CN113737205A - Method for directly preparing ammonia gas by electrochemical reduction of nitrite (nitrite) - Google Patents

Method for directly preparing ammonia gas by electrochemical reduction of nitrite (nitrite) Download PDF

Info

Publication number
CN113737205A
CN113737205A CN202111138428.9A CN202111138428A CN113737205A CN 113737205 A CN113737205 A CN 113737205A CN 202111138428 A CN202111138428 A CN 202111138428A CN 113737205 A CN113737205 A CN 113737205A
Authority
CN
China
Prior art keywords
nitrite
nitrate
electrochemical reduction
metal
ammonia gas
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CN202111138428.9A
Other languages
Chinese (zh)
Other versions
CN113737205B (en
Inventor
向开松
刘恢
易慧敏
沈锋华
王珠江
刘旭东
付迎雪
伍琳
陈昊
柴立元
李青竹
王庆伟
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Central South University
Original Assignee
Central South University
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Central South University filed Critical Central South University
Priority to CN202111138428.9A priority Critical patent/CN113737205B/en
Publication of CN113737205A publication Critical patent/CN113737205A/en
Application granted granted Critical
Publication of CN113737205B publication Critical patent/CN113737205B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B1/00—Electrolytic production of inorganic compounds or non-metals
    • C25B1/01—Products
    • C25B1/27—Ammonia
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B1/00—Electrolytic production of inorganic compounds or non-metals
    • C25B1/50—Processes
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B11/00—Electrodes; Manufacture thereof not otherwise provided for
    • C25B11/02—Electrodes; Manufacture thereof not otherwise provided for characterised by shape or form
    • C25B11/03—Electrodes; Manufacture thereof not otherwise provided for characterised by shape or form perforated or foraminous
    • C25B11/031—Porous electrodes
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B11/00—Electrodes; Manufacture thereof not otherwise provided for
    • C25B11/04—Electrodes; Manufacture thereof not otherwise provided for characterised by the material
    • C25B11/051—Electrodes formed of electrocatalysts on a substrate or carrier
    • C25B11/052—Electrodes comprising one or more electrocatalytic coatings on a substrate
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B11/00—Electrodes; Manufacture thereof not otherwise provided for
    • C25B11/04—Electrodes; Manufacture thereof not otherwise provided for characterised by the material
    • C25B11/051—Electrodes formed of electrocatalysts on a substrate or carrier
    • C25B11/052—Electrodes comprising one or more electrocatalytic coatings on a substrate
    • C25B11/053—Electrodes comprising one or more electrocatalytic coatings on a substrate characterised by multilayer electrocatalytic coatings
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B11/00—Electrodes; Manufacture thereof not otherwise provided for
    • C25B11/04—Electrodes; Manufacture thereof not otherwise provided for characterised by the material
    • C25B11/051—Electrodes formed of electrocatalysts on a substrate or carrier
    • C25B11/055—Electrodes formed of electrocatalysts on a substrate or carrier characterised by the substrate or carrier material
    • C25B11/057—Electrodes formed of electrocatalysts on a substrate or carrier characterised by the substrate or carrier material consisting of a single element or compound
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B11/00—Electrodes; Manufacture thereof not otherwise provided for
    • C25B11/04—Electrodes; Manufacture thereof not otherwise provided for characterised by the material
    • C25B11/051—Electrodes formed of electrocatalysts on a substrate or carrier
    • C25B11/055—Electrodes formed of electrocatalysts on a substrate or carrier characterised by the substrate or carrier material
    • C25B11/057—Electrodes formed of electrocatalysts on a substrate or carrier characterised by the substrate or carrier material consisting of a single element or compound
    • C25B11/061—Metal or alloy
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B11/00—Electrodes; Manufacture thereof not otherwise provided for
    • C25B11/04—Electrodes; Manufacture thereof not otherwise provided for characterised by the material
    • C25B11/051—Electrodes formed of electrocatalysts on a substrate or carrier
    • C25B11/073—Electrodes formed of electrocatalysts on a substrate or carrier characterised by the electrocatalyst material
    • C25B11/075—Electrodes formed of electrocatalysts on a substrate or carrier characterised by the electrocatalyst material consisting of a single catalytic element or catalytic compound
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B11/00—Electrodes; Manufacture thereof not otherwise provided for
    • C25B11/04—Electrodes; Manufacture thereof not otherwise provided for characterised by the material
    • C25B11/051—Electrodes formed of electrocatalysts on a substrate or carrier
    • C25B11/073—Electrodes formed of electrocatalysts on a substrate or carrier characterised by the electrocatalyst material
    • C25B11/091—Electrodes formed of electrocatalysts on a substrate or carrier characterised by the electrocatalyst material consisting of at least one catalytic element and at least one catalytic compound; consisting of two or more catalytic elements or catalytic compounds
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B15/00—Operating or servicing cells
    • C25B15/02—Process control or regulation

