Abstract: A process is presented for the selective separation and recovery of large normal paraffins from a heavy kerosene boiling point fraction. The process includes passing the heavy kerosene fraction through an adsorption separation system for separating the normal paraffins from the paraffin mixture. The recovered extract and raffinate streams are mixed with a diluent made up of a lighter hydrocarbon. The subsequent diluted extract and raffinate streams are passed through first fractionation columns to separate the desorbent from the diluent and the heavier paraffins. The mixture of the diluent and heavier paraffins is passed through a second set of fractionation columns to separate the diluent and the heavier paraffins.

Abstract: Mixing small amounts of an inorganic halide, such as NaCl, to basic copper carbonate followed by calcination at a temperature sufficient to decompose the carbonate results in a significant improvement in resistance to reduction of the resulting copper oxide. The introduction of the halide can be also achieved during the precipitation of the carbonate precursor. These reduction resistant copper oxides can be in the form of composites with alumina and are especially useful for purification of gas or liquid streams containing hydrogen or other reducing agents. These reduction resistant copper oxides can function at near ambient temperatures.

Abstract: Processes and systems are disclosed that relate to the removal of impurities and separation the light olefins from an MTO product vapor stream. Specifically, the processes and systems relate to recovery of light olefins during regeneration of an adsorber in an oxygenate removal unit. Processes and systems for recovering light olefins during regeneration of an adsorber in an oxygenate removal unit can include recycling residual effluent stream to an upstream operation unit upstream of the oxygenate removal unit. Processes and systems for recovering light olefins during regeneration of an adsorber in an oxygenate removal unit can also include recycling residual effluent gas produced by depressurizing residual effluent in the first adsorber, as well as preferably venting an effluent gas from the first adsorber to a compressor upstream of the oxygenate removal unit.

Abstract: A method is described for processing an olefin-containing product stream (1) that contains, besides ethylene and propylene, longer-chain olefins and compounds of hydrocarbons with oxygen (oxygenates). Such a product stream (I) can occur in particular in olefin synthesis from methanol. The product stream is dewatered in successive process steps, optionally compressed in several steps and dried. Then it is subjected to fractionation. For removal of the undesired oxygenates it is proposed that the oxygenates be washed out of the gaseous product stream after the compression steps and before the drying step in a column (12) with methanol.

Abstract: Fuel is desulfurized with a rapid cycle desulfurization-regeneration method and apparatus. Regeneratable mass separating agents, including metals supported on high surface area materials, are used in a plurality of beds that are rotated into, through, and out of a desulfurization series and a regeneration series by valves and plumbing, which can include a rotary valve apparatus.

Abstract: The process includes at least two adsorptive separation zones to separate para-xylene from a feed stream comprising C8 aromatic hydrocarbons and at least one C9 aromatic hydrocarbon component. An adsorbent comprising X or Y zeolite and a heavy desorbent are used in the first adsorptive separation zone to produce an extract stream comprising para-xylene and a raffinate stream comprising para-xylene depleted C8 aromatic hydrocarbons, the C9 aromatic hydrocarbon, and the desorbent. The raffinate stream is separated in a raffinate distillation zone to produce a stream comprising the first desorbent component and the C9 aromatic hydrocarbon which stream is further separated in a second adsorptive distillation zone to produce a stream comprising the desorbent and a C9 aromatic hydrocarbon stream.

Abstract: The invention relates to a process for removing heavy hydrocarbons and hydrogen sulfide from natural gas. The combination of a silica-gel and an activated carbon adsorber allow for a significant reduction in the overall bed volume required for removal of hydrocarbons.

Abstract: A process for removing carbon monoxide from an olefin-containing hydrocarbon feedstock comprising the steps of: a) passing the said hydrocarbon feedstock over a material comprising nickel deposited on a support material wherein said nickel is present as both nickel oxide and metallic nickel; and b) recovering a hydrocarbon stream having a substantially reduced carbon monoxide content.

Abstract: The invention relates to an improved absorption-type separation and/or purification processes having dual rotary valves.

