CA2623200C - Pyrometallurgical process for treating metal-containing materials - Google Patents
Pyrometallurgical process for treating metal-containing materials Download PDFInfo
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- CA2623200C CA2623200C CA2623200A CA2623200A CA2623200C CA 2623200 C CA2623200 C CA 2623200C CA 2623200 A CA2623200 A CA 2623200A CA 2623200 A CA2623200 A CA 2623200A CA 2623200 C CA2623200 C CA 2623200C
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- 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
- C22B34/30—Obtaining chromium, molybdenum or tungsten
- C22B34/36—Obtaining tungsten
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B32/00—Carbon; Compounds thereof
- C01B32/90—Carbides
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B32/00—Carbon; Compounds thereof
- C01B32/90—Carbides
- C01B32/914—Carbides of single elements
- C01B32/949—Tungsten or molybdenum carbides
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G41/00—Compounds of tungsten
Abstract
A process for forming a salt, such as sodium tungstate, using a pyrometallurgical operation is provided. A slagging operation is performed in which a metal-containing material is melted in the presence of slag formers such as sodium metasilicate and silica. The metal predominantly reports to a denser metal-containing phase. The denser metal-containing phase may then be subjected to gas sparging with a carbon-containing gas in order to form metal carbide, preferably tungsten carbide.
Description
PYROMETALLURGICAL PROCESS FOR TREATING
FIELD OF THE INVENTION
The present invention is directed to the--pyrometallurgical treatment of inetal-containing materials and, in a preferred embodiment, the formation of.tungsten carbide using a two stage pyrometallurgical process.
BACKGROUND OF THE INVENTION
Two stage processes for producing tungsten carbide (WC) are known. For example, in U.S. Patent No. 3,373,097 entitled "Method For Separation Of A Metal-Containing Halide Phase From A Gangue-Containing Silicate Phase and Electrolysis of Halide Phase To Obtain The Metal" by Gomes et al., issued March 12, 1968, a process for producing tungsten carbide is disclosed. The process involves a molten phase separation employing sodium chloride (NaCl) in which the tungsten reports to a less dense upper halide phase while impurity elements such as calcium, manganese and iron are recovered in a denser lower silicate phase.
The separation is effected by heating a mixture of halide salts, concentrates of either scheelite (CaWO
4) or wolframite ((Fe,Mn) W04) , and a slag former such as sodium silicate to 900 C to 1,100 C. After fifteen minutes to an hour at the elevated temperature, the phase separation is completed and the halide phase is decanted for processing by molten salt electrolysis.
U.S. Patent No. 4,489,044 entitled, "Formation Of Tungsten Monocarbide From A Molten Tungstate-Halide Phase By Gas Sparging" by Gomes et al., issued December 18, -1984, reissued as Re 32,612 on February 23, 1988, discloses a
FIELD OF THE INVENTION
The present invention is directed to the--pyrometallurgical treatment of inetal-containing materials and, in a preferred embodiment, the formation of.tungsten carbide using a two stage pyrometallurgical process.
BACKGROUND OF THE INVENTION
Two stage processes for producing tungsten carbide (WC) are known. For example, in U.S. Patent No. 3,373,097 entitled "Method For Separation Of A Metal-Containing Halide Phase From A Gangue-Containing Silicate Phase and Electrolysis of Halide Phase To Obtain The Metal" by Gomes et al., issued March 12, 1968, a process for producing tungsten carbide is disclosed. The process involves a molten phase separation employing sodium chloride (NaCl) in which the tungsten reports to a less dense upper halide phase while impurity elements such as calcium, manganese and iron are recovered in a denser lower silicate phase.
The separation is effected by heating a mixture of halide salts, concentrates of either scheelite (CaWO
4) or wolframite ((Fe,Mn) W04) , and a slag former such as sodium silicate to 900 C to 1,100 C. After fifteen minutes to an hour at the elevated temperature, the phase separation is completed and the halide phase is decanted for processing by molten salt electrolysis.
U.S. Patent No. 4,489,044 entitled, "Formation Of Tungsten Monocarbide From A Molten Tungstate-Halide Phase By Gas Sparging" by Gomes et al., issued December 18, -1984, reissued as Re 32,612 on February 23, 1988, discloses a
-2-process for producing tungsten carbide. The process involves the formation of a sodium chloride/sodium__ tungstate (Na2WO4) phase by molten phase separation, similar to.the process described above. The tungsten monocarbide is produced by sparging the melt of sodium chloride and sodium tungstate with a hydrocarbon gas, particularly methane (CH4) or natural gas. According to the disclosure, other alkali halides can be substituted for sodium chloride.
In May, 1985, Gomes, Raddatz and Caranahan made a presentation at the Third Tungsten Symposium in Madrid, Spain (May 13-17, 1985) regarding a two step technique for producing a granular tungsten carbide powder directly from scheelite or wolframite concentrates. The concentrates were first reacted at 1,050 C with a sodium chloride/sodium metasilicate (NaZSiO3) melt. The reaction produces two immiscible liquids: a lighter tungstate-halide (NaCl-NaZWOy) phase containing 99 percent of the input tungsten and a denser silicate slag phase containing 90 to 96 percent of the iron, manganese and calcium oxides. After phase separation, the tungstate-halide phase is sparged with methane gas in a second step to yield granular tungsten carbide. The tungsten carbide is recovered from the reactor by decanting excess salt, cooling, water leaching 'and scraping. See "Preparation of Tungsten Carbide by Gas Sparging Tungstate Melts", Gomes et al., Journal of Metals, December 1985, pps. 29-32.
In May, 1985, Gomes, Raddatz and Caranahan made a presentation at the Third Tungsten Symposium in Madrid, Spain (May 13-17, 1985) regarding a two step technique for producing a granular tungsten carbide powder directly from scheelite or wolframite concentrates. The concentrates were first reacted at 1,050 C with a sodium chloride/sodium metasilicate (NaZSiO3) melt. The reaction produces two immiscible liquids: a lighter tungstate-halide (NaCl-NaZWOy) phase containing 99 percent of the input tungsten and a denser silicate slag phase containing 90 to 96 percent of the iron, manganese and calcium oxides. After phase separation, the tungstate-halide phase is sparged with methane gas in a second step to yield granular tungsten carbide. The tungsten carbide is recovered from the reactor by decanting excess salt, cooling, water leaching 'and scraping. See "Preparation of Tungsten Carbide by Gas Sparging Tungstate Melts", Gomes et al., Journal of Metals, December 1985, pps. 29-32.
3-The processes described above all include an inztial slagging operation in which a tungsten concentrate is combined with a siliceous flux and sodium chloride (other halide sources can be substituted). The tungsten compounds contained in the concentrate (e.g., calcium, iron, or manganese tungstates) react with the sodium chloride and the sodium silicate to produce two immiscible phases: a molten salt and a molten silicate slag. The tungsten preferentially reports to the molten salt phase, while the majority of the impurities are rejected to the slag phase.
The viscous slag is more dense than the salt and settles to the bottom of the furnace crucible. The salt phase, which chiefly consists of sodium chloride and sodium tungstate, is forwarded to a second stage for processing into tungsten carbide.
A problem with the methods described above is that the lower density tungsten-containing phase also includes a halide salt (e.g., sodium chloride). During subsequent sparging operations, this halide salt volatilizes and deposits within various components of the gas handling system. This accretion of salt eventually leads to downtime in order to clear the obstructions. The sodium chloride also represents an operating cost. Additionally, the sodium chloride is extremely corrosive and its presence increases the cost of the materials due to the need to employ corrosion resistant materials and results in higher operating costs due to the corrosion. Furthermore, the sodium chloride dilutes the sodium tungstate in the
The viscous slag is more dense than the salt and settles to the bottom of the furnace crucible. The salt phase, which chiefly consists of sodium chloride and sodium tungstate, is forwarded to a second stage for processing into tungsten carbide.
A problem with the methods described above is that the lower density tungsten-containing phase also includes a halide salt (e.g., sodium chloride). During subsequent sparging operations, this halide salt volatilizes and deposits within various components of the gas handling system. This accretion of salt eventually leads to downtime in order to clear the obstructions. The sodium chloride also represents an operating cost. Additionally, the sodium chloride is extremely corrosive and its presence increases the cost of the materials due to the need to employ corrosion resistant materials and results in higher operating costs due to the corrosion. Furthermore, the sodium chloride dilutes the sodium tungstate in the
4-sparging operation, effectively reducing the chemical activity of the tungstic oxide (Wo3).
It would be advantageous to provide a method for forming metal carbide (e.g., tungsten carbide) from a metal-containing mineral using a pyrometallurgical process.
Additionally, it would be advantageous to form metal (e.g., tungsten) carbide without the need for forming a fused metal-halide salt. It would be advantageous to provide a process in which a majority of the tungsten input to the system is converted to tungsten carbide. It would be advantageous to provide a process in which tungsten carbide can be formed.efficiently and economically without a large amount of system downtime.
SUMMARY OF THE INVENTION
In accordance with one embodiment of the invention, a method is provided for concentrating the metal in a metal-containing material by employing a pyrometallurgical operation. The pyrometallurgical operation includes a heating step in which the metal-containing material is heated in the presence of at least one sodium or potassium compound to melt the metal-containing material and form a high density metal-containing phase and a low density slag phase. The majority of the metal reports to the high density metal-containing phase. The two phases are immiscible and the high density metal-containing phase separates by gravity from the low density slag phase.
Because of its higher density the high density metal-containing phase will settle to the bottom of a furnace .acjm crucible. The two phases can then be separated.
Preferably, the high density metal-containing phase is , subjected to a second pyrometallurgical operation, i.e., sparging with a carbon-containing gas, to form metal carbide.
Although the methods of the present invention have been found particularly applicable to tungsten-containing materials, the methods can be employed to recover other metals from metal-containing materials. Examples of such other metals are Group III-B metals (e.g., thorium), Group IV-B metals (e.g., titanium, zirconium, hafnium), Group V-B
metals (e.g., vanadium, niobium, tantalum), Group VI-B
metals (e.g., tungsten) and Group VII-B metals (e.g., manganese and rhenium). More preferred are refractory metals such as tungsten, titanium and tantalum. Most preferred are tungsten-containing materials. Examples of tungsten-containing materials include tungsten ores such as huebnerite (MnWO4), scheelite (CaWO4), ferberite (FeWO4) and wolframite ((Fe,Mn)W04). Additionally, the method of the present invention can be effective with other tungsten-containing materials such as flue dusts and various secondary materials (e.g., slag and scrap). While the methods of the present invention are useful in connection with a numberof materials, for purposes of clarity, the following description will be of a preferred embodiment employing a tungsten-containing material. It is to be expressly understood that other materials, such as those listed above, can also be employed.
