RESUMEN
Photocatalytic processes are being studied extensively as potential advanced wastewater treatments for the removal of pharmaceuticals, pesticides and other recalcitrant micropollutants from the effluents of conventional wastewater treatment plants (WWTPs). Oxytetracycline (OTC) is a widespread antibiotic which is frequently detected in surface water bodies as a recalcitrant and persistent micropollutant. This review provides an update on advances in heterogeneous photocatalysis for the degradation of OTC in water under UV light, sunlight and visible-light irradiation. Photocatalysts based on pure semiconducting oxides are rarely used, due to the problem of rapid recombination of electron-hole pairs. To overcome this issue, a good strategy could be the coupling of two different semiconducting compounds with different conduction and valence bands. Several methods are described to enhance the performances of catalysts, such as doping of the oxide with metal and/or non-metal elements, surface functionalization, composites and nano-heterojunction. Furthermore, a discussion on non-oxidic photocatalysts is briefly provided, focusing on the application of graphene-based nanocomposites for the effective treatment of OTC.
Asunto(s)
Nanocompuestos , Oxitetraciclina , Contaminantes Químicos del Agua , Purificación del Agua , Catálisis , Luz , Agua , Purificación del Agua/métodosRESUMEN
The catalytic performance of a perovskite-type lanthanum ferrite LaFeO3 to remove arsenic from water has been investigates for the first time. LaFeO3 was prepared by citrate auto-combustion of dry gel obtained from a solution of the corresponding nitrates poured into citric acid solution. Kinetic studies were performed in the dark with As(V) and in the dark and under UV-C irradiation at pHâ 6-7 with As(III) (both 1â mg L-1 ), and As : Fe molar ratios (MR) of 1 : 10 and 1 : 100 using the LaFeO3 catalyst. As(V) was removed from solution after 60â min in the dark in 7 % and in 47 % for MR=1 : 10 and MR=1 : 100, respectively, indicating the importance of the amount of the iron material on the removal. Oxidation of As(III) in the dark was negligible after 60â min in contact with the solid sample, but complete removal of As(III) was observed within 60â min of irradiation at 254â nm, due to As(III) photooxidation to As(V) and to As(III) sorption to a minor extent. Morphological and microstructural studies of the catalyst complement the catalytic testing. This work demonstrates that LaFeO3 can be used for the removal of As(III) from highly arsenic contaminated water.
RESUMEN
Quantum mechanics density functional calculations provided gas-phase electron distributions and proton affinities for several mono- and diaza[5]helicenes; computational results, together with experimental data concerning crystal structures and propensity to methylation of the nitrogen atom(s), provide a basis for designing azahelicene complexes with transition metal ions.
Asunto(s)
Compuestos Aza/química , Complejos de Coordinación/química , Modelos Químicos , Compuestos Policíclicos/química , Elementos de Transición/química , Algoritmos , Álcalis/química , Compuestos Aza/síntesis química , Simulación por Computador , Complejos de Coordinación/síntesis química , Cristalización , Cristalografía por Rayos X , Enlace de Hidrógeno , Conformación Molecular , Compuestos Policíclicos/síntesis química , Teoría Cuántica , Espectrometría de Masa por Ionización de ElectrosprayRESUMEN
In this work, three compounds having the same organic moiety (N-methyl-5-azahelicenium salts) but different counterions (I-, NO3- and COOCF3-) have been investigated in buffered aqueous solutions and in the presence of DNA to give information on the counterion effects on the binding. In particular, the absorption spectra, fluorescence quantum yields and fluorescence lifetimes in aqueous solution for free organic molecules have been determined by steady-state and time-resolved spectrofluorimetric measurements. The obtained values are compared with those of the chromophores in the presence of increasing concentrations of DNA. The results allow determination of the association constants (K(a)) and the number of base couples per chromophore molecule (n) by means of the McGhee Von Hippel model. The binding parameters are strongly affected by the nature of counterions since the highest K(a) value was determined for the compound having COOCF3-; on the other hand the NO3- derivative is able to interact with the highest number of binding sites. The morphology and structural properties of the DNA-chromophore complexes were investigated by circular dichroism (CD) and atomic force microscopy (AFM). The data revealed that I- and COOCF3- derivatives preferentially form intercalation complexes, while the NO3- salt is able to form intercalation and grove binding complexes at the same time.
Asunto(s)
ADN/metabolismo , Sustancias Intercalantes/química , Sustancias Intercalantes/metabolismo , Compuestos Policíclicos/química , Compuestos Policíclicos/metabolismo , Absorción , Animales , Bovinos , Dicroismo Circular , Sales (Química)/química , Espectrometría de FluorescenciaRESUMEN
In this work microstructure, porosity and hydration degree of cement-based solidified/stabilized wasteforms were studied before assessing their leaching behaviour. 2-Chloroaniline was chosen as a model liquid organic pollutant and included into cement pastes, which were also modified with different admixtures for concrete: a superplasticizer based on acrylic-modified polymer, a synthetic rubber latex and a waterproofing agent. An organoclay, modified with an ammonium quaternary salt (benzyl-dimethyl-tallowammonium, BDMTA), was added to the pastes as pre-sorbent agent of the organic matter. All the samples were dried up to constant weight in order to stop the hydration process at different times during the first 28 days of curing, typically, after 1 day (1d), 7 days (7d) and 28 days. Then, the microstructure of the hardened cement-clay pastes was investigated by powder X-ray diffraction (XRD). The hydration degree and porosity were studied by thermal analysis (TG/DTA) and mercury intrusion porosimetry (MIP), respectively. For samples cured for 28 days a short-term leach test set by Italian regulation for industrial waste recycling (D.M. 5 February 1998) was performed. The best results showed a 5% release of the total initial amount of organic pollutant.
Asunto(s)
Silicatos de Aluminio , Materiales de Construcción , Polímeros/química , Compuestos de Amonio Cuaternario/química , Adsorción , Compuestos de Anilina/química , Carbonato de Calcio/química , Arcilla , Mercurio/toxicidad , Microscopía Electrónica de Rastreo , Compuestos Orgánicos , Permeabilidad , Porosidad , Factores de Tiempo , Agua/química , Difracción de Rayos XRESUMEN
The results of 2-chloroaniline (2-CA) immobilization experiments in cement matrices, using an organophilic clay modified with phenolic resins as pre-sorbent, are shown. The 2-CA suspended in water was kept in contact with the organoclay for 24 h, and the slurry obtained was then admixed with ordinary Portland cement (OPC) without additional water, to obtain a firm solid waste. Six cement-clay pastes were prepared with the same water-to-cement ratio (0.50 wt/wt), but with different slurry composition (water-to-organoclay ratio equal to 10 and 5 wt/wt, respectively) and different amounts of 2-CA suspended in water, namely 5000, 15 000, and 25 000 ppmw (weight). Dynamic leach tests were performed on solidified monoliths in order to assess the successful immobilization of the 2-CA. Moreover, X-ray diffraction, scanning electron microscopy and Fourier transform infrared spectroscopy analyses were carried out.