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2.
F. M. Elzawawy E. A. Saad I. H. Badr 《Journal of Radioanalytical and Nuclear Chemistry》1992,164(3):141-151
Isotope exchange reaction between NaCl-36 and triphenyltin chloride in dioxane-water (8020% w/w) and ethanol-water (9010% w/w) mixed solvents has been studied at 25, 35 and 50 °C. The exchange reaction was found to proceed via a bimolecular SN2, limiting mechanism with reaction rates depending on the solvent used. Inhibition of the exchange in ethanol-water is probably due to solvation of chloride ion through hydrogen bond formation. The rate laws for the exchange reactions are: Re=3.24×109 e–65550/RT [Rh3SnCl] [NaCl] in dioxanewater and Re=6.61×108 e–69600/RT [Ph3SnCl] [NaCl] in ethanol-water, where is the degree of dissociation of NaCl and Re is the rate of exchange in mol l–1 s–1. The activation parameters H*, S* and G* are reported. 相似文献
3.
4.
Saad S. M. Hassan 《Mikrochimica acta》1974,62(1):51-57
Summary A new micromethod for spectrophotometric determination of hydrazine compounds is described. It is based on a reaction withperi-naphthindan-2,3,4-trione hydrate at pH 2.5 to give a red precipitate of dihydroxy-peri-naphthindenone which is dissolved in methanol and measured at 460 nm. The results obtained show an average recovery of 99.8 %, the precision being ± 1 %.
Zusammenfassung Eine neue Mikromethode zur spektrophotometrischen Bestimmung von Hydrazinverbindungen wurde beschrieben. Sie beruht auf der Reaktion mit peri-Naphthindan-2,3,4-trion-hydrat bei pH 2,5, wobei ein roter Niederschlag von Dihydroxy-peri-naphthindenon entsteht, der in Methanol gelöst und bei 460 nm gemessen wird. 99,8% Substanz werden wiedergefunden, die Genauigkeit beträgt ±1%.相似文献
5.
New simple, rapid, accurate, and selective methods are described for microdetermination of the nitro and nitroso groups in organic compounds. These are based on reduction with cadmium metal and 0.05 M HCl whereby 6 and 4 equivalents of the cadmium ions are released per nitro and nitroso groups, respectively. The cadmium ions are measured by atomic absorption spectrometry at 228.8 nm, potentiometrically by titration with EDTA using the cadmium ion selective electrode, and visually by EDTA titration using Eriochrome Black T indicator. Results with an average recovery of 98% and a mean standard deviation of 1.3% are obtainable and no interferences are caused by many nitrogen, oxygen, and sulfur functional groups. 相似文献
6.
The coenzyme pyridoxal-5'-phosphate (PLP) is deiermined by in situ measurement of the rate of ammonia production using a potentiometric gas-sensing membrane electrode. It is shown that the initial rate of ammonia liberation from L-tryptophan by action of tryptophanase apoenzyme and the coenzyme can be linearly related to PLP levels in the nanogram range with minimal interference from related compounds. Calibration data for the 1 × 10-7–2.5 × 10-6 M range for PLP yielded a least-squares equation of rate (mV min-1) = (0.64 ± 0.01) C — 0.01 ± 0.02 with a standard error of 0.02 mV min-1, where concentration, C, is expressed in units of 10-7 mol l-1. 相似文献
7.
Saad S. M. Hassan 《Fresenius' Journal of Analytical Chemistry》1973,266(4):272-274
Summary The solid state ion-selective chloride and bromide electrodes are used for the microdetermination of chlorine and bromine in organic compounds. After combustion in an oxygen-filled flask, potentiometric titration with silver nitrate at pH 5–7 in presence of 50% dioxan is carried out. Results accurate to ±0.3% absolute are obtained with some partially and highly halogenated compounds.
Mikrobestimmung von Chlor und Brom in einigen organischen Verbindungen mit Hilfe von ionenselektiven Elektroden
Zusammenfassung Chlorid- und bromidselektive Festkörperelektroden wurden zur Chlor- und Brombestimmung in teilweise bzw. hochhalogenierten organischen Verbindungen benutzt. Nach Verbrennung im Sauerstoffkolben erfolgt eine potentiometrische Titration mit Silbernitrat bei pH 5–7 in Gegenwart von 50% Dioxan. Die erhaltenen Ergebnisse sind auf ±0,3 % genau.相似文献
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H.?Hussain H.?U.?Rehman Z.?AhmadEmail author 《Journal of Sol-Gel Science and Technology》2005,36(3):239-248
Nano-composites from aramid-silica system have been prepared via sol-gel process. Poly (phenyleneterephthalamide) copolymer
chains were prepared by reacting a mixture of p- and m-phenylenediamines with terephthaloyl chloride in dimethylacetamide used as solvent. The sol-gel process in the polymer
matrix was carried out through hydrolysis and condensation of a mixture of tetraethoxysilane and (3-glycidoxypropyl) trimethoxysilane.
The latter was used to develop linkage, on one hand with silica network structure using alkoxy groups and on the other hand
with aramid chains at its secondary amine groups through glycidal groups of silane. Mutual interaction between the two disparate
phases aramid and silica network was thus created. Thin films of the composites containing different proportions of silica
ranging from 5.0 to 25.0-wt% were cast by the solvent elution technique. The α-relaxation temperature associated with the
glass transition was measured by the dynamic mechanical thermal analysis. The results showed an increase in the glass transition
temperature from 328°C for the pure aramid to 352°C for the hybrid materials containing 25-wt% silica, an indicative of the
increased interfacial interaction between the two phases. Films having relatively low silica content were flexible and transparent,
but those with high silica content were opaque and brittle. These films were tested for their tensile strength, modulus and
toughness. The mechanical strength of the composites as compared to the pure aramid increased initially but with further addition
of silica the strength decreased. The initial increase can be explained due to increased interfacial interaction between the
two phases, however agglomeration of silica particles was responsible for decreasing strength at higher silica contents. 相似文献
10.
S. M. Al-Jobori R. K. Itawi A. Saad K. M. Shihab M. Jalil S. S. Farhan 《Journal of Radioanalytical and Nuclear Chemistry》1990,144(3):229-239
As a part of the Iraqi Food Analysis Programme /I.F.A.P./ the concentration of Na, Mg, P, Cl, K, Ca, Zn, Se, Br, Rb and I in natural milk collected from different regions of Iraq, and in milk powder samples have been determined by using the NAA technique. It was found that except for the elements I, Rb and Br the concentration of the elements was approximately identical in both the natural milks and milk powders. 相似文献