Abstract: Where side stream distillate strippers are used in the distillation of hydrocarbons, the required size of the distillation column and the amount of stripping gas or vapor required are reduced by passing components stripped from the distillates through a plurality of strippers in series, rather than directly back to the distillation zone.

Abstract: The separation of ethyl tertiobutyl ether from mixtures with ethanol is based on heteroazeotropic distillation with water as the entrainer using two distillation columns, coupled with an overhead decanter. Purified ethanol is collected from the bottom of the first column and purified ETBE from the bottom of the second column. The separation method may be incorporated into an ETBE production unit in which isobutene (contained in a C.sub.4 -cut from steam cracking, catalytic cracking, or dehydrogenation of isobutane) is etherified by ethanol. Ethanol separated from the ETBE is then recycled to the etherification zone.

Abstract: Purification of crude sulfolane to remove color imparting and turbidity imparting impurities therefrom is achieved by a two-pass distillation process wherein purified sulfolane is withdrawn from the bottom of a column in the second distillation pass.

Abstract: The present invention provides a continuous method of purifying eicosapentaenoic acid and esters of eicosapentanoic acid, comprising (a) fractionally distilling a starting mixture containing eicosapentaenoic acid or esters of eicosapentaenoic acid using a system of at least three distillation columns connected in flow arrangement to separate a fraction containing eicosapentaenoic acid or esters of eicosapentaenoic acid and other C.sub.20 fatty acids from a fraction containing lower-number carbon fatty acids and from a fraction containing higher-number carbon fatty acids, and (b) continuously collecting the fraction containing eicosapentaenoic acid or esters of eicosapentaenoic acid, wherein the pressure in the distillation columns is maintained at 10 Torr or below and wherein the bottom temperature of the distillation columns is maintained at 210.degree. C. or below.

Abstract: A process for separating an aromatic from a mixture containing also nonaroma includes distilling off the nonaromatics from the top of the extractive distillation column as a top product, drawing the aromatic and selective solvent from the extractive distillation column and subsequently separating the selective solvent from the aromatic in a separator column. The extractive distillation column is provided with a separate top product distillation column for recovery of a selective solvent residue from the separated nonaromatics. The entry hydrocarbon mixture is heated prior to admission to the extractive distillation column by an indirect heat exchange with selective solvent drawn from the separator column and heated to a temperature of from 130.degree. to 150.degree. C.The heated entry hydrocarbon mixture is depressurized to form a liquid phase and a vapor phase and these phases are separately fed into the extractive distillation column, the vapor phase entry point being below the liquid phase entry point.

Abstract: Disclosed is a process for the recovery of purified hydroxypivalyl hydroxypivalate (HPHP) from a crude, HPHP containing material containing inorganic catalyst residues and low-boiling and high-boiling (with respect to the boiling point of HPHP) impurities. The purification process employs two distillation zones, a first distillation zone wherein inorganic and high-boiling impurities are removed and a second distillation zone wherein low- and high-boiling impurities are removed.

Abstract: For the separation of tert. butyl ethyl ether from mixtures with ethanol, there are provided two distillation stages, the first being carried out at a pressure p.sub.1 equal to or higher than 1 bar, the second at a pressure p.sub.2 below p.sub.1 by a value .DELTA.p or 0.5 to 12 bars, p.sub.2 then being 0.5 to 10 bars. The second column distillate is partly supplied as reflux to the head of the second column and is in part recycled to the head of the first column. The purified TBEE is collected at the bottom of the first column and the purified ethanol at the bottom of the second column.This separation process can be integrated into a TBEE production unit comprising etherification by ethanol of the isobutylene contained in a C.sub.4 fraction from a catalytic cracking or steam cracking stage. The ethanol separated from the TBEE is then recycled to the etherification zone.

Abstract: The present invention provides an improved process for the separation of impurities from a lower alkylene oxide, such as propylene oxide, by a process wherein the impure propylene oxide is first fractionally distilled to separate higher and lower boiling impurities, then the partially purified alkylene oxide is subjected to extractive distillation to separate additional impurities, the purified propylene oxide being separated as an overhead fraction.

