DE10028636A1 - Verfahren zur Herstellung von Alkanolaminen - Google Patents
Verfahren zur Herstellung von AlkanolaminenInfo
- Publication number
- DE10028636A1 DE10028636A1 DE10028636A DE10028636A DE10028636A1 DE 10028636 A1 DE10028636 A1 DE 10028636A1 DE 10028636 A DE10028636 A DE 10028636A DE 10028636 A DE10028636 A DE 10028636A DE 10028636 A1 DE10028636 A1 DE 10028636A1
- Authority
- DE
- Germany
- Prior art keywords
- reaction
- temperature
- catalyst
- reaction space
- range
- 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- Withdrawn
Links
- 238000006243 chemical reaction Methods 0.000 title claims abstract description 144
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 title claims abstract description 112
- 239000003054 catalyst Substances 0.000 title claims abstract description 68
- 229910021529 ammonia Inorganic materials 0.000 title claims abstract description 56
- 125000002947 alkylene group Chemical group 0.000 title claims abstract description 53
- 230000001105 regulatory effect Effects 0.000 title claims abstract description 15
- 238000004519 manufacturing process Methods 0.000 title abstract description 18
- 238000000034 method Methods 0.000 claims abstract description 183
- 238000009826 distribution Methods 0.000 claims abstract description 12
- 230000033228 biological regulation Effects 0.000 claims abstract description 11
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims description 28
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 25
- 239000000203 mixture Substances 0.000 claims description 25
- 239000010457 zeolite Substances 0.000 claims description 24
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 22
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims description 21
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims description 19
- 238000000926 separation method Methods 0.000 claims description 11
- 229910021536 Zeolite Inorganic materials 0.000 claims description 10
- 238000002360 preparation method Methods 0.000 claims description 10
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 7
- 239000002638 heterogeneous catalyst Substances 0.000 claims description 7
- 150000001336 alkenes Chemical class 0.000 claims description 6
- 239000007789 gas Substances 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 239000001301 oxygen Substances 0.000 claims description 3
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 239000000047 product Substances 0.000 description 37
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 18
- 239000010936 titanium Substances 0.000 description 16
- 229910052719 titanium Inorganic materials 0.000 description 13
- 239000012071 phase Substances 0.000 description 12
- 239000007858 starting material Substances 0.000 description 12
- 238000004821 distillation Methods 0.000 description 11
- 150000004756 silanes Chemical class 0.000 description 11
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 10
- 239000002826 coolant Substances 0.000 description 10
- 239000000463 material Substances 0.000 description 10
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 9
- 239000011541 reaction mixture Substances 0.000 description 9
- 239000011148 porous material Substances 0.000 description 7
- 238000009835 boiling Methods 0.000 description 6
- 150000002169 ethanolamines Chemical class 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 5
- 238000009529 body temperature measurement Methods 0.000 description 5
- 239000007795 chemical reaction product Substances 0.000 description 5
- 230000017525 heat dissipation Effects 0.000 description 5
- 239000000376 reactant Substances 0.000 description 5
- 229910000077 silane Inorganic materials 0.000 description 5
- IJOOHPMOJXWVHK-UHFFFAOYSA-N chlorotrimethylsilane Chemical compound C[Si](C)(C)Cl IJOOHPMOJXWVHK-UHFFFAOYSA-N 0.000 description 4
