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

Types of Step-Growth Polymers: Polyesters01:20

Types of Step-Growth Polymers: Polyesters

2.3K
The introduction of polyesters has brought major development to the textile industry. The wrinkle-free behavior of polyester blends has eliminated the need for starching and ironing clothes.
Polyesters are commonly prepared from terephthalic acid and ethylene glycol; the crude product is known as poly(ethylene terephthalate) or PET. However, polyesters are synthesized industrially by transesterification of dimethyl terephthalate with ethylene glycol at 150 °C. The two reactants and the...
2.3K
Olefin Metathesis Polymerization: Overview01:13

Olefin Metathesis Polymerization: Overview

2.2K
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...
2.2K
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)00:53

Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)

2.0K
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...
2.0K
Free-Radical Chain Reaction and Polymerization of Alkenes02:35

Free-Radical Chain Reaction and Polymerization of Alkenes

8.0K
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.
8.0K
Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

3.6K
Step-growth or condensation polymerization is a stepwise reaction of bi or multifunctional monomers to form long-chain polymers. As all the monomers are reactive, most of the monomers are consumed at the early stages of the reaction to form small chains of reactive oligomers, which then combine to form long polymer chains in the late stages. Hence, the reaction has to proceed for a long time to achieve high molecular weight polymers.
Many natural and synthetic polymers are produced by...
3.6K
Ziegler–Natta Chain-Growth Polymerization: Overview01:17

Ziegler–Natta Chain-Growth Polymerization: Overview

3.4K
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...
3.4K

You might also read

Related Articles

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

Sort by
Same author

Functional and Network PHAs via Stereoselective Polymerization and Tailored Post-Transformation.

Angewandte Chemie (International ed. in English)·2026
Same author

Positional Isomer of P3HB by Stereoselective Polymerization of Racemic α-Methyl-β-propiolactone Delivers Polyethylene-like Properties.

Journal of the American Chemical Society·2026
Same author

Counterintuitive Compatibilization of Poly(δ-valerolactone) and Poly(l‑lactic acid) by Statistical Copolymers toward Compostable and Recyclable Packaging.

ACS sustainable chemistry & engineering·2026
Same author

Alkylidene functionalization produces highly recyclable and scalable polyhydroxyalkanoates.

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

Two-Dimensional Hybrid Framework Based on Weakley-Type POM as a Heterogeneous Catalyst for Glycolysis of PET and Various Polyesters.

Inorganic chemistry·2026
Same author

A Circular and Tacticity-Independent Crystalline Mono-Substituted Nylon-6 Platform: Unexpected Large Positional Effects on Crystallizability and Performance.

Angewandte Chemie (International ed. in English)·2026

Related Experiment Video

Updated: Aug 1, 2025

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

Dual Recycling of Depolymerization Catalyst and Biodegradable Polyester that Markedly Outperforms Polyolefins.

Xin-Lei Li1, Ryan W Clarke2, Hai-Yan An1

  • 1State Key Laboratory of Fine Chemicals, Department of Chemistry, School of Chemical Engineering, Dalian University of Technology, Dalian, 116024, China.

Angewandte Chemie (International Ed. in English)
|April 27, 2023
PubMed
Summary

This study presents a novel dual catalyst/polymer system for sustainable recycling. Inorganic phosphomolybdic acid enables efficient depolymerization of high-performance poly(δ-valerolactone) into its monomer at low temperatures, closing the circular economy loop.

Keywords:
Inorganic PolyacidMetal-CatalystRecyclable PolyesterRing-Opening PolymerizationThermoplastic

More Related Videos

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

3.4K
The Effect of Construction and Demolition Waste Plastic Fractions on Wood-Polymer Composite Properties
09:06

The Effect of Construction and Demolition Waste Plastic Fractions on Wood-Polymer Composite Properties

Published on: June 7, 2020

8.1K

Related Experiment Videos

Last Updated: Aug 1, 2025

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
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

3.4K
The Effect of Construction and Demolition Waste Plastic Fractions on Wood-Polymer Composite Properties
09:06

The Effect of Construction and Demolition Waste Plastic Fractions on Wood-Polymer Composite Properties

Published on: June 7, 2020

8.1K

Area of Science:

  • Polymer Chemistry
  • Materials Science
  • Sustainable Chemistry

Background:

  • Chemically recyclable polymers are gaining attention for sustainability.
  • Developing recyclable catalysts and high-performance polymers simultaneously presents a challenge.
  • Circular economy principles necessitate efficient polymer and catalyst recovery.

Purpose of the Study:

  • To introduce a dual catalyst/polymer recycling system.
  • To achieve selective depolymerization of high-performance biodegradable polymers.
  • To demonstrate the recovery and reuse of both polymer and catalyst.

Main Methods:

  • Utilized recyclable inorganic phosphomolybdic acid as a catalyst.
  • Catalyzed selective depolymerization of poly(δ-valerolactone) in bulk phase.
  • Investigated mechanical properties and recyclability of the polymer and catalyst.

Main Results:

  • Achieved selective depolymerization of poly(δ-valerolactone) at 100°C with quantitative monomer yield.
  • The resulting polymer exhibited outstanding mechanical performance (tensile strength ≈66.6 MPa, fracture strain ≈904%, toughness ≈308 MJ m⁻³).
  • Recovered monomer was repolymerized to the original polymer, and the catalyst retained activity after repeated use.

Conclusions:

  • The developed system enables efficient, low-temperature, and selective depolymerization of high-performance polymers.
  • This approach successfully closes the circular loop for both the polymer and the catalyst.
  • The recyclable catalyst and polymer system offers a sustainable alternative to conventional materials.