US2372109A - Recovery of vanadium - Google Patents
Recovery of vanadium Download PDFInfo
- Publication number
- US2372109A US2372109A US387700A US38770041A US2372109A US 2372109 A US2372109 A US 2372109A US 387700 A US387700 A US 387700A US 38770041 A US38770041 A US 38770041A US 2372109 A US2372109 A US 2372109A
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- United States
- Prior art keywords
- vanadium
- fraction
- bitumen
- ash
- water
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- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 title description 56
- 229910052720 vanadium Inorganic materials 0.000 title description 54
- 238000011084 recovery Methods 0.000 title description 14
- 239000010426 asphalt Substances 0.000 description 33
- 238000000034 method Methods 0.000 description 26
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 24
- 239000002956 ash Substances 0.000 description 23
- 239000003208 petroleum Substances 0.000 description 23
- 239000003921 oil Substances 0.000 description 21
- 238000002485 combustion reaction Methods 0.000 description 16
- 239000007787 solid Substances 0.000 description 14
- 238000009835 boiling Methods 0.000 description 12
- 239000000571 coke Substances 0.000 description 11
- 239000000428 dust Substances 0.000 description 11
- 239000002245 particle Substances 0.000 description 11
- 239000003546 flue gas Substances 0.000 description 10
- 239000007788 liquid Substances 0.000 description 10
- 150000003682 vanadium compounds Chemical class 0.000 description 10
- 239000007789 gas Substances 0.000 description 9
- 238000005406 washing Methods 0.000 description 9
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 8
- GNTDGMZSJNCJKK-UHFFFAOYSA-N divanadium pentaoxide Chemical compound O=[V](=O)O[V](=O)=O GNTDGMZSJNCJKK-UHFFFAOYSA-N 0.000 description 8
- XHCLAFWTIXFWPH-UHFFFAOYSA-N [O-2].[O-2].[O-2].[O-2].[O-2].[V+5].[V+5] Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[V+5].[V+5] XHCLAFWTIXFWPH-UHFFFAOYSA-N 0.000 description 7
- 238000001816 cooling Methods 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- 229910001935 vanadium oxide Inorganic materials 0.000 description 7
- 239000000463 material Substances 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 230000003647 oxidation Effects 0.000 description 5
- 238000007254 oxidation reaction Methods 0.000 description 5
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 4
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 4
- 239000003153 chemical reaction reagent Substances 0.000 description 4
- 239000010779 crude oil Substances 0.000 description 4
- 238000004821 distillation Methods 0.000 description 4
- 229910052742 iron Inorganic materials 0.000 description 4
- 230000001590 oxidative effect Effects 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 239000000567 combustion gas Substances 0.000 description 3
- PNXOJQQRXBVKEX-UHFFFAOYSA-N iron vanadium Chemical compound [V].[Fe] PNXOJQQRXBVKEX-UHFFFAOYSA-N 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 238000005204 segregation Methods 0.000 description 3
- 239000011343 solid material Substances 0.000 description 3
- 229910000628 Ferrovanadium Inorganic materials 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 235000019270 ammonium chloride Nutrition 0.000 description 2
- UNTBPXHCXVWYOI-UHFFFAOYSA-O azanium;oxido(dioxo)vanadium Chemical compound [NH4+].[O-][V](=O)=O UNTBPXHCXVWYOI-UHFFFAOYSA-O 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 239000010881 fly ash Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- HWSZZLVAJGOAAY-UHFFFAOYSA-L lead(II) chloride Chemical compound Cl[Pb]Cl HWSZZLVAJGOAAY-UHFFFAOYSA-L 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- 238000005292 vacuum distillation Methods 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 229910000640 Fe alloy Inorganic materials 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- KSECJOPEZIAKMU-UHFFFAOYSA-N [S--].[S--].[S--].[S--].[S--].[V+5].[V+5] Chemical group [S--].[S--].[S--].[S--].[S--].[V+5].[V+5] KSECJOPEZIAKMU-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- -1 alkaline earth metal carbonates Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- UYJXRRSPUVSSMN-UHFFFAOYSA-P ammonium sulfide Chemical compound [NH4+].[NH4+].[S-2] UYJXRRSPUVSSMN-UHFFFAOYSA-P 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 239000003575 carbonaceous material Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000011221 initial treatment Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 238000005272 metallurgy Methods 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 239000011301 petroleum pitch Substances 0.000 description 1
- 239000011295 pitch Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000012716 precipitator Substances 0.000 description 1
- 230000003134 recirculating effect Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- CMZUMMUJMWNLFH-UHFFFAOYSA-N sodium metavanadate Chemical compound [Na+].[O-][V](=O)=O CMZUMMUJMWNLFH-UHFFFAOYSA-N 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000003886 thermite process Methods 0.000 description 1
- LSGOVYNHVSXFFJ-UHFFFAOYSA-N vanadate(3-) Chemical compound [O-][V]([O-])([O-])=O LSGOVYNHVSXFFJ-UHFFFAOYSA-N 0.000 description 1
- 150000003681 vanadium Chemical class 0.000 description 1
- 229910000166 zirconium phosphate Inorganic materials 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G31/00—Compounds of vanadium
-
- 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
- C22B34/00—Obtaining refractory metals
- C22B34/20—Obtaining niobium, tantalum or vanadium
- C22B34/22—Obtaining vanadium
Definitions
- the present invention is concerned with the recovery of vanadium.
