Abstract: A process for the production of a high quality gasoline blending components from refinery process streams by the alkylation of light isoparaffins with olefins using an ionic liquid catalyst is disclosed. The alkylation process comprises contacting a hydrocarbon mixture comprising at least one olefin having from 2 to 6 carbon atoms and at least one isoparaffin having from 3 to 6 carbon atoms under alkylation conditions, said catalyst comprising a mixture of at least one acidic ionic liquid and at least one alkyl halide. The alkylhalide by reacting to at least a portion of the olefin with a hydrogen halide.

Abstract: An alkylation process comprising contacting a first hydrocarbon feed comprising at least one olefin having from 2 to 6 carbon atoms and a second hydrocarbon feed comprising at least one isoparaffin having from 3 to 6 carbon atoms with a halide-based acidic ionic liquid catalyst under alkylation conditions to produce an alkylate containing an organic halide and contacting at least a portion of the alkylate with a hydrotreating catalyst in the presence of hydrogen under hydrotreating conditions to reduce the concentration of the organic halide is disclosed.

Abstract: CO2 emissions Gas-to-Liquids (GTL) facilities such as, for example, Fischer-Tropsch facilities, are minimized by using recovered hydrogen as a fuel in at least one furnace in the GTL facility. A process for manufacturing hydrocarbonaceous products from a methane-containing feedstock in a GTL facility comprising at least one furnace generating reduced CO2 emissions comprises forming syngas from a methane-containing feedstock by means of a partial oxidation reaction. A hydrogen rich fuel is used in at least one furnace in the GTL facility to reduce CO2 emissions generated by the facility.

Abstract: A blend useful as a diesel fuel, as well as a method for its production, comprising a high quality Fischer-Tropsch derived distillate boiling in the range of a diesel fuel blended with a cracked stock boiling in the range of a diesel fuel wherein the final blend contains 10-35 wt. % aromatics and 1-20 wt. % polyaromatics and produces low regulated emissions levels.

Abstract: Provided is a process for converting CO2-rich natural gas into liquid fuel. The process includes introducing a CO2-rich natural gas feed stream into a synthesis gas formation reactor and then forming a synthesis gas. At least a portion of the synthesis gas is then introduced into a Fischer-Tropsch reactor. A Fischer-Tropsch process is conducted generating a Fischer-Tropsch product. A naphtha is separated from the Fischer-Tropsch product and introduced into a naphtha reformer. Hydrogen by-product is generated by reforming the naphtha to obtain a C6-C10 product having a hydrogen to carbon ratio less than about 2.0. At least a portion of the hydrogen by-product is recirculated and mixed with the CO2-rich natural gas feed stream.

Abstract: Metal hydride compounds, which are prepared by mixing together from about 1 to about 10 parts by molecular weight of at least one metal selected from the group consisting of silicon, aluminum, tin, and zinc; from about 1 to about 3 parts by molecular weight of an alkali metal hydroxide; and from about 5 to about 10 parts by molecular weight of water and allowing this mixture to stand for a time sufficient to form a metal hydride, can be used for making fuel additives, treating sour gas, enhancing oil refining, extracting oil from tar sands and shale, increasing production of hydrogen from a hydrogen plant, treating oil and gas wells to enhance production, eliminate PCBs, cleaning soil contaminated by hydrocarbons and/or heavy metals, controlling odors, cleaning polluting stack emissions, extracting edible and essential oils, and eliminating bacteria, fungicides, and parasites from vegetation.

Abstract: Provided is a process for reducing CO2 emissions generated by a Fischer-Tropsch GTL facility. The process includes introducing a synthesis gas into a Fischer-Tropsch reactor and performing a Fischer-Tropsch process to produce a Fischer-Tropsch product and CO2. At least a portion of the CO2 from the Fischer-Tropsch reactor is fed into at least one of a feed stream being fed to a synthesis gas formation reactor, producing the synthesis gas, or the synthesis gas being fed into the Fischer-Tropsch reactor. In addition, naphtha is obtained from the Fischer-Tropsch product and is fed into a naphtha reformer. Naphtha reforming is conducted, generating hydrogen by-product and C6-C10 product. At least a portion of the hydrogen by-product, generated during naphtha reforming, is fed into the feed stream, converting at least a portion of the CO2 in the feed stream into additional CO. Finally, the additional CO is converted into hydrocarbons in the Fischer-Tropsch reactor.

