US3617536A - Process for the distillation of petroleum crude - Google Patents
Process for the distillation of petroleum crude Download PDFInfo
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- US3617536A US3617536A US806089A US80608969A US3617536A US 3617536 A US3617536 A US 3617536A US 806089 A US806089 A US 806089A US 80608969 A US80608969 A US 80608969A US 3617536 A US3617536 A US 3617536A
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- 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 an improved process for the distillation of petroleum crude and more particularly to an improved method for achieving bottoms product specifications in such a distillation process.
- the crude In the distillation of petroleum crude oil the crude is generally heated in a restricted stream to a temperature of around 700 to 725 F. It is then discharged into the vaporizing zone of a fractionating tower where it is flash distilled to separate the lower boiling fractions from the higher boiling fractions in the crude.
- the lighter, low-boiling fractions pass upwardly through the tower where they are fractionated into a number of refinery products and the heavier, high-boiling fractions are collected in the bottom of the tower as crude botv toms liquid.
- Product specifications for refinery products set an upper limit on the amount of vapor that can be evolved from a product under specified conditions.
- product specifications require that only a very small percentage, generally around p.p.m., of volatile hydrocarbons or light ends be present in the final bottoms product.
- Stripping columns generally operate at a temperature around 650' to 750 F. which is above the normal cracking point of most crudes. Thermocracking of the hot hottoms liquid, therefore, can occur in the stripping zone of the column resulting in the formation of additional light ends. While most of these light ends are removed by stripping, further cracking can also occur downstream of the stripping zone, and particularly in the bottoms holdup portion of the column and in the lines leading to coolers for the final bottoms product. Thermocracking of the hot bottoms liquid in the stripping column therefore has made it extremely difficult to obtain a final bottoms product that meets required product specifications.
- an improved process for the distillation of petroleum crude and more particularly an improved method for achieving bottoms product specifications can be provided by collecting and withdrawing the hot bottoms liquid at the bottom of the vaporizing zone in a fractionating tower, cooling the hot bottoms liquid in a cooling zone to a temperature below its cracking point and thereafter introducing the cooled liquid into a stripping zone where it is stripped of dissolved light ends to meet required products specifications.
- a separate cooling zone By reducing the temperature of the hot bottoms liquid in a separate cooling zone, further cracking of the liquid in the stripping zone and particularly in regions downstream of the stripping zone is prevented, permitting the final bottoms product specifications to be achieved, in a simple, efficient, and economical manner.
- the hot bottoms liquid withdrawn from the bottom of the vaporizing zone is at a temperature around 700 F.
- the heat value removed from the hot bottoms liquid is recovered and used to preheat the crude before it is heated to vaporization temperature, thus further increasing the efficiency of the present distillation process.
- the drawing is a schematic diagram showing an overall distillation process embodying the improvement of this invention.
- crude petroleum is heated in a pipe still 10 to a temperature sufficient to vaporize all but the higher boiling fractions and generally to a temperature of around 725 F.
- the heated crude is then fed into the vaporizing zone 12 of a fractionating tower 14.
- the fractionating tower 14 is of conventional design and includes a plurality of gas-liquid contact elements such as perforated plates 18 that provide intimate contact between ascending vapors and condensed reflux liquid. From the top of tower 14 the lightest vapors of the crude are removed through line 20 where they flow through a condenser 22. Generally a portion of this condensate is returned to tower 14 as reflux at 24 and a portion removed at 26 as a light gasoline product.
- gas-liquid contact elements such as perforated plates 18 that provide intimate contact between ascending vapors and condensed reflux liquid.
- side streams can also be withdrawn at various places along the height of the tower.
- Gasoline for example, can be withdrawn at 28 near the top of the tower, fuel oil at 30 and a lube oil at 32 immediately above vaporizing zone 12.
- Additional plates 18 may also be provided below the vaporizing zone 12 for stripping the higher boiling liquid fraction in a high-temperature stripping zone 34 before the hot bottoms liquid is collected on drawoff tray 16.