- the invention more particularly relates to a process for the segregation and recovery of vanadium from petroleum oils.
- vanadium is recovered from petroleum oils by segregating a high boiling solid or semi-solid fraction from the feed oil, followed by burning and oxidizing the segregated solid fraction under controlled conditions.
- vanadium is present in various petroleum oils. However, due to the fact that the concentration of the same is relatively small, operations directed for its recovery from these oils have not, been commercially successful. I have, however, now discovered an operation by which the vanadium may be readily and efficiently recovered, utilizing a particular arrangement and sequence of distillation and oxidizing stages. The process of my invention may be readily understood by reference to the drawing illustrating one particular embodiment of the same.
- the feed oil is a Venezuelan crude oil.
- the feed oil is introduced into initial heating and distillation zone 2 by means of feed line I.
- Temperature and pressure conditions in zone 2 are adapted to remove the relatively lower boiling hydrocarbon constituents overhead by means of lines 3 and 4 respectively and to remove by means of line 5 a reduced crude fraction.
- This fraction is passed into a secondary heating and distillation zone 6.
- the secondary distillation zone 6 comprises a vacuum distillation or equivalent zone.
- Temperature and pressure conditions in zone 6 are adapted to remove relatively low boiling constituents by means of lines 1 and 8 and to segregate a high boiling bitumen fraction which is removed as a bottoms product by means of line 9.
- This fraction is cooled in cooling zone I0 and ,solldrierd by contact with water as it passes to the storage pile II.
- the solid material is withdrawn from zone Il by Lvmeans of line I2 whichmay comprise any. suitable conveying means, and passed to feed hopper I3.
- the material is passed into rotary burner Il where it rolls on the lining of the burner.
- Excess air is supplied to the burner at feeder outlet I5. under conditions to promote combustion of the residuum within the burner and to maintain the temperature below the point at which the burner lining would fuse with the partially burned bitumen.
- Air is supplied to the burner through air 4box 3l by means of forced air fan I8.
- the residuum is introduced into the burner by conveying means I6 which together with the main burner shell I4, is powered by driving gear Il.
- the hot gases pass from the burner to a boiler iire box and thence around tubes I9 and are withdrawn by means of flue gas duct 2l.
- Tubes I9 comprise an integral part of boiler 20.
- the residuum is coked and largely burned in burner i4.
- the incompletely burned particles pass from the burner with the combustion gases into the boiler ilre box where they are subjected to roasting, further oxidizing the carbon content and increasing the vanadium percentage content.
- contain considerable vanadium dust. This dust is preferably removed from the flue gases by means of a circulated liquid and the dissolved vanadium compound precipitated from the liquid.
- the flue gases are passed to stack 22 through ilue gas scrubber 23 wherein the ue gases are contacted with a washing liquid which is introduced by means of line ⁇ 24.
- the washing liquid preferably comprises Water.
- the water containing vanadium bearing dust suspended or dissolved therein, is removed by means of line 25 and passed to settling zone 26 in which zone the dust is separated from the water and removed by means of line 21, while the washing liquid is' recirculated to scrubber 23 by means of pump 34.
- a part of the vanadium remains with the dust and may be recovered therefrom in subsequentA operations.
- a part of the vanadium is also dissolved in the wash water. The concentration of vanadium may be increased by the water recirculation.
- a portion of the water is withdrawn from settling zone 26 by means of line 28 and passed to vanadium precipitating zone 29 wherein a reagent is added and the vanadium compound precipitated from the water.
- a reagent is added and the vanadium compound precipitated from the water.
- 'I'he vanadium compound is removed from zone 29 by means of line 20, while the water is removed by means of line 3l.
- Additional water suicient to make up for the water withdrawn by means of line 28 is supplied to the system by means of line 32.
- the process of the present invention may be widely varied.
- the invention is essentially directed to a method for recovering vanadium from petroleum oils by utilizing a solid or semi-solid petroleum oil fraction.
- the invention essentially comprises burning the segregated solid or semisolid fraction under conditions to produce an ash product having sufficiently high vanadium con.
- the fraction segregated trom the crude oil preferably comprises high softening point bitumen bottoms, such as these having softening points in the range above 300 F., preferably those having softening points in the range from about 350 F. to 425 F.. as determined by test DSG-26 A. S. T. M. method, "softening Point of Bituminous Materials-Ring and Ball Method.”
- a particularly desirable operation comprises segregating brittle bitumen representing from about to 20% bottoms of Venezuelan crudes, which pitches have softening points in the range from about 250 F. to 450 F., and which preferably have softening points of about 350 F.
- the bituminous product segregated may be burned in lthe solid form eitherl as lumps or granules in a special burner such as the one described or as powder from a modified coal pulverizer, through a water-cooled burner nozzle, and the product of initial combustion roasted to produce ash high in vanadium oxide content.
- the coke particles produced in the initial combustion of bitumen are first introduced from the burner into the boiler fire box, they contain an excessive amount of carbon.
