PL105881B1 - Sposob krystalizacji surowego zwiazku kompleksowego 2,2-dwu-/4-hydroksyfenylo/-propanu z fenolem - Google Patents
Sposob krystalizacji surowego zwiazku kompleksowego 2,2-dwu-/4-hydroksyfenylo/-propanu z fenolem Download PDFInfo
- Publication number
- PL105881B1 PL105881B1 PL18436775A PL18436775A PL105881B1 PL 105881 B1 PL105881 B1 PL 105881B1 PL 18436775 A PL18436775 A PL 18436775A PL 18436775 A PL18436775 A PL 18436775A PL 105881 B1 PL105881 B1 PL 105881B1
- Authority
- PL
- Poland
- Prior art keywords
- phenol
- crystallization
- water
- weight
- propane
- Prior art date
Links
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 title claims description 66
- 238000000034 method Methods 0.000 title claims description 49
- 238000002425 crystallisation Methods 0.000 title claims description 40
- 230000008025 crystallization Effects 0.000 title claims description 38
- 150000001875 compounds Chemical class 0.000 title claims description 26
- -1 4-HYDROXYPHENYL Chemical class 0.000 title description 2
- 239000001294 propane Substances 0.000 title description 2
- 239000000203 mixture Substances 0.000 claims description 43
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 36
- 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 31
- 239000007788 liquid Substances 0.000 claims description 15
- 239000013078 crystal Substances 0.000 claims description 13
- 239000012452 mother liquor Substances 0.000 claims description 13
- 239000012808 vapor phase Substances 0.000 claims description 4
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- KLSLBUSXWBJMEC-UHFFFAOYSA-N 4-Propylphenol Chemical compound CCCC1=CC=C(O)C=C1 KLSLBUSXWBJMEC-UHFFFAOYSA-N 0.000 claims 2
- PBEHQFUSQJKBAS-UHFFFAOYSA-N 4-[2-(4-hydroxyphenyl)propan-2-yl]phenol;phenol Chemical compound OC1=CC=CC=C1.C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 PBEHQFUSQJKBAS-UHFFFAOYSA-N 0.000 claims 1
- 239000012141 concentrate Substances 0.000 claims 1
- 238000009738 saturating Methods 0.000 claims 1
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 18
- 238000004821 distillation Methods 0.000 description 11
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 238000001816 cooling Methods 0.000 description 5
- 239000012535 impurity Substances 0.000 description 5
- 239000012071 phase Substances 0.000 description 5
- 238000009833 condensation Methods 0.000 description 4
- 230000005494 condensation Effects 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 238000000926 separation method Methods 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- BUZMJVBOGDBMGI-UHFFFAOYSA-N 1-phenylpropylbenzene Chemical compound C=1C=CC=CC=1C(CC)C1=CC=CC=C1 BUZMJVBOGDBMGI-UHFFFAOYSA-N 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 238000002955 isolation Methods 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 241001550224 Apha Species 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000003377 acid catalyst Substances 0.000 description 2
- 238000005119 centrifugation Methods 0.000 description 2
- 239000012043 crude product Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229920005668 polycarbonate resin Polymers 0.000 description 2
- 239000004431 polycarbonate resin Substances 0.000 description 2
- 239000012451 post-reaction mixture Substances 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000012429 reaction media Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- WJASVEQGPTWZHE-UHFFFAOYSA-N 2-phenylphenol propane Chemical compound CCC.OC1=C(C=CC=C1)C=1C=CC=CC1 WJASVEQGPTWZHE-UHFFFAOYSA-N 0.000 description 1
- MILSYCKGLDDVLM-UHFFFAOYSA-N 2-phenylpropan-2-ylbenzene Chemical class C=1C=CC=CC=1C(C)(C)C1=CC=CC=C1 MILSYCKGLDDVLM-UHFFFAOYSA-N 0.000 description 1
- 125000004203 4-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000001728 carbonyl compounds Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 230000017525 heat dissipation Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- KSSNXJHPEFVKHY-UHFFFAOYSA-N phenol;hydrate Chemical compound O.OC1=CC=CC=C1 KSSNXJHPEFVKHY-UHFFFAOYSA-N 0.000 description 1
- 231100000719 pollutant Toxicity 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 238000005221 zone crystallization Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
- C07C37/68—Purification; separation; Use of additives, e.g. for stabilisation
