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    二氧化锰晶相对低温微波催化矿化甲苯的影响研究

    Study on the Influence of MnO2 Crystal Phases on Low-Temperature Microwave Catalytic Mineralization of Toluene

    • 摘要: 发展低温区催化矿化技术是治理挥发性有机污染物(VOCs)的重要研究方向。选取甲苯作为研究对象,将兼具催化氧化活性和微波利用能力的MnO2与微波耦合,成功在100~200 ℃低温下将甲苯有效矿化为CO2和H2O。通过水热法成功制备了α-MnO2、β-MnO2、δ-MnO2和γ-MnO2 4种不同晶相的MnO2,并从物化特性和微波特性角度量化评估其氧化活性和微波利用潜力。XRD结果表明成功合成了4种不同晶相的MnO2;SEM和BET结果显示由于δ-MnO2的多孔结构,其具有更大的比表面积(115.3 m2/g)和孔容(0.458 cm3/g);通过升温实验发现,δ-MnO2表现出优异的微波转化能力,在微波功率为400 W下,δ-MnO2从室温升至300 ℃需要600 s,低于另3种MnO2。结合矢量网络测试结果,δ-MnO2具有最强的反射损耗、阻抗匹配和最大的衰减常数,表明δ-MnO2具有最好的微波吸收和利用能力;在反应空速为18 000 h−1时,对比微波辐照下甲苯的矿化效果,发现晶相对MnO2的催化活性有显著影响,δ-MnO2表现出更为优异的低温矿化性能,达到超过90%矿化效率所需的温度为195 ℃;甲苯矿化的活性次序被确定为δ-MnO2 > α-MnO2 > γ-MnO2 > β-MnO2。此外,δ-MnO2具有良好的稳定性,随着反应时间的增加,甲苯矿化率保持稳定。之后通过GC-MS分析在不同反应温度下甲苯降解产物,结果表明,甲苯降解的副产物主要为酯、酮等有机物,且随着反应温度的升高,副产物数量逐渐减少;当温度为200 ℃时,甲苯被完全氧化为CO2和H2O。综合表征分析、电磁特性和实验结果,发现δ-MnO2优异的低温氧化特性与其独特的微观结构(如结晶度、比表面积、孔容、孔径等)密切相关;同时,其丰富的孔隙结构增强了对微波的吸收和衰减能力,使其最终呈现出最佳的微波吸收和利用特性。

       

      Abstract: Developing low-temperature catalytic mineralization technology has become an important research direction for the treatment of volatile organic pollutants (VOCs). Using toluene as the model pollutant, we combine MnO2, which has both catalytic oxidation activity and microwave absorption ability, with microwave irradiation to mineralize toluene into CO2 and H2O at low temperatures ranging from 100 ℃ to 200 ℃. Four different crystalline phases of MnO2 catalysts (α-MnO2, β-MnO2, δ-MnO2, and γ-MnO2) were successfully synthesized by the hydrothermal method. The catalytic oxidation activity and microwave utilization potential of the different catalysts were evaluated quantitatively, considering both physicochemical and microwave properties. XRD results confirm the successful synthesis of the four distinct crystalline phases. SEM and BET results show that δ-MnO2 has a higher specific surface area (115.3 m2/g) and larger pore volume (0.458 cm3/g) due to its porous structure. Through the heating experiment, it was found that δ-MnO2 shows better microwave conversion ability. When the microwave output power was 400 W, 600 s was required for δ-MnO2 to rise from room temperature to 300 ℃, which was lower than that of α-MnO2, β-MnO2, and γ-MnO2. Combined with the vector network test results, we found that δ-MnO2 exhibits the strongest reflection loss, impedance matching, and maximum attenuation constant, indicating better microwave absorption and utilization ability. By comparing the mineralization performance under microwave irradiation, we conclude that the crystalline structure significantly affects the catalytic activity of MnO2. δ-MnO2 exhibits a superior low-temperature mineralization performance, achieving complete mineralization temperature at 195 ℃ with a gas hourly space velocity (GHSV) of 18 000 h−1. The order of toluene mineralization activity is determined to be: δ-MnO2 > α-MnO2 > γ-MnO2 > β-MnO2. Moreover, δ-MnO2 shows an outstanding stability, whose toluene mineralization efficiency remains stable with increasing reaction time. Moreover, we used GC-MS to analyze the degradation products of toluene at different catalytic temperatures. GC-MS results reveal that the main by-products of toluene degradation are esters, ketones, and other organic compounds. The type of toluene degradation by-products decreases as the reaction temperature increases. At a temperature of 200 ℃, toluene is completely oxidized to CO2 and H2O without the generation of organic products. Through comprehensive characterization, analysis of electromagnetic properties, and experimental results, we found that the excellent low-temperature oxidation characteristics of δ-MnO2 are related to its unique microstructure, including crystallinity, specific surface area, pore volume, and pore size. The rich void structure of δ-MnO2 enhances the absorption and attenuation of microwaves, exhibiting optimal microwave absorption and utilization properties.

       

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