The present research involves removing copper and nickel ions from synthesized wastewater by using a simple, cheap, cost-effective, and sustainable activated green waste tea residue (AGWTR) adsorption coupled with electrocoagulation (ADS/EC) process in the presence of iron electrodes. By considering previous studies, their adsorbents used for treating their wastewaters firstly activate them by applying either chemicals or activating agents. However, our adsorbent was prepared without applying neither chemicals nor any activating agents. The operating parameters such as pH, hydraulic retention time, adsorbent dose, initial concentration, current density, and operating cost for both metals were optimized. In ADS/EC, the removal efficiency was obtained as 100% for copper and 99.99% for nickel ions. After the ADS/EC process, Fourier transform infrared (FT-IR) spectroscopy, Scanning Electron Microscopy (SEM) and Energy-dispersive X-ray spectroscopy (EDS) analysis were used to characterize the adsorbent green waste tea residue. The adsorption isotherm and kinetic model results showed that the Langmuir and the pseudo-second-order were well-fitted to the experimental adsorption data better than the Freundlich and pseudo-first-order models for both Cu2+ and Ni2+ with their maximum adsorption capacity of 15.6 and 15.9 mg g−1, respectively. The above results give an option to recycle the metal-based industrial effluents, tea industry-based wastes, enabling a waste-to-green technique for adsorbing and removing the heavy metals and other pollutants in water.
Humic acid (HA) and iron oxide (such as Fe3O4) nanoparticles are widely distributed in soil, and their complex embedded in soil might affect the transport and fate of Cu2+ in the vadose zone, while Cu2+ is a serious threat to the underlying groundwater. In this study, we synthesized a composite of Fe3O4 nanoparticles coated with HA (HA@NPs) using as an amendment a packed sand matrix in the transport column experiments. The impacts of HA content and ion strength (IS) on Cu2+ transport in the unsaturated columns were investigated. The results showed that HA exhibited a stronger inhibition effect on Cu2+ transport, and a higher IS enhanced the mobility of Cu2+ in an unsaturated porous medium in the presence of HA@NPs. The recovery ratio (Rr) of Cu2+ breakthrough in the column decreased from 66.56% to 3.94% while the mass concentration ratio CHA/CNPs increased from 0 to 50 in the HA@NPs complex. The Rr increased by 1.64 times while the IS increased from 0 to 100 mM. Batch adsorption experiments, kinetics and isotherm models, and Fourier transform infrared (FTIR) spectra analysis were implemented to elucidate the underlying mechanism. It was found that HA embedded in the sand matrix could bind Cu2+ by forming stable chelate, while the IS-dependent Cu2+ transport could be attributed to the competitive adsorption between Na+ and Cu2+. Our study demonstrates that the physicochemical environment, as well as the presence of iron oxide nanoparticles and natural organic matter, can significantly impact Cu2+ transport in unsaturated porous medium.
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