Abstract: A microchip is provided. The microchip includes a substrate structure including a fluid channel configured to contain a sample solution, wherein the fluid channel is maintained at a pressure lower than atmospheric pressure prior to injection of the sample solution into the fluid channel.

Abstract: Provided is a method for fabricating a microchip for nucleic acid amplification reaction that is capable of simple and highly accurate analysis. Provided is a method for fabricating a microchip for nucleic acid amplification reaction, the method including a solidification step of drying a reagent solution including at least a part of substances required for a nucleic acid amplification reaction, and a containment step of arranging the reagent solution including the solidified substance in wells that serve as a reaction site for a nucleic acid amplification reaction. In the microchip for nucleic acid amplification reaction fabricated by the fabrication method, since substances required for the nucleic acid amplification reaction are contained by being solidified, non-specific amplification is suppressed in a nucleic acid amplification reaction, which enables highly accurate analysis.

Abstract: A process of preparing a lamination film comprising two or more layers of a fixed cholesteric liquid-crystal phase is disclosed. The process comprises (a) applying a coating liquid of a curable liquid crystal composition comprising a rod-like liquid crystal compound, an alignment-control agent capable of controlling an alignment of the rod-like liquid crystal compound and a solvent to a surface; (b) drying the applied curable liquid crystal composition to form a cholesteric liquid-crystal phase; (c) carrying out a curing reaction of the composition and fixing the cholesteric liquid-crystal phase, thereby to form a lower layer; and (d) repeating the steps (a) to (c) on the lower layer, thereby to form an upper layer; wherein at least a part of the alignment-control agent in the lower layer diffuses into the upper layer.

Abstract: According to one embodiment, there is provided a battery including a positive electrode, and a negative electrode. The positive electrode contains a lithium-cobalt composite oxide and a lithium-manganese composite oxide. The negative electrode contains a lithium titanium composite oxide. The battery satisfies the following formula (1). In addition, an open circuit voltage (OCV) of the positive electrode when the battery is discharged to 1.8 V at 0.2 C is 3.6 V (Li v.s. Li+) or more. (Qp/Qn)>1.1??(1) Qp is a charge capacity (mAh/m2) of the positive electrode per unit area, and Qn is a charge capacity (mAh/m2) of the negative electrode per unit area.

Abstract: A display apparatus includes a multiplexer circuit, a driving unit, a first control line and a second control line. The multiplexer circuit includes a plurality of switch units. The first control line is electrically connected with the switch units and the driving unit. The second control line is electrically connected with the switch units and the driving unit. A maximum time constant from the driving unit to the switch units is less than R*C/4, wherein R represents the equivalent resistance of the portion of the first control line between the two switch units which are the farthest from each other, and C represents the equivalent capacitance of the portion of the first control line between the two switch units which are the farthest from each other.

Abstract: A microchip is provided. The microchip includes a substrate structure including a fluid channel configured to contain a sample solution, wherein the fluid channel is maintained at a pressure lower than atmospheric pressure prior to injection of the sample solution into the fluid channel.

Abstract: A display device comprises a display area, a plurality of data buses located in the display area, a controller, a first de-multiplexer, and a second de-multiplexer. The controller is adapted to provide a first data signal and a second data signal. The first de-multiplexer has a first de-multiplexer ratio, and is adapted to output the first data signal received from the controller to a plurality of first data buses of the data buses. The second de-multiplexer has a second de-multiplexer ratio, and is adapted to output the second data signal received from the controller to a plurality of second data buses of the data buses. The first de-multiplexer ratio is different from the second de-multiplexer ratio.

Abstract: Provided is a hydrometallurgical process of recovering Ni from nickel oxide ore using a high pressure acid leaching, in which abrasion of the facilities caused by an ore slurry is suppressed, the amount of a final neutralized residue is reduced, and impurity components are separated and recovered for recycling. The hydrometallurgical process includes, as steps of the high pressure acid leaching, at least one step selected from step (A): separating and recovering chromite particles in the ore slurry; step (B-1): through leaching step and a solid-liquid separation step, performing neutralization of a leachate obtained after the solid-liquid separation step using a Mg-based alkali such as Mg(OH)2; and step (B-2): through leaching step and a solid-liquid separation step, performing neutralization of a leachate obtained after the solid-liquid separation step using a Mg-based alkali such as Mg(OH)2, and then recovering hematite particles.

Abstract: A microchip is provided. The microchip (A) includes a substrate structure including a fluid channel (2) configured to contain a sample solution, wherein the fluid channel is maintained at a pressure lower than atmospheric pressure prior to injection of the sample solution into the fluid channel.

Abstract: There is provided a microchip including a plurality of substrate layers, and bonding layers provided at boundary surfaces between the substrate layers and configured to include a silicon compound. At least one of the bonding layers is configured to include an organic silicon compound.

