A Comparative Study of the Biodurability and Persistence of Gold, Silver and Titanium Dioxide Nanoparticles Using the Continuous Flow through System.

The potential for nanoparticles to cause harm to human health and the environment is correlated with their biodurability in the human body and persistence in the environment. Dissolution testing serves to predict biodurability and nanoparticle environmental persistence. In this study, dissolution testing using the continuous flow through system was used to investigate the biodurability and persistence of gold nanoparticles (AuNPs), silver nanoparticles (AgNPs) and titanium dioxide nanoparticles (TiO2 NPs) in five different simulated biological fluids and two synthetic environmental media to predict their behaviour in real life situations. This study examined the physicochemical properties and agglomeration state of gold, silver and titanium dioxide nanoparticles before and after dissolution tests using three different techniques (UV-vis, XRD and TEM). The UV-vis spectra revealed that all three nanoparticles shifted to higher wavelengths after being exposed to simulated fluids. The titanium powder was found to be mixed with both rutile and anatase, according to XRD examination. The average diameter of gold nanoparticles was 14 nm, silver nanoparticles were 10 nm and titanium dioxide nanoparticles were 25 nm, according to TEM images. The gold and silver nanoparticles were observed to be spherical, but the titanium dioxide nanoparticles were irregular in shape, with some being spherical. The level of dissolved nanoparticles in simulated acidic media was higher in magnitude compared to that dissolved in simulated alkaline media. The results obtained via the continuous flow through dissolution system also displayed very significant dissolution rates. For TiO2 NPs the calculated half-times were in the range of 13-14 days, followed by AuNPs ranging between 4-12 days, significantly longer if compared to the half-times of AgNPs ranging between 2-7 days. AuNPs and TiO2 NPs were characterized by low dissolution rates therefore are expected to be (bio)durable in physiological surroundings and persistent in the environment thus, they might impose long-term effects on humans and the environment. In contrast, AgNPs have high dissolution rates and not (bio)durable and hence may cause short-term effects. The results suggest a hierarchy of biodurability and persistence of TiO2 NPs > AuNPs > AgNPs. It is recommended that nanoparticle product developers should follow the test guidelines stipulated by the OECD to ensure product safety for use before it is taken to the market.

Trends in Innovations and Recent Advances in Membrane Protected Extraction Techniques for Organics in Complex Samples.

Membrane protected extraction is an ongoing innovation for isolation and pre-concentration of analytes from complex samples. The extraction process, clean-up and pre-concentration of analytes occur in a single step. The inclusion of solid sorbents such as molecularly imprinted polymers (MIPs) after membrane extraction ensures that selective double extraction occurs in a single step. The first step involves selective extraction using the membrane and diffused analytes are trapped on the solid sorbent enclosed in the membrane. No further clean-up is required even for very dirty samples like plant extracts and wastewaters samples. Sample clean-up occurs during extraction in the first process and not as additional step since matrix components are prevented from trapping on the sorbent. This can be referred to as prevention is better than cure approach. In this work, the analytical methods that employed membrane protected extraction for various organics such as pesticides, polycyclic aromatic hydrocarbons, and pharmaceuticals are reviewed. The designs of these analytical methods, their applications, advantages and drawbacks are discussed in this review. Literature suggests that the introduction of solid sorbents in membrane creates the much-needed synergy in selectivity. Previous reviews focused on membrane combinations with MIPs while discussing micro-solid-phase extraction. The scope of this review was broadened to include other sample preparation aspects such as membrane protected stir bar solvent extraction and membrane protected solid-phase microextraction. In addition, novel sample preparation methods for solid samples which include Soxhlet membrane protected molecular imprinted solid phase extraction and membrane protected ultra sound assisted extracted are discussed.

Dissolution kinetics of silver nanoparticles: Behaviour in simulated biological fluids and synthetic environmental media.

