MXPA06008616A - Procedimiento para la fosgenacion en fase gaseosa. - Google Patents
Procedimiento para la fosgenacion en fase gaseosa.Info
- Publication number
- MXPA06008616A MXPA06008616A MXPA06008616A MXPA06008616A MXPA06008616A MX PA06008616 A MXPA06008616 A MX PA06008616A MX PA06008616 A MXPA06008616 A MX PA06008616A MX PA06008616 A MXPA06008616 A MX PA06008616A MX PA06008616 A MXPA06008616 A MX PA06008616A
- Authority
- MX
- Mexico
- Prior art keywords
- channels
- amines
- heat exchangers
- heat
- amine
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 30
- 150000001412 amines Chemical class 0.000 claims abstract description 59
- 238000001704 evaporation Methods 0.000 claims description 23
- 230000008020 evaporation Effects 0.000 claims description 23
- 238000010438 heat treatment Methods 0.000 claims description 20
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 claims description 18
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 claims description 16
- 239000012948 isocyanate Substances 0.000 claims description 15
- 150000002513 isocyanates Chemical class 0.000 claims description 15
- 239000007788 liquid Substances 0.000 claims description 10
- 238000013021 overheating Methods 0.000 claims description 10
- RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 6
- DZIHTWJGPDVSGE-UHFFFAOYSA-N 4-[(4-aminocyclohexyl)methyl]cyclohexan-1-amine Chemical compound C1CC(N)CCC1CC1CCC(N)CC1 DZIHTWJGPDVSGE-UHFFFAOYSA-N 0.000 claims description 5
- HMJBXEZHJUYJQY-UHFFFAOYSA-N 4-(aminomethyl)octane-1,8-diamine Chemical compound NCCCCC(CN)CCCN HMJBXEZHJUYJQY-UHFFFAOYSA-N 0.000 claims description 3
- 125000003277 amino group Chemical group 0.000 claims description 3
- 238000005192 partition Methods 0.000 claims 1
- 230000008016 vaporization Effects 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 description 20
- 239000007789 gas Substances 0.000 description 14
- 239000002904 solvent Substances 0.000 description 12
- 239000000203 mixture Substances 0.000 description 11
- VIKNJXKGJWUCNN-XGXHKTLJSA-N norethisterone Chemical compound O=C1CC[C@@H]2[C@H]3CC[C@](C)([C@](CC4)(O)C#C)[C@@H]4[C@@H]3CCC2=C1 VIKNJXKGJWUCNN-XGXHKTLJSA-N 0.000 description 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
- 238000009835 boiling Methods 0.000 description 6
- 239000012442 inert solvent Substances 0.000 description 6
- 239000000376 reactant Substances 0.000 description 6
- 239000011261 inert gas Substances 0.000 description 5
- 238000012546 transfer Methods 0.000 description 5
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical group [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 4
- 238000009833 condensation Methods 0.000 description 4
- 230000005494 condensation Effects 0.000 description 4
- 238000000354 decomposition reaction Methods 0.000 description 4
- 150000004985 diamines Chemical class 0.000 description 4
- 229910000831 Steel Inorganic materials 0.000 description 3
- -1 aliphatic diamines Chemical class 0.000 description 3
- 229910021529 ammonia Inorganic materials 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000003085 diluting agent Substances 0.000 description 3
