US2064479A - Sintering zinc concentrates - Google Patents
Sintering zinc concentrates Download PDFInfo
- Publication number
- US2064479A US2064479A US49508A US4950835A US2064479A US 2064479 A US2064479 A US 2064479A US 49508 A US49508 A US 49508A US 4950835 A US4950835 A US 4950835A US 2064479 A US2064479 A US 2064479A
- Authority
- US
- United States
- Prior art keywords
- cadmium
- sintering
- coke
- elimination
- zinc
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
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
- C22B1/00—Preliminary treatment of ores or scrap
- C22B1/14—Agglomerating; Briquetting; Binding; Granulating
- C22B1/16—Sintering; Agglomerating
- C22B1/20—Sintering; Agglomerating in sintering machines with movable grates
-
- 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
- C22B19/00—Obtaining zinc or zinc oxide
- C22B19/02—Preliminary treatment of ores; Preliminary refining of zinc oxide
Definitions
- This invention relates to the sintering of zinc ores containing cadmium and particularly concerns certain improvements by'which a markedly increased elimination of cadmium is readily 5 obtained ⁇ t
- the present invention relies on none of these proposals but employs an entirely difierent concept resulting in a marked increase in elimination of cadmium during the sintering operation at practically no increase of cost. It is based upon 4 the discovery that the character of the carbonaceous fuel which is mixed with the preroasted concentrates to form the sinter charge exerts a most critical influence on the percentage of cadmium elimination during the sintering operation.
- the zinc a5 concentrates which may analyze, say, approximately 55% zinc, 0.5% cadmium and 30% sulphur, are treated in a Ropp or Skinner roaster to reduce the sulphur content to between 5% and 7.5%.
- the preroasted concentrates are then mixed with 4-5.5% coke and 18-25% returned sinter fines 5 and charged to the bed of a sintering machine of the Dwight-Lloyd type.. It is not-unusual to include in the charge up to 4 or 5% of dust from the masters which is relatively high in cadmium.
- the charge that is the preroasted concentrates, 10 coke and returned fines with or without the dust, is sintered in the usual manner which results in decreasing the sulphur content in the sintered product to well below 1%, say 0.4-0.7%.
- 40-45% of the cadmium is elim- 15 inated and appropriately collected, the remainder being retained in the zinc sinter.
- bituminous coal used in various ways.
- bituminous coal of average or intermediate volatile content is to be preferred in sintering most zinc ores.
- these figures are not to be regarded in a limiting sense as many other factors are'to be considered in the operation.
- the fineness of the bituminous coal ten. 5 mesh has given excellent results
- theincreased temperature of the gases not only as same affects cadmium elimination but filtration of same for cadmium recovery as well
- the percentage of returned sinter fines in the charge and other fac- 5 tors all influence the operation and the amount of coke replaced by bituminous coal.
Description
Patented Dec. 15, 1956 UNITED STATES x PATENT OFFICE A g 2,064,479 g SINTERING ZINC CONCENTRATES v Stuart-H. Levisom Forest Hills, N. Y and Emil J. Bruderlin} Amarillo, Tex., assignors to American Smelting' and Refining Company, New York, N. Y., a corporation of New Jersey No Drawing. Application November 13, 1935,
( l Serial No. 49,508
4 Claims. (Cl. 75-5 This invention relates to the sintering of zinc ores containing cadmium and particularly concerns certain improvements by'which a markedly increased elimination of cadmium is readily 5 obtained} t In treating zinc ores, it is common practice to subject the concentrates to a preliminary roast to eliminate a major portion of the sulphur content after which the partially roasted concentrates are mixed with a suitable amount of coke and sintered, the sintered product then being charged to a reduction retort for the production and recovery of zinc metal.