- the coke particles are allowed to accumulate on the floor of the ilre box and excess air is supplied for their oxidation. Under these conditions the coke particles will be roasted and further decarbonized.
- the solid petroleum material is discharged into the burner o ⁇ r kiln the volatile components are disengaged almost instantly thereby contributing their heat to the burner or kiln.
- the coke resulting from this initial combustion is difficult to burn but is eventually oxidized in accordance with the present process to ash by being retained in the furnace for an appreciable period of time at elevated temperatures. In the roasting process the coke loses-the major portion of its carbon content, resulting in an ash having a relatively high concentration of vanadium.
- Vanadium bearing brittle bitumen or petroleum pitch may be introduced into the ilre box by blowing means or by a chute or by employing mechanical means.
- the larger particles of coke produced in the initial flash combustion are preferentially disposed in the furnace so as to permit continued oxidation under the influence of a high furnace temperature and excess air either in the roasting zone or combustion zone.
- the auxiliary air is supplied preierably through the floor on which the coke is roasting, if the latter operation be employed.
- the auxiliary air is supplied at the burner inlet. The use of both sources of air may be desirable.
- Venezuelan crude oil contains about 0.03% oi' vanadium and that the bitumen produced by vacuum distillation of the reduced crude or uncracked crude contains about 0.13% of vanadium.
- the bitumen loses 50% to 80% of its weight almost instantaneously and the remaining coke is very diilicult to burn.
- such a coke representing about 46% of the bitumen requires roasting of about one hour at a temperature of l500 F'. in the presence of a considerable excess of air, in order to oxidize the ash.
- the ash produced as described contains from about 10% to 30% of vanadium oxide.
- the ily ash containing an appreciable amount of vanadium may be recovered in any satisfactory manner, as for example, by Cottrell precipitator or by means of a cyclone dust separator. It is, however, preferred to recover the ily ash by washing the flue gases, preferably with a washing solvent comprising water. In accordance with a preferred operation, the water is reclrculated to contact additional portions of the flue gases in order to increase the concentration therein of dissolved vanadium compounds since more water is needed to remove dust from flue gas than is required to dissolve all the available vanadium
- the dissolved vanadium compounds may be recovered by any suitable method, such as by precipitation, utilizing a reagent as for example lead chloride or an equivalent reagent.
- a reagent as for example lead chloride or an equivalent reagent.
- Vanadium pentoxide is soluble in cold water to the extent of 0.8 part by weight per parts. In order to secure this concentration it is desirable to recirculate the water from about ilve to twenty-live times, employing a usual rate of water supply as, for example, 15 to 25 pounds of water per 1,000 cubic feet of flue gas. 'I'he solvent is removed from the scrubber and passed to the settler wherein the ily ash is deposited and where a clarified liquid is separated and recirculated to the scrubber. A portion of the clarified liquid is withdrawn continuously and treated for vanadium recovery, .usually by treating with a solvent such as lead chloride or by cooling, and the like.
- a solvent such as lead chloride or by cooling, and the like.
- Example 1 Lump bitumen representing about 18% bottoms of a Venezuelan crude and having a softening point of about 350 F. was fed into a horizontal rotary kiln which discharged into a boiler setting. It was found that the coke formed by the initial ilash combustion was in the form of light flakes containing 1.5% vanadium oxide. These flakes were further oxidized in the kiln before being blown out onto the floor of the boiler. The floor dust and the ily ash were oxidized under these conditions to vanadium oxide content of 7.5% to 14.5% respectively. In the same equipment operated with less excess air, the kiln temperatures rose to about 2200 F., which caused 4.5% vanadium oxide.
- Example 2 In an operation in which lump bitumen of the character described was fed into a hammer type pulverizer and then discharged into a boiler setting through a water-cooled burner, it was found that the floor dust averaged about 5.0% vanadium oxide and the fly ash averaged about 8% vanadium oxide.
- the vanadium-containing ash may be handled by any suitable method.
- the ash or iiue dust may be mixed with a suitable uxing reagent, such as alkali and alkaline earth metal carbonates, and roasted in a reverberatory furnace.
- a preferred iluxing agent comprises sodium carbonate.
- the slag thus formed is leached with water, after which the water solution may be treated chemically for removal of vanadium or may be evaporated and the residue so obtained reduced to ferro vanadium.
- Thermite process may also be used as a suitable means of converting the vanadium to ferro vanadium.
- the vanadium may be segregated from the concentrated ash by treating with fuming hydrochloric acid in the presence of ethyll alcohol.
- the solution thus obtained is filtered, in which case metallic compounds insoluble in the above treatment will remain as a residue, and the filtrate evaporated with excess acid.
- 'I'he residue so obtained may be treated with an alkali metal hydroxide solution such as a sodium hydroxide solution, the vanadium contained therein oxidized with a suitable oxidizing agent such as chlorine, after which ammonium vanadate is precipitated by the addition of ammonium chloride to the solution.
- This precipitate represents a rather pure material, and if desired may be converted to vanadium pentoxide by suitable ignition.
- the vanadium concentrate so obtained may be employed directly in processing of iron while making various steels.
