Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Oxidation of Phenols to Quinones01:17

Oxidation of Phenols to Quinones

3.2K
In the presence of oxidizing agents, phenols are oxidized to quinones. Quinones can be easily reduced back to phenols using mild reducing agents. The electron-donating hydroxyl group enhances the reactivity of the aromatic ring, enabling oxidation of the ring even in the absence of an α hydrogen.
o-hydroxy phenols are oxidized to o-quinones and p-hydroxy phenols to p-quinones. Such redox reactions involve the transfer of two electrons and two protons. The reversible redox...
3.2K
Hydrolysis of Chlorobenzene to Phenol: Dow Process01:10

Hydrolysis of Chlorobenzene to Phenol: Dow Process

2.9K
Simple aryl halides do not react with nucleophiles under normal conditions. However, the reaction can proceed under drastic conditions involving high temperatures and high pressure to give the substituted products. For example, chlorobenzene is converted to phenol using aqueous sodium hydroxide at 350 °C under high pressure by the Dow process. The reaction follows an elimination-addition mechanism involving a benzyne intermediate. Here, the chloride ion is...
2.9K
Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis01:13

Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis

3.0K
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...
3.0K
Preparation of Diols and Pinacol Rearrangement01:57

Preparation of Diols and Pinacol Rearrangement

3.5K
Compounds bearing two hydroxyl groups are known as diols. When the hydroxyl groups are located on adjacent carbon atoms, the diols are called vicinal diols or glycols. Under acidic conditions, vicinal diols undergo a specific reaction called pinacol rearrangement.
The reaction begins with transferring a proton from the acid catalyst to one of the hydroxyl groups, producing an oxonium ion.
3.5K
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Overview01:20

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

18.3K
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.
18.3K
Vicinal Diols via Reductive Coupling of Aldehydes or Ketones: Pinacol Coupling Overview01:27

Vicinal Diols via Reductive Coupling of Aldehydes or Ketones: Pinacol Coupling Overview

1.8K
Wilhelm Rudolph Fittig discovered the pinacol coupling reaction in 1859. It is a radical dimerization reaction and involves the reductive coupling of aldehydes or ketones in the presence of hydrocarbon solvent to yield vicinal diols.
1.8K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Application of a cancer pain belief modification program for patients with oral cancer in China: a mixed methods study.

Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer·2026
Same author

Rethinking the detail-preserved completion of complex tubular structures based on point cloud: A dataset and a benchmark.

Medical image analysis·2026
Same author

Hard Lewis Base-Driven Crystallization Control for Efficient All-Perovskite Tandem Solar Cells.

Advanced materials (Deerfield Beach, Fla.)·2026
Same author

The LEF1-LAG3 axis regulates CD4<sup>+</sup> T cell function during Plasmodium yoelii NSM infection.

Parasites & vectors·2026
Same author

Designing Mentorship for Constrained Systems: Reframing Workforce Development in Rural and Remote Health.

International journal of environmental research and public health·2026
Same author

A polymer-coated nanowire sponge-based contact electrocatalytic system for simultaneous disinfection and removal of multiple micropollutants.

Nature communications·2026

Related Experiment Video

Updated: Jul 24, 2025

Extraction of Lignin with High &#946;-O-4 Content by Mild Ethanol Extraction and Its Effect on the Depolymerization Yield
10:18

Extraction of Lignin with High β-O-4 Content by Mild Ethanol Extraction and Its Effect on the Depolymerization Yield

Published on: January 7, 2019

20.7K

Selective Depolymerization of Lignin Towards Isolated Phenolic Acids Under Mild Conditions.

Wenbo Peng1, Hanxi Bao2, Yigui Wang3

  • 1School of Chemical & Biomolecular Engineering Renewable Bioproduct Institute, Georgia Institute of Technology, Atlanta, GA 30318, USA.

Chemsuschem
|July 7, 2023
PubMed
Summary

Researchers developed a novel graphene oxide-urea hydrogen peroxide (GO-UHP) catalyst for efficient lignin conversion into valuable phenolic acids (PA) under mild conditions. This method achieves high yields, offering a sustainable route for biomass valorization and biofuel production.

Keywords:
density functional theorygraphene oxidelignin valorizationphenolic acidsselective oxidation

More Related Videos

Designed for Molecular Recycling: A Lignin-Derived Semi-aromatic Biobased Polymer
10:22

Designed for Molecular Recycling: A Lignin-Derived Semi-aromatic Biobased Polymer

Published on: November 30, 2020

3.5K
Ultrafast Lignin Extraction from Unusual Mediterranean Lignocellulosic Residues
09:22

Ultrafast Lignin Extraction from Unusual Mediterranean Lignocellulosic Residues

Published on: March 9, 2021

6.7K

Related Experiment Videos

Last Updated: Jul 24, 2025

Extraction of Lignin with High &#946;-O-4 Content by Mild Ethanol Extraction and Its Effect on the Depolymerization Yield
10:18

Extraction of Lignin with High β-O-4 Content by Mild Ethanol Extraction and Its Effect on the Depolymerization Yield

Published on: January 7, 2019

20.7K
Designed for Molecular Recycling: A Lignin-Derived Semi-aromatic Biobased Polymer
10:22

Designed for Molecular Recycling: A Lignin-Derived Semi-aromatic Biobased Polymer

Published on: November 30, 2020

3.5K
Ultrafast Lignin Extraction from Unusual Mediterranean Lignocellulosic Residues
09:22

Ultrafast Lignin Extraction from Unusual Mediterranean Lignocellulosic Residues

Published on: March 9, 2021

6.7K

Area of Science:

  • Biomass Valorization
  • Catalysis
  • Green Chemistry

Background:

  • Lignin's complex structure hinders selective conversion to high-value biochemicals like phenolic acids (PA).
  • Current PA isolation from lignin is inefficient (<5 wt.%) and requires harsh conditions.

Purpose of the Study:

  • To develop an effective and mild catalytic route for selective lignin conversion into isolated phenolic acids.
  • To achieve high yields of PA from lignin, maximizing biomass utilization.

Main Methods:

  • Utilized a low-cost graphene oxide-urea hydrogen peroxide (GO-UHP) catalyst for lignin depolymerization.
  • Employed pre-acetylation of lignin followed by catalytic conversion under mild conditions (<120°C).
  • Investigated reaction mechanisms involving Cα activation and oxidative transformation of intermediates.

Main Results:

  • Achieved high yields of isolated PA (up to 20 wt.% of lignin) from sweet sorghum and poplar lignin.
  • Demonstrated high lignin conversion (up to 95%) with remaining oils suitable for aviation fuel.
  • Successfully avoided undesired side reactions like the Dakin reaction through strategic pre-acetylation.

Conclusions:

  • The GO-UHP catalytic system provides an efficient and mild pathway for selective lignin side-chain cleavage.
  • This approach enhances the sustainable utilization of lignin for producing valuable biochemicals and biofuels.
  • Opens new avenues for lignin valorization under environmentally friendly conditions.