首页> 外文OA文献 >Adsorção dos gases NH3, NO e H2S em fosfato de vanadila, hidrogeno fosfato de vanadila e fosfatos de vanadila dopados por Al, Co, Mn e Cr
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Adsorção dos gases NH3, NO e H2S em fosfato de vanadila, hidrogeno fosfato de vanadila e fosfatos de vanadila dopados por Al, Co, Mn e Cr

机译:Al,Co,Mn和Cr掺杂的磷酸氧钒,磷酸氢氧钒和磷酸氧钒中NH3,NO和H2S气体的吸附

摘要

In this work were synthesized the materials called vanadyl phosphate, hydrogenvanadyl phosphate and vanadyl phosphate doped by transition metals with the aim inadsorption the following compounds: ammonia, hydrogen sulfide and nitrogen oxide. Tocharacterize the starting compounds was used DRX, FTIR, FRX and TG analysis. After thecharacterization of substrates, proceeded de adsorption of NH3 and H2S gases in reactor,passing the gases with continuous flow for 30 min and room temperature. Gravimetric dataindicate that the matrices of higher performance in adsorption of ammonia was those dopedby aluminum and manganese, obtaining results of 216,77 mgNH3/g and 200,40 mgNH3/g ofmatrix, respectively. The matrice of higher performance in adsorption of hydrogen sulfidewas that doped by manganese, obtaining results of 86,94 mgH2S/g of matrix. The synthesis ofsubstrates VOPO4.2H2O and MnVOPO4.2H2O with nitrogen oxide was made in solution,aiming the final products VOPO4.G.nH2O and MnVOPO4.G.nH2O (G = NO and n = numberof water molecules). The thermo analytical behavior and the infrared spectroscopy areindicative of formation of VOPO4.2,5NO.3H2O compound. Results of scanning electronmicroscopy (SEM) and Energy dispersive spectroscopy (EDS) of materials vanadyl phosphateand vanadyl phosphate modified after reaction in solid state or in solution with the gases showmorphology changes in substrates, beyond the formation of orthorhombic sulfur crystals overtheir respective hosts when these adsorb hydrogen sulfide
机译:在这项工作中,合成了过渡金属掺杂的材料,分别称为磷酸氧钒,磷酸氢氧钒和磷酸氧钒,目的是吸收以下化合物:氨,硫化氢和氮氧化物。为了表征起始化合物,使用了DRX,FTIR,FRX和TG分析。对底物进行表征后,在反应器中进行NH3和H2S气体的脱附,使气体在室温下连续流动30分钟。重量数据表明,较高的吸附氨的基质是铝和锰掺杂的基质,分别得到216,77 mgNH3 / g和200,40 mgNH3 / g基质的结果。锰掺杂了较高性能的硫化氢吸附基质,得到的结果为86.94 mgH2S / g基质。在溶液中用氮氧化物合成了底物VOPO4.2H2O和MnVOPO4.2H2O,最终产物为VOPO4.G.nH2O和MnVOPO4.G.nH2O(G = NO,n =水分子数)。热分析行为和红外光谱表明VOPO4.2,5NO.3H2O化合物的形成。固态或在与气体的溶液中反应后改性的磷酸氧钒和磷酸氧钒的材料的扫描电子显微镜(SEM)和能量色散谱(EDS)结果表明,当这些物质吸附后,基质在基质上的形态发生了变化,超出了在其各自主体上形成的正交晶硫晶体硫化氢

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