Interfacial Behavior of Perchlorate versus Chloride Ions in Aqueous Solutions

2009 ◽  
Vol 113 (48) ◽  
pp. 15843-15850 ◽  
Author(s):  
Marcel D. Baer ◽  
I-Feng William Kuo ◽  
Hendrik Bluhm ◽  
Sutapa Ghosal
1986 ◽  
Vol 51 (11) ◽  
pp. 2437-2443
Author(s):  
František Kopecký ◽  
Mária Vojteková ◽  
Milan Pešák

The conventional activity of chloride ions was measured by an ion-selective electrode at 25 °C in aqueous solutions of benflurone, i.e. 5-(2-(N,N-dimethylamino)ethoxy)-7-oxo-7H-benzo(c)fluorene hydrochloride, without or with additions of KCl. These results suggest a gradual association of benflurone; the formation of a hetero-associate, (BH+)2Cl-, followed by higher associates was evaluated in the measured range up to 0.1 mol l-1.


1994 ◽  
Vol 59 (6) ◽  
pp. 1311-1318 ◽  
Author(s):  
Ladislav Svoboda ◽  
Petr Vořechovský

The properties of cellulose chelating ion exchangers Ostsorb have been studied in the sorption of cadmium and lead from aqueous solutions. The Cd(II) and Pb(II) ions are trapped by the Ostsorb OXIN and Ostsorb DETA ion exchangers most effectively in neutral and alkaline media but at these conditions formation of stable hydrolytic products of both metals competes with the exchange equilibria. From this point of view, Ostsorb DTTA appears to be a more suitable sorbent since it traps the Pb(II) and Cd(II) ions in acidic media already. Chloride ions interfere with the sorption of the two metals by Ostsorb DTTA whereas the ionic strength adjusted by the addition of sodium perchlorate does not affect the exchange capacity of this ion exchanger.


2005 ◽  
Vol 34 (4) ◽  
pp. 427-441 ◽  
Author(s):  
H. López-González ◽  
M. Solache-Ríos ◽  
M. Jiménez-Reyes ◽  
J. J. Ramírez-García ◽  
A. Rojas-Hernández

2012 ◽  
Vol 9 (6) ◽  
pp. 558 ◽  
Author(s):  
Lei Wu ◽  
Xuefeng Hu

Environmental context Aromatic amines are widely used chemicals, which show enhanced toxicity and longer environmental persistence when halogenated. We investigated the chlorination of aniline in seawater and in natural aqueous solutions containing Fe3+ and Cl–, under simulated sunlight irradiation. The results increase our understanding of the transformation pathway of typical nitrogen-containing aromatic contaminants in the environment. Abstract Photochlorination of aniline was observed in aqueous solutions containing dissolved FeIII and chloride ions under simulated solar light irradiation. Effects of O2, Cl–, Fe3+ and pH on the formation of chloroanilines (CAs) were investigated. para-chloroaniline (4CA) was identified as the main chlorinated product. The formation of 4CA is enhanced with increased concentrations of Cl– or Fe3+, and decreased pH, whereas oxygen plays a negligible role in the process. The results indicate that, Cl• is formed mainly by the photodissociation of FeCl2+–FeCl2+ complexes, and reacts with Cl– to produce Cl2•–. Aniline is then oxidised by Cl2•– into an anilino radical cation, which further reacts with Cl2•– to generate CAs. The photochlorination of aniline in natural seawater was also observed. Other phototransformation products of aniline were detected and a transformation pathway was proposed. This work provides evidence for the photochemical chlorination path of aniline-based aromatic amines in aqueous solutions.


CORROSION ◽  
1984 ◽  
Vol 40 (4) ◽  
pp. 186-189 ◽  
Author(s):  
P. Mayer ◽  
A. V. Manolescu ◽  
E. M. Rasile

Abstract The accelerated internal corrosion in boiler evaporators results from an unfavorable coincidence of adverse thermohydraulic conditions, boiler water contamination, and fabrication defects. Boiler tube material (medium carbon steel, Type SA210) was exposed in static autoclaves to aqueous solutions of HF, FeF3, and NiF2 at 300 C, and the rate of attack and morphology of the resulting scales were established. For comparison, parallel tests were conducted in aqueous solutions containing chloride ions. This work establishes the role played by fluoride contamination of the boiler water.


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