Abstract:
The present invention describes an integrated process for carbon dioxide capture, sequestration and utilisation, which comprises: a) providing an aqueous slurry comprising an aqueous solution and a particulate solid comprising an activated magnesium silicate mineral; b) in a dissolution stage, contacting a CO2-containing gas stream with the aqueous slurry to dissolve magnesium from the mineral to provide a magnesium ion enriched aqueous solution and a magnesium depleted solid residue; c) recovering at least a portion of the magnesium depleted solid residue; d) in a separate acid treatment stage, reacting the recovered portion of the magnesium depleted solid residue with a solution comprising a mineral acid or acid salt to further dissolve magnesium and other metals and to provide an acid-treated solid residue; e) recovering the acid-treated solid residue; and f) in a separate precipitation stage, precipitating magnesium carbonate from the magnesium ion enriched aqueous solution.
Abstract:
A method for modifying a fine particle dispersion liquid with which dispersibility and dispersion stability can be improved includes performing filtration to remove impurities in a dispersion liquid using a dispersion liquid modifying device provided with a removal unit that uses a filtration membrane. The quantity of impurities is reduced from a first region until said quantity reaches a second pH-dependent region. In the second pH-dependent region, the dispersibility of the fine particles in the dispersion liquid is in a range in which the dispersibility depends more on a change in dispersion liquid pH than on a change in the quantity of impurities in the dispersion liquid. With the quantity of impurities reduced to the second pH-dependent region, the dispersibility of the fine particles is controlled by adjusting the pH of the fine particle dispersion liquid.
Abstract:
A method for preparing a niobium, titanium or vanadium metal oxide nanostructured material is provided. The method comprises providing an aqueous reagent comprising (i) a soluble metal oxalate, and/or (ii) oxalic acid and a metal oxide precursor, adding a buffering agent to the aqueous reagent to form a mixture, and heating the mixture under hydrothermal conditions to obtain the metal oxide nanostructured material. The metal oxide nanostructured material may also be doped with a dopant metal such as titanium to enhance capacity and cycling stability. An electrode comprising the metal oxide nanostructured material, and an electrochemical cell containing the electrode are also provided.
Abstract:
An object of the present invention is to provide a method for producing oxide particles with controlled color characteristics and to provide oxide particles with controlled color characteristics. The present invention provides a method for producing oxide particles, comprising controlling color characteristics of the oxide particles by controlling the ratio of M-OH bonds, the binding of one or more different elements (M) other than oxygen or hydrogen with hydroxyl group (OH), in oxide particles selected from metal oxide particles and metalloid oxide particles. According to the present invention, oxide particles having controlled color characteristics of any one of reflectance, transmittance, molar absorption coefficient, hue, or color saturation can be provided by controlling the percentage of the M-OH bonds contained in metal oxide particles or metalloid oxide particles.
Abstract:
A method of forming composition-modified barium titanate ceramic particulate includes mixing a plurality of precursor materials and a precipitant solution to form an aqueous suspension. The plurality of precursors include barium nitrate, titanium chelate, and a metal or oxometal chelate. The precipitant solution includes tetraalkylammonium hydroxide and tetraalkylammonium oxalate. The method further includes treating the aqueous suspension at a temperature of at least 150° C. and a pressure of at least 200 psi, and separating particulate from the aqueous suspension after treating.
Abstract:
Described herein are methods for forming inorganic composite oxides. Such methods include combining, at a substantially constant pH of between about 5 and about 6.75 over a period of at least about 5 minutes, an acidic precursor composition and a basic composition to form a precipitate composition, wherein the acidic precursor composition comprises an alumina precursor, a ceria precursor, a zirconia precursor and optionally one or more dopant precursors; stabilizing the precipitate by increasing the pH of the precipitate composition to between about 8 and about 10; and calcining the stabilized precipitate to form an inorganic composite oxide. Also described are inorganic composite oxides formed using such methods.