Abstract: The process for rectification of phenol prepared from crude phenol being the product of decomposition of cumene hydroperoxide and having previously been distilled to remove large portions of acetone, cumene and alpha methylstyrene which includes:feeding the column overhead vapors to a condenser, thereby condensing a major portion of the overhead vapors;withdrawing a small portion of the overhead vapors from the condenser while still in a vapor state, the small portion being relatively enriched in lights and laden with light acids;returning the condensate from the condenser to the phenol distillation column as reflux; andwithdrawing product phenol from at least one-theoretical stage below the top of the phenol distillation column, the product phenol having improved clarity when dispersed in water, clarity being at least 93 percent light transmission as measured by an electrophotometer in a water light test.

Abstract: A process for the recovery of methoxyisopropylamine from the reaction of methoxyisopropanol and ammonia under amination conditions. Water is produced as a byproduct and in the distillation separation an azeotrope is formed which includes about 14% water and 86% methoxyisopropylamine. The improvement for enhancing separation of the azeotrope includes initially distilling the mixture of methoxyisopropylamine, methoxyisopropanol and water under sufficient elevated pressure wherein an azeotrope of water and methoxyisopropylamine overhead and an essentially water free bottoms of methoxyisopropylamine and methoxyisopropanol are formed. The overhead from this initial distillation column is charged to a second distillation column operated at reduced pressure wherein an organic free bottoms containing primarily water is obtained.

Abstract: A thermally-integrated extractive distillation process for recovering anhydrous ethanol from fermentation or synthetic feedstocks has a distillation train of four columns. Two columns are preconcentrators operated in parallel. The remaining columns are an extractive distillation dehydrating tower, and an entrainer-recovery column. The two preconcentrators and the dehydrating tower are operated at three successively increasing pressures so that the condensing vapors of the overhead product of the dehydrating tower supply the necessary heat to the reboiler of the intermediate-pressure preconcentrator. The overhead vapors of this preconcentrator are, in turn, used to supply the required heat to the reboiler of the lowest-pressure preconcentrator. The bottom product from each preconcentrator is used to preheat the dilute feed. Additional energy savings are accomplished by the appropriate heat exchange between the various feeds, overheads, and bottoms.

Abstract: A hydrocarbon material of the starting product is separated in an extractive distillation column in which an N-substituted morpholine whose substituents do not have more than seven carbon atoms is used as a selective solvent. The overhead product comes down as a top product of the extractive distillation and is fed through a coalescer in which the sump product comes down with a solvent content of 20 to 75% by weight at a temperature of 20.degree. to 70.degree. C. and subsequent to that is fed into a separating vessel. There it is separated into a heavier and lighter phase. After that the heavier phase is conducted into an extractive distillation column and the lighter phase into the overhead product distillation column.

Abstract: Small amounts of a medium-boiling fraction are removed from a liquid mixture by distillation using a distillation column (main column) having a rectifying part and a stripping part, the liquid mixture containing relatively large amounts of lower-boiling and higher-boiling components, and the rectifying part being connected to the upper end of a second distillation column (side column) and the stripping part to the lower end of the said column, and the medium-boiling fraction being removed in vapor or liquid form from its middle section, by a process in which the concentration of the medium-boiling fraction in the liquid mixture is less than 2%, preferably less than 0.1%, and the amount of vapor passed into the lower end of the side column from the main column is 1-20%, preferably 3-10%, based on the amount of vapor in the main column at the relevant point.

Abstract: Provided by this invention is a process for producing a purified hydrazine hydrate having a low total organic carbon concentration and which involves:a first step which includes distilling an aqueous solution of hydrazine hydrate in the presence of at least one salt selected from the group consisting of chloride, sulfate, phosphate and carbonate of (a) the metals of Group Ia and IIa of the Periodic Table of the Elements, (b) ammonium or (c) hydrazinium to concentrate the aqueous solution of hydrazine hydrate by distilling water and the majority of the total organic carbon constituents off and separating the resultant concentrate as a bottom product, anda second step which includes distilling the resultant concentrate to recover a purified aqueous solution of hydrazine hydrate as a top product and separating an aqueous solution of the above salt as a bottom product.

