NO328297B1 - Fremgangsmate til fremstilling av etere, typisk THF - Google Patents
Fremgangsmate til fremstilling av etere, typisk THF Download PDFInfo
- Publication number
- NO328297B1 NO328297B1 NO20040081A NO20040081A NO328297B1 NO 328297 B1 NO328297 B1 NO 328297B1 NO 20040081 A NO20040081 A NO 20040081A NO 20040081 A NO20040081 A NO 20040081A NO 328297 B1 NO328297 B1 NO 328297B1
- Authority
- NO
- Norway
- Prior art keywords
- cycle gas
- zone
- stream
- reaction
- catalyst
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 51
- 150000002170 ethers Chemical class 0.000 title abstract description 4
- 238000002360 preparation method Methods 0.000 title abstract 2
- 238000006243 chemical reaction Methods 0.000 claims abstract description 120
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims abstract description 100
- 239000007789 gas Substances 0.000 claims abstract description 77
- 239000003054 catalyst Substances 0.000 claims abstract description 68
- 239000000047 product Substances 0.000 claims abstract description 63
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims abstract description 54
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims abstract description 50
- 238000001704 evaporation Methods 0.000 claims abstract description 38
- 230000008020 evaporation Effects 0.000 claims abstract description 38
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 28
- 239000001257 hydrogen Substances 0.000 claims abstract description 27
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 27
- 238000005984 hydrogenation reaction Methods 0.000 claims abstract description 25
- 150000008064 anhydrides Chemical class 0.000 claims abstract description 23
- 239000000203 mixture Substances 0.000 claims abstract description 22
- 239000006227 byproduct Substances 0.000 claims abstract description 20
- 150000001991 dicarboxylic acids Chemical class 0.000 claims abstract description 15
- 239000013067 intermediate product Substances 0.000 claims abstract description 15
- 238000006356 dehydrogenation reaction Methods 0.000 claims abstract description 14
- 150000002596 lactones Chemical class 0.000 claims abstract description 14
- 150000005690 diesters Chemical class 0.000 claims abstract description 4
- 239000000463 material Substances 0.000 claims description 46
- LDCRTTXIJACKKU-ARJAWSKDSA-N dimethyl maleate Chemical compound COC(=O)\C=C/C(=O)OC LDCRTTXIJACKKU-ARJAWSKDSA-N 0.000 claims description 42
- 238000007670 refining Methods 0.000 claims description 29
- 238000004519 manufacturing process Methods 0.000 claims description 21
- 150000002148 esters Chemical class 0.000 claims description 17
- -1 y-butyrolactone Chemical compound 0.000 claims description 10
- MUXOBHXGJLMRAB-UHFFFAOYSA-N Dimethyl succinate Chemical compound COC(=O)CCC(=O)OC MUXOBHXGJLMRAB-UHFFFAOYSA-N 0.000 claims description 8
- 125000005907 alkyl ester group Chemical group 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 5
- 150000004292 cyclic ethers Chemical group 0.000 claims description 5
- NKHAVTQWNUWKEO-UHFFFAOYSA-N fumaric acid monomethyl ester Natural products COC(=O)C=CC(O)=O NKHAVTQWNUWKEO-UHFFFAOYSA-N 0.000 claims description 5
- 239000003960 organic solvent Substances 0.000 claims description 5
- 238000004064 recycling Methods 0.000 claims description 5
- LOLKAJARZKDJTD-UHFFFAOYSA-N 4-Ethoxy-4-oxobutanoic acid Chemical compound CCOC(=O)CCC(O)=O LOLKAJARZKDJTD-UHFFFAOYSA-N 0.000 claims description 4
- 230000015572 biosynthetic process Effects 0.000 claims description 4
- XLYMOEINVGRTEX-UHFFFAOYSA-N fumaric acid monoethyl ester Natural products CCOC(=O)C=CC(O)=O XLYMOEINVGRTEX-UHFFFAOYSA-N 0.000 claims description 4
