MXPA02009453A - Procedimiento para la preparacion de bisfenoles. - Google Patents
Procedimiento para la preparacion de bisfenoles.Info
- Publication number
- MXPA02009453A MXPA02009453A MXPA02009453A MXPA02009453A MXPA02009453A MX PA02009453 A MXPA02009453 A MX PA02009453A MX PA02009453 A MXPA02009453 A MX PA02009453A MX PA02009453 A MXPA02009453 A MX PA02009453A MX PA02009453 A MXPA02009453 A MX PA02009453A
- Authority
- MX
- Mexico
- Prior art keywords
- bisphenol
- phenol
- crystallization
- adduct
- crystals
- Prior art date
Links
- 229930185605 Bisphenol Natural products 0.000 title claims abstract description 74
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 49
- 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 title abstract description 17
- 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 abstract description 120
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims abstract description 74
- 239000013078 crystal Substances 0.000 claims abstract description 53
- 238000002425 crystallisation Methods 0.000 claims description 74
- 230000008025 crystallization Effects 0.000 claims description 72
- 238000000034 method Methods 0.000 claims description 56
- 239000007788 liquid Substances 0.000 claims description 12
- 150000002989 phenols Chemical class 0.000 claims description 11
- 238000002360 preparation method Methods 0.000 claims description 11
- 239000012452 mother liquor Substances 0.000 claims description 2
- 239000007787 solid Substances 0.000 claims description 2
- 206010012335 Dependence Diseases 0.000 claims 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 26
- 239000000725 suspension Substances 0.000 description 25
- 238000006243 chemical reaction Methods 0.000 description 17
- 239000000243 solution Substances 0.000 description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
- 238000000926 separation method Methods 0.000 description 15
- 239000011541 reaction mixture Substances 0.000 description 12
- 229920000515 polycarbonate Polymers 0.000 description 11
- 239000004417 polycarbonate Substances 0.000 description 11
- 238000000746 purification Methods 0.000 description 9
- 238000004821 distillation Methods 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- 238000001816 cooling Methods 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 230000005540 biological transmission Effects 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 238000003795 desorption Methods 0.000 description 4
- 238000001914 filtration Methods 0.000 description 4
- 150000002500 ions Chemical class 0.000 description 4
- 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 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 239000006227 byproduct Substances 0.000 description 3
- -1 for example Substances 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 238000001953 recrystallisation Methods 0.000 description 3
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000003377 acid catalyst Substances 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 150000001728 carbonyl compounds Chemical class 0.000 description 2
- 238000006555 catalytic reaction Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- OASFYFTVWALXTH-UHFFFAOYSA-L disodium;diphenoxide Chemical compound [Na+].[Na+].[O-]C1=CC=CC=C1.[O-]C1=CC=CC=C1 OASFYFTVWALXTH-UHFFFAOYSA-L 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 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 2
- 239000012535 impurity Substances 0.000 description 2
- 239000000543 intermediate Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000011403 purification operation Methods 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 230000017105 transposition Effects 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- YQDJQYVIHZYJSE-UHFFFAOYSA-N 1-phenyl-2,3-dihydroindene-1,2-diol Chemical class OC1CC2=CC=CC=C2C1(O)C1=CC=CC=C1 YQDJQYVIHZYJSE-UHFFFAOYSA-N 0.000 description 1
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Natural products C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-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
