US1672801A - Pressure-still process - Google Patents
Pressure-still process Download PDFInfo
- Publication number
- US1672801A US1672801A US186719A US18671927A US1672801A US 1672801 A US1672801 A US 1672801A US 186719 A US186719 A US 186719A US 18671927 A US18671927 A US 18671927A US 1672801 A US1672801 A US 1672801A
- Authority
- US
- United States
- Prior art keywords
- pressure
- draw
- oil
- line
- still
- 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 - Lifetime
Links
- 238000000034 method Methods 0.000 title description 19
- 239000003921 oil Substances 0.000 description 32
- 238000005336 cracking Methods 0.000 description 10
- 239000002904 solvent Substances 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 3
- 239000000571 coke Substances 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- 238000011010 flushing procedure Methods 0.000 description 3
- 230000005484 gravity Effects 0.000 description 3
- 238000009834 vaporization Methods 0.000 description 3
- 230000008016 vaporization Effects 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 238000004097 X-ray Buerger Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000009825 accumulation Methods 0.000 description 1
- 230000001174 ascending effect Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000008774 maternal effect Effects 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 238000007790 scraping Methods 0.000 description 1
Images
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
- C10G9/14—Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils in pipes or coils with or without auxiliary means, e.g. digesters, soaking drums, expansion means
-
- 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
- C10G7/00—Distillation of hydrocarbon oils
Definitions
- This invention relates to pressure still processes; and comprises a process of flushing out the tar draW -ofl' of a pressure still by the introduction under pressure through I such draw-01f and at intervals of a quantity of solvent, advantageously some of the pressure still distillate; all as more fully hereinafter set forth and as claimed.
- oil is passed continuously through a.
- the invention is illustratedv in combination with an oil cracking process in which charge oil is heated and vaporized in tubes, the products of such heating are delivered from such tubes to a separating chamber, resulting vapors are dephlegmated, and Outgoing vapors scrubbed with charge oil, the charge oil and reflux condensate delivered to the inlet side of the heating coils, the vapors passing reflux condensation are condensed, and residual oil is withdrawn from the separating chamber substantially as fast as it accumulates therein.
- FIG. 1 indicates a furnace provided with a stack 2 and with means for heating, such as oil burners or the like, located at 3.
- the coil 4 which, for the purpose of illustration, is shown as a continuous coil having the feed end 5 and discharge 6.
- the charge oil is vaporized in the coils 4 and the vapors with, perhaps, a slight amount of unvaporized oil, aredelivered by the discharge 6 to the lower end of a separating chamber 7, heat-insulated particularly at its upper part by insulation 8.
- the upper part of the chamber is provided with a plurality of baflles 9 and 10 and with the air cooled condenser 11.
- the vapors pass througli pressure release valve 13 to the condensing coil 14 and by means of line 15.to the receiving house.
- - Oil to be cracked is forced by means of pump pressure into the separating chamber, preferably at a mid-point through inlet 16 and serves to scrub the ascending vapors in such chamher.
- the baflies provide for good contact of oil and vapors and deliver charge oil and condensate to a collecting trap 17 which is provided with pipe 18 leading to the inlet end 5 of the heating and vaporizin coil. Pump18 is provided for forcing tie oil through the coil.
- the separating chamber 7 need not be insulated at the lower end since it is not the purpose to cause any reaction or conversion of any incidentaloil which may accumulate in the lower'section of the separating chamber.
- residuum or tar draw-off 20 leading past valve 21 to the pumping-out line 22.
- 23 indicates the charging line leading to a source of raw oil supply and is used when the still is first put on a run.
- the valve line 24 leading through cooler 25 may be used as a sampling connection. This may be of smaller diameter than the other lines.
- inlet line 26 leading to a source of solvent which may well be, and preferably is, pressure distillate usually of about 54 B. gravity.
- the cracking process may berun in any commercial way, necessary pressures being maintained by means of pressure valve 13 or 15. In fact, the pressure on the vapors from the cracking tubes may be released before such oil and vapors enter the separating chamber 7 by valve 6".
- the discharge line 20 becomes clogged. This is particularly so with some classes of charging stock containing a relatively high proportion of carbon to hydrogen, or in other words generally heavy gravity stocks.
- the clogging occurs because of the formation of granular coke, solid asphaltic binder and tarry matters, referred to as residuum.
- residuum granular coke, solid asphaltic binder and tarry matters.
- I have found that the formation of the residuum in the draw-off in such operations often clogs the pipe in anywhere from to 200 hours and correspondingly limits the length of a run.
