ABSTRACT
Expression of Concern for 'Palladium supported on mixed-metal-organic framework (Co-Mn-MOF-74) for efficient catalytic oxidation of CO' by Reda S. Salama et al., RSC Adv., 2021, 11, 4318-4326, https://doi.org/10.1039/D0RA09970H.
ABSTRACT
[This corrects the article DOI: 10.1021/acsomega.1c03693.].
ABSTRACT
[This corrects the article DOI: 10.1039/D0RA03591B.].
ABSTRACT
Mono-(Fe) and bimetallic Cox-Fe1-x-MOF with different Co and Fe contents was successfully synthesized by the solvothermal method. The structural properties of the prepared samples were characterized by X-ray diffraction, transmission electron microscopy (TEM), Brunauer-Emmett-Teller specific surface area, and Fourier transform infrared spectroscopy. The results revealed the successful formation of mono and mixed Cox-Fe1-x-MOF. Also, the results of TEM displayed that the particle structure of Cox-Fe1-x-MOF changed to octahedral after the addition of cobalt. The surface acidity results illustrated that the samples showed both Lewis and Brønsted acid sites, and Cox-Fe1-x-MOF possessed more surface acidity than Fe-MOF. The catalytic performance of the prepared samples was tested by synthesis of 14-phenyl-14H-dibenzo [a, j] xanthene (xanthene), and bimetallic Cox-Fe1-x-MOF showed higher activity compared to monometallic Fe-MOF. The sample with Co0.50-Fe0.50-MOF gave the highest yield of xanthene with 90.2%. In addition, the prepared samples were used for removal of Pb2+ and Cd2+ ions from the aqueous solution. The sample with Co0.50-Fe0.50-MOF showed the highest removal efficiency compared with mono- and other bimetallic samples. The results illustrated that the addition of Co to Fe enhanced the structural properties, acidity, and catalytic performance of the prepared samples due to the synergistic effect between Fe and Co ions. According to the obtained results, the prepared samples showed great potentials for the synthesis of pharmacologically active compounds and environmental protection.
ABSTRACT
The study used a one-step hydrothermal method to prepare Fe3O4-FeVO4 and xRGO/Fe3O4-FeVO4 nanocomposites. XRD, TEM, EDS, XPS, DRS, and PL techniques were used to examine the structurally and morphologically properties of the prepared samples. The XRD results appeared that the Fe3O4-FeVO4 has a triclinic crystal structure. Under hydrothermal treatment, (GO) was effectively reduced to (RGO) as illustrated by XRD and XPS results. UV-Vis analysis revealed that the addition of RGO enhanced the absorption in the visible region and narrowed the band gap energy. The photoactivities of the prepared samples were evaluated by degrading methylene blue (MB), phenol and brilliant green under sunlight illumination. As indicated by all the nanocomposites, photocatalytic activity was higher than the pure Fe3O4-FeVO4 photocatalyst, and the highest photodegradation efficiency of MB and phenol was shown by the 10%RGO/Fe3O4-FeVO4. In addition, the study examined the mineralization (TOC), photodegradation process, and photocatalytic reaction kinetics of MB and phenol.
Subject(s)
Nanocomposites , Sunlight , Graphite/chemistry , Lighting , Methylene Blue/chemistry , Nanocomposites/chemistry , Phenol/chemistryABSTRACT
Pure and modified mesoporous TiO2 nanoparticles with different loadings of NiO (3-20.0 wt %) were prepared through the surfactant-assisted sol-gel approach with the use of cetyltrimethylammonium bromide as a template. The optical and structural properties of different samples were examined using N2 adsorption-desorption analysis, energy-dispersive spectroscopy, scanning electron microscopy, transmission electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, UV-vis spectroscopy, Fourier transform infrared spectroscopy, and photoluminescence (PL) spectroscopy. X-ray diffraction results confirmed the insertion of Ni2+ into the lattice of TiO2, and the crystallite size reduced remarkably after the addition of NiO. The diffuse reflectance spectroscopy spectra displayed obvious red shift in the absorption edges, and new absorption bands appeared in the visible region when NiO was added, which indicates the formation of surface defects and oxygen vacancies. The optical band gap of TiO2 reduced sharply when the contents of NiO were increased. The increase in the surface defects as well as oxygen vacancies were examined using PL spectroscopy. The photocatalytic performance of the as-synthesized samples was investigated over photodegradation of brilliant green (BG) and phenol and hydrogen generation under visible light. 10% NiO/TiO2 exhibited the highest photocatalytic efficiency. The photocatalytic activity was improved due to the creation of a p-n junction at the interface of NiO/TiO2, which efficiently promotes the separation of photogenerated electron/hole pairs and consequently enhances its photodegradation activity. According to the photocatalytic activity results, NiO contents were considered one of the most important factors affecting the photodegradation of BG and phenol and H2 evolution. Also, we discussed the mechanism of photodegradation, mineralization (total organic carbon), and photocatalytic reaction kinetics of BG and phenol.
