208 results about "Ferric ion" patented technology

The invention relates to the technical field of water treatment agent preparation and environmental governance material processing, in particular to polymeric ferric sulfate and a preparation method thereof.The preparation method comprises the steps that steam condensation recycled water of a thermal power plant of an aluminum factory is mixed with ferrous sulfate and concentrated sulfuric acid to form a reaction solution, oxygen is introduced for an oxidative polymerization reaction, and a liquid intermediate is generated; gradient cooling is carried out on the liquid intermediate to control the molar ratio of ferric ions to hydroxyl, and a porous solid precursor is formed through concentration and closed aging; crushing the precursor, performing graded drying by adopting a rotary kiln and flash drying, and synchronously spraying a hydrophobic modifier to reduce the surface hydroxyl activity; the powdery product is secondarily dried in a nitrogen inert environment, and moisture absorption and agglomeration are inhibited. The invention solves the problems of mixed crystal forms, delayed release of effective components and secondary pollution in the traditional process. The obtained product is uniform in crystal form, concentrated in particle size distribution, remarkably improved in dissolution rate and storage stability, and suitable for black and odorous water body treatment and industrial sewage treatment.

The invention provides a leakage point pressure difference response high-strength blocking agent based on iron ion dynamic cross-linked latex and a preparation method thereof, and the raw materials comprise the following components in parts: 60-120 parts of latex, 60-120 parts of deionized water, 5-15 parts of an activator, 5-10 parts of a defoamer, 100 parts of a terminator, 100 parts of a stabilizer, 10 parts of a 20% ferric chloride solution, and the balance of water. Rubber particles are dynamically crosslinked through ferric ions, and the plugging strength is remarkably improved. Compared with a traditional differential pressure plugging agent, the plugging strength for small holes with the diameter of 0.5 mm reaches 35.67 MPa and is improved by about 238%, and the plugging strength for large holes with the diameter of 1 mm reaches 9.68 MPa and is improved by about 428%. And the plugging device is suitable for plugging conditions with higher leakage point pressure difference. In addition, the plugging agent can realize rapid and high-strength plugging of an underground pipe column, and provides a more efficient and more reliable solution for well site construction.

The invention discloses a production method of ferrous dihydrogen phosphate, which comprises the following steps of: changing an iron source of iron-process iron phosphate from traditional iron blocks or iron powder into oxide scale, compounding phosphoric acid and sulfuric acid into mixed acid, and controlling the granularity of the oxide scale and the components and acidity of the mixed acid to solve the problems of dissolution and passivation of the oxide scale. According to the method, iron oxide scale can be better dissolved, the residual problem of ferric ions is solved by reducing excessive iron blocks or iron powder, undissolved impurities such as carbon, silicon and iron are removed by filtering, and finally, the stability problem of a reaction system is solved by adjusting the pH value of the system through industrial phosphoric acid and pure water, so that a ferrous dihydrogen phosphate solution required for producing iron phosphate is obtained. The production cost of an iron source required by iron phosphate is greatly reduced, other impurities are not contained, and mixed acid-containing filtrate and washing water generated in the production process can be recycled through an evaporation device.

The present invention relates to the technical field of test and detection, and particularly to an on-line measurement method and device for total iron in power station water vapor. A catalytic reagent is added to the water sample to be measured and acts through an ultraviolet light oxidizer, so as to completely convert the colloidal iron in the water sample into ferric ions. The dissolution and conversion of the colloidal iron are completed without adding acid throughout the process. Since no acid is added during the process of converting the whole colloidal iron into dissolved iron, only a chromogenic reagent needs to be added to accurately measure the total iron content in the water sample, and it is also easier to realize the on-line measurement of total iron in the water sample. When the total iron content in the water sample is less than 10 μg / L, the water sample enters the concentration system for concentration and then optical measurement, so that the low-concentration total iron in the water sample can also be accurately measured. This measurement method can automatically measure the total content in the water sample on-line, avoid manual sampling and detection, can monitor the total iron in the water sample in real time, and has a lower detection limit and more accurate detection results, which is beneficial to the adjustment of the water condition during the start-up and shutdown stages of the power station.

