Sensing the physicochemical nature of he and ne in micropores by adsorption measurements

He and Ne in contact with molecular sieves in the form of crystalline A zeolites and amorphous carbon molecular sieves fibers (CMSF) were studied by adsorption measurements. Classification of the effective enclosure of zeolitic apertures and of graphitic constrictions, as determined by recent temperature-programmed desorption mass spectrometry (TPD-MS) studies of adsorption of He and Ne onto these materials, was utilized in making a prudent choice of samples and experimental conditions. In view of the former TPD information, the behaviors of adsorption and volumetric measurements reported herein are straightforwardly interpreted. The combined TPD, adsorption isotherms, and dead volume data deepen the understanding of the physicochemical nature of adsorbed gas, where gas adsorption in the vicinity of pore constrictions and/or apertures as well as on the inner surface areas of pores and/or cages could be resolved. Previous conclusions that the huge activation energies measured for Ne/CMSF at high temperatures are unlikely to characterize chemical desorption but reflect those required for overcoming the barrier of effectively constricted apertures were confirmed by the volumetric data presented here. At 77 K, considerable He adsorption was observed in the porous solids and found to be responsible for abnormal deduced values of dead volumes. The occurrence of significant adsorption of He onto A zeolites and CMSF at 77 K warrants the realization that in cases concerning porous materials, volumetrically deduced quantities should not be taken for granted, but should be carefully considered and uniquely interpreted in relation to the specific experimental conditions under which they are taken.     

Electron-impact induced rearrangements in isomeric pyridine aldoximes

The mass spectra of α-, β- and γ-pyridine aldoximes and the respective O-methyl ethers were studied. The mass spectral behaviour of α-pyridine aldoxime is characterized by the elimination of NO, while the molecular ion of the γ-isomer expels H₂ CN. In the case of the β-isomer the formation of the m/e 67 ion (C₄H₅N) in a concerted process is the main feature. In the α-pyridine aldoxime methyl ether, in sharp contrast to the hydroxy analog, the M-30 peak was found to be due to the elimination of CH₂O, the expulsion of NO being absent. The mechanism of the fragmentation reactions is discussed, the conclusion drawn being based on the high resolution measurements as well as on the spectra of the respective deuterioanalogs and on the metastable transitions.     

Multichannel homogeneous immunoassay for detection of 2,4,6-trinitrotoluene (TNT) using a microfabricated capillary array electrophoresis chip

A high-throughput homogeneous immunoassay for the sensitive detection of 2,4,6-trinitrotoluene (TNT) has been developed using radial capillary array electrophoresis microdevices. Samples consisting of equilibrium mixtures of anti-TNT antibody (Ab), fluorescein-labeled TNT, and various concentrations of unlabeled TNT were electrokinetically injected into 48 channels of a radial capillary array electrophoresis microchannel plate. The rapid electrophoretic separation allows us to analyze the equilibrium ratio formed by the competition between the labeled and the unlabeled TNT for Ab binding. The simultaneous parallel TNT separations facilitate determination of a calibration curve for the TNT assay, which has high sensitivity (LOD, 1 ng/mL) and a wide dynamic range (1-300 ng/mL).     

A new route of oxygen isotope exchange in the solid phase: demonstration in CuSO4.5H2O

Temperature-programmed desorption mass spectrometry (TPD-MS) measurements on [(18)O]water-enriched copper sulfate pentahydrate (CuSO(4).5H(2)(18)O) reveal an unambiguous occurrence of efficient oxygen isotope exchange between the water of crystallization and the sulfate in its CuSO(4) solid phase. To the best of our knowledge, the occurrence of such an exchange was never observed in a solid phase. The exchange process was observed during the stepwise dehydration (50-300 degrees C) of the compound. Specifically, the exchange promptly occurs somewhere between 160 and 250 degrees C; however, the exact temperature could not be resolved conclusively. It is shown that only the fifth, sulfate-associated, anionic H(2)O molecule participates in the exchange process and that the exchange seems to occur in a preferable fashion with, at the most, one oxygen atom in SO(4). Such an exchange, occurring below 250 degrees C, questions the common conviction of unfeasible oxygen exchange under geothermic conditions. This new oxygen exchange phenomenon is not exclusive to copper sulfate but is unambiguously observed also in other sulfate- and nitrate-containing minerals.     

Oxidation of Ascorbate by Ni(III) Complexes with Tetraaza-macrocyclic Ligands in Neutral Aqueous Solutions. A Pulse-Radiolysis Study

Abstract

The mechanisms and kinetics of oxidation of ascorbate, AH^?, by Ni(III)Lⁱ _aq and by LⁱNi(III) (HPO₄)₂ ^? complexes (L¹ = meso-(5,12)-7,7,14,14-hexamethyl-1,4,8,11-tetraazacyclotetradecane; L² = 1,8-dimethyl-1,3,6,8,10,13-hexaazacyclotetradecane) in neutral aqueous solutions have been investigated.

