KR20010023221A - 바나듐-인 촉매를 제조하는 방법, 및 말레산 무수물의제조를 위해 이들 촉매를 사용하는 방법 - Google Patents
바나듐-인 촉매를 제조하는 방법, 및 말레산 무수물의제조를 위해 이들 촉매를 사용하는 방법 Download PDFInfo
- Publication number
- KR20010023221A KR20010023221A KR1020007001850A KR20007001850A KR20010023221A KR 20010023221 A KR20010023221 A KR 20010023221A KR 1020007001850 A KR1020007001850 A KR 1020007001850A KR 20007001850 A KR20007001850 A KR 20007001850A KR 20010023221 A KR20010023221 A KR 20010023221A
- Authority
- KR
- South Korea
- Prior art keywords
- precursor
- vanadium
- volume
- temperature
- phosphorus
- 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- Withdrawn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
- 239000003054 catalyst Substances 0.000 title claims abstract description 82
- 238000000034 method Methods 0.000 title claims abstract description 70
- 230000008569 process Effects 0.000 title claims abstract description 37
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 title claims abstract description 24
- JKJKPRIBNYTIFH-UHFFFAOYSA-N phosphanylidynevanadium Chemical compound [V]#P JKJKPRIBNYTIFH-UHFFFAOYSA-N 0.000 title claims abstract description 15
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 13
- 238000002360 preparation method Methods 0.000 title abstract description 10
- 238000001354 calcination Methods 0.000 claims abstract description 48
- 239000002243 precursor Substances 0.000 claims abstract description 38
- 230000003647 oxidation Effects 0.000 claims abstract description 28
- 238000007254 oxidation reaction Methods 0.000 claims abstract description 28
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 claims abstract description 21
- 239000012298 atmosphere Substances 0.000 claims abstract description 21
- 239000007789 gas Substances 0.000 claims abstract description 19
- 239000000203 mixture Substances 0.000 claims abstract description 19
- 239000011261 inert gas Substances 0.000 claims abstract description 15
- 229910052698 phosphorus Inorganic materials 0.000 claims abstract description 15
- 239000011574 phosphorus Substances 0.000 claims abstract description 15
- -1 phosphorus compound Chemical class 0.000 claims abstract description 14
- 238000001035 drying Methods 0.000 claims abstract description 12
- 150000003682 vanadium compounds Chemical class 0.000 claims abstract description 9
- 239000003960 organic solvent Substances 0.000 claims abstract description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 5
- 238000006243 chemical reaction Methods 0.000 claims description 38
- 239000012018 catalyst precursor Substances 0.000 claims description 28
- 238000010438 heat treatment Methods 0.000 claims description 26
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 23
- 239000001301 oxygen Substances 0.000 claims description 23
- 229910052760 oxygen Inorganic materials 0.000 claims description 23
- 229910052720 vanadium Inorganic materials 0.000 claims description 23
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 claims description 23
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 claims description 16
- 239000001273 butane Substances 0.000 claims description 12
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 claims description 12
- 229930195733 hydrocarbon Natural products 0.000 claims description 11
- 150000002430 hydrocarbons Chemical class 0.000 claims description 11
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 8
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 8
