CA3141668A1 - Method and system for slag vitrification of toxic elements - Google Patents
Method and system for slag vitrification of toxic elements Download PDFInfo
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- CA3141668A1 CA3141668A1 CA3141668A CA3141668A CA3141668A1 CA 3141668 A1 CA3141668 A1 CA 3141668A1 CA 3141668 A CA3141668 A CA 3141668A CA 3141668 A CA3141668 A CA 3141668A CA 3141668 A1 CA3141668 A1 CA 3141668A1
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- molten slag
- target elements
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- arsenic
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- 239000002893 slag Substances 0.000 title claims abstract description 82
- 238000000034 method Methods 0.000 title claims abstract description 37
- 238000004017 vitrification Methods 0.000 title claims abstract description 28
- 231100000701 toxic element Toxicity 0.000 title description 8
- 239000008188 pellet Substances 0.000 claims abstract description 45
- 238000002844 melting Methods 0.000 claims abstract description 29
- 230000008018 melting Effects 0.000 claims abstract description 28
- 229910052840 fayalite Inorganic materials 0.000 claims abstract description 19
- 229910001948 sodium oxide Inorganic materials 0.000 claims abstract description 13
- 238000002156 mixing Methods 0.000 claims abstract description 12
- 238000005453 pelletization Methods 0.000 claims abstract description 12
- KKCBUQHMOMHUOY-UHFFFAOYSA-N sodium oxide Chemical compound [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 claims abstract description 12
- 238000001816 cooling Methods 0.000 claims abstract description 6
- 229910052785 arsenic Inorganic materials 0.000 claims description 59
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 claims description 54
- 239000000203 mixture Substances 0.000 claims description 43
- 239000010949 copper Substances 0.000 claims description 28
- 239000011521 glass Substances 0.000 claims description 27
- 229910052802 copper Inorganic materials 0.000 claims description 26
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 23
- 238000003723 Smelting Methods 0.000 claims description 19
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 claims description 18
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 16
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 14
- 239000011133 lead Substances 0.000 claims description 13
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 13
- 239000011734 sodium Substances 0.000 claims description 13
- 239000011575 calcium Substances 0.000 claims description 12
- 239000010953 base metal Substances 0.000 claims description 10
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 9
- 235000013980 iron oxide Nutrition 0.000 claims description 9
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 7
- 229910052791 calcium Inorganic materials 0.000 claims description 7
- 239000000377 silicon dioxide Substances 0.000 claims description 7
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 7
- 229910052681 coesite Inorganic materials 0.000 claims description 6
- 229910052906 cristobalite Inorganic materials 0.000 claims description 6
- 239000003500 flue dust Substances 0.000 claims description 6
- 238000010438 heat treatment Methods 0.000 claims description 6
- 229910052682 stishovite Inorganic materials 0.000 claims description 6
- 229910052905 tridymite Inorganic materials 0.000 claims description 6
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims description 5
- 229910052787 antimony Inorganic materials 0.000 claims description 5
- 229910052793 cadmium Inorganic materials 0.000 claims description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- 229910052742 iron Inorganic materials 0.000 claims description 5
- 239000011701 zinc Substances 0.000 claims description 5
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 3
- 229910052782 aluminium Inorganic materials 0.000 claims description 3
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims description 3
- 229910052737 gold Inorganic materials 0.000 claims description 3
- 239000010931 gold Substances 0.000 claims description 3
- VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 claims description 3
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims description 3
- 235000012239 silicon dioxide Nutrition 0.000 claims description 3
- 238000003756 stirring Methods 0.000 claims description 3
- 229910052725 zinc Inorganic materials 0.000 claims description 3
- 239000004115 Sodium Silicate Substances 0.000 claims description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 2
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 claims description 2
- 229910052911 sodium silicate Inorganic materials 0.000 claims description 2
- 239000011573 trace mineral Substances 0.000 claims description 2
- 235000013619 trace mineral Nutrition 0.000 claims description 2
