Physicochemical and microbial community dynamics of Kocho fermented from different enset varieties in South West Ethiopia.

Enset (Ensete ventricosum (Welw.) Cheesman) is an indigenous multipurpose plant in Ethiopia. More than 20 % of people in Ethiopia rely on enset for their subsistence livelihood. Its fermentation produces a starchy food named Kocho, which is yet poorly studied. In this study, physicochemical and microbial community dynamics of Kocho fermented from different enset varieties (Maziya, Genna, and Arkiya) were collected at Dawro Zone (Southern Ethiopia). Samples were collected at various fermentation times (days 1-60) for physicochemical and microbial (culture-dependent and culture-independent) characterization. Results showed that increasing fermentation time has a significantly strong positive (R2 = 0.768, p = 0.004) correlation between titrable acidity, and a significantly strong negative association with pH (R2 = -0.715, p = 0.009), moisture (R2 = -0.982, p < 0.05), ash (R2 = -0.932, p < 0.05), fat (R2 = -0.861, p < 0.05), fiber (R2 = -0.981, p < 0.05) and carbohydrate (R2 = -0.994, p < 0.001) contents. An increasing or decreasing trend of physicochemical parameters observed during enset fermentation is significantly associated with microbial community dynamics. Shifts of microbial community observed during culture-dependent analysis were also confirmed by metagenomic results. During fermentation, Firmicutes (39-68 %) > Proteobacteria (7-53 %) > Cyanobacteria (7-24 %) were dominant phyla in the three enset varieties. Gamma (traditional starter culture) is dominated by Lactobacillus plantrum and Lactobacillus manihotivorans most probably the two species that play a significant role in initiating enset fermentation.

Simultaneous adsorption and oxidation of Sb(III) from water by the pH-sensitive superabsorbent polymer hydrogel incorporated with Fe-Mn binary oxides composite.

In this work, the superabsorbent polymer hydrogel (SPH) of Poly(potassium acrylate-co-acrylamide (PPAA)) incorporated with Fe-Mn binary oxides (FMBOs) was synthesized and used for the removal of Sb(III) from water. Characterization analysis proved that FMBO3 was successfully encapsulated into the SPH. The Fe/Mn oxide species in the composite SPH comprised FeO(OH), Fe2O3, MnO(OH), and MnO2. The functional groups including N-H, -OH, carboxy as well as Fe atoms were confirmed adsorption sites through ligand exchange and inner-sphere complexes formation. Mn oxides can partially oxidize Sb(III) to Sb(V). Compared with the pseudo-first-order model, the pseudo-second-order model could better describe the adsorption kinetics. And the swelling degree of the composite SPH had a positive impact on the removal rate. The Langmuir-Freundlich model was the most suitable isotherm model to analyze the experimental data. According to thermodynamic parameters, the adsorption process was a spontaneous exothermic reaction. The maximum adsorption capacity of the composite SPH for Sb(III) could be up to 105.59 mg/g at 288 K. In addition, a stable removal rate can be achieved over a wide pH range of 3-10, with little metal leaching even under acidic conditions. Furthermore, coexisting ions and DOM displayed an insignificant influence on the adsorption of Sb(III).

Enhanced removal of oxytetracycline antibiotics from water using manganese dioxide impregnated hydrogel composite: Adsorption behavior and oxidative degradation pathways.

The present work provides the first attempt of using manganese dioxide loaded poly(sodium acrylate) hydrogel (MnO2@PSA) to address potential threats posed by oxytetracycline (OTC) antibiotics in aqueous environment. The MnO2@PSA was prepared via a facile approach and demonstrated enhanced removal performance even under extremely high concentrations of OTC. The outstanding performance exhibited by MnO2@PSA was attributed to synergetic effects of adsorption oxidative degradation. The synthesized composite was characterized evaluated under varying conditions. The adsorption pH was optimized at pH 5, at which the removal efficiency OTC was reached 91.46%. According to the kinetics study, the pseudo-second-order kinetic model was the best to explain the adsorption data, implying the interaction mechanisms were dominated by chemisorption. The Langmuir isotherm model was the best to explain the isotherm data, and the corresponding maximum adsorbed amount of OTC was 1150.4 mg g-1. The MnO2@PSA was highly selective for OTC adsorption and degradation under the presence of natural organic matter and common environmental metal ions. The oxidative degradation study indicated that OTC molecules were structurally degraded into 15 intermediate products via six reaction pathways. Both the theoretical models and spectroscopic methods demonstrated the removal mechanism of OTC onto MnO2@PSA was governed by ion exchange, cation-π bonding, hydrogen-bonding, and π-π electron donor-acceptor. Overall, MnO2@PSA is an excellent and environmentally sustainable material to remove OTC from water and wastewater via the combined effects of adsorption and oxidative degradation.