The oxidation of ascorbate by the LⁱNi(III) (HPO₄)₂ ^? and Ni(III)L¹ _aq proceeds via two consecutive reactions well separated in time. The products of the first reaction are the A^.? radical anion and the corresponding Ni(II) complex. The oxidations by the LⁱNi(III)(HPO₄)₂ ^? complexes proceed via the outer sphere mechanism, whereas the detailed mechanism of reaction of Ni(III)L¹ _aq cannot be determined. The rate of reaction decreases with the increase in the concentration of phosphate, thus indicating that LⁱNi(III)(HPO₄)(H₂O)⁺ and LⁱNi(III)OH²⁺ are stronger oxidizing agents than LⁱNi(III)(HPO₄)^? ₂.

The oxidation of ascorbate by Ni(III)L² _aq proceeds via three consecutive reactions which are well separated in time. Thus the results clearly point out that this process occurs via the inner sphere mechanism. The first transient observed is tentatively identified as L²(H₂O)Ni(II)(A^.?)²⁺, i.e., an unexpected complex of the ascorbate anion radical. Also in this process the last transient observed is the A^.? anion radical. The stabilization of the ascorbyl radical in a transient complex might be of biological significance.     

Black Holes Are One-Dimensional

The holographic principle has revealed that phyical systems in 3-D space, black holes included, are basically two-dimensional as far as their information content is concerned. This conclusion is complemented by one sketched here: as far as entropy or information flow is concerned, a black hole behaves as a one-dimensional channel. We define a channel in flat spacetime in thermodynamic terms, and contrast it with common entropy emitting systems. A black hole is more like the former: its entropy output is related to the emitted power as it would be for a one-dimensional channel, and disposal of an information stream down a black hole is limited by the power invested in the same way as for a one-dimensional channel.     

On whistling of pipes with a corrugated segment: Experiment and theory

Corrugated pipes are commonly used because of their local rigidity combined with global flexibility. The flow through such a pipe can induce strong whistling tones, which is an environmental nuisance and can be a threat to the mechanical integrity of the system. This paper considers the use of a composite pipe: a shorter corrugated pipe segment embedded between smooth pipe segments. Such a pipe retains some flexibility, while the acoustical damping in the smooth pipe reduces whistling tones. Whistling is the result of coherent vortex shedding at the cavities in the wall. This vortex shedding is synchronized by longitudinal acoustic waves traveling along the pipe. The acoustic waves trigger the vortex shedding, which reinforces the acoustic field for a critical range of the Strouhal number values. A linear theory for plane wave propagation and the sound production is proposed, which allows a prediction of the Mach number at the threshold of whistling in such pipes. A semi-empirical approach is chosen to determine the sound source in this model. This source corresponds to a fluctuating force acting on the fluid as a consequence of the vortex shedding. The functional form of the Strouhal number dependency of the dimensionless sound source amplitude is based on numerical simulations. The magnitude of the source and the Strouhal number range in which it can drive whistling are determined by matching the model to results for a specific corrugated pipe segment length. This semi-empirical source model is then applied to composite pipes with different corrugated segment lengths. In addition, the effect of inlet acoustical convective losses due to flow separation is considered. The Mach number at the threshold of whistling is predicted within a factor 2.     

Scale-invariant correlations in dynamic bacterial clusters

In Bacillus subtilis colonies, motile bacteria move collectively, spontaneously forming dynamic clusters. These bacterial clusters share similarities with other systems exhibiting polarized collective motion, such as bird flocks or fish schools. Here we study experimentally how velocity and orientation fluctuations within clusters are spatially correlated. For a range of cell density and cluster size, the correlation length is shown to be 30% of the spatial size of clusters, and the correlation functions collapse onto a master curve after rescaling the separation with correlation length. Our results demonstrate that correlations of velocity and orientation fluctuations are scale invariant in dynamic bacterial clusters.     

Scheduling programs with repetitive projects: A comparison of a simulated annealing,a genetic and a pair-wise swap algorithm

We address the problem of scheduling in programs involving the production of multiple units of the same product. Our study was motivated by a construction program for fast naval patrol boats. Other applications of this problem include procurement of multiple copies of aircraft, spacecraft, and weapon systems. In this problem we must decide how many units of the product to assign to each of a number of available crews (individuals, teams, subcontractors, etc.). These types of problems are characterized by two potentially conflicting considerations: 1) the need to complete each unit by its contractual due date, and 2) learning effects. Because of the first consideration, there is a tendency to use multiple crews for simultaneous production, so that meeting due dates is assured. However, the second consideration encourages assigning many units to a single crew so that learning effects are maximized. We study this scheduling problem with two different penalty cost structures and develop models for both versions. The models trade-off the penalty associated with late deliveries and the savings due to learning (and possibly incentive payments for early completion). We discuss different heuristic algorithms — simulated annealing, a genetic algorithm, and a pair-wise swap heuristic — as well as an exhaustive search to determine a baseline for comparisons. Our computational results show that the pair-wise swap algorithm is the most efficient solution procedure for these models.     

Propagation of avalanches in Mn12-acetate: magnetic deflagration

Local time-resolved measurements of fast reversal of the magnetization of single crystals of Mn12-acetate indicate that the magnetization avalanche spreads as a narrow interface that propagates through the crystal at a constant velocity that is roughly 2 orders of magnitude smaller than the speed of sound. We argue that this phenomenon is closely analogous to the propagation of a flame front (deflagration) through a flammable chemical substance.