EP2105489A1 - Oxidative Entschwefelung von Brennstofföl - Google Patents

Oxidative Entschwefelung von Brennstofföl Download PDF

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Publication number
EP2105489A1
EP2105489A1 EP09156238A EP09156238A EP2105489A1 EP 2105489 A1 EP2105489 A1 EP 2105489A1 EP 09156238 A EP09156238 A EP 09156238A EP 09156238 A EP09156238 A EP 09156238A EP 2105489 A1 EP2105489 A1 EP 2105489A1
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EP
European Patent Office
Prior art keywords
sulfur
fuel oil
containing fuel
component
salts
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Withdrawn
Application number
EP09156238A
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English (en)
French (fr)
Inventor
Grigorii Lev Soloveichik
John Mathew Bablin
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General Electric Co
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General Electric Co
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Classifications

    • 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
    • C10G27/00—Refining of hydrocarbon oils in the absence of hydrogen, by oxidation
    • C10G27/04—Refining of hydrocarbon oils in the absence of hydrogen, by oxidation with oxygen or compounds generating oxygen
    • C10G27/12—Refining of hydrocarbon oils in the absence of hydrogen, by oxidation with oxygen or compounds generating oxygen with oxygen-generating compounds, e.g. per-compounds, chromic acid, chromates
    • 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
    • C10G21/00—Refining of hydrocarbon oils, in the absence of hydrogen, by extraction with selective solvents
    • 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
    • C10G21/00—Refining of hydrocarbon oils, in the absence of hydrogen, by extraction with selective solvents
    • C10G21/003—Solvent de-asphalting

Definitions

  • the invention includes embodiments that generally relate to a method for purifying sulfur-containing fuel oil using a catalyst, a water-soluble acid and a peroxide.
  • Raw/fossil fuels such as fuel oil including a crude oil and oil distillates and refinery products like gasoline, kerosene, diesel fuel, naphtha, heavy fuel oil, natural gas, liquefied natural gas and liquefied petroleum gas, and like hydrocarbons, are useful for a number of different processes, particularly as a fuel source, and most particularly for use in a power plant. Virtually all of these fuels contain relatively high levels of naturally occurring, organic sulfur compounds, such as, but not limited to, sulfides, mercaptans and thiophenes.
  • Hydrogen generated in the presence of such sulfur compounds has a poisoning effect on catalysts used in many chemical processes, particularly catalysts used in fuel cell processes, resulting in shortening the life expectancy of the catalysts.
  • sulfur compounds When present in a feed stream in a fuel cell process, sulfur compounds may also poison the fuel cell stack itself. Because of the relatively high levels of sulfur compounds that may be present in many crude fuel feed streams, it is necessary that these feed streams be desulfurized.
  • ODS oxidative desulfurization
  • the present invention provides a method for purifying a sulfur-containing fuel oil comprising: (a) contacting in a first reaction mixture the sulfur-containing fuel oil with an exogenous binary catalyst, hydrogen peroxide, and a water-soluble acid at a temperature in a range of from about 25°C to about 120°C to provide a first oxidized mixture; and (b) separating at least one oxidized sulfur compound from the first oxidized mixture to provide a purified fuel oil.
  • the present invention provides a method for purifying a sulfur-containing fuel oil comprising (a) contacting in a first reaction mixture the sulfur-containing fuel oil with a hydrocarbon diluent, an exogenous binary catalyst, hydrogen peroxide, and a water-soluble acid at a temperature in a range of from about 25°C to about 110°C to provide a first oxidized mixture; and (b) separating at least one oxidized sulfur compound from the first oxidized mixture; and (c) recovering the hydrocarbon diluent to provide a purified fuel oil.
  • the present invention provides a method for purifying a sulfur-containing fuel oil comprising (a) contacting in a first reaction mixture the sulfur-containing fuel oil comprising benzothiophene, dibenzothiophene, alkyl substituted benzothiophenes, and alkyl substituted dibenzothiophenes with petroleum ether, an exogenous binary catalyst, hydrogen peroxide, and a water-soluble acid at a temperature in a range of from about 25°C to about 120°C to provide a first oxidized mixture comprising sulfoxides and sulfones of benzothiophene, dibenzothiophene, alkyl substituted benzothiophenes, and alkyl substituted dibenzothiophenes; (b) separating at least one oxidized sulfur compound from the first oxidized mixture; and (c) recovering petroleum ether to provide a purified fuel oil.
