• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    A fluidifier and stabilizer additive, particularly suitable for coal suspensions in water, based on sulphonated tar, wherein sulphonated and salified tar results to be also oxidized, the oxidation being evidenced by the development of SO2 to the extent of 2 to 60% by wt, w.r.t. the tar during the sulphonation reaction. Also there is a method for the preparation of the additive, consisting in contacting tar with liquid or gaseous SO3, tar and/or SO3 being preferably dissolved in an halogenated organic solvent; the solvent is recovered and the oxidized sulphonated additive is salified.
    公开号:SU1516015A3
    申请号:SU853912356
    申请日:1985-05-28
    公开日:1989-10-15
    发明作者:Преведелло Альдо；Платоне Эдоардо；Пичинини Карло
    申请人:Снампрогетти С.П.А. (Фирма)；
    IPC主号:
    专利说明:

    This invention relates to methods for making a fluidizing and stabilizing additive for coal-water slurries.
    The aim of the invention is to improve the quality of the target product.
    This goal is achieved by sulphonating coal tar or
    petroleum refining resins with a density of 1.025-1.190 g / cm at 20 C with liquid or gaseous sulfur trioxide with a mass ratio of sulfur trioxide and a smlly of 0.41-3.36: 1.0 in the presence of a halogenated hydrocarbon, inert and not

    C / 1
    15160
    mixing or poorly mixing-PierocH with water at a temperature of from room temperature to 90 ° C, ending the reaction at 80-140 ° C and controlling the quality of the liberated sulfur dioxide in the range of 3-50 wt.% with respect to the weight of the resin, followed by neutralization with sulfonated and oxidized resin
    an aqueous solution of sodium hydroxide fQ
    to pH 7, removal of the solvent by decantation and / or evaporation, both of which can be carried out in the opposite direction.
    EXAMPLE 2 The same equipment was used as in Example 1. 43 g of resin diluted with 100 cm of carbon tetrachloride were charged to a flask, while 51.7 g of SOj diluted with 100 cm of carbon tetrachloride were introduced into the feed funnel. After 2 h, a solution of sulfur trioxide is added with external water cooling (temperature T5pha in a flask of 15–18 ° C), then the reaction
    the solution containing the desired product, the mixture is left for 1 h at room temperature
    Sodium sulfate, g 16.6 SOj, g2,1
    EXAMPLE 2 The same equipment was used as in Example 1. 43 g of resin diluted with 100 cm of carbon tetrachloride were charged to a flask, while 51.7 g of SOj diluted with 100 cm of carbon tetrachloride were introduced into the feed funnel. After 2 h, a solution of sulfur trioxide is added with external water cooling (temperature T5pha in a flask of 15–18 ° C), then the reaction
    the mixture is left for 1 hour at room temperature.
    concentration or drying.
    Example 1. The equipment consists of a four-neck flask with a capacity of 500 cm, equipped with a mechanical stirrer with polytetrafluoroethylene blades, a thermometer, a water-cooled ball cooler, and a charging funnel.
    The flask is charged with 44 g of resin diluted with 100 cm of tatrachlorethylene, and 53 g of liquid sulfur trioxide in 100 cm of tetrachlorethylene are simultaneously poured into the feed funnel.
    A solution of triprioxidum sulfur is introduced into the reaction flask for approximately 2 hours, while the reaction flask and the flask is continuously cooled to maintain the TeNJnepaTypH in the flask at a level of 10-15 ° C.
    At the end of the addition of sulfur trioxide, the temperature in the flask is allowed to rise to 20-25 ° C and then for 1 h the reaction mixture is heated with reflux ((approximately 120 ° C) and maintained at this temperature for 1 h.
    Then the reaction mixture is cooled, diluted with water and the resulting
    A resin diluted with 100 cm of tetrachlorethylene (TCE) is charged to the flask, and sulfur trioxide diluted with an additional 100 cm of TCE is added to the H9 feed funnel. The purified product is added. The reactions are transferred
    in a beaker, where its neutral SO solution is continued to be tempered to a pH of 7 with an aqueous solution of ca. 90 m of acid with a battery (132 g) then the whole mass is distilled at atmospheric pressure to recover the solvent
    cooling the reaction flask (the temperature in the flask is 10-15 0).
    Then, holding the reaction mixture in the form of an anisotropic water / tetravay mixture at room temperature (chlorine ethylene, approximately 20–30 0) for 1 h.
