Dimethacrylic/epoxy interpenetrating polymer networks including octafunctional POSS

This investigation presents the synthesis of simultaneous interpenetrating polymer networks based on dimethacrylic/epoxy resins with or without polyhedral oligomeric silsesquioxane (POSS) via in situ polymerization. The curing behavior was studied using differential scanning calorimetry (DSC). The influence of the organic groups from the POSS cages on the curing kinetics of the IPNs was also studied by FT-IR spectrometry. The homogeneous phase structure of the cured IPN was proved by DMA tests. Additionally the integrity of the IPN was also demonstrated by thermal decomposition which occurs in one single step.     

Investigation of LSPR Coupling Effects toward the Rational Design of CsxWO3–δ Based Solar NIR Filtering Coatings

The optical range of localized surface plasmon resonance (LSPR) is extended into the infrared region, thanks to the development of highly doped semiconductor nanocrystals. Particularly, the near-infrared (NIR) range holds a significant interest in managing solar radiation. However, practical applications necessitate the arrangement of particles, which is known to possibly impact their optical properties through LSPR coupling effects. How such coupling modifies the LSPR response in semiconductor hosts remains largely unexplored. In this study, a protocol for producing composite coatings composed of cesium-doped tungsten bronze nanocrystals embedded in a silica matrix is presented. Achieving individual dispersion of nanocrystals is made possible through careful selection of a surface polyglycerol ligand exchange. This allows to tune the interparticle distance by adjusting the nanocrystal volume fraction in the composite. The findings demonstrate that LSPR coupling effects significantly influence the LSPR intensity of nanocrystals in the composite when the nanocrystal-to-nanocrystal distance matches their size. Beyond elucidating the LSPR coupling effect, this study provides insights into the potential use of Cs-HTB nanocrystals for solar control applications. Through the optimization of morphology and film structure, remarkable selectivity is obtained in terms of maintaining good transparency in the visible range while achieving high absorption in the NIR.     

New use of size exclusion chromatography in kinetics of mechanical degradation of polymers in solution

A new method to investigate the mechanical degradation of polymers in solution is described that uses size exclusion chromatograms of the initial polymer and of the degraded sample. The incipient parts of these chromatograms are analyzed to obtain kinetic data about degradation at the level of infinitesimal fractions. The procedure is based on the fact that mechanical degradation of the polymers is a first-order reaction and macromolecules are cleaved mostly in their central region. The rate constant and the variation in the rate constant with molecular weight are determined in a single experiment, avoiding additional fractionation steps. Moreover, the slope of the size exclusion chromatographic calibration curve is derived, opening new ways to determine polydispersities or even to make rapid calibration for unknown polymers. To verify the method, the rate constant and the molecular weight dependence of the rate constant were determined for the sonic degradation of polystyrene in toluene. The rate constant is found to vary with the square of the molecular weight, and its value is in good agreement with results reported using much more laborious methods. © 1993 John Wiley & Sons, Inc.     

Effect of LaCoO3 perovskite deposition on ceria-based supports on total oxidation of VOC

Supported LaCoO₃ perovskites with 10 wt.% loading were prepared by impregnation of different supports containing ceria with a solution of La and Co nitrates and citric acid. All precursors were calcined at 700 °C for 5 h. XRD investigations indicated the perovskite formation via “citrate” precursor only on ceria support. All catalysts were tested for toluene total oxidation in the temperature range 100–600 °C. In spite of a large surface area, alumina-supported perovskites showed a lower global activity. It appears then the necessity of the presence of a perovskite phase for good oxidative activity. In terms of reaction rates higher reaction rates per perovskite weight were observed for all supported catalysts when compared to bulk LaCoO₃.     

Computationally Efficient Formulation of Sparse Color Image Recovery in the JPEG Compressed Domain

Sparse representations provide a powerful framework for various image processing tasks, among which image recovery seems to be an already classical application. While most developments of image recovery applications are focused on finding the best dictionary, the possibility of using already existing sparse image representations tends to be ignored. This is the case of the JPEG compressed image representation, which is a sparse image representation in terms of the discrete cosine transform (DCT) dictionary. The development of sparse frameworks directly on the JPEG encoded image representation can lead to computationally efficient approaches. Here we introduce a DCT-based JPEG compressed domain formulation of the color image recovery process within a sparse representation framework and we prove mathematically and experimentally not only its numerical efficiency as compared to the pixel level formulation (the processing time is reduced up to 40 %), but also the good quality of the restoration results.     

