CA1113244A - Single stage process for flashing to produce improved carbonaceous fuel and condensed liquids - Google Patents
Single stage process for flashing to produce improved carbonaceous fuel and condensed liquidsInfo
- Publication number
- CA1113244A CA1113244A CA336,213A CA336213A CA1113244A CA 1113244 A CA1113244 A CA 1113244A CA 336213 A CA336213 A CA 336213A CA 1113244 A CA1113244 A CA 1113244A
- Authority
- CA
- Canada
- Prior art keywords
- alcohol
- flashing
- vapors
- fluid material
- coal
- 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
Links
- 239000000446 fuel Substances 0.000 title claims abstract description 20
- 238000000034 method Methods 0.000 title claims abstract description 20
- 239000007788 liquid Substances 0.000 title claims description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 44
- 239000007787 solid Substances 0.000 claims abstract description 23
- 230000000694 effects Effects 0.000 claims abstract description 4
- 239000000463 material Substances 0.000 claims description 26
- 239000012530 fluid Substances 0.000 claims description 23
- 238000010438 heat treatment Methods 0.000 claims description 17
- 239000002245 particle Substances 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 8
- 239000011236 particulate material Substances 0.000 claims description 7
- 230000008016 vaporization Effects 0.000 claims description 7
- 239000006227 byproduct Substances 0.000 claims description 6
- 230000035699 permeability Effects 0.000 claims description 6
- 238000009834 vaporization Methods 0.000 claims description 6
- 238000009833 condensation Methods 0.000 claims description 4
- 230000005494 condensation Effects 0.000 claims description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
- 238000005086 pumping Methods 0.000 claims description 3
- 229910052717 sulfur Inorganic materials 0.000 claims description 3
- 239000011593 sulfur Substances 0.000 claims description 3
- YZCKVEUIGOORGS-UHFFFAOYSA-N Hydrogen atom Chemical compound [H] YZCKVEUIGOORGS-UHFFFAOYSA-N 0.000 claims description 2
- 229940000425 combination drug Drugs 0.000 claims 1
- 239000003245 coal Substances 0.000 abstract description 32
- 239000002002 slurry Substances 0.000 abstract description 7
- 239000003575 carbonaceous material Substances 0.000 abstract description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 8
- 229910052799 carbon Inorganic materials 0.000 description 8
- 238000000926 separation method Methods 0.000 description 6
- 150000001298 alcohols Chemical class 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 229930195733 hydrocarbon Natural products 0.000 description 5
- 150000002430 hydrocarbons Chemical class 0.000 description 5
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 238000001311 chemical methods and process Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 239000011261 inert gas Substances 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 239000003077 lignite Substances 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 125000001741 organic sulfur group Chemical group 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 239000011343 solid material Substances 0.000 description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- RHZUVFJBSILHOK-UHFFFAOYSA-N anthracen-1-ylmethanolate Chemical compound C1=CC=C2C=C3C(C[O-])=CC=CC3=CC2=C1 RHZUVFJBSILHOK-UHFFFAOYSA-N 0.000 description 1
- 239000003830 anthracite Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 238000005112 continuous flow technique Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000013467 fragmentation Methods 0.000 description 1
- 238000006062 fragmentation reaction Methods 0.000 description 1
- 239000011344 liquid material Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- -1 paraffins Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 230000003334 potential effect Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Landscapes
- Solid Fuels And Fuel-Associated Substances (AREA)
Abstract
ABSTRACT
A method of producing dry, pulverulent, low-density, high-poros-ity, high-permeability, highly-reactive carbonaceous fuel from slurries of coal and alcohol or stabilized suspensoids of coal and alcohol by single stage flashing. The slurries or suspensoids are heated under pressure to a temperature sufficient to effect single stage flashing of substantially all of the alcohol. The product resulting from flashing then is separated into vapors and solid particulate carbonaceous material. The vapors are con-densed into alcohol for reuse and the particulate carbonaceous material is processed further or used as desired.
