167 results about "Sodium cyanate" patented technology

The invention provides an early-strength water reducer for recycled aggregate concrete, which is suitable for the field of building materials. The the early-strength water reducer comprises the following raw materials by weight percent: 20-25% of a polycarboxylic acid water reducer, 1-6% of tri-isopropanolamine, 0.5-2% of triethanolamine, 5-15% of sodium sulfocyanate, 3-10% of calcium formate, and 42-70.5% of water. The early-strength water reducer provided by the invention is low in dosage, good in early-strength effect, free from chloride ions, resistant to the corrosion of steel bars, suitable for recycled concrete, and capable of enhancing the early strength of a recycled concrete product and improving the peaceability of a recycled concrete mixture.

The invention relates to metal oxide semiconductor 2 (MoS2), in particular to a graphene/MoS2 nano self-lubricating composite material and a preparation method thereof. The composite material is prepared through the following steps that: graphene oxide nanosheets are placed into mixed solution which is formed by molybdate, sodium thiocyanate, sodium chloride and deionized water to obtain mixed solution 1, the pH value of the mixed solution 1 is adjusted through hydrogen chloride (HCl) and sodium hydroxide (NaOH) to 1 to 6, the mixed solution 1 is transferred to a hydrothermal reactor which is lined with polytetrafluoroethylene after being ultrasonically treated and uniformly mixed, the mixed solution 1 has hydrothermal reaction under 180 to 200 DEG C after the reactor is well sealed, products are centrifuged and collected after 24 to 48 hours, the products are washed by the deionized water and the absolute ethyl alcohol, and the dried products are heat treated for 2 hours under 800 to 900 DEG C under the protection of the nitrogen (N2)/hydrogen (H2) atmosphere to obtain the graphene/MoS2 nano self-lubricating composite material.

The invention relates to a preparation method of a low-toxic environment-friendly type novel precious metal beneficiation agent. Raw materials of the low-toxic environment-friendly type novel precious metal beneficiation agent comprise a cyanate, sodium hydroxide, sodium sulfate, sodium ferrocyanide, a bromide, and a lead salt. The preparation method comprises following steps: sodium cyanate, sodium hydroxide, sodium sulfate, and sodium ferrocyanide are mixed at a certain ratio; an obtained mixture is delivered into a smelting pot which is heated to be slightly red, and is heated to 650 to 750 DEG C so as to obtain a fused material, temperature is maintained to be 750 DEG C for 30 to 50min of reaction, and then an obtained product is collected and cooled; the obtained product is smashed, the bromide and the lead salt are added for stirring, and the environment-friendly type precious metal beneficiation agent is obtained via combination. The environment-friendly type precious metal beneficiation agent can be widely used for precious metal beneficiation metallurgy of nonferrous metals ores, contains no hypertoxic compounds, is safe for human and animal, and is friendly to the environment. Compared with other metal beneficiation agents, the environment-friendly type precious metal beneficiation agent is excellent in effects, stable in performance, and low in production cost; the preparation method is simple; and environmental protection can be realized.

The invention provides a gold extracting agent and a preparation method thereof, and belongs to the technical field of gold extraction. The gold extracting agent comprises the raw material components in parts by weight: 12-12.4 parts of sodium hexametaphosphate, 7-7.4 parts of sodium cyanate, 9.4-9.8 parts of sodium ferrocyanide, 10.3-10.7 of sodium sulfide, 13.3-13.7 parts of sulphur, 10.4-10.8 parts of sodium bromide, 6.3-6.7 parts of sodium chloride, 8.2-8.6 parts of manganese dioxide, 11.8-12.2 parts of urea, and 9.3-9.7 parts of industrial sodium carbonate. The gold extracting agent is alkaline, and has the advantages of low toxicity, environmental protection, short leaching time and convenient transportation and keeping and the like; in addition, the gold extracting rate is high; and the gold extracting agent is quite suitable for use as a novel gold extracting agent for heap leaching, pond leaching and carbon paste production processes of micro-fine particle gold-containing oxidized ores.

The invention relates to a salt bath formula for treating a high-speed steel air conditioning compressor blade by salt bath nitriding treatment and a treatment method. The salt bath formula comprises the following compositions in percentage by weight: 15-25 percent of potassium cyanate, 5-20 percent of sodium cyanate, 3-10 percent of lithium carbonate, 8-20 percent of sodium carbonate, 10-40 percent of potassium carbonate and 1-10 percent of sodium chloride. The invention has the advantages that because Li ions and Cl ions are added in the formula, the melting point of salt bath is lowered, and nitridation can be carried out under lower temperature; the activity is favorable, and good appearance and good diffusion layer thickness can be achieved without introducing ammonia; and the K/Na concentration proportion is enhanced, and a white layer is not easy to form on the surface of a workpiece.

