JPH0558611B2 - - Google Patents
Info
- Publication number
- JPH0558611B2 JPH0558611B2 JP5633588A JP5633588A JPH0558611B2 JP H0558611 B2 JPH0558611 B2 JP H0558611B2 JP 5633588 A JP5633588 A JP 5633588A JP 5633588 A JP5633588 A JP 5633588A JP H0558611 B2 JPH0558611 B2 JP H0558611B2
- Authority
- JP
- Japan
- Prior art keywords
- bisphenol
- mother liquor
- phenol
- reaction
- sub
- 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.)
- Expired - Lifetime
Links
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims description 177
- 239000013078 crystal Substances 0.000 claims description 65
- 238000006243 chemical reaction Methods 0.000 claims description 64
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 60
- 239000012452 mother liquor Substances 0.000 claims description 60
- 238000000034 method Methods 0.000 claims description 48
- 239000007788 liquid Substances 0.000 claims description 24
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 22
- 239000003054 catalyst Substances 0.000 claims description 19
- 238000004519 manufacturing process Methods 0.000 claims description 17
- JAGRUUPXPPLSRX-UHFFFAOYSA-N 4-prop-1-en-2-ylphenol Chemical compound CC(=C)C1=CC=C(O)C=C1 JAGRUUPXPPLSRX-UHFFFAOYSA-N 0.000 claims description 16
- 238000000926 separation method Methods 0.000 claims description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 14
- 239000002002 slurry Substances 0.000 claims description 9
- 238000001816 cooling Methods 0.000 claims description 7
- 239000012295 chemical reaction liquid Substances 0.000 claims description 2
- 239000006227 byproduct Substances 0.000 description 20
- 238000002425 crystallisation Methods 0.000 description 15
- 230000008025 crystallization Effects 0.000 description 15
- 239000012535 impurity Substances 0.000 description 14
- 238000003776 cleavage reaction Methods 0.000 description 12
- 239000002994 raw material Substances 0.000 description 10
- 230000007017 scission Effects 0.000 description 10
- 239000000126 substance Substances 0.000 description 10
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
- 235000013824 polyphenols Nutrition 0.000 description 8
- 238000011084 recovery Methods 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- 150000008442 polyphenolic compounds Chemical class 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 6
- 239000003729 cation exchange resin Substances 0.000 description 6
- 238000004040 coloring Methods 0.000 description 6
- 239000011541 reaction mixture Substances 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 239000003463 adsorbent Substances 0.000 description 4
- 239000007795 chemical reaction product Substances 0.000 description 4
- 238000007710 freezing Methods 0.000 description 4
- 230000008014 freezing Effects 0.000 description 4
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 4
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 4
- 150000007522 mineralic acids Chemical class 0.000 description 4
- 238000004064 recycling Methods 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000009825 accumulation Methods 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 3
- 238000011109 contamination Methods 0.000 description 3
- -1 hydrochloric acid Chemical class 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 229920005668 polycarbonate resin Polymers 0.000 description 3
- 239000004431 polycarbonate resin Substances 0.000 description 3
- 239000011973 solid acid Substances 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- 239000003377 acid catalyst Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 238000007664 blowing Methods 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 238000005215 recombination Methods 0.000 description 2
- 230000006798 recombination Effects 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- YZUPZGFPHUVJKC-UHFFFAOYSA-N 1-bromo-2-methoxyethane Chemical compound COCCBr YZUPZGFPHUVJKC-UHFFFAOYSA-N 0.000 description 1
- MLCQXUZZAXKTSG-UHFFFAOYSA-N 2-[2-(4-hydroxyphenyl)propan-2-yl]phenol Chemical compound C=1C=CC=C(O)C=1C(C)(C)C1=CC=C(O)C=C1 MLCQXUZZAXKTSG-UHFFFAOYSA-N 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000003426 co-catalyst Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000012467 final product Substances 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
- 238000010438 heat treatment Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000011949 solid catalyst Substances 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- 238000007738 vacuum evaporation Methods 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63056335A JPH01230538A (ja) | 1988-03-11 | 1988-03-11 | 高純度ビスフェノールaの製造方法 |
US07/321,218 US4954661A (en) | 1988-03-11 | 1989-03-09 | Process for preparing high-purity bisphenol A |
KR1019890002928A KR910004133B1 (ko) | 1988-03-11 | 1989-03-10 | 고순도 비스페놀 a의 제조방법 |
DE89104252T DE68906690T2 (de) | 1988-03-11 | 1989-03-10 | Verfahren zur Herstellung von hochreinem Bisphenol A. |
EP89104252A EP0332203B1 (de) | 1988-03-11 | 1989-03-10 | Verfahren zur Herstellung von hochreinem Bisphenol A |
CA000593304A CA1311498C (en) | 1988-03-11 | 1989-03-10 | Process for preparing high-purity bisphenol a |
ES89104252T ES2054905T3 (es) | 1988-03-11 | 1989-03-10 | Proceso para la preparacion de bisfenol a de alta pureza. |
CN89101325A CN1022560C (zh) | 1988-03-11 | 1989-03-11 | 高纯度双酚a的制造方法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63056335A JPH01230538A (ja) | 1988-03-11 | 1988-03-11 | 高純度ビスフェノールaの製造方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01230538A JPH01230538A (ja) | 1989-09-14 |
JPH0558611B2 true JPH0558611B2 (de) | 1993-08-27 |
Family
ID=13024335
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63056335A Granted JPH01230538A (ja) | 1988-03-11 | 1988-03-11 | 高純度ビスフェノールaの製造方法 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01230538A (de) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2009242316A (ja) * | 2008-03-31 | 2009-10-22 | Mitsubishi Chemicals Corp | ビスフェノールaの製造方法 |
JPWO2014002787A1 (ja) * | 2012-06-28 | 2016-05-30 | 出光興産株式会社 | ビスフェノールaの製造方法 |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5446067B2 (ja) * | 2006-01-25 | 2014-03-19 | 三菱化学株式会社 | ビスフェノールaの製造方法 |
WO2007086239A1 (ja) * | 2006-01-25 | 2007-08-02 | Mitsubishi Chemical Corporation | ビスフェノールaの製造方法 |
JP5247184B2 (ja) * | 2008-02-21 | 2013-07-24 | 三井化学株式会社 | ビスフェノールaの製造方法 |
-
1988
- 1988-03-11 JP JP63056335A patent/JPH01230538A/ja active Granted
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2009242316A (ja) * | 2008-03-31 | 2009-10-22 | Mitsubishi Chemicals Corp | ビスフェノールaの製造方法 |
JPWO2014002787A1 (ja) * | 2012-06-28 | 2016-05-30 | 出光興産株式会社 | ビスフェノールaの製造方法 |
Also Published As
Publication number | Publication date |
---|---|
JPH01230538A (ja) | 1989-09-14 |
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Legal Events
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