3D‐morphology reconstruction of nanoscale phase‐separation in polymer memory blends

In many organic electronic devices functionality is achieved by blending two or more materials, typically polymers or molecules, with distinctly different optical or electrical properties in a single film. The local scale morphology of such blends is vital for the device performance. Here, a simple approach to study the full 3D morphology of phase‐separated blends, taking advantage of the possibility to selectively dissolve the different components is introduced. This method is applied in combination with AFM to investigate a blend of a semiconducting and ferroelectric polymer typically used as active layer in organic ferroelectric resistive switches. It is found that the blend consists of a ferroelectric matrix with three types of embedded semiconductor domains and a thin wetting layer at the bottom electrode. Statistical analysis of the obtained images excludes the presence of a fourth type of domains. The criteria for the applicability of the presented technique are discussed. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2015 , 53, 1231–1237     

Preparing Science Teachers in an Era of Reform: Practitioners' Perspectives of Methods Courses

With recent national calls for the reform of science education have come standards that delineate not only science content but also assessment, pedagogy, and teachers’ professional development. If teachers must teach science differently, then teacher preparation must change. This study asked 31 inservice secondary science teachers to complete a survey about topics for inclusion in a secondary science methods course. Respondents ranked a list of prespecified topics and had an opportunity to suggest other topics for inclusion in the course. Results showed that the majority of prespecified potential topics were judged important enough by these teachers to warrant inclusion in a methods course, though no individual added topic appeared on more than two surveys. Results demonstrate that these teachers believe teaching many of the traditional topics in science methods courses is still needed. In addition, they advocated the inclusion of several topics that either represent recent technological and theoretical advances, or longstanding ideas that have recently received considerable attention.     

Fast atom bombardment mass spectra of keto acid and keto ester phosphoranes

Positive-ion fast atom bombardment mass spectra of 13 keto acid and keto ester phosphoranes were examined. All compounds gave a protonated molecular ion and characteristic peaks at m/z 303, 279, 262 and 201.     

Collision Avoidance in Bi-Directional AGV Systems

The use of a bi-directional, as opposed to a one-way, transportation system, can increase the operational efficiency of automated guided vehicles in both manufacturing and warehousing environments. However, the full potential will only be realized if the routeing algorithms pay particular attention to the problem of collision avoidance. This paper is concerned with the development of such an algorithm. The method is based on the use of delays and deviations to avoid collisions that could arise when using the shortest routes for each vehicle, and is applicable to any transportation system which can be represented as a network with known travel times.     

Monofunctionalised resorcinarenes

A convenient methodology for introducing single functional groups to the lower rim of resorcinarenes is described. The methodology allows for very convenient differential protection or derivatisation of the upper and lower rims, and a wide range of functional groups (alcohol, carboxylic acid, thiol, amine, carbamate, alkyl halide) can be incorporated as a single unit at the lower rim, opening up the way to further modification at this point and generally widening the scope for further utilising resorcinarenes. Furthermore, our approach has enabled us to link two resorcinarenes together to form novel resorcinarene dimers.     

Determination of 11 aminoglycosides in meat and liver by liquid chromatography with tandem mass spectrometry

A method using liquid chromatography with tandem mass spectrometry was developed for the determination of 11 commonly used aminoglycoside antibiotics in meat. The proposed method is sufficiently sensitive (detection limits of 15 to 40 ppb for the various antibiotics) and highly selective. It is suitable for the quantitation and confirmation of aminoglycosides in a variety of matrixes (pork muscle, fish, and veal liver). Any multiresidue method for aminoglycosides must take into account their high affinity toward sample proteins and the significantly different pK values of the various analytes. The developed method uses a low-pH extraction with trichloracetic acid to ensure complete extraction of the analytes from the matrix. An anion-exchange step is used to remove the acid from the centrifuged extract. Aminoglycosides in this solution of low ionic strength can be quantitatively retained and afterwards eluted from a weak cation-exchanger solid-phase extraction (SPE) cartridge. The highly selective SPE steps produce clean extracts, which minimize possible suppression of the mass spectrometer signal.     

