EP0120499A2 - Method for the removal of iron pyrites from coal and carbon structures during ash removal by chemical means - Google Patents
Method for the removal of iron pyrites from coal and carbon structures during ash removal by chemical means Download PDFInfo
- Publication number
- EP0120499A2 EP0120499A2 EP84103390A EP84103390A EP0120499A2 EP 0120499 A2 EP0120499 A2 EP 0120499A2 EP 84103390 A EP84103390 A EP 84103390A EP 84103390 A EP84103390 A EP 84103390A EP 0120499 A2 EP0120499 A2 EP 0120499A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- coal
- removal
- pyrites
- carbon structures
- chemical means
- 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.)
- Withdrawn
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L9/00—Treating solid fuels to improve their combustion
- C10L9/02—Treating solid fuels to improve their combustion by chemical means
Definitions
- the present invention relates to a method for the removal of iron pyrites from coal and carbon structures during ash removal by chemical means.
- Pyrites is commonly distributed within the coal matrix as pyrites particles laminated to the organic coal matrix, often with intermediate bonding by inorganic mineral matter such as aluminosilicates.
- Our invention has as its objective a method which liberates pyrites from coal without the necessity for fine grinding.
- the invention provides a method for liberating pyrites from coal comprising crushing coal to a suitable particle size; leaching the crushed coal with hydrofluoric acid, and treating the leached solids using otherwise conventional pyrites removal s.
- the suitable particle size range varies from coal to coal, however it is coarser in size than.that necessary for satisfactory conventional liberation of pyrites.
- the hydrofluoric acid dissolves most of the inorganic minerals within the coal matrix, including the predominant aluminosilicates, but not the pyrites thereby breaking the bond between the pyrites and the organic coal matrix, and liberating the pyrites particles.
- Conventional pyrites removal methods such as gravity separation, magnetic separation, and flotation can then be employed. Gravity separation is particularly enhanced as the organic coal matrix achieves a lower than normal density after hydrofluoric acid leaching, due to the dissolution of ash-forming minerals, thereby increasing the density difference between the pyrites refuse and the coal accepts.
- hydrofluoric acid leaching conditions are not critical with respect to acid concentration, temperature or leaching time. We have successfully employed acid concentrations of about 3 to 70 w/w%, temperatures of 20 to 100°C and leaching times from about 10 minutes to 48 hours.
- the raw coal must be crushed to a particles size suitable for hydrofluoric acid leaching. It is necessary to reduce the particle size only to that extent required to provide access for the hydrofluoric acid leach liquor to the mineral matter associated with the coal matrix. It is not necessary to completely liberate the mineral particles, which would require finer grinding. Accordingly, relatively coarse coal particles can be acid leached and then treated for pyrites removal. Liberation of pyrites by grinding alone would only be achieved at much finer particle sizes. We have achieved excellent pyrites removal from coal by hydrofluoric acid leaching raw coal at particle sizes as coarse as 5mm, and then using conventional separation methods.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Combustion & Propulsion (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Solid Fuels And Fuel-Associated Substances (AREA)
Abstract
The invention relates to a method for the removal of iron pyrites from coal and carbon structures during ash removal by chemical means. The method includes crushing raw coals to a proper particle size, leaching said crushed coals with hydrofluoric acid, and separating said leached solids.
Description
- The present invention relates to a method for the removal of iron pyrites from coal and carbon structures during ash removal by chemical means.
- Iron pyrites (FE S2) is an undesirable impurity in coal.
- The most commonly employed methods for pyrite removal from coal rely on differences in physical properties between pyrites and coal particles. Flotation relies on surface properties, gravity separation relies on density, and magnetic separation relies on magnetic properties.
- Therefore, in order to remove most pyrites from coal, it is necessary to liberate the pyrites particles from the organic coal matrix, that is, to separate the pyrites particles from the coal particles.
- Pyrites is commonly distributed within the coal matrix as pyrites particles laminated to the organic coal matrix, often with intermediate bonding by inorganic mineral matter such as aluminosilicates.
- Conventional removal methods achieve pyrites liberation by grinding the coal, the finer the grind the more complete is the liberation. However, fine grinding is expensive and often introduces downstream processing or utilisation disadvantages.
- Our invention has as its objective a method which liberates pyrites from coal without the necessity for fine grinding.
- In its broadest form the invention provides a method for liberating pyrites from coal comprising crushing coal to a suitable particle size; leaching the crushed coal with hydrofluoric acid, and treating the leached solids using otherwise conventional pyrites removal s.
- The suitable particle size range varies from coal to coal, however it is coarser in size than.that necessary for satisfactory conventional liberation of pyrites. The hydrofluoric acid dissolves most of the inorganic minerals within the coal matrix, including the predominant aluminosilicates, but not the pyrites thereby breaking the bond between the pyrites and the organic coal matrix, and liberating the pyrites particles. Conventional pyrites removal methods such as gravity separation, magnetic separation, and flotation can then be employed. Gravity separation is particularly enhanced as the organic coal matrix achieves a lower than normal density after hydrofluoric acid leaching, due to the dissolution of ash-forming minerals, thereby increasing the density difference between the pyrites refuse and the coal accepts.
