Magnetophoretic mole-ratio method in solvent extraction systems

2020 ◽  
Vol 1111 ◽  
pp. 60-66
Author(s):  
Hitoshi Watarai ◽  
Mariko Kurahashi
2020 ◽  
Vol 45 (4) ◽  
Author(s):  
O. V. Ikpeazu ◽  
I. E. Otuokere ◽  
K. K. Igwe

Cefotaxime, a β-lactam antibiotic, has a structure which enables it to act as a chelating agent. The formation of Fe(III) complex with cefotaxime has been studied colorimetrically at an absorption maximum of 480 nm at different temperatures. The data showed that Fe(III) and cefotaxime combine in the molar ratio of 1:1  at pH 7.4 with ionic strength maintained using 0.1M KNO3. The stability constants of the complex were calculated to be 1.56 - 1.90 x 104 by continuous variation method and 1.34 - 1.71 x 104 by mole ratio method at 25 and 40 oC respectively. ∆HƟ values for the complex were calculated to be -1.02 x 104 and -1.05 x 104 J by continuous variation method and mole ratio method respectively. ∆GƟ of the complex were calculated to be -2.44 – (-2.51) x 104 J by continuous variation method and -2.41- (- 2.48)  x 104 J by mole ratio method at 25 and 40 oC.  ∆SƟ of the complex were calculated to be 2.44 - 2.51 x 104 J/K by continuous variation method and -2.41 -2.48) x 104 J/K by mole ratio method at 25 and 40 oC respectively. Cefotaxime is a good chelating agent and can be an efficient antidote in the therapy of copper overload or poisoning.  


1980 ◽  
Vol 35 (1) ◽  
pp. 45-56 ◽  
Author(s):  
Karl-Heinz Tytko ◽  
Georgios Petridis ◽  
Bernd Schönfeld

The system H+/MoO42- was investigated by Raman spectroscopy in the range Z = 0 to 1.14 at initial concentrations CMoO₄ 2- = 0.02 to 2M and concentrations of the ionic medium CMe+ = 2CMoO₄ 2- to 3M Me(Cl,NO3) (Me=Li, Na, K,NH4 , Mg/2). The mole-ratio method and intensity difference diagrams do not indicate any species between MoO42- and Mo7O246- contrary to propositions in recent papers. A detailed evaluation of the extensive data shows the possible portion of such species to be < 3 % , this value having a statistical certainty of 95%. Comparing the solutions having Z = 1.1 by fingerprint procedures, in all cases Mo7O246- is the first main product (detectable by static methods) irrespective of the nature and concentration of the ionic medium. Thus, Mg2+ ions do not influence the course of aggregation of molybdate ions as has been proposed in the literature. This is in accordance with theoretical investigations since the Mo7O246- ion has the distinction of a number of favourable structural parameters in the system that become operative in case of scarcity of H+ ions.


1970 ◽  
Vol 48 (9) ◽  
pp. 1414-1419 ◽  
Author(s):  
Byron Kratochvil ◽  
Robert Long

In acetonitrile, iron(II) forms stable 1:1 complexes with chloride, bromide, and iodide and both 1:1 and 1:2 complexes with thiocyanate. Stepwise formation constants for the complexes were determined spectrophotometrically by a mole-ratio method. The log K values are: FeCl+, 5.8; FeBr+, 5.5; FeI+,4.3; Fe(SCN)+, 5.5; and Fe(SCN)2, 3.7.


Author(s):  
Datta B. Mandhare ◽  
Vasant D. Barhate

Objective: A simple spectrophotometric method has been developed for the determination of Iron (III) by using Schiff base 2-[(2-hydroxyphenylimino) methyl]-4-nitrophenol [HPIMNP].Methods: HPIMNP extracts Fe (III) quantitatively (99.95%) into chloroform from an aqueous solution of pH range 4.0-6.0.Results: The chloroform extracts show maximum absorption at 510 nm (λ max). Beer’s Law is obeyed over the Fe (III) concentration range of 0.5 to 20.0 µg/ml. The Molar absorptivity and Sandell’s sensitivity for Fe–HPIMNP system is 5000 L mol ˉ1 cmˉ1 and 0.011 µg cmˉ2respectively. The composition of extracted species is found to be 1: 3 [Fe-HPIMNP] by Job’s continuous variation and Mole-ratio method. Interference by various ions has been studied.Conclusion: The proposed method is rapid, sensitive, reproducible and accurate and it has been satisfactory applied for the determination of Iron in Pharmaceutical Samples.


