2864 results about "Sodium sulfite" patented technology

The invention discloses a temperature resistant salt tolerant high efficiency gel and a preparation method and application thereof. The preparation method is characterized in that the preparation method comprises the following steps: preparing a comb-shaped associated copolymer PAH containing macromonomers and functional hydrophobic monomers into an aqueous solution having the concentration of 0.1 to 4g / L, the crosslinking agent concentration of 0.01 to 1.0g / L, the surfactant concentration of 0.01 to 8mmol / L and the sodium sulfite thermal stabilizer concentration of 0.005 to 1.0g / L; adding the aqueous solution into a mixing container with a stirring device; stirring the aqueous solution evenly at the room temperature; regulating the pH value of the solution to be equal to between 4 and 11, and obtaining a temperature resistant salt tolerant high efficiency gel polymer solution system used for tertiary oil recovery and scavenge, displacement modification, profile modification or water shutoff. The polymer solution system has micro-crosslinking to form the gel during the flowage inside the oil reservoir. The gel has good elasticity, not easy dehydration, stable gelling performance, and excellent tackification, temperature resistance, salt tolerance, shearing resistance and ageing resistance.

The invention relates to method for preparing taurine, comprising the following steps: (1) reacting epoxy ethane with sodium sulfite under 0.05 to 0.1MPa, with pH value of 6.5 to 7.5 and at temperature between 75 and 85 DEG C to obtain hydroxyethyl sodium sulfonate; (2) carrying out ammonolysis reaction on the hydroxyethyl sodium sulfonate and liquid ammonia under 14 to 21MPa and at temperature between 160 and 280 DEG C to obtain ammonolysis solution containing sodium taurate; (3) introducing the ammonolysis solution into a single flash evaporator for primary flash evaporating at a temperature between 160 and 200 DEG C and under 1.3 to 2.0MPa; introducing the flash evaporated liquid into a secondary flash evaporating and falling film evaporator, using the primary flash vapor as a heating medium to carry out flash evaporating and falling film evaporating on the primary flash evaporated liquid in the secondary flash evaporating and falling film evaporator at a temperature between 110 and 140 DEG C and at 0.1 to 0.6MPa; evaporating and concentrating the flash evaporated liquid subjected to secondary flash evaporating and falling film evaporating with flash vapor and steam as heating media in a multi-effect flash evaporating and falling film evaporator; and (4) neutralizing the sodium taurate by sulphuric acid to obtain the taurine. The method for preparing the taurine has the advantages of short time, high yield and low cost, and is easy for industrialized production. In addition, by primary flash evaporating and secondary flash evaporating processes, almost all the ammonia and 40% to 60% of water in the flash evaporated liquid can be removed, thus having double effects of removing ammonia and condensing.

The invention discloses acrylamide modified polymer micro-crosslinking gel and a preparation method thereof. The preparation method is characterized in that the method comprises the following steps that: acrylamide modified polymer PAE containing functional macro monomer is prepared into an aqueous solution with the concentration between 0.1 and 4g / L, the concentration of crosslinking agent between 0.01 and 1.0g / L, the concentration of surface active agent between 0.01 and 8mmol / L and the concentration of heat stabilizer sodium sulfite between 0.005 and 1.0g / L; the aqueous solution is added in a mixing container with a stirring device and is stirred evenly at room temperature; the pH value of the solution is adjusted between 4 and 11 to prepare a polymer solution system of the acrylamide modified polymer micro-crosslinking gel used for tertiary oil recovery and displacement, oil displacement modification, profile modification or water plugging; and the polymer solution system undergoes micro crosslinking during flowing inside an oil layer to form the gel. The acrylamide modified polymer micro-crosslinking gel has ideal elasticity, difficult dehydration, stable performance and excellent performances on tackifying, temperature resistance, salt resistance, shearing resistance and ageing resistance.

