Single-Step Hydrothermal Synthesis of Biochar from H3PO4-Activated Lettuce Waste for Efficient Adsorption of Cd(II) in Aqueous Solution.

Developing an ideal and cheap adsorbent for adsorbing heavy metals from aqueous solution has been urgently need. In this study, a novel, effective and low-cost method was developed to prepare the biochar from lettuce waste with H3PO4 as an acidic activation agent at a low-temperature (circa 200 °C) hydrothermal carbonization process. A batch adsorption experiment demonstrated that the biochar reaches the adsorption equilibrium within 30 min, and the optimal adsorption capacity of Cd(II) is 195.8 mg∙g-1 at solution pH 6.0, which is significantly improved from circa 20.5 mg∙g-1 of the original biochar without activator. The fitting results of the prepared biochar adsorption data conform to the pseudo-second-order kinetic model (PSO) and the Sips isotherm model, and the Cd(II) adsorption is a spontaneous and exothermic process. The hypothetical adsorption mechanism is mainly composed of ion exchange, electrostatic attraction, and surface complexation. This work offers a novel and low-temperature strategy to produce cheap and promising carbon-based adsorbents from organic vegetation wastes for removing heavy metals in aquatic environment efficiently.

Enhanced catalytic performance of atomically dispersed Pd on Pr-doped CeO2 nanorod in CO oxidation.

Single-atom noble metal catalysts have been widely studied for catalytic oxidation of CO. Regulating the coordination environment of single metal atom site is an effective strategy to improve the intrinsic catalytic activity of single atom catalyst. In this work, single atom Pd catalyst supported on Pr-doped CeO2 nanorods was prepared, and the performance and nature of Pr-coordinated atomic Pd site in CO catalytic oxidation are systematically investigated. The structure characterization using AC-HAADF-STEM, EXAFS, XRD and Raman spectroscopy demonstrate the formation of single atom Pd site and abundant surface oxygen vacancies on the surface of Pr-doped CeO2 nanorod. With the combination of the XPS characterization and DFT calculations, the oxidation state of Pd on Pr-doped CeO2 nanorod is determined lower than that on CeO2 nanorod. The turnover frequency of CO oxidation is markedly increased from 8.4 × 10-3 to 31.9 × 10-3 s with Pr-doping at 130 ºC and GHSV of 70,000 h-1. Combined with kinetic studies, DRIFT and DFT calculations, the doped-Pr atoms reduced the formation energy of oxygen vacancies and generate more oxygen vacancies around the atomically dispersed Pd sites on the surface of cerium oxide, which reduces the dissociation energy of oxygen, thereby accelerating the reaction rate of CO oxidation.

Single-Step Preparation of Ultrasmall Iron Oxide-Embedded Carbon Nanotubes on Carbon Cloth with Excellent Superhydrophilicity and Enhanced Supercapacitor Performance.

Nanocomposites consisting of carbon materials and metal oxides are generally preferred as anodes in electrochemical energy storage. However, their low capacitance limits the achieved energy density of supercapacitors (SCs) in aqueous electrolytes. Herein, we propose a rapid combustion strategy to construct a novel electrode architecture-ultrasmall Fe2O3 anchoring on carbon nanotubes (FeO-CNT)-as a superhydrophilic and flexible anode for SCs. In 1 M Na2SO4 aqueous electrolyte, such an FeO-CNT-20 anode presents a high capacitance of 483.4 mF cm-2 (326 F g-1) at 1 mA cm-2. The aqueous asymmetric supercapacitor devices (ASCs) assembled by FeO-CNT-20 and MnO2 present a maximum operating potential of 2.0 V with a high areal energy density of 0.11 mWh cm-2 at a power density of 0.5 mW cm-2. The flexible solid-state ASCs display an energy density of 0.99 mWh cm-3 at 14.3 mW cm-3. The rapidly prepared FeO-CNT not only offers an attractive electrode for SCs but also would open up exciting new avenues to the rational design and large-scale preparation of Fe2O3-based nanocomposites for electrochemical energy storage.

Nitrogen-Doped Porous Carbon Materials Derived from Graphene Oxide/Melamine Resin Composites for CO2 Adsorption.

CO2 adsorption in porous carbon materials has attracted great interests for alleviating emission of post-combustion CO2. In this work, a novel nitrogen-doped porous carbon material was fabricated by carbonizing the precursor of melamine-resorcinol-formaldehyde resin/graphene oxide (MR/GO) composites with KOH as the activation agent. Detailed characterization results revealed that the fabricated MR(0.25)/GO-500 porous carbon (0.25 represented the amount of GO added in wt.% and 500 denoted activation temperature in °C) had well-defined pore size distribution, high specific surface area (1264 m2·g-1) and high nitrogen content (6.92 wt.%), which was mainly composed of the pyridinic-N and pyrrolic-N species. Batch adsorption experiments demonstrated that the fabricated MR(0.25)/GO-500 porous carbon delivered excellent CO2 adsorption ability of 5.21 mmol·g-1 at 298.15 K and 500 kPa, and such porous carbon also exhibited fast adsorption kinetics, high selectivity of CO2/N2 and good recyclability. With the inherent microstructure features of high surface area and abundant N adsorption sites species, the MR/GO-derived porous carbon materials offer a potentially promising adsorbent for practical CO2 capture.