US3684697A - Petroleum coke production - Google Patents

Petroleum coke production Download PDF

Info

Publication number
US3684697A
US3684697A US99319A US3684697DA US3684697A US 3684697 A US3684697 A US 3684697A US 99319 A US99319 A US 99319A US 3684697D A US3684697D A US 3684697DA US 3684697 A US3684697 A US 3684697A
Authority
US
United States
Prior art keywords
coke
feedstock
coking
asphaltene
asphaltene content
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
Application number
US99319A
Inventor
Bernard William Gamson
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Martin Marietta Corp
Original Assignee
Bernard William Gamson
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Bernard William Gamson filed Critical Bernard William Gamson
Application granted granted Critical
Publication of US3684697A publication Critical patent/US3684697A/en
Assigned to MARTIN MARIETTA CORPORATION, A CORP OF MD reassignment MARTIN MARIETTA CORPORATION, A CORP OF MD ASSIGNMENT OF ASSIGNORS INTEREST. Assignors: MARTIN MARIETTA ALUMINUM INC., A CORP OF CA
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10BDESTRUCTIVE DISTILLATION OF CARBONACEOUS MATERIALS FOR PRODUCTION OF GAS, COKE, TAR, OR SIMILAR MATERIALS
    • C10B55/00Coking mineral oils, bitumen, tar, and the like or mixtures thereof with solid carbonaceous material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10BDESTRUCTIVE DISTILLATION OF CARBONACEOUS MATERIALS FOR PRODUCTION OF GAS, COKE, TAR, OR SIMILAR MATERIALS
    • C10B57/00Other carbonising or coking processes; Features of destructive distillation processes in general
    • C10B57/04Other carbonising or coking processes; Features of destructive distillation processes in general using charges of special composition

