69 results about "Alkylation unit" patented technology

The invention discloses efficient coalescence-separation equipment for an alkylating device, and belongs to the field of oil-water separation of petrochemical industry. The efficient coalescence-separation equipment comprises a housing and an internal part; a mixed liquid inlet part, a water (acid) phase outlet part, and an oil phase outlet part are formed in the housing; a liquid distributor is arranged at the mixed liquid inlet part; an oil collecting chamber above which an oil phase outlet is formed is arranged at the oil phase outlet part; a rectifying and uniform distributing device, a coarse graining coalescence section, a modified corrugated and reinforced separation section and a nanofiber deep separation section are arranged in the housing along the direction the mixed liquid flows; a position gauge is also arranged in the housing. According to the efficient coalescence-separation equipment for the alkylating device, the shallow pool theory and coarse graining technology are integrated, so that high oil-water (-acid) separation efficiency can be realized; compared with the existing single filler oil-water separation equipment, the efficient coalescence-separation equipment, disclosed by the invention, has obvious characteristics of being high in separation efficiency, high in processing capability, high in operation flexibility, small in floor area, small in one-time investment for equipment, etc.

A process for producing cumene comprising converting plastics to hydrocarbon liquid and pyrolysis gas; feeding hydrocarbon liquid to hydroprocessor to yield hydrocarbon product and first gas stream; feeding hydrocarbon product to reforming unit to produce reforming product, second gas stream, and hydrogen; separating reforming product into non-aromatics recycle stream and second aromatics stream (C₆+ aromatics); recycling non-aromatics recycle stream to reforming unit; separating second aromatics stream into benzene, C₇, C₈, C₉, C₁₀, and C₁₁+ aromatics; contacting C₇, C₉, and/or C₁₀ aromatics with a disproportionation&transalkylation catalyst/H2 to yield benzene&xylenes; conveying C₁₁+ aromatics to hydroprocessor; introducing pyrolysis gas, first and/or second gas stream to first separator to produce first propylene stream, first C₂&C₄ unsaturated stream, and saturated gas (H₂ and C_1-4 saturated hydrocarbons); introducing first C₂&C₄ unsaturated stream to metathesis reactor to produce second propylene stream; and feeding benzene, and first and/or second propylene stream to alkylation unit to produce cumene.

The present invention provides an integrated process for the production of p-xylene, comprising the steps of A) separating a mixed feedstock containing benzene, toluene, C₈ aromatic hydrocarbons, C₉ and higher aromatic hydrocarbons, and non-aromatic hydrocarbons from a reforming unit, to obtain a first benzene stream, a first toluene stream, a first C₈ aromatic hydrocarbon stream, a stream of C₉ and higher aromatic hydrocarbons, and a stream of non-aromatic hydrocarbons; B) feeding the stream of C₉ and higher aromatic hydrocarbons from step A) to a C₉ and higher aromatic hydrocarbon dealkylation unit, where dealkylation reaction occurs in the presence of hydrogen, and separating the reaction effluent to obtain a second benzene stream, a second toluene stream, and a second C₈ aromatic hydrocarbon stream; C) feeding both the first toluene stream and the second toluene stream to a toluene selective disproportionation unit, where toluene selective disproportionation reaction occurs in the presence of hydrogen to produce a stream containing C₈ aromatic hydrocarbons including p-xylene and benzene, which stream is separated to obtain a third C₈ aromatic hydrocarbon stream, a third toluene stream, and a third benzene stream, with the third toluene stream being returned to an inlet of this unit; D) feeding both the first C₈ aromatic hydrocarbon stream and the second C₈ aromatic hydrocarbon stream to an adsorption separation unit, to obtain a first p-xylene product stream and a fifth C₈ aromatic hydrocarbon stream, with the fifth C₈ aromatic hydrocarbon stream being passed to an isomerization unit; E) feeding the third C₈ aromatic hydrocarbon stream to a crystallization separation unit, to obtain a fourth C₈ aromatic hydrocarbon stream and a second p-xylene product stream, with the fourth C₈ aromatic hydrocarbon stream being passed to the adsorption separation unit or the isomerization unit; and F) feeding an effluent of the isomerization unit to an inlet of the adsorption separation unit.

