Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
  • C07C2/54—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition of unsaturated hydrocarbons to saturated hydrocarbons or to hydrocarbons containing a six-membered aromatic ring with no unsaturation outside the aromatic ring
  • C07C2/56—Addition to acyclic hydrocarbons
  • C07C2/58—Catalytic processes
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
  • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
  • B01J31/0277—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature
  • B01J31/0278—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature containing nitrogen as cationic centre
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
  • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
  • B01J31/0277—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature
  • B01J31/0278—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature containing nitrogen as cationic centre
  • B01J31/0281—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature containing nitrogen as cationic centre the nitrogen being a ring member
  • B01J31/0284—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature containing nitrogen as cationic centre the nitrogen being a ring member of an aromatic ring, e.g. pyridinium
• • 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
  • C10G29/00—Refining of hydrocarbon oils, in the absence of hydrogen, with other chemicals
  • C10G29/20—Organic compounds not containing metal atoms
  • C10G29/205—Organic compounds not containing metal atoms by reaction with hydrocarbons added to the hydrocarbon oil
• • 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
  • C10G57/00—Treatment of hydrocarbon oils, in the absence of hydrogen, by at least one cracking process or refining process and at least one other conversion process
  • C10G57/005—Treatment of hydrocarbon oils, in the absence of hydrogen, by at least one cracking process or refining process and at least one other conversion process with alkylation
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
  • B01J2231/40—Substitution reactions at carbon centres, e.g. C-C or C-X, i.e. carbon-hetero atom, cross-coupling, C-H activation or ring-opening reactions
  • B01J2231/42—Catalytic cross-coupling, i.e. connection of previously not connected C-atoms or C- and X-atoms without rearrangement
• • 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
  • C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
  • C10G2300/10—Feedstock materials
  • C10G2300/1081—Alkanes
• • 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
  • C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
  • C10G2300/10—Feedstock materials
  • C10G2300/1088—Olefins
  • C10G2300/1092—C2-C4 olefins
• • 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
  • C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
  • C10G2300/40—Characteristics of the process deviating from typical ways of processing
  • C10G2300/4081—Recycling aspects
• • 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
  • C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
  • C10G2300/70—Catalyst aspects

Definitions

• the invention relates to a method for producing alkylated oil by ionic liquid catalyzed alkylation reaction, and belongs to the field of petrochemical industry. Background technique
• alkylation of isobutane with butene is one of the important processes for the production of clean high-octane gasoline blending components.
• the catalyst used in the alkylation reaction may include cyanuric acid, concentrated sulfuric acid, and an ionic liquid, of which hydrofluoric acid and concentrated sulfuric acid are conventional industrial catalysts for this process.
• hydrofluoric acid and concentrated sulfuric acid show good performance in terms of activity, selectivity and catalyst life, environmental pollution, equipment corrosion and personal injury caused by hydrofluoric acid and concentrated sulfuric acid during the production process make C4 Industrial applications of alkylation are severely limited.
• ionic liquids are environmentally friendly, have low corrosivity, low toxicity, acidity and physicochemical properties, easy separation from products, and high cycle utilization. This makes it possible to become an ideal new type of catalytic material to replace liquid strong acids such as hydrofluoric acid and concentrated sulfuric acid to catalyze the C4 alkylation reaction.
• U.S. Patent No. 7,285,698, the Chinese patent CN 1500764A discloses the use of a composite ionic liquid as a catalyst to catalyze the alkylation of isobutane with butene. The yield of the alkylated oil of the product can reach 170- of the olefin feed volume.
• the proportion of >C8 in alkylated oil can reach 60-80%, the outstanding advantage is that the proportion of tridecylpentane in C8 component is more than 70%, RON (research octane number) Can reach 93-98.
• Chinese Patent Application No. 200710063459. 6 discloses a method for prolonging the life of a catalyst by using aluminum metal or aluminum trichloride as an aluminum source to supplement aluminum chloride lost due to oil phase entrainment and ionic liquid hydrolysis. .
• the inventors of the patent found that the main reason for the deactivation of the chloroaluminate ionic liquid catalyst is that the loss of reactivity is caused by the loss of aluminum trichloride as an active component, and the main cause of the loss of aluminum trichloride is the reaction raw material. The inevitable water causes the hydrolysis of aluminum trichloride.
