445results about How to "Reduce the amount of adsorption" patented technology

The invention discloses a novel lepidolite flotation method including primary rough selection, secondary fine selection and secondary scavenging. During the flotation, sodium silicate is added as an inhibitor with the amount ranging from 1400g/t to 1900g/t; an anionic collector is sodium oleate or oxyparaffin soap 731 with the amount ranging from 480g/t to 700g/t; and a cationic collector is dodecylamine or coconut oil amine with the amount ranging from 130g/t to 160g/t. The adding sequence of collectors is the anionic collector first and the cationic collector second, or the anionic collector and the cationic collector are added together. By the method, the lepidolite is selected through the combination of the anionic and the cationic, good flotation effect can be realized, flotation efficiency is high, and meanwhile, the synergistic effect is generated between the anionic collector and the cationic collector, and results from joint action of three mechanisms of coadsorption, charge compensation and function complementation.

The invention relates to a multifunctional plating assisting additive for a hot dipping metallization process and a preparation and application method thereof, and belongs to the metal material anticorrosive technical field for providing multiple plating assisting efficacy. The technical proposal of the invention comprises that: a plurality of cations or an amphoteric surfactant ( an equivalent concentration of a quaternary ammonium group is between 0.1 and 2 mol/L) and nonionics (an equivalent concentration of a polyoxyethylene group is between 0.5 and 5 mol/L) are dissolved in deionized water. The method can improve the wetting quality between a liquid-state metal and a workpiece, and the adhesive uniformity and continuity of the plating assisting additive, reduces the drying time, prevents the liquid-state metal from falling and splashing, shortens the dipping and plating time, saves raw materials, improves a residue form, reduces an ash content, increases an ash discharge speed, isolates air, stops oxidation, disperses residual dirt and is suitable for a plurality of processes of hot galvanizing, hot plating zinc-aluminum alloy, hot plating aluminum, etc. The preparation steps comprise dissolution, cubage determination, cooling, keeping stand and filling; when the multifunctional plating assisting additive is used, the multifunctional plating assisting additive is directly added into a plating assisting additive solution and is evenly stirred.

The invention relates to long-carbon-chain amide glycine betaine clean fracturing fluid and a preparation method thereof. The glycine betaine amphiprotic surface active agent long-carbon-chain (more than 18 carbons) amide glycine betaine is used as a main agent, the carbon chain of the glycine betaine is long, the glycine betaine is dissolved in the water and is likely to form gel after being stirred, so that the fracturing fluid is good in viscosity. In addition, the clean fracturing fluid by adopting the long-carbon-chain (more than 18) amide glycine betaine as the main agent adsorbs less rock stratum, the consumption of the surface active agent is effectively reduced, the calcium resistance is strong, the gel is thorough to break, no residue exists, and the harm on the stratum is small. The prepared long-carbon-chain amide propyl glycine betaine clean fracturing fluid can be well applied to an oil field and plays an important role in increasing the yield of the oil-gas field.

The invention discloses extraction equipment for rose essential oil and rose hydrosol which mainly includes a distillation still, a steam conduit, a condenser and an oil-water separator, wherein, the distillation still is connected with the oil-water separator by the steam conduit and the condenser; the lower end of the interior of the distillation still is provided with a steam heating coil; and the upper part of the steam heating coil is provided with a transverse plate sieve which can be opened freely. An adsorption plant is arranged between the top of the distillation still and the steam conduit and internally filled with active ceramic rings serving as an absorbent. The extraction equipment of the invention has the advantages of simple operation, convenient use and high production efficiency, and can greatly enhance the quality of the rose essential oil and the rose hydrosol.

The invention relates to a fracturing fluid system used in an oil and gas field, in particular to a fracturing fluid system of CO2 cleaning foam. The fracturing fluid system comprises the following components in percentage by weight: 0.3-0.8 percent of water-soluble hydrophobic association polymer, 0.25-0.55 percent of rheological auxiliary agent, 0.5-3.0 percent of clay stabilizer, 0.1-0.5 percent of foaming agent, 0.01-0.2 percent of gel breaker, 30.0-80.0 percent of liquid CO2 and the balance of water. Compared with the prior art, in the fracturing fluid system of the CO2 cleaning foam, a cross-linking agent is not needed, the foamability is good, the foam stability is high, the sand-carrying capability is strong, gel breaking is easy to control, no residue is generated after gel breaking, the superficial/interfacial tension of gel-breaking liquid is low, and the damage to the formation is less, and therefore, the fracturing fluid system can be used for fracturing modification of hypoisotonic, low-pressure and water-sensitive storage layers at the temperature of 60-140 DEG C.

