US2797158A - Process for producing lead from lead sulfide containing materials - Google Patents
Process for producing lead from lead sulfide containing materials Download PDFInfo
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- US2797158A US2797158A US455353A US45535354A US2797158A US 2797158 A US2797158 A US 2797158A US 455353 A US455353 A US 455353A US 45535354 A US45535354 A US 45535354A US 2797158 A US2797158 A US 2797158A
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- 239000000463 material Substances 0.000 title claims description 40
- 238000000034 method Methods 0.000 title claims description 26
- 229910052981 lead sulfide Inorganic materials 0.000 title claims description 15
- 229940056932 lead sulfide Drugs 0.000 title claims description 15
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 28
- 229910052760 oxygen Inorganic materials 0.000 claims description 28
- 239000001301 oxygen Substances 0.000 claims description 28
- 238000006243 chemical reaction Methods 0.000 claims description 22
- 229910052717 sulfur Inorganic materials 0.000 claims description 18
- 238000005245 sintering Methods 0.000 claims description 17
- 239000011593 sulfur Substances 0.000 claims description 17
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 16
- 230000001590 oxidative effect Effects 0.000 claims description 12
- 238000010438 heat treatment Methods 0.000 claims description 11
- WABPQHHGFIMREM-UHFFFAOYSA-N lead(0) Chemical compound [Pb] WABPQHHGFIMREM-UHFFFAOYSA-N 0.000 claims description 10
- 239000000446 fuel Substances 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 230000000717 retained effect Effects 0.000 claims description 6
- 150000003464 sulfur compounds Chemical class 0.000 claims description 5
- XCAUINMIESBTBL-UHFFFAOYSA-N lead(ii) sulfide Chemical compound [Pb]=S XCAUINMIESBTBL-UHFFFAOYSA-N 0.000 claims description 3
- 239000000047 product Substances 0.000 description 33
- 239000012141 concentrate Substances 0.000 description 16
- 238000007792 addition Methods 0.000 description 12
- 239000002893 slag Substances 0.000 description 12
- 238000003723 Smelting Methods 0.000 description 11
- 239000010881 fly ash Substances 0.000 description 11
- 239000000203 mixture Substances 0.000 description 11
- 230000007812 deficiency Effects 0.000 description 6
- 239000000571 coke Substances 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 4
- 239000000428 dust Substances 0.000 description 4
- 238000001704 evaporation Methods 0.000 description 4
- 230000008020 evaporation Effects 0.000 description 4
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 235000011941 Tilia x europaea Nutrition 0.000 description 3
- 238000005188 flotation Methods 0.000 description 3
- 239000004571 lime Substances 0.000 description 3
- KEQXNNJHMWSZHK-UHFFFAOYSA-L 1,3,2,4$l^{2}-dioxathiaplumbetane 2,2-dioxide Chemical compound [Pb+2].[O-]S([O-])(=O)=O KEQXNNJHMWSZHK-UHFFFAOYSA-L 0.000 description 2
- 235000019738 Limestone Nutrition 0.000 description 2
- 229910052924 anglesite Inorganic materials 0.000 description 2
- 239000000292 calcium oxide Substances 0.000 description 2
- 235000012255 calcium oxide Nutrition 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- YADSGOSSYOOKMP-UHFFFAOYSA-N dioxolead Chemical compound O=[Pb]=O YADSGOSSYOOKMP-UHFFFAOYSA-N 0.000 description 2
- 239000013067 intermediate product Substances 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 239000006028 limestone Substances 0.000 description 2
- 206010021143 Hypoxia Diseases 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 241001062472 Stokellia anisodon Species 0.000 description 1
- 239000002956 ash Substances 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 235000011116 calcium hydroxide Nutrition 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 230000001427 coherent effect Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 229910000464 lead oxide Inorganic materials 0.000 description 1
- PIJPYDMVFNTHIP-UHFFFAOYSA-L lead sulfate Chemical compound [PbH4+2].[O-]S([O-])(=O)=O PIJPYDMVFNTHIP-UHFFFAOYSA-L 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000005272 metallurgy Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- -1 such as Substances 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B13/00—Obtaining lead
-
- 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
- C22B13/00—Obtaining lead
- C22B13/02—Obtaining lead by dry processes
Definitions
- the present invention relates to an improved process for producing lead from materials containing lead sulfide such as ores, concentrates, intermediate products or waste products containing lead sulfide, and is particularly adapted to the production of lead from such materials having a high content of lead sulfide, for example, from concentrates containing 65 to 85% of lead.
