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21.
M. I. Zaki G. A. M. Hussien R. B. Fahim 《Journal of Thermal Analysis and Calorimetry》1985,30(1):129-134
The kinetics of the solid-state reaction between alumina and strontium carbonate were studied by thermogravimetry. The effects of the structure ( or) and/or doping (with Li+ or Cd2+) of the alumina on the kinetics of the reaction were examined. The results obtained were correlated with the phase composition and structural changes, followed by a number of physicochemical analyses (DTA, XRA and IRA) throughout the course of the reaction.
Zusammenfassung Die Kinetik der Festkörperreaktion zwischen Aluminiumoxid und Strontium-carbonat wurde thermogravimetrisch untersucht. Die Effekte der Struktur ( und) und/oder des Dopens des Aluminiumoxids (mit Li+ oder Cd2+) auf die Kinetik der Reaktion wurde untersucht. Die erhaltenen Ergebnisse wurden mit der Phasenzusammensetzung und mit durch physikalisch-chemische Analysenverfahren (DTA, XRA und IRA) während des Reaktionsverlaufs verfolgten strukturellen Veränderungen in Beziehung gebracht.
. ( ) Li+ Cd2+ . , , - .相似文献
22.
Rahman Hosseinzadeh Ali Sharifi Kourosh Tabar-Heydar Farshid Mohsenzadeh 《Monatshefte für Chemie / Chemical Monthly》2002,133(11):1413-1415
Summary. N,N-Dimethylhydrazones of ketones and aldehydes undergo facile cleavage to the corresponding carbonyl compounds upon exposure
to microwaves in water containing a catalytic amount of PdCl2–SnCl2 in high yields.
Corresponding authors. E-mail: rahman@umz.ac.ir
Received December 27, 2001. Accepted (revised) February 6, 2002 相似文献
23.
Patterned langmuir-blodgett films of monodisperse nanoparticles of iron oxide using soft lithography 总被引:7,自引:0,他引:7
Langmuir-Blodgett (LB) films of monodisperse iron oxide nanoparticles have been successfully deposited onto patterned poly(dimethylsiloxane) surfaces. These patterned LB films of iron oxide nanoparticles were transferred onto solid substrates using micro contact printing. 相似文献
24.
Norimah Yusof Asnah Hassan M.N. Firdaus Abd Rahman Suzina A. Hamid 《Radiation Physics and Chemistry》2007,76(11-12):1756-1759
Most of the tissue banks in the Asia Pacific region have been using ionising radiation at 25 kGy to sterilise human tissues for save clinical usage. Under tissue banking quality system, any dose employed for sterilisation has to be validated and the validation exercise has to be a part of quality document. Tissue grafts, unlike medical items, are not produced in large number per each processing batch and tissues relatively have a different microbial population. A Code of Practice established by the International Atomic Energy Agency (IAEA) in 2004 offers several validation methods using smaller number of samples compared to ISO 11137 (1995), which is meant for medical products. The methods emphasise on bioburden determination, followed by sterility test on samples after they were exposed to verification dose for attaining of sterility assurance level (SAL) of 10−1. This paper describes our experience in using the IAEA Code of Practice in conducting the validation exercise for substantiating 25 kGy as sterilisation dose for both air-dried amnion and those preserved in 99% glycerol. 相似文献
25.
Ultrasonic slurry sampling electrothermal atomic absorption spectrometry with a metal tube atomizer has been applied to the determination of lead in Bangladeshi fish samples. The slurry sampling conditions, such as slurry stabilizing agent, slurry concentration, pyrolysis temperature for the slurried fish samples, particle size and ultrasonic agitation time, were optimized for electrothermal atomic absorption spectrometry with the Mo tube atomizer. Thiourea was used as the chemical modifier for the interference of matrix elements. The detection limit was 53 fg (3S/N). The determined amount of lead in Bangladeshi fish samples was consistent with those measured in the dissolved acid-digested samples. The advantages of the proposed methods are easy calibration, simplicity, low cost and rapid analysis. 相似文献
26.
The first stable crystalline geminal diol of an aldehyde lacking electron-withdrawing groups on the-carbon was synthesized fromd-sorbitol and characterized by1H and13C nuclear magnetic resonance (NMR) and single-crystal x-ray studies. Each hydroxyl is a donor for a single, unique intermolecular hydrogen bond. Only one hydroxyl acts as an acceptor. No intramolecular hydrogen bonding is observed in the crystal. 相似文献
27.
trans-1,2,3,4,4a,5,6,10b-Octahydrophenanthridine, the 9-methoxy analog, and 5-methyl derivatives ( 6a,6b ) of each have been synthesized from trans-phenylcyclohexylamines ( 2a,2b ) and ethyl chloroformate followed by cyclization and reduction or by cyclization, N-methylation and reduction. The oximes ( la,1b ) of 2-phenylcyclohexanone and the m-methoxy relative, a mixture of the syn and anti isomers, were reduced to 2a and 2b with sodium and ethanol. Hydrogenation (platinum oxide-acetic acid) of 1a gave in addition to 2a , a small yield of 2-cyclohexylcyclohexyl-amine. Similar hydrogenation of 1b gave only this fully reduced compound. 相似文献
28.
