Stabilities of the 2-mercaptoethylamine complexes of trivalent metal ions and divalent metal ions in aqueous solution

1995 ◽  
Vol 231 (1-2) ◽  
pp. 159-165 ◽  
Author(s):  
Yuejin Li ◽  
Arthur E. Martell
2016 ◽  
Vol 7 (1) ◽  
pp. 66-76 ◽  
Author(s):  
Ashim Kumar Basumatary ◽  
R. Vinoth Kumar ◽  
Kannan Pakshirajan ◽  
G. Pugazhenthi

This study aimed to assess the performance of three zeolite membranes in the removal of trivalent metal ions from aqueous solution using a cross-flow mode of operation. Three types of zeolite membrane, MCM-41, MCM-48 and FAU, were prepared on a low-cost, circular ceramic support by hydrothermal treatment. The three zeolite membranes were characterized by using X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM) and contact angle measurements. The XRD results confirmed the formation of zeolites. The deposition of zeolite on the ceramic support and hydrophilicity of zeolite membranes were monitored by FESEM and contact angle measurement, respectively. The pore size of the MCM-41, MCM-48 and FAU membrane was found to be 0.173 μm, 0.142 μm, and 0.153 μm, respectively, which was lower than that of the support (1.0 μm). The fabricated zeolite membranes were used to investigate the separation behavior of trivalent metal ions (Al3+ and Fe3+) from aqueous solution at various applied pressures. It was observed that an increase of applied pressure leads to a slight decrease in the removal efficiency. Among the various zeolite membranes, the FAU membrane showed the maximum rejection of 88% and 83% for Fe3+ and Al3+ separation, respectively.


2010 ◽  
Vol 10 (5) ◽  
pp. 3538-3542 ◽  
Author(s):  
Young In Yang ◽  
Inhee Choi ◽  
Surin Hong ◽  
Suseung Lee ◽  
Taewook Kang ◽  
...  

1980 ◽  
Vol 33 (7) ◽  
pp. 1511 ◽  
Author(s):  
KN Pearce

centration formation constants for magnesium and calcium citrate complexes have been redetermined from pH titrations of citric acid in the absence and presence of the divalent metal ions in aqueous solution at 2° Values for the constants, corrected for the presence of potassium citrate complex, are presented and critically compared with literature values. Values for the formation constants of strontium and barium citrate complexes are also reported.


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