A raw material solution containing trivalent iron ions, or trivalent iron ions and ions of a metal element that partially substitutes Fe sites, and an alkaline aqueous solution for neutralizing the raw material solution are added to a reaction system to adjust the pH of the reaction system from 1.0 to 3.0 or lower. Hydroxycarboxylic acid is added to the obtained reaction solution and the pH of the reaction system is then neutralized from 7.0 to 10.0 or lower. The obtained precipitate of a substituent metal element-containing iron oxyhydroxide is coated with silicon oxide, followed by heating so as to form particles of ε-iron oxide in which Fe sites are partially substituted by other metal elements, and then, a slurry containing the particles is classified. The iron-based oxide magnetic powder has a particle shape close to a perfect sphere and is suitable for use in a magnetic recording medium.

The invention discloses a preparation method of polydihydroxyindole and application of the polydihydroxyindole in hair dyeing, and belongs to the field of functional materials and the field of daily cosmetics. The polydihydroxyindole is obtained in the mode that Boc-true melanin is formed after true melanin is protected through phenolic hydroxyl groups, the Boc-true melanin is subjected to oxidative degradation, separation and purification and then deprotection, the true melanin is naturally extracted melanin or chemically synthesized melanin or melanin synthesized through a microbiological method, and the oxidative degradation method is an enzymatic oxidative degradation method. The obtained polydihydroxyindole is moderate in molecular weight and has excellent permeability on hair, a strong alkaline condition is not needed in the oligomer dyeing process, and hair quality damage can be reduced; the polydihydroxyindole is oxidized again in the hair dyeing process to generate melanin, and under the condition that the pH is 5-7, and in the presence of ferric ions, the polydihydroxyindole can be more tightly combined with keratin on the hair to coat the outer layer of the hair, so that the hair color is deepened, and the effects of dyeing and protecting the hair are achieved.

The invention provides coal gangue-based artificial soil as well as a preparation method and application thereof. The preparation method of the coal gangue-based artificial soil comprises the following steps: S1, modifying coal gangue by adopting a solution containing citric acid and ethylenediamine tetraacetic acid to obtain modified coal gangue; s2, preparing the modified coal gangue into artificial soil. According to the invention, the citric acid can dissolve carbonate in the coal gangue, the released carbonate can be combined with heavy metals, and citrate ions and ferric ions can form a complex to destroy the outer layer of ferric oxide of the heavy metals; ethylenediamine tetraacetic acid can permeate into mineral lattices of the coal gangue, lattice bound state heavy metal is released through octahedral Al-O bond breakage, the ethylenediamine tetraacetic acid can capture heavy metal combined with citric acid, a more stable heavy metal complex is formed, the heavy metal complex carries strong negative charges, and the heavy metal complex can be separated from the coal gangue. And electrostatic repulsion can be generated on the surface of the coal gangue with negative electricity, so that the heavy metal removal effect is improved.

The invention belongs to the technical field of biological pharmacy, and particularly relates to a preparation method and application of a nano-drug carrier. The invention provides a preparation process based on a pre-polymerization-coordination-shaping sequence, which comprises the following steps: firstly, slightly combining chitosan and polyphenol under a near-neutral condition to form small particles with uniform size and good dispersity, so that adhesion among the particles is effectively reduced; then ferric ions are slowly introduced under the regulation and control of a weak chelating agent, so that the ferric ions are uniformly coordinated on the surfaces of the particles, and an inner layer which is compact in structure and has responsiveness to an acid environment or a competitive ligand is constructed; and finally, sodium alginate is introduced, crosslinking is performed through slow-release calcium ions, a flexible outer layer is formed, and the layer and the inner layer have a synergistic effect, so that the dilution resistance and the protein adsorption resistance of the carrier are remarkably enhanced.

A method of recovering active materials from a rechargeable battery comprises placing an active material of a rechargeable battery in a cathode chamber comprising a cathode of an electrochemical cell comprising the cathode chamber, an anode chamber comprising an anode, and a membrane separating the cathode chamber from the anode chamber, contacting the active material in the cathode chamber with an electrolyte comprising an acid, ferric ions, and ferrous ions, and dissolving at least one of lithium and cobalt from the active material into the electrolyte. Related apparatuses for recovering metals from active materials of rechargeable batteries are also disclosed.

