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Dehydroaromatization of methane in the absence of oxygen over modified W/HZSM-5 catalyst

机译:改性的W / HZSM-5催化剂在无氧条件下甲烷脱氢芳构化

摘要

The direct conversion of methane to aromatics, mainly benzene without using oxygen, was studied. In prior, a comparison was conducted for the catalytic properties of W/USY, W/Al2O3, W/H , and W/HZSM-5. Among all the support used, the W/HZSM-5 catalyst showed the best activity and stability with highest methane conversion of 8.4%, corresponding to aromatics selectivity of 97.54% at 973 K and 1 atm. Meanwhile, almost 7% of methane was converted on the other W-supported catalysts, which were drastically deactivated. Further study was performed to investigate the role of acidity of the W/HZSM-5 catalyst. The acidic properties of the catalysts have undergone changes due to the introduction of Li ion. The catalytic properties for those catalysts with Li contents, including 3W/HZSM-5, 3W/Li-HZSM-5(10), 3W/Li-HZSM-5(12), 3W/Li-HZSM-5(46), and 3WLiZSM-5 catalysts were tested at 1073 K and 1 atm. The results demonstrated that the introduction of a certain amount of Li into the ZSM-5 catalyst influences the catalytic performance of dehydroaromatization of methane under the non-oxidative condition. Over W/HZSM-5, a maximum methane conversion achieved was 16%, but decreased considerably to 8% over 320 min. of time on stream. Furthermore, the corresponding aromatic selectivity dropped rapidly from 93% to 56%. While, over the 3W/Li-HZSM-5(10) catalyst which contains 74% of strong acid sites of the parent HZSM-5 resulted in a slight decrease in methane conversion from 18% to 12%, with corresponding to aromatics from 91% to 85%, that was observed after 320 min. of time on stream. However, in the case of more Li content was added, the activity of the catalyst decreased as shown those on the 3W/Li-HZSM-5(12), 3W/Li-HZSM-5(46), and 3W/Li-ZSM-5 catalysts. Also it was found that the catalyst performance could be improved by reducing the amount of the strong acid sites, but considerable reduction in the amount of acidic sites, particularly the Brönsted acid sites, is unfavorable for the non-oxidative methane dehydroaromatization. The 3W/Li-HZSM-5(10) catalyst is found to be suitable catalyst as it has the optimum Brönsted acid sites and consequently, gives the maximum methane conversion and selectivity to aromatics. These results suggest that Li modified W/HZSM-5 catalysts is bifunctional catalyst in which both W active sites and Brönsted acid sites of HZSM-5 support are crucial factors for good catalytic performance.
机译:研究了不使用氧气将甲烷直接转化为芳烃(主要是苯)的过程。先前,对W / USY,W / Al2O3,W / H和W / HZSM-5的催化性能进行了比较。在所有使用的载体中,W / HZSM-5催化剂显示出最佳的活性和稳定性,最高的甲烷转化率为8.4%,相当于在973 K和1 atm时芳烃的选择性为97.54%。同时,在其他W负载的催化剂上,将近7%的甲烷被转化,从而使催化剂急剧失活。进行了进一步的研究,以研究W / HZSM-5催化剂的酸度作用。由于引入锂离子,催化剂的酸性性质发生了变化。具有锂含量的那些催化剂的催化性能,包括3W / HZSM-5(3)/ Li-HZSM-5(10),3W / Li-HZSM-5(12),3W / Li-HZSM-5(46),和3WLiZSM-5催化剂在1073 K和1个大气压下进行了测试。结果表明,在非氧化条件下,向ZSM-5催化剂中引入一定量的Li影响了甲烷脱氢芳构化的催化性能。在W / HZSM-5上,最高甲烷转化率为16%,但在320分钟内降低到8%。时间流逝。此外,相应的芳族选择性从93%迅速下降至56%。而在3W / Li-HZSM-5(10)催化剂上,母体HZSM-5的强酸位点占74%,甲烷转化率从18%略微降低到12%,对应于芳烃从91%降低。在320分钟后观察到的%至85%。时间流逝。但是,如果添加更多的Li,则催化剂的活性会降低,如3W / Li-HZSM-5(12),3W / Li-HZSM-5(46)和3W / Li- ZSM-5催化剂。还发现可以通过减少强酸位点的量来改善催化剂性能,但是对于非氧化甲烷脱氢芳构化来说,酸性位点,特别是布朗斯台德酸位点的大量减少是不利的。发现3W / Li-HZSM-5(10)催化剂是合适的催化剂,因为它具有最佳的布朗斯台德酸中心,因此可提供最大的甲烷转化率和对芳烃的选择性。这些结果表明,Li修饰的W / HZSM-5催化剂是双功能催化剂,其中HZSM-5载体的W活性位和布朗斯台德酸位都是良好催化性能的关键因素。

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