Search results for "SEAWATER"
showing 10 items of 386 documents
Application of solar energy to seawater desalination in a pilot system based on vacuum multi-effect membrane distillation
2020
Abstract The evaluation of a novel solar seawater desalination system implemented at the University of Almeria (Spain) is presented. It integrates a solar thermal field based on static collectors and a thermal desalination system based on the vacuum multi-effect membrane distillation technology. The distillation unit has a particular innovation to increase its thermal performance, using a seawater flow to condense the steam and preheat the feed. Experiments were made under different environmental conditions to assess the role of the thermal storage system for minimizing the effect of disturbances in solar radiation. Thermal energy could be delivered at a stable temperature to the distillati…
Assessment of a pilot system for seawater desalination based on vacuum multi-effect membrane distillation with enhanced heat recovery
2018
Abstract This work presents the evaluation of an innovative system based on vacuum multi-effect membrane distillation modules (V-MEMD) for seawater desalination at pilot scale. This four-effect unit introduces a remarkable modification from previous V-MEMD systems, consisting of the use of the seawater feed flow as cooling in the condenser, rather than a separate circuit. Preheating the feed in the condenser improved heat efficiency (maximum gained output ratio obtained for seawater was 3.2). Maximum distillate fluxes reached 8.5 l h−1 m−2 for hot feed temperature 75 °C and feed flow rate 150 l h−1. Increasing both parameters to raise the productivity was hindered by the inability of the co…
Speciation of polyelectrolytes in natural fluids Protonation and interaction of polymethacrylates with major components of seawater.
2002
Acid–base properties of two sodium polymethacrylates (W= 4000 and 5400 Da) were studied potentiometrically in aqueous solution at 25 °C. Measurements were made in different salt solutions: LiCl 0.1–1.5, NaCl 0.1–2, KCl 0.1–2, Et4NI 0.1–0.75 mol l − 1 , and in artificial seawater in the salinity range 10 S 45. Protonation data were analysed by two different models and the dependence of the relative parameters on ionic strength were calculated. Measurements performed in interacting media (alkali metal chlorides and artificial seawater) were interpreted in terms of complex formation, and the relative formation parameters are reported. Previous data on the interaction of a higher molecular weig…
Speciation of Low Molecular Weight Carboxylic Ligands in Natural Fluids: Protonation Constants and Association with Major Components of Seawater of O…
1999
Abstract The interaction of oxydiacetate and citrate with the major components of seawater has been studied potentiometrically, at 25°C, in an artificial seawater (containing Na+, K+, Ca2+, Mg2+, Cl− and SO42−) at different salinities (5–45‰). Apparent protonation constants were calculated, from potentiometric data, and estimated, using an appropriate complex formation model. Formation constants of complexes formed by oxydiacetate and citrate and the cation of seawater (the inorganic content of seawater being considered as a single 1 : 1 salt) were determined. The single salt approximation for the major inorganic components of seawater, which is a good tool in estimating the mean strength o…
Chemical speciation of organic matter in natural waters. Interaction of nucleotide 5′ mono-, di- and triphosphates with major components of seawater
2004
AbstractThe interactions of nucleotide 5’ mono-, di- and triphosphates in a multicomponent ionic medium simulating the macro-composition of seawater (Na+, K+, Ca2+, Mg2+, Cl-, SO42-, Synthetic Sea Water, SSW) have been investigated at different ionic strengths and at T= 25°C. A chemical speciation model, according to which all the internal interactions between the components of the ionic medium are taken into account, was applied to determine the effective formation constants of species in the nucleotide-seawater system. The results were compared to protonation parameters calculated from single electrolyte systems. A simpler model (SSW considered as a single salt BA, with Bz+ and Az-), repr…
Equilibrium studies in natural fluids: interactions of -PO43−, -P2O74−and -P3O105−with the major constituents of sea water
1998
AbstractThe interaction of PiO(i+2)−(3i+1) (i = 1,2,3) with the major components of seawater has been studied potentiometrically, at 25°C, in an artificial seawater (Na+, K, Ca2+, Mg2+, Cl− and SO42−) at different salinities (5—45%o). Apparent protonation constants have been calculated, from potentiometric data, and estimated, using an appropriate complex formation model. Formation constants of complexes formed by phosphates and the cation of seawater (the inorganic content of seawater being considered as a single 1:1 salt) have been determined. The comparison between experimental and estimated results showed that a suitable complexation model can be used with a fairly good accuracy in pred…
Modelling of natural synthetic polyelectrolyte interactions in natural waters by using SIT, Pitzer and Ion Pairing approaches
2006
Abstract In this paper SIT and Pitzer models are used for the first time to describe the interactions of natural and synthetic polyelectrolytes in natural waters. Measurements were made potentiometrically at 25 °C in single electrolyte media, such as Et 4 NI and NaCl (for fulvic acid 0.1 − 1 S single salt ” BA, with cation B and anion A representing all the major cations (Na + , K + , Mg 2+ , Ca 2+ ) and anions (Cl − , SO 4 2− ) in natural sea water, respectively. The ion pair formation model was also applied to fulvate and alginate in artificial sea water by examining the interaction of polyanions with the single sea water cation. Results were compared with those obtained from previous sp…
Increased sulfate availability in saline water promotes hydrogen sulfide production in fish organic waste
2020
The risk of hydrogen sulfide (H2S) production can be a challenge in marine land-based recirculating aquaculture systems (RAS). Hydrogen sulfide is a toxic gas that can cause massive fish mortality even at low concentrations, and in addition, serious odour problems in the surroundings. It is a bacterial by-product originating from the degradation of organic matter in sulfur-rich waters such as marine waters. In order to hinder H2S production in marine land-based RAS, more information on the H2S production conditions and the associated microbiology is needed. In this study, the production of H2S from rainbow trout (Oncorhynchus mykiss) organic waste was examined using a novel H2S measurement …
In-tube solid-phase microextraction coupled by in valve mode to capillary LC-DAD: Improving detectability to multiresidue organic pollutants analysis…
2009
Abstract A simple and fast capillary chromatographic method has been developed to identify and quantify organic pollutants at sub-ppb levels in real water samples. The major groups of pesticides (organic halogens, organic phosphorous, and organic nitrogen compounds), some hydrocarbons (polycyclic aromatic hydrocarbons), phthalates and some phenols such as phenol and bisphenol A (endocrine disruptors) were included in this study. The procedure was based on coupling, in-tube solid-phase microextraction (IT-SPME) by using a conventional GC capillary column (95% methyl–5% phenyl substituted backbone, 80 cm × 0.32 mm i.d., 3 μm film thickness) in the injection valve to capillary liquid chromatog…
Environmentally relevant precursors of carbonyl sulfide in aquatic systems
1997
Seawater solutions of environmentally relevant organosulfur compounds, commercial humic acid (HA), and natural dissolved organic matter (DOM) were incubated with and without UV light in order to determine the carbonyl sulfide (COS) producing capabilities of these compounds. COS dark- and photo-production rate constants were determined for dilute solutions of the organosulfur compounds (μmol l−1) and HA/DOM (mg l−1). Dissolved COS was determined using a purge and cryogenic trap method followed by GC/FPD detection. COS was produced in considerable amounts both non-photochemically and photochemically from the reduced form of free acid of glutathione (GSH) and photochemically from cysteine (CYS…