ABSTRACT
In the context of a regional Chilean project (FIC Taltape project, BIP code 30158422-0), a multi-effect distillation (MED) pilot plant has been built and installed in a small community in the north of Chile (Taltape, Arica) in order to supply treated water for agricultural and domestic purposes. The aim of this paper is to assess the techno-economic feasibility of this system for supplying water with the required quality to the population. The characterization of the feed water and the effluents from the MED pilot plant (distillate and brine), obtained during five months of operation, has been firstly performed. Then, the prediction of the operation of the water treatment system with solar energy has been carried out using a typical meteorological year and the design of a static solar field that cover the thermal energy needs of the water treatment plant. The annual simulations of the MED pilot plant operating with solar energy showed that the water needs can be mostly covered using a static solar thermal field with a total area of 113.2â¯m2, which would generate roughly 46% of the total heat required by the water treatment plant. The technical analysis has been completed with an exhaustive economic assessment. The specific water costs have been determined for the MED pilot plant and the scale factor when the productivity is increased up to 5000â¯m3/day has been evaluated. The cost of distillated water produced by the MED plant varied from 15.0â¯USD$/m3 for the 10â¯m3/day production capacity to 1.25â¯USD$/m3 when this variable is increased to 5000â¯m3/day.
Subject(s)
Agricultural Irrigation/methods , Water Purification/methods , Agricultural Irrigation/economics , Chile , Distillation , Water , Water Purification/economics , Water SupplyABSTRACT
The determination of a single rare earth element in a mixture with other species of this family is a very challenging problem in analytical chemistry due to the close similarity of their chemical properties. In this work, a liquid-solid extraction procedure for praseodymium, neodymium, samarium and yttrium mixtures and subsequent determination by energy dispersive X-ray fluorescence spectrometry is described. The pre-concentration procedure, which involves the use of silica modified with 1-(2-pyridylazo)-2-naphthol, permits complete recovery of the rare earths and significant sensitivity enhancement in comparison with direct determination in the aqueous phase. Determinations in quaternary mixtures show typical precisions and accuracies of 3% and 5%, respectively.
ABSTRACT
Two preconcentration methods has been developed for simultaneous determination of zirconium and hafnium by energy dispersive X-ray fluorescence (EDXRF). The first method is a liquid-solid extraction procedure with the use of an anionic exchange resin modified with xylenol orange. The second is a precipitation procedure carried out in the presence of lanthanum. Both methods permit significant enhancement of sensitivity in comparison with direct measurement in the aqueous phase. The applicability of both procedures for the preconcentration of Zr and Hf prior to their determination by EDXRF was demonstrated by analyzing synthetic mixtures and a sample of zirconium ore. The results obtained with the use of the modified resin show relative standard deviation of about 4% and good agreement with those obtained by spectrographic analysis.
ABSTRACT
The simultaneous determination of lanthanide family elements is one of the greatest problems in analytical chemistry, due to the close similarity of their chemical properties. Spectrophotometric methods are generally of limited use, due to the various mutual spectral interferences involved. By using multivariate calibration methods (partial least-squares regression, PLSR), it was possible to obtain a model that adjusts itself perfectly to the values of the mixture concentrations used in the calibration. The model used absorption spectra in the 290-800 nm range for a set of 20 different mixtures of Ce, Pr, Nd and Sm, and made possible the determination of Ce, Pr and Nd concentrations of a commercial rare-earth product, with significantly greater precision than the conventional univariate calibration method. Determination of the Sm concentrations was not possible, since its concentration was below the concentrations used in the model definition.