JP2916823B2 - フェノールの精製法 - Google Patents
フェノールの精製法Info
- Publication number
- JP2916823B2 JP2916823B2 JP3156167A JP15616791A JP2916823B2 JP 2916823 B2 JP2916823 B2 JP 2916823B2 JP 3156167 A JP3156167 A JP 3156167A JP 15616791 A JP15616791 A JP 15616791A JP 2916823 B2 JP2916823 B2 JP 2916823B2
- Authority
- JP
- Japan
- Prior art keywords
- phenol
- acetophenone
- impurities
- column
- stream
- 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
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 title claims abstract description 40
- 238000000034 method Methods 0.000 title claims abstract description 21
- 238000000746 purification Methods 0.000 title description 6
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 claims abstract description 46
- 238000005336 cracking Methods 0.000 claims abstract description 8
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 claims abstract description 7
- 238000000895 extractive distillation Methods 0.000 claims abstract description 6
- 239000002253 acid Substances 0.000 claims description 3
- 230000002378 acidificating effect Effects 0.000 abstract description 6
- 239000012535 impurity Substances 0.000 description 22
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 14
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 14
- 239000000047 product Substances 0.000 description 13
- 238000004821 distillation Methods 0.000 description 11
- XLSMFKSTNGKWQX-UHFFFAOYSA-N hydroxyacetone Chemical compound CC(=O)CO XLSMFKSTNGKWQX-UHFFFAOYSA-N 0.000 description 10
- 239000000203 mixture Substances 0.000 description 8
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 6
- 150000002989 phenols Chemical class 0.000 description 6
- OZXIZRZFGJZWBF-UHFFFAOYSA-N 1,3,5-trimethyl-2-(2,4,6-trimethylphenoxy)benzene Chemical compound CC1=CC(C)=CC(C)=C1OC1=C(C)C=C(C)C=C1C OZXIZRZFGJZWBF-UHFFFAOYSA-N 0.000 description 5
- 238000000605 extraction Methods 0.000 description 5
- SHOJXDKTYKFBRD-UHFFFAOYSA-N mesityl oxide Natural products CC(C)=CC(C)=O SHOJXDKTYKFBRD-UHFFFAOYSA-N 0.000 description 5
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- BDCFWIDZNLCTMF-UHFFFAOYSA-N 2-phenylpropan-2-ol Chemical compound CC(C)(O)C1=CC=CC=C1 BDCFWIDZNLCTMF-UHFFFAOYSA-N 0.000 description 3
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 3
- 239000006227 byproduct Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 2
- OCKPCBLVNKHBMX-UHFFFAOYSA-N butylbenzene Chemical compound CCCCC1=CC=CC=C1 OCKPCBLVNKHBMX-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000005660 chlorination reaction Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 229930003836 cresol Natural products 0.000 description 2
- 238000004508 fractional distillation Methods 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 238000006396 nitration reaction Methods 0.000 description 2
- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 238000006277 sulfonation reaction Methods 0.000 description 2
- CJWNFAKWHDOUKL-UHFFFAOYSA-N 2-(2-phenylpropan-2-yl)phenol Chemical compound C=1C=CC=C(O)C=1C(C)(C)C1=CC=CC=C1 CJWNFAKWHDOUKL-UHFFFAOYSA-N 0.000 description 1
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- RFRXIWQYSOIBDI-UHFFFAOYSA-N benzarone Chemical compound CCC=1OC2=CC=CC=C2C=1C(=O)C1=CC=C(O)C=C1 RFRXIWQYSOIBDI-UHFFFAOYSA-N 0.000 description 1
- 150000001728 carbonyl compounds Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- -1 dimethyl - phenyl Chemical group 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- FZYCEURIEDTWNS-UHFFFAOYSA-N prop-1-en-2-ylbenzene Chemical compound CC(=C)C1=CC=CC=C1.CC(=C)C1=CC=CC=C1 FZYCEURIEDTWNS-UHFFFAOYSA-N 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 239000002904 solvent Substances 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
