Structural,electrical and electrochemical properties of polyacrylonitrile-ammonium hexaflurophosphate polymer electrolyte system

Polyacrylonitrile (PAN) based polymer electrolyte membranes complexed with Ammonium hexafluorophosphate (NH₄PF₆) with different molar concentration are prepared by solution casting method. Increase in the amorphous nature by the addition of Ammonium salt and the formation of polymer-salt complex are confirmed by X ray diffraction studies and infrared spectroscopy respectively. The glass transition temperature is measured for all membranes and it showed a lowest value for the PAN complexed with 20 mol% of NH₄PF₆. Electrical properties are studied by AC impedance spectroscopy. An ionic conductivity of the order of 10^?3 Scm^?1 is obtained for the 80 PAN / 20 NH₄PF₆ polymer electrolyte. Conductivity, dielectric and modulus spectra from the impedance data are analysed to understand the ionic transport mechanism. Transference number measurement is done to study the ionic contribution to the charge transport. A proton battery with the configuration, Zn+ ZnSO₄. 7H₂O /80 PAN / 20 NH₄PF₆ / PbO₂ +V₂O₅ has been constructed and its discharge characteristics are studied.     

Studies on Egg Shell and SiC Reinforced Hybrid Metal Matrix Composite for Tribological Applications

Silicon - The hybrid metal matrix composite is developed through stir casting process. In theAl7075 aluminium matrix material, two different combination of reinforcements are used to make hybrid...     

Comparative study of arsenic removal by iron using electrocoagulation and chemical coagulation

This research studied As(III) and As(V) removal during electrocoagulation (EC) in comparison with FeCl₃ chemical coagulation (CC). The study also attempted to verify chlorine production and the reported oxidation of As(III) during EC. Results showed that As(V) removal during batch EC was erratic at pH 6.5 and the removal was higher-than-expected based on the generation of ferrous iron (Fe²⁺) during EC. As(V) removal by batch EC was equal to or better than CC at pH 7.5 and 8.5, however soluble Fe²⁺ was observed in the 0.2-μm membrane filtrate at pH 7.5 (10-45%), and is a cause for concern. Continuous steady-state operation of the EC unit confirmed the deleterious presence of soluble Fe²⁺ in the treated water. The higher-than-expected As(V) removals during batch mode were presumed due to As(V) adsorption onto the iron rod oxyhydroxides surfaces prior to the attainment of steady-state operation. As(V) removal increased with decreasing pH during both CC and EC, however EC at pH 6.5 was anomalous because of erratic Fe²⁺ oxidation. The best adsorption capacity was observed with CC at pH 6.5, while lower but similar adsorption capacities were observed at pH 7.5 and 8.5 with CC and EC. A comparison of As(III) adsorption showed better removals during EC compared with CC possibly due to a temporary pH increase during EC. In contrast to literature reports, As(III) oxidation was not observed during EC, and As(III) adsorption onto iron hydroxides during EC was only 5-30% that of As(V) adsorption. Also in contrast to literature, significant Cl₂ was not generated during EC, in fact, the rods actually produced a significant chlorine demand due to reduced iron oxides on the rod. Although Cl₂ generation and As(III) oxidation are possible using a graphite anode, a combination of graphite and iron rods in the same EC unit did not produce As(III) oxidation. However, a two-stage process (graphite anode followed by iron anode in separate chambers) was effective in As(III) oxidation and removal. The competing ions, silica and phosphate interfered with As(V) adsorption during both CC and EC. However, the degree of interference depends on the concentration and presence of other competing ions. In particular, the presence of silica lowered the effect of phosphate with increasing pH due to silica’s own significant effect at high pHs.     

Senescent CD4+CD28− T Lymphocytes as a Potential Driver of Th17/Treg Imbalance and Alveolar Bone Resorption during Periodontitis

Senescent cells express a senescence-associated secretory phenotype (SASP) with a pro-inflammatory bias, which contributes to the chronicity of inflammation. During chronic inflammatory diseases, infiltrating CD4⁺ T lymphocytes can undergo cellular senescence and arrest the surface expression of CD28, have a response biased towards T-helper type-17 (Th17) of immunity, and show a remarkable ability to induce osteoclastogenesis. As a cellular counterpart, T regulatory lymphocytes (Tregs) can also undergo cellular senescence, and CD28⁻ Tregs are able to express an SASP secretome, thus severely altering their immunosuppressive capacities. During periodontitis, the persistent microbial challenge and chronic inflammation favor the induction of cellular senescence. Therefore, senescence of Th17 and Treg lymphocytes could contribute to Th17/Treg imbalance and favor the tooth-supporting alveolar bone loss characteristic of the disease. In the present review, we describe the concept of cellular senescence; particularly, the one produced during chronic inflammation and persistent microbial antigen challenge. In addition, we detail the different markers used to identify senescent cells, proposing those specific to senescent T lymphocytes that can be used for periodontal research purposes. Finally, we discuss the existing literature that allows us to suggest the potential pathogenic role of senescent CD4⁺CD28⁻ T lymphocytes in periodontitis.     