Abstract: The process for production of an aromate concentrate for use as a blending component for gasification fuel includes subjecting another feed hydrocarbon mixture to an extractive distillation using N-substituted morpholines as selective solvent in a extractive distillation column. Low-boiling non-aromates with a boiling range up to about 105.degree. C. practically completely and higher-boiling non-aromates with a boiling range between about 105.degree. and 160.degree. C. to a substantial extent are discharged as a raffinate from the top of the extractive distillation column. The extract bottoms from the extractive distillation are fed to a solvent stripping column where the solvent is at least partially recovered from other hydrocarbons. To eliminate condensation and polymerization products due to components with a boiling point over 170.degree. C.

Abstract: 1,3-Butadiene is isolated from a C.sub.4 -hydrocarbon mixture containing 1,3-butadiene and small amount of propyne and C.sub.5 -hydrocarbons by extractive distillation with a selective solvent and subsequent distillative purification of the crude 1,3-butadiene obtained in the extractive distillation.

Abstract: A fractional distillation system is provided for fractionating unequal liquid mixtures with lower heat throughput and lower energy consumption. For mixtures in which the heavy fraction is predominant (FIG. 1), a stripper (2) pre-fractionates part of the mixture at lower pressure and at no extra energy cost by being reboiled by an intermediate condenser (3). The pre-fractionator temperature range is preferably nested within (overlapped by) the distillation column (6) temperature range.

Abstract: A method for cleaning and reclassifying electrical apparatus designed for use with PCB fluid electrolytes is described which is capable of operation on the site of the equipment being cleaned and while said equipment is energized.

Abstract: The instant invention relates to a process for the purification of dimethylether, which contains impurities, by feeding a mixture which contains the dimethylether at specific trays to a distillation column and withdrawal of the dimethylether and of impurities at specific trays of the same column.

Abstract: In the purification of ethylene oxide from an ethylene oxide-containing reaction formation gas produced by catalytic gas-phase oxidation of ethylene with a molecular oxygen containing gas, external thermal energy required for heating an ethylene oxide refiner is economized by a method which utilizes the diffusate obtained from the top of an ethylene oxide stripper as a heat source for the refiner. Further, the bottom liquid of the stripper can be used as a heat source for ethylene oxide refiner and/or a light ends stripper.

Abstract: A process is described for the production of substantially pure gamma-butyrolactone from a feed mixture containing a major amount of gamma-butyrolactone and a minor amount of diethyl succinate which comprises fractionally distilling the mixture in a fractionation zone in the presence of added diethyl maleate and recovering from the fractionation zone an overhead vaporous product comprising gamma-butyrolactone which is substantially free from diethyl succinate and a liquid bottom product comprising diethyl maleate and diethyl succinate in admixture one with another. This procedure can be used to separate a gamma-butyrolactone rich fraction obtained by distillation in one or more stages of a crude reaction product obtained by hydrogenation of a C.sub.

Abstract: An aqueous effluent is supplied to a stripping column (total stripping column) from which a mixture that is rich in NH.sub.3, CO.sub.2 and H.sub.2 S is withdrawn as a head product. In at least one additional stripping column the mixture is separated into a mixture which is rich in NH.sub.3 and a mixture which is rich in the sour gaes CO.sub.2 and H.sub.2 S. The mixture which is rich in NH.sub.3 is scrubbed with liquid ammonia. The overhead product from the total stripping column is cooled in a condenser under a pressure of 1 to 7 bars and is thus transformed into a liquid phase to such an extent that the liquid phase contains 70 to 100% of the NH.sub.3 which has been supplied to the condenser. The liquid phase is supplied at a temperature of 30.degree. to 90.degree. C. to a second stripping column (NH.sub.3 stripping column), which is operated under a pressure of 1 to 4 bars and from which a gas mixture that is rich in NH.sub.3 is withdrawn as a head product.