- 229910052745 lead Inorganic materials 0.000 claims 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- 238000002474 experimental method Methods 0.000 description 8
- 239000000292 calcium oxide Substances 0.000 description 7
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 7
- 235000017550 sodium carbonate Nutrition 0.000 description 6
- 238000007496 glass forming Methods 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 229910000413 arsenic oxide Inorganic materials 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 238000005188 flotation Methods 0.000 description 3
- 230000004927 fusion Effects 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 230000009919 sequestration Effects 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- IKWTVSLWAPBBKU-UHFFFAOYSA-N a1010_sial Chemical compound O=[As]O[As]=O IKWTVSLWAPBBKU-UHFFFAOYSA-N 0.000 description 2
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 2
- 229960002594 arsenic trioxide Drugs 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 2
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 2
- 238000010908 decantation Methods 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 238000002386 leaching Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000010587 phase diagram Methods 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 238000005549 size reduction Methods 0.000 description 2
- DJHGAFSJWGLOIV-UHFFFAOYSA-K Arsenate3- Chemical compound [O-][As]([O-])([O-])=O DJHGAFSJWGLOIV-UHFFFAOYSA-K 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 229910000272 alkali metal oxide Inorganic materials 0.000 description 1
- 229940000489 arsenate Drugs 0.000 description 1
- AQLMHYSWFMLWBS-UHFFFAOYSA-N arsenite(1-) Chemical compound O[As](O)[O-] AQLMHYSWFMLWBS-UHFFFAOYSA-N 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000012717 electrostatic precipitator Substances 0.000 description 1
- 238000005538 encapsulation Methods 0.000 description 1
- 239000000383 hazardous chemical Substances 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910000464 lead oxide Inorganic materials 0.000 description 1
- HTUMBQDCCIXGCV-UHFFFAOYSA-N lead oxide Chemical compound [O-2].[Pb+2] HTUMBQDCCIXGCV-UHFFFAOYSA-N 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- NOTVAPJNGZMVSD-UHFFFAOYSA-N potassium monoxide Inorganic materials [K]O[K] NOTVAPJNGZMVSD-UHFFFAOYSA-N 0.000 description 1
- 239000010970 precious metal Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000001029 thermal curing Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B5/00—Treatment of metallurgical slag ; Artificial stone from molten metallurgical slag
- C04B5/06—Ingredients, other than water, added to the molten slag or to the granulating medium or before remelting; Treatment with gases or gas generating compounds, e.g. to obtain porous slag
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B09—DISPOSAL OF SOLID WASTE; RECLAMATION OF CONTAMINATED SOIL
- B09B—DISPOSAL OF SOLID WASTE NOT OTHERWISE PROVIDED FOR
- B09B3/00—Destroying solid waste or transforming solid waste into something useful or harmless
- B09B3/20—Agglomeration, binding or encapsulation of solid waste
- B09B3/25—Agglomeration, binding or encapsulation of solid waste using mineral binders or matrix
- B09B3/29—Agglomeration, binding or encapsulation of solid waste using mineral binders or matrix involving a melting or softening step
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C1/00—Ingredients generally applicable to manufacture of glasses, glazes, or vitreous enamels
- C03C1/002—Use of waste materials, e.g. slags
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C3/00—Glass compositions
- C03C3/04—Glass compositions containing silica
- C03C3/062—Glass compositions containing silica with less than 40% silica by weight
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B18/00—Use of agglomerated or waste materials or refuse as fillers for mortars, concrete or artificial stone; Treatment of agglomerated or waste materials or refuse, specially adapted to enhance their filling properties in mortars, concrete or artificial stone
- C04B18/02—Agglomerated materials, e.g. artificial aggregates
- C04B18/023—Fired or melted materials
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/20—Recycling
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Ceramic Engineering (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Civil Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Environmental & Geological Engineering (AREA)
- Processing Of Solid Wastes (AREA)
Abstract
A method for slag vitrification of target elements, comprising forming target elements-containing pellets having a melting temperature lower than a melting temperature of a molten slag, mixing the target elements-containing pellets with the molten slag; and cooling. Vitrification of target elements using molten fayalite slag, comprising pelletizing the target elements with sodium oxide, mixing resulting pellets with the molten slag; and cooling is described.
