An efficient protocol for the rapid room temperature deacetylation of carbohydrate derivatives using CuFe 2 O 4 nanoparticles as an inexpensive and reusable catalyst is presented. After separation of the catalyst with an external magnet, the reaction products are easily obtained in good purity and excellent yields.

The use of amphiphilic macrosurfactants as emulsifying agents has shown to have higher efficiency than that of low molecular weight surfactants. Compared to traditional surfactants, polymeric surfactants have lower critical micelle concentrations and lower diffusion coefficients. In this paper, we present a well defined copolymer based on lauryl methacrylate and poly(ethylene glycol) methyl ether methacrylate, prepared by solution radical copolymerization. The product was characterized by NMR and FTIR spectroscopies and the weight-average molecular weight and polydispersity index were analyzed by SEC. The thermal transitions and decomposition temperatures of the copolymers were determined by DSC and TGA, respectively. Due to the hydrophobic and hydrophilic nature of the monomer units, emulsification studies were performed. DLS experiments showed different sizes of the formed micelles depending on solvent polarity due to polymer-polymer or polymer-solvent interactions. Rheological characterization was undertaken to study the viscoelastic properties of the dispersed systems. Finally, two types of experiments to evaluate the polymer abilities as surfactant have been carried out. Firstly, the amphiphilic characteristics of this material allowed the incorporation of small amounts of an organic solvent in water forming only one phase, as well as the incorporation of small amounts of water in the organic solvent forming an emulsified phase. Then, the amphiphilic properties of this macrosurfactant have been fully exploited in order to form highly stable dispersions of carbon nanotubes in water.

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Responsive interfacial architectures of practical interest commonly require the combination of conflicting properties in terms of their demand upon material structure. Switchable stiffness, wettability, and permeability, key features for tissue engineering applications, are in fact known to be exclusively interdependent. Here, we present a nanoarchitectonic approach that decouples these divergent properties by the use of thermoresponsive microgels as building blocks for the construction of three-dimensional arrays of interconnected pores. Layer-by-layer assembled poly( N-isopropylacrylamide- co-methacrylic acid) microgel films were found to exhibit an increase in hydrophobicity, stiffness, and adhesion properties upon switching the temperature from below to above the lower critical solution temperature, whereas the permeability of redox probes through the film remained unchanged. Our findings indicate that the switch in hydrophilicity and nanomechanical properties undergone by the microgels does not compromise the porosity of the film, thus allowing the free diffusion of redox probes through the polymer-free volume of the submicrometer pores. This novel approach for decoupling conflicting properties provides a strategic route for creating tailorable scaffolds with unforeseen functionalities.

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A simple experiment to determine the real I-V characteristics of three commercially available p-n junction devices is described. The aim of the experiment is to identify the conduction mechanisms present in real p-n devices i.e. recombination currents in the space charge zone, diffusion or ideal currents and high injection currents. Also the influence of series resistance is analysed. The difference between current limitation due to high injection and series resistance is pointed out.

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