65 results about "Mercury intrusion" patented technology

A zirconia-based powder material, wherein [(Vp10-100) / (Vp100-6000)] satisfies the following Formula [1], provided that in a pore diameter distribution determined by a mercury intrusion method, a pore volume in a range of a pore diameter of X nm or more and less than Y nm is taken as VpX-Y:0.4≤[(Vp1⁢0-1⁢0⁢0) / (Vp100-6⁢0⁢0⁢0)]≤1.Formula [1]

The invention relates to the technical field of geological sequestration, in particular to a method and a system for predicting breakthrough pressure of a CO2 geological sequestration mudstone cover layer. The prediction method comprises the following steps: acquiring a mercury injection curve of the CO2 geological sequestration mudstone cover layer; obtaining a calibrated mercury injection curve by using the mercury injection curve; based on the calibrated mercury injection curve, a relation curve of the porosity and the mercury injection pressure is obtained; obtaining a predicted value of the breakthrough pressure through the relation curve; and predicting the breakthrough pressure of the CO2 geological sequestration mudstone cover layer according to the predicted value. On the basis of deep research and wide coverage of characteristics of various mudstone samples, a scientific and reasonable prediction model is established, and low-cost, high-aging and high-precision prediction of the breakthrough pressure of the mudstone cover layer is realized.

The invention relates to a pore throat structure style analysis method and device based on a fractal theory, and the method comprises the steps: obtaining a rock sample mercury injection curve through a mercury injection experiment, and obtaining mercury intrusion dynamic parameters of a plurality of test points; calculating a mercury intrusion dynamic parameter logarithm value according to the rock sample mercury intrusion curve; fitting the mercury intrusion dynamic parameter logarithm value to obtain a linear regression fitting straight line; calculating the pore fractal dimension of the rock according to the slope of the linear regression fitting straight line; and analyzing the pore throat structure style according to the pore fractal dimension to obtain an analysis result. The fractal theory and the mercury injection experiment are combined, and classification characterization and three-dimensional simulation of the reservoir complex pore throat structure style can be achieved through reservoir pore fractal dimension determination.

The invention relates to a shale full pore size distribution and connectivity quantitative characterization method. The method comprises the following steps: respectively determining a two-dimensional nuclear magnetic resonance T1-T2 spectrum and a nuclear magnetic resonance T2 spectrum of a dry sample core and a saturated oil core, carrying out a high-pressure mercury injection test on a parallel sample of the core, completing benchmarking of T2 and pore throat radius, and determining core communication aperture distribution; (2) splitting the rock core into sheets along the lamella, determining a two-dimensional nuclear magnetic resonance T1-T2 spectrum of the sheet-shaped dry sample rock core, comparing the two-dimensional nuclear magnetic resonance T1-T2 spectrum with the T1-T2 spectrum of the dry sample rock core, and calculating the distribution of the disconnected seams of the rock core; (3) grinding the rock core into 200-mesh particles, measuring the two-dimensional nuclear magnetic resonance T1-T2 spectrum of the granular dry sample rock core, comparing the two-dimensional nuclear magnetic resonance T1-T2 spectrum with the T1-T2 spectrum of the sheet-shaped dry sample rock core, and calculating the distribution of disconnected holes of the rock core; and (4) calculating shale full pore size distribution and connectivity. According to the method, nuclear magnetic resonance testing is carried out on shale in different states and forms, and quantitative characterization of shale full pore size distribution and connectivity of different storage spaces is achieved.

The invention discloses a method for characterizing changes of carbon dioxide salt water layer sealing pore permeability along with time based on a carbon dioxide-water-rock reaction. The method for characterizing the change of the carbon dioxide salt water layer sealing pore permeability along with the time based on the carbon dioxide-water-rock reaction comprises the following steps: carrying out a static CO2-water-rock reaction simulation experiment on a saturated core by adopting experimental formation water to obtain the particle sizes of suspended matters under different pressures; performing dynamic CO2-water-rock reaction experiments in the injection process under different pressures by adopting different research area stratum cores, and performing mercury injection test, porosity test and permeability test on the research area stratum cores before and after the experiments to obtain porosity and permeability change rate charts after CO2-water-rock reaction under different pressures; the long-term CO2-water-rock reaction pore permeability change is simulated through multi-field coupling of the model, and the quantification of the change of the pore permeability along with the time in the whole sealing process of injecting the carbon dioxide into the salt water layer is obtained.