Abstract: Clean distillate useful as a jet fuel or jet blending stock is produced from Fischer-Tropsch wax by separating wax into heavier and lighter fractions; further separating the lighter fraction and hydroisomerizing the heavier fraction and that portion of the light fraction above about 475° F. The isomerized product is blended with the untreated portion of the lighter fraction to produce high quality, clean, jet fuel.

Abstract: This invention is related to a catalytically cracked or thermally cracked naphtha stream. The naphtha stream is contacted with a catalyst containing from about 10 to 50 wt. % of a crystalline zeolite having an average pore diameter less than about 0.7 nanometers at reaction conditions which include temperatures from about 500° C. to about 650° C. and a hydrocarbon partial pressure from about 10 to 40 psia. The resulting product is a high octane naphtha.

Abstract: A process comprises separating a naphtha feed into a fraction comprising C7− hydrocarbons and a heavy C8+ fraction, separating the C8+ fraction into a light fraction comprising C8 and/or C8-C9 which then is reformed to produce gasoline and/or a desired distribution of aromatics.

Abstract: Catalyst activation of a platinum reforming catalyst system contained in a multiple reactor system by simultaneously reducing the catalyst with hydrogen while introducing a nonmetallic chlorine-containing compound into a reactor of the multiple reactor system in an amount to add from about 0.05 to about 0.3 weight percent chlorine to the catalyst and thereafter purging the system with about 100 to about 50,000 cubic feet of hydrogen per cubic foot of catalyst resulting in a reforming system having increased activity and providing enhanced RON values with reduced cracking of feedstock.

Abstract: A method for the isomerization of a hydrocarbonic charge containing a substantial quantity of paraffin base hydrocarbons with 5 or 6 carbon atoms and a benzene content that is greater than or equal to 2% by weight, in which the charge to be treated passes, in the presence of hydrogen, at a total pressure greater than or equal to 10.105 Pa (10 bars) and at an average temperature ranging between 100 and 200° C., through at least one reactor (5) containing a catalyst. An adjunctive fluid is introduced in the upstream section of the reaction zone; a fluid that at 40° C. and under atmospheric pressure (1.0134.105 Pa), is in a gaseous phase and has a density that is less than or equal to that of the normal-pentane taken into account under the same conditions.

Abstract: A diesel fuel having at least 50% C10 to C20 paraffins, wherein the iso-paraffin to normal paraffin mole ratio is up to 21:1 and higher. This diesel fuel can be produced from a feed containing at least 90% C10+ normal paraffins. This diesel fuel is produced by contacting a feed in an isomerization reaction zone a feed with a catalyst comprising a SAPO-11 and platinum in the presence of hydrogen (hydrogen:feed ratio of from 1,000 to 10,000 SCFB) at a temperature of from 340° C. to 420° C., a pressure of from 100 psig to 600 psig, and a liquid hourly space velocity of from 0.1 hr−1 to 1.0 hr−1.

Abstract: A method for the isomerization of a hydrocarbonic charge containing a substantial quantity of paraffin base hydrocarbons with 5 or 6 carbon atoms and a benzene content that is greater than or equal to 2% by weight, in which the charge to be treated passes, in the presence of hydrogen, at a total pressure greater than or equal to 10.105 Pa (10 bars) and at an average temperature ranging between 100 and 200° C., through at least one reactor (5) containing a catalyst. An adjunctive fluid is introduced in the upstream section of the reaction zone; a fluid that at 40° C. and under atmospheric pressure (1.0134.105 Pa), is in a gaseous phase and has a density that is less than or equal to that of the normal-pentane taken into account under the same conditions.

Abstract: A process comprises separating a naphtha feed into a fraction comprising C731 hydrocarbons and a heavy C8+ fraction, separating the C8+ fraction into a light fraction comprising C8 and/or C8-C9 which then is reformed to produce gasoline and/or a desired distribution of aromatics.

