EP1713751A1 - Procede pour produire du bisphenol a presentant une teneur reduite en soufre - Google Patents

Procede pour produire du bisphenol a presentant une teneur reduite en soufre

Info

Publication number
EP1713751A1
EP1713751A1 EP05701120A EP05701120A EP1713751A1 EP 1713751 A1 EP1713751 A1 EP 1713751A1 EP 05701120 A EP05701120 A EP 05701120A EP 05701120 A EP05701120 A EP 05701120A EP 1713751 A1 EP1713751 A1 EP 1713751A1
Authority
EP
European Patent Office
Prior art keywords
phenol
bisphenol
washing
adduct
sulfur
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.)
Withdrawn
Application number
EP05701120A
Other languages
German (de)
English (en)
Inventor
Rainer Neumann
Ulrich Blaschke
Stefan Westernacher
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Covestro Deutschland AG
Original Assignee
Bayer MaterialScience AG
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Bayer MaterialScience AG filed Critical Bayer MaterialScience AG
Publication of EP1713751A1 publication Critical patent/EP1713751A1/fr
Withdrawn legal-status Critical Current

Links

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
    • C07C37/11—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by reactions increasing the number of carbon atoms
    • C07C37/20—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by reactions increasing the number of carbon atoms using aldehydes or ketones
    • 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
    • C07C37/70—Purification; separation; Use of additives, e.g. for stabilisation by physical treatment
    • C07C37/82—Purification; separation; Use of additives, e.g. for stabilisation by physical treatment by solid-liquid treatment; by chemisorption
    • 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
    • C07C39/00—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring
    • C07C39/12—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring polycyclic with no unsaturation outside the aromatic rings
    • C07C39/15—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring polycyclic with no unsaturation outside the aromatic rings with all hydroxy groups on non-condensed rings, e.g. phenylphenol
    • C07C39/16—Bis-(hydroxyphenyl) alkanes; Tris-(hydroxyphenyl)alkanes
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G64/00—Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
    • C08G64/04—Aromatic polycarbonates
    • C08G64/06—Aromatic polycarbonates not containing aliphatic unsaturation