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Automation & Control Theory (AREA)
  • Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)

Abstract

The invention discloses a method for preparing ammonia by electrochemical direct reduction of nitrate (nitrite), which is to electrochemically reduce electrolyte containing nitrite and/or nitrate by a porous membrane electrode to generate ammonia; the method can realize the efficient and high-selectivity conversion of nitrate (nitrite) ions into ammonia gas, and the method can convert ammonium ions in the solution into ammonia gas and realize separation without adding alkali, thereby greatly reducing the cost for separating ammonia gas, being capable of being carried out under the conditions of normal temperature and normal pressure, having simple operation and being convenient for large-scale application.

Description

Method for directly preparing ammonia gas by electrochemical reduction of nitrite (nitrite)
Technical Field
The invention relates to a method for directly preparing ammonia by electrochemical reduction of nitrite (nitrite) and particularly relates to a method for realizing resource utilization of ammonia by converting nitrite (nitrite) in denitration waste liquid or nitrate sewage by a wet process into high-economic-value ammonia with high selectivity through electrochemical reduction, belonging to the technical field of resource treatment of nitrate sewage.
Background
The large amount of nitrate nitrogen wastewater generated in industrial activities seriously threatens the water ecology. With increasingly stringent environmental requirements, the harmless treatment of nitrate-nitrogen wastewater becomes the key point of environmental supervision, and the traditional treatment method mainly converts nitrate-nitrogen into stable and harmless nitrogen through denitrification by a microbiological method. On the other hand, if the nitro-nitrogen is used as an important form of nitrogen resource and can be converted into the ammonia resource which is needed urgently at present, the win-win situation of environmental improvement and resource recovery can be realized.
In recent years, methods for converting nitrate nitrogen into ammonium ions have been reported in succession, but subsequent reports for extracting nitrate nitrogen into ammonia gas have not been reported yet. The reason for this is that the electrolysis of (nitrite) -containing waste water to ammonium nitrogen, the main method for separating ammonium nitrogen from water, is to consume large amounts of alkali to adjust the pH to alkaline and then to let ammonia escape by heating or large amounts of aeration, the escaped ammonia still needs to be further concentrated, which is not cost-effective.
Disclosure of Invention
Aiming at the defects in the prior art, the invention aims to provide a method for directly obtaining ammonia by electrochemically reducing nitrate (nitrite) by using a porous membrane electrode, the method has high efficiency and high selectivity for reducing nitrate into ammonia, can be carried out under the conditions of normal temperature and normal pressure, has mild conditions, low energy consumption, simple operation and green and environment-friendly process, has almost zero ammonia separation cost, is beneficial to large-scale popularization and application, and provides a new solution for recycling industrial nitrate (nitrite) wastewater.
In order to achieve the technical purpose, the invention provides a method for directly preparing ammonia by electrochemical reduction of nitrate (nitrite), which comprises the steps of electrochemically reducing an electrolyte containing nitrite and/or nitrate by a porous membrane electrode to generate ammonia; the porous membrane electrode has a catalytic effect on the electrochemical reduction of nitrite and nitrate; when the pH value of the electrolyte containing nitrite and/or nitrate is greater than or equal to 7 and less than 13, the current density of the electrode in the electrochemical reduction process is greater than 10mA/cm2When the pH value of the electrolyte containing nitrite and/or nitrate is more than 1 and less than 7, the current density of the electrode in the electrochemical reduction process is more than 50mA/cm2。
The technical scheme of the invention is that nitrite and/or nitrate-containing electrolyte is electrochemically reduced to generate ammonium ions, and the key is that protons on the surface of the porous membrane electrode can be consumed under appropriate current density by controlling the current density of the porous membrane electrode and utilizing the hydrophobic and porous structures of the porous membrane electrode, so that local high-concentration hydroxide radicals are generated on the surface of the porous membrane electrode, and the ammonium ions are promoted to be converted into free ammonia on the interface of the porous membrane electrode.
Preferably, when the electrolyte containing nitrite and/or nitrate is neutral or alkaline (pH is greater than or equal to 7 and less than 12), the electrode current density in the electrochemical reduction process is preferably 10-200 mA/cm2When the electrolyte containing nitrite and/or nitrate is acidic (the pH is more than 1 and less than 7), the current density of the electrode in the electrochemical reduction process is more than 50-300 mA/cm2. Too high a pH is detrimental to the reduction of nitrite and/or nitrate to ammonia, e.g. pH 13, current density 10mA/cm2In the process, the ammonia process has the first efficiency of 11 percent and the separation rate of 90 percent; too low a pH leads to severe hydrogen evolution during electrolysis and it is difficult to achieve a high pH at the gas-liquid interface under low current conditions, e.g.pH 0.5 and current density 10mA/cm2The ammonia process had 54% of efficiency, and almost no ammonia was separated. In the preferred current density range, the higher the current density, the more favorable the evolution of ammonia gas.