Abstract: A method of transforming a normally gaseous composition containing at least one hydrogen source, at least one oxygen source and at least one carbon source into a normally liquid fuel, wherein said gaseous composition consists at least in part of carbon dioxide as said carbon source and said oxygen source, and of methane as said hydrogen source and as a second carbon source; the method comprising the steps of feeding the composition into a reactor including a first electrode means, a second electrode means and at least one layer of a normally solid dielectric material positioned between the first and the second electrode means; submitting the composition within the reactor in the presence of a normally solid catalyst to a dielectric barrier discharge, wherein said normally solid catalyst is a member selected from the group of zeolites, aluminophosphates, silicoaluminophosphates, metalloaluminophosphates and metal oxides containing OH groups; and controlling the dielectric barrier discharge to convert the gaseo

Abstract: Process for the catalytic steam reforming of a hydrocarbon feed stock with a content of higher hydrocarbons and oxygen comprising the steps of catalytic pre-reforming the feed stock and steam reforming the pre-reformed feed stock, the pre-reforming step is carried out in presence of a fixed bed catalyst comprising at least a portion of a noble metal catalyst being active in oxidation of hydrocarbons to carbon oxides and conversion of higher hydrocarbons to methane, wherein the noble metal catalyst is supported on a carrier of MgO and/or MgAl2O4 spinel.

Abstract: Clean distillate useful as a jet fuel or jet blending stock is produced from Fischer-Tropsch wax by separating wax into heavier and lighter fractions; further separating the lighter fraction and hydroisomerizing the heavier fraction and that portion of the light fraction above about 475° F. The isomerized product is blended with the untreated portion of the lighter fraction to produce high quality, clean, jet fuel.

Abstract: Disclosed are silicoaluminates (SAPOs) having unique silicon distributions, a method for their preparation and their use as naphtha cracking catalysts. More particularly, the new SAPOs have a high silica:alumina ratio and favorable Si atom distribution.

Abstract: A process combination is disclosed to selectively upgrade hydrocarbons in a manner to essentially eliminate olefins in product from the combination. Preferably the hydrocarbons comprise naphtha which is reformed to upgrade its octane number and/or to produce aromatic intermediates, followed by hydrogenation of olefins in the reformate. Olefin saturation optimally is effected by catalytic reaction on an olefin-containing reformate taken at an intermediate point from the effluent side of the reforming-process feed-effluent heat exchanger. Saturation is performed in a defined temperature range which results in selective hydrogenation.

Abstract: A process for the separation of isobutene, otherwise inseparable from butene-1 by fractionation, in high purity from butenes contained in a mixed hydrocarbon stream containing butene-1, butene-2 and small amounts of butadiene in which the mixed hydrocarbon stream is fed to distillation column reactor containing an alumina supported palladium oxide catalyst. The column is operated to tend to exclude butene-2 from contact with the catalyst and to maintain butene-1 in contact with the catalyst to isomerize the butene-1 to butene-2. As butene-2 is produced it is distilled away from the catalyst, upsetting the equilibrium and allowing for a greater than equilibrium amount of butene-2. The isobutene and isobutane are concurrently separated from the butene-2. Additionally, any butadiene in the feed is hydrogenated to butenes. The bottoms is rich in butene-2.

Abstract: A method for optimizing the yield of light olefins in a process for the conversion of a heavy hydrocarbon stream to aromatics and light olefins by contacting the heavy hydrocarbon stream with a zeolite catalyst along with the controlled introduction of a paraffin stream co-feed.

Abstract: A composition is prepared by a method which comprises mixing a first solid material comprising a platinum group metal, a rhenium component, a porous carrier material and, optionally, a halogen component and a second solid material comprising silica and bismuth. The thus-obtained composition is employed as a catalyst in the conversion of hydrocarbons to aromatics. In an alternate embodiment, hydrocarbons are converted to aromatics by sequentially contacting the hydrocarbons with the first solid material and then the second solid material.

Abstract: A process for converting undesirable olefinic hydrocarbon streams to hydrogen and petrochemical feedstock e.g. light olefins in C.sub.2 -C.sub.4 range and aromatics especially toluene and xylenes, which comprises simultaneous cracking and reforming at olefin rich hydrocarbons using a catalyst consisting of dehydrogenating metal components, shape selective zeolite components and large pore acidic components in different proportions in a circulating fluidized bed reactor-regenerator system having reactor temperature within 450-750.degree. C. and WHSV of 0.1-60 hour.sup.-1.

Abstract: This process relates to reforming a full-boiling range hydrocarbon feed in two parallel stages while maximizing the catalyst life of the heavy cut reformer and/or reducing the complexity of the plant by preferentially sending the higher purity Aromax.RTM. hydrogen to the heavy cut reformer.

