EP0089766A1 - A process for making coal-water slurries and product thereof - Google Patents
A process for making coal-water slurries and product thereof Download PDFInfo
- Publication number
- EP0089766A1 EP0089766A1 EP83301195A EP83301195A EP0089766A1 EP 0089766 A1 EP0089766 A1 EP 0089766A1 EP 83301195 A EP83301195 A EP 83301195A EP 83301195 A EP83301195 A EP 83301195A EP 0089766 A1 EP0089766 A1 EP 0089766A1
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- EP
- European Patent Office
- Prior art keywords
- slurry
- coal
- mmd
- particles
- water
- 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.)
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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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- 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
-
- 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/12—Inorganic compounds
- C10L1/1283—Inorganic compounds phosphorus, arsenicum, antimonium containing compounds
-
- 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/24—Organic compounds containing sulfur, selenium and/or tellurium
- C10L1/2431—Organic compounds containing sulfur, selenium and/or tellurium sulfur bond to oxygen, e.g. sulfones, sulfoxides
- C10L1/2437—Sulfonic acids; Derivatives thereof, e.g. sulfonamides, sulfosuccinic acid esters
Definitions
- This invention relates to the production of fuel slurries of coal in water which can be injected directly into a furnace as a combustible fuel.
- a high fuel value coal-water slurry can supplant large quantities of increasingly expensive fuel oil presently being used by utilities, factories, ships and other commercial enterprises. Since the inert water vehicle reduces fuel value in terms of BTU/lb (J/kg), it is desirable to minimize its concentration for efficient use of the slurry as a fuel. High coal content also improves the combustion characteristics of the slurry.
- the slurry be loadable with finely divided coal in amounts as high, for example, as about 50% to 70% of the slurry.
- the slurry must be sufficiently fluid to be pumped and sprayed into the furnace.
- the coal particles must also be uniformly dispersed.. The fluidity and dispersion must be stably maintained during storage.
- An object of the invention is to provide an improved process for producing a slurry suitable for the purpose.
- a process for making substantially stable coal-water slurries which comprises a process for making substantially stable coal-water slurries comprising:
- fluid pourable slurries somprising up to about 70% or higher of coal stably dispersed in water are produced by admixing finely-divided coal having a critical distribution of particle sizes, water, and an organic dispersant in a high shear rate mixer.
- An inorganic buffer salt may also be added.
- fluid as used in this specification and claims means a slurry which is fluid and pourable both at rest and in motion or a slurry which gels or flocculates into a substantially non-pourable composition at rest and becomes pourably fluid with stirring or other application of relatively low shear stress.
- the particle size mixture necessary for fluidity of the highly loaded slurry comprises ultrafine (UF) particles having a maximum size of up to about 10 u MMD (mass median diameter), preferably about 1 u to 8 u MMD and larger particles hereafter defined as (F/C), having a size range of from 20 ⁇ to 200 ⁇ MMD, preferably 20 ⁇ to 150 ⁇ MMD.
- UF particles should comprise more than 30 and up to 50% by wt of the slurry.
- the actual degree of coal loading is not critical and will vary with the given use and operating equipment.
- concentration of coal successfully incorporated into a given slurry varies with such factors as the relative amounts of UF and F/C particles, size of the F/C particles used within the effective range, and the like. In general, percentage loading increases with increasing F/C size.
- An organic dispersant is essential to maintain the coal particles in stable dispersion. It has been found that the highly-loaded slurries are very sensitive to the particular type of surfactant used, especially with respect to fluidity and storage- ability.
- the dispersants which have proven to be effective in producing stable fluid mixes are high molecular weight alkaline earth metal (e. g. Ca, Mg) organosulfonates in which the organic moiety is polyfunctional. Molecular weight of the organosul- fonate is desirably about 1, 000 to 25, 000.
- the surfactant is used in minor amount, e. g. about 0. 5 to 5 pph of coal, preferably
- an inorganic, alkali metal (e. g. Na. K) buffer salt to stabilize pH of the slurry in the range of about pH5 to 8, preferably about pH 6 to 7. 5.
- the salt improves aging stability, pourability and handling characteristics of the slurry. It may be that the buffer counteracts potentially adverse effects of acid leachates from the coal.