The invention relates to a reproduction method for sodium-base flue gas desulfurization liquid, which is characterized in that the flue gas desulfurization liquid containing sodium sulphite and sodium bisulfite is oxidized to a solution containing sodium sulfate, the solution containing sodium sulfate is electrolyzed to a sodium hydroxide solution and a sulfuric acid solution by using bipolar membrane electrodialysis. According to the invention, the electrolytic conversion rate of sodium sulfate can reach more than 90%, the obtained sodium hydroxide solution can be used as absorption liquid for a flue gas desulfurization tower, the sulfuric acid by-product is produced simultaneously. By-product sulfuric acid can be used as sulfuric acid for treating high hardness and high alkalinity. The reproduction method for sodium-base flue gas desulfurization liquid is capable of achieving the purposes of strong brine zero-draining, comprehensive resource utilization and cost reduction.

The invention provides a comprehensive recycling method of a waste and old lithium-ion battery, and relates to the lithium-ion battery. The method comprises the following steps of: performing explosion-proof magnetic smashing and atomized spraying smashing on the waste and old lithium-ion battery, thereby separating an outer shell and a battery material; carbonizing and roasting in a constant-temperature roaster at high temperature and under negative pressure, thereby removing an isolated membrane and a cathode; recycling the outer shell and an anode material in a grading manner by using a centrifugal disintegrator, thereby separating the outer shell and the anode material containing nickel and cobalt; leaching out by adding sodium sulfite into H2SO4 at the normal pressure by utilizing the characteristics of the anode material; regulating the pH value by adding carbonate into an leaching liquid; preliminarily removing Ca and Mg by adding a fluoride salt; extracting and removing impurities by using P2O4, thereby removing the impurities such as Fe, Cu, Zn, Ca, Mg and the like; performing selective extraction for cobalt-nickel separation by using P507, thereby obtaining a high-purity nickel sulfate solution and a high-purity cobalt sulfate solution in which the content of the Fe, the Cu, the Zn, the Ca and the Mg is respectively less than or equal to 2.0mg / L. The method is efficient, simple and convenient and low in production cost, and has wide applicability and a high additional value.

The invention relates to a gel plugging agent for deep profile control of a higher temperature oil reservoir, and a preparation method of the gel plugging agent. The gel plugging agent comprises 0.3-0.8 percent of nonionic polyacrylamide, 0.6-1.3 percent of a cross-linking agent A, 0.45-1.44 percent of a cross-linking agent B, 0.02-0.04 percent of a temperature stabilizer and 0.01-0.08 percent of a pH value regulator, wherein the cross-linking agent A is methenamine; the cross-ling agent B is hydroquinone or resorcinol; the temperature stabilizer is sodium thiosulfate, sodium bisulfite or sodium sulfite; and the pH regulator is sodium hydroxide, potassium hydroxide, sodium carbonate or sodium bicarbonate. The gel plugging agent disclosed by the invention has strong temperature resisting performance and can be used for the profile control operation of the high temperature oil reservoir with 100-160DEG C; the gel plugging agent has the characteristics of high strength after being gelatinized, stronger plugging capability for the stratum and favorable thermal stability; and in addition, after the gel plugging agent is stood at the temperature of 130 DEG C for 90 days, the strength change is little and gel breaking and hydration are avoided.

The invention discloses a deep desulfurization method of sulfate acid tail gas. The method additionally arranges a desulfurization tower behind a second adsorption tower of a sulphuric acid device; after the waste gas discharged from the second adsorption tower enters the desulfurization tower, an ammoniation absorbent is used for adsorbing SO2 in the waste gas to generate ammonium sulfite; the tail gas after the desulfurization passes through a demisting layer in the tower to eliminate acid fog; the purified tail gas is discharged through a chimney at high altitude; the ammonium sulfite in the absorbent is aerated and oxidized to be ammonium sulfate solution at the bottom of the tower; and after the concentration of circulation liquid ammonium sulfate meets the requirement, the circulation liquid ammonium sulfate is sent to a follow-up process to be processed and used. The deep desulfurization method of sulfate acid tail gas can cause the concentration of the SO2 in the tail gas to be lower than 100mg / m<3> in a standard state, greatly reduces the emission of the SO2 in the tail gas, is beneficial to the improvement of the atmospheric environment quality, meets the construction principles of energy conservation, emission reduction and sustainable development and has good social benefits; in addition, the deep desulfurization method can increase the recovery amount of the ammonium sulfate, and has certain economic benefits.

