EP0093883A2 - Carbonaceous materials in water slurries - Google Patents
Carbonaceous materials in water slurries Download PDFInfo
- Publication number
- EP0093883A2 EP0093883A2 EP83103530A EP83103530A EP0093883A2 EP 0093883 A2 EP0093883 A2 EP 0093883A2 EP 83103530 A EP83103530 A EP 83103530A EP 83103530 A EP83103530 A EP 83103530A EP 0093883 A2 EP0093883 A2 EP 0093883A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- water
- condensate
- ammonium
- carbonaceous materials
- composition
- 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- Withdrawn
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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
- C10L1/00—Liquid carbonaceous fuels
- C10L1/32—Liquid carbonaceous fuels consisting of coal-oil suspensions or aqueous emulsions or oil emulsions
- C10L1/326—Coal-water suspensions
Definitions
- This invention relates to carbonaceous materials in water slurries and more particularly to coal in water slurries stabilized with ammonium salts of naphthalenesulfonic acid formaldehyde condensates.
- Transport is one of the major problems involved in use of particulate carbonaceous materials such as coal.
- One method of transport involves aqueous slurries.
- aqueous slurries of finely ground coal containing over 55 weight percent solids are difficult to pump with slurry pumps. This is because as the solids level is increased above 50 weight percent, water and solids tend to separate causing coal particles to build up in various areas in the pumping system. This dewatering of the slurry causes blockage and jamming in the pumping system.
- Stabilized carbonaceous materials in water slurries having reduced viscosity and improved pumpability are obtained by having present an ammonium salt of naphthalenesulfonic acid formaldehyde condensate as a stabilizer, the ammonium condensate being present in an amount sufficient to reduce viscosity of the aqueous carbonaceous slurry and to improve its pumpability.
- ammonium condensate for convenience, is present in the slurry in amounts sufficient to reduce viscosity of the slurry and improve its pumpability.
- Concentration of the ammonium condensate added can be up to 10% by weight, preferably from about 0.01% by weight to about 5.0% by weight.
- from about 0.05% by weight to about 0.5% by weight of the ammonium condensate, based on the total weight of the slurry, i.e., solids plus water, can be used.
- Amount of the ammonium condensate is easily determined by introducing the condensate in an amount sufficient to form a soft sediment.
- the resulting slurries will generally have from about 50 to about 80% by weight solids or higher with the balance being water.
- Ammonium salts of naphthalenesulfonic acid formaldehyde condensates have the following advantages over sodium or other metal salts of these condensates:
- Ammonium condensates are introduced into slurries at any convenient point during their preparation.
- carbonaceous materials encompasses solid particulate carbonaceous fossil fuel materials which may have been powdered or pulverized to a size where at least 80% will pass through a 200 mesh screen (U.S. Series).
- Useful carbonaceous materials include bituminous and anthracite coals, coke, petroleum coke, lignite, charcoal, peat, admixtures thereof and the like. These materials are crushed and milled to obtain finely divided particles suitable for use in pumpable water slurries.
- Water used in slurries may be taken from any available source such as mine, well, river, or lake water or desalinated ocean water having a sufficiently low mineral salt content such that the electrochemistry of the bound water layer and carrier water interface can be controlled and corrosion of milling facilities, pipelines and furnaces will be minimized and controllable.
- ammonium salt of naphthalenesulfonic acid formaldehyde condensate may be prepared by reacting naphthalene with formaldehyde and sulfuric acid and ultimately treating with ammonium hydroxide.
- Useful processes are described in U.S. Patent No. 2,141,569 - Tucker et al - December 27, 1938; U.S. Patent No. 3,193,575 - Nebel et al - July 6, 1965 and U.S. Patent No. 3,277,162 - Johnson - October 4, 1966.
- a naphthalenesulfonic acid formaldehyde condensate is a mixture of condensation products of naphthalenesulfonic acid and formaldehyde. It can be chromatographed by size exclusion chromatography through a column containing pore sizes which selectively separate molecular volumes according to size. The solvent chosen for the acid in chromatography should minimize solute- packing interaction and solute-solute interaction. The chromatogram gives a true molecular volume profile when the eluents are displayed on a detector-strip chart recorder display.
