Production of okara and soy protein concentrates using membrane technology

Microfiltration (MF) membranes with pore sizes of 200 and 450 nm and ultrafiltration (UF) membranes with molecular weight cut off of 50, 100, and 500 kDa were assessed for their ability to eliminate nonprotein substances from okara protein extract in a laboratory cross-flow membrane system. Both MF and UF improved the protein content of okara extract to a similar extent from approximately 68% to approximately 81% owing to the presence of protein in the feed leading to the formation of dynamic layer controlling the performance rather than the actual pore size of membranes. Although normalized flux in MF-450 (117 LMH/MPa) was close to UF-500 (118 LMH/MPa), the latter was selected based on higher average flux (47 LMH) offering the advantage of reduced processing time. Membrane processing of soy extract improved the protein content from 62% to 85% much closer to the target value. However, the final protein content in okara (approximately 80%) did not reach the target value (90%) owing to the greater presence of soluble fibers that were retained by the membrane. Solubility curve of membrane okara protein concentrate (MOPC) showed lower solubility than soy protein concentrate and a commercial isolate in the entire pH range. However, water absorption and fat-binding capacities of MOPC were either superior or comparable while emulsifying properties were in accordance with its solubility. The results of this study showed that okara protein concentrate (80%) could be produced using membrane technology without loss of any true proteins, thus offering value addition to okara, hitherto underutilized. Practical Application: Okara, a byproduct obtained during processing soybean for soymilk, is either underutilized or unutilized in spite of the fact that its protein quality is as good as that of soy milk and tofu. Membrane-processed protein products have been shown to possess superior functional properties compared to conventionally produced protein products. However, the potential of membrane technology has not been exploited for the recovery of okara protein. Our study showed that protein content of okara extract could be improved from approximately 68% to approximately 81% without losing any true proteins in the process.     

Essential oil extracted from peach (Prunus persica) kernel and its physicochemical and antioxidant properties

Peach kernel oil was extracted using Soxhlet extraction with different solvents (petroleum ether, ethyl ether, chloroform and hexane). The physicochemical properties (acid value, iodine value, peroxide value and saponification value), the fatty acid composition, phenolic constituents and contents, and antioxidant activities of peach kernel oil were examined. As per our results, oil extracted with hexane has better overall quality. Its acid, peroxide, iodine and saponification values were 0.895 mg KOH/g oil, 0.916 mg/g oil, 36.328 mg/100 g oil and 101.836 mg KOH/g oil, respectively. Large proportions of unsaturated fatty acid (91.27%) and high content of phenolic compounds (4.1593 mg GAE/g), which contribute to considerably strong antioxidant activity, were found in oil. The main fatty acids found in the peach kernel oil were oleic acid (61.87 g/100 g oil) and linoleic acid (29.07 g/100 g oil). The HPLC analysis of phenolic compounds showed that rutin, (-)-epicatechin gallate, hydrocinnamic acid, sinopinic acid, dithiothreitol and caffeic acid were major constituents. The results suggested that peach kernel oil is a good source of the unsaturated fatty acid, phenolic compounds with strong antioxidant activity, and has the potential to be used as nutrient rich food oil. The results also verified that peach kernel meals contained higher amounts of total phenolic and stronger antioxidant activities than oils, enabling their application as ingredients for functional or enriched foods.     

Open dumping site in Asian developing countries: a potential source of polychlorinated dibenz-p-dioxins and polychlorinated dibenzofurans

