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These data replicate findings that indicate that AWS exhibit slower manual inhibition latency, and suggest that these inhibition differences may be associated with an individual’s negative experience with stuttering rather than stuttering severity.

These data replicate findings that indicate that AWS exhibit slower manual inhibition latency, and suggest that these inhibition differences may be associated with an individual’s negative experience with stuttering rather than stuttering severity.A novel sol-gel method was employed in this study to efficiently synthesize SnO2 nanoparticles to catalyze the ozonation of acetaminophen (ACT) from aqueous solutions. The influence of various parameters including Sn source, type of capping and alkaline agents, and calcination temperature on the catalytic activity of the SnO2 preparations was investigated. The SnO2 nanoparticles prepared by tin tetrachloride as Sn source, NaOH as gelatin agent, CTAB as capping agent and at calcination temperature of 550 °C (SnNaC-550) exhibited the maximum performance in the catalysis of ACT. The optimized catalyst (SnNaC-550) had spherical-homogeneous and cubic-shaped nanocrystalline particles with 5.5 nm mean particle size and a BET surface area of 81 m2/g, which resulted in 98% degradation and 84% mineralization of 50 mg/L ACT at 20 and 30 min reaction time, respectively when combined with ozonation (COP). Based on the radical scavenger experiments, •OH was the major oxidizing agent involved in the removal of ACT. LC/MS analysis showed that short-chain carboxylic acids were the main intermediates. Furthermore, the SnNaC-550 catalytic activity was preserved after four successive cycles. Collectively, the new method has the potential to efficiently synthesize stable and reusable SnO2 nanoparticles to catalyze the ozonation of ACT from aquatic environments.The adsorption of Cr(VI) on biochars can be suppressed by coexisting anions, but the roles of O-containing functional groups and in particular N-containing functional groups are unclear. In this study, we combined spectroscopic and molecular simulation approaches to investigate the selective adsorption of Cr(VI) on the O-rich (PB, UB1) and N-rich (UB3, UB5) biochars under strong competition of anions. The elemental analysis and pyrolysis-gas chromatography/mass spectrometry indicated that the structures of PB and UB1 were similar, and so were the UB3 and UB5. Quantification of functional groups showed that for UB1, 75.3% of Cr(VI) removal was attributed to O-containing groups, while 53.3-72.7% of that was mediated by N-containing groups in UB3 and UB5. X-ray photoelectron spectra and density functional theory calculations confirmed that for O-rich biochars, surface complexation and strong H-bonds between carboxyl/hydroxyl and HCrO4- improved Cr(VI) removal in the presence of anions, while for N-rich biochars, Cr(VI) adsorption was depressed by coexisting anions in the order of Cl->NO3- >SO42- because of the weaker H-bond between protonated amino groups and HCrO4-. This study presents a novel approach for quantitative, molecular-level evaluation of the roles of biochar functional groups in the Cr(VI) removal from complex environmental systems.A novel class of hybrid solvents (mEIPTetz) comprising of N-methylated ethylene imine polymer (mEIP) and 1-ethyl-3-methylimidazolium tetrazolate ([Emim][Tetz]) were developed for the highly efficient and reversible capture of SO2. The synergistic interactions rather than simple mixing between mEIP and [Emim][Tetz] were confirmed by Fourier transform infrared spectroscopy (FTIR), nuclear magnetic resonance (NMR) and density functional theory (DFT) calculations. Besides, it was experimentally demonstrated that mEIPTetz mixtures exhibited improved kinetics for SO2 absorption, and the production of viscous solids were completely eliminated, compared with using mEIP alone. More significantly, an exceedingly high solubility of 0.308 g SO2·g-1 absorbent in 2mEIP8Tetz was received for trapping SO2 from simulated flue gas containing 2000 ppm SO2, which was much higher than most of the results reported in previous literatures under the same conditions. Finally, the absorption and desorption mechanisms were proposed according to the results of FTIR and 1H NMR analysis.The development of magnesium oxychloride cement (MOC) can convert wastes in the potash industry into valuable products and reduce CO2 emission. The use of acid radicals has the potential to enhance the water resistance of MOC. selleck chemicals However, because of the internal stress formed during the crystallization process, the occurrence of cracks accompanied by a significant decrease in the mechanical properties is inevitable. Inspired by the sandcastle worm and organic-inorganic copolymerization, a novel strategy was proposed, which employed phytic acid (PA) to copolymerize with phase 5 crystals to reduce the internal stress and prevent crack generation. XPS and TG-DSC analyses revealed that organic-inorganic copolymers were successfully produced. Furthermore, the compressive strength (CS) and water resistance of MOC-PA were significantly enhanced. The enhanced properties were associated with the coordination bonds and high tension of the rigid rings in phytic acid, which was sufficient to overcome the internal stress. Additionally, the repeated hydrolysis of rod-like phase 5 generated a gel-like phase from the outside inward, enhancing their water resistance. Compared with MOC-0, MOC-0.6 showed a 17.8% increase in CS and a 102.3% increase in water resistance. The microscopic mechanisms of the enhanced CS and water resistance of high-performance greener cements were proposed.In this study, peroxydisulfate (PDS) was used as electron acceptor to improve the photocatalytic activity of WO3. The results indicated that the degradation of carbamazepine by UVA-LED/WO3/PDS process followed pseudo-first order and PDS addition significantly enhanced the degradation rate by inhibiting the recombination of electrons and holes. The observed pseudo-first order rate constant (kobs) was in linear relationship with the dosage of WO3, while inversely proportional to the initial concentration of CBZ. PDS decreased the kobs slightly when its concentration exceeded 0.5 mM. The 365 nm UVA-LED performed much better than 385 nm or 405 nm even though its energy efficiency was the lowest. Based on the steady-state kinetic model, sulfate radical was the dominant radical. The effects of water matrix were complex bicarbonate ion and humic acid showed strong inhibitory effect; increasing the pH above 7 led to significant drop in CBZ removal; sulfate ion slightly decreased the kobs while 5 mM chloride ion more than doubled the kobs.