Methane aromatization over 2 wt% Mo/HZSM-5 in the presence of O2 and NO
被引:48
|
作者:
Tan, PL
论文数: 0引用数: 0
h-index: 0
机构:Hong Kong Baptist Univ, Dept Chem, Kowloon Tong, Hong Kong, Peoples R China
Tan, PL
Leung, YL
论文数: 0引用数: 0
h-index: 0
机构:Hong Kong Baptist Univ, Dept Chem, Kowloon Tong, Hong Kong, Peoples R China
Leung, YL
Lai, SY
论文数: 0引用数: 0
h-index: 0
机构:Hong Kong Baptist Univ, Dept Chem, Kowloon Tong, Hong Kong, Peoples R China
Lai, SY
Au, CT
论文数: 0引用数: 0
h-index: 0
机构:
Hong Kong Baptist Univ, Dept Chem, Kowloon Tong, Hong Kong, Peoples R ChinaHong Kong Baptist Univ, Dept Chem, Kowloon Tong, Hong Kong, Peoples R China
Au, CT
[1
]
机构:
[1] Hong Kong Baptist Univ, Dept Chem, Kowloon Tong, Hong Kong, Peoples R China
[2] Hong Kong Baptist Univ, Ctr Surface Anal & Res, Kowloon Tong, Hong Kong, Peoples R China
[3] Chinese Univ Hong Kong, Dept Phys, Shatin, Hong Kong, Peoples R China
methane aromatization;
Mo/HZSM-5;
oxygen and nitric oxide addition;
D O I:
10.1023/A:1014956501472
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
In the non-oxidative aromatization reaction (temperature = 770degreesC, flow rate = 34 ml min(-1)), 2 wt% Mo/HZSM-5 deactivated after 4 h due to severe coking. We observed that with a suitable amount of O-2 (less than or equal to5.3 vol%) in the methane feed, the catalyst could last for more than 6 h with a ca. 4% yield of aromatics at 770degreesC. Depending on the concentration of O-2 or the reaction temperature, there are three reaction zones in the catalyst bed: (i) methane oxidation; (ii) methane reforming; and (iii) methane aromatization. CO and H-2 produced in the first two zones are accountable for stability amelioration of the catalyst. The addition of NO exhibited similar effects on the reaction. Further increase in O-2 (greater than or equal to8.4 vol%) or NO (greater than or equal to14.2 vol%) concentration would result in CO and CO2 being the predominant carbon-containing products; C2H4 and C2H6 were generated in small amounts and no aromatics were detected.