717 results about "Hydrogen sulphide" patented technology

The invention discloses a rectification mechanism and a carbon disulfide production system containing the same. The rectification mechanism comprises an integrated rectification tower, and an inner cavity of a shell of the integrated rectification tower is sequentially divided into a function-integrated pre-separation and sulfur removal area, a main rectification and hydrogen sulfide removal area and a condensation reflux area from bottom to top in the vertical direction; the pre-separation and sulfur removal area comprises a settling tank arranged at the lower part of the shell, a gathering cover arranged above the inner wall of the settling tank, and a gas rising pipe I arranged above the gathering cover; the invention belongs to the technical field of chemical separation, and achieves the technical effects that multi-stage functions of pre-separation, main rectification, precise purification, final condensation and the like are innovatively integrated in a single tower, so that the fundamental simplification and compactness of the equipment structure are realized; in the traditional process, separate coarse removal, fine removal and finished product towers are replaced by unique expanded settling tanks in the towers, filler layers of integrated plate heat exchangers, tower tops with spiral condensation channels and side-draw systems.

The invention discloses a method for preparing 12-mercaptan through solid organic acid catalysis, belongs to the technical field of 12-mercaptan preparation, and aims to solve the problems of low catalyst activity, harsh reaction conditions, serious pollution, high cost and dependence on import in the prior art. N-dodecanol and hydrogen sulfide are used as raw materials and are mixed according to the molar ratio of 1: 1.2-1: 1.3; the method comprises the following steps: gasifying n-dodecanol, mixing with purified hydrogen sulfide, preheating to 210-240 DEG C, introducing into a fixed bed reactor filled with a solid organic acid catalyst, and reacting at-0.08-3.0 MPa for 3.5-4 hours; and cooling and condensing the reaction product, carrying out gas-liquid separation, rectifying and purifying the liquid product to obtain 12-mercaptan with the purity of more than or equal to 99.5%, and recycling unreacted hydrogen sulfide. The solid organic acid can be a catalyst of p-toluenesulfonic acid and the like or mesoporous silica loaded nickel, cobalt and molybdenum metal oxides. The method has the advantages of high catalytic activity, mild reaction conditions, high product yield (the conversion rate of n-dodecanol is greater than or equal to 94.5%), environmental protection and low cost, can realize the domestic mass production of 12-mercaptan, and meets the market demand.

The invention relates to a spherical hydrotalcite phase desulfurization adsorbent as well as a preparation method and application thereof, the preparation method comprises the following steps: mixing an iron source, a nickel source and organic carboxylate, and then carrying out hydrothermal carbonization reaction to obtain the spherical hydrotalcite phase desulfurization adsorbent. The nickel source and the iron source are selected as the raw materials, hydroxide radicals of laminates and carbonate ions between the laminates of the prepared hydrotalcite phase desulfurization adsorbent can increase the alkalinity of the surface of the desulfurization adsorbent and improve the adsorption capacity to hydrogen sulfide, and meanwhile, the hydrotalcite phase desulfurization adsorbent can react with hydrogen sulfide in a catalytic oxidation manner, so that the removal efficiency is improved. Organic carboxylate is selected as a hydrothermal auxiliary agent, carboxylate radicals can chelate metal ions through multidentate coordination to form a stable complex, so that the nucleation rate of hydrotalcite is delayed, the particle size uniformity is improved, meanwhile, a carbon coating layer is generated through hydrothermal carbonization, and pores in the carbon coating layer and pores in hydrotalcite can form hierarchical pore channels, so that the composite material is prepared. The mass transfer efficiency is synergistically improved, so that the adsorption capacity of the adsorbent is improved.

A method for synergistically preparing lithium sulfide by vacuum molten salt based on hydrogen sulfide-lithium salt reaction belongs to the technical field of battery materials, and comprises the following steps: placing a lithium salt solid in a reactor, introducing a molten salt medium on the surface of the lithium salt or in a reaction system, introducing purified hydrogen sulfide gas under a vacuum auxiliary condition, controlling the reaction temperature to be 200-500 DEG C, and reacting for 1-2 hours; and adjusting the flow rate of hydrogen sulfide to be 50-1000mL / min and the retention time to be 5-180min, continuously exhausting gas to discharge water vapor in the reaction process, stopping introducing hydrogen sulfide gas after the reaction is finished, cooling the system to room temperature under the protection of inert gas, taking out the product, washing to remove residual fused salt, and carrying out vacuum drying to obtain the high-purity lithium sulfide. The prepared lithium sulfide has high purity (greater than or equal to 99.90%), low defect density and an excellent crystal structure, and can be widely applied to lithium-sulfur batteries, all-solid-state batteries and novel energy storage technologies, so that the energy density is improved, the cycle life is prolonged, and the energy consumption is reduced.

