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1.
Summary Extraction of scandium and calcium radioactivities with 1% HDEHP in benzene from nitric acid solution was investigated. The effect of potassium titanium oxalate concentration on the extraction from 1.5M nitric acid was studied. From the data obtained, two procedures based on batch solvent extraction and extraction chromatography were developed for separation and production of radioscandium from a neutron-irradiated potassium titanium oxalate target. The radiochemical purity of the separated scandium radioactivities was more than 98%.
Zusammenfassung Die Extraktion der Aktivitäten des Scandiums und Calciums aus salpetersaurer Lösung mit 1% Diäthylhexylphosphorsäure in Benzol wurde untersucht. Der Einfluß der Kalium-Titanoxalat-Konzentration auf die Extraktion aus 1,5-m Salpetersäure wurde geprüft. Auf Grund der Ergebnisse wurden zwei Verfahren zur Trennung und Gewinnung von Radio-Scandium aus einem neutronenbestrahlten Kalium-Titanoxalat-Target ausgearbeitet, die auf einmaliger Extraktion mit dem Lösungsmittel bzw. auf Extraktionschromatographie beruhen. Die radiochemische Reinheit der Sc-Aktivitäten war besser als 98%.相似文献
2.
Synergistic extraction of samarium with TTA(HA) and TPPO or TOPO (B) mixtures were investigated. The extracted complex was proved to have the general formula SmA3 · 2B. A graphical determination for the formation constants of these complexes gave the values 3.9 × 1013 and 8.2 × 1010 for SmA3 · 2TOPO and SmA3 · 2TPPO in benzene, respectively. 相似文献
3.
Ramadan Ahmed Mekheimer Kamal Usef Sadek Hisham Ahmed Abd El‐Nabi Afaf Abd El‐Hameid Mohamed Ehab Anwer Ebraheem Michael B. Smith 《Journal of heterocyclic chemistry》2005,42(4):567-574
Ethyl 3‐amino‐4‐chlorothieno[3,2‐c]quinoline‐2‐carboxylate ( 4 ) is a versatile synthon, prepared by reacting an equimolar amount of 2,4‐dichloroquinoline‐3‐carbonitrile ( 1 ) with ethyl mercaptoacetate ( 2 ). Ethyl 5‐alkyl‐5H‐1‐thia‐3,5,6‐triazaaceanfhrylene‐2‐carboxylates 9a‐c , novel perianellated tetracyclic heteroaro‐matics, were prepared by refluxing 4 with excess of primary amines 7a‐c to yield the corresponding amino‐thieno[3,2‐c]quinolines 8a‐c . Subsequent reaction with an excess of triethyl orthoformate (TEO) furnished 9a‐c . Reaction of 4 with TEO in Ac2O at reflux, gave the simple acetylated compounds, thieno[3,2‐c]‐quinolines 12 and 13 . Refluxing 4 with benzylamine ( 7d ) gave 10 , and subsequent treatment with TEO gave the tetracyclic compound 11 . Refluxing 13 with an excess of alkylamines 7a‐d gave the fhieno[3,2‐c]quino‐lines 15 . Refluxing the aminothienoquinolines 8b with an excess of triethyl orthoacetate gave thieno[3,2‐c]quinoline 17 , while heating with Ac2O gave 18 and 19 , with small amounts of 16 . Reaction of 8a,b with ethyl chloroformate and phenylisothiocyanate generated the new 1‐thia‐3,5,6‐triazaaceanthrylenes 20a,b and 21a,b , respectively. Diazotization of 8a‐c afforded the novel tetracyclic ethyl 5‐alkyl‐5H‐1‐fhia‐3,4,5,6‐tetraazaaceanthrylene‐2‐carboxylates 22a‐c in good yields. 相似文献
4.
Hisham J. Y. El-Aila 《Journal of Dispersion Science and Technology》2013,34(9):1208-1211
In this article, a mononuclear Mn(Niten)2H2O complex was prepared to catalyze hydrolysis of p-nitrophenyl acetate (PNPA) in presence of Cetyltrimethylammonium bromide (CTAB) micellar system in different pH range from 6.5–10 at 25°C. These results obtained indicate that the complex exhibits good catalytic function. It also appears the complex accelerates the hydrolytic cleavage of PNPA in cationic CTAB micellar solution which may be due to coordinating ability of substrate to complex, electrostatic interaction between micelles and complex and due to electrostatic interaction between micelles with reactant. 相似文献
5.
A 1H NMR spectroscopic study of tetra-n-butylammonium halides (TBAX: X = Cl? , Br? or I? ) in CDCl3 solutions was conducted. Complexation studies of TBAX salts with different host molecules using 1H NMR in CDCl3 have previously revealed that the reference residual CHCl3 proton signal had been shifted downfield. The aim of the study was to quantify the extent of these chemical shift changes with TBAX salts. Linear concentration–chemical shift relationships in each case were obtained from the resulting titration plots obtained from the addition of the TBAX salts alone to CDCl3. Interactions in the solid state as determined by X-ray crystallography support the solution-state investigations indicating halide ion–chloroform proton interactions. 相似文献
6.
