CN1411429A - 二(4-羟基芳基)链烷烃 - Google Patents
二(4-羟基芳基)链烷烃 Download PDFInfo
- Publication number
- CN1411429A CN1411429A CN00817281A CN00817281A CN1411429A CN 1411429 A CN1411429 A CN 1411429A CN 00817281 A CN00817281 A CN 00817281A CN 00817281 A CN00817281 A CN 00817281A CN 1411429 A CN1411429 A CN 1411429A
- Authority
- CN
- China
- Prior art keywords
- gas
- phenol
- hydroxyaryl
- desorption tower
- adducts
- 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.)
- Granted
Links
- 150000001335 aliphatic alkanes Chemical class 0.000 title abstract 3
- 238000003795 desorption Methods 0.000 claims abstract description 34
- 238000000034 method Methods 0.000 claims abstract description 19
- -1 aromatic hydroxy compounds Chemical class 0.000 claims abstract description 14
- 238000004821 distillation Methods 0.000 claims abstract description 8
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 36
- 239000007789 gas Substances 0.000 claims description 36
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 21
- 229930195733 hydrocarbon Natural products 0.000 claims description 16
- 150000002430 hydrocarbons Chemical class 0.000 claims description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- 239000007788 liquid Substances 0.000 claims description 10
- 229910052757 nitrogen Inorganic materials 0.000 claims description 10
- 150000002989 phenols Chemical class 0.000 claims description 8
- KLSLBUSXWBJMEC-UHFFFAOYSA-N 4-Propylphenol Chemical compound CCCC1=CC=C(O)C=C1 KLSLBUSXWBJMEC-UHFFFAOYSA-N 0.000 claims description 7
- 238000005406 washing Methods 0.000 claims description 7
- 238000000926 separation method Methods 0.000 claims description 6
- 238000001816 cooling Methods 0.000 claims description 4
- 239000000919 ceramic Substances 0.000 claims description 3
- 239000000454 talc Substances 0.000 claims description 3
- 229910052623 talc Inorganic materials 0.000 claims description 3
- 235000012222 talc Nutrition 0.000 claims description 3
- 230000005465 channeling Effects 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims 1
- 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 description 30
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 24
- 238000002425 crystallisation Methods 0.000 description 13
- 230000008025 crystallization Effects 0.000 description 13
- 239000000155 melt Substances 0.000 description 11
- 239000000047 product Substances 0.000 description 11
- 239000002253 acid Substances 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 7
- 239000000470 constituent Substances 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- 239000012530 fluid Substances 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 239000006227 byproduct Substances 0.000 description 4
- 238000006555 catalytic reaction Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 239000012452 mother liquor Substances 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- PBEHQFUSQJKBAS-UHFFFAOYSA-N 4-[2-(4-hydroxyphenyl)propan-2-yl]phenol;phenol Chemical class 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 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-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
- 230000002411 adverse Effects 0.000 description 2
- 229910010293 ceramic material Inorganic materials 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 229920000515 polycarbonate Polymers 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 238000005245 sintering Methods 0.000 description 2
- MDFLZWDNYLIUMV-UHFFFAOYSA-N 1-phenyl-2,3-dihydroinden-1-ol Chemical compound C1CC2=CC=CC=C2C1(O)C1=CC=CC=C1 MDFLZWDNYLIUMV-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
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- JGDWYKQLFQQIDH-UHFFFAOYSA-N 2-phenyl-3,4-dihydrochromen-2-ol Chemical compound C1CC2=CC=CC=C2OC1(O)C1=CC=CC=C1 JGDWYKQLFQQIDH-UHFFFAOYSA-N 0.000 description 1
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- 239000004697 Polyetherimide Substances 0.000 description 1