In accordance with another embodiment of the present invention, tungsten carbide is formed from a tungsten _ mineral concentrate. The tungsten mineral concentrate is heated in the presence of a sodium or potassium compound to a temperature from about 900 C to about 1,200 C in order to obtain a first melt. The first melt is maintained at temperature until it separates into a higher density tungsten-containing phase and a lower density slag phase.
The higher density tungsten-containing phase is then separated from the lower density slag phase. The higher density tungsten-containing phase is heated to a temperature of about 1,050"C to about 1,200 C to obtain a second melt. Methane gas is then sparged through the second melt to form tungsten carbide. The tungsten carbide enriched portiori of the second melt is removed and purified in order to obtain purified tungsten carbide. Preferably, the first melt is formed in the substantial absence of sodium chloride. In a preferred embodiment, a portion of a sparged, spent salt-containing mate"rial is recycled from the second melt to the first melt in order to aid in the separation of the higher density tungsten-containing phase from the lower density slag phase and to recycle tungsten not converted to tungsten carbide in the sparging stage.
BRIEF DESCRIPTION OF THE DRAWINGS
Figure 1 is a flow diagram of one embodiment of the process of the present invention.
Figure 2 is a ternary phase diagram of the WO3- NaZ0-SiOZ system at 1,200 C.
o~
Figure 3 is an illustration of a pilot scale slagging system in accordance with an embodiment of the present ~
invention.
Figure 4 is an illustration of a pilot scale sparging system in accordance with an embodiment of the present invgntion.
DETAILED DESCRIPTION OF THE INVENTION
In accordance with one embodiment of the present invention, a pyrometallurgical process is provided for forming a tungstate salt, for example, sodium tungstate or potassium tungstate and preferably sodium tungstate, from a tungsten-containing material. Preferably, the tungsten-containing material is a tungsten ore such as huebnerite (MnWO4) , scheelite (CaWO4) , ferberite (FeWO4) and wolframite ((Fe,Mn)WO4) or a tungsten-containing material such as flue dust and various secondary materials_ (e.g., slag and scrap). The pyrometallurgical slagging process comprises heating the tungsten-containing material in the presence of a slag forming silicate (preferably 'silica and an alkali metal silicate). The melt separates into two immiscible phases, a denser tungsten-containing phase, preferably sodium or potassium tungstate, and a less dense slag phase.
In accordance with another embodiment of the present invention, a process for forming tungsten carbide from a tungsten-containing material is provided. Preferably, the process includes two pyrometallurgical stages, a first slagging stage and a second sparging stage.
Figure 1 illustrates a flow diagram of a preferred embodiment of the present invention. A tungsten-containing =
concentrate 12 together with silica 14 and sodium silicate 16-are introduced into a slagging furnace 18. The slagging furnace 18 is heated to a temperature in the range from about 900 C to about 1,200 C, preferably from about 1,050 C
to about 1,150 C and more preferably to approximately 1,050 C for approximately 0.5 to 2.0 hours. The feed materials separate into two immiscible phases. A higher density tungsten-containing phase (tungstate) 20 settles to the bottom of the furnace crucible due to gravity and a less dense slag phase (silicate) 22 segregates to the upper portion of the furnace crucible. The higher density tungsten-containing phase 20 is introduced into a sparging furnace 24. The lower density slag phase 22 can be disposed of, or subjected to further treatment. The higher density tungsten-containing phase 20 can be separated from the lower density slag phase 22 by any number of appropriate processes. For example; the higher density phase 20 and lower density phase 22 can be poured sequentially from the mouth of a tilting or rotating furnace into separate appropriate vessels such as ladles.
Alternatively, an outlet can be provided in the crucible to draw off the higher density tungsten-containing phase 20.
Gas 26 from the slagging furnace 18 can be subjected to particulate control 28. The recovered particulate matter can be recycled to the slagging furnace 18 and the treated gas 32 can be vented to the atmosphere.
The higher density tungsten-containing phase 20 is introduced into a sparging furnace 24. The higher density tungsten-containing phase 20 is heated to a temperature in the range of from about 1,050 C to about 1,200 C, preferably from about 1,050 C to about 1,150'C and more preferably to a temperature of approximately 1,100 C. A
carbon-containing gas 34, such as methane, is introduced into the sparging furnace 24. The carbon-containing gas 34 is cracked at the sparging furnace temperatures and the carbon is available for the formation of tungsten carbide.
Gas 36 from the sparging furnace 24 can be subjected to an afterburner 38 with the addition of an oxygen-containing gas such as air 40 and a hydrocarbon, such as methane 42.
The afterburner gas 44 can be subjected to particulate control 46. Recovered particulate matter 48 can be recycled to the slagging furnace 18 and treated gas 50 can be vented to the atmosphere. Sparged, spent salt 51 can be recycled to the slagging furnace 18.
The sparging step 24 results in a crude tungsten carbide product 52 which resembles a gray sintered material. The crude tungsten carbide product 52 is subjected to a water leaching step 54 after addition of water 55, followed by solid/liquid separation 56. The liquid portiori 58 is fed to a crystallizer 60 and the crystals 62 can be recycled to the sparging furnace 24.
The solid crude tungsten carbide crystals 64 are comminuted 66 in water 68 and subjected to acid leaching 70 with a suitable acid 72 (e.g., HC1). In a preferred embodiment, Z(lm the comminution 66 and acid leaching 70 take place in a single operation. The comminution 66 is preferably conducted in a ball mill using tungsten carbide grinding media. The crude tungsten carbide crystals 64 are first slurried in a dilute aqueous 68 solution of hydrochloric acid 72, and the comminution 66 is continued for a period of time sufficient to liberate and solubilize impurities.
The comminuted and acid leached suspension 74 is subjected to solid/liquid separation 76. The solid high purity tungsten carbide 78 preferably has a purity level of at least 90 percent tungsten carbide, more preferably at least 95 percent tungsten carbide, and more preferably at least 99 percent tungsten carbide. The liquor 80 is subjected to neutralization and precipitation 82 of solid materials 84.
The solid precipitate 84, after drying, can be recycled to the slagging furnace 18.
In the first pyrometallurgical operation, a furnace charge consisting of a blend of tungsten concentrate and siliceous flux is treated at approximately 1,050 C. The tungsten compounds contained in the concentrate (e.g., calcium, iron, or manganese tungstates) react with the siliceous flux (preferably sodium silicate and silica) to produce two immiscible phases: a molten salt and molten silicate slag. The tungsten is preferentially segregated in the molten salt phase, while the majority of the impurities are rejected in the slag. The salt is more dense than the slag and settles to the bottom of the furnace crucible. The salt phase, which chiefly consists of sodium tungstate, is then forwarded to the second s-eage of pyrometallurgical processing, i.e., sparginga The concentrate used in the examples contained huebnerite (MnWO4) as the primary tungsten mineral. When a blended charge is treated as described above, the following chemical reaction ensues:
MnWO4(c) + NaZSiO3(c) = Mn0=SiOZ(i) + Na2W04M
Segregation of the salt and slag phases is predicated upon the exploitation of the immiscibility region existing within the tungstic oxide-sodium oxide-silica system shown in Figure 2. When the tungsten concentrates enter the 1,050 C melt, they react with the sodium silicate to produce sodium tungstate and slag. At this temperature, the slag and tungstate are immiscible, and they separate by gravity. .
The precise chemistry of the slag will depend upon the relative amounts of excess silica and sodium oxide in the system. Sodium oxide is a desirable slag constituent because its presence reduces the slag melting point sufficiently to ensure the formation of a completely liquid phase. In the absence of sodium oxide or another flux compound which will effectively lower the slag's melting point, a liquid slag cannot be formed in the manganese oxide-silica system at temperatures below approximately 1,250 C.
An example of a slagging system is illustrated in Fig.
3. With the exception of a gas injection system, the same basic furnace configuration useful in the sparging m12 operatzon (described below) can be employed for the slagging operation. Because the slagging operation is simply a melting and separating exercise, no gas lances or nitrogen purge lines are required.
The second pyrometallurgical process effects the crystallization of tungsten carbide within the molten salt phase. This feat is accomplished by heating the tungsten-bearing molten salt from the first stage to within the range of approximately 1,080 to 1,100 C and then sparging with a large stoichiometric excess of hydrocarbon gas, such as methane or propane. Under these conditions, the hydrocarbon gas cracks and provides the reductant and carbon source necessary for forming the tungsten carbide.
The tungsten carbide phase forms as micron-sized crystals, which are insoluble in the molten salt phase. The crystals are also denser than the salt and are segregated near the bottom of the reactor. At the conclusion of the sparging operation, the spent salt is decanted from the crystals.
When methane is employed as the hydrocarbon source, the net chemical reaction leading to the formation of the tungsten carbide (WC) product is believed to be:
4CH 4(g) + NaZWO4M = WC(s) + 3CO(9) + 8H 2(g) + Na2O(1) Because a large stoichiometric excess of hydrocarbon gas is needed, some of the excess gas also cracks to produce carbon and hydrogen gas, as illustrated by the following reaction:
CH4(9) C(S) + 2HZ(9) l3-The hydrogen gas and much of the elemental carbon are oxidized in the afterburner. However, some of the carbon remains as a contaminant within the salt phase. Thus, minimization of excess carbon formation in the sparging furnace is desirable.
Other hydrocarbon gases, such as propane or ethylene (CZH4), can be used in place of methane. For instance, the use of ethylene might enhance the sparging efficiency (i.e., increase the yield of tungsten carbide per unit of carbon added to the melt).
After separation of the free-flowing spent salt phase, the resultant tungsten carbide crystals are contained in a separate phase having a gray, sintered appearance. The gray material retains appreciable quantities of salt. The salt and other impurities are removed via a process of dry and/or wet grinding and sequential leaching in hydrochloric acid, caustic, and water. After this treatment, the resultant crystals can assay between approximately 99.3 and 99.4% tungsten carbide. However, the tungsten carbide produced in preliminary tests contains substantially higher impurity concentrations. The elevated impurity concentrations, mainly chromium and nickel, are believed to result from chemical attack of the fused salt on the reaction crucible.