A method of making a ceramic honeycomb wall-flow filter substrate supporting an on-wall coating, a fragment of which on-wall coated filter substrate analysed by mercury porosimetry has a volume of pores of 005 to 0.5 µm diameter as a percentage of a mercury intrusion volume of the fragment of at least 15.0%, comprises the steps of: (i) preparing a slurry comprising water, a carboxylic acid, inorganic oxide particles or a mixture of two or more inorganic oxide particles having a D(v, 0.9) of 8 to 20 µm; and 10 to 35 % by weight relative to 100% weight of the inorganic oxide particles of a particulate insoluble cellulose pore former of non-uniform morphology and having an equivalent spherical diameter D(v, 0.5) of 0.5 to 14 µm and a modal aspect ratio (width / length) of 0.3 to 0.9; (ii) coating the slurry on at least first channels of the substrate, wherein the substrate has a mean pore size (D50) of 6 to 15 µm prior to any coating and a porosity less than 60% prior to any coating; and (iii) drying and calcining the slurry-coated substrate, whereby sufficient slurry is coated on the substrate so that the product of step (iii) has a coating loading of 0.07 to 0.4 g / in3 (4.3 to 24.4 g / L), relative to a substrate weight prior to step (ii) and wherein a mean average on- wall coating thickness of the coated substrate is 5 to 70 µm.

The invention provides a method for determining the pore diameter lower limit and the effective pore volume ratio of movable fluid. The method comprises the steps that the temperature of each sample under the stratum in-situ condition is calculated according to the ground temperature gradient and the burial depth; correcting the surface tension coefficient of the water by using the calculated temperature; determining an average contact angle of water and shale; calculating capillary force, enabling the capillary force to be equal to reservoir fluid pressure, and calculating the lower limit of the aperture of the movable water; carrying out carbon dioxide adsorption, liquid nitrogen adsorption and mercury injection experiments on the sample to obtain connectivity pore volume-pore size distribution, and calculating effective pore volume in combination with a movable water pore size lower limit; carrying out a low-field nuclear magnetic resonance experiment, calculating the total pore volume of macropores, obtaining the total pore volume of small pores in combination with a carbon dioxide experiment, and finally calculating the total pore volume; and calculating the pore volume ratio of the effective pores by using the pore volume of the effective pores and the total pore volume. According to the method, the evaluation precision of the lower limit of the pore diameter of the shale reservoir movable fluid and the pore volume ratio of the effective pores is effectively improved, and the test cost is reduced.

The invention relates to a rock pore throat coordination number calculation method and device based on pore fractal dimension, and the method comprises the steps: obtaining a rock sample mercury injection curve through a mercury injection experiment, and obtaining mercury intrusion dynamic parameters of a plurality of test points; calculating a mercury intrusion dynamic parameter logarithm value according to the rock sample mercury intrusion curve; fitting the mercury intrusion dynamic parameter logarithm value to obtain a linear regression fitting straight line; calculating the pore fractal dimension of the rock according to the slope of the linear regression fitting straight line; and calculating the rock pore throat coordination number according to the pore fractal dimension to obtain an interval calculation result of the rock pore throat coordination number. According to the method, the rock pore throat coordination number can be rapidly and quantitatively determined based on the pore fractal dimension, and the fluctuation range of the pore throat coordination number can be accurately given.

The invention discloses a glutenite reservoir pore throat structure quantitative identification method and device, a medium and computing equipment, and the method comprises the steps: analyzing a pre-processed sample based on nuclear magnetic resonance and mercury intrusion test, and obtaining a full-scale pore throat radius data set corresponding to a full-band nuclear magnetic resonance spectrum; analyzing the full-scale pore throat radius data set to obtain a turning point of the fractal dimension curve; based on the turning point of the fractal dimension curve, determining the pore throat space type of the pre-treated sample; and based on the pore throat space type and the content corresponding to the pore throat space type, quantitatively identifying different modal pore throat structures of the pre-treated sample. The method and the device aim at improving the accuracy of quantitative recognition of different modal pore throat structures by performing full-scale characterization on the pre-processed sample.

According to an embodiment, an electrode containing an active material containing a titanium oxide is provided. The active material has an average primary particle size of 200 nm or more and 600 nm or less. Regarding the specific surface area S of the electrode based on the nitrogen adsorption method A and the pore specific surface area S based on the mercury intrusion method B satisfy the relationship of 0.3 ≤ S A / S B < 0.6.