Definitions

  • This invention relates to a process for the production of petroleum coke, more particularly sponge-type petroleum coke.
  • the coke which is produced is either a dense, hard particulate product with very low internal porosity coke or a porous low density product called sponge coke.
  • Shot coke is used principally as fuel and in steep production. The latter is used in the manufacture of graphite and carbon electrodes used in the aluminum industry. The former type of coke does not produce satisfactory electrodes because their use results in electrodes with high resistivities.
  • the pitch conventionally used to form the massive carbon bodies used as electrodes in aluminum production has poor binding characteristics for shot coke and results in a product with low compressive and tensile strengths. Oxidation of the electrode during aluminum production causes spalling of major pieces, resulting in shorter elec' trode life and difliculties in operation because of the portions of the electrode dropping into the cell.
  • sponge petroleum coke is ordinarily preferred over shot petroleum coke as a product of a coking operation because of the greater economic value of sponge coke. Therefore, in conventional coking operations, unless a feedstock is employed which from past experience is known to produce only shot coke, coking conditions are usually selected which promote the formation of sponge coke. However, it is well known that certain feedstocks will produce only shot coke, irrespective of the process conditions employed in the coking operation.
  • a third type of coke i.e., needle coke, is produced by employing special coking procedures. See The Oil and Gas Journal, pp. 73-77, Sept. 14, 1970. This invention is not related to this specialized coking operation nor to the coke produced by that process.
  • sponge coke is produced from coking feedstock which normaly produces shot coke in a conventional coking operation by:
  • the maximum asphaltene content of the mixture of feed stocks employed in the coking process of this invention which will still result in the production of shot coke depends in part on the coking conditions employed. As is known, in a conventional coking operation conditions can be selected which promote the formation of sponge coke, e.g., higher pressures, lower feed rates, longer residence time and higher recycle ratios. Because the desired product of the coking process of this invention is sponge coke, those conventional coking conditions which promote the production of sponge coke should therefore be employed. The higher the asphaltene content of the feedstock mixture employed in this process, the more important it is that conditions promoting sponge coke formation be employed.
  • Petroleum coking feedstock which normally produce shot coke in a conventional coking operation are those having asphaltene contents above about 13%, e.g.,
  • Hydrocarbon bottoms which have low asphaltene contents and which can be used with the above-described feedstocks which normally produce shot coke are petroleum hydrocarbons, e.g.,
  • coal tar hydrocarbons e.g., aromatic coal tar hydrocarbon.
  • Pressure tars are those produced in the thermal cracking of catalytically cracked cycle stock.
  • Aromatic oils are the heavy bottom residues from thermally cracked, catalytically cracked cycle stock. These residues are used in the manufacture of filler carbon black because of their high aromatic content.
  • Typical API gravity is 1, initial B.P., 650 F., and asphaltene content, 1.5%.
  • Deasphalted hydrocarbons are prepared by propane deasphalting, sulfur dioxide treatment and related processes.
  • Synthetic hydrocarbon residues are the liquid or solid (at room temperature) by-prdoucts of hydrocarbon syntheses, including polyolefin, e.g., polybutadiene, polyethylene, polypropylene, etc., production, and cracking processes for olefins, dienes, acetylenic and aromatic hydrocarbons.
  • polyolefin e.g., polybutadiene, polyethylene, polypropylene, etc.
  • production, and cracking processes for olefins, dienes, acetylenic and aromatic hydrocarbons are the liquid or solid (at room temperature) by-prdoucts of hydrocarbon syntheses, including polyolefin, e.g., polybutadiene, polyethylene, polypropylene, etc.
  • Preferred low asphaltene-containing residues are those which are substantially asphaltene-free, i.e., containing no more than 3% and preferably 2% asphaltene.
  • Particular preferred are petroleum hydrocarbon residues, especially the aromatic oils.
  • the asphaltene content of the feedstocks is determined in the conventional manner, i.e., measuring the percent of the feedstock which is soluble in an aromatic oil and the percent thereof soluble in pentane, the percent asphaltene content being the difference in the two figures.
  • a feedstock which is completely soluble in an aromatic oil and 83% soluble in pentane has an asphaltene content of 17%, as determined according to ASTM Test No. D2006.
  • substantially asphaltene-free feedstock which is blended with the shot coke forming feedstock to ensure the production of sponge coke will depend on the asphaltene content of the shot coke forming feedstock and the low-asphaltene content hydrocarbon bottoms used therewith.
  • substantially asphaltene-free hydrocarbon bottoms about 540% by volume will sufiice with all except the shot coke forming feedstock of very high asphaltene content, e.g., above 25%.
  • the process conditions employed in a conventional coking operation designed to produce sponge coke are employed in the process of this invention.
  • the feedstock is heated to up to about 900 F. and pumped into a coking drum at a rate which fills the drum in about 8 to hours, with a recycle ratio of about 1.2 to about 2.5, preferably about 1.5.
  • the coke is cooled with steam and the cooled coke removed with high pressure water jets. Total cycle time is about 26 hours.
  • EXAMPLE 1 Shot coke forming feedstock Vacuum virgin residual oil, 15% asphaltene content; initial B.P., 600 F.; API gravity, 4; Watson Characterization Factor, 10.8.
  • Aromatic oil (1.5% asphaltene content; initial B.P., 650 F.; API gravity, -1; Watson Characterization Factor, 9.0.
  • the shot coke forming feedstock and the aromatic oil blending stock are separately preheated to 915 F. and then separately fed to a coking drum (20' diameter, 80' high) at a rate of 350 barrels/hr. and 100 barrels/hr., respectively, with a recycle ratio of 1.5 (total feed/fresh feed). Pressure in the drum is 45 p.s.i.g. Coking time is 12 hours with a total cycle time of 24 hours.
  • the coke produced is high porosity sponge coke with a bulk density 1" crushed coke with about +4 mesh solids) of about 43 lbs./ft. Hydrogen content is about 39%, sulfur content, 1.15%; and ash, 0.27%. Total surface area (1" particle) is about 400-600 ft. /ft. Shot coke of comparable size has a surface area of 75- 100 ft. /ft.
  • sponge coke is prdouced according to the procedure of Example 1 employing as shot coke forming feedstock the residue of a solvent hydrocarbon extraction (25% asphaltene content) or a hydrocarbon asphalt (35 asphaltene content) in combination with a proportion of aromatic oil which provides a total asphaltene content of about 10%.
  • Sponge coke is also produced according to the procedure of Example 1 by substituting as low-asphaltene content hydrocarbon bottoms, the same proportion of pressure tar (1.5% asphaltene content); bottoms of refined deasphalted hydrocarbons (0.3% asphaltene content); the residues of polyethylene production (0% asphaltene content) or coal tar bottoms (0.1% asphaltene content).
  • a process for the production of porous, low density sponge coke from coking feedstock which produces dense, hard particulate shot coke in a conventional delayed coking operation which comprises the steps of:
  • a process according to claim 2 wherein the shot coke forming feedstock is selected from the group consisting of (a) atmospheric distilled virgin residual hydrocarbons;
  • hydrocarbon bottoms is selected from the group consisting of:
  • a process according to claim 8 wherein the shot coke forming feedstock is selected from the group consisting of:
  • hydrocarbon asphalts wherein the hydrocarbon bottoms is selected from the group consisting of:

Abstract

PETROLEUM SPONGE COKE IS PRODUCED FROM HYDROCABON FEEDSTOCK WHICH FORMS SHOT COKE IN A CONVENTIONAL DELAYED COKING PROCESS BY BLENDING THE FEEDSTOCK WITH ANOTHER FEEDSTOCK RELAITELY FREE OF ASPHALTENE TO FORM A BLENDED FEEDSTOCK HAVING AN ASPHALTENE CONTENT BELOW ABOUT 15%.

