Effect of Pasteurization and Retort Processing on Spectral Characteristics,Morphological, Thermal,Physico‐Mechanical,Barrier and Optical Properties of Nylon‐Based Food Packaging Materials

The effect of pasteurization and retort processing on spectral, morphological, thermal, physico‐mechanical, barrier and optical properties of three different packaging materials viz., PP/N6/PP, PET/N6/cPP and SiO_x‐PET/N6/cPP were studied. These packaging materials were packed with distilled water, which acted as a food simulant. Subsequently, these pouches were subjected to different thermal processing conditions such as pasteurization and retort processing. Both the processing techniques found to have retained the mechanical properties of all packaging materials. Water vapour transmission rate (WVTR) and oxygen transmission rate (OTR) of nylon‐based combinations were increased after processing. Gloss found to decrease invariably irrespective of the material and increases with the severity of the treatment. XRD diffractogram shows changes in crystal structure as a result of thermal processing, and SEM analysis shows the crystal fragmentation. Absorption of water by the amide group of nylon 6 was observed, which could be a reason for the increase in OTR and WVTR. Copyright © 2014 John Wiley & Sons, Ltd.     

Starch Hydrolysate,an Optimal and Economical Source of Carbon for the Secretion of Citric Acid by Yarrowia lipolytica (DS-1)

Using Yarrowia lipolytica (DS-1), secretion of citric acid is studied as a function of carbon sources such as glucose, fructose, hydrol, sucrose, cane sugar molasses, kerosene (all available commercially) and tapioca starch hydrolysate, invert sucrose and invert cane sugar molasses (all prepared in laboratory). On the basis of their acceptability by DS-1 for citric and isocitric acid secretion, it is concluded that (a) sucrose and cane sugar molasses (with/without inversion) served as poor carbon sources, (b) fructose, hydrol, impure tapioca starch hydrolysate (96 DE w/w) and invert sucrose served as relatively better carbon sources and (c) purified tapioca starch hydrolysate (96 DE w/w) was the best carbon source to substitute glucose by giving comparable (75%) efficiency of conversion and economical advantage.     

Suppression of fuel and air stream diluted methane–air partially premixed flames in normal and microgravity

The effects of fuel and air stream dilution (ASD) with carbon dioxide on the suppression of normal and microgravity laminar methane–air partially premixed coflow jet flames were experimentally and numerically investigated. Experiments were conducted both in our normal-gravity laboratory and at the NASA Glenn Research Center 2.2 s drop tower. Measurements included flame topology and liftoff heights of diluted flames, critical diluent mole fractions for flame blowout, and the radiant heat loss from flames. The flames were also simulated using an axisymmetric unsteady numerical code that utilizes detailed chemistry and transport models. In addition, counterflow flame simulation results were used to examine similitude between the counterflow and coflow flame suppression, and further characterize the effectiveness of fuel stream versus ASD on flame extinction. A smaller relative fuel stream dilution (FSD) extinguishes partially premixed flames (PPFs) with increasing premixing as compared to dilution of the air stream. Conversely, smaller ASD is required to extinguish PPFs as they become less premixed and approach nonpremixed (NP) behavior. Fuel stream diluted PPFs and air stream diluted NP flames extinguish primarily through a reactant dilution effect while fuel stream diluted NP flames and air stream diluted PPF are extinguished primarily by a thermal cooling effect. Normal gravity flames lift off and blow out with a smaller diluent mole fraction than microgravity flames. The difference between the fuel and ASD effectiveness increases as the gravitational acceleration is reduced. Radiation heat losses are observed to increase with increasing diluent mole fraction and decreasing gravity.     

Role of cadmium on corrosion resistance of Zn-Ni alloy coatings

Cadmium (Cd) catalyzed Zn-Ni alloy plating has been accomplished galvanostatically on mild steel (MS) using gelatin and glycerol as additives. The effect of addition of Cd into Zn-Ni bath has been examined in terms of nickel (Ni) content and corrosion resistance of Zn-Ni-Cd ternary alloy coatings. The process and product of electrolysis under different concentrations of additives and Cd have been investigated by cyclic voltammetry (CV). The effects of current density (c.d.) on Ni content of the alloy have been studied by spectrophotometric method, supported by EDX analysis. The deposition has been carried out under different concentrations of Cd ranging from 0.004 to 0.1 M. The corrosion rates (CR) of Zn-Ni alloy coatings have been found to decrease drastically with addition of Cd. It has been also revealed that the CR of binary Zn-Ni alloy coatings decreased with the increase of Cd concentration only up to a certain optimal concentration, i.e., up to 0.02 M, and then remained unchanged. An effort to change the anomalous type of codeposition into normal one by changing the molar ratios of the metal ions, i.e. [Cd²⁺]/[Ni²⁺] as 0.01, 0.05 and 0.25 has remained futile. CV study demonstrated an important role of Cd in mutual depositions of Zn²⁺ and Ni²⁺ ions by its preferential adsorption, thus leading to the increased Ni content of the alloy. The bath composition and operating parameters have been optimized for deposition of bright and uniform Zn-Ni-Cd alloy coatings. Changes in the surface morphology and phase structure of Zn-Ni alloy coatings due to addition of Cd has been confirmed by Scanning Electron Microscopy (SEM) and X-Ray Diffraction (XRD) study respectively. Experimental investigations so as to identify the role of Cd in codeposition Zn-Ni alloy coatings have been carried out and the results are discussed.     

