16 results about "Chlorite" patented technology

A method for evaluating contribution of each component to shale oil reservoir resistivity at high temperature and high pressure is applied to the field of oil exploration and development. The method comprises the following steps: (1) analyzing the volume percentage of each clay mineral, the pore water content and the mineralization degree of the shale oil reservoir pressure-maintaining closed core; (2) when the fluid pressure is greater than 23MPa, measuring the resistivity of the pressure-maintaining closed rock core at each temperature point; (3) carrying out water balance treatment on pure clay minerals, namely kaolinite, montmorillonite, illite and chlorite, and measuring the resistivity at each temperature point when the fluid pressure is greater than 23MPa; (4) when the fluid pressure is greater than 23MPa, measuring the resistivity of each temperature point of the solution consistent with the mineralization degree of the pore water; and (5) constructing a resistivity evaluation model, and evaluating the contribution of each component to the resistivity of the shale oil reservoir under the condition of high temperature pressure.

A method for calculating a formation temperature of a mineral based on a chlorite spectrum includes: S1, recording characteristic data of each chlorite sample; S2, acquiring a Fe—OH wavelength value of each chlorite sample; S3, calculating a formation temperature of and contents of major elements in each chlorite sample; and S4, according to the formation temperature and major element contents obtained in the step S3, determining a formation environment and a category of a corresponding chlorite sample. The calculation of a formation temperature of a chlorite mineral is based on characteristic wavelength parameters acquired by field short-wave infrared spectroscopy instead of traditional calculation based on major element data acquired by laboratory electron microprobe analysis (EMPA), which facilitates the rapid identification of a formation environment and an alteration zone of a mineral and greatly improves a working efficiency of mineral exploration.

The invention discloses a process method for preparing sintered pavement bricks by low-temperature slow firing, which is characterized in that mill tailings and clay auxiliary materials are used as main raw materials, the main components of the tailings are quartz and feldspar, the content of the feldspar is not less than 30%, and the auxiliary materials contain at least one clay mineral of kaolinite, chlorite and montmorillonite; mixing the tailings and auxiliary materials according to the weight ratio of (6: 4)-(9: 1), and adding water and a fluxing agent to obtain a mixture, wherein the fluxing agent is selected from industrial solid wastes such as boric sludge, lithium slag or spodumene tailings; pressing and forming the mixture to obtain a green body, drying the green body to constant weight, finally sintering by adopting a low-temperature slow sintering process, controlling the sintering temperature at 900-1000 DEG C, and cooling along with a furnace after heating and heat preservation stages to obtain a finished product. According to the invention, industrial solid waste is used as a raw material, and the sintered pavement brick with the compressive strength reaching the standard is prepared while the energy consumption is reduced through an optimized raw material ratio and a low-temperature sintering process, so that the unification of solid waste recycling, energy conservation and consumption reduction and high performance of a product is realized.

The application discloses grass-wood-ash black glaze and a preparation method thereof, and relates to the technical field of glaze preparation. The grass-wood-ash black glaze is prepared from the following raw materials in parts by weight: 50-60 parts of silicon dioxide, 9-12 parts of aluminum oxide, 7-10 parts of calcium oxide, 1-3 parts of magnesium oxide, 4-6 parts of diiron trioxide, 2-6 parts of potassium oxide, 3-8 parts of fluorcarbonate, 5-10 parts of lithium mica, 12-15 parts of quartz stone, 2-4 parts of potassium feldspar, 5-8 parts of plagioclase, 7-10 parts of calcite, 30-35 parts of dolomite, 20-25 parts of illite, 6-9 parts of illite-smectite mixed layer, 5-8 parts of chlorite, 3-5 parts of kaolinite and 10-20 parts of grass-wood-ash. The glaze surface of the grass-wood-ash black glaze has a unique artistic effect of blue-violet kiln-change flow lines on a dark green base, has the advantages of high color saturation, low sintering temperature, unique artistic effect and the like, and has good environmental protection and antibacterial properties.