A method of producing dry, pulverulent, low-density, high-poros-ity, high-permeability, highly-reactive carbonaceous fuel from slurries of coal and alcohol or stabilized suspensoids of coal and alcohol by single stage flashing. The slurries or suspensoids are heated under pressure to a temperature sufficient to effect single stage flashing of substantially all of the alcohol. The product resulting from flashing then is separated into vapors and solid particulate carbonaceous material. The vapors are con-densed into alcohol for reuse and the particulate carbonaceous material is processed further or used as desired.
Description
Z~
Specification Method Of Producing Pulverulent Carbonaceous Fuel This application is related to United States Patent No. 4,146,366, filed November 22, 1977.
Field of the Invention This invention relates to a process of separating coal particles from alcohol by single stage flashing.
Description of the Prior Art United States Patent No. 4,030,893 refers to my United States Patent No. 4,045,092 which discloses and claims a stabilized pseudo-thixotropic suspensoid of coal and alcohol which is employed to solve the problem of transporting coal through a pipeline. The coal and alcohol suspensoid also is described in the newsletter, Energy Studies, published by the Center for Energy Studies, at the University of Texas at Austin, Volume 3, No. 2, November - December 1977.
From an economical standpoint it is desirable to ~-separate the transported coal from the alcohol carrier and use only the coal as a fuel. Prom a practical standpoint, the separation process must be an economical one whlch allows separation of large quantitles of materials.
United States Patent No. 4,030,893 discloses a separation process called "flash mg" which is well known in the prior art. Basically the flashing process consist of ; dropping the pressure of a heated liquid to a sufficiently ; low pressure so that a portion of the liquid spontaneously ;
- -, ~ .. , . . ~ .. -. ,-: , ' .
.- - . . .
:
... , . . . , : . .
. : . . . -~.~13Z44 vaporizes) therefore effecting a drop in temperature which stabilizes the remaining liquid at its saturation pressure condition imposed by the process.
Only a relatively small percentage of the liquid phase material may be converted to vapor in conventional flashing. Therefore, in order to convert most, or perhaps all, of a mass of liquid to vapor, several sequential cycles of liquid pressurizing, heating, then pressure reduction, followed by removal of the vaporized portion must be performed.
Such a process requiring a number of sequential cycles is not economi-cal for separating the coal from the alcohol carrier particularly when large quantities of material are involved which would be the case in the pipeline transportation of the material.
SUMMARY OF THE INVENTION
It is an object of the present invention to economically separate coal or other carbonaceous fuel from alcohol by a single stage flashing process.
It is a further object of the present invention to produce a dry, highly-reactive, pulverulent particulate fuel of low density, high porosity, and high permeability from the single stage flashing process.
The present invention provides a method of producing dry, pulverulent, highly-reactive particulate fuel of low density, high porosity, and high permeability from a fluid material comprising carbonaceous fual particles and alcohol, comprising the steps of: pressurizing said fluid material to a level sufficient to prevent vaporization of liquids or solids during heating, heating said pressurized material under pressure to a temperature sufficient to effect single stage flashing of substantially all of the alcohol, passing said heated fluid material to expansion means to reduce the pressure rapidly to initiate flashing and vaporization of substantially all of the alcohol in said fluid ~; material as well as other volitized materials, passing the resulting solid particulate material and vapor mixture from said expansion means to a gas-.
solids separator means, heated to prevent condensation of vapors, to separate the vapors from the solid particulate material, and removing the separated vapors and solid particulate material from said separator.
BRIEF DESCRIPTION OF DRAWINGS
The Figure shown is a flow diagram of the present invention.
::
;~
~: :
- 2a -.. . ... . . . . . . . . . . . .
:: , : . : , . ;, ~3Z44 Description of the Preferred Embodiments The coal that is employed in this invention may be any of the com-mercially available coals, ranging from the relatively pure and high carbon content anthracite coal through the bituminous coals to and including the less desirable soft coals, lignite and the like.
For transportation through a pipeline, the coal is crushed, pul-verized, and worked in the presence of alcohol to form the suspensoid of coal in alcohol as described in United States Patent No. 4,045,092 men-tioned above, and in the newsletter, Energy Studies, also mentioned above.
