Trace Metals, Crude Protein, and TGA-FTIR Analysis of Evolved Gas Products in the Thermal Decomposition of Roasted Mopane Worms, Sweet Corn, and Peanuts.

The thermal behavior of mopane worms (Imbrasia belina), roasted peanuts (Arachis hypogaea L.), and sweet corn (Zea mays L. saccharata) was investigated under inert conditions using the TGA-FTIR analytical technique heated from 64 to 844°C at a heating rate of 20°C/min. The degradation patterns of the food samples differed as sweet corn and peanuts exhibited four degradation stages 188, 248, 315, and 432°C and 145, 249, 322, and 435°C, respectively. Mopane worms displayed three (106, 398, and 403°C). The different decomposition patterns together with the types of evolved gases shown by FTIR analysis justified the varied biochemical and chemical composition of foods. The common evolved gas species between the food samples were H2O, CO2, P=O, CO, and CH4 but mopane worms showed two extra different bands of C-N and N-H. Higher volumes of evolved gases were recorded at temperatures between 276 and 450°C, which are higher than the usual cooking temperature of 150°C. This means that the food maintained its nutritional value at the cooking temperature. Mopane worms were found to contain twice and four times crude protein content than peanuts and corn, respectively. Only total arsenic metal was reported to be above threshold limits.

A Critical Review on the Synthesis and Application of Ion-Imprinted Polymers for Selective Preconcentration, Speciation, Removal and Determination of Trace and Essential Metals from Different Matrices.

The presence of toxic trace metals and high concentrations of essential elements in the environment presents a serious threat to living organism. Various methods have been used for the detection, preconcentration and remediation of these metals from biological, environmental and food matrices. Owing to the complexicity of samples, methods with high selectivity have been used for detection, preconcentration and remediation of these trace metals. These methods are achieved by the use of ion-imprinted polymers (IIPs) due to their impressive properties such as selectivity, high extraction efficiency, speciation capability and reusability. Because of the increase of toxic trace and essential metals in the environment, IIPs have attracted great use in analytical chemistry. This review, provide a brief background on IIPs and polymerization method that are used for their preparation. Recent applications of IIPs as adsorbents for preconcentration, removal, speciation and electrochemical detection of trace and essential metal is also discussed.

Determination of furanic compounds in Mopane worms, corn, and peanuts using headspace solid-phase microextraction with gas chromatography-flame ionisation detector.

A headspace-solid phase microextraction - gas chromatography-flame ionisation detector (HS-SPME-GC/FID) method was developed for the simultaneous determination of furan, 2-methylfuran and 2-furaldehyde in thermally processed Mopane worms, corn, and peanuts. The optimal HS-SPME conditions with polydimethylsiloxane/carboxen/divinylbenzene (PDMS/CAR/DVB) fiber were 30 °C, 40 min and 600 rpm stirring speed. The recoveries, detection and quantification limits for the analytes in food samples were 67-106%, 0.54-3.5 µg kg-1, and 1.8-12 µg kg-1, respectively. These results showed that the developed method was accurate, reproducible, and sensitive for the determination of furan, 2-methylfuran and 2-furaldehyde in complex food matrices with limited interference from other components. The optimised analytical method was applied for monitoring the presence of the furanic compounds in heat-processed South African foods. Although 2-furaldehyde was not detected in food samples, the maximum concentrations of 24 and 95 µg kg-1 were found for furan and 2-methylfuran, respectively.

Multi-ion imprinted polymers (MIIPs) for simultaneous extraction and preconcentration of Sb(III), Te(IV), Pb(II) and Cd(II) ions from drinking water sources.

Simultaneous extraction and preconcentration of several potentially toxic metal ions have received great attention because of their toxicological effects on aquatic life and human beings. Multi-ion imprinted polymers (MIIP) have proved to be promising adsorbents with excellent specific recognition performance than single-ion imprinted polymer. Therefore, in this study, the MIIP strategy was employed for simultaneous extraction and enrichment of Sb(III), Cd(II), Pb(II) and Te(IV) ions from drinking water sources. MIIPs was used as a sorbent material in ultrasound-assisted dispersive solid phase extraction combined with inductively coupled plasma optical emission spectrometry (UA-DSPE/ICP-OES). The experimental parameters that affect the extraction efficiency and recovery of Sb(III), Cd(II), Pb(II) and Te(IV) were investigated using response surface methodology. Under optimum conditions, the enhancement factors, linear range, limit of detection (LOD) and limit of quantification (LOQ) were 37.7-51.1, 0.04-100 µg L-1, 0.011-0.28 µg L-1, 0.037-093 µg L-1, respectively. The intra-day (n = 10) and inter-day (n = 5) precision expressed as relative standard deviations (%RSDs,) were 3% and 5%, respectively. The proposed UA-DSPE/ICP-OES method was applied for preconcentration and determination of the trace metal ions in environmental samples. Furthermore, the accuracy of the method was evaluated using spiked recovery experiments and the percentage recoveries ranged from 95% to 99.3%.

A comparative study of acid-treated, base-treated, and Fenton-like reagent-treated biomass for Cr(VI) sequestration from aqueous solutions.