- 229910001882 dioxygen Inorganic materials 0.000 claims description 7
- 239000011541 reaction mixture Substances 0.000 claims description 6
- 239000004215 Carbon black (E152) Substances 0.000 claims description 5
- 239000011368 organic material Substances 0.000 claims description 5
- 238000012546 transfer Methods 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 239000012808 vapor phase Substances 0.000 claims description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 abstract description 3
- 230000036961 partial effect Effects 0.000 abstract description 3
- 238000011084 recovery Methods 0.000 abstract 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 13
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 10
- 230000000694 effects Effects 0.000 description 7
- 239000007788 liquid Substances 0.000 description 7
- 229910052757 nitrogen Inorganic materials 0.000 description 7
- 238000010992 reflux Methods 0.000 description 7
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 6
- GNTDGMZSJNCJKK-UHFFFAOYSA-N divanadium pentaoxide Chemical compound O=[V](=O)O[V](=O)=O GNTDGMZSJNCJKK-UHFFFAOYSA-N 0.000 description 6
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical compound [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 description 5
- 235000011180 diphosphates Nutrition 0.000 description 5
- 235000011007 phosphoric acid Nutrition 0.000 description 5
- LSGOVYNHVSXFFJ-UHFFFAOYSA-N vanadate(3-) Chemical compound [O-][V]([O-])([O-])=O LSGOVYNHVSXFFJ-UHFFFAOYSA-N 0.000 description 5
- LJYCJDQBTIMDPJ-UHFFFAOYSA-N [P]=O.[V] Chemical compound [P]=O.[V] LJYCJDQBTIMDPJ-UHFFFAOYSA-N 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 230000001590 oxidative effect Effects 0.000 description 4
- 239000002244 precipitate Substances 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- DLYUQMMRRRQYAE-UHFFFAOYSA-N tetraphosphorus decaoxide Chemical compound O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 3
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 3
- 150000008064 anhydrides Chemical class 0.000 description 3
- 239000010439 graphite Substances 0.000 description 3
- 229910002804 graphite Inorganic materials 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 235000021317 phosphate Nutrition 0.000 description 3
- 238000000746 purification Methods 0.000 description 3
- 239000012429 reaction media Substances 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 230000004913 activation Effects 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 239000003125 aqueous solvent Substances 0.000 description 2
- 235000019445 benzyl alcohol Nutrition 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 239000003607 modifier Substances 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 150000003018 phosphorus compounds Chemical class 0.000 description 2
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 2
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-L Phosphate ion(2-) Chemical compound OP([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-L 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- XHCLAFWTIXFWPH-UHFFFAOYSA-N [O-2].[O-2].[O-2].[O-2].[O-2].[V+5].[V+5] Chemical class [O-2].[O-2].[O-2].[O-2].[O-2].[V+5].[V+5] XHCLAFWTIXFWPH-UHFFFAOYSA-N 0.000 description 1
- LOUBVQKDBZRZNQ-UHFFFAOYSA-M [O-2].[O-2].[OH-].O.[V+5] Chemical compound [O-2].[O-2].[OH-].O.[V+5] LOUBVQKDBZRZNQ-UHFFFAOYSA-M 0.000 description 1