Microstructural investigation on mechanical behavior of soil-geosynthetic interface in direct shear test

Interface shear strength between soil and geosynthetics mainly depends on the mechanical and physical properties of soil, geosynthetics and the normal stress acting at the interface. This paper presents results of an extensive experimental investigation carried out on sand-geosynthetic interface using modified large direct shear box. The study focusses on the shearing mechanism at the sand-geosynthetic interface and the effect of different parameters on the shearing mechanism. Smooth HDPE geomembrane, nonwoven needle punched geotextile and two types of sand having different mean particle size, have been used in the present study. Microstructural investigation of deformed specimen through Field Emission Scanning Electron Microscope (FESEM) reveals the shearing mechanism which includes interlocking and fiber stretching for sand-geotextile while sliding, indentation and plowing for sand-geomembrane interface. The shearing mechanism for sand-geomembrane interface highly depends on the normal stress and degree of saturation of sand. The critical normal stress that demarcates the sliding and plowing mechanism for sand-geomembrane interface is different for dry and wet sand. The amount of scouring (or plowing) of the geomembrane surface reduces with increase in the mean particle size of sand. FESEM images revealed that the sand particles get adhered to the geotextile fibers for tests involving wet sands. The present microstructural study aided in understanding the shearing mechanism at sand-geosynthetic interface to a large extent.     

Experimental investigation on the effect of MgO and TiO2 nanoparticles in stepped solar still

This work aims at augmenting the amount of potable water using MgO and TiO₂ in stepped solar still. Experiments were carried out for the climatic conditions of Chennai, India, with two different concentrations of nanofluids inside a stepped basin under three different cases. Results show that there is an improvement in yield of fresh water from stepped solar still by 33.18% and 41.05% using 0.1% and 0.2% volume concentration of TiO₂ nanofluid, respectively, whereas the freshwater yield from stepped still with MgO nanofluids improved by 51.7% and 61.89%. Furthermore, the economic analysis revealed that the cost of potable water from the modified solar still reduced from 0.029 to 0.016 $/kg. Similarly, the useful annual energy, yearly cost per kilogram, and annual cost per kilowatt hour are significantly profitable with the use of MgO nanofluid in the stepped basin and found as 512.46 kWh, 0.025 $/kg, and 0.026 $/kWh, respectively. It is also found that the cost of potable water from the modified still significantly increases as the amount of fresh water produced is decreased with increased fabrication cost of the solar still.     

Experimental study on conventional solar still integrated with inclined solar still under different water depth

This study primarily focuses on comparative experimental analysis on standalone conventional solar still (CSS), inclined solar still (ISS), and integrated conventional and inclined solar still (CSS‐ISS) for different parameters that affect the freshwater yield. For enhancing the freshwater yield only a few studies are available on still‐still integration. The present novel study provides a greater improvement in improving the freshwater yield by integrating ISS with CSS. This experimental work mainly concentrates on the importance of water depth (d _w) and mass flow rate of water ( m _w) in the solar still. Water depth inside the conventional still varied from 0.02 to 0.06 m whereas, water is constantly flown with a mass flow rate of 8.33 kg/hour in an ISS with baffles. The experimental result shows that the accumulated freshwater yield from CSS‐ISS, ISS, and CSS were 6.2, 5.04, and 4.24 kg, respectively. CSS‐ISS and ISS produced 46.23% and 18.87% higher productivity than the CSS. From the experimental investigation, it is also identified that the water temperature is significantly improved by 20% using integration as compared with CSS without integration under the same water depth of d _w = 0.02 m. The overall improvement in yield was higher in the case of CSS‐ISS. The deviations between experimental and theoretical values of yield from the conventional and modified solar still were in the range of ±7%.     

Green fire retardant finishing and combined dyeing of proteinous wool fabric

Flame retardancy was imparted to a scoured and bleached, proteinous woollen textile by using banana pseudostem sap, an ecofriendly waste agricultural product, at different pH levels. The flame retardancy characteristics of both the control and the treated fabrics were analysed in terms of the limiting oxygen index and the vertical flammability measurement. Thermal degradation and fire retardancy mechanisms were studied using thermogravimetry, scanning electron microscopy, and energy dispersive X‐ray analysis. Moreover, the charring mechanism of both the control and the banana‐pseudostem‐sap‐treated fabrics with varying pH was analysed and reported in detail. The wool fabric was also dyed with CI Acid Blue 25 using banana pseudostem sap as well as water as the medium. The fabric dyed with the banana pseudostem sap medium at pH 5.5 showed more colour exhaustion, colour strength, and thermal stability compared with the control wool fabric. The mechanism by which superior fire retardancy and colour strength are imparted to the woollen textile by the application of banana pseudostem sap is proposed.     

Coalescence of bubbles and stability of foams in aqueous solutions of Tween surfactants

Coalescence of air bubbles and stability of foams in aqueous solutions of Tween 20, 40, 60 and 80 are reported in this work. Adsorption of the surfactants at air–water interface was studied by measuring the surface tension of the surfactant solutions. The surface tension profiles were fitted using a surface equation of state derived from the Gibbs and Langmuir adsorption equations. The critical micelle concentration and surface tension at this concentration were determined. The effect of surfactant concentration on coalescence of air bubbles at flat air–water interface was studied. The role of steric force on coalescence time was investigated. The coalescence time distributions were fitted by the stochastic model. The mean values of the distributions were compared with the predictions of seven film-drainage models. Stability of foams was analyzed by the Ross–Miles test. The initial and residual foam heights were measured at different surfactant concentrations. The stability of foams was compared with the coalescence time of the bubbles.