Abstract:
A production method for metal oxide particles includes: obtaining precursor particles of a metal oxide by performing a synthesis reaction of the precursor particles in the presence of an organic compound; and converting the obtained precursor particles into metal oxide particles by heating an aqueous solution containing the precursor particles to 300° C. or higher and pressurizing the aqueous solution at a pressure of 20 MPa or higher.
Abstract:
The present invention is directed to a method of making metal oxide and mixed metal oxide particles. The method includes treating a mixture formed from a metal source, such as metal alkoxide, a surfactant, and a first alcohol in an aqueous media at a very high metal oxide yield. The mixture is reacted using a catalyst to form metal oxide particles having a desired particle size in said mixture. By washing the particles with an aprotic solvent, the residual carbon content of the particles can be significantly reduced. The method is particularly suitable for forming silica particles. The metal oxide particles can then be heat treated to form synthetic fused metal oxides such as, for example, synthetic fused silica.
Abstract:
A method for producing isolatable oxide microparticles or hydroxide microparticles using an apparatus that processes a fluid between processing surfaces of processing members that are arranged opposite each other so as to be able to approach to or separate from each other and such that at least one can rotate relative to the other. At least two fluids are mixed and oxide microparticles or hydroxide microparticles are separated, said two fluids including: a fluid containing a microparticle raw material solution comprising a microparticle raw material mixed into a solvent, and a fluid containing a microparticle-separation solution. Immediately thereafter, the following are mixed to obtain isolatable oxide microparticles or hydroxide microparticles: a fluid containing the separated oxide microparticles or hydroxide microparticles; and a fluid containing a microparticle-treatment-substance-containing solution that contains a microparticle-treatment substance that adjusts the dispersibility of the separated oxide microparticles or hydroxide microparticles.
Abstract:
A method and structure for making magnetite nanoparticle materials by mixing iron salt with alcohol, carboxylic acid and amine in an organic solvent and heating the mixture to 200–360 C is described. The size of the particles can be controlled either by changing the iron salt to acid/amine ratio or by coating small nanoparticles with more iron oxide. Magnetite nanoparticles in the size ranging from 2 nm to 20 nm with a narrow size distribution are obtained with the invention. The invention can be readily extended to other iron oxide based nanoparticle materials, including M Fe2O4 (M=Co, Ni, Cu, Zn, Cr, Ti, Ba, Mg) nanomaterials, and iron oxide coated nanoparticle materials. The invention also leads to the synthesis of iron sulfide based nanoparticle materials by replacing alcohol with thiol in the reaction mixture. The magnetite nanoparticles can be oxidized to γ-Fe2O3, or α-Fe2O3, or can be reduced to bcc-Fe nanoparticles, while iron oxide based materials can be used to make binary iron based metallic nanoparticles, such as CoFe, NiFe, and FeCoSmx nanoparticles.
Abstract translation:描述了通过将铁盐与醇,羧酸和胺在有机溶剂中混合并将混合物加热至200-360℃来制备磁铁矿纳米颗粒材料的方法和结构。 颗粒的大小可以通过将铁盐改变成酸/胺的比例或通过用更多的氧化铁涂覆小的纳米颗粒来控制。 通过本发明获得尺寸范围为2nm至20nm且具有窄尺寸分布的磁铁矿纳米颗粒。 本发明可以容易地扩展到其它基于氧化铁的纳米颗粒材料,包括M Fe 2 O 4(M = Co,Ni,Cu,Zn,Cr,Ti,Ba ,Mg)纳米材料和氧化铁涂覆的纳米颗粒材料。 本发明还导致通过在反应混合物中用硫醇代替醇来合成基于硫化铁的纳米颗粒材料。 磁铁矿纳米粒子可被氧化成γ-Fe 2 O 3 3或α-Fe 2 O 3 3, 或可以还原成bcc-Fe纳米颗粒,而基于氧化铁的材料可用于制备二元铁基金属纳米颗粒,例如CoFe,NiFe和FeCoSmx纳米颗粒。