- 238000010924 continuous production Methods 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 229910052605 nesosilicate Inorganic materials 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 150000004762 orthosilicates Chemical class 0.000 description 4
- 229910052710 silicon Inorganic materials 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 238000004817 gas chromatography Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000002955 isolation Methods 0.000 description 3
- 238000004898 kneading Methods 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
- 125000004103 aminoalkyl group Chemical group 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 230000001276 controlling effect Effects 0.000 description 2
- 229910021488 crystalline silicon dioxide Inorganic materials 0.000 description 2
- MROCJMGDEKINLD-UHFFFAOYSA-N dichlorosilane Chemical compound Cl[SiH2]Cl MROCJMGDEKINLD-UHFFFAOYSA-N 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 229910052758 niobium Inorganic materials 0.000 description 2
- 239000010955 niobium Substances 0.000 description 2
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 239000005051 trimethylchlorosilane Substances 0.000 description 2
- 229910052720 vanadium Inorganic materials 0.000 description 2
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- GHOKWGTUZJEAQD-ZETCQYMHSA-N (D)-(+)-Pantothenic acid Chemical compound OCC(C)(C)[C@@H](O)C(=O)NCCC(O)=O GHOKWGTUZJEAQD-ZETCQYMHSA-N 0.000 description 1
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- VXEGSRKPIUDPQT-UHFFFAOYSA-N 4-[4-(4-methoxyphenyl)piperazin-1-yl]aniline Chemical compound C1=CC(OC)=CC=C1N1CCN(C=2C=CC(N)=CC=2)CC1 VXEGSRKPIUDPQT-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 241000640882 Condea Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 1
- 229910004283 SiO 4 Inorganic materials 0.000 description 1
- 229910010413 TiO 2 Inorganic materials 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229910000323 aluminium silicate Inorganic materials 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000003729 cation exchange resin Substances 0.000 description 1
- 101150091051 cit-1 gene Proteins 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 229910002026 crystalline silica Inorganic materials 0.000 description 1
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 229910052733 gallium Inorganic materials 0.000 description 1
- 229910052732 germanium Inorganic materials 0.000 description 1
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 description 1
- 239000002815 homogeneous catalyst Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- -1 hydroxy, carboxyl Chemical group 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 238000010327 methods by industry Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 238000004886 process control Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 229910052761 rare earth metal Inorganic materials 0.000 description 1
- 238000000066 reactive distillation Methods 0.000 description 1
- 238000009666 routine test Methods 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000005049 silicon tetrachloride Substances 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 1
- 229910052714 tellurium Inorganic materials 0.000 description 1
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- ZDHXKXAHOVTTAH-UHFFFAOYSA-N trichlorosilane Chemical compound Cl[SiH](Cl)Cl ZDHXKXAHOVTTAH-UHFFFAOYSA-N 0.000 description 1
- 239000005052 trichlorosilane Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052845 zircon Inorganic materials 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C213/00—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton
- C07C213/04—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton by reaction of ammonia or amines with olefin oxides or halohydrins
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/582—Recycling of unreacted starting or intermediate materials
