Recent progress in electrochemical oxidation of saccharides at gold and copper electrodes in alkaline solutions

This article reviews the progress made in the past 10 years, on electrochemical oxidation of saccharides in alkaline media for gold and copper electrodes. The mechanism and processes associated with the electrochemical oxidation of saccharides at native and surface coated electrodes continues to be of great interest. Despite the effort and various mechanisms proposed, still the need for an electrochemically active material that understands the complexity associated with saccharides continues to increase as their detection poses a challenge for bioanalytical chemistry and liquid chromatography

Incorporation of Ni(II)-dimethylglyoxime ion-imprinted polymer into electrospun polysulphone nanofibre for the determination of Ni(II) ions from aqueous samples

Ni(II)-dimethylglyoxime ion-imprinted polymer (Ni(II)-DMG IIP) was encapsulated in polysulphone and electrospun into nanofibres with diameters ranging from 406 to 854 nm. The structures of the Ni(II)-DMG encapsulated-IIP nanofibre, non-imprinted encapsulated-polymer nanofibre and polysulphone nanofibre mats were observed by scanning electron microscopy and evaluated by infrared spectroscopy. Electrospinning increased the specific surface area of the Ni(II)-DMG encapsulated-IIP nanofibre mats, as was evidenced by the low masses of the Ni(II)-DMG encapsulated-IIP nanofibre mats used. The accuracy of the method was validated by analysing a custom solution of certified reference material (SEP-3); the concentration of Ni(II) obtained was close to the certified one. The limit of detection was found to be 4.0x10-4 μg∙mℓ−1 while the limit of quantification was found to be 1.2x10-3 μg∙mℓ−1. The recovery of Ni(II) achieved using the Ni(II)-DMG imprinted nanofibre mats in water samples was found to range from 83 to 89%, while that of non-imprinted nanofibre mats was found to range from 59 to 65%, and that of polysulphone from 55 to 62%

A colorimetric probe for the detection of Ni2+ in water based on Ag-Cu alloy nanoparticles hosted in electrospun nanofibres

A Ni2+ based colorimetric probe based on glutathione-stabilized silver/copper nanoparticles (GSH-Ag-Cu alloy NPs) in an electrospun polymer matrix is reported. Glutathione-Ag-Cu alloy NPs were characterized by ultraviolet-visible spectroscopy (UV-vis), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The freshly synthesized GSH-Ag-Cu alloy NPs in a polymer matrix were black in colour due to an intense surface plasmon absorption band at 424 nm. However the electrospun nanocomposite fibres were green in colour and in the presence of Ni2+ the green GSH-Ag-Cu alloy NP fibres were discoloured. The sensitivity of the GSH-Ag-Cu alloy NPs towards other representative transition, alkali and alkali earth metal ions was negligible. The effect of the concentration of Ni2+ on the nanocomposite fibres was evaluated and the ‘eye-ball’ limit of detection was found to be 5.8 μg/mL.Keywords: colorimetric probes, alloy nanoparticles, electrospun nanofibres, heavy metal determinatio

Selective removal of chromium (VI) from sulphates and other metal anions using an ion-imprinted polymer