- Modern flotation processes yield lead ore concentrates which hardly contain any gangue and in which the lead content has been concentrated to 65 to 85%.
- concentrates are obtained containing 80% lead, 14% sulfur and 6% gangue.
- the smelting of such concentrates in the generally used shaft furnace processes requires a preliminary sintering with the addition of the supplements required for the shaft furnace.
- the lead concentrate is then reduced by the addition of coke and the agglomerate is reduced to raw lead and slag.
- the reduction in the shaft furnace only pro eeeds without disturbances if the lead content of the charge is at most 50%, as, with higher lead contents, the charge bakes together and becomes impermeable to gas before it has completely reacted.
- the object of the present invention is a process for the efiicient recovery of lead from materials rich in lead without the necessity of using coke and without having to add any substantial quantities of foreign materials, particularly reducing material such as coke, and in which the lead is produced at only one point and in which the product of dust is minimized.
- lead could be obtained from fine grained sulfidic lead ores or concentrates by granulating such ores or concentrates, if desired, with the addition ofoxidic lead ore, and partially roasting and sintering to produce a mixture of lead sulfide and oxide and possibly lead sulfate which contains a sufiicient quantity of chemically bound oxygen that it can be converted to lead and sulfur dioxide in a suitable furnace without further'addition of oxygen by the so-called roasting-reaction process.
- the sintering roasting can be effected in a known manner on a moving'sintering grate.
- a small quantity of finely divided lime in the form of limestone, hydrated or unslaked lime can be admixed with the charge to be sintered.
- the sulfide-sulfur content of the charge to be sintered is adjusted in order to beable to operate with the optimum sintering temperature. With most high percentage lead ores or concentrates a 5-9, preferably about 7%, is suitable.
- the sintering is effected with oxygen containing gases, such as, air or air in admixture with recycled gas, care being taken that suflicient free oxygen is present therein to produce a sinter in which the molar ratio of bound oxygen to
- oxygen containing gases such as, air or air in admixture with recycled gas
- suflicient free oxygen is present therein to produce a sinter in which the molar ratio of bound oxygen to
- the ore, and especially the composition of its gangue, requies it can, in exceptional cases, beneeessary to add small quantities of additional materials such as sand, soda, limestone or iron containing materials (pyrites, roasted pyrites, iron ores) in order to assure the production of a good and sufficiently liquid slag.
- additional materials such as sand, soda, limestone or iron containing materials (pyrites, roasted pyrites, iron ores) in order to assure the production of a good and sufficiently liquid slag.
- additional materials such as sand, soda, limestone or iron containing materials (pyrites, roasted pyrites, iron ores) in order to assure the production of a good and sufficiently liquid slag.
- additional materials such as sand, soda, limestone or iron containing materials (pyrites, roasted pyrites, iron ores)
- the rapid heating to the high temperatuers is exceptionally advantageously carried out in a rotary drum flame furnace rotating about a horizontal axis, especially one whose length is no greater than about twice its diameter, and preferably one whose length is about equal to that of its diameter.
- a rotary drum flame furnace rotating about a horizontal axis, especially one whose length is no greater than about twice its diameter, and preferably one whose length is about equal to that of its diameter.
- sintered products containing an excess of oxygen and sintered products containing a deficiency in oxygen are alternately produced and by mixing such sintered products the optimum 0:8 ratio is produced before the charge is introduced into the rotary flame furnace.
- the oxygen content in the sintered product can be varied by adjusting the velocity of the grate, the quantity of recycled material admixed with the charge, the thickness of the charge as well as the pressure differential above and below the charge. It is furthermore also possible to smelt with an oxidizing flame. and compensate for the oxidizing degree of the flame by a corresponding oxygen deficiency in the solid sinter charged into the smelting furnace.