Competitive formation of helical cycloocta- and cyclododecapyrroles

In connection with a study aimed at the evaluation of electronic effects in spiro-dicorrole (1a) and its binuclear Ni(II) complex (1b) we became interested in gem-dimethyl-substituted cyclotetrapyrrole (2a) and the corresponding Ni(II) complex (2b). Attempts to prepare 2a as the 12,13,16,17-tetraethyl-2,3,7, 8-tetramethyl derivative (5) by an acid-catalyzed (1 + 1) condensation of dimethyldipyrrylmethane 3 and diformylbipyrrole 4 resulted in the formation of the (2 + 2) and (3 + 3) condensation products, i.e., the cyclooctapyrrole 6 and the cyclododecapyrrole 7, respectively, rather than in that of the desired gem-dimethyl cyclotetrapyrrole. The cyclododecapyrrole 7, isolated as the major product, is among the largest cyclopolypyrroles known to date. These two new macrocycles have been structurally characterized by variable temperature 1D and 2D NMR experiments, as well as by single-crystal X-ray diffraction analysis. In solution both the cyclooctapyrrole 6 and cyclododecapyrrole 7 exhibit dynamic behavior. At 337 K 6 adopts a D(2)-symmetric conformation, whereas at 196 K two equivalent C(2) conformers that interconvert through the D(2)-symmetric intermediate are observed. The energy barrier for the interconversion process between these two degenerate conformers is found to be 10.6 kcal mol(-)(1). The solution dynamics of 7 could be described in an analogous manner, with the time-averaged conformation at 378 K displaying D(3)(h)() symmetry. X-ray analyses showed that for both macrocycles, 6 and 7, the solid state structures were nearly identical to the low-temperature solution conformers.     

Fundamental studies of mixed-gas inductively coupled plasmas

The effects of adding foreign gases to the central-gas flow or the intermediate-gas flow of an argon inductively coupled plasma are presented. In particular, the influence of up to 16.7% added helium, nitrogen or hydrogen on radially-resolved electron number density, electron temperature, gas-kinetic temperature and calcium ion emission profiles is examined. It is shown that these gases affect not only the fundamental parameters and bulk properties of the plasma, but also how energy is coupled and transported through the discharge and how that energy interacts with the sample. For example, added helium causes an increase in the gas-kinetic temperature, most likely due to the higher thermal conductivity of helium compared to argon but, in general, does not appear to affect significantly either the electron temperature or electron concentration. The shift in the calcium ion emission profile towards lower regions in the discharge with added helium may be attributable to higher droplet desolvation and particle vaporization rates. In contrast, the addition of nitrogen or hydrogen to an Inductively Coupled Argon Plasma (Ar ICP) results in dramatic changes in all three fundamental plasma parameters: electron number density, electron temperature, and gas-kinetic temperature. The net effect of these molecular gases (N₂ or H₂) on calcium ion emission and on the fundamental plasma parameters is shown to be dependent on the amount of gas added to the plasma and whether the gas is introduced as part of the central- or intermediate-gas flow. In general, nitrogen added to the central-gas flow causes a significant reduction in the number of electrons throughout most of the discharge (over an order of magnitude in certain regions), mainly in the central and upper zones of the ICP. A drop of 3000–5000 K in the central channel electron temperature and a smaller drop in the gas-kinetic temperature are also observed when N₂ is added to the central-gas flow. In contrast, the introduction of nitrogen in the intermediate flow causes about a 1 × 10¹⁵ electrons cm⁻³ increase in the electron concentration in the low, toroidal regions of the plasma and an increase in the gas-kinetic temperature of around 1000 K throughout most of the discharge. As seen with the addition of nitrogen to the central-gas flow, the electron temperature is found to increase in the toroidal zones of the plasma when N₂ is added to the intermediate flow. These combined effects cause a 20-fold depression in the calcium ion emission intensity only a 1.7-fold depression when N₂ is added to the central- or intermediate-gas flows, respectively. On the other hand, hydrogen causes a depression in the electron concentration in the upper areas of the plasma when this gas is added to the central flow but increases the number of electrons in the same region when added to the intermediate flow. Hydrogen also causes a dramatic effect on the electron and gas-kinetic temperatures, significantly increasing both of these parameters throughout the discharge. An increase in the calcium ion emission intensity, accompanied by a downward shift, elongation and broadening of the calcium ion emission profile is also observed with H₂ addition.     

Analysis of betamethasone, dexamethasone and related compounds by liquid chromatography/electrospray mass spectrometry

A reversed-phase high-performance liquid chromatography/electrospray ionisation mass spectrometry (HPLC/ESI-MS) method has been developed to conclusively differentiate the epimers betamethasone and dexamethasone and various esterification products (betamethasone and dexamethasone 21-acetate, betamethasone and dexamethasone 21-phosphate, betamethasone 17-valerate, betamethasone 21-valerate and betamethasone 17,21-dipropionate) in counterfeit drugs. Good separation with baseline resolution of all epimers or isomers was obtained on a Zorbax Eclipse XDB or Luna C8 column, using a step gradient with mobile phases of 0.05 M ammonium acetate and acetonitrile. Betamethasones can also be distinguished by the relative abundance of their m/z 279 ion in the positive electrospray tandem mass spectra. The LC/MS or LC/MS/MS method developed was successfully applied to the analysis of drug product samples, i.e. creams and tablets.