A gas sensing element includes a solid electrolyte body having oxygen ionic conductivity, a measured gas side electrode provided on one surface of the solid electrolyte body, and a reference gas side electrode provided on the other surface of the solid electrolyte body. The measured gas side electrode is positioned in a chamber space. The gas sensing element has an introducing hole connecting the chamber space to a measured gas atmosphere outside of the gas sensing element. The introducing hole is filled with a porous member having an average pore diameter of 2 to 30 μm.

The invention relates to a continuous wastewater treatment device utilizing membrane capacitive deionization. An upper cover plate and a lower cover plate are coaxially installed at the upper end and the lower end of a cylindrical shell, a water inlet nozzle and a water outlet nozzle which are communicated with the interior of the shell are respectively formed in the axis part of the upper cover plate and the axis part of the lower cover plate, a water collecting plate is coaxially installed on the upper cover plate in the shell, conducting rods are uniformly and axially distributed on the periphery of the shell at intervals, a lower distribution board and an upper distribution board are coaxially installed in the shell between the water collecting plate and a water distributing plate and are of a pair of metal boards, and a plurality of groups of processing module components are coaxially installed between the two distribution boards, wherein each group of processing module component comprises an upper current collecting plate, a membrane carbon positive electrode, a diaphragm, a membrane carbon negative electrode and a lower current collecting plate. According to the continuous wastewater treatment device, the membrane electrode is integral and is prepared by a carbon electrode and an ion membrane through spraying a cation exchange coating on a cathode and spraying an anion exchange coating on an anode, the thickness of the ion exchange layer is less than 10mu, and the membrane electrode has small resistance and large capacitance compared with those of a membrane electrode on which an ion membrane is directly added.

The invention belongs to the field of synthesis and application of molecular sieves, and discloses a preparation method of a silanization-modified molecular sieve. The method comprises the following steps: transferring a molecular sieve subjected to acid-alkali alternate treatment, an accelerator and a silanization reagent dissolved in an organic solvent into a reactor, carrying out silanization modification on the molecular sieve in a nitrogen protective sealed environment under the conditions of certain temperature and high pressure, filtering, washing, and drying to obtain the silanization-modified molecular sieve. The preparation method disclosed by the invention can effectively enhance the silanization efficiency, does not have great influence on the pore structure of the molecular sieve, and has the advantages of low cost, simple technique and high silanization degree.

The invention belongs to the technical field of preparation of functional high polymer materials, and particularly relates to a natural high polymer material modified adsorption resin for the adsorption of heavy metal ions and a preparation method for the adsorption resin. The heavy metal ion adsorption resin comprises the following components in percentage by weight: 10.0 to 15.0 percent of chitosan (Chit), 25.0 to 50.0 percent of acrylic acid (AA), 20 to 45 percent of acrylamide (AM), 0.1 to 0.4 percent of N,N-methylene-bisacrylamide (NMBA), 1.0 to 3.0 percent of potassium persulfate (KPS) and 0.0 to 15.0 percent of wood meal. By the heavy metal ion adsorption resin, Pb2+ can be efficiently adsorbed and separated, the cost of a chitosan modified adsorption resin can be lowered, adsorption capacity can be improved, the number of reuse times can be increased, and the adsorptive selectivity of the resin can be improved.

[OBJECT] The present invention provides a method for selecting and eliminating endotoxin selectively from a solution where a highly acidic substance such as heparin co-exists, and an adsorbent used therefor.

[MEANS FOR SOLVING] The present invention also provides a method for providing the endotoxin adsorbent, which comprises partially modifying amino groups contained within an amino group-containing molecule used as a ligand of the endotoxin adsorbent, with a molecule that is capable of reacting with an amino group.

The invention discloses a functional polymer containing phosphorylcholine and PEG and a method for forming a biological pollution resistant interface. The polymer is a functional polymer that contains multiple function groups on a side chain and has a controllable proportion; a PEG flexible chain with larger steric hindrance and outer cell membrane phosphorylcholine hydrophilic group interact to achieve good anti-pollution effect; the polymer contains less than 10% of catechol group, and can be strongly combined with surfaces of various polydopamine-mediated base materials to form a stable hydrophilic monomolecular coating, so that the functional modification of material surfaces is implemented. The method for forming coatings is simple; the coatings can exist on the surface of any base material, so that the ability of resisting adhesion and pollution of multiple biological ingredients of the material surface is improved.