Description

United States Patent 3,684,697 PETROLEUM COKE PRODUCTION Bernard William Gamson, 129 S. Alta Vista Blvd., Los Angeles, Calif. 90036 No Drawing. Filed Dec. 17, 1970, Ser. No. 99,319 Int. Cl. Cg 9/14 US. Cl. 208-131 12 Claims ABSTRACT OF THE DISCLOSURE Petroleum sponge coke is produced from hydrocarbon feedstock which forms shot coke in a conventional de' layed coking process by blending the feedstock with another feedstock relatively free of asphaltene to form a blended feedstock having an asphaltene content below about 15%.
BACKGROUND OF THE INVENTION This invention relates to a process for the production of petroleum coke, more particularly sponge-type petroleum coke.
In a conventional petroleum coking operation, the coke which is produced is either a dense, hard particulate product with very low internal porosity coke or a porous low density product called sponge coke. Shot coke is used principally as fuel and in steep production. The latter is used in the manufacture of graphite and carbon electrodes used in the aluminum industry. The former type of coke does not produce satisfactory electrodes because their use results in electrodes with high resistivities. The pitch conventionally used to form the massive carbon bodies used as electrodes in aluminum production has poor binding characteristics for shot coke and results in a product with low compressive and tensile strengths. Oxidation of the electrode during aluminum production causes spalling of major pieces, resulting in shorter elec' trode life and difliculties in operation because of the portions of the electrode dropping into the cell.
Thus, sponge petroleum coke is ordinarily preferred over shot petroleum coke as a product of a coking operation because of the greater economic value of sponge coke. Therefore, in conventional coking operations, unless a feedstock is employed which from past experience is known to produce only shot coke, coking conditions are usually selected which promote the formation of sponge coke. However, it is well known that certain feedstocks will produce only shot coke, irrespective of the process conditions employed in the coking operation.
A third type of coke, i.e., needle coke, is produced by employing special coking procedures. See The Oil and Gas Journal, pp. 73-77, Sept. 14, 1970. This invention is not related to this specialized coking operation nor to the coke produced by that process.
OBI ECT S OF THE INVENTION It is an object of this invention to provide a method whereby the production of sponge coke in a conventional coking operation is assured. Another object is the provision of a process whereby feedstocks which heretofore could not produce sponge coke can be employed in the production thereof. Other objects will be apparent to those skilled in the art to which this invention pertains.
SUMMARY OF THE INVENTION According to this invention, sponge coke is produced from coking feedstock which normaly produces shot coke in a conventional coking operation by:
(a) measuring the asphaltene content of a coking feed- 3,684,697 Patented Aug. 15, 1972 DETAILED DISCUSSION It has been found that coking feedstocks which usually or always produce shot coke in a conventional coking operation can be used to consistently produce sponge coke if blended with a hydrocarbon bottoms, e.g., having a low asphaltene content, e.g., less than 8%, preferably 05%, more preferably O-2%, in a proportion such that the resulting mixture of feed stocks has an asphaltene content of less than about 13%, preferably less than 10%.
The maximum asphaltene content of the mixture of feed stocks employed in the coking process of this invention which will still result in the production of shot coke depends in part on the coking conditions employed. As is known, in a conventional coking operation conditions can be selected which promote the formation of sponge coke, e.g., higher pressures, lower feed rates, longer residence time and higher recycle ratios. Because the desired product of the coking process of this invention is sponge coke, those conventional coking conditions which promote the production of sponge coke should therefore be employed. The higher the asphaltene content of the feedstock mixture employed in this process, the more important it is that conditions promoting sponge coke formation be employed.
Petroleum coking feedstock which normally produce shot coke in a conventional coking operation are those having asphaltene contents above about 13%, e.g.,
(a) atmospheric distilled virgin residual hydrocarbons; (b) vacuum distilled virgin residual hydrocarbons; (c) solvent extracted residual hydrocarbons; and
(d) hydrocarbon asphalts.
Of these, those having asphaltene contents of about 13 to 25% are preferred as feedstocks for the coking process of this invention, especially atmospheric and vacuum distilled virgin residual hydrocarbons.
Hydrocarbon bottoms which have low asphaltene contents and which can be used with the above-described feedstocks which normally produce shot coke are petroleum hydrocarbons, e.g.,
(a) pressure tars;
(b) aromatic oils;
(c) deasphalted hydrocarbons;
(d) synthetic hydrocarbon residues; and
(e) the residual aliphatic hydrocarbons of a crude oil which is substantially asphaltene-free;
and coal tar hydrocarbons, e.g., aromatic coal tar hydrocarbon. Pressure tars are those produced in the thermal cracking of catalytically cracked cycle stock. Aromatic oils are the heavy bottom residues from thermally cracked, catalytically cracked cycle stock. These residues are used in the manufacture of filler carbon black because of their high aromatic content. Typical API gravity is 1, initial B.P., 650 F., and asphaltene content, 1.5%. Deasphalted hydrocarbons are prepared by propane deasphalting, sulfur dioxide treatment and related processes. Synthetic hydrocarbon residues are the liquid or solid (at room temperature) by-prdoucts of hydrocarbon syntheses, including polyolefin, e.g., polybutadiene, polyethylene, polypropylene, etc., production, and cracking processes for olefins, dienes, acetylenic and aromatic hydrocarbons.
Preferred low asphaltene-containing residues are those which are substantially asphaltene-free, i.e., containing no more than 3% and preferably 2% asphaltene. Especially preferred are petroleum hydrocarbon residues, especially the aromatic oils.
The asphaltene content of the feedstocks is determined in the conventional manner, i.e., measuring the percent of the feedstock which is soluble in an aromatic oil and the percent thereof soluble in pentane, the percent asphaltene content being the difference in the two figures. Thus, a feedstock which is completely soluble in an aromatic oil and 83% soluble in pentane has an asphaltene content of 17%, as determined according to ASTM Test No. D2006.
The proportion of substantially asphaltene-free feedstock which is blended with the shot coke forming feedstock to ensure the production of sponge coke will depend on the asphaltene content of the shot coke forming feedstock and the low-asphaltene content hydrocarbon bottoms used therewith. When using the preferred, substantially asphaltene-free hydrocarbon bottoms, about 540% by volume will sufiice with all except the shot coke forming feedstock of very high asphaltene content, e.g., above 25%.