The apparatus includes an alkylation unit connected to a first benzene recycle conduit, a feed conduit and an alkylation effluent conduit; a transalkylation unit connected to an polyalkylbenzene recycle conduit, a second benzene recycle conduit, and a transalkylation effluent conduit. A dividing wall distillation column is in fluid communication with the transalkylation effluent conduit, the alkylation effluent conduit, a product stream, a bottoms stream conduit and first and second benzene recycle conduits. A polyalkylbenzene fractionation column is connected to the bottoms stream conduit, the polyalkylbenzene recycle conduit and a heavy component conduit.

The invention relates to lead-free aviation gasoline. The lead-free aviation gasoline contains components as follows: A) 55wt%-90wt% of alkylation unit oil, B) 5wt%-15wt% of pentane component oil, C) 0-20wt% of C7 aromatic component oil, D) 0-15wt% of cumene and E) 0-15wt% of an alkyl ether antiknock agent, wherein the alkylation unit oil is prepared from a reaction product distillate C4 obtained through alkylation of 1-butene and/or 2-butene and iso-butane as well as light components shown in the specification; the content of arylamine compounds in the lead-free aviation gasoline does not exceed 0.5wt%, and further, the lead-free aviation gasoline contains lead which does not exceed 0.01 g/L and contains at least one of the component C and the component D. The gasoline does not contain the arylamine compounds basically, so that environmental pollution caused by the aviation gasoline is greatly reduced, moreover, an octane value and a heat value realize good balance, a net heating value at least reaches 43.5 MJ/kg, and a motor octane value is not smaller than 91.

The invention discloses a p-xylene fluid catalyst prepared by performing alkylation of methylbenzene methyl alcohol and a preparation method of the p-xylene fluid catalyst. The p-xylene fluid catalyst is prepared by modeling mixed spray of ZSM-5, matrix and amorphous binding agent, modifying by alkaline-earth metals, non-metals or/and rare earth metals and modifying by a siloxy group compound to prepare corresponding catalysts. The catalyst is used in methylbenzene methyl alcohol alkylation reaction; based on full conversion of methanol, methylbenzene conversion rate is more than 20 percent, and the once through yield of p-xylene in the product is up to 25 percent.

A process for the preparation of alkylate and middle distillate, the process comprising: (a) catalytically cracking a first hydrocarbon feedstock by contacting the feedstock with a cracking catalyst comprising a shape-selective additive at a temperature in the range of from 450 to 650° C. within a riser or downcomer reaction zone to yield a first cracked product comprising middle distillate and a spent cracking catalyst; (b) regenerating the spent cracking catalyst to yield a regenerated cracking catalyst; (c) contacting, within a second reaction zone, at least part of the regenerated cracking catalyst obtained in step (b) with a second hydrocarbon feedstock at a temperature in the range of from 500 to 800° C. to yield a second cracked product and a used regenerated catalyst, the second feedstock comprising at least 70 wt % C₅₊ hydrocarbons obtained in a Fischer-Tropsch hydrocarbon synthesis process; (d) using the used regenerated catalyst as at least part of the cracking catalyst in step (a); and (e) alkylating at least a portion of the second cracked product in an alkylation unit to obtain alkylate.

A process for producing propylene and cumene comprising converting plastics to hydrocarbon liquid and pyrolysis gas in pyrolyzer; feeding hydrocarbon liquid to hydroprocessor to yield hydrocarbon product and first gas stream; introducing hydrocarbon product to second separator to produce first C₆ aromatics and refined product; feeding refined product to steam cracker to produce steam cracker product; introducing steam cracker product to third separator to produce second C₆ aromatics, third propylene stream, second C₂&C₄ unsaturated stream, C_1-4 saturated gas, and balance hydrocarbons product; introducing pyrolysis gas and/or first gas stream to first separator to produce first propylene stream, first C₂&C₄ unsaturated stream, and saturated gas stream; feeding first and/or second C₂&C₄ unsaturated stream to metathesis reactor to produce second propylene stream; feeding first and/or second C₆ aromatics, and first, second, and/or third propylene stream to alkylation unit to produce cumene; and conveying balance hydrocarbons product to pyrolyzer and/or hydroprocessor.

