US1788933A - Process for cracking oil - Google Patents
Process for cracking oil Download PDFInfo
- Publication number
- US1788933A US1788933A US676141A US67614123A US1788933A US 1788933 A US1788933 A US 1788933A US 676141 A US676141 A US 676141A US 67614123 A US67614123 A US 67614123A US 1788933 A US1788933 A US 1788933A
- Authority
- US
- United States
- Prior art keywords
- vapors
- oil
- tubes
- still
- pipe
- 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 8
- 238000005336 cracking Methods 0.000 title description 2
- 239000003921 oil Substances 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 230000000087 stabilizing effect Effects 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 230000008016 vaporization Effects 0.000 description 3
- 239000010779 crude oil Substances 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000009834 vaporization 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
Definitions
- the process generally comprises subject ing a body of crude oil in an ordinary topping still to suitable temperatures to vapor- 'ize it, preferably in the neighborhood of 400 f to 450 F. After the natural gasoline and higher fractions pass off to suitable condensers, the vapors are then passed to superheating coils beneath the still which are 0 preferably long narrow pipes in which they are subjected, without increase of pressure,
- Fig. 2 is a plan view of the coils and stabilizing tubes.
- pipe 11 connects the ends of the stabiliaing' tubes 10 oppositethe' ends at which the superheated vapors" are admittechthereto, and the pipe ncommu'nicates with apipe "1 2 which is connected on the condenser side er'thevalvearo thetakeoff 4.
- a A valve 13 is'located in pipe 12 between the junctureof pipes 12 ah d' f'andithe pipe 11. a complete stabilization, but without the dep-
- the operation of the device is as follows:
- tor-r i t is f the" common practice, and to: which no claim is made, s e V After the natural gasoline and the higher 5 is closed and the valve'13 opened. Upon continued heating of the liquid in the still c9 5 fractions have beenthus removed, the valve I at a temperature in the neighborhood of 450 7 F., orslightly greater, depending'upo'n the;
- the vapors pass through the pipe 8 into the super-heating coil 7 where'they are subjected to a temperature in the neighborhood of 1000 to 1300 F. ,The influence causes the complete vaporization and super-heating of the vapors. From the coil 7 they pass by means of the connection 9 into the stabilizing tubes 10 Where,because of the larger diameteriot' j 1 these latter tubes, the velocity of the vapors is considerably retarded, although the pressure is still substantially only a'few pounds above atmospheric pressure. In theselarger tubes a complete stabilization of the vapors is achieved Without deposition of carbon or further the breaking' up of the hydrocarbon molecules. The vaporsthen pass-through the pipes 11 and 12 into the takeofi pipe 4 whence they pass to the condenser 6.
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)
Description
Jan. 13, 1931. VANDE R. 1,788,933
I PROCESS FOR CRACKING OIL Original Filed Nov. 21, 1923 Inven for:
Frank C. 'WzndeT Vizter,
Patented Jan. 13, 1931' FRANK o. VANDEYWA'IER, 0F nnwBuReH, innwtYonx, nssrenoaro Eastman LABORATORIES, me, or NEWBURGH, NEW 203x, aoosroanmon' on NEW YORK rnoozsss FOR onsoxrivs on;
Application filed November 21, 1923, Serial no. eza'ig Renewed r tra r iv, 30.
pressures with a minimum production of un- ,desirable products such as carbon and diolefines.
The process generally comprises subject ing a body of crude oil in an ordinary topping still to suitable temperatures to vapor- 'ize it, preferably in the neighborhood of 400 f to 450 F. After the natural gasoline and higher fractions pass off to suitable condensers, the vapors are then passed to superheating coils beneath the still which are 0 preferably long narrow pipes in which they are subjected, without increase of pressure,
to a temperature in the neighborhood of 1000 to 1300 F., depending upon the stage of the run, character of the chargingstock and character of the product desired. From the super-heating coils the vapors are passed to tubes of much largerodiameter, and subjected to substantially the same temperature in which the vapors, still at substan- 0 tia-lly atmospheric pressure, aresubjected to osition of carbon in appreciable quantities V or further the breaking down of the hydro- 7 carbon molecules. 7
A preferred apparatus .by which the process can be brought into practice is shown in the drawings of which,- 1 Figure 1 is a side elevation of the apparatus partly in section, and
Fig. 2 is a plan view of the coils and stabilizing tubes.
