Abstract: The present invention relates to a method of purifying waste hydrochloric acid, and more particularly, to a method of purifying waste hydrochloric acid which includes preparing an extraction solution by dissolving an extractant in an organic solvent (S1), extracting metallic components with the organic solvent by adding the extraction solution to the waste hydrochloric acid (S2), separating a waste hydrochloric acid layer and the organic solvent containing the metallic components (S3), and obtaining purified hydrochloric acid by recovering the separated (fractionated) waste hydrochloric acid layer (S4), wherein the extractant is used in an amount of 40 moles or more based on 1 mole of iron (Fe) included in the waste hydrochloric acid, and the waste hydrochloric acid and the extraction solution are mixed in a volume ratio of 1:0.1 to 1:1.

Abstract: A purified hydrochloric acid composition is prepared from a stream of a contaminated hydrochloric acid composition by a process comprising a distillation treatment, wherein at least a first distillation column is operated at a first pressure and a second distillation column is operated at a second pressure, which second pressure is lower than the first pressure; wherein the contaminated hydrochloric acid composition comprises water, contaminants and hydrochloric acid in a first hydrochloric acid concentration of above the azeotropic composition of hydrochloric acid and water at the first pressure; wherein a part of the stream of the contaminated hydrochloric acid composition is fed into the first distillation column to yield a first bottom product comprising water and hydrochloric acid with a hydrochloric acid concentration below the first hydrochloric acid concentration and a first top product comprising hydrochloric acid in a concentration above the azeotropic hydrochloric acid composition at the first pres

Abstract: The present invention relates to a method and a system for separating and treating impurities from a hydrogen chloride liquid mixture from the process for preparing isocyanate with phosgenation including sending hydrogen chloride liquid mixture into a gas-liquid separation column for separation to yield a liquid phase flow with impurities at the bottom of the gas-liquid separation column, neutralizing the liquid phase flow comprising impurities with an alkaline liquid in the neutralization tank to yield a neutralized solution, and sending the neutralized solution into a waste liquid treatment device from said neutralization tank for treatment.

Abstract: Extraction of anhydrous hydrogen fluoride from its aqueous solution is provided. A method provides hydrogen fluoride from aqueous solutions, including the reduction of water component of the aqueous solution at an elevated temperature into carbon oxide, carbon dioxide and hydrogen. The condensation and distillation of the obtained hydrogen fluoride and water vapor are characterized by the fact that the mixture of hydrogen fluoride and water is reduced at a temperature of 800 K and above, the molar ratio of carbon to water in the reducing agent is from 0.5 to 4, and using a reducing agent of the general formula CnHmOk, where k?0, m>0, and n>0, and the reducing agent may be saturated, unsaturated, aromatic hydrocarbons, oxygen-containing organic compounds, their isomers and their mixtures. The method makes it possible to extract hydrogen fluoride from its mixtures with water in any ratio and from azeotropic mixtures.

Abstract: The invention pertains to a method for recovering HCl from a HCl containing gas stream wherein a HCl containing gas stream with a temperature of ?20 to 25° C. is provided to an adiabatic absorption unit where it is contacted with water as an absorbent, resulting in the formation of a top gas stream and a aqueous HCl product solution, wherein the temperature of the top gas stream is at least 70° C. and wherein the aqueous HCl product solution has a HCl concentration in the range of 5-20 wt. %. It is preferred for the HCl-containing gas stream to be derived from a hydrogenation step wherein a feed comprising monochloroacetic acid (MCA) and dichloroacetic acid (DCA) is reacted with hydrogen to form a HCl-containing gas stream and a product stream comprising MCA and a reduced amount of DCA. The HCl product solution is preferably diluted to a concentration of 1-8 wt.