- IEPRKVQEAMIZSS-UHFFFAOYSA-N Di-Et ester-Fumaric acid Natural products CCOC(=O)C=CC(=O)OCC IEPRKVQEAMIZSS-UHFFFAOYSA-N 0.000 claims description 3
- IEPRKVQEAMIZSS-WAYWQWQTSA-N Diethyl maleate Chemical compound CCOC(=O)\C=C/C(=O)OCC IEPRKVQEAMIZSS-WAYWQWQTSA-N 0.000 claims description 3
- DKMROQRQHGEIOW-UHFFFAOYSA-N Diethyl succinate Chemical compound CCOC(=O)CCC(=O)OCC DKMROQRQHGEIOW-UHFFFAOYSA-N 0.000 claims description 3
- 235000013305 food Nutrition 0.000 claims description 3
- 150000002431 hydrogen Chemical class 0.000 claims description 3
- NKHAVTQWNUWKEO-IHWYPQMZSA-N methyl hydrogen fumarate Chemical compound COC(=O)\C=C/C(O)=O NKHAVTQWNUWKEO-IHWYPQMZSA-N 0.000 claims description 3
- XLYMOEINVGRTEX-ONEGZZNKSA-N (e)-4-ethoxy-4-oxobut-2-enoic acid Chemical compound CCOC(=O)\C=C\C(O)=O XLYMOEINVGRTEX-ONEGZZNKSA-N 0.000 claims description 2
- JDRMYOQETPMYQX-UHFFFAOYSA-M 4-methoxy-4-oxobutanoate Chemical compound COC(=O)CCC([O-])=O JDRMYOQETPMYQX-UHFFFAOYSA-M 0.000 claims description 2
- XLYMOEINVGRTEX-ARJAWSKDSA-N Ethyl hydrogen fumarate Chemical compound CCOC(=O)\C=C/C(O)=O XLYMOEINVGRTEX-ARJAWSKDSA-N 0.000 claims description 2
- JDRMYOQETPMYQX-UHFFFAOYSA-N butanedioic acid monomethyl ester Natural products COC(=O)CCC(O)=O JDRMYOQETPMYQX-UHFFFAOYSA-N 0.000 claims description 2
- IEPRKVQEAMIZSS-AATRIKPKSA-N diethyl fumarate Chemical compound CCOC(=O)\C=C\C(=O)OCC IEPRKVQEAMIZSS-AATRIKPKSA-N 0.000 claims description 2
- LDCRTTXIJACKKU-ONEGZZNKSA-N dimethyl fumarate Chemical compound COC(=O)\C=C\C(=O)OC LDCRTTXIJACKKU-ONEGZZNKSA-N 0.000 claims description 2
- 229960004419 dimethyl fumarate Drugs 0.000 claims description 2
- 229940074369 monoethyl fumarate Drugs 0.000 claims description 2
- NKHAVTQWNUWKEO-NSCUHMNNSA-N monomethyl fumarate Chemical compound COC(=O)\C=C\C(O)=O NKHAVTQWNUWKEO-NSCUHMNNSA-N 0.000 claims description 2
- 229940005650 monomethyl fumarate Drugs 0.000 claims description 2
- 235000013348 organic food Nutrition 0.000 claims description 2
- 238000011084 recovery Methods 0.000 abstract 1
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 64
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 56
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 18
- 150000002009 diols Chemical class 0.000 description 14
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 9
- 229910052802 copper Inorganic materials 0.000 description 9
- 239000010949 copper Substances 0.000 description 9
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 6
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 6
- JGDFBJMWFLXCLJ-UHFFFAOYSA-N copper chromite Chemical compound [Cu]=O.[Cu]=O.O=[Cr]O[Cr]=O JGDFBJMWFLXCLJ-UHFFFAOYSA-N 0.000 description 5
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 5
- 239000011541 reaction mixture Substances 0.000 description 5
- 238000009834 vaporization Methods 0.000 description 5
- 230000008016 vaporization Effects 0.000 description 5
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 4
- 230000002378 acidificating effect Effects 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 239000012043 crude product Substances 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 4
- 230000032050 esterification Effects 0.000 description 4
- 238000005886 esterification reaction Methods 0.000 description 4
- 239000012808 vapor phase Substances 0.000 description 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 3
