A one-step dispersion copolymerization technique is demonstrated to fabricate biphasic particles as an approach to streamline the production of particles with complex morphology. The model system studies a monomer feed of hydrophobic styrene and hydrophilic, zwitterionic sulfobetaine methacrylate (SBMA) in a water/isopropanol cosolvent mixture. The resulting particles have a core-shell morphology that can be transformed, simply by washing the particles with water, into particles with a single surface opening connected to an interior cavity. Results indicate that particle morphology is dependent on the presence of nanoscopic SBMA-rich aggregates in the initial reaction mixture to act as nucleation sites, forming an SBMA-rich core encased in a styrene-rich shell. Systematic study of the morphology evolution reveals that the difference in monomer solubility profile can be exploited to control compositional drift of the particle composition during copolymerization yielding copolymer with sufficiently different composition to form phase-separated particle morphology. When SBMA is replaced with various ionic comonomers, the cavity-forming morphology is observed when reaction conditions result in low solubility of the comonomer in the cosolvent mixture. Based on these results, design guidelines are developed that may be applied to a variety of systems requiring complex and responsive particles made from chemically distinct comonomer pairings.
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http://dx.doi.org/10.1002/marc.202200873 | DOI Listing |
ACS Macro Lett
January 2025
Faculty of Materials Science and Engineering, South China University of Technology, Guangzhou 510640, People's Republic of China.
Efficient synthesis of cyclic polymers remains a frontier challenge. We report here that macromolecular transesterification during a pseudoblock copolymerization process can be utilized for such a purpose. Organobase-catalyzed ring-opening alternating copolymerization of 3,4-dihydrocoumarin and epoxide is conducted with four-armed poly(ethylene oxide) (PEO) as a macroinitiator.
View Article and Find Full Text PDFACS Nano
January 2025
Hunan Province Key Laboratory for Advanced Carbon Materials and Applied Technology, College of Materials Science and Engineering, Hunan University, Changsha 410082, China.
SiO-based anodes, considered the most promising candidate for high-energy density batteries, have long been bothered by mechanical integrity issues. Research efforts focus on particle modifications, often overlooking the enhancement of interparticle connections, which can reduce the active material content within the electrode. Herein, an integrated electrode with strong covalent bonding at the electrode scale is designed, achieving excellent mechanical stability with ∼95 wt.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Department of Chemical and Biomolecular Engineering, National University of Singapore, 117585, Singapore.
Int J Biol Macromol
January 2025
School of Environmental Engineering, Wuhan Textile University, Wuhan 430073, China; Engineering Research Centre for Clean Production of Textile Dyeing and Printing, Ministry of Education, Wuhan Textile University, Wuhan 430073, China.
Natural lignocellulose-based materials have numerous strengths such as abundance, cheap price and biodegradability, which indicates a brilliant prospect for environmental protection. This work aimed to design an efficient sorbent (NaSS-PSD) by pine sawdust (PSD) for the surveillance and management of enrofloxacin (ENR). In the study, sodium styrenesulfonate (NaSS) was chosen as an effective monomer to ameliorate the performance of PSD by graft copolymerization.
View Article and Find Full Text PDFBiomacromolecules
January 2025
Chair of Macromolecular Chemistry, Julius-Maximilians-Universität Würzburg, Röntgenring 11, 97070 Würzburg, Germany.
Postpolymerization modifications are valuable techniques for creating functional polymers that are challenging to synthesize directly. This study presents aliphatic polycarbonates with pendant thiol-reactive groups for disulfide formation with mercaptans. The reductive responsive nature of this reaction allows for reversible postpolymerization modifications on biodegradable scaffolds.
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