- the chromatogram for a sample of the sulfonic acid used in the examples is the same as that for the sodium naphthaleneformaldehyde sulfonate in U.S. Patent No. 3,954,491 - Adrian et al - May 4, 1976, and the two anionic materials are identical. That is, the anionic materials from the sulfonic acid have the same profile as the anionic materials from the sodium naphthaleneformaldehyde sulfonate having lowest elution volumes of from about 61 to about 70% of the total elution volume and equivalent elution volumes of from about 61 to about 70% of the total elution volume.
- the additive solution used as a control was a 34% sodium condensate solution.
- the other two additive solutions were a 40% ammonium condensate solution having a pH of 6.5 and a 42.3% ammonium condensate solution having a pH of 4.0. Samples of the blank, control and ammonium condensate treated slurries were then evaluted by the procedure described above to obtain the following results:
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- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Liquid Carbonaceous Fuels (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
Abstract
Description
- This invention relates to carbonaceous materials in water slurries and more particularly to coal in water slurries stabilized with ammonium salts of naphthalenesulfonic acid formaldehyde condensates.
- Transport is one of the major problems involved in use of particulate carbonaceous materials such as coal. One method of transport involves aqueous slurries. However, aqueous slurries of finely ground coal containing over 55 weight percent solids are difficult to pump with slurry pumps. This is because as the solids level is increased above 50 weight percent, water and solids tend to separate causing coal particles to build up in various areas in the pumping system. This dewatering of the slurry causes blockage and jamming in the pumping system.
- On the other hand, decreasing the weight percent of water in aqueous coal slurries is desirable because water is a major contributor to the cost of transport and processing operations. The less water transported the greater is the volume of coal that can be moved, resulting in transport efficiencies. Further, water resources are limited. Also, during burning of coal, a significant amount of heat is required to vaporize the water. As the weight percent of water decreases, the efficiency of the coal burning process increases. Hence, use of higher weight percent solids aqueous carbonaceous slurries than were heretofore feasible would be of great importance.
- U.S. Patent No. 4,282,006 - Funk, August 4, 1981, describes a pipeline pumpable coal water slurry having a high content of coal particles with a minimum of void spaces and a maximum of particle surface area to enhance dispersing effects generated by electrolytes and/or dispersing agents added to the slurry. For dispersing agents, see Column 29, line 53 to Column 31, line 9, including condensed mononaphthalene sulfonic acid and its sodium and ammonium salts (Column 30, lines 19 and 20).
- Stabilized carbonaceous materials in water slurries having reduced viscosity and improved pumpability are obtained by having present an ammonium salt of naphthalenesulfonic acid formaldehyde condensate as a stabilizer, the ammonium condensate being present in an amount sufficient to reduce viscosity of the aqueous carbonaceous slurry and to improve its pumpability.
- The ammonium salt of naphthalenesulfonic acid formaldehyde condensate, hereinafter referred to as ammonium condensate for convenience, is present in the slurry in amounts sufficient to reduce viscosity of the slurry and improve its pumpability. Concentration of the ammonium condensate added, based on the total weight of the carbonaceous materials water slurry, can be up to 10% by weight, preferably from about 0.01% by weight to about 5.0% by weight. For example, from about 0.05% by weight to about 0.5% by weight of the ammonium condensate, based on the total weight of the slurry, i.e., solids plus water, can be used. Amount of the ammonium condensate is easily determined by introducing the condensate in an amount sufficient to form a soft sediment. The resulting slurries will generally have from about 50 to about 80% by weight solids or higher with the balance being water. Ammonium salts of naphthalenesulfonic acid formaldehyde condensates have the following advantages over sodium or other metal salts of these condensates:
- (a) Ammonium condensates do not contribute to ash or slag formation during combustion of slurry;
- (b) Ammonium condensates have improved performance as slurry stabilizers;
- (c) Solutions of ammonium condensates have lower manufacturing cost; and
- (d) Solutions of ammonium condensates have improved cold storage stability.
- Ammonium condensates are introduced into slurries at any convenient point during their preparation.
- The term "carbonaceous materials", as used herein, encompasses solid particulate carbonaceous fossil fuel materials which may have been powdered or pulverized to a size where at least 80% will pass through a 200 mesh screen (U.S. Series). Useful carbonaceous materials include bituminous and anthracite coals, coke, petroleum coke, lignite, charcoal, peat, admixtures thereof and the like. These materials are crushed and milled to obtain finely divided particles suitable for use in pumpable water slurries.
