Sorption of uranium and arsenic onto iron hydroxide/oxide modified zeolite
A dissertation submitted to the Faculty of Science, University of the Witwatersrand in fulfilment of the requirements for the award of Master of Science degree, 2017. === Mining is an integral sector of most developing countries and it is a highly lucrative industry that has been in existence for ce...
Main Author: | |
---|---|
Format: | Others |
Language: | en |
Published: |
2018
|
Subjects: | |
Online Access: | Nekhunguni, Pfano Mathews (2017) Sorption of uranium and arsenic onto iron hydroxide/oxide modified zeolite, University of the Witwatersrand, Johannesburg, <http://hdl.handle.net/10539/23603> http://hdl.handle.net/10539/23603 |
Summary: | A dissertation submitted to the Faculty of Science, University of the Witwatersrand in fulfilment of the requirements for the award of Master of Science degree, 2017. === Mining is an integral sector of most developing countries and it is a highly lucrative industry that has been in existence for centuries, and assumes an essential part in their economies. However, the legacy of mining in these countries has posed a threat to underground and surface water as a result of contamination arising from Acid Mine Drainage (AMD). Bearing in mind the environmental and ecological impairment posed by AMD there is a need for innovation in the treatment of AMD, to enable financially savvy treatment of the contaminated waters.
This research is focused on the extraction of U(VI), As(III) and As(V) from synthetic metal solutions as well as field removal of these metal ions by application of iron hydroxide/oxide-modified zeolite. Batch experiments were performed to evaluate the effectiveness of iron hydroxide/oxide-modified zeolite as a potential low-cost sorbent for extracting As(III), U(VI) and As(V) from AMD. The research approach was based on the possible changes that can occur to a zeolite surface that has been in contact with an iron-laden solution. Zeolite is a commonly used adsorbent, but fewer studies have explored changes that it undergoes as an adsorbent on contact with iron solutions. Thus, the study involved modifying zeolite with iron hydroxide/oxide, which are the main precipitates of iron in the environment and which can possibly alter the adsorption properties of zeolite. Batch extraction studies were performed using the modified zeolite.
In paper I, the synthesis of iron (hydr) oxide modified zeolite was achieved through precipitation of iron on the zeolite. The kinetic data for As(V) adsorption by iron (hydr) oxide-modified zeolite model fit well into pseudo second-order and the adsorption capacity was obtained as 0.080 mg g-1. The application of iron (hydr) oxide modified zeolite on AMD for As(V) recovery showed that > 99% of As(V) was extracted from the solution. The high removal efficiency of oxyanionic arsenic species was attributed to arsenic forming complexes with iron oxyhydroxide surface on the surface of the sorbent.
Paper II dealt with adsorption of U(VI) from aqueous solution by application of iron hydro (oxide)-modified zeolite in a single-component system. Parameters such as: solution pH, contact time, adsorbent dosage, initial concentration and temperature were optimized before field application to real acid mine drainage. The optimum parameters for U(VI) adsorption were: adsorbent dosage (3.0 g), solution pH (6 ±0.1) and contact time (30 min). Optimum parameters where then applied to acid mine drainage were the effluent was found to be cleaner than the influent.
In Paper III, iron oxide-coated zeolite (IOCZ) nanocomposite was prepared and fully characterized. This sorbent was then used for extraction of U(VI) and As(III) from aqueous solutions by application of batch techniques. Batch study results were modelled best by the pseudo second-order kinetic model and Freundlich isotherm. The adsorption capacity of both U(VI) and As(II) was dependent on the temperature. The presence of Cd2+, Co2+ and Cr3+ ions enhance the adsorption of As(III) whereas the opposite trend was observed for U(VI) sorption onto IOCZ nanocomposite. === XL2018 |
---|