A method for producing and using an alkaline aqueous ferric iron carbonate solution is disclosed. The method broadly comprises reacting at least one ferric iron salt reagent with at least one alkali metal carbonate salt reagent and forming an alkaline aqueous ferric iron carbonate solution comprising an aqueous-soluble, ferric iron carbonate complex. The reacting generally includes reacting a solid with an aqueous solution. The reacting may include reacting a solid comprising one or both of the ferric iron salt reagent and alkali metal carbonate salt reagent with an aqueous solution. A method for removing reduced sulfur compounds from a reduced sulfur-containing fluid is also disclosed.

A method for producing and using an alkaline aqueous ferric iron carbonate solution is disclosed. The method broadly comprises reacting at least one ferric iron salt reagent with at least one alkali metal carbonate salt reagent and forming an alkaline aqueous ferric iron carbonate solution comprising an aqueous-soluble, ferric iron carbonate complex. The reacting generally includes reacting a solid with an aqueous solution. The reacting may include reacting a solid comprising one or both of the ferric iron salt reagent and alkali metal carbonate salt reagent with an aqueous solution. A method for removing reduced sulfur compounds from a reduced sulfur-containing fluid is also disclosed.

The present disclosure provides a method for separating iron element in brine and application thereof. The method for separating iron element in brine comprises: adding a pH adjusting agent to brine, to adjust pH of the brine to 6.0-7.0, and controlling the temperature of the brine to 75° C.-90° C.; introducing an oxygen-containing gas into the brine, to covert the iron element in the brine into magnetic iron oxide; and separating the magnetic iron oxide from the brine by magnetic adsorption to obtain an iron-removed brine.

An object of the present invention is to provide ferrite particles having a high magnetic permeability in a frequency band of 1 MHz to 1 GHz. Another object is to provide a resin composition containing the ferrite particles and an electromagnetic wave shielding material composed of the resin composition. The ferrite particles are composed of a single crystalline body having an average particle size of 1 to 2000 nm and has a spherical particle shape, wherein the ferrite particles contain substantially no Zn, 3 to 25 wt % of Mn, and 43 to 65 wt % of Fe, and a real part μ′ of a complex magnetic permeability measured using a molding composed of the ferrite particles and a binder resin has a maximal value in a frequency band of 100 MHz to 1 GHz.

An object of the present invention is to provide ferrite particles having a high magnetic permeability in a frequency band of 1 MHz to 1 GHz. Another object is to provide a resin composition containing the ferrite particles and an electromagnetic wave shielding material composed of the resin composition. The ferrite particles are composed of a single crystalline body having an average particle size of 1 to 2000 nm and has a spherical particle shape, wherein the ferrite particles contain substantially no Zn, 3 to 25 wt % of Mn, and 43 to 65 wt % of Fe, and a real part μ′ of a complex magnetic permeability measured using a molding composed of the ferrite particles and a binder resin has a maximal value in a frequency band of 100 MHz to 1 GHz.

A lithium-ion conducting composite material includes a Li binary salt, a Li-ion conductor with a chemical composition of Li.sub.2−3x+y−zFe.sub.xO.sub.y(OH).sub.1−yCl.sub.1−z, and at least two of: a first inorganic compound with a chemical composition of (Fe.sub.1−xM1.sub.x)O.sub.1−y(OH).sub.yCl.sub.1−x; a second inorganic compound with a chemical composition of M2OX; and a defected doped inorganic compound with a chemical composition of (M3OX)′. The value of n is 1 or 2, x is greater than 0 and less than or equal to 0.25, and y is greater than or equal to 0 and less than or equal to 0.25. Also, M1 is at least one of Mg and Ca, M2 and M3 are each at least one of Fe, Al, Sc, La, and Y, and X is at least one of F, Cl, Br, and I.

Techniques including methods and apparatuses for selective measurement and monitoring of halide concentrations in processing solutions for iron triad metals and their alloys are provided. Methods include monitoring of a halide ion, for example, based on a first analytical method such as conductivity with a compensation of the results for a main metal concentration such as a second analytical measurement of concentration of an iron triad metal (e.g., nickel (Ni)). From such measurements, a concentration of certain halide ions can be selectively determined.

Preparation, characterization, and an electrochemical study of Mg.sub.0.1V.sub.2O.sub.5 prepared by a novel sol-gel method with no high-temperature post-processing are disclosed. Cyclic voltammetry showed the material to be quasi-reversible, with improved kinetics in an acetonitrile-, relative to a carbonate-, based electrolyte. Galvanostatic test data under a C/10 discharge showed a delivered capacity >250 mAh/g over several cycles. Based on these results, a magnesium anode battery, as disclosed, would yield an average operating voltage ˜3.2 Volts with an energy density ˜800 mWh/g for the cathode material, making the newly synthesized material a viable cathode material for secondary magnesium batteries.

Various embodiments relate to an acidic ferrate composition and methods of making ferrate. A method of forming ferrate includes treating an iron source with an oxidizer in an aqueous solution having a pH of less than 7 under conditions sufficient to form ferrate.

A method of rapid treatment of heavy metal sludge and preparation of ferrite magnets comprises following steps of: providing a sludge, the sludge at least having zinc metal and ferrous metal; adding an iron-containing substance to the sludge; pickling the sludge and the iron-containing substance with sulfuric acid to obtain a pickling solution with zinc ions and iron ions; neutralizing the pickling solution with sodium hydroxide to form hydroxide precipitates; and airing and heating the neutralized pickling solution by an ultrasonic-microwave method so that the hydroxide precipitates undergoing a ferrite magnet reaction, thereby obtaining ferrite magnets with a spathic structure.