...
首页> 外文期刊>Solid state ionics >Synthesis of alumina supported nickel nanoparticle catalysts and evaluation of nickel metal dispersions by temperature programmed desorption
【24h】

Synthesis of alumina supported nickel nanoparticle catalysts and evaluation of nickel metal dispersions by temperature programmed desorption

机译:氧化铝负载的镍纳米粒子催化剂的合成和通过程序升温脱附对镍金属分散体的评估

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

The purpose of this study was to synthesize highly dispersed Ni/Al2O3 catalysts and to develop a suitable hydrogen -temperature programmed desorption (H,-TPD) method for the determination of nickel metal surface area, dispersion, and crystallite sizes. Several highly dispersed Ni/Al2O3 catalysts with a Ni loading between 15 and 25wt.% were synthesized. The reducibility of catalysts was determined by temperature programmed reduction (TPR) experiments. All catalysts exhibited a single reduction peak with a maximum rate of H, consumption (T-max in TPR) occurring below 450 degrees C. Three different H-2-TPD methods were employed to determine the amount of H, chemisorbed. In TPD-1, a 10% H-2/Ar mixture was used for catalyst pre-reduction and surface saturation by cooling down from T,,,,, in TPR to room temperature. In TPD-2, the catalyst surface after pre-reduction was flushed with Ar at T-max in TPR+ 10 degrees C. The TPD-3 was similar to the TPD-2, but used 100% H, instead of 10% H-2/Ar mixture. In all three TPD methods, the profiles exhibited 2 domains of H-2 desorption peaks, one below 450 degrees C, referred to as type-1 peaks, and attributed to H-2 desorbed from exposed fraction of Ni atoms, and the other above 450 degrees C, denoted as type-2 peaks, and assigned to the desorption of H-2 located in the subsurface layers and/or to spillover H-2. Flushing the reduced catalyst surface in Ar at T-max in TPR+ 10 degrees C in TPD-2 and TPD-3 removed most of the H-2 located in the subsurface layers/spillover H2. The amount of H, chemisorbed to form a monolayer on the reduced Ni/Al2O3 catalysts was determined quantitatively from the TPD peak areas of type-1 peaks in TPD-1, and from both type-1 and type-2 peaks in TPD-2 and TPD-3. The Ni metal surface area, dispersions and crystallite sizes were calculated from the chemisorption data and the values were compared with those obtained using the static chemisorption method. Both TPD-2 and TPD-3 gave chernisorption results similar to that obtained from the static method. (c) 2006 Elsevier B.V. All rights reserved.
机译:这项研究的目的是合成高度分散的Ni / Al2O3催化剂,并开发出一种合适的氢温度程序解吸(H,-TPD)方法,用于测定镍金属的表面积,分散度和微晶尺寸。合成了几种高分散的Ni / Al2O3催化剂,其Ni含量在15%至25%(重量)之间。催化剂的还原性通过程序升温还原(TPR)实验确定。所有催化剂均表现出一个单一的还原峰,其中最大的H消耗速率(TPR中的T-max)低于450摄氏度。三种不同的H-2-TPD方法用于测定化学吸附的H量。在TPD-1中,通过从TPR中的T冷却至室温,将10%H-2 / Ar混合物用于催化剂的预还原和表面饱和。在TPD-2中,将预还原后的催化剂表面在TPR + 10摄氏度下的T-max处用Ar冲洗。TPD-3与TPD-2相似,但使用的是100%H,而不是10%H- 2 / Ar混合物。在所有三种TPD方法中,这些谱图均显示2个H-2解吸峰域,一个在450摄氏度以下,称为1型峰,并归因于Ni原子暴露部分解吸的H-2,另一个在上方。 450摄氏度(表示为2型峰),分配给位于地下层的H-2解吸和/或溢出H-2。在TPD-2和TPD-3中,在TPR + 10°C的T-max下,用Ar冲洗还原的催化剂表面时,除去了位于地下层/溢出H2中的大部分H-2。根据TPD-1中1型峰的TPD峰面积以及TPD-2中1型和2型峰的化学定量确定在还原的Ni / Al2O3催化剂上化学吸附形成单层的H的量。和TPD-3。从化学吸附数据计算出Ni金属的表面积,分散体和微晶尺寸,并将其与使用静态化学吸附方法获得的值进行比较。 TPD-2和TPD-3的吸附结果与静态方法相似。 (c)2006 Elsevier B.V.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号