In the case of zinc concentrates containing cadmium, the elimination of the cadmium prior to making up the charge .for the reduction retorts is of considerable importance as otherwise the cadmium will appear as a contaminant in the recovered zinc met'al. At best the separation of cadmium from zinc metal is an expensive operation and for this reason together with the fact that the cadmium itself is a metal of considerable value, a great many proposals have been made in the past to improve the cadmium elimination during the preroasting and sintering operations for the dual purpose of preventing contamination of the zinc metal and promoting economical recovery of the cadmium itself. Among these proposals may be mentioned the chloridiz- .ing roast, the provision of a greater proportion of fuel in the lower portion of the sintering bed and the mechanical separation of the lower portion of the sinter bed in which the cadmium elimination tends to decrease.
The present invention relies on none of these proposals but employs an entirely difierent concept resulting in a marked increase in elimination of cadmium during the sintering operation at practically no increase of cost. It is based upon 4 the discovery that the character of the carbonaceous fuel which is mixed with the preroasted concentrates to form the sinter charge exerts a most critical influence on the percentage of cadmium elimination during the sintering operation.
45 Thus, while the art has long since employed coke as the carbonaceous constituent of the sinter charge, it has 'also assumed that other carbonaceous fuels, such as coal, are equivalents. That this assumption was, for the most part, an erro- 50 neous one will be readily perceived as the present description proceeds.
What may be termedstandard practice in some of the largest zinc sintering plants on this con tinent may be briefly outlined as follows: the zinc a5 concentrates which may analyze, say, approximately 55% zinc, 0.5% cadmium and 30% sulphur, are treated in a Ropp or Skinner roaster to reduce the sulphur content to between 5% and 7.5%. The preroasted concentrates are then mixed with 4-5.5% coke and 18-25% returned sinter fines 5 and charged to the bed of a sintering machine of the Dwight-Lloyd type.. It is not-unusual to include in the charge up to 4 or 5% of dust from the masters which is relatively high in cadmium. The charge, that is the preroasted concentrates, 10 coke and returned fines with or without the dust, is sintered in the usual manner which results in decreasing the sulphur content in the sintered product to well below 1%, say 0.4-0.7%. At the same time only 40-45% of the cadmium is elim- 15 inated and appropriately collected, the remainder being retained in the zinc sinter.
It has now been found and actually demonstrated on a commercial scale that cadmium elimination can be increased 50% or more by re- 20 placing not less than one-third of the coke normally used in the charge with bituminous coal. While the reason for this phenomenal increase in cadmium elimination through the use of a substantial proportion of bituminous coal is not altogether clear; it is believed that the presence of the volatile hydrocarbons derived therefrom is a factor of major importance in obtaining the marked increase in cadmium elimination.
In comparative tests which were identical ex- 30 cept for the replacement of a portion of the coke with bituminous coal, it was found that no appreciable increase in cadmium elimination was ob tained until approximately 30%-35% of the coke. was so replaced. For example, using a fuel mixture of only 25% coal and the balance coke, cadv mium elimination was only 43.6% as against 42.9% using all coke. Varied and repeated commercial runs in which from 50-90% of the coke was replaced by bituminous coal gave cadmium eliminations ranging between 55% and 88%.
Obviously, variations in the type of bituminous coal used will, of course, influence the amount used. Present indications are that 50-75% bituminous coal of average or intermediate volatile content is to be preferred in sintering most zinc ores. However, these figures are not to be regarded in a limiting sense as many other factors are'to be considered in the operation. For example, the fineness of the bituminous coal (ten. 5 mesh has given excellent results), theincreased temperature of the gases not only as same affects cadmium elimination but filtration of same for cadmium recovery as well, the percentage of returned sinter fines in the charge, and other fac- 5 tors all influence the operation and the amount of coke replaced by bituminous coal.
The marked increase in cadmium elimination which characterizes the present invention is appropriately exemplified by the following results secured in commercial runs. In the first, 1000 tons of preroasted concentrates containing 0.46% cadmium were sintered as hereinbefore described with of the coke being replaced with bituminous coal which resulted in a cadmium elimination of 65% In another run using a fuel mixture of bituminous coal and 40% coke, the cadmium elimination was 71.5%.
While certain novel features of the invention have been disclosed and are pointed out in the annexed claims, it will be understood that various omissions, substitutions and changes may be made by those skilled in the art without departing from the spirit of the invention.
