124 results about "Low chloride" patented technology

The invention relates to an early strength fast hardening terminated anchor mortar material, which is characterized in that the material is formed by mixing and stirring cement, sand, porous fine sand, finely ground steel slag powder, fly ash, an early strength agent, rubber powder, silicon ash, a water reducing agent and an excitant. The parts by weight of the components are as follows: 100 parts of cement, 30-250 parts of sand, 5-25 parts of porous fine sand, 5-30 parts of finely ground steel slag powder, 10-30 parts of fly ash, 0.1-3 parts of early strength agent, 1-10 parts of rubber powder, 0-8 parts of silicon ash, 0.2-2 parts of water reducing agent and 1-5 parts of excitant. Finely ground converter slag which is naturally stored for 3-6 months is adopted for the finely ground steel slag powder and the specific surface area is 400-800m/kg; the content of magnesium oxide is 8-15%; the porous fine sand is shale ceramic sand or fly ash ceramic sand or the mixture of the shale ceramic sand and the fly ash ceramic sand based on random mixture ratio, with grain size of 0.10-2.6mm. The material provided by the invention has good mechanical property and adhesive property, low chloride ion content and shrinkage property, and high impermeability and anti-cracking performance, thereby preventing the prestressed reinforcement of track slabs from rusting.

The invention relates to the field of hydrometallurgy, in particular to a preparation method of low-chloride high-purity germanium dioxide. According to the process, coarse germanium tetrachloride is subject to repeated steaming and rectification to obtain high-purity germanium tetrachloride, and a brand new method is adopted in the hydrolysis section of the high-purity germanium tetrachloride, wherein high-purity nitrogen is adopted for gasifying the high-purity germanium tetrachloride into germanium tetrachloride gas, then the germanium tetrachloride gas is led into a special hydrolysis device, vacuum filtration and germanium dioxide washing are carried out after hydrolysis is finished, then germanium dioxide is dried, the germanium dioxide is dried secondly, and drying is carried out secondly. The low-chloride high-purity germanium dioxide obtained through the process method has the beneficial effects that the purity can reach 99.9999% or above, the chlorine content is lower than 0.0030%, and the germanium dioxide direct recovery rate reaches 92.0% or above.

The invention discloses an activated sludge culture method suitable for high-salt sewage, and the culture method comprises the following steps of: (1) aeration; (2) intermittent water charging to improve chloride ion loading; (3) continuous water charging. Sewage with a low chloride ion concentration is cultured firstly; after activated sludge suitable for the low chloride ion concentration is successfully cultured, the chloride ion concentration is increased gradually (intermittent water charging); after activated sludge suitable for a high chloride ion concentration is generated, the hydraulic loading is increased (continuous water charging), and thus activated sludge which can treat high-salt sewage is obtained. The method can culture activated sludge which can treat sewage with a chloride ion concentration of below 7000 mg/L; the sludge concentration reaches 2500-4000 mg/L; certain removing effect on COD, TN, ammonia nitrogen, and the like is realized; and the effluent quality meets the national discharge grade one B standard. The invention effectively solves the problem of difficult biochemical treatment of high-salt municipal sewage in coastal regions, and has the characteristics of simple culture and low cost.

An apparatus for the selective production of electrolyzed water is provided, wherein the apparatus allows for the production and discharge of either electrolyzed acidic water or electrolyzed basic water to be independently without the corresponding production and discharge of the other. In certain embodiments, the present invention can provide a low chloride electrolyzed acidic water or a low chloride electrolyzed basic water.

The invention relates to a device and a method for oxidizing and removing elemental mercury by using wet flue gas desulfurization wastewater. The device comprises a boiler, wherein the boiler is connected with a SCR (Selective Catalytic Reduction) denitration device through a coal economizer; the SCR denitration device is connected with a limestone-gypsum wet desulphurization tower through an air pre-heater and a dust remover; a chimney is arranged on the limestone-gypsum wet desulphurization tower; atomizing nozzles are distributed in a flue between the coal economizer and the SCR denitration device; the atomizing nozzles are connected with a desulfurization wastewater tank through a slurry pump; an air compressor is connected with the atomizing nozzles and used for supplying compressed air for the atomizing nozzles in the atomizing process. By virtue of the device and the method, the problem that combustion low-chloride coal elemental mercury is difficultly discharged is solved, and the problem of treatment of the desulfurization wastewater is solved.