Preferably, the concentration of the nitrite and/or nitrate containing electrolyte is 10. mu. mol/L to 1.0 mol/L.
Preferably, the porous membrane electrode is made of a hydrophobic material and a catalytic material supported on the surface of the hydrophobic material or made of a hydrophobic catalytic material.
As a preferable scheme, the hydrophobic material is selected from PTFE, PEEK, PP, PE, carbon cloth or porous carbon paper, or is formed by performing surface hydrophobic treatment on a porous material matrix; the porous material matrix is selected from a metal material, an inorganic non-metal material or an organic polymer material. The electrode substrate material can be made of metal materials such as copper foam and nickel foam, inorganic non-metal materials such as porous carbon materials and carbon cloth, organic polymer materials such as net-shaped PTFE, PEEK, PP, PE and the like, and hydrophobic materials or hydrophilic materials can be further subjected to surface hydrophobic treatment to improve hydrophobicity.
As a preferable scheme, the surface hydrophobic treatment is surface modification treatment by hydrophobic macromolecules or hydrophobic small molecules or surface micro-nano scale processing treatment. The surface modification treatment is performed by hydrophobic macromolecules or hydrophobic small molecules, specifically, PTFE, biological wax or octadecanethiol and the like are used for surface modification of a porous material matrix, for example: and (3) soaking the porous material with the gap size of 0.1mm in an ethyl acetate solution in which 1% octadecanethiol is dissolved for 1-5 minutes, and naturally drying to obtain the porous material. The method comprises the following specific steps of surface micro-nano scale processing treatment, for example: a porous material with the gap size of 0.1mm is subjected to anodic oxidation in a 3mol/L potassium hydroxide solution to construct a nano array with the needle-shaped length of about 2 microns in situ, so that the surface of the nano array is hydrophobic.
As a preferable scheme, the catalytic material is at least one of a metal simple substance, a metal sulfide, a metal selenide, a metal phosphide, a metal nitride and boron-doped diamond; the preferred elemental metal is selected from at least one of copper, cobalt, iron, nickel, gold, silver, platinum or palladium. Preferred metal sulfides are selected from at least one of copper, cobalt, iron, nickel, gold, silver, platinum or palladium sulfides. Preferred metal selenides are selected from at least one of copper, cobalt, iron, nickel, gold, silver, platinum or palladium selenides; preferred metal phosphides are selected from at least one of copper, cobalt, iron, nickel, gold, silver, platinum or palladium phosphides. Preferred metal nitrides are selected from at least one of the nitrides of copper, cobalt, iron, nickel, gold, silver, platinum or palladium. These catalytic materials are catalytic materials that are common in the art and have a catalytic effect on the electrochemical reduction of nitrite and nitrate.
In a preferred embodiment, the hydrophobic catalytic material is at least one selected from copper, cobalt, iron, nickel, gold, silver, platinum and palladium, or is at least one of copper, cobalt, iron, nickel, gold, silver, platinum and palladium subjected to surface hydrophobic treatment. The surface hydrophobic treatment is, for example, surface modification treatment by hydrophobic macromolecules or hydrophobic small molecules or surface micro-nano scale processing treatment.
In a preferred embodiment, during the electrochemical reduction process, an electrolyte containing nitrite and/or nitrate is used as a cathode chamber electrolyte, a porous membrane electrode is used as a working electrode, one side of the porous membrane electrode faces the electrolyte, and the other side faces a gas collection chamber.
The electrolyte containing nitrite and/or nitrate radical can adopt wet denitration waste liquid or nitrate nitrogen sewage to realize resource utilization.
The invention directly prepares ammonia by electrochemically reducing nitrate (nitrite) through a porous membrane electrode, and the implementation process comprises the following steps: a three-electrode system is adopted for carrying out nitrate radical electrochemical reduction, sulfur dioxide absorption liquid is taken as electrolyte of a cathode chamber, a membrane electrode is taken as a working electrode, and two surfaces of a catalyst membrane respectively face an electrolyte and a gas collecting chamber. A saturated calomel electrode is used as a reference electrode to construct a three-electrode system taking nitrate as electrolyte. The pH value of the electrolyte is preferably controlled to be more than 7, and the current density is preferably controlled to be more than 10mA/cm2. At this time, ammonia gas can be obtained in the gas collection chamber.
Compared with the prior art, the technical scheme of the invention has the beneficial technical effects that:
1) the technical scheme of the invention realizes the high-selectivity electro-catalytic reduction of nitrate (nitrite) to ammonia gas by adopting the porous membrane electrode for the first time, and compared with the prior art, the technical scheme of the invention has incomparable advantages in the separation cost of ammonia gas.