- 239000008246 gaseous mixture Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 2
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 235000019270 ammonium chloride Nutrition 0.000 description 2
- 239000002199 base oil Substances 0.000 description 2
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 229940117389 dichlorobenzene Drugs 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 238000010494 dissociation reaction Methods 0.000 description 2
- 230000005593 dissociations Effects 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 2
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 2
- 238000009434 installation Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 230000000630 rising effect Effects 0.000 description 2
- GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 description 1
- JTPNRXUCIXHOKM-UHFFFAOYSA-N 1-chloronaphthalene Chemical compound C1=CC=C2C(Cl)=CC=CC2=C1 JTPNRXUCIXHOKM-UHFFFAOYSA-N 0.000 description 1
- RLYCRLGLCUXUPO-UHFFFAOYSA-N 2,6-diaminotoluene Chemical compound CC1=C(N)C=CC=C1N RLYCRLGLCUXUPO-UHFFFAOYSA-N 0.000 description 1
- FZZMTSNZRBFGGU-UHFFFAOYSA-N 2-chloro-7-fluoroquinazolin-4-amine Chemical compound FC1=CC=C2C(N)=NC(Cl)=NC2=C1 FZZMTSNZRBFGGU-UHFFFAOYSA-N 0.000 description 1
- MHQULXYNBKWNDF-UHFFFAOYSA-N 3,4-dimethylbenzene-1,2-diamine Chemical compound CC1=CC=C(N)C(N)=C1C MHQULXYNBKWNDF-UHFFFAOYSA-N 0.000 description 1
- RQEZWDLDUAVUSM-UHFFFAOYSA-N 4-(aminomethyl)octane-1,8-diamine;nonane-1,1,1-triamine Chemical compound CCCCCCCCC(N)(N)N.NCCCCC(CN)CCCN RQEZWDLDUAVUSM-UHFFFAOYSA-N 0.000 description 1
- BDBZTOMUANOKRT-UHFFFAOYSA-N 4-[2-(4-aminocyclohexyl)propan-2-yl]cyclohexan-1-amine Chemical compound C1CC(N)CCC1C(C)(C)C1CCC(N)CC1 BDBZTOMUANOKRT-UHFFFAOYSA-N 0.000 description 1
- CNPURSDMOWDNOQ-UHFFFAOYSA-N 4-methoxy-7h-pyrrolo[2,3-d]pyrimidin-2-amine Chemical compound COC1=NC(N)=NC2=C1C=CN2 CNPURSDMOWDNOQ-UHFFFAOYSA-N 0.000 description 1
- 229910000851 Alloy steel Inorganic materials 0.000 description 1
- CKDWPUIZGOQOOM-UHFFFAOYSA-N Carbamyl chloride Chemical compound NC(Cl)=O CKDWPUIZGOQOOM-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000005700 Putrescine Substances 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N carbonic acid monoamide Natural products NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- 238000001311 chemical methods and process Methods 0.000 description 1
- 238000007385 chemical modification Methods 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- ZZTCPWRAHWXWCH-UHFFFAOYSA-N diphenylmethanediamine Chemical compound C=1C=CC=CC=1C(N)(N)C1=CC=CC=C1 ZZTCPWRAHWXWCH-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229910000856 hastalloy Inorganic materials 0.000 description 1
- 239000011551 heat transfer agent Substances 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 229910001026 inconel Inorganic materials 0.000 description 1
