UA80097C2 - Process for the production of triptane - Google Patents
Process for the production of triptane Download PDFInfo
- Publication number
- UA80097C2 UA80097C2 UA2004032372A UA2004032372A UA80097C2 UA 80097 C2 UA80097 C2 UA 80097C2 UA 2004032372 A UA2004032372 A UA 2004032372A UA 2004032372 A UA2004032372 A UA 2004032372A UA 80097 C2 UA80097 C2 UA 80097C2
- Authority
- UA
- Ukraine
- Prior art keywords
- carbon atoms
- hydrocarbon
- vol
- acid
- hydrocarbons
- Prior art date
Links
- ZISSAWUMDACLOM-UHFFFAOYSA-N triptane Chemical compound CC(C)C(C)(C)C ZISSAWUMDACLOM-UHFFFAOYSA-N 0.000 title claims abstract description 34
- 238000000034 method Methods 0.000 title claims abstract description 27
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 55
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract description 55
- 239000004215 Carbon black (E152) Substances 0.000 claims abstract description 39
- 239000003054 catalyst Substances 0.000 claims abstract description 27
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 13
- 238000006317 isomerization reaction Methods 0.000 claims abstract description 12
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 7
- 239000001257 hydrogen Substances 0.000 claims abstract description 7
- 239000000463 material Substances 0.000 claims description 31
- 125000004432 carbon atom Chemical group C* 0.000 claims description 21
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 15
- 239000007858 starting material Substances 0.000 claims description 15
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 claims description 12
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 12
- 239000010457 zeolite Substances 0.000 claims description 11
- QWHNJUXXYKPLQM-UHFFFAOYSA-N 1,1-dimethylcyclopentane Chemical class CC1(C)CCCC1 QWHNJUXXYKPLQM-UHFFFAOYSA-N 0.000 claims description 10
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 claims description 10
- 229910052751 metal Inorganic materials 0.000 claims description 9
- 239000002184 metal Substances 0.000 claims description 9
- 150000001491 aromatic compounds Chemical class 0.000 claims description 8
- 239000002841 Lewis acid Substances 0.000 claims description 7
- 150000007517 lewis acids Chemical class 0.000 claims description 7
- 238000007142 ring opening reaction Methods 0.000 claims description 7
- 239000007848 Bronsted acid Substances 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 5
- 125000005843 halogen group Chemical group 0.000 claims description 5
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 claims description 5
- QEGNUYASOUJEHD-UHFFFAOYSA-N 1,1-dimethylcyclohexane Chemical compound CC1(C)CCCCC1 QEGNUYASOUJEHD-UHFFFAOYSA-N 0.000 claims description 4
- XAZKFISIRYLAEE-UHFFFAOYSA-N 1,3-dimethylcyclopentane Chemical compound CC1CCC(C)C1 XAZKFISIRYLAEE-UHFFFAOYSA-N 0.000 claims description 4
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 claims description 4
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 claims description 4
- IFTRQJLVEBNKJK-UHFFFAOYSA-N Ethylcyclopentane Chemical compound CCC1CCCC1 IFTRQJLVEBNKJK-UHFFFAOYSA-N 0.000 claims description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 4
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 claims description 4
- OCKPCBLVNKHBMX-UHFFFAOYSA-N butylbenzene Chemical compound CCCCC1=CC=CC=C1 OCKPCBLVNKHBMX-UHFFFAOYSA-N 0.000 claims description 4
- IIEWJVIFRVWJOD-UHFFFAOYSA-N ethylcyclohexane Chemical compound CCC1CCCCC1 IIEWJVIFRVWJOD-UHFFFAOYSA-N 0.000 claims description 4
- UQSQSQZYBQSBJZ-UHFFFAOYSA-N fluorosulfonic acid Chemical compound OS(F)(=O)=O UQSQSQZYBQSBJZ-UHFFFAOYSA-N 0.000 claims description 4
- GDOPTJXRTPNYNR-UHFFFAOYSA-N methylcyclopentane Chemical compound CC1CCCC1 GDOPTJXRTPNYNR-UHFFFAOYSA-N 0.000 claims description 4
- 150000004965 peroxy acids Chemical class 0.000 claims description 4
- 238000009835 boiling Methods 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 3
- 230000000737 periodic effect Effects 0.000 claims description 3
- ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical compound OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 claims description 3
- RIRARCHMRDHZAR-UHFFFAOYSA-N 1,2-dimethylcyclopentane Chemical compound CC1CCCC1C RIRARCHMRDHZAR-UHFFFAOYSA-N 0.000 claims description 2
- -1 for example Chemical compound 0.000 claims description 2
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 claims description 2
- HLTMUYBTNSVOFY-UHFFFAOYSA-N pentylcyclohexane Chemical compound CCCCCC1CCCCC1 HLTMUYBTNSVOFY-UHFFFAOYSA-N 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 238000002203 pretreatment Methods 0.000 claims 1
- 238000012876 topography Methods 0.000 claims 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract description 2
- BZHMBWZPUJHVEE-UHFFFAOYSA-N 2,4-dimethylpentane Chemical compound CC(C)CC(C)C BZHMBWZPUJHVEE-UHFFFAOYSA-N 0.000 description 8
- WGECXQBGLLYSFP-UHFFFAOYSA-N (+-)-2,3-dimethyl-pentane Natural products CCC(C)C(C)C WGECXQBGLLYSFP-UHFFFAOYSA-N 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 7
- JVSWJIKNEAIKJW-UHFFFAOYSA-N 2-Methylheptane Chemical compound CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 6
- 239000003085 diluting agent Substances 0.000 description 5
- CXOWYJMDMMMMJO-UHFFFAOYSA-N 2,2-dimethylpentane Chemical compound CCCC(C)(C)C CXOWYJMDMMMMJO-UHFFFAOYSA-N 0.000 description 4
- GXDHCNNESPLIKD-UHFFFAOYSA-N 2-methylhexane Chemical compound CCCCC(C)C GXDHCNNESPLIKD-UHFFFAOYSA-N 0.000 description 4
- AEXMKKGTQYQZCS-UHFFFAOYSA-N 3,3-dimethylpentane Chemical compound CCC(C)(C)CC AEXMKKGTQYQZCS-UHFFFAOYSA-N 0.000 description 4
- AORMDLNPRGXHHL-UHFFFAOYSA-N 3-ethylpentane Chemical compound CCC(CC)CC AORMDLNPRGXHHL-UHFFFAOYSA-N 0.000 description 4
- VLJXXKKOSFGPHI-UHFFFAOYSA-N 3-methylhexane Chemical compound CCCC(C)CC VLJXXKKOSFGPHI-UHFFFAOYSA-N 0.000 description 4
- AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 4
- QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 description 4
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 150000001923 cyclic compounds Chemical class 0.000 description 3
- 125000004122 cyclic group Chemical group 0.000 description 3
- PFEOZHBOMNWTJB-UHFFFAOYSA-N 3-methylpentane Chemical compound CCC(C)CC PFEOZHBOMNWTJB-UHFFFAOYSA-N 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 229910021536 Zeolite Inorganic materials 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000002336 sorption--desorption measurement Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- ODNBVEIAQAZNNM-UHFFFAOYSA-N 1-(6-chloroimidazo[1,2-b]pyridazin-3-yl)ethanone Chemical compound C1=CC(Cl)=NN2C(C(=O)C)=CN=C21 ODNBVEIAQAZNNM-UHFFFAOYSA-N 0.000 description 1
- LNKQQZFLNUVWQQ-UHFFFAOYSA-N 1-chloro-2,2-bis(4'-chlorophenyl)ethylene Chemical compound C=1C=C(Cl)C=CC=1C(=CCl)C1=CC=C(Cl)C=C1 LNKQQZFLNUVWQQ-UHFFFAOYSA-N 0.000 description 1
- KLZUFWVZNOTSEM-UHFFFAOYSA-K Aluminium flouride Chemical compound F[Al](F)F KLZUFWVZNOTSEM-UHFFFAOYSA-K 0.000 description 1
- 229910021630 Antimony pentafluoride Inorganic materials 0.000 description 1
- GUNJVIDCYZYFGV-UHFFFAOYSA-K Antimony trifluoride Inorganic materials F[Sb](F)F GUNJVIDCYZYFGV-UHFFFAOYSA-K 0.000 description 1
- 239000005935 Sulfuryl fluoride Substances 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 229910000323 aluminium silicate Inorganic materials 0.000 description 1
- VBVBHWZYQGJZLR-UHFFFAOYSA-I antimony pentafluoride Chemical compound F[Sb](F)(F)(F)F VBVBHWZYQGJZLR-UHFFFAOYSA-I 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000003729 cation exchange resin Substances 0.000 description 1
- 229940023913 cation exchange resins Drugs 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000000975 co-precipitation Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000020335 dealkylation Effects 0.000 description 1
- 238000006900 dealkylation reaction Methods 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
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 238000007580 dry-mixing Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000005755 formation reaction Methods 0.000 description 1
