Abstract: Provided is an alumina-based composite oxide having a large initial specific surface area and a small initial mean pore size, with excellent heat resistance of the specific surface area and pore volume; and a production method therefor. Specifically, provided is an alumina-based composite oxide wherein the initial crystallite diameter is 10 nm or less and the initial specific surface area is 80 m2/ml or more; after calcination at 1200° C. for 3 hours in air, the specific surface area is 10 m2/ml or more; the initial mean pore size is 10 nm or more and 50 nm or less; and after calcination at 1200° C. for 3 hours in air, the pore volume retention rate is 10% or more, which is determined by (P1/P0)×100 wherein P0 represents an initial pore volume (ml/g), and P1 represents a pore volume (ml/g) after calcination at 1200° C. for 3 hours in air.

Abstract: Provided is an alumina-based composite oxide having a large initial specific surface area and a small initial mean pore size, with excellent heat resistance of the specific surface area and pore volume; and a production method therefor. Specifically, provided is an alumina-based composite oxide wherein the initial crystallite diameter is 10 nm or less and the initial specific surface area is 80 m2/ml or more; after calcination at 1200° C. for 3 hours in air, the specific surface area is 10 m2/ml or more; the initial mean pore size is 10 nm or more and 50 nm or less; and after calcination at 1200° C. for 3 hours in air, the pore volume retention rate is 10% or more, which is determined by (P1/P0)×100 wherein P0 represents an initial pore volume (ml/g), and P1 represents a pore volume (ml/g) after calcination at 1200° C. for 3 hours in air.

Abstract: Provided is an alumina-based composite oxide having a large initial specific surface area and a small initial mean pore size, with excellent heat resistance of the specific surface area and pore volume; and a production method therefor. Specifically, provided is an alumina-based composite oxide wherein the initial crystallite diameter is 10 nm or less and the initial specific surface area is 80 m2/ml or more; after calcination at 1200° C. for 3 hours in air, the specific surface area is 10 m2/ml or more; the initial mean pore size is 10 nm or more and 50 nm or less; and after calcination at 1200° C. for 3 hours in air, the pore volume retention rate is 10% or more, which is determined by (P1/P0)×100 wherein P0 represents an initial pore volume (ml/g), and P1 represents a pore volume (ml/g) after calcination at 1200° C. for 3 hours in air.

Abstract: Provided is an alumina-based composite oxide having a large initial specific surface area and a small initial mean pore size, with excellent heat resistance of the specific surface area and pore volume; and a production method therefor. Specifically, provided is an alumina-based composite oxide wherein the initial crystallite diameter is 10 nm or less and the initial specific surface area is 80 m2/ml or more; after calcination at 1200° C. for 3 hours in air, the specific surface area is 10 m2/ml or more; the initial mean pore size is 10 nm or more and 50 nm or less; and after calcination at 1200° C. for 3 hours in air, the pore volume retention rate is 10% or more, which is determined by (P1/P0)×100 wherein P0 represents an initial pore volume (ml/g), and P1 represents a pore volume (ml/g) after calcination at 1200° C. for 3 hours in air.

Abstract: An accumulator and state of charge evaluation method for preparing, during charging and discharging, models for each of deterioration degrees, each representing a relationship between terminal voltage, current and state of charge, for selecting respective models for the times during charging and discharging in accordance with a total charging/discharging amount (Ah), a deterioration degree or an elapsed time of an operation of the accumulator, for further estimating state of charge from current accumulation, and for determining a final state of charge from estimated states of charge including a present state of charge estimated from the models for the times during charging and discharging of the accumulator, while using a time or a total charging/discharging amount (Ah) from a time of full-charging by equal charging of the accumulator up to present time to determine the final state of charge from the plurality of states of charge.

Abstract: An exhaust gas purifying catalyst of the present invention includes: a first metal oxide selected from the group of praseodymium oxide, terbium oxide, and a combination thereof; a second metal oxide that is neodymium oxide; a third metal oxide that is zirconia or a combination of zirconia and ceria; and a fourth metal oxide selected from the group of lanthanum oxide, yttrium oxide, barium oxide, calcium oxide, strontium oxide, silicon oxide and a combination thereof.

Abstract: A vehicle exterior component includes a honeycomb structure having an inner plate portion arranged in the vicinity of an engine compartment, an outer plate portion arranged at an outer side of the inner plate portion, and a honeycomb portion held between the plate portions. The honeycomb portion includes a plurality of partition walls and a plurality of cells, which are separated from one another by the partition walls. Each of the partition walls of each cell has communication holes, to allow communication between the engine compartment and the interior space of the cell. Each partition wall has an absorbing portion. When external force acting inward is applied to the partition wall, the absorbing portion absorbs energy produced by the external force through deformation of the partition wall at positions corresponding to the peripheries of the communication holes, of the partition wall.

Abstract: An exhaust gas purifying catalyst of the present invention includes: a first metal oxide selected from the group of praseodymium oxide, terbium oxide, and a combination thereof; a second metal oxide that is neodymium oxide; a third metal oxide that is zirconia or a combination of zirconia and ceria; and a fourth metal oxide selected from the group of lanthanum oxide, yttrium oxide, barium oxide, calcium oxide, strontium oxide, silicon oxide and a combination thereof.

Abstract: While a control method is established which can maximize the lifetime of an storage battery based on a SOC capable of maximizing the lifetime of the storage battery under a temperature condition and a wind condition at an electricity generation site and on currently known ones of other operational conditions, a control system is constructed which can feedback to an actual wind power generation and storage battery system.

