Methods of isolating phenols from phenol-containing media. The methods include combining a phospholipid-containing composition with the phenol-containing medium to generate a combined medium, incubating the combined medium to precipitate phenols in the combined medium and thereby form a phenol precipitate phase and a phenol-depleted phase, and separating the phenol precipitate phase and the phenol-depleted phase. The methods can further include extracting phenols from the separated phenol precipitate phase. The extracting can include mixing the separated phenol precipitate phase with an extraction solvent to solubilize in the extraction solvent at least a portion of the phenols originally present in the phenol precipitate phase.

Described herein are methods and systems for performing liquid-liquid extraction in bulk tankage. According to certain embodiments, the liquid-liquid extraction can occur in a bulk tank via a circulation loop, in which a solvent mixture is injected with the hydrocarbon ahead of mix valves on the circulation loop. According to other embodiments, a misting system is installed in the vapor or head space of bulk tankage. The misting system distributes small micro-drops of a solvent mixture so as to cause a uniform lay down over the entire top surface area of hydrocarbon. The solvent mixture migrates from the top surface of the hydrocarbon to the bottom of the bulk tank, reacting during migration to cause liquid-liquid extraction.

Methods of isolating phenols from phenol-containing media. The methods include combining a phospholipid-containing composition with the phenol-containing medium to generate a combined medium, incubating the combined medium to precipitate phenols in the combined medium and thereby form a phenol precipitate phase and a phenol-depleted phase, and separating the phenol precipitate phase and the phenol-depleted phase. The methods can further include extracting phenols from the separated phenol precipitate phase. The extracting can include mixing the separated phenol precipitate phase with an extraction solvent to solubilize in the extraction solvent at least a portion of the phenols originally present in the phenol precipitate phase.

The invention relates to a method for transferring a target substance (5), particularly a target molecule (5), between two liquid phases (4, 6; 6, 8; 6, 11), of which at least one phase (4, 6) comprises the target substance (5) to be transferred and at least one phase (4, 8, 11) is an aqueous phase, where at least the aqueous phase (4, 8, 11) is arranged in one of two electrode chambers (1a, 1b, 10a, 10b) which are electroconductively connected, preferably by charge carrier exchange, and separated in terms of the volumes thereof, preferably where the phases (4, 6; 6, 8; 6, 11) are arranged together in one of two electrode chambers (1a, 1b, 10a, 10b) which are electroconductively connected and separated in terms of the volumes thereof, and a pH-value modification is generated by the H and/or OH ions created during the electrolysis in the aqueous phase (4, 8, 11), said modification initiating a transfer process of the target substance (5) between the phases (4, 6; 6, 8; 6, 11). The invention also relates to the use of the method for enrichment and subsequent isolation of the target substance (5).

The disclosure includes a method, comprising passing a fluid into a co-current contactor, passing a solvent into the co-current contactor, dividing the solvent into solvent droplets having a first average droplet size, placing the fluid in contact with the solvent droplets to create a combined stream, coalescing at least a portion of the solvent droplets to create solvent droplets having a second average droplet size, wherein the second average droplet size is greater than the first average droplet size, and separating the fluid and the solvent.

The disclosure includes a method, comprising passing a fluid into a co-current contactor, passing a solvent into the co-current contactor, dividing the solvent into solvent droplets having a first average droplet size, placing the fluid in contact with the solvent droplets to create a combined stream, coalescing at least a portion of the solvent droplets to create solvent droplets having a second average droplet size, wherein the second average droplet size is greater than the first average droplet size, and separating the fluid and the solvent.

The disclosure includes a method, comprising passing a fluid into a co-current contactor, passing a solvent into the co-current contactor, dividing the solvent into solvent droplets having a first average droplet size, placing the fluid in contact with the solvent droplets to create a combined stream, coalescing at least a portion of the solvent droplets to create solvent droplets having a second average droplet size, wherein the second average droplet size is greater than the first average droplet size, and separating the fluid and the solvent.

The present disclosure relates to the technical field of chemical engineering, and specifically discloses a method for removing oxygenated compounds from a Fischer-Tropsch oil having a high carbon number. A reaction-extraction combined process is used in this method for removing oxygenated compounds from a Fischer-Tropsch oil having a high carbon number, wherein the Fischer-Tropsch oil (C5-C20) is firstly subjected to alkaline washing with an alkaline aqueous solution to convert acidic substances into water-soluble salts. The Fischer-Tropsch oil is subjected to a primary extraction with a carbonate-based extractant to remove alcohols and esters therein, and subsequently subjected to a secondary extraction with propylene carbonate to remove ketones and aldehydes impurities therein, thereby removing oxygenated compounds in the Fischer-Tropsch oil. After extraction, the content of the oxygenated compounds in the Fischer-Tropsch oil may be down to 1-60 ppm, and the yield of oil product may be kept 90% or more.

The present invention discloses a circulating magnetoelectric-induction reaction system and application thereof. The system comprises an alternating induction voltage unit, an alternating induction magnetic field unit, a low-frequency power supply, and a feed liquid container. The alternating induction voltage unit is mainly composed of a closed iron core, a primary coil, a secondary coil, and an induction voltage cavity. The alternating induction magnetic field unit is mainly composed of a C-shaped iron core, a primary coil, and a magnetic field cavity. The low-frequency power supply is connected to the primary coils in the alternating induction voltage unit and the alternating induction magnetic field unit and provides excitation voltage for the primary coils. The secondary coil comprises an insulating pipeline, which serves as a feed liquid circulating pipeline, and has both ends exposed out of the induction voltage cavity, with one end as a feed inlet and the other as a discharge outlet. The feed liquid container communicates with the feed liquid circulating pipelines in the alternating induction voltage unit and the alternating induction magnetic field unit to form a feed liquid circulation loop. Through the application, continuous-flow processing can be achieved, electrochemical reaction and ionic polarization can be avoided, and production and processing can be conducted efficiently and rapidly in a large scale.

Briefly, the invention provides a method for magnetically assisting demulsification of extraction phases, the method having the steps of contacting a first solution of a first solvent and a solvated paramagnetic metal ion with a second solvent, where the second solvent is immiscible with the first solvent; mixing the first and second solutions to create an emulsion having a first phase of the first solvent and second phase comprising the second solvent where the phases of the emulsion contain different concentrations of the paramagnetic metal ion; and applying a magnetic field gradient to the first and second phases of the emulsion to accelerate separation of the first phase from the second phase. Also provided is a system for demulsifying phases used in the extraction of paramagnetic moieties from solution having a lumen with an interior region, an interior surface, and exterior surface; and a magnetic field gradient present within the interior region.