- 239000003701 inert diluent Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 229910001092 metal group alloy Inorganic materials 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- NTNWKDHZTDQSST-UHFFFAOYSA-N naphthalene-1,2-diamine Chemical compound C1=CC=CC2=C(N)C(N)=CC=C21 NTNWKDHZTDQSST-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- DYFXGORUJGZJCA-UHFFFAOYSA-N phenylmethanediamine Chemical compound NC(N)C1=CC=CC=C1 DYFXGORUJGZJCA-UHFFFAOYSA-N 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- KJAMZCVTJDTESW-UHFFFAOYSA-N tiracizine Chemical compound C1CC2=CC=CC=C2N(C(=O)CN(C)C)C2=CC(NC(=O)OCC)=CC=C21 KJAMZCVTJDTESW-UHFFFAOYSA-N 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- XJIAZXYLMDIWLU-UHFFFAOYSA-N undecane-1,1-diamine Chemical compound CCCCCCCCCCC(N)N XJIAZXYLMDIWLU-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C263/00—Preparation of derivatives of isocyanic acid
- C07C263/10—Preparation of derivatives of isocyanic acid by reaction of amines with carbonyl halides, e.g. with phosgene
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Silicon Compounds (AREA)
- Vaporization, Distillation, Condensation, Sublimation, And Cold Traps (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102005036870A DE102005036870A1 (de) | 2005-08-02 | 2005-08-02 | Verfahren zur Gasphasenphosgenierung |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MXPA06008616A true MXPA06008616A (es) | 2007-12-06 |
Family
ID=37451220
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MXPA06008616A MXPA06008616A (es) | 2005-08-02 | 2006-07-31 | Procedimiento para la fosgenacion en fase gaseosa. |
Country Status (12)
| Country | Link |
|---|---|
| US (2) | US20070043233A1 (enExample) |
| EP (1) | EP1754698B1 (enExample) |
| JP (1) | JP5226940B2 (enExample) |
| KR (1) | KR101337846B1 (enExample) |
| CN (1) | CN1907964B (enExample) |
| AT (1) | ATE417820T1 (enExample) |
| CA (1) | CA2554850C (enExample) |
| DE (2) | DE102005036870A1 (enExample) |
| ES (1) | ES2317376T3 (enExample) |
| MX (1) | MXPA06008616A (enExample) |
| PL (1) | PL1754698T3 (enExample) |
| RU (1) | RU2440333C2 (enExample) |
Families Citing this family (47)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2009037179A1 (de) * | 2007-09-19 | 2009-03-26 | Basf Se | Verfahren zur herstellung von isocyanaten |
| DE102007056511A1 (de) | 2007-11-22 | 2009-05-28 | Bayer Materialscience Ag | Verfahren zur Herstellung aromatischer Diisocyanate in der Gasphase |
| EP2128127A1 (de) * | 2008-05-31 | 2009-12-02 | Bayer MaterialScience AG | Ammoniumchloridabtrennung aus der Gasphase |
| ATE550317T1 (de) | 2008-08-07 | 2012-04-15 | Basf Se | Verfahren zur herstellung von aromatischen isocyanaten |
| EP2364294B1 (de) * | 2008-11-07 | 2013-07-03 | Basf Se | Verfahren zur herstellung von isocyanaten |
| DE102008061686A1 (de) | 2008-12-11 | 2010-06-17 | Bayer Materialscience Ag | Verfahren zur Herstellung von Isocyanaten in der Gasphase |
| DE102008063728A1 (de) | 2008-12-18 | 2010-06-24 | Bayer Materialscience Ag | Verfahren zur Herstellung von Isocyanaten in der Gasphase |
| DE102008063991A1 (de) * | 2008-12-19 | 2010-06-24 | Bayer Materialscience Ag | Verfahren zur Herstellung von Isocyanaten in der Gasphase |
| JP5771535B2 (ja) * | 2009-03-06 | 2015-09-02 | ビーエーエスエフ ソシエタス・ヨーロピアBasf Se | イソシアネートの製造方法および製造装置 |