- the ash obtained by the present operation particularly when utilizing a Venezuelan crude oil, also contains various other metallic elements such as nickel, aluminum, and iron.
- the vanadium concentrate may be added directly to operations involved in the metallurgy of iron, particularly the iron ore going to blast furnaces, in
- the vanadium may also be recovered from the ash by chemical treatment involving an initial treatment with nitric acid.
- the solution so ob-l tained is freed of foreign elements such as lead by a suitable means known to the art as, for example, with aqueous and ammonium sulfide.
- the precipitate formed at this point is removed and the filtrate acidied, whereupon a precipitate of vanadium sulfide forms which is separated. Further purication or processing of the vanadium so obtained may be followed.
- the product may be roasted, followed by an alkali fusion so that the vanadium salt will be formed.
- the sodium vanadate so obtained is crystallized out of solution as ammonium vanadate by the addition of ammonium chloride.
- the vanadate may be heated to produce vanadium pent/oxide.
- Process for the recovery of vanadium from peroleum oils which comprises treating the petroleum oil in a manner to segregate a relatively high boiling fraction of semi-solid to solid mate rial, burning said high boiling fraction in the presence of sufficient air to burn a maior proportion of the combustible materials in said high boiling fraction, segregating the resulting ash and recovering the vanadium therefrom.
- Process for the recovery of vanadium from petroleum oils containing the same which comprises treating the petroleum oil in a manner to segregate a bitumen fraction having a softening point in the range from about 250 F. to 450 F., cooling said bitumen fraction and granulating the same, subjecting the granulated bitumen fraction to oxidizing conditions at elevated temperatures in the presence of excess air sufficient to oxidize substantially all of the carbonaceous content of said bitumen fraction, removing the resulting ash and recovering the vanadium therefrom.
- bitumen fraction has a softening point of about 350 F. and in which said fraction is subjected to oxidation at a temperature of 1500 F. to 2000 F. for a period of about one hour.
- Process for the segregation of vanadium from petroleum oils containing the same which comprises treating said petroleum oil in a manner to segregate a semi-solid to solid bitumen 40 fraction having a softening point in the range from about 250 F. to 450 F., burning said bitumen fraction at elevated temperatures in the presence of excess air sufficient to oxidize substantially all of the carbonaceous content of said bitumen fraction, removing the carboniferous ash and recovering the vanadium therefrom, removing the gases from the oxidation zone, and treating the same to remove vanadium compounds therefrom.
- a process for the recovery of vanadium from petroleum oils containing the same which comprises treating the petroleum oil in a manner to segregate a relatively high boiling fraction of semi-solid to solid material, subjecting said high boiling fraction to combustion in at least two stages to burn a major proportion of the combustible materials contained in said high boiling fraction, separating the resultant ash and recovering the vanadium therefrom.
- a process for the recovery of vanadium from petroleum oils containing the same which comprises treating the petroleum oil in a manner to segregate a semi-solid to solid bitumen fraction having a softening point in the range from about 250 F. to about 450 F., cooling said bitumen fraction and finely subdividing the same,
- bitumen fraction subjecting the nely subdivided bitumen to combustion in at least two stages in the presence of excess air to burn a major proportion of the combustible materials contained in said bitumen fraction, separating the resultant ash and recovw ering vanadium therefrom.
- a process for the recovery of vanadium from petroleum oils containing the same which comprises treating the petroleum oils in a manner to segregate a bitumen fraction having a softening point in the range from about 250 F. to 450 F., cooling said bitumen fraction and finely subdividing the same, subjecting the iinely subdivided bitumen to combustion with an excess of air, collecting the incompletely burned particles produced in this combustion in a heated zone, supplying excess air thereto, roasting and decarbonizing the same, separating the ash formed and recovering the vanadium.
- a process for the recovery of vanadium from petroleum oils containing the same which comprises treating the petroleum oils in a manner to segregate a bitumen fraction having a softening point in the range from about 250 F. to 450 F., cooling said bitumen fraction and nely subdividing the same, subjecting the finely subdivided bitumen to combustion with an excess of air, collecting the incompletely burned particles y washing liquid through the scrubber in order to' produced in this combustion in a heated zone, supplying excess air thereto, roasting and decarbonizing the same. passing the combustion gases and entrained ash particles through a scrubber, ⁇
- a process for the recovery of vanadium from petroleum oils containing the same which comprises treating the petroleum oils in a manner to segregate a bitumen fraction having a softening point in the range from about 250 F. to 450 F., cooling said bitumen fraction and finely subdividing the same, subjecting the nely subdivided bitumen to combustion with an excess of air, collecting the incompletely burned particles produced in this combustion in a heated zone, supplying excess air thereto, roasting and decarbonizing the same, passing the combustion gases and entrained ash particles through a scrubber, washing the said gases with a liquid capable of dissolving vanadium pentoxide, recirculating the increase the concentration of vanadium compounds dissolved therein, and recovering the vanadium therefrom.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Inorganic Chemistry (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Manufacture And Refinement Of Metals (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Description
Patented Mar. 20, 1945 RECOVERY F VANADIUM Henry M. Noel, Summit, N. J assignor to Standard Oil Development Company, a corporation of Delaware Application April 9. 1941, Serial No. 387,700
. 14 Claims.