The invention relates to a polyurethane material with protein adsorption resistance and cell adhesion resistance and a preparing method thereof. The material comprises a substrate and a modification layer. The substrate is made of polyurethane. The modification layer is obtained by polymerizing a vinyl pyrrolidone monomer on the surface of the substrate by utilization of an atom transfer radical polymerization technology. The material is prepared by steps of: subjecting the polyurethane to isocyanic acid esterification, performing amination, fixing a bromine initiator, and initiating graft polymerization of the vinyl pyrrolidone on the surface of the material. The surface of the polyurethane material prepared by the method has good hydrophilicity, good resistance to bovine serum fibrinogen adsorption, bovine serum albumin adsorption and lysozyme adsorption, and a function of resisting cell adhesion of mouse fibroblast cells (L-929), so that the polyurethane material is suitable for preparing biomedical catheter materials with complex shape structures.

The invention relates to a special effect boron adsorption resin and a synthetic method and application thereof, belonging to the fields of high molecules and waste water treatment. The general structural formula of the resin is shown in the specifications, wherein n=1,000-2,000. The method comprises the following steps of: (1) preparing 2-amino-1,3-propylene glycol; (2) preparing chloromethylated styrene-divinylbenzene copolymerized spheres; and (3) preparing the special effect boron adsorption resin from the 2-amino-1,3-propylene glycol and the chloromethylated styrene-divinylbenzene copolymerized spheres. The special effect boron adsorption resin can be used for extracting and recovering boric acid from an acid aqueous solution. In the invention, the special effect boron adsorption resin which is suitable for a strongly acid environment is synthesized by taking 1,3-propylene glycol as a functional group.

The present invention is process of preparing citicoline sodium. The preparation process includes the biotransformation of material including 5'-cytidylate, phosphorylcholine, potassium hydroxide and glucose with yeast as the biocatalyst; extraction and separation with active carbon as the adsorbing carrier, Cl- type ion exchange resin as the separating carrier and re-compounded water-alcohol mixture as the analyzing reagent; and product purification with alcohol solvent as the crystallizing solvent. Compared with available technology, the present invention has the advantages of high product yield and high product purity.

A high-activity red mud adsorbent used for treating the P contained sewage is prepared from the red mud rejected in preparing alumina through proportionally mixing it with acid solution, heating by water bath while reacting to generate solid product, water washing, filtering and baking. It has high adsorptive volume.

The invention relates to a method of in-situ ore leaching and leachate discharge of ion adsorption type ore; the leachate is collected in a vacuum mode; a porous capillary leachate-guiding layer is disposed between the ore body and a vacuum leachate outlet and has the function of obstructing air; the leachate is transferred from the ore body to the vacuum leachate outlet under the vacuum pressure conducted by capillary action. The invention also provides a system for realizing the method. The method and system of the invention facilitate the improvement of vacuum leachate discharge area and system vacuum degree, greatly decrease the energy consumption required for maintaining vacuum, thus reduce the moisture capacity of the ore layer, enlarge the control range, and increase the leachate discharge efficiency.

The invention relates to the field of metal organic framework materials, and provides a metal organic framework material and a preparation method and application thereof. The chemical formula of the metal organic framework material provided by the invention is [Cu(dps)2(SiF6)].6H2O or [Cu(dps)2(GeF6)].6H2O, wherein the dps is bipyridine sulfur. The metal organic framework material provided by theinvention contains fluorine adsorption sites, so that the metal organic framework material can adsorb a large amount of acetylene, but has very small adsorption capacity on other gases with similar sizes, such as ethylene, carbon dioxide and ethane, so that the metal organic framework material provided by the invention can be used for high-selectivity adsorption of acetylene. Results of embodiments show that the adsorption capacity of the metal organic framework material provided by the invention to acetylene under the same condition is far greater than that to ethylene, carbon dioxide and ethane.

The invention discloses a citric acid and chitosan modified biocompatible polyurethane and a preparation method thereof. A main chain of the polyurethane disclosed by the invention is a polyurethane long chain, the two ends of the long chain are respectively an anticoagulative citric acid structure covalently grafted with the long chain, and a chitosan structure is selectively grafted on the citric acid structure. The preparation method comprises the following steps: firstly, adding isocyanate, polyethylene glycol and a catalyst into a reactor, and carrying out stirring reaction for 2-5 h in the presence of nitrogen; then, adding a citric acid, and heating for reacting for 12-18 h, so that a citric acid modified polyurethane is obtained; and activating the citric acid modified polyurethane by using carbodiimide, and soaking the obtained object into a chitosan-acetic acid solution to carry out acid-amide condensation reaction, so that the modified biocompatible polyurethane is obtained. According to the citric acid and chitosan modified biocompatible polyurethane disclosed by the invention, the citric acid structures with biocompatibility and the chitosan structure are covalently bonded in the polyurethane long chain, so that the polyurethane has good chemical stability and biocompatibility, and can be used as a biomedical material; and the preparation method has the advantages of simple and easily-controlled process, low cost, and the like.