Silver nanoparticles offer a wide range of benefits including their application in several fields such as medical, food, health care, consumer, and industrial purposes. However, unlocking this potential requires a responsible and co-ordinated approach to ensure that potential challenges emanating from the use of silver nanoparticles are being addressed. In this study body fluids and environmental media were used to investigate the effects of citrate coated silver nanoparticles (cit-coated AgNPs) to mimic their behaviour in real life situations. Understanding the dissolution kinetics and behaviour of cit-coated AgNPs in simulated biological fluids and synthetic environmental media helps us predict their fate and effects on human health and the environment. The cit-coated AgNPs behaviour significantly varied in acidic and alkaline simulated fluids. Low pH and high ionic strength accelerated the rate and degree of dissolution of AgNPs in simulated fluids. Following exposure to simulated fluids cit-coated AgNPs demonstrated significant changes in agglomeration state and particle reactivity however, the morphology remained unaltered. The slow dissolution rates observed for highly agglomerated cit-coated AgNPs in simulated blood plasma, Gamble's and intestinal fluids, and freshwater indicate that there is a greater likelihood that the particles will be the cause of the observed adverse effects. In contrast, the fast dissolution rates observed for cit-coated AgNPs in simulated gastric and phagolysosomal fluid and synthetic seawater, the release of the silver ions at a fast rate, will be the cause of their short-term effects.

Dissolution of titanium dioxide nanoparticles in synthetic biological and environmental media to predict their biodurability and persistence.

Investigating the biodurability and persistence of titanium dioxide nanoparticles (TiO2 NPs) is of paramount importance because these parameters influence the particles' impact on human health and the environment. Contrary to most research conducted so far, the present study elucidates the dissolution kinetics, namely the dissolution rates, rate constants, order of reaction and half-times of TiO2 NPs in five different simulated biological fluids and two synthetic environmental media to predict their behaviour in real life situations. Results have shown that the dissolution of TiO2 NPs in all simulated fluids was limited. Of all the simulated biological media tested, acidic media such as phagolysosomal and gastric fluid produced the highest dissolution of TiO2 NPs compared to alkaline media such as blood plasma, Gamble's fluid, and intestinal fluid. Furthermore, when the particles were exposed to simulated environmental conditions, the dissolution was higher in high ionic strength seawater compared to freshwater. The dissolution kinetics of titanium dioxide nanoparticles followed first order reaction kinetics and were generally characterized by low dissolution rates and long half-times. These findings indicate that TiO2 NPs are very insoluble and will remain unchanged in the body and environment over long periods of time. Therefore, these particles are most likely to cause both short and long-term health effects and will remain persistent following release into the environment.

First biomonitoring of microplastic pollution in the Vaal river using Carp fish (Cyprinus carpio) "as a bio-indicator".

Fish inhabiting freshwater environments are susceptible to the ingestion of microplastics (MPs). Knowledge regarding MPs in freshwater fish in South Africa is very limited. In this study, the uptake of MPs by common carp (Cyprinus carpio) in the Vaal River in South Africa was assessed. MPs were detected in all of the twenty-six fish examined, 682 particles of MPs were recovered from the gastrointestinal tracts of the fish with an average of 26.23 ± 12.57 particles/fish, and an average abundance of 41.18 ± 52.81 particles/kg. The examination of the physical properties of MPs revealed a predominance on fibers (69%), small-sized particles of less than 0.5 mm (48%), as well as prevelance of coloured MPs (94%), mostly green, blue, and black. Using Raman Spectroscopy, the following plastic polymers were identified: high density polyethylene (HDPE), low density polyethylene (LDPE), polypropylene (PP), polyethylene terephthalate (PET), and polytetrafluoroethylene (PTFE). To the best of our knowledge, this study, is the first to report MPs uptake by freshwater biota in the Vaal River using common carp as a target organism. It provided evidence of MP contamination in the Vaal.

In Situ Decarboxylation-Pressurized Hot Water Extraction for Selective Extraction of Cannabinoids from Cannabis sativa. Chemometric Approach.