- CAUHCBDRRFADDB-UHFFFAOYSA-A [V+5].[V+5].[V+5].[V+5].[O-]P([O-])(=O)OP([O-])([O-])=O.[O-]P([O-])(=O)OP([O-])([O-])=O.[O-]P([O-])(=O)OP([O-])([O-])=O.[O-]P([O-])(=O)OP([O-])([O-])=O.[O-]P([O-])(=O)OP([O-])([O-])=O Chemical compound [V+5].[V+5].[V+5].[V+5].[O-]P([O-])(=O)OP([O-])([O-])=O.[O-]P([O-])(=O)OP([O-])([O-])=O.[O-]P([O-])(=O)OP([O-])([O-])=O.[O-]P([O-])(=O)OP([O-])([O-])=O.[O-]P([O-])(=O)OP([O-])([O-])=O CAUHCBDRRFADDB-UHFFFAOYSA-A 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- UNTBPXHCXVWYOI-UHFFFAOYSA-O azanium;oxido(dioxo)vanadium Chemical compound [NH4+].[O-][V](=O)=O UNTBPXHCXVWYOI-UHFFFAOYSA-O 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 230000002860 competitive effect Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000000374 eutectic mixture Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 235000013373 food additive Nutrition 0.000 description 1
- 239000002778 food additive Substances 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 229940035429 isobutyl alcohol Drugs 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- FISRGBICZQXBOD-UHFFFAOYSA-N methane phosphoric acid Chemical compound C.C.OP(O)(O)=O FISRGBICZQXBOD-UHFFFAOYSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- UXCDUFKZSUBXGM-UHFFFAOYSA-N phosphoric tribromide Chemical compound BrP(Br)(Br)=O UXCDUFKZSUBXGM-UHFFFAOYSA-N 0.000 description 1
- 229910001392 phosphorus oxide Inorganic materials 0.000 description 1
- 239000012688 phosphorus precursor Substances 0.000 description 1
- LFGREXWGYUGZLY-UHFFFAOYSA-N phosphoryl Chemical class [P]=O LFGREXWGYUGZLY-UHFFFAOYSA-N 0.000 description 1
- 235000010333 potassium nitrate Nutrition 0.000 description 1
- 239000004323 potassium nitrate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000006722 reduction reaction Methods 0.000 description 1
- 238000010405 reoxidation reaction Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000010344 sodium nitrate Nutrition 0.000 description 1
- 239000004317 sodium nitrate Substances 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000012258 stirred mixture Substances 0.000 description 1
- MJNHIYILRDOOTC-UHFFFAOYSA-N tetrachlorophosphanium Chemical compound Cl[P+](Cl)(Cl)Cl MJNHIYILRDOOTC-UHFFFAOYSA-N 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 150000003681 vanadium Chemical class 0.000 description 1
- 229910001935 vanadium oxide Inorganic materials 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
- C07C51/21—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
- C07C51/215—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of saturated hydrocarbyl groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Furan Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BE9800475 | 1998-06-23 | ||
| BE9800475A BE1012101A6 (fr) | 1998-06-23 | 1998-06-23 | Procede de conversion a haut rendement de n-butane en anhydride maleique par recyclage des gaz uses. |
| PCT/EP1999/004301 WO1999067021A1 (en) | 1998-06-23 | 1999-06-21 | Process for the preparation of improved vanadium-phosphorus catalysts and use thereof for the production of maleic anhydride |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20010023221A true KR20010023221A (ko) | 2001-03-26 |
Family
ID=3891316
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020007001850A Withdrawn KR20010023221A (ko) | 1998-06-23 | 1999-06-21 | 바나듐-인 촉매를 제조하는 방법, 및 말레산 무수물의제조를 위해 이들 촉매를 사용하는 방법 |
