602 results about "Perchlorate ion" patented technology

A method is provided for forming silicon oxide layers during the processing of semiconductor devices by applying a SOG layer including polysilazane to a substrate and then substantially converting the SOG layer to a silicon oxide layer using an oxidant solution. The oxidant solution may include one or more oxidants including, for example, ozone, peroxides, permanganates, hypochlorites, chlorites, chlorates, perchlorates, hypobromites, bromites, bromates, hypoiodites, iodites, iodates and strong acids.

A method for preparing highly stabilized and dispersible zero valent iron nanoparticles and using the nanoparticles as a remediation technology against inorganic chemical toxins in contaminated sites. The method employs a composition containing select polysaccharides (starch or cellulose) as a stabilizer for the iron nanoparticles in a liquid carrier, and results in suspensions of iron nanoparticles of desired size and mobility in water, brine, soils or sediments. The stabilizer facilitates controlling the dispersibility of the iron nanoparticles in the liquid carrier. An effective amount of the composition is delivered to a contaminated site so that the zero valent iron nanoparticles can remediate one or more toxins such as an arsenate, a nitrate, a chromate, or a perchlorate in the contaminated site.

The invention discloses a transforming solution for preparing anti-corrosion compound oxidation film on an aluminum alloy surface and a using method for the oxidation film. The invention is characterized in that, the transforming solution is a film-forming promoter containing rare-earth salt (nitrate or sulfate and compound salt of cerium, praseodymium, and neodymium), such compound oxidant as radical of permanganate, nitrate and perchlorate, etc., film-forming promoter of vanadium salt and strontium salt, etc.; the transforming solution contains no sexavalent chromium, is environmental friendly; the reaction speed is improved by the compound oxidant and the film-forming promoter, no heating is needed for the chemical transforming, the treating time is 1-5 min. The invention can rapidly prepare under room temperature compound oxidation film comprising compound rare-earth oxide, alumina and manganese oxide with good resistance to corrosion on aluminum alloy surface. The treating solution from the invention is of rapid film-forming speed, simple process, even film layer, high resistance to corrosion, and low environmental pollution, etc.

A magnesium ion containing non-aqueous electrolyte in which magnesium ions and aluminum ions are dissolved in an organic etheric solvent, and which is formed by: adding metal magnesium, a halogenated hydrocarbon RX, an aluminum halide AlY3, and a quaternary ammonium salt R1R2R3R4N+Z− to an organic etheric solvent; and applying a heating treatment while stirring them (in the general formula RX representing the halogenated hydrocarbon, R is an alkyl group or an aryl group, X is chlorine, bromine, or iodine, in the general formula AlY3 representing the aluminum halide, Y is chlorine, bromine, or iodine, in the general formula R1R2R3R4N+Z− representing the quaternary ammonium salt, R1, R2, R3, and R4 represent each an alkyl group or an aryl group, and Z− represents chloride ion, bromide ion, iodide ion, acetate ion, perchlorate ion, tetrafluoro borate ion, hexafluoro phosphate ion, hexafluoro arsenate ion, perfluoroalkyl sulfonate ion, or perfluoroalkyl sulfonylimide ion.

A gas generating system devoid of a booster chamber. The inflator includes a composition having a metal chlorate as a first oxidizer, a primary fuel selected from carboxylic acids, dicarboxylic acids, and mixtures thereof, and a second oxidizer not having perchlorate character. The metal chlorate is provided at about 10-20 wt %, the primary fuel is provided at about 15-45 wt %, and the second oxidizer is provided at about 30-50 wt % stated by weight of the total composition.

The invention relates to an etchant composition and an etching method, wherein, the etchant composition comprises any two components of oxidants, acid and salt, and the pH value of the etchant composition is between 1 and 7. The oxidant components are selected from hydrogen peroxide, ammonium persulfate, potassium persulfate and ceric ammonium nitrate; the acid components are selected from chloric acid, perchlorate, acetic acid, nitric acid, hydrofluoric acid, sulfuric acid and oxalic acid, and the salt components are selected from ammonium fluoride, ammonium bifluoride, diammonium phosphate, ammonium phosphate, ammonium chloride and perfluorinated octyl sulfanilic acid (C8F17SO3NH4).

