US3069251A - Synthesis gas generation with recovery of naturally-occurring metal values - Google Patents
Synthesis gas generation with recovery of naturally-occurring metal values Download PDFInfo
- Publication number
- US3069251A US3069251A US42197A US4219760A US3069251A US 3069251 A US3069251 A US 3069251A US 42197 A US42197 A US 42197A US 4219760 A US4219760 A US 4219760A US 3069251 A US3069251 A US 3069251A
- Authority
- US
- United States
- Prior art keywords
- carbon
- reaction
- naturally
- heavy
- recovery
- 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
- 229910052751 metal Inorganic materials 0.000 title description 21
- 239000002184 metal Substances 0.000 title description 21
- 230000015572 biosynthetic process Effects 0.000 title description 8
- 238000011084 recovery Methods 0.000 title description 7
- 238000003786 synthesis reaction Methods 0.000 title description 7
- 229910052799 carbon Inorganic materials 0.000 description 42
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 41
- 229930195733 hydrocarbon Natural products 0.000 description 30
- 150000002430 hydrocarbons Chemical class 0.000 description 30
- 229910001385 heavy metal Inorganic materials 0.000 description 27
- 239000007789 gas Substances 0.000 description 24
- 238000006243 chemical reaction Methods 0.000 description 20
- 150000002736 metal compounds Chemical class 0.000 description 18
- 239000004215 Carbon black (E152) Substances 0.000 description 17
- 239000000446 fuel Substances 0.000 description 13
- 238000000034 method Methods 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 11
- 238000010791 quenching Methods 0.000 description 10
- 238000007254 oxidation reaction Methods 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- 239000007787 solid Substances 0.000 description 9
- 239000007795 chemical reaction product Substances 0.000 description 8
- 239000000470 constituent Substances 0.000 description 8
- 239000003208 petroleum Substances 0.000 description 8
- 229910052720 vanadium Inorganic materials 0.000 description 8
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 8
- 150000002739 metals Chemical class 0.000 description 7
- 230000003647 oxidation Effects 0.000 description 7
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 6
- 229910002091 carbon monoxide Inorganic materials 0.000 description 6
- 238000002309 gasification Methods 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 229910052759 nickel Inorganic materials 0.000 description 6
- 239000001301 oxygen Substances 0.000 description 6
- 229910052760 oxygen Inorganic materials 0.000 description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
- 239000010779 crude oil Substances 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 4
- 239000011819 refractory material Substances 0.000 description 4
- -1 bitnmins Substances 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000010426 asphalt Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 150000001721 carbon Chemical class 0.000 description 1
- 150000001722 carbon compounds Chemical class 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 230000003628 erosive effect Effects 0.000 description 1
- 239000002737 fuel gas Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229910001092 metal group alloy Inorganic materials 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000005201 scrubbing Methods 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B3/00—Extraction of metal compounds from ores or concentrates by wet processes
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/20—Recycling
Definitions
- Both liquid and semi-solid heavy hydrocarbons containing heavy metal constituents can be gasificd 'in accordance with the method of this invention.
- the non-catalytic partial oxidation of hydrocarbons by reaction with free oxygen and steam at elevated temperature to produce carbon monoxide and hydrogen is of considerable commercial importance.
- Both liquid and semi-solid hydrocarbons may be gasified by reaction of the hydrocarbon at an autogenously maintained temperature above about 2,000 F. with steam and an oxygencontaining gas to produce a gas mixture comprising carbon monoxide and hydrogen.
- nitrogen is desirable in the product gas, for example, for ammonia synthesis, or is relatively innocuous, as in fuel gas or reducing gas
- air or oxygenenriched air may be used for the gasification reaction.
- Carbon monoxide produced in the reaction may be subjected to reaction with steam in a separate water gas shift reaction step to produce an equivalent quantity of hydrogen.
- Petroleum particularly heavy crude oils, bitnmins, and asphalt commonly contain small quantities of naturallyoccurring heavy metal compounds.
- Heavy crude oils and crude residua from refinery operations often have relatively high contents of metals in the form of their compounds.
- the most common heavy metals contained in petroleum are vanadium, nickel, iron, chromium, and molybdenum.
