Comparison of the activities of C2N and BCNO towards Congo red degradation

An n-type organic carbon nitride semiconductor, C2N, was synthesized by the pyrolysis of uric acid, and its properties were investigated by scanning electron and transmission electron microscopies, X-ray powder diffraction, and vibrational, UV-visible and X-ray photoelectron spectroscopies. This novel material, composed of crystalline flakes, featured a broad absorption centered at 700¿nm, possibly due to charge transfer, and a 2.49¿eV band gap. Its catalytic performance was assessed for the treatment of effluents with the diazo dye Congo red, comparing it with that of boron carbon nitrogen oxide, BCNO. Both wide band gap semiconductors exhibited decolorizing activity in the dark, although the mechanisms were different and were not photocatalytic: BCNO was more effective towards the adsorption-coordination due to the presence of B-O, while C2N was effective towards the adsorption and the advancement of the oxidation reaction. Their kinetic constants (0.19 and 0.02 min-1 for BCNO and C2N, respectively) were comparable to those of intermetallic compounds studied for azo dyes degradation in dark conditions. In view of the high color removal efficiency (97% after 20¿min) and good reusability of BCNO, this study suggests a potential application of this catalyst for wastewater treatment, alone or in combination with C2N

Fabrication of Reduced Ag Nanoparticle Using Crude Extract of Cinnamon Decorated on ZnO as a Photocatalyst for Hexavalent Chromium Reduction

The crude extract of cinnamon (after abbreviated as KM) was used to produce silver nanoparticles (AgKM). This was subsequently utilized for the hydrothermal production of a composite consisting of AgKM decorated on zinc oxide (AgKM/ZnO) as a photocatalyst for reducing hexavalent chromium (Cr(VI)). Several methods e.g., XRD, SEM, TEM, XPS, PL, and RDB-PAS were used to analyze the optical and physicochemical properties of ZnO/AgKM samples in order to better comprehend the impact of the development of the AgKM-ZnO heterojunction in comparison to pure ZnO. In 60 min, the optimized ZnO/AgKM reduced Cr(VI) by more than 98%, with a rate constant 63 times faster than that of pure ZnO. The enhancement of the separation and transportation of photogenerated electron-hole pairs, as proven by a decrease in photoluminescence intensity when compared with ZnO, was attributed to the composite’s higher Cr(VI) reduction rate. Also, the formation of a new electronic level was created when AgKM are loaded on the surface of ZnO in the composites, as shown by the energy-resolved distribution of the electron trap (ERDT) pattern resulting to enhancement of light absorption ability by narrowing the energy band gap. Thus, ZnO/AgKM composite’s photocatalytic efficacy was enhanced by its narrow energy band gap and reduced charge recombination. Therefore, the newly produced ZnO/AgKM composite can be used as a photocatalyst to purify Cr(VI)-containing wastewater

Copper Zinc Sulfide (CuZnS) Quantum Dot-Decorated (NiCo)–S/Conductive Carbon Matrix as the Cathode for Li–S Batteries

Sulfur composites consisting of electrochemical reactive catalysts/conductive materials are investigated for use in lithium–sulfur (Li–S) batteries (LSBs). In this paper, we report the synthesis, physicochemical and electrochemical properties of CuZnS quantum dots (CZSQDs) decorated with nickel–cobalt–sulfide ((NiCo)–S)) mixed with reduced graphene oxide (rGO)/oxidized carbon nanotube (oxdCNT) (rGO/oxdCNT) ((NiCo)–S@rGO/oxdCNT) composites. These composites are for the purpose of being the sulfur host cathode in Li–S batteries. The as-prepared composites showed a porous structure with the CZSQDs being uniformly found on the surface of the rGO/oxdCNT, which had a specific surface area of 26.54 m2/g. Electrochemical studies indicated that the (NiCo)–S@rGO/oxdCNT cells forming the cathode exhibited a maximum capacity of 1154.96 mAhg−1 with the initial discharge at 0.1 C. The smaller size of the CZSQDs (~10 nm) had a positive effect on the CZSQDs@(NiCo)–S@rGO/oxdCNT composites in that they had a higher initial discharge capacity of 1344.18 mAhg−1 at 0.1 C with the Coulombic efficiency being maintained at almost 97.62% during cycling. This latter property is approximately 1.16 times more compared to the absence of the Cu–Zn–S QD loading. This study shows that the CuZnS quantum dots decorated with a (NiCo)–S@rGO/oxdCNT supporting matrix-based sulfur cathode have the potential to improve the performance of future lithium–sulfur batteries

Fabrication of Reduced Ag Nanoparticle Using Crude Extract of Cinnamon Decorated on ZnO as a Photocatalyst for Hexavalent Chromium Reduction

The crude extract of cinnamon (after abbreviated as KM) was used to produce silver nanoparticles (AgKM). This was subsequently utilized for the hydrothermal production of a composite consisting of AgKM decorated on zinc oxide (AgKM/ZnO) as a photocatalyst for reducing hexavalent chromium (Cr(VI)). Several methods e.g., XRD, SEM, TEM, XPS, PL, and RDB-PAS were used to analyze the optical and physicochemical properties of ZnO/AgKM samples in order to better comprehend the impact of the development of the AgKM-ZnO heterojunction in comparison to pure ZnO. In 60 min, the optimized ZnO/AgKM reduced Cr(VI) by more than 98%, with a rate constant 63 times faster than that of pure ZnO. The enhancement of the separation and transportation of photogenerated electron-hole pairs, as proven by a decrease in photoluminescence intensity when compared with ZnO, was attributed to the composite’s higher Cr(VI) reduction rate. Also, the formation of a new electronic level was created when AgKM are loaded on the surface of ZnO in the composites, as shown by the energy-resolved distribution of the electron trap (ERDT) pattern resulting to enhancement of light absorption ability by narrowing the energy band gap. Thus, ZnO/AgKM composite’s photocatalytic efficacy was enhanced by its narrow energy band gap and reduced charge recombination. Therefore, the newly produced ZnO/AgKM composite can be used as a photocatalyst to purify Cr(VI)-containing wastewater

Efficient Mercury Removal at Ultralow Metal Concentrations by Cysteine Functionalized Carbon-Coated Magnetite

This work reports the preparation and utility of cysteine-functionalized carbon-coated Fe3O4 materials (Cys-C@Fe3O4) as efficient sorbents for remediation of Hg(II)-contaminated water. Efficient removal (90%) of Hg(II) from 1000 ppb aqueous solutions is possible, at very low Cys-C@Fe3O4 sorbent loadings (0.01 g sorbent per liter of Hg(II) solution). At low metal concentrations (5–100 ppb Hg(II)), where adsorption is typically slow, Hg(II) removal efficiencies of 94–99.4% were achievable, resulting in final Hg(II) levels of <1.0 ppb. From adsorption isotherms, the Hg(II) adsorption capacity for Cys-C@Fe3O4 is 94.33 mg g−1, around three times that of carbon-coated Fe3O4 material. The highest partition coefficient (PC) of 2312.5 mgg−1µM−1 was achieved at the initial Hg (II) concentration of 100 ppb, while significantly high PC values of 300 mgg−1µM−1 and above were also obtained in the ultralow concentration range (≤20 ppb). Cys-C@Fe3O4 exhibits excellent selectivity for Hg(II) when tested in the presence of Pb(II), Ni(II), and Cu(II) ions, is easily separable from aqueous media by application of an external magnet, and can be regenerated for three subsequent uses without compromising Hg(II) uptake. Derived from commercially available raw materials, it is highly possible to achieve large-scale production of the functional sorbent for practical applications