General contribution of nonspecific interactions to fluorescence intensity

Many chemical compounds, including nonfluorescent ones, induce changes in the fluorescence spectra of certain probes, such as berberine cation and Reichardt's betaine, both in the absence and the presence of solvent, that affect almost exclusively emission intensity. In this work, the application of fluorescence detection by intensity changes (FDIC) to HPLC and TLC chromatographic systems with fluorescence detectors has been studied. FDIC detection is of special interest in detecting nonfluorescent analytes, either in HPLC or in TLC mode. It does not involve covalent interactions, and the dielectric permittivity (epsilon) of the medium plays an important role. The balance between nonspecific and specific interactions produces either an increase or a decrease in fluorescence intensity. Therefore, the influence of chromatographic conditions and chemical structure of analytes on the sign and magnitude of fluorescence peaks for sample detection in HPLC and TLC systems has been discussed. In general, probe nature and concentration determine response and detection sensitivity for a given sample in TLC and HPLC. As solubility and fluorescence properties in solvents determine the operating conditions for a FDIC probe in HPLC mode, nature and flows of mobile phase and solvent are important for chromatographic response and detection sensitivity.     

Macroporous hydrogels based on 2-hydroxyethyl methacrylate. Part 5: Hydrolytically degradable materials

Macroporous hydrogels based on 2-hydroxyethyl methacrylate, 2-ethoxyethyl methacrylate and N-(2-hydroxypropyl)methacrylamide, methacrylic acid and [2-(methacryloyloxy)ethyl]trimethylammonium chloride crosslinked with N,O-dimethacryloylhydroxylamine were prepared. Hydrogels were degraded in a buffer of pH 7.4. Completely water-soluble polymers were obtained over time periods ranging from 2 to 40 days. The process of degradation was followed gravimetrically and by optical and electron microscopy. In vivo biological tests with hydrogels based on copolymers of 2-ethoxyethyl methacrylate/N-(2-hydroxypropyl)methacrylamide were performed.     

Chiral switching by spontaneous conformational change in adsorbed organic molecules

Self-assembly of adsorbed organic molecules is a promising route towards functional surface nano-architectures, and our understanding of associated dynamic processes has been significantly advanced by several scanning tunnelling microscopy (STM) investigations. Intramolecular degrees of freedom are widely accepted to influence ordering of complex adsorbates, but although molecular conformation has been identified and even manipulated by STM, the detailed dynamics of spontaneous conformational change in adsorbed molecules has hitherto not been addressed. Molecular surface structures often show important stereochemical effects as, aside from truly chiral molecules, a large class of so-called prochiral molecules become chiral once confined on a surface with an associated loss of symmetry. Here, we investigate a model system in which adsorbed molecules surprisingly switch between enantiomeric forms as they undergo thermally induced conformational changes. The associated kinetic parameters are quantified from time-resolved STM data whereas mechanistic insight is obtained from theoretical modelling. The chiral switching is demonstrated to enable an efficient channel towards formation of extended homochiral surface domains. Our results imply that appropriate prochiral molecules may be induced (for example, by seeding) to assume only one enantiomeric form in surface assemblies, which is of relevance for chiral amplification and asymmetric heterogenous catalysis.     

Effects of ethanol-blended gasoline on emissions of regulated air pollutants and carbonyls from motorcycles

The emission characteristics of regulated air pollutants and carbonyls from motorcycles using gasoline blended with 3% ethanol (E3) and gasoline (E0) were investigated in this study. Nine motorcycles were operated on a chassis dynamometer and driven according to the ECE driving cycle for air pollutant measurements. In addition, durability testing was performed on two brand-new motorcycles of the same model, using E3 in one and E0 in the other, to assess the effects of E3 usage on motorcycle emissions. The results show that average emission factors of CO and THC decreased by 20.0% and 5.27%, respectively, using E3 fuel. However, NO_x and CO₂ emission increased by 5.22% and 2.57%. The results of paired t-tests indicate that only the reduction of CO emission is statistically significant (p-value = 0.006). The emission factors of ∑15 carbonyls for the nine test motorcycles were 1289 ± 502 and 1579 ± 368 μg/km for E0 and E3, respectively. Carbonyl emission increased by 22.5% using E3 substituted for E0. However, the differences in ∑15 carbonyl emission between E0 and E3 were not statistically significant (p-value = 0.137). Among the 15 analyzed carbonyls, only the emission of acetaldehyde was significantly higher (p-value = 0.014) with E3. The results of durability tests show that deterioration coefficients for E3 were 1.50, 1.45, 0.84, 0.94 and 1.06 for CO, THC, NO_x, CO₂ and carbonyls, respectively. Statistical tests exhibit that using E3 as fuel does not increase the regulated air pollutants, nor carbonyl emissions for the durability test.     