Isolation of the therapeutic cannabinoid compounds from Cannabis Sativa L. (C. Sativa) is important for the development of cannabis-based pharmaceuticals for cancer treatment, among other ailments. The main pharmacological cannabinoids are THC and CBD. However, THC also induces undesirable psychoactive effects. The decarboxylation process converts the naturally occurring acidic forms of cannabinoids, such as cannabidiolic acid (CBDA) and tetrahydrocannabinolic acid (THCA), to their more active neutral forms, known as cannabidiol (CBD) and tetrahydrocannabinol (THC). The purpose of this study was to selectively extract cannabinoids using a novel in situ decarboxylation pressurized hot water extraction (PHWE) system. The decarboxylation step was evaluated at different temperature (80-150 °C) and time (5-60 min) settings to obtain the optimal conditions for the decarboxylation-PHWE system using response surface methodology (RSM). The system was optimized to produce cannabis extracts with high CBD content, while suppressing the THC and CBN content. The identification and quantification of cannabinoid compounds were determined using UHPLC-MS/MS with external calibration. As a result, the RSM has shown good predictive capability with a p-value < 0.05, and the chosen parameters revealed to have a significant effect on the CBD, CBN and THC content. The optimal decarboxylation conditions for an extract richer in CBD than THC were set at 149.9 °C and 42 min as decarboxylation temperature and decarboxylation time, respectively. The extraction recoveries ranged between 96.56 and 103.42%, 95.22 and 99.95%, 99.62 and 99.81% for CBD, CBN and THC, respectively.

Development and evaluation of a DGT sampler using functionalised cross-linked polyethyleimine for the monitoring of arsenic and selenium in mine impacted wetlands.

Arsenic and selenium are both carcinogenic and their presence in fresh water has attracted the development of robust and accurate monitoring techniques. A new diffusive gradients in thin-films (DGT) sampler was developed and evaluated for the in situ measurements of arsenic and selenium. The binding layer was made from a mixture of sulphonated and phosphonated cross-linked polyethylenimine (SCPEI and PCPEI, respectively). The optimum ratio of a SCPEI and PCPEI resin mixture was determined. The DGT sampler was calibrated under laboratory conditions to determine the influence of sample turbulence, concentration and pH. The optimised DGT passive sampler was field deployed in a mine impacted dam for 12 days. Binding layer optimisation shows that the polymers had to be mixed in a specific ratio of 80% sulphonated and 20% phosphonated per 0.8 g of the resin mixture, in the loose polymer form. Embedding the resin mixture in agarose gel reduced the uptake of both arsenic and selenium dramatically. At sample pH 3.0 and 5.0, the DGT sampler did not show significant differences in uptake of the two elements during the 15 day deployment. The passive sampler had limited adsorption capacity and was found better suited for dilute solutions, with concentrations below 0.5 mg L-1 of the target metals. This effect was more pronounced when exposed to dam water which had competing cations. Cations may have reduced the capacity by binding to the PEI backbone via the large number of amine groups. Nonetheless, these cations did not show linear uptake.

Selective Extraction of Cannabinoid Compounds from Cannabis Seed Using Pressurized Hot Water Extraction.

Phytochemicals of Cannabis sativa mainly for the use in the different industries are that of delta-9-tetrahydrocannabinol (THC) and cannabidiol (CBD). Pressurized hot water extraction (PHWE) is seen as an efficient, fast, green extraction technique for the removal of polar and semi-polar compounds from plant materials. The PHWE technique was applied to extract cannabinoid compounds from Cannabis sativa seed. Response surface methodology was used to investigate the influence of extraction time (5-60 min), extraction temperature (50-200 °C) and collector vessel temperature (25-200 °C) on the recovery of delta-9-tetrahydrocannabinol (THC), cannabinol (CBN), cannabidiol (CBD), cannabichromene (CBG) and cannabigerol (CBC) from Cannabis sativa seed by PHWE. The identification and semi quantification of cannabinoid compounds were determined using GCXGC-TOFMS. The results obtained from different extractions show that the amount of THC and CBN was drastically decreasing in the liquid extract when the temperature rose from 140 to 160 °C in the extraction cell and the collector's vessel. The optimal conditions to extract more CBD, CBC, and CBG than THC and CBN were set at 150 °C, 160 °C and 45 min as extraction temperature, the temperature at collector vessel, and the extraction time, respectively. At this condition, the predicted and experimental ratio of THCt (THC + CBN)/CBDt (CBD + CBC+ CBG) was found to be 0.17 and 0.18, respectively. Therefore, PHWE can be seen as an alternative to the classic extraction approach as the efficiency is higher and it is environmentally friendly.

