Cationic hydrogels for toxic arsenate removal from aqueous environment

Poly(3-acrylamidopropyl)trimethylammonium chloride (p(APTMACl)) hydrogels were synthesized and utilized as absorbents for the removal of toxic arsenate from aqueous medium. The pH-dependent swelling characteristics of the hydrogel were studied, and the experimental parameters that affect the absorption efficiency were investigated. Our results demonstrate that these types of hydrogels are highly effective in removing arsenate(V) anions from the aqueous environment. A removal efficiency of approximately 99.7% was obtained be immersing 1.5g/l hydrogel in a solution containing 50ppm As(V) at pH 9 for 360min. Moreover, the hydrogels are very easy to handle upon absorption, avoiding issues related to the separation of traditional powder absorbents from water after absorption.     

The impact of the Gulf crisis on Qatar's humanitarian sector

The 2017 Gulf crisis is one of the most challenging episodes faced by Qatar since its independence in 1971, with major economic, social, and political impacts on the Arab Gulf nation. Its economic prognosis has been brought into doubt, the map of regional alliances has been redrawn, and any prospects of deeper regional integration have been dashed. This paper analyses the little-documented impact of the crisis on Qatar's humanitarian sector, which has unfolded as the small, gas-rich emirate has striven to become a major humanitarian donor. It concludes that while there have been disruptions to humanitarian operations and regional coordination, the Gulf crisis has triggered and in some cases accelerated already intended reforms across the Qatari humanitarian sector. In the long term, the reorganisation and adaptation implemented to weather the storm of the crisis may help Qatar to emerge from the crisis with a more sustainable and resilient humanitarian sector.     

Reconstruction under siege: the Gaza Strip since 2007

This paper examines the siege of the Gaza Strip, a self-governing Palestinian territory, since 2007. Research on sieges tends to concentrate on the coping strategies of besieged communities, humanitarian issues associated with the impacts, humanitarian access, and the prioritisation of needs, with little or no attention paid to reconstruction. However, Gaza is unusual as a siege environment within which reconstruction has become a high priority in the aftermath of its three destructive wars with Israel. Following an overview of research on sieges in contemporary warfare and a brief contextualisation of Gaza, this paper examines why reconstruction outcomes have varied over time through the application of a theoretical framework that stipulates the importance of four key factors: time; needs; scarcity; and political context. Based on an analysis of these variables, Gaza was found to be a most-likely case for reconstruction under siege. Nonetheless, the large-scale reconstruction necessary to transform Gaza has not been actualised.     

Determination of etoxazole residues in fruits and vegetables by SPE clean-up and HPLC-DAD

A method for determination of etoxazole residues in apples, strawberries and green beans was developed and validated. The analyte was extracted with acetonitrile from foodstuff and a charcoal-celite cartridge was used for clean-up of raw extracts. Reversed phase high performance liquid chromatography with photodiode array detector (HPLC-DAD) was used for the determination and quantification of etoxazole residues in the studied samples. The calibration graphs of etoxazole in a solvent or three blank matrixes were linear within the tested intervals 0.01–2 mg L^?1, with correlation coefficient of determination >0.999. The combined solid phase extraction (SPE) clean-up and the chromatographic method steps were sensitive and reliable for simultaneous determination of etoxazole residues in the studied samples. The average recoveries of etoxazole in the tested foodstuffs were between 93.4 to 102% at spiking levels of 0.01, 0.10, and 0.50 mg kg^?1, with relative standard deviations ranging from 2.8 to 4.7%, in agreement with directives for method validation in residue analyses. The limit of detection (LOD) of the HPLC-DAD system was 100 pg. The limit of quantification of the entire method was 0.01 mg kg^?1.     

Recovery of metal values from zinc solder dross

Zinc solder dross containing 14.8% Sn, 16.3% Pb, 0.41% Al and 64.5% Zn was leached with 3% H₂SO₄ at 45°C for 1 h. Zinc and aluminum went into solution, whereas lead and tin remained with the residue. Aluminum was selectively precipitated as calcium aluminum carbonate by treating the sulphate leachate with limestone at pH 4.8. Zinc sulphate solution was either evaporated to obtain zinc sulphate crystals or precipitated as basic zinc carbonate at pH 6.8. The undissolved lead and tin were leached with 5 M hot hydrochloric acid. The major part of lead chloride ( 73%) was separated by cooling the leached products down to room temperature. From the soluble fraction, tin was recovered as hydrated tin oxide by alkylation with caustic soda at pH 2.4, while the remaining lead was separated at pH 8.5 as lead hydroxide. A process flowsheet had been suggested which involved two-stage hydrometallurgical treatment. Parameters affecting the recovery efficiency of the suggested method such as temperature, time, pH and acid: solid stoichiometric ratio were investigated. Results obtained revealed that the optimum leaching conditions were achieved by using 20 ml of 3% H₂SO₄ acid/g dross for 1 h at 45°C. Recovery efficiency of the metal salts was 99.1, 99.4, 99.6 and 99.5% for Zn, Al, Pb and Sn respectively. Recovery efficiency was related to the solubility of the concerned salts under the given experimental conditions.     

Chemical characterization of naturally weathered oil residues in arid terrestrial environment in Al-Alamein, Egypt.

The main objective of this study was to investigate compositional changes in a range of source- and weathering-dependent molecular parameters in oil residues in the arid terrestrial environment of Al-Alamein, Egypt. The results of aromatic hydrocarbon analysis demonstrated the stability of several aromatic hydrocarbon ratios in oil residues over a wide range of weathering and hydrocarbon concentrations. The ratios of C2-dibenzothiophenes/C2-phenanthrenes (C2-DBTs/C2-PHENs), C3-dibenzothiophenes/C3-phenanthrenes (C3-DBTs/C3-PHENs), C2-chrysenes/C1-chrysenes (C2-CHRYs/C1-CHRYs), and C2-dibenzothiophenes/C1-dibenzothiophenes (C2-DBTs/C1-DBTs) were nearly constant in oil residues of varying degrees of weathering. Biomarker ratios of hopanes and steranes were useful for source identification even for severely weathered oil residues. The data confirmed previous observations that C29 20S/(20S + 20R) and C29 betabeta/(betabeta+ alphaalpha) sterane epimer ratios, and C29/C30, C30 alphabeta(alphabeta + 3alpha), C31 22S/(22S + 22R) hopane ratios correlate well even after extensive weathering of spilled oils, although some exceptions were encountered for an extensively weathered surface sample. The data provided clear evidence of correlation between samples of the weathered oil residues and the possible source oil. Moreover, the results of biomarker compositions were in good agreement with weathering classification based on alkanes and aromatic hydrocarbons. In general, samples with lowest pregnane indices (PI) and tricyclic terpane indices (TriTI) showed the lowest concentrations of n-alkanes and alkylated polycyclic aromatic hydrocarbon (PAH) homologues, the highest weathering ratios (WRs), the highest values of unresolved complex mixture (UCM)/total resolved peak (TRP) ratios, and the highest ratios of C2 and C3-alkylated CHRYs to their counterparts in the PHEN and DBT series.