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Priority Applications (8)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10028636A DE10028636A1 (de) | 2000-06-09 | 2000-06-09 | Verfahren zur Herstellung von Alkanolaminen |
| EP01945265.5A EP1289927B1 (de) | 2000-06-09 | 2001-06-07 | Verfahren zur herstellung von ethanolaminen |
| PCT/EP2001/006481 WO2001094290A1 (de) | 2000-06-09 | 2001-06-07 | Verfahren zur herstellung von alkanolaminen |
| CNB018109306A CN1202074C (zh) | 2000-06-09 | 2001-06-07 | 制备链烷醇胺的方法 |
| JP2002501807A JP4996031B2 (ja) | 2000-06-09 | 2001-06-07 | アルカノールアミンの製造方法 |
| US10/297,052 US7119231B2 (en) | 2000-06-09 | 2001-06-07 | Method for producing alkanolamines |
| MYPI20012675A MY137615A (en) | 2000-06-09 | 2001-06-08 | Preparation of alkanolamines |
| TW90113982A TW574181B (en) | 2000-06-09 | 2001-06-08 | Preparation of alkanolamines |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10028636A DE10028636A1 (de) | 2000-06-09 | 2000-06-09 | Verfahren zur Herstellung von Alkanolaminen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE10028636A1 true DE10028636A1 (de) | 2001-12-13 |
Family
ID=7645267
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE10028636A Withdrawn DE10028636A1 (de) | 2000-06-09 | 2000-06-09 | Verfahren zur Herstellung von Alkanolaminen |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US7119231B2 (enExample) |
| EP (1) | EP1289927B1 (enExample) |
| JP (1) | JP4996031B2 (enExample) |
| CN (1) | CN1202074C (enExample) |
| DE (1) | DE10028636A1 (enExample) |
| MY (1) | MY137615A (enExample) |
| TW (1) | TW574181B (enExample) |
| WO (1) | WO2001094290A1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN114315612A (zh) * | 2021-12-27 | 2022-04-12 | 万华化学集团股份有限公司 | 一种连续化生产异丙醇胺的工艺 |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101475496B (zh) * | 2009-01-19 | 2012-05-02 | 佳化化学股份有限公司 | 一种制备链烷醇胺的方法 |
| CN101475494B (zh) * | 2009-01-19 | 2012-01-18 | 佳化化学股份有限公司 | 一种链烷醇胺的生产工艺 |
| EP2547648B1 (de) * | 2010-03-18 | 2013-07-10 | Basf Se | Verfahren zur herstellung nebenproduktarmer aminocarboxylate |
| CN102952024B (zh) * | 2011-08-24 | 2014-05-28 | 岳阳蓬诚科技发展有限公司 | 一种乙烯一步法制备乙醇胺的方法 |
| CN103271238B (zh) * | 2013-05-10 | 2014-04-02 | 中国科学院亚热带农业生态研究所 | 一种饲料添加剂一乙醇胺的制备方法及应用 |
| EP2784058A1 (de) | 2013-08-15 | 2014-10-01 | Basf Se | Verfahren zur Verbesserung der Farbstabilität eines Ethanolamins |
| CN105085283B (zh) * | 2014-05-14 | 2017-07-14 | 中国石油化工股份有限公司 | 生产三乙醇胺的方法 |
| CN104710123B (zh) * | 2015-02-03 | 2017-06-06 | 辽宁鑫隆科技有限公司 | 一种改性二乙醇单异丙醇胺盐水泥助磨剂 |
| MY190173A (en) | 2016-03-18 | 2022-03-31 | Nippon Catalytic Chem Ind | Process for producing alkanolamine |
| EP3619190B1 (en) * | 2017-05-03 | 2021-08-04 | Basf Se | Process for the conversion of ethylene oxide to monoethanolamine and ethylenediamine employing a zeolite |
| CN107338072B (zh) * | 2017-07-26 | 2019-09-13 | 徐文忠 | 重整装置用缓蚀剂及其制备方法 |
| WO2019154647A1 (de) * | 2018-02-06 | 2019-08-15 | Basf Se | Verfahren zur herstellung von c2-c4-monoalkanolaminen mittels eines sauren kationenaustau-schers als katalysator |
| WO2023135035A1 (en) | 2022-01-14 | 2023-07-20 | Basf Se | Method for the manufacture or conversion of alkanolamines |
| CN115010611B (zh) * | 2022-04-27 | 2024-02-20 | 北京金隅节能科技有限公司 | 一种二乙醇单异丙醇胺的生产工艺 |
| AU2023266064A1 (en) | 2022-05-02 | 2024-11-14 | Basf Se | Process for making ethanolamines, polyethylenimine and ammonia based on non-fossil energy |
| WO2024180261A2 (en) | 2023-03-02 | 2024-09-06 | Basf Se | Environmenal friendly ethylene oxide, propylene oxide and downstream products |
| CN120936657A (zh) | 2023-04-12 | 2025-11-11 | 巴斯夫欧洲公司 | 具有低氘含量的乙酸乙烯酯 |
Family Cites Families (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE298636C (enExample) | ||||
| US3697598A (en) | 1968-08-20 | 1972-10-10 | Mo Och Ab | Continuous process for preparing monoalkanolamines from ammonia and alkylene oxides |
| BE834514A (nl) | 1974-10-24 | 1976-04-15 | Werkwijze ter bereiding van dialkanolaminen | |