- the exact chemical compositions of the compounds comprising the naturally-occurring heavy metals are somewhat in doubt. It is generally agreed, however, that the metals are present, at least in part, in the form of oil-soluble metallo-organic compounds. Petroleum fuels containing naturally-occurring heavy metal compounds are referred to herein as ash-forming hydro carbons.
- Ash-forming hydrocarbons are unsatisfactory as fuels for many purposes because of the corrosive nature of their ash.
- the corrosiveness of the ash is due primarily to oxidation products of the naturally-occurring metal compounds.
- the ash from such heavy hydrocarbons has been found to be particularly detrimental to oxidic refractory materials available for high temperature service, e.g. 2,000 to 3500 F., as required for a successful direct partial oxidation of hydrocarbons to carbon monoxide and hydrogen.
- the present invention provides a method for protection of gas generation and simultaneous recovery of metal values contained in the ash-forming hydrocarbons.
- Heavy metals occur in petroleum in varying amounts ranging from a trace to as much as 2,000 parts per million by weight based upon the weight of the metal, per se. Many of the heavy hydrocarbon crude oils contain heavy metals in concentration on the order of 200 parts per million. A Venezuelan crude contains as much as 1200 p.p.m. vanadium. Hydrocarbons containing in excess of In one of its more specific as- 50 p.p.m. vanadium are generally not satisfactory as fuels because of the corrosive, or erosive, nature of the ash both to high temperature refractory and to metal alloys. In contrast, petroleum hydrocarbons containing higher concentrations of heavier metals are preferred as charge for the process of this invention.
- Heavy metal constitucuts of petroleum may be concentrated by distillation, the heavy metal compounds largely remaining in the distillation residues.
- the process of this invention is particularly applicable to recovery of the metals from such distillation residues which are of limited value as fuel.
- the residue from propane deasphalting and solvent refinery operations often comprise heavy metal-rich residues suitable as charge stock for the present process.
- High temperature refractories may be protected from attack by heavy metal compounds of petroleum as is disclosed in United States patent by Du Bois Eastman, 2,976,135.
- This application discloses a process in which hydrocarbon oil containing metal constituents is subjected to partial combustion with oxygen and steam at a temperature above 2,000 F. under conditions such that carbon contained in said hydrocarbon is liberated as free carbon in an amount at least equal to fifty times the combined weights of the vanadium and nickel metals contained in the hydrocarbon so that metallic constituents of the hydrocarbon combine with the carbon without damage to the refractory walls of the reaction vessel.
- Carbon containing the heavy metal compounds is separated from the product gas by washing the gas stream with water.
- the present invention provides a method of gasifying petroleum fuels containing naturally-occurring heavy metal compounds in which complete utilization of the carbon content of the fuel is accomplished while at the same time protecting the refractory walls of the reaction vessel from attack by oxidation products of metals contained in the fuel.
- the present invention also permits recovery of heavy metals or their compounds in concentrated form, substantially free from carbon. The concentrate so obtained is a valuable by-product of the gasification process which may be used in steel manufacture.
- hydrocarbons containing heavy metals can be gasified with no net production of carbon while still protecting the refractory materials of the reaction chamber from attack by heavy metal compounds. This is accomplished by carrying out the partial oxidation of the carbonaceous fuel with an insufficient quantity of free oxygen for complete conversion of carbon contained in the fuel carbon compounds so that carbon in an amount within the range of 1 to 5 percent of the carbon contained in said hydrocarbon, preferably 2 to 3 percent, is liberated as free carbon. Apparently the freshly formed carbon occludes ash resulting from the partial oxidation of the ash-forming hydrocarbon.
- Th s carbon, containing said ash, is returned to the partial oxidation reaction zone wherein the carbon is consumed to form additional carbon monoxide while the metal content of said carbon, comprising heavy metal compounds, is liberated from the carbon. It has been found, unexpectedly, that when the heavy metals or their compounds are so liberated from the carbon they do not attack the refractory materials of the generator. The liberated heavy metal compounds are removed from the gas stream and from the free carbon combined with heavy metal compounds contained in the gas stream by means of water as described hereinafter.
- the liberated carbon containing naturally-occurring heavy metal compounds is recycled to the synthesis gas generator wherein the carbon is converted to carbon monoxide and hydrogen by reaction with steam and oxygen while the metals, mostly in the form of water-insoluble sulfides, are liberated in liquid or solid form and discharged from the gas generation zone with the gas stream.