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 238000011143 downstream manufacturing Methods 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical class [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 229910002090 carbon oxide Inorganic materials 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 229910000423 chromium oxide Inorganic materials 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- ALOUNLDAKADEEB-UHFFFAOYSA-N dimethyl sebacate Chemical compound COC(=O)CCCCCCCCC(=O)OC ALOUNLDAKADEEB-UHFFFAOYSA-N 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000011976 maleic acid Substances 0.000 description 2
- 150000002688 maleic acid derivatives Chemical class 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- 238000005809 transesterification reaction Methods 0.000 description 2
- 238000011144 upstream manufacturing Methods 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- 239000011787 zinc oxide Substances 0.000 description 2
- LNETULKMXZVUST-UHFFFAOYSA-N 1-naphthoic acid Chemical class C1=CC=C2C(C(=O)O)=CC=CC2=C1 LNETULKMXZVUST-UHFFFAOYSA-N 0.000 description 1
- NMPJHMFXHISVBR-UHFFFAOYSA-N 4-(oxolan-2-yloxy)butan-1-ol Chemical compound OCCCCOC1CCCO1 NMPJHMFXHISVBR-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 229910000975 Carbon steel Inorganic materials 0.000 description 1
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 1
- 239000005751 Copper oxide Substances 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- VIJYFGMFEVJQHU-UHFFFAOYSA-N aluminum oxosilicon(2+) oxygen(2-) Chemical compound [O-2].[Al+3].[Si+2]=O VIJYFGMFEVJQHU-UHFFFAOYSA-N 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000010962 carbon steel Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000003889 chemical engineering Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229910000431 copper oxide Inorganic materials 0.000 description 1
- 230000009849 deactivation Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 229940014772 dimethyl sebacate Drugs 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 238000007327 hydrogenolysis reaction Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- GBMDVOWEEQVZKZ-UHFFFAOYSA-N methanol;hydrate Chemical compound O.OC GBMDVOWEEQVZKZ-UHFFFAOYSA-N 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229910000510 noble metal Inorganic materials 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 230000000750 progressive effect Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000007086 side reaction Methods 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
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 150000003900 succinic acid esters Chemical class 0.000 description 1
- 230000000153 supplemental effect Effects 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/04—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D307/06—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to ring carbon atoms
- C07D307/08—Preparation of tetrahydrofuran
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Furan Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0117090.1A GB0117090D0 (en) | 2001-07-12 | 2001-07-12 | Process |
| PCT/GB2002/003195 WO2003006446A1 (en) | 2001-07-12 | 2002-07-10 | Process for the production of ethers, typically thf |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NO20040081L NO20040081L (pt) | 2004-01-08 |
| NO328297B1 true NO328297B1 (no) | 2010-01-25 |
Family
ID=9918421
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20040081A NO328297B1 (no) | 2001-07-12 | 2004-01-08 | Fremgangsmate til fremstilling av etere, typisk THF |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US6936727B2 (pt) |
| EP (1) | EP1404660B1 (pt) |
| JP (1) | JP4391816B2 (pt) |
| KR (1) | KR100607120B1 (pt) |
| CN (1) | CN1309714C (pt) |
| AR (1) | AR036338A1 (pt) |