- Stripping gas if required in high-temperature stripping zone 34, can be added at 36 above drawoff tray 16.
- the hot bottoms liquid collected on drawoff tray 16 and normally at a temperature of around 700 F. is withdrawn through line 40, and passed through a heat exchanger 42 where the temperature of the bottoms liquid is reduced to below its cracking temperature, generally below 600 F. and preferably to about 550 F.
- Stripping zone 46 also includes a plurality of gas-liquid contact plates 18. It may comprise a separate column but preferably, and as shown in the drawing, fon'ns a part of the base of fractionating tower 14. Zone 46 is separated from vaporizing zone 12 of the tower by drawoff plate 16.
- stripping zone 46 the cooled bottoms liquid descends over the plates 18 while stripping gas, such as steam, introduced into the bottom of the zone through line 48, rises in contact with the descending liquid.
- stripping gas such as steam
- the stripped bottoms liquid which is primarily heavy lubricating oil that has been stripped of practically all light ends is collected in bottoms holdup section 52 at the bottom of stripping zone 46 and then withdrawn through line 54 and pumped at 55 to a cooler 56 where its temperature is reduced to about 250 F.
- the hot bottoms liquid withdrawn from the bottom of fractionating tower 14 is passed in heat exchange relationship at 42 with the crude oil feed to fractionating tower 14 to simultaneously cool the hot bottoms liquid and preheat the feed before it is heated in pipe still 10.
- the invention thus provides an improved process for the distillation of petroleum crude in which final bottoms product specifications are more readily achieved by substantially preventing cracking and the formation of light ends in a stripping zone in a simple, economical and effective manner.
- the practice of the process of this invention not only prevents the formation of light ends in a stripping zone but also contributes to the overall efficiency of the process by reducing the amount of heat required to heat the crude oil prior to flash distillation
- a specific example of it is set forth below. This example, however, is merely illustrative and is not intended to limit the scope and underlying principles of this vinvention in any way.
- EXAMPLE Petroleum crude is withdrawn from a storage tank (not shown) at room temperature and pumped through heat exchanger 42 where it is heated to a temperature of about 150 F. by indirect heat exchange with hot bottoms liquid withdrawn from the bottom of a distillation tower. From heat exchanger 42 the crude passes to pipe still where it is heated to a temperature of about 725 F.
- the heated crude is discharged into the vaporizing zone 12 of the fractionating tower where it is flash distilled with the vapors rising through the tower while the hot bottoms liquid collects on a drawofi' tray at the bottom of the tower.
- the hot bottoms liquid is then withdrawn from the tower at a temperature of about 700 F. and passed through a heat exchanger where it is reduced to a temperature of around 550 F.
- the hot bottoms liquid After the hot bottoms liquid is cooled, it is returned to the stripping zone of the tower where it is steam stripped to remove dissolved, light ends. Following steam stripping the bottoms product is collected and withdrawn at the bottom of the stripping zone, generally at a temperature of about 530 F., and then cooled to a temperature of about 250 F.
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- 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)
- Vaporization, Distillation, Condensation, Sublimation, And Cold Traps (AREA)
Abstract
An improved process for the distillation of petroleum crude is provided in which hot bottoms liquid, remaining after flash distillation of crude in a fractionating tower, is withdrawn from the tower and passed to a cooling zone to cool the liquid to a temperature below its cracking temperature before it is returned to the stripping zone of the tower. Stripping the hot bottoms liquid at this reduced temperature, prevents cracking of the liquid in the stripping zone and avoids the formation of light ends thereby permitting bottoms product specifications to be more readily achieved.
Description
United States Patent inventors Lonnie S. Saylor Parsippany, N.J.; Arthur R. Campbell, Sarnia, Ontario, Canada Appl. No. 806,089
Filed Mar. 11, 1969 Patented Nov. 2, 1971 Assignee Esso Research and Engineering Company PROCESS FOR THE DISTILLATION OF PETROLEUM CRUDE 3 Claims, 1 Drawing Fig.
