The determination and temperature-dependence of the stability constant of the calcium—catechol-4-sulfonate complex in alkaline aqueous media

1982 ◽  
Vol 138 ◽  
pp. 237-243 ◽  
Author(s):  
Harvey H. Westervelt ◽  
W.J. Frederick ◽  
Earl W. Malcolm ◽  
Dwight B. Easty
Keyword(s):  
Stability Constant ◽  
Temperature Dependence ◽  
Aqueous Media ◽  
The Stability

Discontinuous spectrocolorimetric titration method for determining stability constants of fulvic acid - iron complexes

Soil Research ◽  
1997 ◽  
Vol 35 (6) ◽  
pp. 1279 ◽  
Author(s):  
S. B. Pandeya ◽  
A. K. Singh
Keyword(s):  
Stability Constant ◽  
Stability Constants ◽  
Aqueous Media ◽  
Poultry Manure ◽  
Fulvic Acids ◽  
Titration Method ◽  
Binding Ability ◽  
Press Mud ◽  
Determining Factors ◽  
The Stability

The stability constants for the complexes formed between iron species existing in ambient soil environment and fulvic acids (FA) extracted from organic wastes like sewage sludge, farm yard manure (FYM), poultry manure, and press mud were determined in aqueous media of pH 5·0 and 8·5 by discontinuous spectrocolorimetric titration method. The values of stability constant (log K) of Fe–FA complexes estimated at pH 5·0 were 6·026, 6·212, 6·270, and 6·342 for FYM, sludge, poultry manure, and press mud, respectively. The respective values at pH 8·5 were 6·145, 6·276, 6·350, and 6·940. The order of the values of log K for different preparations of fulvic acids was press mud > poultry manure > sludge > FYM. The functional group contents, their pH of neutralisation, and electrostatic properties of the FA such as pKINT, pKm, and 0·868 nW, were found to be the determining factors for maximum binding ability of FA for metal cations and the stability constant of Fe–FA for different FA preparations. The basic assumptions and the limitations of the discontinuous spectrocolorimetric estimation of stability constants for Fe–FA are discussed.

scholarly journals Electrochemical Studies on Complexation and Speciation of Copper(II) in ppb Level with 1,10-Phenanthroline in Aqueous Media

1970 ◽  
Vol 46 (2) ◽  
pp. 219-224 ◽  
Author(s):  
N Nahar ◽  
NP Mona ◽  
MN Abser
Keyword(s):  
Stability Constant ◽  
Copper Complexes ◽  
Anodic Stripping Voltammetry ◽  
Aqueous Media ◽  
Stripping Voltammetry ◽  
Differential Pulse ◽  
Experimental Conditions ◽  
Overall Stability ◽  
The Stability ◽  
And Diffusion

Complexation and speciation of copper (II) in ppb level with 1,10-phenanthroline (L) in aqueous media have been investigated by differential pulse anodic stripping voltammetry using thin mercury film glassy carbon electrode (TMFGCE). The work was carried out at constant ionic strength of 0.01 mol dm-3 using NaNO3 at ambient temperature. The pH was kept constant at 9.12 ± 0.10 by the addition of borate buffer. Applying the concept of DeFord and Hume, the stability constants of different species of copper with 1,10-phenanthroline were calculated from the variation of peak potential and diffusion current of simple and complexed metal ions under the present experimental conditions. It was found that copper(II) form three complexes (1:1, 1:2 and 1: 3; metal : ligand) with 1,10-phenanthroline. The overall stability constant of copper complexes, MLn can be defined as βMLn= [MLn ]/[M2+][L]n in which M2+ = Cu2+ and L = 1,10-phenanthroline; n is an integer. The values of the stability constant of different copper complexes with 1,10-phenanthroline were found to be 109.33, 1015.10 and 1020.48 for CuL, CuL2 and CuL3, respectively (the overall charges were omitted for simplicity). The high values of overall stability constant indicate that the complexes are highly stable. Using the values of stability constant of copper complexes and hydrolysis constant of copper, the percentage of all possible copper species under present experimental conditions were calculated. Keywords: Electrochemical; Speciation; Complexation; Copper 1,10-phenanthroline. DOI: http://dx.doi.org/10.3329/bjsir.v46i2.8188 Bangladesh J. Sci. Ind. Res. 46(2), 219-224, 2011

Host-Guest Interactions on Electrode Surfaces for Immobilization of Molecular Catalysts

2020 ◽  
Author(s):  
Laurent Sévery ◽  
Jacek Szczerbiński ◽  
Mert Taskin ◽  
Isik Tuncay ◽  
Fernanda Brandalise Nunes ◽  
...  
Keyword(s):  
Aqueous Media ◽  
Heterogeneous Systems ◽  
Catalytic Systems ◽  
New Approach ◽  
Molecular Systems ◽  
Electrode Surfaces ◽  
Catalytic Surfaces ◽  
Oxide Electrodes ◽  
The Stability ◽  
Molecular Catalysts

The strategy of anchoring molecular catalysts on electrode surfaces combines the high selectivity and activity of molecular systems with the practicality of heterogeneous systems. The stability of molecular catalysts is, however, far less than that of traditional heterogeneous electrocatalysts, and therefore a method to easily replace anchored molecular catalysts that have degraded could make such electrosynthetic systems more attractive. Here, we apply a non-covalent “click” chemistry approach to reversibly bind molecular electrocatalysts to electrode surfaces via host-guest complexation with surface-anchored cyclodextrins. The host-guest interaction is remarkably strong and allows the flow of electrons between the electrode and the guest catalyst. Electrosynthesis in both organic and aqueous media was demonstrated on metal oxide electrodes, with stability on the order of hours. The catalytic surfaces can be recycled by controlled release of the guest from the host cavities and readsorption of fresh guest. This strategy represents a new approach to practical molecular-based catalytic systems.

