Near-surface ion distribution and buffer effects during electrochemical reactions

The near-surface ion distribution at the solid-liquid interface during the Hydrogen Oxidation Reaction (HOR)/Hydrogen Evolution Reaction (HER) on a rotating platinum disc electrode is demonstrated in this work. The relation between reaction rate, mass transport and the resulting surface pH-value is used to theoretically predict cyclic voltammetry behaviour using only thermodynamic and diffusion data obtained from the literature, which were confirmed by experimental measurements. The effect of buffer addition on the current signal, the surface pH and the ion distribution is quantitatively described by analytical solutions and the fragility of the surface pH during reactions that form or consume H(+) in near-neutral unbuffered solutions or poorly buffered media is highlighted. While the ideal conditions utilized in this fundamental study cannot be directly applied to real scenarios, they do provide a basic understanding of the surface pH concept for more complex heterogeneous reactions.     

Numerical analysis of Debye screening effect in electrode surface potential mapping by scanning electrochemical potential microscopy

We investigate the effects of the probe apex geometry, overlap of the electric double layers (EDLs) and Debye screening on surface potential mapping with scanning electrochemical potential microscopy (SECPM). The simulation consists of scanning a tip parallel to the electrode surface over a charged hemispherical nano-particle adsorbed on the electrode surface. As expected, a clear dependence of the apparent size of the imaged particle on the probe apex geometry has been noticed. The Debye screening has a significant effect on the probe sensitivity, while the electrolyte concentration affects the observed size of the imaged particles.     

Injector-internal thermal desorption from edible oils. Part 1: visual experiments on sample deposition on the liner wall

Injector-internal thermal desorption from edible oils or fats enables the analysis of a wide range of compounds in oils or extracts of fatty food without prior removal of the sample matrix. The oil or fat is deposited onto the wall of the injector liner. The solutes of interest are evaporated, leaving behind the sample matrix. The injector is kept at a temperature volatilizing the solutes of interest, but minimizing evaporation of the bulk material of the oil. This technique was optimized regarding sample deposition on the liner wall (Part 1) and desorption of high boiling compounds, such as migrants from food packaging materials into simulant D (olive oil) or fatty food (Part 2). The sample liquid should be transferred to the liner wall and spread to a thin film in order to facilitate the release of high boiling components. Visual experiments with perylene-containing solutions showed that the oil must be diluted to reduce the viscosity (separation from the needle tip). The oil concentration should not exceed 20% in order to rule out that squirting sample liquid drops to the bottom of the vaporizing chamber. Further dilution to about 10% oil improves spreading of the liquid to a thin film. A rather high boiling solvent should be used, such as n-butyl acetate, to prevent thermospray at the needle exit and violent evaporation from the liner wall with sputtering liquid. Using a 5-mm ID liner, 5-10-microL injections of 10-20% oil solutions were at the upper limit.     

LC-GC analysis of the aromatics in a mineral oil fraction: Batching oil for jute bags

Aromatics of a C₁₅? C₃₀ mineral oil fraction, the “batching oil” used for producing jute fabrics, were analyzed for estimating the toxicity of oil transferred from jute bags to foods. Group-type pre-separation according to ring systems occurred on a LC NH₂ column with pentane and small additions of methanol as eluent. LC fractions were characterized by LC-GC-MS and quantitated by LC-GC-FID. The oil contained 23% aromatics and 1% “polars”; some 99.5% of the aromatics were alkylated.     

Zur ma?analytischen Bestimmung des Zinns

Ohne Zusammenfassung     

Truncated resolution model structures

Using the dual of Bousfield-Friedlander localization, we colocalize resolution model structures on cosimplicial objects over a left proper model category to get truncated resolution model structures. These are useful for studying realization and moduli problems in algebraic topology.     

Noncovalent Chirality Sensing Ensembles for the Detection and Reaction Monitoring of Amino Acids,Peptides, Proteins,and Aromatic Drugs

Ternary complexes between the macrocyclic host cucurbit[8]uril, dicationic dyes, and chiral aromatic analytes afford strong induced circular dichroism (ICD) signals in the near‐UV and visible regions. This allows for chirality sensing and peptide‐sequence recognition in water at low micromolar analyte concentrations. The reversible and noncovalent mode of binding ensures an immediate response to concentration changes, which allows the real‐time monitoring of chemical reactions. The introduced supramolecular method is likely to find applications in bioanalytical chemistry, especially enzyme assays, for drug‐related analytical applications, and for continuous monitoring of enantioselective reactions, particularly asymmetric catalysis.