The Solvent Extraction Behavior of Inorganic Compounds. III. Variation of the Distribution Quotient with Metal Ion Concentration

1957 ◽  
Vol 61 (1) ◽  
pp. 75-81 ◽  
Author(s):  
R. M. Diamond
Keyword(s):  
Solvent Extraction ◽  
Metal Ion ◽  
Inorganic Compounds ◽  
Ion Concentration ◽  
Extraction Behavior

The Solvent Extraction Behavior of Inorganic Compounds: Molybdenum(VI)

1955 ◽  
Vol 59 (8) ◽  
pp. 710-718 ◽  
Author(s):  
I. Nelidow ◽  
R. M. Diamond
Keyword(s):  
Solvent Extraction ◽  
Inorganic Compounds ◽  
Extraction Behavior

scholarly journals N-n-octylaniline as a new reagent for analytical liquid-liquid extraction of yttrium(III) from matrices of various metal ions

2011 ◽  
Vol 30 (2) ◽  
pp. 151
Author(s):  
Balasaheb N. Kokare ◽  
Aniruddha M. Mandhare ◽  
Sanjay S. Kolekar ◽  
Mansing A. Anuse*
Keyword(s):  
Solvent Extraction ◽  
Hydrochloric Acid ◽  
Metal Ion ◽  
Liquid Extraction ◽  
Alizarin Red ◽  
Slope Analysis ◽  
Binary Separation ◽  
Extraction Behavior ◽  
Liquid Liquid Extraction ◽  
Species Being

A systematic study of solvent extraction behavior of yttrium(III) with N-n-octylaniline from salicylate media was carried out. Yttrium(III) was quantitatively extracted from 0.02–0.05 mol dm–3 NaSal at pH 9.7 – 10.5 with 0.17 mol dm–3 N-n-octylaniline in xylene. The extraction was found to proceed by an anion exchange mechanism with the extraction species being [CH3(CH2)7(C6H5)NH2+Y(C7H4O3)2–] ascertained on the basis of slope analysis. The extracted metal ion was separated by selective stripping with hydrochloric acid or perchloric acid from the metal loading organic phase and estimated spectrophotometrically following a complexation with Alizarin Red S. A binary separation of yttrium(III) from Th(IV), U(VI), Zr(IV), Nb(V), La(III), Nd(III), Ce(IV) and Gd(III) is discussed.

scholarly journals Liquid-liquid extraction of Zr(IV) from sulphuric acid medium using tri-n-octyl amine in kerosene

2018 ◽  
Vol 9 (3) ◽  
pp. 222-227 ◽  
Author(s):  
Jaykishon Swain ◽  
Amit Sahoo ◽  
Bhikari Charana Bhatta
Keyword(s):  
Sulphuric Acid ◽  
Metal Ion ◽  
Ion Concentration ◽  
Effect Of Temperature ◽  
Salting Out ◽  
Extraction Behavior ◽  
Liquid Liquid Extraction ◽  
Quantitative Extraction ◽  
Octyl Amine ◽  
Sulphuric Acid Medium

The extraction behavior of Zr(IV) with tri-n-octyl amine (TOA) in kerosene was studied through a new method of solvent extraction. The mechanism of extraction and the species extracted were identified. Quantitative extraction of Zr(IV) with TOA in kerosene was studied by changing different parameters such as acid variation, diluent effect, metal concentration variation, extractant variation, effect of salting out reagent concentration and effect of temperature. It was observed that the percentage of extraction of Zr(IV) increased when the concentration of TOA and the percentage of extraction also increased when the metal ion concentration increased. The percentage of Zr(IV) became 97.4% with 0.1 M TOA from 3.0 M sulphuric acid. Kerosene was found to be effective diluent for the extraction of Zr(IV) with TOA.

Use of agro-waste (Musa paradisiaca peels) as a sustainable biosorbent for toxic metal ions removal from contaminated water

2019 ◽  
Author(s):  
Chem Int
Keyword(s):  
Heavy Metal ◽  
Metal Ions ◽  
Contact Time ◽  
Metal Ion ◽  
Equilibrium Concentration ◽  
Ion Concentration ◽  
Contaminated Water ◽  
Musa Paradisiaca ◽  
Percentage Removal ◽  
Adsorbent Dose