Abstract: A process is presented for the selective separation and recovery of large normal paraffins from a heavy kerosene boiling point fraction. The process includes passing the heavy kerosene fraction through an adsorption separation system for separating the normal paraffins from the paraffin mixture. The recovered extract and raffinate streams are mixed with a diluent made up of a lighter hydrocarbon. The subsequent diluted extract and raffinate streams are passed through first fractionation columns to separate the desorbent from the diluent and the heavier paraffins. The mixture of the diluent and heavier paraffins is passed through a second set of fractionation columns to separate the diluent and the heavier paraffins.

Abstract: The invention concerns a process for separating meta-xylene from a hydrocarbon feed comprising isomers containing 8 carbon atoms, comprising: a step for bringing said feed into contact with a faujasite type zeolite adsorbant, the percentage of water in the adsorbant being in the range 0 to 8% by weight and the adsorption temperature being from 25° C. to 250° C.; a desorption step employing a solvent selected from tetraline and its alkylated derivatives; a step for separating meta-xylene from the desorbant.

Abstract: Process for separation of a feedstock F by adsorption in a simulated moving bed in an SMB device that comprises a zone 1 for desorption of compounds produced by extraction, a zone 2 for desorption of compounds produced with a raffinate, a zone 3 for adsorption of compounds produced by extraction, and a zone 4 that is located between the draw-off of the raffinate and the supply of the desorbent, whereby the device comprises external bypass lines Li/i+1 directly joining two successive plates Pi, Pi+, that are equipped with non-automated means for adjusting flow rate and closing means, in which the degree of opening of the restriction means of the scavenging flow rate of the bypass lines Li/i+1 is adjusted so as to obtain the best performance of the SMB.

Abstract: Provided is a process for adsorptive separation of p-xylene from an aromatic hydrocarbon mixture comprising other isomers of xylene, and a device used therein. More specifically, the present invention provides a separation process employing simulated moving bed (SMB) adsorptive chromatography, characterized by subjecting the extracts eluted from a plurality of adsorption chambers arranged in parallel, to a crystallizer for additional separation, thereby improving productivity, and a device used therein.

Abstract: Provided is a process for adsorptive separation of p-xylene from an aromatic hydrocarbon mixture comprising other isomers of xylene, and a device used therein. More specifically, the present invention provides a separation process employing simulated moving bed (SMB) adsorptive chromatography, characterized by pretreating a fluid mixture, i.e. the feed, by using single adsorption chamber so as to raise the concentration of a component to be separated, and then carrying out the simulated moving bed adsorptive separation, thereby improving productivity, and a device used therein.

Abstract: A saturated hydrocarbon compound is brought into contact at least with a first adsorbent and a second adsorbent to obtain a liquid for immersion exposure containing the saturated hydrocarbon compound with a purity of 99.5 wt % or more.

Abstract: A process for co-producing para-xylene and styrene from a feed (1) of hydrocarbons containing xylenes and ethylbenzene is described, the process comprising the following succession of steps: a step for separating the feed in a simulated moving bed in an adsorption column (6) containing beds of an adsorbent, from which an extract that is rich in para-xylene (7a) of at least 99.7% purity and at least one raffinate (7b) containing ethylbenzene, ortho-xylene, meta-xylene and a very small quantity of para-xylene is withdrawn; a step for dehydrogenating (10) the ethylbenzene contained in the raffinate (7b) to styrene; at least one step for primary separation of the stream (11) from the dehydrogenation step (10), to eliminate by-products; a step for separating the purified mixture (18) derived from the stream (11) containing styrene, unconverted ethylbenzene, meta-xylene and ortho-xylene, from which a stream (21a) that is rich in styrene of at least 99.

Abstract: A process for removing a contaminant from a hydrocarbon containing a first quantity of the at least one contaminant, including contacting the hydrocarbon with a clay packed in a column, at least a portion of the contaminant bing sorbed by the clay and forming a clay-contaminant adduct; removing the hydrocarbon from the column, the removed hydrocarbon having a second, reduced quantity of the at least one contaminant; heating the clay and the clay-contaminant adduct in the column to regenerate the clay material, the heating being carried out without removing the clay from the column; and re-using the regenerated clay material in further iterations of the process.

