Related Experiment Video
Updated: Jan 11, 2026

Development of Heterogeneous Enantioselective Catalysts using Chiral Metal-Organic Frameworks MOFs
Published on: January 17, 2020
Adding Yttrium to SO4 2-/ZrO2 Catalysts To Improve the Synthesis Performance of Esters for Electrical Insulating Oils
Byeong Sub Kwak1, Eunyoung Kim1, Taehyun Jun1
1Korea Electric Power Research Institute, Korea Electric Power Corporation, 105 Munji-Ro, Yuseong-Gu, Daejeon 34056, Republic of Korea.
Abstract:
Synthetic ester insulating oils exhibit excellent electrical insulating properties, biodegradability, and oxidative stability, rendering them attractive alternatives to conventional mineral- and vegetable-based insulating oils. Typically, synthetic ester insulating oils are prepared via esterification reactions between fatty acids and alcohols using various catalysts. In particular, the solid acid catalyst SO4 2-/ZrO2 is commonly used in this process. In this study, a small amount of yttrium was substituted into a ZrO2-catalyst support to form oxygen vacancy structures in the framework. This modification was intended to alter the interactions with SO4 2- ions and improve both the distribution of acid sites and catalytic activity for esterification. Using the sol-gel method, the synthesized catalyst was calcined at 600 °C for 3 h to promote crystallization. The structural and surface properties of the catalyst, as well as its chemical states, thermal stability, electronic structure, and acidity, were investigated using various advanced characterization techniques, including XRD, XPS, and NH3-TPD. The catalytic performance was evaluated through the esterification of fatty acids (decanoic acid (capric acid) and 2-ethylhexanoic acid) and alcohol at 220 °C. Among the fabricated catalysts, the SO4 2-/ZrO2(0.98)-Y2O3(0.02) catalyst demonstrated the highest conversion of 95.5%. Thus, our developed catalyst could contribute to improving the efficiency of synthetic ester production processes for insulating oil applications.
More Related Videos
Related Concept Videos
Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis
During hydrolysis, the ester is first activated towards nucleophilic attack through the protonation of the carboxyl oxygen atom by the acid catalyst. The protonation makes the ester carbonyl carbon more electrophilic. In the next step, water acts as a nucleophile and adds to the...
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Overview
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Mechanism
Esters to Carboxylic Acids: Saponification
The reaction requires a base in stoichiometric amounts, which participates in the reaction and is not regenerated later. So, the base acts as a...
Sharpless Epoxidation
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide

