دورية أكاديمية

Dry Reforming of Methane over Ni-Supported SBA-15 Prepared with Physical Mixing Method by Complexing with Citric Acid

التفاصيل البيبلوغرافية
العنوان: Dry Reforming of Methane over Ni-Supported SBA-15 Prepared with Physical Mixing Method by Complexing with Citric Acid
المؤلفون: Hua-Ping Ren, Shao-Peng Tian, Si-Yi Ding, Qiang Ma, Wen-Qi Song, Yu-Zhen Zhao, Zhe Zhang, Zongcheng Miao, Wei Wang
المصدر: Catalysts, Vol 13, Iss 9, p 1252 (2023)
بيانات النشر: MDPI AG, 2023.
سنة النشر: 2023
المجموعة: LCC:Chemical technology
LCC:Chemistry
مصطلحات موضوعية: physical mixing, reforming of methane, carbon dioxide, nickel, citric acid, Chemical technology, TP1-1185, Chemistry, QD1-999
الوصف: Ni-supported SBA-15 catalysts were prepared by physical mixing of Ni(NO3)2·6H2O and SBA-15 (Ni/SBA-15-M) and in the presence of citric acid as the complexing agent (Ni/SBA-15-M-C). Moreover, an Ni-supported SBA-15 catalyst was also prepared by the conventional incipient impregnation method (Ni/SBA-15-I). All the catalysts were systematically evaluated for carbon dioxide reforming of methane (CDR) at CO2/CH4 = 1.0, gas hourly space velocity of 60,000 mL·g−1·h−1, and reaction temperature of 700 °C. The characterization results show that the Ni particle size of Ni/SBA-15-M-C is significantly smaller than that of Ni/SBA-15-M due to the coordination effect of citric acid and Ni2+. Consequently, the Ni/SBA-15-M-C exhibits superior anti-coking and anti-sintering during the CDR-operated period because of the higher Ni dispersion and stronger Ni–support interaction. Compared to the Ni/SBA-15-I, the physical mixing of nickel salt and mesoporous material for preparing of Ni-based catalyst is easy to operate, although the crystal size and catalytic performance of Ni/SBA-15-C are very similar to that of Ni/SBA-15-M-I. Thus, the efficient and easily controlled catalyst structure makes the physical mixing strategy very promising for preparing highly active and stable CDR catalysts.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2073-4344
Relation: https://www.mdpi.com/2073-4344/13/9/1252; https://doaj.org/toc/2073-4344
DOI: 10.3390/catal13091252
URL الوصول: https://doaj.org/article/336c08aab865475fa6c368b9cbcde506
رقم الأكسشن: edsdoj.336c08aab865475fa6c368b9cbcde506
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:20734344
DOI:10.3390/catal13091252