Search results for "Malachite green"
showing 5 items of 5 documents
Disappearance of malachite green residues in fry of rainbow trout (Oncorhynchus mykiss) after treatment of eggs at the hatching stage
2009
Abstract The disappearance of malachite green (MG) residues was determined in fry of rainbow trout (Oncorhynchus mykiss) after six repeated treatments of the eggs at the hatching stage with MG oxalate at exposure levels of 1, 3 and 6 mg l− 1 for 30 min. Fry samples were taken from newly hatched fry (0 days post-hatch, d.p.h.) and at regular time intervals at 16, 31, 43, 57 and 96 d.p.h. The residues of MG and its major metabolite, leucomalachite green (LMG), were found to accumulate in the fry after MG treatments of eggs, with the highest residue levels being determined in the newly hatched fry. After exposures of 3 mg l− 1 MG, mean concentrations of 1170 ± 106 µg kg− 1 and 276 ± 38.6 µg kg…
Über Umsetzungen an Poly-p-lithiumstyrol 2. Mitt. Derivate des poly-p-vinyl-di- und Triphenylmethans
1959
Das kurzlich von uns beschriebene Poly-p-lithiumstyrol stellt eine sehr reaktionsfahige makromolekulare metallorganische Verbindung dar. Es wird uber einige Umsetzungen mit Carbonylverbindungen berichtet. Die Reaktion mit Benzaldehyd und einigen p-substituierten Benzaldehyden fuhrt mit hohen Umsetzungsgraden zu Polyvinyldiphenylmethylcarbinolen. Die Reaktion mit Benzophenon liefert Polyvinyltriphenylmethylcarbinol. Diese Verbindung ist in konz. Schwefelsaure loslich als polymeres Analogon des Triphenylmethylkations, was aus der Untersuchung der Absorptionsspektren folgt. Mit MICHLERS Keton last sich ein polymeres Derivat des Malachitgruns darstellen, dessen spektroskopische, Untersuchung in…
Cation and anion electrochemically assisted solid-state transformations of malachite green
2020
[EN] The possibility of the electrochemical promotion of different solid-to-solid transformations including the performance of successive cation and anion insertion processes has been tested using malachite green, a triphenylmethane dye, in contact with aqueous NaCl electrolyte. Electrochemical data using the voltammetry of microparticles methodology reveal significant differences with the solution phase electrochemistry of the dye. Voltammetric data, combined with atomic force microscopy, focusing ion beam-field emission scanning electron microscopy, and high-resolution field emission scanning electron microscopy permit characterization of the oxidative dissolution, oxidation with anion in…
Novel Au NPs/Preyssler acid/TiO 2 nanocomposite for the photocatalytic removal of azo dye
2014
Abstract In this study, we introduced a novel nanocomposite consisting of Au nanoparticles decorated TiO 2 and Preyssler acid as a multifunctional photocatalyst linker molecule, in which gold ions reduced locally on the TiO 2 surface. The obtained nanocomposite has been characterized using Fourier Transform Infrared (FTIR), X-ray Diffraction (XRD), Electron Dispersive X-ray (EDX) Spectroscopy, Transmission Electron Microscopy (TEM) and Scanning Electron Microscope (SEM). Also, their photocatalytic activity has been studied for the degradation of model organic azo dye Malachite Green under UV light irradiation.
Decarboxylation and alkaline colour fading reactions in presence of humic substances.
2002
Humic substances (HSs) can substantially influence velocity of reactions in the environment as shown on example of decarboxylation and alkaline colour (e.g., malachite green and crystal violet) fading reactions. In colour fading and decarboxylation reactions of 6-nitrobenzisoxazole-3-carboxylic acid HS act as inhibitors, but additions of surfactants change the pattern of reaction. The inhibitory activity of HSs much depends on their origin. The velocity of studied reactions depends also on pH, temperature and concentration of HS used. Possible micellar catalysis mechanism has been suggested.