| AT (1) | ATE296816T1 (pt) |
| AU (1) | AU2002314385B2 (pt) |
| BR (1) | BR0211085B1 (pt) |
| CA (1) | CA2451595C (pt) |
| DE (1) | DE60204464T2 (pt) |
| EA (1) | EA005339B1 (pt) |
| ES (1) | ES2240759T3 (pt) |
| GB (1) | GB0117090D0 (pt) |
| MX (1) | MX234385B (pt) |
| MY (1) | MY129064A (pt) |
| NO (1) | NO328297B1 (pt) |
| TW (1) | TWI318975B (pt) |
| WO (1) | WO2003006446A1 (pt) |
| ZA (1) | ZA200309001B (pt) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0329152D0 (en) * | 2003-12-16 | 2004-01-21 | Davy Process Techn Ltd | Process |
| GB0421928D0 (en) | 2004-10-01 | 2004-11-03 | Davy Process Techn Ltd | Process |
| GB0614823D0 (en) * | 2006-07-26 | 2006-09-06 | Davy Process Techn Ltd | Process |
| ZA200901193B (en) * | 2006-08-22 | 2010-06-30 | Dorf Ketal Chemicals I Private | Method of removal of calcium from hydrocarbon feedstock |
| WO2009113095A2 (en) | 2008-01-24 | 2009-09-17 | Dorf Ketal Chemicals (I) Private Limited | Method of removing metals from hydrocarbon feedstock using esters of carboxylic acids |
| GB0803663D0 (en) * | 2008-02-28 | 2008-04-09 | Davy Process Techn Ltd | Process |
| US9186599B2 (en) | 2010-09-24 | 2015-11-17 | Basf Se | Process for isolating tetrahydrofuran |
| EP2619193B1 (de) | 2010-09-24 | 2014-11-12 | Basf Se | Verfahren zur gewinnung von tetrahydrofuran |
| WO2013076747A1 (en) | 2011-11-25 | 2013-05-30 | Conser Spa | Process for producing 1,4- butanediol by hydrogenating dialkyl maleate in mixed liquid/vapor phase |
| US20130296585A1 (en) | 2012-03-30 | 2013-11-07 | Basf Corporation | Catalyst For Tetrahydrofuran Synthesis |
| GB201318175D0 (en) | 2013-10-14 | 2013-11-27 | Johnson Matthey Davy Technologies Ltd | Process |
| JP6716574B2 (ja) | 2015-01-09 | 2020-07-01 | ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ | テトラヒドロフラン、１，４−ブタンジオール又はγ−ブチロラクトンの製造方法 |
Family Cites Families (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2000705A1 (pt) * | 1968-01-25 | 1969-09-12 | Mitsubishi Petrochemical Co | |
| US4451677A (en) | 1981-08-20 | 1984-05-29 | Davy Mckee (London) Limited | Multistage aldehyde hydrogenation |
| JPS60114017A (ja) * | 1983-11-26 | 1985-06-20 | Victor Co Of Japan Ltd | 帰還型くし形フイルタ |
| GB8331793D0 (en) | 1983-11-29 | 1984-01-04 | Davy Mckee Ltd | Process |
| US4584491A (en) * | 1984-01-12 | 1986-04-22 | Motorola, Inc. | TTL to CMOS input buffer circuit for minimizing power consumption |
| BR8507068A (pt) * | 1984-11-21 | 1987-07-14 | Davy Mckee London | Processo para a producao de butano-1,4-diol |
| GB8514002D0 (en) | 1985-06-04 | 1985-07-10 | Davy Mckee Ltd | Process |
| US4626604A (en) | 1985-09-11 | 1986-12-02 | Davy Mckee (London) Limited | Hydrogenation process |
| EP0277168A1 (en) | 1986-08-01 | 1988-08-10 | DAVY McKEE (LONDON) LIMITED | PROCESS FOR THE CO-PRODUCTION OF BUTANE-1,4-DIOL AND $i(GAMMA)-BUTYROLACTONE |
| GB8618888D0 (en) | 1986-08-01 | 1986-09-10 | Davy Mckee Ltd | Process |
| GB8618890D0 (en) | 1986-08-01 | 1986-09-10 | Davy Mckee Ltd | Process |
| GB8717992D0 (en) | 1987-07-29 | 1987-09-03 | Davy Mckee Ltd | Process |
| GB8717993D0 (en) | 1987-07-29 | 1987-09-03 | Davy Mckee Ltd | Process |
| GB8811009D0 (en) | 1988-05-10 | 1988-06-15 | Bp Chem Int Ltd | Chemical process |
| JP2921977B2 (ja) | 1989-01-17 | 1999-07-19 | デイヴイ・プロセス・テクノロジー・リミテッド | プロセス及び装置 |
| GB8917859D0 (en) | 1989-08-04 | 1989-09-20 | Davy Mckee London | Process |
| GB8917864D0 (en) | 1989-08-04 | 1989-09-20 | Davy Mckee London | Process |
| GB8917862D0 (en) * | 1989-08-04 | 1989-09-20 | Davy Mckee London | Process |
| US5254318A (en) | 1992-07-20 | 1993-10-19 | Stone & Webster Engineering Corporation | Lined reformer tubes for high pressure reformer reactors |