- C07C37/70—Purification; separation; Use of additives, e.g. for stabilisation by physical treatment
- C07C37/84—Purification; separation; Use of additives, e.g. for stabilisation by physical treatment by crystallisation
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7440170A FR2289476A1 (fr) | 1974-10-31 | 1974-10-31 | Procede de cristallisation d'un complexe de di(hydroxy-4 phenyl) 2,2 propane et de phenol |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL105881B1 true PL105881B1 (pl) | 1979-11-30 |
Family
ID=9145723
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL18436775A PL105881B1 (pl) | 1974-10-31 | 1975-10-30 | Sposob krystalizacji surowego zwiazku kompleksowego 2,2-dwu-/4-hydroksyfenylo/-propanu z fenolem |
Country Status (13)
| Country | Link |
|---|---|
| JP (1) | JPS5191240A (en:Method) |
| BE (1) | BE835077A (en:Method) |
| CA (1) | CA1062283A (en:Method) |
| CS (1) | CS188977B2 (en:Method) |
| DD (1) | DD121099A5 (en:Method) |
| DE (1) | DE2548470C2 (en:Method) |
| FR (1) | FR2289476A1 (en:Method) |
| GB (1) | GB1482498A (en:Method) |
| IT (1) | IT1047633B (en:Method) |
| NL (1) | NL7512667A (en:Method) |
| PL (1) | PL105881B1 (en:Method) |
| RO (1) | RO72879A (en:Method) |
| SU (1) | SU594891A3 (en:Method) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS58135832A (ja) * | 1982-02-08 | 1983-08-12 | Mitsui Toatsu Chem Inc | ビスフエノ−ルａとフエノ−ルとの付加物の晶析方法 |
| US4492807A (en) * | 1983-04-22 | 1985-01-08 | General Electric Company | Method for purification of bisphenol A |
| US4529823A (en) * | 1984-04-02 | 1985-07-16 | General Electric Company | Purification of bisphenol-A |
| JPH066542B2 (ja) * | 1987-05-06 | 1994-01-26 | 三井東圧化学株式会社 | ビスフェノ−ルａの製造方法 |
| JPH01146839A (ja) * | 1987-12-04 | 1989-06-08 | Mitsui Toatsu Chem Inc | 高純度の２，２−ビス（４−ヒドロキシフェニル）プロパンを製造する方法 |
| JPH01213246A (ja) * | 1988-02-22 | 1989-08-28 | Mitsui Toatsu Chem Inc | ビスフェノールａとフェノールとの付加物の晶出方法 |
| US4927978A (en) * | 1988-12-16 | 1990-05-22 | Shell Oil Company | Method of purifying bisphenols |
| EP0522700B1 (en) * | 1991-07-10 | 1997-01-29 | Chiyoda Corporation | Process for the production of crystalline adduct of bisphenol A and phenol and apparatus therefor |
| US5368827A (en) * | 1991-07-10 | 1994-11-29 | Chiyoda Corporation | Process for the production of crystalline adduct of bisphenol A and phenol and apparatus therefor |
| JP5216748B2 (ja) * | 2009-11-02 | 2013-06-19 | 本州化学工業株式会社 | １，１−ビス（４−ヒドロキシフェニル）−３，３，５−トリメチルシクロヘキサンの製造方法 |
| JP5705168B2 (ja) * | 2012-06-04 | 2015-04-22 | 本州化学工業株式会社 | １，１−ビス（４−ヒドロキシフェニル）−３，３，５−トリメチルシクロヘキサンの製造方法 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AT259547B (de) * | 1965-06-11 | 1968-01-25 | Bayer Ag | Verfahren zur Gewinnung besonders reinen 2,2-Bis-(phenylol)-propans |
| BE759937A (en:Method) * | 1969-12-15 | 1971-06-07 | Shell Int Research |
-
1974
- 1974-10-31 FR FR7440170A patent/FR2289476A1/fr active Granted
-
1975
- 1975-09-30 IT IT5156575A patent/IT1047633B/it active
- 1975-10-09 GB GB4148775A patent/GB1482498A/en not_active Expired
- 1975-10-28 RO RO7583734A patent/RO72879A/ro unknown
- 1975-10-28 CA CA238,718A patent/CA1062283A/fr not_active Expired
- 1975-10-29 JP JP50130299A patent/JPS5191240A/ja active Granted
- 1975-10-29 DE DE19752548470 patent/DE2548470C2/de not_active Expired
- 1975-10-29 NL NL7512667A patent/NL7512667A/xx not_active Application Discontinuation
- 1975-10-30 BE BE161432A patent/BE835077A/xx not_active IP Right Cessation
- 1975-10-30 PL PL18436775A patent/PL105881B1/pl unknown
- 1975-10-30 DD DD18913575A patent/DD121099A5/xx unknown
- 1975-10-30 SU SU752185055A patent/SU594891A3/ru active
- 1975-10-31 CS CS735375A patent/CS188977B2/cs unknown
Also Published As
| Publication number | Publication date |
|---|---|
| FR2289476B1 (en:Method) | 1979-05-11 |
| FR2289476A1 (fr) | 1976-05-28 |
| DE2548470A1 (de) | 1976-05-06 |
| JPS5191240A (en) | 1976-08-10 |
| RO72879A (ro) | 1982-02-01 |
| BE835077A (fr) | 1976-04-30 |
| DE2548470C2 (de) | 1982-04-08 |
| IT1047633B (it) | 1980-10-20 |
| GB1482498A (en) | 1977-08-10 |
| CS188977B2 (en) | 1979-03-30 |
| JPS5246946B2 (en:Method) | 1977-11-29 |
| SU594891A3 (ru) | 1978-02-25 |
| NL7512667A (nl) | 1976-05-04 |
| CA1062283A (fr) | 1979-09-11 |
| DD121099A5 (en:Method) | 1976-07-12 |
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