187 results about "Chloric acid" patented technology

An aqueous solution of metal chlorate, mineral acid and a reducing agent are continuously or intermittently sprayed, in a pattern to achieve intimate mixing, into a spherical chamber creating an aqueous foam reaction mixture generating chlorine dioxide which is removed in a direction 90 degrees to the axis of the spray nozzles. A baffle plate may be used to reduce the open cross sectional area of the exit port to increase reaction efficiency. The reactants are a mineral acid and an alkali metal chlorate or chloric acid and a reducing agent such as hydrogen peroxide. The mineral acid is either diluted or concentrated sulfuric acid, hydrochloric acid, acetic acid, nitric acid or a blend thereof. The ratio of acid is greater than one and less than 3 kg acid per kg of ClO2 formed. The chlorine dioxide may be removed with a stripper column.

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).

Belonging to the technical field of sulfur recovery, the invention relates to a catalyst for selective reduction desulphurization, its preparation method and application. The catalyst is characterized in that: a catalyst active component is loaded on a carrier by means of an isometric immersion method, a multiple immersion method and an immersion precipitation method so as to obtain the catalyst; the catalyst carrier consists of coconut-shell activated carbon, fruit-shell activated carbon and coal-based activated carbon; the oxidation modifier of the catalyst carrier is one or a mixture of any of chloric acid, nitric acid, hydrogen peroxide or concentrated sulfuric acid; the active component of the catalyst is one or a mixture of any of CuO, NiO, Fe2O3, ZnO, Cr2O3, Co2O3, MnO2, and V2O5. The desulfurizer of the invention employs a selective reduction desulphurization technology to convert SO2 in flue gas into elemental sulfur. The preparation technology of the catalyst has the advantages of simplicity, easy control, low cost and long service life. Adoption of the activated carbon-based catalyst prepared in the invention for selective reduction desulphurization not only realizes high efficiency SO2 conversion rate and sulfur selectivity, but also effectively prevents secondary pollution.

An apparatus for treating water by electrolysis method is composed of DC power supply controller, water supply-discharge unit, two electrolyzing cathode bathes, electrically isolating plate unit, water scale depositing unit, and two electrolyzing anode bathes. The electrolytic reaction of water can make the calcium carbonate and the hydroxide of heavy metals to be deposited in anode bathes and the Cl2, O2, the radicals of hypochlorous acid and chloric acid, and ozone to be generated in cathode bathes.

This invention describes a process for producing gypsum whiskers, which includes the the following processes: a)purification of chemical gypsum into dihydrate gypsum; b)levigation of the purified chemical gypsum, and then injection of the slurry thus obtained into an enamelled reactor; c)adding chloric acid or salts into the reactor, and boiling to the dissolution of the gypsum; d)stirring and cooling the solution to the recrystallization into dihydrate gypsum whiskers; e)swing-drying the recrystallization product; and f)neutralizing the swing-dried dihydrate gypsum to obtain a first product of wet dihydrate gypsum whiskers. In this invention the estimated production cost of the gypsum whiskers produced is 800-1900 RMB per ton, only 1/40-1/200 the price of the whiskers in the market. Besides, the overall process of this invention is easy to operate, and all the equipment utilized is common chemical equipment. The produced gypsum whiskers are mainly used for paper manufacturing and the corresponding paper products, while a minor part of them are used for reinforced materials of rubber and plastic products.

The invention discloses a simple and rapid method for preparing Au-Ag complex nanometer particles, which adopts one-step liquid phase deoxidizing method at room temperature to prepare Au-Ag complex nanometer particles. The specific method is that: sequentially add gold chloric acid solution and sodium citrate solution into colorimetric tube; then, respectively add silver nitrate solution into the colorimetric tube, making that Au3+: Ag+ in the tube is 1:9 to 9:1; then add ascorbic acid and shake, thus the Au-Ag complex nanometer particles is obtained. The method has the advantages that: 1) comparing with the current method, the preparation method is simple with mild reaction conditions, and does not need the assistant means of laser induction and ultrasonic processing; the Au-Ag complex nanometer particles can be prepared at room temperature, and the diameter of nanometer particles can be regulated by regulating the proportion of Au and Ag; 2) the deoxidizing agent of ascorbic acid and the stabilizing agent of sodium citrate solution are easily obtained with low cost.

