Fe3+负载介孔丝光沸石吸附脱除二氯甲烷废气的研究

王心愿, 张佳, 王鹏飞, 余金鹏

现代化工 ›› 2023, Vol. 43 ›› Issue (S2) : 159 -163.

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现代化工 ›› 2023, Vol. 43 ›› Issue (S2) : 159-163. DOI: 10.16606/j.cnki.issn0253-4320.2023.S2.031
科研与开发

Fe3+负载介孔丝光沸石吸附脱除二氯甲烷废气的研究

    王心愿, 张佳, 王鹏飞, 余金鹏
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Adsorptive removal of dichloromethane exhaust on Fe3+ loaded mesopore mordenite

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摘要

用NaOH、H2C2O4和Fe(NO3)3对丝光沸石依次进行改性,连续改性不会破坏丝光沸石拓扑结构。先碱后酸的改性方式可以提升丝光沸石的比表面积、孔容和引入介孔,使比表面积从255 m2/g增加到356 m2/g,孔容从0.135 cm3/g提升到0.249 cm3/g,对二氯甲烷废气吸附穿透容量从45 mg/g提升到148 mg/g。继续在丝光沸石上负载Fe3+,孔容随着负载铁质量分数的增加而下降,对二氯甲烷废气吸附穿透容量与负载铁质量分数呈现倒"U"关系,负载0.98%的铁时吸附穿透容量达到163 mg/g。原位漫反射傅里叶变换红外测试结果表明,二氯甲烷分子与丝光沸石之间作用较弱,主要是被孔道捕获;而负载的Fe3+会与氯原子相互作用而吸附二氯甲烷分子。

Abstract

Mordenite is successively modified by NaOH,H2C2O4 and Fe(NO3)3,which does not destroy the topology structure of mordenite.Such a modification operation can help mordenite to increase its specific surface area and pore volume,and generate mesopore.After the modification,the specific surface area of mordenite rises from 255 m2·g-1 to 356 m2·g-1,the pore volume increases from 0.135 cm3·g-1 to 0.249 cm3·g-1,the breakthrough adsorption capacity for dichloromethane exhaust increases from 45 mg·g-1 to 148 mg·g-1.If the modified mordenite is continuously loaded with Fe3+,the pore volume decreases with the increasing loading content of Fe3+.The relation between the breakthrough adsorption capacity for dichloromethane exhaust and the loading content of iron inverts a "U",and the breakthrough adsorption capacity reaches 163 mg·g-1 when the loading content of iron is 0.98%.The in situ diffuse reflectance Fourier transform infrared spectroscopy result indicates that the dichloromethane molecules weakly interact with mordenite,and the molecules are mainly hunted by pores;the loaded Fe3+ interact with chlorine to adsorb dichloromethane molecules.

关键词

丝光沸石 / 金属离子 / 吸附 / 改性 / 二氯甲烷

Key words

mordenite / metal iron / adsorption / modification / dichloromethane

Author summay

王心愿(1991-),男,硕士生,研究方向为分子筛合成和应用,csuwxy17@163.com。

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Fe3+负载介孔丝光沸石吸附脱除二氯甲烷废气的研究[J]. 现代化工, 2023, 43(S2): 159-163 DOI:10.16606/j.cnki.issn0253-4320.2023.S2.031

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