Macromolecules · 2022 · 21 citations · 61 references
Natural SciencesChemical EngineeringMaterials SciencePolymer ChemistryPolymer EngineeringPolymer MaterialsNanoparticle DispersionsPolymer PhysicsPolymeric NanomaterialsPolymeric NanoparticlesPolymerization ChemistryPolymerization ProcessesBimodal Molecular Weight DistributionsDispersion PolymerizationDispersionsDispersity ControlPolymer DispersantsPolymers In Solid DispersionsReversible Addition-fragmentation Chain Transfer PolymerizationSolution Polymerization
We report the synthesis of sterically-stabilized diblock copolymer particles at 20% w/w solids via reversible addition–fragmentation chain transfer (RAFT) aqueous dispersion polymerization of N,N′-dimethylacrylamide (DMAC) in highly salty media (2.0 M (NH4)2SO4). This is achieved by selecting a well-known zwitterionic water-soluble polymer, poly(2-(methacryloyloxy)ethyl phosphorylcholine) (PMPC), to act as the salt-tolerant soluble precursor block. A relatively high degree of polymerization (DP) can be targeted for the salt-insoluble PDMAC block, which leads to the formation of a turbid free-flowing dispersion of PDMAC-core particles by a steric stabilization mechanism. 1H NMR spectroscopy studies indicate that relatively high DMAC conversions (>99%) can be achieved within a few hours at 30 °C. Aqueous GPC analysis indicates high blocking efficiencies and unimodal molecular weight distributions, although dispersities increase monotonically as higher degrees of polymerization (DPs) are targeted for the PDMAC block. Particle characterization techniques include dynamic light scattering (DLS) and electrophoretic light scattering (ELS) using a state-of-the-art instrument that enables accurate ζ potential measurements in a concentrated salt solution. 1H NMR spectroscopy studies confirm that dilution of the as-synthesized dispersions using deionized water lowers the background salt concentration and hence causes in situ molecular dissolution of the salt-intolerant PDMAC chains, which leads to a substantial thickening effect and the formation of transparent gels. Thus, this new polymerization-induced self-assembly (PISA) formulation enables high molecular weight water-soluble polymers to be prepared in a highly convenient, low-viscosity form. In principle, such aqueous PISA formulations are highly attractive: there are various commercial applications for high molecular weight water-soluble polymers, while the well-known negative aspects of using a RAFT agent (i.e., its cost, color, and malodor) are minimized when targeting such high DPs.
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CRC Handbook of Chemistry and Physics
Devendra Leena P · Journal of Molecular Structure · 1992 · 9.4K citations
Natural Sciences, Chemistry, Physics +12
Living Radical Polymerization by the RAFT Process
Graeme Moad, Ezio Rizzardo, San H. Thang · Australian Journal of Chemistry · 2005 · 2.2K citations