The invention discloses a preparation method of a special antibacterial wool fiber for a wool hat. The preparation method comprises the steps of dipping the wool fiber in acetone, airing after washing, adding into a mixed aqueous solution of sodium cyanate and hydrogen peroxide, airing after dipping, and irradiating through an ultraviolet light to obtain a pretreated wool fiber; adding thiourea, urea and butyl titanate into absolute ethyl alcohol for mixing, adjusting a pH value, adding deionized water for stirring until a Tyndall effect occurs, standing for ageing, drying, grinding, and calcining to obtain modified nanometer titania; adding chitosan into an acetic acid aqueous solution, adjusting a pH value, adding the modified nanometer titania, adjusting a system pH value, adding glutaraldehyde after temperature rising, standing for reacting, centrifuging, washing, and drying to obtain modified chitosan; adding the modified chitosan, a plant extract, beta-cyclodextrin and a silane coupling agent KH-550 into the deionized water, and stirring to obtain an antibacterial solution; adding the pretreated wool fiber into the antibacterial solution for padding processing, and baking after drying.

The invention discloses a preparation method of 2-chloro-4-amido-6,7-dimethoxy quinazoline. The preparation method comprises the following steps: 3,4-dimethoxy benzaldehyde is taken as an initial raw material, then the following reactions are sequentially carried out: oxidizing reaction between the 3,4-dimethoxy benzaldehyde and oxydol, nitration reaction between the 3,4-dimethoxy benzaldehyde and nitric acid, reduction reaction of the 3,4-dimethoxy benzaldehyde and hydrogen ion obtained by iron powder and hydrochloric acid, reaction between the 3,4-dimethoxy benzaldehyde and sodium cyanate, chlorination reaction between the 3,4-dimethoxy benzaldehyde and phosphorus oxychloride, ammoniation reaction between the 3,4-dimethoxy benzaldehyde and ammonia liquor, etc., then the 2-chloro-4-amido-6,7-dimethoxy quinazoline is obtained. The synthetic method takes the commercialized 3,4-dimethoxy benzaldehyde as the initial raw material, and potassium permanganate is not used in the oxidizing reaction process, organic solvents (glacial acetic acid, DMF) are not used in the refining process, the noxious solvent N, N-amino dimethylbenzene or the organic solvent N, N-dimethyl formamide with high boiling point is not used in the chlorination process, so the use amounts of the organic solvents and the phosphorus oxychloride are reduced, thus reducing the production cost, simplifying the production process, protecting the health of operators, reducing 'three wastes' pollution, protecting the environment and greatly improving the reaction yield and the production efficiency.

The invention discloses an antibacterial mildew-resistant finishing agent for wool caps. The antibacterial mildew-resistant finishing agent comprises, by weight, 2-10 parts of sodium cyanate, 2-10 parts of hydrogen peroxide, 10-35 parts of modified chitosan, 2-10 parts of eucommia extract, 3-9 parts of bamboo leaf extract, 1-5 parts of cortex dictamni extract, 2-10 parts of pomegranate peel extract, 3-16 parts of radix lithospermi extract, 3-18 parts of beta-cyclodextrin, 0.1-1.2 parts of transglutaminase, 1-5 parts of amino siloxane, 2-10 parts of citric acid and 2-4 parts of hydrophilic surfactant. The antibacterial mildew-resistant finishing agent can endow the wool caps with excellent antibacterial performance and mildew resistance, feltability of the wool caps is lowered, and the woolcaps are enabled to be soft in hand feel and gentle in gloss.

The invention provides a method for preparing a D-(+)-biotin intermediate. The method comprises the steps of: taking L-cysteine monohydrochloride as a starting material; using benzaldehyde and sodium cyanate as a ring closure reagent to synthesize (7aR)-3-phenyl-6-benzyl-1H, 3H-imidazo[1, 5-C]thiazole-(6H, 7aH)-5, 7-dione through the cyclization; then utilizing benzyl bromide to perform benzyl protection on N atoms; then taking zinc as a reducing agent to perform ring-opening synthesis on N, N-dibenzyl-L-sulfhydryl hydantoin; introducing a side chain through an esterification reaction with monomethyl adipate acyl chloride; and taking titanium as the reducing agent to perform reductive ring closure to generate the intermediate. According to the method, the cheap and readily available sodium cyanate is used as the ring closure reagent to replace sodium isocyanate which is toxic and difficult to purchase in an original method, reaction conditions are optimized and reaction order is adjusted, so the disadvantages of harsh reaction conditions and low yield in the original method of ring opening first and then benzyl protection are overcome by the method of performing benzyl protection on the N atoms of an imidazole part first and then performing ring opening; and the total yield reaches 34.0-38.0 percent.