11.8. C1 208/352, 208/353, 208/355, 208/356 Int. Cl 801d 3/06, C 1 0g 7/00 Field of Search 208/347,
[56] References Cited UNITED STATES PATENTS 1,655,603 1/1928 Hanns 208/347 2,064,757 12/1936 Keith 208/352 2,107,156 2/1938 Kuhn et a1. 208/347 2,319,750 5/1943 Schonberg et a1. 208/356 2,426,110 8/1947 McCorquodale et al. 208/354 2,853,439 9/1958 Ernst 208/355 Primary Examiner- Herbert Levine A!t0rneys Pearlman and Stahl and Wayne Hoover ABSTRACT: An improved process for the distillation of petroleum crude is provided in which hot bottoms liquid, remaining after flash distillation of crude in a fractionating tower, is withdrawn from the tower and passed to a cooling zone to cool the liquid to a temperature below its cracking temperature before it is returned to the stripping zone of the tower. Stripping the hot bottoms liquid at this reduced temperature, prevents cracking of the liquid in the stripping zone and avoids the formation of light ends thereby permitting bottoms product specifications to be more readily achieved.
ARTHUR R CAMPBELL LONNIE s} SAYLOR ATTORNEYS PROCESS FOR THE DISTILLATION F PETROLEUM CRUDE This invention relates to an improved process for the distillation of petroleum crude and more particularly to an improved method for achieving bottoms product specifications in such a distillation process.
In the distillation of petroleum crude oil the crude is generally heated in a restricted stream to a temperature of around 700 to 725 F. It is then discharged into the vaporizing zone of a fractionating tower where it is flash distilled to separate the lower boiling fractions from the higher boiling fractions in the crude. The lighter, low-boiling fractions pass upwardly through the tower where they are fractionated into a number of refinery products and the heavier, high-boiling fractions are collected in the bottom of the tower as crude botv toms liquid.
Product specifications for refinery products set an upper limit on the amount of vapor that can be evolved from a product under specified conditions. For heavy materials, such as crude bottoms liquid from a fractional distillation process, product specifications require that only a very small percentage, generally around p.p.m., of volatile hydrocarbons or light ends be present in the final bottoms product.
While a large portion of these light ends are removed by flash distillation in the fractionating tower, the bottoms liquid is never completely free of all light ends and must be subsequently steam stripped to meet product specifications. Stripping is conventionally accomplished by passing the hot bottoms liquid through a stripping column where the hot liquid descends through the column and steam is passed upwardly in contact with descending liquid.
Stripping columns, however, generally operate at a temperature around 650' to 750 F. which is above the normal cracking point of most crudes. Thermocracking of the hot hottoms liquid, therefore, can occur in the stripping zone of the column resulting in the formation of additional light ends. While most of these light ends are removed by stripping, further cracking can also occur downstream of the stripping zone, and particularly in the bottoms holdup portion of the column and in the lines leading to coolers for the final bottoms product. Thermocracking of the hot bottoms liquid in the stripping column therefore has made it extremely difficult to obtain a final bottoms product that meets required product specifications.
To alleviate the difficulty attempts have been made to recycle cooled bottoms product as a quench in the stripper column and, thereby, lower the temperature of the hot bottoms liquid below its cracking point. While this stops the cracking reaction in the stripping zone, recycle of cooled product reduces final product yield, lowers the efiiciency of the stripping column and the bottoms coolers because the recycled product must be both restripped and recooled, and further results in a loss of high-level heat from the hot bottom liquid. Such a system, therefore, has not proven entirely satisfactory for use in a petroleum crude distillation process.
