Stoichiometry and Stability Constant Values for Copper (II) Chelates with Ethylene Diamine in Deep Eutectic Solvents (DES) (Ethaline) Solutions

In this study we used the deep eutectic solvents (ionic liquids) to investigate the reaction between copper (II) with ethylene diamine (en). Two of the existing methods for analyzing spectrophotometric measurements have been applied for establishing, the stoichiometry and whenever possible, the stability constants of the chelates formed. The method of continuous variations was necessary to determine first whether, the metal ion and the ligand ethylene diamine form one or more than one chelate, when more than one chelate formed, the results obtained depend on the wavelength and for meaningful conclusions the wavelengths were carefully selected. The empirical formulae of the chelates were further substantiated by the molar ratio method. The effect of time and temperature on the formation and stability of these chelates in solution is also studied. The stability constants, K1 and K2 for the copper (II) chelates were calculated, though reliable, and are comparable to literature values.

Determination of Stability Constants of Cadmium-Glycine Complexes by a Unified Treatment for Potentiometric and Polarographic Data

The cadmium（Ⅱ）-glycine system was studied by the two experimental techniques, ion sensitive electrode （ISE） and differential pulse polarography （DPP）, and the experimental data obtained were used by a unified mathematical treatment to calculate the complex stability constants. The combination of the two techniques is of many advantages as ISE can be performed at low [LT]：[MT] ratios and significantly higher [MT], whereas DPP could be used well at large [LT]：[MT] ratios and much smaller [MT]. This makes it possible to study a metal-ligand system in a relatively broader range of experimental conditions that, in turn, provides more information about the metakligand system of interest. Applying the unified mathematical treatment to the cadmium-glycine system, two new complexes MHL and ML2（OH） as well as three complexes ML, ML2 and ML3, reported in literatures, could be modeled and all their stability constants have been refined.

Stability Constants and Fluorescence of Terbium(Ⅲ) Complexes with Polyaminopolycarboxylates in Aqueous Solution

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Magnesium (II) Adsorption from Aqueous Solutions on China Clay and the Stability Constants for Complex Formation

China clay was employed as an adsorbent for the removal of Mg 2+ from water at pH 7.0 within the temperature range of 303～328 K. The linearity of the plots indicated Langmuir type isotherms. The reaction was exothermic. A maximum removal of 35% was obtained at 0.50 mmol L -1 metal concentration and a pH of 7.0 at 303 K. The H + rel /Mg 2+ ads ratio changed from a fractional value to 2.5. Strong chemical bondings took place between oxygen atom of the surface and Mg 2+ , resulting in a surface complex species. Temperature had a significant effect on H + rel , and the stability constants also increased with increasing temperature.

Thermodynamics of Stability Constant of Binary Complex of Nicotinamide with Mn^(++)

The stability constants of the binary complexes of Mn2+ with nicotinamide (NA) were determined from potentiometric pH titrations data at 15.0 , 25.0 and 35.0oC and I = 0.1,0.2,0.4 mol L-1 (NaClO4). The formation of binary 1:1 , 1:2 NA-Mn complexes at three different temperatures and the influence of three different ionic strength on their stability were reported. The thermodynamic parameters (DGof, DSof, DHof) for the complex formation reaction were estimated from stability constant at different temperatures.

Stability constants of Sb^5+with Cl−and thermodynamics of Sb−S−Cl−H2O system involving complex behavior of Sb with Cl

The stability constants of Sb^5+with Cl−as well as thermodynamics of the Sb−S−Cl−H2O system were calculated.The stability constants of Sb5+with Cl−were obtained by theoretical calculations of the absorbance of a Sb5+-containing solution at different Cl^−concentrations,which was detected by spectrophotometric analysis at certain wavelengths of light(380 nm).The logarithmic values versus 10 of stability constants of Sb^5+with Cl−were 1.795,3.150,4.191,4.955,5.427 and 5.511,respectively,and partly filled the data gaps in the hydrometallurgy of antimony.The presence and distribution of pentavalent antimony compounds under different conditions were analyzed based on equilibrium calculations.Thermodynamic equilibrium calculations were performed for Sb−S−Cl−H2O system,which included the complex behavior of Sb with Cl,and the equilibrium equations of related reactions in this system were integrated into the potential−pH diagram.

Method of Calculation of Stability Constants of Fulvic Complexes on the Example of Copper

On the example of copper fulvate, it is discussed the method of calculation of stability constants of fulvic complexes. At pH = 8, the complex formation of copper（ll） ions with fulvic acids was studied by the solubility method. Fulvic acids were separated from the river Mtkvari by the adsorption-chromotographic method. The charcoal （BAU, Russia） was used as a sorbent. The suspension of copper（If） hydroxide was used as the solid phase, on which was added the increasing quantity of standard solution of fulvic acids. In diluted solutions, at pH = 8 the dominant form of copper（lI） is copper dihydroxo complex Cu（OH）^zO. It was established that in the Cu（OH）2 （solid）-Cu（OH）^20 （solution）-FA^2-H20 system, dominates copper dyhydroxo fulvate complex with the structure 1：1, [Cu（OH）2FA]^2. The average stability constant of copper dyhydroxo fulvate complex was calculated based on experimental data fl [Cu（OH）2FAJ^2 = 4.5× l0^5.