The present invention is concerned with the recovery of vanadium. The invention more particularly relates to a process for the segregation and recovery of vanadium from petroleum oils. In accordance with the present invention, vanadium is recovered from petroleum oils by segregating a high boiling solid or semi-solid fraction from the feed oil, followed by burning and oxidizing the segregated solid fraction under controlled conditions.
It is known in the art that vanadium is present in various petroleum oils. However, due to the fact that the concentration of the same is relatively small, operations directed for its recovery from these oils have not, been commercially successful. I have, however, now discovered an operation by which the vanadium may be readily and efficiently recovered, utilizing a particular arrangement and sequence of distillation and oxidizing stages. The process of my invention may be readily understood by reference to the drawing illustrating one particular embodiment of the same.
Referring specifically to the drawing, it is as sumed for the purpose of description that the feed oil is a Venezuelan crude oil. The feed oil is introduced into initial heating and distillation zone 2 by means of feed line I. Temperature and pressure conditions in zone 2 are adapted to remove the relatively lower boiling hydrocarbon constituents overhead by means of lines 3 and 4 respectively and to remove by means of line 5 a reduced crude fraction. This fraction is passed into a secondary heating and distillation zone 6. For purposes of description it is assumed that the secondary distillation zone 6 comprises a vacuum distillation or equivalent zone. Temperature and pressure conditions in zone 6 are adapted to remove relatively low boiling constituents by means of lines 1 and 8 and to segregate a high boiling bitumen fraction which is removed as a bottoms product by means of line 9. This fraction is cooled in cooling zone I0 and ,solldiiled by contact with water as it passes to the storage pile II. The solid material is withdrawn from zone Il by Lvmeans of line I2 whichmay comprise any. suitable conveying means, and passed to feed hopper I3.
The material is passed into rotary burner Il where it rolls on the lining of the burner. Excess air is supplied to the burner at feeder outlet I5. under conditions to promote combustion of the residuum within the burner and to maintain the temperature below the point at which the burner lining would fuse with the partially burned bitumen. Air is supplied to the burner through air 4box 3l by means of forced air fan I8. The residuum is introduced into the burner by conveying means I6 which together with the main burner shell I4, is powered by driving gear Il.
. The hot gases pass from the burner to a boiler iire box and thence around tubes I9 and are withdrawn by means of flue gas duct 2l. Tubes I9 comprise an integral part of boiler 20. The residuum is coked and largely burned in burner i4. The incompletely burned particles pass from the burner with the combustion gases into the boiler ilre box where they are subjected to roasting, further oxidizing the carbon content and increasing the vanadium percentage content. Under the conditions of theoperation, the flue gases removed by flue gas duct 2| contain considerable vanadium dust. This dust is preferably removed from the flue gases by means of a circulated liquid and the dissolved vanadium compound precipitated from the liquid. If this operation be employed, the flue gases are passed to stack 22 through ilue gas scrubber 23 wherein the ue gases are contacted with a washing liquid which is introduced by means of line` 24. The washing liquid preferably comprises Water. The water containing vanadium bearing dust suspended or dissolved therein, is removed by means of line 25 and passed to settling zone 26 in which zone the dust is separated from the water and removed by means of line 21, while the washing liquid is' recirculated to scrubber 23 by means of pump 34. A part of the vanadium remains with the dust and may be recovered therefrom in subsequentA operations. A part of the vanadium is also dissolved in the wash water. The concentration of vanadium may be increased by the water recirculation. A portion of the water is withdrawn from settling zone 26 by means of line 28 and passed to vanadium precipitating zone 29 wherein a reagent is added and the vanadium compound precipitated from the water. 'I'he vanadium compound is removed from zone 29 by means of line 20, while the water is removed by means of line 3l. Additional water suicient to make up for the water withdrawn by means of line 28 is supplied to the system by means of line 32.
The process of the present invention may be widely varied. The invention is essentially directed to a method for recovering vanadium from petroleum oils by utilizing a solid or semi-solid petroleum oil fraction. The invention essentially comprises burning the segregated solid or semisolid fraction under conditions to produce an ash product having sufficiently high vanadium con.
centratien from which it is possible to recover efficiently the same, and in which process vanadium loss as vanadium dust in the flue gases is substantially entirely prevented.
Although the operation may be adapted for the segregation and recovery of vanadium from any petroleum oil containing it, itis particularly adapted for the removal of vanadium from asphaltio type crudas such as Lake Venezuela crudes. The fraction segregated trom the crude oil preferably comprises high softening point bitumen bottoms, such as these having softening points in the range above 300 F., preferably those having softening points in the range from about 350 F. to 425 F.. as determined by test DSG-26 A. S. T. M. method, "softening Point of Bituminous Materials-Ring and Ball Method."
A particularly desirable operation comprises segregating brittle bitumen representing from about to 20% bottoms of Venezuelan crudes, which pitches have softening points in the range from about 250 F. to 450 F., and which preferably have softening points of about 350 F. The bituminous product segregated may be burned in lthe solid form eitherl as lumps or granules in a special burner such as the one described or as powder from a modified coal pulverizer, through a water-cooled burner nozzle, and the product of initial combustion roasted to produce ash high in vanadium oxide content.