  • Approximating language may be applied to modify any quantitative representation that could permissibly vary without resulting in a change in the basic function to which it is related. Accordingly, a value modified by a term or terms, such as “about” and “substantially”, are not to be limited to the precise value specified. In at least some instances, the approximating language may correspond to the precision of an instrument for measuring the value.
  • range limitations may be combined and/or interchanged, such ranges are identified and include all the sub-ranges contained therein unless context or language indicates otherwise.
  • the present invention provides a method for purifying a sulfur-containing fuel oil comprising, (a) contacting in a first reaction mixture the sulfur-containing fuel oil with an exogenous binary catalyst, hydrogen peroxide, and a water-soluble acid at a temperature in a range of from about 25°C to about 150°C to provide a first oxidized mixture; and (b) separating at least one oxidized sulfur compound from the first oxidized mixture to provide a purified fuel oil.
  • the sulfur-containing fuel oil is a crude oil, for example Saudi sweet crude oil, West Texas Intermediate crude oil, Dubai crude oil, and Brent crude oil.
  • the sulfur-containing fuel oil is a crude oil, which has been subjected to asphaltene removal.
  • the sulfur-containing fuel oil is a distillate or other refinery products of a crude oil like gasoline, kerosene, diesel fuel, naphtha, heavy fuel oil, natural gas, liquefied natural gas and liquefied petroleum gas.
  • the sulfur-containing fuel oil comprises dibenzothiophene, benzothiophene, alkyl substituted dibenzothiophenes, and alkyl substituted benzothiophenes.
  • the sulfur-containing fuel oil comprises less than 5 weight percent sulfur based on the weight of sulfur-containing fuel oil. In another embodiment, the sulfur-containing fuel oil comprises less than 3 weight percent sulfur based on the weight of sulfur-containing fuel oil. In another embodiment, the sulfur-containing fuel oil comprises less than 2 weight percent sulfur based on the weight of sulfur-containing fuel oil.
  • the phrase "exogenous binary catalyst” means an "external binary catalyst” that is combined in a first reaction mixture with a sulfur-containing fuel oil.
  • the exogenous binary catalyst comprises a first component, a catalyst and a second component, a promoter.
  • the binary catalyst comprises a first component selected from the group consisting of phosphate salts, and oxides, acids and salts of molybdenum, tungsten, manganese, and combinations thereof; and the second component is selected from the group consisting of oxides and salts of cerium, iron, vanadium, titanium, manganese, cobalt, nickel, copper and combinations thereof.
  • the first component comprises an oxide or a salt of molybdenum.
  • the molybdenum containing first component is a molybdenum isopolyacid or heteropolyacid or its salt with different cations, for example, ammonium or alkali metal.
  • the isopolyacid means a polyacid having a polynuclear structure wherein a single oxo-acid is condensed.
  • the heteropolyacid means a polyacid having a polynuclear structure wherein two or more kinds of oxo-acids may be condensed.
  • the heteropolyacid has a structure comprising a condensed structure of an acid forming the skeleton (skeleton acid) and a small number of other kinds of atoms (hetero atom) contained in the center thereof and the like.
  • the first component comprises an oxide or a salt of manganese.
  • the second component comprises an oxide or a salt of cobalt.
  • the second component comprises an oxide or a salt of cerium.
  • the second component comprises an oxide or a salt of iron.
  • the exogenous binary catalyst may comprise oxides or salts of molybdenum as the first component and oxides or salts of cerium as the second component.
  • the binary catalyst may comprise oxides or salts of manganese as the first component and oxides or salts of iron, cobalt, or nickel as the second component.
  • the binary catalyst may comprise a phosphate salt, for example ammonium hydrophosphate as the first component and oxides or salts of iron, cobalt, or nickel as the second component.
  • the total amount of the first component and the second component used in the first reaction mixture is in a range of from about 0.5 weight percent to about 10 weight percent based on the amount of sulfur-containing fuel oil. In another embodiment, the total amount of the first component and the second component used in the first reaction mixture is in a range of from about 0.5 weight percent to about 5 weight percent based on the amount of sulfur-containing fuel oil. In yet another embodiment, the total amount of the first component and the second component used in the first reaction mixture is in a range of from about 1 weight percent to about 3 weight percent based on the amount of sulfur-containing fuel oil.
