Anis Shaheen Fatima, Singaravel Gnanapragasam, Hashaikeh Raed
Department of Chemical Engineering, Khalifa University of Science and Technology, Masdar Institute P. O. Box 54224 Abu Dhabi United Arab Emirates
ADNOC Refining Research Centre, ADNOC Refining Abu Dhabi United Arab Emirates.
RSC Adv. 2018 May 8;8(30):16703-16715. doi: 10.1039/c8ra02662a. eCollection 2018 May 3.
In this work, a hydrocracking catalyst, nano zeolite Y-NiO-WO is reshaped into nanofibrous form. This novel composite fiber show good mechanical strength together with a uniform elemental distribution for both the acidic and hydrogenation components as confirmed through scanning transmission electron microscopy. The catalyst is tested for -heptane hydrocracking in a continuous flow fixed-bed reactor at reaction temperatures of 350 °C and 400 °C with a time on stream of 180 minutes. The fibers produced from nano zeolite-Y show superior performance with a total conversion of 98.81 wt% and 96.8 wt% at 350 °C and 400 °C respectively. In addition, a low amount of coke (0.40 wt% and 1.05 wt% at 350 °C and 400 °C respectively) was formed with the nano zeolite Y fibers. This superior performance is related to the enhanced accessibility due to the nanofiber shape where the non-woven mesh/network of catalytic fibers prevents the agglomeration of the nanoparticles. Agglomeration is a major cause of hindered accessibility of the reactants to the catalyst active sites. The zeolite particle size, and the shape of the fibrous catalyst, together with its mesoporous character (as confirmed through BET analysis) enhances diffusion and improves accessibility for the reactants to react on the catalytic active sites as proven by the high total -heptane conversions and high hexane and iso hexane selectivity for -heptane hydrocracking.
在这项工作中,一种加氢裂化催化剂,纳米沸石Y-NiO-WO被重塑成纳米纤维形式。通过扫描透射电子显微镜证实,这种新型复合纤维具有良好的机械强度,并且酸性和加氢组分的元素分布均匀。该催化剂在连续流动固定床反应器中于350℃和400℃的反应温度下进行庚烷加氢裂化测试,反应时间为180分钟。由纳米沸石Y制成的纤维表现出优异的性能,在350℃和400℃时的总转化率分别为98.81 wt%和96.8 wt%。此外,纳米沸石Y纤维形成的焦炭量较低(在350℃和400℃时分别为0.40 wt%和1.05 wt%)。这种优异的性能与纳米纤维形状导致的可及性增强有关,其中催化纤维的非织造网/网络可防止纳米颗粒的团聚。团聚是反应物难以到达催化剂活性位点的主要原因。沸石粒径、纤维状催化剂的形状及其介孔特性(通过BET分析证实)增强了扩散,并改善了反应物在催化活性位点上反应的可及性,这一点已由高的总庚烷转化率以及庚烷加氢裂化中高的己烷和异己烷选择性所证明。