Y-Mn-O负载的Ni基催化剂用于乙酸自热重整产氢
Y-Mn-O Supported Ni-Based Catalyst for Hydrogen Production via Auto-thermal Reforming of Acetic Acid
作者单位E-mail
胡晓敏 成都理工大学材料与化学化工学院, 成都 610059  
陈慧 成都理工大学材料与化学化工学院, 成都 610059  
贾玄弈 成都理工大学材料与化学化工学院, 成都 610059  
王巧 成都理工大学材料与化学化工学院, 成都 610059  
黄利宏 成都理工大学材料与化学化工学院, 成都 610059 huanglihong06@cdut.cn 
摘要: 为了有效地从生物质衍生的乙酸中获得高氢气产率,通过水热法合成了一系列的NiMnY催化剂并用于乙酸自热重整(ATR)过程中,并采用X射线衍射(XRD)、N2吸附-脱附测试、H2程序升温还原(H2-TPR)探究催化剂中的内在联系。在Ni 0.39Mn0.61YO3.11±δ催化剂中,经焙烧后形成了类钙钛矿型(Ni,Mn) YO3物相;经氢气还原后,转化为含有MnO、Y2O3和高分散Ni纳米粒子的热稳定的Ni-Mn-Y-O物种。Ni0.39Mn0.61YO3.11±δ具有高效稳定的产氢催化性能,乙酸转化率高达100%,氢气产率达到2.68 mol H 2 ·mol HAc-1
关键词: 生物质  非均相催化  氢能    钙钛矿相
基金项目: 国家自然科学基金(No.21276031)、四川省科技计划项目(No.2019YFH0181)和四川省国际科技合作计划项目(No.2015HH0013)资助。
Abstract: To effectively achieve high hydrogen yield from biomass-derived acetic acid (HAc), a series of NiMnY catalysts were prepared by hydrothermal method and tested in auto-thermal reforming (ATR) of HAc. X-ray diffraction (XRD), N2 adsorption-desorption test and H2-temperature-programmed reduction (H2-TPR) were carried out to explore the internal relationship within these NiMnY catalysts. Over the Ni0.39Mn0.61YO3.11±δ catalyst, perovskite-like (Ni, Mn)YO3 phase was formed after calcination, and converted into thermostable Ni-Mn-Y-O species after reduction in H 2, along with the highly dispersed nickel nanoparticles. As a result, over the promoted Ni0.39Mn0.61YO3.11±δ catalyst, a stable catalytic performance with high HAc conversion (100%) and hydrogen yield (2.68 molH 2 ·mol HAc -1) was recorded, showing potential for hydrogen production.
Keywords: biomass  heterogeneous catalysis  hydrogen energy  nickel  perovskite phases
投稿时间:2020-09-16 修订日期:2020-12-04
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胡晓敏,陈慧,贾玄弈,王巧,黄利宏.Y-Mn-O负载的Ni基催化剂用于乙酸自热重整产氢[J].无机化学学报,2021,37(3):555-560.
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