Biochar as an effective material for acetone sorption and the effect of surface area on the mechanism of sorption.

Walnut shells and apricot pits were used to produce non-activated, air-activated and steam-activated biochar. The specific surface area decreased in the order steam-activated (500-727 m 2.g-1), air-activated (59-514 m2.g-1) and non-activated biochars (1.71-236 m2.g-1). The results indicated that water steam created a multi-layer block structure with a well-developed porous structure, especially at 900 °C, while activation with air resulted in a more fragmented structure with a higher amount of coarse pores, leading to lower specific surface values. Acetone sorption experiments were performed in order to determine the acetone sorption capacity and to evaluate the acetone sorption kinetics of the biochars, as well as to identify the possible mechanism of sorption. The maximum sorption capacity estimated from the adsorption isotherms up to a relative pressure of 0.95 ranged from 60.3 to 277.3 mg g-1, and was highest in the steam-activated biochar with the largest surface area. The acetone adsorption isotherms were fitted with different adsorption models, where the Fritz-Schlunder model showed the best fitting results. The adsorption kinetics was evaluated using two kinetics models - pseudo first order and pseudo second order. The results indicated that the biochars with a large surface area exhibited physical sorption through van der Waals forces as the dominant mechanism, while acetone sorption on samples with a smaller surface area can be attributed to a mixed dual sorption mechanism, which combines physical sorption and chemisorption on oxygen functional groups. The perfect reusability of the biochars was confirmed by four consecutive adsorption-desorption cycles.

Correction: Poly(acrylic acid)-mediated synthesis of cerium oxide nanoparticles with variable oxidation states and their effect on regulating the intracellular ROS level.

Correction for 'Poly(acrylic acid)-mediated synthesis of cerium oxide nanoparticles with variable oxidation states and their effect on regulating the intracellular ROS level' by Xiaohui Ju et al., J. Mater. Chem. B, 2021, 9, 7386-7400, DOI: 10.1039/D1TB00706H.

Poly(acrylic acid)-mediated synthesis of cerium oxide nanoparticles with variable oxidation states and their effect on regulating the intracellular ROS level.

Cerium oxide nanoparticles (CeNPs) possess multiple redox enzyme mimetic activities in scavenging reactive oxygen species (ROS) as a potential biomedicine. These enzymatic activities of CeNPs are closely related to their surface oxidation state. Here we have reported a synthetic method to modify CeNPs' surface oxidation state by changing the conformation of the poly(acrylic acid) (PAA) polymers adsorbed onto the CeNP surface. The synthesized PAA-CeNPs exhibited the same core size, morphology, crystal structure, and colloidal stability, with the only variation being their surface oxidation state (Ce3+ percentage). The modification mechanism can be attributed to the polymers chemisorbed onto the metal oxide surface forming a metal complexation structure. Such adsorption further modified CeNPs' surface oxidation state in a temperature-dependent manner. The series of PAA-CeNPs exhibited multiple redox enzyme mimetic activities (superoxide dismutase, catalase, peroxidase, and oxidase) directly related to their surface oxidation state. In vitro experiments showed no cytotoxic effect of these PAA-CeNPs on the osteoblastic cell line SAOS-2 at high loadings. Microscopic images confirmed the internalization of PAA-CeNPs in the cells. All tested PAA-CeNPs can reduce the basal and hydrogen peroxide-induced intracellular ROS level in the cells, indicating their effective intracellular ROS scavenging effect. However, we did not observe a positive correlation between the CeNP surface oxidation state and their capacities to reduce the intracellular ROS levels. We propose that CeNPs can maintain a dynamic state of Ce3+/Ce4+ during their catalytic activities, exhibiting a non-linear correlation between the CeNP surface oxidation state and their effect on regulating the intracellular ROS level.

Electrical mobility of silver ion in Ag2O-B2O3-P2O5-TeO2 glasses.

The effect of adding TeO(2) into (100 - x)[0.5Ag(2)O - 0.1B(2)O(3) - 0.4P(2)O(5)] - xTeO(2), with 0-80 mol % TeO(2) glass, on the structural changes and electrical properties has been investigated. DSC and thermodilatomery were used to study their thermal behavior, structure was studied by Raman spectroscopy, and electrical properties have been studied by impedance spectroscopy over a wide temperature and frequency range. The introduction of TeO(2) as a third glass former to the glass network causes the structural transformation from TeO(3) (tp) to TeO(4) (tbp) which contributes to the changes in conductivity. The glasses with low TeO(2) content show only a slow decrease in dc conductivity with addition of TeO(2) due to the increase of the number of nonbridging oxygens, which increases the mobility of Ag(+) ions. The steep decrease in conductivity for glasses containing more than 40 mol % TeO(2) is a result of decrease of the Ag(2)O content and stronger cross-linkage in glass network through the formation of more Te-(eq)O(ax)-Te bonds in TeO(4) tbp units. The glasses obey ac conductivity scaling with respect to temperature, implying that the dynamic process is not temperature dependent. On the other hand, the scaling of the spectra for different glass compositions showed the deviations from the Summerfield scaling because of the local structural disorder which occurs as a result of the structural modifications in the tellurite glass network.