Cytochemical assessment of phosphopeptides derived from casein as potential ingredients for functional food

Phosphopeptides derived from casein hydrolysis are suggested to have beneficial effects beyond their mere nutritive value by enhancing availability of dietary minerals, especially calcium, iron and zinc. Apart from a possible positive action the potential may exist for adverse effects that could impose restrictions to their widespread application in functional foods for human nutrition. In the present work, various case-inophosphopeptide (CPP) preparations were assessed using different human cell culture model systems in order to estimate their cytotoxic potential and their influence on epithelial properties and differentiation of human intestinal cells (Caco-2). The general cytotoxic potential of CPPs was tested using the AlphaTox NR assay. Structural and functional differentiation of intestinal Caco-2 cells was determined by measuring transepithelial electrical resistance and activity of brush border associated alkaline phosphatase over an extended cultivation period. No loss in cell viability with respect to membrane integrity could be detected, as uptake and retention of neutral red dye (AlphaTox assay) into HeLa cells was not affected by the presence of CPPs. Cytochemical assays conducted on epithelial cells (Caco-2) showed no disturbance of normal cell development and differentiation with respect to structural as well as functional differentiation markers. As all CPPs tested did not provoke any adverse effects in terms of cytotoxicity and showed no impairment of cell differentiation and monolayer integrity of human intestinal cells, it may be supposed that CPPs do not provoke a cytotoxic response in vivo in the cells assayed in the present study.     

Role of black carbon in the sorption of polychlorinated dibenzo-p-dioxins and dibenzofurans at the Diamond Alkali superfund site, Newark Bay, New Jersey

The sorption of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) to organic carbon (OC) and black carbon (BC) was measured in two sediment cores taken near the Diamond Alkali superfund site (DA) in the Passaic River and Newark Bay, New Jersey (U.S.A.). An OC partitioning model and a BC-inclusive, Freundlich distribution model were used to interpret measurements of freely dissolved PCDD/Fs using passive samplers in sediment incubations, together with measured sedimentary concentrations of OC, BC, and PCDD/Fs. Samples were also analyzed for polycyclic aromatic hydrocarbons (PAHs) as controls on the two distribution models. The OC partitioning model underpredicted the distribution of PAHs and PCDD/Fs by 10-100-fold. The Freundlich model predicted the distribution of PAHs at the DA to within a factor of 2-3 of observations. Black carbon-water partition coefficients (K(iBC)) for PCDD/Fs, derived from literature results of both field and laboratory studies differed up to 1000-fold from values derived from this study. Contrary to expectations, PCDDs displayed stronger sorption than either PCDFs or PAHs relative to their subcooled liquid aqueous solubilities. Even though the presence of BC in the sediments reduced the overall bioavailability of PCDD/Fs by >90%, the sediments at 2 m depth continue to display the highest pore water activities of PCDD/Fs.     

Synthesis of heat exchanger networks at subambient conditions with compression and expansion of process streams

This article presents an optimization formulation for the synthesis of heat exchanger networks where pressure levels of process streams can be adjusted to improve heat integration. Especially important at subambient conditions, this allows for the interconversion of work, temperature, and pressure‐based exergy and leads to reduced usage of expensive cold utility. Furthermore, stream temperatures and pressures are tuned for close tracking of the composite curves yielding increased exergy efficiency. The formulation is showcased on a simple example and applied to a case study drawn from the design of an offshore natural gas liquefaction process. Aided by the optimization, it is demonstrated how the process can extract exergy from liquid nitrogen and carbon dioxide streams to support the liquefaction of a natural gas stream without additional utilities. This process is part of a liquefied energy chain, which, supplies natural gas for power generation while facilitating carbon dioxide sequestration. © 2010 American Institute of Chemical Engineers AIChE J, 2011     

Combining coal gasification, natural gas reforming, and solid oxide fuel cells for efficient polygeneration with CO2 capture and sequestration

Several polygeneration process systems are presented which convert natural gas and coal to gasoline, diesel, methanol, and electricity. By using solid oxide fuel cells as the primary electricity generator, the presented systems improve upon a recently introduced concept by which natural gas is reformed inside the radiant cooler of a gasifier. Simulations and techno-economic analyses performed for a wide range of process configurations and market conditions show that this strategy results in significant efficiency and profitability improvements when CO₂ capture and sequestration are employed. Market considerations for this analysis include variations in purchase prices of the coal and natural gas, sale prices of the products, and CO₂ emission tax rates.     