Definitions

  • the present application relates to low-sulfur bisphenol A and a process for its preparation.
  • Bisphenols as condensation products of phenols and carbonyl compounds are starting materials or intermediates for the production of a large number of commercial products.
  • BPA 2,2-bis (4-hydr )xyphenyl) propane
  • BPA serves as a starting material for the production of various types of polymeric materials such as polyarylates, polyetherimides, polysulfones and modified phenol-formaldehyde resins. Preferred areas of application are in the production of epoxy resins and polycarbonates.
  • Divinylbenzene is normally used as the crosslinker, but other crosslinkers such as divinylbiphenyl can also be used.
  • a cocatalyst can be used. These are usually thiols which carry at least one SH function and have a positive influence on both the selectivity and the reactivity of the reaction.
  • the cocatalyst can either be dissolved homogeneously in the reaction solution or, in the case of the acidic ion exchangers, can be fixed on the catalyst itself.
  • Homogeneous cocatalysts are, for example, mercaptopropionic acid, hydrogen sulfide, alkyl sulfides such as ethyl sulfide and similar compounds.
  • Cocatalysts are aminoalkylthiols and pyridylalkylthiols which are ionically bound to the catalyst, where the SH function can be protected and is only released during or after fixation on the catalyst, such as, for example, in the case of dimethylthiazolidine.
  • the cocatalyst can be covalently bound to the catalyst as alkyl or aryl thiol.
  • a product mixture is formed which, in addition to unreacted phenol and optionally acetone, contains primarily BPA and water.
  • typical by-products of the con- densationsreaktioh on such as 2- (4-hydroxyphenyl) -2- (2-hydroxyphenyl) propane (o, p-BPA), substituted indanes, hydroxyphenyl indanols, hydroxyphenyl chromanes, spirobisindanes, substituted rindenols, substituted xanthenes and more condensed Compounds with three or more phenyl rings in the molecular framework.
  • self-condensation of the acetone and reaction with impurities in the raw materials can result in the formation of further secondary components such as anisole, mesityl oxide, mesitylene and diacetone alcohol.
  • the reaction is usually carried out in such a way that 100% conversion of the acetone is not achieved and 0.1-0.6% by weight of acetone are still present in the reactor outlet.
  • high purity requirements are placed on the raw material BPA.
  • a work-up and purification method of BPA is carried out by separating BPA from the reaction mixture in the form of an approximately equimolar crystalline adduct with phenol by cooling the reaction mixture with crystallization of the BPA-phenol adduct in a suspension crystallization.
  • the BPA-phenol adduct crystals are then separated from the liquid phase by a suitable apparatus for solid-liquid separation, such as rotary filters or centrifuges, and sent for further purification.
  • Adduct crystals obtained in this way typically have a purity of> 99% by weight of BPA, based on the sum of BPA and the secondary components, with a phenol content of approximately 40% by weight.
  • the adduct crystals can be freed from impurities adhering to the surface.
  • suitable solutions typically contain one or more components from the group consisting of acetone, water, phenol, BPA and secondary components
  • the liquid stream (mother liquor) obtained in the solid-liquid separation contains phenol, BPA, water formed in the reaction, unreacted acetone and is enriched in the secondary components typically obtained in the production of BPA.
  • This mother liquor stream is usually returned to the reaction unit.
  • water previously formed is removed by distillation. any acetone still present is removed from the mother liquor.
  • the dewatered reaction stream thus obtained is supplemented by phenol, acetone and optionally cocatalyst and returned to the reaction unit.
  • the phenol can also be added in whole or in part before dewatering.
  • before performing the Suspension crystallization of the BPA-phenol adduct water and acetone are removed by distillation.
  • a partial amount of the phenol present in the reaction solution and, depending on the type of cocatalyst, this can also be separated off wholly or in part by distillation, if appropriate.
  • part or all of the circulating stream after the solid-liquid separation and before or after the separation of water and residual acetone can be passed through a rearrangement unit filled with an acidic ion exchanger.
  • This unit is generally operated at higher temperatures than the reaction unit.
  • this rearrangement unit under the prevailing conditions, some of the secondary components of the BPA production present in the recycle stream are isomerized to BPA, so that the overall yield of BPA can be increased.
  • the resin can also be subjected to a thermal, acidic or basic catalyzed cleavage.
  • the phenol released and possibly also isopropenylphenol can be separated off by distillation and returned to the reaction.
  • the BPA-phenol adduct crystals obtained after the above-described suspension crystallization of the reaction solution and solid-liquid separation are passed on to further purification steps, with the separation of phenol and possibly a reduction in the concentration of secondary components being achieved.
  • the BPA-phenol adduct crystals can thus be purified from phenol, organic
  • Solvents water or mixtures of the solvents mentioned, optionally also
  • BPA and its isomers can be recrystallized according to a suspension crystallization.