Synthesis and solvatochromic studies of 2- amino-3-phenolazo1-(4-sulfophenyl)-3-methyi-5-pyrozolone and use it for the determination of trace amount of Nickel (II) in blood samples

2016 ◽  
Vol 5 (10) ◽  
pp. 4920
Author(s):  
Amar M. Ali ◽  
Hussain. J. Mohammed*
Keyword(s):  
Stability Constant ◽  
Trace Amount ◽  
Benzenesulfonic Acid ◽  
Determination Method ◽  
Blood Samples ◽  
Determination Of Nickel ◽  
Normal Human ◽  
The Stability ◽  
Normal Human Blood

A new, simple, sensitive and rapid spectrophotometric method is proposed for the determination of trace amount of Nickel (II). The method is based on the formation of a 1:2 complex with 4-(4-((2-hydroxy-6-nitrophenyl) diazenyl) -3-methyl-5-oxo-2, 5-dihydro-1H-pyrazol-1-yl) benzenesulfonic acid (2-ANASP) as a new reagent is developed. The complex has a maximum absorption at 516 nm and εmax of 1. 84 X 105 L. mol-1. cm-1. A linear correlation (0. 25 – 4. 0μg. ml-1) was found between absorbance at λmax and concentration. The accuracy and reproducibility of the determination method for various known amounts of Nickel (II) were tested. The results obtained are both precise (RSD was 1. 2 %) and accurate (relative error was 0. 787 %). The effect of diverse ions on the determination of Nickel (II) to investigate the selectivity of the method were also studied. The stability constant of the product was 0. 399 X 106 L. mol-1. The proposed method was successfully applied to the analysis of diabetes blood and normal human blood. 

Temperature dependence of the stability of tobramycin mixed with penicillins in human serum

1982 ◽  
Vol 39 (6) ◽  
pp. 1005-1008
Author(s):  
Kimberly A. O'Bey ◽  
Lucia K. Jim ◽  
Joseph P. Gee ◽  
Robert M. Johnson
Keyword(s):  
Temperature Dependence ◽  
Human Serum ◽  
The Stability

Electrical Conductivity of Chloro(phenyl)glyoxime and Its Co(II), Ni(II) and Cu(II) Complexes

2003 ◽  
Vol 68 (7) ◽  
pp. 1233-1242 ◽  
Author(s):  
Orhan Turkoglu ◽  
Mustafa Soylak ◽  
Ibrahim Belenli
Keyword(s):  
Electrical Conductivity ◽  
Temperature Dependence ◽  
Electric Conductivity ◽  
Crystal Structures ◽  
Elemental Analysis ◽  
Analysis Data ◽  
Elemental Analysis Data ◽  
The Stability ◽  
Xrd Patterns ◽  
Metal Ligand

Chloro(phenyl)glyoxime, a vicinal dioxime, and its Ni(II), Cu(II) and Co(II) complexes were prepared. XRD patterns of the complexes point to similar crystal structures. IR and elemental analysis data revealed the 1:2 metal-ligand ratio in the complexes. The Co(II) complex is a dihydrate. Temperature dependence of electrical conductivity of the solid ligand and its complexes was measured in the temperature range 25-250 °C; it ranged between 10-14-10-6 Ω-1 cm-1 and increased with rising temperature. The activation energies were between 0.61-0.80 eV. The Co(II) complex has lower electric conductivity than the Ni(II) and Cu(II) complexes. This difference in the conductivity has been attributed to differences in the stability of the complexes.

Determination of the Stability Constant of the Calcium Dioxalate Complex

Urolithiasis ◽  
1981 ◽  
pp. 447-451
Author(s):  
John R. Burns ◽  
Birdwell Finlayson ◽  
Arthur Smith
Keyword(s):  
Stability Constant ◽  
The Stability

SODIUM CHELATES OF ETHYLENEDIAMINETETRAACETIC ACID

1963 ◽  
Vol 41 (1) ◽  
pp. 18-20 ◽  
Author(s):  
Vladimir Palaty
Keyword(s):  
Stability Constant ◽  
Stability Constants ◽  
Ethylenediaminetetraacetic Acid ◽  
Glass Electrode ◽  
Neutral Solution ◽  
Experimental Conditions ◽  
The Stability ◽  
Sensitive Method

The stability constant of the sodium chelate of EDTA was determined by means of a sodium-sensitive glass electrode. It appears that a hydrogen chelate of the formula NaHY2− is formed in the neutral solution of EDTA, but is very unstable. The stability constants, pKNaY = −2.61 and pKNaHY = 0.03, are comparable to the value obtained by Schwarzenbach and Ackermann under different experimental conditions by a less sensitive method.

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