High resolution scanning gate microscopy measurements on InAs/GaSb nanowire Esaki diode devices

Gated transport measurements are the backbone of electrical characterization of nanoscale electronic devices. Scanning gate microscopy （SGM） is one such gating technique that adds crucial spatial information, accessing the localized properties of semiconductor devices. Nanowires represent a central device concept due to the potential to combine very different materials. However, SGM on semiconductor nanowires has been limited to a resolution in the 50-100 nm range. Here, we present a study by SGM of newly developed III-V semiconductor nanowire InAs/GaSb heterojunction Esaki tunnel diode devices under ultra-high vacuum. Sub-5 nm resolution is demonstrated at room temperature via use of quartz resonator atomic force microscopy sensors, with the capability to resolve InAs nanowire facets, the InAs/GaSb tunnel diode transition and nanoscale defects on the device. We demonstrate that such measurements can rapidly give important insight into the device properties via use of a simplified physical model, without the requirement for extensive calculation of the electrostatics of the system. Interestingly, by precise spatial correlation of the device electrical transport properties and surface structure we show the position and existence of a very abrupt （〈10 nm） electrical transition across the InAs/GaSb junction despite the change in material composition occurring only over 30-50 nm. The direct and simultaneous link between nanostructure composition and electrical properties helps set important limits for the precision in structural control needed to achieve desired device performance.     

A model for the prediction of liquid–liquid interfacial energies

A model for the calculation of liquid–liquid interfacial energies is presented. It is based on the assumption that the interface can be treated as a separate thermodynamic phase. Its derivation has been performed in an analogous way as the derivation of the Butler equation for the surface tension of liquid alloys. It requires as input parameters the excess free energy and the compositions of the bulk phases as functions of temperature. In addition, it also requires the partial molar volumes of the components. Comparison with existing experimental data for Al–Pb, Al–In, and Cu–Co in a non-equilibrium state shows very good agreements. For Al–Bi, the experimental data are either over or underestimated by a factor of ≈1.7, depending on which of the two thermodynamic assessments is used. For the Al-based systems, the calculated Al-mole fraction in the interface layer is close to the arithmetic average of the Al-mole fractions of the bulk phases.     

Effect of four different size reduction methods on the particle size,solubility enhancement and physical stability of nicergoline nanocrystals

Nicergoline, a poorly soluble active pharmaceutical ingredient, possesses vaso-active properties which causes peripheral and central vasodilatation. In this study, nanocrystals of nicergoline were prepared in an aqueous solution of polysorbate 80 (nanosuspension) by using four different laboratory scale size reduction techniques: high pressure homogenization (HPH), bead milling (BM) and combination techniques (high pressure homogenization followed by bead milling HPH?+?BM, and bead milling followed by high pressure homogenization BM?+?HPH). Nanocrystals were investigated regarding to their mean particles size, zeta potential and particle dissolution. A short term physical stability study on nanocrystals stored at three different temperatures (4,?20 and 40?°C) was performed to evaluate the tendency to change in particle size, aggregation and zeta potential. The size reduction technique and the process parameters like milling time, number of homogenization cycles and pressure greatly affected the size of nanocrystals. Among the techniques used, the combination techniques showed superior and consistent particle size reduction compared to the other two methods, HPH?+?BM and BM?+?HPH giving nanocrystals of a mean particle size of 260 and 353?nm, respectively. The particle dissolution was increased for any nanocrystals samples, but it was particularly increased by HPH and combination techniques. Independently to the production method, nicergoline nanocrystals showed slight increase in particle size over the time, but remained below 500?nm at 20?°C and refrigeration conditions.