An example of a suitable system for slagging (Fig. 3) and sparging (Fig. 4) includes a tilting furnace 110 with a cover at the top which has room for two sparging lances 112, 114, two thermocouples 116, 118, one dedicated*
el~o nitrogen line 120, one exhaust line 122, and one pressure gauge 124. The main component is a 12.9 kW resistance- =
heated furnace 110. The furnace 110 has a hot zone 0.914 meter long by 12.7 cm diameter; it can attain a maximum operating temperature of about 1,200 C. Within the furnace shell, the process reaction vessel, or crucible 126, is constructed of 10.2 cm diameter Inconel 600 pipe; the maximum bath depth is about 45.7 cm. The crucible 126 may be removed for cleaning or maintenance by opening the hinged split shell furnace.
The same furnace can be employed for slagging (Fig. 3) and sparging (Fig. 4). In either slagging or sparging operations, the initial charge is typically added to the cold crucible 126, and then power is applied to the furnace 110 in order to elevate the bath temperature to the desired target. Subsequent charges can be made to the hot furnace 110. To facilitate removal of molten products, the furnace 110 can be tilted a full 180 degrees from its vertical = operating position to pour products into ladles.
For operation in the gas sparging mode (Fig. 4), a facility was designed with the capability to purge the crucible 126'with nitrogen 127 and sparge the molten bath with methane, propane, ethylene or any mixture of these hydrocarbon -source gases 128. Seven access ports are located in the reactor lid. Two of the ports admit gas lances 112, 114 during sparging operations. Hydrocarbon gases 128 are injected into the crucible 126 through one of the lances 112, with the other lance 114 held in reserve in case the first lance 112 becomes obstructed.
Preferably, the lances 112, 114 have a relatively small w.
inner diameter (e.g., 0.14 cm) to provide relatively high velocity flow, thus minimizing cracking in the lances 112, 114. The inlet hydrocarbon gases 126 are directly injected intq the melt at a point approximately 5 cm above the crucible 126 bottom. During each sparging test, nitrogen 120 can also be injected through a third inlet port at a point approximately 2.5 cm below the reactor lid. The dedicated nitrogen lance 120 assures positive pressure inside the freeboard to prevent air from entering the crucible 126. All of the inlet gas flows are controlled by flow meters 130, 132, 134. Three other lid ports serve as thermocouple wells, and the main (central) port 122 serves as the process gas offtake.
A primary concern in the system design is to ensure efficient transport of the nascent hydrogen, which is formed by cracking or as a product of the sparging reaction to the afterburner 136. Preferably, in one embodiment, the pressure inside the furnace 110 is first adjusted to 0.25 to 0.50 millimeters (mm) of water by balancing the flow of reacting gas with the extraction draft. Then the pressure is increased to 2.5 to 5.0 mm of water by adjusting the flow of the dedicated nitrogen lance 120. Note that the tip of this lance 120 is positioned only about 5 cm from the top of the crucible 126 so that most of the draft is utilized to extract the reaction product gases and not nitrogen. In this way, most of the nitrogen flows through the top cover, maintaining an inert atmosphere at the top of the crucible 126 and preventing any air from contacting__ the product gases inside the furnace 110. The reaction gases are drawn into the afterburner 136 and combusted to HZ0 and COZ. Carryover salt can be collected at the baghouse 138 or scrubber 140. The afterburner 136 offgases can be air cooled 142 to 120 C before reaching the baghouse 138 or scrubber 140. When the baghouse 138 is employed, the gases go through the scrubbing system; then they can be discharged into the atmosphere. In the embodiment shown in Figure 4, the afterburner 136 offgas passes through the scrubber 140, while the baghouse 138 is used to treat possible fugitive emissions from the furnace 110.
Process gases exit the crucible 126 through the single exit port 122 leading to the gas handling system. The gases are fed directly into a 20.3 cm diameter by 55.9 cm long natural gas-fired, stainless steel afterburner 136 through a 5 cm diameter pipe. The afterburner 136 is designed to operate with a pressure pilot burner which remains ignited throughout the tests. Oxygen 144 is fed into the afterburner 136 at a controlled rate for combustion of the nascent hydrogen, residual hydrocarbon gases, and carbon fines entrained in the offgas stream.
After exiting the afterburner 136, the gases pass through a ball valve 146 (used to balance the system gas pressure profile) and then into the scrubber 140.
The scrubber 140 is constructed of a 208-liter polymer drum and polyvinyl chloride (PVC) piping. The scrubber is filled with approximately 114 liters of water; the afterburner discharge gases are bubbled into the reservoir to condense and remove any soluble material in the gas stream. The afterburner exhaust gases are cooled by air dilution 142 and by an external chiller coil system 148 before entering the scrubber 140. Gases are pulled through the scrubbing system by a 25 cm diameter blower 150. Exit gases from the blower 150 can be vented to the atmosphere.
An external baghouse 138 and blower assembly was set up to collect fugitive emissions from the crucible lid.
The baghouse 138 was fitted with two inlet hoses, each 10.2 cm in diameter, that were placed near the crucible lid.
Fugitive emissions were thus drawn into the baghouse 138, filtered, and then blown into the atmosphere.
Temperature was monitored at several key points throughout the system. Readings were measured by two thermocouples 116, 118 which are placed through two separate lid ports. One thermocouple 116 measured the melt temperature near the point of gas injection, while the other thermocouple 118 was used to monitor the temperature of the head space, or freeboard, in the crucible 126 above the melt.
Examples and Comparative Tests The tungsten concentrate sample used in the following examples was shipped from a commercial source. The 817 kg sample was packed in two unlined 30 gallon metal drums.
The contents of both drums were thoroughly blended together prior to initiating any testing. Approximately half of the sample was stored in a plastic-lined 55 gallon drum. The remaining half of the sample was split into lots of approximately 45 kg. Subsamples were drawn from three of the lots for comparative analysis to ascertain the efficiency of the blending operation. Duplicate samples were retained on inventory for verification analyses. The blended master samples were then stored in sealed containers pending their use in the various tests.
The three subsamples of the tungsten concentrate were initially screened by semiquantitative analytical methods, such as x-ray diffraction (XRD), x-ray fluorescence (XRF), and emission spectrography, to approximate its mineralogy and chemical composition. Subsequently, all major and minor components detected by the screening methods were analyzed by more exacting techniques, including wet quantitative analytical chemistry, atomic absorption spectroscopy (AA), and inductively-coupled plasma spectroscopy (ICP). In some cases, multiple analytical techniques were employed in order to firmly establish the chemical composition of the concentrate sample. In addition to the chemical analysis, the tungsten concentrate sample characterization also included a limited amount of physical characterization.
Comparative Tests A, B and C
Three comparative slagging tests, designated as A, B
and C, were completed within a 5 kW induction furnace system. In view of the huebnerite mineralogy of the concentrate sample, the tests were performed to obtain a preliminary indication of the behavior of the MnO-NazO-Si02 system slag. The charge components included varying amounts of concentrate, sodium chloride, and slag-formers s.odlum silicate and silica. These were added according to the respective charge compositions detailed in Table I.
f During these experiments, excessive salt fumes were evident at times, and thin layers of salt condensed on the internal surface of the dome of the bell jar induction furnace containment.
Table I. Charge Compositions for Comparative Slagging Tests A, B and C
Charge Component Test A Test B Test C
and Mass Concentrate, g 10.73 10.68 12.10 NaCl, g 16.36 16.40 18.64 Na Si0=9H 0, g 23.03 28.93 16.89 Si0 , g 3.36 3.37 0 Visual inspection of the slag and salt products indicated no problems with phase separation. The three slag samples had a vitreous appearance and were tinted green, ranging from light green in Test A to emerald green in Test C. Most of the sodium chloride was volatilized during the first test, leaving a deposit of dark solids on the slag surface. In the other two tests, the halide phase was off-white with a yellow tint on each surface. The slag and halide phase samples produced in each test were recovered and submitted for XRF analysis; the amount of s20-halide phase recovered from Test A was insufficient for XRF
analysis.
The XRF data, summarized in Table II, suggest that a fav-orable partitioning of the tungsten between the slag and the halide phase occurred in two of the three tests. The tungstic oxide (WO3) concentrations in the slag samples generated in Tests A and C were 0.5 and 0.7%, respectively, while the tungstic oxide concentration in the B slag was 1.8%.
Table II. XRF Analysis of Slag Samples from Comparative Slagging Tests Compound A B C
Weight % Weight % Weight %
NaCl 7.1 8.7 3.1 A1 O 3.5 2.6 1.2 FeO 0.7 0.5 0.9 MnO 14.4 10.2 28.7 Na O 22.7 21.2 14.4 Si0 47.7 51.2 42.4 WO 0.5 1.8 0.7 Total 96.6 96.2 91.4 As shown in Table III, the halide phase samples from Tests B and C consisted primarily of chlorine, sodium, and tungsten. According to the XRF data, the halide phase samples from Tests B and C contained 39 and 40% tungstic oxide, respectively. The iron and manganese concentrations were each below 0.1 % in both halide samples. Trace levels of several other elements were also detected.
21~
Table III. XRF Analysis of Halide Phase Samples from Preliminary Slagging Tests Element B C
Weight ~ Weight %
C1 46.5 44.5 Na 23.0 23.3 W 31.0 32.0 Total 100.5 99.8 Example 1 Sodium Tungstate Production Example 1 is designed to demonstrate the feasibility of forming a discrete sodium tungstate phase in the absence of sodium chloride in the charge. For the test to be successful, it is necessary that the sodium tungstate and slag would be present as immiscible liquids at the temperature of interest. This test was conducted in a 5 kW
induction furnace. This charge composition is presented in Table IV.
Table IV. Charge Components and Masses for Sodium Tungstate Production Charge Component Example 1 and Mass Concentrate, grams 66.57 NaCl, grams 0 Na Si0 , grams 62.16 S i0 ,' grams 21.27 Total, grams 150.00 m22 Visual inspection of the test products indicates the formation of two distinct phases, sodium tungstate and slag. The slag phase has a dark green appearance and is at the-top, while the sodium tungstate phase is off-white and located at the bottom of the crucible. The fact that the sodj-um tungstate phase is located at the bottom of the crucible is due to its higher density and its immiscibility with the lower density slag phase.