In accordance with the present invention, it has been found that an improved process for the distillation of petroleum crude and more particularly an improved method for achieving bottoms product specifications can be provided by collecting and withdrawing the hot bottoms liquid at the bottom of the vaporizing zone in a fractionating tower, cooling the hot bottoms liquid in a cooling zone to a temperature below its cracking point and thereafter introducing the cooled liquid into a stripping zone where it is stripped of dissolved light ends to meet required products specifications. By reducing the temperature of the hot bottoms liquid in a separate cooling zone, further cracking of the liquid in the stripping zone and particularly in regions downstream of the stripping zone is prevented, permitting the final bottoms product specifications to be achieved, in a simple, efficient, and economical manner.
Generally, the hot bottoms liquid withdrawn from the bottom of the vaporizing zone is at a temperature around 700 F. v
and this temperature is reduced, according to the process of the present invention, to below 600 F. and generally to about 550 F. to prevent further cracking of the liquid before it is passed to the stripping zone. Preferably, the heat value removed from the hot bottoms liquid is recovered and used to preheat the crude before it is heated to vaporization temperature, thus further increasing the efficiency of the present distillation process.
It is to be understood that both the foregoing general description and the following detailed description are exemplary and explanatory but are not restrictive of the invention.
The accompanying drawing which is incorporated in and constitutes a part of this'specification illustrates a preferred embodiment of the invention and together with the description serves to explain the principles of the invention.
The drawing is a schematic diagram showing an overall distillation process embodying the improvement of this invention.
As shown in the drawing crude petroleum is heated in a pipe still 10 to a temperature sufficient to vaporize all but the higher boiling fractions and generally to a temperature of around 725 F.
The heated crude is then fed into the vaporizing zone 12 of a fractionating tower 14. The lighter, low-boiling fractions that immediately vaporize upon release of pressure rise through the tower while the heavier, high-boiling fractions collect as a liquid at the bottom of the tower on drawoff tray 16.
The fractionating tower 14 is of conventional design and includes a plurality of gas-liquid contact elements such as perforated plates 18 that provide intimate contact between ascending vapors and condensed reflux liquid. From the top of tower 14 the lightest vapors of the crude are removed through line 20 where they flow through a condenser 22. Generally a portion of this condensate is returned to tower 14 as reflux at 24 and a portion removed at 26 as a light gasoline product.
As further shown in the drawing, side streams can also be withdrawn at various places along the height of the tower. Gasoline, for example, can be withdrawn at 28 near the top of the tower, fuel oil at 30 and a lube oil at 32 immediately above vaporizing zone 12. Additional plates 18 may also be provided below the vaporizing zone 12 for stripping the higher boiling liquid fraction in a high-temperature stripping zone 34 before the hot bottoms liquid is collected on drawoff tray 16. Stripping gas, if required in high-temperature stripping zone 34, can be added at 36 above drawoff tray 16.
In accordance with the process of this invention the hot bottoms liquid collected on drawoff tray 16 and normally at a temperature of around 700 F. is withdrawn through line 40, and passed through a heat exchanger 42 where the temperature of the bottoms liquid is reduced to below its cracking temperature, generally below 600 F. and preferably to about 550 F.
The cooled bottoms liquid is then introduced through line 44 into the top of a stripping zone 46. Stripping zone 46 also includes a plurality of gas-liquid contact plates 18. It may comprise a separate column but preferably, and as shown in the drawing, fon'ns a part of the base of fractionating tower 14. Zone 46 is separated from vaporizing zone 12 of the tower by drawoff plate 16.
In stripping zone 46 the cooled bottoms liquid descends over the plates 18 while stripping gas, such as steam, introduced into the bottom of the zone through line 48, rises in contact with the descending liquid. As the bottoms liquid flows downwardly through the stripping zone 46 the light ends dissolved in the liquid are revaporized, with the vapors and steam ascending through perforations 50 in drawoff plate 16 and into vaporizing zone 12 of tower 14.
The stripped bottoms liquid which is primarily heavy lubricating oil that has been stripped of practically all light ends is collected in bottoms holdup section 52 at the bottom of stripping zone 46 and then withdrawn through line 54 and pumped at 55 to a cooler 56 where its temperature is reduced to about 250 F.
