US1623797A - Method of converting nickel-containing matte - Google Patents
Method of converting nickel-containing matte Download PDFInfo
- Publication number
- US1623797A US1623797A US96443A US9644326A US1623797A US 1623797 A US1623797 A US 1623797A US 96443 A US96443 A US 96443A US 9644326 A US9644326 A US 9644326A US 1623797 A US1623797 A US 1623797A
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- matte
- nickel
- converting
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- converter
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B23/00—Obtaining nickel or cobalt
- C22B23/02—Obtaining nickel or cobalt by dry processes
- C22B23/025—Obtaining nickel or cobalt by dry processes with formation of a matte or by matte refining or converting into nickel or cobalt, e.g. by the Oxford process
Definitions
- 2 presents such a converter having tuyeres 3 supplied with air or gases from a wmd-box 4, to which supply pipe 5 leads.
- This pipe 5 connects with the hollow trunnion at t e right of the figure, to which pipe 6 leads from a blowing engine or compressor. 7
- a. supply pipe 8 leads from a three-way valve 9, and when the valve is in the position shown, air is forced into the wind-box and tuyeres in the usual way.
- low pressure air pipe 10 leads to a fuel burner 11, projecting toward the 0 en mouth of the converter. Air is force through this trunnion by any suitable blower, such as shown at 12, and in the form shown, fuel is supplied to the burnerthroughipipe 13.
- the strongly oxidizing blast to the tuyeres is then replaced by a mildly oxidizing, neutral, or even slightly reducing blast.
- this is done by using the exit gases of the converter itself.
- the three-Way valve 9 is turned 90, so that exit gas from the converter, cooled and scrubbed, is sucked into the compressor 71nd forced to the tuyeres.
- the temperature of the exit gas is reduced, the dust is precipitated. and sub stantially all of the sulphur dioxide is absorbed by the water.
- the air should be changed, to reduce the free oxygen earlier than with a Monel metal matte.
- the change to exit gases should be made in such case when the Sulphur is down to about 4%.
- the oxygen content in the exit gas should be lower for nickel matte than for Monel'metal, While the temperature should be kept higher.
- the blown metal may be refined in an electric furnace; the way of reducing the oxygen content may be changed, other lining material may be used; and other changes may be made Without departing from my invention.
- the steps consisting of forcing air through the molten matte and later in the blow forcing waste gases of combustion through the matte.
- the step consisting of withdrawing a part of the exit gases'and forcing them through the charge in the later stage of the blow.
- the step consisting of withdrawing a part of the exit gases and forcing them through the charge in the later stage of the blow, while supplying heat above the level of the bath.
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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
A ril 5 192% p o. LELLEP METHOD OF CONVERTING NICKEL CONTAINING MATTE Filed March 22. 1926 cessfully converted by adding heat to that Patented Apr. 5, 1927.
UNITED STATES PATENT OFFICE.
OTTO LELLEP, OF EGYPT, PENNSYLVANIA, ASSIGNOR TO THE INTERNATIONAL v NICKEL COMPANY, OF NEW YORK, N. Y., A CORPORATION NEW JERSEY.
METHOD OF CON VEBTIN' G NIOIIEL-CONTAINING IATTE.
Application filed March 22, 1926, Serial No. 96,443, and in Canada July 7, 1826.
generally denied in the metallurgical art.
All publications relative thereto show that attempts to convert nickel-containing mattes in the same way as copper mattes' have failed. Such failures have been due to the preferential oxidationofthemetal or alloy after the sulphur has been lowered to a certain extent in the molten bath.
After long experimenting on a large scale, I have found that such mattes can be sucdeveloped-by the converting action itself and by lowering the oxygen, content of the blast during the last stages of converting.
In my previous patent applications, Serial No. 630,618 filed April 7, 1923 and Serial No. 671,496, filed October 29, 1923, I have disclosed several methods of adding heat beyond that developed by the convertingaction. In further work, I have found that the best. method for this'purpose is to use a burner. projecting a flame into the converter above the level of the molten bath. I have also found that excessive oxidation of metal, which otherwise takes place after the sulphur has been largely reduced, can be avoided by greatly lowering the percentage of oxygen 'in the blast in the last stages of converting. I have also found the use of slag-forming material is important if not essential to successful large scale operation, to prevent dust losses during converting;
' and have found a highly refractory material which will sufiiciently withstand "the .high
, temperature and erosive action of the charge,
this being preferably fused alumina bonded with china play. Close control of the temperature is also an important feature. Pure nickel matte converts most successfully at a temperature of about 1600 (1., while a matte containing copper and nickel in the ratio of 1 to 3 will be converted-at about 1500 C. My process is preferably carried out in a fuel-heated Bessemer converter of the type commonl used in making Bessemer steel.
Referring to the diagrammatic 'figure'of the drawing, 2 presents such a converter having tuyeres 3 supplied with air or gases from a wmd-box 4, to which supply pipe 5 leads.