Abstract: A process is provided for recovering a heavy metal from a waste stream resulting from a process for producing aromatic carboxylic acid by liquid-phase oxidation of an aromatic feedstock compound in the presence of a heavy metal catalyst. The process comprises: (a) producing a carbonate salt precipitate of the heavy metal by adding a source of metal ions and carbonate or bicarbonate ions into the waste stream; (b) separating the precipitate from the waste stream; (c) washing the precipitate with an alkali solution having metal ions therein, wherein at least a portion of the metal ions in the alkali solution are the same as at least a portion of metal ions in the source of metal ions and carbonate or bicarbonate ions; and, (d) recovering the washed precipitate wherein the washed precipitate comprises the heavy metal ions. In one embodiment, the aromatic carboxylic acid comprises terephthalic acid.

Abstract: The subject matter of the present invention is a method to extract or recover hydrochloric acid from hydrochloric acid solutions containing metal by means of pyrohydrolytic treatment, followed by absorption and/or condensation of the gaseous hydrogen chloride thus formed in order to form hydrochloric acid. According to the invention, a first partial flow of the hydrochloric acid solution containing metal undergoes pyrohydrolytic treatment and a second partial flow of the metal-containing solution is fed to the absorption column. A device for implementing the process according to the invention is also the subject of the present invention.

Abstract: A method for recovering hydrochloric acid and metal oxides from a chloride liquor is described. The method uses a chloride liquor including the metal and mixing the liquor and a matrix solution to produce a reaction mixture, wherein the matrix solution assists oxidation/hydrolysis of the metal with HCl production. In a preferred embodiment the matrix solution includes zinc chloride in various stages of hydration and an oxygen containing gas is added to the mix. A method where the improvement is the mixing of a liquor and a matrix solution where the solution assists hydrolysis of the metal with HCl production is also disclosed. The reactor is a column reactor in a preferred embodiment. Further disclosed is the method of using the matrix solution and a reactor for recovering hydrochloric acid and for oxidizing/hydrolysis of a metal.

Abstract: A method including: (a) contacting lime with an extract including an S1 solvent carrying a contaminant load to form a lime treated extract; and (b) reducing the contaminant load by removing solids.

Abstract: The invention relates to a process for purifying chlorosilanes by distillation, which includes providing a boron-containing mixture of chlorosilanes containing TCS, DCS and STC and purifying the mixture of chlorosilanes by distillation in a plurality of distillation columns, wherein low-boiling boron compounds are branched off from the distillation columns by overhead streams containing boron-enriched DCS and high-boiling boron compounds are branched off by a boron-enriched bottom stream containing high boilers.

Abstract: Processes of and systems for removing free bromine from gaseous anhydrous HBr contaminated with free bromine are described. In one type of process the gaseous contaminated HBr is fed into countercurrent contact with at least one liquid alkylaromatic hydrocarbon within a packed section of a column while maintaining the packed section under free radical bromination conditions so that one or more than one liquid a-bromoalkylaromatic compound is produced along with one mole of gaseous HBr per mole of a-bromoalkylaromatic compound produced. In another type of process the gaseous anhydrous HBr is fed into countercurrent contact through at least two scrubbers so that the gaseous anhydrous HBr is scrubbed substantially free of bromine by passage through these at least two scrubbers, each of which contains a different specified type of scrubbing liquid. In one embodiment the liquid alkylaromatic hydrocarbon comprises 1,2-diphenylethane.

Abstract: A method for concentrating metal chlorides in and separating same from an iron(III) chloride-containing hydrochloric acid solution is described, wherein iron is precipitated from the solution as iron oxide, preferably haematite and filtered off in a filtration device, and the now further concentrated non-hydrolysable metal chlorides are removed from at least a part of the hydrochloric acid filtrate.

Abstract: Process for degrading organic substances in an aqueous composition comprising a step (a) wherein, in a liquid reaction medium, said aqueous composition is reacted with at least one composition comprising hydroxide ions (OH?) and hypochlorite in a molar ratio between hydroxide and hypochlorite higher than or equal to 0.001 and lower than 1.5, in order to oxidize said organic substances.