Description
TITLE OF THE INVENTION
Method and system for slag vitrification of toxic elements FIELD OF THE INVENTION
[0001] The present invention relates to disposal of toxic elements. More specifically, the present invention is concerned with a method and system for slag vitrification of toxic elements.
BACKGROUND OF THE INVENTION
Method and system for slag vitrification of toxic elements FIELD OF THE INVENTION
[0001] The present invention relates to disposal of toxic elements. More specifically, the present invention is concerned with a method and system for slag vitrification of toxic elements.
BACKGROUND OF THE INVENTION
[0002] Base metals such as copper, zinc, nickel or cobalt for example are extracted by smelting from row ores that typically contain toxic elements such as arsenic (As), antimony (Sb), lead (Pb) and cadmium (Cd), sometimes in large amounts. During the smelting process, such toxic elements are typically volatilized as oxides and carried with flue dusts. Electrostatic precipitators or baghouses may be used to collect the flue dusts, which then need be disposed of safely due to their toxic content, which may be as high as 60% in the case of arsenic for instance. After the base metals have been smelted from the raw ores, a molten slag is left over. Arsenic for example is found in the smelter dust from copper, gold, and lead smelters, and is recovered primarily from copper refinement dust. In the case of copper smelting, the separation of the copper metal during smelting is incomplete and the final molten slag may contain a few per cents of entrained copper. As currently practiced, this final molten slag is cooled down and submitted to flotation after size reduction by crushing in order to recover metallic values remaining therein.
[0003] The safe disposal of flue dusts from smelting or roasting operation may be achieved by vitrification with recovery of the base or precious metals prior to glass formation.
Sequestration of arsenic may be achieved with a glass composition comprising an iron oxide agent that prevents excessive volatilization of the arsenic during the fusion for glass formation.
Sequestration of arsenic may be achieved with a glass composition comprising an iron oxide agent that prevents excessive volatilization of the arsenic during the fusion for glass formation.
[0004] There is still a need in the art for a method and a system for slag vitrification of toxic elements.
SUMMARY OF THE INVENTION
SUMMARY OF THE INVENTION
[0005] More specifically, in accordance with the present invention, there is provided a method for slag vitrification of target elements, comprising forming target elements-containing pellets having a melting temperature lower than a melting temperature of a molten slag, mixing the target elements-containing pellets with the molten slag; and cooling.
[0006] There is further provided a method for the vitrification of target elements using molten fayalite slag, comprising pelletizing the target elements with sodium oxide, mixing resulting pellets with the molten slag; and cooling.
[0007] Other objects, advantages and features of the present invention will become more apparent upon reading of the following non-restrictive description of specific embodiments thereof, given by way of example only with reference to the accompanying drawings.
BRIEF DESCRIPTION OF THE DRAWINGS
BRIEF DESCRIPTION OF THE DRAWINGS
[0008] In the appended drawings:
[0009] FIG. 1 to FIG. 7 show pages of "Phase Diagram for Ceramists" by E.M
Levine and al 1964, The American Ceramic Society.
DESCRIPTION OF ILLUSTRATIVE EMBODIMENTS
Levine and al 1964, The American Ceramic Society.
DESCRIPTION OF ILLUSTRATIVE EMBODIMENTS
[0010] The present invention is illustrated in further details by the following non-limiting examples relating to disposal of arsenic resulting from copper smelting. All compositions herein are in weight percentage unless otherwise indicated.
[0011] The molten slag resulting from copper smelting is mostly an iron silicate (Fe2-)2SiO4 with amounts of oxides of calcium and aluminum, lead, copper, zinc, arsenic and trace elements. Such fayalite (Fe2SiO4) has a typical composition of: 5i02: 25%; Fe: 46%; A1203: 2.8%; CaO: 7.0%; As: 0.55%; Cu:
2.5%; Zn: 2.6%; Pb: 0.6%, or :
2FeO.5i02Ø3Ca0 on an approximate molar basis.
