Magnetic activated carbon from spent coffee grounds: iron-catalyzed CO2 activation mechanism and adsorption of antibiotic lomefloxacin from aqueous medium.

The facile fabrication of low-cost adsorbents possessing high removal efficiency and convenient separation property is an urgent need for water treatment. Herein, magnetic activated carbon was synthesized from spent coffee grounds (SCG) by Fe-catalyzed CO2 activation at 800 °C for 90 min, and magnetization and pore formation were simultaneously achieved during heat treatment. The sample was characterized by N2 adsorption-desorption, XRD, VSM, SEM, and FTIR. Batch adsorption experiments were conducted using lomefloxacin (LMO) as the probing pollutant. Preparation mechanism was revealed by TG-FTIR and XRD. Experimental results showed that Fe3O4 derived from Fe species can be reduced to Fe by carbon at high temperatures, followed by subsequent reoxidation to Fe3O4 by CO2, and the redox cycle between Fe and Fe3O4 favored the formation of pores. The promotion effects of Fe species on CO2 activation can be quantitatively reflected by the yield of CO as the signature gaseous product, and the suitable activation temperate range was determined to be 675 to 985 °C. The BET surface area, total pore volume, and saturated magnetization value of the product were 586 m2 g-1, 0.327 cm3 g-1, and 11.59 emu g-1, respectively. The Langmuir model was applicable for the adsorption isotherm data for LMO with the maximum adsorption capacity of 95 mg g-1, and thermodynamic analysis revealed that the adsorption process was endothermic and spontaneous. This study demonstrated that Fe-catalyzed CO2 activation was an effective method of converting SCG into magnetic separable adsorbent for LMO removal from aqueous medium.

3D carbon aerogel from waste corrugated cardboard as a photothermal reservoir for solar steam generation.

Three-dimensional carbon aerogel (CA800) was prepared from waste corrugated cardboard (WCC) by the procedure of slurrying, solvent replacement, drying, and carbonization in turn, and the product was explored as an all-in-one evaporator for solar steam generation without bulk water. Carbonization of the precursor was investigated using thermogravimetric analyzer coupled with Fourier transform infrared spectrometer. Results showed that CO2, CO, furfural, and levoglucosan were released during pyrolysis of WCC within the range of 300 to 390 °C, while polymerization of newly formed char between 390 and 580 °C mainly resulted in the formation of CO2 and CO. Both pyrolysis and polymerization reactions can be described by diffusion-controlled mechanisms, and the activation energies were 155.62 and 11.17 kJ mol-1, respectively. CA800 possessed a BET surface area of 210 m2 g-1. Light can be effectively absorbed and converted into heat by CA800, and its surface temperature achieving 73 °C under 1 kW m-2 irradiation. CA800 had outstanding wettability due to the presence of hydrophilic minerals in carbon matrix, and it was able to store as much as 15 times its own weight in water due to its abundant interconnected channels and hierarchical nanopores. Solar-driven water evaporation rate over CA800 achieved 1.72 kg m-2 (normalized to projection area), which was nearly 6 times higher than the value achieved by the bare water system. The photothermal conversion efficiency was calculated to be 118 %, and the overestimated efficiency was caused by the environmental energy gained by the cold evaporation surface of CA800.

Ammonia-nitrogen and phosphates sorption from simulated reclaimed waters by modified clinoptilolite.

This paper presents the investigation of the ammonia-nitrogen and phosphates sorption from simulated reclaimed wastewater by modified clinoptilolite. The results showed that the modified clinoptilolite has a high sorption efficiency and removal performance. The ammonia-nitrogen and phosphates removal rate of the modified clinoptilolite reached to 98.46% and 99.80%, respectively. The surface of modified clinoptilolite became loose and some pores appeared, which enlarged the specific surface area; the contents of Na and Fe increased, and the contents of Ca and Mg decreased. The modified clinoptilolite possesses rapid sorption and slow balance characteristics and ammonia-nitrogen and phosphates sorption is more consistent with the Langmuir isotherm model. The adsorption kinetics of ammonia-nitrogen and phosphates follows the Elovich adsorption dynamics equation, which describes the sorption of ammonia-nitrogen and phosphates in aqueous solution as mainly a chemical sorption. Results from the thermodynamics experiment involving ammonia-nitrogen and phosphates sorption reveal that the process is a spontaneous and endothermic process, and is mainly driven by entropy effect.

Continuous removal of ore floatation reagents by an anaerobic-aerobic biological filter.

A laboratory scale up-flow anaerobic-aerobic biological filter was constructed to treat synthetic ore floatation wastewater. Volcanic stone was applied as packing media for aerobic section. Biodegradation of some common ore floatation reagents as potassium ethyl xanthate dithiophosphate and turpentine were evaluated. An average COD reduction rate of 88.7% for potassium ethyl xanthate by the biofilter was obtained at HRT of 6h, air water flow ratio of 10:1 and pH of 7. Its effluent COD concentration varied between 17 and 43 mg/L. Xanthates and dithiophosphate were found to be easily biodegradable, whereas turpentine was not favorable for microorganism to digest. The performance of the reactor fluctuated slightly within the temperature range of 10-35 °C. Operation of the biofilter was sensitive to influent pH values. A neutral to weak basic influent was preferred for biofilter to maintain an efficient operation. Anaerobic treatment was able to enhance the biodegradability of influents significantly.