The invention relates to the manufacture of titanium hydride powder using continuous or semi-continuous process, and using titanium slag or synthetic rutile as raw materials, while hydrogen, titanium tetrachloride, titanium trichloride, titanium dichloride, and hydrogen chloride are participate as intermediate reaction products. The continuous comprises: (a) reduction of TiCl₄ to low titanium chlorides followed by cooling a mixture, (b) separating of residual TiCl₄ from solid low chlorides by heating the mixture in argon or vacuum up to 150° C. followed by removing the titanium tetrachloride from the mixture, (c) dissociation of TiCl₃ to TiCl₂ at 450° C. in vacuum followed by removal of gaseous titanium tetrachloride from the reaction zone, condensation to the liquid, and returning back into the reaction retort, (d) dissociation of TiCl₂ in vacuum at 750-850° C. to manufacture fine powder of metallic titanium and titanium tetrachloride, whereby hydrogen heated up to 1000° C. is used to accelerate this reaction, and (e) saturation of the fine titanium powder by hydrogen at 400-640° C. to manufacture final product of titanium hydride powder which is free of oxygen or nitrogen. The semi-continuous process includes the Kroll's process as the very first step.

The invention relates to a low-chloride phosphorus potassium fertilizer and a preparation method thereof, in particular to a method for preparing the low-chloride phosphorus potassium fertilizer by melting and sintering potassium chloride, phosphorite powder and quartz sand, and the invention belongs to the production field of phosphorus potassium compound fertilizer. In the method, the potassium chloride, the phosphorite powder, the quartz sand or diatomite, insoluble potassic ore and boric anhydride are used as raw materials; coal, heavy oil or natural gas are used as fuel; or an electric cooker is used as a high-temperature heat source; and the phosphorus potassium fertilizer is produced by melting and sintering in steam atmosphere. The reaction is carried out in a blast furnace, an open hearth or the electric cooker, and the melting temperature is 800-1600 DEG C. The method produces the phosphorus potassium fertilizer by the potassium chloride and the phosphorite powder directly and has simplified process; the prepared phosphorus potassium fertilizer has high total nutrient and the low content of chloride and can be used for chlorophobic crops; the phosphorus potassium fertilizer contains two elements of phosphor and potassium required by the crops in large amount at the same time; the percentage content of K2O is 10%-18%; the percentage content of P2O5 is 15%-30%; the content of chlorine ion is less than 3%; and the total nutrient is 30%-45%.

The invention relates to a snowmelt agent, which is a composite snowmelt agent and comprises the following components and contents (weight) in percentage by weight: 80 to 95 percent of acetate and 5 to 20 percent of chloride. Compared with the prior art, the snowmelt agent has good snow removing effect and low chloride content, can reduce the corrosivity of the snowmelt agent obviously, effectively protects pavement and bridges, prolongs the service life of public facilities and reduces the cost while achieving excellent snow removing effect.

The invention discloses a method for treating waste water polluted by composite chlorophenol with coordination of visible light-laccase, comprising the following steps: regulating the pH value of waste water polluted by the composite chlorophenol; mixing the laccase and the waste water to be treated, and carrying out the following processes such as photocatalysis treatment, light-tight treatment,photocatalyst extraction, filter, separation and recovery and the like. The laccase is utilized to catalyze low chloride chlorophenols in the waste water to enable the low chloride chlorophenols to fast aggregate to form sedimentation; and high chloride chlorophenols in the waste water are treated by photocatalysis and oxidation through visible lights to achieve the purpose of completely purifyingcomposite chlorophenol waste water with high efficiency.

The invention belongs to the technical field of wet metallurgy, in particular relates to a method for purifying and separating chloride ions from a chlorine-containing zinc sulfate solution generated in a zinc electrolyzing process. The method comprises the following steps: (1) forming an organic extraction phase by using trialkyl tertiary amine, octyl alcohol and sulfonated kerosene 260 #, and stirring and mixing the organic extraction phase into an acid solution containing chloride zinc sulfate, thereby separating out a chloride-loaded organic phase and a low-chloride-content extraction raffinate; (2) deoiling and adsorbing the low-chloride-content extraction raffinate and then sending to an electric zinc accumulating process; (3) mixing the chloride-loaded organic phase into an extraction raffinate in a zinc extracting process, and sending an obtained subsequent fluid in which SO42 is removed into an zinc extracting system to perform a mineral leaching while stirring and mixing an obtained organic phase into a sodium carbonate solution to perform a reverse extraction; (4) returning a no-load organic phase obtained by the reverse extraction process to the step (1) to be recycled; utilizing two-hydrated alkali type zinc carbonate (a reverse extraction sediment) as a zinc mineral resource; separating out a two-hydrated alkali type zinc carbonate sediment from a reverse extraction subsequent fluid; carrying out a recycling reverse extraction by adding sodium carbonate to a clear solution; and after enabling the chloride (Cl) to reach a setting concentration, evaporating and crystallizing the chloride to obtain an industry body NaCl (sodium chloride). The method provided by the invention is low in cost, high in efficiency and easy to control and free of the discharge of 'three wastes'.