Abstract: Provided is a stock oil composition for a carbonaceous material for a negative electrode of a lithium-ion secondary battery which composition is useful for achieving excellent high-speed charge and discharge characteristics. The stock oil composition for a carbonaceous material for a negative electrode of a lithium-ion secondary battery uses a bottom oil of residue fluid catalytic cracking apparatus as a raw material. The stock oil composition comprises, of a saturated component, an aromatic component, a resin component and an asphaltene component detectable by development of the stock oil composition using thin-layer chromatography, the saturated component ranging from 30 to 50% by weight and the aromatic component ranging from 50 to 70% by weight; and has an average molecular weight of from 400 to 600.

Abstract: A process according to the invention is a process to separate an initial fluid stream comprising phosgene and hydrogen chloride in at least a first and a second fluid stream, said first fluid stream being a hydrogen chloride enriched and phosgene depleted gaseous stream, said second fluid stream being a hydrogen chloride depleted and phosgene enriched stream.

Abstract: It is intended to provide methods of producing a chlorine gas having a small bromine content, an aqueous sodium hypochlorite solution having a small bromic acid content, and liquid chlorine having a small bromine content. More specifically, a chlorine gas is produced by a method comprising the steps of: (A) washing a chlorine gas that contains bromine, in a gas washing unit composed of a packed column or a tray tower, wherein the chlorine gas introduced via a lower part of the gas washing unit is brought into counterflow gas/liquid contact with a liquid chlorine introduced via an upper part of the gas washing unit; and (B) taking out a purified chlorine gas thus washed, via the upper part of the gas washing unit, wherein a weight ratio of the chlorine gas and the liquid chlorine introduced in the step (A) is 1/1.0 to 1/0.3.

Abstract: Disclosed herein are processes for separation of 2,3,3,3-tetrafluoropropene and hydrogen fluoride using azeotropic distillation. Additionally, disclosed are processes for separating mixtures of 2,3,3,3-tetrafluoropropene, hydrogen fluoride and 1,1,1,2,3-pentafluoropropane (HFC-245eb) and/or 1,1,1,2,2-pentafluoropropane (HFC-245cb) by azeotropic distillation.

Abstract: The invention enables processing waste sludge after galvanic treatment of metals, and particularly recycling spent pickling acids after pickling. Provided is an environmentally friendly process, which yields acids for reuse, and pure nano-sized iron pigments as a side product.

Abstract: A new, highly selective way of removing bromine contamination from a gaseous stream comprised of hydrogen bromide and bromine is described. Such process technology involves non-catalyzed free radical (benzylic) bromination of an alkylene-bridged aromatic hydrocarbon and/or certain alkyl-substituted aromatic hydrocarbons and recovering the purified gaseous HBr. Because of the high selectivity of the bromination on the aliphatic bridges or side-chains, virtually no ring bromination occurs, and this enables recovery of the bromine values in the form of HBr. Thus preferably, the bromine is recovered as HBr from the scrubbing liquid by subjecting the scrubbing liquid to thermal or catalytic dehyrobromination. In plant operations, the gaseous HBr purified in the process can then be introduced into a compressor to produce either liquid or gaseous HBr for storage under pressure. Alternatively, the purified gaseous HBr can be fed directly into one or more reactions in which HBr is used as a reactant.

Abstract: A method for producing of ultra-clean and High-purity electronic grade reagents is disclosed. The industrial grade reagents are chemically pretreated and filtered, and the colature is rectified. Heating the steam during the rectification to overheated steam, and filtering the overheated steam used the microporous membrane to remove the solid particulates. Condensing the overheated steam and the secondarily filter to remove the dust in the product. Due to the adoption of the technical scheme, the ultra-clean and High-purity isopropanol produced is in conformity with standard SEMI-C12 and the hydrochloric acid to standard SEMI-C8. And the method is applicable for the large-scale continuous production.