A study of removal of heavy metal ions from heavy metal contaminated water using agro-waste was carried out with Musa paradisiaca peels as test adsorbent. The study was carried by adding known quantities of lead (II) ions and cadmium (II) ions each and respectively into specific volume of water and adding specific dose of the test adsorbent into the heavy metal ion solution, and the mixture was agitated for a specific period of time and then the concentration of the metal ion remaining in the solution was determined with Perkin Elmer Atomic absorption spectrophotometer model 2380. The effect of contact time, initial adsorbate concentration, adsorbent dose, pH and temperature were considered. From the effect of contact time results equilibrium concentration was established at 60minutes. The percentage removal of these metal ions studied, were all above 90%. Adsorption and percentage removal of Pb2+ and Cd2+ from their aqueous solutions were affected by change in initial metal ion concentration, adsorbent dose pH and temperature. Adsorption isotherm studies confirmed the adsorption of the metal ions on the test adsorbent with good mathematical fits into Langmuir and Freundlich adsorption isotherms. Regression correlation (R2) values of the isotherm plots are all positive (>0.9), which suggests too, that the adsorption fitted into the isotherms considered.

scholarly journals Chemical Composition and Corrosion Behavior of a-C:H/DLC Film-Coated Titanium Substrate in Simulated PEMFC Environment

Coatings ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 820
Author(s):  
Beibei Han ◽  
Mengyuan Yan ◽  
Dongying Ju ◽  
Maorong Chai ◽  
Susumu Sato
Keyword(s):  
Corrosion Resistance ◽  
Corrosion Behavior ◽  
Metal Ion ◽  
Ion Beam ◽  
Titanium Substrate ◽  
Corrosion Current ◽  
Ion Concentration ◽  
Bipolar Plates ◽  
High Adhesion ◽  
Corrosion Behaviors

The amorphous hydrogenated (a-C:H) film-coated titanium, using different CH4/H2 and deposition times, was prepared by the ion beam deposition (IBD) method, which has the advantage of high adhesion because of the graded interface mixes at the atomic level. The chemical characterizations and corrosion behaviors of a-C:H film were investigated and evaluated by SEM, AFM, Raman spectroscopy, EPMA, TEM and XPS. An a-C:H film-coated titanium was corroded at 0.8 V, 90 °C in a 0.5 mol/L H2SO4 solution for 168 h. The metal ion concentration in the H2SO4 corrosion solution and the potentiodynamic polarization behavior were evaluated. Results indicate that a higher CH4/H2 of 1:0 and a deposition time of 12 h can result in a minimum ID/IG ratio of 0.827, Ra of 5.76 nm, metal ion concentration of 0.34 ppm in the corrosion solution and a corrosion current of 0.23 µA/cm2. The current density in this work meets the DOE’s 2020 target of 1 µA/cm2. Electrical conductivity is inversely proportional to the corrosion resistance. The significant improvement in the corrosion resistance of the a-C:H film was mainly attributed to the increased sp3 element and nanocrystalline TiC phase in the penetration layer. As a result, the a-C:H film-coated titanium at CH4/H2 = 1:0 with improved anti-corrosion behavior creates a great potential for PEMFC bipolar plates.

Membrane transport systems. II. Transport of alkali metal ions against their concentration gradients

1981 ◽  
Vol 59 (12) ◽  
pp. 1734-1744 ◽  
Author(s):  
Thomas M. Fyles ◽  
Virginia A. Malik-Diemer ◽  
Dennis M. Whitfield
Keyword(s):  
Alkali Metal ◽  
Metal Ions ◽  
Metal Ion ◽  
Complex Function ◽  
Membrane System ◽  
Ion Concentration ◽  
Transport Systems ◽  
Alkali Metal Ions ◽  
Concentration Gradients ◽  
Membrane Transport Systems

An artificial membrane system based on a series of macrocyclic polyether carriers (crown ethers) is described. Under the influence of a proton gradient the carriers move alkali metal ions from basic to acidic solution through a chloroform membrane phase. Transport occurs against the concentration gradient of the transported ion as a result of a coupled counterflow of protons. Different transport behaviors are observed depending upon the metal ion concentration. At high metal ion concentration the amount transported is a linear function of time; at lower metal ion concentration the amount transported is a complex function of time which may be described as the result of a pair of consecutive first order processes. Effects of metal ion, carrier, and proton concentration on transport rate are considered. The rate increases with increasing metal ion or carrier concentration but is essentially independent of the pH of either aqueous phase. Increased lipophilicity of the carrier also results in a rate increase. Carriers derived from 18-crown-6 transport potassium selectively and all ions more rapidly than 15-crown-5 derivatives which are, however, selective for sodium. The overall efficiency of the system is discussed in terms of competing "leak" reactions, either of cations from the basic phase or of anions from the acidic phase.

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