The invention relates to an aromatic hydrocarbon liquid phase alkylation method, for mainly solving the problem that a catalyst is easily inactivated and poor in stability in the prior art. According to the technical scheme, a mixture containing saturated alkane, aromatic hydrocarbon and olefin is taken as a raw material, silicon-aluminum crystal zeolite is taken as a catalyst, and the raw material comes into contact with the catalyst to react to generate an alkylation liquid containing alkylbenzene and polyalkylbenzene under the conditions that the reaction temperature is 100-210 DEG C, the reaction pressure is 1.5-5.0MPa, the mole ratio of aromatic hydrocarbon to olefin is 1:10 and the weight space velocity of olefin is 0.1-1.0 hour<-1>, wherein the saturated alkane is at least one of ethane, propane, n-butane, iso-butane, pentane, cyclopentane, methylcyclopentane, hexane or cyclohexane, and the content of the saturated alkane is 1-80% of the weight of the reaction mixture. Due to adoption of the technical scheme, the problem in the prior art is well solved. The aromatic hydrocarbon liquid phase alkylation method can be applied to industrial production of aromatic hydrocarbon liquid phase alkylation.

Systems and methods to produce branched alkyl aromatic hydrocarbons are described. Systems may include an olefin isomerization unit, an olefin dimerization unit, a dehydrogenation-isomerization unit, an alkylation unit, a dehydrogenation unit, a hydrogenation unit and/or combinations thereof. Methods for producing branched alkyl aromatic hydrocarbons may include isomerization of olefins in a process stream. The isomerized olefins may be used to alkylate aromatic hydrocarbons. After alkylation of the aromatic hydrocarbons, unreacted components from the alkylation process may be separated from the alkyl aromatic hydrocarbons. The unreacted components from the alkylation process may be recycled back into a process stream or sent to other processing units.

Methods are described for the simultaneous dehydrogenation of ethylbenzene and ethane in the presence of oxygen or carbon dioxide via a mixed metal oxide (MMO) catalyst or lithium-promoted sulfated zirconia catalyst to prepare styrene monomer from benzene and ethane. An alkylation unit produces ethyl benzene from ethylene and benzene, and an oxydehydrogenation unit produces styrene and ethylene from ethane, ethylbenzene and an oxidizing agent such as oxygen or carbon dioxide. The ethylene produced in the oxydehydrogenation unit is separated and used as feed to the alkylation unit.

The invention discloses a method for synthesizing diethyltoluenediamine through alkylation of toluenediamine catalyzed by ionic liquid. The method is characterized in that toluenediamine and alkylation reagents such as chloroethane and ethylene are used as raw materials, and acidic ionic liquid is used as catalyst; positive ions of the ionic liquid catalyst come from hydrogen halide of amine containing alkyl, or hydrogen halide of phosphorus containing alkyl or halide containing imidazole or a pyridine ring, and negative ions come from one or more metal halides. The method has the advantages of low reaction temperature and reaction pressure, short reaction time, safer process, high toluenediamine conversion rate and high diethyltoluenediamine selectivity. The invention additionally discloses an alkylation device for synthesizing diethyltoluenediamine under the catalytic effect of ionic liquid. The alkylation device at least comprises a reaction unit, a separation unit and a fractionation unit.

The invention relates to a method for adjusting product composition during coked crude benzene refining. Coked crude benzene hydrogenated oil is premixed with alkylation reagent methanol. The mixture undergoes heat exchange with a material leaving an alkylation reactor and then is heated. After the temperature of the mixture reaches a reaction temperature, in the presence of a molecular sieve based catalyst, the mixture undergoes alkylation reaction so as to obtain a product. After the alkylation reaction is completed, the product is cooled by water and then undergo extraction, rectification and separation so as to obtain benzene, toluene and xylene, which leave the reaction system as target products. The method has simple procedures and can achieve the aim of reducing the benzene production amount and increasing the production amount of the toluene and the xylene by only increasing an alkylation unit without changing the main low-temperature hydrofining procedures of coked crude benzene.