  • the atomic ratio of the first component to the second component is 6:1. In another embodiment, the atomic ratio of the first component is 9:1. In yet another embodiment, the atomic ratio of the first component to the second component is 12:1.
  • a physical mixture of the first and the second components may be used as the binary catalyst. In another embodiment, a pre-synthesized complex compound comprising the first and the second components, for example a heteropolyanion salt may be used as the exogenous binary catalyst.
  • the water-soluble acid may be selected from the group consisting of formic acid, acetic acid, propionic acid, butyric acid, sulfuric cid, phosphoric acid, and mixtures of two or more of the foregoing acids.
  • the acid is acetic acid.
  • the acid is formic acid.
  • the acid is sulfuric acid.
  • acetic acid anhydride may be used to generate acetic acid in situ in the first reaction mixture.
  • the amount of water-soluble acid employed in the oxidation reaction is in a range of from about 15 volume percent to about 40 volume percent based on the amount of the sulfur-containing fuel oil. In another embodiment, the amount of water-soluble acid employed in the oxidation reaction is in a range of from about 20 volume percent to about 35 volume percent based on the amount of the sulfur-containing fuel oil. In another embodiment, the amount of water-soluble acid employed in the oxidation reaction is in a range of from about 25 volume percent to about 30 volume percent based on the amount of the sulfur-containing fuel oil.
  • the amount of hydrogen peroxide (calculated as 100 percent) employed in the oxidation reaction is in a range of from about 4 weight percent to about 20 weight percent based on the amount of the sulfur-containing fuel oil. In another embodiment, the amount of hydrogen peroxide employed in the oxidation reaction is in a range of from about 5 weight percent to about 15 weight percent based on the amount of the sulfur-containing fuel oil. In yet another embodiment, the amount of hydrogen peroxide employed in the oxidation reaction is in a range of from about 6 weight percent to about 10 weight percent based on the amount of the sulfur-containing fuel oil. In one embodiment, hydrogen peroxide may be added as an aqueous solution having a concentration in a range of from about 15 weight percent to about 30 weight percent. In various embodiments, hydrogen peroxide may be added to the first reaction mixture using methods known to one skilled in the art, such as for example, in a continuous manner or in portions.
  • the at least one oxidized sulfur compound may be separated from the first oxidized mixture using a solid-liquid extraction process, for example an adsorption process, to provide the purified fuel oil.
  • the at least one oxidized sulfur compound may be separated from the first oxidized mixture using a liquid-liquid extraction process, to provide the purified fuel oil.
  • the method for purifying the sulfur-containing fuel oil further comprises a step of recovering the binary catalyst.
  • the binary catalyst is recovered from the first oxidized mixture by filtration or centrifuging/decantation, using methods known to one skilled in the art.
  • the first oxidized mixture is contacted with a porous silica adsorbent material, wherein the adsorbent material is characterized by a Brunauer-Emmett-Teller (BET) surface area value (total) of at least about 15 m 2 /g; and a Barrett-Joyner-Halenda (BJH) pore volume (total) of at least about 0.5 cc/g.
  • BET Brunauer-Emmett-Teller
  • BJH Barrett-Joyner-Halenda
  • the first reaction mixture further comprises a phase transfer catalyst.
  • the phase transfer catalyst comprises a quaternary ammonium salt or a phosphonium salt.
  • suitable phase transfer catalysts may be selected from the group consisting of methyltrioctylammonium chloride (Aliquat 336 TM ), tetraalkylammonium bromide, trialkylmethylammonium bromide, and hexaethylguanidium bromide.
  • the phase transfer catalyst comprises a quaternary ammonium or a phosphonium salt comprising an heteropolyanion M 1 n M 2 mO q p , wherein M 1 is selected from the group consisting of phosphorus, cerium, vanadium, manganese, iron, and cobalt, M 2 is selected from the group consisting of molybdenum, tungsten and vanadium or their mixture, "n” is an integer having a value 1 to 2, “m” is an integer having a value 6 to 18, “p” is an integer having a value 24 to 62, and “q” is an integer having a value 3 to 6.
