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Responsive hybrid microcapsules by the one-step interfacial thiol-ene photopolymerization
Dandan Liu1, Bing Yu, Xuesong Jiang
1School of Chemistry and Chemical Engineering, State Key Laboratory for Metal Matrix Composite Materials, Shanghai Jiao Tong University, Shanghai 200240, People's Republic of China.
A novel method fabricates hybrid microcapsules using one-step thiol-ene photopolymerization. These thermoresponsive microcapsules offer tunable sizes and controlled dye dispersion for applications like drug delivery.
Area of Science:
- Materials Science
- Polymer Chemistry
- Nanotechnology
Background:
- Microcapsule fabrication often involves complex, multi-step processes.
- Developing robust and versatile methods for hybrid microcapsule synthesis is crucial for advanced applications.
Purpose of the Study:
- To demonstrate a general, convenient, and robust method for fabricating hybrid microcapsules (HMCs).
- To characterize the morphology, size, and wall thickness of the synthesized HMCs.
- To investigate the thermoresponsive properties and encapsulation capabilities of the HMCs.
Main Methods:
- One-step thiol-ene photopolymerization at the toluene-water interface.
- Utilized amphiphilic polyhedral oligomeric silsesquioxane (POSS) with thiol groups (PTPS) as reactive surfactants.
- Employed trimethylolpropane triacrylate (TMPTA) as a cross-linker.
- Characterization using SEM, TEM, AFM, and CLSM.
Main Results:
- Uniform HMCs with tunable diameters (2-4 μm) and wall thicknesses (55-120 nm) were successfully fabricated.
- HMC size increased with toluene content; wall thickness decreased with toluene but increased with TMPTA.
- HMCs exhibited thermoresponsive behavior in aqueous solutions.
- Demonstrated encapsulation of both hydrophobic and hydrophilic dyes with controlled dispersion.
Conclusions:
- The developed one-step photopolymerization method provides a simple and robust route to hybrid microcapsules.
- The tunable properties and encapsulation abilities of HMCs suggest potential in controlled dispersion and drug delivery systems.
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