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The interaction of the Zn2+ and Ni2+ ions at the iron (III) hydroxiede/solution interface was studied as a function of the constant initial pH and over the metal ion concentration range 1-6 ppm. For each mole of heavy metal ion adsorbed, approximately two moles of H+ ions were displaced from the interface. These results are used for expressing the adsorption data as a function of the solution concentration of both H+ and metal ions. The results obtained permit the interfacial reaction to be described by the equation: 2SH + M2+ = S2M + 2H+ Were S represents a surface site. read more
IKRAM UL HAQ ,S MUSTAFA ,
- 18 Aug 2011
- Volume Detail: VOLUME 7, NO2, JUN 1985
- Pages: 71
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Detailed mass spectrometric fragmentation pattern and structure of 14-membered cyclopeptide alkaloids; sativanine-A (1) and sativanine-B (2) are discussed. read more
R TSCHESCHE ,G ECKHARDT ,A H SHSH ,
- 18 Aug 2011
- Volume Detail: VOLUME 7, NO2, JUN 1985
- Pages: 79
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The geminal anisochronism of the isobutyl groups indicate that the aryl ring is twisted out of the imino plane leading to a chiral conformation. Barriers to rotation around the aryl-imino bond were found by dynamic NMR to lie in the range 16.9-17.9 kcal mol-1 read more
SALIM S AL-SHOWIMAN ,
- 18 Aug 2011
- Volume Detail: VOLUME 7, NO2, JUN 1985
- Pages: 85
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Not availableread more
M KALEEM BALOCH ,NOOR AHMAD ,
- 28 Aug 2011
- Volume Detail: VOLUME 7, NO2, JUN 1985
- Pages: 89
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The kinetics of the reaction between iodine and hydrazine was studied spectrophotometrically for full understanding of the proper conditions under which the reaction is fast and quantitative. The hydrogen ions were fond to exert an enormous influence to and by the system that results in positive errors of the reaction order. The reaction was found to be complete within twenty seconds just above pH 4.5.A suitable buffer is recommended to be used for governing the pH decrease during the titration. Hydrazine free base acts as the active reductant and iodine as a two electron oxidant. Nitrogen gas (N2) was detected by mass spectrometry as the major product for hydrazine oxidation. A possible mechanism for the reaction under certain conditions was suggested. read more
S A AL-TAMRAH ,A M AL-HAJJAJI ,A M AZIZ AL RAHMAN ,SALIM M SULTAN ,I Z AL-ZAMIL ,
- 28 Aug 2011
- Volume Detail: VOLUME 7, NO2, JUN 1985
- Pages: 93
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Condensation of cyclopropyl methyl ketone with aromatic aldehydes gave 1-Aryl-3-cyclopropyl-prop-1-ene-3-ones (I). Addition reactions of bromine, hydrazine, and some active methylene compounds to (I) have been investigated. Structures of the products have been established by elemental analysis, IR, and PMR spectroscopic methods. read more
M A HASSAN ,A A HAMED ,
- 28 Aug 2011
- Volume Detail: VOLUME 7, NO2, JUN 1985
- Pages: 101
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Interactions between T1+, UO22+, Th4+ and (L)2-amino-butanedioic acid-4-amide have been investigated at different temperature 25o, 35o and 45oC and ionic strengths u = [0m0, 0.1, 0.2, 0.5 and 1.0M KNO3] in aqueous media using a pH titration technique. The data suggest the formation of 1:1 complex with T1+ and UO22+ and 1:1 and 1:2 complexes with Th4+ ions in the pH range 6.3-9.2, 3.3-6.0 and 2.5-5.5 respectively. Formation constants have been evaluated employing Calvin and Melchior’s extension of Bjerrum’s method. The thermodynamic stability constants and other function –D Go, D Ho and D So accompanying complexation have also been evaluatedread more
K K SAXENA ,R S SAXENA ,S SHARMA ,
- 29 Aug 2011
- Volume Detail: VOLUME 7, NO2, JUN 1985
- Pages: 105
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Cinnamanilide (I), the N(p-chloro) (XVI) and 4-chloro (XXVII) derivatives by reaction with chlorosulphonic acid gave the sulphonyl chlorides (II, XVII, XXVIII); these were reacted with nucleophiles, e.g. amines, azide ion and hydrazine to give 28 compounds. Oxalanilide (XXXV), the 4, 4'-di-chloro derivative (XLV) and malonanilide (LIV; X=H) similarly afforded the sulphonyl chlorides (XXXVI, XLVI and LV) which were characterized as 30 derivatives. In contrast, 4,4'-dichloromalonanilide (LIV; X=Cl) failed to give the sulphonyl chloride with chlorosulphonic acid. The spectral data of selected compounds are briefly discussed. read more
O SHODE ,R J CREMLYN ,J G BLOY ,K PATHAK ,F J SWINBOURNE ,
- 29 Aug 2011
- Volume Detail: VOLUME 7, NO2, JUN 1985
- Pages: 111
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Not availableread more
SUMBAL MAHMUD ,A RASHID KAUSAR ,
- 29 Aug 2011
- Volume Detail: VOLUME 7, NO2, JUN 1985
- Pages: 125
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- 29 Aug 2011
- Volume Detail: VOLUME 7, NO2, JUN 1985
- Pages: 129
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