CA1126674A - Process for removing sulfur from coal - Google Patents

Process for removing sulfur from coal

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Publication number
CA1126674A
CA1126674A CA329,013A CA329013A CA1126674A CA 1126674 A CA1126674 A CA 1126674A CA 329013 A CA329013 A CA 329013A CA 1126674 A CA1126674 A CA 1126674A
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CA
Canada
Prior art keywords
coal
leachant
sulfur
sodium
water
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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
Application number
CA329,013A
Other languages
French (fr)
Inventor
Allan V. Marse
Donald B. Anthony
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Standard Oil Co
Original Assignee
Standard Oil Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Standard Oil Co filed Critical Standard Oil Co
Priority to CA329,013A priority Critical patent/CA1126674A/en
Application granted granted Critical
Publication of CA1126674A publication Critical patent/CA1126674A/en
Expired legal-status Critical Current

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Abstract

(5082) PROCESS FOR REMOVING SULFUR FROM COAL
ABSTRACT OF THE DISCLOSURE
Inorganic and organic sulfur are removed from coal by contacting the coal with gun blueing solution, namely an aqueous solution of sodium nitrate, sodium nitrite and sodium hydroxide.

1.

Description

' ?~tii'7~

BACKGROUND OF THE INVENTION
The present invention relates to a novel chemical leaching process for significantly reducing the sulfur con-tent of coal.
Processes for removing sulfur from coal by chem-ical leaching operations are well known. Examples of such processes are TRW's Meyer's process (U.S. 3,768,988) and Battelle's hydrothermal process.
Although each of these processes is capable of removing significant quantities of sulfur from coal, they each suffer significant disadvantages. For example, the TRW's Meyer's process is effective only in removing inor-ganic sulfur from coal. Moreover, the Battelle process is disadvantageous because high pressures and temperatures are required.
Accordingly, it is an ob~ect of the present in-vention to provide a novel process for removing sulfur from coal which is effective in removing both organic and inor-ganic sulfur and which can be carried out at comparatively low temperatures and pressures.

SUMMARY OF THE INVENTION
This and other ob~ects are accomplished by the present invention which is based on the discovery that significant amounts of both organlc and inorganic sulfur contained in coal can be removed therefrom by contacting the coal with an aqueous solution containing sodium nitrate, sodium nitrite and sodium hydroxide.
Thus, the present invention provides a process for removing sulfur from coal comprising contacting the coal with an aqueous solution containing sodium nitrate, sodium nitrite and sodium hydroxide.

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~s~ 7 ~ (50~2) DETAILED DESCRIPTION
In accordance with the present invention, both organlc and inorganic sulfur contained in coal can be re-moved therefrom by chemically leaching the coal with an aqueous solution of sodium nitrate, sodium nitrite and sodium hydroxide.
The inventive process is applicable to all types of coal. In this regard, it is well known that the chemical composition of coals obtained from different locations can vary widely. The inventive process can be practiced on all types of coal, although the amount of desulfurization at-tainable varies with the particular coal being processed.
The coal to be treated by the inventive process can be of any size although it should be in particulate form since this increases the contact of the aqueous sulfite solution with the coal mass. Preferably, the particulate coal should have a particle size of no more than 1/8 inch since the efficiency of the process decreases at higher particle sizes. Below this value, however, it has been found that there is no particular criticality in the par-ticle size of the coal, essentially the same results being obtained regardless of particle size. It is desirable, however, to avold using coal of too fine a particle size, since as is well known, physical separation of extremely fine particles from an aqueous liquid can be difficult.
Particle siz~s above 1/8 inch, e.g. 1/4 inch, can be used if desired, while particle sizes on the order of -325 mesh to 1/8 inch, more preferably about 60 mesh, have been found most convenient.
The leachant used to process coal in accordance with the present invention is an aqueous solution containing sodium nitrate, sodium nitrite, and sodium hydroxide. Such ~ 7~ (5082) solutlons have been used in the past to treat gun barrels and hence are known as "gun bluelng solutions". The concen-tration of sodium nitrate, sodium nitrite and sodium hydroxide in the aqueous solution are not particularly crltical and can vary over wide limits. Normally, the concentration Or each of sodium nitrate and sodium nitrite should be between 0.1 normal and the saturation value and the concentration of sodium hydroxide should be between 1 and 12 normal in order that the sulfur removal capabilities of the leachant solu-tion are significant. Any concentrations of sodium nitrate, sodium nitrite and sodium hydroxide within these ranges can be employed with facility. Preferably, the concentration of sodium nitrate is about 0.5 to 1 normal, the concentration of sodium nitrite is about 0.5 to 1 normal and the concen-tration of sodium hydroxide is about 5 normal. While higher concentrations of sodium nitrate, sodium nitrite and sodium hydroxide can be employed, no significant improvement in sulfur removal efficiency is obtained.
The leachant solution of course can contain other dissolved materials which do not interfer with the sulfur removal procedure as well as inert suspended materials, if desired.
The amount of leachant contacted with a given amount of coal is also not critical. As a practical matter, the coal/leachant ratio should be at least 1/20 in order for the process to be economic, although lower coal~leachant ratios can be employed if desired. Furthermore, when the coal/leachant ratio exceeds about 1.5/13 the mixture becomes too viscous. Therefore, it is preferable to operate with a coal/leachant ratio between about 1/20 to 1.5/1. Preferably the coal/leachant ratio is about 1/5.