The invention discloses a synthesis and post-treatment method of high-purity N-carbamylglutamic acid and belongs to the field of organic chemistry and fine chemical engineering. According to the method, sodium glutamate and sodium cyanate are adopted as raw materials to prepare N-carbamoyl sodium glutamate, acidification is performed with sulfuric acid after reaction is completed, then heating is performed to 40-50 DEG C, and filtration is performed to obtain a high-purity product after even stirring; a mother solution is cooled to 0-5 DEG C, a byproduct sodium sulfate decahydrate is obtained through filtration, the mother solution is regulated to be neutral with a sodium hydroxide solution for recycled usage. The problems of high cost, low purity, difficult wastewater treatment and the like in the N-carbamylglutamic acid production process are solved, the product purity is up to 99% or above, and a feasible way is provided for industrial production of the N-carbamylglutamic acid.

A method for diffusing titanium and nitride into a base material having a coating thereon using conventional surface treatments or coatings. The method generally includes the steps of providing a base material having a coating thereon; providing a salt bath which includes sodium dioxide and a salt selected from the group consisting of sodium cyanate and potassium cyanate; dispersing metallic titanium formed by electrolysis of a titanium compound in the bath; heating the salt bath to a temperature ranging from about 430° C. to about 670° C.; and soaking the base material in the salt bath for a time of from about 10 minutes to about 24 hours. In accordance with another aspect of the present invention, titanium and nitride may be diffused into a base material without a coating. The treated base material may further be treated with conventional surface treatments or coatings.

The invention discloses an environment-friendly high-efficiency gold leaching agent synthesis method. The environment-friendly high-efficiency gold leaching agent synthesis method comprises the specific steps that iron salt, sodium cyanate and sodium carbonate are mixed and placed in a reactor, the reaction atmosphere is controlled according to the volume ratio of N2: CO2: O2 being [5-25]:[5-30]:[45-90], slowly heating is carried out to reach 400-900 DEG C, the temperature is kept for 10-50min, and cooling is carried out to normal temperature to obtain an environment-friendly high-efficiency gold leaching agent; and the mass ratio of iron salt, sodium cyanate and sodium carbonate is [2-30]:[40-85]:[5-40]. According to the environment-friendly high-efficiency gold leaching agent synthesis method, by controlling the reaction atmosphere, the metathesis reaction in the high-temperature process can be effectively reduced, the utilization rate of reactants is greatly improved, the generationof cyanate is promoted, the chelation of cyanate and iron salt is catalyzed, the generation of cyanide is inhibited, so that the total cyanide concentration in gold leaching tail liquid is greatly reduced, and the leaching rate is ensured.

The invention discloses a clean production process of m-carbamidoaniline hydrochloride. The clean production process comprises the following steps of: dissolving m-phenylenediamine into a sodium chloride salt water reaction system; adding an auxiliary agent into the reaction system; controlling a reaction temperature at -5 DEG C to 25 DEG C; then adding sodium cyanate and hydrochloric acid for reaction; and after the reaction is completed, carrying out post-treatment on a resulting substance to obtain m-carbamidoaniline hydrochloride, wherein the auxiliary agent is nitric acid or nitrate. According to the clean production process, salt water, instead of pure water, is used as base water, m-carbamidoaniline hydrochloride produced in the reaction can be separated out in time by using salt precipitation effects of sodium chloride, a byproduct diurea is not generated, the purity of the obtained m-carbamidoaniline hydrochloride is more than 98%, the yield is more than 95%, the content is 75%-80%, the sewage quantity is reduced by 50%, and the process is simple and high in automation degree.

The invention discloses an environment-friendly gold leaching agent, which comprises the following components in parts by mass: 20-60 parts of urea, 5-20 parts of thiourea, 8-40 parts of sodium cyanate, tetraoxide 5-25 parts of triiron, 5-30 parts of sodium carbonate, 20-30 parts of sodium hydroxide. The environment-friendly leaching agent of the present invention comprehensively utilizes the cooperation between sulfur urine and iron ions, the coordination of nitrogen atoms in urea and Au3+ to produce a new mixture, and the reaction of urea and salts to generate soluble gold cyanate. The multiple action mechanisms of gold make it electrochemically react with the gold in the ore under the environment of the inhibitory control agent, thus becoming a new type of gold leaching agent with fast gold leaching speed, good leaching effect and high recovery rate of gold in the ore dressing agent. Environmentally friendly leaching agent.