- Water used in slurries may be taken from any available source such as mine, well, river, or lake water or desalinated ocean water having a sufficiently low mineral salt content such that the electrochemistry of the bound water layer and carrier water interface can be controlled and corrosion of milling facilities, pipelines and furnaces will be minimized and controllable.
- The ammonium salt of naphthalenesulfonic acid formaldehyde condensate may be prepared by reacting naphthalene with formaldehyde and sulfuric acid and ultimately treating with ammonium hydroxide. Useful processes are described in U.S. Patent No. 2,141,569 - Tucker et al - December 27, 1938; U.S. Patent No. 3,193,575 - Nebel et al - July 6, 1965 and U.S. Patent No. 3,277,162 - Johnson - October 4, 1966.
- A naphthalenesulfonic acid formaldehyde condensate is a mixture of condensation products of naphthalenesulfonic acid and formaldehyde. It can be chromatographed by size exclusion chromatography through a column containing pore sizes which selectively separate molecular volumes according to size. The solvent chosen for the acid in chromatography should minimize solute- packing interaction and solute-solute interaction. The chromatogram gives a true molecular volume profile when the eluents are displayed on a detector-strip chart recorder display. The chromatogram for a sample of the sulfonic acid used in the examples is the same as that for the sodium naphthaleneformaldehyde sulfonate in U.S. Patent No. 3,954,491 - Adrian et al - May 4, 1976, and the two anionic materials are identical. That is, the anionic materials from the sulfonic acid have the same profile as the anionic materials from the sodium naphthaleneformaldehyde sulfonate having lowest elution volumes of from about 61 to about 70% of the total elution volume and equivalent elution volumes of from about 61 to about 70% of the total elution volume. The teachings in U.S. Patent No. 3,954,491 relating to chromatography are incorporated by reference herein. This chromatographic method was described by Dr. Harold Edelstein in a paper entitled, "Aqueous Gel Permeation Chromatograph of Some Naphthalene Sulfonic Acid Formaldehyde Condensates" presented at the Mini Symposium of the North Jersey Chromatography Group Subsection of the A.C.S. on March 6, 1978 at Hoffman La Roche Auditorium, Clifton N.J.
- The following procedure is used in the evaluation of ammonium salts of naphthalenesulfonic acid formaldehyde condensates in aqueous coal slurries in the examples given below. This procedure determines ability of these ammonium condensates to disperse or suspend coal dust uniformly in water by measuring viscosity.
-
- 8-oz. paint can
- Low shear mechanical mixer with a double blade Spatula
- Stormer viscometer
-
- Water of known record hardness
- Coal dust - Reference coal is Pittston Coal, 80% through 200 mesh (U.S. Series). Other types of coal and grind sizes can be substituted.
- Stabilizing agent
-
- 1. A slurry of coal dust in water is prepared as follows. Coal dust is slowly added to water under agitation by a low shear mechanical mixer with a double blade. Sides of the container are scraped regularly while mixing. The slurry is agitated for an additional hour to ensure uniformity. The weight % solids in the slurry is determined by difference.
- 2. Viscosity of the aqueous coal slurry is determined by weighing out 200 gram samples of the slurry into 8 oz. paint cans. A specific quantity of the ammonium condensate is added to each can under vigorous agitation. A concentration range of ammonium condensate of from 0.10 to 1 gram/200 grams is used. Each can can is closed tightly to prevent evaporation of water.
- 3. Each can is opened and each slurry is stirred with a spatula before viscosity measurements are made with a Stormer Viscometer. Weights are adjusted in order to find a reading as close as possible to 30 seconds and the correct weight for a 30-second viscosity is determined. Readings are repeated twice after stirring each time. Readings should not differ by more than 2 seconds. Readings are repeated until consistent and the average of two readings taken. Readings on slurries covering a broad concentration range of ammonium condensate are taken to the point where the ammonium condensate no longer reduces viscosity of the slurry and/or coal precipitates from the slurry.
- 4. Seconds and weight are converted into krebs units. Krebs units are then converted to centipoise readings.
- For a fuller understanding of the nature and advantages of this invention, reference may be made to the following examples. These examples are given merely to illustrate the invention and are not to be construed in a limiting sense. All quantities, proportions and percentages are by weight and all references to temperature are °C unless otherwise indicated.
