A magnetic nanoparticle, and composites thereof, comprising a ternary host compound comprising a transition metal oxide of size 2-30 nm having two transition metal dopants atom incorporated therein, such that the nanoparticle is converted from superparamagnetic or weak ferromagnetic to strong ferromagnetic material. The strong permanent magnets are formed from non-rare earth materials. The composite material can also include undoped nanoparticles.

It has been found, that when co-absorbing substances are added to intrinsic laser-absorbing bismuthoxide, the marking performance with a Nd.YAG-laser is improved or at least kept at the same level by reducing the costs. It is suspected, that the co-absorbing additive is not simply adding a contrast to the polymer by carbonizing the surrounding polymer but helping the bismuthoxide to couple the laser radiation and to ease the color change of this additive. This so found effect helps to cheapen the replacement of antimony trioxide and therewith have a safer and more sustainable solution for the current and future technology of laser marking.

Aluminium-containing iron oxide pigments of the formula Fe.sub.2-xAl.sub.xO.sub.3 with x values from 0.01 to 0.25, characterized in that they possess an a* value of 30.5 to 32.5 CIELAB units and a b* value of 25.5 to 30.5 CIELAB units, measured in each case as full shade in the alkyd resin according to DIN EN ISO 787-25: 2007.

A method for modifying a fine particle dispersion liquid has excellent dispersibility and dispersion stability. In this method for modifying a fine particle dispersion liquid having improved fine particle dispersibility, impurities included in an agglomeration of fine particles contained in the fine particle dispersion liquid are released into the dispersion liquid by applying physical energy to the agglomeration and performing dispersion processing for dispersion into particles that are smaller than the agglomeration of fine particles. The impurities are removed from the dispersion liquid by means of a removal unit provided with a filtration membrane before reagglomeration is caused by the impurities.

A method for modifying a fine particle dispersion liquid has excellent dispersibility and dispersion stability. In this method for modifying a fine particle dispersion liquid having improved fine particle dispersibility, impurities included in an agglomeration of fine particles contained in the fine particle dispersion liquid are released into the dispersion liquid by applying physical energy to the agglomeration and performing dispersion processing for dispersion into particles that are smaller than the agglomeration of fine particles. The impurities are removed from the dispersion liquid by means of a removal unit provided with a filtration membrane before reagglomeration is caused by the impurities.

A solid electrolyte assembly is obtained by joining a solid electrolyte layer having oxide ion conductivity and containing lanthanum and a first electrode layer made of an oxide that is represented by ABO.sub.3−δ and has a cubic perovskite structure to each other, where A represents an alkaline-earth metal element, B represents a transition metal element, and δ represents a fraction that occurs depending on the valences and amounts of A, B, and O. The oxide contains lanthanum at a part of the A site, and an atom ratio of lanthanum to all the elements occupying the A site is 0.01 or greater and 0.80 or less.

A thermoelectric material, having a formula Tb.sub.xM1.sub.y-xM2.sub.zO.sub.w where M1 is one of Ca, Mg, Sr, Ba and Ra, M2 is at least one of Co, Fe, Ni, and Mn, x ranges from 0.01 to 5; y is 1, 2, 3, or 5; z is 1, 2, 3, or 4; and w is 1, 2, 3, 4, 5, 7, 8, 9, or 14. The thermoelectric material is chemically stable within 5% for one year and is also non-toxic. The thermoelectric material can also be incorporated into a thermoelectric system which can be used to generate electricity from waste heat sources or to cool an adjacent region.

An absorber coating is provided for solar heat power generation that has excellent thermal oxidation resistance and a high spectral absorptance and manufacturing method thereof. The absorber coating for solar heat power generation has a network structure of composite particles comprising: particles of metal oxide containing mainly two or more metals selected from Mn, Cr, Cu, Zr, Mo, Fe, Co and Bi, and titanium oxide partly or entirely coating on the surface of the particle of the metal oxide. The arithmetic mean estimation of the surface of the coating is 1.0 μm or more, and a ratio of a network area of the composite particle to a plane area of the coating is 7 or more.

A disordered rocksalt lithium metal oxide and oxyfluoride as in manganese-vanadium oxides and oxyfluorides well suited for use in high capacity lithium-ion battery electrodes such as those found in lithium-ion rechargeable batteries. A lithium metal oxide or oxyfluoride example is one having a general formula: Li.sub.xM′.sub.aM″.sub.bO.sub.2-yF.sub.y, with the lithium metal oxide or oxyfluoride having a cation-disordered rocksalt structure of one of (a) or (b), with (a) 1.09≤x≤1.35, 0.1≤a≤0.7, 0.1≤b≤0.7, and 0≤y≤0.7; M′ is a low valent transition metal and M″ is a high-valent transition metal; and (b) 1.1≤x≤1.33, 0.1≤a≤0.41, 0.39≤b≤0.67, and 0≤y≤0.3; M′ is Mn; and M″ is V or Mo. The oxides or oxyfluorides balance accessible Li capacity and transition metal capacity. An immediate application example is for high energy density Li-cathode battery materials, where the cathode energy is a key limiting factor to overall performance. The second structure (b) is optimized for maximal accessible Li capacity.

Methods for removing reduced sulfur compounds, such as hydrogen sulfide, from fluids employing a ferric iron salt that exhibits unusually high solubility in aqueous, alkaline solutions and has strong affinity for capture and oxidation of reduced sulfur compounds. Alkaline aqueous ferric iron salt and solutions thereof useful for removing reduced sulfur compounds from fluids and various methods of production of such salts and solutions. In addition, methods of regenerating the alkaline aqueous ferric iron salt solutions after capture of hydrogen sulfide or other reduced sulfur compounds, generally by exposure to oxygen in air. The alkali metal carbonate salt preferably comprises potassium carbonate and/or potassium bicarbonate. The alkaline aqueous ferric iron salt solutions generally comprise ferric ions, potassium ions, carbonate ions, and bicarbonate ions, optionally with one or more organic additives. In addition, aqueous-soluble, ferric iron salts and ferric iron containing solids prepared by removal of aqueous medium from solutions herein.