The suspensoid may be described as a mechanically stabilized pseudo-thixo-tropic suspensoid of particulate carbon-hydrocarbon particles derived from coal or other carbonaceous materials suspended in alcohol as a base fluid or carrier and suspended in a ratio of solids to liquids that essentially precludes the possibility of settling. Pipeline transportation of coal-alcohol as a suspensoid is economical, since it takes less energy per unit of fuel to pump the suspensoid and ln addition two-thirds of the material by weight is carbon.
The alcohol employed for forming the suspensoid preferab;ly is a methyl fuel which is a mixture of crude alcohols predominantly methanol and which may include smaller amounts of ethanol, n-propanol or iso-butanol.
These alcohols all include one to four carbon atoms. If the coal is to be used for chemical processes, gassification, or as a dried combustion fuel which is either burned by itself or mixed with other hydro-carbon fuels, the coal particles in alcohol will be of a size range predominantly from 10 to 100 microns.
Referring now to the drawing, there will be .
. ~
, . .
. , :.............................................. : :. .
.: . . . . ~: , . .
. . - . . . . .
,: ~ . . ~ : ~ .-~3~:~4 described the method of the present invention for separa~ing the coal from the alcohol carrier. Ref erence numeral 21 depicts a pipeline, in which the sus-pensoid of coal particles in alcoh~l is transp~rted from a distant location, or a storage facility where the fluid suspensoid is stored after being transported from the distant location through a pipeline. From the facility 21, the suspensoid is pumped continuously by pumping means 23 to a heating means 25. The pumping means provides high pressures and high volume capacity flow rates for the fluid. The pressures employed are sufficient to prevent vaporization during heating and may be from a few hundred pounds per square inch, to over -~
1000 pounds per square inch, depending on the nature of the volatilizable materials in the fluids. From the heating means 25, the heated fluid is flowed to a controllable pressure reduction device 27 to maintain back-pressure on the heating means and to instantaneously drop the pressure exiting the device 27 to near-atmos-pheric pressure to allow flashing to vapor. The out-put of the pressure-reduction device 27 comprises a mixture of saturated dry vapor and dry solids. This output mixture is flowed to a gas/solids separator device 29, heated to prevent condensation of vapors, to remove the particulate solids from the gas stream either as a single product or divided by settling vel-ocity separation into various particle-size fractions which may be defined for example, as fine, medium and coarse. From the separator 29 the solids are collected in hoppers intergral with the separator and purged of alcohol vapors by hot inert gas, then removed to stor-age means 31 for storage under inert gas i.e. CO2 or N2. The separated vapors are applied to sequential condensers 33, 35, and 37 as will be described subse-quently.
' ' ,.
. . . ~ , :
~ ; . .
,. ; .
:
.
3;~44 In the heating means 25 the fluid suspensoid is heated to a temperature sufficient to allow single stage flashing to take place in the pressure-reduction device 27. For this to occur, the fluid suspensoid must be heated to a temperature of at least about 200 F
above the original fluid temperature and which is app-roximately the mini~lum for complete vaporization of the alcohols. By dropping the pressure rapidly from sev-eral hundred pounds per square inch (to over one thousand pounds per square inch) down to atmospheric pressure, the enthalpy that has been put into the carbon mater-ial by heating is sufficient, in addition to the heat energy that is in the alcohol, to effect total flashing to complete dry vapor of substantially 100% of the alcohol in single stage flashing. Thus separation of th coal particles from the vapors by way of the separator 29 is economical since sequential cycles are not required and separation can be carried out in a continuous flow process.
In the heating means 25, the fluid suspensoid may be heated to temperatures above the minimum required for single stage flashing to occur, for example up to 600 F to 800F above ambient or higher for the purpose of vaporizing and recovering valuable by-products or for the purpose of recovering organic compounds from th~ coal. As the temperature of the suspensoid is increased, more by-products can be recovered from the materials that are contained within the coal structure other than alcohol and which are volitizable such as waxes, paraffins, resins, etc. At about 700 F to 800 F
above ambient the alcohol will begin breaking down into atomic hydrogen and carbon monoxide. When this happens, the hydrogen will attack those chemicals present from which it has the greatest affinity or greatest poten-tial for chemical reactlon. For example, atomic . .. ..