The invention belongs to the technical field of iron ion detection, and particularly relates to a rapid detection method for ferric ions in water, which comprises the following steps: a fluorescent probe preparation step: taking trihydrate of copper nitrate and tryptamine, adding into a centrifuge tube in sequence, adding ultrapure water, performing ultrasonic dissolution, transferring into a high-pressure reaction kettle, and performing hydrothermal reaction to obtain a fluorescent probe; cooling to room temperature, centrifuging the obtained yellow green solution in a centrifugal machine, and filtering the supernate through a microfiltration membrane to obtain a copper-doped carbon quantum dot CuCDs stock solution, namely the fluorescent probe; analyzing and determining Fe < 3 + >: taking the diluent of the prepared CuCDs solution, adding the diluent into a centrifugal tube containing a Fe < 3 + > standard solution, uniformly mixing, carrying out fluorescent quantitative analysis and detection, and exploring the change rule of the fluorescence intensity ratio of CuCDs; according to the rapid detection method for Fe < 3 + > provided by the invention, the synthesized CuCDs have high sensitivity, can realize on-site rapid detection of Fe < 3 + > in a water medium, and shows a wide application prospect in the field of environmental monitoring.

The invention relates to the technical field of wastewater treatment and resource recovery, and discloses an organophosphorus degradation and recovery system based on double-cathode electro-Fenton reaction, comprising: an electrolytic tank for accommodating organophosphorus wastewater to be treated; the anode is arranged in the electrolytic tank and is electrically connected with an anode of a power supply; the oxidizing agent generating cathode is arranged in the electrolytic tank and is used for generating hydrogen peroxide in situ under a power-on condition; the metal reduction cathode is arranged in the electrolytic tank and is used for adsorbing and reducing ferric ions; the metal source is composed of zero-valent iron or iron alloy, is not directly and electrically connected with the power source, and is arranged in an electric field acting area established by the anode and the at least one cathode. Through the design of inductive slow-release iron supply and double-cathode collaborative circulation, a series of problems of uncontrollable iron ion release, high iron sludge yield, low catalyst utilization efficiency, difficulty in resource recovery and the like in the traditional electro-Fenton technology are effectively solved.

The invention belongs to the technical field of electrode materials, and particularly discloses a self-supporting electrolyzed water catalytic electrode material, a preparation method and application thereof, the self-supporting electrolyzed water catalytic electrode material comprises a foamed nickel-molybdenum alloy as a substrate, and the surface of the foamed nickel-molybdenum alloy is covered with a two-dimensional layered nickel-iron metal hydroxide. The nickel-molybdenum alloy self-supporting nickel-iron double-metal hydroxide obtained by the technology is used as a bifunctional catalyst for hydrogen evolution and oxygen evolution reaction in a non-acidic medium. The foamed nickel-molybdenum alloy is used as a raw material of a current collector and a catalytic active site at the same time, a fresh crystal nucleus is formed on the surface of the foamed nickel-molybdenum alloy through one-step ferric ion etching, then the foamed nickel-molybdenum alloy is placed in air, and the catalytic activity of the nickel-molybdenum alloy is improved under the combined action of water and oxygen. The nickel element from the foamed nickel-molybdenum alloy and the adsorbed iron element spontaneously grow on the surface of the nickel-molybdenum alloy to form the layered double-metal hydroxide nanosheet.