A linear copolymer was prepared from 4-vinylpyridine and styrene. An ion-imprinted polymer (IIP) specific for Cr (VI) adsorption was prepared by copolymerisation of the quaternised linear copolymer (quaternised with 1,4-chlorobutane), 2-vinylpyridine functional monomer and ethylene glycol dimethacrylate (EGDMA), as the cross-linking monomer, in the presence of 1,1’-azobis(cyclohexanecarbonitrile) as initiator. Ammonium dichromate and aqueous methanol were used as a template and porogenic solvent, respectively. Leaching of the chromate template from the polymer particles was achieved with successive stirring of the ion-imprinted polymer (IIP) particles in 4 M HNO3 solutions to obtain leached materials, which were then used for selective rebinding of Cr (VI) ions from aqueous solutions. Similarly, the non-imprinted polymer/ control polymer (NIP/CP) material was also prepared under exactly the same conditions as the IIP but without the chromate anion template. Various parameters, such as solution pH, initial concentration, aqueous phase volume, sorbent dosage, contact time and leaching solution volumes, were investigated. Scanning electron microscopy (SEM), Fourier Transform Infrared (FTIR) spectroscopy, BET surface area and pore size analysis were used for the characterisation of IIP (both unleached and leached) and CP materials. Optimal parameters were as follows: solution pH, 3; contact time, 120 min; eluent, 20 mℓ of 0.1 M NaOH; and sorbent amount, 125 mg. Maximum retention capacity of IIP and CP was 37.58 and 25.44 mg∙g-1, respectively. The extraction efficiencies of the IIP and CP were compared using a batch and SPE mode of extraction. In the absence of high concentrations of ions, especially sulphate ions, both CP and IIP demonstrated no differences in binding of Cr (VI), which was almost 100%. However, in the presence of high concentrations of sulphate ions, the selectivity on the CP completely collapsed. The study clearly demonstrates the suitably of the developed IIP for selective extraction of Cr (VI) in complex samples such as those from acid mine drainage. The selectivity was also compared by direct injection of the real-world sample, both spiked and non-spiked, into that obtained after IIP selective extraction. Despite the method’s very low detection limits for direct injection (below 1 μg∙ℓ-1), no Cr (VI) was obtained. However, after IIP selective extraction, spiked Cr (VI) was detected in the spiked sample

Dimethylglyoxime based ion-imprinted polymer for the determination of Ni(II) ions from aqueous samples

A Ni(II)-dimethylglyoxime ion-imprinted polymer {Ni(II)-DMG IIP} was synthesised by the bulk polymerisation method. The morphology of the Ni(II)-DMG IIP and non-imprinted polymer were observed by scanning electron microscopy and the chemical structures were evaluated by infrared spectroscopy. Selectivity of the Ni(II)-DMG IIP was studied by analysing, using an inductively coupled plasma-optical emission spectrometer, for Ni(II) ions that were spiked with varying concentrations of Co(II), Cu(II), Zn(II), Pd(II), Fe(II), Ca(II), Mg(II), Na(I) and K(I) in aqueous samples. The studies revealed Ni(II) recoveries ranging from 93 to 100% in aqueous solutions with minimal interference from competing ions. Enrichment factors ranged from 2 to 18 with a binding capacity of 120 μg∙g−1. Co(II) was the only ion found to slightly interfere with the determination of Ni(II). Selectivity studies confirmed that the Ni(II)-DMG IIP had very good selectivity, characterised by %RSD of less than 5%. The limits of detection and quantification were 3x10-4 μg∙mℓ−1 and 9x10-4 μg∙mℓ−1, respectively. The accuracy of the method was validated by analysing a custom solution of certified reference material (SEP-3) and the concentration of Ni(II) obtained was in close agreement with the certified one. The Ni(II)-DMG IIP was successfully employed to trap Ni(II) ions from a matrix of sea, river and sewage water. It is believed that the Ni(II)-DMG IIP has potential to be used as sorbent material for pre-concentration of Ni(II) ions from aqueous solutions by solid-phase extraction

Extraction of Pesticides from Plants using Solid Phase Microextraction and QuEChERS