,...
~., _ ... . _.
,:
:
hydrogen will combine with organic sulfur to remove it from practically any other compound. Not only the organic sulfur will be removed but also some of the inorganic sulfur will be removed.
The heating preferably i5 done in a mono-tube or parallel-tube heat exchanger in which sufficient fluid velocity is maintained to insure good heating transfer rates, and turbulence is introduced, or effected, to provide uniform heating of the fluid, both the liquid materials and the solid materials. Sufficient retention time is provided to allow heating throughout the individual particles of solid material. This is desired for providing the energy required for vaporiæing, pre-ssuring, and removing the volitizable materials from within the particles and for effecting increased porosity and permeability and also for effecting further comm-inution by fragmentation during the next phase of pro-cessing which is the pressure reduction. The pressure reduction device 27 may be either an adjustable venturi restriction, or an expansion motor, or some other flow-restricting device to drop the pressure and intiate flashing and evaporation. The separator 29 is a gas~
solids separator such as a bag house, cyclonic separator, multiclone cyclonic separator, etc.
As mentioned above, the product resulting from flashing will be a mixture of saturated dry vapor and dry solid. The solids resulting from the flashing and which are separated by the separator are of a different nature than the crushed and pulverized carbon worked with the alcohol to form suspensoid. In this respect, the flashing ~ffects the surface texture, the internal pore space, the internal surface area, and the permeability of the particles and this results in the production of dry, pulverulent, low-density, high porosity, high permeability, high-reactivity particles.
The resulting separated solids can be used as fuels, .
"' ' `""'~' ' `' ';
. , . ~ : . . . .
.
Z4~
as feed stock for gasslfication, for chemical processes or for mixture with other hydrocarbon fuels such as diesel fuel. From the separator, the solids may be separated into different grades of sizes depending upon the usage desired.
The vapors from the separator are applied to the `
sequential condensers 33, 35 and 37 which are commer-cially available condensers which gradually drop the temperature for sequential condensation. The first stage condenser removes water or if any is present, hydrocarbons and by-products.chemicals which condense at the 180 F to 220 F range and most of the particulate carbon which is not removed by the separator 29. The second stage, or intermediate, condenser 35 removes the alcohols and lower boiling-temperature hydrocarbons, and also some by-product chemical compounds, depending on the nature of the coal or lignite source. It is desirable to recover all of the alcohols since they are more costly than the other matert~ls and can be used at the destination location for commercial purposes or sent back to the distant location by way of a second pipeline to be used again as a carrier for transporting the coal from the distant location to - the final destination point. The last stage condenser 37 may strip any low-boiling hydrocarbons and traces of alcohol and may be operated lower than ambient tempera-ture or at elevated pressure (both) if found feasible for some materials. From the condenser 37 the non-condensible gas is pumped out and exhausted to the atmosphere. These gases may be treated to remove con-taminants if required or necessary. They may also be burned as an additive fuel, if high enough in fuel value.
Although the preferred embodiment has been described , . .. ... .
~i ...... -.-- -- , . .
' ..................... . ~ ~ '`
~' ~
. : :
, ~3Z4~
as a process for single stage flashing of a stable sus-pensoid of coal particles and alcohol, it is to be understood that the process could be employed ~or single stage flashing of a slurry comprising a mixture of coal particles and alcohol of the same type as mentiond above. The temperature at which the slurry of coal and alcohol would be heated for single stage flashing may be slightly higher than that of the stable suspen-soid of coal and alcohol because of the difference of specific heat in the carbon and alcohol. In this respect, the carbon has a specific heat of approximately .2 while that of alcohol is about .6. The specific heat of the stable suspensoid of carbon and alcohol is about .33 since it is about two-thirds of carbon in weight.
A slurry cannot be efectively handled at a ratio of more than about 50% solids to liquid. Thus the specific heat for the coal alcohol slurry would be slightly higher than that of the stable suspensoid of coal and alcohol and would require a somewhat higher temperature for flashing.