The invention discloses a fluorescent covalent organic framework material for hydrogen sulfide detection as well as a preparation method and application thereof, relates to a covalent organic framework material as well as a preparation method and application thereof, and aims to solve the technical problems that an existing porous material for H2S detection is few in structure type, unstable in COFs (Covalent Organic Frameworks) structure, high in detection limit and harsh in detection environment. The periodic structure fragment of the fluorescent covalent organic framework material for hydrogen sulfide detection is shown in the specification. 3-(5, 10-diamino-1H-phenanthrene) [9, 10-d] imidazole-2-yl) phenol and 2, 4, 6-tri (4-formylphenoxy)-1, 3, 5-triazine are subjected to a reaction to obtain a hydroxyl intermediate, the hydroxyl intermediate is modified with 2, 4-dinitrofluorobenzene, and the fluorescent material is used for qualitative detection of H2S. The method is not interfered by amino acids and anions in the environment, and is not influenced by an acid-base environment. The method can be used in the field of H2S detection.

Provided is a hydrogen sulfide removing agent that can be stably used while maintaining hydrogen sulfide removing ability equivalent to that of a hydrogen sulfide removing agent comprising an amorphous iron oxyhydroxide. This iron oxyhydroxide-based hydrogen sulfide removing agent contains amorphous iron oxyhydroxide and a crystalline component. The content of the amorphous iron oxyhydroxide is not less than the content of the crystalline component.

The present invention provides a method for preparing lithium sulfide and lithium sulfide, so as to prepare a high-purity lithium sulfide without increasing the purification cost. The method includes: keeping thiourea and lithium hydroxide warm under a first condition to obtain a mixture; wherein, the first condition includes a heat preservation temperature of 130-180 °C; reacting the mixture with hydrogen sulfide under a second condition to obtain lithium sulfide; wherein, the second condition includes a temperature condition of 500-760 °C.

The present invention relates to a method for preparing lithium sulfide, according to the present invention, when preparing lithium sulfide by a reaction between a lithium raw material and hydrogen sulfide, the reaction is carried out under relatively mild conditions compared to the prior art, so that frequent maintenance or replacement due to corrosion and failure of a reactor and various pipes is not required, thereby improving the economical efficiency of the process. Further, by reusing the unreacted hydrogen sulfide from which moisture has been removed and the solvent, process costs can be reduced, and economical efficiency can be ensured during mass production. Furthermore, moisture and water vapor generated in the lithium sulfide generation reaction are effectively removed, thereby preventing a reverse reaction for generating lithium hydroxide, promoting a positive reaction, and producing high-quality lithium sulfide with high purity and high yield. In addition, the particle size can be adjusted in units, and a separate pulverizing space or pulverizing table is not required, so that convenience and mass productivity are excellent.

The invention belongs to the technical field of coke oven gas purification treatment, and particularly discloses a method for removing hydrogen sulfide in coke oven gas through photocatalysis, generation of oxygen vacancies is promoted by adopting a synthesis concept of synergistic effect of silver doping and polyethyleneimine, polyethyleneimine provides an alkaline condition on one hand, lone electron pairs on nitrogen are coordinated with zinc on the other hand, and the hydrogen sulfide in the coke oven gas is removed through photocatalysis. The preparation method comprises the following steps: by taking H2S and polyethyleneimine as raw materials, generating abundant oxygen vacancies under the synergistic effect of the H2S and silver, preventing agglomeration of generated ZnO and increasing reaction sites by taking polyethyleneimine as a surfactant, and then promoting a cascade reaction between ZnO < 1-x > and H2S by taking abundant oxygen vacancies, so that a 1D / 3D-ZnS / ZnO heterojunction is generated in situ to further reduce recombination of photo-generated electron holes; the catalyst converts H2S into elemental sulfur through photo-induced electrons and holes, and a carbon disulfide solution is used for cleaning the catalyst to realize regeneration of the catalyst. The method provided by the invention not only improves the removal efficiency of H2S, but also reduces the operation cost and reduces environmental pollution.