• the patent application provides a method for continuously producing an alkylating oil agent by continuously regenerating an ionic liquid catalyst, using aluminum metal or aluminum trichloride as an aluminum source, supplementing the loss due to oil phase entrainment and ionic liquid hydrolysis. A1C1 3 , thus achieving continuous aluminum supplementation to extend catalyst life.
• the patent application also recognizes that the process simultaneously reduces the amount of HC1 in the catalytic reaction system, maintains the selectivity of the target product isooctane in the product at a higher level, and reduces the corrosivity due to the presence of HC1.
• the main technical problem solved by the present invention is to provide an alkylation reaction method using an ionic liquid as a catalyst, and to catalyze the mechanism of alkylation reaction by an acidic ionic liquid, by reinjecting a hydrocarbon-rich fraction into the reaction system. Achieving the purpose of effectively extending the life of the ionic liquid catalyst while reducing the hydrocarbon content in the alkylated oil product.
• the present invention provides an alkylation reaction method using an ionic liquid as a catalyst for synthesizing an alkylated oil, wherein the reaction raw material is carbon 4 during the alkylation reaction.
• the olefin and the carbon 4 alkane, the carbon 4 alkane are in excess and are separated from the product for recycling, the method further comprising, during the alkylating reaction, separating the hydrocarbon-rich reaction product from the alkylation reaction product.
• the fraction is injected back into the reaction system, and the cation of the ionic liquid catalyst in the alkylation reaction is derived from a hydride of an alkyl group-containing amine, a hydrohalide of imidazole or a hydrohalide of pyridine, and the anion is derived from a The above metal compound.
• the ionic liquid catalyzed alkylation reaction follows a positive ion mechanism in which the Lewis acid of the ionic liquid and Br6ns ted (also known as B acid) act together.
• the inventors of the present invention have shown through research that when the ionic liquid hemostatic agent is selected to contain a compound component, the BrSns ted acid acidity of the ionic liquid is mainly provided by hydrogen halide, in the process of ionic liquid catalyzed alkylation reaction, !
• the chloroalkane formed by the hydrogenation of the hydrogen as an auxiliary with the carbon 4 olefin is an intermediate for the reaction of the initial normal carbon ion.
• the alkylated oil product will be continuously taken out of the reaction system, which will not only cause a higher hydrocarbon content in the alkylated oil, but also cause an ionic liquid. Briins ted acid loss and even catalyst deactivation.
• the present invention provides an effective extension of the life of the ionic liquid catalyst.
• the method for reducing the content of halogenated hydrocarbons in the alkylated oil product that is, in the alkylation reaction process using an ionic liquid as a catalyst, separating or enriching from the alkylation reaction system by means of distillation or adsorption separation Contained! A 3 ⁇ 4 generation hydrocarbon fraction, and then the halogenated hydrocarbon fraction is fed back to the reaction system.
• the ionic liquid catalyst may be various ionic liquids which have been reported or recognized to be capable of catalyzing alkylation reaction, and may be the aforementioned simple ionic liquid, It may be a composite ionic liquid catalyst, that is, the anion of the ionic liquid comes from two or more metal compounds, at least one metal compound is selected from the chloride or bromide of aluminum, and the other metal compound is derived from aluminum, copper, iron, zinc, Nickel, titanium or silver! 3 ⁇ 4 compound, sulfate or nitrate.
• the selection, preparation and use of the ionic liquid catalyst are carried out in accordance with the prior art prior to the present invention, and the invention will not be specifically described herein.
• the alkylation reaction used in the present invention also refers to the reaction between carbon 4 alkane and carbon 4 olefin, especially the C4 alkylation reaction of isobutane with butene, that is, the raw material of the alkylation reaction is basically It is a mixture of isobutane and a C4 olefin (butene); wherein the butene raw material may be one of 1-butene, 2-butene and isobutylene normal or isoolefin or a mixture thereof.
• a hydrocarbon raw material containing the carbon 4 alkane and carbon 4 olefin as a main component may be used, and a small amount of propylene may be allowed in the raw material.
• the conditions and parameters of the alkylation reaction process can be completely adopted by the currently reported or employed processes.
• Isobutane usually requires an excess in the preparation (may also allow a small amount of alkanes such as propane, pentane and the like), that is,
• the molar ratio of alkylene in the reaction raw material should be greater than 1, generally 1:1-40:1; the reaction temperature can be determined at -20-100 ° C, generally 0-50. C;
• the reaction pressure should be selected to ensure that the reaction material is kept in a liquid state as a lower limit, generally 0.1-1. 6Mpa.