The invention discloses a method for separating vanadium and iron in a high-iron-vanadium electrolyte. The method comprises the steps of pH regulation and control, iron removal, vanadium extraction and vanadium reverse extraction. In the step of iron removal, an iron ion targeted complexing agent and a solid phase adsorbent are added into the high-iron vanadium electrolyte with the pH adjusted, reaction is conducted for 10-15 min under stirring, then direct filtering is conducted, and low-iron vanadium electrolyte and a solid phase are obtained; in the vanadium extraction step, vanadium in the low-iron vanadium electrolyte is extracted by adopting a mixed solvent of pretreated P204, TBP and sulfonated kerosene, and a vanadium-containing organic solution is obtained; and the vanadium reverse extraction comprises the step of carrying out reverse extraction on the vanadium-containing organic solution through a sulfuric acid solution with the concentration of 2.0-5.0 mol / L to obtain a vanadium electrolyte. The method can be used for treating iron ions in all valence states, particularly ferric ions which are easier to extract than vanadium ions, qualified vanadium electrolyte with the iron ion concentration meeting the industrial standard can be directly obtained after reverse extraction, and a complexing agent and an adsorbent can be recycled.

The invention discloses a recycling method of NF3 residual electrolysis liquid, and relates to the technical field of residual electrolysis liquid recycling treatment. The method comprises the following steps: step 1, removing Fe ions in the electrolytic residual liquid: firstly, adding hydrogen peroxide or oxygen into the electrolytic residual liquid for reaction, oxidizing ferrous ions into ferric ions, then adding ammonia water and sodium hydroxide or ammonium bicarbonate and sodium hydroxide into the solution for reaction, precipitating ferric ions in the form of ferric hydroxide; 2, hydrofluoric acid is added into the electrolyte solution obtained after iron removal to adjust the pH of filtrate to 3-12, the filtrate enters an extraction system, the nickel element in ammonium hydrogen fluoride is extracted out, and ammonium hydrogen fluoride is purified; and step 3, the nickel element separated from the electrolyte enters a second section to be extracted and synthesized into a nickel sulfate product.

The invention discloses a method for measuring the content of ferric ions in an iron-chromium flow battery electrolyte, which comprises the following steps: before the content of the ferric ions is measured, pretreating the electrolyte to be measured to remove the influence of Cr ions and other impurity ions in the electrolyte on an experimental result, and then titrating with a sodium thiosulfate standard solution; the method has the advantages that the method is suitable for directly measuring the content of the ferric ions under the coexistence condition of a large amount of ferrous ions, the problems that in the prior art, when a large amount of ferrous ions and a trace amount of ferric ions coexist, the error is large, and the accuracy is low are solved, and a technical guarantee is provided for capacity recovery and efficiency improvement of the electrolyte of the flow battery.

The invention relates to the field of preparation of micro-emulsions, in particular to a polysaccharide-protein composite stable high-bioavailability ferrous micro-emulsion as well as a preparation method and application thereof. The preparation method of the polysaccharide-protein composite stable high-bioavailability ferrous microemulsion comprises the following steps: adding mineral substances into water, mixing, and carrying out first stirring treatment to obtain a core material solution; adding starch sodium octenylsuccinate, whey protein isolate and polysaccharides into water, mixing, and sequentially carrying out heating treatment and second stirring treatment to obtain a wall material solution; mixing the core material solution, the wall material solution and an emulsifier, and sequentially carrying out third stirring treatment and homogeneous emulsification treatment to obtain an emulsion; and carrying out spray drying treatment on the emulsion to obtain the product. The polysaccharide-protein compounded stable high-bioavailability ferrous microemulsion has excellent embedding rate and storage stability, can effectively protect ferrous ions and reduce the generation of ferric ions, and is beneficial to improving the bioavailability of ferrous iron.

The invention discloses a method for reducing the content of iron in rare earth chloride, which comprises the following steps: step 1, adding alkali slurry into heavy sand slurry containing ferrous ions to adjust the pH value to 1-2, then adding an oxidizing agent, and reacting for 2-3 hours at the temperature of 30-45 DEG C to oxidize the ferrous ions into ferric ions to obtain first rare earth slurry, the concentration of ferrous ions is 0.1-0.2 g / L; 2, the pH value of the first rare earth slurry is adjusted to 3.8-4.2, a reaction is conducted for 1.5-2.5 h at the temperature of 62-68 DEG C, so that ferric ions form precipitates, and second rare earth slurry is obtained; 3, carrying out solid-liquid separation on the second rare earth slurry to obtain an optimal solution filtrate and a filter cake; and step 4, performing removal, solid-liquid separation, evaporation and concentration on the optimal solution filtrate to obtain a rare earth chloride product with the iron content lower than 0.05%. The invention aims to introduce hydrogen peroxide in the thorium neutralization and deposition stage to reduce the accumulation of iron impurities in the circulation process.

