Aflatoxin B1: Chemistry, Environmental and Diet Sources and Potential Exposure in Human in Kenya

Cancer incidences and mortality in Kenya are increasing according to recent reports and now number among the top five causes of mortality in the country. The risk factors responsible for this increase in cancer incidences are assumed to be genetic and/or environmental in nature. The environmental factors include exposure to carcinogenic contaminants such aflatoxins (AFs). However, the exact causes of the increase in cancer incidences and prevalence in many developing countries are not fully known. Aflatoxins are known contaminants produced by the common fungi Aspergillus flavus and the closely related Aspergillus parasiticus which grow as moulds in human foods. Aflatoxin B1 (AFB1) is most common in food and is 1000 times more potent when compared with benzo(a)pyrene, the most potent carcinogenic polycyclic aromatic hydrocarbon (PAH). Aflatoxins have therefore drawn a lot of interest in research from food safety and human health point of view. In this chapter, the chemistry, synthesis, identification, toxicology and potential human health risks of AFB1 in Kenya are discussed

Modular polyoxometalate-layered double hydroxides as efficient heterogeneous sulfoxidation and epoxidation catalysts

Selective sulfoxidation of sulfides and epoxidation of olefins are two types of important organic reactions and the corresponding products of sulfoxides, sulfones and epoxides are widely used as raw materials in industrial processes. The fabrication of one efficient catalyst for both reactions, remains a challenging task. In this paper, we report the preparation of a highly efficient heterogeneous catalyst of Mg3Al-ILs-La(PW11)2 using an exfoliation/assembly approach. The catalyst was characterized by FT-IR, XRD, TG/DTA, BET, XPS, 29Si CP/MAS NMR, the 27Al-MAS NMR, SEM, HRTEM, EDX etc. The designed catalyst showed high efficiency and selectivity for sulfoxidation of sulphides and epoxidation of olefins under mild conditions at a production rate of 208 mmol g-1 h-1 and 31 mmol g-1 h-1, respectively. Moreover, the Mg3Al-ILs-La(PW11)2 can be recycled and reused at least 5 times without obvious decrease of its catalytic activity. The scaled-up experiments revealed that the catalyst retained its efficiency and robustness, demonstrating the catalyts' great potential for industrial applications

Use of lanthanide-containing polyoxometalates to sensitise the emission of fluorescent labelled serum albumin

Monitoring the interaction of biomolecules is important, and the use of energy transfer is a principal technique in elucidating nanoscale interactions. Lanthanide compounds are promising luminescent probes for biological samples as their emission is longer-lived than any native autofluorescence. Polyoxometalates (POMs) are interesting structural motifs to incorporate lanthanides, offering low toxicity and a size pertinent for biological applications. Here, we employ iso-structured POMs containing either terbium or europium and assess their interaction with serum albumin by sensitisation of a fluorescent tag on the protein via LRET (luminescence resonance energy transfer) by exciting the lanthanide. Time-resolved measurements showed energy transfer with an efficiency of over 90 % for the POM–protein systems. The Tb–POM results were relatively straightforward, while those with the iso-structured Eu–POM were complicated by the effect of protein shielding from the aqueous environment

A Mn(III) polyoxotungstate in the oxidation of organosulfur compounds by H2O2 at room temperature: an environmentally safe catalytic approach

The tetrabutylammonium (TBA) salt of a Keggin-type polyoxometalate (POM), with the chemical formula TBA4H2[BW11Mn(H2O)O39]{\textperiodcentered}H2O, TBABW11Mn, was evaluated as a catalyst in the oxidation by hydrogen peroxide of several organosulfur compounds, namely benzothiophene (BT), 2-methylbenzothiophene (2-MBT), 3-methylbenzothiophene (3-MBT), dibenzothiophene (DBT), 4-methyldibenzothiophene (4-MDBT) and 4,6-diethyldibenzothiophene (4,6-DEDBT), in acetonitrile at room temperature. All compounds were oxidized to their corresponding sulfones with high conversion and selectivity. Following the excellent results achieved, the BW11Mn/H2O2 in CH3CN system was tested in the oxidation of model fuels (MFs) consisting of a mixture of BTs and DBTs in hexane (MF1 containing mainly BTs and MF2 containing predominantly DBTs). In both cases, the organosulfur compounds from the model fuels were fully converted into their corresponding sulfones. Envisaging the development of a promising desulfurization procedure, the extraction of sulfur compounds from MF2 was attempted after the catalytic oxidation process. More than 98 mol% was removed using an ethanol/H2O mixture

Design and Synthesis of Reusable Nanoparticles for Reversible Chemisorption of Hexavalent Chromium Anions from Aqueous Media and Catalysis

A magnetically active nanocomposite material has been synthesized from the reaction mixture of magnetite core iron nanoparticles electrostatically coated with SiO2, hydrotalcite nanosheets ([Eu8 (OH)20 (H2O)n]4+), and decatungstophosphate anion ([α-PW10O367−]). The resulting nanocomposite material, denoted as Fe3O4@SiO2@LEuH@PW10, is demonstrated to effectively adsorb chromate anions from aqueous solutions. The adsorption isotherms fit the Langmuir model with a capacity of 23 mmol·g−1 after 42 minutes at 25°C. The reaction is spontaneous at room temperature with 44.22 kJ·mol−1 of activation energy required. In addition, heating the chromate-adsorbed nanocomposite material at 40°C results in dissociation of the chromate anions from the nanocomposite material. As such, the recycled adsorbent Fe3O4@SiO2@LEuH@PW10 is reused for chromate removal in aqueous solutions for at least ten times without obvious loss of activity. This spontaneous reversible chemisorption mechanism for chromate adsorption provides a new pathway for separation and cleaning of industrial wastewater contaminated with chromate ions. The robust catalytic activity of the nanocomposite is also demonstrated

Trace Metal Detection in Aqueous Reservoirs Using Stilbene Intercalated Layered Rare-Earth Hydroxide Tablets

Contamination of aquatic reservoirs with metal ions is a slow gradual process that is not easy to detect. Consequences of the metal ions, especially the ones with high atomic numbers (heavy metals) at high concentrations, are severe and irreversible in aquatic reservoirs. As such, early detection mechanisms, especially at trace concentration, are essential for mitigation measures. In this work, a new, robust, and effective tool for trace metal detection and monitoring in aqueous solutions has been developed. Tablets (1 mm thick and similar to medicinal tablets) were manufactured from a powder comprising stilbene intercalated into gallery spaces of lanthanide-containing layered double hydroxides. The tablets were placed in a water column having different concentrations of Pb2+ and Cu2+ ions, and the water was allowed to flow for 45 minutes at a flow rate of 100 ml/s. Thereafter, the tablets were dried and made to powder, and their phosphorescence was measured. The gradual stilbene phosphorescence turnoff in the tablets from various concentrations of metal ions was correlated with sorption amounts. The tablets were able to detect effectively metal ions (up to Pb2+ 1.0 mmol/L and Cu2+ 5.0 mmol/L) in the aqueous media. As such, the concentrations of Pb2+ and Cu2+ ions at trace levels were determined in the test solutions. This method provides a real-time metal ion analysis and does not involve sampling of water samples for analysis in the laboratory