Tailoring Wetting Properties at Extremes States to Obtain Antifogging Functionality

Fog formation decreases light transmission of optically clear materials. A promising approach to address this problem is to control the wetting properties of the material at extremes states, which requires imparting micro and nano morphology features on the surface. However, such features may affect the optical properties of the surface. In this work, superhydrophobic and superhydrophilic surfaces, with different morphology characteristics ranging from nanoscale to hierarchical micro-nanoscale are fabricated and evaluated in order to investigate which wetting extreme and surface morphology is more suitable to preserve the light-transmitting properties and exhibit antifogging functionalities. The performance of the aforementioned surfaces is compared for the first time in two different testing modes: under intense fog flow and no surface cooling, and under no-flow and surface cooling, which enhances dew condensation on the surfaces. It is demonstrated that superhydrophilic surfaces with nanoscale morphology maintain their optical transmittance under fog flow for more than 20 min. This duration is one of the longest reported in the literature revealing the long-term antifogging functionality of the proposed surfaces. Finally, by tailoring the morphology and the surface wetting properties, an optically switching surface (initially “milky” which becomes “clear”) when exposed to humidity is demonstrated.     

Evaluation of hydrogen producing cultures using pretreated food waste

In order to enhance bio-hydrogen production from food waste, pretreatment methods are widely used. The influence of the initial pH and autoclaving were investigated in batch experiments. Fermentative studies showed that pure cultures like Clostridium beijerinckii could directly utilize raw food waste to produce hydrogen, while other cultures (Clostridium butyricum and Clostridium pasteurianum) could produce hydrogen only after pH adjustment. In this case, the optimal starting pH of the culture was found to be 7. Autoclaving could further enhance hydrogen yields due to increased hydrolysis of food waste. The maximum hydrogen yield was achieved by C. butyricum (38.9 mL-H₂/g-VS_added) after autoclaving food waste with pH adjustment at 7. In addition, the ratio acetic to butyric acid was decreased by autoclaving pretreatment, because butyrate metabolic pathway was favored in the fermentation process. However, suitable pH for bacteria growth and the low ammonia production could be achieved from autoclaving food waste.     

Deploying LiveWN Grids in the Greek School Network

A determinant factor for the introduction of grid technologies in production domains of scale can be the design of easy, fast and, from an operational point of view, realizable deployment procedures. Remote system management technologies, typically used to monitor and manage IT environments, are designed to offer remote software installation functionality that exhibits the aforementioned characteristics; however, previous work has shown that even valuable systems can fail to perform in heterogeneous, geographically distributed environments, especially if they are maintained by organizations affiliated to the public sector. The deployment of grid technologies throughout the Greek School Network can be achieved by combining OpenRSM, a novel open source solution capable to support usable, configurable, infrastructure management use cases in heterogeneous environments and LiveWN, a grid scavenging solution that integrates live technologies with gLite grids.     

Electrochemical oxidation of stabilized landfill leachate on DSA electrodes

The electrochemical oxidation of stabilized landfill leachate with 2960 mg L(-1) chemical oxygen demand (COD) over a Ti/IrO(2)-RuO(2) anode was investigated in the presence of HClO(4) as the supporting electrolyte. Emphasis was given on the effect of electrolysis time (up to 240 min) and temperature (30, 60 and 80°C), current density (8, 16 and 32 mA cm(-2)), initial effluent's pH (0.25, 3, 5 and 6), HClO(4) concentration (0.25 and 1M) and the addition of NaCl (20 and 100mM) or Na(2)SO(4) (20mM) as source of extra electrogenerated oxidants on performance; the latter was evaluated regarding COD, total carbon (TC), total phenols (TPh) and color removal. Moreover, the anode was studied by scanning electron microscopy and cyclic voltammetry. The main parameters affecting the process were the effluent's pH and the addition of salts. Treatment for 240 min at 32 mA cm(-2) current density, 80°C and the pH adjusted from its inherent value of 0.25 (i.e. after the addition of HClO(4)) to 3 yielded 90% COD, 65% TC and complete color and TPh removal at an electricity consumption of 35 kWh kg(-1) COD removed. Comparable performance (i.e. 75% COD reduction) could be achieved without pH adjustment but with the addition of 100mM NaCl consuming 20 kWh kg(-1) COD removed.     