- the salt such as sodium or potassium phosphate or carbonate, including their acid salts, is used in minor amounts sufficient to provide the desired pH, e. g. about 0.1 to 2% based on the water.
- the inorganic salts also serve to reduce gaseous sulfur pollutants by forming non-gaseous sulfur compounds.
- the ultrafine and larger F/C coal particles, water, dispersant, and inorganic salt components are mixed in a blender or other mixing device which can deliver high shear rates.
- High shear mixing e, g. at shear rates of at least about 100 sec 1 , preferably at least about 500 sec -1 , is essential for producing a stable slurry free from substantial sedimentation.
- the use of high shear mixing and the dispersant appears to have a synergistic effect.
- Dispersant with low shear mixing results in an extremely viscous, non-pourable slurry, while high shear mixing without dispersant produces a slurry which is unstable towards settling. With both dispersant and high shear mixing a fluid, pourable, stable slurry can be obtained.
- the slurries are viscous, fluid dispersion which can generally be characterized as thixotropic or Bingham fluids having a yield point.
- the slurries may gel or flocculate when at rest into substantially non-pourable compositions but are easily rendered fluid by stirring or other application of relatively low shear stress.
- The can be stored for considerable period of time without excessive settling or sedimentation.
- the slurries can be employed as fuels by injection directly into a furnace previously brought up to ignition temperature of the slurry.
- the finely divided state of the coal particles improves combustion efficency. Since the dispersants are organic compounds, they may be biodegraded with time. This can readily be prevented by addition of a small amount ofbiocides.
- the ultrafine coal particles can be made in any suitable device, such as a ball mill or attritor, which is capable of very fine comminution.
- a ball mill or attritor which is capable of very fine comminution.
- the coal . is milled with water so that the UF particles are in water slurry when introduced into the mixer.
- Some of the dispersant can be included, if desired, in the UF milling operation to improve flow and dispersion characteristics of the UF slurry.
- the required larger size coal particles (20 ⁇ to 200 u MMD) can be made from crushed coal in a comminuting device such as a hammerhill equipped with a grate having appropriately sized openings. Excessively sized coal residue can be used for making the UF particles.
- coal concentrations as used in the specification and in the following examples is on a dried coal basis which normally equals 98. 5% by weight of bone dried coal.
- Sedimentation measurement which is based on Stoke's Law giving the relationship between particle size and settling velocity, was used experimentally in all cases to determine sub-sieve particle sizes.
- the particular sedimentation technique employed is one conventially known as centrifugal sedimentation.
- the sedimentometer used was the MSAParticle Size Analyzer (C. F. Casello & Co Regent House, Britania Walk, London NI).
- centrifugal sedimentation the local acceleration due to.gravity g, is multiplied by w 2 r/g where w is rotational velocity and r is radius of rotation.
- the "two layer” method was used in the experimental procedures. All of the coal powder is initially concentrated in a thin layer floating on top of the suspending water fluid in a centrifuge tube.
- the amount of sedimenting powder is measured as a function of time at a specified distance from the surface of the fluid.
- the cumulative size distribution was determined by plotting the fractional weights settled out . against the free-falling Stoke's diameter.
- crushed coal 50% by wt, crushed coal, 1% calcium lignosulfonate (Marasperse C-21) and 49% water were ball milled for 2 hours to give ultrafine 3. 6 ⁇ MMD coal particles.
- Crushed coal was comminuted in a hammer mill at 3, 450 rpm with a 27 HB grate to give a 110 u MMD coal particulate product.
- a 65% coal slurry comprising 32. 5% 3. 6 u MMD and 32. 5% 110 ⁇ MMD coal particles by wt of the slurry, 0. 65% Marasperse C-21, and 34. 35% water, was prepared in a high speed blender at 6000 RPM (shear rate approximately 1000 sec -1 ).
- the resulting slurry was a soft thixotropic gel with a yield point of 49 dynes/cm 2 . With light stirring to overcome the yield point, the slurry was fluid and pourable. It had a Brookfield - viscosity of 1,440 cp at 60 RPM. After 14 days the slurry was still substantially uniformly dispersed. It had a slight supernatant, was free of hard-packed sediment, and could easily be stirred to uniformity and pourability.
