A high-temperature and high-pressure microscopic visual flowing device and an experimental method are provided by the present disclosure, comprising a seepage simulation system, a micro-displacement and metering system connected to the seepage simulation system, and an image acquisition and analysis system; the seepage simulation system consists of a visual high-temperature and high-pressure kettle, a microscopic core model placed in the visual high-temperature and high-pressure kettle, and glass carriers arranged above and below the microscopic core model; the glass carriers are provided with sealing rubber sleeves, and the visual high-temperature and high-pressure kettle is provided with an annular heating jacket; an outlet of the microscopic core model is provided with a microflow channel which is connected to the micro-displacement and metering system through a pipe, effectively reducing the metering error caused by the dead volume of the pipe.

A method of estimating a material mechanical property of a porous material, for an application or objective with a specific application frequency and application strain amplitude, includes estimating an application frequency and an application strain amplitude for use in a targeted application or objective, and constructing a frequency transfer function relating the material mechanical property to measurement frequencies, the measurement frequency range including a measurement frequency different from the application frequency. The method also includes constructing a strain amplitude transfer function relating the material mechanical property at the measurement strain amplitude and the material mechanical property at the application strain amplitude, the measurement strain amplitude different from the application strain amplitude, deriving the material mechanical property from the frequency transfer function using the application frequency, and predicting the material mechanical property from the strain amplitude transformation function using the derived material mechanical property.

A classified characterization method for connectivity of organic matter (OM)-hosted pores in shale includes: scanning a shale sample according to a preset imaging area through a scanning electron microscope to acquire a 2D image of the shale sample; extracting pore parameters of each OM in the 2D image by Avizo software; acquiring a class number of OM sets according to the pore parameters; performing 3D reconstruction on each class of OM sets through a focused ion beam-helium ion microscope to acquire reconstructed 3D models of the OM; acquiring a pore connectivity parameter by the Avizo software; and acquiring an evaluation index for overall connectivity of the OM-hosted pores in the shale based on the pore connectivity parameter. The classified characterization method is based on the morphologically quantitative classification of the OM-hosted pores, and can realize the 3D characterization of connectivity of pores below 10 nm.

Methods of combining mineral composition and laboratory test results for reservoir rock samples to predict future responses to secondary and tertiary oil recovery treatments are disclosed. Particular, SEM and EDS will be combined to produce a mineral map, including mineral distribution around the rock's pore space, for comparison with laboratory data to predict and/or interpret how certain mineral distributions will respond to various fluid-rock interactions.

Estimating permeability enhancement of a subterranean formation due to presence of an oxidizer in a fracturing fluid, including determining kerogen volume percent in the subterranean formation and estimating fractured kerogen porosity, wherein the fractured kerogen porosity is associated with presence of the oxidizer. The technique includes determining an increase in connected porosity in the subterranean formation correlative with the kerogen vol % and the fractured kerogen porosity.

The present disclosure provides a high-pressure helium shale porosity testing device and method. The device comprises a reference cylinder, a pressure cylinder, a sample cylinder, a differential pressure sensor, a pressure gauge, an venting and vacuumizing system, a temperature control system and a tubing and valve system, wherein the reference cylinder is respectively connected with a helium source, the pressure cylinder and the sample cylinder through the tubing and valve system, the differential pressure sensor is configured to measure changes of pressure difference between the sample cylinder and the pressure cylinder, the pressure gauge is configured to measure pressure at the pressure cylinder, the sample cylinder is further connected with the venting and vacuumizing system through the tubing and valve system, and the temperature control system is used for controlling the temperature of the whole device.

Systems and methods relate to generating a self-consistent sediment model. Initially, void ratio extrema are determined for each sediment layer in a sediment column based on historical data or a direct measurement of the sediment column. Initial stress is determined for each sediment layer based on the void ratio extrema. A porosity model is generated for each sediment layer based on the void ratio extrema and the initial stress. At this stage, measured data is obtained for each sediment layer from a data collection device positioned at or near a geographic location of the sediment column. The porosity model of each of the sediment layer is combined with the measured data of the sediment layer to generate the self-consistent sediment model for each sediment layer. The porosity model and the self-consistent sediment model of each sediment layer is updated based on updated measured data obtained from the data collection device.

Disclosed is a characterization method of closed pores and connectivity of coal measure composite reservoirs, including collecting samples of coal seams and shales reservoirs, carrying out low-field NMR experiments and NMR freeze-thaw experiments on plunger samples and crushed samples with different particle sizes to obtain cumulative pore volume distribution and differential pore size distribution of the crushed samples, comparing crushed samples with plunger samples for optimal crushed particle sizes, and preliminarily determining a distribution range of closed pores; carrying out SAXS experiments on crushed samples to obtain size distribution and volume of total pores of 1-100 nanometers; calculating pore volume of total pores and closed pore volume in composite reservoirs by low-field NMR experiments results; carrying out non-steady overburden permeability experiments and variable factors on plunger samples of coal seams, shales and tight sandstone to characterize the connectivity under influence of pores development and lithologic combinations.

The present disclosure recognizes a correlation between zeolitic surface area (ZSA) of a catalyst composition and its catalytic activity. Particularly, the disclosure provides catalyst articles for diesel NO.sub.x abatement, including a substrate and a washcoat layer containing metal-promoted molecular sieves, wherein the zeolitic surface area (ZSA) of the catalyst article is about 100 m.sup.2/g or greater, the volumetric surface area is about 900 m.sup.2/in.sup.3 or greater, and/or the total zeolitic surface area (tZSA) is about 1200 m.sup.2 or greater. The disclosure further relates to methods for evaluating ZSA, volumetric ZSA, and tZSA, e.g., including the steps of coating a catalyst composition comprising metal-promoted molecular sieves onto a substrate; calcining and aging the catalyst composition; determining the ZSA (or volumetric ZSA or tZSA) thereof; and correlating the ZSA (or volumetric ZSA or tZSA) with catalyst composition NO.sub.x abatement activity to determine whether the catalyst composition is suitable for an intended use.

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.