2.5%; Zn: 2.6%; Pb: 0.6%, or :
2FeO.5i02Ø3Ca0 on an approximate molar basis.
[0012] In a nutshell, the method as exemplified in the present disclosure comprises using the molten slag resulting from smelting of bases metals from arsenic-containing ores, as a glass forming material for vitrification of the arsenic in the flue dusts resulting from the smelting of the bases metals.
[0013] The method basically uses the molten slag resulting from smelting of bases metals from arsenic-containing ores, available on site, as a source of iron and silicate for the vitrification of arsenic. A challenge is the presence of amounts of calcium typically added in the flue dusts in order to abate their acidity.
[0014] Typically, when one ton of a copper ore comprising 5% arsenic is treated in a smelter, up to 50 Kg of arsenic is volatilized and carried in the flue dusts with about 50 Kg of other minerals. The amount of molten slag produced is around one ton per ton of ore as an order of magnitude. 250 Kg of this molten slag allows obtaining an arsenical glass containing 20% arsenic. If all the molten slag is used as a glass forming material, the total corresponding glass produced may contain about 5% arsenic.
[0015] In case when the recovery of copper remining in the molten slag is done by decantation or flotation, after reduction of size by crushing and grounding, vitrification of the arsenic being effective even in presence of a few per cents of entrained copper remaining in the slag prior to the vitrification, the arsenic-containing flue dusts are pelletized into arsenic-containing pellets, for example with lime in order to produce arsenite or arsenate of calcium, and the arsenic-containing pellets are dissolved in the molten slag to produce a glass containing up to 20% arsenic, a number of issues occur. First, due to the size reduction by crushing and grounding prior to the vitrification performed for recovery of copper remaining in the molten slag by decantation or flotation as mentioned hereinabove, any still remaining copper becomes integrated within the structure of the glass and thus cannot be recovered therefrom. Moreover, the sequestration of arsenic in the glass phase is poor. A second problem originates from the arsenic present as a salt of calcium in the molten slag.
[0016] Indeed, as shown in Fig. 80 of FIG. 1, the melting point of fayalite 2FeO.Si02 is in the range between about 1000 C and about 1150 C. The presence of amounts of other oxides may change the melting temperature of the fayalite slag. For instance, alkali oxides such as K20 and Na2O, and lead oxide result in a decrease of the melting temperature as shown by Fig. 397 (FIG. 2), Fig. 487 (FIG. 3) and Fig. 496 (FIG. 4) respectively. In contrast, in presence of CaO (Fig. 586 in FIG. 5), MgO (Fig 682 in FIG. 6) and A1203 (Fig 872 in FIG. 7) the melting point is raised.
[0017] Thus, the molten slag resulting from copper smelting has a melting temperature comprised, depending on minor components, in a range between about 950 C and about 1250 C.
[0018] Upon mixing the molten slag and the arsenic oxides-containing pellets, the calcium oxide at the surface of the pellets increases. This local increase in calcium, from 2FeO.Si02Ø3Ca0 in the slag to values much richer in CaO on the surface of the pellets, results in a local increase of the melting temperature, to above 1250 C, at the surface of the pellets, thus resulting in a surface crust, which in turn makes the dissolution of the pellets in the molten slag difficult and/or incomplete.
[0019] In order to circumvent these difficulties, in an embodiment of a method of the present disclosure, the arsenic-containing flue dusts are pelletized prior to their mixing with the molten slag. In an experiment, the following glass forming composition was selected (w/w): flue dusts: 35%; silica 26.4%;
fayalite: 23.6%, sodium carbonate (soda ash Na2CO3): 15.5%. The silica, fayalite and sodium carbonate were ground to 100 microns before being wet mixed with the flue dusts that contain arsenious oxide in a range between about 50 and about 60% (w/w). The resulting mixture was then pelletized and submitted to thermal curing at 200 C.
fayalite: 23.6%, sodium carbonate (soda ash Na2CO3): 15.5%. The silica, fayalite and sodium carbonate were ground to 100 microns before being wet mixed with the flue dusts that contain arsenious oxide in a range between about 50 and about 60% (w/w). The resulting mixture was then pelletized and submitted to thermal curing at 200 C.