- I can dissolve this asphaltic binder and flush the solid carbon back into the still. This cleans out the pipe and can be done while the still is in operation withoutinterfering at all with the normal operation, thereby prolonging in definitely the length of a run, or at least preventing limitation ofa run due to clogging of the draw-off.
- the draw-off line 20 commences to clog. This can be ascertained by observing the operation of the pump-outline 22 or by observations of samples from line 24.
- the valve on line 22 is closed (the valves on lines 20, 23 and 24 are normally open during a run) and the valve on line 26 is opened, whereupon the solvent-best pressure still distillateis pumped in through line 26 and through the draw-off line 20.
- This pressure still distillate dissolves the asphaltic binder which is formed, loosens coke, tar and heavy residuum and forces them back into the still. It takes only a few minutes to pump in the necessary amount of pressure still distillate, an average of 5 barrels each time being about all that is necessary. As soon as this pressure still distillate is flushed out of the tar drawoff the valve on line 26 is closed and the valve on line 22 is opened and the draw-off of the pressure still tar or residuum through lines 20 and 22 is continued.
- the rocess which comprises intermittently, uring the pressure distilation, forcing through the draw-off line in a direction opposed to the normal draw-off a quantity of solvent oil of about o ravity at a pressure greater than that pnevailing at the point of normal drawforcing therethrough into the chamber an ofi. i oil capable of dissolving asphaltic binding 4.
- a pressure process'in whic oil accumulates In testimony whereo I have hereunto af- 6 in a chamber and from which chamber the fixed my signature.
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)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Description
Ju'ne5, 1928. 1,672,801
c. B. BUERGER w .PRESSURE STILL PROGES S Filed April 26, 1927 Patented June 5, 1928.
4 UNITED STATES PATENT OFFICE.
CHARLES B. BUEBGEB, OF PITTSBURGH, PENNSYLVANIA, ABSIGNOR TO GULF DEFINING- GOIPANY, OF PITTSBURGH, PENNSYLVANIA, A CORPORATION OF TEXAS.
PRESSURE-STILL PROCESS.
Application filed April 26, 1927. Serial No. 188,719.
This invention relates to pressure still processes; and comprises a process of flushing out the tar draW -ofl' of a pressure still by the introduction under pressure through I such draw-01f and at intervals of a quantity of solvent, advantageously some of the pressure still distillate; all as more fully hereinafter set forth and as claimed.
- According to some commercial methods of cracking petroleum hydrocarbons now in use, oil is passed continuously through a.
heating zone and then delivered to a ClIaIIF her from which vapors are continuously removed. Usually the process is performed under pressure and usually unvaporized 011 is continuously removed from the chamber. Particularly in processes in which the chamber is used as a reaction zone where vaporization and conversion occur, there is an ac- :0 cumulation in the chamber of tar, tarry matters, asphaltic matters, coke and heavy residuum. These tend to clog the draw-oil pipe and to that extent shorten the length of a run. In a process where a large part of :6 the cracking and vaporization occurs in the tubes and where the products of the cracking and vaporization are delivered to a separating chambergthere is some small accumulation of heavy residuum, tar and cokein the chamber. In such a process where the chamber receiving the heated products, is kept substantially empty of liquid oil the same tendency to clog the draw-oil pipe exists. Attempts have been made to keep the draw-oil open .by using mechanical scraping, cutting or drilling devices at intervals, but there are inherent disadvantages in the use of such appliances. It is difiicult to operate them and keep the stufling boxes used in connection with them leak-proof and the operation involves the loss of considerable time as well as the employment of several workmen.
In accordance with my invention, during.
ly greater than the pressure prevailing in the chamber.
In the accompanying illustration I have shown more or less diagrammatically a cracking unit in which pressure distillation may be carried on, provided with connections adapting the unit for the performance of my process.
The invention is illustratedv in combination with an oil cracking process in which charge oil is heated and vaporized in tubes, the products of such heating are delivered from such tubes to a separating chamber, resulting vapors are dephlegmated, and Outgoing vapors scrubbed with charge oil, the charge oil and reflux condensate delivered to the inlet side of the heating coils, the vapors passing reflux condensation are condensed, and residual oil is withdrawn from the separating chamber substantially as fast as it accumulates therein.