Open landfill dumping areas for municipal wastes in Asian developing countries have recently received particular attention with regard to environmental pollution problems. Because of the uncontrolled burning of solid wastes, elevated contamination by various toxic chemicals including dioxins and related compounds in these dumping sites has been anticipated. In this study, concentrations of polychlorinated dibenzo-p-dioxins (PCDDs), polychlorinated dibenzofurans (PCDFs), and coplanar polychlorinated biphenyls (PCBs) were determined in soils from dumping sites in the Philippines, Cambodia, India, and Vietnam. Residue concentrations of PCDD/Fs and coplanar PCBs in dumping site soils were apparently greater than those in soils collected in agricultural or urban areas far from dumping sites, suggesting that dumping sites are potential sources of PCDD/Fs and related compounds. Observed PCDD/F concentrations in soils from dumping sites in the Philippines and Cambodia were comparable or higher than those reported for dioxin-contaminated locations in the world (e.g., near the municipal waste incinerators and open landfill dumping sites). Homologue profiles of PCDD/Fs in dumping site soils from the Philippines and, to a lesser extent, from Cambodia and India reflected patterns of samples representing typical emissions, while profiles of agricultural or urban soils were similar to those of typical environmental sinks. This result suggests recent formation of PCDD/Fs in dumping site areas and that open dumping sites are a potential source of dioxins in Asian developing countries. Uncontrolled combustions of solid wastes by waste pickers, generation of methane gas, and low-temperature burning can be major factors for the formation of dioxins in dumping sites. Elevated fluxes of PCDD/Fs to soils in dumping sites were encountered in the Philippines, Cambodia, India, and Vietnam-Hanoi, and these levels were higher than those reported for other countries. Considerable loading rates of PCDD/Fs in the dumping sites of these countries were observed, ranging from 20 to 3900 mg/yr (0.12-35 mg TEQ/yr). PCDD/F concentrations in some soil samples from the Philippines, Cambodia, India, and Vietnam-Hanoi exceeded environmental guideline values, suggesting potential health effects on humans and wildlife living near these dumping sites. The estimated intakes of dioxins via soil ingestion and dermal exposure for children were higher than those for adults, suggesting greater risk of dioxin exposure for children in dumping sites. To our knowledge, this is the first comprehensive study on PCDD/Fs contamination in open dumping sites of Asian developing countries. On the basis of the result of this study, we have addressed a new environmental issue that open dumping sites are potential sources of PCDD/Fs and related compounds, and dioxin contamination in dumping sites may become a key environmental problem in developing countries.     

Application of Proteomics in Pancreatic Ductal Adenocarcinoma Biomarker Investigations: A Review

Pancreatic ductal adenocarcinoma (PDAC), a highly aggressive malignancy with a poor prognosis is usually detected at the advanced stage of the disease. The only US Food and Drug Administration-approved biomarker that is available for PDAC, CA 19-9, is most useful in monitoring treatment response among PDAC patients rather than for early detection. Moreover, when CA 19-9 is solely used for diagnostic purposes, it has only a recorded sensitivity of 79% and specificity of 82% in symptomatic individuals. Therefore, there is an urgent need to identify reliable biomarkers for diagnosis (specifically for the early diagnosis), ascertain prognosis as well as to monitor treatment response and tumour recurrence of PDAC. In recent years, proteomic technologies are growing exponentially at an accelerated rate for a wide range of applications in cancer research. In this review, we discussed the current status of biomarker research for PDAC using various proteomic technologies. This review will explore the potential perspective for understanding and identifying the unique alterations in protein expressions that could prove beneficial in discovering new robust biomarkers to detect PDAC at an early stage, ascertain prognosis of patients with the disease in addition to monitoring treatment response and tumour recurrence of patients.     

Enhanced photoluminescence of CoWO<Subscript>4</Subscript> in CoWO<Subscript>4</Subscript>/PbWO<Subscript>4</Subscript> nanocomposites

CoWO₄/PbWO₄ nanocomposites were successfully synthesized at room temperature (RT) by co-precipitation route without using any templates or surfactants and sintered at 600 °C for good crystallization. The sintered samples were characterized by X-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy and Zeta potential measurements. UV–Visible diffuse reflectance spectroscopy, photoluminescence (PL) and PL lifetime were studied at RT. The results indicate that the composites have two-phase composition: CoWO₄ and PbWO₄. SEM micrograph and zeta potential measurements reveal particle agglomeration. The intrinsic PL peak emission at 467 nm of CoWO₄ nano sample was enhanced upto four times by optimizing the atomic ratio of Pb/Co concentration. The interconnected interface of CoWO₄/PbWO₄ nanocomposites could have led to increase in number of recombination of electron hole pairs in CoWO₄ and enhanced its intrinsic PL emission intensity. The mechanism of enhanced PL emission for the CoWO₄/PbWO₄ nanocomposites can be attributed to charge transfer between [WO₄]^2? and [WO₆]^6? complexes due to intra particle agglomeration leading to possible interface.     

