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Surfactant-modified biosolid-derived materials as efficient H2S removal media: Synergistic effects of carbon phase properties and inorganic phase chemistry on reactive adsorption

机译:表面活性剂改性的生物透镜衍生材料作为高效H2S去除介质:碳相质的协同作用和无机相化学对反应性吸附

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A new H2S reactive adsorbent was prepared from a biosolid by the addition of pluronic surfactant F127 prior to a simple pyrolysis at 950 degrees C at two heating regimes. The materials were extensively characterized and tested as H2S removal media from air. The results show an over 250% increase in the H2S removal efficiency compared to the adsorbent obtained without the surfactant addition. Hydrogen sulfide was converted mainly to elemental sulfur. While the surfactant increased the carbon content and volume of mesopores, slow pyrolysis additionally contributed to the development of micropores, increased a carbon structural order, and resulted in an enhanced dispersion of catalytic centers (Ca and Fe oxides) on the surface. It also increased the amount of nitrogen in pyridinic configurations. All of these facilitated electron transfers, thus promoting oxidation reactions, and provided the sites increasing H2S interactions with the surface and also those acting as a storage system for elemental sulfur.
机译:通过在两个加热状态下在950℃下在950℃下加入Pluronic表面活性剂F127,从生物溶解剂中由生物溶解剂制备新的H 2 S反应性吸附剂。这些材料被广泛表征和测试,因为H2S从空气中去除介质。结果表明,与没有表面活性剂加入的吸附剂相比,H2S去除效率的增加超过250%。硫化氢主要转化为元素硫。虽然表面活性剂增加了中孔的碳含量和体积,但慢热解另外导致微孔的发育,增加碳结构秩序,并导致催化中心(Ca和Fe氧化物)的分散在表面上。它还增加了吡啶型构造中的氮气量。所有这些促进的电子转移,从而促进氧化反应,并提供了与表面的H2S相互作用增加的位点,以及作为元素硫的储存系统的那些。

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