EP0244902A2 - Wässrige Kohlesuspension und Verfahren zu deren Herstellung - Google Patents

Wässrige Kohlesuspension und Verfahren zu deren Herstellung Download PDF

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Publication number
EP0244902A2
EP0244902A2 EP87200771A EP87200771A EP0244902A2 EP 0244902 A2 EP0244902 A2 EP 0244902A2 EP 87200771 A EP87200771 A EP 87200771A EP 87200771 A EP87200771 A EP 87200771A EP 0244902 A2 EP0244902 A2 EP 0244902A2
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EP
European Patent Office
Prior art keywords
coal
range
comprised
aqueous
weight
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.)
Granted
Application number
EP87200771A
Other languages
English (en)
French (fr)
Other versions
EP0244902A3 (en
EP0244902B1 (de
Inventor
Salvatore Meli
Nello Passarini
Antonio Vettor
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Eni Tecnologie SpA
Original Assignee
Eniricerche SpA
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Publication date
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Priority to AT87200771T priority Critical patent/ATE64610T1/de
Publication of EP0244902A2 publication Critical patent/EP0244902A2/de
Publication of EP0244902A3 publication Critical patent/EP0244902A3/en
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Publication of EP0244902B1 publication Critical patent/EP0244902B1/de
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Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS 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
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/32Liquid carbonaceous fuels consisting of coal-oil suspensions or aqueous emulsions or oil emulsions
    • C10L1/324Dispersions containing coal, oil and water
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS 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
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/32Liquid carbonaceous fuels consisting of coal-oil suspensions or aqueous emulsions or oil emulsions
    • C10L1/326Coal-water suspensions