It suppresses the decrease in conductivity and charge / discharge efficiency. [Solution] The porous silicon material has a Si phase and a conductive phase which is a silicide phase containing Cr and V and may also contain Al, and may also have an SiO2 phase. When the total of the Si phase, conductive phase and SiO2 phase is considered to be 100% by mass, the conductive phase is contained in an amount of 12% by mass or more and 60% by mass or less, the SiO2 phase content is 12% by mass or less, the porosity determined by the mercury intrusion method is 45% by volume or more and the average pore diameter is 100 nm or less.

The present invention relates to the technical field of oil and gas field development, and specifically relates to a method for converting the transverse relaxation time distribution into the capillary pressure distribution. The present invention proposes a correction coefficient for converting the high-pressure mercury intrusion pore throat radius into the transverse relaxation time, and then obtains the conversion coefficient by using linear interpolation and volume ratio weighting, and establishes a method for converting the transverse relaxation time distribution into the capillary pressure distribution, providing a technical reference for studying the microscopic structure and properties of reservoirs.

The present invention discloses an apparatus and method for artificially preparing structural soil samples capable of controlling the strength of their structural properties. The apparatus belongs to the field of geotechnical engineering and comprises a low-temperature forming module, a carbonization module, and a terminal device. The method, based on the apparatus, obtains the percentage of pores in each pore size interval of natural loess through a mercury intrusion test, air-dries and crushes the sample, adds CaO, and mixes uniformly. Distilled water is sprayed on the CaO-added soil material and stirred to generate Ca(OH)2, thereby preparing a mixed soil material. Dry ice pellets are prepared based on the percentage of pores in each pore size interval obtained through the mercury intrusion test, mixed uniformly with the mixed soil material, and pressed into a sample of the desired size. The sample is placed in a CO2 environment for curing, and CaCO3 cementation, similar to that of natural loess, is formed between the soil particles. The generated CaCO3 content controls the structural properties by varying the CaO incorporation ratio. Furthermore, the present invention enables non-destructive monitoring of the carbonization process during sample preparation and can control the moisture content of the prepared sample.

The present invention pertains to a hardened body of a hydraulic composition, the hardened body comprising alkali-resistant fibers, calcium silicate, and calcium aluminate, and the ratio of the pore volume in the range of 11-300,000 nm to the pore volume in the range of 6-10 nm in the pore diameter distribution of the hardened body as determined by mercury intrusion method being 14 or less.

Surface-treated calcium carbonate of the present invention contains calcium carbonate subjected to surface treatment with a fatty acid-based surface treatment agent, and satisfies a certain BET specific surface area (Sw), certain loss on heat per unit area (As), a certain lightness maintenance ratio (%), a certain average pore diameter at which an increase in a mercury intrusion amount reaches a maximum value in a certain pore distribution in a mercury intrusion method (Dxp), and a certain average pore diameter amount (maximum value of increase in mercury intrusion amount (Dyp) / average pore diameter (Dxp)).

This invention provides a quantitative calculation method for reservoir throat length based on constant-rate mercury intrusion porosimetry (CRMP) experiments, belonging to the field of oil and gas field development data information processing technology. The method includes: calculating the endpoint values ​​of the mercury intrusion intervals of each throat level based on CRMP experimental data; determining the mercury intrusion saturation of each throat level based on the endpoint values ​​of the interval radius and the mercury intrusion curve data determined by CRMP experiments; obtaining the mercury intrusion volume of each interval based on the calculated mercury intrusion saturation and the pore volume of the rock sample; calculating the mercury intrusion volume of a single throat interval using the interval mercury intrusion volume and the number of throats; and finally, quantitatively calculating the length of each throat level based on the throat radius. This invention provides a quantitative calculation method for throat length, offering a new technical approach for determining reservoir throat length and providing strong data support for research on reservoir throat length and its variation patterns, reservoir throat geometry, and reservoir throat network simulation.

The purpose of the present invention is to provide an exhaust gas purification catalyst capable of improving exhaust gas diffusivity and reactivity with respect to diffused exhaust gas, and to provide an exhaust gas purification catalyst (1) provided with a metal honeycomb substrate (10) and a catalyst layer (20) provided on the metal honeycomb substrate (10), the catalyst layer (20) contains a noble metal element, Ce-based oxide particles, and Ce-Zr-based composite oxide particles, and in a logarithmic differential pore volume distribution curve of the catalyst layer (20) obtained by a mercury intrusion method, a first peak value is present in the range of a pore diameter of 5-15 nm inclusive, a second peak value is present in the range of a pore diameter of 200-3200 nm inclusive, the first peak value is 0.060 mL / g or more, the second peak value is not less than 0.060 mL / g, and the third peak value is not less than 0.060 mL / g. The second peak value is 0.018 mL / g or more.

