GB818836A - Improvements in or relating to reforming naphtha - Google Patents
Improvements in or relating to reforming naphthaInfo
- Publication number
- GB818836A GB818836A GB32991/57A GB3299157A GB818836A GB 818836 A GB818836 A GB 818836A GB 32991/57 A GB32991/57 A GB 32991/57A GB 3299157 A GB3299157 A GB 3299157A GB 818836 A GB818836 A GB 818836A
- Authority
- GB
- United Kingdom
- Prior art keywords
- line
- reformate
- naphtha
- hydrogen
- vol
- 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
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/04—Liquid carbonaceous fuels essentially based on blends of hydrocarbons
- C10L1/06—Liquid carbonaceous fuels essentially based on blends of hydrocarbons for spark ignition
-
- 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
- C10G59/06—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 parallel 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
<PICT:0818836/IV (b)/1> A naphtha is reformed by first distilling to obtain a light naphtha boiling up to about 200 DEG F. and a heavy naphtha which latter is reformed over a platinum-alumina catalyst and the reformate distilled to obtain a light reformate boiling up to about 200 DEG F. which is combined with the light naphtha and reformed over an alkalized chromia-alumina catalyst at 0-200 p.s.i.g. in the presence or absence of hydrogen and the reformate so obtained blended with the heavy platinum reformate. The naphtha is fed into distillation tower 11 from which C4 and lighter hydrocarbons are removed overhead, a C5-C7 fraction having an end point of 200 \sB 15 DEG F. is removed by line 13, a 200-360 DEG F. fraction by line 14 and heavier materials as bottoms. The fraction in line 14 may be desulphurized before reforming; the charge to the reforming stage 16 may contain 5-30 p.p.m. sulphur, 1-10 p.p.m. chloride, 2-20 p.p.m. water and less than 5 p.p.m. nitrogen. It is reformed over a platinum catalyst in the presence of hydrogen at 100-400 p.s.i.g. and 850-1000 DEG F. with a space velocity of 0.1-10 vol./vol./hr. and a hydrogen recycle rate of 1000-8000 S.C.F./barrel of hydrogen employing three heater-reactor stages. The reformate is debutanized and then fractionated in tower 22, the heavier product being removed by line 29 and the C5-200 DEG F. overhead being recycled by line 28 to join the light naphtha charge in line 13. This light feed is reformed over an alkalized chromia-alumina catalyst containing for example 18 per cent Cr2O3, 4 per cent K2O, 4 per cent SiO2 and 74 per cent Al2O3. Conditions employed are 0-200 p.s.i.g., preferably about 25 p.s.i.g., 975-1125 DEG F. and a space velocity of 0.1-10 vol./vol./hr. Hydrogen may be recycled if a fluidized catalyst is used. The reformate is debutanized and led by line 35 to be blended with the heavy platinum reformate in line 29.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US619547A US2918422A (en) | 1956-10-31 | 1956-10-31 | Reforming-hydroforming system |
Publications (1)
Publication Number | Publication Date |
---|---|
GB818836A true GB818836A (en) | 1959-08-26 |
Family
ID=24482351
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB32991/57A Expired GB818836A (en) | 1956-10-31 | 1957-10-22 | Improvements in or relating to reforming naphtha |
Country Status (5)
Country | Link |
---|---|
US (1) | US2918422A (en) |
DE (1) | DE1062859B (en) |
FR (1) | FR1210653A (en) |
GB (1) | GB818836A (en) |
NL (1) | NL104749C (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3017344A (en) * | 1958-05-05 | 1962-01-16 | Texaco Inc | Serial reforming of hydrocarbons |
US3016344A (en) * | 1958-08-27 | 1962-01-09 | Houdry Process Corp | Upgrading natural gasoline |
US4246094A (en) * | 1979-06-11 | 1981-01-20 | Standard Oil Company (Indiana) | Process for upgrading naphtha hydrocarbons |
US4347123A (en) * | 1980-05-05 | 1982-08-31 | Exxon Research & Engineering Co. | Reforming with multimetallic catalysts |
US9890335B2 (en) | 2014-07-22 | 2018-02-13 | Uop Llc | Methods and systems for removing sulfur compounds from a hydrocarbon stream |
WO2019191113A1 (en) * | 2018-03-27 | 2019-10-03 | Phillips 66 Company | Catalytic activation of isopentane-enriched mixtures |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2349045A (en) * | 1939-09-18 | 1944-05-16 | Standard Oil Co | Dehydro-aromatization |
US2409695A (en) * | 1943-01-30 | 1946-10-22 | Standard Oil Dev Co | Method for improving aviation fuels |
US2573149A (en) * | 1948-11-20 | 1951-10-30 | Universal Oil Prod Co | Three-stage catalytic process for the reforming of gasoline |
US2653175A (en) * | 1951-05-04 | 1953-09-22 | Sun Oil Co | Preparation of aromatic hydrocarbons |
US2758062A (en) * | 1951-09-04 | 1956-08-07 | Exxon Research Engineering Co | Two-stage hydroforming process |
FR1067976A (en) * | 1951-09-04 | 1954-06-21 | Standard Oil Dev Co | Two-stage hydroformation process |
BE516505A (en) * | 1951-12-28 | |||
US2767124A (en) * | 1952-04-29 | 1956-10-16 | Phillips Petroleum Co | Catalytic reforming process |
NL92559C (en) * | 1952-10-07 |
-
0
- NL NL104749D patent/NL104749C/xx active
-
1956
- 1956-10-31 US US619547A patent/US2918422A/en not_active Expired - Lifetime
-
1957
- 1957-10-22 GB GB32991/57A patent/GB818836A/en not_active Expired
- 1957-10-29 FR FR1210653D patent/FR1210653A/en not_active Expired
- 1957-10-30 DE DEST13111A patent/DE1062859B/en active Pending
Also Published As
Publication number | Publication date |
---|---|
NL104749C (en) | |
FR1210653A (en) | 1960-03-10 |
US2918422A (en) | 1959-12-22 |
DE1062859B (en) | 1959-08-06 |
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