Abstract: Use of mordenite zeolite and zeolite Y as adsorbents enables a dimethylnaphthalene isomer mixture to be efficiently separated. A feedstock oil containing a dimethylnaphthalene isomer mixture including an ?,?-isomer, an ?,?-isomer, and a ?,?-isomer is passed through an adsorbent layer (A) including mordenite zeolite together with a developing solvent. Subsequently, a liquid discharged from the adsorbent layer (A) is passed through an adsorbent layer (B) including zeolite Y. An eluent is passed through the adsorbent layer (B). The solvent is removed from the resultant eluate to obtain the ?,?-isomer of dimethylnaphthalene. Similarly, the ?,?-isomer of dimethylnaphthalene is obtained from the adsorbent layer (A).

Abstract: An improved process for the production capacity and feedstock handling flexibility of a simulated moving bed adsorptive separation process by introducing a second feed stream to the adsorbent chamber comprising a feed material of a different concentration of the desired compound than the concentration of the desired compound in the first feed material stream. The introduction of this second feed material stream may be performed at any location on the adsorbent chamber between (i) a transfer point located immediately upstream of the point of the raffinate material stream withdrawal from the adsorbent chamber to (ii) a transfer point located immediately downstream of the point of extract material stream withdrawal from the adsorbent chamber. A recycle stream may be introduced into the system at a location having a concentration similar to the concentration of the first feed material stream.

Abstract: Process for separation of metaxylene, with at least 99% by weight of purity of an aromatic feedstock F, in a single adsorption stage in a simulated moving bed in an SMB device that comprises 12, 13 or 15 adsorbent beds with different numbers of beds being employed in zone 1 between the supply of the desorbent D and the draw-off of the extract E; zone 2 between the draw-off of the extract E and the supply of the feedstock F; zone 3 between the supply of the feedstock and the draw-off of the raffinate R; and zone 4 between the draw-off of the raffinate R and the supply of the desorbent D whereby the process is carried out according to a configuration of zones (a, b, c, d), whereby a, b, c, and d represent the number of adsorbent beds that operate respectively in zones 1, 2, 3, 4 in which there is used: Either an SMB of 12 adsorbent beds operating according to the configuration (2, 5, 3, 2), Or an SMB of 13 adsorbent beds operating according to the configuration (2, 5, 4, 2), Or an SMB of 15 adsorbent beds op

Abstract: Process for separating paraxylene with a purity that is at least equal to 99.5% by weight from an aromatic feedstock F in a single adsorption stage in a simulated moving bed (SMB), comprising different numbers of beds, allocated to a zone 1 between the supply of the desorbent D and the draw-off of the extract E; a zone 2 between the draw-off of the extract E and the supply of the feedstock F; a zone 3 between the supply of the feedstock and the draw-off of the raffinate R; a zone 4 between the draw-off of the raffinate R and the supply of the desorbent D, wherein an SMB of 12 adsorbent beds has bed configuration (2, 5, 3, 2), an SMB of 15 adsorbent beds has bed configuration (3, 6, 4, 2), or an SMB of 19 adsorbent beds has bed configuration (4, 7, 6, 2), wherein the desorbent in this latter case is paradiethylbenzene.

Abstract: The raw natural gas is deacidized and dehydrated in units DA and DH. The treated gas is then purified by adsorption of the mercaptans in first enclosure A1. Part of the purified gas is heated in E1, then fed into second enclosure A2 so as to discharge the water adsorbed by the adsorbent material contained in this second enclosure. A steam-rich stream is fed into third enclosure A3 containing a mercaptan-laden adsorbent material. In A3, the mercaptans are desorbed and replaced by the steam.

Abstract: A method for separating a mixture of hydrocarbons into fractions enriched in linear, mono-branched, or multi-branched hydrocarbons is disclosed. In particular, mono-branched alkanes are separated from a mixture of alkanes containing multi-branched, mono-branched and linear alkanes, by selectively adsorbing the mono-branched alkanes on a zeolitic adsorbent. The zeolitic adsorbent MCM-22 is particularly suitable for carrying out the method.