- 238000013467 fragmentation Methods 0.000 description 1
- 238000006062 fragmentation reaction Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910001512 metal fluoride Inorganic materials 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- 229910052680 mordenite Inorganic materials 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 238000006462 rearrangement reaction Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000007086 side reaction Methods 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
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- OBTWBSRJZRCYQV-UHFFFAOYSA-N sulfuryl difluoride Chemical compound FS(F)(=O)=O OBTWBSRJZRCYQV-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C9/00—Aliphatic saturated hydrocarbons
- C07C9/14—Aliphatic saturated hydrocarbons with five to fifteen carbon atoms
- C07C9/16—Branched-chain hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/22—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by isomerisation
- C07C5/27—Rearrangement of carbon atoms in the hydrocarbon skeleton
- C07C5/2702—Catalytic processes not covered by C07C5/2732 - C07C5/31; Catalytic processes covered by both C07C5/2732 and C07C5/277 simultaneously
- C07C5/271—Catalytic processes not covered by C07C5/2732 - C07C5/31; Catalytic processes covered by both C07C5/2732 and C07C5/277 simultaneously with inorganic acids; with salts or anhydrides of acids
- C07C5/2718—Acids of halogen; Salts thereof; complexes thereof with organic compounds
- C07C5/2721—Metal halides; Complexes thereof with organic compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C7/00—Purification; Separation; Use of additives
- C07C7/148—Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound
- C07C7/163—Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound by hydrogenation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
- C07C2523/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of noble metals
- C07C2523/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of noble metals of the platinum group metals
- C07C2523/44—Palladium
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
- C07C2523/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of noble metals
- C07C2523/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of noble metals of the platinum group metals
- C07C2523/46—Ruthenium, rhodium, osmium or iridium
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
- C07C2523/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of the iron group metals or copper
- C07C2523/74—Iron group metals
- C07C2523/745—Iron
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
- C07C2523/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of the iron group metals or copper
- C07C2523/74—Iron group metals
- C07C2523/75—Cobalt
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
- C07C2523/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of the iron group metals or copper
- C07C2523/74—Iron group metals
- C07C2523/755—Nickel
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2527/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- C07C2527/02—Sulfur, selenium or tellurium; Compounds thereof
- C07C2527/03—Acids of sulfur other than sulfhydric acid or sulfuric acid, e.g. halosulfonic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2527/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- C07C2527/06—Halogens; Compounds thereof
- C07C2527/08—Halides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- C07C2531/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- C07C2531/025—Sulfonic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- C07C2531/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- C07C2531/04—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing carboxylic acids or their salts
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2400/00—Products obtained by processes covered by groups C10G9/00 - C10G69/14
- C10G2400/02—Gasoline
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Analytical Chemistry (AREA)