Abstract: A display device comprises a display area, a plurality of data buses located in the display area, a controller, a first de-multiplexer, and a second de-multiplexer. The controller is adapted to provide a first data signal and a second data signal. The first de-multiplexer has a first de-multiplexer ratio, and is adapted to output the first data signal received from the controller to a plurality of first data buses of the data buses. The second de-multiplexer has a second de-multiplexer ratio, and is adapted to output the second data signal received from the controller to a plurality of second data buses of the data buses. The first de-multiplexer ratio is different from the second de-multiplexer ratio.

Abstract: Provided is a microchip which enables to easily confirm, from the outside of the microchip, filling of a solution into an analysis region. The microchip includes: an introduction part for introducing a liquid; an analysis region in which a substance contained in the liquid or a reaction product of the substance is analyzed; an indication region to indicate that the analysis region has completely been filled with the liquid; and a flow channel to connect the introduction part, the analysis region, and the indication region. In the microchip, the flow channel is configured in such a manner that an amount of time it takes for the liquid introduced from the introduction part to reach the indication region is longer than an amount of time it takes for the liquid introduced from the introduction part to fill up the analysis region.

Abstract: A light reflection layer, comprising a first liquid crystal layer obtained by fixing a first curable liquid crystal composition through curing in a state of a cholesteric liquid crystal phase, wherein the first curable liquid crystal composition contains a polymerizable liquid crystal compound, a fluoroalkyl group-containing alignment control agent, and a hydrophilic group-containing coating property imparting agent exhibits low haze, excellent heat shielding properties and improved coating properties when the light reflection layer obtained by fixing the cholesteric liquid crystal phase on the light reflection layer is laminated and coated.

Abstract: A sample liquid supply device includes a container tip into which the sample liquid is introduced, a hollow needle provided at one end of the container tip such that a hollow part thereof communicates with inside of the container tip, and a sealing member that covers an opening from which the sample liquid is introduced, wherein the sealing member has a puncture-sealing property achieved by elastic deformation.

Abstract: Provided is a method for fabricating a microchip for nucleic acid amplification reaction that is capable of simple and highly accurate analysis. Provided is a method for fabricating a microchip for nucleic acid amplification reaction, the method including a solidification step of drying a reagent solution including at least a part of substances required for a nucleic acid amplification reaction, and a containment step of arranging the reagent solution including the solidified substance in wells that serve as a reaction site for a nucleic acid amplification reaction. In the microchip for nucleic acid amplification reaction fabricated by the fabrication method, since substances required for the nucleic acid amplification reaction are contained by being solidified, non-specific amplification is suppressed in a nucleic acid amplification reaction, which enables highly accurate analysis.

Abstract: Provided is a microchip including: an inlet part to which a liquid is injected; a plurality of analysis areas to which the liquid is supplied from the inlet part; and a flow channel which is formed to supply the liquid to the plurality of analysis areas at the same time.

Abstract: In general, according to one embodiment, a positive electrode is provided. The positive electrode includes a positive electrode current collector and a positive-electrode-mixture layer formed on the positive electrode current collector. The positive-electrode-mixture layer includes first pores and second pores. Pore size diameters D1 and D2 of the first and the second pores satisfy relationship: 0.03<D1/D2<0.8. Total volumes V(D1) and V(D2) of the first and the second pores satisfy the following relationship: 2<log V(D1)/log V(D2)<6.

Abstract: According to one embodiment, there is provided a battery including a positive electrode, and a negative electrode. The positive electrode contains a lithium-cobalt composite oxide and a lithium-manganese composite oxide. The negative electrode contains a lithium titanium composite oxide. The battery satisfies the following formula (1). In addition, an open circuit voltage (OCV) of the positive electrode when the battery is discharged to 1.8 V at 0.2 C is 3.6 V (Li v.s. Li+) or more. (Qp/Qn)>1.1??(1) Qp is a charge capacity (mAh/m2) of the positive electrode per unit area, and Qn is a charge capacity (mAh/m2) of the negative electrode per unit area.

Abstract: A liquid injecting jig is provided. The liquid injecting jig includes a jig configuration including a plurality of parts adapted to be in cooperative engagement so as to position a channel within the jig configuration, wherein the jig configuration is adapted to fit an opening through which the channel is adapted to be received so as to expose the channel from the jig configuration. A jig set, a microchip case, and a microchip set are also provided.

Abstract: The present disclosure relates to a method and apparatus for separating nucleic acids. A carrier may include a porous microbead having cation-exchangeable groups attached to the surface of the porous microbead. Capturing chains modified with positively charged functional groups and having a base sequence complementary to a target nucleic acid chain sequence are immobilized on to the surface of the porous microbead. In various embodiments, capturing chains are immobilized on to the surface of the porous microbead through an ion exchange bond or a covalent bond with the cation-exchangeable groups of the porous microbead. In some cases, the porous microbead has a number of through pores adapted to permit a solution to pass rapidly through the through pores and a number of diffusive pores adapted to permit a solute of the solution to diffuse into the diffusive pores.