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Related Concept Videos

Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

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.
Many natural and synthetic polymers are produced by...
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...
Radical Chain-Growth Polymerization: Overview01:10

Radical Chain-Growth Polymerization: Overview

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...
Types of Step-Growth Polymers: Polyesters01:20

Types of Step-Growth Polymers: Polyesters

The introduction of polyesters has brought major development to the textile industry. The wrinkle-free behavior of polyester blends has eliminated the need for starching and ironing clothes.
Polyesters are commonly prepared from terephthalic acid and ethylene glycol; the crude product is known as poly(ethylene terephthalate) or PET. However, polyesters are synthesized industrially by transesterification of dimethyl terephthalate with ethylene glycol at 150 °C. The two reactants and the polymer...

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Related Experiment Video

Updated: Jun 19, 2026

20 mJ, 1 ps Yb:YAG Thin-disk Regenerative Amplifier
10:17

20 mJ, 1 ps Yb:YAG Thin-disk Regenerative Amplifier

Published on: July 12, 2017

Subsecond grating growth in a photorefractive polymer.

S M Silence, C A Walsh, J C Scott

    Optics Letters
    |October 2, 2009
    PubMed
    Summary
    This summary is machine-generated.

    This study explores a new photorefractive polymer, showing significantly faster grating formation than previous materials. Findings suggest the presence of mobile charge carriers beyond holes and potential shallow traps.

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    Area of Science:

    • Materials Science
    • Polymer Chemistry
    • Optoelectronics

    Background:

    • Photorefractive polymers are crucial for optical data storage and processing.
    • Existing epoxy-based photorefractive polymers exhibit relatively slow response times.
    • A new class of photorefractive polymer requires investigation into its dynamic properties.

    Purpose of the Study:

    • To investigate the photorefractive effect dynamics in a novel methyl methacrylate copolymer.
    • To characterize grating growth times and understand charge transport mechanisms.
    • To compare the performance with existing photorefractive polymer systems.

    Main Methods:

    • Synthesis of a methyl methacrylate copolymer doped with p-nitroaniline and diethylaminobenzaldehyde diphenylhydrazone.
    • Measurement of photorefractive grating growth dynamics under varying light intensities.
    • Analysis of grating competition and revelation effects.
    • Evaluation of the dependence of growth rate on writing intensity.

    Main Results:

    • Grating growth times were significantly reduced, falling below 1 second at high intensities.
    • Observed grating competition and revelation effects indicate the mobility of charge carriers other than holes.
    • A sublinear relationship between growth rate and writing intensity suggests the presence of shallow traps.
    • The material represents a new class of high-performance photorefractive polymer.

    Conclusions:

    • The novel photorefractive polymer demonstrates exceptionally fast response times.
    • Charge transport involves mobile species beyond photogenerated holes.
    • Shallow traps likely influence the photorefractive dynamics.
    • This material offers potential for advanced optoelectronic applications.