The invention discloses a triazine desulfurizer and a preparation method thereof, and belongs to the technical field of gas purification. The triazine desulfurizer is mainly prepared from the following raw materials in percentage by weight: 20 to 50 weight percent of triazine derivative, 10 to 15 weight percent of sterically hindered amine, 3 to 7 weight percent of stabilizer, 1 to 3 weight percent of synergist, 0.5 to 1.5 weight percent of penetrant, 0.5 to 1.5 weight percent of inhibitor, 1 to 2 weight percent of additive and the balance of water, the preparation method of the triazine derivative comprises the following steps: adding 2-(diphenylphosphino) ethylamine into a toluene solvent, adding a paraformaldehyde aqueous solution in batches under a stirring condition, and reacting for 2-8 hours to obtain the triazine derivative. According to the triazine desulfurizer and the preparation method thereof provided by the invention, the triazine derivative and the sterically hindered amine are taken as a host, and the stabilizer, the synergist, the penetrant, the inhibitor and the assistant are compounded, so that the scaling trend of the triazine desulfurizer in an oil and gas well can be slowed down, the dissolution rate of hydrogen sulfide and the mass transfer rate in a solution are increased, and the desulfurization reaction is promoted; the desulfurization effect and the desulfurization rate are improved, and meanwhile, a very good scale inhibition effect is also achieved.

The invention provides a BDO (1, 4-butanediol) wastewater treatment process with high sulfate content, which comprises the following steps: carrying out electrochemical oxidation treatment on BDO (1, 4-butanediol) wastewater with high sulfate content; introducing the obtained BDO wastewater into an anaerobic reaction device for anaerobic reaction to reduce sulfate ions into hydrogen sulfide and oxidize organic matters to reduce COD (Chemical Oxygen Demand); effluent sequentially flows back to the circulating desulfurization device and the air floatation device; carrying out aeration treatment in the circulating desulfurization device so as to oxidize hydrogen sulfide into elemental sulfur; elemental sulfur is recycled in the air flotation device, and part of effluent of the air flotation device and part of effluent of the anaerobic reaction device flow back to inlet water of the anaerobic reaction device; part of effluent of the air floatation device and part of effluent of the anaerobic reaction device are combined and then are sequentially introduced into an aerobic activated sludge tank with a membrane bioreactor and an ozone catalytic oxidation tank. Effluent can enter a subsequent ultrafiltration reverse osmosis membrane system to be purified, and water produced by the membrane system is recycled as reclaimed water.

The invention relates to the technical field of corrosion prevention of oil field pipes, and particularly discloses electroplating liquid for a high-tungsten-content hydrogen sulfide corrosion resistant sleeve coating and a preparation process of the electroplating liquid. The invention discloses electroplating liquid for a high-tungsten-content hydrogen sulfide corrosion-resistant sleeve coating. The electroplating liquid comprises the following raw materials: 60-90 parts of a composite tungsten source; 40-70 parts of a nickel-cobalt main salt; 35-55 parts of a composite complexing agent; 1-5 parts of carboxylated graphene quantum dots; 1 to 5 parts of an aminated ZIF-8 derived carbon nanocage; 1-5 parts of a rare earth stabilizer; 1-4 parts of sodium hypophosphite; 1-4 parts of sodium citrate; 1-3 parts of a surfactant; 15 to 25 parts of a buffering agent; and 350 to 450 parts of deionized water. According to the single-layer electroplated layer, the interface stress of the multi-layer structure can be eliminated, so that other interface problems such as plating layer cracking caused by underground temperature fluctuation are avoided, it is guaranteed that the thickness of the plating layer reaches the standard, and then it is guaranteed that the plating layer has excellent corrosion resistance.

The invention belongs to the field of microorganisms, and relates to lactobacillus paracasei. In particular discloses a lactobacillus paracasei strain HNGD-AL1, the taxonomic name is Lactobacillus paracasei, the lactobacillus paracasei strain HNGD-AL1 is preserved in China Center for Type Culture Collection on February 27, 2025, the preservation number is CCTCC M 2025303, and the preservation address is No. 299 on eight road in Wuchang District, Wuhan, Hubei. The method for degrading the sulfur-containing amino acid by adopting the lactobacillus paracasei is found for the first time, the effect of degrading 53.39% of the sulfur-containing amino acid can be achieved by culturing the probiotics in a fermentation culture medium for 24 hours, and the probiotics can be colonized in intestinal tracts and play a role in degrading the sulfur-containing amino acid in intestinal contents; the content of metabolite hydrogen sulfide of sulfur-containing amino acid in the intestinal tract is reduced by 60.92%, intestinal tract tissue damage, permeability and inflammatory response are reduced, and the purpose of improving ulcerative colitis is achieved. The preparation method has a wide application prospect in the aspects of preparation of low-sulfur-content amino acid foods and probiotic preparations for improving colitis.