- the optimum 0:8 ratio in the charge when employing an oxidizing flame during the smelting is 1.90 to 1.95 mol 0:1 mol S.
- the simplest procedure is to adjust the 0:8 ratio, only approximately, by mixing the different sintered products and to adjust such ratio to the desired value during the smelting operation with reference to the oxidizing degree of the flame employed by small appropriate additions of sinter with excess or deficiency in oxygen content or, if desired, with dead roasted or unroasted sulfidic material.
- This mode of operation is advantageous in that it is simpler to adjust the composition of the charge with reference to the oxidizing degree of the flame employed by suitable additions of solid materials to the charge than to adjust the oxidizing .degree of the flame to conform to that required for the charge.
- the procedure according to the invention furthermore renders it practical to employ an oxidizing flame for the smelting operation so that the highest temperature attainable with the fuel employed can be attained so that rapid heating of the charge with correspondingly lower evaporation losses is promoted.
- Inthetreatment of some ores asmall quantity of a slag like lead containing residue can, remain. after completition of the smelting reaction.
- the residue preferably.
- Example 16.6 parts by weight of a sulfidic lead ore of the composition I Percent Pb 80.2 S 14.36 Zn 3.2 CaO 0.5
- the fly ash mixture contained 71.3% Pb and 8.0% S. This mixture was admixed with 20 parts. by weight of recycled sintered material of a grain size of 4l2 mm. with the addition of 6-7% of H20 based upon the whole admixture.
- the recycled sintered material contained 81.0% Pb of which 40.6% was metallic Pb, 16.4% was in the form of PbS (18.9% PbS), 13.6% was in the form of PbO (14.7% PbO) and 10.4% was in the form of PbSO4 (15.2% PbSOt).
- the resulting admixture was sintered in the following manner on a sintering apparatus:
- a grate covering of finished sintered product from a previous charge of the same composition of the recycled sintered material in the charge about 20 mm. thick was first applied to the moving grate of the sintering apparatus.
- the grain size of such grate covering was 12-20 mm.
- An ignition layer 30 mm. thick of the some composition as the charge to be sintered except that the fly ash was omitted was applied over the grate covering.
- This ignition layer was ignited under the ignition hood of the sintering apparatus while air was drawn downwardly therethrough. Thereafter a mm. layer of the admixture to be sintered was applied over the ignited ignition layer and the entire charge on the grate was sintered while air was passed upwardly through the charge.
- the finished sintered product was of the same composition as that indicated above for the recycled sintered material admixed with the charge to be sintered.
- the weight ratio of oxygen bound to lead to sulfur bound to lead in the sintered product was 1.05:1 which corresponds to a molar ratio of 2.1:1.
- a process for the production of metallic lead from materials containing lead sulfide with a content of at least 50% Pb which comprises sintering said lead sulfide containing material without addition of fuel in admixture with at least one material selected from the group consisting of fly ash and recycled sintered material under oxidizing roasting conditions to provide about a sufficient quantity of oxygen bound to lead in the sintered product to react upon heating with the sulfur bound to lead retained in the sintered product, and heating a charge of the sintered product without addition of fuel to reaction temperatures to produce metallic lead and volatile sulfur compounds.
- a process in accordance with claim 1 comprising in addition adding small quantities of a material selected from the group consisting of lead bound oxygen and lead bound sulfur containing material while the sintered product is heated to reaction temperatures to adjust the lead bound oxygen to lead bound sulfur in the charge.
- a process in accordance with claim 1 comprising in addition admixing a small quantity of lime with the admixture to be sintered.
- a process for the production of metallic lead from materials containing lead sulfide with a content of at least Pb which comprises sintering said lead sulfide containing material without addition of fuel in admixture with at least one material selected from the group consisting of fly ash and recycled sintered material under oxidizing roasting conditions to provide about a sufiicient quantity of oxygen bound to lead in the sintered product to react upon heating with the sulfur bound to lead retained in the sintered product, and rapidly heating a charge of the sintered product Without addition of fuel to reaction temperatures over 1100" C. to produce metallic lead and volatile sulfur compounds.