2) The technical scheme of the invention adopts the membrane electrode with porous structure and high catalytic activity to realize the electrochemical reduction of nitrate (nitrite) electrolyte, and can quickly and selectively separate the ammonia generated in the reduction process from the electrolyte, thereby promoting the chemical reaction balance of the whole electrochemical reduction reaction to move towards the direction favorable for generating the ammonia, and being favorable for improving the Faraday efficiency and the gas purity of the ammonia.
3) According to the technical scheme, the high-efficiency conversion of the nitrate (nitrite) can be realized only by controlling proper current density at room temperature and normal pressure, the Faraday efficiency of ammonia gas can reach more than 90%, the long-time catalytic stability can be kept, the reaction condition is mild, the energy consumption is low, and the industrial application is facilitated; the reaction process can be separated to generate high-concentration ammonia gas without adding other chemical agents, no waste salt is generated, no energy is consumed in the separation process, and the advantages of environmental protection and energy consumption are obvious.
Detailed Description
The following examples are intended to further illustrate the present invention, but not to limit the scope of the claims.
Nitrate (nitrite) electrolyte in the following examples is electrochemically reduced by using a three-electrode system, a cathode chamber and an anode chamber of the three-electrode system are separated by using a dupont N117 proton membrane or a cation exchange membrane, the electrolyte in the cathode chamber is nitrate (nitrite) electrolyte, a membrane electrode is used as a working electrode, Pt is used as a counter electrode, saturated mercurous sulfate is used as a reference electrode, and a proper current density is controlled by a constant current or constant potential mode according to the pH of the electrolyte.
The membrane electrode preparation process in the following examples takes Cu/PTFE and Ag-Cu/stainless steel wire mesh as examples:
(1) Cu/PTFE: cleaning a commercial PTFE breathable film by using 0.1M hydrofluoric acid, and airing; treating the film with an oxygen plasma at a power of 5W for 5 minutes; the membrane was immersed in a copper sulfate (10 g/L)/sodium tartrate (50g/L) solution, the pH was adjusted to 12 using sodium hydroxide, a formaldehyde solution (10g/L) was added, and the mixture was allowed to stand at room temperature for 1 hour to control the thickness of the plating layer to about 20 μm.
(2) Ag-Cu/stainless Steel wire mesh: cleaning a commercial 1000-mesh stainless steel wire net with 0.1M dilute hydrochloric acid and acetone, and airing; covering one surface of a stainless steel wire mesh with a raw material belt, contacting the uncovered surface with a 1% v/v octadecanethiol/ethyl acetate solution page for 5min, taking out, and drying in an oven at 50 ℃; tearing off the raw material belt, immersing the stainless steel screen membrane in a copper sulfate (10 g/L)/sodium tartrate (50g/L) solution, adjusting the pH to 12 by using sodium hydroxide, adding a formaldehyde solution (10g/L), standing for 1 hour at room temperature, and controlling the thickness of a plating layer to be about 20 mu m to obtain a Cu/stainless steel screen; placing the Cu/stainless steel wire net in 1mM AgNO3Standing the solution for 5min, taking out, cleaning and drying the solution to obtain the Ag-Cu/stainless steel wire mesh with one hydrophobic surface.
The following examples illustrate the effectiveness of the invention using Cu/PTFE and Ag-Cu/stainless steel wire mesh as examples. The chemical reagents used are all conventional commercial products, and are analytically pure reagents.
Example 1
10mL of nitrate electrolyte (0.1mol/L) was used as catholyte, 10mL of an aqueous solution of anhydrous sodium sulfate (1.0mol/L) was used as anolyte, and 2mol/L of sodium hydroxide solution was used to adjust the pH of the catholyte to 10. A three-electrode system is adopted for electrochemical reduction of nitrate, Cu/PTFE is used as a working electrode, and the catalyst side and the non-catalyst side of the catalyst membrane respectively face an electrolyte and a gas collecting chamber. The reduction voltage is set to-0.8V (vs Hg/Hg)2SO4) Constant potential electrolysis with current density of about 25mA/cm2And ammonia gas is generated in the gas collecting chamber, the Faraday efficiency is 92%, and the separation efficiency is 99%.
Example 2
10mL of nitrate electrolyte (0.1mol/L) was used as a catholyte, and 10mL of an aqueous solution of anhydrous sodium sulfate (1.0mol/L) was used as an anolyte. A three-electrode system is adopted for electrochemical reduction of nitrate, Cu/PTFE is used as a working electrode, and the catalyst side and the non-catalyst side of the catalyst membrane respectively face an electrolyte and a gas collecting chamber. Constant current electrolysis with current density set at 50mA/cm2And ammonia gas is generated in the gas collecting chamber, the Faraday efficiency is 93 percent, and the separation efficiency is 98 percent. The ammonia gas can be obtained without adding alkali liquor.
Example 3
10mL of nitrate electrolyte (0.1mol/L) was used as catholyte, 10mL of an aqueous solution of anhydrous sodium sulfate (1.0mol/L) was used as anolyte, and the pH of the catholyte was adjusted to 5 with a 0.1mol/L sulfuric acid solution. A three-electrode system is adopted for electrochemical reduction of nitrate, Cu/PTFE is used as a working electrode, and the catalyst side and the non-catalyst side of the catalyst membrane respectively face an electrolyte and a gas collecting chamber. Constant current electrolysis with current density set at 100mA/cm2And ammonia gas is generated in the gas collecting chamber, the Faraday efficiency is 89%, and the separation efficiency is 90%.