The invention relates to a method for degrading organic pollutants in water by gradient ozone catalytic oxidation, and relates to a gradient ozone catalytic oxidation combination method for degrading organic pollutants in water. By the method, the problem that the conventional advanced oxidation technology has defects during individual use, the problem that the organic pollutants in the water cannot be removed efficiently, the problem that the influence of the pH value and temperature of the water on the method is large, and the problem that high-toxicity byproducts are formed are solved. In the method, water treatment is realized by combining two or three of a process for treating O3 individually, an enhanced catalytic oxidation process for O3 and an O3 / ultraviolet (UV) process sequentially. By the reasonable optimizing and gradient combination of the three treatment modes, the method is suitable for wide pH values and a wide temperature range, the pollutants with intermediate toxicity are controlled to be formed, the toxicity of the pollutants is reduced, the pollutants in the water is degraded efficiently and completely, and the content of oxidative species in effluent is controlled. An efficient oxidation treatment effect is kept at low temperature, and the generation of bromate, nitroso dimethylamine, chlorate, perchlorate, iodate and periodate can be controlled greatly.

The invention discloses a preparation method of modified micron zero-valent iron and an application method of the modified micron zero-valent iron in remediation of heavy metal contaminated soil. The preparation method of the modified micron zero-valent iron comprises the steps of cleaning of iron raw materials, preparation of micro iron, ultrafine grinding and modifying treatment. A modifying agent composed of water, xanthan gum, sulfide, a stabilizing agent, zeolite and blast furnace slag is adopted in the step of modifying treatment. The preparation method of the modified micron zero-valent iron has the beneficial effects that the production process of the modified micron zero-valent iron is simple, and the effect similar or superior to micron zero-valent iron is achieved while the cost is reduced; and in addition, the reaction activity is controlled, the oxidation rate is decreased, excellent stability is obtained, and the acting time of the micron zero-valent iron is longer. By the adoption of the application method of the modified micron zero-valent iron, the remediation cost of heavy metal contaminated underground water is further reduced. According to the preparation method of the modified micron zero-valent iron and the application method of the modified micron zero-valent iron in remediation of heavy metal contaminated soil, organic fertilizer is added in the soil treatment process so that the fertility of soil can be improved, the structure of soil can be improved through humic acid produced by the organic fertilizer, heavy metal elements, such as lead, chromium and arsenic, in underground water can be removed, and the concentration of pollutants such as nitrate and perchlorate can be reduced.

The invention consists of a water treatment process using selective and regenerable weak base anion exchange resins to remove any number of complex anions, especially oxyanions including perchlorate, nitrate, chlorate, arsenate, selenate, and chromate, from aqueous solutions. The treatment process is comprised of three key processes including 1) pretreatment to lower pH, 2) ion exchange, and 3) post treatment to adjust pH and alkalinity. The invention also includes processes for regenerating weak base anion resins and treatment of the residuals generated. This invention employs pressurized treatment, carbon dioxide management, and reuse of regenerating solution to minimize pumping and treatment costs.

A method for removing perchlorate or other anionic contaminates from ground water which comprises the step of passing the ground water over activated carbon, wherein the activated carbon has been either preloaded with an organic cation functional group or organic cation polymer or cationic monomer, or tailored with ammonium or other reduced nitrogen-containing compound.

The invention discloses a preparation and application method for conversion liquid of a corrosion resistant oxide film on magnesium alloy surface, which is characterized in that: the conversion liquid adopts rare-earth-containing salt, permanganate, persulphate, nitrate and perchlorate as composite oxidant, zirconium salt, vanadic salt and strontium salt as film forming promoter, boric acid, aminoacetic acid-hydrochloric acid solution as pH buffer regulator, pyridine, thiourea and derivatives, tannins, phytic acid and the salt compound as corrosion inhibitor, sodium dodecyl benzene sulfonate and dodecyl phenol polyoxyethlene ether (OP-10) as wetting agent; the conversion liquid is free from hexavalent chromium and environment-friendly; heating is not required for chemical conversion treatment, and the treatment time is 1 to 5min; composite oxide film with good corrosion resistance performance comprising rare-earth composite oxide, magnesia and manganese oxide can be rapidly prepared at on magnesium alloy surface at ambient temperature. The preparation method for conversion liquid of a corrosion resistant oxide film on magnesium alloy surface has the advantages of fast film forming, simple process, uniform film, strong corrosion resistance and less environmental pollution.

