EP0091047A2 - Combustible pour moteur à carburation - Google Patents

Combustible pour moteur à carburation Download PDF

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Publication number
EP0091047A2
EP0091047A2 EP83103030A EP83103030A EP0091047A2 EP 0091047 A2 EP0091047 A2 EP 0091047A2 EP 83103030 A EP83103030 A EP 83103030A EP 83103030 A EP83103030 A EP 83103030A EP 0091047 A2 EP0091047 A2 EP 0091047A2
Authority
EP
European Patent Office
Prior art keywords
phenol
coal oil
oil
light coal
benzene
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
EP83103030A
Other languages
German (de)
English (en)
Other versions
EP0091047B1 (fr
EP0091047A3 (en
Inventor
Alfons Dr.Rer.Nat. Jankowski
Werner Dr.-Ing. Döhler
Ulrich Dr.-Ing. Graeser
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.)
Veba Oel AG
RAG AG
Original Assignee
Ruhrkohle AG
Veba Oel AG
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Ruhrkohle AG, Veba Oel AG filed Critical Ruhrkohle AG
Publication of EP0091047A2 publication Critical patent/EP0091047A2/fr
Publication of EP0091047A3 publication Critical patent/EP0091047A3/de
Application granted granted Critical
Publication of EP0091047B1 publication Critical patent/EP0091047B1/fr
Expired legal-status Critical Current

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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
    • C10L1/04—Liquid carbonaceous fuels essentially based on blends of hydrocarbons
    • C10L1/06—Liquid carbonaceous fuels essentially based on blends of hydrocarbons for spark ignition
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G19/00—Refining hydrocarbon oils in the absence of hydrogen, by alkaline treatment
    • C10G19/02—Refining hydrocarbon oils in the absence of hydrogen, by alkaline treatment with aqueous alkaline solutions

Definitions

  • the invention relates to a method for producing a low-benzene, environmentally friendly gasoline from light coal oil.
  • the conversion of coal to gasoline (gasoline) is preferably done in two stages. In the first stage, the bottom phase, the coal is converted into an intermediate product (medium oil and crude gasoline) in the presence of finely divided catalysts using hydrogen under suitable pressure and temperature, which is then converted into gasoline fuel in subsequent stages using further catalysts.
  • Carburetor fuels obtained in this way are highly aromatic due to the molecular structure of the coal from condensed aromatics.
  • the benzene content in particular is between 10 and 20% by weight. This high benzene content is undesirable because of the toxic properties of benzene. In some countries there is a limit to the benzene content in petrol or is the goal. E.g. the benzene content in gasoline in the Federal Republic of Germany should be limited to 5 percent by weight.
  • this is achieved in that a core fraction of the boiling point 145-185 ° C. is distilled off from the crude light coal oil via a packed column.
  • the fraction contains most of the phenol contained in coal oil.
  • the phenol can be separated from this core fraction and extracted by extraction with aqueous sodium hydroxide solution or sodium phenolate solution in a three-stage mixer-settler extractor.
  • the remaining phenol-free raffinate of the core fraction is mixed with the portion of light coal oil, boiling up to 145 ° C, and refined e.g. Pressure 60 bar, temperature 410 ° C load 1.5 kg oil / kg cat. H) prepared for reformer application specification. Reforming (e.g. pressure 15 bar, temperature 480 ° C, load 1.5 kg oil / kg cat. H) results in a low-gasoline gasoline fuel with a high octane number.
  • FIG. 1 shows the procedure of the method according to the invention.
  • a core fraction in the boiling range 145-185 ° C. which contains the main amount of the phenol present in the light coal oil
  • This core fraction is de-phenolized by 3-stage extraction with 69 parts of 12% aqueous NaOH in a mixer-settler extractor and the fraction freed from phenol is then mixed again with the light coal oil (boiling point - 145 ° C.).
  • the phenol-free light coal oil is processed by refining and reforming on gasoline. The procedure described lowers the benzene content of the gasoline fuel to 2.6% by weight. If the light coal oil is not de-phenolized before processing in the refiner and reformer, the benzene content in the gasoline is 17.1% by weight.
  • the feed oil for the refiner / reformer still contains 0.8% by weight of phenol. Due to the extraction of the phenol, only 84 parts of the original 100 parts of light coal oil have to be processed in the refiner / reformer, i.e. this system is relieved in terms of quantity.
  • the hydrogen consumption in the refining is reduced by 130 1 / kg feed oil compared to the processing of the raw, non-de-phenolic light coal oil, since the phenol has been removed and the hydrogen requirement for the hydrogenating phenol removal is thus eliminated.
  • a 3-stage mixer-settler extraction apparatus is used in accordance with FIG. 3 to remove phenols from light coal oil using aqueous sodium hydroxide solution.
  • stage I fresh sodium hydroxide solution is introduced into the mixer zone by means of a metering pump and pre-extracted light coal oil via a forced flow in stage II.
  • stage II fresh sodium hydroxide solution is introduced into the mixer zone by means of a metering pump and pre-extracted light coal oil via a forced flow in stage II.
  • the mass transfer between the two, almost insoluble, phases is brought about until the phase equilibrium is established, ie the phenols contained in the coal oil dissolve in the aqueous sodium hydroxide solution.
  • the inhomogeneous mixture separates into the lighter, organic raffinate (de-phenolic carbon oil) and the heavy extract (phenol-containing sodium hydroxide solution) due to different densities.
  • the two phases are subtracted separately.
  • the upper phaq is the desired, phenol-free raffinate, the lower phase flows to stage II.
  • stage II the simply pre-extracted light coal oil from stage III is extracted with the stage I extract, which is partly loaded with phenols, using the procedure already described.
  • stage III the raw coal light oil is conveyed by means of a metering pump and pre-extracted with the extract (phenol-containing sodium hydroxide solution) from the first two stages.
  • the lighter, organic phase is led to stage II.
  • the heavy phase is removed from the process as a phenol-containing extract to recover the phenols.
  • the light coal oil to be refined is introduced into the reaction system by means of a metering pump 1.
  • Compressed make-up hydrogen is metered in before the preheater 2, in which the components are heated to a temperature slightly below the reaction temperature.
  • the implementation takes place in a fixed bed reactor, which is electrically heated by a heating jacket with several control loops.
  • On the catalytic converter all organic sulfur, nitrogen and oxygen compounds contained in the oil are converted into hydrogen sulfide, ammonia, water and hydrocarbons, and gas is also formed shaped degradation products.
  • the product stream leaving the reactor is separated into gas and liquid phases in high-pressure separator 5.
  • the gas phase is expanded via a gas expansion valve 8. It mainly consists of excess hydrogen, hydrogen sulfide and small amounts of C 1 -C 4 gases.
  • the system according to FIG. 4 includes control loops with mass measurement WIR, volume measurement FIR, pressure measurement PI, temperature measurement TIRC, maintenance LIRC and pressure control PRC. Since, when the refined light coal oil is reformed, the reformer contact is quickly deactivated by oxygen and excessive water vapor partial pressure, the feed oil according to FIG. 5 is pumped through a deoxidizer 11 and dryer 12 by means of a pump 10. Subsequently, compressed hydrogen is added before a preheater 13, which heats the mixture to the reaction temperature. The following fixed bed reactor 14 must be heated from the outside to maintain the reaction. In the reforming, aromatics are formed from paraffinic and naphthenic hydrocarbons with the evolution of hydrogen.
  • the oil After expansion, the oil is pumped into a stabilizing column 18 by means of expansion valve 17, in which low-boiling hydrocarbons are removed by distillation.
  • the too associated pump is designated 19.
  • the distillation sump is the aromatic-rich reformate.
  • the gaseous phase from the high-pressure separator is freed of organic constituents under system pressure in a gas scrubber and gas dryer 20 and is returned as a cycle gas by means of a cycle gas compressor 21.
  • the hydrogen formed during the reforming leaves the process via a valve 22 as excess gas.
  • control devices belonging to the system according to FIG. 5 have the same designations as the control devices according to FIG. 4.