Abstract: Methods for producing silicon tetrafluoride by acid digestion of fluoride salts of alkali metal or alkaline earth metal and aluminum, optionally, in the presence of a source of silicon; methods for producing silane that include acid digestion of by-products of silane production to produce silicon tetrafluoride.

Abstract: A process for regenerating a used acidic catalyst which has been deactivated by conjunct polymers by removing the conjunct polymers so as to increase the activity of the catalyst is disclosed. Methods for removing the conjunct polymers include addition of a basic reagent and alkylation. The methods are applicable to all acidic catalysts and are described with reference to certain ionic liquid catalysts.

Abstract: Polymers useful as catalysts in non-enzymatic saccharification processes are provided. Provided are also methods for hydrolyzing cellulosic materials into monosaccharides and/or oligosaccharides using these polymeric acid catalysts.

Abstract: The invention provides an organic phase composition comprising: a. a first component selected from the group consisting of quaternary amines; b. a second component selected from: b1. The group consisting of category B organic acids; b2. The group consisting of a mixtures of category B organic acids and category C organic acids at a B/C molar ratio of RB/C; and b3. The group consisting of a mixtures of category A organic acids and category C organic acids at an A/C molar ratio of RA/C; c. a third component selected from the group consisting of solvents for said first component and for said second component, wherein (i) all three components are oil-soluble and water-insoluble; (ii) the molar concentration of each of said first component and said second component is greater than 0.6 mol/Kg; (iii) the molar ratio between said second component and said first component is greater than 0.

Abstract: The present invention provides an organic phase composition comprising (f) a first solvent (S1) characterized by water solubility of less than 10% and by at least one of (a1) having a polarity related component of Hoy's cohesion parameter (delta-P) between 5 and 10 mPa1/2 and (b1) having a Hydrogen bonding related component of Hoy's cohesion parameter (delta-H) between 5 and 20 MPa1/2; (g) a second solvent (S2) characterized by water solubility of at least 30% and by at least one of (a2) having a delta-P greater than 8 MPa1/2 and (b2) having a delta-H greater than 12 MPa1/2; (h) water (i) HCl, and (j) a chloride salt.

Abstract: The present invention provides an organic phase composition comprising: (a) a first solvent (S1) characterized by a water solubility of less than 10% and by at least one of (a1) having a polarity related component of Hoy's cohesion parameter (delta-P) between 5 and 10 MPa1/2 and (b1) having a Hydrogen bonding related component of Hoy's cohesion parameter (delta-H) between 5 and 20 MPa1/2; (b) a second solvent (S2) characterized by a water solubility of at least 30% and by at least one of (a2) having a delta-P greater than 8 MPa1/2 and (b2) having a delta-H greater than 12 MPa1/2; (c) water; (d) HCl; and (e) a carbohydrate.

Abstract: For a graphite sheet, a peak intensity ratio (P100/002) of a (100) diffraction peak and a (002) diffraction peak by X-ray diffractometry, and a peak intensity ratio (P110/002) of a (110) diffraction peak and a (002) diffraction peak thereby are set at 10 or more. The graphite sheet is manufactured through a step of preparing a polymer liquid which contains a polymer having carbon in its molecular chains and develops optical anisotropy, a step of unidirectionally orienting the molecular chains of the polymer, a step of obtaining a compact from the polymer liquid in the state that the orientation of the molecular chains of the polymer is maintained, and a step of carbonizing and thereafter graphitizing the compact.

Abstract: A fluoride ion cleaning method includes generating hydrogen fluoride (HF) gas in-situ in a cleaning retort; contacting a part in need of cleaning with the generated HF gas; scrubbing an initial effluent stream in-situ to substantially remove residual HF gas therefrom; and passing the scrubbed effluent gas stream out of the cleaning retort. In an exemplary method, a liquid or gaseous halogenated feedstock is introduced into a cleaning retort; hydrogen gas is introduced into the cleaning retort, HF gas is generated by a reaction of the feedstock with hydrogen gas at a sufficient temperature. In an exemplary method, only HF gas generated in-situ or reconstituted in-situ is utilized in the cleaning process.

