No abstract

Core/shell nanoparticles containing the fungicide tebuconazole were prepared from amphiphilic copolymers of gelatin grafted with MMA. The grafting was performed in water at levels of 1.5–15 wt.‐% solids based on matrix mass, to give core/shell nanoparticles with median diameters ranging from ≈200 to 400 or ≈10 to 100 nm depending on composition, conditions used, and work‐up. The biocide‐containing nanoparticles were delivered into wood in up to 85% efficiency. Wood blocks treated with tebuconazole‐containing nanoparticles leached less tebuconazole than wood blocks treated with tebuconazole solutions. The best nanoparticle formulations afforded wood blocks with a biological efficacy comparable to solution‐treated wood block controls in soil jar decay tests.

No abstract

In this paper, small angle X-ray scattering has been used to study a series of ionic liquids, alkylammonium alkanoates ([N0 0 0 n][CmCO2]), with varying alkyl chain lengths in the cation and the anion. We investigate the behaviour and the structure of such ionic liquids in their neat state, and in binary mixtures with water. To the best of our knowledge, this is the first structural study dealing with the behaviour of propylammonium propanoate [N0 0 0 3][C2CO2], butylammonium propanoate [N0 0 0 4][C2CO2], propylammonium butanoate [N0 0 0 3][C3CO2] and butylammonium butanoate [N0 0 0 4][C3CO2] when mixed in water. Generally, in the ionic liquids containing alkyl chains on both the cation and the anion, the correlation distance and the resulting scattering peak, which signal intermediate range order, are affected equally by both of the chains. The interesting result obtained regarding these systems is that the shift of the pre- and principal peaks with the addition of water depends on the overall molar concentration of the chains and is generally cumulative. Although, for a given sum of cation and anion chain lengths, the shift is reliant on the cation-anion combination in the neat state, it is not the case in their mixtures with water. In some recent papers, it has been reported that with addition of water, the pre-peak position remains constant, but our results show a shift in both pre- and principal Q peaks.

The nanostructural organisation of mixtures of the ionic liquid (butylammonium butanoate) and water at several mole fractions of water has been investigated using small and wide angle X-ray scattering (S-WAXS) and molecular dynamics (MD) simulations. The presence of a first sharp diffraction peak (FSDP) in the pure ionic liquid has been observed, experimentally and theoretically, suggesting the possibility of segregation of domains of different polarity in the system. With increasing dilution in water, the prepeak is shifted towards smaller Q values, and becomes very weak, while the principal peak moves towards larger Q values. These phenomena suggest the disruption of the hydrogen-bonded network of the ionic liquid, primarily through hydrogen bonding of the anion to water, a conclusion supported by MD simulations.