| KR1020007001856A Expired - Fee Related KR100622167B1 (ko) | 1998-06-23 | 1999-06-21 | ｎ-부탄으로부터 말레산 무수물을 제조하는 고생산성 방법 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020007001856A Expired - Fee Related KR100622167B1 (ko) | 1998-06-23 | 1999-06-21 | ｎ-부탄으로부터 말레산 무수물을 제조하는 고생산성 방법 |
Country Status (13)
| Country | Link |
|---|---|
| US (2) | US6040460A (https=) |
| EP (2) | EP1007499B1 (https=) |
| JP (2) | JP2002518172A (https=) |
| KR (2) | KR20010023221A (https=) |
| CN (2) | CN1119205C (https=) |
| AT (1) | ATE235452T1 (https=) |
| AU (2) | AU745774B2 (https=) |
| BE (1) | BE1012101A6 (https=) |
| BR (2) | BR9906553B1 (https=) |
| CA (2) | CA2301048A1 (https=) |
| DE (1) | DE69906224T2 (https=) |
| ES (1) | ES2196826T3 (https=) |
| WO (2) | WO1999067194A1 (https=) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6281378B1 (en) * | 1995-06-08 | 2001-08-28 | Nippon Shokubai Co., Ltd. | Vanadium-containing catalysts, process for manufacturing and use of the same |
| DE69916217T2 (de) | 1998-11-27 | 2005-04-07 | Mitsubishi Chemical Corp. | Verfahren zur Herstellung von Maleinsäureanhydrid |
| EP1055670B1 (en) | 1999-05-25 | 2008-02-20 | Mitsubishi Chemical Corporation | Process for the production of maleic anhydride |
| US6858561B2 (en) * | 2003-05-15 | 2005-02-22 | Scientific Design Company, Inc. | Phosphorus/vanadium catalyst preparation |
| DE10334582A1 (de) * | 2003-07-28 | 2005-02-24 | Basf Ag | Verfahren zur Herstellung von Maleinsäureanhydrid |
| US7399456B2 (en) * | 2005-02-25 | 2008-07-15 | Conocophillips Company | Process for the removal of heavy metals from gases, and compositions therefor and therewith |
| US8143461B2 (en) * | 2006-09-05 | 2012-03-27 | Huntsman Petrochemical Llc | Maleic anhydride catalyst and method for its preparation |
| EP2205353B1 (en) * | 2007-10-22 | 2019-12-18 | Huntsman Petrochemical LLC | Improved oxidation catalyst for maleic anhydride production |
| CN102015104A (zh) * | 2008-03-25 | 2011-04-13 | 巴布考克日立株式会社 | 抑制铁化合物影响的排气净化催化剂 |
| DE102008025834A1 (de) * | 2008-05-29 | 2009-12-03 | Bayer Technology Services Gmbh | Verfahren zur Herstellung von Maleinsäureanhydrid |
| US7972415B2 (en) * | 2008-12-11 | 2011-07-05 | Spx Corporation | Membrane-based compressed air breathing system |
| CN101531650B (zh) * | 2009-03-19 | 2010-04-21 | 江苏钟腾化工有限公司 | 一种从含顺酐气体中回收顺酐的部分冷凝工艺 |
| WO2011023646A1 (de) | 2009-08-26 | 2011-03-03 | Basf Se | Katalysator-precursor für die herstellung von maleinsäureanhydrid und verfahren zu dessen herstellung |
| FR2958185B1 (fr) * | 2010-03-30 | 2012-04-20 | Arkema France | Procede d'oxydation selective de monoxyde de carbone |
| MY188403A (en) * | 2010-09-10 | 2021-12-07 | Huntsman Petrochemical Llc | Improved vpo catalyst with low vanadium oxidation state for maleic anhydride production |
| CN104096376B (zh) * | 2014-06-27 | 2016-03-09 | 常州瑞华化工工程技术有限公司 | 一种防止顺酐装置氧化产物冷凝器堵塞的方法和装置 |
| CN104177317B (zh) * | 2014-07-31 | 2017-04-19 | 常州瑞华化工工程技术有限公司 | 防止顺酐循环尾气露点腐蚀的方法 |
| CN105001185A (zh) * | 2015-07-21 | 2015-10-28 | 宁波浙铁江宁化工有限公司 | 一种顺酐尾气处理设备及其工艺 |
| CN105617959A (zh) * | 2016-01-15 | 2016-06-01 | 湖南弘润化工科技有限公司 | 甲苯液相空气氧化法连续生产苯甲酸的反应装置 |
| US11289700B2 (en) | 2016-06-28 | 2022-03-29 | The Research Foundation For The State University Of New York | KVOPO4 cathode for sodium ion batteries |
| GB201616119D0 (en) * | 2016-09-22 | 2016-11-09 | Johnson Matthey Davy Technologies Limited | Process |
| CN109046412B (zh) * | 2018-08-23 | 2021-05-25 | 常州新日催化剂股份有限公司 | 一种正丁烷氧化制顺酐催化剂及其制备方法 |