ABSTRACT
Immobilization of inorganic metal quantum dots (especially, noble transition metals) onto organic polymers to synthesize nanometal-polymer composites (NMPCs) has attracted considerable attention because of their advanced optical, electrical, catalytic/photocatalytic, and biological properties. Herein, novel, highly efficient, stable, and visible light-active NMPC photocatalysts consisting of silver quantum dots (Ag QDs) immobilized onto polymeric chitosan-polyethylene oxide (CTS-PEO) blend sheets have been successfully prepared by an in situ self-assembly facile casting method as a facile and green approach. The CTS-PEO blend polymer acts as a reducing and a stabilizing agent for Ag QDs which does not generate any environmental chemical pollutant. The prepared x wt % Ag QDs/CTS-PEO composites were fully characterized through X-ray diffraction, Fourier transform infrared spectroscopy, transmission electron microscopy (TEM), thermogravimetric analysis, and UV/visible spectroscopy. The characterization results indicated the successful synthesis of the Ag QDs/CTS-PEO composites by the interactions and complexation between x wt % Ag QDs and CTS-PEO blend sheets. TEM images revealed small granules randomly distributed onto the CTS-PEO blend sheets, indicating the immobilization of Ag QDs onto CTS-PEO composites. The presence of a surface plasmon resonance (SPR) band and the shifting of the absorption edge toward higher wavelengths in the UV/vis spectra indicated the formation of x wt % Ag QDs/CTS-PEO composites. The Ag QDs in the polymeric blend matrix led to remarkable enhancement in the optical, thermal, electrical, and photocatalytic properties of x wt % Ag QDs/CTS-PEO composites. The photocatalytic efficiency of the prepared composites was evaluated by the photodegradation of p-nitrophenol (PNP) under simulated sunlight. The maximum photocatalytic degradation reached 91.1% efficiency within 3 h for the 12.0 wt % Ag QDs/CTS-PEO photocatalyst. Generally, the Ag QDs immobilized onto CTS-PEO blend composites significantly enhance the SPR effect and the synergistic effect and reduce the band gap, leading to a high photocatalytic activity.
ABSTRACT
Successful monometallic and bimetallic metal-organic frameworks with different Co/Mn ratios have been synthesized under solvothermal conditions. The as-synthesized MOFs followed by deposition of Pd nanoparticles with 0.5 to 7 wt%. The XRD, BET, SEM, TEM, EDAX and FT-IR characterization results reveal that bimetallic MOFs and Pd nanoparticles were finely dispersed on the prepared MOFs surfaces. XRD results confirm the formation of the desire MOFs and show the high degree of dispersion of Pd nanoparticles. TEM images show that Pd nanoparticles are nano-sized with almost uniform shape. EDAX shows that Pd nanoparticles successfully loaded on Co0.5-Mn0.5-MOF-74 catalyst. CO oxidation as a model reaction was then used to assess the catalytic performance of the prepared catalysts. The catalytic activity results show enhancement in the catalytic activities of monometallic MOFs after introducing another metal in the same framework and show an excellent improvement in CO conversion after loading with Pd nanoparticles. Furthermore, the samples that contain Pd nanoparticles exhibits higher catalytic activities which raised with increasing the content of Pd nanoparticles.
ABSTRACT
In the present study, a bimetallic Cr-Mg-MOF was successfully synthesized by the solvothermal method and then modified by loading different amounts of phosphomolybdic acid (PMA) using a simple wet impregnation technique. The morphological and structural properties of the prepared samples were investigated using X-ray diffraction, TEM, SEM, BET and FTIR spectroscopy. Importantly, Mg doping not only caused the Cr-Mg-MOF to have a higher surface area than MIL-101 (Cr) or MOF-74 (Mg), but the strategy of doping metal ions can be an effective way to improve the adsorption performance of MOFs. The surface acidity and the acid strength of the samples were determined using potentiometric titration and the FTIR of pyridine adsorption. The incorporation of PMA crystals gradually enhances both the surface acidity and the acid strength of the PMA/Cr-Mg-MOF catalysts up to 75 wt%. The catalytic performances of the prepared catalysts were tested in two acid-catalyzed organic transformations, namely, 7-hydroxy-4-methyl coumarin and 3,4-dihydropyrimidinone. In the two reactions, the catalytic activity attains the maximum value at 75 wt% PMA loading. The PMA catalysts supported on Cr-Mg-MOF are potentially promising heterogeneous catalysts for acid-catalyzed organic transformations in environmentally friendly processes, to replace the use of conventional homogeneous PMA catalysts.