  • the phenol present in the adduct crystals can also be removed in whole or in part by the choice of suitable solvents. Any phenol remaining in the BPA after recrystallization is then completely separated off by suitable distillative, desorptive or extractive methods. Alternatively, the phenol can also be removed from the BPA-phenol adduct crystals by means of a melting process.
  • a bisphenol A melt is obtained, which can be used without prior solidification for the production of polycarbonate by the transesterification process (melt polycarbonate).
  • the bisphenol A melt can also be produced by known processes, such as e.g. can be solidified after the prilling process or by desquamation, for sale or recycling.
  • the melt can be dissolved in sodium hydroxide solution and used for the production of polycarbonate by the phase interface process.
  • the phenol-free bisphenol A can be subjected to a purification step such as melt crystallization, distillation and / or recrystallization from phenol, water or an organic solvent such as toluene or mixtures of these substances before further processing.
  • a purification step such as melt crystallization, distillation and / or recrystallization from phenol, water or an organic solvent such as toluene or mixtures of these substances before further processing.
  • sulfur-containing compounds are carried over into the end product bisphenol A and can therefore lead to quality problems in the color.
  • These compounds can be degradation products of the sulfonic acid ion exchanger, such as sulfuric acid, arylsulfonic acids, oligomeric polystyrene sulfonic acids, finely divided catalyst and the like.
  • Cocatalysts present homogeneously in the reaction mixture such as, for example, mercaptopropionic acid, silylmethane thiols, hydrogen sulfide, alkyl sulfides, such as, for example, ethyl sulfide and similar compounds, can be present in their original form or in the form of their degradation products or secondary products.
  • the SH group can be alkylated, but it can also be compounds such as dimethyl sulfide or disulfide compounds, elemental sulfur, thioether, H 2 S as a cleavage product from the cocatalyst and other compounds.
  • cocatalysts fixed to the catalyst such as, for example, thiazolidines, amino (alkyl) thiols (the aforementioned compounds can also be in the form of their hydrochlorides and / or with, for example, SH function masked by acyl, benzyl or tert.-butyl groups, in which but this is easily releasable, come into use), pyridyl (alkyl) thiols, alkylcarbamoylalkylthioesters, covalently bonded aryl or alkylthiols. These can be split off and / or decomposed and / or simply washed out in the case of the ionically bound cocatalysts.
  • the object of the present invention was therefore to provide a process for the preparation of bisphenol A in which the sulfur content in the end product bisphenol A can be reduced. It was also an object of the present invention to provide bisphenol A with a residual sulfur content of ⁇ 2 ppm.
  • the invention relates to a process for the preparation of bisphenol A, in which
  • Bisphenol A with sulfur contents of ⁇ 2 ppm (measured by medium chemiluminescence) can be produced with the method according to the invention.
  • the sulfur content means the total sulfur content calculated as the mass of the sulfur atoms, although it is not essential whether the sulfur is elementary or in the form of inorganic or organic sulfur compounds.
  • filter media are used in step b) after the reaction mixture has left the reactor with the sulfonic acid ion exchanger.
  • sulfur-containing particles can be fed out and / or acidic components neutralized, absorbed and / or adsorbed.
  • reaction mixture is then subjected to suspension crystallization to separate the
  • BPA phenol adduct crystals fed The cooling can be done by heat exchangers but also by evaporation of existing or possibly added in the reaction mixture Solvents such as phenol, water, alkanes or mixtures thereof can be achieved.
  • Solvents such as phenol, water, alkanes or mixtures thereof can be achieved.
  • the crystallization can take place in one or more crystallizers connected in series. The total residence time of the reaction mixture in this crystallization step should preferably be over 3 hours. With a correspondingly slow crystallization, the inclusion of the reaction mixture or the incorporation of impurities into the BPA-phenol adduct crystals can be largely prevented.
  • all or part of the water present can be freed from the reaction mixture by (vacuum) distillation before the suspension crystallization.
  • sulfur-containing components can be separated further from the reaction mixture.
  • the mixed crystals bisphenol A-phenol are separated from the mother liquor by using filter media suitable for the separation of solids. Washing of the separated solid is preferably also possible in or on these apparatuses. This can be achieved, for example, on appropriate centrifuges such as peeler centrifuges, sieve screw centrifuges or push centrifuges, but also on rotary filters, belt filters and (vacuum) disc filters. Rotary pressure filters, particularly preferably rotary vacuum filters, are preferably used.
  • the filter cake made of the bisphenol A-phenol mixed crystals is also preferably washed with fresh phenol. This reduces the residual sulfur-containing mother liquor in the mixed crystals.
  • the amount of fresh phenol for washing the filtered bisphenol A-phenol mixed crystals is preferably selected so that the flushing amount corresponds to 50-150% by weight of the filter cake or the amount filtered off.
