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Title: Distribution of Chains in Polymer Brushes Produced by a “Grafting From” Mechanism

Abstract

The molecular weight and polydispersity of the chains in a polymer brush are critical parameters determining the brush properties. However, the characterization of polymer brushes is hindered by the vanishingly small mass of polymer present in brush layers. In this study, in order to obtain sufficient quantities of polymer for analysis, polymer brushes were grown from high surface area fibrous nylon membranes by ATRP. We synthesized the brushes with varying surface initiator densities, polymerization times, and amounts of sacrificial initiator, then cleaved from the substrate, and analyzed by GPC and NMR. Characterization showed that the surface-grown polymer chains were more polydisperse and had lower average molecular weight compared to solution-grown polymers synthesized concurrently. Furthermore, the molecular weight distribution of the polymer brushes was observed to be bimodal, with a low molecular weight population of chains representing a significant mass fraction of the polymer chains at high surface initiator densities. Moreover, the origin of this low MW polymer fraction is proposed to be the termination of growing chains by recombination during the early stages of polymerization, a mechanism confirmed by molecular dynamics simulations of brush polymerization.

Authors:
 [1];  [2];  [3];  [1]
  1. Univ. of Connecticut, Storrs, CT (United States)
  2. Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)
  3. Univ. of Akron, OH (United States)
Publication Date:
Research Org.:
Oak Ridge National Laboratory (ORNL), Oak Ridge, TN (United States). Oak Ridge Leadership Computing Facility (OLCF)
Sponsoring Org.:
USDOE Office of Science (SC); National Science Foundation (NSF)
OSTI Identifier:
1261508
Grant/Contract Number:  
AC05-00OR22725; CHE-1310453; DMR-1004576
Resource Type:
Accepted Manuscript
Journal Name:
Macromolecules
Additional Journal Information:
Journal Volume: 49; Journal Issue: 2; Journal ID: ISSN 0024-9297
Publisher:
American Chemical Society
Country of Publication:
United States
Language:
English
Subject:
36 MATERIALS SCIENCE

Citation Formats

Martinez, Andre P., Carrillo, Jan-Michael Y., Dobrynin, Andrey V., and Adamson, Douglas H. Distribution of Chains in Polymer Brushes Produced by a “Grafting From” Mechanism. United States: N. p., 2016. Web. doi:10.1021/acs.macromol.5b02261.
Martinez, Andre P., Carrillo, Jan-Michael Y., Dobrynin, Andrey V., & Adamson, Douglas H. Distribution of Chains in Polymer Brushes Produced by a “Grafting From” Mechanism. United States. https://doi.org/10.1021/acs.macromol.5b02261
Martinez, Andre P., Carrillo, Jan-Michael Y., Dobrynin, Andrey V., and Adamson, Douglas H. Mon . "Distribution of Chains in Polymer Brushes Produced by a “Grafting From” Mechanism". United States. https://doi.org/10.1021/acs.macromol.5b02261. https://www.osti.gov/servlets/purl/1261508.
@article{osti_1261508,
title = {Distribution of Chains in Polymer Brushes Produced by a “Grafting From” Mechanism},
author = {Martinez, Andre P. and Carrillo, Jan-Michael Y. and Dobrynin, Andrey V. and Adamson, Douglas H.},
abstractNote = {The molecular weight and polydispersity of the chains in a polymer brush are critical parameters determining the brush properties. However, the characterization of polymer brushes is hindered by the vanishingly small mass of polymer present in brush layers. In this study, in order to obtain sufficient quantities of polymer for analysis, polymer brushes were grown from high surface area fibrous nylon membranes by ATRP. We synthesized the brushes with varying surface initiator densities, polymerization times, and amounts of sacrificial initiator, then cleaved from the substrate, and analyzed by GPC and NMR. Characterization showed that the surface-grown polymer chains were more polydisperse and had lower average molecular weight compared to solution-grown polymers synthesized concurrently. Furthermore, the molecular weight distribution of the polymer brushes was observed to be bimodal, with a low molecular weight population of chains representing a significant mass fraction of the polymer chains at high surface initiator densities. Moreover, the origin of this low MW polymer fraction is proposed to be the termination of growing chains by recombination during the early stages of polymerization, a mechanism confirmed by molecular dynamics simulations of brush polymerization.},
doi = {10.1021/acs.macromol.5b02261},
journal = {Macromolecules},
number = 2,
volume = 49,
place = {United States},
year = {Mon Jan 11 00:00:00 EST 2016},
month = {Mon Jan 11 00:00:00 EST 2016}
}

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