Abstract: In a process for the dehydrocyclization of a dehydrocyclizable hydrocarbon contained in a dehydrocyclization feed stream which comprises contacting said dehydrocyclizable hydrocarbon in a dehydrocyclization zone under dehydrocyclization conditions in the presence of a dehydrocyclization catalyst, the improvement comprises carrying out said dehydrocyclization process in the presence of a metal chloride additive in said dehydrocyclization feed stream, said metal chloride additive being present in an amount sufficient to inhibit deactivation of such dehydrocyclization catalyst.

Abstract: A process is provided for producing high purity benzene and high purity paraxylene from a hydrocarbon feed. In one aspect, the process comprises: (a) reforming a hydrocarbon feed using either a monofunctional catalyst or a bifunctional catalyst to provide one or more reformate streams; (b) fractionating the reformate stream to provide a toluene stream, a benzene stream, and a xylene stream; (c) subjecting the toluene stream to disproportionation; (d) purifying the benzene stream by extraction followed by distillation to provide a high purity benzene product; and (e) purifying the xylene stream by simulated moving bed countercurrent adsorption followed by crystallization to provide a high purity paraxylene product.

Abstract: The invention concerns a process for the isomerization of an aromatic C8 cut using a catalyst containing mordenite, cerium and at least one metal from group VIII. It also concerns a catalyst containing 2-98% by weight of mordenite, 7-40% by weight of cerium, and 0.01-3% by weight of at least one metal from group VIII, the cerium being deposited on the mordenite, and the percentages being with respect to the weight of catalyst.

Abstract: In a process for preparing olefinically unsaturated compounds such as styrene by oxidative dehydrogenation of corresponding hydrocarbons using a previously oxidized oxygen transferer acting as catalyst in the absence of molecular oxygen and reoxidation of the oxygen transferer in at least two reactors, the dehydrogenation and regeneration takes place alternately in time in the two reactors and the reactors are connected to one another in terms of heat via heat exchangers and a common circuit for heat transfer medium.

Abstract: In the present invention, dimethylbutanes are removed from the raffinate component of the feed to a dehydrocyclization process. Thus, according to a preferred embodiment, a process is provided for producing aromatics by the following steps:(a) contacting fresh paraffins rich feed hydrocarbons, containing 0.1 to 20.0 wt. % dimethylbutanes with a highly selective dehydrocyclization catalyst in a reaction zone, under dehydrocyclization reaction conditions, to convert paraffins to aromatics and obtain an aromatics rich effluent;(b) separating aromatics from the effluent to obtain an aromatics lean raffinate;(c) removing dimethyl butanes from the raffinate to obtain a raffinate of reduced dimethylbutane content; and(d) recycling the raffinate of reduced dimethylbutane content to the reaction zone.Preferably, the dehydrocyclization catalyst used is a nonacidic, monofunctional catalyst. Platinum on L zeolite is a particularly preferred highly selective dehydrocyclization catalyst for use in the process.

Abstract: A catalyst composition and a process for converting a hydrocarbon stream such as, for example, a C.sub.9 + aromatic compound to C.sub.6 to C.sub.8 aromatic hydrocarbons such as xylenes are disclosed. The catalyst composition comprises an aluminosilicate, and a metal wherein the weight ratio of aluminum to silicon is in the range of from about 0.002:1 to about 0.6:1. The process comprises contacting a hydrocarbon stream with the catalyst composition under a condition sufficient to effect the conversion of a hydrocarbon to a C.sub.6 to C.sub.8 aromatic hydrocarbon.

Abstract: The present invention relates to new crystalline zeolite SSZ-42 prepared by processes for preparing crystalline molecular sieves, particularly large pore zeolites, using an organic templating agent selected from the group consisting of N-benzyl-1,4-diazabicyclo?2.2.2!octane cations and N-benzyl-1-azabicyclo?2.2.2!octane cations.

Abstract: A process for converting at least one olefin and at least one isoparaffin to a diesel fuel blending component comprising the steps of contacting the olefin and the isoparaffin with a catalyst comprising an acidic solid comprising a Group IVB metal oxide modified with an oxyanion of a Group VIB metal to provide a diesel fuel. Process conditions can be varied to favor the formation of gasoline, distillate, lube range products or mixtures thereof.

