Phosphorus speciation in the surface sediment and river water from the Orontes (Asi) River, Turkey.

The paper presents the results of the distribution of phosphorus bioavailability (total, organic, and inorganic phosphorus) in surface sediment and river water from the Orontes (Asi) River (Samandag, Antakya, Turkey) in March 2008. Speciation of inorganic phosphorus was carried out using a method on sequential extractions, with each releasing four forms of inorganic phosphorus-loosely sorbed phosphorus, phosphorus bound to aluminum (P-AL), phosphorus bound to iron (P-Fe), and phosphorus bound to calcium (P-Ca). Total phosphorus concentrations are, on average, 3.

A sequential extraction to determine the distribution of phosphorus in the seawater and marine surface sediment.

The distribution of phosphorus species among environmental compartments (e.g., between water and sediment), significantly affects the bioavailability of these species to organisms.

Sorption behaviour of uranium(VI) with N,N-dibutyl-N'-benzoylthiourea Impregnated in Amberlite XAD-16.

The sorption of U(VI) by N, N-dibutyl, N'-benzoylthiourea (DBBT) impregnated resin has been studied. DBBT impregnated resin was prepared by direct adsorption of chelating ligand onto macroporous support, Amberlite XAD-16. The adsorption of DBBT on the macroporous support is shown by FTIR spectroscopy to be the result of only weak chelating ligand-support interactions.

Effect of structural modifications of diaza-18-crown-6 on the extractability and selectivity of univalent metal picrates.

The solvent extraction of univalent metal cations with N,N'-dibenzyl-1,4,10,13-tetraoxa-7,16 diaza-2,3,11,12-dibenzocycloocta deca-2,11-diene (L(1)), N,N' didodecyl-1,4,10,13-tetraoxa-7,16-diaza-2,3-benzocylooctadeca-2 ene (L(2)) and N,N'-dibenzyl-1,4,10,13-tetraoxa-7,16 diaza-2,3,11,12-dibenzocyclo octadeca-2,11-diene (L(3)) with picrate anion into dichloromethane has been studied at 25 degrees C by UV-visible spectroscopy. The extractability and selectivity of univalent metal picrates (Li(+), Na(+), Ag(+), PhCH(2)NH(3)(+), NH(4)(+)) was evaluated as a function of [ligand]/[metal cation]. L(2) showed the highest extractability and selectivity for Li(+) over the larger studied cations, and also exhibited the highest [Li(+)]/[NH(4)(+)] selectivity as L/M=1.

The solvent extraction of alkali metal picrates with 4,13-N,N'-dibenzyl-4,13-diaza-18-crown-6.

Extraction of alkali metal picrates with N,N'-dibenzyl-18-crown-6 was carried out, with dichloromethane as water-immiscible solvent, as a function [ligand]/[metal cation]. The extractability of metal picrates (Li(+), Na(+), K(+), Rb(+), Cs(+)) was evaluated as a function of [L]/[M(+)]. The extractability of complex cation-picrate ion pairs decreases in this sequence: Li(+)>Rb(+)>Cs(+)>K(+)>Na(+).