Example 4 (comparative example)
10mL of nitrate electrolyte (0.1mol/L) was used as a catholyte, 10mL of an aqueous solution of anhydrous sodium sulfate (1.0mol/L) was used as an anolyte, and 0.1mol/L of sulfur was usedThe acid solution adjusted the catholyte pH to 0.5. A three-electrode system is adopted for electrochemical reduction of nitrate, Cu/PTFE is used as a working electrode, and the catalyst side and the non-catalyst side of the catalyst membrane respectively face an electrolyte and a gas collecting chamber. Constant current electrolysis with current density set at 10mA/cm2The Faraday efficiency was 54%, but the gas collection chamber was ammonia-free and no ammonia was separated by the membrane.
Example 5 (comparative example)
10mL of nitrate electrolyte (0.1mol/L) was used as catholyte, 10mL of an aqueous solution of anhydrous sodium sulfate (1.0mol/L) was used as anolyte, and the pH of the catholyte was adjusted to 13 with 2mol/L sodium hydroxide solution. A three-electrode system is adopted for electrochemical reduction of nitrate, Cu/PTFE is used as a working electrode, and the catalyst side and the non-catalyst side of the catalyst membrane respectively face an electrolyte and a gas collecting chamber. Constant current electrolysis with current density set at 10mA/cm2Faraday efficiency is 11%, a small amount of ammonia gas is contained in the gas collection chamber, and the ammonia separation efficiency is 90%.
Example 6
10mL of nitrate electrolyte (0.1mol/L) was used as a catholyte, and 10mL of an aqueous solution of anhydrous sodium sulfate (1.0mol/L) was used as an anolyte. A three-electrode system is adopted for electrochemical reduction of nitrate, Cu/PTFE is used as a working electrode, and the catalyst side and the non-catalyst side of the catalyst membrane respectively face an electrolyte and a gas collecting chamber. Constant current electrolysis with current density set at 100mA/cm2And ammonia gas is generated in the gas collecting chamber, the Faraday efficiency is 90 percent, and the separation efficiency is 97 percent.
Example 7
10mL of nitrate electrolyte (0.1mol/L) was used as a catholyte, and 10mL of an aqueous solution of anhydrous sodium sulfate (1.0mol/L) was used as an anolyte. A three-electrode system is adopted for electrochemical reduction of nitrate, Cu/PTFE is used as a working electrode, and the catalyst side and the non-catalyst side of the catalyst membrane respectively face an electrolyte and a gas collecting chamber. Constant current electrolysis with current density set at 150mA/cm2And ammonia gas is generated in the gas collection chamber, the Faraday efficiency is 85 percent, and the separation efficiency is 97 percent.
Example 8
In 10mL of nitrate radicalThe electrolyte (0.1mol/L) was a catholyte, and 10mL of an aqueous solution of anhydrous sodium sulfate (1.0mol/L) was an anolyte. A three-electrode system is adopted for electrochemical reduction of nitrate, Cu/PTFE is used as a working electrode, and the catalyst side and the non-catalyst side of the catalyst membrane respectively face an electrolyte and a gas collecting chamber. Constant current electrolysis with current density set at 200mA/cm2And ammonia gas is generated in the gas collecting chamber, the Faraday efficiency is 80 percent, and the separation efficiency is 97 percent.
Example 9
10mL of nitrate electrolyte (0.1mol/L) was used as a catholyte, and 10mL of an aqueous solution of anhydrous sodium sulfate (1.0mol/L) was used as an anolyte. A three-electrode system is adopted for carrying out nitrate electrochemical reduction, an Ag-Cu/stainless steel wire mesh is used as a working electrode, the Ag-Cu side of the catalyst film faces to an electrolyte, and the hydrophobic treatment side faces to a gas collection chamber. Constant current electrolysis with current density set at 100mA/cm2And ammonia gas is generated in the gas collection chamber, the Faraday efficiency is 83 percent, and the separation efficiency is 91 percent.
Example 10
10mL of nitrate electrolyte (1.0mol/L) was used as a catholyte, and 10mL of an aqueous solution of anhydrous sodium sulfate (1.0mol/L) was used as an anolyte. A three-electrode system is adopted for electrochemical reduction of nitrate, Cu/PTFE is used as a working electrode, and the catalyst side and the non-catalyst side of the catalyst membrane respectively face an electrolyte and a gas collecting chamber. Constant current electrolysis with current density set at 100mA/cm2And ammonia gas is generated in the gas collection chamber, the Faraday efficiency is 91 percent, and the separation efficiency is 97 percent. The invention is equally applicable to the conversion of high-concentration nitrate wastewater and the separation of ammonia.
Example 11
10mL of nitrite electrolyte (0.1mol/L) was used as a catholyte, and 10mL of an aqueous solution of anhydrous sodium sulfate (1.0mol/L) was used as an anolyte. A three-electrode system is adopted for electrochemical reduction of nitrate, Cu/PTFE is used as a working electrode, and the catalyst side and the non-catalyst side of the catalyst membrane respectively face an electrolyte and a gas collecting chamber. Constant current electrolysis with current density set at 100mA/cm2And ammonia gas is generated in the gas collection chamber, the Faraday efficiency is 88 percent, and the separation efficiency is 93 percent. The invention relates to nitrous acidRoot conversion is equally applicable to ammonia separation.

