Related Experiment Video
Updated: Jul 6, 2025

Two-way Valorization of Blast Furnace Slag: Synthesis of Precipitated Calcium Carbonate and Zeolitic Heavy Metal Adsorbent
Published on: February 21, 2017
Synthesis and Optimization of Glycerol Carbonate from Crude Glycerol Using Sodium Carbonate (Na2CO3) as a
Bantita Saelim1, Thanate Ratanawilai2, Sukritthira Ratanawilai1
1Department of Chemical Engineering, Faculty of Engineering, Prince of Songkla University, Hat Yai, Songkhla 90110, Thailand.
Abstract:
The essential need for sustainable energy sources to replace fossil fuels has fueled interest in renewable energy and biorefinery processes. Biodiesel production generates a considerable amount of crude glycerol (CG), which poses a challenge for the industry. This study aims to address this challenge by purifying CG through acidification. The acidification process successfully purified crude glycerol (PCG), resulting in a purity of 98.4 wt %. Subsequently, synthesizing glycerol carbonate (GC) from PCG and dimethyl carbonate (DMC) was undertaken by using heterogeneous catalysts. Sodium carbonate (Na2CO3) emerges as the most promising catalyst, considering its suitability in the presence of impurities such as 0.72 wt % of water and 0.57 wt % of matter organic nonglycerol (MONG) in PCG. The optimum catalyst dosage of Na2CO3 was determined as 2.1% mol of PCG. The experiments were carried out using a central composite design (CCD) methodology. By employing the response surface method (RSM), the optimal reaction conditions were determined to be a PCG/DMC molar ratio of 1:2.37 and a reaction time of 1.83 h. Under these conditions, an observed GC yield of 72.13% and PCG conversion of 78.39% were achieved. Despite the purification process, PCG still contains residual water, making Na2CO3 a suitable catalyst capable of tolerating a water content up to 3 wt %. This study not only enhances the effective utilization of CG within the biodiesel industry but also offers valuable insights for further exploration of sustainable chemical processes in future research.
Related Concept Videos
Alkylation of β-Diester Enolates: Malonic Ester Synthesis
Ketones with Nonenolizable Aromatic Aldehydes: Claisen–Schmidt Condensation
As the self-condensation of ketones is generally not favored in basic conditions, the self-condensed products do not form in the reaction between ketones and benzaldehyde. The general reaction of Claisen–Schmidt...
Loss of Carboxy Group as CO2: Decarboxylation of Malonic Acid Derivatives
Preparation of Alcohols via Addition Reactions
The acid-catalyzed addition of water to the double bond of alkenes is a large-scale industrial method used to synthesize low-molecular-weight alcohols. An acidic atmosphere is required to allow the hydrogen in the water molecule to act as an electrophile and attack the double bond in an alkene. The addition of a proton to the double bond creates a carbocation intermediate. The proton preferentially bonds to the less substituted end of the double bond to create a more stable carbocation...
Aldol Condensation with β-Diesters: Knoevenagel Condensation
Preparation of Aldehydes and Ketones from Carboxylic Acid Derivatives
Carboxylic acid derivatives like acid chlorides and esters are more easily reducible than the corresponding acids. The derivatives reduce in the presence of mild reducing agents to give aldehydes. Aldehydes can also be prepared by Rosenmund reduction, that is, the reduction of...