- the 3.6 ⁇ MMD ultrafine coal component was made in accordance with Example 1, except that 1% Lomar UDG, a calcium napthalene sulfonate containing 11. 5% Ca as CaS0 4 , was substituted for the Marasperse C-21.
- a 110 ⁇ MMD coal component was prepared as in Example 2.
- a 65% coal slurry comprising 32, 5% 3. 6 ⁇ MMD and 32. 5% 110 ⁇ MMD coal particles by wt of the slurry, 0, 65% Lomar UDG, and 34. 35% water, was prepared in a high speed blender at 6000 RPM.
- the resulting slurry was a soft thixotropic gel with a yield point of 30 dynes/cm 2 . With light stirring to overcome the yield point, the slurry was fluid and pourable. It had a Brook- . field viscosity of 1, 915 cp at 60 RPM. After 14 days, the slurry was free of hard-packed sediment, and could easily be stirred to uniformity and pourability.
- the ultrafine 3. 6 ⁇ MMD coal component was prepared by mixing 60 wt% coal with 0,6% Marasperse C-21, 0.28% Na2HPO 4 , and 39,12% water and ball milling for 2 hours as in Example 1.
- the phosphate buffer salt was included to facilitate the grinding.
- a 110 ⁇ MMD coal fraction was-prepared by hammer-milling as in Example 1.
- a 65% coal slurry comprising 50% 3. 6 ⁇ MMD and 15% 110 ⁇ MMD coal particles by wt of the slurry, Marasperse C-21 0. 65%, 0,23% Na 2 HPO 4 , and 34.12% water was prepared in a high speed blender at 6000 RPM.
- the resulting slurry was a unifomly dispersed thixotropic gel after 5 days which became fluid and pourable with light stirring.
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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)
- Colloid Chemistry (AREA)
- Output Control And Ontrol Of Special Type Engine (AREA)
- Fuel-Injection Apparatus (AREA)
Abstract
Description
- This invention relates to the production of fuel slurries of coal in water which can be injected directly into a furnace as a combustible fuel. Such a high fuel value coal-water slurry can supplant large quantities of increasingly expensive fuel oil presently being used by utilities, factories, ships and other commercial enterprises. Since the inert water vehicle reduces fuel value in terms of BTU/lb (J/kg), it is desirable to minimize its concentration for efficient use of the slurry as a fuel. High coal content also improves the combustion characteristics of the slurry.
- It is important, therefore, that the slurry be loadable with finely divided coal in amounts as high, for example, as about 50% to 70% of the slurry. Despite such high solids loading, the slurry must be sufficiently fluid to be pumped and sprayed into the furnace. The coal particles must also be uniformly dispersed.. The fluidity and dispersion must be stably maintained during storage.
- An object of the invention is to provide an improved process for producing a slurry suitable for the purpose.
- According to the present invention there is provided a process for making substantially stable coal-water slurries which comprises a process for making substantially stable coal-water slurries comprising:
- a. Admixing:
- (i) ultrafine coal particles having a maximum size (as determined by a sedimentation technique based on Stoke's law) of 10µm MMD (Mass Median Diameter) in an amount comprising more than 30% and up to 50% by weight of the slurry,
- (ii) larger coal particles within the size range of from 20 to 200µm MMD in an amount sufficient to provide a desired total coal concentration in the slurry,
- (iii) water, and,
- (iv) a minor amount of dispersant consisting of an alkaline earth metal salt of organo-sulfonate in which the organic moiety is multi-functional, and
- b. subjecting the mixture to high shear at a rate of at least 100 sec-1.
- Thus, fluid pourable slurries somprising up to about 70% or higher of coal stably dispersed in water are produced by admixing finely-divided coal having a critical distribution of particle sizes, water, and an organic dispersant in a high shear rate mixer. An inorganic buffer salt may also be added. The term "fluid" as used in this specification and claims means a slurry which is fluid and pourable both at rest and in motion or a slurry which gels or flocculates into a substantially non-pourable composition at rest and becomes pourably fluid with stirring or other application of relatively low shear stress.