The present invention is a method for the preparation of electrostatographic toner including the following steps. A polymer material is dissolved in an organic solvent to form an organic phase. The organic phase is dispersed in an aqueous phase that includes a particulate stabilizer and a salt including an anion selected from chloride, oxychloride, sulfate, perchlorate, nitrate, dihydrogen phosphate, lactate, trifluoromethylsulfonate, and trifluromethylhydrate and a cation selected from aluminum, iron (III), tin (II) and zirconium (IV), to form a dispersion. The dispersion is homogenized. The organic solvent is evaporated from the dispersion and the resultant product is recovered, washed and dried. In an alternate method the salt is added directly to the dispersion.

An explosive composition comprises a porous fuel and an oxidizer. The porous fuel is a solid with a structure size measuring between about 2 nm and 1000 nm and has a porosity that lies between 10% and 98%. The oxidizer is solid or liquid at room temperature and is incorporated into the pores of the porous fuel. The oxidizer is selected, in an amount of at least 50% by weight relative to a total quantity of the oxidizer, from the group consisting of hydrogen peroxide, hydroxyl ammonium nitrate, organic nitro compounds or nitrates, alkali metal nitrates or earth alkali metal nitrates as well as metal nitrites, metal chlorates, metal perchlorates, metal bromates, metal iodates, metal oxides, metal peroxides, ammonium perchlorate, ammonium nitrate and mixtures thereof.

The invention relates to a system and method to reduce perchlorate in wastewater utilizing perchlorate-reducing bacteria, sulfur as an electron donor and mollusk shells as alkalinity agent. Embodiments of the invention include a perchlorate-reduction system comprising a bioreactor unit having perchlorate-reducing media comprising elemental sulfur, oyster shells and a microbial community, and can further include an optional pretreatment unit, wastewater-catchment and / or post-treatment components. Embodiments of the method include multiple steps utilizing the system and additional process steps that achieve enhanced perchlorate reduction.

The organic electroluminescence device (OELD) includes packaging structure. The packaging structure includes a layer of thick film formed from polymeric material. Dryer is doped in the layer of thick film. The dryer includes alkali metals, alkaline earth metal and at least one object selected from following matters: metallic oxide, zeolite, and metal alcoholates with hydrocarbon in long chain, sulfate, halide, and perchlorate. The packaging structure is located at one side or two sides of OELD. The invention simplifies packaging technique, reduces defects in preparing procedures, raising flexibility and performance for obstructing water and oxygen so as to raise service life of device.

A method is provided for removing an inorganic ionic species or organometallic ion contaminant, or combination contaminants, including such as arsenic, chromium, bromide, bromate, perchlorate, and / or others from water which contains an unacceptably high concentration of the contaminant(s). The method includes treating the water with an ion exchange resin, preferably a magnetic ion exchange resin such as MIEX® Resin, which is capable of adsorbing the inorganic ionic species contaminant(s), and regenerating and recycling the ion exchange resin back to the process. The method produces potable water from ground water containing such contaminants and eliminates breakthrough and chromatographic peaking problems observed with conventional ion exchange systems.

A method is provided for forming silicon oxide layers during the processing of semiconductor devices by applying a SOG layer including polysilazane to a substrate and then substantially converting the SOG layer to a silicon oxide layer using an oxidant solution. The oxidant solution may include one or more oxidants including, for example, ozone, peroxides, permanganates, hypochlorites, chlorites, chlorates, perchlorates, hypobromites, bromites, bromates, hypoiodites, iodites, iodates and strong acids.

