chemical physics of discharges - Argonne National Laboratory
chemical physics of discharges - Argonne National Laboratory chemical physics of discharges - Argonne National Laboratory
S ~ l ~ o n~pg:ading r is the result of two important factors. r l ~ s t , the 201 irrit holling range has been narrowod and, secondly, the 5ol~ent has S E ~ ~ ,cabilised I by removal of its less refractory (readllv crached, ,,mponents. qolvent improve 1cb stahilitv. Continued use and recycle-of this A hciff dlscuaslon of the variables in coal solution and coking of its deasned ~olutlon wlll outline the reasons for the improvemenrs -e:.ireri by the channes In solvent boiling range and composition noted
383 ash content of the initial high volatile bituminous coal. Thus, it has been repeatedly demonstrated in the bench and pilot solvent deashing studies on coal samples with ash contents varying from 5 to 20 weight percent that final ash values of 0.1 to 0.3 could be obtained in the treated coal extracts. Lisewise , inorganic chlorides have been iargely eliminated with the ash. Coals containing 0.25 and 0.15 weight percent chlorine were reduced to values of 0.004 to 0.003, respectively. It is assumed that coals of considerably higher inorganic chloride contents could be reduced to similar low values. The harmful corrosive effects of ash and chlorides on furnace operation are well known and their effective reduction is obviously very desirable. Sulfur Reduction The degree of bituminous coal desulfurization by solvent deashing has proven to be a function of the original ratio of inorganic sulfate and pyritic sulfur to the organic forms. Original total sulfur contents of 1 t o 4 percent are reduced to values of 0.4 to 1 weight percent in the extracts. It is known that this ratio increases with coals of increasing total sulfur content, i.e., in the lower grade coals of correspondingly higher ash. The final sulfur of the deashed coal therefore relates to the original organic sulfur which is only partially removed in the process, whereas the inorganic sulfur is removed substantially quantitatively. Thus, in Table 1, complete elimination of the pyritic and sulfate sulfurs has been achieved with an accompanying 26 percent reduction in organic sulfur, for an overall sulfur reduct- ion of about 50 percent. Delayed Coking The original 1957 concept of the coal deashing process was to prepare a coal solution which, after filtration for removal of its ash, sulfur and other contaminants, would be charged to the conventional Lummui delayed petroleum coking process. The coke drum vapor would pass to the combination fractionation tower for separation of gas and light and medium distillate from a tower bottom cycle oil which would be re-used for fresh coal solution. The bench and pilot coking of the deashed coal Solution proved to be almost routine. This charge stock resembled in many of its characteristics a low temperature carbonization pitch. Lummus had previously in bench scale and pilot plant delayed coking apparatus successfully coked both low and high temperature carbon- ization pitches as well as Gilaonite and Athabasca tar sand pitches. n
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- Page 370 and 371: 369 ' i 1. REFERENCES Berber, John
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- Page 394 and 395: TABLE 4 390 DELAYED COKING OF DEASH
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- Page 406 and 407: 402 HYDROGEN CYANIDE PRODUCED FROM
- Page 408 and 409: 404 Before startup, the system is p
- Page 410 and 411: 4 OL. ' , I. . TesCs. With.Coals .o
- Page 412 and 413: Table 3.- Product Gas Analyses and
- Page 414 and 415: 410 BIBLIOGRAPHY 1. American Public
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- Page 420 and 421: 0. E c .4 7 .. .c . I ( - Low tempe
- Page 422 and 423: 418 cual. A mjor aa\;antage or' the
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- Page 426 and 427: 422 Table 3. Room-texperature M'dss
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- Page 430 and 431: Table 4. Room-?;ergerature isomer s
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- Page 434 and 435: Brooks J.D. and Sternhell S. (1957)
383<br />
ash content <strong>of</strong> the initial high volatile bituminous coal. Thus,<br />
it has been repeatedly demonstrated in the bench and pilot solvent<br />
deashing studies on coal samples with ash contents varying from 5<br />
to 20 weight percent that final ash values <strong>of</strong> 0.1 to 0.3 could be<br />
obtained in the treated coal extracts.<br />
Lisewise , inorganic chlorides have been iargely eliminated<br />
with the ash. Coals containing 0.25 and 0.15 weight percent chlorine<br />
were reduced to values <strong>of</strong> 0.004 to 0.003, respectively. It is<br />
assumed that coals <strong>of</strong> considerably higher inorganic chloride contents<br />
could be reduced to similar low values. The harmful corrosive<br />
effects <strong>of</strong> ash and chlorides on furnace operation are well known and<br />
their effective reduction is obviously very desirable.<br />
Sulfur Reduction<br />
The degree <strong>of</strong> bituminous coal desulfurization by solvent<br />
deashing has proven to be a function <strong>of</strong> the original ratio <strong>of</strong><br />
inorganic sulfate and pyritic sulfur to the organic forms. Original<br />
total sulfur contents <strong>of</strong> 1 t o 4 percent are reduced to values <strong>of</strong><br />
0.4 to 1 weight percent in the extracts.<br />
It is known that this ratio increases with coals <strong>of</strong><br />
increasing total sulfur content, i.e., in the lower grade coals <strong>of</strong><br />
correspondingly higher ash. The final sulfur <strong>of</strong> the deashed coal<br />
therefore relates to the original organic sulfur which is only<br />
partially removed in the process, whereas the inorganic sulfur is<br />
removed substantially quantitatively.<br />
Thus, in Table 1, complete elimination <strong>of</strong> the pyritic<br />
and sulfate sulfurs has been achieved with an accompanying 26<br />
percent reduction in organic sulfur, for an overall sulfur reduct-<br />
ion <strong>of</strong> about 50 percent.<br />
Delayed Coking<br />
The original 1957 concept <strong>of</strong> the coal deashing process<br />
was to prepare a coal solution which, after filtration for removal<br />
<strong>of</strong> its ash, sulfur and other contaminants, would be charged to the<br />
conventional Lummui delayed petroleum coking process. The coke<br />
drum vapor would pass to the combination fractionation tower for<br />
separation <strong>of</strong> gas and light and medium distillate from a tower<br />
bottom cycle oil which would be re-used for fresh coal solution.<br />
The bench and pilot coking <strong>of</strong> the deashed coal Solution<br />
proved to be almost routine. This charge stock resembled in many<br />
<strong>of</strong> its characteristics a low temperature carbonization pitch.<br />
Lummus had previously in bench scale and pilot plant delayed coking<br />
apparatus successfully coked both low and high temperature carbon-<br />
ization pitches as well as Gilaonite and Athabasca tar sand pitches.<br />
n