Example 1 was conducted without difficulty and phase separation was excellent. The products of this experiment were submitted for analysis to determine their respective tungsten and manganese distribution between the two product phases. As shown in Table V, the analytical results for Example 1 confirmed the feasibility of favorable tungsten and manganese distributions between the slag and salt phases. Judging from these results, the separation of tungsten from the concentrate as sodium tungstate, in the absence of sodium chloride, presents an attractive alternative.
Table V. Analytical Results from Example I
Charge Composition Chemical Analysis Species Weight t Element ~ in Salt o in Slag Na Si0 41.45 Mg 0.06 0.34 Si0 14.17 Na 12.80 16.70 MnWO 44.38 W 59.25 0.10 Mn 2.05 12.40 cl Si 0.21 19.50 Comuarative Tests D. E. F and G
Variation of the Manganese-to-Sodium Silicate Ratio in the Charge The objective of Comparative Test D is to evaluate the effect of a high manganese-to-sodium silicate (Mn:Na2Si03) ratio on the distribution of tungsten and manganese between the slag and salt phases. While not wishing to be bound by any theory, it is believed that is important to maintain a certain level of sodium in the system. In conducting tests where the slag composition was the independent variable, the respective distribution of manganese between the salt and slag phases was adversely affected as the manganese oxide level of the slag increased. This problem became apparent when the molar ratio of manganese to sodium silicate in the charge was raised above 1. It is believed that this phenomena occurred because an insufficient amount of sodium was present to complete the following reaction:
MnWO4(s) + NaZSiO3(s) = Mn0= Si02(,) + Na2WO4(0.
If Mn:Na2SiO3 molar ratios of greater than one are desired to reduce flux consumption, additional sources of sodium are needed to maximize the formation of sodium tungstate and minimize the dissolution of unreacted manganese tungstate into the salt phase. The additional source of sodium utilized in this experiment was sodium hydroxide (NaOH) according to the composition presented in Table VI.
Table VIo Charge Composition for Test D
Compound Test D
Concentrate, grams 41.23 NaCl, grams 64.33 Na Si0 , grams 12.26 NaOH, grams 3.24 Total, grams 121.06 Although two distinct phases were again formed, the appearance of the slag was different than that observed in previous experiments. The slag in this test had a sandy appearance which, when observed under the microscope (30X
magnification), gave evidence of different phases and incomplete fusion of the charge. The halide phase had the same appearance as in the previous tests. As evidenced from the analytical results given in Table VII, the use of sodium hydroxide yielded unsatisfactory tungsten and manganese distributions in both the slag and salt phases.
Three additional induction furnace tests were conducted to further explore the effect of altering the Mn:NazSi03 ratio in the furnace charge, and to investigate the use of alternative sources of sodium and silica. The specific objective of Test E was to study the effects of a slag composition with a Mn:Na2SiO3 molar ratio of one on the distributions of tungsten and manganese between the halide and slag phases. As indicated in Table VII, the 0.55%
concentration of tungsten in the slag and the 0.14%
concentration of manganese in the halide indicate' that reduction in flux consumption to realize a slag molar ratio of Mn:NazSiO3 of less than or equal to one is feasible and worth pursuing.
In Test F, an attempt was made to increase the manganese:silicon ratio to 1.35, under conditions similar to those of Test D but using sodium carbonate (Na2CO3) instead of sodium hydroxide as the additional sodium source. The objective was to determine whether the choice of,.additional sodium source had any significant effect on the tungsten and manganese distributions. As seen in Table VII, a tungsten -concentration of 1.08% in the slag suggests, when compared to 3.9% from Test D, that the source of additional sodium can have an effect on the distribution of tungsten in the halide phase.
In Test G the objective was to study the feasibility of using silica and sodium carbonate as the sole sources of sodium and silica in an attempt to substitute less expensive raw materials for sodium metasilicate. As shown in Table VII, the 0.13% tungsten concentration in the slag and the 0.03% manganese concentration in the halide suggested that the substitution is feasible.
Table Vleo AnaWtical Results for Comparative Tests D. E, F.
and G
Charge Composition Chemical Analysis Test Comments Species Weight % Element % in % in Salt Slag Comparative NaZSiO$ 10.13 Mg 0.01 1.35 Test D NaOH used Si02 0.00 Na 34.90 5.82 as MnWO4 34.05 W 17.50 9.44 additional sodium NaCI 53.14 Mn 0.22 33.60 source for a NaOH 2.68 CI 46.00 0.75 basic slag.
Si 0.19 11.90 Comparative Na2SiO3 20.24 Mg 0.01 0.69 Test E Mn:NazSiO3 Si02 0.00 Na 30.70 14.80 molar ratio MnWO4 31.40 W 25.60 0.55 of one in the slag.
NaCI 48.36 Mn 0.14 24.50 CI 37.00 0.06 L Si 0.12 12.30 Comparative Na2SiO3 13.89 Mg 0.01 0.39 Test F Na2CO3 0.00 Na 30.30 11.10 used as MnWO4 32.56 W 23.40 1.08 additional sodium NaCi 50.28 Mn 0.10 32.70 source Na2CO3 3.27 CI 38.00 0.39 (basic slag).
Si 0.31 12.40 Comparative NaZSiO3 0.00 Mg 0.03 0.72 Test G Si0Z and Si0Z 18.85 Na 30.50 15.60 Na 2CO3 as MnWO4 24.20 W 23.60 0.13 sole sources of NaCI 37.36 Mn 0.03 13.20 silicon and Na2C03 19.59 CI 40.50 0.10 sodium.
Si 0.17 16.95 Example 2 27=.
In Example 2, no sodium chloride was included in the chargeo The slag composition was selected to ensure the.
formation of two immiscible liquids. The formation of the two immiscible phases, as well as the favorable distributions of tungsten and manganese in the salt and slac, was predicted by the results of Example 1.
The mass balance for Example 2 is shown in Table VIII.
The mass closure for this Example was 96.8%. A tungsten mass balance indicates that 92.9% of the charged tungsten reported to the halide phase and 3.3% to the slag. Only 3.8% of the tungsten in the charge was unaccounted.
Table VIII. Mass Balance for Slagging Example 2 Material In Kilograms Material Out Kilograms Concentrate 4.43 Halide Phase 3.94 Silica 1.41 Slag 5.74 Sodium Metasilicate 4.15 Total 10.00 Total 9.68 The tungsten distribution for Example 2, as calculated from the analytical data, indicates that approximately 97%
of the input tungsten was segregated in the tungstate phase, with the difference reporting to the slag. While these results siuggest that an efficient slagging operation in the absence of sodium chloride is indeed possible, those skilled in the art can improve the tungsten distribution without undue experimentation. Entrainment of salt from the reactor walls during slag pouring may have contributed o28e to the relatively high tungsten concentration in the slag from Example 2.
From an operational point of view, although the sodium tungstate phase was segregated below the slag in the reactor (due to the higher density of the salt), it poured first, due to its lower viscosity and the geometry of the reactor. There were only a few minor traces of slag entrained in the salt, and these had floated to the surface before the salt solidified in the ladle.
Example 3 Recycling Sparged, Spent Salt to the Slagging Operation This Example is designed to demonstrate the effectiveness of recycling the spent salt from the sparging unit operation to the slagging unit operation. This practice is desirable for two reasons. First, the spent salt typically contains an appreciable concentration of tungsten (approximately 15% by weight) which is not converted to tungsten carbide during the sparging step.
Returning the salt to the slagging operation keeps the tungsten within the processing circuit and is useful in achieving economic levels of tungsten recovery in the overall operation. Second, it is believed that the sodium oxide in the sparged salt can serve as the sodium source in the production of sodium tungstate during the slagging operation. Therefore, recycling the spent salt is expected to reduce the consumption of raw materials. This Example was designed to determine whether recycling the spent salt would affect the distribution of tungsten between the salt -and slag phases.
The Example consists of three charging cycles conducted sequentially. The Cycle 1 charge represents a typi-cal slagging operation charge without salt recycled from the sparging operation and consists of a 5 kg blend of 260% huebnerite concentrate, 24.7% sodium metasilicate (Na2Si03), 8.4% silica (Si0Z) and 40.6% sodium chloride (NaC1). The Cycle 2 charge consisted of 1 kg of spent salt (generated during a previous sparging test) plus 4 kg of the same components used in Cycle 1, mixed in the identical proportions. The Cycle 3 charge contained 2 kg of spent salt plus 4 kg of the components used in Cycle 1, again mixed according to the Cycle 1 proportions.
At the beginning of each test cycle, the charge materials were blended together, added to the furnace, and processed at a nominal temperature of 1,O50 C for one hour.
The fused salt was then removed by tilting the furnace and pouring the melt into a ladle where it was allowed to solidify. The furnace was restored to its vertical operating position, and the process was repeated with the next charge. The slag phase was not removed until all three cycles had been completed. The slag was then poured into a ladle and allowed to solidify. Samples of the slag and of each of the three salt products were prepared and submitted for chemical analysis.
G3Qe The analyses of the slag and salt products are summarized in Table IX. As calculated from the measured-_ product weights and associated tungsten analyses, approximately 99.1% of the tungsten reported to the salt.
Comparison of the salt analyses from Cycles 1, 2 and 3 indicates favorably low concentrations of impurities in all three cycles.
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G~~o Examples 4 and 5 Sparging Sodium Tungstate to Produce Tungsten Carbide It has been demonstrated that tungsten carbide of reasonably high purity can be obtained by sparging a molten mixture of sodium tungstate and sodium chloride with methane. However, elimination of the sodium chloride from the operation improves the process for several reasons.
Consequently, two additional Examples are presented to demonstrate whether crystalline tungsten carbide powder can be produced by sparging molten sodium tungstate with methane gas.
In each Example, the initial melt consists of sodium tungstate produced in previous slagging tests. During the Examples, the sodium tungstate bath is maintained at approximately 1,100 C, while methane gas is injected below its surface at a flow rate of approximately 11.4 liters per minute. Methane sparging is continued for three hours in Example 4 and for 90 minutes in Example 5. At the conclusion of each Example, the molten products are poured into a steel ladle and allowed to solidify.