Provided is a molded body of a basic functional group-containing resin, wherein the total basic functional group amount per 1 g of the molded body is 2.5 mmol or more, the neutral salt decomposition capacity per 1 g of the molded body is 0.1 mmol or more, the specific surface area per 1 g of the molded body as measured by mercury intrusion is 10 m2 or more, the pore capacity per 1 g of the molded body as measured by mercury intrusion is 0.5 cm3 or more, and the average pore diameter of the molded body as measured by mercury intrusion is 100 nm to 1000 nm.

1. A method for making a ceramic honeycomb wall-flow filter substrate supporting an on-wall coating, wherein a section of the on-wall coated filter substrate analyzed by mercury porosimetry has a pore volume of 0.05 to 0.5 μm diameter as a percentage of the mercury intrusion volume of at least 15.0% of the section, and (i) an equivalent spherical diameter D(v,0.5) of 0.5 to 1 μm, which is equal to 10 to 35 wt. % of water, carboxylic acid, inorganic oxide particles, or a particulate insoluble cellulose pore former of heterogeneous morphology, with D(v,0.9) of 8 to 20 μm, relative to 100 wt. % of inorganic oxide particles. 4 μm and having a modal aspect ratio (width / length) of 0.3 to 0.9; (ii) coating the slurry onto at least first channels of a substrate, the substrate having an average pore size (D50) of 6 to 15 μm and a porosity of less than 60% before any coating; and (iii) drying and calcining the slurry-coated substrate, wherein the product of step (iii) has a porosity of 0.07 to 0.4 g / in based on the substrate weight before step (ii). 3 A method wherein sufficient slurry is coated onto a substrate to have a coating loading of (4.3-24.4 g / L) and an average on-wall coating thickness of the coated substrate is 5-70 μm.

Disclosed is a metal nonwoven fabric which contains metal fibers and has liquid permeability. The average fiber diameter of the metal fibers is 20 nm or more and 10 [mu] m or less. The metal nonwoven fabric has a pore distribution peak top diameter of 30 [mu] m or less as measured by mercury intrusion method. The metal nonwoven fabric preferably has a gap distribution peak top diameter of 0.01 [mu] m or more as measured by a mercury intrusion method. The arithmetic mean value of X / Y values, which is the ratio of X to Y in three boundary regions when the length is quartered in the direction of extension of the metal fiber, is preferably 4 or less, where X is the length in the direction of extension of the metal fiber and Y is the length in the direction orthogonal to the direction.

Silica particles having a d50 median particle size from 8 to 20 μm, a sphericity factor (S80) of at least 0.9, a BET surface area from 0.1 to 8 m2 / g, a total mercury intrusion pore volume from 0.35 to 0.8 cc / g, and a loss on ignition from 3 to 7 wt. %, are disclosed, as well as methods for making these silica particles, and dentifrice compositions containing the silica particles.

Provided are: a porous spherical silica having a large number of pore diameters, a high pore volume, and a narrow pore diameter distribution; and a method for producing the porous spherical silica. [Solution] A porous spherical silica characterized by having a pore volume as determined by mercury intrusion method of 0.5-8 ml / g, a mode pore diameter as determined by mercury intrusion method of 5-50 nm, and a ratio of a pore volume in the range of + / -5 nm of the mode pore diameter to the total pore volume of 40% or more. A fumed silica dispersion, which is dispersed so that the particle size distribution reaches a prescribed range, is formed into a spherical shape by an emulsion method and then gelled, thereby being able to be produced.

The adsorption filter according to the present invention is formed from a molded body including activated carbon and a binder, the pore volume of pores having a diameter of 10 μm or greater in terms of the volume of the adsorption filter as measured through mercury intrusion being 0.10 cm3 / cc to 0.39 cm3 / cc.

The invention relates to the technical field of characterization of unconventional shale reservoirs, and discloses a method for determining the primary porosity of a shale oil reservoir, which comprises the following steps of: measuring the oil-containing porosity of shale, namely testing the porosity of a fresh rock sample according to means such as a helium method, a nuclear magnetic method or a mercury intrusion method to obtain the porosity of the shale sample when the shale sample contains oil; acquiring the porosity of different hydrocarbon components in the shale sample, namely acquiring the porosity of a light oil component (S1-1), the porosity of a medium oil component (S1-2) and the porosity of a heavy oil component (S2-1); the shale primary porosity is quantified, that is, the primary porosity of the shale oil reservoir is quantitatively calculated by combining the porosity of the shale sample when the shale sample contains oil, the porosity of the light oil component, the porosity of the medium oil component and the porosity of the heavy oil component when the shale sample does not contain oil.