Abstract: A glass substrate chemically strengthened, includes a primary surface that has a compressive stress layer formed in an uppermost surface layer thereof. The compressive stress layer is configured to enhance strength of the glass substrate due to a compressive stress generated in the compressive stress layer. The compressive layer consists of a layer of a potassium ion concentration equal to or less than 5000 parts per million (ppm).

Abstract: A vehicle exterior component includes a honeycomb structure having an inner plate portion arranged in the vicinity of an engine compartment, an outer plate portion arranged at an outer side of the inner plate portion, and a honeycomb portion held between the plate portions. The honeycomb portion includes a plurality of partition walls and a plurality of cells, which are separated from one another by the partition walls. Each of the partition walls of each cell has communication holes, to allow communication between the engine compartment and the interior space of the cell. Each partition wall has an absorbing portion. When external force acting inward is applied to the partition wall, the absorbing portion absorbs energy produced by the external force through deformation of the partition wall at positions corresponding to the peripheries of the communication holes, of the partition wall.

Abstract: A grid plate for a lead acid storage battery including a frame section having a pair of quadrangular contour shape, and longitudinal and lateral grid strands forming a frame section grid. The longitudinal and lateral grid strands have thick strands of smaller thickness than the frame section, and thin strands of smaller width and thickness than the thick strands. Strands adjacent to the thick strands are thin strands, and space allows flow of active material to sides of the thick strands. Ends of the thick strands in the thickness direction are positioned further inward from end faces of the frame section in the thickness direction, and the end portions of one end side of the thin strands in the thickness direction are positioned offset to one end side of the thick strands in the thickness direction, and active material is packed into the reverse surface side of the grid plate.

Abstract: A glass substrate chemically strengthened, includes a primary surface that has a compressive stress layer formed in an uppermost surface layer thereof. The compressive stress layer is configured to enhance strength of the glass substrate due to a compressive stress generated in the compressive stress layer. The compressive layer consists of a layer of a potassium ion concentration equal to or less than 5000 parts per million (ppm).

Abstract: The life of a lead acid storage battery is extended by changing an over-frequency equalized charge interval performed on a lead acid storage battery, in accordance with a transition situation of a state of charge (SOC) of the lead acid storage battery. The lead acid storage battery is also made to be advantageous in terms of cost by reducing the equalized charge with a low degree of urgency to reduce the power and cost for equalized charge, and by reducing the number of stops of a natural energy storage system. A lead acid storage battery and a lead acid storage battery system whose operational management can be easily performed are achieved by a method in which the future timing when the equalized charge is performed can be grasped by people operating the lead acid storage battery.

Abstract: A lead acid storage battery composed of plates, the lead acid storage battery being obtained by packing an active material into a grid plate provided with a frame section having a quadrangular profile shape, and lateral grid strands and longitudinal grid strands that form a grid inside the frame section. The lateral grid strands are composed of thick lateral strands having a thickness equal to the thickness of the frame section, and thin lateral strands of smaller width and thickness than the thick strands, the longitudinal grid strands being composed of thick longitudinal strands that have a thickness that is less than thickness of the frame section, one end in the thickness direction being arranged in the same plane as one end of the frame section in the thickness direction, and thin longitudinal strands of smaller width and thickness than the thick longitudinal strands.

Abstract: A glass substrate chemically strengthened, includes a primary surface that has a compressive stress layer formed in an uppermost surface layer thereof. The compressive stress layer is configured to enhance strength of the glass substrate due to a compressive stress generated in the compressive stress layer. The compressive layer consists of a layer of a potassium ion concentration equal to or less than 5000 parts per million (ppm).

Abstract: A lead acid storage battery composed of plates, the lead acid storage battery being obtained by packing an active material into a grid plate provided with a frame section having a quadrangular profile shape, and lateral grid strands and longitudinal grid strands that form a grid inside the frame section. The lateral grid strands are composed of thick lateral strands having a thickness equal to the thickness of the frame section, and thin lateral strands of smaller width and thickness than the thick strands, the longitudinal grid strands being composed of thick longitudinal strands that have a thickness that is less than thickness of the frame section, one end in the thickness direction being arranged in the same plane as one end of the frame section in the thickness direction, and thin longitudinal strands of smaller width and thickness than the thick longitudinal strands.

Abstract: A glass substrate chemically strengthened, includes a primary surface that has a compressive stress layer formed in an uppermost surface layer thereof. The compressive stress layer is configured to enhance strength of the glass substrate due to a compressive stress generated in the compressive stress layer. The compressive layer consists of a layer of a potassium ion concentration equal to or less than 5000 parts per million (ppm).

Abstract: A lead acid storage battery composed of plates, the lead acid storage battery being obtained by packing an active material into a grid plate provided with a frame section having a quadrangular profile shape, and lateral grid strands and longitudinal grid strands that form a grid inside the frame section.

Abstract: There is provided a method for operating a lead acid storage battery in order to compensate for fluctuations in the amount of power generated by a solar power generation apparatus, a wind power generation apparatus, or another natural energy power generation device, the lead acid storage battery being charged by a power generation device and discharged to a load. The state of charge of the lead acid storage battery is maintained in a range of 30 to 90% where the fully charged state of the lead acid storage battery is 100%; and the lead acid storage battery is charged and discharged while the battery voltage is kept in a specified range of 1.80 to 2.42 V per cell to extend the service life of the battery. A reference temperature of 25° C. is established, and when the ambient temperature has risen above or fallen below the reference temperature, the upper and lower limit values of a specified range are corrected within a range of ?4 mV/° C. to ?6 mV/° C.