• the hydrocarbon-rich fraction is injected back to
• the method of the reaction system may include:
• the fraction enriched in 3 ⁇ 4 hydrocarbons of the alkane is mixed with the ionic liquid catalyst before entering the reactor;
• the fraction rich in 3 ⁇ 4 hydrocarbons is mixed with the carbon 4 alkane feedstock recycled in the alkylation reaction and injected into the reactor.
• the inventors of the present invention found through research that the alkylene hydrocarbons contained in the alkylated oil products are mostly C3 ⁇ C5 monosubstituted hydrocarbons, of which C4 halogenated hydrocarbons are dominant, and the boiling points of these halogenated hydrocarbons are mainly concentrated.
• the C5 ⁇ C7 fraction of the alkylation product such as: 2-chloropropane, boiling point 35 'C; 2-chloro-2-methylpropane, boiling point 51 ° C; 1-chloro-2-pyridyl propane , boiling point 69 °C; 2-chloro-2-indenyl butane, boiling point 87 °C, and so on, fractionation of alkylated oil products
• the C5-C7 fraction is concentrated at 28 °C ⁇
• the C6 fraction is concentrated at 50 °C - 69 ° (:.
• the hydrocarbon-rich fraction can be determined as C5 ⁇ C7 obtained by distillation collection of the alkylation reaction product.
• the fraction is more preferably determined to be a C6 fraction.
• the separated fraction is first mixed with the alkylation reaction raw material, and then enters the reactor to further prolong the life of the acidic ionic liquid, thereby increasing the throughput per unit weight of the catalyst. .
• a distillation column or a related fractionation apparatus may be disposed in the alkylation reaction system, and the alkylation product may be subjected to a fraction cutting treatment, that is, the distillation of the alkylation reaction product may be
• the alkylation reaction product is introduced into a distillation column, and the fraction rich in the hydrocarbon generation is collected and taken out from the side line of the distillation column.
• a single column or multiple columns may be provided, and the reaction product may be subjected to one or more stages of distillation separation, for example, the alkylation reaction product is introduced into a distillation column, and the distillation column is collected and taken out from the side line of the distillation column.
• a hydrocarbon-rich fraction primary distillation separation
• Reinjecting into the reaction system or, introducing the alkylation reaction product into a distillation column of two or more stages in series, collecting and extracting the halogenated hydrocarbon-rich fraction from the side line of the last stage distillation column, and reinjecting it into In the reaction system.
• single-sided line collection can be used, in order to obtain a more concentrated fraction (for example, when the C6 fraction is dominant), or multi-side line collection.
• the alkylation product may also be subjected to a de-treatment to collect a halogenated hydrocarbon or a halogenated hydrocarbon-rich component therein and to reinject it into the reaction system. That is, the fraction rich in deuterated hydrocarbons may also be adsorbed and enriched by adsorbing and enriching halogenated hydrocarbons from the alkylation reaction product, and then adsorbing and enriching the hydrocarbons using carbon 3 to carbon 6 A fraction obtained by dehydration of a hydrocarbon, the molecular sieve, activated carbon, activated alumina, porous silica gel, adsorption resin, activated carbon fiber, acid clay or any mixture thereof.
• the C3 ⁇ C5 monosubstituted halogenated hydrocarbons contained in the alkylated oil product can utilize, for example, molecular sieves, Adsorbent materials such as activated carbon, activated alumina, porous silica gel, adsorption resin, activated carbon fiber, acid white clay or some substances capable of dehydrocarbonation are adsorbed from the alkylated oil product as an adsorbent and concentrated on the adsorbent.
• Adsorbent materials such as activated carbon, activated alumina, porous silica gel, adsorption resin, activated carbon fiber, acid white clay or some substances capable of dehydrocarbonation are adsorbed from the alkylated oil product as an adsorbent and concentrated on the adsorbent.
• the 3 ⁇ 4 generation hydrocarbons can be desorbed and regenerated by using appropriate light hydrocarbon fractions, and the hydrocarbon-containing light hydrocarbon fraction can be obtained.
• the appropriate adsorption materials can be selected to obtain higher adsorption and desorption results, which is consistent with the above.