[0020] The molar composition of the resulting pellets was about: 5.5. SiO2;
1.59 FeO; 1.0 Na2O; and 0.2 CaO, beside arsenic oxide. Fig. 487 in FIG. 3 indicates that the melting temperature of such composition is below 1000 C, which is typically much lower than the melting point of fayalite, i.e.
of the slag. As a result, fusion of the resulting pellets efficiently occurs in contact with the molten slag, resulting in efficient mixing of phases and incorporation of the arsenic in the glass composition independently of the mixing sequence, namely either when the slag is added to the pellets or when the pellets are added in the slag. Adding the pellets to the slag may be preferred so as to avoid introducing pelletized arsenic in an empty hot reactor.
1.59 FeO; 1.0 Na2O; and 0.2 CaO, beside arsenic oxide. Fig. 487 in FIG. 3 indicates that the melting temperature of such composition is below 1000 C, which is typically much lower than the melting point of fayalite, i.e.
of the slag. As a result, fusion of the resulting pellets efficiently occurs in contact with the molten slag, resulting in efficient mixing of phases and incorporation of the arsenic in the glass composition independently of the mixing sequence, namely either when the slag is added to the pellets or when the pellets are added in the slag. Adding the pellets to the slag may be preferred so as to avoid introducing pelletized arsenic in an empty hot reactor.
[0021] To obtain an homogeneous and inert arsenic glass, the viscosity of the molten slag is to be taken into account. In case the relatively cold pellets, of a typical temperature in a range between about 100 C and about 200 C, are added to the molten slag, which is at a temperature in the range between about 1000 C and about 1150 C, part of the molten slag is expected to freeze around the pellets unless some form of stirring is used; even with the presently discussed low-melting pellets (melting temperature below 1000 C), and achieving homogeneity may be a lengthy process. In an embodiment of an aspect of the present disclosure, to overcome this issue, a rotating tilting furnace or a hot gas circulation through the reaction mass may be used to control the temperature of the mixture. Moreover, depending on the composition and temperature of the molten slag and on the composition and temperature of the pellets, direct heating of the mixture may be used to maintain the fluidity of the mixture for a period of time in order to obtain the target homogeneity of the glass.
[0022] In a first experiment, arsenic-containing flue dusts pelletization was done using calcium oxide as taught in L.G. Twidwell, (Journal of Hazardous Materials, 8 (1983) 85-90). A fayalite having the following composition (w/w):
As: 0.32%; Si: 22.44%; Fe: 18.94%; Ca: 2.10%; Na: 10.33% and Cu: 0.25% was melted at 1200 C. Arsenic-containing pellets (60g) prepared from the arsenic-containing flue dusts and having the following composition (w/w):
As: 33.43%; Ca: 25.79%; Fe: 0.13%; Si: 0.09% and Cu: 0.95%, were added to the melted fayalite (160g). After two hours, the mixture was cooled. The resulting glass was lumpy and heterogenous and the EPA acetic acid test (TCLP 131) indicated a high leaching value of 277 mg of arsenic, a maximum standardly admitted being 5 mg of As.
The arsenic content in the glass was 14% w/w.
As: 0.32%; Si: 22.44%; Fe: 18.94%; Ca: 2.10%; Na: 10.33% and Cu: 0.25% was melted at 1200 C. Arsenic-containing pellets (60g) prepared from the arsenic-containing flue dusts and having the following composition (w/w):
As: 33.43%; Ca: 25.79%; Fe: 0.13%; Si: 0.09% and Cu: 0.95%, were added to the melted fayalite (160g). After two hours, the mixture was cooled. The resulting glass was lumpy and heterogenous and the EPA acetic acid test (TCLP 131) indicated a high leaching value of 277 mg of arsenic, a maximum standardly admitted being 5 mg of As.
The arsenic content in the glass was 14% w/w.