- Gas generated in the synthesis gas generation zone is quench-cooled by direct contact with water in a quench zone.
- the metal compounds contained in the gas stream are accumulated in the form of small granular particles in the quench zone. These particles are retained in the water in the quench zone. The solid particles settle to the bottom of the quench water which also contains carbon separated from the gas stream.
- the heavy metal compounds are readily separated from the carbon-containing quench water by settling.
- the liberated heavy metals or heavy metal compounds are heavier than the carbon and have a higher settling rate than the settling rate of the carbon.
- Carbon remains suspended in the quench water due to the agitation of the water by the hot gas from the generator whereas the heavier metal compounds settle to the bottom of the quench vessel and may be withdrawn therefrom with a small amount of water.
- Carbon removed from the synthesis gas stream in the quenching and scrubbing operation is separately recovered from the quench water and recycled to the gas generator.
- This carbon contains some of the heavy metal compounds. It may be admixed with the liquid hydrocarbon feed to the gas generator, for example by the method described in US. Patent 2,665,980 to Charles R. Carkeek or recycled in other suitable manner. It has been found, contrary to expectations, that so long as sufficient carbon is produced from the hydrocarbon liquid to sequester the metal originally present in the hydrocarbon, i.e.
- a process for the generation of synthesis gas and simultaneous recovery of metal values from heavy hydrocarbon fuels containing naturally-occurring metal constituents comprising vanadium and nickel which oomprises subjecting said fuel to partial oxidation in a reaction zone at a temperature in the range of 2000 to 3500 F.
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Geochemistry & Mineralogy (AREA)
- Geology (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Environmental & Geological Engineering (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Hydrogen, Water And Hydrids (AREA)
Description
United States Patent 'Ofiice 3,069,251 Patented Dec. 18, 1962 3,069,251 SYNTHESIS GAS GENERATION WITH RECOVERY OF NATURALLY-OCCURRING METAL VALUES Du Bois Eastman, Whittier, Roger M. Dille, La Habra, and Ronald W. Chapman, Whittier, Califi, assignors to Texaco Inc., New York, N.Y., a corporation of Delaware No Drawing. Filed July 12, 1960, Ser. No. 42,197 1 Claim. (Cl. 48-+215) This invention relates to a method for the gasification of heavy hydrocarbons. pects, it relates to the recovery of metal values from hydrocarbons containing naturally-occurring heavy metal constituents. Both liquid and semi-solid heavy hydrocarbons containing heavy metal constituents can be gasificd 'in accordance with the method of this invention. The non-catalytic partial oxidation of hydrocarbons by reaction with free oxygen and steam at elevated temperature to produce carbon monoxide and hydrogen is of considerable commercial importance. Both liquid and semi-solid hydrocarbons may be gasified by reaction of the hydrocarbon at an autogenously maintained temperature above about 2,000 F. with steam and an oxygencontaining gas to produce a gas mixture comprising carbon monoxide and hydrogen. Generally, it is desirable to carry out the gasification reaction with steam and substantially pure oxygen, i.e. oxygen of at least 95 volume percent purity. If nitrogen is desirable in the product gas, for example, for ammonia synthesis, or is relatively innocuous, as in fuel gas or reducing gas, air or oxygenenriched air may be used for the gasification reaction. Carbon monoxide produced in the reaction may be subjected to reaction with steam in a separate water gas shift reaction step to produce an equivalent quantity of hydrogen.
Petroleum, particularly heavy crude oils, bitnmins, and asphalt commonly contain small quantities of naturallyoccurring heavy metal compounds. Heavy crude oils and crude residua from refinery operations often have relatively high contents of metals in the form of their compounds. The most common heavy metals contained in petroleum are vanadium, nickel, iron, chromium, and molybdenum. The exact chemical compositions of the compounds comprising the naturally-occurring heavy metals are somewhat in doubt. It is generally agreed, however, that the metals are present, at least in part, in the form of oil-soluble metallo-organic compounds. Petroleum fuels containing naturally-occurring heavy metal compounds are referred to herein as ash-forming hydro carbons. Ash-forming hydrocarbons, particularly crude oil, crude residua, and heavy distillates from crude oils, are unsatisfactory as fuels for many purposes because of the corrosive nature of their ash. The corrosiveness of the ash is due primarily to oxidation products of the naturally-occurring metal compounds. The ash from such heavy hydrocarbons has been found to be particularly detrimental to oxidic refractory materials available for high temperature service, e.g. 2,000 to 3500 F., as required for a successful direct partial oxidation of hydrocarbons to carbon monoxide and hydrogen. The present invention provides a method for protection of gas generation and simultaneous recovery of metal values contained in the ash-forming hydrocarbons.