- Samples of coal water slurries were treated with the quantities of solutions of sodium condensate (sodium salt of naphthalenesulfonic acid formaldehyde condensate) and ammonium condensate (ammonium salt of naphthalenesulfonic acid formaldehyde condensate) shown in the table below. The coal water slurries were 60% by weight slurries of Pittston coal dust in tap water. A sample of coal slurry on drying was found to contain 59.1% solids. Quantity in the table is the quantity of additive solution added to 200 g of coal water slurry. An untreated sample of the coal slurry was used as the blank and samples treated with sodium condensate were used as the control. The additive solution used as a control was a 34% sodium condensate solution. The other two additive solutions were a 40% ammonium condensate solution having a pH of 6.5 and a 42.3% ammonium condensate solution having a pH of 4.0. Samples of the blank, control and ammonium condensate treated slurries were then evaluted by the procedure described above to obtain the following results:
- While the invention has been described with reference to certain specific embodiments thereof, it is understood that it is not to be so limited since alterations and changes may be made therein which are within the full intended scope of the appended claims.
Claims (8)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US37741282A | 1982-05-12 | 1982-05-12 | |
US377412 | 1982-05-12 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0093883A2 true EP0093883A2 (en) | 1983-11-16 |
EP0093883A3 EP0093883A3 (en) | 1985-04-03 |
Family
ID=23489000
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP83103530A Withdrawn EP0093883A3 (en) | 1982-05-12 | 1983-04-12 | Carbonaceous materials in water slurries |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP0093883A3 (en) |
JP (1) | JPS58199032A (en) |
AU (1) | AU554665B2 (en) |
CA (1) | CA1179132A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1994001684A1 (en) * | 1992-07-06 | 1994-01-20 | Eniricerche S.P.A. | Process for recovering and causing highly viscous petroleum products to flow |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5478365A (en) * | 1986-11-13 | 1995-12-26 | Chevron U.S.A. Inc. | Heavy hydrocarbon emulsions and stable petroleum coke slurries therewith |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4330301A (en) * | 1979-07-26 | 1982-05-18 | Kao Soap Co., Ltd. | Dispersant for aqueous slurry of coal powder |
-
1982
- 1982-07-05 CA CA000406586A patent/CA1179132A/en not_active Expired
-
1983
- 1983-04-12 EP EP83103530A patent/EP0093883A3/en not_active Withdrawn
- 1983-04-15 AU AU13561/83A patent/AU554665B2/en not_active Ceased
- 1983-04-18 JP JP58068258A patent/JPS58199032A/en active Pending
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4330301A (en) * | 1979-07-26 | 1982-05-18 | Kao Soap Co., Ltd. | Dispersant for aqueous slurry of coal powder |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1994001684A1 (en) * | 1992-07-06 | 1994-01-20 | Eniricerche S.P.A. | Process for recovering and causing highly viscous petroleum products to flow |
US5445179A (en) * | 1992-07-06 | 1995-08-29 | Eniricerche S.P.A. | Process for recovering and causing highly viscous petroleum products to flow |
Also Published As
Publication number | Publication date |
---|---|
JPS58199032A (en) | 1983-11-19 |
AU1356183A (en) | 1983-11-17 |
AU554665B2 (en) | 1986-08-28 |
EP0093883A3 (en) | 1985-04-03 |
CA1179132A (en) | 1984-12-11 |
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Legal Events
Date | Code | Title | Description |
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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 |
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AK | Designated contracting states |
Designated state(s): AT BE CH DE FR GB IT LI LU NL SE |
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PUAL | Search report despatched |
Free format text: ORIGINAL CODE: 0009013 |
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AK | Designated contracting states |
Designated state(s): AT BE CH DE FR GB IT LI LU NL SE |
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RAP1 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: DIAMOND SHAMROCK CHEMICALS COMPANY |
|
17P | Request for examination filed |
Effective date: 19851001 |
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17Q | First examination report despatched |
Effective date: 19861106 |
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STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN |
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18D | Application deemed to be withdrawn |
Effective date: 19870317 |
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RIN1 | Information on inventor provided before grant (corrected) |
Inventor name: VILLA, JOSE L. |