Claims (8)

1. A method for directly preparing ammonia by electrochemical reduction of nitrite (nitrite) is characterized in that: the electrolyte containing nitrite and/or nitrate is electrochemically reduced through a porous membrane electrode to generate ammonia gas; the porous membrane electrode has a catalytic effect on the electrochemical reduction of nitrite and nitrate; when the pH value of the electrolyte containing nitrite and/or nitrate is greater than or equal to 7 and less than 13, the current density of the electrode in the electrochemical reduction process is greater than 10mA/cm2When the pH value of the electrolyte containing nitrite and/or nitrate is more than 1 and less than 7, the current density of the electrode in the electrochemical reduction process is more than 50mA/cm2。
2. The method for directly preparing ammonia gas by electrochemical reduction of nitrite (nitrite) according to claim 1, which is characterized in that: the concentration of the electrolyte containing nitrite and/or nitrate is 10 mu mol/L-1.0 mol/L.
3. The method for directly preparing ammonia gas by electrochemical reduction of nitrite (nitrite) according to claim 1, which is characterized in that: the porous membrane electrode is made of hydrophobic materials and catalytic materials loaded on the surface of the hydrophobic materials, or made of hydrophobic catalytic materials.
4. The method for directly preparing ammonia gas by electrochemical reduction of nitrite (nitrite) according to claim 3, which is characterized in that: the hydrophobic material is selected from PTFE, PEEK, PP, PE, carbon cloth or porous carbon paper, or is formed by performing surface hydrophobic treatment on a porous material matrix; the porous material matrix is selected from a metal material, an inorganic non-metal material or an organic polymer material.
5. The method for directly preparing ammonia gas by electrochemical reduction of nitrite (nitrite) according to claim 4, which is characterized in that: the surface hydrophobic treatment is surface modification treatment through hydrophobic macromolecules or hydrophobic small molecules or surface micro-nano scale processing treatment.
6. The method for directly preparing ammonia gas by electrochemical reduction of nitrite (nitrite) according to claim 3, which is characterized in that:
the catalytic material is at least one of metal simple substances, metal sulfides, metal selenides, metal phosphides, metal nitrides and boron-doped diamond;
the metal elementary substance is at least one selected from copper, cobalt, iron, nickel, gold, silver, platinum or palladium;
the metal sulfide is at least one of copper sulfide, cobalt sulfide, iron sulfide, nickel sulfide, gold sulfide, silver sulfide, platinum sulfide or palladium sulfide;
the metal selenide is at least one of copper, cobalt, iron, nickel, gold, silver, platinum or palladium selenide;
the metal phosphide is at least one of phosphide of copper, cobalt, iron, nickel, gold, silver, platinum or palladium;
the metal nitride is at least one of copper, cobalt, iron, nickel, gold, silver, platinum or palladium nitride.
7. The method for directly preparing ammonia gas by electrochemical reduction of nitrite (nitrite) according to claim 3, which is characterized in that: the hydrophobic catalytic material is at least one selected from copper, cobalt, iron, nickel, gold, silver, platinum or palladium, or is formed by at least one selected from copper, cobalt, iron, nickel, gold, silver, platinum or palladium which is subjected to surface hydrophobic treatment.
8. The method for directly preparing ammonia gas by electrochemical reduction of nitrite (nitrite) according to claim 1, which is characterized in that: in the electrochemical reduction process, electrolyte containing nitrite and/or nitrate is used as electrolyte in a cathode chamber, a porous membrane electrode is used as a working electrode, one side of the porous membrane electrode faces the electrolyte, and the other side faces a gas collection chamber.
CN202111138428.9A 2021-09-27 2021-09-27 Method for directly preparing ammonia gas by electrochemical reduction of nitrite Active CN113737205B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202111138428.9A CN113737205B (en) 2021-09-27 2021-09-27 Method for directly preparing ammonia gas by electrochemical reduction of nitrite