The invention relates to a beneficiation method, in particular to a beneficiation method for separating the polymetallic sulphide ore containing copper, lead, zinc and tin. The method comprises the following steps: (1) carrying out ore grinding on the raw ore before carrying out bulk flotation on copper, lead and sulphur, using diethyl mixed with xanthate as collecting agent of copper and lead mineral, using zinc sulphate and sodium sulfite as inhibitor of zinc mineral; (2) carrying out phase-2 ore grinding and selection; (3) separating copper, lead and sulphur, using sodium sulfite and sodium thiosulfate as the inhibitor of the lead and sulphur mineral, using Z-200 as collecting agent for separation and scavenging and then carrying out lead flotation after the separation and scavenging; (4) carrying out zin flotation on the bulk flotation tailings; and (5) finally, carrying out reselection on the zinc flotation tailings to recover tin. The metalliferous mineral of the invention has the advantages of good separating effect, high metal recovery rate, more complete comprehensive recovery of useful minerals, low cost of medicament, simple method, easy operation and energy conservation.

The invention discloses a method for desulfurizing high-concentration flue gas. The high-concentration flue gas is desulfurized through a sodium sulfite method, and meanwhile, the sodium sulfite is recovered as a by-product, wherein the flue gas needs to be deoxidized before being desulfurized through the sodium sulfite method. In the method for desulfurizing high-concentration flue gas disclosedby the invention, by deoxidizing the flue gas through an appropriate pretreatment process, the purity of the by-product sodium sulfite produced by the subsequent flue gas desulfurization process of the sodium sulfite method can be obviously improved, and the value of the by-product is improved, thereby obviously improving the comprehensive economic benefits. The pretreatment process of the flue gas is performed by using the sulfite and / or the hydrosulfite produced by the reaction of SO2 contained in the flue gas and alkali to react with oxygen without using any other deoxidizer. The method disclosed by the invention has simple production process and is easy to operate.

The invention relates to a copper-zinc separation beneficiation method which comprises the following steps: (1) primary grinding, that is, adopting a combined depressant comprising lime, sodium sulfide, zinc sulfate, and sodium sulfite under the condition that the size and the content of grinding particles are respectively -0.074 mm and 65 to 70 percent; (2) copper rough concentrates regrinding and concentration, that is, selecting out high-quality copper concentrates which contain high-grade copper and silver, but low zinc by adopting single groove speed flotation method and continually using the combined depressant constituted by lime, sodium sulfide, zinc sulfate, and sodium sulfite, so as to realize the zinc depressing and copper flotation; (3) zinc-sulfur separation, that is, using butyl xanthate as a collecting agent to float zinc, obtaining zinc-sulphur bulk concentrate, conducting pulp conditioning by adding lime so as to depress sulfur and float copper and obtain zinc concentrates and partial sulfur concentrates, conducting the iso-flotation on the tailings and further adding the butyl xanthate to conduct flotation and obtain partial sulfur concentrate. The invention has the advantages of adopting the processes of ore blending, primary grinding, copper rough concentrates regrinding and concentration, and zinc-sulphur iso-flotation technological process, thereby better solving the problem that the copper concentrates contain too much zinc or the copper content in the zinc concentrates is over standard.

The invention relates to a process for separating and recovering selenium from a selenium-containing material. The process comprises the following steps: dissolving the selenium-containing material into a sulfuric acid solution, adding 10% H2O2 into the mixture, filtering and separating to get leachate and residue containing silver, lead, copper and other valuable metals; separating the selenium from tellurium in the oxidation leachate by using sodium hydroxide; and acidifying the selenium leachate with hydrochloric acid, adding sodium sulfite to reduce the settled selenium, washing and drying to get crude selenium with the grade of not lower than 90%. The crude selenium which is separated by the process is higher in purity and can be directly refined, so that the process flow of recovering selenium is shortened, the recovery rate of selenium is improved, the production cost is reduced and the energy is saved; and the sodium sulfite is used for substituting sulfur dioxide to perform reduction, the control is easy and the environmental pollution is further reduced. The process has very important significance in both aspects of recovering resources and protecting an environment.

The invention relates to a display and quantitative detection method of residual austenite or island martensite-austenite (MA island for short) in TRIP steel. The method comprises the steps: (1) a TRIP tapping sample is prepared into a metallographic specimen; (2) after grinding and polishing, the metallographic specimen is light etched for 5 to 8 seconds in Nital of 1 to 3 percent by weight, and water is sprinkled on a flannel polishing disk for 1 to 2 seconds; sodium pyrosulfite water solution of 1 to 3 percent by weight and picral of 2 to 6 percent by weight are mixed by volume ratio of 1:1 to prepare corrosive liquid, then the metallographic specimen is put into the corrosive liquid for etching of 55 to 65 seconds; (3) the structure of the TRIP steel is observed under a metallurgical microscopy: the delta ferrite is minus blue, the residual austenite or MA island is white, and bainite is brownish-black; and (4) each phase in the structure is carried out quantitative analysis. The method presents different colors, each phase of structure has distinct layers which are easy to distinguish; and a quantitative image analysis method is utilized to fix amount of the feature object structure, which is objective and accurate and has good repeatability.

The invention discloses a brewing process of apple unblended wine and a preparation method of apple unblended series wine. The brewing process of the apple unblended wine comprises the following steps of: selecting various apples as raw materials and mixing according to the proportion to use; during fermentation, fermenting full apples without adding sodium sulfite and other antioxidants; and after fermenting for enzymolysis, adding complex peptide so as to improve the brewing efficiency and enhance the nutrition of the apple unblended wine. Compared with the traditional brewing process, the brewing process of the apple unblended wine has the advantages of high brewing efficiency, production cost saving, and the like. In addition, a series of apple wine products can be developed on the basis of high-quality apple unblended wine produced by the process, including apple sweet wine, apple foaming wine, apple brandy, apple heath-care wine and the like.

The invention discloses a composite reducing agent for dye, comprising the following compositions in weight portion: 8 to 20 portions of vat powder, 5 to 40 portions of thiourea dioxide, and 5 to 15 portions of sodium sulfite. The invention also discloses a method for dyeing by the reducing agent, comprising the following steps that: a reducing agent and sodium hydrate are used for reducing the dye by a vatting method; the weight ratio of a reducing solution to the dye is 37.5: 0.8 to 2.0 and the mixture is for later use; a leveling agent and the fiber penetrating swelling agent are added to dye or a buffering agent is added to adjust the pH value and is dyed by vat acid, the temperature is reduced and the mixture is washed; the mixture is subjected to oxidization to develop color, fixing, reducing temperature and washing; the fresh water bath is performed, the dye composite reducing agent is reduced and washed, and the temperature is reduced and the fiber penetrating swelling agent is produced. The composite reducing agent for the dye is a special reducing agent used for reducing the dye, a sulfur dye, a perylene dye and a leuco body, and improves the stability of the leuco body, color yield percentage, the color reproducibility, the color fixation and the color evenness degree, meanwhile, the dye composite reducing agent avoids the harm of formaldehyde on the environment and the human body.

The invention relates to a pemetrexed disodium lyophilized powder injection, which consists of pemetrexed disodium, mannitol and sodium sulfite in the following weight portions: 50 portions of the pemetrexed disodium, 10 to 50 portions of mannitol, and 0.1 to 1 portions of sodium sulfite; and the pH value of the pemetrexed disodium lyophilized powder injection is between 7.0 and 8.0. The process for preparing the pemetrexed disodium lyophilized powder injection comprises the following steps: placing the mannitol in a sterile chamber; adding 80 percent of water for injection into the sterile chamber to dissolve the mannitol; adding the sodium sulfite to the mixture after the water for injection is cooled to a temperature of between 15 and 25 DEG C, and evenly stirring the solution for dissolving the sodium sulfite; then, adding the pemetrexed disodium into the solution, and stirring the solution to completely dissolve the pemetrexed disodium and evenly mixing the pemetrexed disodium, and adjusting the pH value of the solution to between 7.0 and 8.0; decarbidizing; after an intermediate compound passes examination, carrying out volume fixing, filtering, filling, partially stopping, traying, lyophilizing, nitrogen aerating, stopping and unboxing, sealing by a plastic-aluminum combined cap, and packaging after passes quality inspection to obtain the pemetrexed disodium lyophilized powder injection. The invention has the advantages of simple preparation process, convenience and practicality, good repeatability and low production cost, and can realize industrial large-scale production easily.