Reducing the temperature of thecrude bottoms liquid in a cooling zone apart from the vaporizing zone in accordance with the present invention, and thereafter returning the cooled bottoms liquid to the stripping zone at reduced temperature, prevents cracking and theundesirable formation of light ends in the stripping zone. All the light ends remaining in the crude bottoms liquid after vaporization, therefore, can be completely stripped out in the stripping zone and no more light ends are.
formed downstream of the stripper, particularly in the bottoms holdup portion or coolers. This permits final bottoms product specifications to be more readily achieved. By the process of this invention color degradation of the volatile product, due to the formation of coke when cracking occurs in the stripping section, is also reduced since cracking has been substantially eliminated in the stripping zone.
Further, by cooling the hot bottoms liquid from the vaporizing zone in a separate cooling zone, high-level heat can be recovered from the hot bottoms liquid and used to further increase the efficiency of the distillation process.
in accordance with the preferred embodiment of this invention and as shown in the drawing, the hot bottoms liquid withdrawn from the bottom of fractionating tower 14 is passed in heat exchange relationship at 42 with the crude oil feed to fractionating tower 14 to simultaneously cool the hot bottoms liquid and preheat the feed before it is heated in pipe still 10.
The invention thus provides an improved process for the distillation of petroleum crude in which final bottoms product specifications are more readily achieved by substantially preventing cracking and the formation of light ends in a stripping zone in a simple, economical and effective manner. The practice of the process of this invention not only prevents the formation of light ends in a stripping zone but also contributes to the overall efficiency of the process by reducing the amount of heat required to heat the crude oil prior to flash distillation For a clearer understanding of this invention, a specific example of it is set forth below. This example, however, is merely illustrative and is not intended to limit the scope and underlying principles of this vinvention in any way.
EXAMPLE Petroleum crude is withdrawn from a storage tank (not shown) at room temperature and pumped through heat exchanger 42 where it is heated to a temperature of about 150 F. by indirect heat exchange with hot bottoms liquid withdrawn from the bottom of a distillation tower. From heat exchanger 42 the crude passes to pipe still where it is heated to a temperature of about 725 F.
The heated crude is discharged into the vaporizing zone 12 of the fractionating tower where it is flash distilled with the vapors rising through the tower while the hot bottoms liquid collects on a drawofi' tray at the bottom of the tower. The hot bottoms liquid is then withdrawn from the tower at a temperature of about 700 F. and passed through a heat exchanger where it is reduced to a temperature of around 550 F.
After the hot bottoms liquid is cooled, it is returned to the stripping zone of the tower where it is steam stripped to remove dissolved, light ends. Following steam stripping the bottoms product is collected and withdrawn at the bottom of the stripping zone, generally at a temperature of about 530 F., and then cooled to a temperature of about 250 F.
Analysis of the final bottoms product, a heavy lubricating oil, shows that strict product specifications, setting a limit on the amount of dissolved light ends that can be present in the product have been met.
The invention in its broader aspects is not limited to the specific details shown and described and departures may be made from such details without departing from the principles of the invention and without sacrificing its chief advantages.
What is claimed is: 1. An improved process for the distillation of whole petroleum crude which comprises:
heating said crude m a heating zone to a temperature sufficient to vaporize at least a proportion of the lower boiling fractions in said crude:
discharging the heated crude into a vaporizing zone of a fractionating tower to flash distill the lower boiling fractions;
passing the distilled vapors from the vaporizing zone through a rectifying zone;
stripping the hot liquid which collects at the bottom of the vaporizing zone in a high-temperature stripping zone; collecting and withdrawing said stripped hot liquid from said high-temperature stripping zone;
cooling said stripped hot liquid to a temperature below about 600 F. by passing said hot liquid in'heat exchange relationship with the whole crude before it is heated in said heating zone;
thereafter stripping the cooled bottoms liquid in a separate low-temperature stripping zone.