Determination of Composition and Stability Constant of Praseodymium(Pr^(3+))Complex with Tribromoarsenazo(TBA)by Dual-Series Linear Regression Method

A new method,dual-series linear regression method,has been used to study the complexation equilibrium of praseodymium(Pr^(3+))with tribromoarsenazo(TBA)without knowing the accurate concentra- tion of the complexing agent TBA.In 1.2 mol/L HCl solution, Pr^(3+)reacts with TBA and forms 1:3 com- plex,the conditional stability constant(lgβ_3)of the complex determined is 15.47,and its molar absorptivity(ε_3^(630))is 1.48×10~5 L·mol^(-1)·cm^(-1).

The Stability Constants of Complexes of BDBPH- Metals and Species Distributions

The stability constants of the mononuclear complexes of BDBPH-Zn(II), Cd(II) and Mn (II) were determined by the potentiometric equilibrium measurements, and species distributions were also discussed. The metal ions do not combine with the ligand until the first two protons of the ligand have almost been completely neutralized. The main species were mononuclear complexes with the diprotonated ligand, MH,L. The three metal ions also form mono- and noprotonated (fully deprotonated) complexes, MHL, ML. The relative order of stabilities of the mononuclear complexes, ML, is Zn(II) > Cd(II) > Mn(II). The ligand has strong tendency to form mononuclear complexes with Zn(II), Cd(II) and Mn(II), and it can also form dinuclear complexes at high pH.

Mobile Equilibrium Method for Determining Composition and Stability Constant of Coordination Compounds of the Form M_mR_n

A new method is proposed for determining the composition and stability constant of coordination compounds of the form M m R n ; it can be used to differentiate mono and poly nuclear coordination compounds. The equation derived is lg( A i/(A max - A i) m)=n lg c′ R+lg( m·β(c M/A max ) ( m -1) ). The method is based on Bent French limited logarithm method. The demonstration of the proposed method has yielded correct results for Sc 3+ chlorophosphonazo Ⅲ system and Fe 3+ Chromazurol S system.

The Study on the Stability Constant and Species Distribution of Eu (III) and Tb (III) Complexes with BDBPH

The stability constants and species distributions of complexes of two lanthanide ions, Eu（Ⅲ） and Tb（Ⅲ）, with a macrocyclic ligand, BDBPH, in 1：1 and 2：lsystem, were determined potentiometrically at 25.0 ℃ and I=0.100 mol L^-l. The two metal ions could form deprotonated mono- or dinuclear complexes with BDBPH after the first two protons of the ligand completely neutralized. At higher pH values, Eu（Ⅲ） could not form hydroxy complexes with BDBPH, while Tb（Ⅲ） could form hydroxy complexes in the type of M2L（OH）, M2L（OH）2, and M2L（OH）3.

The Determination of Average Stability Constant of NickeI-FA Complex at pH = 8,0 by the Solubility Method

At pH = 8, the complex formation process of Ni（Ⅱ） ions with FA was studied by the solubility method. FA were separated from the river Mtkvari by the adsorption-chromotographic method. The charcoal （BAU, Russia） was used as a sorbent. The old suspension of Ni（Ⅱ） hydroxide was used as the solid phase, on which was added the increasing quantity of standard solution of FA. In diluted solutions, at pH = 8.0 the dominant form of Ni（Ⅱ） is nickel dihydroxocomplex Ni（OH）2^0. It was established that in the Ni（OH）2（solid）-Ni（OH）2^0（solution）-FA2-H20 system dominates nickel dyhydroxofulvate complex with the structure 1：1, [Ni（OH）2FA]2-. The average stability constant of nickel dyhydroxofulvate complex was calculated based on experimental data flNi（OH）2FA2＂ = 5.3 × 105.

DETERM INATION OF THE STABILITY CONSTANTS OF COMPLEXES OF HISTIDINE,SOME DIPEPTIDES AND TRIGLYCINE WITH Zn(Ⅱ)AND Cd(Ⅱ)USING SMALL-SCALE PH-METRIC TITRATIONS

A potentiometric study on the complexes of His,Gly-His,ALa-His,Gly-Gly and Gly—Gly—Gly with Zn(Ⅱ)and Cd(Ⅱ)has been reported.Small-scale potentiometric titrations were car- ried out to determine stabil ity constants of complexes at 25℃ with I=0.10 mol dm^(-3)(KNO_3).The com- puter programs SUPERQUAD were applied for data treatment with satisfactory results.

DETERMINATION OF STABILITY CONSTANTS OF THE COORDINATION COMPOUNDS OF Au(Ⅲ)-2-MERCAPTOPYRIDINE-1-OXIDE AND METHYL DERIVATIVES——METHOD OF DUAL-WAVELENGTH CORRESPONDING SOLUTIONS

In this paper,we report the deductive formula used for the method of dual-wavelength corresponding solutions under condition of having ligand interference and the stability constants of three new coordination compounds [AuL_2]^+determined with this method.The stability of the three compounds,the necessity of controlling pH in experimental systems and the advantage of this method are discussed in detail.

