JP2010248193A5 - - Google Patents
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- Publication number
- JP2010248193A5 JP2010248193A5 JP2010095077A JP2010095077A JP2010248193A5 JP 2010248193 A5 JP2010248193 A5 JP 2010248193A5 JP 2010095077 A JP2010095077 A JP 2010095077A JP 2010095077 A JP2010095077 A JP 2010095077A JP 2010248193 A5 JP2010248193 A5 JP 2010248193A5
- Authority
- JP
- Japan
- Prior art keywords
- alkali metal
- metal chloride
- reaction waste
- aqueous solution
- containing reaction
- 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
- 238000000034 method Methods 0.000 claims description 36
- 229910001514 alkali metal chloride Inorganic materials 0.000 claims description 27
- 238000006243 chemical reaction Methods 0.000 claims description 22
- 239000002699 waste material Substances 0.000 claims description 22
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 18
- 239000007864 aqueous solution Substances 0.000 claims description 18
- 239000000243 solution Substances 0.000 claims description 14
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 12
- 239000012528 membrane Substances 0.000 claims description 12
- 238000004821 distillation Methods 0.000 claims description 11
- 230000003204 osmotic effect Effects 0.000 claims description 11
- 238000005868 electrolysis reaction Methods 0.000 claims description 9
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 8
- 239000000460 chlorine Substances 0.000 claims description 8
- -1 diaryl carbonate Chemical compound 0.000 claims description 7
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical group [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 6
- 239000002585 base Substances 0.000 claims description 6
- 238000000926 separation method Methods 0.000 claims description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 claims description 4
- 239000003463 adsorbent Substances 0.000 claims description 4
- 229910052783 alkali metal Inorganic materials 0.000 claims description 4
- 150000001340 alkali metals Chemical class 0.000 claims description 4
- 239000003054 catalyst Substances 0.000 claims description 4
- 229910052801 chlorine Inorganic materials 0.000 claims description 4
- 229910001902 chlorine oxide Inorganic materials 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 229910001510 metal chloride Inorganic materials 0.000 claims description 3
- 238000000746 purification Methods 0.000 claims description 3
- 239000011780 sodium chloride Substances 0.000 claims description 3
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 2
- 239000012267 brine Substances 0.000 claims description 2
- 229910002091 carbon monoxide Inorganic materials 0.000 claims description 2
- 238000009792 diffusion process Methods 0.000 claims description 2
- 238000006056 electrooxidation reaction Methods 0.000 claims description 2
- 238000000605 extraction Methods 0.000 claims description 2
- 239000007789 gas Substances 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical group 0.000 claims description 2
- 150000002431 hydrogen Chemical group 0.000 claims description 2
- 229910052757 nitrogen Inorganic materials 0.000 claims description 2
- 230000001590 oxidative effect Effects 0.000 claims description 2
- 229910052708 sodium Inorganic materials 0.000 claims description 2
- 239000011734 sodium Substances 0.000 claims description 2
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 claims description 2
- 239000002904 solvent Substances 0.000 claims description 2
- FGUUSXIOTUKUDN-IBGZPJMESA-N C1(=CC=CC=C1)N1C2=C(NC([C@H](C1)NC=1OC(=NN=1)C1=CC=CC=C1)=O)C=CC=C2 Chemical compound C1(=CC=CC=C1)N1C2=C(NC([C@H](C1)NC=1OC(=NN=1)C1=CC=CC=C1)=O)C=CC=C2 FGUUSXIOTUKUDN-IBGZPJMESA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- BSWWXRFVMJHFBN-UHFFFAOYSA-N 2,4,6-tribromophenol Chemical compound OC1=C(Br)C=C(Br)C=C1Br BSWWXRFVMJHFBN-UHFFFAOYSA-N 0.000 description 2
- HFZWRUODUSTPEG-UHFFFAOYSA-N 2,4-dichlorophenol Chemical compound OC1=CC=C(Cl)C=C1Cl HFZWRUODUSTPEG-UHFFFAOYSA-N 0.000 description 1
- 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 1
- HVXRCAWUNAOCTA-UHFFFAOYSA-N 4-(6-methylheptyl)phenol Chemical compound CC(C)CCCCCC1=CC=C(O)C=C1 HVXRCAWUNAOCTA-UHFFFAOYSA-N 0.000 description 1
- JSFITYFUKSFPBZ-UHFFFAOYSA-N 4-(7-methyloctyl)phenol Chemical compound CC(C)CCCCCCC1=CC=C(O)C=C1 JSFITYFUKSFPBZ-UHFFFAOYSA-N 0.000 description 1
- GZFGOTFRPZRKDS-UHFFFAOYSA-N 4-bromophenol Chemical compound OC1=CC=C(Br)C=C1 GZFGOTFRPZRKDS-UHFFFAOYSA-N 0.000 description 1
- WXNZTHHGJRFXKQ-UHFFFAOYSA-N 4-chlorophenol Chemical compound OC1=CC=C(Cl)C=C1 WXNZTHHGJRFXKQ-UHFFFAOYSA-N 0.000 description 1