The invention discloses a process for treating dinaphthol wastewater by using a complexation extraction method. A process core includes that trioctylamine or trialkyl tertiary amine serves as a complexing agent, sulfonated kerosene serves as a diluent, and chloric acid tributyl ester serves as a chaotropic agent to be mixed according to a certain ratio into an extraction agent, the extraction agent comprises, by volume, 20% to 30% of the complexing agent, 60% to 70% of the diluent and 5% to 15% of the chaotropic agent. Dinaphthol production wastewater is extracted when the temperature is in a range of 20 DEG C to 30 DEG C and the pH is 1, aqueous phase: oil phase is 1: 1 (volume ratio), the removal rate of first extraction CODcr can reach 97%, naphthalene sulfonate in wastewater can be extracted through multistage extraction, and simultaneously water is discharged up to standard. Water phases of back extraction can be recycled as production materials; and organic phases are mixtures of the extraction agent and the diluent and can be recycled.

The object is to provide an etching liquid for a conductive polymer having excellent etching capability toward a conductive polymer, and a method for patterning a conductive polymer employing the etching liquid for a conductive polymer. The conductive etching liquid of the present invention is selected from the group consisting of (1) an etching liquid comprising greater than 0.5 wt % but no greater than 70 wt % of (NH₄)₂Ce(NO₃)₈ or at least 0.5 wt % but no greater than 30 wt % of Ce(SO₄)₂, (2) an etching liquid comprising greater than 0.5 wt % but no greater than 30 wt % of (NH₄)₄Ce(SO₄)₄, (3) an etching liquid comprising a hypochlorous acid salt aqueous solution having an effective chlorine concentration of at least 0.06 wt % and a pH of greater than 3 but less than 8, (4) an etching liquid comprising nitrosyl chloride which comprises at least 5 wt % of hydrochloric acid and at least 20 wt % of nitric acid, a (hydrochloric acid concentration+0.51×nitric acid concentration) value being no greater than 35 wt %, and a (hydrochloric acid concentration+0.5×nitric acid concentration) value being at least 30 wt %, (5) an etching liquid comprising at least 3 wt % but no greater than 40 wt % of a bromic acid compound and at least 4 wt % of an inorganic acid, (6) an etching liquid comprising at least 6 wt % but no greater than 40 wt % of a chloric acid compound and at least 7 wt % of a hydrogen halide, (7) an etching liquid comprising at least 0.001 wt % but no greater than 20 wt % of a permanganic acid compound, and (8) an etching liquid comprising at least 3 wt % but no greater than 30 wt % of a hexavalent chromium compound.

The invention discloses a detection method of heavy metal in soil. The detection method comprises the following steps: weighing soil, adding an alkali solution containing an ammonia solution, performing shaking and microwave treatment, adding an acid solution containing chloric acid, adjusting a pH valve, and performing ultrasonic extraction and centrifugation so as to obtain a crude extract; then performing concentration and microfiltration, and setting volumes so as to obtain a sample solution; preparing a blank solution; performing quantitative determination on the obtained sample solution by an extra-high efficient liquid chromatography. According to the detection method disclosed by the invention, an alkaline hydrolysis acid extraction method is adopted for pre-treating samples, so that losses and air pollution of heavy metal elements are avoided. Besides, the detection method has the advantages of being high in recovery rate, precision, and treatment speed, simple and convenient to operate, wide in application range and the like. According to the detection method disclosed by the invention, after the samples are pretreated, the determination of varied heavy metal elements can be performed on the pretreated samples, and performing separate sample pretreatment on each heavy metal element is not needed, so that the workload is reduced. The detection method disclosed by the invention is very acute for determining the content of the heavy metal in the soil, and has a relatively high detection efficiency.

The invention relates to a method for observing the epidermal and internal microstructures of a leaf by using a transparent leaf, which has low cost and can accurately observe the microstructures of leaf. The technical scheme in the method comprises the following steps: firstly, processing the leaf, and cleaning and soaking the leaf in ethanol to remove chlorophyll; then soaking in alkaline solution to break the mesophyll cells; decolorizing in sodium hypochlorite; rinsing with flowing water; placing in hydrated chloric acid; taking out the leaf; rinsing with flowing water; dewatering with alcohol solutions with gradient concentrations; placing in xylene solution to enable the leaf to be transparent; and sealing with neutral balsam or water; and observing and picking images with optical microscope to observe the internal and external structure at different levels of the leaf. The method has the advantages of less material selection, low cost, less work load, high success rate and good effect, and is suitable for observation of various leaves.