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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)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
EP83103030A 1982-04-08 1983-03-26 Combustible pour moteur à carburation Expired EP0091047B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19823213220 DE3213220A1 (de) 1982-04-08 1982-04-08 Vergaserkraftstoff
DE3213220 1982-04-08

Publications (3)

Publication Number Publication Date
EP0091047A2 true EP0091047A2 (fr) 1983-10-12
EP0091047A3 EP0091047A3 (en) 1985-01-09
EP0091047B1 EP0091047B1 (fr) 1987-03-04

Family

ID=6160604

Family Applications (1)

Application Number Title Priority Date Filing Date
EP83103030A Expired EP0091047B1 (fr) 1982-04-08 1983-03-26 Combustible pour moteur à carburation

Country Status (8)

Country Link
EP (1) EP0091047B1 (fr)
AU (1) AU556607B2 (fr)
CA (1) CA1206908A (fr)
DE (2) DE3213220A1 (fr)
IN (1) IN158910B (fr)
NZ (1) NZ203807A (fr)
SU (1) SU1172452A3 (fr)
ZA (1) ZA832467B (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3410455A1 (de) * 1984-03-22 1985-10-03 Ruhrkohle Ag, 4300 Essen Verfahren zur herstellung eines vergaserkraftstoffes aus kohleleichtoel

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101429446B (zh) * 2007-11-09 2012-10-10 丁冉峰 一种催化烃重组制备高质量汽油的设备及其方法
CN101429449B (zh) * 2007-11-09 2012-10-10 丁冉峰 一种催化烃重组制备高质量汽油的设备及其方法
CN101475835B (zh) * 2009-01-22 2012-09-05 北京金伟晖工程技术有限公司 一种组分炼油烃重组后加氢制备高质量汽油的系统和方法

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB107454A (en) * 1916-07-31 1917-07-05 George Edward Heyl Improvements in Liquid Fuels.
US4319981A (en) * 1980-11-12 1982-03-16 The United States Of America As Represented By The United States Department Of Energy Process for preparing a liquid fuel composition

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3410455A1 (de) * 1984-03-22 1985-10-03 Ruhrkohle Ag, 4300 Essen Verfahren zur herstellung eines vergaserkraftstoffes aus kohleleichtoel

Also Published As

Publication number Publication date
SU1172452A3 (ru) 1985-08-07
AU1309483A (en) 1983-10-13
DE3370022D1 (en) 1987-04-09
CA1206908A (fr) 1986-07-02
NZ203807A (en) 1986-02-21
ZA832467B (en) 1983-12-28
EP0091047B1 (fr) 1987-03-04
IN158910B (fr) 1987-02-14
EP0091047A3 (en) 1985-01-09
AU556607B2 (en) 1986-11-13
DE3213220A1 (de) 1983-10-13

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