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1718 results about "Liquid ratio" patented technology

Liquid ratio is a thermodynamic ratio of a liquid obtained by dividing boiling point by melting point of a substance in absolute temperature scales (in kelvin or rankine scales). This ratio is used for defining range of kinetic stability of its liquid state.

Preparation and use method of microbial immobilized material for remedying polluted soil

The invention discloses a method for preparing and using a microbial immobilized material for repairing contaminated soil. The method comprises the following steps: (1) after being dried by air, the waste biomass raw material is pulverized or ground into 1-20mm of particles; (2) the biomass particles are carbonized and sterilized at the temperature of 150-450 DEG C and under limited oxygen condition for 0.5-6 hours to prepare a carrier material; (3) the carrier material is put into bacterium suspension for enrichment culture according to the solid-to-liquid ratio of 0.5-2mL/g, then the microbial immobilized material is produced; (4) the produced microbial immobilized material is added to organic contaminated soil according to the proportion of 1-500 tons per hectare soil, 0-30cm of topsoil is ploughed to cause the microbial immobilized material to be mixed evenly in the soil, simultaneously, the contaminated soil is biologically repaired and safe agricultural products are produced. The method has the advantages that the carrier material contains abundant lignin structures, carbon and nutrient elements, which provides more suitable matrix for microbial growth; and the immobilized material has strong affinity, high immobilization efficiency, strong adsorption capacity and good resistance against the pollutants in the environment; and the immobilized material is a soil fertilizer, and is suitable for large-scale in-situ biological repair of the contaminated soil.
Owner:ZHEJIANG UNIV

Method for preparing fucoidan

InactiveCN101993501AComprehensive utilization value has no impactComprehensive utilization value impactFood additiveLiquid ratio
The invention provides a method for preparing fucoidan, relating to the field of production and application of food additives. The method comprises the following steps of: adding distilled water according to a material to liquid ratio of 1:40-4:80 g / mL with brown algae, such as kelps, undaria pinnatifida, and the like as raw materials; treating by a colloid mill and then carrying out microwave-assisted extraction or ultrasonic wave-assisted extraction, wherein, in the microwave-assisted extraction process, the microwave time lasts 20-40min, the microwave extraction temperature is 60-80 DEG C, and the microwave power is 400-500W; and in the ultrasonic wave-assisted extraction process, the ultrasonic power is 800-100W, the microwave time lasts 20-40min, and the extraction temperature is 60-90 DEG C; and centrifuging an extracting solution, adding a proper amount of 2% CaCl2 solution into a supernatant, stirring, keeping constant temperature for 20-30h at 35-40 DEG C, centrifuging, adding 50-100% ethanol into the supernatant until the ethanol concentration of the solution is 15-20%, stirring, filtering, concentrating, adding 90-100% ethanol into a concentrated solution until the ethanol concentration of the solution is 55-60%, centrifuging again and drying a precipitate in vacuum to obtain white or yellow-white fucoidan powder.
Owner:ZHEJIANG UNIVERSITY OF SCIENCE AND TECHNOLOGY

Method for extracting cobalt and nickel from manganese, cobalt and nickel waste residue

The invention discloses a method for extracting cobalt and nickel from a manganese, cobalt and nickel waste residue. The method sequentially comprises the following steps: a) adding water into the manganese, cobalt and nickel waste residue in a solid-to-liquid ratio of 1:(2-5) to size, and heating and bubbling under stirring to obtain cobalt and nickel foaming slags and ferromanganese sediments; b) heating, pickling and filtering the cobalt and nickel foaming slags to obtain a cobalt and nickel filter cake; c) curing and leaching the cobalt and nickel filter cake by concentrated sulfuric acid to obtain cobalt and nickel liquor; d) removing impurities in the cobalt and nickel liquor to remove impurities such as copper, iron, calcium, magnesium, manganese and zinc, wherein the mass concentration of impurities in the liquor is reduced to below 0.01g / L; e) extracting and separating the cobalt and nickel liquor without impurities by a P507 extractant to obtain nickel sulfate liquor and a cobalt-loaded organic phase; and f) cooling and crystallizing the nickel liquor, and recovering a nickel sulfate product, and carrying out reverse extraction on the cobalt-loaded organic phase by sulfuric acid to obtain cobaltous sulfate liquor. According to the invention, the production condition is relatively simple, efficient grouping is realized, and the recovery rate of cobalt and nickel is high.
Owner:GUANGXI NON FERROUS METALS GROUP HUIYUANMENGYE

Method for pre-treating phosphorite by using acidic waste water in the production process of titanium pigment

