Your browser doesn't support javascript.
loading
Continuous ammonia synthesis from water and nitrogen via contact electrification.
Li, Juan; Xia, Yu; Song, Xiaowei; Chen, Bolei; Zare, Richard N.
Afiliación
  • Li J; Hubei Key Laboratory of Environmental and Health Effects of Persistent Toxic Substances, School of Health and Environment, Jianghan University, Wuhan 430056, China.
  • Xia Y; Hubei Key Laboratory of Environmental and Health Effects of Persistent Toxic Substances, School of Health and Environment, Jianghan University, Wuhan 430056, China.
  • Song X; Department of Chemistry, Stanford University, Stanford, CA 94305.
  • Chen B; Department of Chemistry, Stanford University, Stanford, CA 94305.
  • Zare RN; Hubei Key Laboratory of Environmental and Health Effects of Persistent Toxic Substances, School of Health and Environment, Jianghan University, Wuhan 430056, China.
Proc Natl Acad Sci U S A ; 121(4): e2318408121, 2024 Jan 23.
Article en En | MEDLINE | ID: mdl-38232282
ABSTRACT
We synthesized ammonia (NH3) by bubbling nitrogen (N2) gas into bulk liquid water (200 mL) containing 50 mg polytetrafluoroethylene (PTFE) particles (~5 µm in diameter) suspended with the help of a surfactant (Tween 20, ~0.05 vol.%) at room temperature (25 °C). Electron spin resonance spectroscopy and density functional theory calculations reveal that water acts as the proton donor for the reduction of N2. Moreover, isotopic labeling of the N2 gas shows that it is the source of nitrogen in the ammonia. We propose a mechanism for ammonia generation based on the activation of N2 caused by electron transfer and reduction processes driven by contact electrification. We optimized the pH of the PTFE suspension at 6.5 to 7.0 and employed ultrasonic mixing. We found an ammonia production rate of ~420 µmol L-1 h-1 per gram of PTFE particles for the conditions described above. This rate did not change more than 10% over an 8-h period of sustained reaction.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2024 Tipo del documento: Article País de afiliación: China