Heavy metals occur in petroleum in varying amounts ranging from a trace to as much as 2,000 parts per million by weight based upon the weight of the metal, per se. Many of the heavy hydrocarbon crude oils contain heavy metals in concentration on the order of 200 parts per million. A Venezuelan crude contains as much as 1200 p.p.m. vanadium. Hydrocarbons containing in excess of In one of its more specific as- 50 p.p.m. vanadium are generally not satisfactory as fuels because of the corrosive, or erosive, nature of the ash both to high temperature refractory and to metal alloys. In contrast, petroleum hydrocarbons containing higher concentrations of heavier metals are preferred as charge for the process of this invention. Heavy metal constitucuts of petroleum may be concentrated by distillation, the heavy metal compounds largely remaining in the distillation residues. The process of this invention is particularly applicable to recovery of the metals from such distillation residues which are of limited value as fuel. The residue from propane deasphalting and solvent refinery operations often comprise heavy metal-rich residues suitable as charge stock for the present process.
High temperature refractories may be protected from attack by heavy metal compounds of petroleum as is disclosed in United States patent by Du Bois Eastman, 2,976,135. This application discloses a process in which hydrocarbon oil containing metal constituents is subjected to partial combustion with oxygen and steam at a temperature above 2,000 F. under conditions such that carbon contained in said hydrocarbon is liberated as free carbon in an amount at least equal to fifty times the combined weights of the vanadium and nickel metals contained in the hydrocarbon so that metallic constituents of the hydrocarbon combine with the carbon without damage to the refractory walls of the reaction vessel. Carbon containing the heavy metal compounds is separated from the product gas by washing the gas stream with water.
The present invention provides a method of gasifying petroleum fuels containing naturally-occurring heavy metal compounds in which complete utilization of the carbon content of the fuel is accomplished while at the same time protecting the refractory walls of the reaction vessel from attack by oxidation products of metals contained in the fuel. The present invention also permits recovery of heavy metals or their compounds in concentrated form, substantially free from carbon. The concentrate so obtained is a valuable by-product of the gasification process which may be used in steel manufacture.
It has now been found that hydrocarbons containing heavy metals can be gasified with no net production of carbon while still protecting the refractory materials of the reaction chamber from attack by heavy metal compounds. This is accomplished by carrying out the partial oxidation of the carbonaceous fuel with an insufficient quantity of free oxygen for complete conversion of carbon contained in the fuel carbon compounds so that carbon in an amount within the range of 1 to 5 percent of the carbon contained in said hydrocarbon, preferably 2 to 3 percent, is liberated as free carbon. Apparently the freshly formed carbon occludes ash resulting from the partial oxidation of the ash-forming hydrocarbon. Th s carbon, containing said ash, is returned to the partial oxidation reaction zone wherein the carbon is consumed to form additional carbon monoxide while the metal content of said carbon, comprising heavy metal compounds, is liberated from the carbon. It has been found, unexpectedly, that when the heavy metals or their compounds are so liberated from the carbon they do not attack the refractory materials of the generator. The liberated heavy metal compounds are removed from the gas stream and from the free carbon combined with heavy metal compounds contained in the gas stream by means of water as described hereinafter.
