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

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...
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...
Molecular Shape and Polarity03:37

Molecular Shape and Polarity

Dipole Moment of a Molecule

You might also read

Related Articles

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

Sort by
Same author

Ligand Exchange and Binding at the Surface of PbS Quantum Dots Quantified Using Multimodal Magnetic Resonance.

ACS nano·2025
Same author

Strong Variation of Micelle-Unimer Coexistence as a Function of Core Chain Mobility.

Macromolecules·2023
Same author

Activities of Family 18 Chitinases on Amorphous Regenerated Chitin Thin Films and Dissolved Chitin Oligosaccharides: Comparison with Family 19 Chitinases.

Biomacromolecules·2023
Same author

Chelator-mediated biomimetic degradation of cellulose and chitin.

International journal of biological macromolecules·2020
Same author

Adsorption of Xyloglucan onto Thin Films of Cellulose Nanocrystals and Amorphous Cellulose: Film Thickness Effects.

ACS omega·2019
Same author

Design of Nanofiber Coatings for Mitigation of Microbial Adhesion: Modeling and Application to Medical Catheters.

ACS applied materials & interfaces·2018

Related Experiment Video

Updated: Jul 6, 2026

Automated Lipid Bilayer Membrane Formation Using a Polydimethylsiloxane Thin Film
08:23

Automated Lipid Bilayer Membrane Formation Using a Polydimethylsiloxane Thin Film

Published on: July 10, 2016

Morphological evolution in dewetting polystyrene/polyhedral oligomeric silsesquioxane thin film bilayers.

Rituparna Paul1, Ufuk Karabiyik, Michael C Swift

  • 1Macromolecules and Interfaces Institute and the Department of Chemistry (0212), Virginia Polytechnic Institute and State University, Blacksburg, Virginia 24061, USA.

Langmuir : the ACS Journal of Surfaces and Colloids
|April 11, 2008
PubMed
Summary

This study explores the unique dewetting behaviors of polystyrene (PS) and trisilanolphenyl-POSS (TPP) thin films. Elevated temperatures cause cracking and dewetting, leading to TPP-encapsulated PS droplets.

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

Orientational Transition in a Liquid Crystal Triggered by the Thermodynamic Growth of Interfacial Wetting Sheets
06:26

Orientational Transition in a Liquid Crystal Triggered by the Thermodynamic Growth of Interfacial Wetting Sheets

Published on: May 15, 2017

Related Experiment Videos

Last Updated: Jul 6, 2026

Automated Lipid Bilayer Membrane Formation Using a Polydimethylsiloxane Thin Film
08:23

Automated Lipid Bilayer Membrane Formation Using a Polydimethylsiloxane Thin Film

Published on: July 10, 2016

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

Orientational Transition in a Liquid Crystal Triggered by the Thermodynamic Growth of Interfacial Wetting Sheets
06:26

Orientational Transition in a Liquid Crystal Triggered by the Thermodynamic Growth of Interfacial Wetting Sheets

Published on: May 15, 2017

Area of Science:

  • Materials Science
  • Polymer Science
  • Surface Science

Background:

  • Thin film dewetting is crucial for microelectronics and nanotechnology.
  • Understanding polymer/inorganic material interfaces is key for novel material design.

Purpose of the Study:

  • Investigate the morphological evolution of polystyrene (PS) and trisilanolphenyl-POSS (TPP) thin film bilayers during dewetting.
  • Analyze the effects of annealing temperature and time on dewetting morphologies.

Main Methods:

  • Optical Microscopy (OM) for real-time observation of crack formation and dewetting.
  • Atomic Force Microscopy (AFM) for high-resolution surface morphology analysis.
  • X-ray Photoelectron Spectroscopy (XPS) to determine layer dewetting progression.

Main Results:

  • Unique dewetting morphologies observed in PS/TPP bilayers at elevated temperatures, differing from polymer/polymer systems.
  • Cracking of the upper TPP layer initiated at ~130°C due to tensile stress.
  • At >160°C, dewetting of both TPP and PS layers occurred, exposing the substrate.
  • Cracks in TPP acted as nucleation sites for rapid dewetting and aggregation.
  • Complete dewetting of both layers and formation of TPP-encapsulated PS droplets observed after 90 min at 200°C.

Conclusions:

  • The PS/TPP bilayer system exhibits distinct dewetting behavior compared to traditional polymer bilayers.
  • Annealing temperature and time are critical parameters controlling the complex morphological evolution.
  • The study provides insights into the interfacial dynamics and phase separation during thin film dewetting.