  • the bisphenol A with low sulfur contents produced by the process according to the invention shows particularly positive properties if the amount of fresh, that is to say externally introduced phenol, selected for washing the bisphenol A-phenol mixed crystals is more than 70% by weight of the total corresponds to the process of fresh phenol supplied from outside.
  • the washing is preferably carried out at a temperature of the phenol of 40-70 ° C.
  • the washed mixed crystals are then preferably melted and the melt obtained is freed from the phenol.
  • the melt is preferably treated by evaporation and residual phenol desorption at temperatures between 160-210 ° C., phenol and sulfur compounds being separated off.
  • This two-stage procedure in which the melt is exposed both to a vacuum and elevated temperature in the first step and to a higher temperature and a desorption gas, preferably nitrogen, in the second step, not only the phenol but also sulfur compounds in particular can be effectively separated.
  • a suitable washing liquid such as water, sulfur compounds still present can be separated off in this way.
  • the sulfur content in bisphenol A can be further reduced by a prilling process.
  • the bisphenol A is solidified by free fall in the cooled nitrogen countercurrent in drop form. It was observed that the nitrogen discharges any sulfur still present in the product. This effect is not achieved when using other consolidation processes such as scale rollers.
  • the invention also relates to bisphenol A with a sulfur content of ⁇ 2 ppm, which is preferably in the form of prills.
  • Bisphenol A with a low sulfur content of ⁇ 2 ppm which was produced, for example, by the process according to the invention, can be reacted with phosgene according to the phase interface process or with diaryl carbonates, preferably diphenyl carbonate, according to the melt process to polycarbonate.
  • phosgene according to the phase interface process
  • diaryl carbonates preferably diphenyl carbonate
  • Phenol and acetone are reacted on Lewatit SC 104 ® from Bayer Chemicals AG as a sulfonic acid ion exchanger and with 300 ppm mercaptopropionic acid as a cocatalyst.
  • the reaction solution is filtered at 75 ° C using a bag filter made of polypropylene with a pore size of 50 ⁇ m.
  • the BPA-phenol adduct crystals obtained in the acid-catalyzed reaction of phenol and acetone with subsequent suspension crystallizations are separated from the liquid phase by means of a rotary filter and then cleaned and a separation unit for separating BPA from phenol fed.
  • the rotary filter housing is inertized under a slight excess pressure of 10 mbar with nitrogen ( ⁇ 1 ppm oxygen).
  • Circulating nitrogen quantity (oxygen content ⁇ 1 ppm) and the suction openings of the control disc are set so that the residual moisture in the filter cake is ⁇ 15% based on the quantity of mixed crystals.
  • the roundness of the drum and the orientation of the peeling knife allow a maximum peeling knife distance to the drum of about 5 mm over the entire filter surface.
  • Pure phenol at a temperature of 55 ° C. is used for rinsing the filter cake in the washing zone, the rinsing quantity for filter cake cleaning being 100%, based on the filter cake.
  • the amount of fresh phenol used to rinse the filter cake corresponds to 74% of the total amount of fresh phenol added to the process.
  • the washed filter cake is flowed through with nitrogen (oxygen content ⁇ 1 ppm), which is circulated, about 7% of the circulating amount being continuously fed out and replaced by pure nitrogen and the circulating nitrogen being washed with demineralized water.
  • nitrogen oxygen content ⁇ 1 ppm
  • the mixed crystals are melted on a heating coil under inert conditions (oxygen content ⁇ 1 ppm), the melt flows immediately into a collecting container in order to minimize the contact time of the crystals on the hot stainless steel surface (1.4571).
  • the surface temperature of the heating coil is approximately 160 ° C.
  • the phenol is removed by distillation at temperatures of 120-140 ° C. and a vacuum of 100-140 mbar by distillation to a phenol content of 15% by weight.
  • the mixed crystal melt with a phenol content of 15% by weight is then pumped into a desorber.
  • the temperature of the melt in the desorber is adjusted to 190 ° C. by the melt inlet and heating, the temperature of the heating surfaces being 200 ° C.
  • Nitrogen (N2) is used for desorption, the amount of nitrogen being 200 m 3 / m 3 BPA / phenol mixture and the ⁇ temperature being set to 195 ° C. by preheating before entering the desorber. After desorption, the nitrogen is circulated, cooled and separated from the phenol and sulfur-containing compounds, washed and cleaned of BPA or BPA phenol sublimate by filtration. In relation to the circulating current, an amount of 3% of N2 is withdrawn.
  • the nitrogen is passed through a desorber filled with packing in countercurrent to the melt running down from above.
  • An overpressure of about 20 mbar is set at the head of the desorber, the level in the desorber is set at 15 cm above the inlet and the packing.
  • the oxygen content in the circle 'running nitrogen is ppm of less than 1 and is freed of the cycle nitrogen from metallic and ceramic solids fines in sintered filter cartridges, as well as the melt flow is filtered to and from the desorber.
  • the bisphenol A melt thus obtained has a residual sulfur content of ⁇ 2 ppm.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Polyesters Or Polycarbonates (AREA)

