Development of a Glacio-hydrological Model for Discharge and Mass Balance Reconstruction

The reconstruction of glacio-hydrological records for the data deficient Himalayan catchments is needed in order to study the past and future water availability. The study provides outcomes of a glacio-hydrological model based on the degree-day approach. The model simulates the discharge and mass balance for glacierised Shaune Garang catchment. The degree-day factors for different land covers, used in the model, were estimated using daily stake measurements on Shaune Garang glacier and they were found to be varying between 2.6?±?0.4 and 9.3?±?0.3 mm °C^?1day^?1. The model is validated using observed discharge during ablation season of 2014 with coefficient of determination (R²) 0.90 and root mean square error (RMSE) 1.05 m³ sec^?1. The model is used to simulate discharge from 1985 to 2008 and mass balance from 2001 to 2008. The model results show significant contribution of seasonal snow and ice melt in total discharge of the catchment, especially during summer. We observe the maximum discharge in July having maximum contribution from snow and ice melt. The annual melt season discharge shows following a decreasing trend in the simulation period. The reconstructed mass balance shows mass loss of 0.89 m we per year between 2001 and 2008 with slight mass gain during 2000/01 and 2004/05 hydrological years.     

Space-based bacterial production of hydrogen

This paper deals with the electrochemical production of hydrogen by depolarizing the oxygen evolution reaction using human feces and urine, which contains 30-40% bacteria and yeast. The electroactivity of graphite, tungsten carbide, perovskite and RuO2-coated Ebonex (Ti4O7) as anode materials are compared. The scale-up of the process in a laboratory-scale three-dimensional packed bed cell is discussed.     

Utilization of Oil Industry Residues for the Production of Rhamnolipids by Pseudomonas indica

In the present work, a new strain Pseudomonas indica MTCC 3714 was studied for the production of biosurfactants using various rice‐bran oil industry residues viz. rice‐bran, de‐oiled rice‐bran, fatty acids and waxes. Among all the carbon sources, a maximum reduction in surface tension (26.4 mN/m) was observed when the media were supplemented with rice‐bran and the biosurfactant was recovered using the ultrasonication technique as one of the steps in the extraction process. Biosurfactants were obtained in yields of about 9.6 g/L using rice‐bran as the carbon source. The structure of the biosurfactants as characterized by FT‐IR, NMR (¹H and ¹³C) and LC–MS analysis revealed that the majority of the biosurfactants were di‐rhamnolipids. The biosurfactants produced were able to emulsify various hydrocarbons and showed excellent potential in microbial enhanced oil recovery, as it was able to recover kerosene up to 70 % in a sandpack test.     

Selective interfacial localization in conducting polycaprolactam/ethylene vinyl acetate/carbon black composites

Unusual electrical conductivity was demonstrated by ethylene vinyl acetate/polycaprolactam/carbon black (CB) composites. The critical exponent value was 1.2 ± 0.2 for ternary composites and was greater than 2.0 for the binary composites, indicating two‐dimensional electrical conduction in ternary composites. The ternary composites also showed inverted U‐shaped conductivity curves when CB weight fraction was greater than 10 wt%. However, at 10 wt% CB, a discontinuous conductivity curve showing conductivity only when polycaprolactam content was greater than 50% was observed, suggesting substantial variation in the interfacial characteristics with the change in the blend composition. Small‐angle X‐ray scattering studies pointed out that ternary composites can be viewed as a two‐phase system with sharp boundaries, and that interface layer in the composites does not exist. Differential scanning calorimetry studies suggested composition dependent variation in the crystallinity of polycaprolactam phase, partially contributing to the increase in the composites' conductivity at higher polycaprolactam fractions. POLYM. COMPOS., 34:912–919, 2013. © 2013 Society of Plastics Engineers     

Corrosion and Fire Protective Behavior of Advanced Phosphatic Geopolymeric Coating on Mild Steel Substrate