- reaction temperatures are between 1200 C. and 1250 C 10.
- heating to reaction temperatures is effected in rotary flame furnaces rotating about a horizontal axis.
- a process in accordance with claim 8 comprising in addition separating the lead produced from any slag produced and heating such slag in admixture with further quantities of said sintered product to reaction temperatures to produce lead and volatile sulfur compounds.
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- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Manufacture And Refinement Of Metals (AREA)
Description
United States Patent PROCESS FOR PRODUCING LEAD FROM LEAD SULFIDE CONTAINING MATERIALS vor der Hohe, Werner Carl-August Maelzer,
No Drawing. Application September 10, 1954, Serial No. 455,353
Claims priority, application Germany September It), 1953 13 Claims. (Cl. 75--77) The present invention relates to an improved process for producing lead from materials containing lead sulfide such as ores, concentrates, intermediate products or waste products containing lead sulfide, and is particularly adapted to the production of lead from such materials having a high content of lead sulfide, for example, from concentrates containing 65 to 85% of lead.
Modern flotation processes yield lead ore concentrates which hardly contain any gangue and in which the lead content has been concentrated to 65 to 85%. For example, concentrates are obtained containing 80% lead, 14% sulfur and 6% gangue. The smelting of such concentrates in the generally used shaft furnace processes requires a preliminary sintering with the addition of the supplements required for the shaft furnace. In the shaft furnace the lead concentrate is then reduced by the addition of coke and the agglomerate is reduced to raw lead and slag. The reduction in the shaft furnace only pro eeeds without disturbances if the lead content of the charge is at most 50%, as, with higher lead contents, the charge bakes together and becomes impermeable to gas before it has completely reacted. It is consequently customary to admix slag, lime and/ or silica with the concentrate either before or after the roasting before the charge is introduced into the shaft furnace in order that it be diluted to a lead content of 50%. It is just such diluents which are separated in the flotation or in the shaft furnace, so that the advantages obtained by the concentration during flotation, except for savings in transportation, are substantially reduced as the throughput through the shaft furnace is lowered proportionately to the dilution and the heat required per ton of lead produced is correspondingly increased.
One process for smelting of concentrates Without dilution has been proposed, namely, the roasting-reaction process on Newman hearths or Schlippenbach plants. With such a process, about 60% of'the lead contained in the ore is converted to raw lead on a hearth furnace. The gray slag obtained in the hearth furnace is sintered and then smelted-in a shaft furnace with the addition of coke with a conversion of a further 30% of the lead content of the ore into raw lead. A considerable quantity of dust occurs both in the hearth furnace as well as in the shaft furnace. Such dust approximately contains about of the lead originally contained in the ore and must be recovered by electrostatic gas cleaning apparatus. The high incidence of intermediate products rich in lead renders it necessary to split up the manufacturing process into several streams which entails an increase in labor costs. Also, as the flow of material is divided into several streams, the apparatuses do not operate uniformly and it is difiicult to avoid danger to the operators from the large quantities of lead containing dust which occurs. Furthermore, the process entails the use of coke for the smelting of the gray lead containing slag in the shaft furnace.
bound sulfur is about 2:1.
, 2,797,158 Patented June 25 1957 The object of the present invention is a process for the efiicient recovery of lead from materials rich in lead without the necessity of using coke and without having to add any substantial quantities of foreign materials, particularly reducing material such as coke, and in which the lead is produced at only one point and in which the product of dust is minimized.
In accordance with the invention it has been found that lead could be obtained from fine grained sulfidic lead ores or concentrates by granulating such ores or concentrates, if desired, with the addition ofoxidic lead ore, and partially roasting and sintering to produce a mixture of lead sulfide and oxide and possibly lead sulfate which contains a sufiicient quantity of chemically bound oxygen that it can be converted to lead and sulfur dioxide in a suitable furnace without further'addition of oxygen by the so-called roasting-reaction process.