- JGDWYKQLFQQIDH-UHFFFAOYSA-N 2-phenyl-3,4-dihydrochromen-2-ol Chemical class C1CC2=CC=CC=C2OC1(O)C1=CC=CC=C1 JGDWYKQLFQQIDH-UHFFFAOYSA-N 0.000 description 1
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical class C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 1
- 241001550224 Apha Species 0.000 description 1
- 239000007848 Bronsted acid Substances 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- GFHNAMRJFCEERV-UHFFFAOYSA-L cobalt chloride hexahydrate Chemical compound O.O.O.O.O.O.[Cl-].[Cl-].[Co+2] GFHNAMRJFCEERV-UHFFFAOYSA-L 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 239000002826 coolant Substances 0.000 description 1
- 230000009849 deactivation Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical class O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
- 125000003454 indenyl group Chemical class C1(C=CC2=CC=CC=C12)* 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920001467 poly(styrenesulfonates) Polymers 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920001230 polyarylate Polymers 0.000 description 1
- 229920001601 polyetherimide Polymers 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000000066 reactive distillation Methods 0.000 description 1
- 230000003134 recirculating effect Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000011144 upstream manufacturing Methods 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 229920001285 xanthan gum Polymers 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
-
- 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
- C07C37/685—Processes comprising at least two steps in series
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10015014A DE10015014A1 (de) | 2000-03-27 | 2000-03-27 | Verfahren zur Herstellung von Bisphenolen |
| PCT/EP2001/002845 WO2001072677A1 (de) | 2000-03-27 | 2001-03-14 | Verfahren zur herstellung von bisphenolen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MXPA02009453A true MXPA02009453A (es) | 2003-04-10 |
Family
ID=7636449
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MXPA02009453A MXPA02009453A (es) | 2000-03-27 | 2001-03-14 | Procedimiento para la preparacion de bisfenoles. |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US6828465B2 (enExample) |
| EP (1) | EP1268379B9 (enExample) |
| JP (2) | JP5419314B2 (enExample) |
| KR (1) | KR100781863B1 (enExample) |
| CN (1) | CN1179931C (enExample) |
| AU (1) | AU2001248347A1 (enExample) |
| BR (1) | BR0109539A (enExample) |
| DE (2) | DE10015014A1 (enExample) |
| ES (1) | ES2217134T5 (enExample) |
| MX (1) | MXPA02009453A (enExample) |
| TW (1) | TWI252224B (enExample) |
| WO (1) | WO2001072677A1 (enExample) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10015014A1 (de) * | 2000-03-27 | 2001-10-04 | Bayer Ag | Verfahren zur Herstellung von Bisphenolen |
| US6703530B2 (en) | 2002-02-28 | 2004-03-09 | General Electric Company | Chemical reactor system and process |
| KR20050098870A (ko) | 2003-03-27 | 2005-10-12 | 미쓰이 가가쿠 가부시키가이샤 | 비스페놀 ａ의 제조 방법 |
| DE102004005723A1 (de) * | 2004-02-05 | 2005-08-25 | Bayer Materialscience Ag | Herstellung von Bisphenol A mit verringertem Schwefelgehalt |
| JP4517656B2 (ja) * | 2004-02-05 | 2010-08-04 | 三菱化学株式会社 | ビスフェノールａの製造方法 |
| US20100048942A1 (en) * | 2006-12-11 | 2010-02-25 | Basf Se | Process for preparing isocyanates |
| DE102007001427A1 (de) | 2007-01-09 | 2008-07-10 | Bayer Materialscience Ag | Kristallisationsverfahren zur Herstellung von Bisphenol A |
| WO2008129757A1 (ja) * | 2007-03-30 | 2008-10-30 | Mitsubishi Chemical Corporation | ビスフェノールａの製造方法 |
| DE102007021935A1 (de) * | 2007-05-10 | 2008-11-20 | Bayer Materialscience Ag | Verfahren und Herstellung von Bisphenol A mit verlängerter Standzeit in der Kristallisation |
| JP5655397B2 (ja) * | 2010-07-01 | 2015-01-21 | 三菱化学株式会社 | ビスフェノールａの製造方法 |
| CN108137456B (zh) * | 2015-11-19 | 2021-01-12 | 株式会社Lg化学 | 制备双酚a的装置和方法 |
| US10570076B2 (en) | 2016-07-22 | 2020-02-25 | Sabic Global Technologies B.V. | Method for the continuous manufacture of bisphenol A |
