利用枯草芽孢杆菌生物膜支撑的锰-铈/沸石催化剂高效降解甲苯

Muhammad Zubair Mohsin, Ali Mohsin, Waqas Qamar Zaman, Xiaojuan Zhu, Xihua Zhao, Zain Abbas, Muhammad Hammad Hussain, Ali Shan, Salim ur-Rehman, Muhammad Asif Nawaz, Rabia Omer, Yingping Zhuang, Meijin Guo, Jiaofang Huang
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引用次数: 0

摘要

本研究探讨了一种合成枯草芽孢杆菌生物膜支撑的锰-铈/沸石催化剂以降解气态甲苯的新方法。在沸石纳米颗粒上以不同的锰(Mn)和铈(Ce)比例合成了四种不同的金属氧化物纳米催化剂(ZMn、ZMnCe-10%、ZMnCe-20% 和 ZMnCe-30%)。利用 TEM、SEM、XRD、BET、XPS 和 EDX 图谱对这四种样品以及简单的沸石进行了研究。根据这些分析,在介质阻挡放电(DBD)反应器中采用非热等离子体(NTP)技术测试了制备的 ZMn、ZMnCe-10%、ZMnCe-20% 和 ZMnCe-30% 样品在完全氧化甲苯和甲苯中间产物方面的催化活性。其中,ZMnCe-20% 在低浓度(200 ppm)和湿度(50%)条件下的甲苯降解效率最高(89%)。随后,将枯草芽孢杆菌生物膜野生型(WT)和工程型枯草芽孢杆菌生物膜 EPS 与 ZMnCe-20% 催化剂结合,制备出高效疏水性纳米生物催化剂。EPS 是生物膜基质中的主要成分,在影响生物膜稳定性、电子传递、表面粗糙度和疏水性等特性方面起着关键作用。与 WT 枯草芽孢杆菌生物膜相比,过表达 EPS 的枯草芽孢杆菌生物膜在 ZMnCe-20% 纳米催化剂上表现出更强的生长和发育能力。此外,装有 ZMnCe-20%/ 生物膜(EPS+)纳米生物催化剂的 NTP 系统在甲苯浓度(250 ppm)和湿度增加(90%)的情况下,甲苯降解活性最高(99%),二氧化碳选择性(83%),氮氧化物浓度降低(高达 50%),臭氧分解完全。NTP 系统中产生的高能电子会打断甲苯分子环间的 C-H 和 C-C 键,形成多种副产品,这些副产品随后会与 O-、OH- 和 O3 等活性自由基物种发生反应,并进一步转化为最终降解产物(CO2 和 H2O)。研究结果表明,ZMnCe-20% 催化剂具有超疏水、抗 H2O、改善表面粗糙度和电子生成等先进特性,可成功实现生物膜的发育和生长。总之,该研究方法结合了生物工程和材料科学,开发出了可持续的纳米生物催化剂,用于去除工业和环境中的挥发性有机化合物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Efficient Toluene Degradation using Bacillus subtilis Biofilm Supported Mn-Ce/Zeolite Catalysts

Efficient Toluene Degradation using Bacillus subtilis Biofilm Supported Mn-Ce/Zeolite Catalysts

This study investigated a new approach for synthesizing Bacillus subtilis biofilm-supported Mn-Ce/Zeolite catalysts for the degradation of gaseous toluene. Four different metal oxide nano-catalysts (ZMn, ZMnCe-10%, ZMnCe-20%, and ZMnCe-30%) were synthesized with varying ratios of manganese (Mn) and cerium (Ce) on zeolite nanoparticles. TEM, SEM, XRD, BET, XPS, and EDX mapping were used to examine these four samples, as well as simple zeolite. Based on these analyses, the catalytic activity of the prepared samples ZMn, ZMnCe-10%, ZMnCe-20%, and ZMnCe-30% for the complete oxidation of toluene and toluene intermediate products were tested with Non-thermal plasma (NTP) technology in a dielectric barrier discharge (DBD) reactor. Among all, ZMnCe-20% showed the highest toluene degradation efficiency (89%) at low concentrations (200 ppm) and humidity (>50%). Later, highly efficient and hydrophobic nano-biocatalysts were prepared by combining B. subtilis biofilm wild-type (WT) and engineered B. subtilis biofilm EPS with ZMnCe-20% catalyst. EPS is the main component found in biofilm matrix and plays a key role in influencing properties such as biofilm stability, electron transfer, surface roughness and hydrophobicity. Compared to WT B. subtilis biofilm, EPS overexpressed B. subtilis biofilm showed stronger growth and development on ZMnCe-20% nanocatalyst. Moreover, the NTP system packed with ZMnCe-20%/biofilm (EPS+) nano-biocatalyst exhibited the highest toluene degradation activity (99%) with (83%) CO2 selectivity, (up to 50%) reduction in NOx concentration and complete ozone decomposition at (250 ppm) toluene concentrations and increased humidity (>90%). High-energy electrons generated in the NTP system break the C-H and C-C bond between the rings of the toluene molecule, forming several byproducts which are later reacted with active radical species such as O•, OH•, and O3 and further converted into final degradation products (CO2 and H2O). The results demonstrated successful biofilm development and growth on the ZMnCe-20% catalyst with advanced features such as superhydrophobicity, H2O resistance, improved surface roughness, and electron generation. In short, the study's approach combines bioengineering and material science to develop sustainable nano-biocatalysts for removing VOCs in industrial and environmental settings.

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