- 150000001728 carbonyl compounds Chemical class 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000012295 chemical reaction liquid Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 230000002779 inactivation Effects 0.000 description 1
- 125000003454 indenyl group Chemical class C1(C=CC2=CC=CC=C12)* 0.000 description 1
- 238000006317 isomerization reaction Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- QDLAGTHXVHQKRE-UHFFFAOYSA-N lichenxanthone Natural products COC1=CC(O)=C2C(=O)C3=C(C)C=C(OC)C=C3OC2=C1 QDLAGTHXVHQKRE-UHFFFAOYSA-N 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen(.) Chemical compound [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- XDTRNDKYILNOAP-UHFFFAOYSA-N phenol;propan-2-one Chemical compound CC(C)=O.OC1=CC=CC=C1 XDTRNDKYILNOAP-UHFFFAOYSA-N 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
- 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
- 239000002994 raw material Substances 0.000 description 1
- 230000008707 rearrangement Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 238000006277 sulfonation reaction 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
-
- 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Devices And Processes Conducted In The Presence Of Fluids And Solid Particles (AREA)
Abstract
Description
Claims (7)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19961566.7 | 1999-12-20 | ||
DE19961566A DE19961566A1 (de) | 1999-12-20 | 1999-12-20 | Bis(4-hydroxyaryl)alkane |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1411429A true CN1411429A (zh) | 2003-04-16 |
CN100360488C CN100360488C (zh) | 2008-01-09 |
Family
ID=7933488
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNB008172811A Expired - Fee Related CN100360488C (zh) | 1999-12-20 | 2000-12-07 | 二(4-羟基芳基)链烷烃 |
Country Status (12)
Country | Link |
---|---|
US (1) | US6919487B2 (zh) |
EP (1) | EP1242349B1 (zh) |
JP (1) | JP5260816B2 (zh) |
KR (2) | KR20070110447A (zh) |
CN (1) | CN100360488C (zh) |
AU (1) | AU3363101A (zh) |
BR (1) | BR0016494A (zh) |
DE (1) | DE19961566A1 (zh) |
ES (1) | ES2401772T3 (zh) |
MX (1) | MXPA02006090A (zh) |
TW (1) | TW526190B (zh) |
WO (1) | WO2001046104A1 (zh) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113926216A (zh) * | 2021-11-19 | 2022-01-14 | 中国海洋石油集团有限公司 | 一种双酚a加合物结晶分离装置及分离工艺 |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6545187B1 (en) * | 2001-09-19 | 2003-04-08 | General Electric Company | Production of low-particulate bisphenol and use thereof in the manufacturing of polycarbonate |
DE102005025788A1 (de) * | 2005-06-04 | 2006-12-07 | Bayer Materialscience Ag | Verfahren zur Herstellung von hochreinem Bisphenol A |
DE102007026548A1 (de) | 2007-06-08 | 2008-12-18 | Bayer Materialscience Ag | Vermeidung von Feststoffablagerungen in Tropfenabscheidern durch Eindüsung von geeigneten Flüssigkeiten |
Family Cites Families (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IT974747B (it) * | 1972-12-22 | 1974-07-10 | Sir Soc Italiana Resine Spa | Procedimento perfezionato per la produzione di 2 2 4 4 dii drossidifenilpropano |
DE2928464A1 (de) * | 1979-07-13 | 1981-01-29 | Bayer Ag | Verwendung von speziellen rohbisphenolen zur herstellung von polycarbonaten |
US4294994A (en) * | 1980-04-21 | 1981-10-13 | General Electric Company | Purification of bisphenol-A |
US4931146A (en) * | 1988-04-05 | 1990-06-05 | Mitsui Toatsu Chemicals, Inc. | Process for obtaining high-purity bisphenol A |
JPH085828B2 (ja) * | 1988-04-05 | 1996-01-24 | 三井東圧化学株式会社 | 高純度ビスフェノールaの製造方法 |
PL164289B1 (pl) * | 1990-11-24 | 1994-07-29 | Inst Ciezkiej Syntezy Orga | Sposób otrzymywani blsfenolu A PL PL |
JP2887300B2 (ja) * | 1991-08-01 | 1999-04-26 | 千代田化工建設株式会社 | 高品位ビスフェノールaの製造方法 |
CN1059428C (zh) * | 1991-07-10 | 2000-12-13 | 千代田化工建设株式会社 | 高品位双酚a的制造方法 |
JP3190388B2 (ja) * | 1991-10-25 | 2001-07-23 | 千代田化工建設株式会社 | 高品位ビスフェノールaの製造方法 |
EP0643032B1 (en) * | 1991-07-16 | 1997-02-05 | Chiyoda Corporation | Condensation process for recovery of bisphenol A and phenol |
CN1050828C (zh) * | 1993-02-16 | 2000-03-29 | 中国石油化工总公司 | 制备高品位聚碳酸脂级双酚a的脱酚新方法 |