The research objectives of this study were to investigate and compare corrosion and fire protective properties of conventional and advanced phosphatic geopolymeric coating on mild steel substrate using spray coating technique For these studies two composition were developed using conventional geopolymerisation route by adding alkali activator solution to fly ash and six compositions were developed using advanced geopolymerisation process in which water was added to solid precursor powder obtained by together co-ginding of raw materials for a period of 8 h. Coated plates were tested for adhesion strength, water resistance, fire protection and corrosion resistance. Results indicated that coating developed from two passes with thickness 100 ± 15 μm showed better adhesion as compared to single pass and also proved to be promising corrosion protective coating material for mild steel substrate under sea water conditions. The developed material is able to withstand flame for more than 45 min and also no cracks were observed in coating by direct heating on liquefied petroleum gas flame. Thus developed phosphatic geopolymeric material is well suited for protecting the mild steel structures from fire and corrosion.     

One Scaffold,Different Organelle Sensors: pH-Activable Fluorescent Probes for Targeting Live Microglial Cell Organelles**

Targeting live cell organelles is essential for imaging, understanding, and controlling specific biochemical processes. Typically, fluorescent probes with distinct structural scaffolds are used to target specific cell organelles. Here, we have designed a modular one-step synthetic strategy using a common reaction intermediate to develop new lysosomal, mitochondrial, and nucleus-targeting pH-activable fluorescent probes that are all based on a single boron dipyrromethane scaffold. The divergent cell organelle targeting was achieved by synthesizing probes with specific functional group changes to the central scaffold resulting in differential fluorescence and pK_a. Specifically, we show that the functional group transformation of the same scaffold influences cellular localization and specificity of pH-activable fluorescent probes in live primary microglial cells with pK_a values ranging from ∼3.2–6.0. We introduce a structure-organelle-relationship (SOR) framework to target nuclei ( NucShine ), lysosomes ( LysoShine ), and mitochondria ( MitoShine ) in live microglia. This work will result in future applications of SOR beyond imaging to target and control organelle-specific biochemical processes in disease-specific models.     

Effect of moisture and nitrogen levels on the decomposition of wheat straw in soil

Two per cent of wheat straw was mixed with samples of a slightly degraded chernozem soil, and its decomposition was studied at 10, 20, and 30 per cent moisture content of the soil with the addition of 160, 240, and 400 ppm of NH4 + -N. The overall decomposition, measured as CO2 production, and total carbon loss from the soil at 28 degrees C was enhanced by the added nitrogen at all levels of moisture in proportion to the quantity added. Maximum mineralization of the straw carbon was observed at 30 per cent moisture content but there was no significant difference between the amount of carbon mineralized at 20 and 30 per cent moisture levels. No stabilization of the substrate took place in the soil except at 240 and 400 ppm of applied nitrogen at 30 per cent moisture level towards the end of the incubation period. More straw carbon was mineralized when the soil samples were subjected to daily measurements of CO2 evolved than when CO2 measurements were made at intervals over the same period of incubation.     

Evidences of solvent‐induced miscibility in polychloroprene‐co‐ethylene‐propene diene terpolymer blends

Solvent dependent changes in the compatibility behavior of Polychloroprene/Ethylene–propylene–diene terpolymer blends (CR/EPDM) have been investigated using dilute solution viscometry and solvent permeability analysis. To predict the compatibility of rubber blends of different compositions in solvents of different cohesive energy densities, Huggins interaction parameter (ΔB), hydrodynamic interaction (Δη) and Sun's parameter (α) were evaluated from the analysis of the specific and reduced viscosity data of two and three‐component polymer solutions. Miscibility criteria were not satisfied for CR/EPDM blends over the entire composition range in toluene, xylene, and carbon tetrachloride (CCl₄), however, a narrow miscibility domain was observed in chloroform (CHCl₃) for CR/EPDM/CHCl₃ system. These results were further corroborated with the analysis of heat of mixing (ΔH_m) and polymer–polymer interaction parameter (χ₁₂), for all rubber blend compositions. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2009