Various aspects of the present invention pertain to methods of sorption of various materials from an environment, including radioactive elements, chlorates, perchlorates, organohalogens, and combinations thereof. Such methods generally include associating graphene oxides with the environment. This in turn leads to the sorption of the materials to the graphene oxides. In some embodiments, the methods of the present invention also include a step of separating the graphene oxides from the environment after the sorption of the materials to the graphene oxides. More specific aspects of the present invention pertain to methods of sorption of radionuclides (such as actinides) from a solution by associating graphene oxides with the solution and optionally separating the graphene oxides from the solution after the sorption.

A new and useful way of treating oxidized-contaminant-containing water, soil, rock, other geological or non-geological matrix formation (such as a landfill) is provided. A bioreactor is provided that includes elemental sulfur and a microbial population capable of oxidizing sulfur and reducing pertechnate (TcO4−), arsenate (H2AsO4−), chromate (CrO42−), bromate (BrO3−), chlorite (ClO2−), chlorate (ClO3−), perchlorate (ClO4−), and uranium(VI) oxide, with biological reduction of these oxidized contaminants in the matrix containing the oxidized contaminant performed by the bioreactor, with the elemental sulfur as the electron donor.

The invention provides a metal-organic framework material for separating acetylene and ethylene, and a method for separating ethylene and acetylene. The metal-organic framework material has the advantages of good stability, high adsorption capacity, good adsorption separation selectivity, simple preparation method and low preparation cost. The structural general formula of the metal-organic framework material is Cu2(pzdc)2L.2H2O, pzdc in the formula is pyrazine-2,3-dicarboxylic acid, and the material is a three-dimensional network structure formed by copper ions, the pyrazine-2,3-dicarboxylicacid and an organic ligand A through a coordination bond or an intermolecular action force. The preparation method comprises the following steps: (1) mixing and reacting an inorganic salt, the pyrazine-2,3-dicarboxylic acid, an alkali and the organic ligand in proportion, wherein the inorganic salt is chloride, nitrate, acetate, sulfate or perchlorate of the copper ions; and (2) sequentially washing a product obtained after the reaction is finished with ionized water and anhydrous methanol, and then carrying out vacuum drying to obtain the metal-organic framework material. The metal-organic framework material is used as an adsorbent to adsorb and separate a mixed gas containing ethylene and acetylene.

The invention discloses a method for preparing bis(sulfonyl fluoride) imine and (perfluoroalkyl sulfonyl fluorine sulfonyl) imine alkali metal salt. According to the method, sulfamide is utilized to take reaction with thionyl chloride and chlorosulfonic acid for preparing bis(sulfonyl fluoride) imine or (perfluoroalkyl sulfonyl fluorine sulfonyl) imine, then, the bis(sulfonyl fluoride) imine or (perfluoroalkyl sulfonyl fluorine sulfonyl) imine takes reaction with antimony trifluoride and potassium (rubidium or caesium and the like) carbonate, and corresponding high-purity bis(sulfonyl fluoride) imine potassium (rubidium or caesium) salt or (perfluoroalkyl sulfonyl fluorine sulfonyl) imine potassium (rubidium or caesium) salt can be obtained; and the double decomposition exchange reaction of the potassium (rubidium or caesium) salt and lithium (or sodium) perchlorate or lithium (or sodium) tetrafluoroborate and the like in aprotic polar solvents is utilized to obtain corresponding high-purity lithium (or sodium) salt. The method provided by the invention has the characteristics that the operation step is simple, the products can be easily separated and purified, the purity and the yield are high, the environment pollution is avoided, the method is suitable for industrial mass production, and the like.

The invention discloses stereospecific synthesis of beta-artemether by using artemisinin as a raw material through a one-pot method, which comprises the following steps of: in a system of alkaline solution of dichloromethane, taking sodium borohydride as a reducing agent and aluminium tert-butoxide as a catalyst, and reducing to obtain dihydroartemisinin; and separating out a water phase, adding methanol, sodium acid sulfate, aluminum perchlorate nonahydrate, nickelousperchlorate and the like serving as catalysts for methyl etherification, and reacting at room temperature for 2 hours to obtain the beta-artemether, wherein the maximum yield rate of the beta-artemether is 85 percent and the maximum total yield rate of artemether is 93.5 percent. The method has the characteristics of low cost, high yield, short time and simple and safe operation, and is completely suitable for industrial production.