Abstract: The Invention provides a process for the recovery of gaseous HCl comprising: a) providing an HCl-carrying extractant comprising: (i) an oil soluble amine which amine is substantially water insoluble both in free and in salt form; and (ii) a solvent for the amine and organic acid; b) contacting the HCl-carrying extractant with at least one non-volatile mineral acid, and c) stripping gaseous HCl, whereby HCl-depleted extractant and gaseous HCl are formed.

Abstract: A method for producing concentrated HCl vapor from an aqueous solution of HCl, including: (a) introducing an aqueous feed liquor to an evaporation chamber containing a mother liquor, the feed liquor having an initial, super-azeotropic HCl concentration; (b) directly contacting a liquor of these liquors with a heat-laden heat transfer fluid, to transfer heat from the fluid; (c) utilizing the heat to evaporate HCl, within the chamber, to produce the concentrated HCl vapor and to produce the mother liquor, the mother liquor including an aqueous phase having a reduced concentration of HCl, with respect to the initial HCl concentration; (d) subjecting the mother liquor to a liquid-liquid separation to produce a liquid phase containing HCl, and another liquid phase containing the heat transfer fluid in a heat-depleted state, with respect to the heat transfer fluid in step (b); (e) heating the heat transfer fluid in the heat-depleted state, to regenerate the heat-laden heat transfer fluid, and (f) returning this hea

Abstract: Steam stripper off gas from chemical pulp mills, for example kraft or sulphite pulp mills is rich in methanol and totally reduced sulphur (TRS) compounds. This gaseous stream is usually burned to avoid further handling of this TRS-rich, odorous stream. We found that once this gaseous stream is condensed, it can be used as a reducing agent in the chlorine dioxide generator, in place of purchased methanol. Surprisingly, we found that, in addition to the methanol component, the TRS components act as reducing agents during the production of chlorine dioxide or, at the very least, do not consume chlorine dioxide. The use of this stream in the ClO2 generator will allow pulp mills to reduce or eliminate the consumption of purchased methanol while providing a new approach to deal with TRS compounds in the chlorine dioxide generator rather than employing a dedicated TRS incinerator or any other combustion device.

Abstract: The present technology provides compositions that are intimate mixtures of hydrogen fluoride and a polyacrylate-polyacrylamide cross-linked copolymer, as well as methods and preparing and using such compositions. The compositions are less hazardous and, therefore, more conveniently stored, transported, and handled in comparison to pure hydrogen fluoride. Further, the hydrogen fluoride may be readily recovered from the compositions of the invention for use.

Abstract: A process and apparatus are described for converting a feed that is substantially comprised of halogenated materials, and especially byproduct and waste chlorinated hydrocarbons as are produced from a variety of chemical manufacturing processes, to one or more higher value products via a partial oxidation reforming reaction step. These products can be in the form of a useful or salable acid product and/or a product synthesis gas comprised of carbon monoxide and hydrogen, or the reaction product including the same hydrogen halide, carbon monoxide and hydrogen components can be employed as a feed in the synthesis of a different useful or salable product.

Abstract: Processes for forming ferric chloride solutions that are stable at relatively low temperatures and suitable for transportation without precipitation are provided. The stable ferric chloride solutions have an iron content of about 16 to about 23 weight percent and a hydrochloric acid content of about 11 to about 17 weight percent, wherein the ferric chloride solution is a stable solution and/or reversibly freezes at ?10° C. Also disclosed are processes for reconstituting the stable ferric chlorides solutions to provide a final iron content of 10 to 14 weight percent and lower the concentration of hydrochloric acid contained therein.

