Evaluating polymerization kinetics using microrheology

Monitoring the kinetic evolution of molecular weight for growing polymers is critical to understand and optimize polymerization reactions for materials development and discovery. In this work, we propose the use of passive probe microrheology as a facile and low-cost method to monitor polymer growth...

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Veröffentlicht in:Polymer chemistry 2024-04, Vol.15 (17), p.1758-1766
Hauptverfasser: Salas-Ambrosio, Pedro, Gupit, Caidric I, Urueña, Juan Manuel, Luo, Yimin, Hankett, Jeanne M, Gupta, Rohini, Valentine, Megan T, Maynard, Heather D, Helgeson, Matthew E
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container_end_page 1766
container_issue 17
container_start_page 1758
container_title Polymer chemistry
container_volume 15
creator Salas-Ambrosio, Pedro
Gupit, Caidric I
Urueña, Juan Manuel
Luo, Yimin
Hankett, Jeanne M
Gupta, Rohini
Valentine, Megan T
Maynard, Heather D
Helgeson, Matthew E
description Monitoring the kinetic evolution of molecular weight for growing polymers is critical to understand and optimize polymerization reactions for materials development and discovery. In this work, we propose the use of passive probe microrheology as a facile and low-cost method to monitor polymer growth kinetics by indirectly tracking the molecular weight evolution of a polymerizing reaction mixture using time-resolved measurements of sample viscosity. To do so, a recently developed Brownian probe microrheology method based on differential dynamic microscopy (DDM) was applied to a model system of dimethylacrylamide undergoing reversible addition-fragmentation chain-transfer (RAFT) polymerization. The polymerization rate constants extracted from microrheology were within 20% of those obtained from conventional nuclear magnetic resonance (NMR) spectroscopy and size-exclusion chromatography (SEC) measurements. A simple and intuitive workflow based on a single-point Mark-Houwink analysis was then used to estimate an apparent viscosity from NMR and SEC data and, equivalently, an apparent molecular weight from microrheology data. Over the expected range of validity of the analysis, the results are in reasonable quantitative agreement with the corresponding independently measured values. The results demonstrate the ease and reliability of inferring the molecular weight from viscosity data and highlight the capability of DDM microrheology to monitor polymerization of polymer systems. High-throughput microrheology and simple viscosity modeling can be used to continuously monitor the kinetic evolution of polymer molecular weight during controlled polymerizations.
doi_str_mv 10.1039/d4py00188e
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source Royal Society Of Chemistry Journals 2008-
subjects Addition polymerization
Evolution
Kinetics
Molecular weight
NMR
NMR spectroscopy
Nuclear magnetic resonance
Polymerization
Polymers
Rate constants
Size exclusion chromatography
Viscosity
Workflow
title Evaluating polymerization kinetics using microrheology
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