- Controlled distribution of coal particles sizes is essential for both fluidity and stability. The particle size mixture necessary for fluidity of the highly loaded slurry, comprises ultrafine (UF) particles having a maximum size of up to about 10 u MMD (mass median diameter), preferably about 1 u to 8 u MMD and larger particles hereafter defined as (F/C), having a size range of from 20µ to 200µ MMD, preferably 20µ to 150µ MMD. For stability of the slurry, the UF particles should comprise more than 30 and up to 50% by wt of the slurry.
- The actual degree of coal loading is not critical and will vary with the given use and operating equipment. The concentration of coal successfully incorporated into a given slurry varies with such factors as the relative amounts of UF and F/C particles, size of the F/C particles used within the effective range, and the like. In general, percentage loading increases with increasing F/C size. An organic dispersant is essential to maintain the coal particles in stable dispersion. It has been found that the highly-loaded slurries are very sensitive to the particular type of surfactant used, especially with respect to fluidity and storage- ability. The dispersants which have proven to be effective in producing stable fluid mixes are high molecular weight alkaline earth metal (e. g. Ca, Mg) organosulfonates in which the organic moiety is polyfunctional. Molecular weight of the organosul- fonate is desirably about 1, 000 to 25, 000. The surfactant is used in minor amount, e. g. about 0. 5 to 5 pph of coal, preferably about 1 to 2 pph.
- In some cases, particularly at higher coal loadings, it has been found desirable to add an inorganic, alkali metal (e. g. Na. K) buffer salt to stabilize pH of the slurry in the range of about pH5 to 8, preferably about pH 6 to 7. 5. The salt improves aging stability, pourability and handling characteristics of the slurry. It may be that the buffer counteracts potentially adverse effects of acid leachates from the coal. The salt, such as sodium or potassium phosphate or carbonate, including their acid salts, is used in minor amounts sufficient to provide the desired pH, e. g. about 0.1 to 2% based on the water. The inorganic salts also serve to reduce gaseous sulfur pollutants by forming non-gaseous sulfur compounds.
- The ultrafine and larger F/C coal particles, water, dispersant, and inorganic salt components are mixed in a blender or other mixing device which can deliver high shear rates. High shear mixing, e, g. at shear rates of at least about 100 sec 1, preferably at least about 500 sec-1, is essential for producing a stable slurry free from substantial sedimentation. The use of high shear mixing and the dispersant appears to have a synergistic effect. Dispersant with low shear mixing results in an extremely viscous, non-pourable slurry, while high shear mixing without dispersant produces a slurry which is unstable towards settling. With both dispersant and high shear mixing a fluid, pourable, stable slurry can be obtained.
- The slurries are viscous, fluid dispersion which can generally be characterized as thixotropic or Bingham fluids having a yield point. In some cases, the slurries may gel or flocculate when at rest into substantially non-pourable compositions but are easily rendered fluid by stirring or other application of relatively low shear stress. The can be stored for considerable period of time without excessive settling or sedimentation. The slurries can be employed as fuels by injection directly into a furnace previously brought up to ignition temperature of the slurry. The finely divided state of the coal particles improves combustion efficency. Since the dispersants are organic compounds, they may be biodegraded with time. This can readily be prevented by addition of a small amount ofbiocides.
- The ultrafine coal particles can be made in any suitable device, such as a ball mill or attritor, which is capable of very fine comminution. Preferably, though not essentially, the coal . is milled with water so that the UF particles are in water slurry when introduced into the mixer. Some of the dispersant can be included, if desired, in the UF milling operation to improve flow and dispersion characteristics of the UF slurry.
- The required larger size coal particles (20µ to 200 u MMD) can be made from crushed coal in a comminuting device such as a hammerhill equipped with a grate having appropriately sized openings. Excessively sized coal residue can be used for making the UF particles.
- The coal concentrations as used in the specification and in the following examples is on a dried coal basis which normally equals 98. 5% by weight of bone dried coal.
- 3. 6µ MMD UF particles employed in Examples were prepared in accordance with Example 1 and the UF particles were introduced -in the form of the Example 1 aqueous slurry containing a portion of the dispersant. The total amount of dispersant given in the Examples includes the portion introduced in this way.
