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Eco-friendly, renewable Hochst-based adsorbents remove high quantities of Zn in water. | LitMetric

Eco-friendly, renewable Hochst-based adsorbents remove high quantities of Zn in water.

J Environ Health Sci Eng

Universidade Estadual do Oeste do Paraná (UNIOESTE), Faculdade Street, 645 - Jardim La Salle, Toledo, State of Paraná 85903-000 Brazil.

Published: December 2020

AI Article Synopsis

Article Abstract

Although not considered poisonous and with natural occurrence, Zn contamination is mainly related to anthropic actions. This research aim was to develop, from crambe wastes, adsorbents with high adsorption capacity of Zn. The crambe biomass was modified with HO, HSO and NaOH 0.1 mol L, resulting in four crambe-based adsorbents: C. (unmodified), C. HO, C. HSO and C. NaOH. These were studied by determination of their chemical components, SEM, FTIR, pH, thermal stability (by TG/DTG curves), SSA, pore volume and pore diameter (by BET and BJH). Adsorption studies were also carried out to evaluate its Zn removal capacity. Evaluations were taken on adsorbent dose and the influence of the pH, as well as studies on adsorption kinetics and equilibrium. These results were evaluated by pseudo-first order, pseudo-second order, Elovich, intraparticle diffusion, Langmuir, Freundlich, Dubinin-Radushkevich and Sips (linear and nonlinear models). Results show that the crambe-based adsorbents may have functional groups such as hydroxyls, amides, carbonyls and carboxylates, which may be responsible for the Znadsorption. The materials have heterogeneous structure, allowing the occurrence of mono and multilayer adsorption of Zn. The finest results point out the occurrence of mono and multilayer of Zn (evidenced by Sips-nonlinear model), with an increase in Q of 72% (C. HO), 22% (C. HSO) and 80% (C. NaOH). The developed crambe adsorbents have low cost of production (since the raw material is until now a solid waste) and have high removal ratio of Zn from waters, being a promising technology.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7721775PMC
http://dx.doi.org/10.1007/s40201-020-00505-9DOI Listing

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