دورية أكاديمية
The Effect of Preparation Method of Ni-Supported SiO2 Catalysts for Carbon Dioxide Reforming of Methane
العنوان: | The Effect of Preparation Method of Ni-Supported SiO2 Catalysts for Carbon Dioxide Reforming of Methane |
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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 |
تدمد: | 20734344 |
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DOI: | 10.3390/catal11101221 |