This pipe 5 connects with the hollow trunnion at t e right of the figure, to which pipe 6 leads from a blowing engine or compressor. 7 To this blowing engine, which has'the usual valves, a. supply pipe 8 leads from a three-way valve 9, and when the valve is in the position shown, air is forced into the wind-box and tuyeres in the usual way. I
From the other hollow trunnion at the left of the figure a. low pressure air pipe 10 leads to a fuel burner 11, projecting toward the 0 en mouth of the converter. Air is force through this trunnion by any suitable blower, such as shown at 12, and in the form shown, fuel is supplied to the burnerthroughipipe 13. Over the mouth of the converter when in blowing position In carrying out my process with'such apparatus, 'the nickel-containing matte is blown with air in the usual way, except that extra heat is supplied by the burner which projects a flame into the converter'above the bath, and that slag-forming material such as sand is supplied to flux and form it slag, ;until the sulphur in the charge has been low 'ered to a point where oxidation of the metal =begins. lVhen Monel metalmatte is bein converted, this point is in the neighbor-ho of 2%. Below that percentage, the normal air blast would oxidize a considerable amount of metal while burningout the further sulphur. Hence, if continued, a large percentage of metal would pass into the slag. To prevent this and further reduce the sulphur without materially oxidizing the metal, the strongly oxidizing blast to the tuyeres is then replaced by a mildly oxidizing, neutral, or even slightly reducing blast. In the form -shown, this is done by using the exit gases of the converter itself. At this s'tage,.the three-Way valve 9 is turned 90, so that exit gas from the converter, cooled and scrubbed, is sucked into the compressor 71nd forced to the tuyeres. In thescrubber, the temperature of the exit gas is reduced, the dust is precipitated. and sub stantially all of the sulphur dioxide is absorbed by the water.
- out by proper regulation of the fuel and air fed to the heating burner. An experienced operator can easily determine this by the appearance of the heating flame and can regulate the supplies accordingly.
In practice, about 30% ofthe total air or gases used in converting passes through the tuyeres and about 70% is injected through the burner.
In caseof a substantiallypure nickel matte, the air should be changed, to reduce the free oxygen earlier than with a Monel metal matte. Usually the change to exit gases should be made in such case when the Sulphur is down to about 4%. Also, the oxygen content in the exit gas should be lower for nickel matte than for Monel'metal, While the temperature should be kept higher. p The blown metal may be refined in an electric furnace; the way of reducing the oxygen content may be changed, other lining material may be used; and other changes may be made Without departing from my invention.
I claim:
1. In the converting of nickel-containing matte, the steps consisting of forcing oxy- This.
gen-containing gases through the molten matte, supplying additional heat, and reducing the content of free oxygen in the blast during the later stage of blowing.
4. In the converting of nickel-containing tnatte, the steps consisting of forcing air through the molten matte and later in the blow forcing waste gases of combustion through the matte.
5. In the converting of nickel-containing matte, the steps consisting of forcingair through the molten matte and later in the blow forcing Waste gases of combustion through the matte While supplying additional heat.
6. In the converting of nickel-containing matte, the step consisting of withdrawing a part of the exit gases'and forcing them through the charge in the later stage of the blow.
matte, the step consisting of withdrawing a part of the exit gases and forcing them through the charge in the later stage of the blow, while supplying heat above the level of the bath.
()TTO LELLEP 7. In the converting of nickel cOntaining
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA1623797X | 1926-07-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
US1623797A true US1623797A (en) | 1927-04-05 |
Family
ID=4173829
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US96443A Expired - Lifetime US1623797A (en) | 1926-07-07 | 1926-03-22 | Method of converting nickel-containing matte |
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US (1) | US1623797A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3069254A (en) * | 1960-08-23 | 1962-12-18 | Int Nickel Co | Autogenous pyrometallurgical production of nickel from sulfide ores |
US3139336A (en) * | 1961-05-11 | 1964-06-30 | Mclaughlin John J | Copper refining |
US3516818A (en) * | 1967-04-26 | 1970-06-23 | Int Nickel Co | Fire refining of nickel-containing metallurgical intermediates and scrap |
FR2318233A1 (en) * | 1975-07-16 | 1977-02-11 | Int Nickel Canada | Purifying a nickel matte by oxidn. - to remove e.g. iron, cobalt and lead which have a higher oxygen affinity than nickel |
US4045215A (en) * | 1973-07-16 | 1977-08-30 | Creusot-Loire | Method of refining mattes containing nickel |
WO1985001750A1 (en) * | 1983-10-19 | 1985-04-25 | Commonwealth Scientific And Industrial Research Or | Smelting nickel ores or concentrates |
-
1926
- 1926-03-22 US US96443A patent/US1623797A/en not_active Expired - Lifetime
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3069254A (en) * | 1960-08-23 | 1962-12-18 | Int Nickel Co | Autogenous pyrometallurgical production of nickel from sulfide ores |
US3139336A (en) * | 1961-05-11 | 1964-06-30 | Mclaughlin John J | Copper refining |
US3516818A (en) * | 1967-04-26 | 1970-06-23 | Int Nickel Co | Fire refining of nickel-containing metallurgical intermediates and scrap |
US4045215A (en) * | 1973-07-16 | 1977-08-30 | Creusot-Loire | Method of refining mattes containing nickel |
FR2318233A1 (en) * | 1975-07-16 | 1977-02-11 | Int Nickel Canada | Purifying a nickel matte by oxidn. - to remove e.g. iron, cobalt and lead which have a higher oxygen affinity than nickel |
WO1985001750A1 (en) * | 1983-10-19 | 1985-04-25 | Commonwealth Scientific And Industrial Research Or | Smelting nickel ores or concentrates |
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