scholarly journals ELECTROCHEMICAL OXIDATION OF SYNTHETIC ORGANIC DYES BY FERRATE (VI), USING COMMERCIAL STEEL WOOL ELECTRODES

2018 ◽  
Vol 18 (1) ◽  
pp. 5-15
Author(s):  
Ramiro Escalera Vásquez ◽  
Uli Nicol Hosse Pastor ◽  
Pablo Marcelo Pérez García
2019 ◽  
Vol 328 ◽  
pp. 252-258 ◽  
Author(s):  
L. Santos-Juanes ◽  
S. García-Ballesteros ◽  
R.F. Vercher ◽  
A.M. Amat ◽  
A. Arques

2008 ◽  
Vol 8 (1) ◽  
pp. 73-77 ◽  
Author(s):  
Caio F. Gromboni ◽  
George L. Donati ◽  
Wladiana O. Matos ◽  
Eduardo F. A. Neves ◽  
Ana Rita A. Nogueira ◽  
...  

2015 ◽  
Vol 138 ◽  
pp. 15-19 ◽  
Author(s):  
Luiz Alberto Cesar Teixeira ◽  
Nildo de Abreu Vieira ◽  
Lidia Yokoyama ◽  
Fabiana Valéria da Fonseca

2019 ◽  
Vol 299 ◽  
pp. 01002
Author(s):  
Alexandra Banu ◽  
Madalina Mocirla ◽  
GizemNur Soylu

Methyl orange (MO) is an environmental concern because their degradation products are highly toxic to aquatic microorganisms and carcinogenic, also their degradation products are mutagenic to humans. Electrochemical oxidation is one of the promising technologies for the dye wastewater de-pollution, which are obtained extensively attentions because it holds the advantages of total oxidization of dyes to CO2 and H2O. Titanium dioxide has emerged as the leading candidate to provide complete destruction of organic pollutants via heterogeneous photocatalysis that result in total mineralization of many organic pollutants. Though this process offers actual annihilation of the dye moleculesatavery high efficiency, thepost-treatmentrecoveryof TiO2 canbecostly. The titanium nanotubes are typically produced by anodic oxidation of the titanium foil in various electrolytes.Degradation of methyl orange (MO) was conducted by electrochemical oxidation method with Ti/TiO 2 nanotubes anodes. Were prepared samples of TiO2 nanotubes by anodizing titanium in an electrochemical bath consisting of 1:1 waterglycerol with 0.4% of HF using different conditions: 25V for 8 hours, 30V for 3 hours in the stationary state, 30V 3 hours under ultrasound stirring. The oxidation efficiency was determined by UV-VIS analysis of the electrolyte.


2003 ◽  
Vol 773 ◽  
Author(s):  
Aaron R. Clapp ◽  
Igor L. Medintz ◽  
J. Matthew Mauro ◽  
Hedi Mattoussi

AbstractLuminescent CdSe-ZnS core-shell quantum dot (QD) bioconjugates were used as energy donors in fluorescent resonance energy transfer (FRET) binding assays. The QDs were coated with saturating amounts of genetically engineered maltose binding protein (MBP) using a noncovalent immobilization process, and Cy3 organic dyes covalently attached at a specific sequence to MBP were used as energy acceptor molecules. Energy transfer efficiency was measured as a function of the MBP-Cy3/QD molar ratio for two different donor fluorescence emissions (different QD core sizes). Apparent donor-acceptor distances were determined from these FRET studies, and the measured distances are consistent with QD-protein conjugate dimensions previously determined from structural studies.


2003 ◽  
Vol 773 ◽  
Author(s):  
Xiaohu Gao ◽  
Shuming Nie ◽  
Wallace H. Coulter

AbstractLuminescent quantum dots (QDs) are emerging as a new class of biological labels with unique properties and applications that are not available from traditional organic dyes and fluorescent proteins. Here we report new developments in using semiconductor quantum dots for quantitative imaging and spectroscopy of single cancer cells. We show that both live and fixed cells can be labeled with multicolor QDs, and that single cells can be analyzed by fluorescence imaging and wavelength-resolved spectroscopy. These results raise new possibilities in cancer imaging, molecular profiling, and disease staging.


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