When the coke particles produced in the initial combustion of bitumen are first introduced from the burner into the boiler fire box, they contain an excessive amount of carbon. However, in accordance with the present process the coke particles are allowed to accumulate on the floor of the ilre box and excess air is supplied for their oxidation. Under these conditions the coke particles will be roasted and further decarbonized. When the solid petroleum material is discharged into the burner o`r kiln the volatile components are disengaged almost instantly thereby contributing their heat to the burner or kiln. The coke resulting from this initial combustion is difficult to burn but is eventually oxidized in accordance with the present process to ash by being retained in the furnace for an appreciable period of time at elevated temperatures. In the roasting process the coke loses-the major portion of its carbon content, resulting in an ash having a relatively high concentration of vanadium.
Vanadium bearing brittle bitumen or petroleum pitch may be introduced into the ilre box by blowing means or by a chute or by employing mechanical means. In practicing the present inven tion, it is desirable to water jacket the feed nozzle or burner in orderto prevent the feed stock from melting therein. The larger particles of coke produced in the initial flash combustion are preferentially disposed in the furnace so as to permit continued oxidation under the influence of a high furnace temperature and excess air either in the roasting zone or combustion zone. Ii.' this former operation be employed, the auxiliary air is supplied preierably through the floor on which the coke is roasting, if the latter operation be employed. the auxiliary air is supplied at the burner inlet. The use of both sources of air may be desirable. By operating in this manner a floor dust having a high concentration of vanadium is produced, which dust is recovered as hereinafter described from the fire box and from the ilue gases which contain an appreciable concentration oi' the same. The term "excess air" used herein means a quantity of air greater than that necescompounds therein.
Gli
sary to eiect complete combustion of coke or other carbonaceous materials contained in the oil fraction or residue treated. c
I have found that Venezuelan crude oil contains about 0.03% oi' vanadium and that the bitumen produced by vacuum distillation of the reduced crude or uncracked crude contains about 0.13% of vanadium. By burning this bitumen in .a hot furnace or kiln as described, the bitumen loses 50% to 80% of its weight almost instantaneously and the remaining coke is very diilicult to burn. I have found that such a coke representing about 46% of the bitumen requires roasting of about one hour at a temperature of l500 F'. in the presence of a considerable excess of air, in order to oxidize the ash. The ash produced as described contains from about 10% to 30% of vanadium oxide.
The ily ash containing an appreciable amount of vanadium may be recovered in any satisfactory manner, as for example, by Cottrell precipitator or by means of a cyclone dust separator. It is, however, preferred to recover the ily ash by washing the flue gases, preferably with a washing solvent comprising water. In accordance with a preferred operation, the water is reclrculated to contact additional portions of the flue gases in order to increase the concentration therein of dissolved vanadium compounds since more water is needed to remove dust from flue gas than is required to dissolve all the available vanadium The dissolved vanadium compounds may be recovered by any suitable method, such as by precipitation, utilizing a reagent as for example lead chloride or an equivalent reagent. One distinct advantage of an operation of this character is that the fine particles of fly ash removed by the water solvent are richer in vanadium than the coarser particles and the vanadium is thus more readily recovered.
Vanadium pentoxide is soluble in cold water to the extent of 0.8 part by weight per parts. In order to secure this concentration it is desirable to recirculate the water from about ilve to twenty-live times, employing a usual rate of water supply as, for example, 15 to 25 pounds of water per 1,000 cubic feet of flue gas. 'I'he solvent is removed from the scrubber and passed to the settler wherein the ily ash is deposited and where a clarified liquid is separated and recirculated to the scrubber. A portion of the clarified liquid is withdrawn continuously and treated for vanadium recovery, .usually by treating with a solvent such as lead chloride or by cooling, and the like.
In order to illustrate the invention further, the following examples are given which should not be construed as limiting the same in any manner whatsoever:
Example 1 Lump bitumen representing about 18% bottoms of a Venezuelan crude and having a softening point of about 350 F. was fed into a horizontal rotary kiln which discharged into a boiler setting. It was found that the coke formed by the initial ilash combustion was in the form of light flakes containing 1.5% vanadium oxide. These flakes were further oxidized in the kiln before being blown out onto the floor of the boiler. The floor dust and the ily ash were oxidized under these conditions to vanadium oxide content of 7.5% to 14.5% respectively. In the same equipment operated with less excess air, the kiln temperatures rose to about 2200 F., which caused 4.5% vanadium oxide.
Example 2 In an operation in which lump bitumen of the character described was fed into a hammer type pulverizer and then discharged into a boiler setting through a water-cooled burner, it was found that the floor dust averaged about 5.0% vanadium oxide and the fly ash averaged about 8% vanadium oxide.
The vanadium-containing ash may be handled by any suitable method. For example, the ash or iiue dust may be mixed with a suitable uxing reagent, such as alkali and alkaline earth metal carbonates, and roasted in a reverberatory furnace. A preferred iluxing agent comprises sodium carbonate. The slag thus formed is leached with water, after which the water solution may be treated chemically for removal of vanadium or may be evaporated and the residue so obtained reduced to ferro vanadium. The Thermite process may also be used as a suitable means of converting the vanadium to ferro vanadium.