ActiveCN101759166AReduce processing costsControl the strength of sulfuric acidPhosphoric acidPhosphoric acidSlurry
The invention discloses a method for pre-treating phosphorite of wet process phosphoric acid by using acidic waste water in the production process of titanium pigment, which comprises the following steps: (1), collecting the acidic waste water into an acidic waste water storage groove, controlling the acid degree to be 2 to 5 percent and the total iron concentration to be 0.3 to 0.5 percent; (2), adding the acidic waste water and the milled phosphorite in a solid-to-liquid ratio of 2-5:1 into a reaction groove for reaction; and (3), performing solid-liquid separation on the slurry which is obtained in the step (2) to obtain a solid phase, namely the required phosphorite. The content of magnesium in the phosphorite which is treated by the method is reduced by over 70 percent, the loss ratio of the phosphorus is controlled to be within 1 percent; when the phosphorite which is treated by the process is used for producing the phosphoric acid by a wet method, the consumption of the sulfuric acid for mine per ton is reduced by about 10 percent; and the acidic waste water pretreats phosphorite and then is delivered to a sewage station for treatment, the consumption of lime or other alkaline substance is reduced by 60 percent compared with the mode of directly delivering the waste water to the sewage station, so the economical efficiency of the process is high.
Owner:SICHUAN LOMON TITANIUM IND CO LTD

Passivator for controlling pollutions of heavy metals copper, lead and cadmium on soil and applications thereof

The invention belongs to the technical field of soil heavy metal pollution control and particularly relates to a passivator which is suitable for the in-situ control of the pollutions of heavy metals copper, lead and cadmium on soil and applications thereof. The passivator uses middle-grade and low-grade phosphate ore powder as the main raw material and the heavy metal passivator is prepared to passivate heavy metals in soil. The preparation method of the passivator comprises the following steps: smashing the middle-grade and low-grade phosphate ore of which P2O5 content is 20-30%, sieving with a 100 meshes of screen to obtain phosphate ore powder, mixing the phosphate ore powder with 0.1-0.7mol/L of oxalic acid according to the solid-to-liquid ratio of 1:1-1:20, activating at 28 DEG C for 6 days, and then drying at 50 DEG C for 20-24h to obtain the passivator. 3.97g of the prepared passivator is applied in 1kg of soil which is polluted by heavy metals; and the lettuce which grows for 120 days is harvested, and sampling is performed to measure the content of various forms of heavy metals in soil and the plant absorption amount. The passivator fully utilizes the middle-grade and low-grade phosphate ore resource which is difficult in use in China; and the passivator has the characteristics that the investment is low, the engineering quantity is low, the physicochemical properties of soil can not be damaged and secondary pollution can not be caused.
Owner:HUAZHONG AGRI UNIV

Olfactory analog instrument and on-site analysis method for odor grade of specific substance

The invention provides an olfactory analog instrument and an on-site analysis method for the odor grade of a specific substance. The invention has the following characteristics: 1, a gas sensor array constant temperature operation room, a computer and an autoinjection system are integrated in a test box; 2, utilization of a sample bottle with a volume of 250 ml and 25 ml of a to-be-tested sample enables a gas-liquid ratio to be 9: 1; 3, parallel resistance wires respectively wind in a semi-circle manner to generate 45-W power, so the sample and headspace volatilized gas are heated to a temperature of 80 DEG C in only 8 min and maintained at the temperature for 30 min; 4, 25 ml of an aqueous ethanol solution with a concentration of 100 ppm is used to generate standard reference gas in the sample bottle with a volume of 250 ml, and correction on gas sensors are carried out based on the generated standard reference gas; 5, headspace sampling flow is 500 ml / min, sampling time is 30 s, and gas sensor response signals undergo lowpass filtering and dimensionality reduction pretreatment; and 6, a database is established, and the olfactory analog instrument carries out on-site detection and grade prediction and identification on the odor of specific substances consisting of an adhesive, petroleum wax, leather, glycerin and edible vegetable oil.
Owner:EAST CHINA UNIV OF SCI & TECH

Method for treating highly concentrated ammonian wastewater with poor biodegradability by using a multiple-technique combination

The invention relates to a method for treating highly concentrated ammonian wastewater with poor biodegradability by using a multiple-technique combination, which belongs to the technical field of wastewater treatment. The method is characterized in that: the ammonian wastewater primarily enters a pH adjusting tank for adjusting the pH value to be 11-12.5 and enters a blow-off tower for blowing off with the gas-liquid ratio being 3000-4500, the blown-off wastewater enters a chemical precipitation tank, magnesium salts and phosphates are added according to the mol ratio of Mg : N : P being 1.4-1.7:1:1 for reacting with the wastewater to generate ammonium magnesium phosphate precipitate for removing ammonian, yielding water enters a break point chlorination tank, chlorine-containing oxide is added according to the weight ratio Cl / N being 9-12:1 of active chlorine and ammonian, the wastewater is transferred to a reducing tank after the reaction, reducing agent is added according to 1-1.1 times of theoretical mol value of the yielding water completely reacting with residual chlorine, and the wastewater can be directly discharged after the reaction. The treatment method has simple operation, high reaction speed and low wastewater treatment cost, and can lead ammonian to be recovered without secondary pollution to environment; and the yielding water can reach primary emission standard.
Owner:GUANGZHOU INST OF GEOCHEMISTRY - CHINESE ACAD OF SCI