The invention relates to a method for dyeing cotton fibers by using a natural dye, comprising the following steps of: 1) boiling the cotton fibers and drying the cotton fibers for later use; 2) modifying the cotton fibers; 3) dyeing the cotton fibers; and 4) fixing the color of the cotton fibers, wherein the dosage of a color fixing agent is 1-5% of the mass of the cotton fibers, the temperature of color fixation is 50-85 DEG C, the color fixing agent is added to the cotton fibers obtained in step 3), the time of color fixation is 20-50 min, drying is performed after water washing, and the color fixing agent can be one or two of sodium chloride, sodium sulfite, citric acid and aluminum potassium sulfate dodecahydrate. The food-grade fixing agent is selected in the method; therefore, the troubles caused by synthetic dyes and heavy metals for the health of human are solved, and the fastness of the cotton fibers can be enhanced; as a result, the dyed cotton fibers are natural and soft in color and have no harm to the human body and the environment.

The invention relates to a nitrogen foam fracturing fluid for coal bed methane and a preparation method of the nitrogen foam fracturing fluid. The nitrogen foam fracturing fluid comprises a gas phase and a fluid phase, the gas phase is nitrogen, the fluid phase is an aqueous solution which contains 0.20-0.50 wt.% of a foaming agent, 0.4-1.0 wt. % of a foam stabilizer and 0.10-0.30 wt.% of a gel breaker, the volume ratio of the gas phase to the fluid phase is (2-4):1, and corresponding foam mass is 65%-80%; and the foaming agent is a compound system which is composed of sodium dodecyl sulfate and N-(2-hydroxypropyl) perfluor caprylamide according to the mass ratio of (8-10):1, the foam stabilizer is C16-C20 lauryltrimethylammonium chloride, and the gel breaker is a redox system which is composed of ammonium persulfate and sodium sulfite according to the mass ratio of (1.0-2.0):1. A foam generator is used for obtaining the nitrogen foam fracturing fluid. The nitrogen foam fracturing fluid has the advantages of being simple in fluid preparing, small in harm to a coal bed, low in leak-off, small in friction, rapid in flowback speed, high in sand-carrying capability and the like.

The present application includes a method for inhibiting amine degradation during CO2 capture from flue gas streams. Particularly, the present disclosure relates to a method of inhibiting O2- and / or SO2-induced degradation of amines using sodium sulfite (Na2SO3), potassium sodium tartrate tetrahydrate (KNaC4H4O6.4H2O), ethylenediaminetetraacetic acid (EDTA) or hydroxylamine (NH2OH), or analogs or mixtures thereof during CO2 capture by amines.

A formaldehyde remover for the aldehyde-contained adhesive and the flyboard is prepared from triethanolamine, sodium dimetasulfite, Na2EDTA, 2,3,4,5,6-pentahydroxy hexyaldehyde and distilled water through proportion and compounding. It has high effect on removing formaldehyde from indoor air.

The invention provides a polyethyleneimine jelly profile-control water-blocking agent. The profile-control water-blocking agent is prepared by reacting partially-hydrolyzed polyacrylamide and a cross-linking agent polyethyleneimine. The profile-control water-blocking agent comprises following components by weight: 0.3-0.8% of the partially-hydrolyzed polyacrylamide, 0.2-0.5% of the cross-linking agent polyethyleneimine and 0.3-0.8% of an additive, with the balance being water, wherein the partially-hydrolyzed polyacrylamide adopts anionic polyacrylamide, and the additive is one compound selected from a group of sodium sulfite, sodium bisulfate, and sodium hyposulfite or thiourea, or is a mixture of several compounds selected from the group. The jelly forming time of the profile-control water-blocking agent is adjustable and the jelly has high strength. The profile-control water-blocking agent can block underground water having a temperature lower than 110 DEG C and a NaCl mineralization degree of 50000 mg / L. The profile-control water-blocking agent has good temperature toleration and cannot be dehydrated for 120 days.