Abstract: A process for removing by product acetone from reaction mixtures obtained by reacting methyl acetate and/or dimethylether with carbon monoxide at elevated temperatures to obtain acetic anhydride in the presence of a catalyst system consisting essentially of carbonyl complexes of noble metals belonging to group VIII of the Periodic System of the elements, acetic acid, an organophosphorus or organonitrogen compound, and methyl iodide whereby the acetone obtained as a by-product during the reaction is subjected to condensation at temperatures of 50.degree. to 250.degree. C., under pressures of 0.01 to 150 bars and at a molar ratio as above defined for the catalyst system constituent of 1:(25-500):(10-100):(15-150) so as to obtain predominantly higher-boiling secondary products to be distillatively separated in a successive distillation zone together with volatile constituents of the catalyst system.

Abstract: The separation of homozeotropic mixtures of a paraffin or paraffins of 6-14 carbon atoms and an alcohol or alcohols of 4-8 carbon atoms is conducted in two rectification steps. In a first step, rectification is carried out in the presence of water as the azeotropic agent, and the resultant distillate, after condensation, is separated into two liquid phases. The thus-obtained organic phase is rectified in a further step without the addition of water, and the head product consisting of an alcohol/paraffin mixture is recycled into the first step. The paraffin or paraffins and the alcohol or alcohols are obtained in the lower section of the individual rectifying step or steps. The water which may be present in the starting mixture is removed from the cycle. Low-boiling paraffins and/or low-boiling alcohols are suitable as additional azeotropic agents.

Abstract: In the distillation of fresh water from sea water, the sea water is passed ownwardly in a falling film evaporator through a multiplicity of vertical tube evaporator (VTE) stages and multiple stage flash (MSF) evaporators. After the sea water passes through the first VTE stage where it forms a liquid component and a steam component, the liquid component is distributed evenly into the next VTE stage while the steam component enters an adjoining MSF stage. Condensed fresh water flows downwardly from one MSF stage to the next and experiences flash evaporation. The sea water or brine component and the fresh water distillate flow downwardly through the VTE and MSF stages so that the brine component can be removed from the final VTE stage and the fresh water distillate from the final MSF stage.

Abstract: In a continuous alkoxidation-phosphorylation process for producing tributyl phosphate having low color utilizing excess butanol in the alkoxidation reaction which is heated by an alcohol flasher wherein the excess butanol is recovered after phosphorylation by two stage flash distillation, the bottoms product from the first stage going to the second stage, the overhead product from the second stage returning to the first stage flash distillation, and the bottoms from the second stage distillation going to final product washing and drying process while the overhead from the first stage flash distillation is fed to the process alkoxidation alcohol flasher, the improvement which comprises distilling in a distillation column the overhead product from the first stage flash distillation and then feeding the overhead from the distillation column to the alkoxidation alcohol flasher.

Abstract: Methacrylonitrile higher in purity than that obtained by the conventional process is efficiently produced by the present improved process for producing purified methacrylonitrile in which the reaction mixture formed by the ammoxidation of isobutylene or tert-butyl alcohol is distilled using water as solvent to obtain a crude methacrylonitrile solution which contains methacrylonitrile as major constituent, methacrolein, hydrogen cyanide, and isobutyronitrile, and the crude methacrylonitrile solution is then purified in a product column, wherein the improvement comprises first removing isobutyronitrile from said crude solution, then feeding the remaining solution to the product column, withdrawing from the top a vapor containing methacrolein, condensing the vapor, returning a greater part of the condensate to the product column while removing the remainder from the distillation system, and withdrawing purified methacrylonitrile from the middle or lower section, preferably from a point lower than the feeding sta

Abstract: Improved process for the separation of a hydrocarbon-containing feedstream comprising monomer, comonomer and diluent into separate product streams which comprises subjecting the feedstream to two-stage distillation provided with a common accumulation zone wherein the condensate from the accumulation zone serves as the source of feed for the second distillation and reflux for the first distillation. In a specific embodiment, a feed comprising ethylene, 1-hexene, and isobutane is separated into separate streams of 1-hexene, ethylene and isobutane, and isobutane for recycle to polymerization.