The process conditions employed in a conventional coking operation designed to produce sponge coke are employed in the process of this invention. The feedstock is heated to up to about 900 F. and pumped into a coking drum at a rate which fills the drum in about 8 to hours, with a recycle ratio of about 1.2 to about 2.5, preferably about 1.5. When the coking drum is filled with coke, the coke is cooled with steam and the cooled coke removed with high pressure water jets. Total cycle time is about 26 hours.
Without further elaboration, it is believed that one skilled in the art can, using the preceding description, utilize the present invention to its fullest extent. The following preferred specific embodiments are, therefore, to be constructed as merely illustrative, and not limitative of the remainder of the disclosure in any way whatsoever.
EXAMPLE 1 Shot coke forming feedstock: Vacuum virgin residual oil, 15% asphaltene content; initial B.P., 600 F.; API gravity, 4; Watson Characterization Factor, 10.8.
Low aspheltene-content hydrocarbon bottoms: Aromatic oil, (1.5% asphaltene content; initial B.P., 650 F.; API gravity, -1; Watson Characterization Factor, 9.0.
The shot coke forming feedstock and the aromatic oil blending stock are separately preheated to 915 F. and then separately fed to a coking drum (20' diameter, 80' high) at a rate of 350 barrels/hr. and 100 barrels/hr., respectively, with a recycle ratio of 1.5 (total feed/fresh feed). Pressure in the drum is 45 p.s.i.g. Coking time is 12 hours with a total cycle time of 24 hours.
The coke produced is high porosity sponge coke with a bulk density 1" crushed coke with about +4 mesh solids) of about 43 lbs./ft. Hydrogen content is about 39%, sulfur content, 1.15%; and ash, 0.27%. Total surface area (1" particle) is about 400-600 ft. /ft. Shot coke of comparable size has a surface area of 75- 100 ft. /ft.
Large anodes for alumina electrolytic reduction cells formed from this sponge coke are comparable in every respect to those formed from sponge coke produced from conventional sponge coke forming feedstock.
EXAMPLE 2 Following the procedure of Example 1, sponge coke having substantially the same properties is produced by substituting as the shot coke forming feedstock atmospheric virgin residual hydrocarbons (11% asphaltene content; API gravity, 14.5; Watson Characterization Factor, 11.1).
Similarly, sponge coke is prdouced according to the procedure of Example 1 employing as shot coke forming feedstock the residue of a solvent hydrocarbon extraction (25% asphaltene content) or a hydrocarbon asphalt (35 asphaltene content) in combination with a proportion of aromatic oil which provides a total asphaltene content of about 10%.
Sponge coke is also produced according to the procedure of Example 1 by substituting as low-asphaltene content hydrocarbon bottoms, the same proportion of pressure tar (1.5% asphaltene content); bottoms of refined deasphalted hydrocarbons (0.3% asphaltene content); the residues of polyethylene production (0% asphaltene content) or coal tar bottoms (0.1% asphaltene content).
What is claimed is:
1. A process for the production of porous, low density sponge coke from coking feedstock which produces dense, hard particulate shot coke in a conventional delayed coking operation which comprises the steps of:
(a) measuring the asphaltene content of a coking feedstock having an asphaltene content above about 13% and which normally produces shot coke in a conventional delayed coking process; and
(b) using a mixture of said shot coke forming coking feedstock and a hydrocarbon bottoms having an asphaltene content below about 8%, in a proportion such that the total asphaltene content of the mixture is below about 13%, as the coking feedstock in said conventional delayed coking operation.
2. A process according to claim 1 wherein the shot coke forming feedstock has about 13-25% asphaltene content.
3. A process according to claim 2 wherein the shot coke forming feedstock is selected from the group consisting of (a) atmospheric distilled virgin residual hydrocarbons;
(b) vacuum distilled virgin residual hydrocarbons;
(c) solvent extracted residual hydrocarbons; and
(d) hydrocarbon asphalts.
4. A process according to claim 1 wherein the mixture of feedstocks has an asphaltene content of less than 10%.
5. A process according to claim 1 wherein the hydrocarbon bottoms has an asphaltene content of 02%.
6. A process according to claim 5 wherein the hydrocarbon bottoms is selected from the group consisting of:
(a) pressure tars;
(b) aromatic oils;
(c) deasphalted hydrocarbons;
(d) synthetic hydrocarbon residues;
(e) the residual aliphatic hydrocarbons of a crude oil which is substantially asphaltene-free; and
(f) aromatic coal tar hydrocarbons.
7. A process according to claim 6 wherein the hydrocarbon bottoms is an aromatic oil.
8. A process according to claim 2 wherein the hydrocarbon bottoms has an asphaltene content of 02%, and the mixture thereof and said shot coke forming feedstock has an asphaltene content of less than 10%.
9. A process according to claim 8 wherein the shot coke forming feedstock is selected from the group consisting of:
(at) atmospheric distilled virgin residual hydrocarbons;
(b)- vacuum distilled virgin residual hydrocarbons;
(c) solvent extracted residual hydrocarbons; and
(d) hydrocarbon asphalts, and wherein the hydrocarbon bottoms is selected from the group consisting of:
(a) pressure tars;
(b) aromatic oils;
(0) deasphalted hydrocarbons;
(d) synthetic hydrocarbon residues;
(e) the residual aliphatic hydrocarbons of a crude oil which is substantially asphaltene-free; and
(f) aromatic coal tar hydrocarbons.
10. A process according to claim 8 wherein the hydrocarbon bottoms is an aromatic oil.
I 6 11. A process for the production of porous, low density References Cited sponge coke in a conventional delayed coking operation UNITED STATES PATENTS employing a feedstock which produces dense, hard particulate shot coke, which comprises the steps of: 2775549 12/1256 Shea 208 '131 (a) blending a coking feedstock having an asphaltene 5 2,922,755 1/1960 'Hacldey 208*39 content above about 13% and which normally pro- 3472761 10/1969 Cameron 208 131 duces shot Icloke in da congentiognal deluged coking OTHER REFERENCES process wit a y rocar on ottoms avlng an asphaltene content below about 8%, in a proportion Scott Chemlstry and Industry (London) July 1967 such that the total asphaltene content of the resulting 10 1124-31 mixture of feedstocks is less than about 13%, and
TOBIAS E. LEV-OW, P E (b) using said blend as the feedstock in said convennmary Xammer tional delayed coking operation, A. P. DEMERS, Assistant Examiner 12. A process according to claim 11 wherein the hydrocarbon bottoms has an asphaltene content of 0-5% and 15 the blend has an asphaltene content less than 10%. 208-39 86 UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent NO- 3'. 684. 697 Dated Au ust 15. 1972 V Inventor(s) Bernard William Gamson It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:
Column 1, line after "Calif. 90036" insert ---assignor to Harvey Aluminum (Incorporated), Torrance, Calif. 90509-- Signed and sealed this 17th day of April 1973.
(SEAL) Attest:
EDWARD M.FLETCHER,JR. ROBERT ,GOTTSCHALK Attesting Officer Comm-iss ioner' of Patents FQRM Po-mso (10-69) USCOMM-DC 6037 5-P69 u.s. sovemmsm' PRINTING orncs: i959 o-asssu
US99319A 1970-12-17 1970-12-17 Petroleum coke production Expired - Lifetime US3684697A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US9931970A 1970-12-17 1970-12-17

