GB769346A - Hydrogenation of crude hydrocarbon oils - Google Patents
Hydrogenation of crude hydrocarbon oilsInfo
- Publication number
- GB769346A GB769346A GB34648/54A GB3464854A GB769346A GB 769346 A GB769346 A GB 769346A GB 34648/54 A GB34648/54 A GB 34648/54A GB 3464854 A GB3464854 A GB 3464854A GB 769346 A GB769346 A GB 769346A
- Authority
- GB
- United Kingdom
- Prior art keywords
- line
- catalyst
- oil
- withdrawn
- reactor
- 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
- 239000003921 oil Substances 0.000 title abstract 12
- 238000005984 hydrogenation reaction Methods 0.000 title abstract 5
- 229930195733 hydrocarbon Natural products 0.000 title abstract 3
- 150000002430 hydrocarbons Chemical class 0.000 title abstract 3
- 239000004215 Carbon black (E152) Substances 0.000 title abstract 2
- 239000003054 catalyst Substances 0.000 abstract 16
- 239000002002 slurry Substances 0.000 abstract 6
- 239000007789 gas Substances 0.000 abstract 5
- 239000000203 mixture Substances 0.000 abstract 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 5
- 239000000463 material Substances 0.000 abstract 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract 2
- QZPSXPBJTPJTSZ-UHFFFAOYSA-N aqua regia Chemical compound Cl.O[N+]([O-])=O QZPSXPBJTPJTSZ-UHFFFAOYSA-N 0.000 abstract 2
- 238000001816 cooling Methods 0.000 abstract 2
- 239000002184 metal Substances 0.000 abstract 2
- 229910052751 metal Inorganic materials 0.000 abstract 2
- 230000003716 rejuvenation Effects 0.000 abstract 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 abstract 1
- 239000005864 Sulphur Substances 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 230000003197 catalytic effect Effects 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- KYYSIVCCYWZZLR-UHFFFAOYSA-N cobalt(2+);dioxido(dioxo)molybdenum Chemical compound [Co+2].[O-][Mo]([O-])(=O)=O KYYSIVCCYWZZLR-UHFFFAOYSA-N 0.000 abstract 1
- 238000002485 combustion reaction Methods 0.000 abstract 1
- 239000000356 contaminant Substances 0.000 abstract 1
- 239000010779 crude oil Substances 0.000 abstract 1
- 230000001066 destructive effect Effects 0.000 abstract 1
- 238000004821 distillation Methods 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 239000000446 fuel Substances 0.000 abstract 1
- 239000000295 fuel oil Substances 0.000 abstract 1
- 239000011874 heated mixture Substances 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 150000002739 metals Chemical class 0.000 abstract 1
- 238000002156 mixing Methods 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 230000000737 periodic effect Effects 0.000 abstract 1
- 230000008929 regeneration Effects 0.000 abstract 1
- 238000011069 regeneration method Methods 0.000 abstract 1
- 230000000630 rising effect Effects 0.000 abstract 1
- 238000005406 washing Methods 0.000 abstract 1
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
- C10G47/00—Cracking of hydrocarbon oils, in the presence of hydrogen or hydrogen- generating compounds, to obtain lower boiling fractions
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:0769346/III/1> In the catalytic destructive hydrogenation of crude hydrocarbon oil to obtain gas oil, the temperature of the reaction, which is carried out at a pressure of 200 to 750 p.s.i., is controlled by withdrawing oil from the hydrogenation zone, cooling the withdrawn oil, and then returning the cooled oil to the hydrogenation zone. The catalyst may be a metal of Group IV, V, VI or VIII of the periodic system, an oxide or sulphide of these metals, or a mixture thereof; the catalyst may be supported on activated alumina. The catalyst is separated from the products of hydrogenation, and is then regenerated for re-use by burning off the carbonaceous deposits with an oxygen-containing gas, followed if necessary by treatment with chlorine or with aqua regia which has been diluted with water. A sulphurous crude oil introduced through line 1 and hydrogen-containing gas supplied through line 2 are mixed in line 3; and the mixture is passed through furnace F. To the heated mixture is then added, in line 7, tail gas from reactor 8 and recycle oil together with a slurry of catalyst (cobalt molybdate supported on activated alumina) in oil from line 6. The mixture is charged to the bottom of reactor 8 which is maintained at a temperature of 700 DEG -850 DEG F. and a pressure of about 400 p.s.i.g. The expanded upper part of the