Selective pressurized hot water extraction of nutritious macro-nutrients vs. micro-nutrients in Moringa oleifera leaves-a chemometric approach.

Moringa oleifera leaves are widely used in traditional medicine as a food supplement because they are high in essential and nutritious content. Pressurized hot water extraction (PHWE), which is a green approach, was used for the recovery of the macro-nutrient and micro-nutrient elements from dried leaf powder of Moringa oleifera. In this study, response surface methodology was applied to assess the influence of temperature (50-200 °C) and time (5-60 min) on the extractability pattern of macro-nutrient and micro-nutrient elements from the leaves of Moringa oleifera when processed by PHWE. The quantification of macro-nutrient elements such as Ca, K and Mg and micro-nutrient elements like Al, Co, Cr, Cu, Fe, Ni and Zn from the leaves was determined using inductively coupled plasma optical emission spectroscopy (ICP-OES). Obtained results revealed that the extraction of macro-nutrient elements from the Moringa oleifera leaves was enhanced by increasing the extraction time more than the extraction temperature. On the contrary, the amounts of extractable micro-nutrient elements were increased by increasing the extraction temperature. Hence, the recovery for macro-nutrient elements ranged from 88 to 98% while for micro-nutrients it ranged from 21 to 46%. This implies that macro-nutrient elements are extracted with relatively high selectivity in relation to micro-nutrient elements in Moringa dried leaf powder using the PHWE technique.

Removal of platinum (IV) from aqueous solutions with yeast-functionalised bentonite.

There is a need for cheap but, efficient methods for the removal of precious metals from wastewaters, which are normally lost during mineral processing. Moreover, the disposal of yeast waste from brewing has been a problem in many parts of the world. In this study, the removal of Pt(IV) from aqueous solutions using the readily available bentonite clay functionalised with spent yeast from brewing was investigated. The maximum adsorption capacity of Pt(IV) with 100 mg yeast-functionalised bentonite at pH 2 within 90 min was 255 µg g-1 (98.5% efficiency) but, decreased as pH increased. The adsorption capacity of Pt(IV) was insignificantly (p > 0.05) affected by the presence of competing ions (Fe(III), Ca(II), Mg(II), K(I), Co(II), Ni(II), Hf(IV), Zn(II) and other platinum group metals (PGMs)). Moreover, most of these metals were significantly adsorbed along with Pt(IV). The indicative cost-benefit analysis showed that 1 kg of the yeast-functionalised bentonite can remove ∼700 g Pt(IV) in which a profit of more than USD20000 can be made. The bentonite functionalised with spent yeast from brewing has a potential to recover lost PGMs in wastewater. Since, this is a cheap process, the mining and other industries can make much profit from such recoveries.

A scoping study of component-specific toxicity of mercury in urban road dusts from three international locations.

This scoping study presents an investigation of the total and bioaccessible mercury concentrations in road dust (RD) from three international urban sites, where a one-off sampling campaign was conducted at each. This was done to address the hypothesis that the matrix in which mercury is found influences its ability to become accessible to the body once inhaled. For that purpose, the samples were analysed for total and pulmonary bioaccessible mercury and the data compared to the chemical structure of individual particles by SEM. The results obtained from this study suggest that a high mercury content does not necessarily equate to high bioaccessibility, a phenomenon which could be ascribed to the chemical character of the individual particles. It was found that the Manchester samples contained more pulmonary soluble mercury species (as determined by elemental associations of Hg and Cl) in comparison to the other two samples, Curitiba, Brazil, and Johannesburg, South Africa. This finding ultimately underlines the necessity to conduct a site-specific in-depth analysis of RD, to determine the concentration, chemical structure and molecular speciation of the materials within the complex matrix of RD. Therefore, rather than simply assuming that higher bulk concentrations equate to more significant potential human health concerns, the leaching potential of the metal/element in its specific form (for example as a mineral) should be ascertained. The importance of individual particle behaviour in the determination of human health risk is therefore highlighted.

Mercury accumulation and biotransportation in wetland biota affected by gold mining.

