US1364573A - Granvh - Google Patents
Granvh Download PDFInfo
- Publication number
- US1364573A US1364573A US1364573DA US1364573A US 1364573 A US1364573 A US 1364573A US 1364573D A US1364573D A US 1364573DA US 1364573 A US1364573 A US 1364573A
- Authority
- US
- United States
- Prior art keywords
- sulfur
- sulfuric acid
- ores
- ore
- container
- 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
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 68
- RAHZWNYVWXNFOC-UHFFFAOYSA-N sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 18
- AKEJUJNQAAGONA-UHFFFAOYSA-N Sulfur trioxide Chemical compound O=S(=O)=O AKEJUJNQAAGONA-UHFFFAOYSA-N 0.000 description 16
- 238000000034 method Methods 0.000 description 14
- NINIDFKCEFEMDL-UHFFFAOYSA-N sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 14
- 239000011593 sulfur Substances 0.000 description 14
- 229910052717 sulfur Inorganic materials 0.000 description 14
- 239000007789 gas Substances 0.000 description 8
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 8
- 239000002253 acid Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 125000004122 cyclic group Chemical group 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 238000002144 chemical decomposition reaction Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 238000005868 electrolysis reaction Methods 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
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
- C22B1/02—Roasting processes
-
- 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
- C22B3/00—Extraction of metal compounds from ores or concentrates by wet processes
-
- 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
Definitions
- the invention relates to the process of extracting sulfur and metallic or chemical values from ores by subjecting said ores to dissolution or chemical decomposition by employing ozonized air in a suitable container with ore and sulfuric acid under the influence of heat.
- the object of the invention is to render the extraction more effectual, complete and economical.
- ihis treatment causes the ores to deconr pose and the native values of the said ores to pass into solution or separate out in such a manner that they may be recovered later.
- the sulfids are coir verted to sulfates and at the same time frolsulfur, sulfur dioxid. and sulfur trioxid in gaseous form are evolved.
- the sulfates are removed for subsequent treatment by known methods and fresh batches of sullids supplied While the said gases are treated with ozonized air.
- the free sulfur is precipitated and removed by appropriate methods. while the sulfur dioxid and sulfur trioxid are conveyed into another apparatus where the sulfur trioxid is thrown down, leaving only the sulfur dioxid which is then converted while in transit into sulfuric acid by known methods and this sulfuric acid is then returned to the original ore container for action on fresh batches of ore supplied thereto.
- the sulfur trioxid gas above mentioned is already in condition to form sulfuric acid by the addition of a Water molecule which may he introduced as is well known by a water spray which results in the reaction ()-l- SO H S() the sulfuric acid so formed being recovered from the bottom of the chamber and the sulfur dioxid passing on for further treatment. Some sulfur is probably also deposited with the sulfuric acid but this is separated out in well known ways.
Description
GRANVILLE MOORE, OF SAN FRANCISCO, CALIFORNIA.
METHOD OF TREATING ORES.
No Drawing. Application filed January 14, 1919, Serial No. 271,121.
Specification of Letters Patent.
Patented Jan. 4, 1921 Renewed July 20, 1920. Serial To all wlwmz't may concern Be it known that I, GRANVILLE Moonn, a citizen of the United States, and a. resident of the cit and county of San Francisco, State of California, have invented new and useful Improvements in Methods of Treating Ores, of which the following is a specification.-
The invention relates to the process of extracting sulfur and metallic or chemical values from ores by subjecting said ores to dissolution or chemical decomposition by employing ozonized air in a suitable container with ore and sulfuric acid under the influence of heat.
The object of the invention is to render the extraction more effectual, complete and economical.
In my process sultid ores, or a suitably proportionate mixture of sulfid and non sulfid ores. are treated with sulfuric acid (H 80 in a suitable container undcr the influence of heat. and ozonized air (under pressure or without. as circumstances may re uire.)
ihis treatment causes the ores to deconr pose and the native values of the said ores to pass into solution or separate out in such a manner that they may be recovered later.