Abstract: Clean distillate useful as a jet fuel or jet blending stock is produced from Fischer-Tropsch wax by separating wax into heavier and lighter fractions; further separating the lighter fraction and hydroisomerizing the heavier fraction and that portion of the light fraction above about 475.degree. F. The isomerized product is blended with the untreated portion of the lighter fraction to produce high quality, clean, jet fuel.

Abstract: The present invention relates to new crystalline zeolite SSZ-41 which comprises oxides of (1) silicon or a mixture of silicon and germanium, and (2) zinc, said zinc being present in an amount from about 2 wt % to about 5 wt % of zinc metal based on the total weight of metals in said zeolite. Zeolite SSZ-41 may also optionally contain oxides of aluminum, iron, gallium or mixtures thereof. Zeolite SSZ-41 has the X-ray diffraction lines of Table I and has an argon adsorption capacity of at least about 0.06 cc/gm at 87.degree. K. Also disclosed are methods of making and using zeolite SSZ-41.

Abstract: Provided is a process for catalytic reforming a hydrocarbon feedstock containing at least 20 ppbw sulfur. The process comprises passing the hydrocarbon feedstock through at least two serialy connected reforming zones, with each zone containing a highly sulfur sensitive reforming catalyst. The catalyst in the first reforming zone is more frequently regenerated than the catalyst in the second reforming zone. The result is a highly efficient and simplified process for reforming a sulfur contaminated hydrocarbon feedstock. The process basically employs a minor portion of the highly sulfur sensitive reforming catalyst as both the reforming catalyst and a sulfur removal agent.

Abstract: A catalytic reforming process uses a riser reactor with multiple catalyst injection points to obtain high aromatics yields from a naphtha feedstock. Product from the riser reactor typically is discharged into a fluidized-reforming reactor, in which the reforming reaction is completed and catalyst is separated from hydrogen and hydrocarbons. Hydrocarbons from the reactor are separated to recover an aromatized product. Catalyst is regenerated to remove coke and reduced for reuse in the reforming process.

Abstract: The invention concerns a process for reducing the benzene content of petrol fractions and isomerizing paraffins in the presence of an isomerization catalyst comprising 4 to 15% of at least one halogen and at least one metal from group VIII deposited on a support composed of a mixture of specific proportions of eta alumina and gamma alumina, in which isomerization is carried out on a mixture of a) a feed with the following composition by weight: 40% to 80% of paraffins, 0.5% to 7% of cyclic hydrocarbons and 6% to 45% of aromatics, and with a maximum distillation temperature of between 70.degree. C. and 90.degree. C., b) a C.sub.5 -C.sub.6 cut which is generally a straight run cut, and c) a chlorine-containing compound providing a concentration of 50-5000 ppm of chlorine in the mixture.

Abstract: Provided is a process for catalytically reforming a hydrocarbon feedstock using a highly sulfur sensitive catalyst. The process comprises contacting the hydrocarbon in a reaction zone, with the hydrocarbon feed and catalyst flowing in opposite directions. Once the catalyst has passed through the reaction zone, it is then passed to a regeneration zone for regeneration. The process eliminates the need of passing the hydrocarbon feed through a sulfur sorber prior to entry into the reaction zone, as the spent catalyst which is leaving the reaction zone for regeneration acts as a sulfur sorber and removes the sulfur from the feed entering the reaction zone.

Abstract: Methane is suppressed in a hydroisomerization process without substantial effect on light gas and light liquid yields when carbon dioxide is included with the feed and a Group VIII non-noble metal or Group VI metal catalyst supported on alumina or silica-alumina.

Abstract: Disclosed is a reforming process for the production of gasoline having an increased isoparaffin yield, reduced aromatics content and a constant octane level which comprises passing the gasoline precursor containing greater than 20 vol% aromatics over a reforming catalyst comprising one or more metals from Group VIII and IVA of the Periodic Table on an oxide support, having a total pore volume of about 0.300 to 0.600 cc/g and greater than 85% of the pore volume in pores of diameter less than 100.ANG..

Abstract: A method for producing alkylnaphthalenes in a reformer process unit used to reform a gasoline boiling range hydrocarbonaceous feedstock in the presence of a platinum containing supported catalyst at reforming process conditions, the method comprising spiking said feedstock with up to about 5 vol.% of an additional stream containing a substantial amount of tetralins and decalins, based on the volume of feedstock.

