Cross-linked cationic diblock copolymer worms are superflocculants for micrometer-sized silica particles
A series of linear cationic diblock copolymer nanoparticles are prepared by polymerization-induced self-assembly (PISA) reversible addition-fragmentation chain transfer (RAFT) aqueous dispersion polymerization of 2-hydroxypropyl methacrylate (HPMA) using a binary mixture of non-ionic and cationic ma...
Gespeichert in:
Veröffentlicht in: | Chemical science (Cambridge) 2016-01, Vol.7 (12), p.6894-6904 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | A series of linear cationic diblock copolymer nanoparticles are prepared by polymerization-induced self-assembly (PISA)
reversible addition-fragmentation chain transfer (RAFT) aqueous dispersion polymerization of 2-hydroxypropyl methacrylate (HPMA) using a binary mixture of non-ionic and cationic macromolecular RAFT agents, namely poly(ethylene oxide) (PEO
,
= 4400 g mol
;
/
= 1.08) and poly([2-(methacryloyloxy)ethyl]trimethylammonium chloride) (PQDMA
,
= 31 800 g mol
,
/
= 1.19). A detailed phase diagram was constructed to determine the maximum amount of PQDMA
stabilizer block that could be incorporated while still allowing access to a pure worm copolymer morphology. Aqueous electrophoresis studies indicated that zeta potentials of +35 mV could be achieved for such cationic worms over a wide pH range. Core cross-linked worms were prepared
statistical copolymerization of glycidyl methacrylate (GlyMA) with HPMA using a slightly modified PISA formulation, followed by reacting the epoxy groups of the GlyMA residues located within the worm cores with 3-aminopropyl triethoxysilane (APTES), and concomitant hydrolysis/condensation of the pendent silanol groups with the secondary alcohol on the HPMA residues. TEM and DLS studies confirmed that such core cross-linked cationic worms remained colloidally stable when challenged with either excess methanol or a cationic surfactant. These cross-linked cationic worms are shown to be much more effective bridging flocculants for 1.0 μm silica particles at pH 9 than the corresponding linear cationic worms (and also various commercial high molecular weight water-soluble polymers.). Laser diffraction studies indicated silica aggregates of around 25-28 μm diameter when using the former worms but only 3-5 μm diameter when employing the latter worms. Moreover, SEM studies confirmed that the cross-linked worms remained intact after their adsorption onto the silica particles, whereas the much more delicate linear worms underwent fragmentation under the same conditions. Similar results were obtained with 4 μm silica particles. |
---|---|
ISSN: | 2041-6520 2041-6539 |
DOI: | 10.1039/c6sc03732a |