAOYSA-N 0.000 description 2
- LSQZJLSUYDQPKJ-NJBDSQKTSA-N amoxicillin Chemical compound C1([C@@H](N)C(=O)N[C@H]2[C@H]3SC([C@@H](N3C2=O)C(O)=O)(C)C)=CC=C(O)C=C1 LSQZJLSUYDQPKJ-NJBDSQKTSA-N 0.000 description 2
- 229960003022 amoxicillin Drugs 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 238000009776 industrial production Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229960002510 mandelic acid Drugs 0.000 description 2
- 239000012452 mother liquor Substances 0.000 description 2
- LSQZJLSUYDQPKJ-UHFFFAOYSA-N p-Hydroxyampicillin Natural products O=C1N2C(C(O)=O)C(C)(C)SC2C1NC(=O)C(N)C1=CC=C(O)C=C1 LSQZJLSUYDQPKJ-UHFFFAOYSA-N 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- QBYIENPQHBMVBV-HFEGYEGKSA-N (2R)-2-hydroxy-2-phenylacetic acid Chemical compound O[C@@H](C(O)=O)c1ccccc1.O[C@@H](C(O)=O)c1ccccc1 QBYIENPQHBMVBV-HFEGYEGKSA-N 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- AWZRBUVZMPCWDR-UHFFFAOYSA-N 2-sulfonylpropane Chemical compound CC(C)=S(=O)=O AWZRBUVZMPCWDR-UHFFFAOYSA-N 0.000 description 1
- 229940090248 4-hydroxybenzoic acid Drugs 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 241000282313 Hyaenidae Species 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000005456 alcohol based solvent Substances 0.000 description 1
- GZCGUPFRVQAUEE-SLPGGIOYSA-N aldehydo-D-glucose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-SLPGGIOYSA-N 0.000 description 1
- 229940053195 antiepileptics hydantoin derivative Drugs 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000007809 chemical reaction catalyst Substances 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000012847 fine chemical Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 150000001469 hydantoins Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000004464 hydroxyphenyl group Chemical group 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000012454 non-polar solvent Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 230000004083 survival effect Effects 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
- C08G14/00—Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00
- C08G14/02—Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes
- C08G14/04—Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes with phenols
- C08G14/06—Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes with phenols and monomers containing hydrogen attached to nitrogen
- C08G14/08—Ureas; Thioureas
-
- 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
- C08G14/00—Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00
- C08G14/02—Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes
- C08G14/04—Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes with phenols
- C08G14/06—Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes with phenols and monomers containing hydrogen attached to nitrogen
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Phenolic Resins Or Amino Resins (AREA)
Abstract
Description
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CN201711028512.9A CN107759754B (zh) | 2017-10-29 | 2017-10-29 | 利用对羟基苯海因生产废渣制备海因甲醛树脂的方法 |
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CN201711028512.9A CN107759754B (zh) | 2017-10-29 | 2017-10-29 | 利用对羟基苯海因生产废渣制备海因甲醛树脂的方法 |
Publications (2)
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CN107759754A CN107759754A (zh) | 2018-03-06 |
CN107759754B true CN107759754B (zh) | 2019-07-19 |
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Families Citing this family (3)
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CN108946726A (zh) * | 2018-08-13 | 2018-12-07 | 天津市职业大学 | 一种利用酚类废弃物制备高性能活性炭的方法 |
CN108996502A (zh) * | 2018-08-27 | 2018-12-14 | 天津市职业大学 | 对羟基苯海因生产废母液制备高性能活性炭的方法 |
CN111807877A (zh) * | 2020-07-09 | 2020-10-23 | 定陶三化药业有限公司 | 一种dl-对羟基苯海因及其硫酸脲/硫酸铵生产工艺 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2002193876A (ja) * | 2000-12-25 | 2002-07-10 | Nippon Shokubai Co Ltd | グリオキシル酸系化合物の精製方法および5−アリールヒダントイン類の製造方法 |
JP2002193943A (ja) * | 2000-12-25 | 2002-07-10 | Nippon Shokubai Co Ltd | 5−アリールヒダントイン類の製造方法 |
CN101230123A (zh) * | 2007-12-28 | 2008-07-30 | 天津市职业大学 | 对羟基苯海因生产副产物综合利用方法 |
CN101973941A (zh) * | 2010-11-22 | 2011-02-16 | 天津市职业大学 | 一种制备对羟基苯海因的方法 |
Family Cites Families (1)
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JP6728772B2 (ja) * | 2016-03-01 | 2020-07-22 | 日立化成株式会社 | 電極、鉛蓄電池及びこれらの製造方法 |
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- 2017-10-29 CN CN201711028512.9A patent/CN107759754B/zh active Active
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002193876A (ja) * | 2000-12-25 | 2002-07-10 | Nippon Shokubai Co Ltd | グリオキシル酸系化合物の精製方法および5−アリールヒダントイン類の製造方法 |
JP2002193943A (ja) * | 2000-12-25 | 2002-07-10 | Nippon Shokubai Co Ltd | 5−アリールヒダントイン類の製造方法 |
CN101230123A (zh) * | 2007-12-28 | 2008-07-30 | 天津市职业大学 | 对羟基苯海因生产副产物综合利用方法 |
CN101973941A (zh) * | 2010-11-22 | 2011-02-16 | 天津市职业大学 | 一种制备对羟基苯海因的方法 |
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Effective date of registration: 20210830 Address after: 012000 Bayin 1st Street, Chahar Industrial Park, Jining District, Wulanchabu City, Inner Mongolia Autonomous Region Patentee after: Inner Mongolia tianyuda Biotechnology Co.,Ltd. Address before: 300410 2 Luohe Road, Beichen District, Tianjin Patentee before: TIANJIN VOCATIONAL INSTITUTE |
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Denomination of invention: Method for preparing formaldehyde resin from waste residue of p-hydroxyphenylhydantoin production Granted publication date: 20190719 Pledgee: Bank of China Limited Ulanqab branch Pledgor: Inner Mongolia tianyuda Biotechnology Co.,Ltd. Registration number: Y2025980006161 |
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