GB593778A - Catalytic conversion of oils - Google Patents
Catalytic conversion of oilsInfo
- Publication number
- GB593778A GB593778A GB14916/45A GB1491645A GB593778A GB 593778 A GB593778 A GB 593778A GB 14916/45 A GB14916/45 A GB 14916/45A GB 1491645 A GB1491645 A GB 1491645A GB 593778 A GB593778 A GB 593778A
- Authority
- GB
- United Kingdom
- Prior art keywords
- tower
- refractory
- line
- heavy
- conversion
- 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
- C10G11/00—Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
- C10G11/14—Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils with preheated moving solid catalysts
- C10G11/18—Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils with preheated moving solid catalysts according to the "fluidised-bed" technique
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:0593778/III/1> <PICT:0593778/III/2> In processes for the catalytic conversion of hydrocarbons (including cracking, reforming, hydrogenation, dehydrogenation, isomerisation, polymerisation, desulphurisation) of the kind employing a fluidised catalyst system, improved control of the coke deposition on the catalyst and thus of the heat produced in the regeneration are obtained by feeding and simultaneous conversion of two stocks differing in their refractory nature, a higher boiling less refractory fraction through line 23 into the upper portion of the converter 17 and a lower boiling more refractory fraction through line 7 into the bottom of the catalyst bed. The conversion plant comprises converter 17, regenerator 20, products fractionator 29 and associated preheating furnaces 21, 22 and catalyst standpipes 18, 19, 24, 25. The respective fractions for conversion are obtained by stripping the crude in a tower 3 of gasoline and naphtha which are separated in tower 5. The partly reduced crude is heated in furnace 15 and fractionated in tower 9 to separate heavy naptha, light and heavy gasoil fractions through lines 10, 11, 12 respectively and a reduced crude is recovered as bottoms and passed through a further coil in furnace 15 the products being flashed in a tower 14 at temperatures of 700-840 DEG F. and under a pressure of 100 mm. with slight cracking if desired to recover a heavy flashed condensate which constitutes the less refractory stock fed through line 23 while the naphtha collected at bottom of tower 5 constitutes the more refractory stock fed through line 7. Gasoline is recovered overhead from tower 29 while a heavy aromatic fraction is collected through line 35 and fed to tank 41 where it is mixed with the tarry residues from flasher 14 to constitute a stable fuel oil. The fractionation may be controlled to separate more or less refractory fractions differing in respect to (a) molecular weight (b) content of nitrogen bases (c) naphthenic and olefinic content (d) paraffinic and olefinic content (e) aromatic and paraffinic content. The reactor, Fig. II, is adapted to converting two stocks simultaneously by providing an upper manifold 46 for the less refractory stock and a lower manifold 45 for the more refractory stock.ALSO:In processes for the catalytic conversion of hydrocarbons (including cracking, reforming, hydrogenation, dehydrogenation, isomerization, polymerization, desulphurization) of the kind employing a fluidised catalyst system, improved control of the coke deposition on the catalyst and thus of the heat produced in the regeneration and simultaneous conversion of two stocks differing in their refractory nature, are obtained by feeding the higher boiling less refractory fraction through line 23 into the upper portion of the converter 17 and the lower boiling more refractory fraction through line 7 into the bottom of the catalyst bed. The conversion plant comprises converter 17, regenerator 20, products fractionator 29 and associated preheating furnaces 21, 22 and catalyst standpipes 18, 19, 24, 25. The respective fractions for conversion are obtained by stripping the crude fed through line 1 to the mid-point of tower 3 of gasoline and naphtha which are separated in tower 5. The partly reduced crude is heated in furnace 15 and flashed in tower 9 to separate heavy naphtha, light and heavy gas oil fractions recovered through lines 10, 11, 12 respectively and a reduced crude is recovered as bottoms and passed through a further coil in furnace 15, the products being flashed in tower 14 at temperatures of 700-840 DEG F. under a pressure of 100 mm. with slight cracking if desired to recover a heavy flashed condensate which constitutes the less refractory stock fed through line 23 while the