تحضير ودراسة فاعلية بعض المركبات الاميدية الجديدة
Asma Omar jebril (1-2012)

Ternary systems of 152Eu(III), bulk bentonite and ethylenediaminetetraacetic acid (EDTA) ([Eu] = 7.9 × 10−10 M; pH = 6.0–7.0) have been studied. Without EDTA, there was slow uptake in a two-stage process, with initial rapid sorption of Eu(III) (96%), followed by slower uptake of a much smaller fraction (3.0% over a period of one month). The reversibility of Eu(III) binding was tested by allowing Eu(III) to sorb to bentonite for 1–322 days. EDTA was added to the pre-equilibrated Eu bentonite systems at 0.01 M, a concentration that was sufficient to suppress sorption in a system where EDTA was present prior to the contact of Eu(III) with bentonite. A fraction of the Eu was released instantaneously (30‒50%), but a significant amount remained bound. With time, the amount of Eu(III) retained by the bentonite reduced, with a slow fraction dissociation rate constant of approximately 4.3 × 10−8 s−1 (values in the range 2.2 × 10−8 – 1.0 × 10−7 s−1) for pre-equilibration times ≥7 days. Eventually, the amount of Eu(III) remaining bound to the bentonite was within error of that when EDTA was present prior to contact (4.5% ± 0.6), although in systems with pre-equilibration times >100 days, full release took up to 500 days. Europium interactions with colloidal bentonitewere also studied, and the dissociation rate constant measured by a resin competition method. For the colloids, more Eu was found in the slowly dissociating fraction (60–70%), but the first-order dissociation rate constant was faster, with an average rate constant of 8.8 × 10−7 s−1 and a range of 7.7 × 10−7–9.5 × 10−7 s−1. For both bulk and colloidal bentonite, although slow dissociation was observed for Eu(III), there was no convincing evidence for ‘irreversible’ binding.
RAGIAB ISSA(1-2021)

The thermovoltaic detection (TVD) technique is based on measurement of the EMF generated by two dissimilar metal electrodes in contact with the specimen. This technique has recently been applied when investigating different types of materials involving thermal decomposition reactions which have more normally been studied by conventional thermal analysis techniques, such as DTA, TG, etc. This paper reports the application of the combined TVD and DTA techniques for thermal characterization of materials. The Harrop DTA system has been modified such that measurements by the two techniques can be made simultaneously in the same environment. Data have been obtained on different types of materials, e.g., NiSO,.6H,O and CoSO,.7H,O, etc., at a programmed heating rate of 10” C rnin- ‘. Results obtained by these techniques are discussed and compared with the corresponding values in the literature.
Ragiab Ali Mokhtar(5-1990)