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The Synthesis and Effect of Silver Nanoparticles on the Adsorption of Cu2+ from Aqueous Solutions

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The adsorption of Cu2+ ions from an aqueous solution using AgNPs synthesized from Convolvulus arvensis leaf extract was investigated. The characterization of AgNPs was investigated before and after the adsorption of Cu2+ ions via Fourier-transform infrared spectroscopy (FTIR), energy-dispersive X-ray spectroscopy (EDS), and scanning electron microscopy (SEM) analyses. The adsorbent contained various functional groups in addition to the AgNPs, which contributed to the Cu2+ ions adsorption. The silver nanoparticle surface consisted of spherical particles and deep pores, which adsorbed numerous Cu2+ ions. The influences of dosage, pH, and contact time on adsorption of 10 and 50 mg/L Cu2+ at 298 K, and initial Cu2+ concentrations at 298 and 323 K were studied. It was found that the highest percentage of Cu2+ ions adsorbed from an aqueous solution was 98.99%; the aqueous solution had 10 mg/L of Cu2+ ions and 0.2 g of AgNPs, at pH 12 and 298 K. A pseudo-second kinetics model offered the most accurate description of the process of adsorption. The process of Cu2+ adsorption more resembled a Langmuir rather than a Freundlich isotherm model, including chemical and physical mixed adsorption (mixed adsorption) processes, and was exothermic and spontaneous.
Title: The Synthesis and Effect of Silver Nanoparticles on the Adsorption of Cu2+ from Aqueous Solutions
Description:
The adsorption of Cu2+ ions from an aqueous solution using AgNPs synthesized from Convolvulus arvensis leaf extract was investigated.
The characterization of AgNPs was investigated before and after the adsorption of Cu2+ ions via Fourier-transform infrared spectroscopy (FTIR), energy-dispersive X-ray spectroscopy (EDS), and scanning electron microscopy (SEM) analyses.
The adsorbent contained various functional groups in addition to the AgNPs, which contributed to the Cu2+ ions adsorption.
The silver nanoparticle surface consisted of spherical particles and deep pores, which adsorbed numerous Cu2+ ions.
The influences of dosage, pH, and contact time on adsorption of 10 and 50 mg/L Cu2+ at 298 K, and initial Cu2+ concentrations at 298 and 323 K were studied.
It was found that the highest percentage of Cu2+ ions adsorbed from an aqueous solution was 98.
99%; the aqueous solution had 10 mg/L of Cu2+ ions and 0.
2 g of AgNPs, at pH 12 and 298 K.
A pseudo-second kinetics model offered the most accurate description of the process of adsorption.
The process of Cu2+ adsorption more resembled a Langmuir rather than a Freundlich isotherm model, including chemical and physical mixed adsorption (mixed adsorption) processes, and was exothermic and spontaneous.

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