A method that cyanide barren solution is used for recovering the copper-lead-zinc from cyanide tailing by means of floatation belongs to the field of nonferrous metal separation. The processing procedures of the method are as following: (1) mashing: the cyanide barren solution is added into the cyanide tailing and stirred to ore slurry, the concentration of which is 35 to 40 per cent; (2) lead-zinc preferential flotation: after being stirred, the ore slurry is put into flotation machine and lime, Ethyl thiocarbamate and Sodium n-butyl xanthate synthetic are added in to the ore slurry. The course of once rough floatation, twice scavenging and twice concentration is processed to recover Zinc and Lead; (3) Cu-S separation: after the tailing of lead and zinc bulk flotation is concentrated, the cyanide barren solution is added into the tailing and the tailing is made into the ore slurry with the concentration of 35 to 40 per cent. And then, the ore slurry is put into the floatation machine and sulfate, sodium sulfite, Z-200 and ammonium butyl aerofloat are added into the tailing. The course of once rough floatation, twice scavenging and twice concentration is processed to recover copper. And the tailing can be for sale as sulfur concentrate; (4) Reuse of separation tailing water: the press filtrate of bulk concentrate, the overflow of thickener, the press filtrate of copper concentrate and the press filtrate of the sulfur concentrate return to the buffer slot of the cyanide barren solution to be used for replacement fluid. The invention has the advantages of good flotation effect, high recovery rate of the copper-lead-zinc and zero discharge of waste water and residue.

An adsorption-absorption reaction type formaldehyde removing agent is composed of adsorption-absorption agent (activated carbon, alumina, diatomite, polyamide or water) for adsorbing and absorbing the formaldehyde from indoor air, and reactant (sodium sulfite and ammonium salt or hydroxy amine hydrochloride) for reacting on adsorbed and absorbed formaldehyde to become non-toxic, no-odor and non-pollution substance.

The invention discloses a composite decarbonizing solution for gathering carbon dioxide in mixed gas, belonging to the technical field of gas separation. The composite decarbonizing solution is characterized by consisting of main absorption components including MEA and AEE, auxiliary absorption components including AHPD, AMP, TEA and MDEA, active components including PZ, HEPZ, AEP and DEA, sodium vanadate as an inhibiter, sodium sulfite and copper acetate as antioxidant, and a mixed solvent including NMP, polyethylene glycol and propylene carbonate and water. Because the mixed solvent is used for the composite decarbonizing liquid, on the one hand, the absorption capacity, the purification degree and the desorption rate are improved, and the reaction temperature range is enlarged, and on the other hand, regeneration energy consumption is greatly improved. The invention has the advantages that the composite decarbonizing solution is used for gathering carbon dioxide in various kinds of chemical reaction tail gas, burning stack gas and natural mixed gas and eliminating carbon oxide in city gas, natural gas, and the like, and has social benefit and economic benefit.

The invention relates to a processing method of thionyl chloride acyl-chlorinated tail gas. Mixed tail gas produced by a acyl chlorinating process contains hydrogen chloride and sulfur dioxide; the sulfur dioxide is liquefied under a certain temperature condition; the incondensable hydrogen chloride and a little sulfur dioxide are absorbed in two stages by water; the absorbed tail gas in a first stage is pure hydrogen chloride gas; after being absorbed in a second stage, the qualified chlorhydric acid is obtained; first-stage falling film absorption liquid is resolved by heating; then the tail gas is sent to a liquefying process again; the liquid sulfur dioxide can be canned as a product; or after being vaporized, the liquid sulfur dioxide is absorbed by 30 percent of sodium hydroxide solution to obtain sodium sulfite aqueous solution which is further dried after low temperature crystallization or distillation to obtain 97 percent of sodium sulfite solid. With the method, the hydrogen chloride, the sulfur dioxide and a little thionyl chloride produced by an acyl chlorination synthetic process can be separated out to obtain the chlorhydric acid and the pure sodium sulfite solid. The processing method of the thionyl chloride acyl-chlorinated tail gas of the invention is capable of effectively recovering the thionyl chloride acyl-chlorinated tail gas, which has the advantages of safety process and easy control.