After the products have solidified and cooled sufficiently, two separate phases are observed: a white "spent ash" and a denser, medium gray phase. The two phases are separated and prepared for x-ray diffraction (XRD) analysis. The products from Example 4 were selected for the XRD analysis because they were more easily and cleanly separated after cooling. XRD analysis of the white spent salt indicates that it is predominantly composed of unreacted sodium tungstate (Na2WO4) with trace concentration of another unidentified crystalline phase. Nore==
significantly, the dense graph phase was found to contain sodium tungstate, with lesser concentrations of tungsten carbide (WC) and ditungsten carbide (W2C) and trace concentrations of metallic tungsten and the same unidentified crystalline phase that occurred in the white salt.
Although those skilled in the art will be able to further optimize the process, the x-ray diffraction results demonstrate that it is possible to form tungsten carbide via the methane sparging method.
While various embodiments of the present invention have been described in detail, it is apparent that modifications and adaptations of those embodiments will occur to those skilled in the art. It is to be expressly understood, however, that such modifications and adaptations are within the scope of the present invention, as set forth in the following claims:
-34 , List of Reference Numerals Tungsten-Containing Concentrate 12 Silica 14 Silicate 16 Slagging Furnace 18 Tungstate Salt 20 Slag 22 Sparging Furnace 24 Slagging Furnace Gas 26 Particulate Control 28 Part'iculates 30 Treated Gas 32 Carbon-Containing Gas 34 Sparging Furnace Gas 36 Afterburner 38 Oxygen-Containing Gas 40 Methane 42 Afterburner Gas 44 Particulate Control 46 Particulates 48 Treated Gas 50 Sparged, Spent Salt 51 Crude Tungsten Carbide Product 52 Water Leaching Step 54 Water 55 Solid/Liquid Separation 56 Liquid Portion 58 Crystallizer 60 Crystals 62 Solid Crude Tungsten Carbide Crystals 64 Comminution 66 Water 68 Acid Leaching 70 Acid 72 Comminuted and Acid Leached Suspension 74 Solid/Liquid Separation 76 High Purity Tungsten Carbide 78 Liquor 80 Neutralization and Precipitation 82 Solid Precipitate 84 Tilting Furnace 110 Sparge Lances 112, 114 Thermocouples 116, 118 Nitrogen Line 120 Exhaust Line 122 Pressure Gauge 124 Crucible 126"
Nitrogen 127 Hydrocarbon Gas(es) 128 Flow Meters 130, 132, 134 Afterburner 136 Baghouse 138 Scrubber 140 Cooling Air Intake 142 Oxygen 144 ValVe 146 Chiller Coil System 148 Blower 150
It would be advantageous to provide a method for forming metal carbide (e.g., tungsten carbide) from a metal-containing mineral using a pyrometallurgical process.
Additionally, it would be advantageous to form metal (e.g., tungsten) carbide without the need for forming a fused metal-halide salt. It would be advantageous to provide a process in which a majority of the tungsten input to the system is converted to tungsten carbide. It would be advantageous to provide a process in which tungsten carbide can be formed.efficiently and economically without a large amount of system downtime.
SUMMARY OF THE INVENTION
In accordance with one embodiment of the invention, a method is provided for concentrating the metal in a metal-containing material by employing a pyrometallurgical operation. The pyrometallurgical operation includes a heating step in which the metal-containing material is heated in the presence of at least one sodium or potassium compound to melt the metal-containing material and form a high density metal-containing phase and a low density slag phase. The majority of the metal reports to the high density metal-containing phase. The two phases are immiscible and the high density metal-containing phase separates by gravity from the low density slag phase.
Because of its higher density the high density metal-containing phase will settle to the bottom of a furnace .acjm crucible. The two phases can then be separated.
Preferably, the high density metal-containing phase is , subjected to a second pyrometallurgical operation, i.e., sparging with a carbon-containing gas, to form metal carbide.
Although the methods of the present invention have been found particularly applicable to tungsten-containing materials, the methods can be employed to recover other metals from metal-containing materials. Examples of such other metals are Group III-B metals (e.g., thorium), Group IV-B metals (e.g., titanium, zirconium, hafnium), Group V-B
metals (e.g., vanadium, niobium, tantalum), Group VI-B
metals (e.g., tungsten) and Group VII-B metals (e.g., manganese and rhenium). More preferred are refractory metals such as tungsten, titanium and tantalum. Most preferred are tungsten-containing materials. Examples of tungsten-containing materials include tungsten ores such as huebnerite (MnWO4), scheelite (CaWO4), ferberite (FeWO4) and wolframite ((Fe,Mn)W04). Additionally, the method of the present invention can be effective with other tungsten-containing materials such as flue dusts and various secondary materials (e.g., slag and scrap). While the methods of the present invention are useful in connection with a numberof materials, for purposes of clarity, the following description will be of a preferred embodiment employing a tungsten-containing material. It is to be expressly understood that other materials, such as those listed above, can also be employed.
In accordance with another embodiment of the present invention, tungsten carbide is formed from a tungsten _ mineral concentrate. The tungsten mineral concentrate is heated in the presence of a sodium or potassium compound to a temperature from about 900 C to about 1,200 C in order to obtain a first melt. The first melt is maintained at temperature until it separates into a higher density tungsten-containing phase and a lower density slag phase.
The higher density tungsten-containing phase is then separated from the lower density slag phase. The higher density tungsten-containing phase is heated to a temperature of about 1,050"C to about 1,200 C to obtain a second melt. Methane gas is then sparged through the second melt to form tungsten carbide. The tungsten carbide enriched portiori of the second melt is removed and purified in order to obtain purified tungsten carbide. Preferably, the first melt is formed in the substantial absence of sodium chloride. In a preferred embodiment, a portion of a sparged, spent salt-containing mate"rial is recycled from the second melt to the first melt in order to aid in the separation of the higher density tungsten-containing phase from the lower density slag phase and to recycle tungsten not converted to tungsten carbide in the sparging stage.
BRIEF DESCRIPTION OF THE DRAWINGS
Figure 1 is a flow diagram of one embodiment of the process of the present invention.
Figure 2 is a ternary phase diagram of the WO3- NaZ0-SiOZ system at 1,200 C.
o~
Figure 3 is an illustration of a pilot scale slagging system in accordance with an embodiment of the present ~
invention.
Figure 4 is an illustration of a pilot scale sparging system in accordance with an embodiment of the present invgntion.
DETAILED DESCRIPTION OF THE INVENTION
In accordance with one embodiment of the present invention, a pyrometallurgical process is provided for forming a tungstate salt, for example, sodium tungstate or potassium tungstate and preferably sodium tungstate, from a tungsten-containing material. Preferably, the tungsten-containing material is a tungsten ore such as huebnerite (MnWO4) , scheelite (CaWO4) , ferberite (FeWO4) and wolframite ((Fe,Mn)WO4) or a tungsten-containing material such as flue dust and various secondary materials_ (e.g., slag and scrap). The pyrometallurgical slagging process comprises heating the tungsten-containing material in the presence of a slag forming silicate (preferably 'silica and an alkali metal silicate). The melt separates into two immiscible phases, a denser tungsten-containing phase, preferably sodium or potassium tungstate, and a less dense slag phase.
In accordance with another embodiment of the present invention, a process for forming tungsten carbide from a tungsten-containing material is provided. Preferably, the process includes two pyrometallurgical stages, a first slagging stage and a second sparging stage.
Figure 1 illustrates a flow diagram of a preferred embodiment of the present invention. A tungsten-containing =
concentrate 12 together with silica 14 and sodium silicate 16-are introduced into a slagging furnace 18. The slagging furnace 18 is heated to a temperature in the range from about 900 C to about 1,200 C, preferably from about 1,050 C
to about 1,150 C and more preferably to approximately 1,050 C for approximately 0.5 to 2.0 hours. The feed materials separate into two immiscible phases. A higher density tungsten-containing phase (tungstate) 20 settles to the bottom of the furnace crucible due to gravity and a less dense slag phase (silicate) 22 segregates to the upper portion of the furnace crucible. The higher density tungsten-containing phase 20 is introduced into a sparging furnace 24. The lower density slag phase 22 can be disposed of, or subjected to further treatment. The higher density tungsten-containing phase 20 can be separated from the lower density slag phase 22 by any number of appropriate processes. For example; the higher density phase 20 and lower density phase 22 can be poured sequentially from the mouth of a tilting or rotating furnace into separate appropriate vessels such as ladles.
Alternatively, an outlet can be provided in the crucible to draw off the higher density tungsten-containing phase 20.
Gas 26 from the slagging furnace 18 can be subjected to particulate control 28. The recovered particulate matter can be recycled to the slagging furnace 18 and the treated gas 32 can be vented to the atmosphere.
The higher density tungsten-containing phase 20 is introduced into a sparging furnace 24. The higher density tungsten-containing phase 20 is heated to a temperature in the range of from about 1,050 C to about 1,200 C, preferably from about 1,050 C to about 1,150'C and more preferably to a temperature of approximately 1,100 C. A
carbon-containing gas 34, such as methane, is introduced into the sparging furnace 24. The carbon-containing gas 34 is cracked at the sparging furnace temperatures and the carbon is available for the formation of tungsten carbide.
Gas 36 from the sparging furnace 24 can be subjected to an afterburner 38 with the addition of an oxygen-containing gas such as air 40 and a hydrocarbon, such as methane 42.
The afterburner gas 44 can be subjected to particulate control 46. Recovered particulate matter 48 can be recycled to the slagging furnace 18 and treated gas 50 can be vented to the atmosphere. Sparged, spent salt 51 can be recycled to the slagging furnace 18.
The sparging step 24 results in a crude tungsten carbide product 52 which resembles a gray sintered material. The crude tungsten carbide product 52 is subjected to a water leaching step 54 after addition of water 55, followed by solid/liquid separation 56. The liquid portiori 58 is fed to a crystallizer 60 and the crystals 62 can be recycled to the sparging furnace 24.
The solid crude tungsten carbide crystals 64 are comminuted 66 in water 68 and subjected to acid leaching 70 with a suitable acid 72 (e.g., HC1). In a preferred embodiment, Z(lm the comminution 66 and acid leaching 70 take place in a single operation. The comminution 66 is preferably conducted in a ball mill using tungsten carbide grinding media. The crude tungsten carbide crystals 64 are first slurried in a dilute aqueous 68 solution of hydrochloric acid 72, and the comminution 66 is continued for a period of time sufficient to liberate and solubilize impurities.