[0023] In a second experiment, pelletization of the flue dust was done using sodium oxide. Arsenic-containing pellets (160g) prepared with the arsenic-containing flue dusts and having the following composition (w/w): As: 47.9;
Ca: 0.77%; Fe: 0.15%; Na: 17.71%; Si: 0.07% and Cu: 1.42% were added to the molten fayalite of the same composition (134g) as in the first experiment After two hours at 1200 C, the mixture was cooled. The resulting glass was homogeneous without lumps or pits and the EPA acetic acid test (TCLP
131) indicated a leaching of 2.66 mg of As, below the 5.0 mg As maximum standardly admitted limit. The arsenic content in the glass was 15% w/w.
Ca: 0.77%; Fe: 0.15%; Na: 17.71%; Si: 0.07% and Cu: 1.42% were added to the molten fayalite of the same composition (134g) as in the first experiment After two hours at 1200 C, the mixture was cooled. The resulting glass was homogeneous without lumps or pits and the EPA acetic acid test (TCLP
131) indicated a leaching of 2.66 mg of As, below the 5.0 mg As maximum standardly admitted limit. The arsenic content in the glass was 15% w/w.
[0024] In a third experiment, pelletization of the flue dust was done using recycled glass as a source of sodium, with the following composition: Fe: 0.2%; Mg: 0.9%; Ca: 7.8%; Si:35.2%; Al:
1.0%; Na: 9.35%; K: 0.5%; and B:0.03%. Pellets were prepared containing 70% w/w of this recycled glass composition and 30% w/w of the flue dusts containing 55% w/w of As203. The pellets (60g) were mixed with the molten fayalite (140g) as in the second experiment described hereinabove. A homogenous glass containing 5% As w/w was then obtained with a TCLP 131 value of 1.05 mg of As, which is well below the 5.0 mg As maximum standardly admitted limit of 5.0 mg.
1.0%; Na: 9.35%; K: 0.5%; and B:0.03%. Pellets were prepared containing 70% w/w of this recycled glass composition and 30% w/w of the flue dusts containing 55% w/w of As203. The pellets (60g) were mixed with the molten fayalite (140g) as in the second experiment described hereinabove. A homogenous glass containing 5% As w/w was then obtained with a TCLP 131 value of 1.05 mg of As, which is well below the 5.0 mg As maximum standardly admitted limit of 5.0 mg.
[0025] In a fourth experiment, pelletization of the flue dust was done using sodium/iron oxide. Starting from a molten slag having the same composition as in the second experiment described hereinabove, pellets (60g) having the following composition: Na2CO3: 21.0g; flue dust: 39.0g and fayalite: 3.2g were added to the molten slag (134g) at 1200 C. After heating the resulting mixture for two hours at 1200 C, the obtained glass was casted and cooled.
The glass had the following composition: As: 10.56%; Si: 18.96%; Fe: 10.45%;
Ca:1.46%; Cu: 0.60%; Zn: 0.57%;
Na: 12.19% and Al: 0.47%. The TCLP 131 test indicated 3.64ppm As, below the 5.0 mg As maximum standardly admitted. The weight of casted glass was 176.12g, indicating a volatilization of arsenic at a level of 5.84%.
The glass had the following composition: As: 10.56%; Si: 18.96%; Fe: 10.45%;
Ca:1.46%; Cu: 0.60%; Zn: 0.57%;
Na: 12.19% and Al: 0.47%. The TCLP 131 test indicated 3.64ppm As, below the 5.0 mg As maximum standardly admitted. The weight of casted glass was 176.12g, indicating a volatilization of arsenic at a level of 5.84%.
[0026] Thus, a composition for the pelletized arsenic-containing flue dusts that comprises sodium/iron oxides as stabilizing agent, is found to decrease the refractoriness of the molten slag.
Using such sodium-rich pellets in a mixture with the molten slag, a very homogeneous glass was obtained containing 15% As (w/w), and the EPA acetic acid test (TCLP 131) below 5ppm indicated the arsenic was efficiently sequestrated. A similar result was obtained with sodium oxide/iron oxide pellets: the molten slag, mostly fayalite, was used very efficiently for the encapsulation of arsenic.