Electrochemical cell current requirements for toxic organic waste destruction in Ce(IV)-mediated electrochemical oxidation process

The electrochemical cell for cerium oxidation and reactor for organic destruction are the most important operation units for the successful working mediated electrochemical oxidation (MEO) process. In this study, electrochemical cells with DSA electrodes of two types, single stack and double stack connected in series, were used. The performances towards the electrochemical generation of Ce(IV) in nitric acid media at 80 °C were studied. The current-voltage curves and cerium electrolysis kinetics showed the dependence on number of cell stacks needed to be connected in series for the destruction of a given quantity of organic pollutant. The presence of an optimum region for Ce(III) oxidation with a contribution of oxygen evolution, especially at low Ce(III) concentration (high conversion ratios), was found. The cells were applied for the Ce(IV) regeneration during the organic destruction. The cell and reactor processes were fitted in a simple model proposed and used to calculate the current needed in terms of Ce(III) oxidation rate and the number of cell stacks required for maintaining Ce(IV)/Ce(III) ratio at the same level during the organic destruction. This consideration was based on the kinetic model previously developed by us for the organic destruction in the MEO process.     

Structural and electrochemical impedance spectroscopic studies on reactive magnetron sputtered titanium oxynitride (TiON) thin films

Titanium oxynitride films were deposited onto commercially pure titanium substrates by direct current reactive magnetron sputtering method using Ti targets and an Ar–N₂–O₂ mixture discharge gas. The X-ray photoelectron spectroscopy survey spectra on the etched surfaces of TiON films exhibited the characteristic Ti 2p, N 1s, and O 1s peaks at the corresponding binding energies 454.5, 397.0, and 530.7 eV, respectively. The surface topography of these coatings was studied using atomic force microscopy. The characteristic Raman peaks at 200 and 641 cm⁻¹ for the TiN bonds and at 148, 398 ,and 518 cm⁻¹ for the TiO₂ bonds were observed from the Laser Raman spectrometer. The potentiodynamic polarization studies in simulated bodily fluid were performed and the results are reported in this article.     

Phthalocyanine- and Calixarene-Templating Effect on the Catalytic Performance of Solid Supported Vanadates

Abstract  

Catalytic performance of solid supported monovanadate catalysts toward oxidation of propane is significantly affected by the templating effect of: (1) pretreatment of the solid support with calixarene derivatives before deposition of ammonium vanadate, (2) direct deposition of vanadyl phthalocyanine as the vanadate precursor. This effect is believed to be linked to the accessibility of the active sites, and was studied in comparison with a reference mesoporous support.     

Electrochemical synthesis and characterization of poly(aniline-co-1-amino-9,10-anthraquinone), a nanosized conducting copolymer

The electrochemical copolymerization of aniline (ANI) with 1-amino-9,10-anthraquinone (1-AAQ) was carried out in 4 M sulfuric acid by potential cycling in the potential range of −0.1 V to 1.3 V vs. SCE. Copolymer films were grown from different feed ratios of ANI and 1-AAQ (0.2:0.8, 0.4:0.6, 0.5:0.5, 0.6:0.4, 0.8:0.2) on a glassy carbon electrode (GCE). Studies on the effect of scan rate on the conductivity of the copolymer film confirmed the formation of a stable conducting copolymer film. The FTIR spectrum recorded for the copolymer film provides concrete evidence of copolymer formation, since it indicates the presence of quinone units in the copolymer backbone. XRD data (particle size: 47 nm) and SEM (grain size: 100 nm) micrographs provide a clear picture of the nano-sized polymeric particles formed. It is envisaged that the newly reported copolymer could be a useful material for performing the catalytic reduction of oxygen in an acidic medium—a useful process for fuel cell applications.     

Applications of wittig reactions in dibenzo 18‐crown‐6‐ether substituted phenylenevinylene oligomer—synthesis,photo luminescent,and dielectric properties

Novel phenylenevinylene oligomer substituted dibenzo 18‐crown‐6 ether ring (DB‐OPV) was synthesized using dibenzo 18‐crown‐6 with terephthaldicarboxaldehyde via Wittig reaction. Formation of the oligomer was confirmed by spectral (FT‐IR, ¹H and¹³C‐NMR), gel‐permeation chromatography and elemental analysis. The morphology of the oligomer film of one‐dimensional and three‐dimensional architectures was observed using atomic force microscopy. The oligomer showed excellent photoluminescence with bluish green emission maxima at shorter wavelengths of 505 nm. Stability of the oligomer was analyzed using UV spectroscopy with varying time and temperature. The dielectric properties such as dielectric constant and loss factor for the oligomer have also been studied with respect to change of frequency (50 Hz–5 MHz) and temperature (30–60°C). The value of dielectric constant decreased with increasing frequency, which indicates that the major contribution to the polarization comes from orientation polarization. The value of dielectric constant increased with increasing temperature which is due to greater freedom of movement of the dipole molecular chains within the oligomer at high temperature © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011