- Sedimentation measurement, which is based on Stoke's Law giving the relationship between particle size and settling velocity, was used experimentally in all cases to determine sub-sieve particle sizes. The particular sedimentation technique employed is one conventially known as centrifugal sedimentation. The sedimentometer used was the MSAParticle Size Analyzer (C. F. Casello & Co Regent House, Britania Walk, London NI). In centrifugal sedimentation, the local acceleration due to.gravity g, is multiplied by w2 r/g where w is rotational velocity and r is radius of rotation. The "two layer" method was used in the experimental procedures. All of the coal powder is initially concentrated in a thin layer floating on top of the suspending water fluid in a centrifuge tube. The amount of sedimenting powder is measured as a function of time at a specified distance from the surface of the fluid. The cumulative size distribution was determined by plotting the fractional weights settled out . against the free-falling Stoke's diameter. Thus sub-sieve particle sizes disclosed and claimed herein were obtained by sedimentation measurement.
- 50% by wt, crushed coal, 1% calcium lignosulfonate (Marasperse C-21) and 49% water were ball milled for 2 hours to give ultrafine 3. 6µ MMD coal particles. Crushed coal was comminuted in a hammer mill at 3, 450 rpm with a 27 HB grate to give a 110 u MMD coal particulate product.
- A 65% coal slurry comprising 32. 5% 3. 6 u MMD and 32. 5% 110 µ MMD coal particles by wt of the slurry, 0. 65% Marasperse C-21, and 34. 35% water, was prepared in a high speed blender at 6000 RPM (shear rate approximately 1000 sec-1). The resulting slurry was a soft thixotropic gel with a yield point of 49 dynes/cm2. With light stirring to overcome the yield point, the slurry was fluid and pourable. It had a Brookfield - viscosity of 1,440 cp at 60 RPM. After 14 days the slurry was still substantially uniformly dispersed. It had a slight supernatant, was free of hard-packed sediment, and could easily be stirred to uniformity and pourability.
- The 3.6µ MMD ultrafine coal component was made in accordance with Example 1, except that 1% Lomar UDG, a calcium napthalene sulfonate containing 11. 5% Ca as CaS04, was substituted for the Marasperse C-21. A 110 µ MMD coal component was prepared as in Example 2.
- A 65% coal slurry, comprising 32, 5% 3. 6 µ MMD and 32. 5% 110 µ MMD coal particles by wt of the slurry, 0, 65% Lomar UDG, and 34. 35% water, was prepared in a high speed blender at 6000 RPM. The resulting slurry was a soft thixotropic gel with a yield point of 30 dynes/cm2. With light stirring to overcome the yield point, the slurry was fluid and pourable. It had a Brook- . field viscosity of 1, 915 cp at 60 RPM. After 14 days, the slurry was free of hard-packed sediment, and could easily be stirred to uniformity and pourability.
- The ultrafine 3. 6 µ MMD coal component was prepared by mixing 60 wt% coal with 0,6% Marasperse C-21, 0.28% Na2HPO4, and 39,12% water and ball milling for 2 hours as in Example 1. The phosphate buffer salt was included to facilitate the grinding. A 110 µ MMD coal fraction was-prepared by hammer-milling as in Example 1.
- A 65% coal slurry comprising 50% 3. 6 µ MMD and 15% 110 µ MMD coal particles by wt of the slurry, Marasperse C-21 0. 65%, 0,23% Na2HPO4, and 34.12% water was prepared in a high speed blender at 6000 RPM. The resulting slurry was a unifomly dispersed thixotropic gel after 5 days which became fluid and pourable with light stirring.