Radiation doses to Norwegian heart-transplanted patients undergoing annual coronary angiography

Heart-transplanted patients in Norway undergo annual coronary angiography (CA). The aims of this study were to establish a conversion factor between dose-area product and effective dose for these examinations and to use this to evaluate the accumulated radiation dose and risks associated with annual CA. An experienced cardiac interventionist performed a simulated examination on an Alderson phantom loaded with thermoluminescence dosemeters. The simulated CA examination yielded a dose-area product of 17 Gy cm(2) and an effective dose of 3.4 mSv: the conversion factor between dose-area product and effective dose was 0.20 mSv Gy cm(-2). Dose-area product values from 200 heart-transplanted patients that had undergone 906 CA examinations between 2001 and 2008 were retrieved from the institutional database. Mean dose-area product from annual CA was 25 Gy cm(2), ranging from 2 to 140 Gy cm(2). Mean number of CA procedure was 8 (range, 1-23). Mean accumulated effective dose for Norwegian heart-transplanted patients between 2001 and 2008 was 34 mSv (range, 5-113 mSv). Doses and radiation risks for heart-transplanted patients are generally low, because most heart transplantations are performed on middle-aged patients with limited life expectancy. Special concern should however be taken to reduce doses for young heart-transplanted patients who are committed to lifelong follow-up of their transplanted heart.     

Improving Product Quality and Reliability with Customer Experience Data

Advance technology development and wide use of the World Wide Web have made it possible for new product development organizations to access multi‐sources of data‐related customer complaints. However, the number of customer plaints of highly innovative consumer electronic products is still increasing; that is, product quality and reliability is at risk. This article aims to understand why existing solutions from literature as well as from industry to deal with these increasingly complex multiple data sources are not able to manage product quality and reliability. Three case studies in industry are discussed. On the basis of the case study results, this article also identifies a new research agenda that is needed to improve product quality and reliability under this circumstance. Copyright © 2011 John Wiley & Sons, Ltd.     

Identification of clay minerals by infrared spectroscopy and discriminant analysis

Identification of clay minerals based on chemometric analysis of measured infrared (IR) spectra was suggested. IR spectra were collected using the diffuse reflection technique. Discriminant analysis and principal component analysis were used as chemometric methods. Four statistical models were created for separation and identification of clay minerals. More than 50 samples of various clay mineral standards from different localities were used for the creation of statistical models. The results of this study confirm that the discriminant analysis of IR spectra of clay minerals could provide a powerful tool for identification of clay minerals. Differentiation of muscovite from illite and identification of mixed structures of illite-smectite were achieved.     

Critical Aspects of Alloying of Sintered Steels with Manganese

This study examines the sintering behavior and properties of Fe-0.8Mn-0.5C manganese powder metallurgy steels. The study focuses on the influence of mode of alloying—admixing using either high-purity electrolytic manganese or medium carbon ferromanganese as well as the fully prealloying of water-atomized powder. Three main aspects were studied during the whole sintering process—microstructure development, interparticle necks evolution, and changes in the behavior of manganese carrier particles during both heating and sintering stages. The prealloyed powder shows considerable improvement in carbon homogenization and interparticle neck development in comparison with admixed materials. The first indication of pearlite for the fully prealloyed material was registered at ~1013 K (740 °C) in comparison with ~1098 K (825 °C) in the case of the admixed systems. The negative effect of the oxidized residuals of manganese carrier particles and high microstructure inhomogeneity, which is a characteristic feature of admixed systems, is reflected in the lower values of the mechanical properties. The worst results in this respect were obtained for the system admixed with electrolytic manganese because of more intensive manganese sublimation and resulting oxidation at lower temperatures. According to the results of X-ray photoelectron spectroscopy and high-resolution scanning electron microscopy and energy dispersive X-ray analyses, the observed high brittleness of admixed materials is connected with intergranular decohesion failure associated with manganese oxide formation on the grain boundaries.     

Filtration Efficiency of Functionalized Ceramic Foam Filters for Aluminum Melt Filtration

Metallurgical and Materials Transactions B - The influence of filter surface chemistry on the filtration efficiency of cast aluminum alloys was evaluated for four different filter coating...     

Compensation of Pinhole Defects in Food Packages by Application of Iron‐based Oxygen Scavenging Multilayer Films

To protect sensitive food products from oxidative deterioration, multilayer barrier film systems and also modified atmosphere packaging are widely applied. However, the preservation of food quality in such packaging systems may be compromised by the presence of defects in the sealing layer of the films, especially when these are below a critical size, typically the detection limit of standard leak testers of 10 µm. The addition of an oxygen scavenger (OS) layer in barrier film structures could therefore provide extended protection against O₂ penetration through such defects. In this study, O₂ absorption of different multilayer film structures including an iron‐based OS were investigated under defined gas atmospheres. Measurement cells were thereby covered with plastic films of defined O₂ permeability to simulate conditions in a food package during storage with pinhole defect sizes of 10 and 17 µm. The results indicated that the OS film structures applied could only compensate for a defect size of 10 µm in the sealing layer. Analysis of the O₂ absorption of different multilayer film structures at 85% and 100% relative humidity showed that higher humidity accelerates the activation of the scavenger. After full activation, the scavenger kinetics are the same for 85% and 100% relative humidity. Long‐term storage experiments using the most effective film structure from the preliminary experiments were carried out to compare O₂ absorption of a snack food product in packages with and without an OS. The analyzed linear gradient of the reaction of the OS film and food product, respectively, indicated first‐order reaction kinetics with corresponding reaction constants calculated to be K (food product) 0.021 mg (O₂) mbar (O₂)^?1 day^?1 and K (OS film) 0.066 mg (O₂) mbar (O₂)^?1 day^?1. The reaction velocity of the OS was thus three times faster than that of the food. The applicability of OS multilayer film systems to compensate a critical pinhole defect size of 10 µm for sensitive food products could therefore be confirmed. The measurement of quality parameters for the status of lipid oxidation processes would help to verify this result. Copyright © 2012 John Wiley & Sons, Ltd.