The invention discloses a fluorescent probe for targeting mitochondrial ferric ions as well as preparation and application of the fluorescent probe. The fluorescent probe is prepared by reacting cucurbit [7] uril with (E)-4-(4-(dimethylamino) styryl)-1-(3-(triphenylphosphonium) propyl) pyridine-1-onium bromide according to a molar ratio of 1: 1. The fluorescent probe can be used for detecting Fe < 3 + > ions, and has the characteristics of simple preparation method, convenience in operation, high sensitivity, high selectivity, low cost and rapidness in detection.

The invention discloses a method for testing the concentration of ferric ions in a citric acid cleaning solution, when the cleaning solution is combined with a color developing agent, namely a potassium thiocyanate solution, the cleaning solution is acidized in advance, firstly, citric acid is easy to form a stable complex with Fe < 3 + > at a relatively high pH value to hinder a subsequent color developing reaction and titration, and the concentration of ferric ions in the citric acid cleaning solution is not influenced; the protonated citric acid is subjected to pre-acidification treatment, so that the complexing ability of the protonated citric acid is destroyed, free Fe < 3 + > is released, hydrolysis of Fe < 3 + > is inhibited, and Fe < 3 + > is ensured to participate in subsequent reaction in an ionic state; besides, the acid environment can reduce the oxidation rate of Fe < 2 + >, avoid the introduction of additional errors due to the fact that Fe < 2 + > is oxidized into Fe < 3 + >, and improve the accuracy of a Fe < 3 + > concentration test result, so that the citric acid complexing effect is eliminated through the pre-acidification treatment, meanwhile, the oxidation interference of Fe < 2 + > is inhibited, and the detection precision is improved.

The invention provides a directional recovery method of pickling wastewater. According to the treatment method disclosed by the invention, a decomplexing agent is used for promoting a complex of fluorine, iron, chromium and nickel to be dissociated into free fluorine, then nanofiltration is adopted for realizing separation of the free fluorine, the iron, the chromium and the nickel, and a fluorine removal agent is added into the separated fluorine-rich solution for realizing fluorine recovery, so that the problem that the complex fluorine is difficult to recover is solved; meanwhile, according to the treatment method, a reducing agent is added into a separated solution rich in iron, chromium and nickel to promote ferric ions to be reduced into ferrous ions, then ion exchange resin is used for preferentially adsorbing chromium and nickel, the ion exchange resin containing chromium and nickel is subjected to desorption treatment, and then graded recovery of chromium and nickel is achieved through gradient pH regulation and control. And finally, pH regulation and control are carried out on the effluent obtained after ion exchange resin adsorption, iron recovery can be achieved, and therefore the problem that separation is difficult due to the fact that the pH of iron and chromium precipitates is close is solved.

The invention discloses a method for precipitating iron through ultrasonic enhanced oxidation, and belongs to the technical field of hydrometallurgy. The method comprises the following steps: performing ultrasonic treatment on a mixed system of an iron-containing zinc sulfate solution and an oxidizing agent under an acidic condition, efficiently catalyzing ferrous ions (Fe < 2 + >) to be oxidized into ferric ions (Fe < 3 + >) by utilizing an ultrasonic cavitation effect, and promoting the ferric ions to be stably precipitated in a goethite (alpha-FeOOH) form; after the reaction is completed, carrying out solid-liquid separation to obtain a low-iron zinc sulfate solution and goethite slag; compared with a traditional jarosite method and a hematite method, the method has the advantages that exogenous cations such as potassium and sodium do not need to be introduced, a high-temperature and high-pressure environment is not needed, and the oxidation efficiency can be remarkably improved and the goethite crystal form conversion can be regulated and controlled only based on the ultrasonic cavitation effect, so that the consumption of an oxidizing agent and the zinc content in the slag are effectively reduced; meanwhile, the iron grade and the filtering performance of an iron precipitation product are improved; the method is suitable for various oxidants, is high in process adaptability, has the advantages of high efficiency, greenness and economy, and has wide popularization and application prospects in the field of zinc smelting.