    975 g of an aqueous solution not containing solid particles were obtained and 196 cm of the quantity of 200 cm were recovered. Sodium sulfate,% Ouho active substance, g107
    After that, it is heated with reflux for 1 hour at 120 C. The reaction mass is cooled to room temperature from the initial temperature, diluted with water and then
    do not trapizuyut aqueous solution of caustic soda. Most of the solvent is separated in the form of the lower phase of the final reaction mixture after it is neutral. 70
    five
    Q
    0
    the temperature is then heated | with reflux (g 80 s) for 2 hours, the reaction mass is cooled to room temperature, diluted with water, transferred to a beaker, swept the flask again with water and the reaction mixture is neutralized to pH 7 with an aqueous solution caustic soda (128 g).
    The azeotropic carbon tetrachloride / water mixture is distilled off as the main fraction, and 1176 g of an aqueous solution is obtained as a residue. Sodium sulfate,% 1.7 Dry active substance, g94.5
    Sodium sulfate, g 20 Sour gas, g 2.6 Examples 3-17. These examples were carried out under the same conditions (temperature, dissolution of the resin and sulfur trioxide in a solvent, and the duration of the addition of sulfur trioxide to the resin) as in Example 1.
    A resin diluted with 100 cm of tetrachlorethylene (TCE) is loaded into the flask, and sulfur trioxide diluted with an additional 100 cm of TCE is added to the H9 feed hopper. The addition of a solution of SO is continued for about 90 minutes with
    “” Of the SO solution is continued for about 90 missions with
    cooling the reaction flask (the temperature in the flask is 10-15 0).
    Then the reaction mass is kept at room temperature (approximately 20-30 0) for 1 h.
    51
    and the rest is recovered as an azeotropic mixture with water. Total solvent recovery reaches approximately 96-97%,
    The data relating to these experiments are given in Table 2.
    In all examples, waste gases (consisting mainly of sulfur dioxide and traces of sulfur trioxide) were analyzed by absorbing them after the cooler in a trap containing a titrated aqueous solution of caustic soda.
    Example 18, Equipment is used the same as in example 1,
    Into the reaction flask is charged 80 g of sulfur trioxide, diluted with 100 cm of tetrachlorethylene.
    44 resins diluted with tetrachlorethylene are loaded into the addition funnel.
    The resin solution is poured into the SOE solution for about 50 minutes while gradually increasing the temperature of the reaction mixture from 22 to 12 ° C, and then. the reaction mass is heated to 120 ° C and held at this temperature for 1 hour. Then most of the solvent is decanted at
    80C. After that, the flask is placed in a thermostatic bath at 140 ° C,
    Most of the solvent is recovered within 80 minutes (recovery reaches approximately; 98%), the reaction mixture is neutralized in a hot state (80-85 s) to pI 7 with a 15% sodium hydroxide solution and then diluted with water.
    795 g of aqueous solution was obtained. Sodium sulfate,%. 2.9 The dry active part, g 92.9 Sodium sulfate, g 23.1 Sulfur dioxide during the reaction, g 13 Organic sulfur, g 14.3 Example 19, Equipment similar to Example 1, 44 g of resin diluted with 326 g of TCE was charged to a flask and 81 g of liquid sulfur trioxide was added to an addition funnel. Liquid sulfur trioxide is poured to
    resin solution for 40 minutes without external cooling of the reaction flask. The initial temperature is 23 ° C, then the temperature is raised to a maximum value of 90 ° C, and at the end of the addition is 65 ° C.
    The reaction mixture is heated for 15 minutes to a temperature of 20 ° C and
    0
    about
    five
    0
    five
    ABOUT
    p e
    P
    five
    15"
    maintained at this temperature for 1 h.
    The solvent is then decanted at a temperature of approximately 90 ° C (274 g of TCE is recovered), after which the reaction flask is placed in a thermostatic oil bath with a temperature of 132-134 ° C to recover the solvent by distillation. With this second operation, the remaining TCA is recovered. The remaining mixture is neutralized at a temperature of approximately 80-90 ° C to pH 7 with an aqueous solution of sodium hydroxide. The weight of the final aqueous solution of sulfonated, oxidized and salified resin is 477 g,
    Sodium sulfate,% 6.8% Dry active part, g 97.5% sodium sulfate, g 32.4% separated SOj, g 13.9% organic sulfur, g 7.1 example and 20. Example is carried out analogously to example 1 , 44 g of resin diluted with 327 g of TCE is charged to the reaction flask; 79 g of liquid sulfuric anhydride are added to a dropping funnel.