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202111138428.9A CN113737205B (en) 2021-09-27 2021-09-27 Method for directly preparing ammonia gas by electrochemical reduction of nitrite

Publications (2)

Publication Number Publication Date
CN113737205A true CN113737205A (en) 2021-12-03
CN113737205B CN113737205B (en) 2023-03-10

Family

ID=78741433

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202111138428.9A Active CN113737205B (en) 2021-09-27 2021-09-27 Method for directly preparing ammonia gas by electrochemical reduction of nitrite

Country Status (1)

Country Link
CN (1) CN113737205B (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114436371A (en) * 2022-01-25 2022-05-06 中南大学 Vanadium-titanium magnetite-based electrode and preparation method and application thereof
CN114538592A (en) * 2022-02-28 2022-05-27 河南大学 Ultrathin iron phosphide nano-array electrocatalyst taking titanium sheet as substrate, preparation method and application thereof
CN114657596A (en) * 2022-03-09 2022-06-24 济南大学 Electro-catalytic nitrate radical reduction catalyst Fe-CoS2Preparation method of/CC
CN114832596A (en) * 2022-07-04 2022-08-02 浙江百能科技有限公司 Method and device for preparing ammonia by active molecule oxidation flue gas double-circulation denitration

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110075843A (en) * 2019-04-08 2019-08-02 电子科技大学 A kind of nanometer of copper catalyst and its preparation method and the application in synthesis of acetic acid or ammonia
WO2020028570A1 (en) * 2018-08-03 2020-02-06 The Board Of Trustees Of The Leland Stanford Junior University A method for the electrochemical synthesis of ammonia from nitrates and water
CN113122864A (en) * 2021-03-31 2021-07-16 中南大学 Method for preparing hydrogen sulfide by electrochemical reduction of sulfur dioxide