Toxic effects of metals: modulation of intracellular calcium homeostasis

Metals and metalloids with their organic derivatives are part of the environment occurring naturally or being introduced upon human activity (e.g. industry, agriculture or medicine). Even if they are useful for humans, these chemicals could be highly toxic (e.g. mercury, lead, arsenic, tin) acting as neurotoxins or carcinogens. Several human cases of metal derived intoxication have been documented resulting in health complications or ending with death. The mechanisms of toxicity are not well understood. Since calcium is a universal second messenger in all cell types it is a good candidate to investigate how changes in the intracellular calcium homeostasis are involved in metal(loid) toxicity. In this mini‐overview the interaction of metallic species with channel proteins at the outer cell membrane, as well as with calcium release sides from the calcium stores and the impairment with calcium extrusion mechanism is discussed.     

Ultrastructural evaluation of mesenchymal stem cells from inflamed periodontium in different in vitro conditions

This research aimed to observe the behavior of mesenchymal stem cells (MSCs) isolated from periodontal granulation tissue (gt) when manipulated ex vivo to induce three‐dimensional (3D) spheroid (aggregates) formation as well as when seeded on two bone scaffolds of animal origin. Periodontal gt was chosen as a MSC source because of its availability, considering that it is eliminated as a waste material during conventional surgical therapies. 3D aggregates of cells were generated; they were grown for 3 and 7 days, respectively, and then prepared for transmission electron microscopic analysis. The two biomaterials were seeded for 72 h with gtMSCs and prepared for scanning electronic microscopic observation. The ultrastructural analysis of 3D spheroids remarked some differences between the inner and the outer cell layers, with a certain commitment observed at the inner cells. Both scaffolds showed a relatively smooth surface at low magnification. Macro‐ and micropores having a scarce distribution were observed on both bone substitutes. gtMSCs grew with relative difficulty on the biomaterials. After 72 h of proliferation, gtMSCs scarcely covered the surface of bovine bone scaffolds, demonstrating fibroblast‐like or star‐like shapes with elongated filiform extensions. Our results add other data on the possible usefulness of gtMSC and could question the current paradigm regarding the complete removal of chronically inflamed gts from the defects during periodontal surgeries. Until optimal protocols for ex vivo manipulation of MSCs are available for clinical settings, it is advisable to use biocompatible bone substitutes that allow the development of progenitor cells. Microsc. Res. Tech. 78:792–800, 2015. © 2015 Wiley Periodicals, Inc.     

Synthesis and characterization of glycerol-adipic acid hyperbranched polyesters

The structure and molecular weight of the hyperbranched polyesterification of adipic acid and glycerol were characterized by ¹³C NMR spectroscopy and size-exclusion chromatography as a function of reaction time and reaction stoichiometry. The glycerol substitution patterns and the extent of reaction of both glycerol and adipic acid were determined by NMR. The glycerol species concentrations determined by NMR were used with a Macosko–Miller conditional probability model to predict the hyperbranched polyester weight-average molecular weight. The model accommodated the difference in primary and secondary –OH reactivity and any substituent effects to glycerol –OH reactivity. In all cases, the predicted weight-average molecular weights were in excellent agreement with the absolute molecular weights determined by size-exclusion chromatography with light scattering detection.     

Fabrication of soft,stimulus-responsive structures with sub-micron resolution via two-photon polymerization of poly(ionic liquid)s

Soft, stimulus-responsive 3D structures created from crosslinked poly(ionic liquid)s (PILs) have been fabricated at unprecedented sub-micron resolution by direct laser writing (DLW). These structures absorb considerable quantities of solvent (e.g., water, alcohol, and acetone) to produce PIL hydrogels that exhibit stimulus-responsive behavior. Due to their flexibility and soft, responsive nature, these structures are much more akin to biological systems than the conventional, highly crosslinked, rigid structures typically produced using 2-photon polymerization (2-PP). These PIL gels expand/contract due to solvent uptake/release, and, by exploiting inherited properties of the ionic liquid monomer (ILM), thermo-responsive gels that exhibit reversible area change (30?±?3%, n?=?40) when the temperature is raised from 20?°C to 70?°C can be created. The effect is very rapid, with the response indistinguishable from the microcontroller heating rate of 7.4?°C?s^?1. The presence of an endoskeleton-like framework within these structures influences movement arising from expansion/contraction and assists the retention of structural integrity during actuation cycling.