Preparation of Ti-SO3H/ICG using microwave-assisted for esterification of palm fatty acid distillate to methyl ester

• Main Authors: Saimon, Nur Nazlina, Thavil, Suwew, Jusoh, Mazura, Ngadi, Norzita, Zakaria, Zaki Yamani
• Format: Article
• Language: English
• Published: Italian Association of Chemical Engineering - AIDIC 2018
• Subjects: TP Chemical technology
• Online Access: http://eprints.utm.my/id/eprint/84441/1/ZakiYamaniZakaria2018_PreparationofTi-SO3HICGUsingMicrowave-Assisted.pdf; http://eprints.utm.my/id/eprint/84441/; http://dx.doi.org/10.3303/CET1863078
• Institution: Universiti Teknologi Malaysia

The utilisation of low-cost yet valuable feedstock such as palm fatty acid distillate (PFAD) in the replacement of edible oils have a great potential in solving high-cost problem in biodiesel industries. Heterogeneous solid acid catalyst is the most proficient to esterify the feedstock containing high free fatty acid (FFA). Most of the prepared catalysts from the previous studies were produced using a conventional heating method which is basically time and energy consuming. The development of heterogeneous solid acid catalyst from sulfonated glucose and impregnation with titanium (Ti-SO3H/ICG) was prepared by using a microwave-assisted heating method with various heating time during the sulfonation process. The heating times taken were 3, 5, 7 and 9 min for acid treatment using H2SO4. The catalysts showed an outstanding result in reducing the catalyst separation problem and efficiently producing high percentage yield of biodiesel. The physical and chemical properties of the modified catalyst were analysed by using Temperature Programmed Desorption-Ammonia (TPD-NH3) and Brunauer-Emmett-Teller (BET). 7 min Ti-SO3/ICG showed the best performance catalyst due to its high surface area and acid site density, which were 78.37 m2/g and 15.16 mmol/g. The catalyst showed highest percentage yield and conversion of 98.92 % and 80.24 % at 70 °C, with a molar ratio of methanol to PFAD of 10: 1, 2.5 wt% of catalyst loading and 90 min of reaction time. A kinetic model was studied and the activation energy (Ea) obtained was 13.43 kJ/mol.K, the lowest value recorded as compared with the activation energy from previous studies in related field.