Nanoconfinement degradation in NaAlH4/CMK-1

An ordered mesoporous carbon scaffold (CMK-1) has been synthesized and infiltrated with NaAlH₄ nanoparticles by solvent- and melt-infiltration techniques. Small angle X-ray scattering (SAXS), powder X-ray diffraction (XRD), scanning electron microscopy (SEM), Transmission Electron Microscopy (TEM) and energy dispersive spectroscopy (EDS) are used to characterize the structure, composition and morphology before and after thermal treatment. This study illuminates some of the problems that can be associated with nanoconfinement of hydrogen storage materials including scaffold contamination, residual solvent contamination, sample morphology changes after heating, and other factors that can be detrimental to the application of these systems. Of particular interest is the expulsion of NaAlH₄ decomposition products from the scaffold after heating beyond its melting point under vacuum. This results in the surface of mesoporous carbon particles having arrays of multi-micron-long Al filaments that are >100 nm in diameter.     

Enhanced hydrogen reversibility of nanoconfined LiBH4–Mg(BH4)2

This study shows the hydrogen desorption kinetics and reversible hydrogen storage properties of 0.55LiBH₄–0.45Mg(BH₄)₂ melt-infiltrated in different nanoporous carbon aerogels with different BET surface areas of 689 or 2660 m²/g and pore volumes of 1.21 or 3.13 mL/g. These investigations clearly show a significantly improved hydrogen storage capacity after four cycles of hydrogen release and uptake for bulk 0.55LiBH₄–0.45Mg(BH₄)₂ and infiltrated in carbon aerogel and the high surface area scaffold, where 22, 36 and 58% of the initial hydrogen content remain after four cycles of hydrogen release and uptake, respectively. Nanoconfinement in high surface area carbon aerogel appears to facilitate hydrogen release illustrated by release of 13.3 wt% H₂ (93%) and only 8.4 wt% H₂ (58%) from bulk hydride in the first cycle using the same physical condition. Notably, nanoconfinement also appear to have a beneficial effect on hydrogen uptake, since 8.3 wt% H₂ (58%) is released from the high surface area scaffold and only 3.1 wt% H₂ (22%) from the bulk sample during the fourth hydrogen release.     

Chemometric analysis of mass spectra of cis and trans fatty acid picolinyl esters

Capillary GC of fatty acid methyl esters with MS detection only yields information about the molecular weight of the compound. However, if picolinyl esters of fatty acids are analysed in this way it is possible to obtain more information about their structure, perhaps even the cis or trans configuration. Picolinyl esters of fatty acids are prepared by adding carbonyl-diimidazole, 3-hydroxymethylpyridine and 4-pyrrolidin-o-pyridine to a solution of free fatty acids in dichloromethane. The picolinyl esters dissolved in heptane are then separated by capillary GC on a CP Sil 88 column equipped with a quadropole MS-detector. The mass spectra clearly show the molecular weight and the position of double bonds in the fatty acids, but whether the configuration is cis or trans is impossible to discern visually. However, with the use of principal component analysis, it is possible to distinguish between cis and trans fatty acids of C16:1, C18:1,n-9, C18:1,n-12, C18:2 and C22:1 in two- and three-dimensional score plots. With Soft Independent Modelling of Class Analogy (SIMCA), it is possible to calculate models that can predict from the mass spectra of unknown fatty acids whether they are of the cis or trans configuration, which is demonstrated for C18:1 trans from hardened margarine and butter.     

Enzymatic-fluorometric quantification of cholesterol in bovine milk

The present paper describes an enzymatic-fluorometric method for the determination of cholesterol in milk and other opaque matrices. The initial step of the method is to liberate chemically and physically bound cholesterol from the milk fat globule membrane by enzymatic action. The method is able to discriminate between esterified and free cholesterol in milk. The analysis is cost effective and is developed to work directly on whole, fresh milk thereby eliminating time consuming and tedious pre-treatment procedures of the sample. More than 1000 milk samples were analysed on the day of sampling. The total concentration of milk cholesterol ranged from 80 to 756μM (n=1068; mean 351μM). Milk cholesterol was significantly correlated to milk fat concentration as analysed by mid-infra red spectrometry (r=0.630; n=853) and by an enzymatic-fluorometric method (triacylglycerol) (r=0.611; n=842).     