2. The process of claim 1 wherein the whole petroleum crude oil is heated to about 725 F. in a heating zone prior to discharging said crude into the vaporizing zone.
3. in a process for the distillation of whole petroleum crude wherein the crude is heated and flash distilled in a vaporizing zone to separate it into a lower boiling vapor fraction and a higher boiling liquid fraction, and wherein. the liquid fraction is subsequently stripped in a high temperature stripping zone to remove dissolved lower boiling fractions therefrom, the improvement which comprises collecting and withdrawing the higher boiling liquid fraction from the hightemperature stripping zone, cooling the liquid fraction to a temperature below about 600 F. in a cooling zone by passing said liquid in heat exchange relationship with the whole crude before said crude is heated in said heating zone, and thereafter stripping the cooled liquid fraction in a separate low-temperature stripping zone.
I i 0 i l 5223 UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No. 3,617,536 Dated November 2, 1971 Lonnie S. Saxflor and Arthur 3. Campbell It is certified that error appears in the aboveand that said Letters Patent are hereby corrected as Inventor(s) identified patent shown below:
Column t, Claim 1, line 20; "proportion" should read --portion--.-
"cient to vaporize at least a portion of the lower boiling" Signed and sealed this 30th day of May 1972.
(SEAL) Attest:
EDWARD M.FLFITCHER ,JR.
. ROBERT GOTTSCHALK Attesting Officer Commissionerof Patents
Claims (2)
- 2. The process of claim 1 wherein the whole petroleum crude oil is heated to about 725* F. in a heating zone prior to discharging said crude into the vaporizing zone.
- 3. In a process for the distillation of whole petroleum crude wherein the crude is heated and flash distilled in a vaporizing zone to separate it into a lower boiling vapor fraction and a higher boiling liquid fraction, and wherein the liquid fraction is subsequently stripped in a high temperature stripping zone to remove dissolved lower boiling fractions therefrom, the improvement which comprises collecting and withdrawing the higher boiling liquid fraction from the high- temperature stripping zone, cooling the liquid fraction to a temperature below about 600* F. in a cooling zone by passing said liquid in heat exchange relationship with the whole crude before said crude is heated in said heating zone, and thereafter stripping the cooled liquid fraction in a separate low-temperature stripping zone.
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US806089A US3617536A (en) | 1969-03-11 | 1969-03-11 | Process for the distillation of petroleum crude |
| GB8993/70A GB1294235A (en) | 1969-03-11 | 1970-02-25 | Improved process for the distillation of petroleum crude |
| DE19702010034 DE2010034A1 (en) | 1969-03-11 | 1970-03-04 | Petroleum distillation process |
| NL7003311A NL7003311A (en) | 1969-03-11 | 1970-03-09 | |
| FR7008586A FR2034815A7 (en) | 1969-03-11 | 1970-03-10 | |
| CA077025A CA919115A (en) | 1969-03-11 | 1970-03-10 | Process for the distillation of petroleum crude |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US806089A US3617536A (en) | 1969-03-11 | 1969-03-11 | Process for the distillation of petroleum crude |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3617536A true US3617536A (en) | 1971-11-02 |
Family
ID=25193290
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US806089A Expired - Lifetime US3617536A (en) | 1969-03-11 | 1969-03-11 | Process for the distillation of petroleum crude |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US3617536A (en) |
| CA (1) | CA919115A (en) |
| DE (1) | DE2010034A1 (en) |
| FR (1) | FR2034815A7 (en) |
| GB (1) | GB1294235A (en) |