Publications (1)

Publication Number Publication Date
US3684697A true US3684697A (en) 1972-08-15

Family

ID=22274455

Family Applications (1)

Application Number Title Priority Date Filing Date
US99319A Expired - Lifetime US3684697A (en) 1970-12-17 1970-12-17 Petroleum coke production

Country Status (5)

Country Link
US (1) US3684697A (en)
DE (1) DE2160527A1 (en)
GB (1) GB1332424A (en)
IT (1) IT945444B (en)
NO (1) NO131939C (en)

Cited By (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6048448A (en) * 1997-07-01 2000-04-11 The Coastal Corporation Delayed coking process and method of formulating delayed coking feed charge
US20020179493A1 (en) * 1999-08-20 2002-12-05 Environmental & Energy Enterprises, Llc Production and use of a premium fuel grade petroleum coke
US20040256292A1 (en) * 2003-05-16 2004-12-23 Michael Siskin Delayed coking process for producing free-flowing coke using a substantially metals-free additive
US20050258071A1 (en) * 2004-05-14 2005-11-24 Ramesh Varadaraj Enhanced thermal upgrading of heavy oil using aromatic polysulfonic acid salts
US20050258075A1 (en) * 2004-05-14 2005-11-24 Ramesh Varadaraj Viscoelastic upgrading of heavy oil by altering its elastic modulus
US20050263440A1 (en) * 2003-05-16 2005-12-01 Ramesh Varadaraj Delayed coking process for producing free-flowing coke using polymeric additives
WO2005113708A1 (en) * 2004-05-14 2005-12-01 Exxonmobil Research And Engineering Company Blending of resid feedstocks to produce a coke that is easier to remove from a coker drum
US20050269247A1 (en) * 2004-05-14 2005-12-08 Sparks Steven W Production and removal of free-flowing coke from delayed coker drum
US20050279672A1 (en) * 2003-05-16 2005-12-22 Ramesh Varadaraj Delayed coking process for producing free-flowing coke using low molecular weight aromatic additives
US20050279673A1 (en) * 2003-05-16 2005-12-22 Eppig Christopher P Delayed coking process for producing free-flowing coke using an overbased metal detergent additive
US20060006101A1 (en) * 2004-05-14 2006-01-12 Eppig Christopher P Production of substantially free-flowing coke from a deeper cut of vacuum resid in delayed coking
US20090057192A1 (en) * 2007-08-28 2009-03-05 Leta Daniel P Deasphalter unit throughput increase via resid membrane feed preparation
US20090057203A1 (en) * 2007-08-28 2009-03-05 Leta Daniel P Enhancement of saturates content in heavy hydrocarbons utilizing ultrafiltration
US20090057196A1 (en) * 2007-08-28 2009-03-05 Leta Daniel P Production of an enhanced resid coker feed using ultrafiltration
US20090062590A1 (en) * 2007-08-28 2009-03-05 Nadler Kirk C Process for separating a heavy oil feedstream into improved products
US20090057198A1 (en) * 2007-08-28 2009-03-05 Leta Daniel P Upgrade of visbroken residua products by ultrafiltration
US20090057226A1 (en) * 2007-08-28 2009-03-05 Leta Daniel P Reduction of conradson carbon residue and average boiling points utilizing high pressure ultrafiltration
US20090057200A1 (en) * 2007-08-28 2009-03-05 Leta Daniel P Production of an upgraded stream from steam cracker tar by ultrafiltration
US20090100912A1 (en) * 2004-12-15 2009-04-23 Graham Butler Process For Evaluating Fouling Caused By Refinery Feedstocks
US20090145810A1 (en) * 2006-11-17 2009-06-11 Etter Roger G Addition of a Reactor Process to a Coking Process
US20090152165A1 (en) * 2006-11-17 2009-06-18 Etter Roger G System and Method for Introducing an Additive into a Coking Process to Improve Quality and Yields of Coker Products
US20090184029A1 (en) * 2008-01-22 2009-07-23 Exxonmobil Research And Engineering Company Method to alter coke morphology using metal salts of aromatic sulfonic acids and/or polysulfonic acids
US20090209799A1 (en) * 2006-11-17 2009-08-20 Etter Roger G System and Method of Introducing an Additive with a Unique Catalyst to a Coking Process
US20100170827A1 (en) * 2006-11-17 2010-07-08 Etter Roger G Selective Cracking and Coking of Undesirable Components in Coker Recycle and Gas Oils
WO2010151361A1 (en) * 2009-06-25 2010-12-29 Bp Corporation North America Inc. Hydrocarbon conversion process additive and related processes
US9011672B2 (en) 2006-11-17 2015-04-21 Roger G. Etter System and method of introducing an additive with a unique catalyst to a coking process
US11072745B1 (en) * 2020-04-20 2021-07-27 Saudi Arabian Oil Company Two-stage delayed coking process to produce anode grade coke

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4551232A (en) * 1983-02-09 1985-11-05 Intevep, S.A. Process and facility for making coke suitable for metallurgical purposes
GB2362912B (en) * 2000-06-02 2003-12-24 Kvaerner Cementation Found Ltd Applying crowd force in piling rigs

