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Related Concept Videos

Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis01:13

Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis

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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...
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Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Overview01:20

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

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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.
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Esters to Carboxylic Acids: Saponification01:25

Esters to Carboxylic Acids: Saponification

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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...
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Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Mechanism01:13

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

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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.
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Alkylation of β-Ketoester Enolates: Acetoacetic Ester Synthesis01:07

Alkylation of β-Ketoester Enolates: Acetoacetic Ester Synthesis

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Acetoacetic ester synthesis is a method to obtain ketones from alkyl halides and β-keto esters. The reaction occurs in the presence of an alkoxide base that abstracts the acidic proton of the β-keto esters. The step results in an enolate ion which is doubly stabilized. The enolate then reacts with an alkyl halide via the SN2 process to produce an alkylated ester intermediate with a new C–C bond. The hydrolysis of the intermediate, followed by acidification, results in an...
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Alkylation of β-Diester Enolates: Malonic Ester Synthesis01:14

Alkylation of β-Diester Enolates: Malonic Ester Synthesis

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Malonic ester synthesis is a method to obtain α substituted carboxylic acids from ꞵ-diesters such as diethyl malonate and alkyl halides.
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Experimental Protocol for Biodiesel Production with Isolation of Alkenones as Coproducts from Commercial Isochrysis Algal Biomass
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A Highly Effective Biomass-Derived Solid Acid Catalyst for Biodiesel Synthesis Through Esterification.

Songdang Zhang1, Hu Pan2, Jinshu Huang1

  • 1State Key Laboratory Breeding Base of Green Pesticide and Agricultural Bioengineering, Key Laboratory of Green Pesticide and Agricultural Bioengineering, State-Local Joint Laboratory for Comprehensive Utilization of Biomass, Center for Research and Development of Fine Chemicals, Ministry of Education, Guizhou University, Guiyang, China.

Frontiers in Chemistry
|April 4, 2022
PubMed
Summary
This summary is machine-generated.

A novel biomass-based solid acid catalyst (SiO2@Cs-SO3H) efficiently converts oleic acid to biodiesel. Optimized conditions yielded 98.2% biodiesel, demonstrating a sustainable and reusable catalyst for green fuel production.

Keywords:
biodieselesterificationrenewable bio-based catalystresponse surface methodologysulfonation

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Area of Science:

  • Catalysis
  • Green Chemistry
  • Biomass Valorization

Background:

  • Biodiesel production from renewable biomass is crucial for sustainable energy.
  • Development of efficient and environmentally friendly catalysts is essential.
  • Biomass-derived catalysts offer a sustainable alternative to traditional catalysts.

Purpose of the Study:

  • To synthesize and characterize a highly active biomass-based solid acid catalyst (SiO2@Cs-SO3H) from chitosan.
  • To evaluate the catalytic performance of SiO2@Cs-SO3H for biodiesel production via esterification of oleic acid.
  • To optimize reaction conditions using Response Surface Methodology (RSM) for maximum biodiesel yield.

Main Methods:

  • Synthesis of SiO2@Cs-SO3H catalyst through sulfonation of chitosan.
  • Characterization of the catalyst's properties, including specific surface area and acidity.
  • Catalytic testing for esterification of oleic acid with methanol.
  • Optimization of reaction parameters (temperature, time, catalyst dosage, molar ratio) using RSM.

Main Results:

  • The synthesized SiO2@Cs-SO3H catalyst exhibited a large specific surface area (21.82 m²/g) and high acidity (3.47 mmol/g).
  • Optimized conditions (92°C, 4.1 h, 6.8 wt% catalyst, 31.4 methanol:OA ratio) achieved a biodiesel yield of 98.2%.
  • The catalyst demonstrated good reusability, maintaining 87.0% yield after five cycles.

Conclusions:

  • SiO2@Cs-SO3H is a highly efficient and reusable biomass-based solid acid catalyst for biodiesel production.
  • RSM is a reliable tool for optimizing reaction conditions and predicting outcomes.
  • This catalyst presents a sustainable pathway for the valorization of renewable biomass into high-quality biodiesel.