Abstract: Methods and apparatus for the purification and distribution of acetylene. Acetylene is removed from an acetylene storage device, and provided to a purifier where solvent is removed. The purified acetylene is then provided to a semiconductor processing tool.

Abstract: The present invention discloses a means to improve the production capacity and feedstock handling flexibility of a simulated moving bed adsorptive separation process by introducing a second feed stream to the adsorbent chamber, such second feed stream comprising a feed material of a different concentration of the desired compound than the concentration of such desired compound in the first feed material stream. The introduction of this second feed material stream may be performed at any location on the adsorbent chamber between (i) a transfer point located immediately upstream of the point of the raffinate material stream withdrawal from the adsorbent chamber to (ii) a transfer point located immediately downstream of the point of extract material stream withdrawal from the adsorbent chamber. The specific transfer point used for the introduction of the second feed material stream will depend upon the concentration of the desired component in the second feed material stream.

Abstract: The present invention relates to a novel process for refining the liquefied petroleum gas (LPG) in a commercial scale. The process comprises: sequentially performing fine desulfurization and mercaptan conversion of the LPG after alcohol amine treatment through desulfurizer and catalyst set in fixed bed reactor in the absence of alkali, wherein, during the fine desulfurization, the resultants of reaction between hydrogen sulfide in the LPG and Fe—Ca oxides or their hydrates adhered on the desulfurizer, and during the mercaptan conversion, the mercaptan in the LPG reacts with the residual trace amount of air in the LPG under the action of the catalyst to produce the disulfides; letting the formed disulfides along with the LPG flow out of the fixed bed reactor; rectifying the LPG after the mercaptan conversion to obtain the refined LPG products, with further rectification to obtain the valuable disulfide products.

Abstract: At lower temperatures an acidic molecular sieve adsorbent preferentially adsorbs water and basic organic nitrogen compounds over weakly basic organic nitrogen compounds such as nitrites. Elevated temperatures improve the capacity of acidic molecular sieve adsorbents to adsorb nitrites in the presence of water.

Abstract: In a process for selectively separating 1-butene from a C4 feed stream comprising at least 1-butene, cis-2-butene and trans-2-butene, the feed stream is passed through a first bed of an adsorbent comprising a crystalline microporous material to form a substantially trans-2-butene-free effluent stream. Then, the substantially trans-2-butene-free effluent stream is passed through a second bed of an adsorbent comprising a crystalline microporous material to form a substantially 1-butene-free effluent stream, whereby the 1-butene is separated from the feed stream. The adsorbed 1-butene is then typically desorbed from the second adsorbent bed either by lowering the pressure or raising the temperature of the bed.

Abstract: The present invention is directed to the removal of nitrogen and sulfur containing impurities from high molecular weight petroleum feedstock obtained from fluid cracking catalyst or distillation zone of a petroleum treatment plant. The present process comprises first treating C12 and higher hydrocarbon petroleum feedstock having nitrogen and sulfur containing compounds therein with a porous, particulate adsorbent comprising a silica matrix having an effective amount of metal atoms therein to cause the adsorbent to have Lewis acidity of at least 500 ?mol/g and then treating the resultant feedstock to catalytic hydrodesulfurization to produce a hydrocarbon fuel having low sulfur and nitrogen content.

Abstract: A fuel processing system and method for processing fuel for a fuel cell having a first adsorbent bed for adsorption of high molecular weight organic sulfur-containing compounds and inorganic sulfur-containing compounds, and a second adsorbent bed for adsorption of low molecular weight organic sulfur-containing compounds, where the adsorbent beds are arranged such that the fuel to be processed passes through one of the adsorbent beds and, thereafter through the other adsorbent bed.

Abstract: A process for removal of trace impurities of hydrides of arsenic, phosphorus, antimony, silicon, and boron and sulfur and oxygenates and compounds containing these impurities from a hydrocarbon stream comprising contacting the hydrocarbon stream with an adsorbent material selected from the group consisting of zeolites and promoted alumina to adsorb compounds containing sulfur and/or oxygenates, contacting the hydrocarbon stream with an adsorbent material comprising one or more active metal oxides to remove the hydrides and contacting the hydrocarbon stream with an adsorbent material that removes water.

