preparation-biomass-based-mesoporous-carbon-with-higher-nitrogen

Preparation of Biomass-based Mesoporous Carbon with Higher Nitrogen-/Oxygen-chelating Adsorption for Cu(II) Through Microwave Pre-Pyrolysis

An environment-friendly technique for synthesizing biomass-based mesoporous activated carbon with high nitrogen-/oxygen-chelating adsorption for Cu(II) is ...

Nanjing Agricultural University

Pure N mono- and N/P dual-doped cotton-stalk-derived activated carbon fibers (CSCFs) were synthesized by steam, HNO(CSCF-N), NH(CSCF-A), and (NH)PO(CSCF-N/P) treatments. This study investigated how three different N/P modifiers affected the pore structure, chemical property, HO generation ability, and electrocatalytic activity of methylene blue (MB) degradation of CSCFs in an electric-Fenton system. Results confirmed that the three employed treatments effectively doped N/P in the carbon lattice and slightly changed the pore structures. NH and (NH)PO were the most effective modifiers for the N mono-doping and N/P dual-doping of CSCFs, respectively. Among the fabricated CSCFs, the N/P dual-doped CSCF-N/P demonstrated the highest electrochemical activity in an electro-Fenton system, followed by the N mono-doped CSCF-A, the CSCF-N, and the raw CSCF. In contrast to the CSCF electrode, the CSCF-N/P electrode exhibited enhanced HO, OH generation, and MB degradation efficiency by 42%, 41%, and 35%, respectively. Under optimum conditions, the electrochemical decolorization efficiency of MB (initial concentration, 100 mg L) of the CSCF-N/P reached 93% after 150 min and was 24.1% higher than that of the CSCF. By the tenth cycle, 82.2% of the MB could still be decomposed, suggesting the excellent stability and reusability of the N/P co-doped CSCF electrode. The outstanding electrocatalytic performance of the CSCF-N/P electrode is primarily due to the simultaneous doping of active N/P sites with low activation energy and introduction of mesopores with strong trapping forces for MB. The MB reduction catalyzed by CSCF electrodes followed pseudo-first-order kinetics, and the reaction rate depended on the modifiers.

Effects of N mono- and N/P dual-doping on HO, OH generation, and MB electrochemical degradation efficiency of activated carbon fiber electrodes.

A novel wastewater treatment process, known as an alternating activated sludge reactor (AASR), is proposed to treat wastewater in full-scale operations. The AASR is a technical development based on the sequencing batch reactor (SBR) and cyclic activated sludge technology (CAST). The performance of AASR was evaluated in this study and found to be effective for the removal of pollutants. The average effluent NH-N, TN, TP, and COD concentrations were 0.5, 17, 0.8, and 40 mgL, respectively. The corresponding average removal efficiencies were 97%, 59%, 83%, and 83%, respectively, indicating that the AASR was also a successful operating system for the removal of organic matter. The AASR has many advantages, such as successive filling, high removal efficiency, high stability and reliability, low area requirement, no sludge circulation reflux, and low construction costs. The operation mode of the alternating anoxic, anaerobic, and aerobic conditions displayed a higher efficiency for nitrification than that of conventional SBR. The effective mode for denitrification was a step-feed. The control program of the AASR is highly flexible and can easily be modified by a plant manager to meet various loading requirements.

Performance of nitrogen removal in an alternating activated sludge reactor for full-scale applications.

Controlling of pre-oxidation conditions can effectively enhance the aimed active functional groups via promoting the oxidation and grafting reaction on biochar's surface. Here, the effect of different nitric acid pre-oxidation concentration (NAPOC) was investigated on the type and content of active oxygen-containing functional sites during the pre-oxidation stage, as well as the active nitrogen-containing binding sites for the following grafting process. And the possible reaction mechanisms for introducing nitrogen/oxygen-containing functional groups such as amide, pyridinic, carbonyl, carboxyl, etc., into the surface by ethylenediamine (EDA) were proposed. The samples were characterized by various analyses including N adsorption/desorption, Boehm titration, Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). Results showed that the NAPOC played a crucial role in promoting the formation of oxygen-containing initiators, and difference of NAPOC resulted in different reaction principles. At higher NAPOC, more carbonyl, carboxyl and hydroxyl functional groups were formed, which facilitated the decoration of nitrogen binding active sites of amide and pyridinic for mercury ions adsorption into the carbon lattice of mesoporous biomass-derived biochar (MBB). The proportions of micropore and mesopore remained basically unchanged, indicating that the decorated nitrogen/oxygen sites were highly uniformly dispersed in MBB's frame and thus resulted in high activity. The comparison of adsorption properties of MBB showed that MBB-25-EDA had the highest adsorption capacity of 153 mg g at pH 6, confirming that the 25% was the optimum NAPOC for introducing nitrogen/oxygen functional binding sites for effectively anchoring mercury.

Effect of nitric acid pre-oxidation concentration on pore structure and nitrogen/oxygen active decoration sites of ethylenediamine -modified biochar for mercury(II) adsorption and the possible mechanism.

Kunquan Li

College of Engineering

Nanjing Agricultural University

Preparation of Biomass-based Mesoporous Carbon with Higher Nitrogen-/Oxygen-chelating Adsorption for Cu(II) Through Microwave Pre-Pyrolysis