دورية أكاديمية

The Effect of Preparation Method of Ni-Supported SiO2 Catalysts for Carbon Dioxide Reforming of Methane

التفاصيل البيبلوغرافية
العنوان: The Effect of Preparation Method of Ni-Supported SiO2 Catalysts for Carbon Dioxide Reforming of Methane
المؤلفون: Hua-Ping Ren, Si-Yi Ding, Qiang Ma, Wen-Qi Song, Yu-Zhen Zhao, Jiao Liu, Ye-Ming He, Shao-Peng Tian
المصدر: Catalysts, Vol 11, Iss 10, p 1221 (2021)
بيانات النشر: MDPI AG, 2021.
سنة النشر: 2021
المجموعة: LCC:Chemical technology
LCC:Chemistry
مصطلحات موضوعية: reforming of methane, carbon dioxide, nickel, glycine, SiO2, Chemical technology, TP1-1185, Chemistry, QD1-999
الوصف: Reforming methane to produce syngas is a subject that generates considerable interest. The process requires catalysts that possess high-performance active sites to activate stable C–H bonds. Herein, we report a facile synthetic strategy to prepare Ni-based catalysts by complexation–impregnation (Ni-G/SiO2-C) and precipitation–impregnation (Ni-G/SiO2-P) methods using glycine as a complexing agent. The particle size of Ni in both types of catalysts is decreased by adding glycine in the preparation process. Nevertheless, the preparation methods and amount of glycine play a significant role in the particle size and distribution of Ni over the Ni-based catalysts. The smaller particle size and narrower distribution of Ni were obtained in the Ni-G/SiO2-P catalyst. The catalysts were comparatively tested for carbon-dioxide reforming of methane (CDR). Ni-G/SiO2-P showed better CDR performance than Ni-G/SiO2-C and Ni/SiO2 and increased stability because of the smaller particle size and narrower distribution of Ni. Moreover, a high-performance Ni-based catalyst was prepared by optimizing the amount of glycine added. An unobservable deactivation was obtained over Ni-G-2/SiO2-P and Ni-G-3/SiO2-P for CDR during TOS = 20 h. Thus, a new promising method is described for the preparation of Ni-based catalysts for CDR.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2073-4344
Relation: https://www.mdpi.com/2073-4344/11/10/1221; https://doaj.org/toc/2073-4344
DOI: 10.3390/catal11101221
URL الوصول: https://doaj.org/article/005ea327dcb742438efa95b61374e659
رقم الأكسشن: edsdoj.005ea327dcb742438efa95b61374e659
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:20734344
DOI:10.3390/catal11101221