A method for precisely predicting phase equilibrium from existing phase equilibrium data on the basis of a wide range of phase equilibrium data including binary vapor-liquid equilibrium data; a method or apparatus for designing or controlling a component separator or a refiner using the prediction method; and a program for designing this design or control apparatus. Binary phase equilibrium measurement data is used to calculate an index of proximity ratio to critical points and infinite dilution pressure gradients. The obtained index is correlated with the infinite dilution pressure gradients to newly calculate infinite dilution activity coefficients from the respective index to infinite dilution pressure gradients correlations. The obtained infinite dilution activity coefficients values are used to predict phase equilibrium. Thus, the obtained values are used to design or control a component separator or a refiner, such as a distillation column.

A method for counter-current liquid-liquid extraction in a sub-millimeter conduit is implemented from an initial liquid drop stream. The stream has alternating drops of a first liquid, and a second liquid less wetting than the first liquid and immiscible with the first liquid. One of the liquids includes a component to extract towards the other liquid. A first pressure gradient applied along the conduit generates a visco-inertial flow displacing a first drop stream volume according to the first gradient and generating a film of first liquid displaced along the opposite orientation, the film being located between the drops of second liquid and the conduit. The application of the first pressure gradient is stopped. A second pressure gradient is applied along the conduit, in the opposite orientation to generate a viscous-capillary flow displacing a second volume of according to the second gradient and application of the second pressure gradient stops.

Techniques for separating a fuel on-board a vehicle include mixing an input fuel stream and a fluid solvent; separating the mixture into a first liquid fuel stream and a second liquid fuel stream, the first liquid fuel stream including a first portion of the input fuel stream defined by a first auto-ignition characteristic value and the fluid solvent, the second liquid fuel stream including a second portion of the input fuel stream defined by a second auto-ignition characteristic value that is different than the first auto-ignition characteristic value; separating the first liquid fuel stream into the fluid solvent and the first portion of the input fuel stream; directing the first portion of the input fuel stream to a first fuel tank on the vehicle; and directing the second portion of the input fuel stream to a second fuel tank on the vehicle.

Centrifugal contactors that can be used for mixing or separating materials are described. The contactors include a sensing system including a communications fiber within the shaft of the contactors and access ports providing access from the communications fiber to the mixing/separating zone of the contactor. The sensing system can be utilized during operation of the contactor and can provide for detailed and accurate on-line characterization of a protocol, as well as process control and system modification as necessary during operation.

A solvent extraction settler arrangement comprises a settler (1) having a feed end (2) and a discharge end (3), said settler being arranged to separate solution phases from a dispersion fed from the feed end while the dispersion flows to the discharge end. Elongated discharge launders (4, 5) are arranged at the discharge end (3) of the settler for each solution phase to be separated from the dispersion, each discharge launder (4, 5) including a first end (6), an outlet (7, 8) arranged at the first end, and a closed second end (9). At least one of the discharge launders (4, 5) has a form of a conical tube with a cross-section converging from the first end (6) towards the second end (9) and an inclined bottom (10, 11) descending from the second end (9) towards the first end (6).

This disclosure relates to a method of continuous recovery of (meth)acrylic acid and an apparatus used for the recovery method. The method of continuous recovery of (meth)acrylic acid according to the present invention may effectively remove scum formed in the continuous recovery process of (meth)acrylic acid, and simultaneously recover (meth)acrylic acid with excellent efficiency, thus enabling more stable operation of the continuous process.

An initial introduction control part introduces an aqueous solution containing molybdenum 99 and technetium 99m, and an organic solvent being capable of dissolving the technetium 99m into an extraction tank. A micro-mixing control part micro-mixes the aqueous solution and the organic solvent by heating and stirring a mixed solution of the aqueous solution and the organic solvent introduced into the extraction tank with a heater, while applying ultrasonic to the mixed solution. A separation control part separates the mixed solution micro-mixed into two phases of aqueous solution and an organic solvent. A taking-out introduction control part passes the organic solvent separated into two phases through an adsorption column be capable of adsorbing molybdenum 99 and introduces the organic solvent into an evaporation elution tank. An evaporation control part evaporates the organic solvent and leaves residue by reducing pressure inside the evaporation elution tank and heating the organic solvent introduced into the evaporation elution tank with a heater, while applying ultrasonic to the organic solvent. An elution control part introduces physiological saline solution into the residue and elutes technetium 99m into the physiological saline solution from the residue.

The present invention relates to the field of upgrading biomass, in particular algal biomass, and more specifically the present invention relates to a method for extracting water-soluble compounds from microalgae and/or cyanobacteria, as well as the product obtained by this method and the uses of same, in particular in the food industry or as food supplements.

An initial introduction control part introduces an aqueous solution containing molybdenum 99 and technetium 99m, and an organic solvent being capable of dissolving the technetium 99m into an extraction tank. A micro-mixing control part micro-mixes the aqueous solution and the organic solvent by heating and stirring a mixed solution of the aqueous solution and the organic solvent introduced into the extraction tank with a heater, while applying ultrasonic to the mixed solution. A separation control part separates the mixed solution micro-mixed into two phases of aqueous solution and an organic solvent. A taking-out introduction control part passes the organic solvent separated into two phases through an adsorption column be capable of adsorbing molybdenum 99 and introduces the organic solvent into an evaporation elution tank. An evaporation control part evaporates the organic solvent and leaves residue by reducing pressure inside the evaporation elution tank and heating the organic solvent introduced into the evaporation elution tank with a heater, while applying ultrasonic to the organic solvent. An elution control part introduces physiological saline solution into the residue and elutes technetium 99m into the physiological saline solution from the residue.

A method of inhibiting degradation of an extractant by utilizing several auxiliary means in the DSX process: includes (a) preparing adjustment of the concentration of an extractant of a DSX solvent to a certain range; (b) extracting a metal contained in a pregnant leached solution by adjusting the ratio of the extractant and the diluent in the DSX solvent to a certain range; (c) measuring the pH of the aqueous phase solution by separating mixture into the aqueous phase solution and the organic phase solvent using a settler after step of extracting; (d) controlling the pH by adding soda ash (Na.sub.2CO.sub.3) so as to maintain the pH of the aqueous phase solution to be 3 to 7; and (e) scrubbing with scrubbing solution having a zinc concentration of 2 to 20 g/L by zinc sulfate (ZnSO.sub.4) to remove the manganese from the organic phase solvent containing the extracted metal.