Definitions

  • the present invention relates to an aqueous slurry and to the related preparation processes.
  • an aqueous coal slurry which contains two separate groups of coal particles, wherein the particles of the first group have an average size comprised within the range of from 210 to 60 ⁇ m, the maximum size being not greater than 300 ⁇ m, and the particles of the second group have a size comprised within the range of from 1/6th to 1/20th of those of the first group.
  • a first object of the present invention is an aqueous coal slurry at a concentration comprised within the range of from 60% to 80% by weight, comprising a polyelectrolyte selected from the monovalent cation salts of the polymerized naphthalenesulphonic acids having a molecular weight comprised within the range of from 800 to 3,000, preferably around 2,000, characterized in that on coal surface, which coal is constituted by particles having a granulometry not greater than 300 ⁇ m, a liquid which is obtained by the distillation of pit-coal tar, or a fuel oil derived from mineral oil, is present, in an amount comprised within the range of from 0.1% to 2%, preferably of from 0.2% to 1.2%, by weight, relatively to same coal.
  • the liquid obtained from the distillation of pit-­ coal tar is preferably selected from those having a distillation range comprised within 200 and 400°C, more preferably between 250 and 350°C.
  • creosote oil can be used.
  • the fuel oil deriving from mineral oil is selected from those having a viscosity at 50° preferably not lower than 3°E.
  • Coal can be constituted by one single group of particles, or by two particle groups.
  • the first group may contain particles having an average granulometry comprised within the range of from 210 to 60 ⁇ m, the maximum size being however not greater than 300 ⁇ m;
  • the second group can contain particles having an average granulometry comprised within the range of from 1/6th to 1/20th of the average granulometry of the particles of the first group, by "average granulometry of the particles” the granulometry corresponding to 50% of the cumulative mass distribution of that group being meant.
  • the particles of the first group should preferably be at least 40% of total, more preferably at least 60% by weight of total particles.
  • the cumulative particle distribution curve by resulting from two fractions (i.e., two distinct groups of coal particles), should show, if reported on a bi­logarithmic scale (log-log chart), a flat zone comprised between the values of the average dimensions of component fractions; wherein by "flat zone” a length of the curve is meant, wherein the derivative, computed on a bilogarithmic scale (log-log chart), is lower than 0.4, and preferably lower than or equal to 0.1, and still more preferably equals zero.
  • the cumulative granulometric distribution should hence be such that always two particle size values d1 and d2, comprised between the average values of the diameters of the two fractions exist, for which the numeric value of the following expression is lower than 0.4, preferably lower than or equal to 0.1, and, still more preferably, equals 0.
  • (%CM1) and “(%CM2)” the values are indicated of the cumulative percentages of the mass of particles, respectively having a size lower than d1 and d2.
  • the numerical value of the expression is, obviously, independent from the unit of measure (micrometres or millimetres) according to which the particle size is expressed.
  • the addition of the liquid obtained by means of distillation of pit-coal tar is carried out during the same beneficiation treatment, by performing such a treatment in the presence of a light hydrocarbon of from 4 to 8, preferably from 5 to 6, carbon atoms, said hydrocarbon being flashed off after the agglomeration.
  • n-­pentane and n-hexane we mention here n-­pentane and n-hexane.
  • the Light hydrocarbon is preferably present in a percentage comprised within the range of from 5% to 30% by weight relatively to coal.
  • a second object of the present invention is the process for preparation of the aqueous coal slurries.
  • the process comprises a beneficiation by agglomeration in water of a coal having a granulometry not higher than 300 ⁇ m with a liquid obtained by means of the distillation of pit-coal tar, or with a fuel oil deriving from mineral oil, in an amount comprised within the range of from 0.2% to 2% by weight relatively to coal, and a light hydrocarbon comprising a number of carbon atoms comprised within the range of from 4 to 8, in an amoung ranging from 5% to 30% by weight relatively to coal, the flashing of the light hydrocarbon, after that the prevailingly organic portion has agglomerated and separated from the aqueous solution in which the inorganic components have remained suspended or dissolved, and, finally, the slurrying in an aqueous solution comprising a polyelectrolyte, as the dispersant, selected from the monovalent cation salts of polymerized naphthalenesulphonic acids having a molecular weight of from 800
  • polyelectrolytes there can be used, e.g., the chemical compounds known under the tradename of DAXAD 15 and DAXAD 19 by W.R. Grace, and Reoplast 203 by Fratelli Lamberti S.p.A.
  • the process comprises the slurrying of a coal having a granulometry not greater than 300 ⁇ m, in a solution containing a liquid obtained by means of the distillation of pit-coal tar, or a fuel oil deriving from mineral oil, in an amount comprised between 0,2% and 2% by weight relative to coal, and a light hydrocarbon liquid comprising a number of carbon atoms comprised within the range of from 4 to 8, in an amount comprised within the range of from 50% to 200% by weight relatively to coal, followed by the flashing of the light hydrocarbon and by the forma­tion of an aqueous slurry by means of the addition of a dispersant constituted by a polyelectrolite selected from the monovalent cation salts of polymerized naphthalenesulphonic acids having a molecular weight of from 800 to 3,000, preferably around 2,000, the percent amount of the dispersant being comprised within the range of from 0.05% to 0.5%
  • the preferred liquids obtained from the distillation of pit-­coal tar the preferred fuel oils deriving from mineral oil, the preferred light oils, and the preferred polyelectrolytes, what above said for the aqueous slurries holds true as well.
  • the coal having this granulometry was used for preparing the slurries after being coated with a creosote oil film.
  • the coating by the creosote oil was achieved by diluting this latter oil in n-hexane, subsequenty adding coal, under stirring, and finally flashing off the solvent.
  • the amount of creosote oil added to coal was 0.5% by weight based on dry coal, and the amount of n-hexane was 100% by weight.
  • samples were then prepared and analysed of water-coal slurries, with a solids concentration of 62% by weight, to which 0.2% 0.3% and 0.5% by weight of DAXAD 15, relatively to the suspension, was added.
  • the blend was characterized in terms of its apparent viscosity at 50 sec ⁇ 1.
  • a Polish coal having the following analytical characteristics:
  • the coal with the above described granulometry underwent a beneficiation treatment by selective agglomeration with n-pentane and creosote oil. Used amount of creosote oil equalled 0.5% by weight relatively to coal.
  • the beneficiation step was carried out on a batch equipment having a capacity of 10 litres of slurry, on a coal slurry in water at 20% of solids by weight, by using a concentration of n-hexane of 20% relatively to dry coal.
  • n-pentane was removed by drying under N2 in oven at 40°C.
  • the induction times of the agglomeration phenomenon i.e., the times necessary for agglomeration to begin, resulted sharply shorter: from the 15-minute time of the test with n-pentane only, a decrease to the 8-minute time of the test with n-pentane plus creosote oil as the agglomerating agent were obtained, with obvious advantages from the viewpoint of process economy.
  • n-pentane was removed by oven-drying under N2 at 40°C.
  • Example 15 The same Polish coal as of Example 9-11, with the same bimodal granulometry, not beneficiated, and without creosote oil, was used to prepare slurries to which 0.2% (Example 15), 0.3% (Example 16) and 0.5% by weight (Example 17) of DAXAD had been added.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dispersion Chemistry (AREA)
  • Liquid Carbonaceous Fuels (AREA)
  • Solid Fuels And Fuel-Associated Substances (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Carbon And Carbon Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
EP87200771A 1986-05-02 1987-04-23 Wässrige Kohlesuspension und Verfahren zu deren Herstellung Expired - Lifetime EP0244902B1 (de)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AT87200771T ATE64610T1 (de) 1986-05-02 1987-04-23 Waessrige kohlesuspension und verfahren zu deren herstellung.