In the process of this invention, the liberated carbon containing naturally-occurring heavy metal compounds is recycled to the synthesis gas generator wherein the carbon is converted to carbon monoxide and hydrogen by reaction with steam and oxygen while the metals, mostly in the form of water-insoluble sulfides, are liberated in liquid or solid form and discharged from the gas generation zone with the gas stream. Gas generated in the synthesis gas generation zone is quench-cooled by direct contact with water in a quench zone. The metal compounds contained in the gas stream are accumulated in the form of small granular particles in the quench zone. These particles are retained in the water in the quench zone. The solid particles settle to the bottom of the quench water which also contains carbon separated from the gas stream. The heavy metal compounds are readily separated from the carbon-containing quench water by settling. The liberated heavy metals or heavy metal compounds are heavier than the carbon and have a higher settling rate than the settling rate of the carbon. Carbon remains suspended in the quench water due to the agitation of the water by the hot gas from the generator whereas the heavier metal compounds settle to the bottom of the quench vessel and may be withdrawn therefrom with a small amount of water.
Carbon removed from the synthesis gas stream in the quenching and scrubbing operation is separately recovered from the quench water and recycled to the gas generator. This carbon, as previously explained, contains some of the heavy metal compounds. It may be admixed with the liquid hydrocarbon feed to the gas generator, for example by the method described in US. Patent 2,665,980 to Charles R. Carkeek or recycled in other suitable manner. It has been found, contrary to expectations, that so long as sufficient carbon is produced from the hydrocarbon liquid to sequester the metal originally present in the hydrocarbon, i.e. to produce free carbon in an amount at least equal in weight to 50 times the combined Weight of the vanadium and nickel contained in the hydrocarbon, expressed as pure metals, the refractory lining of the gasification reaction vessel is protected from attack by the ash or slag from the hydrocarbon. This is entirely unexpected since the recycled carbon contains a fairly high percentage of the heavy metal compounds. All of the carbon can be returned to the gasification zone and completely consumed so that there is no net production of carbon in the process.
Obviously, many modifications and variations of the invention as hereinbefore set forth, may be made without departing from the spirit and scope thereof, and therefore only such limitations should be imposed as are indicated in the appended claim.
We claim:
A process for the generation of synthesis gas and simultaneous recovery of metal values from heavy hydrocarbon fuels containing naturally-occurring metal constituents comprising vanadium and nickel which oomprises subjecting said fuel to partial oxidation in a reaction zone at a temperature in the range of 2000 to 3500 F. by reaction with steam and a free oxygen-containing gas in relative proportions such that from about 1 to about 5 percent of the carbon contained in said hydrocarbon is liberated as free carbon together with reaction products of metal constituents comprising vanadium and nickel from said hydrocarbon fuel, separating said liberated free carbon containing said reaction products from gaseous products of reaction, returning said separated free carbon containing said reaction products to said partial oxidation reaction into admixture with said hydrocarbon fuel whereby said carbon is ultimately substantially completely consumed thereby releasing normally solid reaction products of said metal constituents, discharging gaseous products of reaction together with released solid reaction products and said liberated carbon from said reaction zone, quench cooling said gaseous products of reaction containing said released solid reaction products of said metal constituent and said liberated carbon by direct contact with liquid water in excess of the amount vaporizable by the heat contained in said products of reaction eliecting removal of liberated carbon from gaseous products and the formation of dense granular particles of said released solid reaction products comprising vanadium and nickel substantially free from carbon, and recovering said granular particles of released solid reaction products from said water and carbon by sedimentation.
