Crosslinking effect on polydimethylsiloxane elastic modulus measured by custom‐built compression instrument

A macroscopic compression test utilizing a simple custom‐built instrument was employed to measure polydimethylsiloxane (PDMS) elastic modulus. PDMS samples with varying crosslinking density were prepared with the elastomer base to the curing agent ratio ranging from 5 : 1 to 33 : 1. The PDMS network elastic modulus varied linearly with the amount of crosslinker, ranging from 0.57 MPa to 3.7 MPa for the samples tested. PDMS elastic modulus in MPa can be expressed as 20 MPa/PDMS base to curing agent ratio. This article describes a simple method for measuring elastic properties of soft polymeric materials. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 41050.     

Benzophenone vs. Copper/Benzophenone in Light‐Promoted Atom Transfer Radical Additions (ATRAs): Highly Effective Iodoperfluoroalkylation of Alkenes/Alkynes and Mechanistic Studies

Iodoperfluooralkylation of terminal alkenes and alkynes is effectively photo‐promoted by benzophenone 2 (BP) or the photoreducible copper(II) complex 1 . In particular, BP at 1 mol% in methanol upon 365 nm irradiation with a low‐pressure mercury lamp (type TLC=thin layer chromatography, 6 W) results in a fast reaction with excellent reaction yields. Complex 1 and BP 2 exhibited very similar reactivity, suggesting that the reactions involving 1 are likely to be governed by the benzophenone photoactivation processes, rather than copper(I)/(II) redox processes. Mechanistic investigations using transient absorption spectroscopy revealed that a deactivation pathway of the benzophenone triplet (³BP*) is via its reaction with the methanol solvent. We propose that the generated radicals, in particular ^.CH₂OH, play a key role in the initiation step forming R_f^. by reacting with R_fI, R_f^. then entering a radical chain cycle. ¹H NMR studies provided evidence that a substantial amount (∼7% NMR yield) of the hemiacetal CH₃OCH₂OH is formed, i.e., the possible by‐product of the reaction between ^.CH₂OH and R_fI. Finally, DFT calculations indicate that a triplet‐triplet energy transfer (TTET) process from ³BP* to perfluorooctyl iodide (C₈F₁₇I) is unlikely or should be rather slow under the reaction conditions, consistent with the transient absorption studies.

     

I2-Imidazoline Ligand CR4056 Improves Memory,Increases ApoE Expression and Reduces BBB Leakage in 5xFAD Mice

Recent evidence suggests that I2-imidazoline ligands have neuroprotective properties in animal models of neurodegeneration, such as Alzheimer’s disease (AD). We recently demonstrated that the I2-ligand BU224 reversed memory impairments in AD transgenic mice and this effect was not because of reductions in amyloid-β (Aβ) deposition. In this study, our aim was to determine the therapeutic potential of the powerful analgesic I2-imidazoline ligand CR4056 in the 5xFAD model of AD, since this ligand has been proven to be safely tolerated in humans. Sub-chronic oral administration of CR4056 (30 mg/kg for 10 days) led to an improvement in recognition memory in 6-month-old 5xFAD mice, but not in wild-type littermates, without affecting Aβ levels or deposition. Our results also revealed a change in the profile of microglia by CR4056, resulting in a suppression of pro-inflammatory activated microglia, but increased the density of astrocytes and the expression of ApoE, which is mainly produced by these glial cells. In addition, CR4056 restored fibrinogen extravasation, affecting the distribution of markers of astrocytic end feet in blood vessels. Therefore, these results suggest that CR4056 protects against Aβ-mediated neuroinflammation and vascular damage, and offers therapeutic potential at any stage of AD.     

Iron Mobilization from Ferritin in Yeast Cell Lysate and Physiological Implications

Most in vitro iron mobilization studies from ferritin have been performed in aqueous buffered solutions using a variety of reducing substances. The kinetics of iron mobilization from ferritin in a medium that resembles the complex milieu of cells could dramatically differ from those in aqueous solutions, and to our knowledge, no such studies have been performed. Here, we have studied the kinetics of iron release from ferritin in fresh yeast cell lysates and examined the effect of cellular metabolites on this process. Our results show that iron release from ferritin in buffer is extremely slow compared to cell lysate under identical experimental conditions, suggesting that certain cellular metabolites present in yeast cell lysate facilitate the reductive release of ferric iron from the ferritin core. Using filtration membranes with different molecular weight cut-offs (3, 10, 30, 50, and 100 kDa), we demonstrate that a cellular component >50 kDa is implicated in the reductive release of iron. When the cell lysate was washed three times with buffer, or when NADPH was omitted from the solution, a dramatic decrease in iron mobilization rates was observed. The addition of physiological concentrations of free flavins, such as FMN, FAD, and riboflavin showed about a two-fold increase in the amount of released iron. Notably, all iron release kinetics occurred while the solution oxygen level was still high. Altogether, our results indicate that in addition to ferritin proteolysis, there exists an auxiliary iron reductive mechanism that involves long-range electron transfer reactions facilitated by the ferritin shell. The physiological implications of such iron reductive mechanisms are discussed.     