• the light hydrocarbon fraction rich in 3 ⁇ 4 hydrocarbons obtained hereinafter is also referred to as a halogen-rich hydrocarbon fraction in the present invention.
• the above adsorbent materials which can realize the dehydrogenation of hydrocarbons can be selected by a person skilled in the art as needed, and may be molecular sieves and activated alumina.
• the hydrocarbon substance for desorption may be a carbon 3 to carbon 6 alkane or a mixture thereof, such as propane, n-butane, isobutane, C5 alkane and C6 alkane.
• propane, n-butane, isobutane, C5 alkane and C6 alkane propane, n-butane, isobutane, C5 alkane and C6 alkane.
• One or a mixture thereof, combined with the actual production operation, Isobutane is preferred.
• the carbon 3 to carbon 6 light hydrocarbon may be additionally added, or may be derived from a fractionated product of the alkylation product, for example, a part of the recycled isobutane is directly separated from the reaction product and introduced into the adsorption system. The desorbed halogenated hydrocarbon is brought back to the reaction system.
• the adsorption-desorption treatment of the alkylation product may be carried out by first feeding the separated alkylated oil product into an adsorption device (in which an adsorption material is added in advance), and introducing the desorption
• the light hydrocarbon fraction for example, introducing a recycled alkane (isobutane) into the adsorption unit desorbs and carries the deuterated hydrocarbon adsorbed from the alkylated oil back to the alkylation reaction system.
• the above adsorption-desorption treatment may also be combined with the aforementioned distillation process, and the distillate-rich fraction (C5-C7 fraction) extracted from the side line of the distillation column is first sent to the adsorption device, and then the dehydrogenation process is performed to cause the hydrocarbon generation to be Carrying back to the alkylation reaction system.
• the invention can effectively prolong the service life of the acidic ionic liquid catalyst, reduce the acid consumption of the acid ionic liquid catalyst, and improve the catalytic performance of the catalyst by reinjecting the fraction rich in 3 ⁇ 4 hydrocarbons from the alkylation reaction product into the reaction system.
• the amount of raw material treated per unit mass of the catalyst is significantly increased; and the alkylene in the alkylation product is separated, and the hydrocarbon content in the alkylated oil is also effectively reduced.
• hydrocarbons to be collected by distillation and/or adsorption in the process of the invention are predominantly chlorinated or brominated hydrocarbons, depending on the particular choice of ionic liquid catalyst employed.
• the method for reinjecting the reaction system may be that the hydrocarbon-containing fraction in the alkylated oil product is mixed with the raw material and then enters the reactor; in the method of the present invention, The method for reinjecting the reaction system may be that the distillate-containing fraction in the alkylated oil product is mixed with the ionic liquid and then enters the reactor; in the method of the present invention, the method for reinjecting the reaction system may be The halogenated hydrocarbon-containing fraction of the alkylated oil product is directly injected into the reactor; in the method of the present invention, the method of reinjecting the reaction system may be to mix the halogenated hydrocarbon-rich fraction with the recycled isobutane Inject into the reactor.
• the key to the present invention is to provide a pair of acid
• the ionic liquid is a process for industrially producing alkylated oil for the catalyst, and the hydrocarbon in the alkylation product is returned to the alkylation reaction system in the form of a fraction, supplementing the consumption of B acid of the acidic ionic liquid, and prolonging the acid ionic liquid catalyst.
• the service life, the amount of halogenated hydrocarbon or halogenated hydrocarbon-rich fractions is completely dependent on the circulation of the reaction system, which is more advantageous for industrial implementation.
• the implementation of the solution of the present invention only needs to be appropriately modified for the current alkylation reaction device, for example, adding a side-line fractionation design, a adsorption device, and an increase in a distillation column for separating isobutane from an alkylated oil. It is sufficient to feed the extracted fraction into the reaction system, that is, to increase the efficiency of the alkylation reaction without adding more equipment investment.
• the practice of the present invention can effectively extend the service life of the acidic ionic liquid catalyst and reduce the consumption of B acid in the reaction; another outstanding advantage of the method of the present invention is that it can effectively reduce the alkylate oil! 3 ⁇ 4 content, and has no effect on the quality of the alkylated oil; the method provided by the invention is simple to operate and is advantageous for industrial application.
• the present invention provides a process for producing an alkylated oil having a reduced content of a compound, particularly a reduced hydrocarbon content of 13 ⁇ 4.