DE4413396A1 (de) * | 1994-04-18 | 1995-10-19 | Bayer Ag | Verfahren zur Herstellung von ultrareinem Bisphenol-A und dessen Verwendung |
US5783733A (en) * | 1996-06-13 | 1998-07-21 | General Electric Company | Process for manufacture of bisphenol |
CN1178213A (zh) * | 1996-09-13 | 1998-04-08 | 通用电气公司 | 双酚a的制备 |
DE19848026A1 (de) | 1998-10-17 | 2000-04-20 | Bayer Ag | Verfahren zur Herstellung von Bis(4-hydroxyaryl)alkanen |
USH1943H1 (en) * | 1998-12-15 | 2001-02-06 | General Electric Co. | Process for the manufacture of bisphenol-A |
DE19860144C1 (de) * | 1998-12-24 | 2000-09-14 | Bayer Ag | Verfahren zur Herstellung von Bisphenol A |
US6545187B1 (en) * | 2001-09-19 | 2003-04-08 | General Electric Company | Production of low-particulate bisphenol and use thereof in the manufacturing of polycarbonate |
-
1999
- 1999-12-20 DE DE19961566A patent/DE19961566A1/de not_active Withdrawn
-
2000
- 2000-12-07 US US10/149,906 patent/US6919487B2/en not_active Expired - Lifetime
- 2000-12-07 KR KR1020077023912A patent/KR20070110447A/ko not_active Application Discontinuation
- 2000-12-07 MX MXPA02006090A patent/MXPA02006090A/es unknown
- 2000-12-07 KR KR1020027007867A patent/KR100786460B1/ko not_active IP Right Cessation
- 2000-12-07 CN CNB008172811A patent/CN100360488C/zh not_active Expired - Fee Related
- 2000-12-07 WO PCT/EP2000/012324 patent/WO2001046104A1/de active Application Filing
- 2000-12-07 AU AU33631/01A patent/AU3363101A/en not_active Abandoned
- 2000-12-07 ES ES00991585T patent/ES2401772T3/es not_active Expired - Lifetime
- 2000-12-07 JP JP2001546618A patent/JP5260816B2/ja not_active Expired - Fee Related
- 2000-12-07 EP EP00991585A patent/EP1242349B1/de not_active Expired - Lifetime
- 2000-12-07 BR BR0016494-1A patent/BR0016494A/pt not_active Application Discontinuation
- 2000-12-19 TW TW089127151A patent/TW526190B/zh not_active IP Right Cessation
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113926216A (zh) * | 2021-11-19 | 2022-01-14 | 中国海洋石油集团有限公司 | 一种双酚a加合物结晶分离装置及分离工艺 |
Also Published As
Publication number | Publication date |
---|---|
US20020183562A1 (en) | 2002-12-05 |
EP1242349B1 (de) | 2013-02-20 |
KR20020062353A (ko) | 2002-07-25 |
US6919487B2 (en) | 2005-07-19 |
ES2401772T3 (es) | 2013-04-24 |
TW526190B (en) | 2003-04-01 |
EP1242349A1 (de) | 2002-09-25 |
MXPA02006090A (es) | 2003-01-28 |
CN100360488C (zh) | 2008-01-09 |
BR0016494A (pt) | 2002-09-17 |
WO2001046104A1 (de) | 2001-06-28 |
DE19961566A1 (de) | 2001-06-21 |
AU3363101A (en) | 2001-07-03 |
KR20070110447A (ko) | 2007-11-16 |
KR100786460B1 (ko) | 2007-12-17 |
JP2003518048A (ja) | 2003-06-03 |
JP5260816B2 (ja) | 2013-08-14 |
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Effective date of registration: 20120802 Address after: Germany Leverkusen Patentee after: Carcoustics Techconsult GmbH Address before: Germany Leverkusen Patentee before: Bayer Aktiengesellschaft |
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EE01 | Entry into force of recordation of patent licensing contract |
Application publication date: 20030416 Assignee: Bayer Material Science (China) Co., Ltd. Assignor: Carcoustics Techconsult GmbH Contract record no.: 2012990000854 Denomination of invention: Two (4- hydroxy aryl) alkanes Granted publication date: 20080109 License type: Common License Record date: 20121128 |
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LICC | Enforcement, change and cancellation of record of contracts on the licence for exploitation of a patent or utility model | ||
C56 | Change in the name or address of the patentee | ||
CP03 | Change of name, title or address |
Address after: Leverkusen, Germany Patentee after: BAYER MATERIALSCIENCE AG Address before: Germany Leverkusen Patentee before: Carcoustics Techconsult GmbH |
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CF01 | Termination of patent right due to non-payment of annual fee | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20080109 Termination date: 20171207 |