High-Temperature Oxidation of Boron Nitride: I, Monolithic Boron Nitride

High-temperature oxidation of monolithic boron nitride (BN) is examined at 900–1200°C. Hot-pressed BN and both low- and high-density chemically vapor-deposited BN are studied. The oxidation product is B₂O₃( l ) and the oxidation kinetics are sensitive to crystallographic orientation, porosity, and impurity levels. The B₂O₃ product also reacts readily with ambient water vapor in the test furnace (ppm levels) to form the volatile species HBO₂( g ), leading to overall paralinear kinetics. The linear rate constant extracted from these experiments agreed with that predicted from diffusion of HBO₂( g ) across a static boundary layer.     

Influence of clays on the rheology of cement pastes

The fresh state of concrete is becoming increasingly important in furthering the types of applications of today's construction world. Processing techniques have resulted in technologies such as self-consolidating concrete and depend on the microstructural changes that take place during and immediately after mixing and placing. These changes to the microstructure reflect the flocculation behavior between the particles in suspension. The ability to modify this behavior allows control over the balance among flowability and shape-stability of concrete. This study investigates how clay admixtures affect the microstructure of cement pastes from a rheological stand point. Shear and compressive rheology techniques are used to measure how the solids volume fraction of suspensions with different admixtures evolves with stress. Based on these relationships, the effectiveness of clays on the balance between flowability and shape-stability is measured. Results are consistent with green strength tests performed on concrete mixes derived from the cement paste mixes.     

Sodium sulfate: Deposition and dissolution of silica

The hot-corrosion process for SiO₂-protected materials involves deposition of Na₂SO₄ and dissolution of the protective SiO₂ scale. Dew points for Na ₂SO₄ deposition are calculated as a function of pressure, sodium content, and sulfur content. Expected dissolution regimes for SiO₂ are calculated as a function of Na₂SO₄ basicity, hence generated by fuels with 0.5% and 0.05% S. Controlled-condition burner-rig tests on quartz verify some of these predicted dissolution regimes. However, the basicity of Na₂SO₄ is not always a simple function of (Na₂O) show that carbon creates basic conditions in Na₂SO₄, which explains the extensive corrosion of SiO₂-protected materials containing carbon, such as SiC.     

A comparative life cycle assessment of hybrid osmotic dilution desalination and established seawater desalination and wastewater reclamation processes

The purpose of this study was to determine the comparative environmental impacts of coupled seawater desalination and water reclamation using a novel hybrid system that consist of an osmotically driven membrane process and established membrane desalination technologies. A comparative life cycle assessment methodology was used to differentiate between a novel hybrid process consisting of forward osmosis (FO) operated in osmotic dilution (ODN) mode and seawater reverse osmosis (SWRO), and two other processes: a stand alone conventional SWRO desalination system, and a combined SWRO and dual barrier impaired water purification system consisting of nanofiltration followed by reverse osmosis. Each process was evaluated using ten baseline impact categories. It was demonstrated that from a life cycle perspective two hurdles exist to further development of the ODN-SWRO process: module design of FO membranes and cleaning intensity of the FO membranes. System optimization analysis revealed that doubling FO membrane packing density, tripling FO membrane permeability, and optimizing system operation, all of which are technically feasible at the time of this publication, could reduce the environmental impact of the hybrid ODN-SWRO process compared to SWRO by more than 25%; yet, novel hybrid nanofiltration-RO treatment of seawater and wastewater can achieve almost similar levels of environmental impact.     

A simulation environment for performance analysis of HVAC systems

Due to the lack of a building simulation program that can simulate in details the combined heat, vapor, and liquid transfer in porous elements and the HVAC (heating, ventilation and air-conditioning) systems, a flexible computational algorithm has been elaborated in order to integrate models for both HVAC systems and multizone hygrothermal building model. In the algorithm, models for the primary system-composed of chiller, cooling tower, primary pumps, and condensation pumps—have been described. For the secondary system, models for the cooling and dehumidifying coil, humidifier, fan, and mixing box have been considered. Those mathematical models have been integrated into the whole-building PowerDomus simulation environment. The simulation environment is presented, and results show the usability aspects of the proposed computer environment by comparing air- and water-cooled equipment.