Abstract: A process for separating mixtures of hydrocarbon isomers on molecular sieves, including providing columns which include molecular sieves and function alternatively as secondary adsorption, primary adsorption, and desorption devices, feeding the mixtures of hydrocarbon isomers to a column functioning as the primary adsorption device for adsorbing isomers with greater selectivity towards the molecular sieves, feeding effluent of the mixtures from the column functioning as the primary adsorption device to a column functioning as the secondary adsorption device for adsorbing remaining isomers with greater selectivity, discharging isomers with a lower selectivity from the column functioning as the secondary adsorption device and a desorbing agent therein, feeding a desorbing agent to the column functioning as the desorption device, discharging isomers with a greater selectivity towards the molecular sieves and the desorbing agent in the column functioning as the desorption device.

Abstract: There is provided with a process for separating normal paraffins from hydrocarbons of C5-10 using zeolite molecular sieve 5A, which comprises the steps of (a) selective adsorption (b) cocurrent purge (c) countercurrent desorption. The present process employs butane for purge and desorption step to achieve excellent desorption efficiency and recycles butane in liquid phase to reduce the investment cost. The optimum operating conditions for feedstock change and adsorption capacity reduction are determined by NIR system for on-line monitoring and control. The separated normal paraffins can be efficiently applied to raw material for ethylene production and the separated non-normal paraffins can be efficiently applied to raw material for aromatic hydrocarbons production.

Abstract: A process for co-production of paraxylene, metaxylene and/or orthoxylene from a hydrocarbon feedstock (1) that comprises [1] a separation stage of the feedstock in a simulated moving bed in a chromatographic column (9) that contains a number of beds of an adsorbent, interconnected in a loop, is described, whereby said column comprises an injection (3) of the feedstock, a draw-off (10) of an extract that consists of paraxylene and desorbent, an intermediate fraction (11) (extract or raffinate) that contains ethylbenzene, and a raffinate (12) that contains a mixture of metaxylene and orthoxylene that is virtually free of ethylbenzene and paraxylene and [2] a crystallization stage (27) of the metaxylene and/or orthoxylene fraction. Upstream from the adsorption zone and/or upstream from the crystallization zone, it is possible to distill the entering mixture to produce an orthoxylene-enriched fraction at the bottom and a metaxylene-enriched fraction at the top.

Abstract: A process is described for co-producing metaxylene and paraxylene from a hydrocarbon feed comprising two separation steps. The first step of the process is a counter-current simulated moving bed system in a chromatographic column containing at least five zones, comprising injecting the feed and injecting a desorbent and delivering an extract, a raffinate and an intermediate raffinate either continuously or discontinuously. The extract is distilled to obtain a paraxylene with a purity of at least 99.7%. The raffinate, which is richer in metaxylene, is distilled to extract the desorbent and injected into a counter-current simulated moving bed continuously delivering an extract and a raffinate. One of these two streams is enriched in metaxylene. The most metaxylene-rich stream is distilled to obtain metaxylene with a purity of more than 99%.

Abstract: A coproduction process for ortho-xylene and para-xylene starting with a batch of hydrocarbons comprises a simulated counter-current fluidized bed system in a chromatographic column (6) containing at least five zones, comprising injection (1) of the batch and injection (2) of desorption agent and delivering an extract (3), a refined product (5), and an intermediate refined product (4). Refined product (5), richer in ortho-xylene than the intermediate refined product, is distilled (9) to extract desorption agent (15) and is injection, according to the second step of the process, into a simulated counter-current fluidized bed system (17) delivering an extract (18) and a refined product (19) continuously.

Abstract: The invention relates to a process for drying a gaseous or liquid mixture by passing the said mixture into an adsorber, characterized in that the water adsorption equilibrium zone of the adsorber comprises an upstream alumina zone and a downstream molecular sieve zone.