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020028570A1 (en) * 2018-08-03 2020-02-06 The Board Of Trustees Of The Leland Stanford Junior University A method for the electrochemical synthesis of ammonia from nitrates and water
CN110075843A (en) * 2019-04-08 2019-08-02 电子科技大学 A kind of nanometer of copper catalyst and its preparation method and the application in synthesis of acetic acid or ammonia
CN113122864A (en) * 2021-03-31 2021-07-16 中南大学 Method for preparing hydrogen sulfide by electrochemical reduction of sulfur dioxide

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114436371A (en) * 2022-01-25 2022-05-06 中南大学 Vanadium-titanium magnetite-based electrode and preparation method and application thereof
CN114436371B (en) * 2022-01-25 2023-10-03 中南大学 Vanadium titano-magnetite-based electrode and preparation method and application thereof
CN114538592A (en) * 2022-02-28 2022-05-27 河南大学 Ultrathin iron phosphide nano-array electrocatalyst taking titanium sheet as substrate, preparation method and application thereof
CN114657596A (en) * 2022-03-09 2022-06-24 济南大学 Electro-catalytic nitrate radical reduction catalyst Fe-CoS2Preparation method of/CC
CN114832596A (en) * 2022-07-04 2022-08-02 浙江百能科技有限公司 Method and device for preparing ammonia by active molecule oxidation flue gas double-circulation denitration

Also Published As

Publication number Publication date
CN113737205B (en) 2023-03-10

Similar Documents

Publication Publication Date Title
CN113737205B (en) Method for directly preparing ammonia gas by electrochemical reduction of nitrite
RU2479558C2 (en) Electrochemical method of producing nitrogen fertilisers
CN113637989B (en) Method for synthesizing ammonia by electrocatalytic nitrate or nitrite
CN109534453B (en) Chlorine free radical mediated electrochemical filtration system and application thereof
KR20200002278A (en) Electrochemical system for producing ammonia from nitrogen oxides and preparation method thereof
CN113789526B (en) Method for preparing ammonia gas by nitric oxide electrochemical reduction
CN113174600A (en) Porous nickel screen electrolytic water catalytic material and preparation method thereof
CN111792705A (en) Graphene oxide loaded carbon-based copper-nickel electrode, preparation method and application
CN115010217B (en) Preparation method and application of three-dimensional composite electrode for efficiently removing nitrate in water by electrocatalytic reaction
CN113772789A (en) Method and device for electrochemical treatment of organic wastewater and reduction of carbon dioxide
CN112320818A (en) Method for oxidizing sulfite in flue gas desulfurization slurry
CN113122864B (en) Method for preparing hydrogen sulfide by electrochemical reduction of sulfur dioxide
CN114836777A (en) Three-dimensional hydrophobic hierarchical pore electrode and preparation method and application thereof
Li et al. Strategies of selective electroreduction of aqueous nitrate to N2 in chloride-free system: A critical review
CN118007150A (en) Electrolytic-air film coupling system for recycling bromine based on BiOBr electrode and Br-Is recovered by the method of (2)
Machida et al. Electrocatalytic nitrate hydrogenation over an H+-conducting solid polymer electrolyte membrane–modified cathode assembly
CN111996541A (en) Indirect hydrogen sulfide electrolysis method and device for improving hydrogen yield
CN114249399A (en) Photoelectrocatalysis system for efficiently removing nitrate nitrogen in high-salt system and application
CN102002724B (en) Acetylene black cathode provided with waterproof membrane and used for producing hydrogen peroxide and manufacturing method thereof
CN105776439A (en) Foam nickel-based nano-graphite electrode, and preparation method and application thereof
JP3615814B2 (en) Method and apparatus for removing nitrate and / or nitrite nitrogen
CN114752952B (en) Electrocatalytic nitrogen fixation device and method for simultaneously generating nitric acid and ammonia double products
CN114959771B (en) Nickel-based electrocatalyst and hydrogen production synergistic formaldehyde wastewater degradation electrolytic cell
CN113120866B (en) Method for preparing elemental sulfur by using sulfur dioxide
CN117886404B (en) Water treatment method and water treatment system

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant