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Synthesis, Morphology, and Particle Size Control of Acidic Aqueous Polyurethane Dispersions
Ellen J Quane1, Niels Elders2, Anna S Newman1
1School of Mathematical and Physical Sciences, The University of Sheffield, Dainton Building, Brook Hill, Sheffield, South Yorkshire S3 7HF, U.K.
Charge-stabilized aqueous polyurethane (PU) dispersions self-assemble into particles and supramolecular structures. Particle size is controlled by hydrophile content, decreasing with increased PU acidity and influenced by polyether soft-segment molecular weight.
Area of Science:
- Polymer Chemistry
- Materials Science
- Surface Chemistry
Background:
- Aqueous polyurethane (PU) dispersions are versatile materials with tunable properties.
- Understanding the self-assembly behavior of PU chains is crucial for controlling dispersion characteristics.
Purpose of the Study:
- To synthesize and characterize charge-stabilized aqueous PU dispersions.
- To investigate the relationship between PU composition, self-assembly, and particle characteristics.
Main Methods:
- Synthesis of PU dispersions with varying compositions.
- Characterization using mass spectrometry, GPC, SAXS, AFM, and FTIR.
- Analysis of scattering data with a mass conservation model.
Main Results:
- PU dispersions form spherical particles and supramolecular structures.
- Supramolecular structure proportion increases with dimethylolpropionic acid (DMPA) content.
- Particle radius decreases with increased PU acidity, following surface charge density models.
Conclusions:
- PU particle size is governed by hydrophile (DMPA) content and polyether soft-segment molecular weight.
- A critical hydrophile coverage is required for particle stabilization, increasing with polyether molecular weight.
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