Referring now to the'embodiment iilustrated, I have shown a still or :tank 1 of any suitable construction which is placed over or in proximity to a fire-box or chamber 2 superheating which may be superheated by any of the common fuels now in" use, as obviously various circumstances will necessitate the use of various fuels. An aperture 3 is provided in the top of the oil tank through which the same mav be filledwiththe oil to be topped andemkea "The 31111 is rovided; with takeoff 4 within 'which is located a valve 5,"whi ch takeoff leads to a condenser 6 which may be,
ofan'y of the approved types and which is merely illustrated diagrammatically: j
Beneath thestill and in close proximity to theffire-box 2 I providega S lPerheating coil 7 prefera-bly of comparatively small diameter which is connected means of pipe 8 i to the takeoff 4 between the valve 5 and the still l. 'The superhea'tingcoils are connected as by 9 tothe large stabilizing tubes 10 arrangediat each side" of the superheating c oilsfand'al so' in proximity to the fire-box 2. It'will be seen that thesestahi} lizing, tubes 10 are of a much larger diameter than the superheating tubes and that therefore a certain amount of expansion takes place when the" superheated. vapors pass from the coil 7 tofthe pipef10. pipe 11 connects the ends of the stabiliaing' tubes 10 oppositethe' ends at which the superheated vapors" are admittechthereto, and the pipe ncommu'nicates with apipe "1 2 which is connected on the condenser side er'thevalvearo thetakeoff 4. a A valve 13 is'located in pipe 12 between the junctureof pipes 12 ah d' f'andithe pipe 11. a complete stabilization, but without the dep- The operation of the deviceis as follows:
Oil to'be cracked' i's filled into the still 1 through the-aperture the valve 13 closed, valve 51 opened, and the fire started in the fir-bOxQQ Heatis thus applied to the body of time to reinove the natural gasoline "expasses by Sway of pipe time the condenser 6 and is condensed as gasoline? From this 7 i v t 5 'ofoil within the still 1 for a sufficient length "is'ting m me oil frornithe same. This vapor point itemay be taken'to fthe'usual fractionars" ipliriit moments? tor-r i t is f the" common practice, and to: which no claim is made, s e V After the natural gasoline and the higher 5 is closed and the valve'13 opened. Upon continued heating of the liquid in the still c9 5 fractions have beenthus removed, the valve I at a temperature in the neighborhood of 450 7 F., orslightly greater, depending'upo'n the;
fractions it is desired'to drive off, the vapors pass through the pipe 8 into the super-heating coil 7 where'they are subjected to a temperature in the neighborhood of 1000 to 1300 F. ,The influence causes the complete vaporization and super-heating of the vapors. From the coil 7 they pass by means of the connection 9 into the stabilizing tubes 10 Where,because of the larger diameteriot' j 1 these latter tubes, the velocity of the vapors is considerably retarded, although the pressure is still substantially only a'few pounds above atmospheric pressure. In theselarger tubes a complete stabilization of the vapors is achieved Without deposition of carbon or further the breaking' up of the hydrocarbon molecules. The vaporsthen pass-through the pipes 11 and 12 into the takeofi pipe 4 whence they pass to the condenser 6.
It will thus be seen that under this process crude oil can be cracked efficiently without vthe deposition of carbon and the formation of diolefines, in anordinary-toppingstill beneath which the simple cracking and stabilizing tubesare disposed, thus requiring very little addition to the ordinary plant to apply this process. By carrying out the process in this manner and under very low pressures, theusual dangers encounteredin the operation of high pressure plants are avoided.
1. The process of treating liquid hydrocarbons comprising subjecting a body of oil to a vaporizing temperature, subjecting said moving vapors to a super-heatingtemperature in a restricted elongated space, whereby their velocity is increased, and then permitting said vapors to expand to reduce their velocity While subjected to substantially the same temperature, the entire operation taking place at substantially atmospheric pressure. 4 J
2. The process of treating liquid hydrocarbons comprising subjecting a body of oil to a vaporizing temperature in the neighborhood of 450 F., then subjecting said moving vapors to a super-heating temperature in the neighborhood of 1300 F. in a restricted elongated passage whereby their 've'locity is increased, and then permittingsaid vapors to expand to reduce their velocity while subject-ed to substantially the same temperature, the entire operation taking place atsubstaw tially atmospheric pressure. I
In testimony whereof, I afiix my signature.
'- FRANK C. VANDE WATER.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US676141A US1788933A (en) | 1923-11-21 | 1923-11-21 | Process for cracking oil |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US676141A US1788933A (en) | 1923-11-21 | 1923-11-21 | Process for cracking oil |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1788933A true US1788933A (en) | 1931-01-13 |
Family
ID=24713381
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US676141A Expired - Lifetime US1788933A (en) | 1923-11-21 | 1923-11-21 | Process for cracking oil |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1788933A (en) |
-
1923
- 1923-11-21 US US676141A patent/US1788933A/en not_active Expired - Lifetime
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