The adsorption and condensed film formation of cetyltrimethylammonium bromide at the mercury/electrolyte interface

The adsorption of cetyltrimethyammonium bromide (CTAB) on a hanging mercury electrode is studied in various electrolyte systems and temperatures. A condensed film is formed at negative potentials and at room temperature only in the presence of KBr. The decrease of the temperature favors the formation of the condensed film. Hysterisis phenomena are observed during the potential scans at both directions. Capacity time curves at the potentials where the film is formed show a nucleation and growth mechanism, with induction time depending on potential, which has been investigated using Avrami formulation and has been explained as a progressive one-dimensional nucleation with constant growth rate. The nucleation rate increases while moving toward more negative potentials. A linear decrease of the capacitance with time was observed in some cases independent of the measuring potential in a relative large potential range. The different types of micelles can affect the adsorption of CTAB on mercury. An unusual capacitance transient observed at a very narrow negative potential range is attributed to the formation of hemicylinders. The condensed film in the presence of the other electrolytes is observed only at high concentrations (1 M) and very low temperatures (5 degrees C).     

Hyperpolarization of Amino Acids in Water Utilizing Parahydrogen on a Rhodium Nanocatalyst

NMR offers many possibilities in chemical analysis, structural investigations, and medical diagnostics. Although it is broadly used, one of NMR spectroscopies main drawbacks is low sensitivity. Hyperpolarization techniques enhance NMR signals by more than four orders of magnitude allowing the design of new contrast agents. Parahydrogen induced polarization that utilizes the para-hydrogen's singlet state to create enhanced signals is of particular interest since it allows to produce molecular imaging agents within seconds. Herein, we present a strategy for signal enhancement of the carbonyl ¹³C in amino acids by using parahydrogen, as demonstrated for glycine and alanine. Importantly, the hyperpolarization step is carried out in water and chemically unmodified canonical amino acids are obtained. Our approach thus offers a high degree of biocompatibility, which is crucial for further application. The rapid sample hyperpolarization (within seconds) may enable the continuous production of biologically useful probes, such as metabolic contrast agents or probes for structural biology.     

Uniqueness of reconstruction of multiphase morphologies from two-point correlation functions

The restoration of the spatial structure of heterogeneous media, such as composites, porous materials, microemulsions, ceramics, or polymer blends from two-point correlation functions, is a problem of relevance to several areas of science. In this contribution we revisit the question of the uniqueness of the restoration problem. We present numerical evidence that periodic, piecewise uniform structures with smooth boundaries are completely specified by their two-point correlation functions, up to a translation and, in some cases, inversion. We discuss the physical relevance of the results.     

Syntheses and characterization of two dioxygen-reactive dinuclear macrocyclic schiff-base copper(I) complexes

The dinuclear copper(I) complex [Cu(2)L(1)(CH(3)CN)(2)](ClO(4))(2) (1, L(1) = 3,6,9,17,20,23-hexaazatricyclo[23.3.1.1]triaconta-1(29),2,9,11(30),12(13),14,16,23,25,27-decaene) has been structurally characterized. As previously described, intramolecular ligand hydroxylation (at the aromatic ring) was observed when 1 was reacted with dioxygen. A stopped-flow analysis of the reaction of 1 with dioxygen under different conditions did not allow a "dioxygen intermediate" to be spectroscopically detected. Detailed NMR and electrochemical data on 1 are also presented and evaluated for the first time. No copper(II) complexes of L(1) could be characterized due to hydrolysis of the compounds. In contrast, complex 2-differing from 1 only in an increase in the size of the chelate rings-did not undergo intramolecular hydroxylation when it was oxidized. The crystal structure of 2 is also described.     

Safety first portfolio choice based on financial and sustainability returns

The aim of this paper is to expand the methodological spectrum of socially responsible investing by introducing stochastic sustainability returns into safety first models for portfolio choice. We provide a foundation of the notion of sustainability in portfolio theory and establish a general model for generalized safety first portfolio management with probabilistic constraints and three specifications of it. Moreover, we prove theorems about conditions for unique optimal solutions and for the constraints of one model being more restrictive than those of another. In an empirical part, we calculate the costs of investing according to our approach in terms of less financial return.     

Zum Nachweis von Blut

Ohne Zusammenfassung     

Den Nachweis von Minerals?uren in Essig

Ohne Zusammenfassung     

Ma?analytische Bestimmung des Quecksilbers

Ohne Zusammenfassung