What is claimed is: i
1. Intreating preroasted zinc concentrates containing cadmium by sintering the same with coke, the improvement which comprises replacing not less than one-third of the coke content of the charge with bituminous coal and sintering said charge on a machine of the Dwight-Lloyd type thereby materially increasing the percentage of cadmium elimination.
2. The process for treating zinc concentrates containing cadmium which comprises roasting said concentrates to reduce the sulphur content to approximately 5-7.5%, forming same into a si-nter charge with approximately 18-25% returned fines and approximately 4-5.5% carbonaceous fuel of which not less than one-third thereof consists of bituminous coal with the balance coke and sintering said charge on a machine of the Dwight- Lloyd type.
3. The method of increasing cadmium elimination in the sintering of preroasted zinc concentrates which consists in replacing a part and not less than one-third of the coke used in the charge with bituminous coal and sintering said charge.
4. In sintering preroasted zinc concentrates containing cadmium employing coke as a carbonaoeous fuel constituent, the improvement which comprises incorporating bituminous coal as the major portion of the carbonaceous fuel in said charge thereby markedly increasing cadmium elimination during the sintering operation.
STUART H. LEVISON. EMIL J. BRUDERLIN.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US49508A US2064479A (en) | 1935-11-13 | 1935-11-13 | Sintering zinc concentrates |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US49508A US2064479A (en) | 1935-11-13 | 1935-11-13 | Sintering zinc concentrates |
Publications (1)
Publication Number | Publication Date |
---|---|
US2064479A true US2064479A (en) | 1936-12-15 |
Family
ID=21960194
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US49508A Expired - Lifetime US2064479A (en) | 1935-11-13 | 1935-11-13 | Sintering zinc concentrates |
Country Status (1)
Country | Link |
---|---|
US (1) | US2064479A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2612441A (en) * | 1948-11-10 | 1952-09-30 | Residue Company | Method of refining zinc ore |
US2756136A (en) * | 1952-06-14 | 1956-07-24 | Augustin L J Queneau | Method of chloridizing sintering of zinciferous materials with elimination of lead and similar contaminants |
-
1935
- 1935-11-13 US US49508A patent/US2064479A/en not_active Expired - Lifetime
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2612441A (en) * | 1948-11-10 | 1952-09-30 | Residue Company | Method of refining zinc ore |
US2756136A (en) * | 1952-06-14 | 1956-07-24 | Augustin L J Queneau | Method of chloridizing sintering of zinciferous materials with elimination of lead and similar contaminants |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2944883A (en) | Treatment of nickel-containing sulfide ores | |
US2064479A (en) | Sintering zinc concentrates | |
US2523138A (en) | Recovery of iron from its ores | |
US2049633A (en) | Reclamation of battery plate scrap | |
US2221061A (en) | Process of making iron and nickel alloys | |
US3904400A (en) | Segregation roast process for the recovery of nickel from lateritic ore | |
US2004498A (en) | Producing columbium alloys | |
DE1758951A1 (en) | Method of making sponge iron | |
US2159412A (en) | Process relating to the production of nickel carbonyl | |
EP0056880B1 (en) | Process for the production of an agglomerated burden for zinc shaft furnaces | |
US2429416A (en) | Low-temperature carbonization process and product | |
US2759809A (en) | Method of roasting refractory manganese-precious metal ores | |
US2919231A (en) | Process of manufacturing iron-coke | |
US2199654A (en) | Process of treating iron ore | |
US2105037A (en) | Manufacture of nickel carbonyl | |
US1661813A (en) | Process of sintering zinc ores | |
US2913331A (en) | Nickel ore reduction process using asphalt additive | |
US2325176A (en) | Refining of nonferrous metal fume | |
US665744A (en) | Process of treating sulfid ores. | |
US1652184A (en) | Process and apparatus for extracting zinc | |
US1518626A (en) | Treatment of copper-lead matte | |
US2913336A (en) | Process for separating cobalt and nickel from ammoniacal solutions | |
US1803771A (en) | Removal of arsenic from lead bullion | |
US1884339A (en) | Method of producing coke | |
US1494130A (en) | Process of and material for the production of carbide and reduction of ore |