Abstract: A process for separating multibranched paraffins comprised in a hydrocarbon feed comprising hydrocarbons containing 5 to 8 carbon atoms per molecule comprises a separation unit functioning by adsorption and contains at least one zeolitic adsorbent with a mixed structure with principal channels with openings defined by a ring containing 10 oxygen atoms and secondary channels with openings defined by a ring of at least 12 oxygen atoms, the secondary channels only being accessible to the feed to be separated via the principal channels. Particular zeolitic adsorbents of the invention are zeolites with structure types EUO, NES and MWW. NU-85 and NU-86 zeolites are also particularly suitable for carrying out the process of the invention.

Abstract: A pressure swing adsorption process to separate para-xylene and ethylbenzene from a C8 aromatics stream produced by toluene conversion uses a para-selective adsorbent, preferably a non-acidic, medium pore molecular sieve of the MFI structure type, and is operated isothermally in the vapor phase at elevated temperatures and pressures. A fixed bed of adsorbent is saturated with pX and EB, which are preferentially adsorbed, then the feed to the process is stopped. Lowering the partial pressure desorbs the pX and EB giving a pX/EB-rich effluent. A stream of non-adsorbed mX and oX may be obtained before desorbing pX and EB.

Abstract: A pressure swing adsorption process to separate para-xylene and ethylbenzene from C8 aromatics uses a para-selective adsorbent, preferably a non-acidic, medium pore molecular sieve of the MFI structure type, and is operated isothermally in the vapor phase at elevated temperatures and pressures. A fixed bed of adsorbent is saturated with para-xylene and ethylbenzene, which are preferentially adsorbed, then the feed to the process is stopped. Lowering the partial pressure desorbs the para-xylene and ethylbenzene. The process effluent is rich in para-xylene and ethylbenzene. A stream of non-adsorbed meta-xylene and ortho-xylene may be obtained prior to desorption of para-xylene and ethylbenzene.

Abstract: An improved process for recovering hydrocarbons from an inlet inert gas-hydrocarbon vapor mixture is provided. The inlet mixture is caused to flow through a first bed of solid adsorbent whereby hydrocarbon vapors are adsorbed on the bed and a residue gas stream comprised of substantially hydrocarbon-free inert gas is produced. The hydrocarbon-free inert gas is vented and a second bed of solid adsorbent having hydrocarbon vapors adsorbed thereon is evacuated with an ejector operated by a motive liquid. A major portion of the hydrocarbon vapors is desorbed from the bed and an inert gas and hydrocarbon-rich vapor mixture commingled with the motive liquid is produced. The inert gas and hydrocarbon-rich vapor mixture is separated from the motive liquid and conducted to a point of additional processing or disposal.

Abstract: A process is provided for the concentration and recovery of ethylene and heavier components from an oxygenate conversion process. A separation process such as a pressure swing adsorption (PSA) process is used to remove hydrogen and methane from a demethanizer overhead stream comprising hydrogen, methane and C2 hydrocarbons and subsequently return the recovered C2 hydrocarbons to be admixed with the effluent from the oxygenate conversion process. This integration of a separation zone with a fractionation scheme in an ethylene recovery scheme using an initial demethanizer zone resulted in significant capital and operating cost savings by the elimination of cryogenic ethylene-based refrigeration from the overall recovery scheme.

Abstract: Two separate paraffinic hydrocarbon products, such as normal and monomethyl branched C10-C23 paraffins, are recovered from a mixture comprising the product hydrocarbons and many other hydrocarbons in a process employing two adsorptive separation zones in series. A single desorbent comprising a light paraffin is used in both zones and recovered in a single system, thus reducing capital and operating costs. The recovered paraffinic hydrocarbons may then be dehydrogenated and reacted with benzene to form alkylaromatic hydrocarbons useful as a detergent precursor.

