1-D Coordination Polymers of Organotin(IV) Nodes with Alternating Spacers

Coordination compounds of organotin(IV) with diverse dimensionalities are obtained due to the ability of the tin atoms to have different coordination numbers, such as 4, 5, 6, or 7 [1]. [...

Iron-Modified Titanate Nanorods for Oxidation of Aqueous Ammonia Using Combined Treatment with Ozone and Solar Light Irradiation

Sodium titanate nanorods were synthesized by a hydrothermal method and subsequently modified with an iron precursor. For comparison, Fe2O3 nanocubes were also obtained through a similar hydrothermal treatment. Pristine, Fe-modified nanorods and Fe2O3 nanocubes were suspended in diluted ammonia solutions (20 ppm) and exposed to ozone and simulated light irradiation. Ammonia abatement, together with the resulting nitrogen-containing products (NO3−), was monitored by ion chromatography measurements. The generation of reactive oxygen species (·OH and O2−) in the investigated materials and their photoelectrochemical behaviour were also investigated. Morphological and structural characterizations (SEM, XRD, XRF, UV–Vis, H2-TPR, NH3-TPD, PL, PZC) of the studied catalysts were correlated with their activity for ammonia degradation with ozone- and photo-assisted oxidation. An increase in ammonia conversion and a decreasing amount of NO3− were achieved by combining the above-mentioned processes

Iron-Modified Titanate Nanorods for Oxidation of Aqueous Ammonia Using Combined Treatment with Ozone and Solar Light Irradiation

Sodium titanate nanorods were synthesized by a hydrothermal method and subsequently modified with an iron precursor. For comparison, Fe2O3 nanocubes were also obtained through a similar hydrothermal treatment. Pristine, Fe-modified nanorods and Fe2O3 nanocubes were suspended in diluted ammonia solutions (20 ppm) and exposed to ozone and simulated light irradiation. Ammonia abatement, together with the resulting nitrogen-containing products (NO3−), was monitored by ion chromatography measurements. The generation of reactive oxygen species (·OH and O2−) in the investigated materials and their photoelectrochemical behaviour were also investigated. Morphological and structural characterizations (SEM, XRD, XRF, UV–Vis, H2-TPR, NH3-TPD, PL, PZC) of the studied catalysts were correlated with their activity for ammonia degradation with ozone- and photo-assisted oxidation. An increase in ammonia conversion and a decreasing amount of NO3− were achieved by combining the above-mentioned processes

Valmet Chiral Schiff‐Base Ligands And Their Copper(II) Complexes as Organo, Homogeneous and Heterogeneous Catalysts for Henry, Cyanosilylation and Aldol Coupling Reactions

International audienceCyanosilylation, aldol coupling and asymmetric Henry reactions were carried out with L- and D-valmet ligands in different configurations: i) coordinated to sodium ions, as organocatalysts, with week base properties, ii) complexes with copper(II), as homogeneous catalysts, and iii) immobilized copper(II) complexes onto graphene oxide (GO) as heterogeneous catalysts. For the reaction of benzaldehyde and nitromethane in water these afforded an asymmetric Henry reaction, with a spectacular increase of the conversion and ee (92.5 and 95.8 %, respectively) after the deposition on GO. Ligand complexed copper was also effective for cyanosilylation and Aldol coupling reaction

Band-Gap Engineering of Layered Perovskites by Cu Spacer Insertion as Photocatalysts for Depollution Reaction

A multi-step ion-exchange methodology was developed for the fabrication of Cu(LaTa2O7)2 lamellar architectures capable of wastewater depollution. The (001) diffraction line of RbLaTa2O7 depended on the guest species hosted by the starting material. SEM and TEM images confirmed the well-preserved lamellar structure for all intercalated layered perovskites. The UV–Vis, XPS, and photocurrent spectroscopies proved that Cu intercalation induces a red-shift band gap compared to the perovskite host. Moreover, the UV–Vis spectroscopy elucidated the copper ions environment in the Cu-modified layered perovskites. H2-TPR results confirmed that Cu species located on the surface are reduced at a lower temperature while those from the interlayer occur at higher temperature ranges. The photocatalytic degradation of phenol under simulated solar irradiation was used as a model reaction to assess the performances of the studied catalysts. Increased photocatalytic activity was observed for Cu-modified layered perovskites compared to RbLaTa2O7 pristine. This behavior resulted from the efficient separation of photogenerated charge carriers and light absorption induced by copper spacer insertion