A COMPARISON OF THE DETERMINATION OF STABILITY CONSTANTS OF COMPLEXES OF Cd(Ⅱ)WITH AMINO ACIDS AND SIMPLE PEPTIDES USING MICRO—pH—METRIC TITRATIONS AND CYCLIC VOLTAMMETRY

This paper reports the determination of stability constants for complexes of Cd(Ⅱ)with Gly, Ala,Val,Asp,Gly—Asp,Asp Gly,Gly—Gly and Gly—Gly—Gly using both micro—pH—metric titra- tions and the application of convolution—deconvolution cyclic voltammetry at 25℃ and I=0.10 mol· dm^(-3)(KNO_3).Stability constants were calculated from pH—metric data using the SUPERQUAD com- puter program and cyclic voltammograms were collected,stored and manipulated using the EG and G CONDECON 300 software.A considerably larger ligand:metal ratio(e,g.50:1)was possible using voltammetry.Evaluation of results from the two techniques suggests that stability constants for the species[CdL_2]and[CdL_3]are reliable when calculated fromvoltammetry while those for[CdL]are more reliable when determined by pH-metric titration.

STABILITY OF SOME POSITIVE LINEAR OPERATORS ON COMPACT DISK

Recently, Popa and Rata [27, 28] have shown the （in）stability of some classical operators defined on [0, 1] and found best constant when the positive linear operators are stable in the sense of Hyers-Ularn. In this paper we show Hyers-Ulam （in）stability of complex Bernstein-Schurer operators, complex Kantrovich-Schurer operators and Lorentz operators on compact disk. In the case when the operator is stable in the sense of Hyers and Ulam, we find the infimum of Hyers-Ulam stability constants for respective operators.

Short communication Linear analysis on the stability of lanthanide vapor complexes LnAl_3Cl_(12)(Ln=LatoLu)

The reactions LnCl3 (s) + (3/2)Al2Cl6, (g) = LnAl3Cl12 (g) for Ln = La to Lu were studied by quenching experiments in roughly the same temperature and pressure ranges (588-851 K and 0.01-0.22 MPa). Stability constants Kθ of lanthanide complexes LnAl3Cl12 were calculated from the measurements. The values of Ig Kθ change linearly with the ionpotential (Z+/r) of lanthanide(Ⅲ) from La to Gd and from Tb to Lu, respectively, indicating the Gd break. There exist inclined W effect between Ig Kθ and the total angular momentum L of lanthanide(Ⅲ). And hereby lanthanide elements are divided into four segments, La-Nd, Pm-Gd, Tb-Ho, and Er-Lu. In each segment, the linearity is maintained.

Composition, Stability and Probable Structure of a Colourless Organometallic Complex (Gd(III)-Malic Acid)

The formation of colourless gadolinium complexes (x,y,z), between x gadolinium ions, y ligands and z protons, of some organic acids, has been studied in aqueous solution. In this work we present the results of investigations on the interaction of the gadolinium ion (Gd3+) with malic acid (C4H6O5, a-hydroxyl dicarboxylic acid), in dilute aqueous solution for pH values between 5.5 and 7.5. Colourless gadolinium complexes of malate ions have no absorption band UV-visible, the indirect photometric detection (IPD) technique was used and studies have identified a major tri-nuclear complex of malate ion (﹣OOC-CH2-CHOH-COO﹣). The formation of this new colourless complex is derived from three Gd(III) ions that react with two malate ions and two hydronium ions (H3O+), giving for this colourless complex, a (3,2,2) composition and apparent stability constant depends on the acidity of the medium, with logK'322 = 18.88 ± 0.05 at pH = 6.30. To complement previous results and to propose a probable structure for this new complex detected in solution, studies of IR spectroscopy have been conducted to identify the chelation sites for both ligands. The results were analysed and show that this organometallic gadolinium complex, contains two different sites, respectively, two lateral tetradentate mono-nuclear sites and a single central bidentate mono-nuclear site. From these results, the reaction of formation, the stability constant and the probable structure of this new colourless organometallic gadolinium complex are proposed.

Studies on Complexation of ATMP, PBTCA, PAA and PMAAA with Ca^(2+) in Aqueous Solutions

By means of acid-base potentiometric titration and the advanced BEST computer program developed by Martell et al., the deprotonation constants of four inhibitors[Aminotrimethylenephosphoinic acid(ATMP), 2-phosphino-tutane-1,2,4-tricarboxylic acid(PBTCA), polyacrylic acid(PAA, M_w=2000), poly(maleic, acrylic) acid(PMAAA, M_w=3000)], and the stability constants of the complexes of these inhibitors with Ca 2+ have been determined. And the distribution curves of ATMP at different pH values in aqueous solutions have also been given out. The result of this study can be applied to explaining the inhibition mechanism.