The invention belongs to the technical field of hyperspectral remote sensing, and relates to a method for rapidly extracting chlorite minerals by using 02D data of resource I. The method comprises the following steps: step 1, carrying out atmospheric correction and ortho-rectification on the 02D data of the resource I; 2, calculating a single-band mean value image of a first spectral absorption valley of the chlorite altered mineral; 3, calculating a single-band mean value image of a second spectral absorption valley of the chlorite altered mineral; 4, calculating a single-band mean value image of a first spectral reflection peak of the chlorite altered mineral; 5, calculating a single-band mean value image of a second spectral reflection peak of the chlorite altered mineral; 6, calculating chlorite altered mineral single-band images for multiple times by adjusting floating parameters, and storing the chlorite altered mineral single-band images with relatively good extraction effects; and 7, determining a chlorite mineral distribution range by using a density segmentation method, and outputting vector elements. According to the method, the chlorite mineral extraction speed and the chlorite mineral extraction accuracy are improved.

To improve operability and convenience. [Solution] The inner container 11, measured in an atmosphere of 20°C and 90% relative humidity according to JIS Z 0208-1976, has a moisture permeability of 1.5 g / m² at a thickness of 25 μm. 2 The oxygen gas permeability at a thickness of 25 μm was measured at a temperature of 20°C and relative humidity of 65% in an atmosphere based on JIS K 7126 (isobaric method) and was 500 (cm³). 3 / m 2 The outer container 12 is made of a synthetic resin material with a pH of 24h·atm or higher, and the synthetic resin material forming the inner container contains a soluble basic component. The oxygen gas permeability of the outer container 12 at a thickness of 25 μm was measured at a temperature of 20°C and a relative humidity of 65% based on JIS K 7126 (isobaric method) and was 80 (cm³). 3 / m 2 It is made of a synthetic resin material with a humidity of 24h·atm or less, and a chlorine dioxide gas generator 13 containing metal chlorite, an activator, and silicon dioxide is provided between the inner container and the outer container.

The present invention addresses the problem of providing a method for rapidly generating chlorine dioxide gas at a desired time while maintaining the temperature during a reaction at a low temperature. Provided is a method for producing chlorine dioxide gas, comprising a step of reacting a chlorite salt, an amino acid, and an aldehyde compound in a solvent in a container under acidic conditions.

This invention discloses a method for the simultaneous removal of arsenic and chlorine from waste acid based on sodium arsenite minerals, belonging to the field of wastewater treatment and resource recovery technology. The method includes: adding an oxidant to the waste acid solution; supplementing copper, sodium, calcium, and chlorine sources according to the stoichiometric ratio of sodium arsenite (NaCaCu₅(AsO₄)₄Cl·5H₂O); conducting a water bath heating reaction under stirring conditions; adjusting the pH of the solution; and inducing Na₂O. + Ca 2+ In situ, sodium arsenate precipitate (sodium arsenate chlorite) is formed by the coordination precipitation reaction of Cu²⁺, As(V), and Cl⁻. After solid-liquid separation, washing, and drying, the sodium arsenate chlorite mineral is obtained. This invention utilizes the coexistence of arsenic and chlorine in pollutants. By adjusting the ratio of key components and controlling the reaction conditions, both arsenic and chlorine are simultaneously introduced into the mineral lattice, achieving efficient removal and resource conversion of arsenic and chlorine. This invention achieves synergistic removal and resource utilization of pollutants, resulting in significant environmental and economic benefits.

The invention belongs to the technical field of dissolution of bauxite, and particularly relates to a low-alkali-consumption dissolution method for bauxite with high chlorite content. Carrying out phase detection on the bauxite in each ore spot, respectively using the bauxite according to the types of the ore components, independently stacking the bauxite with the chlorite content higher than 10% for use, and independently dissolving out the bauxite. In the high-temperature dissolution process of the high-chlorite bauxite, chlorite does not react with sodium hydroxide to generate sodium silicon slag, the content of sodium oxide in the red mud is low, and alkali consumption in aluminum oxide production is low.

A method of reducing activity of sulfur and / or nitrogen metabolizing bacteria is provided. The method includes adding a composition of an alkali metal salt of chlorite and / or an alkali metal salt of chlorate and hydrogen peroxide to process water of a cooling tower and increasing a concentration of the composition from about 0 ppm to about 300 ppm in about 1 to about 100 minutes.

