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

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.
Molecular Weight of Step-Growth Polymers01:08

Molecular Weight of Step-Growth Polymers

Step growth polymerization involves bi or multifunctional monomers. Bifunctional monomers react to form linear step growth polymers, whereas multifunctional monomers react to form non-linear or branched polymers.
As the step-growth polymerization involves step-wise condensation of monomers, the molecular weight also builds up eventually. Consequently, high molecular weight polymers are obtained at the late stages of the polymerization, where 99% of monomers have been consumed.
The extent of the...
Characteristics and Nomenclature of Copolymers01:24

Characteristics and Nomenclature of Copolymers

Copolymers are the products obtained from the polymerization of multiple monomer species. So, in a polymer chain itself, there can be multiple repeating units that come from different monomers. The process of synthesizing a polymer from different monomer species is called copolymerization. When two monomers are involved, the polymer is known as a bipolymer. Polymers with three and four monomers are termed terpolymers and quaterpolymers, respectively. Figure 1 depicts the copolymerization of...
Determination of Molar Masses of Polymers I01:24

Determination of Molar Masses of Polymers I

Polymerization produces macromolecules with a range of chain lengths due to the random nature of molecular growth processes. As chains form and terminate at different stages, a single polymer sample contains molecules of varying sizes rather than a uniform structure. This variability is described using average molar masses and distribution-related parameters, which together provide a comprehensive understanding of polymer characteristics.The distribution of molar masses plays a critical role in...
Polymer Classification: Architecture01:14

Polymer Classification: Architecture

Polymers are classified as linear or branched on the basis of their chain architecture. The polymer chains in linear polymers have a long chain-like structure with minimal to no branching at all. Even if a polymer features large substituent groups on the monomer, which appear as branches to the skeleton, it is not considered a branched polymer. A branched polymer contains secondary polymer chains that arise from the main polymer chain. The branching occurs when the polymer growth shifts from...
Stress-Strain Diagram - Ductile Materials01:24

Stress-Strain Diagram - Ductile Materials

The stress-strain relationship in ductile materials such as structural steel or aluminium is intricate and progresses through several stages. When a specimen is loaded, it initially exhibits a linear length increase, depicted by a steep straight line on the stress-strain diagram. It indicates the material is elastically deforming and will return to its original shape once unloaded. However, when a critical stress value is reached, plastic deformation begins. This stage sees substantial...

You might also read

Related Articles

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

Sort by
Same author

Patterns and Stability of Coupled Multi-Stable Nonlinear Oscillators.

Chaos, solitons, and fractals·2023
Same author

Parallel replica dynamics simulations of reactions in shock compressed liquid benzene.

The Journal of chemical physics·2019
Same author

Describing nonequilibrium soft matter with mean field game theory.

The Journal of chemical physics·2019
Same author

Three-dimensional imaging of vortex structure in a ferroelectric nanoparticle driven by an electric field.

Nature communications·2017
Same author

Morphology dictated heterogeneous dynamics in two-dimensional aggregates.

Soft matter·2016
Same author

Machine learning bandgaps of double perovskites.

Scientific reports·2016

Related Experiment Video

Updated: Jul 13, 2026

Gyroid Nickel Nanostructures from Diblock Copolymer Supramolecules
08:40

Gyroid Nickel Nanostructures from Diblock Copolymer Supramolecules

Published on: April 28, 2014

Stress distributions in diblock copolymers.

P Maniadis1, T Lookman, E M Kober

  • 1Theoretical Division and Center for Nonlinear Studies, Los Alamos National Laboratory, Los Alamos, New Mexico 87545, USA.

Physical Review Letters
|August 7, 2007
PubMed
Summary

This study applies a generalized self-consistent field theory to AB diblock copolymers, revealing stress reductions at domain interfaces due to interfacial tension and chain connectivity effects in polymer melts.

More Related Videos

Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives
09:22

Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives

Published on: February 7, 2017

Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers
11:42

Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers

Published on: June 20, 2019

Related Experiment Videos

Last Updated: Jul 13, 2026

Gyroid Nickel Nanostructures from Diblock Copolymer Supramolecules
08:40

Gyroid Nickel Nanostructures from Diblock Copolymer Supramolecules

Published on: April 28, 2014

Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives
09:22

Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives

Published on: February 7, 2017

Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers
11:42

Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers

Published on: June 20, 2019

Area of Science:

  • Polymer Physics
  • Materials Science
  • Soft Matter Physics

Background:

  • Understanding the mechanical properties of polymer melts is crucial for material design.
  • Self-consistent field theory (SCFT) is a powerful tool for modeling polymer behavior.
  • Elastic stress and strain fields play a significant role in polymer morphology.

Purpose of the Study:

  • To apply a generalized SCFT, incorporating elastic stress and strain, to AB diblock copolymer melts.
  • To investigate the stress distributions within stable lamellar and hexagonal morphologies.
  • To elucidate the contributions of chain connectivity and interfacial tension to the overall stress profile.

Main Methods:

  • Development and application of a generalized self-consistent field theory.
  • Inclusion of elastic stress and strain fields within the theoretical framework.
  • Analysis of stress distributions under volume-conserving strain loadings for specific morphologies.

Main Results:

  • Local stress is reduced at the domain interface in AB diblock copolymer melts.
  • A slight enhancement of stress is observed in the immediate vicinity of the interface.
  • The overall stress profile results from a balance between chain connectivity (positive contribution) and interfacial tension (negative contribution).

Conclusions:

  • The generalized SCFT provides a robust framework for studying stress in polymer melts.
  • Interfacial tension significantly influences stress distribution, leading to localized reductions.
  • The interplay between chain connectivity and immiscibility governs the mechanical response of diblock copolymers.