The paper describes the synthesis and characterization of novel TiO2–metal hexacyanometallates (MHCMs) composite materials. The starting material, TiO2, was modified by addition of cobalt-hexacyanoferrate (CoHCF) or iron-hexacyanocobaltate (FeHCC) at various concentrations. The resulting composites were characterized as follows: cyclic voltammetry (CV) followed the formation of TiO2–MHCM clusters, TEM micrographs studied their morphology, XAS and XPS data indicated that MHCM bonds to TiO2 through the nitrogen atom of its –CN group and modifies the environment of Ti compared to that of pure anatase. As expected, and confirmed by UV-Vis and XP-valence band data, the electronic properties of TiO2 were substantially modified: the edge in the composite materials shifted by about −2.0 eV relative to TiO2
This paper deals with the synthesis and characterization of iron-hexacyanocobaltate (FeHCC) and its antibacterial properties. The nanoparticles were prepared by a facile co-precipitation technique. Crystal structure, particle morphology, and elemental composition were determined using X-ray Powder Diffraction, X-ray fluorescence spectroscopy, Transmission Electron Microscopy (TEM), and Infrared Spectroscopy (IR). The antibacterial activity of the FeHCC nanoparticles was tested against Escherichia coli and Staphylococcus aureus as models for Gram-negative and Gram-positive bacteria, respectively, by bacterial counting method and microscopic visualization (TEM, FEG-SEM, and fluorescence microscopy). The results showed that the FeHCC nanoparticles bind to the bacterial cells, inhibit bacterial growth in a dose- and time-dependent manner, inducing a loss of the membrane potential, the production of reactive oxygen species and the release of macromolecules (nucleic acids and proteins) in the extracellular environment. To the best of our knowledge, this is the first study reporting the antimicrobial effects of metal-hexacyanometallates suggesting practical uses of these materials in different areas, such as self-cleaning surfaces or food packaging.
The treatment of tannery wastewaters is a complex task due to the complexity of the waste: a mixture of several pollutants, both anionic and cationic as well as organic macromolecules which are very hard to treat for disposal all together. Geopolymers are a class of inorganic binders obtained by alkali activation of aluminosilicate powders at room temperature. Such activation process leads to a cement like matrix that drastically decreases mobility of several components via entrapment. This process taking place in the matrix can be hypothesized to be the in-situ formation of zeolite structures. In this work we use a metakaolin based geopolymer to tackle the problem directly in an actual industrial environment. To obtain a geopolymer, the metakaolin was mixed with 10 wt% of wastewater added with sodium hydroxide and sodium silicate as activating solutions. This process allowed a rapid consolidation at room temperature, the average compressive strength was between 14 and 43 MPa. Leaching tests performed at different aging times confirm a high immobilization efficiency close to 100%. In particular, only the 0.008 and 2.31% of Chromium and Chlorides respectively are released in the leaching test after 7 months of aging.
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