  • the amount of phase transfer catalyst used is in a range of from about 0.1 weight percent to about 10 weight percent based on the amount of sulfur-containing fuel oil. In another embodiment, the amount of phase transfer catalyst used is in a range of from about 0.5 weight percent to about 1 weight percent based on the amount of sulfur-containing fuel oil. In yet another embodiment, the amount of phase transfer catalyst used is in a range of from about 1 weight percent to about 3 weight percent based on the amount of sulfur-containing fuel oil.
  • the temperature at which the oxidation (also referred to as contacting the fuel oil with an exogenous binary catalyst, hydrogen peroxide, and an acid at a temperature in a range of from about 25°C to about 120°C, to provide a first oxidized mixture) is carried out is in a range of from about 25°C to about 110°C. In another embodiment, the temperature at which the oxidation is carried out is in a range of from about 55°C to about 95°C. In yet another embodiment, the temperature at which the oxidation is carried out is in a range of from about 60°C to about 90°C.
  • the sulfur-containing fuel oil is deasphalted prior to contacting the sulfur-containing fuel oil with the binary catalyst and oxygen.
  • Deasphalting of the sulfur-containing fuel oil may be carried out by methods known to one skilled in the art. Typically, deasphalting is carried out by contacting the sulfur-containing fuel oil with an inert diluent and filtering or centrifuging the resultant mixture to separate the fuel oil from the insoluble asphaltenes to provide a deasphalted fuel oil.
  • the inert diluent is selected from the group consisting of liquid saturated hydrocarbons, liquid cyclic hydrocarbons, and mixtures of at least two of the foregoing inert diluents.
  • Suitable non-limiting examples of liquid cyclic hydrocarbons include cyclohexane, cycloheptane, and decalin.
  • Suitable non-limiting examples of liquid saturated hydrocarbons include propane, butane, and petroleum ether.
  • the method for purifying the sulfur-containing fuel oil further comprises a step of recovering the inert diluent.
  • the inert diluent is recovered from the first oxidized mixture by distillation, using methods known to one skilled in the art.
  • the present invention provides a method for purifying a sulfur-containing fuel oil comprising (a) contacting in a first reaction mixture the sulfur-containing fuel oil with a hydrocarbon diluent, an exogenous binary catalyst, hydrogen peroxide, and a water-soluble acid at a temperature in a range of from about 25°C to about 110°C to provide a first oxidized mixture; and (b) separating at least one oxidized sulfur compound from the first oxidized mixture; and (c) recovering the hydrocarbon diluent to provide a purified fuel oil.
  • the present invention provides a method for purifying a sulfur-containing fuel oil comprising (a) contacting in a first reaction mixture the sulfur-containing fuel oil comprising benzothiophene, dibenzothiophene, alkyl substituted benzothiophenes, and alkyl substituted dibenzothiophenes with petroleum-ether, an exogenous binary catalyst, hydrogen peroxide, and a water-soluble acid at a temperature in a range of from about 25°C to about 120°C to provide a first oxidized mixture comprising sulfoxides and sulfones of benzothiophene, dibenzothiophene, alkyl substituted benzothiophene, and alkyl substituted dibenzothiophene; (b) separating at least one oxidized sulfur compound from the first oxidized mixture; and (c) recovering petroleum-ether to provide a purified fuel oil.
  • Reagents and catalysts employed herein were obtained from Aldrich Chemical Company.
  • Examples 1 to 21 and Comparative Examples CE-1 to CE-11 Effect Of Oxidative Desulfurization On A Sulfur-Containing Fuel Oil Model Mixture.
  • the first model mixture was prepared from tetralin and benzothiophene (BT), and dibenzothiophene (DBT) wherein the sulfur-containing compounds were present in a 1:2 weight ratio (mixture #1).
  • the second model mixture was prepared from tetralin and dioctylsulfide (DOS), BT, and DBT wherein the sulfur-containing compounds were present in a 2:2:3 weight ratio (mixture #2).
  • the mixture #1 was used in Examples 1 to 16 and Comparative examples 1 to 7.
  • the mixture #2 was used in Examples 17 to 19 and Comparative examples 8 to 9.
  • the model mixtures were shown to comprise about 3 weight percent sulfur, when tested using a Varian Saturn 2000 GCMS.
  • Hydrogen peroxide (30 weight percent, 2 ml) was then added to each of the vials and the vials were placed in a Thermoline dry block heater and stirrer. The reaction mixture was stirred for about 30 minutes. The vials were removed and cooled in an ice bath. The cooled mixture was filtered through a filter device (Whatman autovial 0.45 micron PTFE). The filtrate was collected in a fresh vial. On standing, the filtrate separated into a top oil layer and a bottom aqueous layer. For analysis, the top oil layer 0.25 ml was diluted with 2.25 ml of acetonitrile containing 0.35 weight percent of biphenyl (internal standard).