| CN115697955A (zh) | 2020-09-17 | 2023-02-03 | 巴斯夫欧洲公司 | 制备乙二醛的方法 |
| CN119327376A (zh) * | 2023-07-20 | 2025-01-21 | 中国石化工程建设有限公司 | 一种正戊烷氧化制顺酐和苯酐的系统和方法 |
| WO2025062466A1 (en) | 2023-09-19 | 2025-03-27 | Conser Spa | Gas recycle maleic anydride process for high productivity and low carbon emissions |
Family Cites Families (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3293268A (en) | 1964-03-23 | 1966-12-20 | Princeton Chemical Res Inc | Production of maleic anhydride by oxidation of n-butane |
| US3864280A (en) * | 1972-06-19 | 1975-02-04 | Chevron Res | Catalyst for a n-butane oxidation to maleic anhydride |
| US4132670A (en) | 1974-11-06 | 1979-01-02 | Chevron Research Company | Method of preparing vanadium (IV) phosphate composition with high intrinsic surface area |
| US3904652A (en) * | 1972-11-16 | 1975-09-09 | Standard Oil Co Indiana | Recycle process for oxidation of n-butane to maleic anhydride |
| US3899516A (en) * | 1973-10-17 | 1975-08-12 | Sun Ventures Inc | Oxidation of butane to maleic anhydride using butane-rich feed |
| US4064070A (en) | 1974-12-23 | 1977-12-20 | Chevron Research Company | Catalyst for producing maleic anhydride |
| US4222945A (en) * | 1978-01-30 | 1980-09-16 | Imperial Chemical Industries Limited | Production of maleic anhydride |
| EP0003431B1 (en) | 1978-01-30 | 1984-04-11 | Imperial Chemical Industries Plc | Production of carboxylic acid anhydrides and catalysts therefor |
| US4231943A (en) * | 1979-05-31 | 1980-11-04 | Chevron Research Company | Maleic anhydride production |
| US4247419A (en) * | 1979-12-13 | 1981-01-27 | Atlantic Richfield Company | Single phase vanadium(IV)bis(metaphosphate) oxidation catalyst with improved intrinsic surface area |
| US4312787A (en) | 1979-12-17 | 1982-01-26 | Standard Oil Company | Coated catalysts containing high loading of active phase, particularly useful in the preparation of maleic anhydride |
| US4333853A (en) | 1980-05-05 | 1982-06-08 | The Standard Oil Company | Mixed vanadium phosphorus oxide catalysts and preparation thereof |
| US4315864A (en) | 1980-10-22 | 1982-02-16 | Standard Oil Company (Ohio) | Preparation of maleic anhydride |
| US4317778A (en) * | 1980-12-29 | 1982-03-02 | Standard Oil Company (Sohio) | Preparation of maleic anhydride using fluidized catalysts |
| US4342699A (en) * | 1981-02-23 | 1982-08-03 | Standard Oil Company (Indiana) | Process for production of maleic anhydride |
| US4392986A (en) | 1981-10-08 | 1983-07-12 | Exxon Research & Engineering Co. | Catalyst for carboxylic anhydride production |
| US4562268A (en) | 1983-12-28 | 1985-12-31 | Monsanto Company | Process for producing maleic anhydride |
| US4632915A (en) | 1985-10-28 | 1986-12-30 | Monsanto Company | Iron/lithium--promoted catalysts for the production of maleic anhydride |
| US5011945A (en) * | 1987-08-31 | 1991-04-30 | Amoco Corporation | Continuous process for the production of maleic anhydride |
| IT1253698B (it) * | 1990-05-31 | 1995-08-23 | Sisas Spa | Procedimento per il recupero di anidride maleica da miscele di reazione |
| US5126463A (en) * | 1990-10-31 | 1992-06-30 | The Boc Group, Inc. | Process for the production of anhydrides |
| US5262547A (en) * | 1990-10-31 | 1993-11-16 | The Boc Group, Inc. | Process for the production of petrochemicals |
| HUT58680A (en) * | 1990-11-14 | 1992-03-30 | Boc Group Inc | Process for producing anhydrides and nitriles |