Cited By (67)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6048448A (en) * 1997-07-01 2000-04-11 The Coastal Corporation Delayed coking process and method of formulating delayed coking feed charge
US20060032788A1 (en) * 1999-08-20 2006-02-16 Etter Roger G Production and use of a premium fuel grade petroleum coke
US20020179493A1 (en) * 1999-08-20 2002-12-05 Environmental & Energy Enterprises, Llc Production and use of a premium fuel grade petroleum coke
US9475992B2 (en) 1999-08-20 2016-10-25 Roger G. Etter Production and use of a premium fuel grade petroleum coke
US20050263440A1 (en) * 2003-05-16 2005-12-01 Ramesh Varadaraj Delayed coking process for producing free-flowing coke using polymeric additives
US7306713B2 (en) 2003-05-16 2007-12-11 Exxonmobil Research And Engineering Company Delayed coking process for producing free-flowing coke using a substantially metals-free additive
US20040256292A1 (en) * 2003-05-16 2004-12-23 Michael Siskin Delayed coking process for producing free-flowing coke using a substantially metals-free additive
US7645375B2 (en) 2003-05-16 2010-01-12 Exxonmobil Research And Engineering Company Delayed coking process for producing free-flowing coke using low molecular weight aromatic additives
US7658838B2 (en) 2003-05-16 2010-02-09 Exxonmobil Research And Engineering Company Delayed coking process for producing free-flowing coke using polymeric additives
US20040262198A1 (en) * 2003-05-16 2004-12-30 Michael Siskin Delayed coking process for producing free-flowing coke using a metals-containing addivitive
US7303664B2 (en) 2003-05-16 2007-12-04 Exxonmobil Research And Engineering Company Delayed coking process for producing free-flowing coke using a metals-containing additive
US20050279672A1 (en) * 2003-05-16 2005-12-22 Ramesh Varadaraj Delayed coking process for producing free-flowing coke using low molecular weight aromatic additives
US20050279673A1 (en) * 2003-05-16 2005-12-22 Eppig Christopher P Delayed coking process for producing free-flowing coke using an overbased metal detergent additive
CN1954047B (en) * 2004-05-14 2010-10-27 埃克森美孚研究工程公司 Blending of resid feedstocks to produce a coke that is easier to remove from a coker drum
US7537686B2 (en) 2004-05-14 2009-05-26 Exxonmobil Research And Engineering Company Inhibitor enhanced thermal upgrading of heavy oils
US20060021907A1 (en) * 2004-05-14 2006-02-02 Ramesh Varadaraj Inhibitor enhanced thermal upgrading of heavy oils
US20050258071A1 (en) * 2004-05-14 2005-11-24 Ramesh Varadaraj Enhanced thermal upgrading of heavy oil using aromatic polysulfonic acid salts
US20060183950A1 (en) * 2004-05-14 2006-08-17 Ramesh Varadaraj Preparation of aromatic polysulfonic acid compositions from light cat cycle oil
US20050269247A1 (en) * 2004-05-14 2005-12-08 Sparks Steven W Production and removal of free-flowing coke from delayed coker drum
US20050258075A1 (en) * 2004-05-14 2005-11-24 Ramesh Varadaraj Viscoelastic upgrading of heavy oil by altering its elastic modulus
US20050284798A1 (en) * 2004-05-14 2005-12-29 Eppig Christopher P Blending of resid feedstocks to produce a coke that is easier to remove from a coker drum
US20050258070A1 (en) * 2004-05-14 2005-11-24 Ramesh Varadaraj Fouling inhibition of thermal treatment of heavy oils
US20060006101A1 (en) * 2004-05-14 2006-01-12 Eppig Christopher P Production of substantially free-flowing coke from a deeper cut of vacuum resid in delayed coking
US7374665B2 (en) 2004-05-14 2008-05-20 Exxonmobil Research And Engineering Company Blending of resid feedstocks to produce a coke that is easier to remove from a coker drum
US7794586B2 (en) 2004-05-14 2010-09-14 Exxonmobil Research And Engineering Company Viscoelastic upgrading of heavy oil by altering its elastic modulus
US7732387B2 (en) 2004-05-14 2010-06-08 Exxonmobil Research And Engineering Company Preparation of aromatic polysulfonic acid compositions from light cat cycle oil
US7727382B2 (en) 2004-05-14 2010-06-01 Exxonmobil Research And Engineering Company Production and removal of free-flowing coke from delayed coker drum
US7704376B2 (en) 2004-05-14 2010-04-27 Exxonmobil Research And Engineering Company Fouling inhibition of thermal treatment of heavy oils
US7594989B2 (en) 2004-05-14 2009-09-29 Exxonmobile Research And Engineering Company Enhanced thermal upgrading of heavy oil using aromatic polysulfonic acid salts
WO2005113708A1 (en) * 2004-05-14 2005-12-01 Exxonmobil Research And Engineering Company Blending of resid feedstocks to produce a coke that is easier to remove from a coker drum
US20050263438A1 (en) * 2004-05-14 2005-12-01 Ramesh Varadaraj Inhibitor enhanced thermal upgrading of heavy oils via mesophase suppression using oil soluble polynuclear aromatics
US7984643B2 (en) * 2004-12-15 2011-07-26 Bp Oil International Limited Process for evaluating fouling caused by refinery feedstocks
US20090100912A1 (en) * 2004-12-15 2009-04-23 Graham Butler Process For Evaluating Fouling Caused By Refinery Feedstocks
