A method of treating a metal carbonate salt includes hydrolyzing a metal halide salt to form a hydrohalic acid and a hydroxide salt of the metal in the metal halide salt. The metal includes an alkaline earth metal or an alkali metal. The method includes reacting the hydrohalic acid with the metal carbonate salt, wherein the metal carbonate salt is a carbonate salt of the alkaline earth metal or alkali metal, to form CO.sub.2 and the metal halide salt. At least some of the metal halide salt formed from the reacting of the hydrohalic acid with the metal carbonate salt is recycled as at least some of the metal halide salt in the hydrolyzing of the metal halide salt to form the hydrohalic acid and the hydroxide salt.

A method of treating a metal carbonate salt includes hydrolyzing a metal halide salt to form a hydrohalic acid and a hydroxide salt of the metal in the metal halide salt. The metal includes an alkaline earth metal or an alkali metal. The method includes reacting the hydrohalic acid with the metal carbonate salt, wherein the metal carbonate salt is a carbonate salt of the alkaline earth metal or alkali metal, to form CO.sub.2 and the metal halide salt. At least some of the metal halide salt formed from the reacting of the hydrohalic acid with the metal carbonate salt is recycled as at least some of the metal halide salt in the hydrolyzing of the metal halide salt to form the hydrohalic acid and the hydroxide salt.

As pellets grow from seed/sand in a fluidized bed pellent reactor, the weight of the reactor is measured and the density of the contents of the reactor is calculated, and the input flow of untreated water, water treatement chemical, and seed/sand are adjusted to provide improved removal of water hardness while reducing fine particulates in the outflow of softened water from the reactor.

A system and method for treating reverse-osmosis (RO) concentrated water with high temporary hardness. The system includes a crystallization unit, a precipitation unit, a dewatering unit, and a programmable logic controller (PLC) system. The crystallization unit, precipitation unit and dewatering unit are connected in series, and the PLC system is configured to control pumps, valves, and displays in the crystallization unit, precipitation unit and dewatering unit. The crystallization unit includes a storage tank and a crystallization reactor communicated therewith. The crystallization reactor is provided with a pH meter, a liquid-level gauge, and a stirrer. A connection pipe between the crystallization reactor and the RO concentrated water is provided with an inlet pump and a inlet valve. A connection pipe between the crystallization reactor and the storage tank is provided with a feeding pump and a feeding valve.

The present invention relates to a method for treating an aqueous liquid effluent containing calcium and carbonate ions and containing precipitation-inhibiting products, said process comprising the following successive steps: a) providing an aqueous liquid effluent supersaturated with CaCO.sub.3 and containing precipitation-inhibiting products; b) having the effluent obtained in step a) pass into a reactor with high solid content with a solid content maintained between 20 and 800 g/l and integrated solid-liquid separation, at a pH comprised between 8 and 9.2 allowing in a single step precipitation in situ of the aragonite polymorph of calcium carbonate and removal of the precipitation-inhibiting products; c) recovering an aqueous liquid supernatant containing a suspended solids content of less than or equal to 0.1% by mass of the solid content in the reactor, advantageously a suspended solids content of less than 50 mg/l, the precipitation-inhibiting products being phosphonates.

The present invention relates to a method for treating an aqueous liquid effluent containing calcium and carbonate ions and containing precipitation-inhibiting products, said process comprising the following successive steps: a) providing an aqueous liquid effluent supersaturated with CaCO.sub.3 and containing precipitation-inhibiting products; b) having the effluent obtained in step a) pass into a reactor with high solid content with a solid content maintained between 20 and 800 g/l and integrated solid-liquid separation, at a pH comprised between 8 and 9.2 allowing in a single step precipitation in situ of the aragonite polymorph of calcium carbonate and removal of the precipitation-inhibiting products; c) recovering an aqueous liquid supernatant containing a suspended solids content of less than or equal to 0.1% by mass of the solid content in the reactor, advantageously a suspended solids content of less than 50 mg/l, the precipitation-inhibiting products being phosphonates.

The present disclosure relates to methods of treating water to remove contaminants, including harmful metal ions, and water treatment plants for practicing such methods. In an embodiment, the process includes adding a sulfur-containing, metal-decreasing agent; an iron (III)-containing, metalloid-decreasing agent; forming a solid precipitate from the contaminated water, wherein the solid precipitate includes a solid metal sulfide, a solid iron metalloid, a solid calcium metalloid, or a combination thereof; and separating the contaminated water from the solid precipitate to form purified water.

Methods of treating animal organic material are disclosed herein. The methods include diluting the animal organic material to produce an organic material slurry, anaerobically digesting the organic material slurry to produce a biogas and a digestate, separating the digestate to produce a digestate solids and a filtrate, removing ammonia from the filtrate, removing organic contaminants and divalent anions from the filtrate, concentrating the filtrate to produce a retentate and a permeate, combining the digestate solids and the retentate to produce a solids product, and returning the permeate to dilute the animal organic material. Systems for treatment of animal organic material are also disclosed herein. The systems include a dilution tank, an anaerobic digester, a first solids-liquid separation subsystem, an ammonia-reducing column, a second solids-liquid separation subsystem, a production water storage tank, and a solids product tank.

Per- and polyfluoroalkyl substances (PFAS) are destroyed by oxidation in supercritical conditions. PFAS in water is concentrated in a reverse osmosis step and salt from the resulting solution is removed in supercritical conditions prior to destruction of PFAS in supercritical conditions.

A method of treating a metal carbonate salt includes hydrolyzing a metal halide salt to form a hydrohalic acid and a hydroxide salt of the metal in the metal halide salt. The metal includes an alkaline earth metal or an alkali metal. The method includes reacting the hydrohalic acid with the metal carbonate salt, wherein the metal carbonate salt is a carbonate salt of the alkaline earth metal or alkali metal, to form CO.sub.2 and the metal halide salt. At least some of the metal halide salt formed from the reacting of the hydrohalic acid with the metal carbonate salt is recycled as at least some of the metal halide salt in the hydrolyzing of the metal halide salt to form the hydrohalic acid and the hydroxide salt.