In the roasting-reaction process, the chemically bound oxygen introduced into the charge during roasting reacts with the chemically bound sulfur retained in the charge to produce metallic lead and sulfur dioxide. The primary reactions involved are represented by the following equations:
In accordance with the present invention it was found that the roasting of the fine grained ore or concentrate to produce a satisfactorily coherent and gas permeable sinter with the desired ratio of chemically bound oxygen to chemically bound sulfur is possible without the necessity of previous granulation of the charge if recycled internal material and/or fly ash is admixed with the fine I grained charge to be sintered. The best results are obtained when the ratio of recycled material and/or fly ash to ore or concentrate is more than 1:1 and preferably 1.5 to 2:1. The term fly ash, as employed herein, is intended to mean such fly :ash as occurs in the metallurgy of lead.
The sintering roasting can be effected in a known manner on a moving'sintering grate. If desired, a small quantity of finely divided lime in the form of limestone, hydrated or unslaked lime can be admixed with the charge to be sintered. The sulfide-sulfur content of the charge to be sintered is adjusted in order to beable to operate with the optimum sintering temperature. With most high percentage lead ores or concentrates a 5-9, preferably about 7%, is suitable. The sintering is effected with oxygen containing gases, such as, air or air in admixture with recycled gas, care being taken that suflicient free oxygen is present therein to produce a sinter in which the molar ratio of bound oxygen to After the sintered product is discharged from the sintering apparatus, the sinter is crushed and sieved. The quantity of sintered product in the desired grain size required for the sinter roasting isrecycled and admixed with the subsequent ore or concentrate to be roasted :and sintered. The remaining sintered product is then charged into a furnace and rapidly heated to reaction temperature to produce metallic lead I tered product to reaction temperatures is etfected in as short a time as possible.
The increase in speed of reaction attained by such high temperatures reduces evaporation losses to a minimum. At the temperatures nor-' mally, employed for such internal reaction for the production of lead, which are under about 1000 C. and usu- 3 ally lie between 800 and 1000" C., considerably greater evaporation. losses occur.
If the nature of the ore, and especially the composition of its gangue, requies it, it can, in exceptional cases, beneeessary to add small quantities of additional materials such as sand, soda, limestone or iron containing materials (pyrites, roasted pyrites, iron ores) in order to assure the production of a good and sufficiently liquid slag. As the gangue content of a good lead ore concentrate does not exceed about 58%, the quantity of additional materials which may be required, if at all, is very small and usually only 2-5% of the quantity of the concentrate.
It has been found that the rapid heating to the high temperatuers is exceptionally advantageously carried out in a rotary drum flame furnace rotating about a horizontal axis, especially one whose length is no greater than about twice its diameter, and preferably one whose length is about equal to that of its diameter. As the flame path reverses in the furnace, the heat introduced thereby into the furnace is rapidly and directly transferred to the furnace charge during rotation of the furnace and substantially lower evaporation losses occur than when the usual flameand rotary furnaces are employed.
It was also found according to the invention that it is expedient not to carry out the preliminary roasting and sintering so that the exact ratio of lead bound sulfur and lead bound oxygen required for the subsequent inner conversion is achieved thereby, as the exact control of such ratio is difficult to achieve upon a commercial scale operation. The roasting and sintering is, however, carried out so that the molar ratio of lead bound oxygen to lead bound sulfur in the resulting sinter is approximately 2:1 but that such sinter contains either an excess or deficiency in oxygen. By making slight changes in the roasting and sintering conditions, sintered products containing an excess of oxygen and sintered products containing a deficiency in oxygen are alternately produced and by mixing such sintered products the optimum 0:8 ratio is produced before the charge is introduced into the rotary flame furnace. The oxygen content in the sintered product can be varied by adjusting the velocity of the grate, the quantity of recycled material admixed with the charge, the thickness of the charge as well as the pressure differential above and below the charge. It is furthermore also possible to smelt with an oxidizing flame. and compensate for the oxidizing degree of the flame by a corresponding oxygen deficiency in the solid sinter charged into the smelting furnace. In practice it was found that the optimum 0:8 ratio in the charge when employing an oxidizing flame during the smelting is 1.90 to 1.95 mol 0:1 mol S. The simplest procedure is to adjust the 0:8 ratio, only approximately, by mixing the different sintered products and to adjust such ratio to the desired value during the smelting operation with reference to the oxidizing degree of the flame employed by small appropriate additions of sinter with excess or deficiency in oxygen content or, if desired, with dead roasted or unroasted sulfidic material. This mode of operation is advantageous in that it is simpler to adjust the composition of the charge with reference to the oxidizing degree of the flame employed by suitable additions of solid materials to the charge than to adjust the oxidizing .degree of the flame to conform to that required for the charge. The procedure according to the invention furthermore renders it practical to employ an oxidizing flame for the smelting operation so that the highest temperature attainable with the fuel employed can be attained so that rapid heating of the charge with correspondingly lower evaporation losses is promoted. V
Inthetreatment of some ores asmall quantity of a slag like lead containing residue can, remain. after completition of the smelting reaction. The residue preferably.
