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Preparation and Characterization of Mn_xO_y-Al2O3 Sorbents for H2S Removal from Biomass Gasification Gas

机译:从生物质气化气体中移除H2S的Mn_XO_Y-Al2O3吸附剂的制备与表征

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A series of Mn_xO_y-A12O3 materials have been prepared either by spray-drying (SD) of Al/Mn precursor solutions or by multiple wet-impregnations of two different Mn precursors on various alumina supports. The two Mn precursors used in the preparation were manganese nitrate (Mn(NO3)2-4H2O) and manganese acetate (Mn(CH3COO)2-4H2O). To study properties relevant for the sorption performance, the calcined materials were characterized using several methods. Textural properties (N2 sorption) of the Mn loaded samples show significant differences when compared to the parent supports. For the samples prepared by multiple wet-impregnations this is due to the relatively high Mn loading (up to 30 wt. %) and the additional heat treatment. For the sample prepared by SD it is the presence of Mn species that modifies the textural properties and affects the way the final material is formed. X-ray diffraction measurements show that the ratio of Mn20O3/Mn3O4 depends on the Mn precursor used when the samples are prepared by the multiple wet-impregnation method. For the samples prepared by the SD method the use of a specific Mn precursor has no influence on the ratio of Mn2O3/Mn30O4 in the final material. UV-Raman spectra strongly indicate the presence of MnO2 on the surface of all Mn_xO_y-A12O3 sorbents. MnO2 was not detected by XRD. The presence of new Mn_xO_y species was also detected by Raman spectroscopy and their existence is ascribed to a specific interaction between Mn_xO_y and A12O3. TPR data show there are three main reduction steps most likely due to the reduction of MnO2 to MnO through intermediate Mn2O3 and Mn3O4. The data, however, indicates that a new species is formed at high temperature (above approx. 550 °C). It is proposed that the additional features observed in the TPR profiles might be due to the formation of the spinel structure MnAl2O4.
机译:通过Al / Mn前体溶液的喷雾干燥(SD)或通过各种氧化铝载体的两种不同Mn前体的多次湿浸渍制备了一系列Mn_XO_Y-A12O3材料。制备中使用的两个Mn前体是硝酸锰(Mn(NO 3)2-4H 2 O)和乙酸锰(Mn(CH 3 COO)2-4H 2 O)。为了研究与吸附性能相关的性质,使用几种方法表征煅烧材料。与父支持相比,Mn加载样品的质地性质(N2吸附)显示出显着的差异。对于多个湿浸渍制备的样品,这是由于相对高的Mn负载(最高30重量%)和附加热处理。对于通过SD制备的样品,存在Mn种类的存在,其改变纹理性质并影响形成最终材料的方式。 X射线衍射测量表明,MN20 O 3 / MN3O4的比例取决于通过多湿浸渍方法制备样品时使用的Mn前体。对于通过SD方法制备的样品,使用特异性Mn前体的使用对最终材料中的Mn 2 O 3 / Mn30 O 4的比率没有影响。 UV-Raman光谱强烈指示所有MN_XO_Y-A12O3吸附剂表面上的MNO2存在。 XRD未检测到MNO2。通过拉曼光谱检测到新MN_XO_Y物种的存在,并且它们的存在归因于MN_XO_Y和A12O3之间的特定相互作用。 TPR数据显示,由于通过中间体Mn2O3和Mn3O4将MnO 2还原为MnO 2至MnO,有三个主要减少步骤。然而,数据表明,新物种在高温下形成(高于约550°C)。提出,在TPR型材中观察到的附加特征可能是由于尖晶石结构Mnal2O4的形成。

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