Natural variation in biomarkers indicating mastitis in healthy cows

Dairy herds are expanding and, with increasing numbers of animals in each herd, there is a need for automatic recording of indicators in milk in order to detect mastitis, inflammation of the udder. A number of biomarkers for mastitis have been suggested over the years. Mastitis usually occurs in one of the four udder quarters and since it is now possible to milk each udder quarter separately in automated milking systems, it is important to evaluate the normal variation in the biomarkers at udder quarter level. This study evaluated the normal variations between milkings for some biomarkers in clinically healthy cows, determined by repeated somatic cell count and bacteriological analysis. The biomarkers studied were serum amyloid A (SAA), haptoglobin (Hp), lactate dehydrogenase (LDH), N-acetyl-β-D-glucosaminidase (NAGase) and alkaline phosphatase (AP), parameters that have been suggested as markers for mastitis. Ten cows were monitored on 42 consecutive milking occasions through collection of udder quarter milk samples and representative cow composite milk samples, giving a total of 2100 individual milk samples. Each cow had its individual profile for the concentrations and variations in the parameters analysed. Although there was relatively large variation between cows for the biomarkers analysed, the variation between milkings in clinically healthy quarters within cows was often below 10%. The biomarker with the lowest variation in this study was LDH. The results suggest that comparing quarters within an individual cow can identify deviations from the natural variations between milkings. This could be a valuable tool instead of, or in combination with, a cut-off value for each parameter in order to detect changes in the milk indicating mastitis.     

Detection of the voltage distribution in photovoltaic modules by electroluminescence imaging

We introduce an approach to determine the operating voltage of individual solar cells in photovoltaic (PV) modules by electroluminescence (EL) imaging. The highest EL signal of each solar cell is proportional to its operating voltage. Moreover the sum of all operating voltages equals the externally applied module voltage. Thus the operating voltage of individual solar cells is determined from the measured EL signal. The reliability of this relation is verified by measurements on specially prepared PV modules allowing us to measure the individual operating cell voltage. The experimentally measured cell voltages are deduced with an uncertainty of ±1% from an EL image. Moreover, the operating cell voltages determined from the EL image are used to calculate the module series resistance. Comparing experimentally determined values from the operating cell voltage and the total current flowing supplied to the module with calculated module series resistances using tabulated material and typical solar cell parameters, a very good correspondence is found. Copyright © 2010 John Wiley & Sons, Ltd.     

Surface-Enhanced Raman Scattering Detection of pH with Silica-Encapsulated 4-Mercaptobenzoic Acid-Functionalized Silver Nanoparticles

Sensors based upon surface-enhanced Raman spectroscopy (SERS) are attractive because they have narrow, vibrationally specific spectral peaks that can be excited using red and near-infrared light which avoids photobleaching, penetrates tissue, and reduces autofluorescence. Several groups have fabricated pH nanosensors by functionalizing silver or gold nanoparticle surfaces with an acidic molecule and measuring the ratio of protonated to deprotonated Raman bands. However, a limitation of these sensors is that macromolecules in biological systems can adsorb onto the nanoparticle surface and interfere with measurements. To overcome this interference, we encapsulated pH SERS sensors in a 30 nm thick silica layer with small pores which prevented bovine serum albumin (BSA) molecules from interacting with the pH-indicating 4-mercaptobenzoic acid (4-MBA) on the silver surfaces but preserved the pH-sensitivity. Encapsulation also improved colloidal stability and sensor reliability. The noise level corresponded to less than 0.1 pH units from pH 3 to 6. The silica-encapsulated functionalized silver nanoparticles (Ag-MBA@SiO(2)) were taken up by J774A.1 macrophage cells and measured a decrease in local pH during endocytosis. This strategy could be extended for detecting other small molecules in situ.