The invention relates to a Raman probe for detecting hydrogen sulfide as well as a preparation method and application of the Raman probe. The gold and silver nanocage (AuAg NCs) is prepared, and after the gold and silver nanocage (AuAg NCs) is modified by a Raman signal molecule 4-ethynylaniline (4EA), it is found that the AuAg-4EANCs shows the strongest Raman enhancement effect at the position of 2010 cm <-1 > located in a cell silence zone. The SERS probe with the tumor targeting capability is developed through the functional modification of a mucoprotein 1 aptamer (MUin1aptamer, MUC1Apt) and polyethylene glycol (PEG), and the SERS probe with the tumor targeting capability is further developed through the functional modification of the mucoprotein 1 aptamer (MUin1aptamer, MUC1Apt) and the PEG (Polyethylene Glycol). In the presence of hydrogen sulfide (H2S) and oxygen, Ag in AuAg-4EANCs rapidly reacts with H2S to generate Ag2S with significantly reduced Raman enhancement performance, resulting in sharp attenuation of 4EA signal intensity. And along with the increase of the H2S concentration, the generation amount of Ag2S is increased, so that a quantitative detection model dependent on the H2S concentration is established.

The invention belongs to the technical field of semiconductor oxide gas sensors, and particularly relates to an rGO / CuO / Li sensitive material, a preparation method thereof and application of the rGO / CuO / Li sensitive material in H2S sensors. The preparation method comprises the following steps: firstly, preparing a graphene oxide nanosheet by using an improved Hummers method, and then preparing the rGO / CuO / Li sensitive material by using copper nitrate, lithium chloride and the prepared graphene oxide nanosheet as raw materials, polyvinylpyrrolidone as a surfactant and N, N-dimethylformamide as a solvent by using a one-step solvothermal method. Under the condition of room temperature, the sensitive material shows a relatively high response value (220.1) and a relatively low detection lower limit (1ppb) on hydrogen sulfide, has good selectivity, repeatability and stability, and has a wide application prospect in trace-level hydrogen sulfide detection in the fields of industrial safety and atmosphere detection.

The invention discloses an intelligent hydrogen sulfide-resistant anticorrosive coating for a coal chemical industry pipeline and a preparation method, and belongs to the technical field of corrosion prevention of coal chemical industry pipelines. The coating is composed of a base material, a functional filler, an intelligent component and an auxiliary agent, the base material improves the mechanical property and chemical stability, the functional filler enhances the hydrogen sulfide corrosion resistance, and the intelligent components achieve the self-repairing function of the coating. The preparation method comprises the steps of microcapsule preparation, component mixing, ultrasonic dispersion, coating and thermocuring. The corrosion resistance of the coating is greater than or equal to 95% under the environment of 80 DEG C, 90% humidity and 1000ppm H2S, the adhesive force reaches grade 1, the tensile strength is 10-20MPa, and the elongation at break is 200-300%. The high-corrosion-resistance and self-repairing pipeline protection material has high corrosion resistance, self-repairing capacity and construction convenience, and is suitable for pipeline protection in a high-concentration hydrogen sulfide environment.

The invention provides a liquid sulfur removal agent and a preparation method thereof, and belongs to the technical field of natural gas hydrogen sulfide removal treatment.The liquid sulfur removal agent comprises, by weight, 36-66% of s-triazine derivatives, 5-8% of sulfolane, 2-5% of a pH control agent, 10-12% of a stabilizer, 5-8% of a scale inhibitor, 1-2% of a bactericide and the balance deionized water; wherein the s-triazine derivative is selected from a mixture of hexahydro-1, 3, 5-triacetyl-hexahydros-triazine, 1, 3, 5-triacetyl-hexahydros-triazine and 1, 3, 5-triazinane-2, 4-diketone, and the structural formula of the s-triazine derivative is shown in the description. The liquid sulfur removal agent is high in sulfur removal efficiency, good in corrosion inhibition and sterilization performance and not prone to scaling.