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
IT20295/86A IT1189094B (it) 1986-05-02 1986-05-02 Sospensione acquosa di carbone e relativi procedimento di preparazione
IT2029586 1986-05-02

Publications (3)

Publication Number Publication Date
EP0244902A2 true EP0244902A2 (de) 1987-11-11
EP0244902A3 EP0244902A3 (en) 1989-01-11
EP0244902B1 EP0244902B1 (de) 1991-06-19

Family

ID=11165506

Family Applications (1)

Application Number Title Priority Date Filing Date
EP87200771A Expired - Lifetime EP0244902B1 (de) 1986-05-02 1987-04-23 Wässrige Kohlesuspension und Verfahren zu deren Herstellung

Country Status (12)

Country Link
EP (1) EP0244902B1 (de)
JP (1) JPS62266313A (de)
AT (1) ATE64610T1 (de)
AU (1) AU599376B2 (de)
CA (1) CA1328735C (de)
DE (1) DE3770867D1 (de)
ES (1) ES2024490B3 (de)
GR (1) GR3002281T3 (de)
IT (1) IT1189094B (de)
PL (1) PL159184B1 (de)
RU (1) RU1838384C (de)
ZA (1) ZA872947B (de)

Cited By (1)

* Cited by examiner, † Cited by third party
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 (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20180124021A (ko) 2016-04-04 2018-11-20 에이알큐 아이피 리미티드 고체-액체 원유 조성물 및 그 분별 방법
US9777235B2 (en) 2016-04-04 2017-10-03 Allard Services Limited Fuel oil compositions and processes

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE822032C (de) * 1950-01-24 1951-11-22 Johann Christian Groeber Dr Kraftstoff fuer Brennkraftmaschinen
IT1211049B (it) * 1981-05-21 1989-09-29 Snam Progetti Sospensione acquosa di carbone.

Cited By (2)

* Cited by examiner, † Cited by third party
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
JPS62266313A (ja) 1987-11-19
ATE64610T1 (de) 1991-07-15
IT8620295A0 (it) 1986-05-02
RU1838384C (ru) 1993-08-30
AU7242387A (en) 1987-11-05
DE3770867D1 (de) 1991-07-25
IT8620295A1 (it) 1987-11-02
EP0244902A3 (en) 1989-01-11
AU599376B2 (en) 1990-07-19
EP0244902B1 (de) 1991-06-19
ZA872947B (en) 1987-10-20
CA1328735C (en) 1994-04-26
GR3002281T3 (en) 1992-12-30
IT1189094B (it) 1988-01-28
ES2024490B3 (es) 1992-03-01
PL265442A1 (en) 1988-05-26
PL159184B1 (pl) 1992-11-30

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