首页|羟基官能化K掺杂g-C3N4光催化海水合成过氧化氢

羟基官能化K掺杂g-C3N4光催化海水合成过氧化氢

扫码查看
从双氰胺出发,以氯化铵、草酸铵为气体模板剂、KC1为热熔盐,经离子热缩聚反应合成了 2种羟基官能化K掺杂g-C3N4(ACCN和AOCN),用于光催化海水合成过氧化氢(H2O2),考察了 ACCN和AOCN的循环使用性能,并通过加入捕获剂探究了 H2O2的合成机理。结果表明,在室温、常压、中性条件下,以空气为分子氧源、乙醇为牺牲剂、模拟太阳光为光源,实现了 ACCN、AOCN光催化海水合成H2O2,6 h时H2O2最高生成速率为1 622 µmol·g-1·h-1;ACCN、AOCN经离心分离后循环使用5次,催化活性基本保持不变。
Photocatalytic Production of Hydrogen Peroxide from Seawater by Hydroxy-Functionalized K-Doped g-C3N4
Taking dicyandiamide as a raw material,ammonium chloride or ammonium oxalate as a gas tem-plate,and KCl as a molten salt,we synthesized two hydroxy-functionalized K-doped g-C3N4(ACCN and AOCN)by ioniothermal condensation reaction,which were used in photocatalytic production of hydrogen peroxide(H2O2)from seawater.Moreover,we investigated the production mechanism of H2O2 by adding trapping a-gents.The results show that,under the conditions of room temperature,atmospheric pressure,and neutral reac-tion,when air is taken as the molecular oxygen source,ethanol as the sacrificial agent,and simulated sunlight as the light source,the maximum H2O2 production rate can reach 1 622 μmol·g-1·h-1 at 6 h photocatalyzed by ACCN and AOCN.After centrifugation,ACCN and AOCN can be reused for 5 recycles,and their catalytic ac-tivities remain basically unchanged.

hydrogen peroxideseawatersolar lightmolecular oxygen reductiong-C3N4

骆盼盼、游锦芳、马诗棋、石芹瑕、杨树、李心忠

展开 >

福州大学环境与安全工程学院,福建 福州 350108

闽江学院材料与化学工程学院,福建 福州 350108

过氧化氢 海水 可见光 分子氧还原 g-C3N4

2025

化学与生物工程
武汉工程大学 湖北省化学化工学会 湖北省化学研究院 湖北省化学工业研究设计院

化学与生物工程

北大核心
影响因子:0.351
ISSN:1672-5425
年,卷(期):2025.42(1)