首页 | 官方网站   微博 | 高级检索  
     


Synthesis of NaX and NaY Zeolites from Tunisian Kaolinite as Base Catalysts: An Investigation of Knoevenagel Condensation
Authors:Yosra Ghrib  Najoua Frini‐Srasra  Ezzeddine Srasra
Affiliation:1. Laboratoire de Physico‐chimie des Matériaux Minéraux et leurs Applications, Centre National des Recherches en Science des Matériaux, Borj Cedria Techno‐Park, BP 95‐2050 Hammam Lif, Tunis, Tunisia, Tel: (+216) 97565917;2. Fax: (+216)72272691;3. Institut National des Sciences Appliquées et de technologie, Université de Carthage;4. Département de Chimie, Faculté des Sciences de Tunis, 1060 Tunis, Tunisia, Université de Tunis El Manar
Abstract:The synthesis of Faujasite‐type zeolites with high purity has been successfully performed from Tunisian kaolinite and the effects of different crystallization parameters on the final products were widely investigated. The alkaline fusion of kaolinite followed by hydrothermal treatment lead to zeolite NaX synthesis whereas the classic hydrothermal transformation of metakaolinite produces NaY zeolite. The results show that an increase in the synthesis temperature and time has improved the crystallization process of the zeolite NaX whereas the SiO2/Al2O3 and the Na2O/SiO2 molar ratios were the key parameters to obtain a pure zeolite NaY. The highest specific surface areas obtained with the optimal crystallization conditions were 554 m2 g?1 and 592 m2 g?1 for respectively NaX and NaY zeolites. The basic properties of NaX and NaY zeolites were explored in the Knoevenagel condensation of benzaldehyde with ethyl cyanoacetate at 140 °C as a test reaction in the absence of solvent. The influence of ion exchange with cesium cation on the catalytic activity of prepared catalysts was also investigated. It was found that the NaX provided higher activity than that of NaY catalyst due to its lower Si/Al ratio whereas a cesium exchange conferred higher basicity to the prepared Na‐faujasite.
Keywords:Kaolinite  Zeolite  Faujasite  Base catalysts  Knoevenagel condensation
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司    京ICP备09084417号-23

京公网安备 11010802026262号