• the alkylated oil having a reduced hydrocarbon content of 3 ⁇ 4 generation is particularly suitable for use as a fuel or fuel co-mixing component which is optionally further treated to remove at least a portion of the residual halogenated hydrocarbon prior to use.
• the halogenated hydrocarbon is recycled back to the reaction system, but the halogenated hydrocarbon can also be removed from the process and subsequently disposed of or used in other processes.
• Figure 1 is a schematic flow diagram of a process for producing an alkylated oil by an alkylation reaction provided by the present invention.
• Figure 2 is a flow diagram of one embodiment of a process for the production of alkylated oils by alkylation using the present invention, wherein fractions of the hydrocarbon-rich fraction fractionated from the reaction product are returned to the reaction feed and passed to the reactor.
• Fig. 3 is a flow chart showing another embodiment of a process for producing an alkylated oil by an alkylation reaction according to the present invention, which is rich in fractionation from the reaction product! The 3 ⁇ 4 generation hydrocarbon fraction is first returned to the ionic liquid catalyst and then to the reactor.
• Figure 4 is a flow diagram of yet another embodiment of a process for the production of alkylated oils by alkylation using the present invention, wherein the fractions rich in halogenated hydrocarbons fractionated from the reaction product are returned directly to the reactor.
• the alkylated product is fractionated by a multi-tower side line, wherein the C6 fraction is fractionated and returned to the reaction raw material. And enter the reactor.
• Fig. 6 is a flow chart showing an embodiment of the method for producing an alkylated oil by an alkylation reaction using an adsorption process for separating a halogenated hydrocarbon from an alkylated oil and reinjecting it into a reaction system.
• Fig. 7 is a flow chart showing an embodiment of a method for producing an alkylated oil by an alkylation reaction in which a distillation and adsorption process are combined. detailed description
• FIG. 1 illustrates the alkylation reaction scheme provided by the present invention.
• the C4 raw material undergoes alkylation reaction in the reaction system under ionic liquid catalysis, and the reaction product is separated from the catalyst in a catalyst separation system (also called a separation system).
• a catalyst separation system also called a separation system.
• the separated ionic liquid catalyst is returned to the reaction system.
• excess C4 alkane isobutane
• the alkylated oil is discharged and collected.
• the above process is a conventional alkylation reaction scheme, and the method provided by the present invention further comprises simultaneously collecting the halogenated hydrocarbon-rich fraction from the product separation system into the reaction system.
• Figure 1 shows several schemes for collecting fractions from the side line of the distillation column to the reaction system: Mixing the raw materials into the reaction system, directly entering the reaction system, mixing with the ionic liquid catalyst, entering the reaction system, and mixing with the recycled isobutane before entering the reaction system (please add a dotted arrow mixed with the recycled isobutane, Should the direction of the arrow when mixing with the ionic liquid should be downward?).
• Figure 1 is only a partial representation of the invention, and the reinjected halogenated hydrocarbon fraction may also be derived from the adsorption and desorption of alkylated oil from the product separation system.
• a more specific embodiment flow can be described with reference to Figures 2-6 and the following examples.
• the acidic ionic liquid catalysts used in the examples were synthesized by the methods described in U.S. Patent No. 7,285,698, USP No. 20040133056 A1 and Chinese Patent No. 02149296.
• the composition of the alkylated oil product was determined by gas chromatography, and the element (chlorine or bromine) in the alkylated oil product was quantitatively analyzed by the microcoulometric method, and the catalyst activity was measured by the conversion ratio of butene.
• Butene conversion is defined as follows:
• C the raw material is a mixture of isobutane and 2-butene, the molar ratio of alkylene is 20:1, and the alkylation product obtained by catalytic alkylation reaction with fresh catalyst is collected, and the composition thereof is analyzed, and the results are shown in Table 1, wherein The ratio of TMP/DMH indicates the quality of the alkylated oil, and the higher the value, the better the quality of the alkylated oil.
• the isobutane alkylation reaction is carried out on a continuous apparatus using an acidic ionic liquid having the same ratio as the catalyst.
• the ionic liquid is stored in an amount of 200 g, the reaction pressure is 0.5 MPa, and the reaction temperature is 30.
• C the raw material is the same as the mixture of isobutane and 2-butene, and the molar ratio of pitene is 20:1.