Abstract: A process for producing anhydrous ethanol from an ethanol-water mixture feedstock comprising subjecting the feedstock to distillation in a first distillation zone to produce an overhead vapor of from about 80 to about 90 weight percent ethanol, subjecting the thus produced overhead vapor to extractive distillation in an extractive distillation zone to produce anhydrous ethanol vapor overhead of about 99.5 weight percent ethanol and a solvent-rich bottom stream, and stripping the solvent-rich bottom stream and recycling the thus produced lean solvent bottom stream to the extractive distillation zone and recycling the thus produced overhead vapor stream to the first distillation zone. Also disclosed is a system for performing the process.

Abstract: Disclosed is a process for recovering a virtually water-free amine from an amine acid salt thereof. The process comprises a unique combination of phase separation stages practiced under mild heating and distillation stages. An amine product containing less than 0.2% water can be achieved by the present process. The feedstock for the process suitably is an acid scrub liquor used to scrub amine from a vapor stream thereof which has been used in a cold-box molding process in the foundry industry or in the cure of vapor permeation curable coatings in the coatings industry.

Abstract: A flow of fermenting liquor from a fermentor is separated into a yeast concentrate flow, which is recirculated to the fermentor, and a yeast-free flow which is separated in a simple evaporator unit into a first ethanol-enriched vapor flow and a first liquid bottom flow. The first vapor flow is treated to produce the desired ethanol while a major part of the first liquid bottom flow is recirculated to the fermentor. A minor, residual part of the latter flow is fed to a stripping unit where it is separated into a second ethanol-enriched vapor flow and a second liquid bottom flow exhausted of ethanol.

Abstract: A novel fractional distillation process and applications thereof to the production of thermal or mechanical energy from two low level heat sources wherein a mixture of two highly non-ideal reactive solutions such, for example, as of the water/ammonia type, is separated into its water and ammonia components in an apparatus comprising a cascade of condensers and evaporators operating respectively at the temperature of the cold source and at the temperature of the hot source and at staggered pressures. The residue and distillate formed are remixed in a mixing apparatus when it is desired to recover the thermal energy of dilution of the solutions.The invention is applicable, in particular, to the heating of buildings from low level thermal energy and from the thermal energy of "cold wind".

Abstract: Disclosed is a process for recovering a virtually water-free amine from an amine acid salt thereof. The process comprises a unique combination of phase separation stages practiced under mild heating and distillation stages. An amine product containing less than 0.2% water can be achieved by the present process. The feedstock for the process suitably is an acid scrub liquor used to scrub amine from a vapor stream thereof which has been used in a cold-box molding process in the foundry industry or in the cure of vapor permeation curable coatings in the coatings industry.

Abstract: This invention relates to a process for purifying crude ethanol, whether produced by fermentation or by the synthetic route, to produce a pure ethanol-water azeotrope. The process uses only two distillation columns for fermentation ethanol or synthetic ethanol eventhough the latter has diethyl ether as impurity. The inventive concept lies in the design and specification of the columns and the specific high pressure and low reflux ratio distillation conditions which enable each of the impurities in ethanol to be reduced below ppm. Ethanol of such purity is most desirable when used for potable or pharmaceutical purposes.

Abstract: In a method for separating a hydrocarbon mixture into relatively difficultly soluble hydrocarbons and relatively easily soluble hydrocarbons by extractive distillation using a polar solvent comprising feeding the starting hydrocarbon mixture to at least two evaporators, an extractive distillation column, a stripping column and a rectifying column; the improvement wherein(1) the polar solvent discharged at a high temperature from the bottom of the stripping column is recycled to the extractive distillation column after it has been cooled to a suitable temperature by giving up heat to a reboiler of the extractive distillation column, a reboiler of the rectifying column and successively to the two or more evaporators, and(2) the starting hydrocarbon mixture is divided into two or more streams and heated in two or more evaporators, one stream being evaporated in a first evaporator to a pressure necessary for introduction into the extractive distillation column and then fed to the extractive distillation column, a

Abstract: A liquid containing a contaminant such as water or polymeric solids is purified. Purification of a liquid containing a contaminant is enhanced by the use of second fractionating column in conjunction with a first fractionating column to recover a portion of the liquid to be purified from the kettle product of the first column. Vapor from a second fractionating column is used to control the total energy input to a first fractionating column.

