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Highly Selective Deep Desulfurization of a Model Gasoline on Amine-Modified SiO2 Hybrid Aerogel

机译:在胺改性的SiO2混合气凝胶上高度选择性的模型汽油的深度脱硫

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Amine-modified SiO2 hybrid aerogel desulfurization adsorbents with varied Si/N molar ratios (SiO2-NH2-n) were prepared via the sol-gel method followed by the atmospheric drying technique. SiO2-NH2-n aerogels were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), in situ Fourier transform infrared (FT-IR), and N-2 adsorption-desorption. The desulfuriza-tion performances of SiO2-NH2-n were studied by the batch and breakthrough adsorption experiments. SiO2-NH2-n exhibited an obvious improvement in adsorption capacity for thiophenics compared with SiO2 aerogel due to the hydrogen bonding between thiophenics and amino groups. Among them, SiO2-NH2-8 had the best performance, and the adsorption capacities for thiophene, benzothiophene, and dibenzothiophene were 6.8, 9.5, and 10.2 mg S/g(ads) respectively. No effect of toluene and cyclohexene on the adsorption of SiO2-NH2-8 for thiophene was observed. The equilibrium adsorption data of SiO2-NH2-8 for thiophene were well fitted by the Freundlich model, indicating that multilayer adsorption occurred on the heterogenetic surface of SiO2-NH2-8. The kinetic adsorption data of SiO2-NH2-8 for thiophene could correlate properly with the pseudo-second-order kinetic model, suggesting that the rate-controlling steps involve surface adsorption. The saturated SiO2-NH2-8 could be regenerated completely via heating at 393 K for 12 h, and the regenerated SiO2-NH2-8 afforded 100% breakthrough adsorption capacity for thiophene.
机译:通过溶胶 - 凝胶法洗涤具有变化的Si / N摩尔比的胺改性的SiO 2杂化气凝胶脱硫吸附剂,然后通过溶胶 - 凝胶法制备大气干燥技术。 SiO2-NH2-N Aerogels的特征在于X射线衍射(XRD),X射线光电子能谱(XPS),扫描电子显微镜(SEM),原位傅里叶变换红外(FT-IR)和N-2吸附 - 解吸。通过批量和突破性吸附实验研究了SiO2-NH2-N的脱硫性能。由于噻吩和氨基之间的氢键合,SiO2-NH2-N与SiO2气凝胶相比,戏剧性的吸附能力显而易见。其中,SiO2-NH2-8具有最佳的性能,以及噻吩,苯并噻吩和二苯甲酸酚的吸附能力分别为6.8,9.5和10.2mg S / G(ADS)。观察到甲苯和环己烯没有对噻吩的吸附的影响。对于噻吩的SiO2-NH2-8的平衡吸附数据由Freundlich模型齐全,表明在SiO 2-NH2-8的异质表面上发生多层吸附。用于噻吩的SiO2-NH2-8的动力学吸附数据可以与伪二阶动力学模型相当相关,表明速率控制步骤涉及表面吸附。饱和的SiO 2-NH2-8可以通过在393k持续12小时的393k中完全再生,并再生SiO 2-NH2-8得到100%的噻吩的突破性吸附能力。

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    Zhejiang Univ Technol Lab Ind Catalysis Coll Chem Engn Hangzhou 310014 Peoples R China;

    Zhejiang Univ Technol Lab Ind Catalysis Coll Chem Engn Hangzhou 310014 Peoples R China;

    Zhejiang Univ Technol Lab Ind Catalysis Coll Chem Engn Hangzhou 310014 Peoples R China;

    Zhejiang Univ Technol Lab Ind Catalysis Coll Chem Engn Hangzhou 310014 Peoples R China;

    Zhejiang Univ Technol Lab Ind Catalysis Coll Chem Engn Hangzhou 310014 Peoples R China;

    Zhejiang Univ Technol Lab Ind Catalysis Coll Chem Engn Hangzhou 310014 Peoples R China;

    Zhejiang Univ Technol Lab Ind Catalysis Coll Chem Engn Hangzhou 310014 Peoples R China;

    Zhejiang Univ Technol Lab Ind Catalysis Coll Chem Engn Hangzhou 310014 Peoples R China;

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