- Water Supply & Treatment (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- General Factory Administration (AREA)
- Automobile Manufacture Line, Endless Track Vehicle, Trailer (AREA)
- Extrusion Moulding Of Plastics Or The Like (AREA)
- Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0121105.1A GB0121105D0 (en) | 2001-08-31 | 2001-08-31 | An improved process for the production of triptane |
| PCT/GB2002/003752 WO2003020668A1 (en) | 2001-08-31 | 2002-08-15 | A process for the production of triptane |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| UA80097C2 true UA80097C2 (en) | 2007-08-27 |
Family
ID=9921281
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| UA2004032372A UA80097C2 (en) | 2001-08-31 | 2002-08-15 | Process for the production of triptane |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US7332638B2 (de) |
| EP (1) | EP1421047B1 (de) |
| JP (1) | JP4307257B2 (de) |
| AT (1) | ATE342876T1 (de) |
| AU (1) | AU2002313548B2 (de) |
| DE (1) | DE60215520T2 (de) |
| ES (1) | ES2272750T3 (de) |
| GB (1) | GB0121105D0 (de) |
| RU (1) | RU2296735C2 (de) |
| UA (1) | UA80097C2 (de) |
| WO (1) | WO2003020668A1 (de) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0320684D0 (en) * | 2003-09-03 | 2003-10-01 | Bp Chem Int Ltd | Process |
| US7825287B2 (en) * | 2008-03-28 | 2010-11-02 | The Regents Of The University Of California | Process for production of triptane and triptene |
| DE102008024891B4 (de) * | 2008-05-16 | 2019-09-12 | Dr. Ing. H.C. F. Porsche Aktiengesellschaft | Kraftfahrzeug |
| DE102008024896B4 (de) * | 2008-05-16 | 2017-03-23 | Dr. Ing. H.C. F. Porsche Aktiengesellschaft | Luftleiteinrichtung |
| DE102008024892B4 (de) * | 2008-05-16 | 2019-06-19 | Dr. Ing. H.C. F. Porsche Aktiengesellschaft | Luftleiteinrichtung |
| DE102008024895B4 (de) * | 2008-05-16 | 2017-03-23 | Dr. Ing. H.C. F. Porsche Aktiengesellschaft | Luftleiteinrichtung |
| BR102019024934B1 (pt) | 2019-11-26 | 2022-02-22 | Petróleo Brasileiro S.A. - Petrobras | Processo para obtenção de compostos, dentre os quais o triptano por reação de acoplamento de álcoois |
| JP7299252B2 (ja) | 2021-01-20 | 2023-06-27 | 本田技研工業株式会社 | トリプタンの製造装置および製造方法 |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3415736A (en) | 1965-09-20 | 1968-12-10 | Mobil Oil Corp | Lithium-containing crystalline aluminosilicate |
| US3766286A (en) * | 1971-06-25 | 1973-10-16 | Exxon Research Engineering Co | Process for the isomerization of hydrocarbons |
| US3878261A (en) * | 1973-08-24 | 1975-04-15 | Phillips Petroleum Co | Hydroisomerization of paraffin hydrocarbon with a supported catalyst of SbF{HD 5 {B and CF{HD 3{B SO{HD 3{B H |
| US3972983A (en) | 1974-11-25 | 1976-08-03 | Mobil Oil Corporation | Crystalline zeolite ZSM-20 and method of preparing same |
| US4714601A (en) | 1984-05-04 | 1987-12-22 | Exxon Research And Engineering Co. | Process for preparing a high silica faujasite aluminosilicate, ECR-4 |
| US4879103A (en) | 1984-05-04 | 1989-11-07 | Exxon Research And Engineering Company | Composition and process for preparing ECR-30 |
| US4931267A (en) | 1987-11-19 | 1990-06-05 | Exxon Research And Engineering Company | Process for preparing a high silica zeolite having the faujasite topology, ECR-32 |
| US5116590A (en) | 1991-07-09 | 1992-05-26 | Exxon Research And Engineering Company | Crystalline zeolite ECR-35 and a method for producing same |
| AU665965B2 (en) * | 1991-10-25 | 1996-01-25 | Mobil Oil Corporation | Combined paraffin isomerization/ring opening process |
| US5763731A (en) | 1995-09-05 | 1998-06-09 | Exxon Research And Engineering Company | Process for selectively opening naphthenic rings |
| WO1997009290A1 (en) | 1995-09-05 | 1997-03-13 | Exxon Research And Engineering Company | Process for selectively opening naphthenic rings |
| GB9623934D0 (en) | 1996-11-18 | 1997-01-08 | Bp Oil Int | Fuel composition |
| EG22450A (en) | 1998-03-26 | 2003-02-26 | Bp Oil Int | Fuel composition |
| DE69903562T2 (de) | 1998-08-04 | 2003-02-20 | Bp Oil International Ltd., London | Delaminierter mikroporöser feststoff |