. . . ~

~ (5082) The temperature at which the coal is contacted with the leachant can also vary widely. ~he process should be conducted at, near or above the boillng point of the leachant, which may be a few 30 or more degrees Centigrade above the boiling point of water. Thus, it is preferred to carry out the process at a temperature of about 80-400C, most preferably 100-150C. Care should be taken not to operate at too high a temperature, however, since the coal organics begin to oxidize under these conditions. In the most preferred embodlment of the inventlon, the process is carried out under reflux conditions, i.e. the leachant is boiling and the vapors driven off the leachant through boillng are condensed and returned to the leachant.
The inventive process can be carried out at any pressure although atmospheric or slightly above atmospheric pressures are preferred. The contact time of the leachant with the coal necessary for significant sulfur removal varies depending on a number of factors such as the concen-tration of sodium sulfite in the leachant and the particular coal being processed. Normally, contact times on the order of l/2 hour to 24 hours are employed.
When the leaching procedure is finished, the processed coal and the leachant are separated from one another. This can be accomplished by any convenient tech-nique such as, for example, filtering.
The treated particulate coal recovered in this manner can be used as is. However, it has been found in accordance with a further feature of the present invention that additional amounts of sulfur can be removed from the coal by washing the coal with water preferably containing an acid. Although not wishing to be bound to any theory, applicants believe that as a result of the inventive leaching .~

~ 7~ ( 5082) procedure, some of-the sulfur in the coal is transformed into sulfates whlch as known have limited solubillty in slightly basic solutions. Since the aqueous leachant is slightly basic, a portion of the sulfates tend to remain in the coal particles when they are separated from the leachant.
By washing the coal particles with water, additional sulfur will be removed. And if the water wash is acidic, still more sulfur will be removed because of the greater solu-bility of sulfates in acidic solutions.
In carrying out an acid wash, any acid can be used, although hydrochloric acid is preferred. Also, it is preferred to avoid using nitric acid as this may oxidize the coal. The concentrat~on of acid in the aqueous acidic wash solution is not critical, concentrations ranging from 1.0 to 6.o normal being preferred as most convenient. Also, if an acid wash is used it is desirable to water wash the coal after the acid wash to remove acid anions which may become entrained therein.
In a particularly preferred embodiment of the in-vention, the inventive process as discussed above is followed by a conventional float-sink operation. In this regard, it is a common commercial practice to process raw coal before it is sold to remove some of the ash content thereof.
This is normally done by a density separation technique wherein ground raw coal is formed into a slurry of an apDropriate liquid and agitated. This causes heavier in-organics in the coal, i.e. ash, to he separated from the remainder of the coal and fall to the bottom of the com-position and the remainder of the coal to float to the top. Choice of the density of the liquid determines how much ash is separated out from the remainder of the coal.

Although many different liquids can be used such as, for ;r ? ~ ( 5 0 8 2 ) example, carbon tet~achlorlde, it ls conventlonal ln com-mercial ODeratiOnS to emDloy water. The "apparent density"
cr the water can be varied either by charging air into the bottom of the composition or by conducting the Drocedure in an apparatus which the water continuously flo~s uDwards in the treating vessel.
In accordance with the present invention, it has been found that inventive treatment process in addition to removing sulfur from the coal will cause additional loosening of the inorganic matrix of the coal in much the same way as a Group I or II metal salt loosens the inorganic matrix in the invention of commonly assigned application (attorney docket 5080). Thus, when coal treated to the inventive Dro-cedure is sub~ected to float-sinking, more ash than would otherwise be possible under a given set of conditions is removed from the coal. This, of course, causes the coal product produced by this procedure to have a higher heat value than the raw coal charged.
In order to more thoroughly illustrate the present invention, the following examples are presented.
Example 1 50 grams of a Pittsburgh seam coal from the Ireland Mine, West Virginia, and containing 5.27 percent sulfur (2.05% pyritic/0.35 sulfate/2.87% organic) was ground to 40 x 60 mesh. The particulate coal so obtained was treated for 6 hours with an aqueous solution o.8N in sodium nitrate 0.4N in sodium nitrite and 5N in sodium hydroxide, the aqueous solution boiling at 134C under reflux. The coal was recovered by filtration, then washed in order with water, an aqueous solution of 2N HCl and again with water. Product coal was analvzed and found to contain 2.70~ sulfur (0.62 (5082) 7~
pyritic~0.07 sulfate/2.01 organic) whlch represents a 49%
sulfur reduction. Moreover~ the ash content of the coal was reduced from 10.6 to 7.7~.
Exam~les 2 to 10 The process of Example 1 was repeated using a number of different coals. The results obtained are set forth ln the following Table I.