The influence of ball milling and subsequent calcination of a 2.5:1 molar mixture of α-Fe2O3 and Li2CO3 on the formation of lithium ferrites has been investigated. Premilling was found to considerably lower the temperature at which the lithium ferrites LiFeO2 and LiFe5O8 are formed. A β-to-α phase transition in LiFe5O8 was found to take place on cooling from ca. 1000°C depending on the milling history and cooling regime. 相似文献
7.
McKeown NB Hanif S Msayib K Tattershall CE Budd PM 《Chemical communications (Cambridge, England)》2002,(23):2782-2783
Network polymers exhibiting large surfaces areas (900-1000 m2g-1) are prepared by the highly efficient dibenzodioxane forming reaction between meso-tetrakis(pentafluorophenyl)porphyrin and a rigid bis(catechol) monomer. 相似文献
8.
Yazicioglu Y Royston TJ Spohnholtz T Martin B Loth F Bassiouny HS 《The Journal of the Acoustical Society of America》2005,118(2):1193-1209
The vibration of a thin-walled cylindrical, compliant viscoelastic tube with internal turbulent flow due to an axisymmetric constriction is studied theoretically and experimentally. Vibration of the tube is considered with internal fluid coupling only, and with coupling to internal-flowing fluid and external stagnant fluid or external tissue-like viscoelastic material. The theoretical analysis includes the adaptation of a model for turbulence in the internal fluid and its vibratory excitation of and interaction with the tube wall and surrounding viscoelastic medium. Analytical predictions are compared with experimental measurements conducted on a flow model system using laser Doppler vibrometry to measure tube vibration and the vibration of the surrounding viscoelastic medium. Fluid pressure within the tube was measured with miniature hydrophones. Discrepancies between theory and experiment, as well as the coupled nature of the fluid-structure interaction, are described. This study is relevant to and may lead to further insight into the patency and mechanisms of vascular failure, as well as diagnostic techniques utilizing noninvasive acoustic measurements. 相似文献
9.
Daniel Schäpper Muhd Nazrul Hisham Zainal Alam Nicolas Szita Anna Eliasson Lantz Krist V. Gernaey 《Analytical and bioanalytical chemistry》2009,395(3):679-695
Biotechnology process development involves strain testing and improvement steps aimed at increasing yields and productivity. This necessitates the high-throughput screening of many potential strain candidates, a task currently mainly performed in shake flasks or microtiter plates. However, these methods have some drawbacks, such as the low data density (usually only end-point measurements) and the lack of control over cultivation conditions in standard shake flasks. Microbioreactors can offer the flexibility and controllability of bench-scale reactors and thus deliver results that are more comparable to large-scale fermentations, but with the additional advantages of small size, availability of online cultivation data and the potential for automation. Current microbioreactor technology is analyzed in this review paper, focusing on its industrial applicability, and directions for future research are presented. 相似文献
10.
S. Hosseini A. B. Mohamad A. H. Kadhum W. R. Wan Daud 《Journal of Thermal Analysis and Calorimetry》2010,99(1):197-202
A study concerned to thermogravimetric analysis is performed in cesium dihydrogen phosphate (CsH2PO4) that was synthesized, using cetyltrimethylammonium-bromide (CTAB), polyoxyethylene-polyoxypropylene (F-68) and mixture of
(F-68:CTAB) with two mole ratio 0.06 and 0.12 as surfactant. The dehydration behavior of particles was studied using thermal
gravimetric analysis and differential scanning calorimetric. Subsequently, the experimental results indicated that the first
dehydration temperature in the range of 237–239 °C upon heating, the second peaks occur at temperature range 290–295 °C and
overlapping in the thermogravimetric events is observed. The mass loss values are obtained in the range of 6.62–6.97 wt% that
is less than reported theoretical value 7.8 wt%. These values show well compatibility of reaction CsH2PO4 to Cs2H2P2O7 with 3.92 wt% whereas mass loss value of CsH2PO4 to CsPO3 is less than theoretical value 7.8 wt%. The activation energy of two steps dehydration are calculated using Kissinger equation
for the samples synthesized via CTAB and (F-68) with minimum value mass loss 6.62% and maximum value mass loss 6.97%, respectively.
The calculation results reveal that the reaction rate in the first step (CsH2PO4 → Cs2H2P2O7) is faster than the second step (CsH2PO4 → CsPO3). The weight loss values of the samples demonstrate that existence of CTAB can be considered as effective factor which prevents
more weight loss during the dehydration process. 相似文献