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Related Concept Videos

Ion Exchange01:17

Ion Exchange

Ion exchange chromatography separates charged molecules from a solution by reversibly exchanging them with mobile, or 'active', ions associated with the oppositely charged stationary phase. This method can be used to separate ions, soften and deionize water, and purify solutions. The polymers comprising the ion-exchange column are high-molecular-weight and chemically stable polymers, crosslinked to be porous and essentially insoluble. They are also functionalized with either acidic or basic...
Preparation and Reactions of Sulfides02:26

Preparation and Reactions of Sulfides

Sulfides are the sulfur analog of ethers, just as thiols are the sulfur analog of alcohol. Like ethers, sulfides also consist of two hydrocarbon groups bonded to the central sulfur atom. Depending upon the type of groups present, sulfides can be symmetrical or asymmetrical. Symmetrical sulfides can be prepared via an SN2 reaction between 2 equivalents of an alkyl halide and one equivalent of sodium sulfide.
Phase Diagrams of Ternary Systems01:28

Phase Diagrams of Ternary Systems

Consider a ternary system, which is composed of three components: water (W), ethanoic acid (E), and trichloromethane (T). Here, Ethanoic acid (E) is fully miscible with both water (W) and trichloromethane (T), meaning it can mix entirely with either of them. However, water and trichloromethane have partial miscibility, meaning they can only mix to a certain extent, beyond which two separate phases will form.The phase diagram of a ternary system is represented as an equilateral triangle, where...
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,...
Intermolecular Forces03:13

Intermolecular Forces

Atoms and molecules interact through bonds (or forces): intramolecular and intermolecular. The forces are electrostatic as they arise from interactions (attractive or repulsive) between charged species (permanent, partial, or temporary charges) and exist with varying strengths between ions, polar, nonpolar, and neutral molecules. The different types of intermolecular forces are ion–dipole, dipole–dipole, hydrogen bonds, and dispersion; among these, dipole–dipole, hydrogen bonds, and dispersion...
Molecular Shape and Polarity03:37

Molecular Shape and Polarity

Dipole Moment of a Molecule

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Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives
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Phase separation and water channel formation in sulfonated block copolyimide.

Chi Hoon Park1, Chang Hyun Lee, Joon-Yong Sohn

  • 1School of Chemical Engineering, Hanyang University, Seoul 133-791, Korea.

The Journal of Physical Chemistry. B
|August 26, 2010
PubMed
Summary

Proton exchange membranes (PEMs) show different microscopic structures impacting fuel cell performance. Weaker microphase separation in sulfonated block copolyimides (SPIs) impedes water channel formation, affecting proton conductivity.

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Published on: October 10, 2016

Area of Science:

  • Materials Science
  • Electrochemistry
  • Polymer Science

Background:

  • Proton exchange membranes (PEMs) are crucial for fuel cell efficiency.
  • Understanding the relationship between microscopic structure and macroscopic properties is key for PEM development.

Purpose of the Study:

  • To compare experimental and simulated data on phase separation and water channel formation in PEMs.
  • To investigate the influence of polymer structure on fuel cell performance.

Main Methods:

  • Utilized experimental and simulation techniques.
  • Studied sulfonated block copolyimides (SPIs) as model polymers and Nafion as a reference.
  • Analyzed microscopic structural differences (atoms, backbone rigidity, sulfonic acid group location).

Main Results:

  • SPIs exhibit weaker microphase separation compared to Nafion.
  • Lower mobility of sulfonic acid groups and hydrogen bonding in SPIs hinder water channel formation.
  • Microscopic structural variations significantly impact macroscopic properties like density, water uptake, and proton conductivity.

Conclusions:

  • Phase separation and water channel formation are critical factors governing PEM macroscopic properties.
  • Microscopic structural differences between SPIs and Nafion explain variations in water uptake and proton transport.
  • Tailoring polymer architecture is essential for optimizing PEMs for fuel cell applications.