The invention relates to a preparation method of a fluorescent molecular probe for detecting fluoride ions through colorimetric detection and fluorescence enhancement and an application of the fluorescent molecular probe to detecting fluoride ions. The fluorescent molecular probe is prepared by protecting 2-hydroxyl-1-naphthaldehyde taken as a raw material with silane and then condensing the raw material and malononitrile. The fluorescent molecular probe is simple and convenient to synthesize, and reaction conditions are mild. The fluorescent molecular probe has the specific characteristics that the probe molecule has stable optical properties and higher synthetic yield; the probe molecule has high fluoride ion detection sensitivity and low lower limit of detection, and the limit of detection is 0.52mu M; the response range is 0-100mu M and the detection range is wide; the probe molecule has good selectivity and has no responses to anions, such as dihydrogen phosphate radicals, acetate radicals, bromide ions, hydrosulfate radicals, chlorate radicals, iodide ions, chloride ions and nitrate radicals; the probe molecule is suitable for colorimetric detection; the fluorescent molecular probe has practical application values in the fields of biochemistry, environmental sciences and the like.

The invention relates to a preparation method of conductive fabric fiber, and belongs to the improved technology of textile. The invention is characterized in that: firstly the fabric fiber is soaked in aniline salt solution with 9 to 12 percent of concentration at a room temperature; then is added with perchloric acid or chloric acid according to a mol ratio of 1: 0.5 to 1.5, and is polymerized for 30 to 60 minutes to generate polyanion on the surface of the fabric fiber, thereby obtaining the conductive fabric fiber with a conductive rate of 10 <-1> to 10 <1> s/cm, and the fabric fiber and the polyanion are bond by a chemical bond. The fabric fiber obtained by the processing of the invention which is bond with the polyanion (PAn) by the chemical bond has the advantages of strong conductivity, good flexibility, corrosion resistance and being washed arbitrarily, additionally having very good anti-oxidation performance and anti-aging performance. The conductivity is 10 <-1> to 10 <1> (s/cm).

Chlorous acid is generated from a chlorite salt precursor, a chlorate salt precursor, or a combination of both by ion exchange. The ion exchange material facilitates the generation of chlorous acid by simultaneously removing unwanted cations from solution and adding hydrogen ion to solution. Chlorine dioxide is generated in a controlled manner from chlorous acid by catalysis. Chlorine dioxide can be generated either subsequent to the generation of chlorous acid or simultaneously with the generation of chlorous acid. For catalysis of chlorous acid to chlorine dioxide, the chlorous acid may be generated by ion exchange or in a conventional manner. Ion exchange materials are also used to purify the chlorous acid and chlorine dioxide solutions, without causing degradation of said solutions, to exchange undesirable ions in the chlorous acid and chlorine dioxide solutions with desirable ions, such as stabilizing ions, and to adjust the pH of chlorous acid and chlorine dioxide solutions.

The invention which is suitable for the technical field of mineral processing provides a cobalt copper sulfide ore processing method. The method comprises the following steps: 1, grinding the cobalt copper sulfide ore, mixing the cobalt copper sulfide ore with sulfurous acid or a sulfite according to a ratio of the total mass of cobalt and copper in the cobalt copper sulfide ore to the mass of sulfurous acid or the sulfite of 1:1-3, adding an acidic solution to adjust the pH value of the obtained system to 0.5-1, and reacting for more than 1h at 65-80DEG C; and 2, maintaining the pH value andthe temperature of the system, adding chloric acid or a chlorate according to a ratio of the total mass of residual cobalt and residual copper in the system to the mass of chloric acid or the chlorate of 1:1-3, and continuously reacting for more than 1h. The cobalt copper sulfide ore processing method of the invention, which allows cobalt and copper in the cobalt copper sulfide ore to be fully leached by carrying out primary leaching with sulfurous acid or the sulfite and carrying out secondary leaching with chloric acid or the chlorate, allows the leaching efficiency of cobalt and copper in the cobalt copper sulfide ore to be substantially improved. Sulfurous acid or the sulfite is used as an oxidant and a reductant in the primary leaching process, and chloric acid or the chlorate is used as an oxidant in the secondary leaching process, so the processing cost is substantially reduced.

