Extraction of cadmium salicylate with some nitrogen-containing organic bases

1978 ◽  
Vol 56 (23) ◽  
pp. 2922-2926 ◽  
Author(s):  
J. M. Singh ◽  
S. N. Tandon

Cd(HSal)2 is extracted from aqueous solutions into n-butanol, but not into non-hydroxylic solvents (such as benzene and chloroform) at pH 4.5 to 6.0. Addition of N bases, which have no effect alone, causes extraction into the latter solvents, apparently by displacement of coordinated water, giving Cd(HSal)2•2B. This synergistic effect varies with B (β-picoline > pyridine > quinoline). Formation and distribution constants are given for the experimental conditions.

1980 ◽  
Vol 58 (15) ◽  
pp. 1558-1561 ◽  
Author(s):  
Bina Jain ◽  
J. M. Singh ◽  
R. N. Goyal ◽  
S. N. Tandon

Zinc and cadmium anthranilates do not extract into non-polar solvents alone in the pH range 4.5–6.5. But their extraction is synergistically enhanced in presence of N bases, apparently by displacement of coordinated water. The synergistic effect varies with the bases in the order β-picoline > pyridine > quinoline. The values of extraction constants suggest that cadmium forms more stable complexes than zinc.


1994 ◽  
Vol 59 (3) ◽  
pp. 582-588
Author(s):  
Jan Souček ◽  
Ladislav Belický ◽  
Josef Havel

The protonation and distribution constants of dibenz[b, f]-1,4-oxazepin (CR) were measured. This substance forms stable ion-associates with Acid Red 88, extractable into chloroform. Reextraction with an aqueous phase containing basic fuchsine or safranine T brings about exchange of the CR cation for the basic dye cation. The associates so formed exhibit higher conditional extraction constants and higher molar absorptivities than the initial associates.


Nanoscale ◽  
2020 ◽  
Vol 12 (2) ◽  
pp. 658-668 ◽  
Author(s):  
Rafael del Caño ◽  
Jose M. Gisbert-González ◽  
Jose González-Rodríguez ◽  
Guadalupe Sánchez-Obrero ◽  
Rafael Madueño ◽  
...  

The highly packed cetyltrimethylammonium bromide bilayer on the surface of gold nanorods synthesized by the seed-mediated procedure hampers the complete ligand exchange under experimental conditions that preserves the stability of the dispersions.


2014 ◽  
Vol 13 (1) ◽  
Author(s):  
Dariusz Wyrzykowski ◽  
Joanna Pranczk ◽  
Dagmara Jacewicz ◽  
Aleksandra Tesmar ◽  
Bogusław Pilarski ◽  
...  

AbstractA potentiometric titration method (PT) and a stopped-flow kinetic technique monitored by a UV−Vis spectroscopy have been used to characterize the stability of series of Co(II)- and Ni(II)-thiodiacetato complexes, M(TDA), in the presence of 1,10-phenanthroline (phen) or 2,2’-bipyridine (bipy) in aqueous solutions. The stability constants of the binary (1:1), ternary (1:1:1) as well as the resulting hydroxo complexes were evaluated and compared to the corresponding oxydiacetate complexes. Based on the species distribution as a function of pH the relative predominance of the species in the system over a pH range was discussed. Furthermore, the kinetic measurements of the substitution reactions of the aqua ligands to phen or bipy in the coordination sphere of the binary complexes M(TDA) were performed in the 288–303 K temperature range, at a constant concentration of phen or bipy and at seven different concentrations of the binary complexes (0.2–0.5 mM). The kinetic stability of the M(TDA) complexes was discussed in relation to the experimental conditions and the kind of the auxiliary ligands (phen/bipy). Moreover, the influence of the type of primary ligand (thiodiacetate/oxydiacetate) on the substitution rate of the auxiliary ligands was also compared.


Attention has previously been directed by one of us to the existence of a differential septum enclosing the seeds of Hordeum (barley). When the seeds are immersed in aqueous solutions of most electrolytes, and of many non-electrolytes, this covering behaves as a very efficient differential septum, water alone entering the seeds under the attractive influence of the finely granulated contents. The rate at which the water enters is considerably affected if substances are dissolved in it, being increased by some and diminished by others; it is also markedly dependent on the temperature of the water or solution in which the seeds are immersed. Variations of the rate at which water enters with alterations of the experimental conditions are presumably due mainly to changes in the water, and the seeds of Hordeum would thus appear to be a very suitable medium for the investigation of the nature of the changes produced in water by the presence of dissolved substances or by alterations of temperature.


1977 ◽  
Vol 55 (14) ◽  
pp. 2613-2619 ◽  
Author(s):  
M. S. El-Ezaby ◽  
M. A. El-Dessouky ◽  
N. M. Shuaib

The interactions of Ni(II) and Co(II) with 2-pyridinecarboxaldehyde have been investigated in aqueous solutions at μ = 0.10 M (KNO3) at 30 °C. The stability constants of different complex equilibria have been determined using potentiometric methods. Spectrophotometric methods were also used in the case of the nickel(II) – 2-pyridinecarboxaldehyde system. It was concluded that nickel(II) and cobalt(II), analogous to copper(II), enhance hyrdation of 2-pyridinecarboxaldehyde prior to deprotonation of one of the geminal hydroxy groups. Complex species of 1:1 as well as 1:2 metal ion to ligand composition exist under the experimental conditions used.


2003 ◽  
Vol 58 (7) ◽  
pp. 658-662 ◽  
Author(s):  
Manal R. Al-Saraj ◽  
Salman M. Saadeh ◽  
Monzir S. Abdel-Latif

Several versions of Cu(II) ion selective electrodes (ISE), based on cyclized N,N'-bis(salicylidene)-o-phenylenediamine (salophen) complexes with Cu(II), were fabricated for determination of Cu(II) in aqueous solutions. The response of the ISE was optimized by variation of membrane composition and evaluation of various experimental conditions. Near Nernstian slopes (~ 28-32 mV/decade) were obtained for some preparations. The linear range of the ISE ranged from 5 × 10-5 to 1 × 10-2M Cu(II). Coated-wire and coated disc ISE resulted practically in a similar response as screen printed electrodes (SPE). The potentiometric selectivity coefficients (Kij) for all electrodes were determined for Na+, NH4+, Ca2+, Mg2+, Ni2+, Pb2+, Zn2+, Cd2+, Co2+, Fe3+, Hg2+, CO32-, H2PO4-, HPO42-, SO42-, CH3COO-, Br-, I-, NO3-, and SCN-. The selectivity coefficients were in the range from 10-2 to 10-3 for all ions tested except Hg2+, I-, and to less extent Fe3+. Fabricated ISE using the Cu(II)-salophen complex are reliable and stable.


1995 ◽  
Vol 60 (5) ◽  
pp. 788-794 ◽  
Author(s):  
Vlasta Brezová ◽  
Alžbeta Blažková ◽  
Mirko Brezňan ◽  
Peter Kottáš ◽  
Michal Čeppan

The photocatalytic mineralization of phenol in aqueous solutions under various experimental conditions was employed, to test the activity of the prepared immobilized fibreglass/TiO2 photocatalysts. The particles of titanium dioxide P25 were coated on the surface of commercial fibreglass fabric by dipping in ethanolic TiO2 suspensions and were fixed by firing 6 h at 500 °C.


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