is retained in the smelting furnace and retreated with the next charge. After several charges the. lead content 4v thereof is decreased to such an extent that it can be discarded.
The following example will serve to illustrate the process according to the invention:
Example 16.6 parts by weight of a sulfidic lead ore of the composition I Percent Pb 80.2 S 14.36 Zn 3.2 CaO 0.5
was mixed with 3.4 parts by weight of an oxidic ore of the following composition and 2.0 parts by weight of a mixture of fly ashes of varying origin primarily fromthe sintering apparatus and the rotary flame smelting furnace. The fly ash mixture contained 71.3% Pb and 8.0% S. This mixture was admixed with 20 parts. by weight of recycled sintered material of a grain size of 4l2 mm. with the addition of 6-7% of H20 based upon the whole admixture. The recycled sintered material contained 81.0% Pb of which 40.6% was metallic Pb, 16.4% was in the form of PbS (18.9% PbS), 13.6% was in the form of PbO (14.7% PbO) and 10.4% was in the form of PbSO4 (15.2% PbSOt).
The resulting admixture was sintered in the following manner on a sintering apparatus:
A grate covering of finished sintered product from a previous charge of the same composition of the recycled sintered material in the charge about 20 mm. thick was first applied to the moving grate of the sintering apparatus. The grain size of such grate covering was 12-20 mm. An ignition layer 30 mm. thick of the some composition as the charge to be sintered except that the fly ash was omitted was applied over the grate covering. This ignition layer was ignited under the ignition hood of the sintering apparatus while air was drawn downwardly therethrough. Thereafter a mm. layer of the admixture to be sintered was applied over the ignited ignition layer and the entire charge on the grate was sintered while air was passed upwardly through the charge.
The finished sintered product was of the same composition as that indicated above for the recycled sintered material admixed with the charge to be sintered. The weight ratio of oxygen bound to lead to sulfur bound to lead in the sintered product was 1.05:1 which corresponds to a molar ratio of 2.1:1.
One part of this sintered product was admixed with 1.2 parts of a sintered product produced in a similar manner having a deficiency in lead bound oxygen containing 80.5% Pb of which 37.4% was in the form of metallic lead, 9.3% was in the form of PbSO4 (13.6% PbSOr), 19.9% was in the form of P138 (23.0% PbS) and 16.6% Was in the form of PbO (17.9% PbO). The molar ratio of lead bound oxygen to lead bound sulfur therein therefore was 1.81:1. The resulting mixed sintered product therefore had a molar ratio of lead bound oxygen to lead bound sulfur of 1.93:1. The slight deficiency in oxygen in the mixed sintered product was found in practice to be the optimum for counteracting the oxidizing action of theflame in the rotary smelting furnace.
kilograms of this mixed sintered product were introducedinto a rotary flame furnace having an internal diameter of 0.7 meter-and'an internal length of 0.7 meter which had been preheated to 1200 C. The period re,-
quired for the charging of the furnace was minutes. The temperature of the furnace which had been reduced by the introduction of the cold charge and the ensuing reaction was again raised to the original 1200 C. in 140 minutes and then maintained at such temperature for a further 10 minutes. The furnace was then tapped. 110 kg. of raw lead, 4.5 kg. of fly ash containing 70.5% Pb and 29.0 kg. of slag containing 28.8% Pb were produced. The yield obtained upon the basis of the 150 kg. charge is not entirely correct as it is impossible to prevent slag from a previous charge to be admixed with the slag of the new charge or to prevent a certain quantity of the slag from being retained in the furnace.