Abstract: Catalytically cracked naphthas containing C.sub.9 + hydrocarbons are hydrocracked over a crystalline zeolite, typically, mildly steamed zeolite beta then subjected to reforming to achieve a gasoline product of reduced end boiling range and higher octane than the feed. A hydrogen stream from the reformer which contains a catalytic promoter, such as chlorine, is separated into a first stream and a second stream. The first stream is treated over a solid sorbent to remove the promoter and recycled promoter to the hydrocracking step while the untreated second hydrogen stream which contains promoter is recycled to the reformer.

Abstract: Provided is a reforming process for producing a high purity benzene product using a non-acidic zeolitic catalyst. The high purity benzene is extracted from a light fraction of reformate that has less than 500 ppm by weight toluene. Generally, a hydrocarbon feed is reformed in a reformer under reforming conditions in the presence of a non-acidic catalyst to produce a reformate. That reformate is separated into a light fraction and a heavy fraction. The extraction unit, preferably an extractive distillation unit, is then used to separate the light fraction into an aromatic extract stream and a nonaromatic raffinate stream.

Abstract: A continuous process for upgrading reformate feedstock or the like to reduce benzene content and increase octane fuel rating. The improved process comprises maintaining a fluidized bed of regenerable acid solid medium pore zeolite catalyst particles in a turbulent regime reaction zone, preferably maintained with a superficial gas velocity of 0.1 to 1 meter/sec. with reformate feedstock being introduced at a bottom portion of the reaction zone at a weight hourly space velocity (WHSV) of 0.1 to 5, based on active catalyst solids; reaction zone total pressure being less than 2000 kPa. The preferred catalyst particles have an average particle size of 20 to 100 microns (.mu.), with about 10 to 25% of the catalyst particles comprising fine particles having a particle size less than 30 microns; and the preferred zeolite catalyst comprises shape selective medium pore aluminosilicate zeolite having a constraint index of 1 to 12. The benzene is reacted by contacting reformate feedstock, such as C.sub.

Abstract: Hydrocarbon lubricants having a high viscosity index (V.I.) and low pour point are produced by hydroisomerizing, over zeolite beta, a waxy lube feed such as a waxy vacuum gas oil whose aromatic components are removed by extraction, e.g. with furfural. The zeolite beta catalyst comprises noble metal, e.g., Pt, and a low acidity zeolite beta, e.g., framework boron-containing zeolite beta.

Abstract: Zeolite L containing caesium is prepared by a process in which said zeolite L is crystallised from a synthesis mixture with a molar composition (expressed as oxides) of:______________________________________ K.sub.2 O/SiO.sub.2 0.15 to 0.40 K.sub.2 O/Cs.sub.2 O 3 to 10 H.sub.2 O/K.sub.2 O 40 to 100 and SiO.sub.2 /Al.sub.2 O.sub.3 7 to 13 ______________________________________and containing 0.5 to 15 ppm (by weight) of divalent metal carbons, e.g. Mg ions. The zeolite L is used in dehydrocyclisation and/or isomerisation processes.

Abstract: This invention is a process of converting n-pentane to cyclopentane. In accordance with a preferred embodiment of the invention, n-pentane feed is converted in dual temperature stage process without interstage processing of the first stage product mixture.

Abstract: Supports for catalytic reforming catalysts are prepared by doping ZrO.sub.2 with tantalum. The catalyst may contain a Group VII or Group VIII metal and/or an acidic component.

Abstract: Processes are disclosed for the separation of hydrogen sulfide from feedstreams containing hydrogen sulfide and hydrocarbons by adsorption using a clinoptilolite adsorbent containing cations having ionic radii of from about 1.10 to 1.40 Angstroms. The processes can provide substantially enhanced adsorption capacities as compared with other adsorbents such as Zeolite 4A. As a result, a throughput of existing sulfur adsorption plants can be increased, e.g., by about 100%. The processes can be operated at elevated adsorption temperatures, e.g., greater than about 200.degree. F., and thus are particularly suitable when integrated with other processing steps such as hydrocarbon conversion reactions that utilize catalysts which are sulfur-sensitive. In addition, the clinoptilolite adsorbents of the present invention have a high tolerance to environments that comprise halides, e.g., HCl.