Hu Mian, Cui Baihui, Xiao Bo, Luo Shiyi, Guo Dabin
College of Environment, Zhejiang University of Technology, Hangzhou 310032, China.
School of Environmental Science & Engineering, Huazhong University of Science and Technology, Wuhan 430074, China.
Nanomaterials (Basel). 2020 Jul 18;10(7):1397. doi: 10.3390/nano10071397.
Ex situ catalytic pyrolysis of biomass using char-supported nanoparticles metals (Fe and Ni) catalyst for syngas production and tar decomposition was investigated. The characterizations of fresh Fe-Ni/char catalysts were determined by TGA, SEM-EDS, Brunauer-Emmett-Teller (BET), and XPS. The results indicated that nanoparticles metal substances (Fe and Ni) successfully impregnated into the char support and increased the thermal stability of Fe-Ni/char. Fe-Ni/char catalyst exhibited relatively superior catalytic performance, where the syngas yield and the molar ratio of H2/CO were 0.91 Nm3/kg biomass and 1.64, respectively. Moreover, the lowest tar yield (43.21 g/kg biomass) and the highest tar catalytic conversion efficiency (84.97 wt.%) were also obtained under the condition of Ni/char. Ultimate analysis and GC-MS were employed to analyze the characterization of tar, and the results indicated that the percentage of aromatic hydrocarbons appreciably increased with the significantly decrease in oxygenated compounds and nitrogenous compounds, especially in Fe-Ni/char catalyst, when compared with no catalyst pyrolysis. After catalytic pyrolysis, XPS was employed to investigate the surface valence states of the characteristic elements in the catalysts. The results indicated that the metallic oxides (MeO) were reduced to metallic Me as active sites for tar catalytic pyrolysis. The main reactions pathway involved during ex situ catalytic pyrolysis of biomass based on char-supported catalyst was proposed. These findings indicate that char has the potential to be used as an efficient and low-cost catalyst toward biomass pyrolysis for syngas production and tar decomposition.
研究了使用炭负载纳米颗粒金属(铁和镍)催化剂对生物质进行非原位催化热解以生产合成气和分解焦油。通过热重分析(TGA)、扫描电子显微镜-能谱分析(SEM-EDS)、布鲁诺尔-埃米特-泰勒(BET)比表面积测定法和X射线光电子能谱(XPS)对新鲜的铁-镍/炭催化剂进行了表征。结果表明,纳米颗粒金属物质(铁和镍)成功浸渍到炭载体中,并提高了铁-镍/炭的热稳定性。铁-镍/炭催化剂表现出相对优异的催化性能,合成气产率和H2/CO摩尔比分别为0.91 Nm3/kg生物质和1.64。此外,在镍/炭条件下还获得了最低的焦油产率(43.21 g/kg生物质)和最高的焦油催化转化效率(84.97 wt.%)。采用元素分析和气相色谱-质谱联用(GC-MS)分析焦油的特性,结果表明,与无催化剂热解相比,尤其是在铁-镍/炭催化剂作用下,芳烃的百分比显著增加,而含氧化合物和含氮化合物明显减少。催化热解后,采用XPS研究催化剂中特征元素的表面价态。结果表明,金属氧化物(MeO)还原为金属Me作为焦油催化热解的活性位点。提出了基于炭负载催化剂的生物质非原位催化热解过程中的主要反应途径。这些发现表明,炭有潜力用作高效低成本的催化剂,用于生物质热解以生产合成气和分解焦油。