| KR20120000078A (ko) | 2009-03-20 | 2012-01-03 | 바스프 에스이 | 이소시아네이트를 제조하기 위한 방법 및 장치 |
| DE102009032413A1 (de) | 2009-07-09 | 2011-01-13 | Bayer Materialscience Ag | Verfahren zur Herstellung von Isocyanaten |
| DE102009032414A1 (de) | 2009-07-09 | 2011-01-13 | Bayer Materialscience Ag | Verfahren zur Herstellung von Isocyanaten in der Gasphase |
| DE102009033639A1 (de) * | 2009-07-17 | 2011-01-20 | Bayer Materialscience Ag | Verfahen zur Herstellung von Isocyanaten in der Gasphase |
| US9249029B2 (en) | 2010-01-22 | 2016-02-02 | Basf Se | Single chamber vaporizer and use thereof in chemical synthesis |
| MX2012008473A (es) * | 2010-01-22 | 2012-08-15 | Basf Se | Evaporador de una camara y su uso en la sintesis quimica. |
| HUE026304T2 (en) * | 2010-02-26 | 2016-06-28 | Basf Se | A method for producing isocyanates in a gas phase |
| US8487127B2 (en) | 2010-02-26 | 2013-07-16 | Basf Se | Process for preparing isocyanates in the gas phase |
| DE102010019342A1 (de) | 2010-05-05 | 2011-11-10 | Bayer Materialscience Ag | Verfahren zur Herstellung von Isocyanaten in der Gasphase |
| CN101912751B (zh) * | 2010-09-03 | 2012-12-12 | 烟台万华聚氨酯股份有限公司 | 一种胺汽化器及其用于制备异氰酸酯的方法 |
| PL214497B1 (pl) | 2010-12-10 | 2013-08-30 | Inst Chemii Przemyslowej Im Prof Ignacego Moscickiego | Sposób otrzymywania toluilenodiizocyjanianu (TDI) w procesie fosgenowania toluilenodiaminy (TDA) w fazie gazowej |
| US8969615B2 (en) * | 2011-03-31 | 2015-03-03 | Basf Se | Process for preparing isocyanates |
| EP2872481B1 (de) | 2012-07-11 | 2016-08-24 | Covestro Deutschland AG | Verfahren zur aufarbeitung von destillationsrückständen aus der isocyanatherstellung |
| WO2014122180A1 (de) | 2013-02-08 | 2014-08-14 | Bayer Materialscience Ag | Verfahren zur abtrennung eines durch phosgenierung eines primären amins in der gasphase hergestellten isocyanats aus dem gasförmigen rohprodukt der phosgenierung |
| EP2829533A1 (de) | 2013-07-26 | 2015-01-28 | Bayer MaterialScience AG | Verfahren zur herstellung von isocyanaten |
| HUE039136T2 (hu) | 2014-03-27 | 2018-12-28 | Covestro Deutschland Ag | Eljárás gázfázisú foszgénezõ rendszer mûködtetésére |
| EP3122719B1 (de) | 2014-03-27 | 2018-05-16 | Covestro Deutschland AG | Verfahren zum betreiben einer gasphasenphosgenierungsanlage |
| EP3129353B1 (de) * | 2014-04-11 | 2024-02-28 | Covestro Deutschland AG | Zusammensetzung zur herstellung transparenter polythiourethan-körper |
| KR102547793B1 (ko) | 2014-09-19 | 2023-06-26 | 코베스트로 도이칠란트 아게 | 1,5-펜탄디이소시아네이트의 기체상 제조 방법 |
| CN107406573B (zh) | 2015-03-16 | 2021-09-03 | 科思创德国股份有限公司 | 基于1,5-五亚甲基二异氰酸酯的多异氰酸酯组合物 |
| CN107438634A (zh) | 2015-04-21 | 2017-12-05 | 科思创德国股份有限公司 | 基于1,5‑二异氰酸根合戊烷的多异氰酸酯混合物 |
| WO2016198404A1 (de) | 2015-06-12 | 2016-12-15 | Covestro Deutschland Ag | Verfahren zur herstellung von diisocyanaten in der gasphase |
| CN107848960B (zh) | 2015-07-16 | 2020-09-22 | 科思创德国股份有限公司 | 用于制备异氰酸酯的方法 |
| CN108290831B (zh) | 2015-12-03 | 2021-11-19 | 科思创德国股份有限公司 | 制备异氰酸酯的方法 |
| CN107556215B (zh) | 2016-06-30 | 2022-04-19 | 科思创德国股份有限公司 | 从氯化氢液体混合物中分离和处理杂质的方法和系统 |
| CN110072845B (zh) | 2016-12-21 | 2022-04-08 | 科思创德国股份有限公司 | 制备异氰酸酯的方法 |
