The method comprises the following steps providing a porous sample containing a first fluid; establishing a steady state profile of a second fluid content in the porous sample by applying a first mechanical load, to create a plurality of regions having different second fluid contents in the porous sample; measuring, in each of the plurality of regions, a local saturation in the first fluid or/and in the second fluid; measuring, in each of the plurality of regions, a corresponding local electrical resistivity and/or conductivity; and determining a value of the representative parameter based on the corresponding values of local saturation and of local electrical conductivity and/or resistivity in each of the plurality of regions.

Provided are a porosity deriving method and a porosity deriving device capable of deriving a porosity of an inspection object being conveyed. The porosity deriving method of deriving a porosity of the inspection object includes: a basis weight measuring step including measuring a basis weight of a specific part of the inspection object being conveyed; a thickness measuring step including measuring a thickness of the specific part of the inspection object being conveyed; and a porosity deriving step including deriving a porosity of the inspection object from the basis weight, the thickness, and a true density of the inspection object.

Provided are a raw material particle size distribution measuring apparatus and a particle size distribution measuring method. Also provided is a porosity measuring apparatus. The raw material particle size distribution measuring apparatus includes: a coarse particle measuring device that acquires information indicating the particle size distribution of the coarse particles; a fine particle measuring device that acquires information indicating the particle size distribution of the fine particles; and an arithmetic device that computes the particle size distribution of the coarse particles using the information indicating the particle size distribution of the coarse particles, computes the particle size distribution of the fine particles using the information indicating the particle size distribution of the fine particles, and computes an overall particle size distribution of the raw material using the particle size distribution of the coarse particles and the particle size distribution of the fine particles.

A synthetic source rock including roasted tea powder and inorganic material. A technique for preparing the synthetic source rock, including grinding tea leaves to give tea powder, roasting the tea powder at a roasting temperature to give a roasted tea powder, and determining composition and porosity of the roasted tea powder.

A system and method for surface characterization of a porous solid or powder sample using flowing gas include mass flow controllers configured to deliver a controllable mass flow of a carrier gas and adsorptive gas to vary concentration of the adsorptive gas flowing through at least one measurement channel containing a sample cell. A concentration detector downstream of the sample cell provides a signal indicative of the adsorptive gas concentration to a controller that determines the amount of adsorptive gas adsorbed and/or desorbed to characterize the surface area, pore volume, pore volume distribution, etc. of the sample material. The detector may include a housing, heat exchanger, thermal conductivity detector, and a temperature regulator.

The method comprises the following steps providing a porous sample containing a first fluid; establishing a steady state profile of a second fluid content in the porous sample by applying a first mechanical load, to create a plurality of regions having different second fluid contents in the porous sample; measuring, in each of the plurality of regions, a local saturation in the first fluid or/and in the second fluid; measuring, in each of the plurality of regions, a corresponding local electrical resistivity and/or conductivity; and determining a value of the representative parameter based on the corresponding values of local saturation and of local electrical conductivity and/or resistivity in each of the plurality of regions.

Provided are a raw material particle size distribution measuring apparatus and a particle size distribution measuring method. Also provided is a porosity measuring apparatus. The raw material particle size distribution measuring apparatus includes: a coarse particle measuring device that acquires information indicating the particle size distribution of the coarse particles; a fine particle measuring device that acquires information indicating the particle size distribution of the fine particles; and an arithmetic device that computes the particle size distribution of the coarse particles using the information indicating the particle size distribution of the coarse particles, computes the particle size distribution of the fine particles using the information indicating the particle size distribution of the fine particles, and computes an overall particle size distribution of the raw material using the particle size distribution of the coarse particles and the particle size distribution of the fine particles.

In the present invention, a method for determining at least one pore-related parameter of a porous structure is provided. In a preferred embodiment, an enhanced evapoporometry (EP) technique is provided to determine pore size distribution of continuous pores of a porous structure. In this enhanced EP technique, a volatile liquid, such as isopropoyl alcohol or water, is supplied to one side of a porous structure in order to enable the volatile liquid to penetrate and saturate the porous structure through capillary force. Thereafter, an immiscible non-volatile liquid, such as glycerol, mineral oils, silicon oils or hydrophilic ionic liquid, is supplied to the one side of the porous structure. As the volatile liquid evaporates progressively from the filled pores, the emptied pores may be immediately filled by the non-volatile liquid drawn upwards by capillary action. This prevents formation of a t-layer formed from the adsorption of vapour emanating from the volatile liquid that is used to saturate the pores.

The present invention relates to a method for measuring the active area of an active material in an electrode, comprising: manufacturing three types of electrodes including a first electrode coated with an electrode mixture including both an electrode active material and a conductive material, a second electrode coated with an electrode mixture which includes the electrode active material as a main ingredient and does not include the conductive material, and a third electrode coated with an electrode mixture which does not include the active material and includes the conductive material as a main ingredient; a cell manufacturing step of manufacturing three types of monocells by using the same types of electrodes; a capacitance measuring step of measuring, from the monocells, capacitance of each electrode used in the monocells; and an active area calculating step of calculating the active area of the electrode active material from the capacitance.

A method for surface characterization of a porous solid or powder sample using flowing gas includes a controller that controls mass flow of a carrier gas and an adsorptive gas to form a mixture having a target concentration of the adsorptive gas over the sample, determining adsorptive gas concentration based on signals from a detector disposed downstream of the sample, automatically repeating the controlling and determining steps for a plurality of different target concentrations, and generating an isotherm for the sample based on the adsorptive gas concentration for the plurality of different target concentrations. The method may include immersing the sample in liquid nitrogen to cool the sample for all, or at least a portion of each of the different target concentrations. The target concentrations may vary from less than 5% to greater than 95%, and may vary in a stepwise manner.