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Influence of Ni/SiO2 catalyst preparation methods on hydrogen production from the pyrolysis/reforming of refuse derived fuel

机译:Ni / siO2催化剂制备方法对垃圾衍生燃料热解/重整制氢的影响

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摘要

Hydrogen production from the pyrolysis/reforming of refuse derived fuel (RDF) was investigated with a series of Ni/SiO2 catalysts. The catalysts were prepared by homogeneous precipitation derived from a sol-gel method (HPG) and compared to Ni/SiO2 catalysts prepared by adding a phase separation step to the HPG process (B-HPG). All the catalysts had a NiO loading of 10 wt.%, and three different calcination temperatures (500 °C, 700 °C and 900 °C) were used for each method. The prepared Ni/SiO 2 catalysts were analysed to determine their surface area, and porosity characteristics; additionally scanning electron microscopy (SEM-EDX), transmission electron microscopy (TEM), infrared spectroscopy (FTIR), and X-Ray diffraction (XRD) analyses were carried out. The results showed that the catalyst prepared by HPG and calcined at 700 °C (HPG700), presented a relatively high surface area (∼347 m2 g-1), large pore diameter (12.50 nm), and also resulted in the highest catalytic activity towards H2 production, attaining ∼60 vol.% hydrogen. The lowest hydrogen concentration of about 42 vol.% was obtained using the catalysts prepared by the combined HPG-phase separation method, and calcined at 900 °C (B-HPG900). It was also observed that at calcination temperatures higher than 700 °C the catalytic activity for hydrogen production was diminished for both preparation methods.
机译:用一系列Ni / SiO2催化剂研究了垃圾衍生燃料(RDF)的热解/重整制氢。通过衍生自溶胶-凝胶法(HPG)的均相沉淀制备催化剂,并将其与通过在HPG工艺中添加相分离步骤(B-HPG)制备的Ni / SiO2催化剂进行比较。所有催化剂的NiO负载量均为10 wt。%,每种方法使用三种不同的煅烧温度(500°C,700°C和900°C)。分析所制备的Ni / SiO 2催化剂,以确定其表面积和孔隙率特性;另外,还进行了扫描电子显微镜(SEM-EDX),透射电子显微镜(TEM),红外光谱(FTIR)和X射线衍射(XRD)分析。结果表明,HPG制备并在700°C下煅烧的催化剂(HPG700)具有相对较高的表面积(〜347 m2 g-1),大孔径(12.50 nm),并具有最高的催化活性。达到H2的产生,氢达到〜60 vol。%。使用通过组合的HPG相分离方法制备的催化剂,并在900°C下煅烧(B-HPG900),可获得最低氢浓度约为42%(体积)。还观察到,在两种以上的制备方法中,在高于700℃的煅烧温度下,产氢的催化活性均降低。

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    Blanco PH; Wu C; Williams PT;

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  • 年度 2014
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  • 正文语种 en
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