This invention provides gold nanoparticles for bio-molecule detection in body fluid and systems therefor. In one embodiment, this invention provides a method for synthesis of gold nanoparticles dispersed in solution. In another embodiment, this invention provides a method for detecting a substance directly from a sample of body fluid with SERS using the gold nanoparticles dispersed in solution. In a further embodiment, this invention provides a system, having the gold nanoparticles dispersed in solution, for on-site detection of a substance directly from a sample of body fluid with SERS.

The disclosed embodiments relate to nanotechnology and to nano-electronics and molecular electronic sensors. In an exemplary embodiment, a nano-sensor having a nanoparticle complex attached at each end to a respective nano-electrode. An exemplary nanoparticle complex includes a biomolecule coupled at each end to a metallic nanoparticle to form a dumbbell-shaped molecular bridge. A method to manufacture single molecule dumbbell nanowires for forming conductive molecular bridges includes the steps of: providing a double-stranded nucleic acid with terminal 3′ thiol modification on both the strands conjugated to a gold (Au) nanoparticle (AuNP) on each end; purifying single biomolecule dumbbells from aggregates using size-exclusion chromatography; imaging the eluted products by electron microscopy to validate formation of single molecule dumbbells; trapping a single molecule dumbbell between a pair of nanoelectrodes on a substrate, the electrodes separated by a nanogap; and measuring the conductivity of a trapped single molecule dumbbell.

The disclosed embodiments relate to nanotechnology and to nano-electronics and molecular electronic sensors. In an exemplary embodiment, a nano-sensor having a nanoparticle complex attached at each end to a respective nano-electrode. An exemplary nanoparticle complex includes a biomolecule coupled at each end to a metallic nanoparticle to form a dumbbell-shaped molecular bridge. A method to manufacture single molecule dumbbell nanowires for forming conductive molecular bridges includes the steps of: providing a double-stranded nucleic acid with terminal 3′ thiol modification on both the strands conjugated to a gold (Au) nanoparticle (AuNP) on each end; purifying single biomolecule dumbbells from aggregates using size-exclusion chromatography; imaging the eluted products by electron microscopy to validate formation of single molecule dumbbells; trapping a single molecule dumbbell between a pair of nanoelectrodes on a substrate, the electrodes separated by a nanogap; and measuring the conductivity of a trapped single molecule dumbbell.

The present invention relates to a bio-electrode for current measurement including silicon carbide (SiC) doped at least partially with nitrogen (N). The bio-electrode for current measurement according to an embodiment of the present invention is a bio-electrode for a current measurement which is contact with an object to be analyzed, which generates a current signal by an electrochemical reaction, and includes silicon carbide (SiC) doped at least partially with nitrogen (N). The electrode may be used in a high-sensitive bio-quantification kit, a high-sensitive bio-quantification device, and an immunoassay device.

The present invention relates to a bio-electrode for current measurement including silicon carbide (SiC) doped at least partially with nitrogen (N). The bio-electrode for current measurement according to an embodiment of the present invention is a bio-electrode for a current measurement which is contact with an object to be analyzed, which generates a current signal by an electrochemical reaction, and includes silicon carbide (SiC) doped at least partially with nitrogen (N). The electrode may be used in a high-sensitive bio-quantification kit, a high-sensitive bio-quantification device, and an immunoassay device.

The present invention relates to a chemically sensitive sensor for detecting volatile organic compounds, the sensor comprising a substrate, an electrode array, a micro-barrier, and a sensing layer comprising a multiplicity of core-shell particles in close-packed orientation, the particles comprising a metal nanoparticle (MNP) core and an organic ligand shell, wherein the MNP core has a mean particle size below about 15 nm. The invention further provides a method for fabrication of the chemically sensitive sensor.

The present invention relates to a chemically sensitive sensor for detecting volatile organic compounds, the sensor comprising a substrate, an electrode array, a micro-barrier, and a sensing layer comprising a multiplicity of core-shell particles in close-packed orientation, the particles comprising a metal nanoparticle (MNP) core and an organic ligand shell, wherein the MNP core has a mean particle size below about 15 nm. The invention further provides a method for fabrication of the chemically sensitive sensor.

The present disclosure relates to a method of preparing a nano-porous powder material. The method includes: firstly removing A in the alloy A.sub.xT.sub.y by using an ultrasonically-assisted de-alloying method to prepare a nano-porous T coarse powder, and then, allowing the nano-porous T coarse powder to perform M-ization reaction with a gas reactant containing M to obtain a nano-porous T-M coarse powder, and finally, further crushing the nano-porous T-M coarse powder using a jet mill to obtain a nano-porous T-M fine powder. The method can achieve low-cost mass production of the nano-porous T-M fine powder, bringing broad application prospects.

The present invention refers to the recovery of high-value metals such as gold and silver from ores containing them by the leaching process that is carried out in tanks or reactors, and to the destruction of cyanide, which is carried out in cyanide destruction (detox) tanks at the end of the leaching process, to avoid damage to the environment. An oxygen diffuser with a specific design is provided which is used in pulp leaching tanks and in cyanide destruction (detox) tanks containing residual pulp, with the application of oxygen, whereby better results are obtained in the recovery of metals, in the application of oxygen and in retention time, among others.

The recovery of noble metal(s) from noble-metal-containing material is generally described. The noble metal(s) can be recovered selectively, in some cases, such that noble metal(s) is at least partially separated from non-noble-metal material within the material. Noble metal(s) may be recovered from noble-metal-containing material using mixtures of acids, in some instances. In some cases, the mixture can comprise nitric acid and/or another source of nitrate ions and at least one supplemental acid, such as sulfuric acid, phosphoric acid, and/or a sulfonic acid. The amount of nitrate ions within the mixture can be, in some instances, relatively small compared to the amount of supplemental acid within the mixture. In some cases, the recovery of noble metal(s) using the acid mixtures described herein can be enhanced by transporting an electric current between an electrode and the noble metal(s) of the noble-metal-containing material. In some cases, acid mixtures can be used to recover silver from particular types of scrap materials, such as scrap material comprising silver metal and cadmium oxide and/or scrap material comprising silver metal and tungsten metal.