US20090152165A1 (en) * 2006-11-17 2009-06-18 Etter Roger G System and Method for Introducing an Additive into a Coking Process to Improve Quality and Yields of Coker Products
US8394257B2 (en) 2006-11-17 2013-03-12 Roger G. Etter Addition of a reactor process to a coking process
US9187701B2 (en) 2006-11-17 2015-11-17 Roger G. Etter Reactions with undesirable components in a coking process
US20090145810A1 (en) * 2006-11-17 2009-06-11 Etter Roger G Addition of a Reactor Process to a Coking Process
US9150796B2 (en) 2006-11-17 2015-10-06 Roger G. Etter Addition of a modified vapor line reactor process to a coking process
US9011672B2 (en) 2006-11-17 2015-04-21 Roger G. Etter System and method of introducing an additive with a unique catalyst to a coking process
US8968553B2 (en) 2006-11-17 2015-03-03 Roger G. Etter Catalytic cracking of undesirable components in a coking process
US8888991B2 (en) 2006-11-17 2014-11-18 Roger G. Etter System and method for introducing an additive into a coking process to improve quality and yields of coker products
US20090209799A1 (en) * 2006-11-17 2009-08-20 Etter Roger G System and Method of Introducing an Additive with a Unique Catalyst to a Coking Process
US20100170827A1 (en) * 2006-11-17 2010-07-08 Etter Roger G Selective Cracking and Coking of Undesirable Components in Coker Recycle and Gas Oils
US8372264B2 (en) 2006-11-17 2013-02-12 Roger G. Etter System and method for introducing an additive into a coking process to improve quality and yields of coker products
US8372265B2 (en) 2006-11-17 2013-02-12 Roger G. Etter Catalytic cracking of undesirable components in a coking process
US8361310B2 (en) 2006-11-17 2013-01-29 Etter Roger G System and method of introducing an additive with a unique catalyst to a coking process
US8206574B2 (en) 2006-11-17 2012-06-26 Etter Roger G Addition of a reactor process to a coking process
US20090062590A1 (en) * 2007-08-28 2009-03-05 Nadler Kirk C Process for separating a heavy oil feedstream into improved products
US20090057198A1 (en) * 2007-08-28 2009-03-05 Leta Daniel P Upgrade of visbroken residua products by ultrafiltration
US7867379B2 (en) 2007-08-28 2011-01-11 Exxonmobil Research And Engineering Company Production of an upgraded stream from steam cracker tar by ultrafiltration
US7871510B2 (en) 2007-08-28 2011-01-18 Exxonmobil Research & Engineering Co. Production of an enhanced resid coker feed using ultrafiltration
US7897828B2 (en) 2007-08-28 2011-03-01 Exxonmobile Research And Engineering Company Process for separating a heavy oil feedstream into improved products
US20090057203A1 (en) * 2007-08-28 2009-03-05 Leta Daniel P Enhancement of saturates content in heavy hydrocarbons utilizing ultrafiltration
US8177965B2 (en) 2007-08-28 2012-05-15 Exxonmobil Research And Engineering Company Enhancement of saturates content in heavy hydrocarbons utilizing ultrafiltration
US7815790B2 (en) 2007-08-28 2010-10-19 Exxonmobil Research And Engineering Company Upgrade of visbroken residua products by ultrafiltration
US20090057192A1 (en) * 2007-08-28 2009-03-05 Leta Daniel P Deasphalter unit throughput increase via resid membrane feed preparation
WO2009032156A1 (en) * 2007-08-28 2009-03-12 Exxonmobil Research And Engineering Company Production of an enhanced resid coker feed using ultrafiltration
US20090057196A1 (en) * 2007-08-28 2009-03-05 Leta Daniel P Production of an enhanced resid coker feed using ultrafiltration
US7736493B2 (en) 2007-08-28 2010-06-15 Exxonmobil Research And Engineering Company Deasphalter unit throughput increase via resid membrane feed preparation
US8864996B2 (en) 2007-08-28 2014-10-21 Exxonmobil Research And Engineering Company Reduction of conradson carbon residue and average boiling points utilizing high pressure ultrafiltration
US20090057200A1 (en) * 2007-08-28 2009-03-05 Leta Daniel P Production of an upgraded stream from steam cracker tar by ultrafiltration
US20090057226A1 (en) * 2007-08-28 2009-03-05 Leta Daniel P Reduction of conradson carbon residue and average boiling points utilizing high pressure ultrafiltration
US20090184029A1 (en) * 2008-01-22 2009-07-23 Exxonmobil Research And Engineering Company Method to alter coke morphology using metal salts of aromatic sulfonic acids and/or polysulfonic acids
US7794587B2 (en) 2008-01-22 2010-09-14 Exxonmobil Research And Engineering Company Method to alter coke morphology using metal salts of aromatic sulfonic acids and/or polysulfonic acids
US20100326880A1 (en) * 2009-06-25 2010-12-30 Bp Corporation North America Inc. Hydrocarbon Conversion Process Additive and Related Processes
WO2010151361A1 (en) * 2009-06-25 2010-12-29 Bp Corporation North America Inc. Hydrocarbon conversion process additive and related processes
US11072745B1 (en) * 2020-04-20 2021-07-27 Saudi Arabian Oil Company Two-stage delayed coking process to produce anode grade coke