The invention discloses an illegal cooking oil lubricant and a preparation method thereof. The illegal cooking oil lubricant comprises the following components in percentage by weight: 40%-60% of illegal cooking oil, 0.5%-1.5% of sodium sulfite, 1%-3% of sorbide oleate, 0.02%-0.04% of antioxidants, 0.2%-0.3% of extreme-pressure antiwear agents, 0.05%-0.1% of formaldehyde, 1.0%-1.2% of sodium hydroxide and the balance of water. Through the illegal cooking oil lubricant disclosed by the invention, the problem that torque and friction resistance are reduced through lubrication in the drilling process of a horizontal well is effectively solved, moreover, a new way is provided for the recycling of the illegal cooking oil, and the preparation cost of the lubricant can be reduced.

The invention relates to a preparation method of a stable iodized plant oil fatty acid ethyl ester, which firstly puts the plant oil into ester exchange reaction with alcohol with the effect of salt catalyst so as to produce plant oil fatty acid ethyl ester which is then put into addition reaction with hydrogen iodide to produce the iodized plant oil fatty acid ethyl ester, then heating and air ventilating methods are used for eliminating unstable iodine being combined in the iodized plant oil fatty acid ethyl ester, and lopsidedness sodium sulfite solution is used for liquid seal of the separated free iodine so as to obtain the iodized plant oil fatty acid ethyl ester with good stability; the preparation method is characterized by small viscosity, good stability and low cost.

The invention discloses a whitening cosmetic composition which comprises, by weight percentage, 0.01-5.00% of glycyrrhiza glabra extract, 0.1-10.00% of whitening compound, 0.01-10.00% of citrus peel extract and 75.00-99.85% of cosmetic auxiliary material substrate, wherein the whitening compound comprises water, butanediol, arbutin, citric acid, sodium sulphite, acetyl tyrosine, saxifraga sarmentosa extract, peony root extract, amino-propanol ascorbic acid phosphate ester, radix scutellariae root extract, glutathione and hydrolyzed mirabalan. The whitening cosmetic composition contains the glycyrrhiza glabra extract, the whitening compound and the citrus peel extract, and the composition has safe and efficient skin whitening effects.

The invention relates to a plugging agent for deep profile control and water plugging and a preparation method thereof. The plugging agent comprises the following raw materials in percentage by weight: 0.10-0.30% of partially hydrolyzed polyacrylamide, 0.09-0.20% of potassium dichromate, 0.15-0.30% of sodium sulfite, 0.08-0.3% of hexamethylenetetramine, 0.06-0.24% of phenol, 0.04-0.14% of ammonium chloride and the balance of water. The invention also provides the preparation method of the plugging agent. The variation of the gelatinization strength of the plugging agent system along with time is in an obvious double-step trend. Thus, the plugging agent can be effectively prevented from leaking into a low-permeability layer in the injection process, and can effectively plug a high-permeability stratum when the plugging agent reaches the deep stratum.

The present invention relates to a graphene oxide / silver complex antibacterial material, the material is a chelate of silver organic or inorganic complex with graphene oxide. The structure formula of the material is as shown in the specification. The preparation method for the graphene oxide / silver complex antimicrobial material comprises the following steps: (1) dispersing graphene oxide powder into deionized water, obtaining a graphene oxide dispersion by ultrasonic fully releasing, adding a large pi bond water-soluble organic substance into the graphene oxide dispersion and mixing completely with ultrasound; (2) dissolving silver nitrate in water and adding sodium sulfite or sodium citrate into the solution to obtain a silver complex after the reactions; and (3)mixing the graphene oxide water solution obtained in step (1) with the silver complex obtained in step (2), and after the reaction, filtering the solution to obtain a precipitate. The stability of the graphene oxide is enhanced by combining small molecules formed by silver and the organic or inorganic complex with the graphene oxide. The anti-bacterial property is prolonged through a slow release performance.