| US4438281A (en) * | 1983-01-24 | 1984-03-20 | Texaco Inc. | Selective production of monoalkanolamines from alkylene oxides and ammonia over acidic inorganic catalysts |
| IT1222868B (it) | 1987-10-12 | 1990-09-12 | Montedipe Spa | Metodo per la preparazione di titanio silicaliti |
| US4939301A (en) * | 1988-12-23 | 1990-07-03 | Texaco Chemical Company | Production of ethanolamine by amination of ethylene oxide over acid activated clays |
| US5244650A (en) | 1989-06-29 | 1993-09-14 | Engelhard Corporation | Large-pored molecular sieves with charged octahedral titanium and charged tetrahedral aluminum sites |
| DD298636A5 (de) | 1989-12-11 | 1992-03-05 | Buna Ag,De | Verfahren zur herstellung von ueberwiegend diethanolamin enthaltenden reaktionsgemischen aus der umsetzung von ethenoxid und ammoniak |
| US5378671A (en) | 1993-06-03 | 1995-01-03 | Mobil Oil Corp. | Method for preparing catalysts comprising zeolites |
| DE4323774A1 (de) | 1993-07-15 | 1995-02-09 | Basf Ag | Hohlkugelartig agglomerierte Pentasilzeolithe |
| US5430000A (en) | 1993-08-25 | 1995-07-04 | Mobil Oil Corporation | Method for preparing titania-bound zeolite catalysts |
| JP2771465B2 (ja) * | 1993-11-02 | 1998-07-02 | 株式会社日本触媒 | アルカノールアミンの製造方法およびこれに用いる触媒 |
| DE69409463T2 (de) | 1993-11-02 | 1998-07-30 | Nippon Catalytic Chem Ind | Verfahren zur Herstellung von Alkanolamin, Katalysator für dieses Verfahren und Verfahren zur Herstellung des Katalysators |
| DE4435688A1 (de) * | 1994-10-06 | 1996-04-11 | Basf Ag | Verfahren zur Herstellung von Oligoaminen oder Polyaminen |
| US5463127A (en) * | 1995-01-17 | 1995-10-31 | The Dow Chemical Company | Process for preparation of halohydroxypropyl-trialkylammonium halides |
| JP2996914B2 (ja) * | 1995-06-07 | 2000-01-11 | 株式会社日本触媒 | アルカノールアミンの製造方法 |
| US5846598A (en) * | 1995-11-30 | 1998-12-08 | International Business Machines Corporation | Electroless plating of metallic features on nonmetallic or semiconductor layer without extraneous plating |
| US6063965A (en) * | 1997-09-05 | 2000-05-16 | Huntsman Petrochemical Corporation | Production of diethanolamine |
| DE19757709A1 (de) | 1997-12-23 | 1999-07-01 | Basf Ag | Verfahren zur Herstellung oxalkylierter Amine |
| JP3154984B2 (ja) * | 1998-03-13 | 2001-04-09 | 株式会社日本触媒 | ジアルカノールアミンの製造方法およびこれに用いる触媒 |
| DE19855383A1 (de) * | 1998-12-01 | 2000-06-08 | Basf Ag | Verfahren zur Reinigung von Triethanolamin |
| DE19954322A1 (de) | 1999-11-10 | 2001-05-17 | Basf Ag | Oxid und Verfahren zu dessen Herstellung |
| DE10015246A1 (de) | 2000-03-28 | 2001-10-04 | Basf Ag | Verfahren zur Umsetzung einer organischen Verbindung mit einem Hydroperoxid |
-
2000
- 2000-06-09 DE DE10028636A patent/DE10028636A1/de not_active Withdrawn
-
2001
- 2001-06-07 US US10/297,052 patent/US7119231B2/en not_active Expired - Fee Related
- 2001-06-07 JP JP2002501807A patent/JP4996031B2/ja not_active Expired - Fee Related
- 2001-06-07 EP EP01945265.5A patent/EP1289927B1/de not_active Expired - Lifetime
- 2001-06-07 WO PCT/EP2001/006481 patent/WO2001094290A1/de not_active Ceased
- 2001-06-07 CN CNB018109306A patent/CN1202074C/zh not_active Expired - Fee Related
- 2001-06-08 TW TW90113982A patent/TW574181B/zh not_active IP Right Cessation
- 2001-06-08 MY MYPI20012675A patent/MY137615A/en unknown
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN114315612A (zh) * | 2021-12-27 | 2022-04-12 | 万华化学集团股份有限公司 | 一种连续化生产异丙醇胺的工艺 |
| CN114315612B (zh) * | 2021-12-27 | 2024-02-02 | 万华化学集团股份有限公司 | 一种连续化生产异丙醇胺的工艺 |
Also Published As
| Publication number | Publication date |
|---|---|
| JP4996031B2 (ja) | 2012-08-08 |
| JP2003535838A (ja) | 2003-12-02 |
| MY137615A (en) | 2009-02-27 |
| EP1289927B1 (de) | 2014-05-14 |
| US7119231B2 (en) | 2006-10-10 |
| US20030149305A1 (en) | 2003-08-07 |
| WO2001094290A1 (de) | 2001-12-13 |
| CN1436164A (zh) | 2003-08-13 |
| TW574181B (en) | 2004-02-01 |
| CN1202074C (zh) | 2005-05-18 |
| EP1289927A1 (de) | 2003-03-12 |
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