Phytoremediation is a cost-effective, eco-friendly technology for the removal of metals from polluted areas. In this study, six different plant species (Datura stramonium, Phragmites australis, Persicaria lapathifolia, Melilotus alba, Panicum coloratum, and Cyperus eragrostis) growing in a gold mine contaminated wetland were investigated as potential phytoremediators of mercury. The accumulation of total mercury and methylmercury in plant tissues was determined during the wet and dry seasons to establish the plants' variability in accumulation. The highest accumulation of total mercury was in the tissues of Phragmites australis with recorded concentrations of 806, 495, and 833 µg kg-1 in the roots, stem, and leaves, respectively, during the dry season. The lowest accumulation levels were recorded for Melilotus alba during both seasons. The highest amount of the methylmercury was found in Phragmites australis during the dry season with a value of 618 µg kg-1. The accumulation and biotransportation were not significantly different between the seasons for some plants. The results of this study indicated that plants growing in wetlands can be used for phytoremediation of mercury and suggest the choice of species for constructed wetlands.

Development of a single format membrane assisted solvent extraction-molecularly imprinted polymer technique for extraction of polycyclic aromatic hydrocarbons in wastewater followed by gas chromatography mass spectrometry determination.

A technique that combines membrane assisted solvent extraction and molecularly imprinted polymer into a single step format has been successfully developed and evaluated for the extraction of the 16 US-EPA priority polycyclic aromatic hydrocarbons in wastewater samples followed by determination using gas chromatography coupled with time of flight mass spectrometry. The technique involves placing the polymer particles into a hydrophobic polypropylene membrane bag which is in contact with an aqueous donor phase. The technique was optimized for various parameters that include presence of an organic modifier in the donor phase, stirring rate and extraction time. The optimum conditions were 25% of dimethyl sulfoxide as an organic modifier and stirring at 1000 rpm for 120 min. The limits of detection using the technique were in the 0.01-0.45 ng mL-1 range. Linearity values determined in the 10-1 000 ng mL-1 calibration range were all above 0.9972. Extraction efficiencies of the sixt analytes calculated as averages for three spiking concentrations ranged from 62.8 to 96.8% (RSD = 3.1-12.3%). The optimized method was tested for the extraction of polycyclic aromatic hydrocarbons in wastewater samples in the presence of surrogate standards. The developed method showed great reproducibility with inter day repeatability values ranging from 0.6 to 24.9%. The analytes were quantified in the nanogram level showing that the developed technique is a viable alternative in the analysis of trace organic compounds in complex aqueous samples.

Assessment of heavy metals in raw food samples from open markets in two African cities.

The present study was performed to assess the level of biologically potent metallic elements (Al, Cd, Cr, Cu, Hg, Mn, Pb and Zn), metalloid (As) and non-metal (Se) in different raw food from open markets in Kinshasa (Democratic Republic of Congo) and Johannesburg (South Africa). Hundred twenty different food samples comprising of cabbage, bean, beef and fish were collected, digested in the microwave system and analysed for trace metals using ICP-OES, ICP-MS and mercury analyser. The obtained results were used to evaluate the health risk of these elements via consumption of foods. The investigation revealed that the mean level of trace elements ranged Al: 1.62 ±â€¯0.32 to 52.10 ±â€¯3.45, As: 1.62 ±â€¯0.32 to 5.33 ±â€¯1.04, Cd: 0.16 ±â€¯0.09 to 3.93 ±â€¯0.12, Cr: 0.58 ±â€¯0.24 to 17.29 ±â€¯2.03, Cu: 0.69 ±â€¯0.15 to 15.70 ±â€¯1.67, Hg: 1.53 ±â€¯0.1 to 2.94 ±â€¯0.23, Mn: 5.34 ±â€¯1.37 to 18.31 ±â€¯3.45, Pb: 0.16 ±â€¯0.09 to 4.14 ±â€¯1.08, Se: 0.18 ±â€¯0.08 to 1.41 ±â€¯0.97, Zn: 5.47 ±â€¯1.83 to 75.12 ±â€¯5.67 mg kg-1. The average values of As, Cd, Cr, Cu, Hg, Mn, Pb, Se and Zn in raw foods collected from Johannesburg market were significantly higher (p < 0.05) than those from the Kinshasa market. While the highest Al contents (p < 0.05) were found in the food sold in Kinshasa open market. The levels of most studied metals in the raw foods were exceeding the recommended maximum acceptable limit proposed by the Joint FAO/WHO Expert Committee on Food. The combined Target Hazard Quotients (THQ) values for all samples from both markets were greater than 1 which indicates a potential health risk to the local consumer.

