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Related Concept Videos

Polymer Classification: Stereospecificity01:26

Polymer Classification: Stereospecificity

Polymerization generates chiral centers along the entire backbone of a polymer chain. Accordingly, the stereochemistry of the substituent group has a significant effect on polymer properties. Polymers formed from monosubstituted alkene monomers feature chiral carbons at every alternate position in the polymer backbone. Relative to the predominant orientation of substituents at the adjacent chiral carbons, the polymer can exist in three different configurations: isotactic, syndiotactic, and...
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...
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...
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,...
Polymers02:34

Polymers

The word polymer is derived from the Greek words “poly” which means “many” and “mer” which means “parts”. Polymers are long chains of molecules composed of repeating units of smaller molecules, known as monomers. They either occur naturally, such as DNA and proteins, or can be constructed synthetically, like plastics. They have varied structural characteristics, such as linear chains, branched chains, or complex networks, that contribute to the properties that they exhibit. Additionally,...

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Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives
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Supramolecular assembly in telechelic polymer blends.

R Elliott1, Glenn H Fredrickson

  • 1Materials Research Laboratory, University of California, Santa Barbara, California 93106, USA. relliott@mrl.ucsb.edu

The Journal of Chemical Physics
|October 17, 2009
PubMed
Summary

Supramolecular assembly in polymer blends depends on bond strength. High affinities lead to longer chains and polydispersity, while specific bonding can form multiblock copolymers and novel phases.

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Area of Science:

  • Polymer Science
  • Materials Science
  • Physical Chemistry

Background:

  • Investigates supramolecular assembly in polymer melts with reversible bonding.
  • Explores how chain bonding affinities influence blend structure and phase behavior.

Purpose of the Study:

  • Theoretically investigate equilibrium supramolecular assembly in telechelic polymer melts.
  • Analyze the impact of homobonding, heterobonding, and mixed bonding on blend properties.

Main Methods:

  • Utilized mean-field theory and developed a new integral equation formalism.
  • Employed random phase approximation and numerical self-consistent field theory.
  • Modeled polymers as Gaussian threads with Flory-Huggins repulsions.

Main Results:

  • Low affinities yield monodisperse chains; high affinities create polydisperse blends and chain assembly.
  • Heterobonding can lead to multiblock copolymers, mesophases, and a novel Lifshitz point indicating emulsification.
  • Mapped phase diagrams for various bonding scenarios.

Conclusions:

  • Bonding strength and type critically control supramolecular assembly in polymer blends.
  • Identified conditions for chain assembly, mesophase formation, and potential emulsification.
  • The theoretical framework provides insights into complex polymer blend phase behavior.