reactor acts as a chamber which causes the catalyst to settle to the lower part, back-mixing being prevented by a plurality of perforated baffles B. The product is withdrawn from the reactor through line 13 and is charged, via pressure-reducing valve V, into distilling column 14, where it is fractionated under atmospheric pressure, steam being introduced into the column through line 16. Light hydrocarbons and steam are withdrawn from the head of the column, gasoline is withdrawn through line 18, and the main product-gas oil-is withdrawn via line 23. These products have a very low sulphur content. A bottoms fraction containing catalyst is taken off through line 24, and a portion of this fraction is pumped through line 27 to cooler 28 which contains coil 29 through which cold water is circulated. A portion of the material in the reactor is withdrawn from a middle-section via line 31, and this also passes through line 27 to the cooler. The cool material leaving the cooler is pumped to the reactor through lines 10 and 6. A portion of the bottoms fraction in line 24 is passed to settler 33, where the catalyst separates out and clear oil is decanted off through line 34. Since it contains a substantial proportion of the metallic contaminants present in the original feed, it is rejected from the system and may be used as fuel. A small proportion of the slurry withdrawn from the base of the settler is rejected through line 36, but the main portion is either returned to the reactor via line 37 and cooler 28, or is passed through cooler 40 to washing vessel 43 together with naphtha introduced through line 41. The naphtha removes heavy oily material from the catalyst. The solution of this heavy oil is withdrawn through line 48; and the naphtha may be recovered from it by distillation. The cleaned catalyst is withdrawn from the bottom of washer 43 as a slurry, part of which is pumped through lines 47 and 6 to the reactor. The remainder of the slurry is carried, by steam, up line 50 and through a reducing-valve into cyclone S. Dry catalyst collects at the base of the cyclone, and a mixture of steam and oil vapours pass off overhead. The dry catalyst is suspended in air in line 51, and is carried to regenerator 53 where it forms a dense fluidized bed while the carbonaceous and sulphurous deposits are removed therefrom by combustion. Cooling means 54 prevents the regeneration-temperature rising above 1200 DEG F. The catalyst may also be subjected to "rejuvenation," i.e. it is allowed to remain in contact with air at 1050 DEG -1200 DEG F. for 4 to 24 hours. The regenerated catalyst is withdrawn from the regenerator via line 56, passed through cooler 57 to cool it to about 600 DEG -800 DEG F., and mixed with feed-oil from line 58. The slurry, so formed, is pumped to the reactor. When regeneration and rejuvenation fail to restore the activity of the catalyst, a portion thereof is withdrawn from line 56 and is mixed in line 61 with aqua regia which has been diluted with water, the mixture being passed to treating zone 63. The treated catalyst is washed with water in zone 65 in order to remove acid; and the catalyst/water slurry is charged, together with feed-oil introduced through line 67 to column 14. Specification 497,382 is referred to.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US769346XA | 1953-12-31 | 1953-12-31 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB769346A true GB769346A (en) | 1957-03-06 |
Family
ID=22135079
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB34648/54A Expired GB769346A (en) | 1953-12-31 | 1954-11-30 | Hydrogenation of crude hydrocarbon oils |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB769346A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2222531A (en) * | 1988-06-30 | 1990-03-14 | Shell Int Research | Regeneration process for a Fischer-Tropsch catalyst |
| EP2199370A4 (en) * | 2007-09-28 | 2015-11-04 | Japan Oil Gas & Metals Jogmec | PROCESS FOR THE PRODUCTION OF SYNTHETIC NAPHTHA |
-
1954
- 1954-11-30 GB GB34648/54A patent/GB769346A/en not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2222531A (en) * | 1988-06-30 | 1990-03-14 | Shell Int Research | Regeneration process for a Fischer-Tropsch catalyst |
| EP2199370A4 (en) * | 2007-09-28 | 2015-11-04 | Japan Oil Gas & Metals Jogmec | PROCESS FOR THE PRODUCTION OF SYNTHETIC NAPHTHA |
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