  • Examples 1 to 21 demonstrate that the process disclosed herein, generally affords satisfactory sulfur removal of greater than about 85 percent. Further, catalyst activity appears to be dependent on the molecular structure of the catalyst. On comparing the conversion efficiency of catalysts in Tables 1 and 2, it can be seen that the binary catalysts having the following combinations Mo/Fe, P/Co, and P/Ni demonstrate good catalytic activity in the presence of acetic acid, while binary catalysts having the following combinations Mo/Ce, Mo/Ni, and Mn/Co demonstrate good catalytic activity in the presence of sulfuric acid.
  • Examples 22 to 26 and Comparative Examples CE-12 to CE-13 Effect Of Oxidative Desulfurization On A Sulfur-Containing Distillate Fuel Oil.
  • 25 ml of Saudi Crude atmospheric distillate fraction 600 - 700 °F (315 - 370 °C), containing 2.255 weight percent sulfur is first mixed with sulfuric or acetic acid and a binary catalyst consisting of about 250 mg of the first component and about 50 mg of the second component and placed into a reaction flask. Hydrogen peroxide (30 weight percent) is then added sequentially in three portions by 3 ml to the flask under stirring. The reaction mixture is stirred for about 30 minutes. The mixture is centrifuged and the oil layer is separated from the aqueous one. The oil layer is washed with 10 ml of acetonitrile to remove oxidized products. The oil layer is analyzed on the Spectro Phoenix II XRF analyzer.
  • the oxidized sulfur compounds may be separated from the crude oil containing reaction mixture (first oxidized mixture) using any of the techniques disclosed herein as being effective for that purpose. Table 4. Sulfur removal from distillate fuel oil and oil yield in the reaction of the oxidation with hydrogen peroxide in the presence of binary catalyst, an acid, and a phase transfer catalyst.
  • Example Catalyst Co-Catalyst Acid Phase transfer catalyst Sulfur in treated oil, perent Sulfur removal, percent Oil yield, percent Formula mg 22 MnSO 4 Co(OAc) 2 53 Sulfuric No 0.49 78.2 59.1 23 (NH 4 ) 6 Mo 7 O 24 Ce(NO 3 ) 3 51 Sulfuric No 0.40 82.3 83.5 24 (NH 4 ) 6 Mo 7 O 24 MnSO 4 52 Acetic No 1.47 34.8 86.0 25 (NH 4 ) 6 Mo 7 O 24 MnSO 4 52 Acetic Yes 1.29 42.8 84.0 CE-12 MnSO 4 None - Sulfuric No 1.03 54.3 85.1 CE-13 (NH 4 ) 6 Mo 7 O 24 None - Sulfuric No 0.41 81.8 50.4
  • Examples 22 to 25 also demonstrate that the process disclosed herein, generally applicable to real oil distillates and affords satisfactory sulfur removal of greater than about 80 percent at satisfactory fuel oil yield.
  • the binary catalyst having the combination Mn/Co demonstrates noticeable improvement in sulfur removal
  • binary catalyst having the combination Mo/Ce demonstrates significant improvement of the process selectivity and the fuel oil yield.
  • the use of a phase transfer catalyst significantly improves the sulfur removal from a fuel oil at about the same oil yield in that is obtained in the presence of acetic acid. It should be noted that the experiments conducted as part of this study were not optimized in all cases. Thus it is believed that much higher conversion of sulfur compounds that those shown in Table 1, 2, 3 and 4 are achievable, by adjusting various reaction parameters which are known to those skilled in the art. Such optimization falls within the scope of the instant invention.
  • the oxidized sulfur compounds may be separated from the reaction mixture (first oxidized mixture) using any of the techniques disclosed herein as being effective for that purpose.
  • the reaction mixture of Example 1 is filtered through a pad of silica gel to remove both the oxidized sulfur compounds and the exogenous binary catalyst which may be recovered therefrom.

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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)
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EP09156238A 2008-03-26 2009-03-26 Oxidative Entschwefelung von Brennstofföl Withdrawn EP2105489A1 (de)

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