Márquez Negro Alejandro, Martí Verónica, Sánchez-Hervás José María, Ortiz Isabel
Unit for Sustainable Thermochemical Valorization, Energy Department, CIEMAT, 28040 Madrid, Spain.
Department of Chemical Engineering and Materials, Faculty of Chemistry, Complutense University of Madrid (UCM), 28040 Madrid, Spain.
Molecules. 2025 Mar 27;30(7):1501. doi: 10.3390/molecules30071501.
The development of sustainable waste management for environmental remediation has highlighted the potential of biochar produced from agricultural wastes as an effective adsorbent for gas pollutant capture. This work focuses on the production and activation of biochar derived from pistachio shells for CO and HS adsorption. Adsorbents were obtained by pyrolysis and subsequently activated through two methods: chemical activation with KOH and physical activation with CO. Adsorption studies were conducted to evaluate the influence of these activation methods on textural properties and adsorption capacities. Chemical activation enhanced microporosity and increased the specific surface area (531 m/g), resulting in a better performance, obtaining adsorption capacities of 87 mgCO/g and 9.6 mgHS/g. Non-linear kinetic models were identified as the most suitable for fitting CO adsorption data, with the Avrami model presenting the best fit results. Dynamic HS adsorption tests revealed the influence of moisture present in the adsorbent, favoring HS dissociation and thus improving capture processes, especially when chemical activation biochar is employed. This enhancement is attributed to the greater development of active centers on its surface, including micropores and heterogeneous atoms introduced though impregnation.
用于环境修复的可持续废物管理的发展凸显了利用农业废弃物生产的生物炭作为捕获气体污染物的有效吸附剂的潜力。这项工作聚焦于由开心果壳衍生的生物炭的制备及其用于吸附一氧化碳和硫化氢的活化处理。通过热解获得吸附剂,随后通过两种方法进行活化:用氢氧化钾进行化学活化和用一氧化碳进行物理活化。开展吸附研究以评估这些活化方法对结构性质和吸附容量的影响。化学活化增强了微孔性并增加了比表面积(531平方米/克),从而带来了更好的性能,一氧化碳和硫化氢的吸附容量分别达到87毫克/克和9.6毫克/克。确定非线性动力学模型最适合拟合一氧化碳吸附数据,其中阿弗拉米模型呈现出最佳拟合结果。动态硫化氢吸附试验揭示了吸附剂中水分的影响,其有利于硫化氢离解,从而改善捕获过程,特别是当使用化学活化生物炭时。这种增强归因于其表面活性中心的进一步发展,包括微孔以及通过浸渍引入的异质原子。