Abstract: The present invention provides apparatus and a process capable of reducing the sulphur content of the gasoline product resulting from the cracking of a high molecular weight hydrocarbon feed comprising sulphur which comprises at least three concurrent steps: (a) passing input fluid comprising pollutant through at least one adsorber to produce a polluted adsorber and a purified fluid stream (of reduced pollutant content), which leaves the adsorber, stopping the flow into said adsorber to leave residual fluid therein, and separating said residual fluid from said adsorber to leave the polluted adsorber of reduced residual fluid content, (0) heating a polluted adsorber with a heated regeneration gas to produce a hot adsorher (of reduced polutant content) and cooler regeneration gas (of increased pollutant content), (c) contacting a heated adsorher (of reduced pollutant content) with a regeneration gas (of a lower temperature than that of said adsorber) to produce a cooler adsorber and a warmer regeneration gas, w

Abstract: A process for the production of at least one isomer of xylenes comprising a simulated moving-bed adsorption (8) of a C8-aromatic feedstock (1) that delivers a paraxylene-rich fraction (9) that is optionally purified after a distillation (16) by at least one high-temperature crystallization (5) and a fraction (10) that is low in paraxylene is described. Fraction (10) is distilled and then isomerized (21) in the presence of an EUO-structural-type catalyst. The lightest hydrocarbons are removed from the isomerization effluent in a first distillation (23) then naphthenes in a second distillation (26), and distilled isomerization effluent (2) that results therefrom is recycled at least in part in adsorption (8). A mother liquor (3) that results from the crystallization stage is recycled at least in part in adsorption (8).

Abstract: A process for co-production of paraxylene and ethylbenzene comprises: (A) an adsorption stage of a feedstock of xylenes and ethylbenzene in a simulated moving bed that produces an extract of pure paraxylene and an ethylbenzene-rich raffinate; (B) an adsorption stage in a simulated moving bed, of raffinate from which desorbent has been removed that supplies an essentially pure ethylbenzene extract and an orthoxylene and metaxylene raffinate that contains desorbent; (C) a recover stage for the desorbent; (D) an isomerization stage for the orthoxylene and metaxylene raffinate in the presence of a catalyst that comprises an EUO-type zeolite; and (E) a stage for recycling the isomerate that is produced with adsorption.

Abstract: For co-production of metaxylene and paraxylene from a feedstock (line-4) of hydrocarbons, there is employed a simulated moving bed chromatographic column 5 having at least five zones and which delivers an extract, a raffinate and an intermediate raffinate. The feedstock has an ethylbenzene content of less than 5% by weight, and the chromatographic column comprises at least twenty-five beds, of which at least five beds are in zone 3B. The raffinate is distilled (31) to recover the metaxylene at a purity of at least 99% and orthoxylene. The extract is distilled (7, 10) to recover the paraxylene at a purity of at least 99.6%. The recovered isomers can be synthesized into isophthalic acid and terephthalic acid.

Abstract: For producing three effluents which are respectively rich in straight chain paraffins, in mono-branched paraffins, and in di-branched and tri-branched paraffins possibly with naphthenic and/or aromatic compounds, from C5-C8 cuts or intermediate cuts (C5-C7, C6-C8, C7-C8, C6-C7, C7 or C8), comprising paraffinic and possibly naphthenic and/or aromatic hydrocarbons, and in some cases olefinic hydrocarbons, a chromatographic separation process uses a separation zone operating by adsorption. The process of the invention is of particular application when coupled with a hydro-isomerization process, which selectively recycles straight chain and mono-branched paraffins, necessary for paraffins containing at least 7 carbon atoms.

Abstract: A process is provided for the concentration and recovery of ethylene and heavier components from an oxygenate conversion process. A separation process such as a pressure swing adsorption (PSA) process is used to remove hydrogen and methane from a demethanizer overhead stream comprising hydrogen, methane, and C2 hydrocarbons and subsequently return the recovered C2 hydrocarbons to be admixed with the effluent from the oxygenate conversion process. This integration of a separation zone with a fractionation scheme in an ethylene recovery scheme using an initial demethanizer zone resulted in significant capital and operating cost savings by the elimination of cryogenic ethylene-based refrigeration from the overall recovery scheme.

Abstract: A molecular sieve used in a process for separating olefinic hydrocarbons from paraffinic hydrocarbons is regenerated in a method which removes diolefins and aromatic hydrocarbons from the molecular sieve. The method comprises contacting the sieve with alkaline water and then drying the sieve with stream of a superheated light paraffin. The molecular sieve may be present in either a guard bed used upstream of a main separation zone or as part of the main adsorptive separation zone.