In the drawing 1 indicates a furnace provided with a stack 2 and with means for heating, such as oil burners or the like, located at 3. In the furnace is mounted the coil 4 which, for the purpose of illustration, is shown as a continuous coil having the feed end 5 and discharge 6. The charge oil is vaporized in the coils 4 and the vapors with, perhaps, a slight amount of unvaporized oil, aredelivered by the discharge 6 to the lower end of a separating chamber 7, heat-insulated particularly at its upper part by insulation 8. The upper part of the chamber is provided with a plurality of baflles 9 and 10 and with the air cooled condenser 11. From the header 12 of the air cooled condenser the vapors pass througli pressure release valve 13 to the condensing coil 14 and by means of line 15.to the receiving house.- Oil to be cracked is forced by means of pump pressure into the separating chamber, preferably at a mid-point through inlet 16 and serves to scrub the ascending vapors in such chamher. The baflies provide for good contact of oil and vapors and deliver charge oil and condensate to a collecting trap 17 which is provided with pipe 18 leading to the inlet end 5 of the heating and vaporizin coil. Pump18 is provided for forcing tie oil through the coil. The separating chamber 7 need not be insulated at the lower end since it is not the purpose to cause any reaction or conversion of any incidentaloil which may accumulate in the lower'section of the separating chamber. At the lower end of the separating chamber there is provided residuum or tar draw-off 20 leading past valve 21 to the pumping-out line 22. 23 indicates the charging line leading to a source of raw oil supply and is used when the still is first put on a run. The valve line 24 leading through cooler 25 may be used as a sampling connection. This may be of smaller diameter than the other lines. In communication with the draw-off line 20 there is provided inlet line 26 leading to a source of solvent which may well be, and preferably is, pressure distillate usually of about 54 B. gravity.
The cracking process may berun in any commercial way, necessary pressures being maintained by means of pressure valve 13 or 15. In fact, the pressure on the vapors from the cracking tubes may be released before such oil and vapors enter the separating chamber 7 by valve 6".
During the continuous run the discharge line 20 becomes clogged. This is particularly so with some classes of charging stock containing a relatively high proportion of carbon to hydrogen, or in other words generally heavy gravity stocks. The clogging occurs because of the formation of granular coke, solid asphaltic binder and tarry matters, referred to as residuum. I have found that the formation of the residuum in the draw-off in such operations often clogs the pipe in anywhere from to 200 hours and correspondingly limits the length of a run. By pumping in a dissolving form of disti late through the inlet 26 I can dissolve this asphaltic binder and flush the solid carbon back into the still. This cleans out the pipe and can be done while the still is in operation withoutinterfering at all with the normal operation, thereby prolonging in definitely the length of a run, or at least preventing limitation ofa run due to clogging of the draw-off.
In practice I pump back pressure still distillate which is about 54 B. gravity and I have found a good practice is to pump back about 5 barrels of such distillate at eight-hour intervals. Of course, the pump pressure for delivering the flushing distillate must be greater than the pressure prevailing in the separating chamber 7. While it is sometimes advantageous to preheat the pressure still distillate I have found that it is not necessary to do so because of the small amount of oil in the separating chamber. In the separating chamber there is only Sufi.- cient oil to cover the inlet of the draw-off-QO. But if the process is runsin such a way that there is a substantial quantity of oil in the chamber 7, I preheat the solvent oil somewhat, and where a high degree o meat advisable I use a higher boiling solvent oil.
The exact character of distillate, the interval of time for flushing, and the amount of distillate pumped in, can of course be varied and need not be closely limited, as all these conditions vary according to the nature of the still operation, the size of the pipe and connections, the working temperature, the particular time of the run and the character of charging stock.
I have found that during the first part of the run it is not necessary to frequently flush out the tar draw-oft but after a duration of about a day, and in some cases a little less, the draw-off line 20 commences to clog. This can be ascertained by observing the operation of the pump-outline 22 or by observations of samples from line 24. When it is desired to flush the draw-off line the valve on line 22 is closed (the valves on lines 20, 23 and 24 are normally open during a run) and the valve on line 26 is opened, whereupon the solvent-best pressure still distillateis pumped in through line 26 and through the draw-off line 20. This pressure still distillate dissolves the asphaltic binder which is formed, loosens coke, tar and heavy residuum and forces them back into the still. It takes only a few minutes to pump in the necessary amount of pressure still distillate, an average of 5 barrels each time being about all that is necessary. As soon as this pressure still distillate is flushed out of the tar drawoff the valve on line 26 is closed and the valve on line 22 is opened and the draw-off of the pressure still tar or residuum through lines 20 and 22 is continued.