A study employing dispersive solid phase extraction in the formof the quick, easy, cheap, effective, rugged and safe (QuEChERS) method and solid phase microextraction (SPME) for the cleanup of pesticides in plant samples from the Okavango Delta (Botswana) is presented. Concentration levels of aldrin, 1,1-dichloro-2,4-bis[chlorophenyl]ethane (DDD), 1,1-dichloro- 2,2-bis[p-chlorophenyl]ethylene(DDE), 1,1,1-trichloro-2,2-bis[p-chlorophenyl]ethane (DDT), dieldrin, endosulfan and endrin were investigated using gas chromatography with electron capture detection (GC-ECD) and confirmedwith gas chromatography with high resolution time of flight mass spectrometry (GC-TOFMS). Parameters affecting the extraction efficiencies of both techniques were optimized. In the absence of CRMs for the plants under investigation, method validation and evaluation of the extraction efficiencies were achieved through spiking of Nymphaea nouchali (Tswii) leaves at two concentration levels with trichlorobenzene as an internal standard. Recoveries for both SPME and QuEChERS were in the range 61–95 %. The calibration plots were reproducible and linear (R2>0.995) with limits of detection ranging from 0.102 to 1.693 μg L–1 for all the pesticides. The optimal conditions for QuEChERS and SPME were applied to the extraction of pesticides residues from the edible parts (leaves, roots and/ or stems) of Asparagus africanus, Cleome hirta and Nymphaea nouchali plants. No pesticides were detected in the leaves and stems of all the plants studied. Aldrin and endosulfan were detected in the Nymphaea nouchali roots at concentrations of 3–21 μg kg–1 and 5–3 μg kg–1, respectively. Pentachlorobenzene (PCB) and hexachlorobenzene (HCB) were also detected but were not quantified.KEYWORDS Gas chromatography, mass spectrometry, pesticide, plant sample, green techniques

Pre-concentration of toxic metals using electrospun amino-functionalized nylon-6 nanofibre sorbent

This paper presents a new approach for pre-concentrating toxic metals (As, Cd, Ni and Pb) in aqueous environments using an amino-functionalized electrospun nanofibre sorbent. The sorbent, composed of nanofibres of average diameter 80 ± 10 nm and specific surface area of 58m2 g–1, exhibited fast adsorption kinetics ( adsorption (0.34)>HNO3+H2O2 (0.23) digestion.Asimilar trend was observed for Ni in river water as well as Ni andCdin tap water samples. Pb ions in the river water samples were pre-concentrated slightly better using the two digestion methods pre-concentration factors ~22) compared to adsorption method (pre-concentration factor ~21). The use of the electrospun amino-functionalized nanofibre sorbent presentsanefficientand cost-effective alternative for pre-concentration of toxic metals inaqueousenvironments

Analysing chemical attraction of gravid Anopheles gambiae sensu stricto with modified BG-Sentinel traps.

BACKGROUND: Cues that guide gravid Anopheles gambiae sensu lato to oviposition sites can be manipulated to create new strategies for monitoring and controlling malaria vectors. However, progress towards identifying such cues is slow in part due to the lack of appropriate tools for investigating long-range attraction to putative oviposition substrates. This study aimed to develop a relatively easy-to-use bioassay system that can effectively analyse chemical attraction of gravid Anopheles gambiae sensu stricto. METHODS: BG-Sentinel™ mosquito traps that use fans to dispense odourants were modified to contain aqueous substrates. Choice tests with two identical traps set in an 80 m(2) screened semi-field system were used to analyse the catch efficacy of the traps and the effectiveness of the bioassay. A different batch of 200 gravid An. gambiae s.s. was released on every experimental night. Choices tested were (1) distilled versus distilled water (baseline) and (2) distilled water versus soil infusion. Further, comparisons were made of distilled water and soil infusions both containing 150 g/l of Sodium Chloride (NaCl). Sodium Chloride is known to affect the release rate of volatiles from organic substrates. RESULTS: When both traps contained distilled water, 45% (95 confidence interval (CI) 33-57%) of all released mosquitoes were trapped. The proportion increased to 84% (95 CI 73-91%) when traps contained soil infusions. In choice tests, a gravid female was twice as likely to be trapped in the test trap with soil infusion as in the trap with distilled water (odds ratio (OR) 1.8, 95% CI 1.3-2.6). Furthermore, the attraction of gravid females towards the test trap with infusion more than tripled (OR 3.4, 95% CI 2.4-4.8) when salt was added to the substrates. CONCLUSION: Minor modifications of the BG-Sentinel™ mosquito trap turned it into a powerful bioassay tool for evaluating the orientation of gravid mosquitoes to putative oviposition substrates using olfaction. This study describes a useful tool for investigating olfactory attraction of gravid An. gambiae s.s. and provides additional evidence that gravid mosquitoes of this species are attracted to and can be baited with attractive substrates such as organic infusions over a distance of several metres