Abstract: Provided is a method of purifying hydrochloric acid by removing an organic substance having a boiling point of ?25° C. to 120° C. under atmospheric pressure from an organic substance-containing hydrochloric acid that contains the organic substance and has a hydrogen chloride concentration higher than an azeotropic hydrogen chloride concentration under atmospheric pressure. The method includes the step of subjecting the organic substance-containing hydrochloric acid to distillation using a distillation tower at an operation pressure set such that an azeotropic hydrogen chloride concentration under the operation pressure is higher than the hydrogen chloride concentration of the organic substance-containing hydrochloric acid, to distill out the organic substance from the top of the distillation tower.

Abstract: A process for the co-production of gaseous HCl and a salt product comprising a cation and an anion, which process comprises the steps of a. providing an aqueous solution comprising protons, chloride anions, and cations and anions of the salt product, b. bringing the solution into contact with a substantially immiscible extractant, the extractant comprising: 1) an oil soluble amine, which amine is substantially water insoluble both in free and in salt form; and 2) a carrier solvent for the amine; whereupon HCl selectively transfers to the extractant to form an HCl-carrying extractant and a chloride depleted aqueous solution containing the salt product; c. separating the HCl-carrying extractant from the chloride-depleted aqueous solution; and d. distilling HCl from the separated HCl-carrying extractant to form gaseous HCl and HCl depleted extractant.

Abstract: Hexachlorodisilane is decomposed into hydrochloric acid, silicon dioxide and water by introducing hexachlorodisilane-containing flue gas into a reaction region without moistening the flue gas and by supplying oxygen-containing gas that also contains a small amount of moisture to the reaction region maintained at a temperature at which hexachlorodisilane decomposes.

Abstract: Process for purifying hydrogen chloride, comprising at least one step of bringing said hydrogen chloride into contact with a scrubbing agent containing at least one chlorohydrin.

Abstract: In a method for recovering acid from an aqueous etching mixture containing HF, HNO3, H2SiF6 and HNO2 which has been used for purifying polycrystalline silicon, the used etching mixture is distilled progressively so that approximately from 20 to 50 wt. % of the mixture is distilled off as dilute acid containing more than 90 wt. % of the silicon dissolved as hexafluorosilicic acid in a first fraction, and the water contained in the used etching mixture having been reduced by approximately 10-30 wt. %, this water-depleted mixture is then concentrated by evaporation to a residue of about 1 to 5 wt. % of the initial amount of used etching mixture during which a second fraction is distilled off, and the residue is disposed of.

Abstract: The present invention provides compositions that are intimate mixtures of hydrogen fluoride and a polyacrylate-polyacrylamide cross-linked copolymer. The compositions of the invention are less hazardous and, therefore, more conveniently stored, transported, and handled in comparison to pure hydrogen fluoride. Further, the hydrogen fluoride may be readily recovered from the compositions of the invention for use.

Abstract: There is provided a process for the recovery of HCI from a dilute solution thereof, comprising bringing a dilute aqueous HCI solution into contact with a substantially water-immiscible extractant, the extractant comprising an oil soluble amine, which amine is substantially water insoluble both in free and in salt form; an oil soluble weak organic acid having a pKa above 3, which acid is substantially water insoluble both in free and in salt form; and a solvent for the amine and organic acid; whereupon HCI selectively transfers to the extractant to form an HCI-carrying extractant, and treating the HCI-carrying extractant to obtain gaseous HCI. Also provided is the extractant composition.

Abstract: (Chloro)hydrocarbon-free hydrogen chloride and phosgene-free (chloro)hydrocarbons are recovered from a hydrogen chloride stream having (chloro)hydrocarbons and phosgene.

Abstract: Wide mesoporous alumina composites are produced by an “in situ reaction” route comprising agglomeration of an alumina powder that is capable of rehydration together with a second reactive powder such as carbonate. In one method of production, the powders are fed to a rotating forming device that is continuously sprayed with liquid under conditions to form particulates. The discharging beads are then subjected to curing and thermal activation to produce the final catalyst or adsorbent. The alumina participates in a pore altering process involving the carbonate component upon formation of hydroxycarbonate intermediates such as Dawsonite. Large fraction of the pore volume of the final product consists of wide mesopores in the 15-50 nanometers range. The alumina composites exhibit a characteristic trimodal pore structure that includes also small micro-meso pores and macropores larger than 200 nanometers.