What I claim is 1. In an oil cracking process in which pressure still tar or residuum tends to clog the draw-off line, the process which comprises intermittently, during the pressure distillation, forcing through the draw-off line in a direction opposed to the normal draw-off, a quantity of solvent at a pressure greater than that prevailing at the point of normal draw-off.
2. In an oil cracking process in which pressure still tar or residuum tends to clog the draw-off line, the process which comprises intermittently, during the pressure distillation, forcing through the draw-off line in a direction opposed to the normal draw-off, a quantity of pressure still distillate at a pressure greater than that prevailat the point of normal draw-ofi.
8. In an oil cracking process in which pressure still tar or residuum tends to clog the draw-off line, the rocess which comprises intermittently, uring the pressure distilation, forcing through the draw-off line in a direction opposed to the normal draw-off a quantity of solvent oil of about o ravity at a pressure greater than that pnevailing at the point of normal drawforcing therethrough into the chamber an ofi. i oil capable of dissolving asphaltic binding 4. In the flistillation-of troleum oils by maternal tending to e10 the draw-0E line. I a pressure process'in whic oil accumulates In testimony whereo I have hereunto af- 6 in a chamber and from which chamber the fixed my signature.
oil is drawn off by means'of a draw-ofi line,
the step ef cleening the draw-ofi line by CHARLES B. BUERGER.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US186719A US1672801A (en) | 1927-04-26 | 1927-04-26 | Pressure-still process |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US186719A US1672801A (en) | 1927-04-26 | 1927-04-26 | Pressure-still process |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1672801A true US1672801A (en) | 1928-06-05 |
Family
ID=22686030
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US186719A Expired - Lifetime US1672801A (en) | 1927-04-26 | 1927-04-26 | Pressure-still process |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1672801A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4203825A (en) * | 1979-02-02 | 1980-05-20 | Exxon Research & Engineering Co. | Method for removing coronene from heat exchangers |
| US4214976A (en) * | 1979-02-02 | 1980-07-29 | Exxon Research & Engineering Co. | Method for removing coronene from heat exchangers |
| US4222852A (en) * | 1979-02-02 | 1980-09-16 | Exxon Research & Engineering Co. | Method for removing coronene from heat exchangers |
-
1927
- 1927-04-26 US US186719A patent/US1672801A/en not_active Expired - Lifetime
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4203825A (en) * | 1979-02-02 | 1980-05-20 | Exxon Research & Engineering Co. | Method for removing coronene from heat exchangers |
| US4214976A (en) * | 1979-02-02 | 1980-07-29 | Exxon Research & Engineering Co. | Method for removing coronene from heat exchangers |
| US4222852A (en) * | 1979-02-02 | 1980-09-16 | Exxon Research & Engineering Co. | Method for removing coronene from heat exchangers |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US1672801A (en) | Pressure-still process | |
| US2093588A (en) | Process of cracking heavy hydrocarbon oils | |
| US2165587A (en) | Cracking hydrocarbon oils | |
| US1940725A (en) | Process for treating carbonaceous material | |
| US2332800A (en) | Process for cleaning petroleum refining equipment | |
| US2064708A (en) | Method for cracking hydrocarbon oils | |
| US2162300A (en) | Process for treatment of hydrocarbons | |
| US1963265A (en) | Treatment of hydrocarbons | |
| CA1314258C (en) | Process for the extraction of low-temperature carbonization oil | |
| US2255060A (en) | Treatment of hydrocarbon and other residues | |
| US1783257A (en) | Process and apparatus for converting hydrocarbons | |
| US1840012A (en) | Apparatus for making gasoline | |
| US1868418A (en) | Process of cracking petroleum hydrocarbons | |
| US1916026A (en) | Process for the manufacture of coke | |
| US1640444A (en) | Process and apparatus for cracking hydrocarbon oils | |
| US1978562A (en) | Treatment of hydrocarbon oils | |
| US2096589A (en) | Converting residuum into charging stock and coke | |
| US1955246A (en) | Process for the distillation of hydrocarbon oils | |
| US1239423A (en) | Manufacture of gasolene. | |
| US1585496A (en) | Process for making gasoline | |
| US1786315A (en) | Process of cracking mineral oil | |
| US1324075A (en) | Process of manufacturing gasolene. | |
| US1636520A (en) | Method of and apparatus for treating petroleum | |
| US1953612A (en) | Treating hydrocarbon oils | |
| US1868738A (en) | Process of destructively distilling bitumen |