Electrochemical platform based on molecularly imprinted polymer with zinc oxide nanoparticles and multiwalled carbon nanotubes modified screen-printed carbon electrode for amaranth determination.

A novel electrochemical platform for amaranth determination has been developed using a rapid, easy, inexpensive, and portable molecularly imprinted polymer technique. The MIP platform was fabricated by electropolymerizing melamine as monomer in the presence of amaranth as template on the surface of ZnO-MWCNT/SPCE. Then, amaranth was completely eluted, leaving imprinted cavities in the polymeric film that could effectively recognize amaranth in solution. The electrochemical platform based on a molecularly imprinted polymelamine was analyzed by scanning electron microscopy (SEM), cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and differential pulse voltammetry (DPV). Under optimum conditions, the developed MIP/ZnO-MWCNT/SPCE platform can be properly used for amaranth determination, with high sensitivity of 96.2 µA µM cm-2, two linear concentration ranges (0.01 to 1 µM and 1 to 1000 µM) and a low limit of detection of 0.003 µM. The anodic peak potential of amaranth was found to be 0.73 V. Additionally, the polymelamine MIP films specifically recognize amaranth molecules, making it possible to detect amaranth in a complex solution with high selectivity, excellent repeatability, reproducibility, and stability. The MIP/ZnO-MWCNT modified screen-printed carbon electrode was successfully applied to determine amaranth in pharmaceutical and water samples, with recovery values ranging from 99.7 to 102% and RSD% values less than 3.2%.

Antibacterial Activity of ZnSe, ZnSe-TiO2 and TiO2 Particles Tailored by Lysozyme Loading and Visible Light Irradiation.

ZnSe, ZnSe-TiO2 microspheres and nanostructured TiO2 obtained by hydrothermal and sol-gel methods were tested against Staphylococcus aureus ATCC 25923 and Micrococcus lysodeikticus ATCC 4698 before and after lysozyme (Lys) loading. Morphological characterization of inorganic matrices and hybrid organic-inorganic complexes were performed by microscopy techniques (SEM, AFM and Dark Field Hyperspectral Microscopy). Light absorption properties of ZnSe, ZnSe-TiO2 and TiO2 powders were assessed by UV-visible spectroscopy and their ability to generate reactive oxygen species (•OH and O2•-) under visible light irradiation was investigated. Antibacterial activity of ZnSe, ZnSe-TiO2, TiO2, Lys/ZnSe, Lys/ZnSe-TiO2 and Lys/TiO2 samples under exposure to visible light irradiation (λ > 420 nm) was tested against Staphylococcus aureus and Micrococcus lysodeikticus and correlated with ROS photogeneration.

Simultaneous determination of anthracene and phenanthrene using a poly-alizarin red S/carbon paste electrode.

A polymer-based carbon paste electrode was constructed by electropolymerized Alizarin Red S (ARS) film on the carbon paste electrode (CPE) surface. The electrochemical properties of poly-ARS/CPE were characterized by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). Scanning electron microscopy (SEM) was utilized for electrode characterization. The electropolymerization cycles for the construction of the sensor and the supporting electrolyte were optimized. With 0.1 M LiClO4 as a supporting electrolyte, poly-ARS/CPE was able to generate oxidation peaks for anthracene (ANT) and phenanthrene (PHE), that were clearly defined and easily distinguished from one to another when operating in square wave voltammetry (SWV). In the simultaneous detection the linear ranges of ANT and PHE were within 80-1000 µM, with detection limits of 24 µM. The variation of peak parameters with scan rate was investigated to determine the nature of electrooxidation and the number of electrons involved in the electrode process. Poly-ARS/CPE was successfully utilized for the detection of ANT and PHE in different water samples and the obtained results suggested the selectivity, stability and reproducibility of the modified electrode.

Rapid and sensitive electrochemical determination of tartrazine in commercial food samples using IL/AuTiO2/GO composite modified carbon paste electrode.

A novel electrochemical sensor based on the modification of carbon paste electrode with an ionic liquid (1-butyl-2,3-dimethylimidazolium tetrafluoroborate) and AuTiO2/GO composite (IL/AuTiO2/GO/CPE) was developed for rapid and sensitive determination of tartrazine by differential pulse voltammetry. Under the optimum experimental conditions, the peak current was linear to concentration of tartrazine in the ranges of 1-400 µmol L-1 and 400-1000 µmol L-1, with sensitivities of 0.008 µA µmol L-1 and 0.002 µA µmol L-1, respectively, and with a limit of detection of 0.33 µmol L-1 (S/N = 3). To demonstrate the performance of the method, the reproducibility was studied and the obtained values of RSD% were 2.72%. The method was applied to the sensitive determination of tartrazine in isotonic drink, mustard and yellow egg dye samples with recovery rates between 98.55% and 103.62%.

A review of catalysts used in microwave assisted pyrolysis and gasification.

The review describes different catalysts and reactor-types used in microwave-assisted thermochemical biomass conversion. We present comparative review of various catalytic experiments and experimental conditions using catalysts in both in situ and ex situ processes. In situ catalytic processes are more frequently used due to simpler experimental set up. However, the process leads to higher catalytic deactivation rate and catalyst recovery is difficult. Catalysts used in ex situ processes require a more complex experimental set-up, the advantage being the fact that optimum temperature can be obtained to achieve best results catalyst recovery is facile, and its deactivation occurs at a lower rate. The catalysts described herein represent just a small part of the catalyst types/family that can be theoretically used. Commonly used catalysts are zeolites, metal oxides, various salts or carbon type materials but other materials or improvements of those mentioned need to be tested in the future.