Abstract

L'invention concerne un bisphénol A, présentant une faible teneur en soufre, ainsi que son procédé de production.
EP05701120A 2004-02-05 2005-01-22 Procede pour produire du bisphenol a presentant une teneur reduite en soufre Withdrawn EP1713751A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102004005723A DE102004005723A1 (de) 2004-02-05 2004-02-05 Herstellung von Bisphenol A mit verringertem Schwefelgehalt
PCT/EP2005/000614 WO2005075395A1 (fr) 2004-02-05 2005-01-22 Procede pour produire du bisphenol a presentant une teneur reduite en soufre

Publications (1)

Publication Number Publication Date
EP1713751A1 true EP1713751A1 (fr) 2006-10-25

Family

ID=34801627

Family Applications (1)

Application Number Title Priority Date Filing Date
EP05701120A Withdrawn EP1713751A1 (fr) 2004-02-05 2005-01-22 Procede pour produire du bisphenol a presentant une teneur reduite en soufre

Country Status (9)

Country Link
US (1) US7112703B2 (fr)
EP (1) EP1713751A1 (fr)
JP (1) JP2007520501A (fr)
KR (1) KR20060130167A (fr)
CN (1) CN1914140A (fr)
DE (1) DE102004005723A1 (fr)
RU (1) RU2006131514A (fr)
TW (1) TW200607793A (fr)
WO (1) WO2005075395A1 (fr)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102010014726A1 (de) 2010-04-13 2011-10-13 Bayer Materialscience Ag Polycarbonatzusammensetzungen mit verbesserten optischen und thermischen Eigenschaften
US20140051803A1 (en) * 2011-05-02 2014-02-20 Sabic Innovative Plastics Ip B.V. High purity bisphenol-a and polycarbonate materials prepared therefrom
WO2012150560A1 (fr) * 2011-05-02 2012-11-08 Sabic Innovative Plastics Ip B.V. Bisphénol a de grande pureté et matériaux de type polycarbonate préparés à partir de celui-ci
EP2705016A1 (fr) * 2011-05-02 2014-03-12 SABIC Innovative Plastics IP B.V. Bisphénol a de grande pureté et matériaux de type polycarbonate préparés à partir de celui-ci
US20140051802A1 (en) * 2011-05-02 2014-02-20 Sabic Innovative Plastics Ip B.V. High purity bisphenol-a and polycarbonate materials prepared therefrom
US8735634B2 (en) 2011-05-02 2014-05-27 Sabic Innovative Plastics Ip B.V. Promoter catalyst system with solvent purification
US9290618B2 (en) 2011-08-05 2016-03-22 Sabic Global Technologies B.V. Polycarbonate compositions having enhanced optical properties, methods of making and articles comprising the polycarbonate compositions
BR112014007755A8 (pt) * 2011-10-27 2018-04-03 Sabic Innovative Plastics Ip Bv Processo para produzir um produto bisfenol a, processo para preparar policarbonato, e, contêiner
US8962117B2 (en) 2011-10-27 2015-02-24 Sabic Global Technologies B.V. Process for producing bisphenol A with reduced sulfur content, polycarbonate made from the bisphenol A, and containers formed from the polycarbonate
EP2810309A1 (fr) 2012-02-03 2014-12-10 SABIC Innovative Plastics IP B.V. Dispositif à diodes électroluminescentes et son procédé de production comprenant de la chimie de matière de conversion
CN104144902A (zh) * 2012-02-29 2014-11-12 沙特基础创新塑料Ip私人有限责任公司 用于生产低硫双酚a的方法、用于生产聚碳酸酯的方法以及由聚碳酸酯制作的制品
CN105206732B (zh) 2012-02-29 2018-11-09 沙特基础全球技术有限公司 塑料模制器件和发光器件
US9346949B2 (en) 2013-02-12 2016-05-24 Sabic Global Technologies B.V. High reflectance polycarbonate
KR101961312B1 (ko) 2012-10-25 2019-03-22 사빅 글로벌 테크놀러지스 비.브이. 발광 다이오드 장치, 이의 제조 방법 및 용도
WO2014186548A1 (fr) 2013-05-16 2014-11-20 Sabic Innovative Plastics Ip B.V. Compositions de polycarbonate ramifié présentant des propriétés chimiques d'un matériau de conversion, et articles associés
US9772086B2 (en) 2013-05-29 2017-09-26 Sabic Innovative Plastics Ip B.V. Illuminating devices with color stable thermoplastic light transmitting articles
KR101739756B1 (ko) 2013-05-29 2017-06-08 사빅 글로벌 테크놀러지스 비.브이. 색 안정성 열가소성 조성물
EP3464470B1 (fr) 2016-05-27 2021-04-07 SHPP Global Technologies B.V. Lentilles en copolycarbonate, procédés pour leur fabrication et applications correspondantes
CN109196048B (zh) 2016-05-27 2021-09-21 高新特殊工程塑料全球技术有限公司 具有增强的光学性质的共聚碳酸酯组合物、由其形成的制品和制造方法
WO2018020425A1 (fr) 2016-07-25 2018-02-01 Sabic Global Technologies B.V. Compositions de copolycarbonate présentant des propriétés optiques améliorées, articles formés à partir desdites compositions et procédés de fabrication
JP2019525942A (ja) * 2016-08-03 2019-09-12 クラリアント・インターナシヨナル・リミテツド 廃液からチタン（ハロ）アルコキシドを回収するための方法
DE102016116078B3 (de) 2016-08-29 2018-01-04 Epc Engineering Consulting Gmbh Verfahren zur Herstellung eines Polycarbonats unter Einsatz einer Strippvorrichtung
US11260378B2 (en) 2017-04-24 2022-03-01 Badger Licensing Llc Catalyst system and process for producing bisphenol-A
KR102349519B1 (ko) * 2017-11-24 2022-01-07 주식회사 엘지화학 비스페놀a의 제조방법
EP3818034A1 (fr) 2018-07-06 2021-05-12 Badger Licensing LLC Traitement de flux résiduels issus de la fabrication de bisphénols
CN112409573B (zh) * 2019-08-23 2023-06-20 南通星辰合成材料有限公司 一种副产多元酚环氧树脂及其制造方法与应用

