6 research outputs found

    Graphene modified Salen ligands for the electrochemical determination of heavy metal ions

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    >Magister Scientiae - MScEnvironmental pollution is a major threat to all life, which needs to be addressed. Heavy metals are well-known environmental pollutants due to their toxicity and, persistence in the environment toxicity for living organisms and having a bioaccumulative nature. Environmentally, the most common hazardous heavy metals are: Cr, Ni, Cu, Zn, Cd, Pb, Hg, and As. Remediation using conventional physical and chemical methods is uneconomical and generates waste chemicals in large quantities. This study focuses on the extraction and determination of heavy metals (Nickel, Copper and Cobalt) by chelating Schiff base ligands of the type [O,N,N,O] with these metal ions. Two Schiff base ligands [N,N’-ethylenebis(salicylimine)] (Salen) and ligand [1,3-bis(salicylideneamino)-2-propanol] (Sal-DAP) were synthesized and characterised using FTIR, 1H and 13C NMR spectrometry and GC-MS techniques. Electrochemical detection of heavy metal ions in this work was achieved via ligand-metal complexation via two approaches. The in-situ method in which the metal and ligands were added to the electrochemical cell and stirred to allow complexation to occur and monitored by square wave voltammetry. While the ex-situ approach involved modifying the electrode surface by depositing a thin film of Schiff base on the electrode surface and immersed into a heavy metal solution to allow the complexation. Three modified GCE were used viz. Salen coated GCE, reduced graphene oxide-Salen coated GCE and a nafion-Salen coated GCE. The two approaches used for the electrochemical detection were successful and effective. The ex-situ approach was selected for the modification of the electrode surface since it demonstrated a higher capacity for heavy metal ion extraction

    Proceedings of the 27th International Symposium on Analytical and Environmental Problems

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    Synthesis of new pyrazolium based tunable aryl alkyl ionic liquids and their use in removal of methylene blue from aqueous solution

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    In this study, two new pyrazolium based tunable aryl alkyl ionic liquids, 2-ethyl-1-(4-methylphenyl)-3,5- dimethylpyrazolium tetrafluoroborate (3a) and 1-(4-methylphenyl)-2-pentyl-3,5-dimethylpyrazolium tetrafluoroborate (3b), were synthesized via three-step reaction and characterized. The removal of methylene blue (MB) from aqueous solution has been investigated using the synthesized salts as an extractant and methylene chloride as a solvent. The obtained results show that MB was extracted from aqueous solution with high extraction efficiency up to 87 % at room temperature at the natural pH of MB solution. The influence of the alkyl chain length on the properties of the salts and their extraction efficiency of MB was investigated

    Anti-angiogenic and toxicity effects of Derris trifoliata extract in zebrafish embryo

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    Introduction: Derris trifoliata has been traditionally used as folk for the treatment of , rheumatic joints, diarrhoea, and dysmenorrhea, and rotenoids isolated from the plant have shown to exhibit anti-cancer properties. This study aimed to assess the toxicity effects and antiangiogenic activity of extract of Derris trifoliata on zebrafish embryo model. Materials and Methods: Zebrafihs embryos were treated with aqueous extract of Derris Trifoliata to evaluate its effects on angiogenesis and zebrafish-toxicity. Angiogenic response was analyzed using whole-mount alkaline phosphatase (AP) vessel staining on 72 hours post fertilization (hpf) zebrafish embryos. Results: 1.0 mg/ml concentration was toxic to zebrafish embryos and embryos exposed to concentrations at 0.5 mg/ml and below showed some malformations. Derris trifoliata aqueous extract also showed some anti-angiogenic activity in vivo in the zebrafish embryo model wereby at high concentration inhibited vessel formation in zebrafish embryo. Conclusions: The anti-angiogenic response of extract of Derris trifoliata in zebrafish in vivo model suggest its therapeutic potential as anti-cancer agent
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