Abstract: A method which especially can safely produce a hypobromous acid or a water-soluble salt thereof, that does not require expensive equipment or the like, does not involve extra work such as pre-mixing or have restrictions such as producing immediately prior to use, and is simple. Further, a method which can efficiently and rapidly form a hypobromous acid or a water-soluble salt thereof which is stable and has high sterilization/anti-microbial effect, and which does not form harmful bromic acid. At least either a hypobromous acid or a water-soluble salt thereof is formed by reacting at least either a hypochlorous acid or a water-soluble salt thereof with a bromide in a liquid to be treated, wherein the at least either hypobromous acid a water-soluble salt thereof is formed by adding a modified chlorite to the liquid to be treated.

Abstract: The invention relates to a process for recovering acids from product streams of organic syntheses, which comprises the steps a) neutralization of the acid with a base, b) removal of the base by means of adsorption, c) recovery of the acid.

Abstract: Methods for purifying an aqueous hydrochloric acid solution waste stream having an impurity fraction comprising an initial Ti fraction, an initial S fraction and an initial Si fraction; that provide purified aqueous hydrochloric acid solutions having a final Ti fraction of less than 250 ppm, a final S fraction of less than 200 ppm, and a final Si fraction of less than 10 ppm, which may be determined with inductively coupled plasma spectroscopy. Process steps in various embodiments include sparging with an gas; mixing the sparged solution with a precipitation agent comprising a sufficient amount of an alkali earth metal salt and, optionally, a phosphoric acid source, to provide a metal salt precipitate; and mixing the initial aqueous acid solution or, optionally, the sparged aqueous acid solution, with a flocculating polymer. A preferred alkali earth metal salt is barium chloride and preferred flocculating polymers are poly(diallyldialkylammonium chloride) homopolymers and copolymers.

Abstract: A process for regenerating a used acidic catalyst which has been deactivated by conjunct polymers by removing the conjunct polymers so as to increase the activity of the catalyst is disclosed. Methods for removing the conjunct polymers include hydrogenation, addition of a basic reagent and alkylation. The methods are applicable to all acidic catalysts and are described with reference to certain ionic liquid catalysts.

Abstract: The present invention provides a method for separating HBr from HBr-containing hydrocarbons (alkenes, aromatics and/or alkanes) to purify the hydrocarbons. Reacting a silica supported metal oxide solid material (MOx/SiO2, MOx=MgO, CoO, Co2O3, CuO and mixture thereof) with HBr in HBr-containing hydrocarbons, so as to ensure that the concentration of HBr is reduced to below 1.87×10?16, and then oxidizing the solid material which reacted with HBr in oxygen or air to regenerate MOx/SiO2, meanwhile Br2 is recycled. Therefore, the purpose of continuous purification of hydrocarbons can be achieved.

Abstract: The present invention is drawn to a method for removing colloidal titanium dioxide and titanium oxychloride from by-product hydrochloric acid. The method includes adding phosphate ion source and quaternary amine to the by-product acid to cause the titanium dioxide and the titanium oxychloride to form a precipitate. The precipitate can then be separated from the acid, thus producing a decontaminated hydrochloric acid product with reduced levels of titanium.

Abstract: The invention provides a process for the recovery of HCl from a dilute solution thereof, comprising: a) bringing a dilute aqueous HCl solution into contact with a substantially immiscible extractant, said extractant comprising: 1) an oil soluble amine which amine is substantially water insoluble both in free and in salt form; 2) an oil soluble organic acid which acid is substantially water insoluble both in free and in salt form; and 3) a solvent for the amine and organic acid; whereupon HCl selectively transfers to said extractant to form an HCl-carrying extractant; and b) treating said HCl-carrying extractant to obtain gaseous HCl.