A solid electrolyte includes lithium, phosphorus, sulfur, and halogen, in which, when the solid electrolyte is measured by TG-MS, a first peak derived from cyclic sulfur appears in a temperature range of 170° C. or higher and lower than 250° C., a second peak derived from the cyclic sulfur appears in a temperature range of 250° C. or higher and lower than 300° C., and a peak intensity P1 of the first peak is higher than a peak intensity P2 of the second peak.

The invention relates to coated effect pigments, wherein the coating comprises a binder which is suitable for powder paints. They comprise a crystalline and an amorphous fraction which is determined by C.sup.13 NMR MAS relaxation measurements, the relaxation of the .sup.13C cores being fitted as a biexponential relaxation according to the formula (II) and the degree of crystallinity c being in a range between 40 to 85%, and relaxation having a short average relaxation time T.sub.1.sup.S and a long average relaxation time T.sub.1.sup.l, and T.sub.1.sup.l being in a range of from 65 to 130 s. The effect pigments coated according to the invention have at least one endothermic peak with a maximum from a range of T.sub.max=100 to 150° C. and an enthalpy ΔH associated with said peak from a range of 15 J/g to 80 J/g in DSC at a feed speed of 5° C./min, the enthalpy being calculated relative to the amount of the binder. The binders are applied to the effect pigment by way of spontaneous precipitation.

The present disclosure relates to methods for producing hydrogen and calcium- or magnesium-bearing carbonates by capturing, converting, and storing carbon dioxide. The methods may include providing one or more calcium- or magnesium-bearing compounds; providing one or more water-soluble oxygenates; providing a plurality of catalysts; and reacting one or more calcium- or magnesium-bearing compounds and one or more water-soluble oxygenates with plurality of catalysts under conditions to produce hydrogen and calcium- or magnesium-bearing carbonates. The methods may include providing one or more calcium- or magnesium-bearing silicates; providing carbon monoxide; providing water vapor; and reacting one or more calcium- or magnesium-bearing silicates, carbon monoxide, and water vapor. The methods may include providing one or more calcium- or magnesium-bearing compounds; providing one or more water-soluble oxygenates; providing a catalyst; and reacting one or more calcium- or magnesium-bearing compounds and one or more water-soluble oxygenates with said catalyst.

The present disclosure provides an aluminum phosphite-based complex with dual-peak thermal gravity decomposition characteristics and a preparation method and use thereof. A structural formula of the complex is as follows: ((HPO.sub.3).sub.3Al.sub.2).((H.sub.2PO.sub.3).sub.3Al).sub.x, wherein x is 0.01-0.5 and represents a molar ratio of (H.sub.2PO.sub.3).sub.3Al to (HPO.sub.3).sub.3Al.sub.2. The dual-peak thermal gravity decomposition characteristics are as follows: a first gravity peak temperature is 460-490° C., and a second gravity peak temperature is 550-580° C. The preparation method includes: uniformly mixing aluminum phosphite and aluminum hydrogen phosphite according to the ratio in the structural formula, and then performing stepwise heating at a rate of 5° C./min to raise the temperature of a mixture from the normal temperature to no more than 350° C. within 1-10 hours, so as to obtain the aluminum phosphite-based complex with the dual-peak thermal gravity decomposition characteristics. The complex may serve as or is configured to prepare a flame retardant or a flame-retardant synergist.

Particulate electrode active material with an average particle diameter in the range of from 2 to 20 μm (D50) having a general formula Li.sub.1+xTM.sub.1−xO.sub.2 wherein TM is a combination of Ni, Co and Al, and, optionally, at least one more metal selected from Mg, Ti, Zr, Nb, Ta, Mo, Mn, and W, with at least 80 mole-% of TM being Ni, and wherein x is in the range of from zero to 0.2, wherein the Co content at the outer surface of the secondary particles is higher than at the center of the secondary particles by a factor of at most 5 or by at most 30 mol-%, referring to TM.

An object of the present invention is to provide composite particles capable of suppressing oxidation over time of a Si—C composite material. Composite particles (B) of the present invention contains composite particles (A) containing carbon and silicon; and amorphous layers coating surfaces thereof, where the composite particles (B) have I.sub.Si/I.sub.G of 0.10 or more and 0.65 or less, and have R value (I.sub.D/I.sub.G) of 1.00 or more and 1.30 or less, when a peak due to silicon is present at 450 to 495 cm.sup.−1, an intensity of the peak is defined as I.sub.Si, an intensity of a G band (peak intensity in the vicinity of 1600 cm.sup.−1) is defined as I.sub.G, and an intensity of a D band (peak intensity in the vicinity of 1360 cm.sup.−1) is defined as I.sub.D in a Raman spectrum, and where the composite particles (B) have a full width at half maximum of a peak of a 111 plane of Si of 3.0 deg. or more using a Cu-Kα ray in an XRD pattern.

The present disclosure relates to a positive electrode active material, a preparing method therefor, and a lithium secondary battery including same. A positive electrode active material according to an embodiment comprises: a core including a lithium nickel composite oxide represented by Chemical Formula 1; and a surface layer present on the core and including at least one of a water-soluble ammonium-based organic compound and a water-soluble amine-based organic compound. The details of Chemical Formula 1 are as defined in the specification.

A positive electrode active material has a small difference in a crystal structure between the charged state and the discharged state. For example, the crystal structure and volume of the positive electrode active material, which has a layered rock-salt crystal structure in the discharged state and a pseudo-spinel crystal structure in the charged state at a high voltage of approximately 4.6 V, are less likely to be changed by charging and discharging as compared with those of a known positive electrode active material. In order to form the positive electrode active material having the pseudo-spinel crystal structure in the charged state, it is preferable that a halogen source such as a fluorine and a magnesium source be mixed with particles of a composite oxide containing lithium, a transition metal, and oxygen, which is synthesized in advance, and then the mixture be heated at an appropriate temperature for an appropriate time.

An electrode material, its manufacturing method, and its use as a cathode material in batteries are provided. The electrode material comprises a plurality of nanoparticles, each having a diameter of approximately 100-400 nm and comprising a core and a shell encapsulating the core. The shell comprises carbon and nitrogen, respectively having a mass fraction of approximately 70-90% and approximately 5-20% relative to a total mass of the shell. The core comprises sulfur, having a mass fraction of approximately 40-97% relative to a total mass of the core. The core has a mass fraction of approximately 50-90% relative to a total mass of each nanoparticle. The electrode material can be used in a cathode of a Li—S battery, which has a good energy storage capacity, a high electrochemical stability, and a low capacity decay.

This invention relates to a process for treating acid mine drainage (AMD). The process includes the steps of adjusting the pH of the AMD to be in the range of 3 to 5; adding maghemite nanoparticles to form a slurry; and a) aerating the slurry obtained in step 3), or b) simultaneously heating and mixing the slurry obtained in step 3). Thereafter maghemite nanoparticles loaded with one or more metals and sulphate and precipitated metals is separated from the slurry.