Di Yonghao, Zhang Xiangwei, Wang Xinlin, Zheng Shuilin
School of Chemical and Environmental Engineering, China University of Mining and Technology (Beijing), Beijing 100083, China.
Materials (Basel). 2021 Oct 28;14(21):6469. doi: 10.3390/ma14216469.
Binary composite was synthesized via coupling BiOCl with alkali leached natural clinoptilolite (40B0/CN), which showed retarded recombination of photo-generated carriers. The clinoptilolite was pretreated with alkali leaching, resulting in a larger pore size and high cation exchange capacity. The modified clinoptilolite was more feasible for the growth of BiOCl and to promote the adsorption ability for formaldehyde (HCHO). In addition, the cation exchange capacity was conducive to anchor Bi, further leading to the reduction of the particle size of BiOCl. The carrier effect of alkali leached natural clinoptilolite promoted the amorphous transformation of BiOCl at low temperature, which simultaneously produced more distortions and defects in the BiOCl lattice. The 40B0/CN composite exhibited the superior light absorption ability with a narrower band gap. The photocatalytic degradation rate for HCHO of 40B0/CN under solar light reached 87.7%, and the reaction rate constant was 0.0166 min, which was 1.6 times higher than that of BiOCl. This paper gave a deep insight into photocatalytic technology to efficiently degrade formaldehyde.
通过将碱浸天然斜发沸石(40B0/CN)与BiOCl偶联合成了二元复合材料,该复合材料显示出光生载流子的复合受到抑制。斜发沸石经过碱浸预处理,导致孔径增大和阳离子交换容量提高。改性后的斜发沸石更有利于BiOCl的生长,并提高了对甲醛(HCHO)的吸附能力。此外,阳离子交换容量有利于锚定Bi,进而导致BiOCl粒径减小。碱浸天然斜发沸石的载体效应促进了BiOCl在低温下的非晶化转变,同时在BiOCl晶格中产生了更多的畸变和缺陷。40B0/CN复合材料表现出优异的光吸收能力,带隙更窄。在太阳光下,40B0/CN对HCHO的光催化降解率达到87.7%,反应速率常数为0.0166 min⁻¹,比BiOCl高1.6倍。本文深入探讨了光催化技术高效降解甲醛的问题。