沸石
介孔材料
微型多孔材料
热重分析
无机化学
化学
酸强度
差示扫描量热法
解吸
催化作用
离子交换
丝光沸石
核化学
吸附
材料科学
有机化学
离子
物理
热力学
作者
Chunshan Song,Wei Chuan Lai,Andrew D. Schmitz,Kondam Madhusudan Reddy
出处
期刊:Preprints of Papers, American Chemical Society, Division of Fuel Chemistry
日期:1996-10-01
卷期号:41 (1): 71-76
被引量:5
摘要
Thermal gravimetric analysis (TGA) and differential scanning calorimetry (DSC) were applied for characterizing the acidic properties of microporous and mesoporous zeolite catalysts through temperature-programmed desorption (TPD) of n-butylamine (n-BA). A flow system was designed with heating and evacuation capability for preparing the n-BA adsorbed sample. The sample was then transferred to TGA (or DSC) apparatus. n-BA desorption conducted on TGA at different temperatures represents the interaction with surface acidic sites of different strength. BAse desorption at 100-240{degrees}C, 240-340{degrees}C, and 340-500{degrees}C, was classified as weak, intramediate, and strong acid sites, respectively. DSC indicates the endothermic nature of the differential thermogravimetric peaks (observed from TGA) in the above temperature regimes, confirming the TPD data. The microporous zeolites examined include three proton-form mordenites, three proton-form and metal-ion exchanged Y-zeolites, and four noble metal catalysts supported on mordenite and Y-zeolite. Four mesoporous zeolites were synthesized and examined by the same TPD method. Both the total acidity (mmol/g) and acid strength distribution depend on the zeolite type. Si/Al ratio, and metal loading. Ni and La ion-exchange decreased the strong acid sites. Pt and Pd loading on an HY decreased the strong acid sites but their loading on an H-mordenite had little effect on its strongmore » acid sites. Mesoporous zeolites showed lower acidity and lower fraction of strong acid sites compared to HY and H-mordenites. However, the acidity of mesoporous zeolites strongly depends on the aluminum source compounds used in the hydrothermal synthesis of the zeolites.« less
科研通智能强力驱动
Strongly Powered by AbleSci AI