References Cited in the file of this patent UNITED STATES PATENTS 2,665,980 Carkeek Jan. 12, 1954 2,920,936 Dille et a1 Jan. 12, 1960 2,976,135 Eastman Mar. 21, 1961
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US42197A US3069251A (en) | 1960-07-12 | 1960-07-12 | Synthesis gas generation with recovery of naturally-occurring metal values |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US42197A US3069251A (en) | 1960-07-12 | 1960-07-12 | Synthesis gas generation with recovery of naturally-occurring metal values |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3069251A true US3069251A (en) | 1962-12-18 |
Family
ID=21920579
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US42197A Expired - Lifetime US3069251A (en) | 1960-07-12 | 1960-07-12 | Synthesis gas generation with recovery of naturally-occurring metal values |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3069251A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3607157A (en) * | 1969-07-23 | 1971-09-21 | Texaco Inc | Synthesis gas from petroleum coke |
| US3620700A (en) * | 1969-08-15 | 1971-11-16 | Warren G Schlinger | Recovery of entrained carbon in synthesis gas |
| US3912464A (en) * | 1971-03-20 | 1975-10-14 | Maschf Augsburg Nuernberg Ag | Method of and device for separating solid components from a hot combustible gas generated in a reactor |
| US4155985A (en) * | 1977-02-14 | 1979-05-22 | Metallgesellschaft Aktiengesellschaft | Process of purifying gases |
| AU665710B2 (en) * | 1993-03-26 | 1996-01-11 | Hoechst Aktiengesellschaft | Process for the production of synthesis gas |
| US5578094A (en) * | 1994-12-08 | 1996-11-26 | Texaco Inc. | Vanadium addition to petroleum coke slurries to facilitate deslagging for controlled oxidation |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2665980A (en) * | 1950-05-05 | 1954-01-12 | Texas Co | Process for generation of carbon monoxide |
| US2920936A (en) * | 1957-05-14 | 1960-01-12 | Texaco Inc | Recovery of heavy metals from hydrocarbons |
| US2976135A (en) * | 1961-03-21 | Generation of carbon monoxide and hydrogen |
-
1960
- 1960-07-12 US US42197A patent/US3069251A/en not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2976135A (en) * | 1961-03-21 | Generation of carbon monoxide and hydrogen | ||
| US2665980A (en) * | 1950-05-05 | 1954-01-12 | Texas Co | Process for generation of carbon monoxide |
| US2920936A (en) * | 1957-05-14 | 1960-01-12 | Texaco Inc | Recovery of heavy metals from hydrocarbons |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3607157A (en) * | 1969-07-23 | 1971-09-21 | Texaco Inc | Synthesis gas from petroleum coke |
| US3620700A (en) * | 1969-08-15 | 1971-11-16 | Warren G Schlinger | Recovery of entrained carbon in synthesis gas |
| US3912464A (en) * | 1971-03-20 | 1975-10-14 | Maschf Augsburg Nuernberg Ag | Method of and device for separating solid components from a hot combustible gas generated in a reactor |
| US4155985A (en) * | 1977-02-14 | 1979-05-22 | Metallgesellschaft Aktiengesellschaft | Process of purifying gases |
| AU665710B2 (en) * | 1993-03-26 | 1996-01-11 | Hoechst Aktiengesellschaft | Process for the production of synthesis gas |
| US5578094A (en) * | 1994-12-08 | 1996-11-26 | Texaco Inc. | Vanadium addition to petroleum coke slurries to facilitate deslagging for controlled oxidation |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3607157A (en) | Synthesis gas from petroleum coke | |
| US3740193A (en) | Hydrogen production by catalytic steam gasification of carbonaceous materials | |
| US3998609A (en) | Synthesis gas generation | |
| US4668429A (en) | Partial oxidation process | |
| US5441990A (en) | Cleaned, H2 -enriched syngas made using water-gas shift reaction | |
| US4668428A (en) | Partial oxidation process | |
| US3920579A (en) | Synthesis gas production by partial oxidation | |
| US4588850A (en) | Process for the production of acetylene and synthesis or reduction gas from coal in an electric arc process | |
| US4141696A (en) | Process for gas cleaning with reclaimed water and apparatus for water reclamation | |
| US4671804A (en) | Partial oxidation process | |
| US4205962A (en) | Process for gas cleaning with reclaimed water | |
| EP0290689B1 (en) | Partial oxidation process | |
| US3232728A (en) | Synthesis gas generation | |
| US3069251A (en) | Synthesis gas generation with recovery of naturally-occurring metal values | |
| US4692172A (en) | Coal gasification process | |
| US4705539A (en) | Partial oxidation process | |
| US6350289B1 (en) | Two-zone molten metal hydrogen-rich and carbon monoxide-rich gas generation process | |
| US4141695A (en) | Process for gas cleaning with reclaimed water | |
| KR100323961B1 (en) | A process for the gasification of a petroleum coke feedstock | |
| US4784670A (en) | Partial oxidation process | |
| US4952380A (en) | Partial oxidation process | |
| US2999741A (en) | Production of carbon monoxide and hydrogen | |
| US4851152A (en) | Prevention of formation of nickel subsulfide in partial oxidation of heavy liquid and/or solid fuels | |
| US4411670A (en) | Production of synthesis gas from heavy hydrocarbon fuels containing high metal concentrations | |
| US3846095A (en) | Reducing gas generation |