Weak Polyampholytes at the Interface of Magnetic Nanocarriers: A Facile Catch-and-Release Platform for Dyes.

We present a platform of charge-invertible core-shell hybrid particles for the selective and reversible adsorption of small charged molecules as model systems. The herein employed carrier systems consist of an iron oxide core coated with different pH-responsive polyampholytes which exhibit varying surface charge depending on the surrounding pH value. The resulting materials were used for electrostatically mediated catch-and-release experiments of either cationic or anionic dyes with the perspective to allow the pH-dependent magnetically guided transport of suitable cargo. The use of three different polyampholyte coatings (poly(2-(imidazol-1-yl)acrylic acid) (PImAA), poly(dehydroalanine) (PDha), and poly(N,N-diallylglutamate) (PDAGA)) enables a deeper understanding about how the surface net charge in combination with the charge and charge density of any cargo influences such processes. The size, surface charge, and aggregation behavior of the herein described particles were investigated via dynamic light scattering (DLS), transmission electron microscopy (TEM), and pH-dependent ζ-potential measurements, whereas adsorption and release studies were investigated via UV-vis.

Effect of poly(acrylic acid) architecture on setting and mechanical properties of glass ionomer cements.

OBJECTIVE: This work focuses on the influence of poly(acrylic acid) (PAA) architecture (linear or branched) on setting behavior and compressive strength of glass ionomer cements (GICs). METHODS: Branched and linear poly(acrylic acid)s were synthesized according to the Strathclyde methodology or by free radical polymerization. They were characterized by 1H-NMR spectroscopy and size exclusion chromatography to determine their molecular weight and size distribution. GIC setting was characterized by oscillating rheometry and time-dependent FTIR spectroscopy. In addition, compressive strength was tested on cylindrical samples (6 × 4 mm; n = 8/cement composition) after storage in deionized water at 37 °C for one day. RESULTS: We used two different routes to prepare PAA. One direct route in order to provide straightforward access to branched PAA and a two-step approach in order to get more control about the PAA molecular weight using tert-butyl acrylate (tBA) for polymerization with subsequent deprotection. Using the second approach we obtained several linear PAA of which a mixture was used in order to mimic the molecular weight and size distribution of branched PAA. This allowed the direct comparison of properties relying only on the polymer architecture. Comparing linear PAA to branched samples in general led to faster setting but at the same time decreased the compressive strength. Increasing molecular weight of branched PAA resulted in even faster GIC setting while increasing compressive strength and this correlates well with the trends reported for linear PAA in literature. Mixing of branched and linear PAA, however, turned out to be an effective way of tailoring GIC properties. SIGNIFICANCE: our results suggest that both molecular weight and dispersity need to be considered when choosing suitable PAA architecture for obtaining specific GIC properties.