Visible light-induced decomposition of monoethanolamine in water using graphitic carbon nitride as a photocatalyst

被引:9
|
作者
Hori, Hisao [1 ]
Wachi, Shohei [1 ]
Iwamura, Kentaro [1 ]
Sano, Taizo [2 ]
机构
[1] Kanagawa Univ, Fac Sci, Dept Chem, 2946 Tsuchiya, Hiratsuka, Kanagawa 2591293, Japan
[2] Natl Inst Adv Ind Sci & Technol, AIST Tsukuba West, 16-1 Onogawa, Tsukuba, Ibaraki 3058569, Japan
关键词
Amine; Degradation; Graphitic carbon nitride; Formic acid; Post-combustion CO2 capture; CO2; CAPTURE; G-C3N4; DEGRADATION; PHOTODEGRADATION; BIODEGRADATION; PERFORMANCE; AMINES; ACTIVATION; CATALYSTS; HYBRID;
D O I
10.1016/j.jphotochem.2017.10.015
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Photochemical decomposition of monoethanolamine (MEA) in the presence of graphitic carbon nitride (g-C3N4) in water under visible-light irradiation was investigated. When aqueous MEA was irradiated by visible light ( >389 nm) in the presence of either TiO2 (P25) and O-2 or g-C3N4 and argon, virtually no decomposition of MEA was observed. In contrast, when aqueous MEA was irradiated by visible light in the presence of g-C3N4 and O-2, the MEA decomposed to produce HCOOH, NO2-, NO3-, and NH3. Although metal (Ag or Pt)-loading onto g-C3N4 enhanced the photocatalytic MEA decomposition slightly, it accelerated the formation of NO2- and NO3-. After the g-C3N4 catalyzed reactions, the recovery of carbon atoms was almost completely accounted for by the remaining MEA and HCOOH formed in the reaction solution, indicating that the carbon atoms in the reacted MEA were predominantly transformed to HCOOH. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:162 / 169
页数:8
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