- QHPQWRBYOIRBIT-UHFFFAOYSA-N 4-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C=C1 QHPQWRBYOIRBIT-UHFFFAOYSA-N 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- QBDSZLJBMIMQRS-UHFFFAOYSA-N p-Cumylphenol Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=CC=C1 QBDSZLJBMIMQRS-UHFFFAOYSA-N 0.000 description 1
- NKTOLZVEWDHZMU-UHFFFAOYSA-N p-cumyl phenol Natural products CC1=CC=C(C)C(O)=C1 NKTOLZVEWDHZMU-UHFFFAOYSA-N 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102009017862A DE102009017862A1 (de) | 2009-04-17 | 2009-04-17 | Verfahren zur Herstellung von Diarylcarbonat |
| DE102009017862.7 | 2009-04-17 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2010248193A JP2010248193A (ja) | 2010-11-04 |
| JP2010248193A5 true JP2010248193A5 (enExample) | 2013-05-23 |
| JP5714240B2 JP5714240B2 (ja) | 2015-05-07 |
Family
ID=42313663
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010095077A Expired - Fee Related JP5714240B2 (ja) | 2009-04-17 | 2010-04-16 | ジアリールカーボネートの製造方法 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US8882984B2 (enExample) |
| EP (1) | EP2241550B1 (enExample) |
| JP (1) | JP5714240B2 (enExample) |
| KR (1) | KR20100115319A (enExample) |
| CN (1) | CN101863772B (enExample) |
| DE (1) | DE102009017862A1 (enExample) |
| RU (1) | RU2536998C2 (enExample) |
| SG (2) | SG10201401571TA (enExample) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2748782T3 (es) | 2015-07-01 | 2020-03-17 | Covestro Deutschland Ag | Procedimiento de destilación osmótica para la concentración de un líquido que contiene cloruro de sodio |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE790369A (fr) | 1971-10-21 | 1973-04-20 | Diamond Shamrock Corp | Procede et appareil pour la preparation d'hydroxydes de metaux alcalins de haute purete dans une cuve electrolytique. |
| US3773634A (en) | 1972-03-09 | 1973-11-20 | Diamond Shamrock Corp | Control of an olyte-catholyte concentrations in membrane cells |
| DE2509036C2 (de) | 1975-03-01 | 1986-05-28 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von symmetrischen Diarylcarbonaten |
| GB2260975B (en) | 1991-10-28 | 1995-07-12 | Chang Shih Chang | The process to recover salt from brine waste water |
| DE4238123C2 (de) | 1992-11-12 | 2000-03-09 | Bayer Ag | Verfahren zur Herstellung von thermoplastischen Polycarbonaten |
| DE19600631A1 (de) | 1996-01-10 | 1997-07-17 | Bayer Ag | Verfahren zur Reinigung von Kohlensäurediarylestern |
| US6258923B1 (en) * | 1999-06-11 | 2001-07-10 | General Electric Company | Method for manufacturing dialkyl carbonate |
| EP1200359B1 (de) | 1999-06-18 | 2004-02-25 | Bayer Aktiengesellschaft | Verfahren zum abbau organischer verbindungen in wasser |
| US6340736B1 (en) | 1999-11-29 | 2002-01-22 | General Electric Company | Method and apparatus for the production of polycarbonates with brine recycling |
| DE10063297A1 (de) | 2000-12-19 | 2002-06-20 | Bayer Ag | Kontinuierliches Verfahren zur Herstellung von Kohlensäurediarylester |
| DE10063296A1 (de) | 2000-12-19 | 2002-06-20 | Bayer Ag | Verfahren zur Herstellung von Kohlensäurediarylester |
| DE10063869A1 (de) * | 2000-12-21 | 2002-06-27 | Bayer Ag | Kontinuierliches Verfahren zur Herstellung von Kohlensäurediarylester |
| JP2003063999A (ja) * | 2001-08-28 | 2003-03-05 | Mitsubishi Heavy Ind Ltd | 有機ハロゲン化物分解処理システム |
| DE10207442A1 (de) * | 2002-02-22 | 2003-09-11 | Bayer Ag | Aufbereitung von Kochsalz enthaltenden Abwässern zum Einsatz in der Chlor-Alkali-Elektrolyse |
| JP4638415B2 (ja) * | 2003-03-05 | 2011-02-23 | ダウ グローバル テクノロジーズ インコーポレイティド | 廃水の清浄化方法 |
| US20050011753A1 (en) * | 2003-06-23 | 2005-01-20 | Jackson John R. | Low energy chlorate electrolytic cell and process |
| JP4137941B2 (ja) * | 2003-06-27 | 2008-08-20 | 旭化成ケミカルズ株式会社 | 芳香族炭酸エステルの製造方法 |
| CA2469769A1 (en) * | 2004-06-04 | 2005-12-04 | Aker Kvaerner Canada Inc. | Apparatus and method for spent alkali metal halide solution concentration using osmotic membrane distillation |
| DE102006041465A1 (de) | 2006-09-02 | 2008-03-06 | Bayer Materialscience Ag | Verfahren zur Herstellung von Diarylcarbonat |
-
2009
- 2009-04-17 DE DE102009017862A patent/DE102009017862A1/de not_active Withdrawn
-
2010
- 2010-04-01 EP EP10003663.1A patent/EP2241550B1/de not_active Not-in-force
- 2010-04-13 US US12/759,074 patent/US8882984B2/en not_active Expired - Fee Related
- 2010-04-14 CN CN201010166642.0A patent/CN101863772B/zh not_active Expired - Fee Related
- 2010-04-15 SG SG10201401571TA patent/SG10201401571TA/en unknown
- 2010-04-15 SG SG201002632-6A patent/SG166070A1/en unknown
- 2010-04-16 KR KR1020100035157A patent/KR20100115319A/ko not_active Withdrawn
- 2010-04-16 RU RU2010115186/04A patent/RU2536998C2/ru not_active IP Right Cessation
- 2010-04-16 JP JP2010095077A patent/JP5714240B2/ja not_active Expired - Fee Related
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