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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...
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...
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,...
Ziegler–Natta Chain-Growth Polymerization: Overview01:17

Ziegler–Natta Chain-Growth Polymerization: Overview

Ziegler–Natta polymerization is another form of addition or chain‐growth polymerization used for synthesizing linear polymers over branched polymers. The catalyst used for polymerization is the Ziegler–Natta catalyst, named after Karl Ziegler and Giulio Natta, who developed it in 1953. This catalyst is an organometallic complex of titanium tetrachloride and triethyl aluminum, with the active form of the catalyst being an alkyl titanium compound. Using the Ziegler–Natta catalyst, high molecular...
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.
Classification and Mechanical Properties of Synthetic Polymers01:28

Classification and Mechanical Properties of Synthetic Polymers

Synthetic polymers are classified as elastomers, fibers, or plastics based on their crystallinity. Crystallinity, the degree of long-range order in the solid state, influences the mechanical properties (stretching or contracting) of elastomers. Elastomers are flexible polymers that can expand or contract easily upon the application of an external force. They have numerous crosslinks that pull them back into their original shape when stress is removed. Silicones, for instance, are highly elastic...

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Microfluidic Preparation of Liquid Crystalline Elastomer Actuators
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Electrically driven alignment and crystallization of unique anisotropic polymer particles.

Kevin P Herlihy1, Janine Nunes, Joseph M Desimone

  • 1Department of Chemistry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27514, USA.

Langmuir : the ACS Journal of Surfaces and Colloids
|July 24, 2008
PubMed
Summary

Researchers explored how electric fields affect polymer particle shapes, finding significant changes in particle chaining and orientation. This study details the behavior of disk, rod, hexnut, and boomerang particles under electric fields.

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Area of Science:

  • Polymer Science
  • Materials Science
  • Soft Matter Physics

Background:

  • Anisotropic polymer particles offer unique properties for advanced materials.
  • Controlling particle assembly is crucial for fabricating functional materials.

Purpose of the Study:

  • To investigate the behavior of various anisotropic polymer particle shapes in aqueous suspensions under alternating electric fields.
  • To understand how electric fields influence particle chaining, packing, and orientation.

Main Methods:

  • Synthesis of micrometer-sized, monodisperse anisotropic polymer particles (disk, rod, hexnut, boomerang) using the particle replication in nonwetting templates (PRINT) process.
  • Application of alternating electric fields (20-50 V ac, 0.5-5.0 kHz) across coplanar electrodes with 1-2 mm gaps.
  • Monitoring particle behavior in aqueous suspensions using fluorescence microscopy.

Main Results:

  • Alternating electric fields induced significant changes in particle packing and orientation for all tested shapes.
  • Disk, rod, and hexnut particles exhibited extensive chaining and altered packing.
  • Boomerang particles showed limited chaining but transitioned from random to ordered packing arrangements.

Conclusions:

  • Electric field manipulation is an effective method for controlling the assembly and orientation of anisotropic polymer particles.
  • Particle shape significantly influences the response to electric fields, affecting chaining and packing behavior.
  • The PRINT process enables the synthesis of diverse anisotropic particles for studying electric-field-induced assembly.