A composite material of one aspect includes a resin matrix phase, and a ruthenium oxide having Ca.sub.2RuO.sub.4 structure and included in the resin matrix phase. The ruthenium oxide may be represented by a general formula (1): Ca.sub.2xR.sub.xRu.sub.1y1M.sub.yO.sub.4+z, in which R may represent at least one element selected from among alkaline earth metals and rare earth elements, M may represent at least one element selected from among Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, and Ga, and the values x, y, and z may satisfy 0x<0.2, 0y<0.3, and 1<z<0.02.

An adsorbent is provided to adsorb ruthenium from aqueous solution for recovery and/or reuse or removal of said ruthenium, and a method for purifying, for example, sea water and/or water containing sodium ions, magnesium ions, calcium ions, chlorine ions or other ions, polluted with a radioactive element, using said adsorbent. The ruthenium adsorbent includes manganese in the form of oxides thereof. The adsorbent can further include at least one additional transition metal element other than manganese, such as copper. The adsorbent soaked in water removes radioactive ruthenium or the like through adsorption, and thereby can purify, for example, sea water and/or water containing sodium ions, magnesium ions, calcium ions, chlorine ions or other ions.

A simple one pot sol-gel method for the synthesis of bi-metal nanostructures is based on non-noble metals (Fe, Co and Sn) and titanium. The method involves the synthesis of mixed metal nanoscale composites using low cost precursors which allow for the synthesis of desired nanocomposite materials with self-scarifying titanium or silica supports. The procedure does not require any surfactant or any need for pH controlled step. Applicants' method involves the in-situ generation of precursors and their simultaneous entrapment in a gel. This simple one pot synthesis allows for the synthesis of homogenous size, shape and distribution of targeted nanostructures. Further, this method can be applied for the preparation of various nanocomposite materials using different choices of metals and self-scarifying supports. Applicants also show that Pd, the noble metal based nanocomposite is feasible.

A simple one pot sol-gel method for the synthesis of bi-metal nanostructures is based on non-noble metals (Fe, Co and Sn) and titanium. The method involves the synthesis of mixed metal nanoscale composites using low cost precursors which allow for the synthesis of desired nanocomposite materials with self-scarifying titanium or silica supports. The procedure does not require any surfactant or any need for pH controlled step. Applicants' method involves the in-situ generation of precursors and their simultaneous entrapment in a gel. This simple one pot synthesis allows for the synthesis of homogenous size, shape and distribution of targeted nanostructures. Further, this method can be applied for the preparation of various nanocomposite materials using different choices of metals and self-scarifying supports. Applicants also show that Pd, the noble metal based nanocomposite is feasible.

A method of producing ceria nanocrystals is provided. The method includes providing a gas that includes ozone to a solution that includes a cerium salt, and obtaining ceria nanocrystals from the solution after the gas is provided to the first solution. A method of producing nanoparticles is provided. The method includes providing a gas that includes ozone to a solution that includes a metal salt that includes at least one of a transition metal or a lanthanide, and producing at least one of metal oxide nanoparticles, metal oxynitrate nanoparticles, or metal oxyhydroxide nanoparticles from the solution after the gas is provided to the solution.

This invention relates to the identification of modified cytosine residues, such as 5-methylcytosine (5mC), 5-hydroxymethylcytosine (5hmC) and 5-formylcytosine (5fC) to be distinguished from cytosine (C) in a sample nucleotide sequence. Methods may comprise oxidizing or reducing a first portion of polynucleotides which comprise the sample nucleotide sequence; treating the oxidized or reduced first portion and a second portion of polynucleotides with bisulfite; sequencing the polynucleotides in the first and second portions of the population following steps ii) and iii) to produce first and second nucleotide sequences, respectively and; identifying the residue in the first and second nucleotide sequences which corresponds to a cytosine residue in the sample nucleotide sequence. These methods may be useful, for example in the analysis of genomic DNA and/or of RNA.

A method of separating Osmium from Iridium, including receiving a powdered mixture of Osmium and Iridium, oxidizing the Osmium of the powdered mixture, capturing the oxidized Osmium in a trapping solution, reducing the oxidized Osmium from the solution to release the Osmium.

A method of separating Osmium from Iridium, including receiving a powdered mixture of Osmium and Iridium, oxidizing the Osmium of the powdered mixture, capturing the oxidized Osmium in a trapping solution, reducing the oxidized Osmium from the solution to release the Osmium.

A solid oxide fuel cell (SOFC) includes a cathode having a yttria stabilized zirconia (YSZ) structure. The YSZ structure is in contact with a solid electrolyte layer. A lanthanum strontium manganite (LSM) structure is deposited on the YSZ structure to form a composite cathode. The cathode includes a catalyst layer. The catalyst layer is a mesoporous nanoionic catalyst material integrated with the YSZ and LSM structures. Alternatively, or in addition to, the mesoporous nanoionic catalyst material may be coated onto the YSZ and LSM structures or embedded into the YSZ and LSM structures. The mesoporous nanoionic catalyst material may form an interconnected fibrous network.

A sodium-containing oxide positive electrode material and a preparation method therefor and use thereof are disclosed. Also disclosed are a positive electrode plate and uses thereof.