Proton Nuclear Magnetic Resonance-Based Method for the Quantification of Epoxidized Methyl Oleate

Epoxidized methyl esters (EMO) with their high oxirane ring reactivity, acts as a raw material in the synthesis of various industrial chemicals including polymers, stabilizers, plasticizers, glycols, polyols, carbonyl compounds, biolubricants etc. EMO has been generally quantified by the gas chromatography (GC) and high-performance liquid chromatography (HPLC) techniques. Taking into the account of the limitations of these techniques, two qHNMR-based equations have been proposed for the quantification of EMO in the mixture of EMO and methylesters (MO). The validity of the proposed method was determined using standard mixtures of MO and EMO having different molar concentrations. The developed equations have been applied on the samples of EMO prepared from oleic acid in two-step process viz., esterification followed by epoxidation. The qHNMR-based EMO quantification showed acceptable agreement with the results obtained from HPLC analysis.     

Nanocomposites based on transition metal oxides in polyvinyl alcohol for EMI shielding application

In the present work, the nanocomposites based on different transition metal oxides like iron oxide (Fe₂O₃), zinc oxide (ZnO), silicon dioxide (SiO₂), zirconium dioxide (ZrO₂), and titanium dioxide (TiO₂) in PVA matrix have been studied for their suitability as electromagnetic interference (EMI) shielding materials in the frequency range of 4–8 GHz (C-band) and 8–12 GHz (X-band). The nanocomposites containing 0.1, 0.5, 1.0, 5.0, and 10.0 wt% of oxides in the matrix were synthesised by solvent casting method. The EMI attenuation studies in 4–12 GHz frequency range were carried out using the Vector Network Analyzer R & S: ZVA40 method by measuring the loss due to reflection. The minimum reflectivity values for the composites containing Fe₂O₃, ZnO, SiO_2, ZrO₂, and TiO₂ in PVA matrix at 10 wt% concentration level in the matrix were found to be ?38.85 dB (10.4 GHz), ?33.65 dB (10.4 GHz), ?41.90 dB (10.4 GHz), ?24.90 dB (11.0 GHz), and ?32.90 dB (9.76 GHz), respectively. Based on these results, the SiO₂- and Fe₂O₃-based composites, which also exhibit high thermal stability and mechanical strength, are found to be low-cost and efficient EMI shielding materials.     

Prevalence,characterization, and genetic diversity of Listeria monocytogenes isolated from foods of animal origin in North East India

Listeria monocytogenes is a pathogenic microorganism infects man mostly through food. A total of 1615 samples of foods of animal origin and water were collected from retail meat shops of North-Eastern India and processed. Sixty-three (3.9%) samples were positive for L. monocytogenes. Animal origin foods showing the highest prevalence was chevon (9.8%) followed by beef (8.9%), chicken (8.5%), pork (2.8%) and milk (1.8%). The prevalence rate in water from retail meat shops was 10%. Recovered L. monocytogenes were distributed into 3 serogroups, of which 74.6% fit in to 1/2a, 3a serogroup, 17.5% to 1/2b, 3b and 7.9 % to 4b, 4d, 4e serogroups. Thirty-five isolates out of 63 possessed all the tested four virulence genes. RAPD- and ERIC -PCR based analyses jointly revealed a discriminative genetic profile for the L. monocytogenes. On the whole, the occurrence of L. monocytogenes in foods of animal origin of North Eastern India displays public health hazard.     

Detecting localized homogeneous anomalies over spatio-temporal data

The last decade has witnessed an unprecedented growth in availability of data having spatio-temporal characteristics. Given the scale and richness of such data, finding spatio-temporal patterns that demonstrate significantly different behavior from their neighbors could be of interest for various application scenarios such as—weather modeling, analyzing spread of disease outbreaks, monitoring traffic congestions, and so on. In this paper, we propose an automated approach of exploring and discovering such anomalous patterns irrespective of the underlying domain from which the data is recovered. Our approach differs significantly from traditional methods of spatial outlier detection, and employs two phases—(i) discovering homogeneous regions, and (ii) evaluating these regions as anomalies based on their statistical difference from a generalized neighborhood. We evaluate the quality of our approach and distinguish it from existing techniques via an extensive experimental evaluation.     

Intensification of Freeze-Drying Rate of Bacillus subtilis MTCC 2396 Using Tungsten Halogen Radiation: Optimization of Moisture Content and α-Amylase Activity

A novel freeze-drying protocol has been explored to render fast and cost-effective freeze drying of hyperamylase producing Bacillus subtilis MTCC2396 employing a tungsten halogen lamp radiator (THLR) as a heat source. Response surface methodology assessed the maximum reduction in moisture content (96.07%) and minimum reduction in α-amylase (EC 3.2.1.1) activity (1.02%) in 4 h drying time at 42.5°C radiation temperature. α-amylase activity (0.046 U) and final moisture content (3.93%) of the optimally freeze-dried bacterial strain appeared satisfactory. The freeze-drying time using THLR (4 h) is remarkably lower compared to that under a conventional conductive plate heater (CPH) (10 h) at otherwise identical conditions. The higher effective moisture diffusivity of 0.0052 to 0.0078 m ²/s under THLR compared to 0.00084 to 0.0015 m ²/s under CPH (corresponding to 20–50°C) advocated the superiority of the THLR heating protocol. The higher efficacy of THLR was also evidenced through lower activation energy (8.42 kJ/mol) of moisture diffusion compared to that (12.051 kJ/mol) of CPH. The optimally freeze-dried bacteria demonstrated the same growth rate in addition to exhibiting excellent retention of bioremedial (Hg²⁺ removal) activity to that of the control.     