| EP3606630B1 (de) | 2017-04-03 | 2021-03-10 | Covestro Intellectual Property GmbH & Co. KG | Reinigungsvorrichtung für gasströme aus der isocyanatherstellung |
| US10836713B2 (en) | 2017-06-08 | 2020-11-17 | Covestro Deutschland Ag | Method for producing isocyanates in the gas phase |
| EP3634946B1 (de) | 2017-06-08 | 2022-09-14 | Covestro Intellectual Property GmbH & Co. KG | Verfahren zur herstellung von isocyanaten |
| EP3524591A1 (en) | 2018-02-13 | 2019-08-14 | Covestro Deutschland AG | Process for the preparation of isocyanates |
| US10626084B2 (en) | 2018-08-03 | 2020-04-21 | Covestro Llc | Method for producing two isocyanates |
| HUE068310T2 (hu) | 2019-09-17 | 2024-12-28 | Covestro Deutschland Ag | Eljárás izocianátok elõállítására |
| EP4151618A1 (en) | 2021-09-20 | 2023-03-22 | Covestro Deutschland AG | Obtaining aliphatic amines from compositions |
| EP4151619A1 (en) | 2021-09-20 | 2023-03-22 | Covestro Deutschland AG | Method for the removal of water from and transport of aliphatic diamines |
| EP4442859A1 (de) | 2023-04-06 | 2024-10-09 | Covestro Deutschland AG | Nachhaltige herstellung von hexamethylendiisocyanat für die produktion von polyurethan |
| EP4480944A1 (de) | 2023-06-20 | 2024-12-25 | Covestro Deutschland AG | Verfahren zur herstellung von aliphatischen diisocyanaten in der gasphase |
| WO2025036923A1 (de) | 2023-08-15 | 2025-02-20 | Covestro Deutschland Ag | Herstellung eines isocyanats im wege einer gasphasenreaktion in mehreren parallel betriebenen gasphasenreaktionsanordnungen |
| EP4545579A1 (de) | 2023-10-24 | 2025-04-30 | Covestro Deutschland AG | Verfahren zur herstellung eines polyisocyanats auf basis von 1,5-pentamethylendiisocyanat |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3714439A1 (de) * | 1987-04-30 | 1988-11-10 | Bayer Ag | Verfahren zur herstellung von (cyclo)aliphatischen diisocyanaten |
| EP0486749A1 (en) | 1990-11-22 | 1992-05-27 | Hodogaya Chemical Co., Ltd. | Triarylmethane compounds and pressure sensitive recording material |
| DE19528781A1 (de) * | 1995-08-04 | 1997-02-06 | Bayer Ag | Verfahren zur Herstellung von Toluylendiisocyanat, spezielle Gemische aus Toluylendiamin und Wasser und deren Verwendung zur Herstellung von Toluylendiisocyanat |
| US6255497B1 (en) * | 1997-04-29 | 2001-07-03 | The Endowment For Research In Human Biology, Inc. | Method for the inhibition of ALDH-I useful in the treatment of alcohol dependence or alcohol abuse |
| DE19800529A1 (de) | 1998-01-09 | 1999-07-15 | Bayer Ag | Verfahren zur Phosgenierung von Aminen in der Gasphase unter Einsatz von Mikrostrukturmischern |
| DE19912541C1 (de) * | 1999-03-19 | 2000-10-26 | Karlsruhe Forschzent | Verfahren zum Abtöten schädlicher Mikroorganismen in Flüssigkeiten durch kurzzeitiges Hocherhitzen |
| US6610113B1 (en) | 1999-09-09 | 2003-08-26 | Kennametal Pc Inc. | Process for heat treating ceramics and articles of manufacture made thereby |
| DE10010397C1 (de) * | 2000-02-28 | 2001-12-06 | Mannesmann Ag | Vorrichtung zum Verdampfen flüssiger Medien |
| DE10133729A1 (de) * | 2001-07-11 | 2003-01-23 | Bayer Ag | Verfahren zur Herstellung von (cyclo)aliphatischen Diisocyanaten |
