苝四羧酸二酰亚胺修饰增强g-C3N4光催化性能

O614.41; 以3,4,9,10-苝四甲酸二酐和L-天冬氨酸为原料,合成水溶性苝二酰亚胺衍生物N,N′-二(2-丁二酸基)-3,4,9,10-苝四羧酸二酰亚胺(PASP).采用水热法将PASP接枝在g-C3 N4上,制备PASP改性g-C3 N4复合光催化剂(g-C3 N4-PASP).通过X射线衍射仪(XRD)、傅里叶变换红外光谱仪(FT-IR)、X射线光电子能谱仪(XPS)、扫描电子显微镜(SEM)、透射电子显微镜(TEM)、紫外-可见光漫反射光谱(UV-Vis DRS)和固体荧光光谱等对g-C3N4-PASP的组成、结构、形貌和光学性质等进行表征,考察g-C3 N4-PASP对水溶液...

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Published in材料工程 Vol. 50; no. 3; pp. 98 - 106
Main Authors 赵卫峰, 郝宁, 张改, 钱慧锦, 马爱洁, 周宏伟, 陈卫星
Format Journal Article
LanguageChinese
Published 西安工业大学材料与化工学院,西安710021 20.03.2022
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ISSN1001-4381
DOI10.11868/j.issn.1001-4381.2021.000057

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Abstract O614.41; 以3,4,9,10-苝四甲酸二酐和L-天冬氨酸为原料,合成水溶性苝二酰亚胺衍生物N,N′-二(2-丁二酸基)-3,4,9,10-苝四羧酸二酰亚胺(PASP).采用水热法将PASP接枝在g-C3 N4上,制备PASP改性g-C3 N4复合光催化剂(g-C3 N4-PASP).通过X射线衍射仪(XRD)、傅里叶变换红外光谱仪(FT-IR)、X射线光电子能谱仪(XPS)、扫描电子显微镜(SEM)、透射电子显微镜(TEM)、紫外-可见光漫反射光谱(UV-Vis DRS)和固体荧光光谱等对g-C3N4-PASP的组成、结构、形貌和光学性质等进行表征,考察g-C3 N4-PASP对水溶液中模型污染物亚甲基蓝(MB)的光催化降解活性.结果表明:g-C3 N4与PASP经水热反应,可通过酰胺键共价结合;相比纯g-C3 N4,g-C3 N4-PASP比表面积显著增大,吸收带边红移至614 nm,同时PASP修饰可促进g-C3 N4材料表面光生电子和空穴分离,进而有效提升光催化活性.在可见光(λ>420 nm)照射下,g-C3 N4-PASP对MB的降解率60 min内可达99.4%,降解速率常数k约为g-C3 N4的2倍.
AbstractList O614.41; 以3,4,9,10-苝四甲酸二酐和L-天冬氨酸为原料,合成水溶性苝二酰亚胺衍生物N,N′-二(2-丁二酸基)-3,4,9,10-苝四羧酸二酰亚胺(PASP).采用水热法将PASP接枝在g-C3 N4上,制备PASP改性g-C3 N4复合光催化剂(g-C3 N4-PASP).通过X射线衍射仪(XRD)、傅里叶变换红外光谱仪(FT-IR)、X射线光电子能谱仪(XPS)、扫描电子显微镜(SEM)、透射电子显微镜(TEM)、紫外-可见光漫反射光谱(UV-Vis DRS)和固体荧光光谱等对g-C3N4-PASP的组成、结构、形貌和光学性质等进行表征,考察g-C3 N4-PASP对水溶液中模型污染物亚甲基蓝(MB)的光催化降解活性.结果表明:g-C3 N4与PASP经水热反应,可通过酰胺键共价结合;相比纯g-C3 N4,g-C3 N4-PASP比表面积显著增大,吸收带边红移至614 nm,同时PASP修饰可促进g-C3 N4材料表面光生电子和空穴分离,进而有效提升光催化活性.在可见光(λ>420 nm)照射下,g-C3 N4-PASP对MB的降解率60 min内可达99.4%,降解速率常数k约为g-C3 N4的2倍.
Author 周宏伟
张改
陈卫星
郝宁
赵卫峰
钱慧锦
马爱洁
AuthorAffiliation 西安工业大学材料与化工学院,西安710021
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ZHANG Gai
CHEN Weixing
ZHOU Hongwei
MA Aijie
HAO Ning
QIAN Huijin
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Keywords 石墨相氮化碳;苝四羧酸二酰亚胺;化学修饰;光催化
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Snippet O614.41; 以3,4,9,10-苝四甲酸二酐和L-天冬氨酸为原料,合成水溶性苝二酰亚胺衍生物N,N′-二(2-丁二酸基)-3,4,9,10-苝四羧酸二酰亚胺(PASP).采用水热法将PASP接枝在g-C3 N4...
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Title 苝四羧酸二酰亚胺修饰增强g-C3N4光催化性能
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