Browsing by Author "Bolender, James"

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    Hydrochemistry and fluoride contamination in Ndali-Kasenda crater lakes, Albertine Graben: Assessment based on multivariate statistical approach and human health risk
    (Groundwater for Sustainable Development, 2021) Ojok, Walter; Wanasolo, William; Wasswa, John; Bolender, James; Ntambi, Emmanuel
    Hydrochemistry of crater lakes (n = 15) in the Ndali-Kasenda cluster was deciphered using standard methods of the American Public Health Association to understand the major ion chemistry; spatial distribution, occurrence, and non-carcinogenic health risks due to exposure to fluoride levels in the lakes in Ndali- Kasenda cluster, Albertine Graben. Numerous economic activities take place in and around the crater lakes which serve as major sources of domestic water whose origin of potential contaminants is ambiguous. In this study, WHO (2017) regulatory limit exceedance included F􀀀 , pH, Ca2+, Fe2+, Mn2+, and TDS. A strong positive correlation was observed between F􀀀 and TDS; F􀀀 and pH; F􀀀 and EC; F􀀀 and HCO3􀀀 . However, concerning hydrogeochemical signature, the lakes are mainly of Ca–HCO3 type and low in Na–K–HCO3 type due to rock water interaction in the geology of the area. Principal component analysis (PCA) performed on Ndali-Kasenda hydrogeochemical data resulted in six principal components (PCs) explaining 88.6% of the total variance. The PCs represented the primary processes that control the crater lake hydrogeochemistry in the Ndali-Kasenda area which include; weathering of rocks reactions, ion exchange, and evaporation processes. The hazard quotient (HQ) for noncarcinogenic health risks associated with exposure to Ndali- Kasenda fluoride levels via ingestion revealed that HQ for infants surpassed the acceptable HQ limit for all the lakes studied, while 86.67 % of the sampled lakes exceeded the HQ value for children via ingestion. Based on the hydrogeochemical parameters analyzed, aside from L. Murigamire and L. Wankenzi, water from the other studied lakes is chemically not acceptable for drinking purposes. An urgent need to take ameliorative action in this area to protect the inhabitants from exposure to excess fluoride in drinking water was recommended.
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    Synthesis and characterization of hematite biocomposite using cassava starch template for aqueous phase removal of fluoride
    (Carbohydrate Polymer Technologies and Applications, 2022) Ojok, Walter; Ntambi, Emmanuel; Bolender, James; Wasswa, John; Wanasolo, William; Moodley, Brenda
    In this study, facile synthesis of α-Fe2O3 biocomposite was mediated by cassava starch as a soft template. Batch mode evaluated its sorption behavior for fluoride removal from aqueous media. Characterization studies using analytical techniques confirmed the existence of porous α- Fe2O3 biocomposite with heterogeneous surfaces having a varied affinity for fluoride. The sorption process was optimized using central composite design (CCD) in response surface methodology (RSM) with a good model prediction (R2 = 0.9066). A study of the interaction effect showed the synergy of process variables on fluoride removal with the result’s intensity indicated by the nature of contour plot curvature. Based on the RSM optimization, an optimum fluoride removal efficiency of 85.26 % can be achieved at an initial fluoride concentration of 55 mg/L, α- Fe2O3 biocomposite dose of 0.55 g, pH of 7.5, and contact time of 95 min. Sorption equilibrium data were well modeled by Freundlich isotherm (0.9916), indicating multilayer sorption on a heterogeneous surface of the sorbent with a varied affinity for fluoride. Presence of co-existing anions reduced fluoride removal efficiency in the order PO43􀀀 > HCO3􀀀 > SO4 2 􀀀 > NO3􀀀 > CƖ􀀀 . At the same time, its kinetics was better modeled by pseudo-second-order kinetics (R2 = 0.9764), showing that the sorption process is rate-limiting. The sorption thermodynamics study showed that the process was spontaneous, exothermic, and entropy-driven physisorption. Hence, the results signify that the green synthesized α- Fe2O3 biocomposite could be a potential sorbent for sustainable defluoridation.