• the C5-C7 fraction obtained in the comparative example is mixed with 100 kg of raw material, and then the continuous alkane is mixed.
• the base reaction was carried out to separate and collect the alkylated oil product (isobutylene and catalyst, the same as in the following examples), and the composition thereof was analyzed. The results are shown in Table 3.
• the C5 ⁇ C7 fraction with higher chlorine content in the alkylated oil product is the same as the comparative example.
• the mixing of the raw materials can significantly prolong the life of the ionic liquid catalyst, and has no significant effect on the quality of the alkylated oil product.
• the ionic liquid is catalyzed by a similar ionic ionic liquid as a catalyst in a continuous apparatus to catalyze the isobutane alkylation reaction, the ionic liquid is 200 g, the reaction pressure is 0. 5 MPa, the reaction temperature is 30 ° C, the raw material The same ratio as the mixture of isobutane and 2-butene, the molar ratio of alkylene is 20:1, and the C5 ⁇ C7 fraction obtained in the comparative example is mixed with 200g of ionic liquid catalyst for continuous alkylation.
• the alkylated oil product obtained by the reaction was analyzed for its composition, and the results are shown in Table 4.
• the chlorine content of the fraction above C8 was measured and found to be 9. 2 mg/L of chlorine. It can be seen that, compared with the comparative example, the C5-C7 fraction with higher chlorine content in the alkylated oil product is mixed with the ionic liquid in advance to significantly prolong the life of the ionic liquid catalyst, and simultaneously to the alkylated oil. The overall quality of the product has no significant effect.
• the ionic liquid is catalyzed by a ionic liquid in the same manner as the catalyst.
• the ionic liquid is 200 g
• the reaction pressure is 0.5 MPa
• the reaction temperature is 30 ° C
• the raw materials are the same.
• the comparative example is a mixture of isobutane and 2-butene
• the molar ratio of alkylene is 20: 1
• the feed rate of the raw material is 500 g / h
• the C5 ⁇ C7 fraction obtained in the comparative example is 4 g / h.
• the rate was directly injected into the reactor, and a continuous alkylation reaction was carried out to separate and collect the alkylated oil product, and the composition thereof was analyzed. The results are shown in Table 5.
• the isobutane alkylation reaction is carried out on a continuous apparatus using an acidic ionic liquid having the same ratio as the catalyst.
• the ionic liquid is stored in an amount of 200 g, the reaction pressure is 0.5 MPa, and the reaction temperature is 30.
• a continuous alkylation reaction is carried out by using an ionic liquid alkylation reaction process as shown in FIG. 1, and a reaction raw material (indicated by a C4 raw material in the drawing) is simultaneously fed into the reactor together with the ionic liquid.
• a reaction raw material indicated by a C4 raw material in the drawing
• Forming an alkylation reaction system the reactants enter the separation system, the ionic liquid is separated and returned to the reaction system, and the alkylation product continues to enter the distillation column, and the distillation operation is controlled to fractionate the C5-C7 fraction or the C6 fraction from the side line to be rich.
• the fraction containing the ?3 ⁇ 4 hydrocarbons is reinjected into the reaction feedstock and enters the reactor together.
• the side line of the distillation column also separates n-butane, and the alkylate oil is separated from the bottom of the column and sent to the product storage tank, respectively.
• the excess isobutane separated is returned to the reactor for continued use.
• the other conditions of the alkylation reaction were the same as in Example 1 except that the C5-C7 fraction continuously fractionated from the alkylation product was collected by a single column single side line to be recycled into the reaction raw material to carry out the continuous operation.
• the ionic liquid alkylation reaction process shown in Fig. 2 was employed.
• the specific embodiment is a single column separation ionic liquid catalytic alkylation reaction process, the distillation tower top separates excess isobutane for recycling, the bottom is an alkylated oil product, and the C5-C7 fraction is rich (deuterated)
• the hydrocarbon fraction) or the C6 fraction is withdrawn from the side line of the distillation column, and is mixed with the ionic liquid catalyst recycled from the catalyst separation system before entering the reaction system for reaction.
• Example 7 As a process change, the distillation conditions are controlled, multi-side line fractionation is carried out in the distillation column, and the C6 fraction is collected in the same manner, and the C5 fraction is collected at the same time, and is used together with the bottoms fraction as an alkylated oil product or alternatively for other purposes.