The invention discloses sulfur-free ring stabilizing agent propellant powder which consists of the following components in parts by weight: 70 parts of an oxidant, 34 parts of a burnable agent, 6 parts of an adhesive, 2 parts of a stabilizing agent, 2 parts of an anti-aging agent, 1 part of a catalyst and 2 parts of an antismoke agent which are uniformly mixed according to a general method, wherein the oxidant is a mixture consisting of potassium perchlorate, amine perchlorate and barium nitrate; the burnable agent is a mixture consisting of potassium hydrogen terephthalate, potassium acid phthalate, nitrocellulose, purified terephthalic acid and hemp stem carbon powder; the stabilizing agent adopts calcium stearate; the anti-aging agent adopts calcium phthalate; the catalyst adopts copper oxide; the antismoke agent adopts aluminum hydroxide; the adhesive is selected from one or a mixture of multiple of phenolic resin, strong adhesive powder, glutinous rice flour and polyvinyl alcohol according to any ratio. The sulfur-free ring stabilizing agent propellant powder is high in power capability and excellent in safety performance indexes and has excellent storage stability, and the environment-friendly performance is greatly improved.

The invention provides a method for preparing an active silver electrode, the method comprises the following steps: firstly, carrying out anode oxidation reaction to the silver electrode to form a silver oxidation state layer on the surface of the silver electrode in water solution with anion,, secondly, changing polarity of the silver electrode, and carrying out cathode oxidation reaction to cathode of the silver electrode to obtain the active silver electrode, wherein anion is compounded by one, or two, or more than two following ions, namely, (1) perchlorate ion, (2) hypochlorous acid ion, (3) hydroxide ion, (4) nitrate ion, (5) sulfate ion, (6) carbonate ion, (7) halide ion, (8) organic acid ion and (9) phenol hydroxyl root ion, the active silver electrode which is obtained according to the method of the invention is not only provided with a more specific surface, but also provided with higher electro-catalysis activity, longer electro-catalysis performance and less power loss, and the obtained active silver electrode can be used to electrolyze 3,4,5,6-tetrachloropicolinic acid and to compound 3,6-dichloropicolinic, which not only has lower energy consumption, but also has higher production efficiency.

The invention discloses a method for separating magnesium and extracting lithium from salt lake brine with a high magnesium-lithium ratio. With adoption of the method, tributyl phosphate is taken as an extractant, number 200 solvent oil or kerosene is taken as a diluent, perchlorate is taken as a co-extraction agent, and water is taken as a stripping agent to form an extraction system; and lithium carbonate is prepared through extraction, reversed-phase extraction and deep magnesium removal by the salt lake brine. The method has the following beneficial effects: 1. the property of the co-extraction agent is stable, lithium magnesium separation can be carried out in neutral brine and the pH value of an aqueous phase needs not to be controlled; 2. the emulsification phenomenon doesn't exist and a third phase doesn't appear in the extraction process, two phases are easy to separate, the reversed-phase extraction is carried out by water and the device has little corrosion; and 3. the whole technique is simple in process, high in lithium extraction rate, good in separation effect and low in economic cost, is suitable for industrial production of the salt lake brine and is low in environmental damage degree because the co-extraction agent in water can be recycled.

The use of volatilization reagents is disclosed for improved detection of inorganic oxidizers such as, but not limited to, chlorates and perchlorates. Detection methods are disclosed whereby a reagent can transfer a proton to the anion (i.e., chlorate, perchlorate, etc.) of an inorganic salt analyte, forming an acid (i.e., chloric acid, perchloric acid) that is easier to detect by a mechanism whereby the acidified reagent is more easily vaporized, and hence, more easily detected. Concurrently, the anion of the acid forms a new salt with the cation released from the salt that was acidified. The reagents can also include acidic salts or cation-donators, more generally. In some embodiments, hydrated reagents or co-reagents that can release water can be employed. In another aspect of the invention, a class of reagents including polmeric acids, polymeric organic acids and polymeric sulfonic acids are disclosed that can carry out this method. In various embodiments, these reagents can be embedded in a swipe or other substrate, delivered as a liquid infused via nebulizer, or otherwise introduced to a sample to be tested for the presence of a target analyte.