    The sulfuric anhydride solution is poured into the resin for 40 minutes without external cooling of the reaction flask (the internal temperature is initially 21 ° C, increases to a maximum of 90 ° C, and at the end of the addition of F3 is 65 ° C).
    Then the reaction mixture is heated to the boiling point of tetrachloroethylene (about 120 ° C) for 15 minutes and kept at this temperature for 1 hour. Then most of the solvent (270 g) is decanted at a temperature of approximately 85 ° C, after which the reaction flask t in a thermostatic oil bath with a temperature of 140 ° C. The solvent is taken off for 2 hours. The solid residue in the flask is neutralized to pH 7 with an aqueous solution of sodium hydroxide. Final weight
    aqueous solution, g 474.4 Sodium sulfate,% 7.4 Dryness active
    part% 93.9 Sodium sulfate, g 35.1 Sulfur dioxide released during the experiment, g 13.1
    7151
    Organic sulfur, g 5.4
    Comparative example. The equipment used is the same as in Example 1. 38.8 g of resin diluted with 200 cm of tetrachloroethylene are loaded into a flask while 43.8 g of liquid sulfuric anhydride are loaded into the feed funnel. The latter was introduced into the reaction flask for approximately 80 minutes, cooled by running water, so that the temperature inside the flask was always 17-20 ° C. The mixture was then stirred for 4 hours. While maintaining the temperature in the flask. Then the mixture of sulfonated resin is neutralized to pH 7 with an aqueous solution of caustic soda.
    The solvent is then distilled off by azeotropic distillation.
    897.3 g of water are obtained.
    solution.
    Sulphate content
    sodium% 3.82
    Suha is active
    part% 63.9
    Sodium sulfate, g 34.3
    Analytical limit sour gas j., We
    Organic sulfur, 9.2 g
    The product thus obtained does not exhibit dispersibility.
    Comparative example 2. Equipment similar to example 1, except that the capacity of the reaction flask is not 500, but 250 cm. 17.0 g of resin diluted with 50 cm of tetrachlorethylene are loaded into the flask. 31.8 g of sulfur trioxide diluted with 50 cm of tetrachloroethylene is poured into the feed funnel. The latter is poured into the reaction flask for approximately 135 minutes while being cooled externally with running water to maintain the temperature in the flask at a level of 16-18. The mixture is then stirred for another 130 minutes all the time at temperatures of approximately. After that, the reaction mixture is neutralized with an aqueous solution of sodium hydroxide to pH 7.
    787.4 g of an aqueous solution of sulfonated sodium salt are obtained.
    Sodium sulfate,% 1.45
    Dry active
    substance, g58,6
    eight
    Sodium sulfate, g 11 | 4
    Released at
    sulphurous reactions
    gas below analytical limit
    Organic sulfur, 9.4 g
    The product thus obtained did not exhibit dispersibility.
    Substrates that are subjected to sulfonation in examples 21-25 include derivatives of oil distillates obtained by the following method: the residue of atmospheric distillation is subjected to vacuum distillation, thus obtaining various fractions, among which are SN-60, SN-150 and SN-450 ( SN - neutral solvent).
    These cuts are refined by extraction with furfurol, the extracts being mostly aromatic compounds and some of the naphthenic compounds present in the original SN fractions. These aromatic extracts (ES AR) are substrates that are subjected to sulfonation.
    The average physico-chemical characteristics of ES AR obtained after the processing of crude oil are given in Table 1.
    Examples 21-25. The equipment used is the same as in Example 1. The examples were carried out under the same experimental conditions with respect to the temperature value, dilution of the oil fraction and SO content, in the TCh and time of addition of the PS in the coal tar.
    Oil fraction diluted with 130 ml TCE. the VO solution diluted with another 70 ml of TCE is introduced into the flask and through the funnel, the SOj solution is poured into the flask for 60 minutes, which is cooled externally with water to maintain the reaction temperature within 20-27 °
    Then the reaction mixture is heated to boiling point (115-120 ° C) for about 30 minutes and kept at this temperature for 60 minutes.
    Waste gas more (mainly consisting of SO and with traces of
    91
    SO. ) are analyzed in all examples by absorbing them down in the direction of flow from a condenser in a trap containing a titrated aqueous solution of NaOH. The reaction mixture is then cooled, diluted with water and neutralized with an aqueous solution of hydrate.