The comminuted and acid leached suspension 74 is subjected to solid/liquid separation 76. The solid high purity tungsten carbide 78 preferably has a purity level of at least 90 percent tungsten carbide, more preferably at least 95 percent tungsten carbide, and more preferably at least 99 percent tungsten carbide. The liquor 80 is subjected to neutralization and precipitation 82 of solid materials 84.
The solid precipitate 84, after drying, can be recycled to the slagging furnace 18.
In the first pyrometallurgical operation, a furnace charge consisting of a blend of tungsten concentrate and siliceous flux is treated at approximately 1,050 C. The tungsten compounds contained in the concentrate (e.g., calcium, iron, or manganese tungstates) react with the siliceous flux (preferably sodium silicate and silica) to produce two immiscible phases: a molten salt and molten silicate slag. The tungsten is preferentially segregated in the molten salt phase, while the majority of the impurities are rejected in the slag. The salt is more dense than the slag and settles to the bottom of the furnace crucible. The salt phase, which chiefly consists of sodium tungstate, is then forwarded to the second s-eage of pyrometallurgical processing, i.e., sparginga The concentrate used in the examples contained huebnerite (MnWO4) as the primary tungsten mineral. When a blended charge is treated as described above, the following chemical reaction ensues:
MnWO4(c) + NaZSiO3(c) = Mn0=SiOZ(i) + Na2W04M
Segregation of the salt and slag phases is predicated upon the exploitation of the immiscibility region existing within the tungstic oxide-sodium oxide-silica system shown in Figure 2. When the tungsten concentrates enter the 1,050 C melt, they react with the sodium silicate to produce sodium tungstate and slag. At this temperature, the slag and tungstate are immiscible, and they separate by gravity. .
The precise chemistry of the slag will depend upon the relative amounts of excess silica and sodium oxide in the system. Sodium oxide is a desirable slag constituent because its presence reduces the slag melting point sufficiently to ensure the formation of a completely liquid phase. In the absence of sodium oxide or another flux compound which will effectively lower the slag's melting point, a liquid slag cannot be formed in the manganese oxide-silica system at temperatures below approximately 1,250 C.
An example of a slagging system is illustrated in Fig.
3. With the exception of a gas injection system, the same basic furnace configuration useful in the sparging m12 operatzon (described below) can be employed for the slagging operation. Because the slagging operation is simply a melting and separating exercise, no gas lances or nitrogen purge lines are required.
The second pyrometallurgical process effects the crystallization of tungsten carbide within the molten salt phase. This feat is accomplished by heating the tungsten-bearing molten salt from the first stage to within the range of approximately 1,080 to 1,100 C and then sparging with a large stoichiometric excess of hydrocarbon gas, such as methane or propane. Under these conditions, the hydrocarbon gas cracks and provides the reductant and carbon source necessary for forming the tungsten carbide.
The tungsten carbide phase forms as micron-sized crystals, which are insoluble in the molten salt phase. The crystals are also denser than the salt and are segregated near the bottom of the reactor. At the conclusion of the sparging operation, the spent salt is decanted from the crystals.
When methane is employed as the hydrocarbon source, the net chemical reaction leading to the formation of the tungsten carbide (WC) product is believed to be:
4CH 4(g) + NaZWO4M = WC(s) + 3CO(9) + 8H 2(g) + Na2O(1) Because a large stoichiometric excess of hydrocarbon gas is needed, some of the excess gas also cracks to produce carbon and hydrogen gas, as illustrated by the following reaction:
CH4(9) C(S) + 2HZ(9) l3-The hydrogen gas and much of the elemental carbon are oxidized in the afterburner. However, some of the carbon remains as a contaminant within the salt phase. Thus, minimization of excess carbon formation in the sparging furnace is desirable.
Other hydrocarbon gases, such as propane or ethylene (CZH4), can be used in place of methane. For instance, the use of ethylene might enhance the sparging efficiency (i.e., increase the yield of tungsten carbide per unit of carbon added to the melt).
After separation of the free-flowing spent salt phase, the resultant tungsten carbide crystals are contained in a separate phase having a gray, sintered appearance. The gray material retains appreciable quantities of salt. The salt and other impurities are removed via a process of dry and/or wet grinding and sequential leaching in hydrochloric acid, caustic, and water. After this treatment, the resultant crystals can assay between approximately 99.3 and 99.4% tungsten carbide. However, the tungsten carbide produced in preliminary tests contains substantially higher impurity concentrations. The elevated impurity concentrations, mainly chromium and nickel, are believed to result from chemical attack of the fused salt on the reaction crucible.
An example of a suitable system for slagging (Fig. 3) and sparging (Fig. 4) includes a tilting furnace 110 with a cover at the top which has room for two sparging lances 112, 114, two thermocouples 116, 118, one dedicated*
el~o nitrogen line 120, one exhaust line 122, and one pressure gauge 124. The main component is a 12.9 kW resistance- =
heated furnace 110. The furnace 110 has a hot zone 0.914 meter long by 12.7 cm diameter; it can attain a maximum operating temperature of about 1,200 C. Within the furnace shell, the process reaction vessel, or crucible 126, is constructed of 10.2 cm diameter Inconel 600 pipe; the maximum bath depth is about 45.7 cm. The crucible 126 may be removed for cleaning or maintenance by opening the hinged split shell furnace.
The same furnace can be employed for slagging (Fig. 3) and sparging (Fig. 4). In either slagging or sparging operations, the initial charge is typically added to the cold crucible 126, and then power is applied to the furnace 110 in order to elevate the bath temperature to the desired target. Subsequent charges can be made to the hot furnace 110. To facilitate removal of molten products, the furnace 110 can be tilted a full 180 degrees from its vertical = operating position to pour products into ladles.
For operation in the gas sparging mode (Fig. 4), a facility was designed with the capability to purge the crucible 126'with nitrogen 127 and sparge the molten bath with methane, propane, ethylene or any mixture of these hydrocarbon -source gases 128. Seven access ports are located in the reactor lid. Two of the ports admit gas lances 112, 114 during sparging operations. Hydrocarbon gases 128 are injected into the crucible 126 through one of the lances 112, with the other lance 114 held in reserve in case the first lance 112 becomes obstructed.
Preferably, the lances 112, 114 have a relatively small w.
inner diameter (e.g., 0.14 cm) to provide relatively high velocity flow, thus minimizing cracking in the lances 112, 114. The inlet hydrocarbon gases 126 are directly injected intq the melt at a point approximately 5 cm above the crucible 126 bottom. During each sparging test, nitrogen 120 can also be injected through a third inlet port at a point approximately 2.5 cm below the reactor lid. The dedicated nitrogen lance 120 assures positive pressure inside the freeboard to prevent air from entering the crucible 126. All of the inlet gas flows are controlled by flow meters 130, 132, 134. Three other lid ports serve as thermocouple wells, and the main (central) port 122 serves as the process gas offtake.
A primary concern in the system design is to ensure efficient transport of the nascent hydrogen, which is formed by cracking or as a product of the sparging reaction to the afterburner 136. Preferably, in one embodiment, the pressure inside the furnace 110 is first adjusted to 0.25 to 0.50 millimeters (mm) of water by balancing the flow of reacting gas with the extraction draft. Then the pressure is increased to 2.5 to 5.0 mm of water by adjusting the flow of the dedicated nitrogen lance 120. Note that the tip of this lance 120 is positioned only about 5 cm from the top of the crucible 126 so that most of the draft is utilized to extract the reaction product gases and not nitrogen. In this way, most of the nitrogen flows through the top cover, maintaining an inert atmosphere at the top of the crucible 126 and preventing any air from contacting__ the product gases inside the furnace 110. The reaction gases are drawn into the afterburner 136 and combusted to HZ0 and COZ. Carryover salt can be collected at the baghouse 138 or scrubber 140. The afterburner 136 offgases can be air cooled 142 to 120 C before reaching the baghouse 138 or scrubber 140. When the baghouse 138 is employed, the gases go through the scrubbing system; then they can be discharged into the atmosphere. In the embodiment shown in Figure 4, the afterburner 136 offgas passes through the scrubber 140, while the baghouse 138 is used to treat possible fugitive emissions from the furnace 110.
Process gases exit the crucible 126 through the single exit port 122 leading to the gas handling system. The gases are fed directly into a 20.3 cm diameter by 55.9 cm long natural gas-fired, stainless steel afterburner 136 through a 5 cm diameter pipe. The afterburner 136 is designed to operate with a pressure pilot burner which remains ignited throughout the tests. Oxygen 144 is fed into the afterburner 136 at a controlled rate for combustion of the nascent hydrogen, residual hydrocarbon gases, and carbon fines entrained in the offgas stream.
After exiting the afterburner 136, the gases pass through a ball valve 146 (used to balance the system gas pressure profile) and then into the scrubber 140.
The scrubber 140 is constructed of a 208-liter polymer drum and polyvinyl chloride (PVC) piping. The scrubber is filled with approximately 114 liters of water; the afterburner discharge gases are bubbled into the reservoir to condense and remove any soluble material in the gas stream. The afterburner exhaust gases are cooled by air dilution 142 and by an external chiller coil system 148 before entering the scrubber 140. Gases are pulled through the scrubbing system by a 25 cm diameter blower 150. Exit gases from the blower 150 can be vented to the atmosphere.
An external baghouse 138 and blower assembly was set up to collect fugitive emissions from the crucible lid.
The baghouse 138 was fitted with two inlet hoses, each 10.2 cm in diameter, that were placed near the crucible lid.
Fugitive emissions were thus drawn into the baghouse 138, filtered, and then blown into the atmosphere.
Temperature was monitored at several key points throughout the system. Readings were measured by two thermocouples 116, 118 which are placed through two separate lid ports. One thermocouple 116 measured the melt temperature near the point of gas injection, while the other thermocouple 118 was used to monitor the temperature of the head space, or freeboard, in the crucible 126 above the melt.
Examples and Comparative Tests The tungsten concentrate sample used in the following examples was shipped from a commercial source. The 817 kg sample was packed in two unlined 30 gallon metal drums.
