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Related Concept Videos

Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis01:13

Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis

Hydrolysis of esters under acidic conditions proceeds through a nucleophilic acyl substitution. In the presence of excess water, the reaction proceeds in a reversible manner, forming carboxylic acids and alcohols.
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 Overview01:20

Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Overview

The Fischer esterification reaction was developed by the German chemist Emil Fischer in 1895. It is a condensation reaction between carboxylic acids and alcohols in an acidic medium to give esters and water.
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Mechanism01:13

Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Mechanism

Carboxylic acids react with alcohols to yield esters via an acid-catalyzed condensation reaction called Fischer esterification. This is a nucleophilic acyl substitution reaction that proceeds via a tetrahedral intermediate, where a water molecule is eliminated as the leaving group.
Esters to Carboxylic Acids: Saponification01:25

Esters to Carboxylic Acids: Saponification

Esters can be hydrolyzed to carboxylic acids under acidic or basic conditions. Base-promoted hydrolysis of esters is a nucleophilic acyl substitution reaction in which esters react with an aqueous base, followed by an acid to give carboxylic acids. This reaction is also known as saponification because it forms the basis for making soaps from fats.
The reaction requires a base in stoichiometric amounts, which participates in the reaction and is not regenerated later. So, the base acts as a...
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation02:17

Reduction of Alkenes: Asymmetric Catalytic Hydrogenation

Catalytic hydrogenation of alkenes is a transition-metal catalyzed reduction of the double bond using molecular hydrogen to give alkanes. The mode of hydrogen addition follows syn stereochemistry.
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Electrophilic Aromatic Substitution: Sulfonation of Benzene01:22

Electrophilic Aromatic Substitution: Sulfonation of Benzene

Sulfonation of benzene is a reaction wherein benzene is treated with fuming sulfuric acid at room temperature to produce benzenesulfonic acid. Fuming sulfuric acid is a mixture of sulfur trioxide and concentrated sulfuric acid.

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Related Experiment Video

Updated: Jun 22, 2026

Tuning the Acidity of Pt/ CNTs Catalysts for Hydrodeoxygenation of Diphenyl Ether
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Tuning the Acidity of Pt/ CNTs Catalysts for Hydrodeoxygenation of Diphenyl Ether

Published on: August 17, 2019

Esterification of acidic oils over a versatile amorphous solid catalyst.

Federica Zaccheria1, Simona Brini, Rinaldo Psaro

  • 1ISTM-CNR, Milano, Italy.

Chemsuschem
|May 30, 2009
PubMed
Summary

A novel amorphous silicon dioxide-zirconium dioxide catalyst efficiently esterifies free fatty acids and transesterifies triglycerides in vegetable oils. This bifunctional catalyst is ideal for low-waste oil deacidification and high-acid feedstock biodiesel production.

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Efficient Synthesis of Polyfunctionalized Benzenes in Water via Persulfate-promoted Benzannulation of α,β-Unsaturated Compounds and Alkynes
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Published on: December 16, 2019

Area of Science:

  • Catalysis
  • Materials Science
  • Green Chemistry

Background:

  • Vegetable oils often contain high free fatty acids (FFAs), complicating downstream processing.
  • Traditional methods for FFA removal or conversion can be inefficient or generate waste.
  • Biodiesel production from high-acid feedstocks requires effective pretreatment or integrated processes.

Purpose of the Study:

  • To evaluate the efficacy of an amorphous SiO(2)-ZrO(2) catalyst for simultaneous FFA esterification and triglyceride transesterification.
  • To assess the catalyst's potential for low-waste deacidification and one-pot biodiesel production.

Main Methods:

  • Synthesis of amorphous silicon dioxide-zirconium dioxide (SiO(2)-ZrO(2)) catalyst.
  • Testing the catalyst's activity in esterification of FFAs in vegetable oils.
  • Evaluating the catalyst's performance in transesterification of triglycerides.

Main Results:

  • The amorphous SiO(2)-ZrO(2) catalyst demonstrated high activity in esterifying FFAs.
  • The catalyst also effectively promoted the transesterification of triglycerides.
  • The bifunctional nature of the catalyst was confirmed.

Conclusions:

  • Amorphous SiO(2)-ZrO(2) is a promising catalyst for simultaneous FFA removal and biodiesel production.
  • The catalyst enables efficient, low-waste pretreatment of high-acid vegetable oils.
  • This catalyst supports a simplified, one-pot biodiesel production pathway.