A connectivity evaluation method and apparatus for a rock pore channel, and a server and a medium. The method comprises: acquiring mercury intrusion pressures and mercury intrusion volumes corresponding to the mercury intrusion pressures at at least two pressure change points for mercury entering a pore channel with a pore structure in rock to be evaluated; and on the basis of a first energy conservation formula, a second energy conservation formula, the mercury injection pressures and the mercury intrusion volumes, determining a connectivity coefficient of the pore channel, wherein the connectivity coefficient is used for evaluating the connectivity degree of the pore channel with the pore structure. Mercury intrusion pressures and mercury intrusion volumes are processed on the basis of the two energy conservation formulas, so as to enable the connectivity coefficient obtained on the basis of the processed mercury intrusion pressures and mercury intrusion volumes to be more accurate, thereby achieving more precise evaluation of the connectivity degree of pore channels in rock to be evaluated.

The present invention provides a method and device for correcting the porosity distribution curve of geotechnical materials. The correction method comprises obtaining the actual porosity n0 of a soil sample, the porosity distribution curve n(r) of the soil sample with respect to the pore size r measured by mercury intrusion, and the measured porosity n of the soil sample, and establishing the porosity n of the pores that are missed in the soil sample when the pore size is r based on the above parameters. 漏 (r) is calculated by using the formula dr to solve the unknown number, and finally the corrected porosity distribution curve n1(r)=n(r)+n 漏 (r). The present invention provides a method for correcting the porosity distribution curve of geomaterials. The porosity distribution curve measured by mercury intrusion injection is added with the missed porosity to obtain a corrected porosity distribution curve. This method can quickly correct the porosity distribution curve measured by mercury intrusion injection, thereby improving the accuracy of the porosity distribution.

The present invention discloses an experimental method for observing the evolution of mesostructure during loess collapse, which relates to the field of mesoscopic observation technology and includes: preparing mesostructure evolution samples of loess samples in the same state; determining the collapse deformation of the original loess samples using a single-line immersion saturation compression method; performing additional tests on samples with significantly different test results from other parallel samples; dividing the collapse stage of the original loess into M stages according to arithmetic differences; taking N evolution samples in the same state, performing a single-line immersion saturation compression test, and removing ring knife samples in stages; freezing and drying the removed samples with liquid nitrogen, and cutting them into observation samples; performing scanning electron microscope observation tests and mercury intrusion tests on the observation samples; and obtaining the evolution characteristics of the loess collapse process based on statistical principles. By obtaining the complete mesostructure evolution characteristics of the entire loess collapse test process, the present invention can characterize the collapse evolution process, predict the macroscopic collapse deformation of loess, and better serve loess engineering.

The resin composition according to the present disclosure contains a resin and hollow silica particles, the 20% breaking pressure of the hollow silica particles as measured by mercury intrusion is 120 MPa or more, or the charge amount of the hollow silica particles is 0.005-0.080 [mu] C / g.

The purpose of the present invention is to provide an exhaust gas cleaning catalyst with which it is possible to realize improved exhaust gas diffusion and improved reactivity with diffused exhaust gas. In order to achieve the foregoing, provided is an exhaust gas cleaning catalyst (1) comprising a metal honeycomb base material (10) and a catalyst layer (20) provided on the metal honeycomb base material (10). The catalyst layer (20) contains a noble metal element, Ce-based oxide particles, and Ce-Zr-based composite oxide particles. A logarithmic differential pore volume distribution curve of the catalyst layer (20) obtained by a mercury intrusion method shows a first peak value in the pore diameter range from 5 nm to 15 nm and a second peak value in the pore diameter range from 200 nm to 3200 nm, the first peak value being 0.060 mL / g or more, and the second peak value being 0.018 mL / g or more.

A zirconia powder containing a stabilizer, and having a specific surface area of 20 m2 / g or more and 60 m2 / g or less and a particle diameter D50 of 0.1 μm or more and 0.7 μm or less, in which in a range of 10 nm or more and 200 nm or less in a pore distribution based on a mercury intrusion method, a peak top diameter in a pore volume distribution is 20 nm or more and 85 nm or less, a pore volume is 0.2 ml / g or more and less than 0.5 ml / g, and a pore distribution width is 40 nm or more and 105 nm or less.