Evaluating the effect of fenton pretreated pyridine wastewater under different biological conditions: Microbial diversity and biotransformation pathways.

Pyridine contamination poses a significant threat to human and environmental health. Due to the presence of nitrogen atom in the pyridine ring, the pi bond electrons are attracted toward it and make difficult for pyridine treatment with biological and chemical methods. In this study, coupling Fenton treatment with different biological process was designed to enhance pyridine biotransformation and further mineralization. After Fenton oxidation process optimized, pretreated pyridine was evaluated under three biological (anaerobic, aerobic and microaerobic) operating conditions. Under optimum Fenton oxidation, pyridine (30-75%) and TOC (5-25%) removal efficiencies were poor. Biological process alone also showed insignificant removal efficiency, particularly anaerobic (pyridine = 8.2%; TOC = 5.3%) culturing condition. However, combining Fenton pretreatment with biological process increased pyridine (93-99%) and TOC (87-93%) removals, suggesting that hydroxyl radical generated during Fenton oxidation enhanced pyridine hydroxylation and further mineralization in the biological (aerobic > microaerobic > anaerobic) process. Intermediates were analyzed with UPLC-MS and showed presence of maleic acid, pyruvic acid, glutaric dialdehyde, succinic semialdehyde and 4-formylamino-butyric acid. High-throughput sequencing analysis also indicated that Proteobacteria (35-43%) followed by Chloroflexi (10.6-24.3%) and Acidobacteria (8.0-29%) were the dominant phyla detected in the three biological treatment conditions. Co-existence of dominant genera under aerobic/microaerobic (Nitrospira > Dokdonella > Caldilinea) and anaerobic (Nitrospira > Caldilinea > Longilinea) systems most probably play significant role in biotransformation of pyridine and its intermediate products. Overall, integrating Fenton pretreatment with different biological process is a promising technology for pyridine treatment, especially the combined system enhanced anaerobic (>10 times) microbial pyridine biotransformation activity.

Hydrous manganese dioxide modified poly(sodium acrylate) hydrogel composite as a novel adsorbent for enhanced removal of tetracycline and lead from water.

In this study, hydrous manganese dioxide (HMO) modified poly(sodium acrylate) (PSA) hydrogel was produced for the first time to remove tetracycline(TC) and lead(Pb(II)) from water. The as-prepared composite was characterized using various techniques, such as SEM-EDS, FTIR, XRD, BET, and XPS, to elucidate the successful loading of HMO and analyze subsequent sorption mechanisms. Different influencing parameters such as adsorbent dose, initial concentration of adsorbates, reaction time, solution pH, and temperature were also investigated. The adsorption kinetic studies of both TC and Pb(II) removal indicated that equilibrium was achieved within 12 h, with respective removal rates of 91.9 and 99.5%, and the corresponding adsorption data were fitted to the second-order kinetics model. According to the adsorption isotherm studies, the sorption data of TC best fitted to the Langmuir isotherm model while the adsorption data of Pb(II) were explained by the Freundlich isotherm model. The maximum adsorption capacities of both TC and Pb(II) were found to be 475.8 and 288.7 mg/g, respectively, demonstrating excellent performances of the adsorbent. The uptake capacity of PSA-HMO was significantly influenced by the level of solution pH, in which optimum adsorption amount was realized at pH 4.0 in the TC and Pb(II) systems, respectively. Thermodynamic studies showed the process of TC and Pb(II) adsorptions were endothermic and spontaneous. Overall this study elucidated that PSA-HMO composite can be a promising candidate for antibiotics and heavy metal removal in water treatment applications.

Application of graphene-based materials for removal of tetracyclines using adsorption and photocatalytic-degradation: A review.

Tetracyclines are extensively used to treat human and animal infectious diseases due to its effective antimicrobial activities. About 70-90% of its parent materials are released into the environment through urine and feces, implying they are the most frequently detected antibiotics in the environment with high ecological risks. Adsorption and photocatalysis have been promising techniques for the removal of tetracyclines due to effectiveness and efficiency. Graphene-based materials provide promising platforms for adsorptive and photocatalytic removal of tetracyclines from aqueous environment owning to distinctive remarkable physicochemical, optical, and electrical characteristics. Herein, we intensively reviewed the available literatures in order to provide comprehensive insight about the applications and mechanisms of graphene-based materials for removal of tetracyclines via adsorption and phototocatalysis. The synthesis methods of graphene-based materials, the tetracycline adsorption and photocatalytic-degradation conditions, and removal mechanisms have been extensively discussed. Finally concluding remarks and future perspectives have been deduced and recommended to stimulate further researches in the subject. The review study can be used as theoretical guideline for further researchers to improve the current approaches of material synthesis and application towards tetracyclines removal.