• Example 7
• the ionic liquid alkylation reaction process shown in Fig. 3 was employed.
• an excess of isobutane is separated at the top of the distillation column, and the bottom is an alkylated oil product, which is rich in a hydrocarbon-rich fraction (C5-C7 fraction). It is taken from the side line of the distillation column and directly injected into the reactor to participate in the alkylation reaction.
• the other conditions of the alkylation reaction were the same as in Example 3, except that the C5-C7 fraction continuously fractionated from the alkylation product was collected by a single column side line and directly injected into the reactor for continuous operation.
• Example 8 According to the comparative example and the comparison result of Example 3, it can be clearly predicted, according to Figure 3.
• the process of alkylation to synthesize alkylated oil not only extends the life of the ionic liquid catalyst, but also reduces the chlorine content of the alkylated oil product.
• Example 8
• Example 5 The process of Example 5 was changed to employ an ionic liquid alkylation reaction process as shown in FIG.
• ionic liquid catalytic alkylation reaction process of multi-tower separation secondary separation
• a series of distillation columns A and B are arranged, and excess isobutane is separated and recycled by distillation column A, and the bottoms fraction enters the distillation column.
• B n-butane is separated from the top of the column, and the C5 and C6 components are respectively taken out from the side line of the distillation column B, and the C5 fraction and the bottom fraction are collectively used as an alkylated oil product, and the C 6 fraction is premixed with the reaction raw material.
• the other conditions of the alkylation reaction were the same as in Example 1 except that the C5-C7 fraction continuously fractionated from the alkylation product was collected by the multi-tower side line to be recycled into the reaction raw material to carry out the continuous operation.
• an ionic liquid alkylation reaction process as shown in FIG. 5 was employed.
• a portion of the excess iso-alkane is separated from the top of the distillation column and directly returned to the reaction raw material for recycling, and the bottom is an alkylated oil, which is alkylated.
• the oil is introduced into the adsorption tank A/B to remove the hydrocarbon-substituted unit (in which an adsorbent material such as one of 13X molecular sieve, NaY molecular sieve or activated alumina is previously disposed), and another portion of the adsorption-saturated adsorption tank is from the top of the distillation tower.
• the recycled isobutane is desorbed and regenerated, and the desorbed isobutane is cooled and then carried with the desorbed hydrocarbon. It is also mixed with the reaction raw material and then enters the reaction body.
• the alkylation reaction is carried out, and the alkylated oil after decoupling the hydrocarbon is discharged as a product.
• the alkylation reaction conditions were the same as in Example 4.
• Example 10 From the results of Comparative Example, Example 1 and Example 4, it can be clearly predicted that the alkylation reaction can be carried out according to the process of Figure 5 and the above-mentioned process to synthesize the alkylated oil, which not only prolongs the life of the ionic liquid catalyst, but also reduces the alkylated oil.
• the chlorine content of the product Example 10
• the ionic liquid alkylation reaction process shown in Fig. 6 was used.
• a portion of the excess isobutane is separated from the top of the distillation column and directly returned to the reaction raw material for recycling.
• the bottom of the column is an alkylated oil product, and the distillation column side line
• the C5-C7 fraction rich in halogenated hydrocarbons and n-butane are taken out, and the hydrocarbon-rich fraction is introduced into the adsorption tank A/B for adsorption removal!
• the fraction after the removal of the hydrocarbon is incorporated into the bottom fraction as the alkylation oil product discharge device, and the adsorption saturated adsorption tank is desorbed and regenerated by another portion of the recycled isobutane from the top of the distillation column. Desorption is carried out with isobutane and then carried away and desorbed!
• the 3 ⁇ 4 generation hydrocarbon is mixed with the reaction raw material and then enters the reaction system for alkylation reaction.
• the alkylation reaction conditions were the same as in Example 4.
• Example 1 and Example 4 From the results of Comparative Example, Example 1 and Example 4, it can be predicted that the alkylation reaction can be carried out according to the process of Figure 6 and the above-mentioned process to synthesize the alkylated oil, which can not only prolong the life of the ionic liquid catalyst, but also reduce the alkylated oil product.
• the chlorine content in the medium It should be noted that the above embodiments are only used to explain the technical solutions of the present invention, and are not limited thereto. Any one skilled in the art can modify or replace the technical solutions of the present invention within the technical scope of the present invention. It is intended to be included within the scope of the appended claims.

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