    &
    sodium oxide,
    TCE is distilled off at atmospheric pressure as an azeotropic mixture with water, resulting in an aqueous solution of the sulfonated-oxidized and the product obtained in the form of a salt.
    Table 3 shows the data obtained in the tests performed, and Table 4 shows the results obtained from the rheological assessment of these dispersing additives.
    The percentage of 50 relative to the resin for all examples is given in Table 5.
    The amount of sodium hydroxide that is needed to neutralize the coal tar-containing suspension, until the pH value is 7, is given in Table 6.
    Water / coal dispersion viscosity measurements.
    In order to evaluate various dispersants, measurements of viscosity at various speed gradients were carried out using an Naak RU 12 rotational viscometer equipped with a MU1 sensor and a M 500 measuring head.
    Measurement of cutting resistance.
    A sample of a dispersant according to the proposed invention is compared with a commercial | Sample (DaxaD 15, Grace Halia) according to a technique called stability as a function of cutting stresses.
    In a glass reactor with 1 liter flanges, height and diameter
    I60i5
    ten
    For this purpose, weigh 70 g of particles with a mesh size of 60 mesh and 5% moisture into a 200 cm chemical beaker and add an aqueous mixture of the tested dispersant in such a quantity as to ultimately get%: 70% by weight of coal, 29.5 by weight of water, 0.5 by weight of a dispersant of a torus.
    Products are mixed using a mixer with two metal loop-shaped blades mi-for 1 min at 650 rpm and for 2 min at
    5 1200 rpm The suspension thus obtained is introduced into the outer measuring cylinder of the viscometer, the temperature of which is constant (20 ° C), and after holding for
    0 5 min at 20 ° C. The values of the cutoff voltage (f) at various velocity gradients (y) (from 3.8 to approximately 150) are determined. The experimental values thus obtained are processed using
    force equations or Ostwald equations
    r to f
    valid for a pseudoplastic state.
    For each series of experimental measurements of f-J, the values of K or the curve - –y with linear regression are calculated. In addition, for the last five tested values, ip is 37.60; 75, 120, and 150 s. The values of the asymptotic viscosity are calculated by quantifying the experimental data.
    The values obtained for some samples in this procedure, as well as for the known additive DaxaD 15, are as follows.
    10 cm, 336 g of dry (moisture less than 0.5%) coal with a particle size of less than 60 mega and a solution of a dispersant in water are placed so that at the end of the load they have,%: 70 by weight of coal; 29.5 by weight of water; 0.5 by weight dispersant.
    The mixture is agitated by opening the reactor to combine with the atmosphere.
    H151
    a stirrer with loop-shaped blades for 2 minutes at 650 rpm and then for 10 minutes at 1200 rpm.
    Fgan (VC is closed at 200 ml. An impeller is placed with a 2 cm flywheel and the mixture is stirred at 200 rpm for 24 hours. Mixing is stopped, the impeller is removed and everything is left alone for three days. and drain the sludge.
    The results are presented in Table 7, in which the following legends are accepted:
     - sludge flows spontaneously;
    - the residue at the bottom can be easily liquefied again with the help of a glass rod or similar tool;
    Thus, the additive according to the proposed eiMOMy method is of better quality, since the suspension with its inclusion can be completely drained without sediment, whereas the suspension with DAXAD 15 must first be moved in order to be able to relatively completely drain.
    权利要求:
    Claims (4)
    [1]
    Claim 30
    .1, A method for producing a fluidizing and stabilizing additive for water-based suspensions based on sulfonation and neutralization reactions, characterized in that, in order to improve the quality of the target product, a coal tar or oil refining resin with a density of 1.025-1.190 g / cm at 20 ° C is reacted with liquid or gaseous sulfur trioxide at a mass ratio of sulfur trioxide
    0.993
    1,005
    1,024
    41
    59
    125
    20
    thirty
    015; 12
    and resin, 0.41–3.36: 1.0 in the presence of a halogenated hydrocarbon, inert and not miscible or poorly miscible with water at a temperature of from room temperature to, ending with 80–140 ° С and control quality of alumina dioxide
    0 sulfur in the range of 3-50 wt.% Relative to the weight of the resin, followed by neutralization of the sulfonated and oxidized smopa with an aqueous solution of sodium hydroxide to pH 7, removing
    5 by decantation and / or evaporation, both of which can be carried out in reverse order by recovering the aqueous solution containing the desired product by concentration or drying.
    [2]
    2, non.l method, which is absent, and using carbon tetrachloride, tetrachlorethylene or dichloroethane as the solvent.