- The hydrofluoric acid leaching conditions are not critical with respect to acid concentration, temperature or leaching time. We have successfully employed acid concentrations of about 3 to 70 w/w%, temperatures of 20 to 100°C and leaching times from about 10 minutes to 48 hours.
- The raw coal must be crushed to a particles size suitable for hydrofluoric acid leaching. It is necessary to reduce the particle size only to that extent required to provide access for the hydrofluoric acid leach liquor to the mineral matter associated with the coal matrix. It is not necessary to completely liberate the mineral particles, which would require finer grinding. Accordingly, relatively coarse coal particles can be acid leached and then treated for pyrites removal. Liberation of pyrites by grinding alone would only be achieved at much finer particle sizes. We have achieved excellent pyrites removal from coal by hydrofluoric acid leaching raw coal at particle sizes as coarse as 5mm, and then using conventional separation methods.
- Using a coal with .9% sulphur, approximately .4 of which is pyritic, the following results were obtained: crushing the coal to 2mm minus and drying, the coal was then subjected to a heavy media wash and it was found sulphur was reduced by approximately .02%. A sample of the same coal crushed to 2mm minus and subjected to the hyrdofluoric wash detailed earlier was then treated to a heavy media wash in the same conditions as the untreated sample; residual sulphur was then found to be 0.4%. More than 99% of the pyritic sulphur was removed.
Claims (4)
1. A method for the removal of iron pyrites from coal and carbon structures comprising the steps of crushing raw coals to a proper particle size, leaching said crushed coals with hydrofluoric acid, and separating said leached solids.
2. The method of clim 1, said leaching with hydrofluoric acid is carried out in the conditions of acid concentrations of about 3 to 70 percent of weight, temperatures of 20 C° to 10 C°, and times from about 10 minutes to 48 hours.
3. The method of claim 1, said crushed coals are at particle sizes up to 5 millimeters.
4. The method of claim 3, said crushed coals are at particle sizes up to 2 millimeters.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU864883 | 1983-03-28 | ||
AU8648/83 | 1983-03-28 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0120499A2 true EP0120499A2 (en) | 1984-10-03 |
EP0120499A3 EP0120499A3 (en) | 1985-10-02 |
Family
ID=3699356
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP84103390A Withdrawn EP0120499A3 (en) | 1983-03-28 | 1984-03-27 | Method for the removal of iron pyrites from coal and carbon structures during ash removal by chemical means |
Country Status (2)
Country | Link |
---|---|
EP (1) | EP0120499A3 (en) |
AU (1) | AU2620084A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003074639A1 (en) * | 2002-03-05 | 2003-09-12 | Karalee Research Pty Ltd | Method for treating carbonaceous materials |
WO2009071284A1 (en) * | 2007-12-05 | 2009-06-11 | Kronos International, Inc. | Method for treating cyclone dust occurring during chlorination of raw materials containing titanium |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BR8605483A (en) * | 1985-02-19 | 1987-04-22 | Oabrand Pty Ltd | METHOD FOR CONTINUOUS CHEMICAL REDUCTION AND REMOVAL OF MINERAL MATERIAL CONTAINED IN CARBON STRUCTURES |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB173072A (en) * | 1920-09-23 | 1921-12-23 | Rudolf Lessing | Treatment of coal to cause or facilitate its breaking up or crushing |
US4169710A (en) * | 1978-03-29 | 1979-10-02 | Chevron Research Company | Process for comminuting and reducing the sulfur and ash content of coal |
EP0016624B1 (en) * | 1979-03-16 | 1983-05-25 | Kinneret Enterprises Limited | Coal de-ashing process |
-
1983
- 1983-03-28 AU AU26200/84A patent/AU2620084A/en not_active Abandoned
-
1984
- 1984-03-27 EP EP84103390A patent/EP0120499A3/en not_active Withdrawn
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB173072A (en) * | 1920-09-23 | 1921-12-23 | Rudolf Lessing | Treatment of coal to cause or facilitate its breaking up or crushing |
US4169710A (en) * | 1978-03-29 | 1979-10-02 | Chevron Research Company | Process for comminuting and reducing the sulfur and ash content of coal |
EP0016624B1 (en) * | 1979-03-16 | 1983-05-25 | Kinneret Enterprises Limited | Coal de-ashing process |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003074639A1 (en) * | 2002-03-05 | 2003-09-12 | Karalee Research Pty Ltd | Method for treating carbonaceous materials |
WO2009071284A1 (en) * | 2007-12-05 | 2009-06-11 | Kronos International, Inc. | Method for treating cyclone dust occurring during chlorination of raw materials containing titanium |
Also Published As
Publication number | Publication date |
---|---|
AU2620084A (en) | 1984-10-04 |
EP0120499A3 (en) | 1985-10-02 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
AK | Designated contracting states |
Designated state(s): DE FR GB IT |
|
PUAL | Search report despatched |
Free format text: ORIGINAL CODE: 0009013 |
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AK | Designated contracting states |
Designated state(s): DE FR GB IT |
|
17P | Request for examination filed |
Effective date: 19860324 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION HAS BEEN WITHDRAWN |
|
18W | Application withdrawn |
Withdrawal date: 19860729 |
|
RIN1 | Information on inventor provided before grant (corrected) |
Inventor name: LLOYD, ROBERT Inventor name: TURNER, MAXWELL JAMES |