Simultaneous Removal of Nitrate and Natural Organic Matter from Drinking Water Using a Hybrid Heterotrophic/Autotrophic/Biological Activated Carbon Bioreactor

Simultaneous removal of nitrate ([Formula: see text]) and natural organic matter (NOM) from drinking water using a hybrid heterotrophic/autotrophic/BAC bioreactor (HHABB) was studied in continuous mode. The HHABB consisted of three compartments: ethanol heterotrophic part, sulfur autotrophic part, and biological activated carbon (BAC)-part (including anoxic and aerobic sections). Experiments were performed with [Formula: see text] concentration 30?mg N/L, [Formula: see text] loading rate 0.72?kg N/m(3)/d, C?:?N ratio 0.53, and three concentrations of NOM (0.6, 2.6, and 5.7?mg C/L). Overall denitrification rate and efficiency of the HHABB were not affected by NOM concentration and were in the suitable ranges of 0.69-0.70?kg N/m(3)/d and 96.0%-97.7%, respectively. NOM removal at concentration 0.6?mg C/L was not efficient because of organic carbon replacement as soluble microbial products. At higher NOM concentrations, total NOM removal efficiencies were 55%-65%, 55%-70%, and 55%-65% for dissolved organic carbon, trihalomethane formation potential, and UV absorbance at 254?nm (UV(254)), respectively. The more efficient compartments of the HHABB for the removal of NOM were the ethanol heterotrophic phase and aerobic BAC-phase. The efficiency of the HHABB in the removal of NOM was considerable, and the effluent dissolved organic carbon and trihalomethane formation potential concentrations were relatively low. This study indicated that the HHABB without the anoxic BAC-phase could be a feasible alternative for simultaneous removal of [Formula: see text] and NOM from drinking water at full scale.     

Aminobenzenesulfonamide functionalized SBA-15 nanoporous molecular sieve: A new and promising adsorbent for preconcentration of lead and copper ions

A rapid method for the extraction and monitoring of nanogram level of Pb²⁺ and Cu²⁺ ions using uniform silanized mesopor (SBA-15) functionalized with aminobenzenesulfonamide groups and flame atomic absorption spectrometry (FAAS) is presented. Aminobenzenesulfonamide functionalized SBA-15 was synthesized according to procedure in the literature and the presence of organic groups in the silica framework was demonstrated by FT-IR spectra. The functionalized product showed the BET surface area 110 m²/g and pore diameter 5.1 nm, based on adsorption-desorption of N₂ at 77 K. The effect of several variables such as (amount of adsorbent, stirring time, pH and presence of other ions in the medium) has been studied. Lead and copper were completely extracted at pH greater than 3 after stirring for 10 min. The maximum capacity of the adsorbent was found to be 191.3 ± 1.4 and 155.0 ± 1.0 μg of lead and copper ions/mg functionalized SBA-15, respectively. The preconcentration factor of the method was found to be 200. The detection limit of the technique was 3.4 and 0.4 ng/mL for Pb²⁺ and Cu²⁺, respectively. The applications of this methodology for real samples were examined by various water type, black tea and pepper samples.     

Control of TAME reactive distillation using Non-Dominated Sorting Genetic Algorithm-II

The control system performs poor in characteristics and even it becomes unstable, if improper values of the controller tuning constants are used. So it becomes necessary to tune the controller parameters to achieve good control performance with the proper choice of tuning constants. Many control problems involve simultaneous optimization of multiple variables that competing with each other. In this paper, the Non-Dominated Sorting Genetic Algorithm-II (NSGA-II) has been successfully applied to optimization of dynamic state of t-amyl-methyl-ether (TAME) reactive distillation process. This paper presents the tuning of Proportional-Integral-Derivative (PID) controllers by minimizing of two objective functions (overshoot and Integral of Absolute Error (IAE)) through the NSGA-II. Results show that genetic algorithm is more suitable method for optimal control of the TAME reactive distillation columns than traditional methods such as Tyreus-Luyben.     

Daily dietary intakes of zinc,copper, lead,and cadmium as determined by duplicate portion sampling combined with either instrumental analysis or the use of food composition tables,Shiraz, Iran

Estimation of essential and toxic element intakes is crucial to evaluate the risks of deficiency or toxicity. The purpose of this study was to investigate and also to compare the dietary intakes of zinc (Zn) and copper (Cu) by adults living in Shiraz, Iran, determined by two procedures: duplicate portion sampling of 21 hospital meals combined with either instrumental analysis (voltammetric measurement) or the use of food composition tables (FCTs). The level of exposure to lead (Pb) and cadmium (Cd) was evaluated as well. The daily Zn intakes of both methods were not significantly different and were higher than the RDA values except the value measured by the instrumental analysis which was lower than the RDA established for a male adult. Daily intake of Cu determined by instrumental analysis was significantly lower and closer to RDA for adults compared with the value estimated by FCTs. The dietary intakes of Pb and Cd were 313 and 61 % of the respective provisional tolerable weekly intakes (PTWIs), respectively. The accuracy of two methods used for estimation of Zn intake was similar. In the case of Cu, the use of FCTs, in which the influence of environmental conditions and dietary habits of meal preparation is not taken into account, overestimated dietary intake. The risk of zinc deficiency was found in adult males. Moreover, the estimated intake of Pb, but not Cd, could be a cause of concern for Shiraz population. Thus, conducting regular periodic studies to assess the dietary intake of mentioned elements are recommended.