The contents of both drums were thoroughly blended together prior to initiating any testing. Approximately half of the sample was stored in a plastic-lined 55 gallon drum. The remaining half of the sample was split into lots of approximately 45 kg. Subsamples were drawn from three of the lots for comparative analysis to ascertain the efficiency of the blending operation. Duplicate samples were retained on inventory for verification analyses. The blended master samples were then stored in sealed containers pending their use in the various tests.
The three subsamples of the tungsten concentrate were initially screened by semiquantitative analytical methods, such as x-ray diffraction (XRD), x-ray fluorescence (XRF), and emission spectrography, to approximate its mineralogy and chemical composition. Subsequently, all major and minor components detected by the screening methods were analyzed by more exacting techniques, including wet quantitative analytical chemistry, atomic absorption spectroscopy (AA), and inductively-coupled plasma spectroscopy (ICP). In some cases, multiple analytical techniques were employed in order to firmly establish the chemical composition of the concentrate sample. In addition to the chemical analysis, the tungsten concentrate sample characterization also included a limited amount of physical characterization.
Comparative Tests A, B and C
Three comparative slagging tests, designated as A, B
and C, were completed within a 5 kW induction furnace system. In view of the huebnerite mineralogy of the concentrate sample, the tests were performed to obtain a preliminary indication of the behavior of the MnO-NazO-Si02 system slag. The charge components included varying amounts of concentrate, sodium chloride, and slag-formers s.odlum silicate and silica. These were added according to the respective charge compositions detailed in Table I.
f During these experiments, excessive salt fumes were evident at times, and thin layers of salt condensed on the internal surface of the dome of the bell jar induction furnace containment.
Table I. Charge Compositions for Comparative Slagging Tests A, B and C
Charge Component Test A Test B Test C
and Mass Concentrate, g 10.73 10.68 12.10 NaCl, g 16.36 16.40 18.64 Na Si0=9H 0, g 23.03 28.93 16.89 Si0 , g 3.36 3.37 0 Visual inspection of the slag and salt products indicated no problems with phase separation. The three slag samples had a vitreous appearance and were tinted green, ranging from light green in Test A to emerald green in Test C. Most of the sodium chloride was volatilized during the first test, leaving a deposit of dark solids on the slag surface. In the other two tests, the halide phase was off-white with a yellow tint on each surface. The slag and halide phase samples produced in each test were recovered and submitted for XRF analysis; the amount of s20-halide phase recovered from Test A was insufficient for XRF
analysis.
The XRF data, summarized in Table II, suggest that a fav-orable partitioning of the tungsten between the slag and the halide phase occurred in two of the three tests. The tungstic oxide (WO3) concentrations in the slag samples generated in Tests A and C were 0.5 and 0.7%, respectively, while the tungstic oxide concentration in the B slag was 1.8%.
Table II. XRF Analysis of Slag Samples from Comparative Slagging Tests Compound A B C
Weight % Weight % Weight %
NaCl 7.1 8.7 3.1 A1 O 3.5 2.6 1.2 FeO 0.7 0.5 0.9 MnO 14.4 10.2 28.7 Na O 22.7 21.2 14.4 Si0 47.7 51.2 42.4 WO 0.5 1.8 0.7 Total 96.6 96.2 91.4 As shown in Table III, the halide phase samples from Tests B and C consisted primarily of chlorine, sodium, and tungsten. According to the XRF data, the halide phase samples from Tests B and C contained 39 and 40% tungstic oxide, respectively. The iron and manganese concentrations were each below 0.1 % in both halide samples. Trace levels of several other elements were also detected.
21~
Table III. XRF Analysis of Halide Phase Samples from Preliminary Slagging Tests Element B C
Weight ~ Weight %
C1 46.5 44.5 Na 23.0 23.3 W 31.0 32.0 Total 100.5 99.8 Example 1 Sodium Tungstate Production Example 1 is designed to demonstrate the feasibility of forming a discrete sodium tungstate phase in the absence of sodium chloride in the charge. For the test to be successful, it is necessary that the sodium tungstate and slag would be present as immiscible liquids at the temperature of interest. This test was conducted in a 5 kW
induction furnace. This charge composition is presented in Table IV.
Table IV. Charge Components and Masses for Sodium Tungstate Production Charge Component Example 1 and Mass Concentrate, grams 66.57 NaCl, grams 0 Na Si0 , grams 62.16 S i0 ,' grams 21.27 Total, grams 150.00 m22 Visual inspection of the test products indicates the formation of two distinct phases, sodium tungstate and slag. The slag phase has a dark green appearance and is at the-top, while the sodium tungstate phase is off-white and located at the bottom of the crucible. The fact that the sodj-um tungstate phase is located at the bottom of the crucible is due to its higher density and its immiscibility with the lower density slag phase.
Example 1 was conducted without difficulty and phase separation was excellent. The products of this experiment were submitted for analysis to determine their respective tungsten and manganese distribution between the two product phases. As shown in Table V, the analytical results for Example 1 confirmed the feasibility of favorable tungsten and manganese distributions between the slag and salt phases. Judging from these results, the separation of tungsten from the concentrate as sodium tungstate, in the absence of sodium chloride, presents an attractive alternative.
Table V. Analytical Results from Example I
Charge Composition Chemical Analysis Species Weight t Element ~ in Salt o in Slag Na Si0 41.45 Mg 0.06 0.34 Si0 14.17 Na 12.80 16.70 MnWO 44.38 W 59.25 0.10 Mn 2.05 12.40 cl Si 0.21 19.50 Comuarative Tests D. E. F and G
Variation of the Manganese-to-Sodium Silicate Ratio in the Charge The objective of Comparative Test D is to evaluate the effect of a high manganese-to-sodium silicate (Mn:Na2Si03) ratio on the distribution of tungsten and manganese between the slag and salt phases. While not wishing to be bound by any theory, it is believed that is important to maintain a certain level of sodium in the system. In conducting tests where the slag composition was the independent variable, the respective distribution of manganese between the salt and slag phases was adversely affected as the manganese oxide level of the slag increased. This problem became apparent when the molar ratio of manganese to sodium silicate in the charge was raised above 1. It is believed that this phenomena occurred because an insufficient amount of sodium was present to complete the following reaction:
MnWO4(s) + NaZSiO3(s) = Mn0= Si02(,) + Na2WO4(0.
If Mn:Na2SiO3 molar ratios of greater than one are desired to reduce flux consumption, additional sources of sodium are needed to maximize the formation of sodium tungstate and minimize the dissolution of unreacted manganese tungstate into the salt phase. The additional source of sodium utilized in this experiment was sodium hydroxide (NaOH) according to the composition presented in Table VI.
Table VIo Charge Composition for Test D
Compound Test D
Concentrate, grams 41.23 NaCl, grams 64.33 Na Si0 , grams 12.26 NaOH, grams 3.24 Total, grams 121.06 Although two distinct phases were again formed, the appearance of the slag was different than that observed in previous experiments. The slag in this test had a sandy appearance which, when observed under the microscope (30X
magnification), gave evidence of different phases and incomplete fusion of the charge. The halide phase had the same appearance as in the previous tests. As evidenced from the analytical results given in Table VII, the use of sodium hydroxide yielded unsatisfactory tungsten and manganese distributions in both the slag and salt phases.
Three additional induction furnace tests were conducted to further explore the effect of altering the Mn:NazSi03 ratio in the furnace charge, and to investigate the use of alternative sources of sodium and silica. The specific objective of Test E was to study the effects of a slag composition with a Mn:Na2SiO3 molar ratio of one on the distributions of tungsten and manganese between the halide and slag phases. As indicated in Table VII, the 0.55%
concentration of tungsten in the slag and the 0.14%
concentration of manganese in the halide indicate' that reduction in flux consumption to realize a slag molar ratio of Mn:NazSiO3 of less than or equal to one is feasible and worth pursuing.
In Test F, an attempt was made to increase the manganese:silicon ratio to 1.35, under conditions similar to those of Test D but using sodium carbonate (Na2CO3) instead of sodium hydroxide as the additional sodium source. The objective was to determine whether the choice of,.additional sodium source had any significant effect on the tungsten and manganese distributions. As seen in Table VII, a tungsten -concentration of 1.08% in the slag suggests, when compared to 3.9% from Test D, that the source of additional sodium can have an effect on the distribution of tungsten in the halide phase.
In Test G the objective was to study the feasibility of using silica and sodium carbonate as the sole sources of sodium and silica in an attempt to substitute less expensive raw materials for sodium metasilicate. As shown in Table VII, the 0.13% tungsten concentration in the slag and the 0.03% manganese concentration in the halide suggested that the substitution is feasible.
Table Vleo AnaWtical Results for Comparative Tests D. E, F.
and G
Charge Composition Chemical Analysis Test Comments Species Weight % Element % in % in Salt Slag Comparative NaZSiO$ 10.13 Mg 0.01 1.35 Test D NaOH used Si02 0.00 Na 34.90 5.82 as MnWO4 34.05 W 17.50 9.44 additional sodium NaCI 53.14 Mn 0.22 33.60 source for a NaOH 2.68 CI 46.00 0.75 basic slag.
Si 0.19 11.90 Comparative Na2SiO3 20.24 Mg 0.01 0.69 Test E Mn:NazSiO3 Si02 0.00 Na 30.70 14.80 molar ratio MnWO4 31.40 W 25.60 0.55 of one in the slag.
NaCI 48.36 Mn 0.14 24.50 CI 37.00 0.06 L Si 0.12 12.30 Comparative Na2SiO3 13.89 Mg 0.01 0.39 Test F Na2CO3 0.00 Na 30.30 11.10 used as MnWO4 32.56 W 23.40 1.08 additional sodium NaCi 50.28 Mn 0.10 32.70 source Na2CO3 3.27 CI 38.00 0.39 (basic slag).
Si 0.31 12.40 Comparative NaZSiO3 0.00 Mg 0.03 0.72 Test G Si0Z and Si0Z 18.85 Na 30.50 15.60 Na 2CO3 as MnWO4 24.20 W 23.60 0.13 sole sources of NaCI 37.36 Mn 0.03 13.20 silicon and Na2C03 19.59 CI 40.50 0.10 sodium.
Si 0.17 16.95 Example 2 27=.