The slurry may be formed specifically for flashing in order to remove the undesirable by-products from the coal in order to produce a clear burning high quality fuel. Similarly the stable suspensoid of coal and alcohol may be also formed specifically for flashing purposes in order to remove the undesirable by-pr~ducts for the purpose of producing a-clean burning high quality fuel.
While first, second and third stages of flashing have been described hereinbefore, any number of stages of flashing can be employed as desired for separating constituents.
Having thus described the invention, it will be understood that such description has been given by way of illustration and e~ample and not by way of limitation, reference for the latter purpose being had to the appended ~, claims.
.
. . . . . ~ ~
Specification Method Of Producing Pulverulent Carbonaceous Fuel This application is related to United States Patent No. 4,146,366, filed November 22, 1977.
Field of the Invention This invention relates to a process of separating coal particles from alcohol by single stage flashing.
Description of the Prior Art United States Patent No. 4,030,893 refers to my United States Patent No. 4,045,092 which discloses and claims a stabilized pseudo-thixotropic suspensoid of coal and alcohol which is employed to solve the problem of transporting coal through a pipeline. The coal and alcohol suspensoid also is described in the newsletter, Energy Studies, published by the Center for Energy Studies, at the University of Texas at Austin, Volume 3, No. 2, November - December 1977.
From an economical standpoint it is desirable to ~-separate the transported coal from the alcohol carrier and use only the coal as a fuel. Prom a practical standpoint, the separation process must be an economical one whlch allows separation of large quantitles of materials.
United States Patent No. 4,030,893 discloses a separation process called "flash mg" which is well known in the prior art. Basically the flashing process consist of ; dropping the pressure of a heated liquid to a sufficiently ; low pressure so that a portion of the liquid spontaneously ;
- -, ~ .. , . . ~ .. -. ,-: , ' .
.- - . . .
:
... , . . . , : . .
. : . . . -~.~13Z44 vaporizes) therefore effecting a drop in temperature which stabilizes the remaining liquid at its saturation pressure condition imposed by the process.
Only a relatively small percentage of the liquid phase material may be converted to vapor in conventional flashing. Therefore, in order to convert most, or perhaps all, of a mass of liquid to vapor, several sequential cycles of liquid pressurizing, heating, then pressure reduction, followed by removal of the vaporized portion must be performed.
Such a process requiring a number of sequential cycles is not economi-cal for separating the coal from the alcohol carrier particularly when large quantities of material are involved which would be the case in the pipeline transportation of the material.
SUMMARY OF THE INVENTION
It is an object of the present invention to economically separate coal or other carbonaceous fuel from alcohol by a single stage flashing process.
It is a further object of the present invention to produce a dry, highly-reactive, pulverulent particulate fuel of low density, high porosity, and high permeability from the single stage flashing process.
The present invention provides a method of producing dry, pulverulent, highly-reactive particulate fuel of low density, high porosity, and high permeability from a fluid material comprising carbonaceous fual particles and alcohol, comprising the steps of: pressurizing said fluid material to a level sufficient to prevent vaporization of liquids or solids during heating, heating said pressurized material under pressure to a temperature sufficient to effect single stage flashing of substantially all of the alcohol, passing said heated fluid material to expansion means to reduce the pressure rapidly to initiate flashing and vaporization of substantially all of the alcohol in said fluid ~; material as well as other volitized materials, passing the resulting solid particulate material and vapor mixture from said expansion means to a gas-.
solids separator means, heated to prevent condensation of vapors, to separate the vapors from the solid particulate material, and removing the separated vapors and solid particulate material from said separator.
BRIEF DESCRIPTION OF DRAWINGS
The Figure shown is a flow diagram of the present invention.
::
;~
~: :
- 2a -.. . ... . . . . . . . . . . . .
:: , : . : , . ;, ~3Z44 Description of the Preferred Embodiments The coal that is employed in this invention may be any of the com-mercially available coals, ranging from the relatively pure and high carbon content anthracite coal through the bituminous coals to and including the less desirable soft coals, lignite and the like.
