Abstract:
Improved electrodialysis (ED) stacks are disclosed having one or more components selected from the group: a) cation exchange membranes having ion exchange groups predominantly sulfonic acid groups and a minor amount of weakly acidic and/or weakly basic groups or membranes which are selective to monovalent cations and simultaneously therewith, cation exchange granules selective to monovalent cations as packing in the dilute compartments; b) anion exchange membranes having as ion exchange groups only quaternary ammonium and/or quaternary phosphonium groups and substantially no primary, secondary and/or tertiary amine and/or phosphine groups or membranes which are selective to monovalent anions simultaneously therewith, anion exchange granules selective to monovalent anions as packing in the dilute compartments; c) as packing in the dilute compartment, anion exchange granules which are selective to monovalent anions, or cation exchange granules which are selective to monovalent cations, or cation exchange granules having as exchange groups a predominant amount of sulfonic acid groups and a minor amount of weakly acidic and/or weakly basic groups, or anion exchange granules consisting of organic polymers having as anion exchange groups only quaternary ammonium and/or quaternary phosphonium groups and almost no primary, secondary and/or tertiary amine and/or phosphine groups.
Abstract:
Metal salts are removed from solution in an electrolyte by subjecting the solution to electrolysis in a cell having an anode that has an anion exchange membrane closely associated therewith which sequesters the anion of the salt. The cathode may also be provided with a closely associated cation exchange membrane that sequesters, at least partially, the cation of the salt. A metal salt solution can be regenerated by reversing the polarity of the electrodes and conducting an electrolysis using fresh electrolyte.
Abstract:
A porous ion exchanger which has a porous structure having ion exchange resin particles bound by a binder polymer, and which has a water permeability of at least 30 kg.multidot.cm.sup.-1 .multidot.hr.sup.-1 under a pressure of 0.35 kg/cm.sup.2.
Abstract:
Improvements on the electrolytic reactor and process of U.S. Pat. No. 5,419,816 and copending U.S. application Ser. No. 08/400,950, filed Mar. 9, 1995, now U.S. Pat. No. 5,609,742, are disclosed for the controlled oxidation and reduction of inorganic and organic species in dilute aqueous solutions. More specifically, other physical forms and additives for the modified ion exchange material can be used in the packed bed electrolytic reactor, including powdered ion exchange materials and solid membranes containing the modified ion exchange materials. Direct contact with only one electrode, the anode for oxidation, and the cathode for reduction, is required for the modified ion exchange resin, instead of with both electrodes. Superior performance is also demonstrated for bipolar operation of the electrolytic reactor in comparison to monopolar operation. Preferably, the polarity of the electrodes is reversed every 1 to 60 minutes. Finally, other point of use applications are disclosed for the electrolytic reactor and process, including sanitization and sterilization, such as useful in the medical, dental and veterinary industries, food and animal disinfection, bacteria control and waste treatment.
Abstract:
An electrolytic process and apparatus is disclosed for oxidizing or reducing inorganic and organic species, especially in dilute aqueous solutions. The electrolytic reactor includes an anode and cathode in contact with a packed bed of particulate ion exchange material which establishes an infinite number of transfer sites in the electrolyte to significantly increase the mobility of the ionic species to be oxidized or reduced toward the anode or cathode, respectively. The ion exchange material is cationic for oxidation and anionic for reduction, or a combination of both for special circumstances. Preferably, the ion exchange material is treated to convert a portion of the transfer sites to semiconductor junctions which act as mini anodes, or cathodes, to significantly increase the capacity of the reactor to oxidize or reduce the species to be treated. Exemplary applications for the disclosed electrolytic process and apparatus are the conversion of halides to halous acids in dilute solutions.
Abstract:
In an electrodeionization apparatus having a cathode compartment and an anode compartment for removing ions from a liquid under the influence of a voltage, the cathode compartment includes electron conductive particles such as metal particles and/or carbon particles.
Abstract:
It concerns a monomer, a polymer obtained from the monomer and a process for obtaining the said polymer. The monomer consists of a polyether containing at least 3 ether units and pyrrole or thiophene units bonded to the ends of the chains of this polyether via, for each of these heterocycic compounds, either their carbon atoms in the 3,3'-positions of their heterocycles or, as regards more particularly the pyrrole groups, via their respective nitrogen atoms, the 2- and 2'-positions of these heterocycles being, however, free of all substitutions or, at the very most, substituted by easily removable groups (protective groups, for example). Application to the purification and recovery of metal ions such as radioactive silver.
Abstract:
Processes and apparatuses for separating ions from an aqueous solution are provided which utilize a first separation by an ion exchange medium in combination with second separation by a D.C. electropotential gradient. The first separation separates the target ion by ion exchange and the second separation effects migration of the ions from the ion exchange medium, through a ion permeable, hydrophobic membrane into a second zone, which may contain a buffer. The hydrophobic membrane substantially resists fouling.
Abstract:
An electrochemical cell for capacitive deionization and electrochemical purification and regeneration of electrodes includes two oppositely disposed, spaced-apart end plates, one at each end of the cell. Two generally identical single-sided end electrodes, are arranged one at each end of the cell, adjacent to the end plates. An insulator layer is interposed between each end plate and the adjacent end electrode. Each end electrode includes a single sheet of conductive material having a high specific surface area and sorption capacity. In the preferred embodiment, the sheet of conductive material is formed of carbon aerogel composite. The cell further includes a plurality of generally identical double-sided intermediate electrodes that are equidistally separated from each other, between the two end electrodes. As the electrolyte enters the cell, it flows through a continuous open serpentine channel defined by the electrodes, substantially parallel to the surfaces of the electrodes. By polarizing the cell, ions are removed from the electrolyte and are held in the electric double layers formed at the carbon aerogel surfaces of the electrodes. As the cell is saturated with the removed ions, the cell is regenerated electrically, thus significantly minimizing secondary wastes.
Abstract:
An electrolytic process and apparatus is disclosed for oxidizing or reducing inorganic and organic species, especially in dilute aqueous solutions. The electrolytic reactor includes an anode and cathode in contract with a packed bed of particulate ion exchange material which establishes an infinite number of transfer sites in the electrolyte to significantly increase the mobility of the ionic species to be oxidized or reduced toward the anode or cathode, respectively. The ion exchange material is cationic for oxidation and anionic for reduction, or a combination of both for special circumstances. Preferably, the ion exchange material is treated to convert a portion of the transfer sites to semiconductor junctions which act as mini anodes, or cathodes, to significantly increase the capacity of the reactor to oxidize or reduce the species to be treated. Exemplary applications for the disclosed electrolytic process and apparatus are the conversion of halides to halous acids in dilute solutions.