Electrolysis using a suitable electrolyte provides a completely nonsludging zinc phosphate conversion coating process that produces a high quality conversion coating in a very short time. The suitable electrolyte contains at least water, dissolved nitric acid, and dissolved zinc cations and optionally also contains m chemically distinct species of cations other than zinc and n chemically distinct species of anions other than anions derivable by ionization of phosphoric and nitric acids, each of m and n independently being zero or a positive integer. Preferably, the liquid composition contains as additive at least one selection from nitrous acid, permanganic acid, peroxysulfuric acid, hydrogen peroxide, chloric acid, perchloric acid, nitrobenzenesulfonic acid, hydroxylamine, starch/phosphoric acid esters, fluorine compounds, and salts of the preceding; and/or the metal substrate is subjected to cathodic electrolysis after the workpiece has been brought into contact with a weakly basic aqueous colloidal solution that contains titanium oxide, titanium hydroxide, and zinc phosphate.

The invention provides a new low-cost oxidation denitrating technology aiming at the problem that the denitrating technology in the prior art is high in cost. The new low-cost oxidation denitrating technology comprises the specific steps as follows: A) preparing aqueous solution with chlorate ion concentration of 50-500g/L by taking lime water and chlorine as raw materials; B) in oxidation section, diluting the prepared aqueous solution to serve as an oxidant, and spraying into the oxidation section from the upper part, so as to contact with smoke entering from the lower part reversely and enable nitric oxide in the smoke to have oxidation reaction; and C) in an absorption section, spraying alkali liquor as an absorbent into the absorption section from the upper part to absorb the oxidized nitric oxide in the smoke to produce corresponding nitrite dissolved in water, thereby achieving the denitration purpose. The new low-cost oxidation denitrating technology has the advantages of being simple in technological flow, low in operation cost and the like.

A main object of the present invention is to provide an organic EL element having members such as an organic EL layer formed highly precisely in a pattern with preferable light emission characteristic of the organic EL layer, and a photocatalyst containing coating solution to be used for the production thereof. To achieve the object, the present invention provides an organic electroluminescent element comprising: a substrate; a first electrode layer formed on the substrate; an organic electroluminescent layer formed on the first electrode layer; and a second electrode layer formed on the organic electroluminescent layer, wherein a photocatalyst containing layer containing a photocatalyst, a characteristic providing agent, and a light emission characteristic improving material having the function of improving the activation of the photocatalyst and the light emission characteristic of the organic electroluminescent layer so as to have the characteristic of the characteristic providing agent changed by the action of the photocatalyst accompanied by the energy irradiation is formed at any position between the substrate and the second electrode layer; and the light emission characteristic improving material is a silver salt of a fluorine or an acid selected from the group consisting of carboxylic acids, sulfonic acids, sulfinic acids, phenols, enols, thiophenols, imides, oximes, primary or secondary nitro compounds, clathrate compounds, a chloric acid and a perchloric acid.

The invention discloses a method for regenerating a precious-metal mercury-free catalyst for acetylene hydrochlorination. The method comprises the following steps: (1) carrying out drying treatment; (2) carrying out treatment by using regeneration reagents such as an acid mixture of hypochlorous acid, chloric acid, perchloric acid, hydrogen peroxide and hydrochloric acid, formic acid, acetic acid and tartaric acid; and (3) carrying out water washing and baking. According to the method, the performance of the deactivated precious-metal mercury-free catalyst can be restored, and the precious-metal mercury-free catalyst can be recycled, so that the use cost is greatly reduced; and the implementation process is environmentally friendly, so that a foundation is laid for non-mercurization of calcium-carbide-process PVC industry.

The present invention provides an electrolysis cell for synthesizing a perchloric acid compound, the electrolysis cell having: a feedstock solution containing a chloride or a chloric acid compound; a cathode; and an anode having an electroconductive diamond as an anode substance, the anode electrolytically oxidizing the chloride or the chloric acid compound to synthesize the perchloric acid compound, and a method for electrolytically synthesizing a perchloric acid compound.