Wiseshore7204

This study investigated the methane production improvement of algal sludge by zerovalent iron (ZVI)-assisted anaerobic digestion. The zerovalent iron added were 0.5, 2, 5, 10, and 20 g·ZVI/g·TS (total solid). The results indicated that the addition of ZVI at 2, 5, 10, and 20 g·ZVI/g·TS has improved the methane production 1.07, 1.24, 1.41, and 1.46 times as compared with no ZVI added. The dewaterability of treated algal sludge has improved 1.06, 1.08, 1.08, and 1.11 times as compared with no ZVI addition. The biochemical methane production test results fitted to both one-substrate and two-substrate models. The one-substrate model indicated that the hydrolysis rate k has increased 8.21, 7.07, 9.39, 3.50, and 5.07 times as compared with R1 where no ZVI was added. The two-substrate model implied that the rapid hydrolysis rate k rapid values were 5.23, 4.5, 5.98, 2.23, and 3.23 times as compared with R1. The one-substrate model predicted that the value of methane production was in high correlation with the actual value (R 2 > 0.98). selleck chemical The addition of ZVI in algal sludge for methane production without an extra pretreatment process has improved the hydrolysis rate and methane production. This has the potential to be developed as an effective and economic technology in resource recovery from algal sludge. Copyright © 2020 American Chemical Society.A precise determination method of azilsartan solubility between 293.15 and 333.15 K in several ordinary solvents and some of their aqueous mixtures was established by high-performance liquid chromatography. In all tested solvents, its solubility shows exponential growth with the increase in temperature. This trend is especially pronounced in methanol and ethanol. The order of solubility of azilsartan can be expressed as ethanol > tetrahydrofuran > ethanol/water (8/2, v/v) > methanol > methanol/water (8/2, v/v) > n-propanol > isopropanol > ethanol/Water (5/5, v/v) > acetonitrile. The solubility data of azilsartan were well correlated by the λh model. Moreover, the thermodynamic data including the dissolving enthalpy, entropy, and Gibbs free energy of azilsartan in each solvent were calculated which is crucial to its preparation technology study. Copyright © 2020 American Chemical Society.The kraft lignin's low molecular weight and too high hydroxyl content hinder its application in bio-based carbon fibers. In this study, we were able to polymerize kraft lignin and reduce the amount of hydroxyl groups by incubating it with the white-rot fungus Obba rivulosa. Enzymatic radical oxidation reactions were hypothesized to induce condensation of lignin, which increased the amount of aromatic rings connected by carbon-carbon bonds. This modification is assumed to be beneficial when aiming for graphite materials such as carbon fibers. Furthermore, the ratio of remaining aliphatic hydroxyls to phenolic hydroxyls was increased, making the structure more favorable for carbon fiber production. When the modified lignin was mixed together with cellulose, the mixture could be spun into intact precursor fibers by using dry-jet wet spinning. The modified lignin leaked less to the spin bath compared with the unmodified lignin starting material, making the recycling of spin-bath solvents easier. The stronger incorporation of modified lignin in the precursor fibers was confirmed by composition analysis, thermogravimetry, and mechanical testing. This work shows how white-rot fungal treatment can be used to modify the structure of lignin to be more favorable for the production of bio-based fiber materials. Copyright © 2020 American Chemical Society.We examine the applicability of urea solutions as a novel cost-effective chemical for enhanced oil recovery processes. Two sandpack flooding experiments were conducted using 5 and 10 wt % urea solutions. Another flooding experiment was also carried out using the same sandpack with fresh water and used as a reference. Supporting experiments such as interfacial tension (IFT), viscosity of water in oil (W/O) emulsions, total acid number (TAN), and Fourier-transform infrared (FTIR) spectroscopy were conducted to confirm the generation of in situ surfactants by reacting urea solutions with the naphthenic acids in bitumen and evaluate their impact on the oil recovery. The analyses of FTIR, IFT, TAN, and viscosity measurements support the generation of in situ surfactants that leads to the formation of stable water in oil emulsions and hence a more stable displacement front resulting in higher oil recovery. Copyright © 2020 American Chemical Society.The physicochemical and hydration properties of mechanically modified flax fibers (FFs) were investigated herein. Raw flax fibers (FF-R) were ball-milled and sieved through mesh with various aperture sizes (420, 210, and 125 μm) to achieve modified samples, denoted as FF-420, FF-210, and FF-125, respectively. The physicochemical and hydration properties of FF-R with variable particle sizes were characterized using several complementary techniques microscopy (SEM), spectroscopy (FT-IR, XRD, and XPS), thermoanalytical methods (DSC and TGA), adsorption isotherms using gas/dye probes, and solvent swelling studies in liquid H2O. The hydration of FF biomass is governed by the micropore structure and availability of active surface sites, as revealed by the adsorption isotherm results and the TGA/DSC profiles of the hydrated samples. Gravimetric water swelling, water retention values, and vapor adsorption results provide further support that particle size reduction of FF-R upon milling parallels the changes in surface chemical and physicochemical properties relevant to adsorption/hydration in the modified FF materials. This study outlines a facile strategy for the valorization and tuning of the physicochemical properties of agricultural FF biomass via mechanical treatment for diverse applications in biomedicine, energy recovery, food, and biosorbents for environmental remediation. Copyright © 2020 American Chemical Society.This work reports the synthesis of nanosilica-coated magnetic carbonaceous adsorbents (MCA@SiO2) using low-temperature hydrothermal carbonization technique (HCT) and the feasibility to utilize it for methylene blue (MB) adsorption. Initially, a carbon precursor (CP) was synthesized from corn starch under saline conditions at 453 K via HCT followed by the magnetization of CP again via HCT at 453 K. Subsequently, MCA was coated with silica nanoparticles. MCA and MCA@SiO2 were characterized using X-ray diffraction, Fourier transform infrared, scanning electron microscopy/energy-dispersive spectroscopy, transmission electron microscopy, and Brunauer-Emmett-Teller (BET) N2 adsorption-desorption isotherms. The BET surface area of MCA and MCA@SiO2 were found to be 118 and 276 m2 g-1, respectively. Adsorption of MB onto MCA@SiO2 was performed using batch adsorption studies and in the optimum condition, MCA@SiO2 showed 99% adsorption efficiency with 0.5 g L-1 of MCA@SiO2 at pH 7. Adsorption isotherm studies predicted that MB adsorption onto MCA@SiO2 was homogeneous monolayer adsorption, which was best described using a Langmuir model with the maximum adsorption capacity of 516.