A method for making an iron-based oxide magnetic powder includes adding raw material solution containing trivalent iron ions, or trivalent iron ions and ions of a metal element that partially substitutes Fe sites, and an alkaline aqueous solution for neutralizing the raw material solution to a reaction system to adjust the pH of the reaction system to 1.0 or higher and 3.0 or lower. Hydroxycarboxylic acid is added to the obtained reaction solution and thereafter the pH of the reaction system is neutralized to 7.0 or higher and 10.0 or lower. The obtained precipitate of a substituent metal element-containing iron oxyhydroxide is coated with silicon oxide and then heated, whereby an iron-based oxide magnetic powder is obtained with a reduced content of fine and coarse particles, a particle shape close to a perfect sphere, and particles of ε-iron oxide in which Fe sites are partially substituted by other metal elements.

The invention provides a red foamed ceramic wall body material. The red foamed ceramic wall body material is prepared from the following raw material components in parts by weight: 50 to 78 parts of waste glass powder, 0 to 20 parts of fly ash, 10 to 20 parts of magnesium-iron hydrotalcite, 10 to 20 parts of limestone and 2 to 5 parts of borax. According to the invention, magnesium iron hydrotalcite is subjected to in-situ decomposition to generate pleonaste, the red color of ferric ions is retained, the red foamed ceramic is prepared, and black ferrous oxide or ferroferric oxide is prevented from being generated.

The invention provides a ferronickel-based oxygen evolution electrode and a preparation method thereof based on interface confinement. The preparation method of the ferronickel-based oxygen evolution electrode comprises the following steps: preparing a precursor solution containing ferrous ions and ferric ions; the foamed nickel substrate is cleaned; the cleaned foamed nickel is tightly attached to the surface of the bottom of the reaction container, the foamed nickel is immersed in the precursor solution, under the room-temperature standing condition, divalent and trivalent iron ions are induced to be subjected to a synergistic hydrolysis and coprecipitation reaction through a physical interface confinement space formed by an attached interface, and the nickel-based composite material is obtained. Therefore, a high-activity and high-uniformity nickel-iron-based (oxygen) hydroxide catalyst layer (DIC-NiFeOOH / NF) is grown on the surface of the foamed nickel in situ. The method is simple in process, green and energy-saving, and the prepared nickel-iron-based oxygen evolution electrode shows excellent performance in oxygen evolution reaction and anion exchange membrane water electrolysis.

The present invention addresses the problem of providing an acidic cleaning solution for an aluminum-based metallic material, the acidic cleaning solution being capable of suppressing foaming while achieving favorable cleaning properties. One embodiment for solving the aforementioned problem is an acidic cleaning solution for an aluminum-based metallic material that comprises 0.01-25 g / L of at least one inorganic acid selected from the group consisting of sulfuric acid, nitric acid, nitrous acid, and phosphoric acid; 0.05-4.0 g / L of trivalent iron ions; and 0.1-10 g / L of a surfactant, wherein the surfactant includes a surfactant A: a polyoxyalkylene alkyl ether having a cloud point of 80°C or more, a surfactant B: a polyoxyalkylene alkyl ether having a cloud point of 50-60°C, and a surfactant C: a polyoxyalkylene alkyl ether having a cloud point of 40°C or less, and wherein the cloud point is measured in accordance with JIS K 3211: 1990.

To provide an acidic cleaning solution for aluminum-based metal materials that can achieve desirable cleaning properties while suppressing foaming. [Solution] An acidic cleaning solution for aluminum-based metal materials comprising: 0.01 g / L to 25 g / L of at least one inorganic acid selected from the group consisting of sulfuric acid, nitric acid, nitrite, and phosphoric acid; 0.05 g / L to 4.0 g / L of trivalent iron ions; and 0.1 g / L to 10 g / L of a surfactant, wherein the surfactant comprises: surfactant A: a polyoxyalkylene alkyl ether with a cloud point of 80°C or higher; surfactant B: a polyoxyalkylene alkyl ether with a cloud point of 50°C to 60°C; and surfactant C: a polyoxyalkylene alkyl ether with a cloud point of 40°C or lower.