Development and optimisation of a novel three-way extraction technique based on a combination of Soxhlet extraction, membrane assisted solvent extraction and a molecularly imprinted polymer using sludge polycyclic aromatic hydrocarbons as model compounds.

A novel technique that integrates extraction and clean-up into a single step format is reported as part of the search for new sample preparation techniques in the analysis of persistent organic pollutants from complex samples. This was achieved by combining the extraction efficiency of the Soxhlet extractor, the selectivity of a size exclusion membrane and the specificity of a molecularly imprinted polymer for the extraction of polycyclic aromatic hydrocarbons from wastewater sludge followed by quantitation using gas chromatography with time-of-flight mass spectrometry. The approach is described as the Soxhlet extraction membrane-assisted solvent extraction molecularly imprinted polymer technique. This technique was optimised for various parameters such as extraction solvent, reflux time and membrane acceptor phase. The applicability of the developed technique was optimised using a wastewater sludge certified reference material and then tested on real wastewater sludge samples. The method detection limits ranged from 0.14 to 12.86 ng/g with relative standard deviation values for the extraction of the 16 US-EPA priority polycyclic aromatic hydrocarbons from wastewater sludge samples ranging from 0.78 to 18%. The extraction process was therefore reproducible and showed remarkable selectivity. The developed technique is a promising prospect that can be applied in the analysis of organic pollutants from complex solid samples.

Synthesis and characterization of a molecularly imprinted polymer for the isolation of the 16 US-EPA priority polycyclic aromatic hydrocarbons (PAHs) in solution.

A smart sorbent consisting of benzo[k]fluoranthene-imprinted and indeno[1 2 3-cd]pyrene-imprinted polymers mixed at 1:1 (w/w) was successfully screened from several cavity-tuning experiments and used in the isolation of polycyclic aromatic hydrocarbons from spiked solution. The polymer mixture showed high cross selectivity and affinity towards all the 16 US-EPA priority polycyclic aromatic hydrocarbons. The average extraction efficiency from a cyclohexane solution was 65 ± 13.3% (n = 16, SD). Batch adsorption and kinetic studies confirmed that the binding of polycyclic aromatic hydrocarbons onto the polymer particles resulted in formation of a monolayer and that the binding process was the rate limiting step. The imprinted polymer performance studies confirmed that the synthesized polymer had an imprinting efficiency of 103.9 ± 3.91% (n = 3, SD). A comparison of the theoretical number of cavities and the experimental binding capacity showed that the overall extent of occupation of the imprinted cavities in the presence of excess polycyclic aromatic hydrocarbons was 128 ± 6.45% (n = 3, SD). The loss of selectivity was estimated at 2.9% with every elution cycle indicating that the polymer can be re-used several times with limited loss of selectivity and sensitivity. The polymer combination has shown to be an effective adsorbent that can be used to isolate all the 16 US-EPA priority polycyclic aromatic hydrocarbons in solution.

Miniaturized pipette-tip-based electrospun polyacrylonitrile nanofibers for the micro-solid-phase extraction of nitro-based explosive compounds.

In this study, a self-assembly of miniaturized pipette-tip-based solid-phase extraction for the simultaneous extraction of nitroaromatic compounds was developed, with electrospun polyacrylonitrile nanofibers used as sorbents. The electrospun polyacrylonitrile nanofibers were characterized by scanning electron microscopy, FTIR analysis and surface area analysis. Good linearities for the four nitroaromatic compounds (2,6-dinitrotoluene, 2-nitrotoluene, 3-nitrotoluene, and 4-nitrotoluene) were obtained in a range of 250-1000 µg/L with coefficients of determination > 0.99. The limits of detection of these analytes were between 21 and 38 µg/L. The results showed that the pipette-tip-based solid-phase extraction was effective in extracting nitrotoluenes in the pH regime of environmental interest (≈ 6). The investigation also revealed that the optimum mass of electrospun polyacrylonitrile nanofibers sorbent was 15 mg and 20 aspirating/dispensing cycles gave the maximum recovery of nitrotoluenes with 200 µL acetonitrile as the best eluting solvent. Moreover, the performance of the present method was studied for the extraction and determination of nitroaromatic compounds in real environmental water samples and good recoveries ranging from 70 to 115% were found, and respective relative standard deviations of <12% were obtained.