-
Claims (12)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/360,523 US4465495A (en) | 1980-10-17 | 1982-03-22 | Process for making coal-water fuel slurries and product thereof |
| US360523 | 1982-03-22 | ||
| AU11831/83A AU556291B2 (en) | 1982-03-22 | 1983-02-24 | Making fuel slurries in water |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP0089766A1 true EP0089766A1 (en) | 1983-09-28 |
| EP0089766B1 EP0089766B1 (en) | 1986-06-04 |
Family
ID=36764395
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP83301195A Expired EP0089766B1 (en) | 1982-03-22 | 1983-03-07 | A process for making coal-water slurries and product thereof |
Country Status (7)
| Country | Link |
|---|---|
| EP (1) | EP0089766B1 (en) |
| JP (1) | JPS58173193A (en) |
| AT (1) | ATE20248T1 (en) |
| AU (1) | AU556291B2 (en) |
| DE (1) | DE3363876D1 (en) |
| NZ (1) | NZ202639A (en) |
| ZA (1) | ZA831302B (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4740329A (en) * | 1984-11-20 | 1988-04-26 | Witton Chemical Company Limited | Dispersing agents for coal slurries |
| EP0281960A3 (en) * | 1987-03-12 | 1989-08-16 | Henkel Kommanditgesellschaft Auf Aktien | Dispersants ant their use in aqueous coal suspensions |
| EP0386943A1 (en) * | 1989-03-06 | 1990-09-12 | Central Research Institute Of Electric Power Industry | Process for production of coal-water mixture |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH04220494A (en) * | 1990-12-21 | 1992-08-11 | Nippon Komu Kk | Manufacture of highly concentrated coal/water slurry |
| EP1879428B1 (en) | 2006-07-14 | 2020-11-18 | WMF Group GmbH | Device to determine the temperature of a medium |
| CN106010693B (en) * | 2016-05-17 | 2018-02-27 | 陕西邦希化工有限公司 | A kind of additive of brown coal water slurry |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1522575A (en) * | 1976-06-24 | 1978-08-23 | Texaco Development Corp | Production of solid fuel-water slurries |
| GB2047267A (en) * | 1979-04-16 | 1980-11-26 | Thermo Electron Corp | Solid Carbon-containing Slurry Fuel and Method and Apparatus for Generating Power from such Fuel |
| WO1981001152A1 (en) * | 1979-10-26 | 1981-04-30 | Univ Alfred Res | Coal-water slurry and method for its preparation |
| EP0050412A2 (en) * | 1980-10-17 | 1982-04-28 | Atlantic Research Corporation | A process for making fuel slurries of coal in water and the product thereof |
-
1982
- 1982-11-26 NZ NZ202639A patent/NZ202639A/en unknown
-
1983
- 1983-02-24 AU AU11831/83A patent/AU556291B2/en not_active Ceased
- 1983-02-25 ZA ZA831302A patent/ZA831302B/en unknown
- 1983-03-07 AT AT83301195T patent/ATE20248T1/en not_active IP Right Cessation
- 1983-03-07 EP EP83301195A patent/EP0089766B1/en not_active Expired
- 1983-03-07 DE DE8383301195T patent/DE3363876D1/en not_active Expired
- 1983-03-22 JP JP58046130A patent/JPS58173193A/en active Granted
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1522575A (en) * | 1976-06-24 | 1978-08-23 | Texaco Development Corp | Production of solid fuel-water slurries |
| GB2047267A (en) * | 1979-04-16 | 1980-11-26 | Thermo Electron Corp | Solid Carbon-containing Slurry Fuel and Method and Apparatus for Generating Power from such Fuel |
| WO1981001152A1 (en) * | 1979-10-26 | 1981-04-30 | Univ Alfred Res | Coal-water slurry and method for its preparation |
| EP0050412A2 (en) * | 1980-10-17 | 1982-04-28 | Atlantic Research Corporation | A process for making fuel slurries of coal in water and the product thereof |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4740329A (en) * | 1984-11-20 | 1988-04-26 | Witton Chemical Company Limited | Dispersing agents for coal slurries |
| EP0281960A3 (en) * | 1987-03-12 | 1989-08-16 | Henkel Kommanditgesellschaft Auf Aktien | Dispersants ant their use in aqueous coal suspensions |
| US5028238A (en) * | 1987-03-12 | 1991-07-02 | Rybinski Wolfgang | Dispersants and their use in aqueous coal suspensions |
| EP0386943A1 (en) * | 1989-03-06 | 1990-09-12 | Central Research Institute Of Electric Power Industry | Process for production of coal-water mixture |
Also Published As
| Publication number | Publication date |
|---|---|
| ATE20248T1 (en) | 1986-06-15 |
| AU556291B2 (en) | 1986-10-30 |
| NZ202639A (en) | 1986-03-14 |
| ZA831302B (en) | 1983-11-30 |
| JPH0330638B2 (en) | 1991-05-01 |
| JPS58173193A (en) | 1983-10-12 |
| DE3363876D1 (en) | 1986-07-10 |
| AU1183183A (en) | 1983-09-29 |
| EP0089766B1 (en) | 1986-06-04 |
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