Synthesis, properties and biomedical applications of poly(glycerol sebacate) (PGS): A review

Poly(glycerol sebacate) (PGS) is a biodegradable polymer increasingly used in a variety of biomedical applications. This polyester is prepared by polycondensation of glycerol and sebacic acid. PGS exhibits biocompatibility and biodegradability, both highly relevant properties in biomedical applications. PGS also involves cost effective production with the possibility of up scaling to industrial production. In addition, the mechanical properties and degradation kinetics of PGS can be tailored to match the requirements of intended applications by controlling curing time, curing temperature, reactants concentration and the degree of acrylation in acrylated PGS. Because of the flexible and elastomeric nature of PGS, its biomedical applications have mainly targeted soft tissue replacement and the engineering of soft tissues, such as cardiac muscle, blood, nerve, cartilage and retina. However, applications of PGS are being expanded to include drug delivery, tissue adhesive and hard tissue (i.e., bone) regeneration. The design and fabrication of PGS based devices for applications that mimic native physiological conditions are also being pursued. Novel designs range from accordion-like honeycomb structures for cardiac patches, gecko-like surfaces for tissue adhesives to PGS (nano) fibers for extra cellular matrix (ECM) like constructs; new design avenues are being investigated to meet the ever growing demand for replacement tissues and organs. In less than a decade PGS has become a material of great scrutiny and interest by the biomedical research community. In this review we consolidate the valuable existing knowledge in the fields of synthesis, properties and biomedical applications of PGS and PGS-related biomaterials and devices.     

A green chemistry approach for the synthesis and characterization of bioactive gold nanoparticles using Azolla microphylla methanol extract

This article reports the environmentally benign synthesis of gold nanoparticles （GNPs） using methanol extract of Azolla microphylla as the stabilizing and reducing agent. The GNPs were characterized by UV-vis spectrophotometry and FTIR, and the morphological characteristics were analyzed by XRD, FESEM-EDX and HRTEM. The GNPs could be formed in very short time, even in less than 30 min. The nanoparticles measured by UV-spectrophotometer demonstrated a peak at 540 nm corresponding to surface plasmon resonance spectra, and the peaks showed by FTIR suggested the presence of organic biomolecules on the surface of the GNPs. XRD results confirmed the crystalline nature of the GNPs, and FESEM-EDX and HRTEM analyses had been performed in the size ranges of 17-40nm and 1.25-17.5nm respectively. The synthesized GNPs showed excellent antioxidant activity. This study shows the feasibility of using plant sources for the biosynthesis of GNPs.     

Bi-phasic bio-conversion of sulfur present in model organo-sulfur compounds and hydro-treated diesel

Bacterial strain of Rhodococcus sp. (JUBT1) isolated from petrol/diesel station has been used for the desulfurization of different model organo-sulfur compounds like DBT, substituted DBT, etc. which are difficult to remove in the conventional hydro-desulfurization of diesel fraction. The initial concentration of organo-sulfur compounds has been varied in the range of 100–1000 mg/dm³. Under the present experimental range, the bacterial growth has been observed to follow Haldane-type kinetics characterizing the presence of substrate inhibition. The extent of inhibition by the substrate has been observed to increase with the number of substituents in the same range of initial concentration of different organo-sulfur compounds. The values of intrinsic kinetic parameters, like maximum desulfurization rate, v_max, half saturation constant, K_S, inhibition constant, K_Si and the maximum substrate concentration, C_Smax, corresponding to the maximum uninhibited rate of desulfurization, have been determined using each organo-sulfur compound having different number of substituents as limiting substrate. Relative changes in the values of the kinetic parameters have been correlated to the number of substitutions. Separate studies have also been conducted to determine the kinetics of bio-desulfurization of a hydro-treated diesel fraction. The concentration of sulfur in diesel was selected in the range of 100–500 mg/dm³.

The effect of aqueous to non-aqueous ratio on the rate of specific desulfurization of hydro-treated diesel fraction in the range from 1:9 to 9:1 has also been studied in the present investigation. Mathematical models have been developed to predict the conversion of sulfur during batch-type bio-desulfurization of model compounds as well as diesel having known distribution of organo-sulfur compounds. The predictions of the model satisfactorily compare with the experimental results.