GB463244A - A process for manufacturing olefines - Google Patents
A process for manufacturing olefinesInfo
- Publication number
- GB463244A GB463244A GB31849/36A GB3184936A GB463244A GB 463244 A GB463244 A GB 463244A GB 31849/36 A GB31849/36 A GB 31849/36A GB 3184936 A GB3184936 A GB 3184936A GB 463244 A GB463244 A GB 463244A
- Authority
- GB
- United Kingdom
- Prior art keywords
- tower
- line
- gases
- distillate
- vapours
- 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
- C10G9/00—Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (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:0463244/IV/1> Olefines containing 3 to 5 carbon atoms per molecule are obtained from a gasoline type hydrocarbon distillate, i.e. a distillate of low aromatic content and of boiling range about 40--200 DEG C. and derived from the distillation, cracking or hydrogenation of carbonaceous materials, by subjecting the distillate and a recycle stock, to a temperature of 525--650 DEG C. for a time sufficient to convert 10--25 per cent of the mixture, quenching the converted mixture, fractionating the products to separate them into a light fraction comprising pentanes and lighter hydrocarbons, an intermediate fraction free from hydrocarbons containing 5 and less carbon atoms in the molecule and a residue, and returning a portion of the intermediate fraction as the recycle stock referred to above. The distillate is heated to 550--650 DEG C. while passing through a coil 2 and then flows into the bottom of a fractioning tower 5 together with quenching oil introduced through a line 51. Residues are removed through a cooler 7 while vapours pass to a tower 10 where they are fractionated into an intermediate stock which is returned through the line 12 as recycle stock and in part as reflux to the tower 5, and vapours which are fractionated in a tower 14 into vapours comprising pentanes and lighter hydrocarbons and bottoms free therefrom. The vapours are compressed and partially liquefied in a condenser 17 and the condensate is separated from gases in a separator 18. The condensate is freed from dissolved gases in a reboiler fractionator 23--24, the separated gases passing with the gases from the separator 18 into an absorption unit comprising an absorber 26, condenser 28, absorption oil recovery tower 34, and p cooler 37, the lean absorption oil being recycled through the line 39. The gasoline fraction obtained as bottoms in the tower 14 is stabilized in a tower 41 and sent to a storage tank 47 from which it is pumped as quenching oil to the line 51 or as reflux to the line 50. The gases obtained from the stabilization are mixed with the olefine fraction passing from the tower 34 and after further fractionation in towers 44, 57 are collected in storage tanks C.ALSO:<PICT:0463244/III/1> Olefines containing 3 to 5 carbon atoms per molecule are obtained from a gasoline type hydrocarbon distillate, i.e. a distillate of low aromatic content and of boiling range about 40--200 DEG C. derived from the distillation, cracking or hydrogenation of carbonaceous materials, by subjecting the distillate and a recycle stock to a temperature of 525--650 DEG C. for a time sufficient to convert 10--25 per cent of the mixture, quenching the converted mixture, fractionating the products to separate them into a light fraction comprising pentanes and lighter hydrocarbons, an intermediate fraction free from hydrocarbons containing 5 and less carbon atoms in the molecule, and a residue, and returning a portion of the intermediate fraction as the recycle stock referred to above. The cracked products may be quenched by contact with water, steam or a distillate produced in the process. The distillate is heated to 550--650 DEG C. while passing through a coil 2 and then flows into the bottom of a fractionating tower 5 together with quenching oil introduced through a line 51. Residues are removed through a cooler 7 while vapours pass to a tower 10 where they are fractionated into an intermediate stock, which is returned through the line 12 as recycle stock and in part as reflux to the tower 5, and vapours which are fractionated in a tower 14 into vapours comprising pentanes and lighter hydrocarbons and bottoms free therefrom. The vapours are compressed and partially liquified in a condenser 17 and the condensate is separated from gases in a separator 18. The condensate is freed from dissolved gases in a re-boiler fractionator 23--24, the separated gases passing with the gases from the separator 18 into an absorbtion unit comprising an absorber 26, condenser 28, absorption oil-recovery tower 34 and cooler 37, the lean absorption oil 23 being recycled through line 39. The gasoline fraction obtained as bottoms in the tower 14 is stabilized in a tower 41 and sent to a storage tank 47 from which it is pumped as quenching-oil to the line 51 or as reflux to the line 50. The gases obtained from the stabilization are mixed with the olefine fraction passing from the tower 34 and after further fractionation in towers 44, 57 are collected in storage tanks C.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US463244XA | 1935-11-29 | 1935-11-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB463244A true GB463244A (en) | 1937-03-24 |
Family
ID=21942842
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB31849/36A Expired GB463244A (en) | 1935-11-29 | 1936-11-20 | A process for manufacturing olefines |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB463244A (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2416227A (en) * | 1944-05-18 | 1947-02-18 | Standard Oil Dev Co | Production of diolefins |
US2420030A (en) * | 1943-04-13 | 1947-05-06 | Standard Oil Dev Co | Motor fuels and preparation thereof |
US2421615A (en) * | 1943-12-28 | 1947-06-03 | Standard Oil Dev Co | Treating hydrocarbon fluids |
US2423374A (en) * | 1943-05-01 | 1947-07-01 | United Gas Improvement Co | Process for producing aromatics and diolefins from petroleum |
US2423835A (en) * | 1942-04-17 | 1947-07-15 | Houdry Process Corp | Inert heat material in contact mass catalysis |
US2431515A (en) * | 1943-12-24 | 1947-11-25 | Standard Oil Dev Co | Production of an aromatic gasoline |
US2434522A (en) * | 1944-05-18 | 1948-01-13 | Standard Oil Dev Co | Production of diolefins |
US2458862A (en) * | 1943-07-24 | 1949-01-11 | Standard Oil Dev Co | Preventing secondary reactions in catalytic processes |
-
1936
- 1936-11-20 GB GB31849/36A patent/GB463244A/en not_active Expired
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2423835A (en) * | 1942-04-17 | 1947-07-15 | Houdry Process Corp | Inert heat material in contact mass catalysis |
US2420030A (en) * | 1943-04-13 | 1947-05-06 | Standard Oil Dev Co | Motor fuels and preparation thereof |
US2423374A (en) * | 1943-05-01 | 1947-07-01 | United Gas Improvement Co | Process for producing aromatics and diolefins from petroleum |
US2458862A (en) * | 1943-07-24 | 1949-01-11 | Standard Oil Dev Co | Preventing secondary reactions in catalytic processes |
US2431515A (en) * | 1943-12-24 | 1947-11-25 | Standard Oil Dev Co | Production of an aromatic gasoline |
US2421615A (en) * | 1943-12-28 | 1947-06-03 | Standard Oil Dev Co | Treating hydrocarbon fluids |
US2416227A (en) * | 1944-05-18 | 1947-02-18 | Standard Oil Dev Co | Production of diolefins |
US2434522A (en) * | 1944-05-18 | 1948-01-13 | Standard Oil Dev Co | Production of diolefins |
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