Alwadai Norah, Abahussain Abdulaziz A M, Vadodariya Dharmesh M, Banabdwin Khaled M, Fakeeha Anis Hamza, Abu-Dahrieh Jehad K, Almuqati Naif S, Alghamdi Ahmad M, Kumar Rawesh, Al-Fatesh Ahmed S
Department of Physics, College of Science, Princess Nourah bint Abdulrahman University P. O. Box 84428 Riyadh 11671 Saudi Arabia.
Chemical Engineering Department, College of Engineering, King Saud University Riyadh 11421 Saudi Arabia
RSC Adv. 2024 Aug 13;14(35):25273-25288. doi: 10.1039/d4ra04781h. eCollection 2024 Aug 12.
Achieving remarkable H yield with significantly high H/CO over Ni-based catalysts through partial oxidation of methane (POM) is a realistic approach to depleting the concentration of CH and using H and CO as synthetic feedstock. This study examined Ni catalysts on titania-zirconia for methane conversion POM at 600 °C and atmospheric pressure. The addition of strontium to the catalyst was explored to improve its performance. Catalysts were characterized by X-ray diffraction, Raman-infrared-UV-vis spectroscopy, and Temperature-programmed reduction-desorption techniques (TPR, TPD). 2.5 wt% Sr addition induced the formation of the highest concentration of extreme basic sites. Interestingly, over the unpromoted catalyst, active sites are majorly generated by hardly reducible NiO species whereas upon 2.5 wt% promoted Sr promotional addition, most of active sites are derived by easily reducible NiO species. 45% CH conversion and 47% H yield with H/CO = 3.5 were achieved over 2.5 wt% Sr promoted 5Ni/30TiO + ZrO catalyst. These results provide insight into the role of basic sites in enhancing activity through switching indirect pathways over direct pathways for POM. Further process optimization was carried out in the range of 10 000-22 000 SV, 0.35-0.75 O/CH and 600-800 °C reaction temperature over 5Ni2.5Sr/30TiO + ZrO by using central composite design under response surface methodology. The optimum activity as high as ∼88% CH conversion, 86-87% yield of H, and 2.92H/CO were predicted and experimentally validated at 800 °C reaction temperature, 0.35O/CH ratio, and 10 000 space velocity.
通过甲烷部分氧化(POM)在镍基催化剂上以显著高的H/CO比实现显著的H产率,是降低CH浓度并将H和CO用作合成原料的一种现实方法。本研究考察了负载于二氧化钛-氧化锆上的镍催化剂在600℃和常压下用于甲烷转化POM的性能。研究了添加锶对催化剂性能的影响。采用X射线衍射、拉曼-红外-紫外-可见光谱以及程序升温还原-脱附技术(TPR、TPD)对催化剂进行了表征。添加2.5 wt%的Sr诱导形成了最高浓度的极端碱性位点。有趣的是,在未促进的催化剂上,活性位点主要由难还原的NiO物种产生,而在添加2.5 wt%促进剂Sr后,大多数活性位点由易还原的NiO物种产生。在2.5 wt% Sr促进的5Ni/30TiO + ZrO催化剂上实现了45%的CH转化率和47%的H产率,H/CO = 3.5。这些结果深入了解了碱性位点在通过将POM的间接途径切换为直接途径来提高活性方面的作用。通过响应面法下的中心复合设计,在10000 - 22000 SV、0.35 - 0.75 O/CH和600 - 800℃反应温度范围内,对5Ni2.5Sr/30TiO + ZrO进行了进一步的工艺优化。预测在800℃反应温度、0.35O/CH比和10000空速下,最佳活性高达约88%的CH转化率、86 - 87%的H产率和2.92H/CO,并通过实验验证。