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Related Concept Videos

Polymer Classification: Crystallinity01:21

Polymer Classification: Crystallinity

Unlike ionic or small covalent molecules, polymers do not form crystalline solids due to the diffusion limitations of their long-chain structures. However, polymers contain microscopic crystalline domains separated by amorphous domains.
Crystalline domains are the regions where polymer chains are aligned in an orderly manner and held together in proximity by intermolecular forces. For example, chains in the crystalline domains of polyethylene and nylon are bound together by van der Waals...
Anionic Chain-Growth Polymerization: Overview01:20

Anionic Chain-Growth Polymerization: Overview

The polymerization process that involves carbanion as an intermediate is called anionic polymerization. It is also a type of addition or chain-growth polymerization. Anionic polymerization gets initiated by a strong nucleophile such as an organolithium or a Grignard reagent. The most commonly used initiator for anionic polymerization is butyl lithium. Monomers involved in anionic polymerization must possess a vinyl group bonded to one or two electron-withdrawing groups. For instance,...
Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

The cationic polymerization mechanism consists of three steps: initiation, propagation, and termination. In the initiation step of the polymerization process, the π bond of a monomer gets protonated by the Lewis acid catalyst, which is formed from boron trifluoride and water. The protonation of the π bond generates a carbocation stabilized by the electron‐donating group. In the propagation step, the π bond of the second monomer acts as a nucleophile and attacks the generated carbocation,...
Determination of Molar Masses of Polymers II01:27

Determination of Molar Masses of Polymers II

Polymer samples typically consist of macromolecular chains with a distribution of lengths, resulting in a range of molar masses rather than a single discrete value. Conventional descriptors such as the number-average molar mass and weight-average molar mass quantify this distribution but do not fully capture polymer behavior in solution..The viscosity-average molar mass provides a more realistic description of polymer behavior in solution because it accounts for the enhanced contribution of...
Anionic Chain-Growth Polymerization: Mechanism01:04

Anionic Chain-Growth Polymerization: Mechanism

The mechanism for anionic chain-growth polymerization involves initiation, propagation, and termination steps. In the initiation step, a nucleophilic anion, such as butyl lithium, initiates the polymerization process by attacking the π bond of the vinylic monomer. As a result, a carbanion, stabilized by the electron‐withdrawing group, is generated. The resulting carbanion acts as a Michael donor in the propagation step and attacks the second vinylic monomer, which acts as a Michael acceptor.
Polymers: Molecular Weight Distribution01:10

Polymers: Molecular Weight Distribution

For any given polymer, the weight average molecular weight (Mw) is higher than, if not equal to, the number average molecular weight (Mn). The only situation in which the weight average molecular weight and the number average molecular weight are equal is when a polymer consists only of chains with equal molecular weight. However, this never happens in a synthetic polymer, since it is difficult to control the polymerization process up to a molecular level with accuracy to a hundred percent.

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Related Experiment Video

Updated: Jun 17, 2026

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

Viscous solvent embrittles long-chain polymer networks.

Haeji Kim1, Diogo Costa1, Junsoo Kim1

  • 1Department of Mechanical Engineering, Northwestern University, Evanston, Illinois, 60208, USA. junsoo.kim@northwestern.edu.

Soft Matter
|June 16, 2026
PubMed
Summary

Toughness in polymer networks can decrease with higher solvent viscosity for long polymer chains. This occurs because increased viscosity limits tension transmission along chains at crack tips, reducing overall toughness.

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Area of Science:

  • Materials Science
  • Polymer Physics
  • Rheology

Background:

  • Polymer network toughness is often linked to viscoelastic energy dissipation.
  • A common design principle suggests higher viscosity enhances toughness.

Purpose of the Study:

  • To investigate the relationship between solvent viscosity and polymer network toughness.
  • To explore how polymer chain length influences this relationship.

Main Methods:

  • Preparation of polyacrylamide hydrogels with identical network structures.
  • Controlled variation of solvent viscosity using glycerol-water mixtures.
  • Mechanical testing including pure shear and trouser tests.

Main Results:

  • Toughness significantly decreases with increasing solvent viscosity for long polymer chains.
  • A master curve for toughness was observed, dependent on the product of viscosity and velocity.
  • Embrittlement is attributed to limited tension transmission along polymer chains at the crack tip.

Conclusions:

  • The inverse relationship between viscosity and toughness in long-chain polymer networks challenges conventional design principles.
  • Understanding tension transmission and viscous dissipation is crucial for predicting polymer network toughness.
  • This study provides new insights into the dynamics of fracture in viscoelastic materials.