naphtha collected at bottom of tower 5 constitutes the more refractory stock fed through line 7. Gasoline is recovered <PICT:0593778/IV/1> <PICT:0593778/IV/2> overhead from tower 29 while a heavy aromatic fraction is collected through line 35 and fed to tank 41 where it is mixed with the tarry residues from flasher 14 to constitute a stable fuel oil. The fractionation may be controlled to separate more or less refractory fractions differing in respect to (a) molecular weight, (b) content of nitrogen bases, (c) naphthenic and olefinic content, (d) paraffinic and olefinic content, (e) aromatic and paraffinic content. The reactor, Fig. II, is adapted to converting two stocks simultaneously by providing an upper manifold 46 for the less refractory stock and a lower manifold 45 for the more refractory stock.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US547445A US2416608A (en) | 1944-07-31 | 1944-07-31 | Catalytic conversion of oils |
Publications (1)
Publication Number | Publication Date |
---|---|
GB593778A true GB593778A (en) | 1947-10-24 |
Family
ID=24184669
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB14916/45A Expired GB593778A (en) | 1944-07-31 | 1945-06-12 | Catalytic conversion of oils |
Country Status (3)
Country | Link |
---|---|
US (1) | US2416608A (en) |
FR (1) | FR938955A (en) |
GB (1) | GB593778A (en) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2461958A (en) * | 1944-12-14 | 1949-02-15 | Standard Oil Dev Co | Treating hydrocarbon fluids |
US2498840A (en) * | 1947-11-14 | 1950-02-28 | Standard Oil Dev Co | Catalytic cracking of diisobutylene |
US2586705A (en) * | 1948-02-14 | 1952-02-19 | Standard Oil Dev Co | Means for distributing solids in gases in catalytic apparatus |
US2689209A (en) * | 1949-12-27 | 1954-09-14 | Phillips Petroleum Co | Catalytic treatment of hydrocarbons |
US2779717A (en) * | 1950-12-15 | 1957-01-29 | Socony Mobil Oil Co Inc | Method of distilling a high boiling hydrocarbon oil for use as a feed in catalytic cracking |
US2762754A (en) * | 1951-12-20 | 1956-09-11 | Gulf Oil Corp | Thermal conversion of reduced crudes |
US2789083A (en) * | 1952-04-09 | 1957-04-16 | Exxon Research Engineering Co | Deashing of hydrocarbon oils |
US2755229A (en) * | 1953-07-02 | 1956-07-17 | Gulf Research Development Co | Stabilization of fuel oil |
NL83381C (en) * | 1953-08-10 | 1956-06-15 | ||
US2890164A (en) * | 1954-12-29 | 1959-06-09 | Pure Oil Co | Catalytic cracking process |
US2913391A (en) * | 1955-05-26 | 1959-11-17 | Exxon Research Engineering Co | Integrated process for production of improved asphalt |
US2923678A (en) * | 1958-06-12 | 1960-02-02 | Lummus Co | Continuous contact coking of two feeds with the second feed entering upstream of the first feed |
US4376038A (en) * | 1979-11-14 | 1983-03-08 | Ashland Oil, Inc. | Use of naphtha as riser diluent in carbo-metallic oil conversion |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2335684A (en) * | 1943-11-30 | Catalytic reforming | ||
US1413260A (en) * | 1919-03-31 | 1922-04-18 | Standard Oil Co | Process of distilling crude petroleum and product thereof |
US2253486A (en) * | 1939-05-20 | 1941-08-19 | Belchetz Arnold | Catalytic conversion of hydrocarbons |
US2324165A (en) * | 1939-09-13 | 1943-07-13 | Standard Oil Co | Dehydroaromatization |
US2338573A (en) * | 1939-09-13 | 1944-01-04 | Kellogg M W Co | Catalytically processing hydrocarbon oils |
US2356611A (en) * | 1939-11-18 | 1944-08-22 | Peters Kurt | Process for catalytic conversion of hydrocarbons |
US2327510A (en) * | 1940-03-30 | 1943-08-24 | Universal Oil Prod Co | Conversion of hydrocarbon oils |
US2377613A (en) * | 1940-12-09 | 1945-06-05 | Standard Oil Co | Powdered catalyst conversion |
US2379966A (en) * | 1940-12-31 | 1945-07-10 | Standard Oil Co | Hydrocarbon conversion system |
US2379711A (en) * | 1941-09-12 | 1945-07-03 | Standard Oil Dev Co | Catalytic conversion of hydrocarbon oils |
US2356697A (en) * | 1941-12-27 | 1944-08-22 | Standard Oil Dev Co | Treating hydrocarbon fluids |
US2385825A (en) * | 1942-07-08 | 1945-10-02 | Graviner Manufacturing Co | Electrical fire preventing system for aircraft |
US2360622A (en) * | 1943-04-30 | 1944-10-17 | Standard Oil Dev Co | Method of producing aviation gasoline |
-
1944
- 1944-07-31 US US547445A patent/US2416608A/en not_active Expired - Lifetime
-
1945
- 1945-06-12 GB GB14916/45A patent/GB593778A/en not_active Expired
- 1945-10-17 FR FR938955D patent/FR938955A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
FR938955A (en) | 1948-10-29 |
US2416608A (en) | 1947-02-25 |
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