A wide variety of biomass materials have been used for the removal of toxic chromium(VI) by biosorption. The current study investigated the efficacy of Macadamia nutshells treated with sodium hydroxide, nitric acid, and the Fenton-like reagent in the removal of Cr(VI). The adsorbents were characterized by FTIR, SEM, TGA, and elemental analysis. Effects of functional parameters influencing the adsorption of Cr(VI), solution pH (pH 1-11), contact time (5-250 min), concentration of adsorbent (1-10 g/L), and adsorbate concentration (10-200 mg/L) were investigated. The optimum conditions for biosorption were pH 1.4, adsorbent dose of 5 g/L, and 160 min of contact time. In all cases, the base-treated adsorbent displayed superior performance compared to others, with highest percent removal of 98%. The adsorbate-adsorbent interactions were better explained by the Freundlich isotherm and the pseudo-first-order rate model. The Macadamia-based adsorbents are potentially useful for Cr(VI) removal from aqueous solutions. PRACTITIONER POINTS: Three different chemical activators were investigated for the modification of Macadamia surface. The base-treated material exhibited the highest specific surface area of 12.1 m2 /g. The Cr(VI) adsorption performance for the base-treated material dwarfed the other materials. Excellent Cr(VI) removal efficiency in the presence of competitors was achieved.

Recent advances in hexavalent chromium removal from aqueous solutions by adsorptive methods.

Chromium exists mainly in two forms in environmental matrices, namely, the hexavalent (Cr(vi)) and trivalent (Cr(iii)) chromium. While Cr(iii) is a micronutrient, Cr(vi) is a known carcinogen, and that warrants removal from environmental samples. Amongst the removal techniques reported in the literature, adsorption methods are viewed as superior to other methods because they use less chemicals; consequently, they are less toxic and easy to handle. Mitigation of chromium using adsorption methods has been achieved by exploiting the physical, chemical, and biological properties of Cr(vi) due to its dissolution tendencies in aqueous solutions. Many adsorbents, including synthetic polymers, activated carbons, biomass, graphene oxide, and nanoparticles as well as bioremediation, have been successfully applied in Cr(vi) remediation. Initially, adsorbents were used singly in their natural form, but recent literature shows that more composite materials are generated and applied. This review focused on the recent advances, insights, and project future directions for these adsorbents as well as compare and contrast the performances achieved by the mentioned adsorbents and their variants.

Adsorptive Removal of Hexavalent Chromium by Diphenylcarbazide-Grafted Macadamia Nutshell Powder.

Macadamia nutshell powder oxidized by hydrogen peroxide solutions (MHP) was functionalized by immobilizing 1,5'-diphenylcarbazide (DPC) on its surface. The effectiveness of grafting was confirmed by the Fourier transform infrared spectrum due to the presence of NH and C=C stretches at 3361, 1591, and 1486 cm-1, respectively, on the grafted material which were absent in the nongrafted material. Thermogravimetric analysis revealed that the presence of DPC on the surface of Macadamia shells lowered the thermal stability from 300°C to about 180°C owing to the volatile nature of DPC. Surface roughness as a result of grafting was appreciated on the scanning electron microscopy images. Parameters influencing the adsorptive removal of Cr(VI) were examined and found to be optimal at pH 2, 120 min, 150 mg/L, and 2.5 g/L. Grafting MHP with DPC leads to an increase in the Langmuir monolayer capacity from 37.74 to 72.12 mg/g. Grafting MHP with DPC produced adsorbent with improved removal efficiency for Cr(VI).

Solvent-solvent fractionations of Combretum erythrophyllum (Burch.) leave extract: Studies of their antibacterial, antifungal, antioxidant and cytotoxicity potentials.

OBJECTIVE: To evaluate the biological activities of Combretum erythrophyllum (C. erythrophyllum) leaf extracts against infectious diseases' pathogenesis and their cytotoxicity potentials. METHODS: Powdered leaf material (300 g) of C. erythrophyllum was extracted (1:10 w/v) using acetone to obtain the crude extract. Liquid-liquid fractionation was performed on the crude acetone extract (30 g) using solvents of different polarity. The bioautographic method was used to detect the inhibition of bacterial and fungal growth by active compounds present in the crude and fractions. The extracts were then tested on bacterial strains: Staphylococcus aureus, Enterococcus faecalis, Escherichia coli, Pseudomonas aeruginosa; fungal strains: Candida albicans (C. albicans), Cryptococcus neoformans, and Aspergillus fumigatus, by microtitre dilution method for MIC determination. RESULTS: The extracts MIC values ranged between 0.08 and 2.50 mg/mL against the tested pathogens. Water fraction had the highest activity against bacteria strains, while the fungal assay revealed crude acetone extract and ethyl acetate fraction to be active against C. albicans (1.25 mg/mL), dichloromethane extract against C. albicans and A. fumigatus (0.16 mg/mL). Extract fractions showed a good antioxidant activity via DPPH, ABTS and hydroxyl radical scavenging assays, in the order: ethyl acetate > water > acetone > dichloromethane > hexane. The toxicity level of crude extract and fractions evaluated in Vero monkey kidney cells ranged from 34 to 223 µg/mL, while doxorubicin (IC50 = 7.19 µg/mL) served as the positive control. CONCLUSIONS: It can be concluded that the extracts of C. erythrophyllum are safe for medicinal use in folk medicine for treating infectious and stress related diseases.

The Baylis-Hillman approach to quinoline derivatives.

Baylis-Hillman reactions of 2-nitrobenzaldehydes with various activated alkenes afford adducts that undergo reductive cyclisation to quinoline derivatives. The chemo- and regioselectivity of cyclisation appears to be influenced by the choice of both the substrate and the reagent system, and competing reactions have been observed.