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Average BIX values for the inlets and outlets were ∼0.8, suggesting limited contributions from autochthonous production of CDOM. Dominant plant species in the wetlands were cattail and bulrush. Humic peaks A and C, along with protein peaks, were observed in plant leachates. Protein peaks rapidly degraded with solar simulator irradiation. Results indicate that most of the wetlands are a net sink for CDOM, possibly due to absorption to sediments. The FS wetland appears to have a source of non-CDOM optically active organic carbon, possibly from a pollutant. In this research, UiO-66 and its composite nanoparticles with thermally oxidized nanodiamond (OND) were synthesized via a simple solvothermal method and utilized as solid adsorbent for the removal of anionic methyl red (MR) dye and cationic malachite green (MG) dye from contaminated water. The synthesized adsorbents were analyzed by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), thermogravimetric analysis (TGA), N2 adsorption-desorption, and zeta potential analyzer. The influences of various factors such as initial concentrations of the dyes, adsorption process time, solution pH, solution temperature and ionic strength on adsorption behavior of MR dye onto OND-UiO hybrid nanoparticle were investigated. The adsorption of MR onto OND-UiO hybrid nanoparticle could be well described by Langmuir isotherm model. Meanwhile, pseudo-second order kinetic model was found to be suitable for illustration of adsorption kinetics of MR onto OND-UiO. Thermodynamic investigation suggested that the adsorption process was spontaneous and endothermic, and controlled by an entropy change instead of enthalpy effect. The experimental adsorption results indicated that OND-UiO hybrid nanoparticle could simultaneously adsorb 59% of MR and 43% of MG from the mixture of both dyes in only 2 min showing synergistic effect compared with single UiO-66 and OND nanoparticles in terms of adsorption rate and removal capacity of anionic dyes. The appropriate removal efficiency, rapid adsorption kinetic, high water stability, and good reusability make OND-UiO hybrid nanoparticle attractive candidate for simultaneously removal of both anionic MR and cationic MG dyes from wastewater. The present study evaluates biodegradation of the polyblends of poly(lactic acid) (PLA), polycaprolactone (PCL) and microcrystalline cellulose (MCC) in different compositions and comparison of the properties of those blends with that of neat PLA and neat PCL. The samples were melt extruded and blended to evaluate the environmental fate of the polyblends under simulated composting conditions following the standard ASTM International D5338-15 protocol. It was seen that blends with a higher concentration of PCL and MCC in the PLA matrix showed higher carbon mineralization percentage in comparison to the blends having low PCL and MCC components. Molecular weight analysis of the samples showed a decrease in their weight due to chain scission mechanism leading to the formation of intermediates. Analytical techniques revealed the formation of microbial biofilms on the blended biopolymeric surfaces. Field emission scanning electron microscopy showed the formation of fibril-like structures by PLA, and the formation of rough patches on the PCL surface re-confirmed biodegradation of the samples. This work fuels interest in the material characterization of PLA/PCL/MCC based polyblends and helps in tuning the biodegradability of the studied samples according to the demands. To investigate how the changes in performance and the microbial community of the co-digestion system of Pennisetum hybrid and pig manure, two co-digestion systems in a semi-continuous mode were established at different grassmanure mixture ratios (5050 and 7525), and at variable organic loading rates (OLRs). The two reactors were in a steady-state at the OLRs of 2.0-5.0 g VS/(L·d), with the specific and volumetric biogas yields of 383.86 ± 65.13 to 574.28 ± 72.04 mL/g VS and 0.87 ± 0.07 to 2.36 ± 0.13 m3/(m3·d), respectively. The co-digestion system with a mixture ratio of 7525 failed at an OLR of 5.5 g VS/(L⋅d). This failure could be attributed to the accumulation of volatile fatty acids (VFAs) owing to the imbalance between acid-production and -oxidation bacteria. By contrast, the co-digestion system with mixture ratio of 5050 failed at an OLR of 7.0 g VS/(L⋅d), which was likely due to mechanical issues or improper reactor configuration. The genus Proteiniphilum contributed to the increase in total ammonia nitrogen. These findings provide useful guidance for optimizing co-digestion system, enhancing reactor performance and improving the wastes treatment. Herein, CeO2 catalysts with nanotube, nanobelt, and wire-in-nanotube morphologies were successfully fabricated by a facile single spinneret electrospinning technique. And catalytic activity of these electrospun CeO2 nanomaterials were evaluated by toluene catalytic combustion reaction. https://www.selleckchem.com/products/Vorinostat-saha.html Among the three morphologies of CeO2 catalysts, CeO2 nanobelt (CeO2-NB) presented the best toluene catalytic combustion performance (T90% = 230 °C) at WHSV = 60,000 mL g-1 h-1, also exhibited the lowest activation energy (Ea = 80.2 kJ/mol). Based on the characterization by TEM, XRD, BET, SEM, XPS, Raman spectroscopy, H2-TPR, and O2-TPD results, the high catalytic activity of CeO2-NB catalyst was attributed to its porous nanobelt morphology with larger specific surface area and the abundance of surface oxygen vacancies. Furthermore, the CeO2-NB catalysts presented an excellent durability by longtime on-stream test (as well as presence of 5% vol. water vapor), suggesting its great potential for practical air pollution control application. The effective removal and recovery of phosphorus from aquatic environments are highly important for successful eutrophication control and phosphorus recycling. Herein, we prepared biochar containing MgO nanoparticles (MgO-biochar) by fast pyrolysis of MgCl2-impregnated corn stalks, probed its phosphate adsorption performance. Through the fast pyrolysis, the MgCl2 promoted the formation of micropores and mesoporous, and decomposed into MgO nanoparticles with the size smaller than 100 nm. The adsorption experiments showed that the adsorption property increased with the increase of Mg content, and had a strong correlation with the external surface area. And the phosphate adsorption was well described by the Langmuir-Freundlich model (maximum adsorption capacity was determined as 60.95 mg P/g). Kinetic analysis and characterization analysis of MgO-biochar for different adsorption time indicated that phosphate adsorption onto MgO-biochar was mainly controlled by rapid binding to the external surface (about 75% of the equilibrium adsorption amount), and the uptake rate was limited by the slow diffusion of phosphate into the biochar interior (about 25% of the equilibrium adsorption amount).