On deformation and tearing of stiffened and un-stiffened square plates subjected to underwater explosion—a numerical study

In modern combat operations warships can be subjected to underwater blast loads capable of causing considerable structural damage. Research in the field of underwater explosion effects on structures has seen systematic developments since world war-I (WW-I) with the increased awareness that the possible underwater explosions and threats from the hunter killer “U” boats could now be countered. Most of the earlier investigations were conducted by military and these were classified. Cole [1] established empirical relations to model the underwater explosion (UNDEX) loading, which were the outcome of numerous experimental investigations done by the military agencies. In the present study the UNDEX load profile has been modeled as an exponentially decaying shock wave, which varies spatially and transiently. The failure modes in high strength (HS) and WELDOX Steel rectangular plates was predicted using an elasto-plastic model with isotropic hardening, strain rate effects and fracture criterion under clamped edge conditions. These models were implemented in the nonlinear finite element code ABAQUS/Explicit. The present study predicts and establishes the failure modes using a 3D FE analysis.     

Hexamethylenetetramine: A New Fuel for Solution Combustion Synthesis of Complex Metal Oxides

Hexamethylenetetramine, (CH₂)₆N₄ (HMT) has been employed as a fuel for the first time to synthesize several binary, ternary, and quaternary oxides by the solution combustion method. Technologically important oxides, namely, zirconia, ceria, and their solid solutions, -Al₂O₃, Cr³⁺-doped -Al₂O₃, spinels, MAl₂O₄ (M = Ca, Mg, Zn and Ni), perovskites, LaMO₃ (M = Mn, Cr and Al), La_0.67Sr_0.33MnO₃, and La_0.67Ca_0.33MnO₃, have been synthesized. The oxides synthesized are characterized by X-ray powder diffraction, resistivity, fluorescence spectra, particle size, and surface area measurements. Decomposition of nickel nitrate-HMT complex has been investigated by TG, DTA, TPD, and evolved-gas analysis to elucidate the mechanism.     

Perturbation-Based Eigenvector Updates for On-Line Principal Components Analysis and Canonical Correlation Analysis

Principal components analysis is an important and well-studied subject in statistics and signal processing. Several algorithms for solving this problem exist, and could be mostly grouped into one of the following three approaches: adaptation based on Hebbian updates and deflation, optimization of a second order statistical criterion (like reconstruction error or output variance), and fixed point update rules with deflation. In this study, we propose an alternate approach that avoids deflation and gradient-search techniques. The proposed method is an on-line procedure based on recursively updating the eigenvector and eigenvalue matrices with every new sample such that the estimates approximately track their true values as would be calculated analytically from the current sample estimate of the data covariance matrix. The perturbation technique is theoretically shown to be applicable for recursive canonical correlation analysis, as well. The performance of this algorithm is compared with that of a structurally similar matrix perturbation-based method and also with a few other traditional methods like Sanger’s rule and APEX.

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The guideline interchange format: a model for representing guidelines

Carboxylate and sulfate groups were introduced at the surface of poly(ethylene) (PE) samples. This was accomplished by coating and immobilizing sodium 10-undecenoate (C11(:)) and 10-undecene sulfate (S11(:)) on the polymer by means of an argon plasma treatment. The composition of the coated surfactant layer was proportional to the composition of the coating solution. The thickness of the surfactant layer on the surface of PE samples, which were precoated from an aqueous solution with a total surfactant concentration of 0.30 M, was about 55 A. The presence of carboxylate and sulfate groups after plasma treatment of the precoated surfaces was confirmed by X-ray photoelectron spectroscopy (XPS). About 20% of the initial amount of functional groups of the coated surfactants was retained at the PE surface. The ratio of carboxylate/sulfate groups at the plasma treated surfaces was dependent on the composition of the precoated surfaces. The minimum surface density of these groups on the resulting samples was about one group per 40 A2.     

Involvement of CD14 and complement receptors CR3 and CR4 in nuclear factor-kappaB activation and TNF production induced by lipopolysaccharide and group B streptococcal cell walls

This study was undertaken to evaluate the role of CD14 and complement receptors type 3 (CR3) and 4 (CR4) in mediating TNF release and NF-kappaB activation induced by LPS and cell wall preparations from group B streptococci type III (GBS). LPS and GBS caused TNF secretion from human monocytes in a CD14-dependent manner, and soluble CD14, LPS binding protein, or their combination potentiated both LPS- and GBS-induced activities. Blocking of either CD14 or CD18, the common beta-subunit of CR3 and CR4, decreased GBS-induced TNF release, while LPS-mediated TNF production was inhibited by anti-CD14 mAb only. Chinese hamster ovary cell transfectants (CHO) that express human CD14 (CHO/CD14) responded to both LPS and GBS with NF-kappaB translocation, which was inhibited by anti-CD14 mAb and enhanced by LPS binding protein. While LPS showed fast kinetics of NF-kappaB activation in CHO/CD14 cells, a slower NF-kappaB response was induced by GBS. LPS also activated NF-kappaB in CHO cells transfected with either human CR3 or CR4 cDNA, although responses were delayed and weaker than those of CHO/CD14 cells. In contrast to LPS, GBS failed to induce NF-kappaB in CHO/CR3 or CHO/CR4 cells. Both C3H/OuJ (Lps[n]) and C3H/HeJ (Lps[d]) mouse peritoneal macrophages responded to GBS with TNF production and NF-kappaB translocation, whereas LPS was active only in C3H/OuJ macrophages. Thus, LPS and GBS differentially involve CD14 and CR3 or CR4 for signaling NF-kappaB activation in CHO cells and TNF release in human monocytes, and engage a different set of receptors and/or intracellular signaling pathways in mouse macrophages.