The vanadium may be segregated from the concentrated ash by treating with fuming hydrochloric acid in the presence of ethyll alcohol. The solution thus obtained is filtered, in which case metallic compounds insoluble in the above treatment will remain as a residue, and the filtrate evaporated with excess acid. 'I'he residue so obtained may be treated with an alkali metal hydroxide solution such as a sodium hydroxide solution, the vanadium contained therein oxidized with a suitable oxidizing agent such as chlorine, after which ammonium vanadate is precipitated by the addition of ammonium chloride to the solution. This precipitate represents a rather pure material, and if desired may be converted to vanadium pentoxide by suitable ignition. The vanadium concentrate so obtained may be employed directly in processing of iron while making various steels. The ash obtained by the present operation, particularly when utilizing a Venezuelan crude oil, also contains various other metallic elements such as nickel, aluminum, and iron. Thus, the vanadium concentrate may be added directly to operations involved in the metallurgy of iron, particularly the iron ore going to blast furnaces, in
order to produce directly a vanadium iron alloy.
The vanadium may also be recovered from the ash by chemical treatment involving an initial treatment with nitric acid. The solution so ob-l tained is freed of foreign elements such as lead by a suitable means known to the art as, for example, with aqueous and ammonium sulfide. The precipitate formed at this point is removed and the filtrate acidied, whereupon a precipitate of vanadium sulfide forms which is separated. Further purication or processing of the vanadium so obtained may be followed. The product may be roasted, followed by an alkali fusion so that the vanadium salt will be formed. The sodium vanadate so obtained is crystallized out of solution as ammonium vanadate by the addition of ammonium chloride. The vanadate may be heated to produce vanadium pent/oxide.
I claim:
1. Process for the recovery of vanadium from peroleum oils, which comprises treating the petroleum oil in a manner to segregate a relatively high boiling fraction of semi-solid to solid mate rial, burning said high boiling fraction in the presence of sufficient air to burn a maior proportion of the combustible materials in said high boiling fraction, segregating the resulting ash and recovering the vanadium therefrom.
2. Process aS defined by claim 1, in which said relatively high boiling fraction has a softening point in the range from about 350 F. to 425 F.
3. Process as dened by claim 1, in which said relatively high boiling fraction comprises from about 10% to 20% bottoms of asphaltic type crudes and in which said product is oxidized at a temperature of about 1500 F. to 2000 F. in the presence of excess air.
4. Process as defined by claim 1, in which said segregated petroleum oil fraction is subjected to oxidation for a period of about one hour at a temperature of 1500 F. to 2000 F. in the presence oi' considerable excess air.
5. Process for the recovery of vanadium from petroleum oils containing the same, which comprises treating the petroleum oil in a manner to segregate a bitumen fraction having a softening point in the range from about 250 F. to 450 F., cooling said bitumen fraction and granulating the same, subjecting the granulated bitumen fraction to oxidizing conditions at elevated temperatures in the presence of excess air sufficient to oxidize substantially all of the carbonaceous content of said bitumen fraction, removing the resulting ash and recovering the vanadium therefrom.
6. Process as defined by claim 5, in which said bitumen fraction has a softening point of about 350 F. and in which said fraction is subjected to oxidation at a temperature of 1500 F. to 2000 F. for a period of about one hour.
7. Process for the segregation of vanadium from petroleum oils containing the same, which comprises treating said petroleum oil in a manner to segregate a semi-solid to solid bitumen 40 fraction having a softening point in the range from about 250 F. to 450 F., burning said bitumen fraction at elevated temperatures in the presence of excess air sufficient to oxidize substantially all of the carbonaceous content of said bitumen fraction, removing the carboniferous ash and recovering the vanadium therefrom, removing the gases from the oxidation zone, and treating the same to remove vanadium compounds therefrom.
8. Process as defined by claim 7, in which said vanadium compounds are removed from said gases by treating with a solvent comprising water.
9. Process as deiined by claim 7, in which said vanadium compounds are removed from the gases by treating with a washing solvent comprising water, which solvent is subsequently treated to precipitate vanadium compounds therefrom.
l0. A process for the recovery of vanadium from petroleum oils containing the same, which comprises treating the petroleum oil in a manner to segregate a relatively high boiling fraction of semi-solid to solid material, subjecting said high boiling fraction to combustion in at least two stages to burn a major proportion of the combustible materials contained in said high boiling fraction, separating the resultant ash and recovering the vanadium therefrom.
11. A process for the recovery of vanadium from petroleum oils containing the same, which comprises treating the petroleum oil in a manner to segregate a semi-solid to solid bitumen fraction having a softening point in the range from about 250 F. to about 450 F., cooling said bitumen fraction and finely subdividing the same,
subjecting the nely subdivided bitumen to combustion in at least two stages in the presence of excess air to burn a major proportion of the combustible materials contained in said bitumen fraction, separating the resultant ash and recovw ering vanadium therefrom.