The invention relates to a ferrate-calcium salt enhanced turbidity removal and water purification method based on ferrous ion activation, and aims to solve the technical problems that the effluent quality is difficult to guarantee when a traditional coagulant is used for treating low-temperature low-turbidity water or algae-laden water, and particularly the turbidity is easy to exceed the standard. The invention discloses a ferrate-calcium salt enhanced turbidity removal and water purification method, which comprises the following steps of: adding a ferrous compound, a calcium salt and ferrate into low-turbidity or high-algae raw water, uniformly stirring, controlling the molar ratio of the ferrous compound to the ferrate to the calcium salt to be (0.5-1.5): 1: (2-10), and standing and precipitating to complete the enhanced turbidity removal and water purification method of the low-turbidity or high-algae raw water. Calcium ions are introduced through calcium salt so as to effectively compress double electric layers on the surface of colloid and promote destabilization and coagulation, multiple synergistic effects of oxidation, coagulation, adsorption and coprecipitation are constructed through directional activation of ferrous ions on ferrate and synergistic interaction of the calcium ions, and therefore when complex water with low temperature, low turbidity, high algae and the like is treated, the treatment effect is good, and the treatment cost is low. The deep and efficient removal of turbidity and organic matters can be synchronously realized.

Provided is an etching liquid composition capable of sufficiently etching a layer containing copper in the depth direction while sufficiently suppressing side etching. An etchant composition for etching a layer containing copper, the etchant composition containing (A) a compound represented by general formula (1) (in general formula (1), R1 and R2 each independently represent a hydrogen atom, an amino group, a thiol group, a phenyl group or a carboxyl group; in the formula, when one of R1 and R2 is a hydrogen atom, the other is a thiol group, a phenyl group, or a carboxyl group. (B) at least one component selected from the group consisting of bivalent copper ions and trivalent iron ions; and (C) an aqueous solution of an acid and water.

This invention discloses an apparatus and process for removing sulfur dioxide from flue gas using siderite slurry, relating to the field of environmental protection technology. The apparatus comprises six major components: desulfurization, slurry circulation, slurry replenishment, oxidation, defoaming emission, and spent slurry treatment. The components are interconnected by pipelines. The process includes siderite pretreatment slurry preparation, slurry replenishment, flue gas desulfurization, sulfite oxidation, flue gas defoaming emission, and spent slurry treatment. Siderite is crushed and ground into a slurry with a specific particle size and solids content, which is then contacted countercurrently with sulfur-containing flue gas. Utilizing ferric carbonate, magnesium carbonate, and calcium carbonate in the slurry as desulfurizing agents, combined with the oxidation effect of air and ferric ions, sulfur dioxide is converted into ferric sulfate and calcium sulfate, achieving desulfurization. This invention has high desulfurization efficiency, with the sulfur dioxide content in the purified flue gas below 50 mg / Nm³. 3 It makes full use of low-grade siderite resources, and the desulfurization by-products can be utilized as resources. The process is simple and has no secondary pollution, resulting in significant economic and environmental benefits.

This invention relates to a method for preparing and applying an acidic medium-based iron ion recognition indicator. The indicator contains an aminoquinoline structure and a sulfosalicylic acid structure. It exhibits excellent dual colorimetric and fluorescence responses to ferric ions. When the sample contains Fe... 3+ At that time, Fe 3+ It can undergo complexation reactions with the -NH-CO-, -OH, and quinoline-N groups in the indicator, changing the solution from colorless to brown. This allows for qualitative analysis of iron ions by naked-eye observation. Simultaneously, the fluorescence weakens, and the fluorescence intensity is similar to that of Fe. 3+ The content exhibits a good linear relationship, reaching the nanomolar level, enabling quantitative detection of iron ions and Fe. 3+ It has extremely excellent selectivity, and can identify and detect iron ions not only in normal environments, but also accurately identify iron ions under extreme conditions of strong acidity. It is stable, can be used in acidic media, and has strong anti-interference ability.