Apparatus and process to provide cooling water for ammonia and or hydrogen productions
US-2024207802-A1 · Jun 27, 2024 · US
US2025101605A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2025101605-A1 |
| Application number | US-202418799181-A |
| Country | US |
| Kind code | A1 |
| Filing date | Aug 9, 2024 |
| Priority date | Sep 22, 2023 |
| Publication date | Mar 27, 2025 |
| Grant date | — |
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An electrolyte for an electrochemical nitrogen reduction reaction and a method for electrochemically preparing ammonia using the same are provided. The electrolyte includes a first lithium salt including at least one selected from the group consisting of a fluoroborate-based lithium salt, a fluorophosphate-based lithium salt, a fluoroarcenate-based lithium salt, and a fluorosulfonylimide-based lithium salt, a second lithium salt different from the first lithium salt, and an organic solvent.
Opening claim text (preview).
What is claimed is: 1 . An electrolyte for an electrochemical nitrogen reduction reaction, the electrolyte comprising: a first lithium salt including at least one selected from the group consisting of a fluoroborate-based lithium salt, a fluorophosphate-based lithium salt, a fluoroarcenate-based lithium salt, and a fluorosulfonylimide-based lithium salt; a second lithium salt different from the first lithium salt; and an organic solvent. 2 . The electrolyte of claim 1 , wherein the first lithium salt includes at least one selected from the group consisting of LiBF 4-x H x , LiPF 6-y H y , LiAsF 6-y H y , LiDFOB (Lithium bis(2,2-difluoro-1,3-dioxolane-4,5-bis (oxalato)borate), LiFSI (Lithium bis(fluorosulfonyl)imide), LiFOB (Lithium difluoro (oxalato)borate), and Li (+) F—SO 2 —N(−) SO 2 —R (in which ‘x’ denotes a real number ranging from 0 to 3, ‘y’ and ‘z’ denote each independently a real number ranging from 0 to 5, and ‘R’ denotes an alkyl group or a fluoroalkyl group having 1 to 6 carbon atoms). 3 . The electrolyte of claim 1 , wherein the first lithium salt includes at least one selected from the group consisting of LiBF 4 , LiPF 6 , LiAsF 6 , and an mixture of LiBF 4 , LiPF 6 , and LiAsF 6 . 4 . The electrolyte of claim 1 , wherein the first lithium salt is contained in an amount of 0.0001 wt % to 10 wt %. 5 . The electrolyte of claim 1 , wherein the organic solvent includes at least one selected from the group consisting of propylene carbonate, ethylene carbonate, dimethyl carbonate, 1,3-dioxolane, dimethoxyethane, tetrahydrofuran, dimethylformamide, acetonitrile, N-methylpyrrolidone, ethanol, 1-propanol, 2-methyl-1-propanol, tert-butyl alcohol, 2-butanol, 2-ethyl-1-butanol, 1-pentanol, 1-hexanol, 1-heptanol, 1-nonanol, benzyl alcohol, phenol, 1-phenylethanol, 2-phenylethanol, 2-chloroethanol, 2,2,2-trifluoroethanol, hexafluoro 2-propanol, 1,3-butanediol, glycerol, triethylene glycol, 1,5-pentanediol, acetic acid, hexane, alkyl alcohol, 2-methoxyethanol, 1-propanediol, methanol, cyclohexanol, 3-butene-1-ol, 2-propanol, 1-butanol, 3-methyl-1-butanol, and a mixture of propylene carbonate, ethylene carbonate, dimethyl carbonate, 1,3-dioxolane, dimethoxyethane, tetrahydrofuran, dimethylformamide, acetonitrile, N-methylpyrrolidone, ethanol, 1-propanol, 2-methyl-1-propanol, tert-butyl alcohol, 2-butanol, 2-ethyl-1-butanol, 1-pentanol, 1-hexanol, 1-heptanol, 1-nonanol, benzyl alcohol, phenol, 1-phenylethanol, 2-phenylethanol, 2-chloroethanol, 2,2,2-trifluoroethanol, hexafluoro 2-propanol, 1,3-butanediol, glycerol, triethylene glycol, 1,5-pentanediol, acetic acid, hexane, alkyl alcohol, 2-methoxyethanol, 1-propanediol, methanol, cyclohexanol, 3-butene-1-ol, 2-propanol, 1-butanol, 3-methyl-1-butanol. 6 . The electrolyte of claim 1 , wherein the second lithium includes at least one selected from the group consisting of lithium perchlorate, lithium dithionate, lithium sulfate, lithium bromide, lithium chloride, lithium bis(oxalato)borate, and a mixture of lithium perchlorate, lithium dithionate, lithium sulfate, lithium bromide, lithium chloride, lithium bis(oxalato)borate. 7 . A method for electrochemically preparing ammonia, the method comprising: synthesizing the ammonia from nitrogen (N 2 ) through an electrochemical nitrogen reduction reaction, by applying a current to a reduction electrode under presence of the electrolyte for the electrochemical nitrogen reduction reaction according to claim 1 . 8 . The method of claim 7 , wherein a layer including lithium fluoride including fluorine ions (F − ) provided from the first lithium salt is formed on a surface of the reduction electrode by applying the current to the reduction electrode. 9 . The method of claim 7 , wherein the applying of the current to the reduction electrode includes: applying the current to the reduction electrode in a range of −1 mA/cm 2 to −100 mA/cm 2 for 15 minutes to 12 hours. 10 . The method of claim 7 , wherein the reduction electrode includes: at least one selected from the group consisting of gold (Au), silver (Ag), copper (Cu), platinum (Pt), zinc (Zn), iron (Fe), titanium (Ti), tin (Sn), indium (In), bismuth (Bi), samarium (Sm), nickel (Ni), molybdenum (Mo), cobalt (Co), stainless steel, graphene, carbon nanotubes, and fullerene. 11 . The method of claim 7 , wherein the nitrogen (N 2 ) reacts with lithium provided from the first lithium salt and the second lithium salt to form lithium nitride (Li x N), in which ‘x’, which is the subscript of Li, denotes a molar ratio of Li element, is a real number of at least ‘1’. 12 . The method of claim 11 , wherein the lithium nitride (Li x N) binding with the layer including the lithium fluoride reacts with hydrogen ions (H + ) to synthesize ammonia (NH 3 ).
Electrodes formed of a single material · CPC title
Means for supplying current; Electrode connections; Electric inter-cell connections · CPC title
Preparation of ammonia by synthesis (preparation or purification of gas mixtures for ammonia synthesis C01B3/025) · CPC title
Processes · CPC title
Supplying or removing reactants or electrolytes; Regeneration of electrolytes · CPC title
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