For transportation through a pipeline, the coal is crushed, pul-verized, and worked in the presence of alcohol to form the suspensoid of coal in alcohol as described in United States Patent No. 4,045,092 men-tioned above, and in the newsletter, Energy Studies, also mentioned above.
The suspensoid may be described as a mechanically stabilized pseudo-thixo-tropic suspensoid of particulate carbon-hydrocarbon particles derived from coal or other carbonaceous materials suspended in alcohol as a base fluid or carrier and suspended in a ratio of solids to liquids that essentially precludes the possibility of settling. Pipeline transportation of coal-alcohol as a suspensoid is economical, since it takes less energy per unit of fuel to pump the suspensoid and ln addition two-thirds of the material by weight is carbon.
The alcohol employed for forming the suspensoid preferab;ly is a methyl fuel which is a mixture of crude alcohols predominantly methanol and which may include smaller amounts of ethanol, n-propanol or iso-butanol.
These alcohols all include one to four carbon atoms. If the coal is to be used for chemical processes, gassification, or as a dried combustion fuel which is either burned by itself or mixed with other hydro-carbon fuels, the coal particles in alcohol will be of a size range predominantly from 10 to 100 microns.
Referring now to the drawing, there will be .
. ~
, . .
. , :.............................................. : :. .
.: . . . . ~: , . .
. . - . . . . .
,: ~ . . ~ : ~ .-~3~:~4 described the method of the present invention for separa~ing the coal from the alcohol carrier. Ref erence numeral 21 depicts a pipeline, in which the sus-pensoid of coal particles in alcoh~l is transp~rted from a distant location, or a storage facility where the fluid suspensoid is stored after being transported from the distant location through a pipeline. From the facility 21, the suspensoid is pumped continuously by pumping means 23 to a heating means 25. The pumping means provides high pressures and high volume capacity flow rates for the fluid. The pressures employed are sufficient to prevent vaporization during heating and may be from a few hundred pounds per square inch, to over -~
1000 pounds per square inch, depending on the nature of the volatilizable materials in the fluids. From the heating means 25, the heated fluid is flowed to a controllable pressure reduction device 27 to maintain back-pressure on the heating means and to instantaneously drop the pressure exiting the device 27 to near-atmos-pheric pressure to allow flashing to vapor. The out-put of the pressure-reduction device 27 comprises a mixture of saturated dry vapor and dry solids. This output mixture is flowed to a gas/solids separator device 29, heated to prevent condensation of vapors, to remove the particulate solids from the gas stream either as a single product or divided by settling vel-ocity separation into various particle-size fractions which may be defined for example, as fine, medium and coarse. From the separator 29 the solids are collected in hoppers intergral with the separator and purged of alcohol vapors by hot inert gas, then removed to stor-age means 31 for storage under inert gas i.e. CO2 or N2. The separated vapors are applied to sequential condensers 33, 35, and 37 as will be described subse-quently.
' ' ,.
. . . ~ , :
~ ; . .
,. ; .
:
.
3;~44 In the heating means 25 the fluid suspensoid is heated to a temperature sufficient to allow single stage flashing to take place in the pressure-reduction device 27. For this to occur, the fluid suspensoid must be heated to a temperature of at least about 200 F
above the original fluid temperature and which is app-roximately the mini~lum for complete vaporization of the alcohols. By dropping the pressure rapidly from sev-eral hundred pounds per square inch (to over one thousand pounds per square inch) down to atmospheric pressure, the enthalpy that has been put into the carbon mater-ial by heating is sufficient, in addition to the heat energy that is in the alcohol, to effect total flashing to complete dry vapor of substantially 100% of the alcohol in single stage flashing. Thus separation of th coal particles from the vapors by way of the separator 29 is economical since sequential cycles are not required and separation can be carried out in a continuous flow process.
In the heating means 25, the fluid suspensoid may be heated to temperatures above the minimum required for single stage flashing to occur, for example up to 600 F to 800F above ambient or higher for the purpose of vaporizing and recovering valuable by-products or for the purpose of recovering organic compounds from th~ coal. As the temperature of the suspensoid is increased, more by-products can be recovered from the materials that are contained within the coal structure other than alcohol and which are volitizable such as waxes, paraffins, resins, etc. At about 700 F to 800 F
above ambient the alcohol will begin breaking down into atomic hydrogen and carbon monoxide. When this happens, the hydrogen will attack those chemicals present from which it has the greatest affinity or greatest poten-tial for chemical reactlon. For example, atomic . .. ..
,...
~., _ ... . _.
,:
:
hydrogen will combine with organic sulfur to remove it from practically any other compound. Not only the organic sulfur will be removed but also some of the inorganic sulfur will be removed.
The heating preferably i5 done in a mono-tube or parallel-tube heat exchanger in which sufficient fluid velocity is maintained to insure good heating transfer rates, and turbulence is introduced, or effected, to provide uniform heating of the fluid, both the liquid materials and the solid materials. Sufficient retention time is provided to allow heating throughout the individual particles of solid material. This is desired for providing the energy required for vaporiæing, pre-ssuring, and removing the volitizable materials from within the particles and for effecting increased porosity and permeability and also for effecting further comm-inution by fragmentation during the next phase of pro-cessing which is the pressure reduction. The pressure reduction device 27 may be either an adjustable venturi restriction, or an expansion motor, or some other flow-restricting device to drop the pressure and intiate flashing and evaporation. The separator 29 is a gas~
solids separator such as a bag house, cyclonic separator, multiclone cyclonic separator, etc.
As mentioned above, the product resulting from flashing will be a mixture of saturated dry vapor and dry solid. The solids resulting from the flashing and which are separated by the separator are of a different nature than the crushed and pulverized carbon worked with the alcohol to form suspensoid. In this respect, the flashing ~ffects the surface texture, the internal pore space, the internal surface area, and the permeability of the particles and this results in the production of dry, pulverulent, low-density, high porosity, high permeability, high-reactivity particles.
The resulting separated solids can be used as fuels, .
"' ' `""'~' ' `' ';
. , . ~ : . . . .
.
Z4~
as feed stock for gasslfication, for chemical processes or for mixture with other hydrocarbon fuels such as diesel fuel. From the separator, the solids may be separated into different grades of sizes depending upon the usage desired.
The vapors from the separator are applied to the `
sequential condensers 33, 35 and 37 which are commer-cially available condensers which gradually drop the temperature for sequential condensation. The first stage condenser removes water or if any is present, hydrocarbons and by-products.chemicals which condense at the 180 F to 220 F range and most of the particulate carbon which is not removed by the separator 29. The second stage, or intermediate, condenser 35 removes the alcohols and lower boiling-temperature hydrocarbons, and also some by-product chemical compounds, depending on the nature of the coal or lignite source. It is desirable to recover all of the alcohols since they are more costly than the other matert~ls and can be used at the destination location for commercial purposes or sent back to the distant location by way of a second pipeline to be used again as a carrier for transporting the coal from the distant location to - the final destination point. The last stage condenser 37 may strip any low-boiling hydrocarbons and traces of alcohol and may be operated lower than ambient tempera-ture or at elevated pressure (both) if found feasible for some materials. From the condenser 37 the non-condensible gas is pumped out and exhausted to the atmosphere. These gases may be treated to remove con-taminants if required or necessary. They may also be burned as an additive fuel, if high enough in fuel value.
Although the preferred embodiment has been described , . .. ... .
~i ...... -.-- -- , . .
' ..................... . ~ ~ '`
~' ~
. : :
, ~3Z4~
as a process for single stage flashing of a stable sus-pensoid of coal particles and alcohol, it is to be understood that the process could be employed ~or single stage flashing of a slurry comprising a mixture of coal particles and alcohol of the same type as mentiond above. The temperature at which the slurry of coal and alcohol would be heated for single stage flashing may be slightly higher than that of the stable suspen-soid of coal and alcohol because of the difference of specific heat in the carbon and alcohol. In this respect, the carbon has a specific heat of approximately .2 while that of alcohol is about .6. The specific heat of the stable suspensoid of carbon and alcohol is about .33 since it is about two-thirds of carbon in weight.
A slurry cannot be efectively handled at a ratio of more than about 50% solids to liquid. Thus the specific heat for the coal alcohol slurry would be slightly higher than that of the stable suspensoid of coal and alcohol and would require a somewhat higher temperature for flashing.
The slurry may be formed specifically for flashing in order to remove the undesirable by-products from the coal in order to produce a clear burning high quality fuel. Similarly the stable suspensoid of coal and alcohol may be also formed specifically for flashing purposes in order to remove the undesirable by-pr~ducts for the purpose of producing a-clean burning high quality fuel.
While first, second and third stages of flashing have been described hereinbefore, any number of stages of flashing can be employed as desired for separating constituents.
Having thus described the invention, it will be understood that such description has been given by way of illustration and e~ample and not by way of limitation, reference for the latter purpose being had to the appended ~, claims.
.
. . . . . ~ ~
Claims (7)
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. A method of producing dry, pulverulent, highly-reactive par-ticulate fuel of low density, high porosity, and high permeability from a fluid material comprising carbonaceous fuel particles and alcohol, compris-ing the steps of:
pressurizing said fluid material to a level sufficient to pre-vent vaporization of liquids or solids during heating, heating said pressurized material under pressure to a temper-ature sufficient to effect single stage flashing of substantially all of the alcohol, passing said heated fluid material to expansion means to reduce the pressure rapidly to initiate flashing and vaporization of substantially all of the alcohol in said fluid material as well as other volitized mate-rials, passing the resulting solid particulate material and vapor mix-ture from said expansion means to a gas-solids separator means, heat to prevent condensation of vapors, to separate the vapors from the solid par-ticulate material, and removing the separated vapors and solid particulate material from said separator.
pressurizing said fluid material to a level sufficient to pre-vent vaporization of liquids or solids during heating, heating said pressurized material under pressure to a temper-ature sufficient to effect single stage flashing of substantially all of the alcohol, passing said heated fluid material to expansion means to reduce the pressure rapidly to initiate flashing and vaporization of substantially all of the alcohol in said fluid material as well as other volitized mate-rials, passing the resulting solid particulate material and vapor mix-ture from said expansion means to a gas-solids separator means, heat to prevent condensation of vapors, to separate the vapors from the solid par-ticulate material, and removing the separated vapors and solid particulate material from said separator.
2. The method of claim 1 comprising the step of condensing the separated vapors from said separator means to recover alcohol.
3. The method of claim 1 comprising the steps of passing the sep-arated vapors from said separator means to sequential condensers to remove by-product materials and alcohol.
4. The method of claim 1 comprising the steps of separating the solid particulate material into different sizes.
5. The method of claim 1 wherein said fluid material is pressurized by a pumping means which pumps said fluid material under pressure to a heating means and then to said expansion means whereby said steps are carried out continuously.
6. The method of claim 1 wherein said fluid material is heated to a temperature of at least about 200° F
above ambient temperature.
above ambient temperature.
7. The method of claim 1 wherein said fluid material is heated to a temperature sufficient to break down the alcohol into atomic hydrogen for combina-tion with sulfur for removal of sulfur from the carbonaceous fuel particles.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA336,213A CA1113244A (en) | 1979-09-24 | 1979-09-24 | Single stage process for flashing to produce improved carbonaceous fuel and condensed liquids |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA336,213A CA1113244A (en) | 1979-09-24 | 1979-09-24 | Single stage process for flashing to produce improved carbonaceous fuel and condensed liquids |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1113244A true CA1113244A (en) | 1981-12-01 |
Family
ID=4115193
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA336,213A Expired CA1113244A (en) | 1979-09-24 | 1979-09-24 | Single stage process for flashing to produce improved carbonaceous fuel and condensed liquids |
Country Status (1)
Country | Link |
---|---|
CA (1) | CA1113244A (en) |
-
1979
- 1979-09-24 CA CA336,213A patent/CA1113244A/en not_active Expired
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