Abstract: A process for producing an unsaturated nitrile with saved energy by which the bottom stream from a recovery column is used as the heat source for at least one distillation column in the process and thereafter used to pre-heat a recovery column feed withdrawn from the bottom of an absorption column, characterized in that the bottom stream of the absorption column is previously heated by at least one source of waste heat in the process, the source being selected from (1) the circulating water in the quenching column, (2) the overhead vapor of the absorption column, (3) the overhead vapor of a dehydration column and (4) the overhead vapor of a product column.

Abstract: A process is provided for the continuous separation of slightly volatile components from a crude phthalic acid anhydride wherein a portion of the crude phthalic acid anhydride is compressed and heated before being reintroduced into a flash evaporator.

Abstract: An improved distillation method and apparatus are provided for recovering anhydrous ethanol from fermentation or synthetic feedstocks. The system includes at least one stripper-rectifier tower, a dehydrating tower, and an azeotropic agent stripping tower. Substantial energy savings are realized by operating the dehydrating tower, and preferably also the azeotropic agent stripping tower, at a higher pressure than the stripper-rectifier tower and by condensing the overhead vapors from the dehydrating tower (or dehydrating tower and azeotropic agent stripping tower) to provide the heat required in the stripper-rectifier tower. In a preferred embodiment, two stripper-rectifier towers are used, one operating at a higher pressure than the other, in which case the higher pressure tower is heated as just described and the overhead vapors from the higher pressure tower are condensed to supply the heat required in the lower pressure tower.

Abstract: In a process for recovering pure methylal from methanol-methylal mixtures, which can optionally contain still further compounds, the separation conducted in a rectification device comprising two rectifying columns. In the first rectifying column, the mixture to be separated is rectified under a pressure lower than that in the second column, into a methylal-rich, methanol-poor distillate, and into a practically methylal-free, methanol-rich sump product. The methylal-rich distillate of the first rectification is then separated in a second rectifying column, operated under a higher pressure than the first rectification column, into a compound stream containing methanol and methylal, which is then recycled to the first rectifying column, and into pure methylal as the sump product.

Abstract: A method is disclosed for preventing the condensation of aluminum chloride (AlCl.sub.3) in a fractional distillation column which is operated to separate a fraction which does not include AlCl.sub.3 from a mixture containing AlCl.sub.3 and other metal chlorides and which is operated at temperatures which include the sublimation or melting points of AlCl.sub.3 at the operating pressure of the column. According to this method, titanium tetrachloride (TiCl.sub.4) is maintained in the column in an amount at least as great, by weight, as the amount of AlCl.sub.3 contained in the mixture.

Abstract: A process for synthesizing ammonia is disclosed comprising the steps of generating the synthesis gas from hydrocarbons by the primary reforming of said hydrocarbon with steam and by the secondary reforming of the resulting gaseous mixture with oxygen; subjecting a portion of the starting hydrocarbon mixed with the steam to a tertiary reforming in which the necessary heat is provided by the gaseous reaction mixture leaving the secondary reforming; causing the ammonia synthesis to occur at low pressure with drying of the gas sent to the synthesis reactor by employing a molecular sieve; causing the ammonia contained in the reacted gas to be absorbed by water; and subjecting the ammonia solution so obtained to a distillation which may be a conventional distillation step or one effected by means of two distillation columns operating at different pressures.

