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

Olefin Metathesis Polymerization: Overview01:13

Olefin Metathesis Polymerization: Overview

2.1K
Recently, the development of olefin metathesis polymerization advanced the field of polymer synthesis. Simply put, the reorganization of substituents on their double bonds between two olefins in the presence of a catalyst is known as the olefin metathesis reaction. The use of metathesis reaction for polymer synthesis is called olefin metathesis polymerization.
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists...
2.1K
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)00:53

Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)

1.9K
Acyclic diene metathesis polymerization or ADMET polymerization involves cross-metathesis of terminal dienes, such as 1,8-nonadiene, to give linear unsaturated polymer and ethylene. As ADMET is a reversible process, the formed ethylene gas must be removed from the reaction mixture to complete the polymerization process.
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
1.9K
Free-Radical Chain Reaction and Polymerization of Alkenes02:35

Free-Radical Chain Reaction and Polymerization of Alkenes

7.8K
The conversion of alkenes to macromolecules called polymers is a reaction of high commercial importance. The structure of the polymer is defined by a repeating unit, while the terminal groups are considered insignificant. The average degree of polymerization represents the number of repeating units in the polymer molecule and is denoted by the subscript n.
7.8K
Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)01:16

Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)

2.6K
Ring-opening metathesis polymerization or ROMP involves strained cycloalkenes as starting materials. The mechanism of ROMP proceeds by reacting cycloalkene with Grubbs catalyst to give metallacyclobutane intermediate which undergoes a ring-opening reaction to form new carbene. The new carbene reacts with another molecule of cycloalkene. Repetition of these steps leads to the formation of an unsaturated open-chain polymer product. All these steps are reversible, however, relieving the ring...
2.6K
Catalysis02:50

Catalysis

26.9K
The presence of a catalyst affects the rate of a chemical reaction. A catalyst is a substance that can increase the reaction rate without being consumed during the process. A basic comprehension of a catalysts’ role during chemical reactions can be understood from the concept of reaction mechanisms and energy diagrams.
26.9K
Ziegler–Natta Chain-Growth Polymerization: Overview01:17

Ziegler–Natta Chain-Growth Polymerization: Overview

3.3K
Ziegler–Natta polymerization is another form of addition or chain‐growth polymerization used for synthesizing linear polymers over branched polymers. The catalyst used for polymerization is the Ziegler–Natta catalyst, named after Karl Ziegler and Giulio Natta, who developed it in 1953. This catalyst is an organometallic complex of titanium tetrachloride and triethyl aluminum, with the active form of the catalyst being an alkyl titanium compound. Using the Ziegler–Natta...
3.3K

You might also read

Related Articles

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

Sort by
Same authorSame journal

Engineering and Application of a Thermostable MHETase for PET Depolymerization.

ACS sustainable chemistry & engineering·2026
Same author

Lignin to adipic acid in a high-yield chemical and biological redox process.

Nature·2026
Same author

Effects of Polymer Morphology on Solvent and Catalyst Accessibility during Polyethylene and Polystyrene Autoxidation.

JACS Au·2026
Same author

Synthesis and Dilute Solution Properties of Precision Short-Chain Branched Poly(ethylene) Block Copolymers Derived from Ring-Opening Metathesis Polymerization.

Macromolecules·2026
Same author

Alkylidene functionalization produces highly recyclable and scalable polyhydroxyalkanoates.

Science (New York, N.Y.)·2026
Same author

Catalytic Autoxidation for Depolymerization of Multilayer Plastic Films.

ChemSusChem·2026
Same journal

Enhancing (Super)hydrophobicity of Natural Fibers: An Overview of Methodologies and Their Sustainability Assessment.

ACS sustainable chemistry & engineering·2026
Same journal

Delamination of Multilayer Plastic Films to Recover Polyethylene with Favorable Mechanical Properties.

ACS sustainable chemistry & engineering·2026
Same journal

Pd-Modified Metal Organic Frameworks Synthesized via Mechanochemical Extrusion: Versatile Materials for Suzuki-Miyaura Cross-Coupling and Electrochemical Hydrogen Evolution Reaction.