Assessment of organochlorine pesticide residues in raw food samples from open markets in two African cities.

This study investigates the level of organochlorine pesticides in the raw food from open markets in Kinshasa, Democratic Republic of Congo (DRC), and Johannesburg, South Africa. It assesses the potential health risks associated with the organochlorine pesticide residues. The Quick, Easy, Cheap, Effective, Rugged, and Safe (QuEChERS) method has been developed for sample preparation. A total of 120 food samples (beans, cabbage, beef, and fish) were obtained from the open markets. The mean concentrations of organochlorine pesticides in raw foods collected from the Johannesburg market were significantly higher (p < 0.05) than those from the Kinshasa market. DDE recorded the highest mean concentration (253.58 ± 4.78 µg kg-1) in beef from Johannesburg, and α-BHC recorded the lowest mean concentration (38.54 ± 7.46 µg kg-1) in beans from Kinshasa. The investigation of health risk estimates revealed that the number of organochlorine pesticides exceeded the reference dose in the collected food samples.

Development of pressurised hot water extraction (PHWE) for essential compounds from Moringa oleifera leaf extracts.

Pressurised hot water extraction (PHWE) is a "green" technology which can be used for the extraction of essential components in Moringa oleifera leaf extracts. The behaviour of three flavonols (myricetin, quercetin and kaempferol) and total phenolic content (TPC) in Moringa leaf powder were investigated at various temperatures using PHWE. The TPC of extracts from PHWE were investigated using two indicators. These are reducing activity and the radical scavenging activity of 2,2-diphenyl-1-picrylhydrazyl (DPPH). Flavonols content in the PHWE extracts were analysed on high performance liquid chromatography with ultra violet (HPLC-UV) detection. The concentration of kaempferol and myricetin started decreasing at 150 °C while that of quercetin remained steady with extraction temperature. Optimum extraction temperature for flavonols and DPPH radical scavenging activity was found to be 100 °C. The TPC increased with temperature until 150 °C and then decreased while the reducing activity increased.

Mercury stable isotope signatures of world coal deposits and historical coal combustion emissions.

Mercury (Hg) emissions from coal combustion contribute approximately half of anthropogenic Hg emissions to the atmosphere. With the implementation of the first legally binding UNEP treaty aimed at reducing anthropogenic Hg emissions, the identification and traceability of Hg emissions from different countries/regions are critically important. Here, we present a comprehensive world coal Hg stable isotope database including 108 new coal samples from major coal-producing deposits in South Africa, China, Europe, India, Indonesia, Mongolia, former USSR, and the U.S. A 4.7‰ range in δ(202)Hg (-3.9 to 0.8‰) and a 1‰ range in Δ(199)Hg (-0.6 to 0.4‰) are observed. Fourteen (p < 0.05) to 17 (p < 0.1) of the 28 pairwise comparisons between eight global regions are statistically distinguishable on the basis of δ(202)Hg, Δ(199)Hg or both, highlighting the potential application of Hg isotope signatures to coal Hg emissions tracing. A revised coal combustion Hg isotope fractionation model is presented, and suggests that gaseous elemental coal Hg emissions are enriched in the heavier Hg isotopes relative to oxidized forms of emitted Hg. The model explains to first order the published δ(202)Hg observations on near-field Hg deposition from a power plant and global scale atmospheric gaseous Hg. Yet, model uncertainties appear too large at present to permit straightforward Hg isotope source identification of atmospheric forms of Hg. Finally, global historical (1850-2008) coal Hg isotope emission curves were modeled and indicate modern-day mean δ(202)Hg and Δ(199)Hg values for bulk coal emissions of -1.2 ± 0.5‰ (1SD) and 0.05 ± 0.06‰ (1SD).