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5436363A (en) * 1977-08-26 1979-03-17 Adeka Argus Chem Co Ltd Polycarbonate resin composition
EP0001863B1 (fr) * 1977-11-09 1981-07-15 Shell Internationale Researchmaatschappij B.V. Préparation de bisphénols
US4935173A (en) * 1987-01-20 1990-06-19 The Dow Chemical Company Process for producing prills
US4847432A (en) * 1987-12-28 1989-07-11 General Electric Company Method for the purification of ion exchange resins used in the production of bisphenol A
US5008470A (en) * 1989-11-30 1991-04-16 Shell Oil Company Process for preparing a bisphenol
US5059721A (en) * 1990-07-31 1991-10-22 Shell Oil Company Process for preparing a bisphenol
EP0552518B1 (fr) * 1992-01-14 1995-09-13 General Electric Company Procédé de récupération de bisphénol-A à partir des écoulements du procédé de fabrication
DE19720541A1 (de) * 1997-05-16 1998-11-19 Bayer Ag Verfahren zur kontinuierlichen Herstellung von Dihydroxydiphenylalkanen
JP4093655B2 (ja) * 1998-10-22 2008-06-04 出光興産株式会社 ビスフェノールａの製造法
DE19860144C1 (de) * 1998-12-24 2000-09-14 Bayer Ag Verfahren zur Herstellung von Bisphenol A
DE19961521A1 (de) * 1999-12-20 2001-06-21 Bayer Ag Bisphenol-Phenol-Addukte
DE10015014A1 (de) * 2000-03-27 2001-10-04 Bayer Ag Verfahren zur Herstellung von Bisphenolen

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO2005075395A1 *

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US7112703B2 (en) 2006-09-26
US20050215833A1 (en) 2005-09-29
JP2007520501A (ja) 2007-07-26
WO2005075395A1 (fr) 2005-08-18
DE102004005723A1 (de) 2005-08-25
TW200607793A (en) 2006-03-01
KR20060130167A (ko) 2006-12-18
CN1914140A (zh) 2007-02-14
RU2006131514A (ru) 2008-03-10

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