Method for recrystallizing and purifying desulphurized gypsum

The invention provides a method for recrystallizing and purifying desulphurized gypsum, which mainly comprises the four steps of acid-washing, dissolution, crystallization and washing, and specifically comprises the following steps of: removing impurities, reacted with acids, in the desulphurized gypsum by the aid-washing, dissolving calcium sulphate in the desulphurized gypsum into the acid solution at a relatively higher temperature by utilizing the characteristic that the solubility of the calcium sulphate in the specific acid solution is remarkably changed with the temperature, performing solid-liquid separation to remove undissolved solid-phase impurities at the high temperature, performing cooling recrystallization and the solid-liquid separation on a liquid phase at a relatively lower temperature, and washing and drying a filter cake to obtain high-purity gypsum, wherein the liquid phase in the dissolution and recrystallization processes can be reused. Through the method provided by the invention, the gypsum with relatively higher purity and whiteness can be prepared by selecting a proper solid-to-liquid ratio, proper temperatures and proper acid concentration and performing dissolution and crystallization for a certain time, and the performance of the desulphurized gypsum is remarkably improved.
Owner:SHANGHAI UNIV

Method for preparing bagasse dissolving pulp and pre-extracting hemicellulose and product thereof

The invention relates to a method for preparing bagasse dissolving pulp and pre-extracting hemicellulose and products thereof; the method comprises the following steps: bagasse preparation which comprises the steps of depithing and washing; prehydrolysis which is carried out in a globe digester or a hydrolysis boiler; wherein, the process conditions are as follows: in the process for depithing and oven-drying bagasse, the solid-to-liquid ratio is 1:0.4-8.0, the hydrolysis temperature is 100-200 DEG C, the hydrolysis time is 15-240min, the pH value of the end point of hydrolysis is 2-5; in the process of the solid-to-liquid separation and washing, the filtrate is collected to prepare extracting solution; dissolving pulp is prepared by residue alkali method. By adopting the method, bagasse dissolving pulp and bagasse extracting solution which is used to prepare oligosaccharides are obtained. Most of pentosan in bagasse can be extracted by controlling the process conditions of the prehydrolysis, the technical route and the process conditions have strong pertinence so that the reactivity and the uniformity of bagasse dissolving pulp can be improved; by improving the traditional dissolving pulp alkali method for pulping, bagasse biorefinery based on dissolving pulp pulping can be realized in engineering so that the production costs for preparing bagasse dissolving pulp and pre-extracting hemicellulose are reduced.
Owner:上海士林纤维材料有限公司

Vanadium-containing non-magnesium hard alloy and preparation method thereof

The invention relates to a nonmagnetic hard alloy material and a preparation method thereof. The alloy comprises (wt %) tungsten carbide 75-90, nickel powder 8-20, chromium carbide 0.5-3.0, and vanadium carbide 0.3-2.5. The preparation method comprises compounding, wet grinding, drying, pressing, sintering and checking, wherein in the wet grinding step, a nonmagnetic alloy lining board wet grinder is used, alcohol or acetone is added as grinding medium, nonmagnetic hard alloy balls is used as grinding material, the ratio of grinding medium to material is 5:1, the solid-to-liquid ratio is 350ml/Kg, and the wet grinding time is 48-56 hours; and pressure sintering is adopted. In the inventive nonmagnetic hard alloy material, fine-particle tungsten carbide powder (1.0-1.5 mum) is used as hard phase, so as to improve the hardness and abrasion resistance of the alloy. The nickel is used as binder, and a small amount of chromium carbide and vanadium carbide are added as tungsten carbide grain growth inhibitor, so as to refine tungsten carbide crystal grains, and further improve the hardness and abrasion resistance of the alloy. The pressure sintering technique accelerates densification speed during sintering process, effectively reduces porosity of the alloy, and remarkably improves the strength of the alloy.
Owner:ZHUZHOU JINGGONG CEMENTED CARBIDE

Method for recovering cobalt from lithium battery anode material

The invention discloses a method for recovering cobalt from a lithium battery anode material. The method is characterized by comprising the following steps of: (1) removing aluminum foil from the anode material, obtaining a black solid matter containing lithium cobalt oxide, roasting the black solid matter to form lithium cobalt oxide powder, (2) weighing and adding the lithium cobalt oxide powder into 119-240g/L of citric acid according to a solid-to-liquid ratio of (20-30):1g/L, adding hydrogen peroxide at a mass fraction of 30% according to a mole ratio of 2:(1-1.05), performing stirring leaching for 5-7h at 80-90 DEG C, filtering to form filtrate containing the cobalt, (3) adding an ammonium oxalate solution into the filtrate to form a cobalt oxalate precipitate, and (4) after drying the cobalt oxalate precipitate, adding lithium carbonate powder according to a mole ratio (1:(1-1.05)) of the cobalt to lithium, grinding uniformly, roasting for 6-8h at 800-850 DEG C, and obtaining lithium cobalt oxide powder capable of directly serving as the electrode material. The method is easy to operate and high in recovery rate, equipment is simple, waste liquid is easy to treat, and the pollution of waste lithium batteries to an environment can be effectively reduced.
Owner:HUAZHONG UNIV OF SCI & TECH WUCHANG BRANCH
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