2017 ◽  
Vol 89 (19) ◽  
pp. 10141-10146 ◽  
Author(s):  
Hitoshi Watarai ◽  
Jiayue Chen

2020 ◽  
Vol 17 (34) ◽  
pp. 689-699
Author(s):  
Mohammed Kareem HAYAWI ◽  
Mohanad Mousa KAREEM ◽  
Luma Majeed AHMED

The spinel structure Mn3O4 and the spinel Mn3O4/ZrO2 nano-composites particles were synthesized successfully as photocatalysts by employing the co-precipitation process and ultrasonic technique, respectively. The morphology of the top mention prepared photocatalysts was distinguished using X-ray diffraction (XRD) technology and atomic force microscopy (AFM) and indicated that the mean crystal sizes and particle sizes for all studied samples were nanometric. In addition, the optical properties of the obtained photocatalysts were investigated using a UV-Visible spectrophotometer with Labsphere diffuse reflectance accessory to measure the bandgaps of them. Based on the Tauc equation, the bandgaps (Bg) for the studied photocatalysts were determined. The bandgaps are indirect for all samples, and it is increased in values for the nanocomposites with the increasing the ratio of ZrO2. So, the sequence of bandgaps values is: Bg spinel Mn3O4 Bg Comp.1 Bg Comp.2 Bg Comp.3 Bg ZrO2, and equal to 2.21 eV 3.15 eV 4.51 eV 4.26 eV 5.29 eV. The research revealed that the spinel Mn3O4 and the spinel Mn3O4 ZrO2 nano-composites particles were quasispherical and spherical particles respectively. Moreover, the incorporation of spinel Mn3O4 particle with ZrO2 particle was successfully carried out that was proved by XRD and AFM analyses. This work discovered that the photocatalytic reaction response via employing Fe(II)-(4,5-Diazafluoren-9-one 11) complex as model material under UV-A lamp with the use of the studied photocatalysts. The primary photo experiments for these photocatalysts found that the decolorization of Fe(II)-(4,5-Diazafluoren-9-one 11) complex is not active without addition of H2O2, that attitude is due to the very high stability of these complex with having an octahedral structure, which was proved with using mole ratio method. Whereas, after the addition of H2O2 to the aqueous solution of these complex, the activity with using the spinel Mn3O4 ZrO2 nanocomposite 3 was found to be the double active than that using the spinel Mn3O4 alone, and the sequence of phootdecolorization efficiency (E%) is being: E% composite 3 E% composite 2 E% composite 1 E% spinel Mn3O4.


2012 ◽  
Vol 12 (1) ◽  
pp. 12-19 ◽  
Author(s):  
Dhananjay B Sarode ◽  
Sopan T Ingle ◽  
Sanjay B Attarde

A new method for determination of stoichiometry of colorless complexes by using atomic absorption spectrophotometric technique in continuous variation method and slope ratio method was described here. This method can be used in same manner as that of mole ratio method and slope ratio method. In this method atomic absorption spectroscopy was used instead of UV-Vis spectrophotometry. Atomic absorption spectrophotometric technique is superior to UV-Vis spectrophotometry as it can be applied to colorless soluble complexes. Pb(II) and n-benzoyl-n-phenyl hydroxylamine react to form colorless complex at pH 6.5, which can be easily determined by this method. It was found that Pb(II) forms 1:2 complex with n-benzoyl-n-phenyl hydroxylamine and is quantitatively extracted back to aqueous solution for AAS analysis.


2010 ◽  
Vol 75 (9) ◽  
pp. 1191-1201 ◽  
Author(s):  
Yan Zhang ◽  
Xingming Wang ◽  
Lisheng Ding

The interaction of the Schiff base (K[HL]) with herring sperm DNA was studied by UV-vis absorption, fluorescence and viscosity methods in a physiological pH environment (pH 7.40), where the Schiff base was derived from vanillin and L-tryptophan. A binding ratio of nK[HL]:nDNA = 5:1 and an apparent molar absorption coefficient of ?K[HL]-DNA = 4.98 ? 105 L?mol-1?cm-1 were confirmed by the mole ratio method. The binding constants of KB ? 28?C = 1.94 ? 105 L?mol-1 and KB ? 37?C = 1.09 ? 105 L?mol-1 were obtained by the double reciprocal method. Thermodynamic parameters suggest that the interaction between K[HL] and DNA is driven mainly by enthalpy. Combined with Scatchard methods and viscosity methods, the results indicate the presence of intercalation and groove binding between K[HL] and DNA.


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