The present invention related to low-chloride alkylated cyclodextrin compositions, along with processes for preparing and using the same. The processes of the present invention provide alkylated cyclodextrins with low levels of drug-degrading agents and chloride.

The invention discloses a method for preparing isocyanate with low chloride content. A reaction is performed between a compound organic salt and crude isocyanate under acidic conditions, a precipitateis removed in a simple filtration mode, the acid content is further reduced in an inert gas stripping mode, and a residual solvent is removed in a vacuum distillation mode. Through the method, the content of a chlorinated derivative impurity is reduced to 0.1% or below, the acid content is reduced to less than 10 ppm, meanwhile, side reactions are avoided, and the yield can reach 90% or above; and the chlorine content of the isocyanate obtained by using the method can be reduced, so that preparation of down-stream products is improved obviously.

The invention relates to a low-chloride AFFF (aqueous film-forming foam) extinguishing agent. The low-chloride AFFF extinguishing agent comprises components in percentage by mass as follows: 12%-30% of a composite carbon-hydrogen surfactant, 2%-5% of a fluorocarbon surfactant, 0.1%-1% of a foam stabilizer, 1%-10% of an anti-freezing agent, 3%-5% of a solubilizer and the balance of water, wherein the composite carbon-hydrogen surfactant is composition of an anionic surfactant and a nonionic surfactant. The low-chloride AFFF extinguishing agent is an environment-friendly AFFF extinguishing agent with low chlorine content, and is mainly used for preventing and fighting hydrocarbon fires. The chlorine ion content of a product is very low, so that the corrosion rate of the product is very low, and corrosion to various storage containers is effectively reduced, so that the product is applicable to various storage containers and is particularly applicable to storage containers made of metal such as stainless steel and the like.

The invention relates to a preparation method of low-chloride high-purity cobalt carbonate. The preparation method is characterized by comprising the following steps: using ammonium bicarbonate as a precipitator, adding ammonium bicarbonate which accounts for 4-6 times of molar ratio of cobalt chloride into a cobalt chloride solution containing a foam inhibitor at one time under the conditions of normal temperature and continuous agitation, standing for at least 12 hours, washing a product obtained, filtering and drying to obtain a high-purity cobalt carbonate product. Content of chlorine in the prepared high-purity cobalt carbonate product is less than 500ppm, but the content of chlorine in the prior art is high than 1000ppm. Meanwhile, the preparation method has a simple technology; by the use of ammonium bicarbonate, there is no introduction of new impurity elements; and with the addition of the foam inhibitor, speed of carbon dioxide overflowing from the solution is reduced so as to achieve the effect of full reaction. Thus, purity of the product is raised; overswelling is avoided; and capacity is greatly increased.

A process for producing N-carboxyanhydrides is disclosed. The process produces N-carboxyanhydrides as a product and HCl as a by-product. The HCl by-product is purged from the reaction mixture by passing a purge gas through the reaction mixture as a carbonylation reagent is reacting with an amino acid or a salt thereof. The N-carboxyanhydrides produced by this process have a relatively lower chloride impurity content, relatively higher yields can be achieved, and the N-carboxyanhydrides can be produced on a larger scale.

The invention provides a preparation method of low iron and low chloride hydroxyethylidene-1,1-diphosphonic acid (HEDP) to meet the requirements of the special industries such as electronics and the like on iron ions, chloride ions and the like in HEDP products. The preparation method is specially characterized by recrystallizing common HEDP solution to obtain the special low iron and low chloride HEDP product. The preparation method has the prominent benefits that by repeatedly recrystallizing common HEDP to remove the iron and chloride ions, the special requirements of the industries such as electronics and the like are met and the application field of HEDP is expanded.

The invention relates to a special compound admixture for marine concrete and a preparation method of the admixture and belongs to the technical application field of inorganic nonmetallic materials. The admixture is prepared from raw materials in percentage by weight as follows: 11%-28% of metakaolin, 16%-32% of refined quartz sand, 12%-31% of waste silica powder, 8%-22% of a chloride ion adsorbent, 4%-6% of sodium nitrite, 3%-6% of sodium sulfate, 5%-9% of calcium sulphoaluminate and 2%-4% of a polycarboxylate superplasticizer. The materials used by the special compound admixture for marine concrete are common and available components, and the marine concrete prepared from the admixture has higher early strength and later strength, higher anti-penetrability performance and sulfate corrosion resistance and low chloride ion diffusion coefficient.

Disclosed and claimed herein are novel thallium-sensitive assays for identifying modulators of ion channels, channel-linked receptors or ion transporters. Further described are novel chloride-free buffers and low chloride cell growth media.