By this treatment the sulfids are coir verted to sulfates and at the same time frolsulfur, sulfur dioxid. and sulfur trioxid in gaseous form are evolved. The sulfates are removed for subsequent treatment by known methods and fresh batches of sullids supplied While the said gases are treated with ozonized air. The free sulfur is precipitated and removed by appropriate methods. while the sulfur dioxid and sulfur trioxid are conveyed into another apparatus where the sulfur trioxid is thrown down, leaving only the sulfur dioxid which is then converted while in transit into sulfuric acid by known methods and this sulfuric acid is then returned to the original ore container for action on fresh batches of ore supplied thereto. The sulfur trioxid gas above mentioned is already in condition to form sulfuric acid by the addition of a Water molecule which may he introduced as is well known by a water spray which results in the reaction ()-l- SO H S() the sulfuric acid so formed being recovered from the bottom of the chamber and the sulfur dioxid passing on for further treatment. Some sulfur is probably also deposited with the sulfuric acid but this is separated out in well known ways.
It will hc seen that I recover a continuous supply of sulfuric acid available for retreatment or recovery as desired and the process is cyclic.
The mineral and chemical values contamed in the solution before mentioned are recover-rd by well known chemical means or by electrolysis.
am aware that it is old in the art to treat sultid ores with sulfuric acid and ozonized air. but I am not aware that it has been proposed to treat the resultant gases in such way as to generate tllelPfl'fllll sulfuric acid for action on fresh batches of ore. thus pro ducing a continuous cyclic process from a single supply of sulfuric acid.
claim:
1. The process of treating sultid ores which consists in subjecting: them in a loscd container to the action of sulfuric acid and ozonized air under the influen e of heat. then converting the resultant sulfur dioxid while in transit into sulfuric acid and rcturning this acid to the ore container for action on fresh batches of ore.
2. The process of treating sullid orcs which consists in subjecting them in a closed container to the action of sulfuric acid and ozonized air under the influence of heat, whereby the sulfids are converted into sulfates and free sulfur. sulfur dioxid. and sulfur trioxid in gaseous form are evolved, then eliminating the free sulfur and sulfur trioxid. and convertingthe sulfur dioxid while in transit into sulfuric acid and returning this acid to the ore container for action on fresh batches of ore.
3. The process of treating sulfid ores which consists in subjecting them in a closed container to the action of sulfuric acid and ozonized air under the influence of heat, whereby the sulfids are converted. into sulfates, and free sulfur. sulfur dioxid. and sulfur trioxid in gaseous form are evolved, then conveying said gases to another container and there subjecting them toozonized air, then eliminating the free sulfur and sulfur trioxid and converting the sulfur dioxid while in transit into sulfuric acid and res turning this acid to the ore container for action on fresh batches of ore.
In testimony whereof, I have hereunto set my hand at San Franc sco, California.
GRANVILLE MOORE.
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1364573A true US1364573A (en) | 1921-01-04 |
Family
ID=3397411
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US1364573D Expired - Lifetime US1364573A (en) | Granvh |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1364573A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2686114A (en) * | 1951-01-19 | 1954-08-10 | Chemical Construction Corp | Elimination of arsenic from metallic arsenide-sulfide concentrates |
| US2746859A (en) * | 1951-12-22 | 1956-05-22 | Chemical Construction Corp | Method of recovering non-ferrous metal values |
| US2772947A (en) * | 1951-03-23 | 1956-12-04 | Wigton Abbott Corp | Process for converting nickel sulfide to nickel sulfate |
| US2776207A (en) * | 1951-04-05 | 1957-01-01 | Bethlehem Steel Corp | Treatment of iron ores |
| US2836490A (en) * | 1952-09-17 | 1958-05-27 | Sherritt Gordon Mines Ltd | Method of treating solutions containing metal values |
| US3174849A (en) * | 1961-10-05 | 1965-03-23 | Sherritt Gordon Mines Ltd | Two-stage oxidation and leaching process |
-
0
- US US1364573D patent/US1364573A/en not_active Expired - Lifetime
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2686114A (en) * | 1951-01-19 | 1954-08-10 | Chemical Construction Corp | Elimination of arsenic from metallic arsenide-sulfide concentrates |
| US2772947A (en) * | 1951-03-23 | 1956-12-04 | Wigton Abbott Corp | Process for converting nickel sulfide to nickel sulfate |
| US2776207A (en) * | 1951-04-05 | 1957-01-01 | Bethlehem Steel Corp | Treatment of iron ores |
| US2746859A (en) * | 1951-12-22 | 1956-05-22 | Chemical Construction Corp | Method of recovering non-ferrous metal values |
| US2836490A (en) * | 1952-09-17 | 1958-05-27 | Sherritt Gordon Mines Ltd | Method of treating solutions containing metal values |
| US3174849A (en) * | 1961-10-05 | 1965-03-23 | Sherritt Gordon Mines Ltd | Two-stage oxidation and leaching process |
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