- C07C37/74—Purification; separation; Use of additives, e.g. for stabilisation by physical treatment by distillation
- C07C37/80—Purification; separation; Use of additives, e.g. for stabilisation by physical treatment by distillation by extractive distillation
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT02051490A IT1248679B (it) | 1990-06-01 | 1990-06-01 | Procedimento per la purificazione di fenolo |
| IT20514A/90 | 1990-06-01 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH04235932A JPH04235932A (ja) | 1992-08-25 |
| JP2916823B2 true JP2916823B2 (ja) | 1999-07-05 |
Family
ID=11168086
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3156167A Expired - Lifetime JP2916823B2 (ja) | 1990-06-01 | 1991-05-31 | フェノールの精製法 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US5262016A (OSRAM) |
| EP (1) | EP0459572B1 (OSRAM) |
| JP (1) | JP2916823B2 (OSRAM) |
| AT (1) | ATE125244T1 (OSRAM) |
| CA (1) | CA2043721A1 (OSRAM) |
| DE (1) | DE69111303T2 (OSRAM) |
| ES (1) | ES2075329T3 (OSRAM) |
| IT (1) | IT1248679B (OSRAM) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1255264B (it) * | 1992-05-22 | 1995-10-25 | Giuseppe Messina | Procedimento per il recupero di fenolo da sue miscele contenenti cumene e alfa-metilstirene |
| US5705039A (en) * | 1995-10-13 | 1998-01-06 | Albemarle Corporation | Process for purifying a 2,6-dialkylphenol |
| JPH10316603A (ja) * | 1997-05-13 | 1998-12-02 | Sumitomo Chem Co Ltd | ｔ−ブチル−メチルフェノール異性体の分離精製方法 |
| DE19913571C2 (de) | 1999-03-25 | 2002-11-07 | Infineon Technologies Ag | Integrierter Speicher mit Speicherzellen, die je einen ferroelektrischen Speichertransistor aufweisen |
| AU2002229090A1 (en) * | 2000-12-14 | 2002-06-24 | Rtimage Inc. | Three-dimensional image streaming system and method for medical images |
| US6576798B1 (en) | 2001-11-29 | 2003-06-10 | General Electric Company | Method and system for purifying cumene hydroperoxide cleavage products |
| US6573408B1 (en) | 2001-11-29 | 2003-06-03 | General Electric Company | System and method for purifying cumene hydroperoxide cleavage products |
| RU2217409C2 (ru) * | 2002-02-08 | 2003-11-27 | Общество с ограниченной ответственностью "Петрофенол" | Способ и катализатор получения паракумилфенола |
| RU2217408C2 (ru) * | 2002-02-08 | 2003-11-27 | Общество с ограниченной ответственностью "Петрофенол" | Способ и катализатор очистки фенола |
| EP1476413A1 (en) * | 2002-02-08 | 2004-11-17 | General Electric Company | Process and catalyst for purifying phenol |
| US20040211657A1 (en) * | 2003-04-11 | 2004-10-28 | Ingelbrecht Hugo Gerard Eduard | Method of purifying 2,6-xylenol and method of producing poly(arylene ether) therefrom |
| WO2016189495A1 (en) | 2015-05-27 | 2016-12-01 | Van Dyke, Marc | Alerting predicted accidents between driverless cars |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2537115A (en) * | 1948-07-23 | 1951-01-09 | Hoffmann La Roche | Extractive distillation of alcohols |
| GB920905A (en) * | 1959-11-20 | 1963-03-13 | Shawinigan Chem Ltd | Improvements in and relating to purification of phenol |
| GB1021759A (en) * | 1963-03-27 | 1966-03-09 | Mitsui Petrochemical Ind | A process for the manufacture of highly pure phenol |
| CH546719A (de) * | 1969-05-02 | 1974-03-15 | Bayer Ag | Verfahren zur herstellung eines wohlriechenden von pchlorphenol freien o-benzyl-p-chlorphenols und seine verwendung als zusatz zu kosmetischen praeparaten. |