ACS sustainable chemistry & engineering·2026
Same journal

A Unified Analytical Method Greenness Score (<i>uAMGS</i>) Quantifies How Microscopic Imaging Is Greener Than Conventional Liquid Chromatography.

ACS sustainable chemistry & engineering·2026
Same journal

Greenhouse Gas Emissions and Cost Trade-Offs of Renewable Feedstocks for Methyl Methacrylate Production.

ACS sustainable chemistry & engineering·2026
See all related articles

Related Experiment Video

Updated: Jun 27, 2025

Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers
08:12

Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers

Published on: December 16, 2022

3.3K

Tandem Heterogeneous Catalysis for Polyethylene Depolymerization via an Olefin-Intermediate Process.

Lucas D Ellis1, Sara V Orski2, Grace A Kenlaw2

  • 1Renewable Resources and Enabling Sciences Center, National Renewable Energy Laboratory, Golden, Colorado 80401, United States.

ACS Sustainable Chemistry & Engineering
|May 6, 2024
PubMed
Summary
This summary is machine-generated.

Researchers developed a heterogeneous catalyst system for plastic recycling. This system efficiently depolymerizes polyethylene (PE) into valuable alkane products, offering a sustainable alternative to traditional methods.

More Related Videos

Ethylene Polymerizations Using Parallel Pressure Reactors and a Kinetic Analysis of Chain Transfer Polymerization
07:28

Ethylene Polymerizations Using Parallel Pressure Reactors and a Kinetic Analysis of Chain Transfer Polymerization

Published on: November 27, 2015

13.2K
Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-phosphinetriyltripiperidine]}palladium Under Mild Reaction Conditions
11:44

Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-phosphinetriyltripiperidine]}palladium Under Mild Reaction Conditions

Published on: March 20, 2014

25.4K

Related Experiment Videos

Last Updated: Jun 27, 2025

Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers
08:12

Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers

Published on: December 16, 2022

3.3K
Ethylene Polymerizations Using Parallel Pressure Reactors and a Kinetic Analysis of Chain Transfer Polymerization
07:28

Ethylene Polymerizations Using Parallel Pressure Reactors and a Kinetic Analysis of Chain Transfer Polymerization

Published on: November 27, 2015

13.2K
Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-phosphinetriyltripiperidine]}palladium Under Mild Reaction Conditions
11:44

Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-phosphinetriyltripiperidine]}palladium Under Mild Reaction Conditions

Published on: March 20, 2014

25.4K

Area of Science:

  • Catalysis
  • Materials Science
  • Polymer Chemistry

Background:

  • Growing plastic waste necessitates advanced chemical recycling solutions.
  • Previous work utilized homogeneous catalysts for polyethylene (PE) depolymerization.
  • Homogeneous catalysts present challenges in separation and reusability.

Purpose of the Study:

  • To develop a fully heterogeneous catalyst system for PE depolymerization.
  • To improve upon existing homogeneous catalytic approaches.
  • To enable selective and versatile polyolefin recycling.

Main Methods:

  • A physical mixture of SnPt/γ-Al2O3 and Re2O7/γ-Al2O3 was employed as a heterogeneous catalyst.
  • The catalyst system was tested on a model C20 alkane (n-eicosane) and a linear PE substrate.
  • Reactions were conducted in n-pentane solvent at 200 °C for 15 hours.

Main Results:

  • The heterogeneous catalyst successfully produced linear alkane products from both n-eicosane and PE.
  • A significant molecular weight reduction of 73% was achieved for the PE substrate.
  • The process demonstrated the effectiveness of tandem dehydrogenation and olefin cross metathesis.

Conclusions:

  • Heterogeneous catalysts offer a viable and potentially more sustainable route for polyolefin chemical recycling.
  • Olefin-intermediate processes provide a selective and versatile method for plastic depolymerization.
  • This approach enables polyolefin breakdown at lower temperatures and shorter times compared to pyrolysis.