The invention relates to a process for the production of alkylated aromatic compounds comprising introducing olefin and aromatic compounds into at least first and second vertically spaced catalytic reaction zones in an alkylation unit under alkylation reaction conditions to provide an alkylated product, wherein the second catalytic reaction zone is positioned above the first catalytic reaction zone; wherein aromatic compound from each of the at least first and second catalytic reaction zones are contacted with a cooling means for re-condensing at least a portion of the aromatic compounds vaporized from the exothermic heat of reaction of the alkylation process; and wherein the olefin is introduced into the at least first and second catalytic reaction zones via respective first and second olefin feed streams at respective olefin feed rates such as to maintain olefin partial pressures at inlets to at least first and second catalytic reaction zones which vary by less than about ten percent. The invention additionally relates to an apparatus for practicing the alkylation process of the invention.

The invention relates to a normal-pressure continuous quantitative feeding system for an alkylating device active agent, and belongs to the technical field of petrochemical engineering. The system comprises a closed unloader, an active agent buffering and micro-negative-pressure dust removal unit, closed dense-phase conveying equipment, an active agent storing and filtering unit, small automatic feeding, metering and conveying equipment, a temporary storing and dust removal unit, a weighing, metering and anti-bonding unit, a double-helix continuous quantitative feeding unit and an emergency shutdown cutting-off unit. According to the normal-pressure continuous quantitative feeding system for the alkylating device active agent, the problems that the active agent is needed to be accurately added and metered, hydrocarbon gas in a reaction kettle is caked and hung on the wall after being in contact with the active agent, and a pipeline is easily blocked are solved; and the problems of environmental pollution and occupational injury to operators caused by active agent dust leakage during agent loading are fundamentally solved.

The invention provides a refinery plant byproduct C4 hydrocarbon and liquefied gas comprehensive processing and utilizing device and method. The device comprises an alkylating unit, an iso-butane dehydrogenation unit and an MTBE unit, wherein the alkylating unit comprises an alkylating device; the iso-butane dehydrogenation unit comprises an iso-butane removal tower and a propane-iso-butane mixeddehydrogenation device; the MTBE unit comprises an MTBE device; the alkylating device, the iso-butane removal tower, the propane-iso-butane mixed dehydrogenation device and the MTBE device communicatesuccessively. The components of C4 hydrocarbon and liquefied gas are processed and utilized. Single component separation of C4 hydrocarbon is avoided by optimizing and configuring a flow, so that thecurrent difficulty of state VI gasoline upgrade of the refinery plant is overcome effectively, the energy consumption is correspondingly reduced and the product quality is ensured; high-octane gasoline components can be produced to the maximum extent, and state VI gasoline upgrade of the refinery plant is achieved.

An alkylation process is described. The alkylation process includes contacting a feed comprising a paraffin or an aromatic with an olefin feed in the presence of a liquid Lewis acid catalyst in an alkylation reaction zone under alkylation conditions to form a reaction mixture comprising alkylation products and the liquid Lewis acid catalyst. The liquid Lewis acid catalyst is the liquid reaction product of a donor molecule and a metal halide. The alkylation products are separated from the liquid Lewis acid catalyst and recovered.

The invention provides a type-Y molecular sieve absorbent as well as a preparation method and method for removing sulfur dioxide in iso-butane. The preparation method of the type-Y molecular sieve absorbent comprises the following steps: performing the de-acidification for a vector to obtain the de-acidified vector; performing the ion exchange loading for the de-acidified vector and a chloride ofa transitional metal to obtain a semi-finished product of the transitional metal type-Y molecular sieve absorbent; drying the semi-finished product of the transitional metal type-Y molecular sieve absorbent, roasting, and obtaining the transitional metal type-Y molecular sieve absorbent; and a loading amount of the transitional metal type-Y molecular sieve absorbent is 0.8 to 9.0 percent. The transitional metal type-Y molecular sieve absorbent provided by the invention is adopted to remove the sulfur dioxide in iso-butane which is incompletely reacted in an alkylation apparatus, the removal rate is higher, and the content of the sulfur dioxide in the iso-butane which is not reacted in the alkylation apparatus can be removed to be 1 mg/kg or more.

One exemplary embodiment can be an alkylation unit. The alkylation unit can include at least one alkylation reaction zone having an alkylation catalyst, at least one cooler communicating with the at least one alkylation reaction zone, a settler communicating with the at least one alkylation reaction zone and the at least one cooler, a fractionation zone receiving an effluent from the settler passing through a line, and a boot coupled to a substantially horizontal portion of the line. Generally, the boot receives an effluent portion rich in the alkylation catalyst.