12. A process for the recovery of vanadium from petroleum oils containing the same, which comprises treating the petroleum oils in a manner to segregate a bitumen fraction having a softening point in the range from about 250 F. to 450 F., cooling said bitumen fraction and finely subdividing the same, subjecting the iinely subdivided bitumen to combustion with an excess of air, collecting the incompletely burned particles produced in this combustion in a heated zone, supplying excess air thereto, roasting and decarbonizing the same, separating the ash formed and recovering the vanadium.
13. A process for the recovery of vanadium from petroleum oils containing the same, which comprises treating the petroleum oils in a manner to segregate a bitumen fraction having a softening point in the range from about 250 F. to 450 F., cooling said bitumen fraction and nely subdividing the same, subjecting the finely subdivided bitumen to combustion with an excess of air, collecting the incompletely burned particles y washing liquid through the scrubber in order to' produced in this combustion in a heated zone, supplying excess air thereto, roasting and decarbonizing the same. passing the combustion gases and entrained ash particles through a scrubber,`
washing the said gases with a liquid capable of dissolving vanadium pentoxide and recovering the vanadium therefrom.
14. A process for the recovery of vanadium from petroleum oils containing the same, which comprises treating the petroleum oils in a manner to segregate a bitumen fraction having a softening point in the range from about 250 F. to 450 F., cooling said bitumen fraction and finely subdividing the same, subjecting the nely subdivided bitumen to combustion with an excess of air, collecting the incompletely burned particles produced in this combustion in a heated zone, supplying excess air thereto, roasting and decarbonizing the same, passing the combustion gases and entrained ash particles through a scrubber, washing the said gases with a liquid capable of dissolving vanadium pentoxide, recirculating the increase the concentration of vanadium compounds dissolved therein, and recovering the vanadium therefrom.
HENRY M. NOEL.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US387700A US2372109A (en) | 1941-04-09 | 1941-04-09 | Recovery of vanadium |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US387700A US2372109A (en) | 1941-04-09 | 1941-04-09 | Recovery of vanadium |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2372109A true US2372109A (en) | 1945-03-20 |
Family
ID=23531028
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US387700A Expired - Lifetime US2372109A (en) | 1941-04-09 | 1941-04-09 | Recovery of vanadium |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2372109A (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE946288C (en) * | 1952-01-01 | 1956-07-26 | British Petroleum Co | Process for the extraction of vanadium |
| US3132920A (en) * | 1960-08-31 | 1964-05-12 | Kerr Mc Gee Oil Ind Inc | Process for recovery of vanadium values from aqueous liquors |
| US3384448A (en) * | 1965-07-23 | 1968-05-21 | Exxon Research Engineering Co | Process for recovering vanadium values from crude residua |
| US3416882A (en) * | 1965-08-25 | 1968-12-17 | Whigham William | Production of vanadium values from crude oil |
| US3522001A (en) * | 1968-01-22 | 1970-07-28 | Universal Oil Prod Co | Recovery of metals from carbonaceous material |
| US4110398A (en) * | 1977-04-08 | 1978-08-29 | Uop Inc. | Metal separation from dragstream material of refining process |
| US4243639A (en) * | 1979-05-10 | 1981-01-06 | Tosco Corporation | Method for recovering vanadium from petroleum coke |
| DE102007010776A1 (en) * | 2007-03-06 | 2008-09-11 | Gfe Metalle Und Materialien Gmbh | Process for the preparation of a heavy metal enriched, low-carbon concentrate from carbon-rich, heavy metal-containing residues, in particular petroleum processing |
-
1941
- 1941-04-09 US US387700A patent/US2372109A/en not_active Expired - Lifetime
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE946288C (en) * | 1952-01-01 | 1956-07-26 | British Petroleum Co | Process for the extraction of vanadium |
| US3132920A (en) * | 1960-08-31 | 1964-05-12 | Kerr Mc Gee Oil Ind Inc | Process for recovery of vanadium values from aqueous liquors |
| US3384448A (en) * | 1965-07-23 | 1968-05-21 | Exxon Research Engineering Co | Process for recovering vanadium values from crude residua |
| US3416882A (en) * | 1965-08-25 | 1968-12-17 | Whigham William | Production of vanadium values from crude oil |
| US3522001A (en) * | 1968-01-22 | 1970-07-28 | Universal Oil Prod Co | Recovery of metals from carbonaceous material |
| US4110398A (en) * | 1977-04-08 | 1978-08-29 | Uop Inc. | Metal separation from dragstream material of refining process |
| US4243639A (en) * | 1979-05-10 | 1981-01-06 | Tosco Corporation | Method for recovering vanadium from petroleum coke |
| DE102007010776A1 (en) * | 2007-03-06 | 2008-09-11 | Gfe Metalle Und Materialien Gmbh | Process for the preparation of a heavy metal enriched, low-carbon concentrate from carbon-rich, heavy metal-containing residues, in particular petroleum processing |
| DE102007010776B4 (en) * | 2007-03-06 | 2008-11-13 | Gfe Metalle Und Materialien Gmbh | Process for the preparation of a heavy metal enriched, low-carbon concentrate from carbon-rich, heavy metal-containing residues, in particular petroleum processing |
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