利用不寻常的商用有机粘土制造多孔粘土纳米结构:作为挥发性有机化合物全氧化过程中稳定催化剂的支撑氧化锰

IF 5.2 2区 化学 Q1 CHEMISTRY, APPLIED Catalysis Today Pub Date : 2024-10-11 DOI:10.1016/j.cattod.2024.115098
Rosana Balzer , Alexander Sachse , Jean-Dominique Comparot , Maria do Carmo Martins Alves , Jonder Morais , Katia Bernardo-Gusmão , Anderson Joel Schwanke
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引用次数: 0

摘要

本报告介绍了利用一种众所周知但却鲜有研究的商用有机粘土 C-20A 实现的粘土纳米结构(PCN)多孔工程。彻底的表征(通过 XRD、TGA、N2 吸附、ICP、SEM、TEM、27Al MAS NMR、DR UV-Vis、XPS、Py-FTIR 和 H2-TPR)证实了一种分层结构,其比表面积为 504 m² g-1,比用作参考的钠钙蒙脱石高出 12 倍,并具有一种新的孔隙系统,其尺寸范围从超微孔到小中孔(1.3-10 nm)。我们评估了这些 PCN 作为氧化锰的支持物在气相全催化氧化挥发性有机化合物 (VOC) 中的作用。与含钠蒙脱石(17 纳米)相比,含 5% 锰的 PCN 产生了更高的纳米颗粒分散度(10 纳米)。含锰量为 10% 的 PCN 的催化活性最高,在 350 °C 的条件下,苯、甲苯和邻二甲苯的氧化率分别为 54%、39% 和 34%。在这些条件下,催化剂的稳定性可达 36 小时。
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Engineering porous clay nanoarchitectures from unusual commercial organoclay: Supported manganese oxide as stable catalysts in the total oxidation of volatile organic compounds
The porous engineering of clay nanoarchitectures (PCN) achieved from a well-known but little-explored commercial organoclay C-20A is reported. Thorough characterizations (by XRD, TGA, N2 sorption, ICP, SEM, TEM, 27Al MAS NMR, DR UV-Vis, XPS, Py-FTIR and H2-TPR) confirmed a delaminated structure presenting a specific surface area of 504 m² g−1, twelve times higher than the sodic montmorillonite used as reference and featuring a new pore system comprising a size range from supermicropores to small mesopores (1.3–10 nm). The role of these PCN as support of manganese oxide for the gas-phase total catalytic oxidation of volatile organic compounds (VOCs) was evaluated. PCN with 5 % of Mn resulted in a higher nanoparticle dispersion (10 nm) compared to the sodic montmorillonite (17 nm). The highest catalytic activity was reached with PCN containing 10 % of Mn achieving a benzene, toluene and ortho-xylene oxidation of 54 %, 39 % and 34 %, respectively, at 350 °C. The catalyst was stable up to 36 h under these conditions.
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来源期刊
Catalysis Today
Catalysis Today 化学-工程:化工
CiteScore
11.50
自引率
3.80%
发文量
573
审稿时长
2.9 months
期刊介绍: Catalysis Today focuses on the rapid publication of original invited papers devoted to currently important topics in catalysis and related subjects. The journal only publishes special issues (Proposing a Catalysis Today Special Issue), each of which is supervised by Guest Editors who recruit individual papers and oversee the peer review process. Catalysis Today offers researchers in the field of catalysis in-depth overviews of topical issues. Both fundamental and applied aspects of catalysis are covered. Subjects such as catalysis of immobilized organometallic and biocatalytic systems are welcome. Subjects related to catalysis such as experimental techniques, adsorption, process technology, synthesis, in situ characterization, computational, theoretical modeling, imaging and others are included if there is a clear relationship to catalysis.
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