We claim:
1. A process for the production of metallic lead from materials containing lead sulfide with a content of at least 50% Pb which comprises sintering said lead sulfide containing material without addition of fuel in admixture with at least one material selected from the group consisting of fly ash and recycled sintered material under oxidizing roasting conditions to provide about a sufficient quantity of oxygen bound to lead in the sintered product to react upon heating with the sulfur bound to lead retained in the sintered product, and heating a charge of the sintered product without addition of fuel to reaction temperatures to produce metallic lead and volatile sulfur compounds.
2. A process in accordance with claim 1 in which the admixture of the lead sulfide containing material is alternately sintered under conditions producing an excess of lead bound oxygen in the sintered product and under conditions producing a deficiency of lead bound oxygen in the sintered product, and mixing the sintered products obtained to produce a sintered product containing an optimum lead bound oxygen to lead bound sulfur before such sintered product is heated to reaction temperatures to produce the metallic lead and volatile sulfur compounds.
3. A process in accordance with claim 1 in which the molar ratio of lead bound oxygen to lead bound sulfur is 1.90 to 1.95 :1 in the sintered product heated to reaction temperatures and the heating to reaction temperatures is efiected With an oxidizing flame.
4. A process in accordance with claim 1 comprising in addition adding small quantities of a material selected from the group consisting of lead bound oxygen and lead bound sulfur containing material while the sintered product is heated to reaction temperatures to adjust the lead bound oxygen to lead bound sulfur in the charge.
5. A process in accordance with claim 1 in which the ratio of the material selected from the group consisting of recycled sintered material and fly ash to the lead sulfide containing material is greater than 1:1.
6. A process in accordance with claim 1 in which the ratio of the material selected from the group consisting of recycled sintered material and fly ash to the lead sulfide containing material is 1.5 to 2:1.
7. A process in accordance with claim 1 comprising in addition admixing a small quantity of lime with the admixture to be sintered.
8. A process for the production of metallic lead from materials containing lead sulfide with a content of at least Pb which comprises sintering said lead sulfide containing material without addition of fuel in admixture with at least one material selected from the group consisting of fly ash and recycled sintered material under oxidizing roasting conditions to provide about a sufiicient quantity of oxygen bound to lead in the sintered product to react upon heating with the sulfur bound to lead retained in the sintered product, and rapidly heating a charge of the sintered product Without addition of fuel to reaction temperatures over 1100" C. to produce metallic lead and volatile sulfur compounds.
9. A process in accordance with claim 8 in which said reaction temperatures are between 1200 C. and 1250 C 10. A process in accordance with claim 8 in which said heating to reaction temperatures is effected in rotary flame furnaces rotating about a horizontal axis.
11. A process in accordance with claim 10 in which the ratio of the diameter to the length of said flame furnace is at most 1:2.
12. A process in accordance with claim 10 in which the ratio of the diameter to the length of said flame furnace is about 1:1.
13. A process in accordance with claim 8 comprising in addition separating the lead produced from any slag produced and heating such slag in admixture with further quantities of said sintered product to reaction temperatures to produce lead and volatile sulfur compounds.
