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Ligia Frunza

Bio: Ligia Frunza is an academic researcher from University of Salamanca. The author has contributed to research in topics: Liquid crystal & Dielectric. The author has an hindex of 14, co-authored 43 publications receiving 726 citations.

Papers
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TL;DR: In this article, the photocatalytic decomposition of ibuprofen down to low ppm concentrations over titania catalyst has been investigated in detail, and the effect of the pH value, oxygen supply and catalyst re-use have been checked.
Abstract: Due to the growing importance of low concentrated pollution of surface, ground and drinking, the photocatalytic decomposition of ibuprofen down to low ppm concentrations over titania catalyst has been investigated in detail. The catalyst was characterized by XRD, TEM, diffuse reflection UV–Vis and nitrogen adsorption measurement. The photocatalytic abatement of ibuprofen was monitored by UV–Vis spectrometry, chromatographic by GC/MS, and HPLC coupled electrospray ionization time-of-flight mass spectrometry (ESI-TOF-MS). Catalytic performance has been studied by varying the catalyst and substrate concentration as well as decreasing the catalyst-to-substrate mass ratio over a wide range. The photocatalytic treatment with titania catalyst leads to rapid mineralization of ibuprofen. Formation of intermediate reaction products has been investigated. It is proposed that intermediates in part form oligomeric species, which are responsible for catalyst poisoning. Additional, the influence of the pH value, oxygen supply and catalyst re-use have been checked.

139 citations

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TL;DR: In this article, a comparison of the two catalytic systems was revealed by a comparative analysis of the data obtained from the adsorption and oxidation tests, showing that only CuO/Al2O3 was effective in the RB5 degradation.
Abstract: CuO/Al2O3 and NiO/Al2O3 catalysts prepared by incipient wetness impregnation were used for the oxidation of Reactive Black 5 (RB5) in aqueous solution. Removal of the dye was assessed by High Performance Liquid Chromatography (HPLC) and Total Organic Carbon (TOC) measurements and the generation of the hydroxyl radicals in the process was evaluated by chemiluminescence measurements. To put in evidence the interaction RB5 – catalyst and the surface species formed onto catalysts during the oxidation, Diffuse Reflectance Infrared Fourier Transform (DRIFT) analysis was performed. A different behavior of the two catalytic systems was revealed by the comparative analysis of the data obtained from the adsorption and oxidation tests. Only CuO/Al2O3 was effective in the RB5 degradation, NiO/Al2O3 acted as a simple adsorbent. In the presence of CuO/Al2O3, at H2O2 concentration of 40 mM the azo dye was totally eliminated from both solution and catalyst surface after 4 h, with a mineralization degree higher than 90%. However, a strong inhibition of the catalytic oxidation of RB5 was observed in the presence of phosphate ions. In the conditions of hydrogen peroxide excess, the rate equation in the case of copper catalyst was simply expressed by a pseudo-first order equation and the model was found to fit well the data. The amount of copper leached from catalyst during the oxidation process was only 1.0–1.6% per cycle leading to the conclusion that the decrease of the dye mineralization with the number of cycles has to be explained mostly by the surface covering with the reaction products, at least to a certain extent.

102 citations

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TL;DR: Ferrite catalysts were prepared following two routes, i.e., the hydrothermal one and the calcination of an oxide mixture as discussed by the authors, and all the samples were fully characterized using chemical analysis, X-ray fluorescence spectroscopy and EDX, nitrogen adsorption-desorption isotherms at −196 ǫ c, XRD, FTIR, scanning electron microscopy and XPS.

83 citations

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TL;DR: In this paper, the photocatalytic experiments were performed by photodegradation of methylene blue in the PCC2 checker apparatus, and it was demonstrated that MB decolorization can serve as a test reaction at least for self cleaning of fabrics.

47 citations

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TL;DR: In this paper, the molecular dynamics of 4-octyl-4-4′-cyanobiphenyl and 4-pentyl, 4-4, 4, 4, 4, 2, 4, 2, 3, 4-1, 4.5, 4.1, 3.5, and 4.6, confined to the mesopores of the molecular sieve AlMCM-41, using broadband dielectric spectroscopy.

45 citations


Cited by
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TL;DR: A thorough review of alternative non-iron Fenton catalysts and their reactivity towards hydrogen peroxide activation is presented, describing in detail the complex mechanisms and emphasizes on practical limitations influencing their environmental applications.

1,618 citations

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TL;DR: In this paper, the authors review the catalytic reactions for the removal of NO and discuss the reduction of NO in the presence of NH3, CO, H-2 or hydrocarbons as well as the decomposition of NO.

1,110 citations

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TL;DR: The functionalized magnetically retrievable catalysts or nanocatalysts that are increasingly being used in catalysis, green chemistry and pharmaceutically significant reactions are summarized in this review.
Abstract: Surface functionalization of nano-magnetic nanoparticles is a well-designed way to bridge the gap between heterogeneous and homogeneous catalysis. The introduction of magnetic nanoparticles (MNPs) in a variety of solid matrices allows the combination of well-known procedures for catalyst heterogenization with techniques for magnetic separation. Magnetite is a well-known material, also known as ferrite (Fe3O4), and can be used as a versatile support for functionalization of metals, organocatalysts, N-heterocyclic carbenes, and chiral catalysts. It is used as a support for important homogeneous catalytically active metals such as Pd, Pt, Cu, Ni, Co, Ir, etc. to obtain stable and magnetically recyclable heterogeneous catalysts. Homogeneous organocatalysts can be successfully decorated with linkers/ligands on the surface of magnetite or alternatively the organocatalysts can be directly immobilized on the surface of magnetite. The functionalized magnetically retrievable catalysts or nanocatalysts that are increasingly being used in catalysis, green chemistry and pharmaceutically significant reactions are summarized in this review.

1,057 citations

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TL;DR: An overview of the state of the art concerning the fundamental properties of electrode polarization of interest in the measurement of high conductivity samples and its implications for both dielectric (DS) and impedance spectroscopy (IS) can be found in this article.
Abstract: In this review, we present an overview of the state of the art concerning the fundamental properties of electrode polarization (EP) of interest in the measurement of high conductivity samples and its implications for both dielectric (DS) and impedance spectroscopy (IS). Initially a detailed description of what constitutes EP is provided and the problems that it induces. Then, we review some of the more popular models that have been used to describe the physical phenomena behind the formation of the ionic double layer. Following this we shall enumerate the common strategies used historically to correct its influence on the measured signals in DS or in IS. Finally we also review recent attempts to employ fractal electrodes to bypass the effects of EP and to offer some physical explanation as to the limitations of their use.

294 citations