Green synthesis of Zinc sulphide (ZnS) nanostructures using S. frutescences plant extract for photocatalytic degradation of dyes and antibiotics

Pollutants such as dyes and pharmaceuticals have become a problem in the environment, thus there is a need to find multifunctional materials that are safe and can be used for the removal of various pollutants. In this study, we report on the synthesis of Zinc sulphide (ZnS) nanostructures and their use as photocatalysts for the degradation of dyes and various antibiotics. Fourier transform infrared spectroscopy(FTIR) confirmed the functional groups found in plants and these were linked to the biomolecules identified through Liquid chromatography-mass spectrometry (LCMS). Ultraviolet-visible spectroscopy (UV-vis) and X-ray diffraction (XRD) confirmed the formation of the ZnS nanostructures. Thermal Gravimetric Analysis (TGA) and Brunner Emmet Teller (BET) confirmed the material was thermally stable up until 480oC and mesoporous in nature, respectively. Scanning electron microscope (SEM) and transmission electron microscope (TEM) showed that the material is spherical in shape and energy dispersive spectroscopy (EDS) further corroborated their formation. From the degradation analysis, 90% of the malachite green (MG) dye could be degraded in 60 min at optimum conditions (pH 6, 25 mg and 10 mg/L) and the holes were responsible for the degradation. Lastly, when tested against antibiotics, the ZnS material managed to degrade both the sulfisoxazole (SSX) and sulfamethoxazole (SMX). These results showed that the ZnS nanoparticles could be used as a multifunctional material for the degradation of various pollutants.

Two transition complexes based on 1H-benzimidazole-5,6-dicarboxylic acid: Synthesis, structure and photocatalytic degradation of dyes

Metal-organic frameworks [Co(Hbidc)(H2O)2] (1) and [Mn(Hbidc)(H2O)] (2), with multidentate 1H-benzimidazole-5,6-dicarboxylic acid (H3bidc) ligand, have been synthesized under hydro/solvothermal conditions and structurally characterized by elemental analysis, IR spectrum, and single-crystal X-ray diffraction. Single-crystal X-ray diffraction analysis revealed that the center Co atom of complex 1 is six-coordinated with three-dimensional supramolecular structure and center Mn of complex 2 is five-coordinated with exhibiting a 2D layered network. The photodegradation of Crystal violet dye and Methylene blue dye were studied firstly by complexes 1 and 2 as photocatalysts. Research result indicates that the degradation rate for complex 1 can reach 89.85% , 90.6% and that for complex 2 can reach 88.28% , 79.48% . At the same time, corresponding to photocatalytic kinetics was performed.

Statistical modeling of methylene blue degradation by yeast-bacteria consortium; optimization via agro-industrial waste, immobilization and application in real effluents

The progress in industrialization everyday life has led to the continuous entry of several anthropogenic compounds, including dyes, into surrounding ecosystem causing arduous concerns for human health and biosphere. Therefore, microbial degradation of dyes is considered an eco-efficient and cost-competitive alternative to physicochemical approaches. These degradative biosystems mainly depend on the utilization of nutritive co-substrates such as yeast extract peptone in conjunction with glucose. Herein, a synergestic interaction between strains of mixed-culture consortium consisting of Rhodotorula sp., Raoultella planticola; and Staphylococcus xylosus was recruited in methylene blue (MB) degradation using agro-industrial waste as an economic and nutritive co-substrate. Via statistical means such as Plackett–Burman design and central composite design, the impact of significant nutritional parameters on MB degradation was screened and optimized. Predictive modeling denoted that complete degradation of MB was achieved within 72 h at MB (200 mg/L), NaNO3 (0.525 gm/L), molasses (385 μL/L), pH (7.5) and inoculum size (18%). Assessment of degradative enzymes revealed that intracellular NADH-reductase and DCIP-reductase were key enzymes controlling degradation process by 104.52 ± 1.75 and 274.04 ± 3.37 IU/min/mg protein after 72 h of incubation. In addition, azoreductase, tyrosinase, laccase, nitrate reductase, MnP and LiP also contributed significantly to MB degradation process. Physicochemical monitoring analysis, namely UV−Visible spectrophotometry and FTIR of MB before treatment and degradation byproducts indicated deterioration of azo bond and demethylation. Moreover, the non-toxic nature of degradation byproducts was confirmed by phytotoxicity and cytotoxicity assays. Chlorella vulgaris retained its photosynthetic capability (˃ 85%) as estimated from Chlorophyll-a/b contents compared to ˃ 30% of MB-solution. However, the viability of Wi-38 and Vero cells was estimated to be 90.67% and 99.67%, respectively, upon exposure to MB-metabolites. Furthermore, an eminent employment of consortium either freely-suspended or immobilized in plain distilled water and optimized slurry in a bioaugmentation process was implemented to treat MB in artificially-contaminated municipal wastewater and industrial effluent. The results showed a corporative interaction between the consortium examined and co-existing microbiota; reflecting its compatibility and adaptability with different microbial niches in different effluents with various physicochemical contents.