The invention relates to the technical field of acid tail gas treatment, and discloses a boron-nitrogen-doped aluminum oxide catalyst as well as a preparation method and application thereof. The method comprises the following steps: (1) mixing an aluminum source, a nitrogen source, a boron source and water to obtain a mixed solution, then adding a peptizing agent to adjust the pH of the mixed solution to be acidic, and then standing and aging; (2) drying the material subjected to standing and aging in the step (1), then roasting under protective gas, and then sequentially carrying out high-temperature nitriding and cooling; and (3) carrying out plasma treatment on the material cooled in the step (2). The catalyst prepared by the method has large specific surface area and catalytic activity, can well capture water and carbonyl sulfide, converts carbonyl sulfide into hydrogen sulfide and improves the purity and yield of enriched hydrogen sulfide, and the preparation method of the catalyst is simple and efficient.

This disclosure relates to systems for hydrogen sulfide mitigation. A battery cell or plurality of battery cells in a battery pack with a solid electrolyte sandwiched between an anode and a cathode are presented. A coating is applied to an interior surface of the sulfur-containing lithium-based rechargeable battery cell. The coating is configured to precipitate hydrogen sulfide gas responsive to moisture ingress in the cathode and exude sulfur dioxide and water external to the sulfur-containing lithium-based rechargeable battery cell.

Embodiments of the present disclosure may include a system and method for enhancing the extraction of lithium from a liquid resource. A volume of midstream-liquid resource may be received from a site like a pipeline, tank, or disposal site where the midstream-liquid resource may undergo a pre-treatment. A treatment regimen may be applied to remove hydrocarbons, organic matter, hydrogen sulfide, ions, and suspended solids along with reduction of excess pre-treatment chemicals and byproducts. Embodiments may further include critical-material extraction. The system for this process includes a pre-treatment station, a filtration station, and a direct-lithium-extraction (DLE) unit, with a reverse-osmosis station to concentrate the lithium product.

Provided is a device for producing lithium sulfide, the lithium sulfide production device being equipped with a reactor 1 for reacting hydrogen sulfide with a lithium source. The reactor 1 has a hydrogen sulfide inlet line 4 for introducing hydrogen sulfide obtained from a desulfurizer 2 into the reactor 1 and a hydrogen sulfide outlet line 5 for releasing unreacted hydrogen sulfide to the outside of the reactor.

The present invention relates to a process for preparing lithium sulfide (LiS) from lithium hydroxide (LiOH) and hydrogen sulfide (HS), characterized in that the lithium hydroxide is sulfided in a reaction zone (9) comprising at least one moving-bed tubular reactor (9a) with an ascending oscillating spiral configuration, in which the lithium hydroxide (4) circulates countercurrently to an anhydrous gas mixture (10) containing hydrogen sulfide and at least one inert gas.

This disclosure relates to hydrogen sulfide mitigation systems. A battery cell or a plurality of battery cells in a battery pack having a solid electrolyte disposed between an anode and a cathode is presented. A coating is applied to an interior surface of the sulfur-containing lithium-based rechargeable battery cell. The coating is configured to precipitate hydrogen sulfide gas in response to moisture ingress into the cathode and to expel sulfur dioxide and water outside the sulfur-containing lithium-based rechargeable battery cell.

The present invention relates to a production method of a solid electrolyte in which adopting a liquid-phase method, a solid electrolyte having a high ionic conductivity, in which the generation of hydrogen sulfide is suppressed, the method including mixing a raw material inclusion containing a lithium element, a sulfur element, a phosphorus element, and a halogen element with a complexing agent containing a compound having at least two tertiary amino groups in the molecule; and an electrolyte precursor constituted of a lithium element, a sulfur element, a phosphorus element, a halogen element, and a complexing agent containing a compound having at least two tertiary amino groups in the molecule.

The invention provides a preparation method of a magnetic recoverable catalyst and a method for synthesizing 3-mercaptopropionic acid, and mainly solves the problem that a large amount of acid and alkali solutions are needed in the existing acrylonitrile-sodium hydrosulfide and acrylic acid-thiourea process routes. The thiohydracrylic acid synthesis catalyst is prepared. The use conditions of the catalyst are as follows: the temperature is 30-80 DEG C, the reaction pressure is 0.5-3 MPa, the mass ratio of the acrylic acid to the solvent is 0.1-5, and the mass ratio of the acrylic acid to the catalyst is 0.2-20. Compared with the prior art, the catalyst disclosed by the invention is used as a synthetic catalyst for preparing thiohydracrylic acid through reaction of acrylic acid and hydrogen sulfide, a solid catalyst and a liquid reaction system can be completely separated by adopting simple methods such as filtration, centrifugation or magnetic separation, and a complicated pickling step is not needed; and the problem that a homogeneous catalyst is difficult to rectify after salification in the use process is avoided.