The invention discloses a flotation separation method of refractory lead-zinc sulfide ore and a sphalerite inhibitor of the refractory lead-zinc sulfide ore, the sphalerite inhibitor is a composition of calcium hypochlorite and carbonized sodium cyanurate, the mass ratio of calcium hypochlorite to carbonized sodium cyanurate is 1: (2 to 4), and the inhibitor composition can have a strong inhibition effect on sphalerite. The invention further provides a flotation separation method of the refractory lead-zinc sulfide ore, the refractory lead-zinc sulfide ore is subjected to ore grinding and grading treatment and size mixing, a sphalerite activating agent, a flotation collecting agent and a foaming agent are added, then inflation flotation is conducted, lead-zinc bulk concentrate dense underflow is obtained through regrinding and thickening, and the sphalerite inhibitor and a galena collecting agent are added for flotation separation; and the separated lead rough concentrate is subjected to sphalerite inhibition and repeated concentration to obtain lead concentrate, the galena collecting agent is added into the separated lead rough concentrate for repeated lead scavenging to obtain zinc concentrate, and therefore the refractory lead-zinc sulfide ore is economically and efficiently separated and enriched, and the method has wide industrial application prospects.

The invention provides a blood virus RAN protective agent and a blood sampling tube. The blood virus RAN protective agent is prepared by dissolving the following components in DEPC (diethyl pyrocarbonate) solution 100-500mg/ml glycine, 1-5mg/ml aprotinin, 1-5mg/ml wortmannin, 10-40mg/ml glutathione, 100-500mg/ml sodium thiocyanate, 1-3mg/ml anticoagulant and 5-20mg/ml membrane protective agent. The blood virus RAN protective agent provided by the invention is capable of supplying long-term protection to virus RNA in blood under room temperature, preventing degradation and pollution of virus RNA and effectively guaranteeing accuracy and validity of blood sample.

The invention discloses an environment-friendly gold and silver leaching agent and a preparation method thereof. The leaching agent is prepared from, by weight, 1-60 parts of sodium cyanate, 1-15 parts of sodium chloride, 1-60 parts of carbamide, 1-40 parts of potassium ferrocyanide, 1-40 parts of tetrasodium hexacyanoferrate, 1-50 parts of soda and 1-15 parts of sodium thiosulfate. The preparation method of the leaching agent comprises the steps that the materials are prepared according to a proportion, and added into a mixing agitator to be evenly stirred, and then the mixture enters a stainless steel reaction still to be subjected to a high-temperature reaction for 3.5 h to 5.5 h at the temperature of 450 DEG C to 860 DEG C; and the mixture is crushed into the size of 0.1 cm to 2 cm through a crusher after being discharged and cooled, and the product is weighed and filled to from a finished product after being inspected to be qualified. According to the environment-friendly gold and silver leaching agent, no harmful or toxic ingredients are included in the product, the leaching rate is high, the applicable mine types are wide, and the raw materials are easy to buy; the technological process of production is short, cost is low, and the product quality is easy to control; and the leaching agent is nonhazardous to production personnel and livestock, and pollution to the ecological environment is avoided.

An improved method is provided for diffusing titanium and nitride into a base material comprising a steel or steel alloy. The composition of the base material generally comprises at least one of the following: more than about 1.95% vanadium, less than about 4.1% chromium, and a presence of cobalt. The method generally includes the steps of providing such a base material; providing a salt bath which includes sodium dioxide and a salt selected from the group consisting of sodium cyanate and potassium cyanate; dispersing metallic titanium formed by electrolysis of a titanium compound in the bath; heating the salt bath to a temperature ranging from about 430° C. to about 670° C.; and soaking the base material in the salt bath for a time of from about 10 minutes to about 24 hours.

The invention discloses a method for synthesizing 1-(2,4-dichlorophenyl)-3-methyl-4-difluoromethyl-1,2,4-triazole-5-ketone. The method takes p-chloroaniline as a raw material, through diazotization, reduction, and salt forming, p-chlorophenylhydrazine hydrochloride is synthesized, p-chlorophenylhydrazine is obtained through alkali neutralization, under condition that tert-butyl alcohol is taken asa solvent, chlorophenylhydrazine, acetaldehyde, sodium cyanate and sodium hypochlorite are subjected to condensation, cyclisation and an oxidation reaction to generate 1-p-chlorophenyl-3-methyl-1H-1,2,4-triazole-5-ketone, and the 1-p-chlorophenyl-3-methyl-1H-1,2,4-triazole-5-ketone is subjected to salt forming, reaction with chlorodifluoromethane, and chlorination to obtain the 1-(2,4-dichlorophenyl)-3-methyl-4-difluoromethyl-1,2,4-triazole-5-ketone (a sulfentrazone intermediate). The synthetic method takes p-chloroanniline as the raw material, the synthetic method is realized by only one-time chlorination, steric hindrance for intermediate synthesis is small, and the impurity is low, so that the yield is increased; in addition, the raw materials required by the synthesis route are easilyacquired, the cost is low, the condition is mild, operation is simple, security is high, and the synthesis method is in favor of realizing industrial production.