Also Published As

Publication number Publication date
NO131939C (en) 1975-08-27
NO131939B (en) 1975-05-20
DE2160527B2 (en) 1975-08-07
DE2160527A1 (en) 1973-02-01
IT945444B (en) 1973-05-10
GB1332424A (en) 1973-10-03

Similar Documents

Publication Publication Date Title
US3684697A (en) Petroleum coke production
US4096097A (en) Method of producing high quality sponge coke or not to make shot coke
US4075084A (en) Manufacture of low-sulfur needle coke
DE2160527C3 (en)
EP0008493A1 (en) Delayed coking process with hydrotreated recycle and graphitized products thereof
US3767564A (en) Production of low pour fuel oils
GB1562447A (en) Process for the production of petroleum coke
US5028311A (en) Delayed coking process
US4235703A (en) Method for producing premium coke from residual oil
US3369992A (en) Low pour point synthetic crude oil
US3284334A (en) Molded carbon bodies
US4720338A (en) Premium coking process
US4130475A (en) Process for making premium coke
US3326796A (en) Production of electrode grade petroleum coke
US3238116A (en) Coke binder oil
EP0285261A1 (en) Premium coking process
US4234387A (en) Coking poor coking coals and hydrocracked tar sand bitumen binder
JP2008504376A (en) A delayed coking process for producing free-flowing coke using low molecular weight aromatic additives.
US4201658A (en) Pour point depressant made from the asphaltene component of thermally treated shale oil
EP0090897A2 (en) Delayed coking of a heat-treated ethylene tar
GB1575279A (en) Process for making premium coke
US4713168A (en) Premium coking process
US5071515A (en) Method for improving the density and crush resistance of coke
US4014781A (en) Method for producing pitch and coke
US4740293A (en) Premium coke from a blend of pyrolysis tar and hydrotreated decant oil

Legal Events

Date Code Title Description
AS Assignment

Owner name: MARTIN MARIETTA CORPORATION, A CORP OF MD

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:MARTIN MARIETTA ALUMINUM INC., A CORP OF CA;REEL/FRAME:004403/0818

Effective date: 19841221