This invention relates to the field of chemical equipment technology, and discloses a lithium sulfide preparation device and method, comprising: an insulated shell; a reactor rotatably disposed inside the insulated shell, with a heating chamber formed between the reactor and the insulated shell; a rotating shaft fixed to one end of the reactor, passing through one end of the insulated shell and rotatably engaging with a support assembly; a rotating assembly connected to the rotating shaft to drive its rotation; and a heat source inlet pipe fixed to one end face of the insulated shell to communicate with the interior of the heating chamber. This invention utilizes a dynamic reactor, causing the solid material to continuously tumble and shift during the reaction process, greatly increasing the contact area between the solid phase and the gaseous hydrogen sulfide, enhancing mass transfer efficiency, significantly improving product purity and reaction efficiency, shortening the production cycle, reducing equipment investment and energy consumption, and facilitating large-scale industrial production of high-purity lithium sulfide.

The battery system (100) comprises a single cell (10) made of a sulfide-based all-solid-state battery, a battery module (200) in which a plurality of single cells (10) are stacked between a pair of restraining members (31, 32), an intermediate plate (60) disposed between the stacked single cells (10), a detection unit configured to detect a load applied to the intermediate plate (60), and an estimation unit (300) configured to estimate the generation of hydrogen sulfide in the single cell (10) based on a change in the load applied to the intermediate plate (60).

The invention belongs to the technical field of coal ethylene glycol, and particularly relates to a process and a device for finely removing impurities from carbon monoxide after cryogenic separation of synthesis gas, the device comprises an impurity removal device, the impurity removal device comprises a desulfurization tank, a dechlorination tank and a decarbonylation tank which are sequentially connected in series, or an adsorption tower which is sequentially filled with desulfurization, dechlorination and decarbonylation adsorbents; the impurity removal device is arranged to remove trace hydrogen sulfide, hydrogen chloride, carbonyl iron and carbonyl nickel in CO after cryogenic separation, so that ppb-level removal of impurities in CO is realized, poisoning of a downstream dimethyl oxalate (DMO) synthesis catalyst is avoided, the service life of the catalyst is prolonged, the production cost of an enterprise is reduced, and the operation stability of the device is improved.

The present invention discloses a method for removing impurities from waste acid and fully recycling the waste acid. The method comprises the following steps: introducing hydrogen sulfide into the waste acid for a sulfidation reaction, removing arsenic sulfide and mercuric sulfide precipitates formed during the reaction; continuing to introduce hydrogen sulfide for a step-by-step sulfidation reaction, adding an iron-containing substance to adjust the reaction pH and ORP, and recovering the copper, lead, and zinc sulfide slag precipitates formed during the reaction in a step-by-step manner; adding an iron-containing substance for a neutralization reaction, controlling the pH and ORP, promoting the reaction between iron ions and arsenate, and removing the ferric arsenate precipitate formed during the reaction; adding an adsorbent for an adsorption reaction, and removing fluorine-containing and thallium-containing components by adsorption; introducing an oxidant for an oxidative hydrolysis reaction, controlling the degree of hydrolysis, and preparing polyferric sulfate. The present invention utilizes the iron-containing substance to remove impurities from waste acid, thereby achieving deep impurity removal and full resource utilization of waste acid.

The utility model relates to the technical field of chemical engineering, in particular to a sodium hydrogen sulfide solution storage tank flushing system which comprises a magnetic turning plate liquid level meter, a remote transmission liquid level meter, a sodium hydrogen sulfide storage tank, a condensation water pipeline, an upper flushing line, a lower flushing line and a remote transmission flushing line. A lower end inlet of the magnetic flap liquid level meter is connected with a lower end drain valve; a first short-circuit wire is led out from the sodium hydrosulfide storage tank to be connected to an outlet in the upper end of the magnetic flap liquid level meter, a second short-circuit wire is led out from the sodium hydrosulfide storage tank to be connected to an outlet in the lower end of the magnetic flap liquid level meter, a third short-circuit wire is led out from the sodium hydrosulfide storage tank to be connected to the remote transmission liquid level meter, and a remote transmission shower valve is arranged on the third short-circuit wire. On-line flushing of the sodium hydrogen sulfide solution storage tank is achieved, when liquid level display is different from remote liquid level, water flushing is carried out, checking is carried out again after flushing, and the operation risk is reduced.