| EP1326947B1 (de) * | 2000-10-11 | 2004-09-22 | Bp Oil International Limited | Isomerizationsverfahren |
-
2001
- 2001-08-31 GB GBGB0121105.1A patent/GB0121105D0/en not_active Ceased
-
2002
- 2002-08-15 RU RU2004109919/04A patent/RU2296735C2/ru not_active IP Right Cessation
- 2002-08-15 WO PCT/GB2002/003752 patent/WO2003020668A1/en active IP Right Grant
- 2002-08-15 AT AT02753142T patent/ATE342876T1/de not_active IP Right Cessation
- 2002-08-15 US US10/487,460 patent/US7332638B2/en not_active Expired - Fee Related
- 2002-08-15 AU AU2002313548A patent/AU2002313548B2/en not_active Ceased
- 2002-08-15 DE DE60215520T patent/DE60215520T2/de not_active Expired - Lifetime
- 2002-08-15 UA UA2004032372A patent/UA80097C2/uk unknown
- 2002-08-15 JP JP2003524941A patent/JP4307257B2/ja not_active Expired - Fee Related
- 2002-08-15 ES ES02753142T patent/ES2272750T3/es not_active Expired - Lifetime
- 2002-08-15 EP EP02753142A patent/EP1421047B1/de not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| RU2004109919A (ru) | 2005-10-20 |
| DE60215520D1 (de) | 2006-11-30 |
| EP1421047B1 (de) | 2006-10-18 |
| US20040249228A1 (en) | 2004-12-09 |
| DE60215520T2 (de) | 2007-09-20 |
| US7332638B2 (en) | 2008-02-19 |
| JP4307257B2 (ja) | 2009-08-05 |
| AU2002313548B2 (en) | 2008-04-24 |
| EP1421047A1 (de) | 2004-05-26 |
| GB0121105D0 (en) | 2001-10-24 |
| JP2005501894A (ja) | 2005-01-20 |
| RU2296735C2 (ru) | 2007-04-10 |
| ES2272750T3 (es) | 2007-05-01 |
| ATE342876T1 (de) | 2006-11-15 |
| WO2003020668A1 (en) | 2003-03-13 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Guisnet et al. | Mechanism of short-chain alkane transformation over protonic zeolites. Alkylation, disproportionation and aromatization | |
| US4886926A (en) | Catalytic dehydrogenation of hydrocarbons over tin-containing crystalline microporous materials | |
| Guisnet et al. | Organic chemistry of coke formation | |
| Smirniotis et al. | Comparison between zeolite β and γ-Al2O3 supported Pt for reforming reactions | |
| US3315007A (en) | Dehydrogenation of saturated hydrocarbons over noble-metal catalyst | |
| US20090163757A1 (en) | Linear olefin isomer isomerization using molecular sieve catalysts | |
| Yao et al. | Pt-promoted and Hβ zeolite-supported Ni2P catalysts for hydroisomerisation of n-heptane | |
| US5968343A (en) | Hydrocarbon conversion catalyst composition and processes therefor and therewith | |
| KR20170084025A (ko) | 혼합 금속 산화물-제올라이트 담체 상의 복분해 촉매 및 그것의 사용을 위한 방법 | |
| UA80097C2 (en) | Process for the production of triptane | |
| US3975299A (en) | Production of acid hydrocarbon conversion catalysts | |
| US20070246400A1 (en) | Zeolite Catalysts | |
| US4177219A (en) | Process for selective ethyl scission of ethylaromatics to methylaromatics | |
| BRPI0615895B1 (pt) | método para produzir etileno e propileno | |
| García-Gutiérrez et al. | Study of selectivity of MoO3-catalyzed C6–C7 hydrocarbons hydroisomerization: Mechanistic insights into the formation of carbonaceous deposits on the catalyst surface | |
| EP3371140B1 (de) | Verfahren zur umwandlung von acyclischen c5-verbindungen in cyclische c5-verbindungen | |
| Weitkamp et al. | Direct conversion of aromatics into a synthetic steamcracker feed using bifunctional zeolite catalysts | |
| AU2002313548A1 (en) | A process for the production of triptane | |
| Shou et al. | Cracking of Butane on a Pt/H-ZSM-5 Catalyst in the Presence of Hydrogen | |
| Jacobs et al. | Comparison of acid-to metal-catalysed conversion of n-decane and cyclodecane on ZSM-5 and faujasite-type zeolites | |
| US20240182796A1 (en) | Production of monoaromatic hydrocarbons from hydrocarbon feedstocks | |
| JP3061897B2 (ja) | 合成結晶アルミノケイ酸塩および石油化学プロセスで炭化水素を触媒反応させる方法 | |
| Csicsery | Reactions of n-butylbenzene over supported platinum catalysts | |
| Khasanova et al. | A study of propane aromatization on a zeolite-containing catalyst with different Si/Al ratios | |
| US6583330B1 (en) | Catalysts containing heteropolyanions usable in processes for conversion of paraffins |