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P) D
O P~
~a H t~ H O O O H O
P~

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D ~D
O ~D

~ ~ 3' 3~ ~ ~ 3H H H 5 3 C O O O ~ ~ C ct P) p~ p~ ~D
D
p) CO
~D
~ 1~
W ~ ~ ~ O ~n c~ C
P~ ~ ~ W ~ o~ o ~ c ~ P~ I_ O~ ~ ~ O ~ CJ~ IJ C

ct 1- 0 1- W O O 1- 1- ~ OQ ~3 3~ 1 . . . . . . . . ~ 3 ~
P~ I w ~rl ~ ~ co ~ ~L) a~ ~ c~ W
3 ~ W ~ a~ I~ W ~ c~ D t' D 3 t~
~D . ~--. H
~0 3 p~ ~ . . . . . . . . 0~ Q
~ w ~ ~ 1~ 3 O

., p, ~ i~

0~ ~
r\~ I~ 1-- ~ W a~ ~ D
W O W 1~ DCO W P~ ~
D

w w ~ ~ ~ ~ c o ~n w o~co o co ~ ~_ * ~t ~
tD ~
~o 3 l~ n 7~ o w o o ~ o or~ 3 ~
1,. 3 w w w ~ I~) w r~ ) Q D
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ct ~:
9.
"

(5082) 11266~4 ~ rom the foregolng, lt can be seen that the inven-tlve process is capable of removlng sulfur from a wlde varlety of dlfferent coals. Thus, the present invention is of signlficant value ln reduclng air pollution caused by the burning of coal. Also, because the coal product of the inventive process has (as illustrated by the examples) a higher heat value than the raw coal, the inventive pro-cess is further advantageous in producing a superior coal product.
Incidentally, although the experimental results above indlcate that no sulfur was removed in Example 8, it is believed that ln fact a small amount of sulfur was re-moved and that the results indlcated are erroneous. In this connectlon, the measurement accuracy of the instruments employed to measure sulfur content ln the examples are not very sensitlve at very low levels of sulfur content.
Although only a few embodlments of the present lnventlon have been descrlbed above, lt should be appre-clated that many modlflcatlons can be made wlthout departing from the spirlt and scope of the lnventlon. For example, bases other than sodium hydroxide such as calcium hydroxide, can be employed ln place of the sodium hydroxide. All such modifications are intended to be included within the scope of the present invention, which is to be llmited only by the followlng clalms.

10 .

Claims (8)

WE CLAIM:
1. A process for removing sulfur from coal com-prising contacting the coal with a leachant comprising an aqueous solution containing sodium nitrate, sodium nitrite and a base.
2. The process of claim 1 wherein said base is sodium hydroxide.
3. The process of claim 2 wherein said leachant is heated to reflux during contact with said coal.
4. The process of claim 2 wherein said coal is particulate in form, substantially all of said coal having a particle size of no larger than 1/8 inch.
5. The process of claim 4 wherein said leachant is at least 0.1 normal in sodium nitrate, 0.1 normal in sodium nitrite and 1 normal in sodium hydroxide.
6. The process of claim 5 further comprising separating said particulate coal from said aqueous leachant and thereafter washing said particulate coal with water.
7. The process of claim 6 wherein said water contains an acid.
8. The process of claim 7 further comprising separating said particulate coal from the acid-containing water and thereafter washing said particulate coal with water.
CA329,013A 1979-06-04 1979-06-04 Process for removing sulfur from coal Expired CA1126674A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CA329,013A CA1126674A (en) 1979-06-04 1979-06-04 Process for removing sulfur from coal

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CA329,013A CA1126674A (en) 1979-06-04 1979-06-04 Process for removing sulfur from coal

Publications (1)

Publication Number Publication Date
CA1126674A true CA1126674A (en) 1982-06-29

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
CA329,013A Expired CA1126674A (en) 1979-06-04 1979-06-04 Process for removing sulfur from coal

Country Status (1)

Country Link
CA (1) CA1126674A (en)

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