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Related Concept Videos

Step-Growth Polymerization: Overview01:03

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Step-growth or condensation polymerization is a stepwise reaction of bi or multifunctional monomers to form long-chain polymers. As all the monomers are reactive, most of the monomers are consumed at the early stages of the reaction to form small chains of reactive oligomers, which then combine to form long polymer chains in the late stages. Hence, the reaction has to proceed for a long time to achieve high molecular weight polymers.
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The skeletal structure of polymers synthesized via radical polymerization is always branched. For example, the polymerization of ethylene by radical polymerization results in a low-density grade of polyethylene with a heavily branched skeletal structure. Here, the radical site abstracts hydrogen from the growing chain, and the radical site shifts from the end (a primary carbon center) to anywhere within the growing chain (a secondary carbon center). Consequently, the part of the chain from the...
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Anionic Chain-Growth Polymerization: Overview01:20

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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,...
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Radical Chain-Growth Polymerization: Overview01:10

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Chain-growth or addition polymerization is successive addition reactions of monomers with a polymer chain. In radical chain-growth polymerization, the reaction proceeds via a free-radical intermediate. The free radical is formed from radical initiators, which spontaneously generate free radicals by homolytic fission. Organic peroxides (such as dibenzoyl peroxide, as shown in Figure 1) or azo compounds are popular radical initiators. A low concentration ratio of radical initiator to monomer is...
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Radical Chain-Growth Polymerization: Mechanism01:09

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The radical chain-growth polymerization mechanism consists of three steps: initiation, propagation, and termination of polymerization. The polymerization initiates when a free radical generated from the radical initiator adds to the unsaturated bond in the monomer. The unpaired electron of the free radical and one π electron in the unsaturated bond creates a σ bond between the free radical and the monomer. As a result, the other π electron in the unsaturated bond converts this...
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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...
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Synthesis of Cyclic Polymers and Characterization of Their Diffusive Motion in the Melt State at the Single Molecule Level
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Toward a 3D physical model of diffusive polymer chains.

Andras Karsai1, Grace J Cassidy2, Aradhya P Rajanala1

  • 1School of Physics, Georgia Institute of Technology, Atlanta, GA, United States.

Frontiers in Physics
|August 4, 2023
PubMed
Summary
This summary is machine-generated.

Researchers created macro-scale polymer analogs using bead chains in a fluidized bed. Bead chain dynamics revealed exponential velocity distributions, differing from typical polymer models due to environmental forces.

Keywords:
3D printingdiscrete element methodsexperimental methodsfluidized bedsgranular mediapolymer physics

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Area of Science:

  • Polymer physics
  • Soft matter physics
  • Biophysics

Background:

  • Macro-scale analogs of microscopic polymer chains like DNA are created using bead chains.
  • These chains exhibit diffusive motion influenced by random fluctuations.
  • Previous models did not fully capture the complex interactions in granular media.

Purpose of the Study:

  • To model and investigate the dynamics of bead chains in a novel stochastic forcing system: an air fluidizing bed.
  • To compare experimental results with Discrete Element Method (DEM) simulations.
  • To understand deviations from expected polymer behavior in non-ideal environments.

Main Methods:

  • Constructing bead chains from spherical resin beads connected by silk thread.
  • Subjecting bead chains to fluidization in a granular media bed with controlled airflow.
  • Utilizing X-ray imaging for dynamic observation and DEM simulations for 3D motion analysis.
  • Varying chain length, bead connection geometry, and stiffness using 3D printing.

Main Results:

  • Bead chain velocity distributions were found to be exponential, not Gaussian as expected for polymers in solution.
  • DEM simulations indicated that environmental force distributions from the fluidized bed cause this deviation.
  • The study successfully created and analyzed macro-scale polymer analogs.

Conclusions:

  • The fluidized bed environment significantly influences bead chain dynamics, leading to non-Gaussian velocity distributions.
  • DEM simulations provide a valuable tool for understanding complex polymer physics in granular media.
  • This research offers insights into the behavior of large biopolymers and complex polymeric systems.