| GB9324753D0 (en) * | 1993-12-02 | 1994-01-19 | Davy Mckee London | Process |
| ZA973972B (en) | 1996-05-14 | 1998-03-23 | Kvaerner Process Tech Ltd | A process for the production of at least one C4 compound selected from butane-1,4-diol, gamma-butyrolactone and tetrahydrofuran. |
| ZA973971B (en) | 1996-05-15 | 1998-03-23 | Kvaerner Process Tech Ltd | A process for the production of at least one C4 compound selected from butane-1,4-diol, gamma-butyrolactone and tetrahydrofuran. |
| ES2158645T3 (es) | 1998-03-23 | 2001-09-01 | Basf Ag | Procedimiento para la preparacion de 1,4-butanodiol, butirolactona y tetrahidrofurano. |
| JP2001048819A (ja) * | 1999-08-04 | 2001-02-20 | Tonen Chem Corp | ジカルボン酸類の二段階水素化法 |
| EP1108702A1 (en) * | 1999-12-13 | 2001-06-20 | Kvaerner Process Technology Limited | Process for the co-production of aliphatic diols and cyclic ethers |
-
2001
- 2001-07-12 GB GBGB0117090.1A patent/GB0117090D0/en not_active Ceased
-
2002
- 2002-07-10 CN CNB028111710A patent/CN1309714C/zh not_active Expired - Lifetime
- 2002-07-10 WO PCT/GB2002/003195 patent/WO2003006446A1/en active IP Right Grant
- 2002-07-10 JP JP2003512218A patent/JP4391816B2/ja not_active Expired - Fee Related
- 2002-07-10 EA EA200400173A patent/EA005339B1/ru not_active IP Right Cessation
- 2002-07-10 CA CA2451595A patent/CA2451595C/en not_active Expired - Fee Related
- 2002-07-10 EP EP02740957A patent/EP1404660B1/en not_active Expired - Lifetime
- 2002-07-10 US US10/483,524 patent/US6936727B2/en not_active Expired - Lifetime
- 2002-07-10 MX MXPA03010841 patent/MX234385B/es active IP Right Grant
- 2002-07-10 DE DE60204464T patent/DE60204464T2/de not_active Expired - Lifetime
- 2002-07-10 ES ES02740957T patent/ES2240759T3/es not_active Expired - Lifetime
- 2002-07-10 AT AT02740957T patent/ATE296816T1/de not_active IP Right Cessation
- 2002-07-10 AU AU2002314385A patent/AU2002314385B2/en not_active Ceased
- 2002-07-10 KR KR20037011701A patent/KR100607120B1/ko active IP Right Grant
- 2002-07-10 BR BRPI0211085-7A patent/BR0211085B1/pt not_active IP Right Cessation
- 2002-07-11 TW TW091115407A patent/TWI318975B/zh not_active IP Right Cessation
- 2002-07-11 MY MYPI20022637A patent/MY129064A/en unknown
- 2002-07-12 AR ARP020102602A patent/AR036338A1/es not_active Application Discontinuation
-
2003
- 2003-11-19 ZA ZA2003/09001A patent/ZA200309001B/en unknown
-
2004
- 2004-01-08 NO NO20040081A patent/NO328297B1/no not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| DE60204464T2 (de) | 2006-05-11 |
| KR100607120B1 (ko) | 2006-08-01 |
| CA2451595A1 (en) | 2003-01-23 |
| US6936727B2 (en) | 2005-08-30 |
| JP2005505516A (ja) | 2005-02-24 |
| CN1309714C (zh) | 2007-04-11 |
| US20040199026A1 (en) | 2004-10-07 |
| KR20040022413A (ko) | 2004-03-12 |
| WO2003006446A1 (en) | 2003-01-23 |
| EP1404660B1 (en) | 2005-06-01 |
| CA2451595C (en) | 2011-01-18 |
| TWI318975B (en) | 2010-01-01 |
| WO2003006446A8 (en) | 2003-08-14 |
| NO20040081L (pt) | 2004-01-08 |
| MY129064A (en) | 2007-03-30 |
| EA200400173A1 (ru) | 2004-06-24 |
| CN1512989A (zh) | 2004-07-14 |
| AU2002314385B2 (en) | 2007-09-20 |
| AR036338A1 (es) | 2004-09-01 |
| JP4391816B2 (ja) | 2009-12-24 |
| ES2240759T3 (es) | 2005-10-16 |
| EP1404660A1 (en) | 2004-04-07 |
| ATE296816T1 (de) | 2005-06-15 |
| GB0117090D0 (en) | 2001-09-05 |
| MXPA03010841A (es) | 2004-02-17 |
| MX234385B (es) | 2006-02-13 |
| BR0211085B1 (pt) | 2013-05-21 |
| BR0211085A (pt) | 2004-06-15 |
| ZA200309001B (en) | 2005-01-26 |
| EA005339B1 (ru) | 2005-02-24 |
| DE60204464D1 (de) | 2005-07-07 |
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