    [3]
    31 Method POP.1, characterized in that the sulphonation reaction is completed while controlling the quality of the liberated sulfur dioxide in the range of 10-35 wt.%, Relative to the weight of the resin,
    [4]
    4. Method pop, 1, differs by the fact that the process is carried out by introducing into the previously grown- BoreHHjTKi in a solvent a sulfur trioxide resin as such or dissolved in a solvent
    5, the method according to claim. I, characterized in that the process is carried out
    40 nyteM pouring out the resin as such or dissolved in the solvent in the solvent dissolved in the solvent sulfur trioxide,
    Table 1
    25
    35
    83 85 88
    00
    - about 1L CNI r-
    oo m o cN o
    in tsi 4t in cs
     vj- about 1 00
    vO g r O LH
    1L vO r. H o o
    "K M" I
    - about vC CU TV -1 CS - "-
    - fO (Tv CVJ O
    CM m r n 00
    - CNJ -i CN -
    00 GO CN OO CTv
    oo f o -
    You v d o y
    About J-CTi
    vO r o vO fO u-i J in
    00
    about o lo
    oo oo - - gg and z
    SL SL C / 3 SL
    SL c / 3 to sya ate
    ij fjj Щ Щ flj
    -;} t vj- f -d- r 4t r
    - CM GO t lO CNI CS CM CM CN
    Coal A: Agi content 1.2 ash 8,522, volatile matter 35.9, fixed
    carbon 54.4, total content. sulfur 0.952. Coal B: Moisture content 9Z, ash 15.52, volatile. 23.72, fixed
    carbon 59.22, total sulfur content 0.642,
    Granulometric curve of both types of coal: maximum size
    250 microns, in the presence of 70-802 less than 74 microns,
    ..
    Example, No. SOjtcMona,% Example I 50: resin,%
     .
    17
    Compiled by T. Vlasov Editor Y. Sereda Tehred A. Kravchuk Proofreader V. Kabatsy
    Order 6299/59
    Circulation 446
    VNIIPI State Committee for Inventions and Discoveries under the State Committee on Science and Technology of the USSR 113033, Moscow, Zh-35, 4/5 Raushsk nab.
    Production and publishing plant Patent, Uzhgorod, st. Gagarin, 101
    1516015 8
    Table
    Subscription
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    引用文献:
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    DE106500C|
    BE373377A|
    US1711448A|1925-04-27|1929-04-30|Peter Reilly|Treatment of tar|
    GB483907A|1935-07-26|1938-04-27|Ladislao D Antal|Improvements in or relating to the treatment of bitumina and allied substances|
    US2227999A|1938-07-07|1941-01-07|Sulphonation of coal tab distillates |
    US3089842A|1959-12-14|1963-05-14|Phillips Petroleum Co|Production of sulfonated asphalt|
    US3374210A|1965-09-20|1968-03-19|Grefco|Sulfonated aromatic resins|
    DE2138637A1|1971-08-02|1973-02-15|Kureha Chemical Ind Co Ltd|Dispersant with low foamability - prepd by pyrolysis of petroleum fractions or coal, and sulphonation|
    DE2256758B2|1972-03-27|1976-07-01|Marathon Oil Co., Findlay, Ohio |USE OF PETROLEUM SULFONATES FOR THE DISPLACEMENT OF CRUDE OIL FROM EARTH FORMATIONS|
    US4416666A|1979-10-26|1983-11-22|Alfred University Research Foundation Inc.|Coal-water slurry and method for its preparation|
    JPS606395B2|1979-07-26|1985-02-18|Kao Soap Co|
    US4441889A|1981-01-29|1984-04-10|Gulf & Western Industries, Inc.|Coal-aqueous mixtures|
    US4432771A|1981-05-15|1984-02-21|International Telephone And Telegraph Corporation|Combustible coal/water mixtures for fuels and methods of preparing the same|
    JPS5823889A|1981-08-03|1983-02-12|Nippon Oil & Fats Co Ltd|Additive for coal-water slurry|
    FR2517671B1|1981-12-07|1984-04-06|Raffinage Cie Francaise|
    US4502868A|1982-09-27|1985-03-05|Texaco Inc.|Coal-water slurries of low viscosity and method for their preparation|
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    法律状态:
    优先权:
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    IT8421140A|IT1206704B|1984-05-29|1984-05-29|FLUIDIFYING AND STABILIZING ADDITIVE AND ITS PREPARATION METHOD.|
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