Using such sodium-rich pellets in a mixture with the molten slag, a very homogeneous glass was obtained containing 15% As (w/w), and the EPA acetic acid test (TCLP 131) below 5ppm indicated the arsenic was efficiently sequestrated. A similar result was obtained with sodium oxide/iron oxide pellets: the molten slag, mostly fayalite, was used very efficiently for the encapsulation of arsenic.
[0027] The method thus comprises vitrification of arsenic oxides by pelletization of the flue dusts with fusible oxides rather, as opposed to refractory oxides, and control of the fluidity of the mixture of the molten slag and the pelletized flue dusts by heating until obtaining a homogeneous glass. An effective sequestration of arsenic is obtained with a significant economy in energy and raw materials as a result of using the slag in fusion, compared with industrial methods for the vitrification of arsenic that consist in mixing pelletized arsenic-loaded flue dusts with glass forming elements.
[0028] Thus, the molten slag is used to vitrify arsenic in arsenic-containing pellets of flue dusts having a lower melting point than the melting point of the slag. The lower melting point of the arsenic-containing pellets of flue dusts is achieved by pelletizing the flue dusts with sodium as opposed to with calcium.
[0029] Thus leveraging the energy and a number of elements already present in the molten slag and that are needed for the vitrification, an efficient and economical vitrification of arsenic is achieved.
[0030] There is thus provided a method comprising using the molten slag from base metals smelting, which is mostly an iron silicate and already in a molten phase, as vitrification agent of arsenic. The method comprises selecting a combination of sodium oxide from sodium carbonate, sodium silicate or recycled glass or iron oxides as such or as iron silicate or a mixture of both sodium oxide and iron oxides, to prepare flue dusts pellets of a melting temperature below 1000 C, from the arsenic-containing flue dusts, and mixing these arsenic-containing pellets with the molten slag.
[0031] In an embodiment of the present disclosure, the method uses flue dust pellets comprising (w/w) FeO/Fe2O3 in a range between about 7 and about 15%; Na2O in a range between about 10 and about 25%; SiO2 in a range between about 15 and about 30%; and CaO in a range between about 1 and about 4%, and having a melting temperature below 1000 00, and a molten slag as defined by the CaO-FeO-SiO2 phase diagrams for a melting temperature in a range between about 950 and about 1250 C, typically between about 1000 C and about 1150 C.
Such use of the molten slag as the vitrification medium for arsenic yields economy of energy and raw materials, in an operational way.
Such use of the molten slag as the vitrification medium for arsenic yields economy of energy and raw materials, in an operational way.
[0032] Arsenic (As), as well as other toxic elements such a antimony (Sb), lead (Pb) and cadmium (Cd), may thus be sequestered by vitrification using the molten slag.
[0033] The scope of the claims should not be limited by the embodiments set forth in the examples, but should be given the broadest interpretation consistent with the description as a whole.
Claims (20)
1. A method for slag vitrification of target elements after base metals have been smelted from ores, the ores containing the base metals and the target elements, the method comprising collecting molten slag and flue dusts resulting from smelting of the base metals from the ores after the base metals have been smelted from the ores; forming a composition of the collected flue dusts, pelletizing the composition of the flue dusts with fusible oxides into target elements-containing pellets, the target elements-containing pellets having a melting temperature lower than a melting temperature of the collected molten slag; mixing the target elements-containing pellets with the collected molten slag;
and cooling the mixture; whereby the collected molten slag is a vitrification agent for the vitrification of the target elements.
and cooling the mixture; whereby the collected molten slag is a vitrification agent for the vitrification of the target elements.
2. The method as in Claim 1, comprising controlling a fluidity of the mixture of the collected molten slag and the target elements-containing pellets by heating.
3. The method as in any one of Claims 1 and 2, wherein the collected molten slag is a fayalite comprising one or more of oxides of calcium and aluminum, lead, copper, zinc, arsenic and trace elements, and having a melting temperature in a range between 950 C and 1250 C.
