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Influence of PVAc/PVA Hydrolysis on Additive Surface Activity
Ophélie Squillace1, Rebecca Fong1, Oliver Shepherd1
1Department of chemistry, Durham University, Stockton road, Durham DH1 3LE, UK.
Polymer matrix hydrophobicity controls small molecule surface behavior. Changes in polymer chemistry dictate additive compatibility and surface activity, influencing material properties.
Area of Science:
- Polymer Science
- Materials Chemistry
- Surface Science
Background:
- Understanding how polymer matrix properties influence small molecule surface behavior is crucial for material design.
- Hydrophobicity of polymer matrices plays a significant role in the surface activity and compatibility of additives.
Purpose of the Study:
- To establish design rules for predicting the influence of polymer matrices on small molecule surface properties.
- To investigate the dependence of additive surface behavior on polymer matrix hydrophobicity and degree of hydrolysis.
Main Methods:
- Systematic modification of polyvinyl acetate (PVAc) to polyvinyl alcohol (PVA) via controlled hydrolysis to alter matrix hydrophobicity.
- Analysis of the surface behavior of model additives (sorbitol, octanoic acid, sodium dodecyl sulfate) in matrices with varying degrees of hydrolysis (DH).
Main Results:
- Sorbitol surface segregation decreased with increasing DH, transitioning from surface blooming in PVAc to plasticization in PVA.
- Octanoic acid (OA) increased PVAc wettability due to high compatibility and reorientation, presenting a hydrophilic surface.
- Sodium dodecyl sulfate (SDS) formed wetting layers across a wide DH range, showing optimal compatibility at intermediate DH.
Conclusions:
- Additive surface segregation is complex, influenced by hydrophobicity, compatibility, surface energy, and component mobility.
- The degree of hydrolysis (DH) is a key parameter for tuning additive behavior and surface properties in polymer matrices.
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