The invention discloses a method for indicating a hydrothermal center based on chlorite short-wave spectrum and Raman parameters, and belongs to the technical field of mineral exploration. The method comprises the following steps: carrying out geological exploration on a target mining area; determining chlorite sample sampling points based on the exploration result; acquiring chlorite SWIR spectral data based on the chlorite sample; analyzing and interpreting SWIR spectrum data, establishing a mining area altered mineral spectrum matching library, and analyzing spectrum parameters of chlorite samples; performing laser Raman spectrum scanning on chlorite samples with different depths to obtain a change curve of Si-Obr-Si telescopic vibration of the chlorite samples along with the depths; sWIR and Raman parameter prospecting indexes are extracted, and comprehensive prospecting indexes are established to determine the hydrothermal center. The method has the characteristics of high recognition degree, convenience in operation, reliable result, short interpretation time, high test speed, relatively strong short wave infrared parameters and Raman spectrum characteristic signals and high signal-to-noise ratio.

A porous matrix substrate that has chlorite reactant distributed therein can be used to produce gaseous chlorine dioxide. Ozone-containing gas can pass through the porous matrix substrate and the ozone can react with the chlorite to produce chlorine dioxide.

This invention provides a continuous preparation device for chlorine dioxide slow-release microspheres, belonging to the field of mechanical device technology. It solves the problems of existing commercially available chlorine dioxide preparation devices, where dust easily comes into contact with the chlorite solution and polymer solution during continuous production, causing a decline in chlorine dioxide quality; and the inaccurate and unstable delivery of the feeding equipment to the designated position during the placement and collection of chlorine dioxide slow-release microspheres, resulting in product loss. This continuous preparation device for chlorine dioxide slow-release microspheres includes a body, a frame, and a base. The body, located at the top of the base, has a rotating unit for loading materials and a preparation unit on one side of the rotating unit. The preparation unit and the rotating unit are separated by a glass plate. Two symmetrical openings are located at the bottom of the glass plate, and a limiting seat is provided at the opening within the preparation unit. This invention has the advantages of dust prevention and continuous manufacturing.

The present application relates to the field of agricultural waste resource utilization and soil improvement material technology, and particularly relates to a chlorite and Mg / Al-LDHs composite modified cow dung hydrothermal carbon and a preparation method and application thereof.A specific technical scheme is as follows: the present application takes cow dung as raw material, and after hydrothermal carbonization, is modified by chlorite co-hydrothermal modification and Mg / Al-LDHs post-treatment modification in sequence.The present application realizes the synergistic composite modification of natural layered silicate mineral and artificial synthesized layered double hydroxide, so that the specific surface area of the material is significantly increased, a rich multi-level pore network is formed, and the theoretical maximum adsorption capacity of the material to phosphorus reaches 1707.72 mg / kg.The material is applied to agricultural production as a soil improvement agent or a phosphorus slow-release material, can significantly promote crop growth, and has important application value in efficient recovery and utilization of livestock and poultry manure phosphorus resources.

The application discloses a chlorine-oxygen double vacancy FeOCl catalyst and a preparation method and application thereof in removal of organic pollutants in water by activating chlorite, and relates to the technical field of organic wastewater treatment. The chlorine-oxygen double vacancy FeOCl catalyst is successfully constructed on the surface of FeOCl through a two-step method (heat treatment + reaction under illumination). The synergistic effect of the chlorine-oxygen double vacancy significantly enhances the activation capacity of FeOCl on chlorite, and the removal rate of the organic pollutants, especially antibiotic organic pollutants, is higher than that of FeOCl materials without illumination treatment. The chlorine-oxygen double vacancy FeOCl catalyst constructed in the application can simultaneously generate selective high-valence metal substances and ClO2 in the chlorite activation advanced oxidation system, realizes selective oxidative degradation of various representative organic pollutants, and can maintain high and stable removal performance in a wide pH range and various water body substrates, and exhibits good environmental adaptability.