4. The method as any one of Claims 1 to 3, wherein the composition comprises elements that decrease the refractoriness of the collected molten slag.
5. The method of any one of claims 1 to 4, wherein said pelletizing the composition of the collected flue dusts comprises pelletizing the composition with one of: sodium, sodium/iron oxides and recycled glass.
6. The method of any one of claims 1 to 5, wherein the target elements-containing pellets comprise at least one of: sodium oxide, sodium carbonate, sodium silicate, recycled glass, iron oxides; and iron silicate.
7. The method as any one of Claims 1 to 6, comprising at least one of:
heating and stirring of the mixture of the target elements-containing pellets and the collected molten slag.
heating and stirring of the mixture of the target elements-containing pellets and the collected molten slag.
8. The method as any one of Claims 1 to 7, comprising controlling the viscosity of the mixture of the target elements-containing pellets and the collected molten slag.
9. The method as any one of Claims 1 to 8, the ores containing copper and at least one of: As, Sb, Cd and Pb, and the collected molten slag is fayalite molten slag.
10. The method as any one of Claims 1 to 9, wherein the molten slag is CaO-Fe0-SiO2 C resulting from copper smelting, the melting temperature of the collected molten slag is in a range between 950 C and 1250 , and the target elements-containing pellets comprise (w/w): FeO/Fe203 in a range between 7 and 15%; Na2O in a range between 10 and 25%; SiO2 in a range between 15 and 30%;
and Ca0 in a range between 1 and 4%.
and Ca0 in a range between 1 and 4%.
11. The method as any one of Claims 1 to 9, wherein the molten slag is CaO-Fe0-5i02 resulting from copper smelting, the melting temperature of the collected molten slag is in a range between 1000 C and 1150 C , and the target elements-containing pellets comprise (w/w): FeO/Fe203 in a range between 7 and 15%; Na2O in a range between 10 and 25%; 5i02 in a range between 15 and 30%; and Ca0 in a range between 1 and 4%.
12. The method as any one of Claims 1 to 11, wherein the target elements comprise at least one of As, Sb, Cd and Pb.
13. A method for the vitrification of target elements using molten slag after smelting of base metals from ores as vitrification agent, the ores comprising one of:
copper, gold, and lead, and the target elements, the smelting also resulting in flue dusts, comprising pelletizing a composition of the flue dust with one of: sodium, sodium/iron oxides and recycled glass into target elements-containing pellets having a melting temperature lower than a melting temperature of the molten slag, mixing the target elements-containing pellets with the molten slag; and cooling the mixture, thereby achieving vitrification of the target elements by the molten slag as a vitrification agent.
copper, gold, and lead, and the target elements, the smelting also resulting in flue dusts, comprising pelletizing a composition of the flue dust with one of: sodium, sodium/iron oxides and recycled glass into target elements-containing pellets having a melting temperature lower than a melting temperature of the molten slag, mixing the target elements-containing pellets with the molten slag; and cooling the mixture, thereby achieving vitrification of the target elements by the molten slag as a vitrification agent.
14. The method as in claim 13, comprising controlling the viscosity of the mixture.
15. The method as in any one of claims 13 and 14, comprising stirring the mixture.
16. The method as in any one of claims 13 to 15, comprising heating the mixture.
17. The method as in any one of claims 13 to 16, wherein the molten slag is fayalite collected after smelting of copper, the melting temperature of the molten slag is in a range between 9500C
and 12500C, and the target elements comprise arsenic.
and 12500C, and the target elements comprise arsenic.
18. The method as in any one of claims 13 to 17, wherein the molten slag is fayalite collected after smelting of copper, the melting temperature of the molten slag is in a range between 1000 C and 11500, and the target elements comprise arsenic.
19. The method as in any one of claims 13 to 18, wherein the target elements comprise at least one of As, Sb, Cd and Pb.
20. The method as in any one of claims 1 to 12, wherein the base metals comprise one of: copper, gold, and lead, and the flue dusts comprise arsenic.
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