Evaluating π-π-Interactions as a Method for Isolation of Polycyclic Aromatic Hydrocarbons from Solution

The polycyclic aromatic hydrocarbon (PAH), chrysene, was linked to the solid support TentaGel S-NH₂ via a linker by means of synthesis. The resulting product 4-(chrysene-1-yloxy)-N-(TentaGel S)butanamide (4) was then evaluated for its ability to isolate PAHs from solution by means of π-π-interactions.     

Development of a Four-Channel Potentiostat for Amperometric Detection in Flow Injection Analysis

Abstract

A four-channel multipotentiostat has been developed for simultaneous voltammetric measurements with microelectrode arrays. To reduce the complexity of electrochemical cell, only one reference and one auxiliary electrode are used. The potential ranges of the four working electrodes may be independently controlled, but they are synchronously scanned by only one DAC. This is accomplished through a microcomputer interfaced with a PCL-711B data acquisition board, which allows the continuous monitoring of the currents and actual potentials of the working electrodes.

The system has been applied to the simultaneous determination of ascorbic and uric acids in synthetic samples. The measurements were carried out with gold microelectrodes modified by deposition of noble metals, which enhance the electrocatalysis and provide an anticipation and a better definition of the oxidation potentials. Recuperation of 98.2% and 97.8% for ascorbic and uric acids, respectively, was obtained by using amperometry.     

Stability of the chromia layer on steels in flowing nonequilibrium H2-H2O-CH4-CO mixtures at 950 °C

The stability of the protective oxide layer formed on Fe-12.5 pct Cr, Fe-18 pct Cr-10 pct Ni, and Fe-25 pct Cr-20 pct Ni was investigated in a flowing nonequilibrium H2-H2O-CH4-CO mixture at 950 °C. The samples were preoxidized in H2-H2O, and subsequently the carbon activity was raised in stepwise manner by adding methane. CO formation occurred on the sample surface by the catalytic reaction CH4 + H2O → CO + 3H2. The conversion of oxide to carbide commenced at the end of the sample wherePco has its highest andPH2O its lowest value. Oxidation, conversion, and catalytic reaction were monitored by gravimetric measurements and CO-determination during the experiments. Partial equilibria can be calculated for (ac)1 =K ₁ P _{ch 4}/(Ph2)2, (ac)2 =K2(PcoPh2)ph{2o}and(Po2)1\2 = K3Ph2o/Ph2. The conversion of oxide to carbide started when the steady state ofac and(Po2)1/2 on the surface approached the value for the equilibrium of chromium oxide and chromium carbide. The results show that this steady state value is much nearer to the point(ac)2-(Po2)1/2 in the thermochemical stability diagram than to the point (ac)1 — (Po ₂)^1/2- The oxide layers were stable even at very high values of (ac)₁ which demonstrates that there is only very little interaction of CH₄ with the oxide surface. P. C. Prasannan formerly Research Scientist at the Max-Planck-Institut für Eisenforschung This paper is based on a presentation made at the “Stephen R. Shatynski Memorial Symposium on Surfaces and Interfaces” held at the 114th annual AIME meeting in New York, February 24-28, 1985, under the auspices of the ASM-MSD Thermodynamic Activity Committee.     

Green State Joining of Silicon Carbide Using Polycarbosilane

Green state joining of SiC was investigated using a paste consisting of polycarbosilane polymer and SiC powder. The joining process and densification were described. Initial experiments resulted in the formation of symmetrical black bands and cracks on both sides of the joint. However, with modifications in processing conditions, the cracks were eliminated and the resulting joints were indistinguishable from the matrix. The flexural strength of joined samples was measured to be 234 MPa, which was comparable to that of the control sample with similar density. As the applied pressure during joining was increased from 34 to 138 MPa, the strength of the joined samples increased from 180 to 250 MPa.     

Intentional ρ-type doping by carbon in metalorganic MBE of GaAs

We report on the intentional ρ-type doping of GaAs layers grown in an UHV system from molecular beams of arsine (AsH₃) and mixtures of frimethyl gallium (TMG) and friethyl gallium (TEG). The entire doping range between 10¹⁴ cm^-3 (growth from pure TEG) and 10²⁰ cm^-3 (growth from pure TMG) can be covered by using mixtures of TMG and TEG. As revealed by SIMS and photoluminescence (PL) carbon is the dominant acceptor in the layers. Comparison of the Hall mobility and of the PL spectra shows that the quality of our films equals that of the best LPE and MBE grown ρ-type GaAs layers.     

Electrorheological properties of kaolinite,polyindole, and polyindole/kaolinite composite suspensions

In this study, polyindole (PIN) and polyindole/kaolinite (PIN/KAO) composite were synthesized by free radical polymerization using FeCl₃ as an initiator. Average particle sizes (d₅₀) of PIN and PIN/KAO composite were determined by dynamic light scattering (DLS) as 7.2 and 6.2 μm, respectively. The samples were characterized by FTIR, elemental analysis, DSC/TGA and SEM measurements. Suspensions of KAO, PIN, and PIN/KAO composite were prepared in silicone oil (SO) and the sedimentation stabilities were determined. Electrorheological (ER) properties of these suspensions were studied as a function of dispersed phase concentration, shear rate, shear stress, and temperature; and yield stresses and excess shear stresses determined. Further, dielectric properties of KAO, PIN, and PIN/KAO composite were investigated. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007     

The reality of fluid-wave resonance frequencies on a cylindrical shell

Summary The existence of a unique axisymmetric non-radiating surface wave near a cylindrical elastic shell submerged in a fluid and described by Kennard's model is proved.     

Review of free software tools for image analysis of fluorescence cell micrographs

An increasing number of free software tools have been made available for the evaluation of fluorescence cell micrographs. The main users are biologists and related life scientists with no or little knowledge of image processing. In this review, we give an overview of available tools and guidelines about which tools the users should use to segment fluorescence micrographs. We selected 15 free tools and divided them into stand‐alone, Matlab‐based, ImageJ‐based, free demo versions of commercial tools and data sharing tools. The review consists of two parts: First, we developed a criteria catalogue and rated the tools regarding structural requirements, functionality (flexibility, segmentation and image processing filters) and usability (documentation, data management, usability and visualization). Second, we performed an image processing case study with four representative fluorescence micrograph segmentation tasks with figure‐ground and cell separation. The tools display a wide range of functionality and usability. In the image processing case study, we were able to perform figure‐ground separation in all micrographs using mainly thresholding. Cell separation was not possible with most of the tools, because cell separation methods are provided only by a subset of the tools and are difficult to parametrize and to use. Most important is that the usability matches the functionality of a tool. To be usable, specialized tools with less functionality need to fulfill less usability criteria, whereas multipurpose tools need a well‐structured menu and intuitive graphical user interface.