| NL (1) | NL7003311A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4776948A (en) * | 1984-01-30 | 1988-10-11 | Williams, Phillips & Umphlett | Fractionation method with quench liquid recycle |
| EP1050570A3 (en) * | 1999-05-05 | 2002-12-18 | Bechtel Corporation | Process for separation of dewaxed lube oil into light and heavyproducts |
| US20050011442A1 (en) * | 2003-06-24 | 2005-01-20 | International Business Machines Corporation | Plasma processing material reclamation and reuse |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2221221B (en) * | 1988-07-29 | 1992-03-18 | Amoco Corp | Apparatus and method for recovering diesel-quality fuel from produced crude oil |
| US5116485A (en) * | 1988-07-29 | 1992-05-26 | Krisa Thomas E | Apparatus and method for recovering diesel-quality fuel from produced crude oil |
| RU2186085C2 (en) * | 1998-07-20 | 2002-07-27 | Общество с ограниченной ответственностью "Интербизнеспроект" | Method of producing motor fuels from hydrocarbon raw materials |
| RU2170755C1 (en) * | 2000-10-19 | 2001-07-20 | Крючков Виктор Алексеевич | Method of processing of secondary heavy hydrocarbon materials |
| RU2170754C1 (en) * | 2000-10-19 | 2001-07-20 | Крючков Виктор Алексеевич | Reactor for processing of secondary heavy hydrocarbon materials |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1655603A (en) * | 1923-03-31 | 1928-01-10 | Standard Oil Co California | Process of distilling petroleum oil |
| US2064757A (en) * | 1934-07-26 | 1936-12-15 | Gasoline Products Co Inc | Process for the treatment of hydrocarbon oil |
| US2107156A (en) * | 1934-05-28 | 1938-02-01 | Texas Co | Mineral oil distillation |
| US2319750A (en) * | 1939-08-12 | 1943-05-18 | Standard Oil Dev Co | Distillation process |
| US2426110A (en) * | 1942-10-14 | 1947-08-19 | Sun Oil Co | Distillation of crude petroleum |
| US2853439A (en) * | 1952-08-01 | 1958-09-23 | Exxon Research Engineering Co | Combination distillation and hydrocarbon conversion process |
-
1969
- 1969-03-11 US US806089A patent/US3617536A/en not_active Expired - Lifetime
-
1970
- 1970-02-25 GB GB8993/70A patent/GB1294235A/en not_active Expired
- 1970-03-04 DE DE19702010034 patent/DE2010034A1/en active Pending
- 1970-03-09 NL NL7003311A patent/NL7003311A/xx unknown
- 1970-03-10 FR FR7008586A patent/FR2034815A7/fr not_active Expired
- 1970-03-10 CA CA077025A patent/CA919115A/en not_active Expired
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1655603A (en) * | 1923-03-31 | 1928-01-10 | Standard Oil Co California | Process of distilling petroleum oil |
| US2107156A (en) * | 1934-05-28 | 1938-02-01 | Texas Co | Mineral oil distillation |
| US2064757A (en) * | 1934-07-26 | 1936-12-15 | Gasoline Products Co Inc | Process for the treatment of hydrocarbon oil |
| US2319750A (en) * | 1939-08-12 | 1943-05-18 | Standard Oil Dev Co | Distillation process |
| US2426110A (en) * | 1942-10-14 | 1947-08-19 | Sun Oil Co | Distillation of crude petroleum |
| US2853439A (en) * | 1952-08-01 | 1958-09-23 | Exxon Research Engineering Co | Combination distillation and hydrocarbon conversion process |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4776948A (en) * | 1984-01-30 | 1988-10-11 | Williams, Phillips & Umphlett | Fractionation method with quench liquid recycle |
| EP1050570A3 (en) * | 1999-05-05 | 2002-12-18 | Bechtel Corporation | Process for separation of dewaxed lube oil into light and heavyproducts |
| US20050011442A1 (en) * | 2003-06-24 | 2005-01-20 | International Business Machines Corporation | Plasma processing material reclamation and reuse |
Also Published As
| Publication number | Publication date |
|---|---|
| CA919115A (en) | 1973-01-16 |
| NL7003311A (en) | 1970-09-15 |
| GB1294235A (en) | 1972-10-25 |
| DE2010034A1 (en) | 1970-09-17 |
| FR2034815A7 (en) | 1970-12-18 |
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