Emulsion copolymerization of 2-(tert-butylamino)ethyl methacrylate (TBAEMA) with divinylbenzene (DVB) cross-linker in the presence of monomethoxy-capped poly(ethylene glycol) methacrylate (PEGMA) at 70 °C afforded sterically stabilized poly[2-(tert-butylamino)ethyl methacrylate] (PTBAEMA) latexes at 10% solids at pH 9. Such particles proved to be an effective Pickering emulsifier at pH 10 for both n-dodecane and n-hexane. (1)H NMR spectroscopy was used to follow the model reaction between the secondary amine of the TBAEMA monomer and the isocyanate groups of tolylene 2,4-diisocyanate-terminated poly(propylene glycol) (PPG-TDI). Cross-linking the PTBAEMA latex particles adsorbed at the n-dodecane/water interface using this oil-soluble PPG-TDI cross-linker at around 0 (o)C led to robust colloidosomes that survived an acid challenge. This resistance to demulsification was confirmed via laser diffraction studies following an in situ switch from pH 10 to 3, since no change was observed in either the oil droplet size or concentration (compared to non-cross-linked PTBAEMA-stabilized Pickering emulsions). Such PTBAEMA colloidosomes survived removal of the internal oil phase on washing with excess ethanol. However, because ethanol is a good solvent for the PTBAEMA chains, imaging the ethanol-treated colloidosomes via electron microscopy proved rather problematic due to partial film formation. Therefore, a series of TBAEMA/styrene copolymer latexes (comprising 10, 30, 50, or 60 mol % styrene) were prepared via emulsion copolymerization at 70 °C in the presence of DVB and PEGMA. The higher glass transition temperatures exhibited by these copolymer particles (and their greater resistance to ethanol swelling) enabled better-quality electron microscopy images to be obtained. The presence of nitrogen atoms at the surface of these copolymer latex particles was confirmed via X-ray photoelectron spectroscopy studies; these secondary amine groups allow covalent cross-linking via PPG-TDI when adsorbed at the surface of n-dodecane droplets at TBAEMA comonomer contents as low as 40 mol %. After removal of the n-hexane oil phase by evaporation, fluorescence microscopy studies indicate that these colloidosomes undergo collapse in their latex form at pH 10 but regain their original spherical morphology in their cationic microgel form at pH 3.5.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/la5033674 | DOI Listing |
Angew Chem Int Ed Engl
November 2024
Department of Physical and Macromolecular Chemistry, Faculty of Science, Charles University, 128 40, Prague 2, Czech Republic.
In recent years, polymerization-induced self-assembly (PISA) has emerged as a powerful method for the straightforward synthesis of polymer nanoparticles at high concentration. In this study, we describe for the first time the synthesis of poly(2-oxazoline) nanoparticles by dispersion cationic ring-opening polymerization-induced self-assembly (CROPISA) in n-dodecane. Specifically, a n-dodecane-soluble aliphatic poly(2-(3-ethylheptyl)-2-oxazoline) (PEHOx) block was chain-extended with poly(2-phenyl-2-oxazoline) (PPhOx).
View Article and Find Full Text PDFACS Sustain Chem Eng
June 2024
Dipartimento Scienza Applicata e tecnologia, Politecnico di Torino, 10129 Torino, Italy.
J Colloid Interface Sci
February 2025
State Key Laboratory of Solidification Processing, Center of Advanced Lubrication and Seal Materials, School of Materials Science and Engineering, Northwestern Polytechnical University, Xi'an 710072, PR China. Electronic address:
Developing stimulus-responsive properties of drug delivery nanocarriers combined with enhanced joint lubrication is an effective synergistic strategy for treating osteoarthritis. Poly(N-isopropylacrylamide) (PNIPAm) is a typical thermo-responsive polymer, which can achieve drug delivery by transition from swollen state to collapsed state. However, undesired transition temperature, limited drug loading capacity, and weakened mechanical properties in joint present obstacles to use as drug delivery nanocarriers.
View Article and Find Full Text PDFPolymers (Basel)
September 2024
College of Materials Science & Engineering, Xihua University, Chengdu 610039, China.
Biomacromolecules
September 2024
Universite Claude Bernard Lyon 1, CPE Lyon, CNRS, UMR 5128, Catalysis, Polymerization, Processes and Materials (CP2M), 43 Bd du 11 Novembre 1918, 69616 Villeurbanne, France.
This work aims at synthesizing tailor-made poly(vinyl alcohol--vinyl acetate) (PVA) amphiphilic copolymers, obtained by alcoholysis of poly(vinyl acetate) (PVAc) that could display improved properties as stabilizers compared to commercially available PVAs. Well-defined PVAs with different alcoholysis degrees were produced from a library of PVAc homopolymers synthesized by macromolecular design via interchange of xanthate polymerization and exhibiting different degrees of polymerization degrees. Subsequently, these PVAs were evaluated as stabilizers in the emulsion copolymerization of VAc and vinyl neodecanoate (VERSA 10, referred to as V10) and compared to a commercially available reference PVA obtained by alcoholysis of PVAc formed by conventional radical polymerization.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!