| CA935441A (en) * | 1971-03-11 | 1973-10-16 | Union Carbide Corporation | Process for the purification and recovery of an aromatic hydroxyl compound |
| US4251325A (en) * | 1978-03-04 | 1981-02-17 | Bp Chemicals Limited | Process for the removal of hydroxyacetone from phenol |
| JPS5814411B2 (ja) * | 1979-11-02 | 1983-03-18 | 三井化学株式会社 | フエノ−ル類の精製法 |
| US4455198A (en) * | 1981-06-22 | 1984-06-19 | Allied Corporation | Extraction and/or extractive distillation of ethanol from aqueous solutions |
| US4501645A (en) * | 1983-11-01 | 1985-02-26 | Lloyd Berg | Separation of methanol from acetone by extractive distillation |
| US4836896A (en) * | 1988-11-14 | 1989-06-06 | Lloyd Berg | Separation of m-diisopropylbenzene from p-diisoproylbenzene by azeotropic distillation with acetophenone |
-
1990
- 1990-06-01 IT IT02051490A patent/IT1248679B/it active IP Right Grant
-
1991
- 1991-05-24 AT AT91201236T patent/ATE125244T1/de not_active IP Right Cessation
- 1991-05-24 DE DE69111303T patent/DE69111303T2/de not_active Expired - Fee Related
- 1991-05-24 EP EP91201236A patent/EP0459572B1/en not_active Expired - Lifetime
- 1991-05-24 US US07/705,395 patent/US5262016A/en not_active Expired - Fee Related
- 1991-05-24 ES ES91201236T patent/ES2075329T3/es not_active Expired - Lifetime
- 1991-05-31 CA CA002043721A patent/CA2043721A1/en not_active Abandoned
- 1991-05-31 JP JP3156167A patent/JP2916823B2/ja not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| IT9020514A1 (it) | 1991-12-01 |
| US5262016A (en) | 1993-11-16 |
| DE69111303D1 (de) | 1995-08-24 |
| IT1248679B (it) | 1995-01-26 |
| DE69111303T2 (de) | 1996-01-18 |
| EP0459572A2 (en) | 1991-12-04 |
| ES2075329T3 (es) | 1995-10-01 |
| EP0459572B1 (en) | 1995-07-19 |
| JPH04235932A (ja) | 1992-08-25 |
| ATE125244T1 (de) | 1995-08-15 |
| CA2043721A1 (en) | 1991-12-02 |
| EP0459572A3 (en) | 1992-07-29 |
| IT9020514A0 (OSRAM) | 1990-06-01 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US5064507A (en) | Distillation process for recovery of high purity phenol | |
| CA1165330A (en) | Process for the recovery of pure acetone from cumene hydroperoxide cleavage reaction product | |
| US5133839A (en) | Lower alkylene oxide purification | |
| JP2916823B2 (ja) | フェノールの精製法 | |
| KR101012157B1 (ko) | 증류에 의한 쿠멘 하이드로퍼옥사이드 분해 생성물의 회수방법 | |
| CA1153017A (en) | Process for producing phenolic compounds | |
| US2992169A (en) | Inven | |
| US4722769A (en) | Process for recovery of acetone | |
| KR100738718B1 (ko) | 아세톤의 정제방법 | |
| US7034192B2 (en) | Method for removal of acetol from phenol | |
| EP2240428B1 (en) | Treatment of phenol | |
| KR20030060979A (ko) | 알킬아릴 하이드로퍼옥사이드의 개열시 생성된 개열생성물 혼합물의 증류에 의한 후처리 방법 및 후처리용 장치 | |
| US3335070A (en) | Phenol purification by base addition and plural distillation | |
| US4634796A (en) | Production of high purity phenol | |
| JP5661466B2 (ja) | フェノール製造の間でのアセトフェノンの回収 | |
| US6583326B2 (en) | Process for separating phenol from a mixture comprising at least hydroxyacetone, cumene, water and phenol | |
| US5567853A (en) | Purification of acetone | |
| US4851086A (en) | Production of high purity phenol by steam distillation | |
| US3896006A (en) | Mesityl oxide removal from high-purity phenol | |
| US3029293A (en) | Phenol purification | |
| CN108602743B (zh) | 纯化苯酚的方法 | |
| US4532012A (en) | Production of high purity phenol by distillation with steam and a solvent | |
| KR830001166B1 (ko) | 페놀 화합물의 제조방법 | |
| US3830708A (en) | Process for the purification of phenol by azeotropic distillation with ethylene glycol | |
| JPS647058B2 (OSRAM) |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 19990303 |