References Cited in the file of this patent UNITED STATES PATENTS 2,416,628 Kalling Feb. 25, 1947 2,660,525 Foster Nov. 24, 1953 FOREIGN PATENTS 482,224 Great Britain Mar. 25, 1938
Claims (1)
1.A PROCESS FOR THE PRODUCTION OF METALLIC LEAD FROM MATERIALS CONTAINING LEAD SULFIDE WITH A CONTENT OF AT LEAST 50% PB WHICH COMPRISES SINTERING SAID LEAD SULFIDE CONTAINING MATERIAL WITHOUT ADDITION OF FUEL IN ADMIXTURE WITH AT LEAST ONE MATERIAL SELECTED FROM THE GROUP CONSISTING OF FLY ASH AND RECYCLED SINTERED MATERIAL UNDER OXIDIZING ROASTING CONDITIONS TO PROVIDE ABOUT A SUFFICIENT QUANTITY OF OXYGEN BOUND TO LEAD IN THE SINTERED PRODUCT TO REACT UPON HEATING WITH THE SULFUR BOUND TO LEAD RETAINED IN THE SINTERED PRODUCT, AND HEATING A CHARGE OF THE SINTERED PRODUCT WITHOUT ADDITION OF FUEL TO REACTION TEMPERATURES TO PRODUCE METALLIC LEAD AND VOLATILE SULFUR COMPOUNDS.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2797158X | 1953-09-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2797158A true US2797158A (en) | 1957-06-25 |
Family
ID=7998574
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US455353A Expired - Lifetime US2797158A (en) | 1953-09-10 | 1954-09-10 | Process for producing lead from lead sulfide containing materials |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2797158A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2926081A (en) * | 1956-05-15 | 1960-02-23 | Dravo Corp | Process of smelting zinc containing lead ores |
| US3149964A (en) * | 1960-12-10 | 1964-09-22 | Metallgesellschaft Ag | Removal of zinc from lead-containing flue dust |
| US3300301A (en) * | 1962-12-14 | 1967-01-24 | Outokumpu Osakeyhtio | Process for the production of metallic lead from materials containing lead oxide |
| US3395010A (en) * | 1967-07-20 | 1968-07-30 | Shoeld Mark | Reclamation of lead-acid storage batteries |
| US4231791A (en) * | 1978-07-04 | 1980-11-04 | Metallurgical Processes Ltd. | Roasting of sulphide materials |
| EP0045531A1 (en) * | 1980-08-06 | 1982-02-10 | Metallgesellschaft Ag | Process for the continuous direct smelting of metallic lead from sulfidic lead concentrates |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB482224A (en) * | 1936-05-16 | 1938-03-25 | Metallgesellschaft Ag | Process for the working up of lead ores |
| US2416628A (en) * | 1941-03-11 | 1947-02-25 | Bolidens Gruv Ab | Method of extracting lead from lead sulphide ores and concentrates |
| US2660525A (en) * | 1952-01-22 | 1953-11-24 | Charles B Foster | Method of extracting lead from its sulfides |
-
1954
- 1954-09-10 US US455353A patent/US2797158A/en not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB482224A (en) * | 1936-05-16 | 1938-03-25 | Metallgesellschaft Ag | Process for the working up of lead ores |
| US2416628A (en) * | 1941-03-11 | 1947-02-25 | Bolidens Gruv Ab | Method of extracting lead from lead sulphide ores and concentrates |
| US2660525A (en) * | 1952-01-22 | 1953-11-24 | Charles B Foster | Method of extracting lead from its sulfides |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2926081A (en) * | 1956-05-15 | 1960-02-23 | Dravo Corp | Process of smelting zinc containing lead ores |
| US3149964A (en) * | 1960-12-10 | 1964-09-22 | Metallgesellschaft Ag | Removal of zinc from lead-containing flue dust |
| US3300301A (en) * | 1962-12-14 | 1967-01-24 | Outokumpu Osakeyhtio | Process for the production of metallic lead from materials containing lead oxide |
| US3395010A (en) * | 1967-07-20 | 1968-07-30 | Shoeld Mark | Reclamation of lead-acid storage batteries |
| US4231791A (en) * | 1978-07-04 | 1980-11-04 | Metallurgical Processes Ltd. | Roasting of sulphide materials |
| EP0045531A1 (en) * | 1980-08-06 | 1982-02-10 | Metallgesellschaft Ag | Process for the continuous direct smelting of metallic lead from sulfidic lead concentrates |
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