| JP2022546022A (ja) | 2019-08-27 | 2022-11-02 | コベストロ・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング・アンド・コー・カーゲー | ヒドロキシアセトンの存在下でビスフェノールａ（ｂｐａ）を作製するプロセス |
| JP2024508777A (ja) | 2021-02-23 | 2024-02-28 | コベストロ、ドイチュラント、アクチエンゲゼルシャフト | 少なくとも２つの不純物の存在下でビスフェノールａ（ｂｐａ）を作製するプロセス |
| WO2022179900A1 (en) | 2021-02-23 | 2022-09-01 | Covestro Deutschland Ag | Process for preparing bisphenol a (bpa) in the presence of 2-methyl benzofuran |
| EP4298083A1 (en) | 2021-02-23 | 2024-01-03 | Covestro Deutschland AG | Process for preparing bisphenol a (bpa) in the presence of acetophenone |
| US20240076256A1 (en) | 2021-02-23 | 2024-03-07 | Covestro Deutschland Ag | Process for preparing bisphenol a (bpa) in the presence of alpha-methylstyrene |
| KR20230149817A (ko) | 2021-02-23 | 2023-10-27 | 코베스트로 도이칠란트 아게 | 벤젠의 존재 하에 비스페놀 a (bpa)를 제조하는 방법 |
| JP2024508775A (ja) | 2021-02-23 | 2024-02-28 | コベストロ、ドイチュラント、アクチエンゲゼルシャフト | クメンの存在下でビスフェノールａ（ｂｐａ）を作製するプロセス |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2775620A (en) * | 1954-07-12 | 1956-12-25 | Shell Dev | Production of bis (hydroxyaryl) substituted compounds |
| JPS6236346A (ja) * | 1985-04-24 | 1987-02-17 | Mitsui Toatsu Chem Inc | アクリルアミド結晶の製造方法 |
| US4859803A (en) * | 1988-05-16 | 1989-08-22 | Shell Oil Company | Preparation of bisphenols |
| JP3171465B2 (ja) * | 1991-10-25 | 2001-05-28 | 千代田化工建設株式会社 | 色相の良好なビスフェノールａ・フェノール結晶アダクトの製造方法 |
| EP0718268B1 (en) | 1991-07-10 | 1998-12-09 | Chiyoda Corporation | Process for the production of crystalline adduct of bisphenol A and phenol |
| JP3413497B2 (ja) * | 1991-10-30 | 2003-06-03 | 三菱化学株式会社 | ビスフェノールａの製造方法 |
| DE4408008A1 (de) * | 1994-03-10 | 1995-09-14 | Bayer Ag | Verfahren zur kontinuierlichen Herstellung von hochreinem Bisphenol-A |
| EP0720976B2 (en) † | 1994-12-09 | 2005-05-18 | The Dow Chemical Company | Process for preparing an adduct of a bisphenol with a phenolic compound |
| DE10015014A1 (de) * | 2000-03-27 | 2001-10-04 | Bayer Ag | Verfahren zur Herstellung von Bisphenolen |
-
2000
- 2000-03-27 DE DE10015014A patent/DE10015014A1/de not_active Withdrawn
-
2001
- 2001-03-14 WO PCT/EP2001/002845 patent/WO2001072677A1/de not_active Ceased
- 2001-03-14 US US10/239,544 patent/US6828465B2/en not_active Expired - Lifetime
- 2001-03-14 MX MXPA02009453A patent/MXPA02009453A/es active IP Right Grant
- 2001-03-14 CN CNB018071686A patent/CN1179931C/zh not_active Expired - Lifetime
- 2001-03-14 AU AU2001248347A patent/AU2001248347A1/en not_active Abandoned
- 2001-03-14 DE DE50101607T patent/DE50101607D1/de not_active Expired - Lifetime
- 2001-03-14 EP EP01921334A patent/EP1268379B9/de not_active Expired - Lifetime
- 2001-03-14 KR KR1020027012693A patent/KR100781863B1/ko not_active Expired - Fee Related
- 2001-03-14 ES ES01921334T patent/ES2217134T5/es not_active Expired - Lifetime
- 2001-03-14 JP JP2001570593A patent/JP5419314B2/ja not_active Expired - Fee Related
- 2001-03-14 BR BR0109539-0A patent/BR0109539A/pt not_active Application Discontinuation
- 2001-03-20 TW TW090106395A patent/TWI252224B/zh not_active IP Right Cessation
-
2013
- 2013-08-09 JP JP2013165930A patent/JP2013249306A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| CN1179931C (zh) | 2004-12-15 |
| BR0109539A (pt) | 2003-06-10 |
| JP5419314B2 (ja) | 2014-02-19 |
| ES2217134T3 (es) | 2004-11-01 |
| EP1268379B9 (de) | 2010-02-24 |
| DE50101607D1 (de) | 2004-04-08 |
| US20040030195A1 (en) | 2004-02-12 |
| JP2013249306A (ja) | 2013-12-12 |
| KR20020084253A (ko) | 2002-11-04 |
| EP1268379B1 (de) | 2004-03-03 |
| AU2001248347A1 (en) | 2001-10-08 |
| EP1268379B2 (de) | 2009-06-17 |
| JP2003528840A (ja) | 2003-09-30 |
| KR100781863B1 (ko) | 2007-12-05 |
| DE10015014A1 (de) | 2001-10-04 |
| US6828465B2 (en) | 2004-12-07 |
| WO2001072677A1 (de) | 2001-10-04 |
| CN1419530A (zh) | 2003-05-21 |
| TWI252224B (en) | 2006-04-01 |
| HK1053106A1 (en) | 2003-10-10 |
| EP1268379A1 (de) | 2003-01-02 |
| ES2217134T5 (es) | 2009-11-17 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG | Grant or registration |