GB775961A - Hydrogenative reforming of gasoline and other naphtha fractions - Google Patents
Hydrogenative reforming of gasoline and other naphtha fractionsInfo
- Publication number
- GB775961A GB775961A GB23277/53A GB2327753A GB775961A GB 775961 A GB775961 A GB 775961A GB 23277/53 A GB23277/53 A GB 23277/53A GB 2327753 A GB2327753 A GB 2327753A GB 775961 A GB775961 A GB 775961A
- Authority
- GB
- United Kingdom
- Prior art keywords
- stage
- halogen
- alumina
- initial
- stages
- 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.)
- Expired
Links
Classifications
-
- 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
- C10G59/00—Treatment of naphtha by two or more reforming processes only or by at least one reforming process and at least one process which does not substantially change the boiling range of the naphtha
- C10G59/02—Treatment of naphtha by two or more reforming processes only or by at least one reforming process and at least one process which does not substantially change the boiling range of the naphtha plural serial stages only
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Abstract
Hydroforming of naphtha or gasoline is effected in several stages in the presence of a platinum catalyst having strong hydrogenatingdehydrogenating activity, in the initial stage there being absent the combination of alumina and gaseous halogen or halide, and in a subsequent stage only there being present with the platinum catalyst an alumina carrier and a minor amount of gaseous halogen or halide mixed with the stream of naphtha and hydrogen, whereby the initial stage is more favourable for hydrogenation than isomerization and the subsequent stage more favourable for isomerization. Platinum on alumina may be used in the initial stage and halogen added only to the effluent passing to the subsequent stage. Alternatively, aromatics formed in the initial stage may be separated, and the residual product only passed with halogen to the subsequent stage, the isomerized product then being recycled to the first stage preferably with fresh naphtha. The amount of halogen is generally at least 0.001 per cent by weight of the naphtha, and preferably 0.005-0.1, using catalysts containing up to 1 per cent Pt on activated alumina. Pressures may be higher in an initial stage or stages and lower in a subsequent stage or stages. Thus, with a C6-C8 charge, initial hydrogen partial pressure is not less than 400, e.g. 450-500 p.s.i., and pressure in a final stage is not above 300, e.g. 250 down to 150 p.s.i. With higher boiling fractions, higher pressures may be used. With cuts boiling over a range of more than 100 DEG F., the final stage pressure should be at 25 per cent less than that of the first stage. Temperatures are in general 850-1050 DEG F., liquid hourly space velocities 0.5-10, and hydrogen to oil molar ratio 3-10, being the same or different in the stages. The feed may be fractionated into higher and lower boiling fractions which are treated in separate series of reactors under different reaction conditions or the higher fraction may by-pass the initial stage subsequent stages. Naphthas of B.R. 180-400 DEG F. are preferably cut at about 260-300 DEG F. In an alternative method of operation, a carrier other than alumina, such as silica gel, activated carbon or other non-acidic carrier having little or no cracking activity is used in the initial stage. Hydrogen-rich gas from the final reactor may then be recycled to the initial one even if halogen is present.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US775961XA | 1953-04-09 | 1953-04-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB775961A true GB775961A (en) | 1957-05-29 |
Family
ID=22139003
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB23277/53A Expired GB775961A (en) | 1953-04-09 | 1953-08-24 | Hydrogenative reforming of gasoline and other naphtha fractions |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB775961A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3110661A (en) * | 1959-01-23 | 1963-11-12 | Texaco Inc | Treatment of hydrocarbons |
EP0027384A1 (en) * | 1979-10-15 | 1981-04-22 | Atlantic Richfield Company | Plural stage reforming with catalysts having a skewed distribution of a platinum-group metal and rhenium |
-
1953
- 1953-08-24 GB GB23277/53A patent/GB775961A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3110661A (en) * | 1959-01-23 | 1963-11-12 | Texaco Inc | Treatment of hydrocarbons |
EP0027384A1 (en) * | 1979-10-15 | 1981-04-22 | Atlantic Richfield Company | Plural stage reforming with catalysts having a skewed distribution of a platinum-group metal and rhenium |
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