Abstract: Provided is a sulfide solid electrolyte containing lithium, phosphorus, sulfur and chlorine, in which a molar ratio of the chlorine to the phosphorus, c (Cl/P), is greater than 1.0 and 1.9 or less, the sulfide solid electrolyte includes an argyrodite-type crystal structure, and a lattice constant of the argyrodite-type crystal structure is 9.820 ? or less.

Abstract: Provided is a sulfide solid electrolyte containing lithium, phosphorus, sulfur and chlorine, in which a molar ratio of the chlorine to the phosphorus, c (Cl/P), is greater than 1.0 and 1.9 or less, the sulfide solid electrolyte includes an argyrodite-type crystal structure, and a lattice constant of the argyrodite-type crystal structure is 9.820 ? or less.

Abstract: A method for producing a sulfide solid electrolyte comprising an argyrodite-type crystal structure, wherein phosphorus sulfide having a phosphorus content of 28.3 mass % or less and containing free sulfur is used as the raw material.

Abstract: Provided is a sulfide solid electrolyte containing lithium, phosphorus, sulfur and chlorine, in which a molar ratio of the chlorine to the phosphorus, c (Cl/P), is greater than 1.0 and 1.9 or less, the sulfide solid electrolyte includes an argyrodite-type crystal structure, and a lattice constant of the argyrodite-type crystal structure is 9.820 ? or less.

Abstract: A method for producing sulfide glass wherein phosphorus sulfide satisfying the following formula (1) is used as a raw material: 100×A/B?37??(1) wherein in the formula, A is peak areas of peaks that appear at peak positions in a range of 57.2 ppm or more and 58.3 ppm or less, and 63.0 ppm or more and 64.5 ppm or less in 31PNMR spectroscopy, and B is the total of peak areas of all peaks measured in 31PNMR spectroscopy.

Abstract: A microorganism concentrator includes a water storage part that stores water sample therein and a filter that partitions the water storage part into a supply side and a drain side for the water sample. The microorganism concentrator concentrates microorganisms that are too large to pass through the filter on the supply side by moving the water sample on the supply side to the drain side of the water storage part. In the microorganism concentrator, the filter is arranged in such a way that no vertically downward force is applied to a surface of the filter on the supply side.

Abstract: An examination apparatus 1 for microorganisms for measuring an amount of microorganisms in a sample solution, the apparatus including stirring and mixing means 7 for stirring and mixing the sample solution into which a sample and a fluorescent staining reagent are added, in a sample container 5 formed of a material allowing light to pass through, an excitation light source 10 including a light source that irradiates an irradiation target surface of the sample container 5 with excitation light while the sample solution is being stirred by the stirring and mixing means 7, light receiving means 14 for detecting light and converting the light resulting from a fluorescent emission caused by excitation light from the excitation light source 10, into an electric signal, and control means 23 for detecting the number of emissions based on the electric signal from the light receiving means 14 and calculating the amount of the microorganisms contained in the sample in the sample container 5 based on the number of emissi

Abstract: A method for producing sulfide glass wherein phosphorus sulfide satisfying the following formula (1) is used as a raw material: 100×A/B?37 ??(1) wherein in the formula, A is peak areas of peaks that appear at peak positions in a range of 57.2 ppm or more and 58.3 ppm or less, and 63.0 ppm or more and 64.5 ppm or less in 31PNMR spectroscopy, and B is the total of peak areas of all peaks measured in 31PNMR spectroscopy.

Abstract: A method for examining microorganisms has a sampling preparation step including a fluorescence staining step of stirring and mixing certain amounts of a sample and a fluorescence staining reagent, a still standing step of leaving the solution after the fluorescence staining step to still stand for a certain time, and a dilution step of diluting the solution after the still standing step with a liquid that emits no fluorescence.

Abstract: A microorganism concentrator includes a water storage part that stores water sample therein and a filter that partitions the water storage part into a supply side and a drain side for the water sample. The microorganism concentrator concentrates microorganisms that are too large to pass through the filter on the supply side by moving the water sample on the supply side to the drain side of the water storage part. In the microorganism concentrator, the filter is arranged in such a way that no vertically downward force is applied to a surface of the filter on the supply side.

Abstract: A method for examining microorganisms has a sampling preparation step including a fluorescence staining step of stirring and mixing certain amounts of a sample and a fluorescence staining reagent, a still standing step of leaving the solution after the fluorescence staining step to still stand for a certain time, and a dilution step of diluting the solution after the still standing step with a liquid that emits no fluorescence.

Abstract: An examination apparatus 1 for microorganisms for measuring an amount of microorganisms in a sample solution, the apparatus including stirring and mixing means 7 for stirring and mixing the sample solution into which a sample and a fluorescent staining reagent are added, in a sample container 5 formed of a material allowing light to pass through, an excitation light source 10 including a light source that irradiates an irradiation target surface of the sample container 5 with excitation light while the sample solution is being stirred by the stirring and mixing means 7, light receiving means 14 for detecting light and converting the light resulting from a fluorescent emission caused by excitation light from the excitation light source 10, into an electric signal, and control means 23 for detecting the number of emissions based on the electric signal from the light receiving means 14 and calculating the amount of the microorganisms contained in the sample in the sample container 5 based on the number of emissi