Abstract: Substantially anhydrous, i.e., absolute, ethanol is distilled at high thermal efficiency from a dilute feedstock such as a fermentate ("beer") containing one or more low boiling components whose removal at least in part prior to anhydrous distillation is necessary in order to achieve an acceptable degree of phase separation in a decanter. Most of the low boiling component(s) are removed from the feed in a rectifying column with the balance of the low boiling component(s), insufficient in amount to seriously interfere with proper operation of the decanter, being removed from the system employing a light-ends column. Both the anhydrous column and the light-ends column are operated at substantially superatmospheric pressure with thermal values recovered from these columns being used in the operation of the rectifying column.

Abstract: A process is disclosed for the recovery of a phenol-free cumene fraction from a mixture thereof with phenol and water. Said mixture is introduced into a first fractionation column at conditions to separate a bottom fraction comprising a major portion of said phenol and an overhead fraction comprising said cumene and water and a residual portion of said phenol. The overhead fraction is condensed to form an aqueous phase containing a minor portion of the residual phenol and a water-saturated organic phase comprising cumene and the balance of said residual phenol. The water-saturated organic phase is then further treated in a second fractionation column whereby cumene is recovered as an overhead fraction substantially free of phenol.

Abstract: A process for the isolation of hydroquinone, pyrocatechol, phenol and carboxylic acid from the reaction mixture containing the same such as one obtained by reaction of phenol with percarboxylic acid is disclosed. The reaction mixture is fed to a first rectification column and subjected to distillation whereby there is obtained a bottoms product containing pyrocatechol, hydroquinone and phenol. The top product is largely condensed and recycled, there being withdrawn from the top of the rectification column a mixture comprising phenol and carboxylic acid. The phenol and carboxylic acid mixture are continuously fed to a second rectification column where carboxylic acid is separated from phenol and substantially pure phenol is withdrawn from the stripping section and/or bottom of the second rectification column.

Abstract: Crude acetonitrile is purifed to 99+ weight percent by a continuous distillation procedure.

Abstract: A flow of fermenting liquor from a fermentor is separated into a yeast concentrate flow, which is recirculated to the fermentor, and a yeast-free flow which is separated in a simple evaporator unit into a first ethanol-enriched vapor flow and a first liquid bottom flow. The first vapor flow is treated to produce the desired ethanol while a major part of the first liquid bottom flow is recirculated to the fermentor. A minor, residual part of the latter flow is fed to a stripping unit where it is separated into a second ethanol-enriched vapor flow and a second liquid bottom flow exhausted of ethanol.

Abstract: Metal chlorides such as aluminum chloride (AlCl.sub.3) are separated from a mixture containing metal chlorides including AlCl.sub.3 and ferric chloride (FeCl.sub.3). In order to effect this separation, the mixture is subjected to a fractional distillation process utilizing an array of distillation columns. According to this process, the mixture is introduced into a first distillation column which is operated at temperatures and pressures sufficient to separate FeCl.sub.3 from the mixture while avoiding the formation of a solid solution of FeCl.sub.3 and AlCl.sub.3 within the column. At least one additional distillation column is then employed to separate metal chlorides from the remaining mixture from the first column.

Abstract: The invention involves a process for substantially separating the components of mixtures of substances at least one of which is of low volatility while the other is of low or no volatility, the process using a compressed gas under supercritical conditions and an entrainer which increases the concentration of said mixture in the gaseous phase as well as the separation factor between the components to be separated. The process operates in two distillation zones the first of which substantially separates the components of low volatility in a process similar to a rectification process while the second distillation zone separates the top product of the first distillation zone from the gas with the aid of the entrainer which is condensed partially and in this state is passed in countercurrent to the gas carrying the separated component of low volatility.

Abstract: A process for the continuous separation of methanol and water from a feed mixture containing predominantly tetrahydrofuran admixed with water, methanol and small amounts of additional compounds, in a rectifying apparatus having at last two rectifying columns, of which two are operated at different pressures which involves feeding the raw material into a first column operated under lower pressure, and introducing the distillate from the column operated under a lower pressure to a second column operated under a higher pressure, while a product stream from the second column operated under a higher pressure is reintroduced into the first column operated under a lower pressure.