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In this study, we investigated different metal pairings of Au nanoparticles (NPs) as potential catalysts for glycerol dehydration for the first time. All of the systems preferred the formation of hydroxyacetone (HYNE). Although the bimetallics that were tested, i.e., Au NPs supported on Ni, Fe and Cu appeared to be more active than the Au/SiO2 system, only Cu supported Au NPs gave high conversion (ca. 63%) and selectivity (ca. 70%) to HYNE. [ABSTRACT FROM AUTHOR]

Energy consumption steadily increases and energy production is associated with many environmental risks, e.g., generating the largest share of greenhouse gas emissions. The primary gas pollution concern is CO2, CH4, and nitrogen oxides (NOx). Environmental catalysis plays a pivotal role in NOx mitigation (DeNOx). This study investigated, for the first time, a collection of ceramic foams as potential catalyst support for selective catalytic NOx reduction (SCR). Ceramic foams could be an attractive support option for NOx removal. However, we should functionalize the surface of raw foams for such applications. A library of ceramic SiC, Al2O3, and ZrO2 foams ornamented with nanorod ZnO and TiO2 as W and V oxide support was obtained for the first time. We characterized the surface layer coating structure using the XPS, XRF and SEM, and TEM microscopy to optimize the W to V molar ratio and examine NO2 mitigation as the SCR model, which was tested only very rarely. Comparing TiO2 and ZnO systems reveals that the SCR conversion on ZnO appeared superior vs. the conversion on TiO2, while the SiC-supported catalysts were less efficient than Al2O3 and ZrO2-supported catalysts. The energy bands in optical spectra correlate with the observed activity rank. [ABSTRACT FROM AUTHOR]

An ultrasound-assisted methodology for the determination of dissolved silicate in water has been developed by combining the miniaturized ion-associated based preconcentration method with energy dispersive X-ray fluorescence spectrometry (EDXRF). The method has been devised for the determination of silicate through molybdenum in the ion-associated complex between 12-molybdosilicate and crystal violet. Because silicate is determined indirectly via molybdenum fluorescent radiation the difficulties resulting from low fluorescence yield and low energy of silicon radiation were successfully overcome. A good ratio of silicon to molybdenum (1 to 41) and a sensitive Kα line of molybdenum make possible the determination of low concentration of silicon in the form of dissolved silicate. Under optimized conditions, good linearity, up to 5 μg of silicon in the form of silicate (r = 0.9990) and a detection limit of 9 ng mL−1 were achieved. The total RSD for the EDXRF determination of silicate, followed by precipitation of the ion-associated complex and its dissolution in a microdrop of isoamyl alcohol, was 6.5%. The enrichment factor was equal to 142. The developed method was used to determine the dissolved silica content in surface waters. The accuracy and repeatability of the proposed procedure were checked by the standard addition method and compared to the results obtained using the ICP-OES technique. The recovery (in the 93–97% range) was satisfactory and indicated the usefulness of the developed procedure. [ABSTRACT FROM AUTHOR]

Sorptive and selective mini-membranes based on TiO2 directly synthesized onto cellulose filters (TiO2@cellulose) have been developed. The in situ synthesis of TiO2@cellulose applied is simple and economically advantageous. The obtained membranes can be useful for (1) separating arsenic(V) and selenium(IV) from other ions and organic matter, (2) speciation of arsenic and selenium, and (3) determining ulratraces of these ions in water samples. The membranes exhibit good stability and high maximum adsorption capacities for Se(IV) (71 mg g−1) and As(V) (41 mg g−1). A monolayer chemical adsorption of analytes on the membranes was confirmed. The structure of membranes was examined with scanning electron microscopy, x-ray diffractometry, and micro energy-dispersive x-ray fluorescence spectrometry (μ-EDXRF). The membranes were characterized by homogenous distribution of TiO2 onto cellulose. The TiO2@cellulose was used as a new sorbent in micro-solid phase extraction for determination of Se(IV) and As(V) by EDXRF. Using direct analysis of mini-membranes after sorption of analytes avoids the elution step. Thus, the proposed procedure is an attractive and solvent-free option for quantitative monitoring of Se(IV) and As(V) in different materials. Both analytes were quantitatively and simultaneously separated/determined from samples at pH 2 with very good recovery (close to 100%), precision (4.5%), and detection limits (0.4 ng mL−1 Se and 0.25 ng mL−1 As). TiO2@cellulose membranes were applied to water analysis. [ABSTRACT FROM AUTHOR]