In Example 2, no sodium chloride was included in the chargeo The slag composition was selected to ensure the.
formation of two immiscible liquids. The formation of the two immiscible phases, as well as the favorable distributions of tungsten and manganese in the salt and slac, was predicted by the results of Example 1.
The mass balance for Example 2 is shown in Table VIII.
The mass closure for this Example was 96.8%. A tungsten mass balance indicates that 92.9% of the charged tungsten reported to the halide phase and 3.3% to the slag. Only 3.8% of the tungsten in the charge was unaccounted.
Table VIII. Mass Balance for Slagging Example 2 Material In Kilograms Material Out Kilograms Concentrate 4.43 Halide Phase 3.94 Silica 1.41 Slag 5.74 Sodium Metasilicate 4.15 Total 10.00 Total 9.68 The tungsten distribution for Example 2, as calculated from the analytical data, indicates that approximately 97%
of the input tungsten was segregated in the tungstate phase, with the difference reporting to the slag. While these results siuggest that an efficient slagging operation in the absence of sodium chloride is indeed possible, those skilled in the art can improve the tungsten distribution without undue experimentation. Entrainment of salt from the reactor walls during slag pouring may have contributed o28e to the relatively high tungsten concentration in the slag from Example 2.
From an operational point of view, although the sodium tungstate phase was segregated below the slag in the reactor (due to the higher density of the salt), it poured first, due to its lower viscosity and the geometry of the reactor. There were only a few minor traces of slag entrained in the salt, and these had floated to the surface before the salt solidified in the ladle.
Example 3 Recycling Sparged, Spent Salt to the Slagging Operation This Example is designed to demonstrate the effectiveness of recycling the spent salt from the sparging unit operation to the slagging unit operation. This practice is desirable for two reasons. First, the spent salt typically contains an appreciable concentration of tungsten (approximately 15% by weight) which is not converted to tungsten carbide during the sparging step.
Returning the salt to the slagging operation keeps the tungsten within the processing circuit and is useful in achieving economic levels of tungsten recovery in the overall operation. Second, it is believed that the sodium oxide in the sparged salt can serve as the sodium source in the production of sodium tungstate during the slagging operation. Therefore, recycling the spent salt is expected to reduce the consumption of raw materials. This Example was designed to determine whether recycling the spent salt would affect the distribution of tungsten between the salt -and slag phases.
The Example consists of three charging cycles conducted sequentially. The Cycle 1 charge represents a typi-cal slagging operation charge without salt recycled from the sparging operation and consists of a 5 kg blend of 260% huebnerite concentrate, 24.7% sodium metasilicate (Na2Si03), 8.4% silica (Si0Z) and 40.6% sodium chloride (NaC1). The Cycle 2 charge consisted of 1 kg of spent salt (generated during a previous sparging test) plus 4 kg of the same components used in Cycle 1, mixed in the identical proportions. The Cycle 3 charge contained 2 kg of spent salt plus 4 kg of the components used in Cycle 1, again mixed according to the Cycle 1 proportions.
At the beginning of each test cycle, the charge materials were blended together, added to the furnace, and processed at a nominal temperature of 1,O50 C for one hour.
The fused salt was then removed by tilting the furnace and pouring the melt into a ladle where it was allowed to solidify. The furnace was restored to its vertical operating position, and the process was repeated with the next charge. The slag phase was not removed until all three cycles had been completed. The slag was then poured into a ladle and allowed to solidify. Samples of the slag and of each of the three salt products were prepared and submitted for chemical analysis.
G3Qe The analyses of the slag and salt products are summarized in Table IX. As calculated from the measured-_ product weights and associated tungsten analyses, approximately 99.1% of the tungsten reported to the salt.
Comparison of the salt analyses from Cycles 1, 2 and 3 indicates favorably low concentrations of impurities in all three cycles.
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v v v a a b 0o ~ g 8 w o a +, v ~ V
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Ei K1 M "'t 't ~ ~cC
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c+1 ~ t3. N N 0 E 6' ~i' LO
G~~o Examples 4 and 5 Sparging Sodium Tungstate to Produce Tungsten Carbide It has been demonstrated that tungsten carbide of reasonably high purity can be obtained by sparging a molten mixture of sodium tungstate and sodium chloride with methane. However, elimination of the sodium chloride from the operation improves the process for several reasons.
Consequently, two additional Examples are presented to demonstrate whether crystalline tungsten carbide powder can be produced by sparging molten sodium tungstate with methane gas.
In each Example, the initial melt consists of sodium tungstate produced in previous slagging tests. During the Examples, the sodium tungstate bath is maintained at approximately 1,100 C, while methane gas is injected below its surface at a flow rate of approximately 11.4 liters per minute. Methane sparging is continued for three hours in Example 4 and for 90 minutes in Example 5. At the conclusion of each Example, the molten products are poured into a steel ladle and allowed to solidify.
After the products have solidified and cooled sufficiently, two separate phases are observed: a white "spent ash" and a denser, medium gray phase. The two phases are separated and prepared for x-ray diffraction (XRD) analysis. The products from Example 4 were selected for the XRD analysis because they were more easily and cleanly separated after cooling. XRD analysis of the white spent salt indicates that it is predominantly composed of unreacted sodium tungstate (Na2WO4) with trace concentration of another unidentified crystalline phase. Nore==
significantly, the dense graph phase was found to contain sodium tungstate, with lesser concentrations of tungsten carbide (WC) and ditungsten carbide (W2C) and trace concentrations of metallic tungsten and the same unidentified crystalline phase that occurred in the white salt.
Although those skilled in the art will be able to further optimize the process, the x-ray diffraction results demonstrate that it is possible to form tungsten carbide via the methane sparging method.
While various embodiments of the present invention have been described in detail, it is apparent that modifications and adaptations of those embodiments will occur to those skilled in the art. It is to be expressly understood, however, that such modifications and adaptations are within the scope of the present invention, as set forth in the following claims:
-34 , List of Reference Numerals Tungsten-Containing Concentrate 12 Silica 14 Silicate 16 Slagging Furnace 18 Tungstate Salt 20 Slag 22 Sparging Furnace 24 Slagging Furnace Gas 26 Particulate Control 28 Part'iculates 30 Treated Gas 32 Carbon-Containing Gas 34 Sparging Furnace Gas 36 Afterburner 38 Oxygen-Containing Gas 40 Methane 42 Afterburner Gas 44 Particulate Control 46 Particulates 48 Treated Gas 50 Sparged, Spent Salt 51 Crude Tungsten Carbide Product 52 Water Leaching Step 54 Water 55 Solid/Liquid Separation 56 Liquid Portion 58 Crystallizer 60 Crystals 62 Solid Crude Tungsten Carbide Crystals 64 Comminution 66 Water 68 Acid Leaching 70 Acid 72 Comminuted and Acid Leached Suspension 74 Solid/Liquid Separation 76 High Purity Tungsten Carbide 78 Liquor 80 Neutralization and Precipitation 82 Solid Precipitate 84 Tilting Furnace 110 Sparge Lances 112, 114 Thermocouples 116, 118 Nitrogen Line 120 Exhaust Line 122 Pressure Gauge 124 Crucible 126"
Nitrogen 127 Hydrocarbon Gas(es) 128 Flow Meters 130, 132, 134 Afterburner 136 Baghouse 138 Scrubber 140 Cooling Air Intake 142 Oxygen 144 ValVe 146 Chiller Coil System 148 Blower 150
Claims (12)
1. A method for forming a metal carbide, comprising:
(a) heating a tungstate salt to a temperature from about 1,050 degrees Celsius to about 1,200 degrees Celsius, wherein the tungstate salt is heated to form a melt lacking any halide salt;
(b) sparging a hydrocarbon gas through the melt to form tungsten carbide; and (c) separating said tungsten carbide from the melt.
(a) heating a tungstate salt to a temperature from about 1,050 degrees Celsius to about 1,200 degrees Celsius, wherein the tungstate salt is heated to form a melt lacking any halide salt;
(b) sparging a hydrocarbon gas through the melt to form tungsten carbide; and (c) separating said tungsten carbide from the melt.
2. The method of claim 1, wherein the tungstate is one of sodium tungstate or potassium tungstate.
3. The method of claim 1, wherein the heating step (a) takes place in the presence of an alkali metal compound.
4. The method of claim 1, wherein the sparging step (b) further comprises forming a sparged melt.
5. The method of claim 1, further comprising:
(d) purifying the tungsten carbide to from a purified tungsten carbide.
(d) purifying the tungsten carbide to from a purified tungsten carbide.
6. The method of claim 5, wherein the purified tungsten carbide is at least percent tungsten carbide.
7. The method of claim 1, wherein step (b) forms a particulate matter, wherein the particulate matter and the remainder of the melt of step (c) are recycled to a slagging furnace.
8. The method of claim 5, wherein step (d) further comprises:
(D1) leaching the tungsten carbide with water to form a water-leached tungsten carbide;
(D2) separating the water-leached tungsten carbide from an aqueous phase;
(D3) comminuting and leaching the water-leached tungsten carbide with a leaching agent to form a purified tungsten carbide; and (D4) separating the purified tungsten carbide from the leaching agent.
(D1) leaching the tungsten carbide with water to form a water-leached tungsten carbide;
(D2) separating the water-leached tungsten carbide from an aqueous phase;
(D3) comminuting and leaching the water-leached tungsten carbide with a leaching agent to form a purified tungsten carbide; and (D4) separating the purified tungsten carbide from the leaching agent.
9. The method of claim 8, wherein the aqueous phase of step (D2) further comprises:
(D2') crystallizing from the aqueous phase a crystalline material; and (D2") recycling the crystalline material to step (a).
(D2') crystallizing from the aqueous phase a crystalline material; and (D2") recycling the crystalline material to step (a).
10. The method of claim 1, wherein the hydrocarbon gas is one of methane, ethylene, propane, or a mixture thereof.
11. The method of claim 1, wherein the hydrocarbon gas is in a stoichiometric excess.
12. The method of claim 1, wherein the sparging is conducted in a crucible or a furnace and wherein the crucible or the furnace is purged with nitrogen.
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/482,129 US5882620A (en) | 1995-06-07 | 1995-06-07 | Pyrometallurgical process for forming tungsten carbide |
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| CA2224185A CA2224185C (en) | 1995-06-07 | 1996-06-07 | Pyrometallurgical process for treating metal-containing materials |
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