| DE10133728A1 (de) | 2001-07-11 | 2003-01-23 | Bayer Ag | Verfahren zur Herstellung von (cyclo)aliphatischen Diisocyanaten |
| DE10138970A1 (de) | 2001-08-08 | 2003-02-20 | Bayer Ag | Rohrreaktor auf Basis eines Schichtstoffes |
| DE10161384A1 (de) * | 2001-12-14 | 2003-06-18 | Bayer Ag | Verbessertes Verfahren für die Herstellung von (/Poly)-isocyanaten in der Gasphase |
| DE10238995A1 (de) * | 2002-08-20 | 2004-02-26 | Basf Ag | Gasphasenphosgenierung bei moderaten Drücken |
| DE10245704A1 (de) | 2002-09-30 | 2004-04-01 | Bayer Ag | Verfahren zum Quenchen eines gasförmigen Reaktionsgemisches bei der Gasphasenphosgenierung von Diaminen |
| DE10326381B4 (de) * | 2003-06-12 | 2005-09-22 | Jähn, Peter | Turbulenzerzeuger |
| DE10335451A1 (de) * | 2003-08-02 | 2005-03-10 | Bayer Materialscience Ag | Verfahren zur Entfernung von flüchtigen Verbindungen aus Stoffgemischen mittels Mikroverdampfer |
| DE10349504A1 (de) | 2003-10-23 | 2005-05-25 | Bayer Technology Services Gmbh | Verfahren zur Herstellung von Isocyanaten in der Gasphase |
| DE10359627A1 (de) * | 2003-12-18 | 2005-07-21 | Bayer Materialscience Ag | Verfahren zur Herstellung von Diisocyanaten |
-
2005
- 2005-08-02 DE DE102005036870A patent/DE102005036870A1/de not_active Withdrawn
-
2006
- 2006-07-21 DE DE502006002363T patent/DE502006002363D1/de active Active
- 2006-07-21 EP EP06015211A patent/EP1754698B1/de not_active Not-in-force
- 2006-07-21 AT AT06015211T patent/ATE417820T1/de not_active IP Right Cessation
- 2006-07-21 PL PL06015211T patent/PL1754698T3/pl unknown
- 2006-07-21 ES ES06015211T patent/ES2317376T3/es active Active
- 2006-07-27 US US11/494,419 patent/US20070043233A1/en not_active Abandoned
- 2006-07-28 CA CA2554850A patent/CA2554850C/en not_active Expired - Fee Related
- 2006-07-31 MX MXPA06008616A patent/MXPA06008616A/es active IP Right Grant
- 2006-08-01 KR KR1020060072449A patent/KR101337846B1/ko not_active Expired - Fee Related
- 2006-08-01 RU RU2006127641/04A patent/RU2440333C2/ru not_active IP Right Cessation
- 2006-08-02 CN CN200610110937XA patent/CN1907964B/zh not_active Expired - Fee Related
- 2006-08-02 JP JP2006211035A patent/JP5226940B2/ja not_active Expired - Fee Related
-
2010
- 2010-08-12 US US12/855,073 patent/US8692016B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| US20100312009A1 (en) | 2010-12-09 |
| KR20070016072A (ko) | 2007-02-07 |
| ES2317376T3 (es) | 2009-04-16 |
| KR101337846B1 (ko) | 2013-12-06 |
| US8692016B2 (en) | 2014-04-08 |
| PL1754698T3 (pl) | 2009-06-30 |
| US20070043233A1 (en) | 2007-02-22 |
| CA2554850A1 (en) | 2007-02-02 |
| DE102005036870A1 (de) | 2007-02-08 |
| CN1907964B (zh) | 2013-03-13 |
| JP2007039459A (ja) | 2007-02-15 |
| EP1754698A3 (de) | 2007-03-07 |
| RU2440333C2 (ru) | 2012-01-20 |
| RU2006127641A (ru) | 2008-02-10 |
| DE502006002363D1 (de) | 2009-01-29 |
| EP1754698B1 (de) | 2008-12-17 |
| CN1907964A (zh) | 2007-02-07 |
| CA2554850C (en) | 2014-11-25 |
| JP5226940B2 (ja) | 2013-07-03 |
| EP1754698A2 (de) | 2007-02-21 |
| ATE417820T1 (de) | 2009-01-15 |
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