Surface modification of nanoscale zero-valent iron (nZVI) using polymer stabilizers (e.g., sodium carboxymethyl cellulose, CMC) is usually used to minimize aggregation, increase stability, and enhance transport of nZVI. We investigated the stability and dynamic aggregation of bare and CMC–nZVI as affected by variations in pH, ionic strength (IS), and nZVI particle concentration. CMC coating of nZVI resulted in smaller hydrodynamic size and larger zeta potential. The largest hydrodynamic size of nZVI was associated with bare nZVI at high IS (100 mM), pH close to the point of zero charge (PZC, 7.3–7.6), and larger particle concentration (1.0 g L⁻¹). The increase in the zeta potential of CMC–nZVI reached one- to four-fold of that for bare nZVI, and was greater at pH values close to PZC, high IS, and larger particle concentration. The stability of CMC–nZVI was increased by 61.8, 93.1, and 57.5% as compared to that of bare nZVI at IS of 1, 50 and 100 mM, respectively. Calculations of Derjaguin, Landau, Verwey and Overbeek (DLVO) interaction energy were in agreement with stability results, and showed the formation of substantial energy barriers at low IS indicating greater nZVI stability. Our results suggest that at IS above 50 mM and nZVI particle concentration larger than 0.1 g L⁻¹, the likelihood of nZVI aggregation is high. Nevertheless, CMC polymer stabilizer would enhance the stability and transport of nZVI even under these unfavorable solution chemistry conditions.

During the last decade, due to an increase in anthropogenic activities, a higher environmental accumulation of heavy metals has been found, which has resulted in disturbed biogeochemical balance. Many kinds of remediation techniques have been practiced to mitigate heavy metal toxicity in the aqueous phase; however, adsorption is the most commonly accepted technique for efficient heavy metal removal. In this study, conocarpus waste was pretreated with 0%, 10%, and 20% kaolinite and pyrolyzed at 600 °C for 1 h to synthesize biochars (BC, BCK10, and BCK20, respectively), while hydrothermalized at 200 °C for 6 h to synthesize hydrochars (HC, HCK10, and HCK20, respectively). After characterization, synthesized materials were employed for the removal of cadmium (Cd), copper (Cu), lead (Pb), and zinc (Zn) from contaminated water. Experimental data was further subjected to isotherm and kinetic models to estimate the adsorption mechanism. Among all the tested adsorbents, kaolinite-synthesized materials revealed comparatively higher adsorption compared to pristine materials. It was found that pH 7 was optimum for the maximum removal of tested heavy metals. Adsorption of tested heavy metals was well explained by Langmuir and Freundlich isotherms, while pseudo-second order and Elovich kinetics models fitted well for adsorption kinetics. The maximum adsorption capacity, as predicted by the Langmuir isotherm, was the highest for BCK20 (63.19 mg g⁻¹ for Cd, 228.05 mg g⁻¹ for Cu, 248.33 mg g⁻¹ for Pb, and 45.79 mg g⁻¹ for Zn) compared to the other tested materials, and for HCK20 (31.93 mg g⁻¹ for Cd, 181.78 mg g⁻¹ for Cu, 231.85 mg g⁻¹ for Pb, and 45.72 mg g⁻¹), it was higher than pristine HC. Isotherm and kinetics modeling data indicated that multiple mechanisms were involved in Cd, Cu, Pb, and Zn removal, such as chemisorption and electrostatic interactions. The amount of oxygen-containing surface functional groups and SiO₂ particles could be responsible for the maximum adsorption of heavy metals by BCK20 and HCK20. Our findings suggest that biochar, hydrochar, and their kaolinite-modified composites possess the excellent potential to remove heavy metals from contaminated aqueous media, and could be further applied to treat wastewater to mitigate heavy metal toxicity for a sustainable environment.

Efficient application of nanoscale zero-valent iron (nZVI) particles in remediation processes relies heavily on the ability to modify the surfaces of nZVI particles to enhance their stability and mobility in subsurface layers. We investigated the effect of sodium carboxy-methyl-cellulose (CMC) polymer stabilizer, pH, particle concentration, and flow rate on the transport of nZVI particles in sand columns. Breakthrough curves (BTCs) of nZVI particles indicated that the transport of nZVI particles was increased by the presence of CMC and by increasing the flow rate. The relative concentration (RC) of the eluted CMC–nZVI nanoparticles was larger at pH 9 as compared to RC at pH 7. This is mainly attributed to the increased nZVI particle stability at higher pH due to the increase in the electrostatic repulsion forces and the formation of larger energy barriers. nZVI particle deposition was larger at 0.1 cm min⁻¹ flow due to the increased residence time, which increases the aggregation and settlement of particles. The amount of CMC–nZVI particles eluted from the sand columns was increased by 52% at the maximum flow rate of 1.0 cm min⁻¹. Bare nZVI were mostly retained in the first millimeters of the soil column, and the amount eluted did not exceed 1.2% of the total amount added. Our results suggest that surface modification of nZVI particles was necessary to increase stability and enhance transport in sandy soil. Nevertheless, a proper flow rate, suitable for the intended remediation efforts, must be considered to minimize nZVI particle deposition and increase remediation efficiency.

Microplastics (MPs) are emerging environmental pollutants worldwide, posing potential health risks. Moreover, MPs may act as vectors for other contaminants and affect their fate, transport, and deposition in the environment. Therefore, efficient and economical techniques are needed for the removal of contemporary MPs and contaminants from the environment. The present research study investigated the sorption of phosphorus (P) and ammonium (NH₄⁺) onto date palm waste-derived biochar (BC) from an aqueous solution in the presence of polyamide (PA) and polyethylene (PE) MPs. The BC was prepared at 600 °C, characterized for physio-chemical properties, and applied for P and NH₄⁺ removal via isotherm and kinetic sorption trials. The results of the sorption trials demonstrated the highest removal of NH₄⁺ and P was obtained at neutral pH 7. The highest P sorption (93.23 mg g⁻¹) by BC was recorded in the presence of PA, while the highest NH₄⁺ sorption (103.76 mg g⁻¹) was found with co-occurring PE in an aqueous solution. Sorption isotherm and kinetics models revealed that P and NH₄⁺ removal by MP-amended BC followed chemisorption, electrostatic interaction, precipitation, diffusion, and ion exchange mechanisms. Overall, co-existing PA enhanced the removal of P and NH₄⁺ by 66% and 7.7%, respectively, while co-existing PE increased the removal of P and NH₄⁺ by 55% and 30%, respectively, through the tested BC. Our findings suggested that converting date palm waste into BC could be used as a competent and economical approach to removing P and NH₄⁺ from contaminated water. Furthermore, microplastics such as PE and PA could assist in the removal of P and NH₄⁺ from contaminated water using BC.