| US5137860A (en) | 1991-06-27 | 1992-08-11 | Monsanto Company | Process for the transformation of vanadium/phosphorus mixed oxide catalyst precursors into active catalysts for the production of maleic anhydride |
| BE1008103A3 (fr) * | 1994-04-22 | 1996-01-16 | Pantochim Sa | Procede de preparation de catalyseurs au vanadium et phosphore et leur utilisation pour la production d'anhydride maleique. |
| IT1269970B (it) * | 1994-06-30 | 1997-04-16 | Sisas Spa | Procedimento di riciclo di gas esausti nel processo di conversione di n-butano ad anidride maleica |
| IT1290407B1 (it) * | 1996-04-29 | 1998-12-03 | Lonza Spa | Procedimento per la trasformazione di un precursore di catalizzatore a base di ossido misto di vanadio/fosforo nel catalizzatore attivo |
-
1998
- 1998-06-23 BE BE9800475A patent/BE1012101A6/fr not_active IP Right Cessation
-
1999
- 1999-06-21 EP EP99931128A patent/EP1007499B1/en not_active Expired - Lifetime
- 1999-06-21 CA CA002301048A patent/CA2301048A1/en not_active Abandoned
- 1999-06-21 CN CN99801207A patent/CN1119205C/zh not_active Expired - Fee Related
- 1999-06-21 EP EP99932707A patent/EP1011859A1/en not_active Withdrawn
- 1999-06-21 AT AT99931128T patent/ATE235452T1/de not_active IP Right Cessation
- 1999-06-21 KR KR1020007001850A patent/KR20010023221A/ko not_active Withdrawn
- 1999-06-21 WO PCT/EP1999/004300 patent/WO1999067194A1/en not_active Ceased
- 1999-06-21 BR BRPI9906553-3A patent/BR9906553B1/pt not_active IP Right Cessation
- 1999-06-21 JP JP2000555698A patent/JP2002518172A/ja not_active Withdrawn
- 1999-06-21 KR KR1020007001856A patent/KR100622167B1/ko not_active Expired - Fee Related
- 1999-06-21 AU AU48998/99A patent/AU745774B2/en not_active Ceased
- 1999-06-21 DE DE69906224T patent/DE69906224T2/de not_active Expired - Fee Related
- 1999-06-21 CN CNB998012084A patent/CN1205162C/zh not_active Expired - Fee Related
- 1999-06-21 ES ES99931128T patent/ES2196826T3/es not_active Expired - Lifetime
- 1999-06-21 BR BR9906554-1A patent/BR9906554A/pt not_active Application Discontinuation
- 1999-06-21 CA CA002301061A patent/CA2301061A1/en not_active Abandoned
- 1999-06-21 AU AU47753/99A patent/AU4775399A/en not_active Abandoned
- 1999-06-21 JP JP2000555850A patent/JP2002518466A/ja active Pending
- 1999-06-21 WO PCT/EP1999/004301 patent/WO1999067021A1/en not_active Ceased
- 1999-06-22 US US09/337,542 patent/US6040460A/en not_active Expired - Lifetime
- 1999-06-22 US US09/337,541 patent/US6174833B1/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| WO1999067021A1 (en) | 1999-12-29 |
| ES2196826T3 (es) | 2003-12-16 |
| JP2002518466A (ja) | 2002-06-25 |
| BE1012101A6 (fr) | 2000-05-02 |
| AU745774B2 (en) | 2002-03-28 |
| BR9906554A (pt) | 2000-08-15 |
| US6040460A (en) | 2000-03-21 |
| CA2301048A1 (en) | 1999-12-29 |
| ATE235452T1 (de) | 2003-04-15 |
| KR20010023227A (ko) | 2001-03-26 |
| EP1007499B1 (en) | 2003-03-26 |
| CN1274301A (zh) | 2000-11-22 |
| DE69906224T2 (de) | 2003-12-11 |
| CN1119205C (zh) | 2003-08-27 |
| JP2002518172A (ja) | 2002-06-25 |
| AU4899899A (en) | 2000-01-10 |
| CN1205162C (zh) | 2005-06-08 |
| US6174833B1 (en) | 2001-01-16 |
| KR100622167B1 (ko) | 2006-09-07 |
| DE69906224D1 (de) | 2003-04-30 |
| CA2301061A1 (en) | 1999-12-29 |
| EP1011859A1 (en) | 2000-06-28 |
| CN1274343A (zh) | 2000-11-22 |
| AU4775399A (en) | 2000-01-10 |
| EP1007499A1 (en) | 2000-06-14 |
| BR9906553A (pt) | 2000-08-15 |
| WO1999067194A1 (en) | 1999-12-29 |
| BR9906553B1 (pt) | 2010-09-08 |
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