Carbon nanoscrolls: a promising material for hydrogen storage

A multiscale theoretical approach was used for the investigation of hydrogen storage in the recently synthesized carbon nanoscrolls. First, ab initio calculations at the density functional level of theory (DFT) were performed in order to (a) calculate the binding energy of H2 molecules at the walls of nanoscrolls and (b) fit the parameters of the interatomic potential used in Monte Carlo simulations. Second, classical Monte Carlo simulations were performed for estimating the H2 storage capacity of "experimental size" nanoscrolls containing thousands of atoms. Our results show that pure carbon nanoscrolls cannot accumulate hydrogen because the interlayer distance is too small. However, an opening of the spiral structure to approximately 7 A followed by alkali doping can make them very promising materials for hydrogen storage application, reaching 3 wt % at ambient temperature and pressure.     

Multiscale modeling reveals poisoning mechanisms of MgO-supported Au clusters in CO oxidation

Catalyst deactivation mechanisms on MgO-supported Au(6) clusters are studied for the CO oxidation reaction via first-principle kinetic Monte Carlo simulations and shown to depend on support vacancies. In defect-poor MgO or in the presence of a Mg vacancy, O(2) does not bind to the clusters and the catalyst is poisoned by CO. On Au clusters interacting with O vacancies of the support, O(2) can be chemisorbed and transient activity is observed. In this case, an unexpected catalyst "breathing" mechanism (restructuring) leads to carbonate formation and catalyst deactivation, rationalizing several experimental observations. Our study underscores the importance of the cluster's charge state and dynamics on catalytic activity.     

Tomographic imaging with polarized light

We report three-dimensional tomographic reconstruction of optical parameters for the mesoscopic light scattering regime from experimentally obtained datasets by using polarized light. We present a numerically inexpensive approximation to the radiative transfer equation governing the polarized light transport. This approximation is employed in the reconstruction algorithm, which computes two optical parameters by using parallel and perpendicular polarizations of transmitted light. Datasets were obtained by imaging a scattering phantom embedding highly absorbing inclusions. Reconstruction results are presented and discussed.     

Synthesis and biological investigation of novel tricyclic benzodiazepinedione-based RGD analogues

Integrins, a widely expressed family of heterodimeric cell surface adhesion proteins, are expressed in a variety of cell types. They play a decisive role in cell-cell adhesion or cell to extracellular matrix adhesion events. Antagonists of alpha(v)beta(3) or alpha(IIb)beta(3) integrin may have a potential use in suppression of pathological processes. We present the synthesis of novel tricyclic benzodiazepinedione-based RGD analogues, which were subsequently tested in a solid-phase receptor assay in order to investigate their binding affinities towards alpha(v)beta(3) and alpha(IIb)beta(3) integrin.     

Aristoforin, a novel stable derivative of hyperforin, is a potent anticancer agent

Hyperforin, a natural product of St. John's wort (Hypericum perforatum L.), has a number of pharmacological activities, including antidepressive and antibacterial properties. Furthermore, hyperforin has pronounced antitumor properties against different tumor cell lines, both in vitro and in vivo. Despite being a promising novel anticancer agent, the poor solubility and stability of hyperforin in aqueous solution limits its potential clinical application. In this study, we present the synthesis of hyperforin derivatives with improved pharmacological activity. The synthesized compounds were tested for their solubility and stability properties. They were also investigated for their antitumor properties, both in vitro and in vivo. One of these hyperforin derivatives, Aristoforin, is more soluble in aqueous solution than hyperforin and is additionally highly stable. Importantly, it retains the antitumor properties of the parental compound without inducing toxicity in experimental animals. These data strongly suggest that Aristoforin has potential as an anticancer drug.