Microemulsion-based synthesis of CeO(2) powders with high surface area and high-temperature stabilities 总被引:2,自引:0,他引:2
Bumajdad A Zaki MI Eastoe J Pasupulety L 《Langmuir : the ACS journal of surfaces and colloids》2004,20(25):11223-11233
Pure ceria powders, CeO(2), were synthesized in heptane-microemulsified aqueous solutions of CeCl(3) or Ce(NO(3))(3) stabilized by AOT (sodium bis(2-ethylhexyl) sulfosuccinate), DDAB (di-n-didodecyldimethylammonium bromide), or DDAB + Brij 35 surfactant mixtures. Micellar DTAB (n-dodecyltrimethylammonium bromide) and vesicular DDAB systems were also used as media for generating CeO(2). Characterization of the powders by X-ray powder diffractometry, laser-Raman spectroscopy, and Fourier transform infrared spectroscopy revealed that in the presence of surfactants almost-agglomerate-free nanosized crystallites (6-13 nm) of anionic vacancy-free cubic CeO(2) were produced. In the absence of surfactants 21-nm-sized crystallites were formed, comparing with the 85-nm-sized crystallites when cubic CeO(2) was created via thermal decomposition of cerium oxalate. Surface characterization, by X-ray photoelectron spectroscopy, N(2) sorptiometry, and high-resolution electron microscopy showed AOT- or (DDAB + Brij 35)-stabilized microemulsions to assist in formation of crystallites exposing surfaces of large specific areas (up to ca. 250 m(2)/g) but of low stability to high-temperature calcination (28-13 m(2)/g at 800 degrees C). In contrast, the double-chained DDAB was found to generate cubic CeO(2) crystallites of lower initial surface areas (144 (microemulsion) to 125 (vesicles) m(2)/g)) but of higher thermal stability (55-45 m(2)/g at 800 degrees C). Hence, the latter cerias could be considered as appropriate components for total oxidation (combustion) catalysts. 相似文献
29.
S. Z. Haider K. M. A. Malik A. Rahman T. Wadsten 《Journal of Thermal Analysis and Calorimetry》1986,31(3):621-631
Six adducts of the tctrakis(8-hydroxyquinolinato) complex of thorium(IV) with 8-hydroxyquinoline, pyridine, urea, dimethylsulphoxide, dimethylformamide and 1,10-phenanthroline were prepared and characterized, the infrared bands for the room-temperature forms are given and their particular thermal properties are reported. The thermal analyses were performed mostly in the presence of air, but in some cases an argon atmosphere was used for comparison. The adducts were lost from the principal complex at temperatures varying between 110 and 290°. Intermediate oxygenated complexes were formed in each case at about 400°. The thermal data suggest the standardization of a procedure for the formation of Th(C9H6NO)4.
We are grateful to the Bangladesh University Grants Commission for a Fellowship Grant to AR. 相似文献
Zusammenfassung Sechs Addukte des Tetrakis(8-hydroxyquinolinato)-Komplexes von Thorium(IV) mit 8-Hydroxyquinolin, Pyridin, Harnstoff, Dimethylsulphoxid, Dimethylformamid und 1,10-Phenanthrolin wurden dargestellt und charakterisiert. Infrarotbanden und spezielle thermische Eigenschaften der Raumtemperatur-Formen sind angegeben. Die thermischen Analysen wurden meist in Luft ausgeführt, in einigen Fällen zu Vergleichszwecken aber auch in Argonatmosphäre. Die Addukte wurden vom Komplex bei Temperaturen zwischen 110 und 290 °C abgegeben. Intermediäre oxydierte Komplexe wurden in jedem Fall bei etwa 400 °C gebildet. Die thermischen Daten ermöglichen die Standardisierung eines Verfahrens zur Darstellung von Th(C9H6NO)4.
-(8- ) (IV) 8- , , , - , 1,10-. - , . , , . 110–290°. 400° . Th(C9H6NO)4.
We are grateful to the Bangladesh University Grants Commission for a Fellowship Grant to AR. 相似文献
30.
Soot deep oxidation catalyzed by molybdena and molybdates: a thermogravimetric investigation 总被引:2,自引:0,他引:2
Molybdena (MoO3) and molybdates of bismuth (Bi2Mo3O12), chromium (Cr2Mo3O12), barium (BaMoO4), manganese (MnMoO4) and copper (Cu3Mo2O9) were synthesized and characterized by X-ray powder diffractometry and infrared spectroscopy. They were then assessed as ‘loose contact' catalysts for soot deep oxidation (combustion) in air by thermogravimetry. A similar assessment was carried out on commercial chromia (Cr2O3) and tungsta (WO3). Observed high oxidation activity of MoO3, as compared to both Cr2O3 and WO3, is attributed to the higher volatility (mobility) of MoOx species. On similar grounds, observed high activity of MoO3 and Cu3Mo2O9, as compared to the other test molybdates, is explained. Relatively speaking, however, a higher activity was observed for Cu3Mo2O9 than MoO3, whereby soot ignition temperature decreased from 571°C (uncatalyzed oxidation) to 430°C, to occur within the temperature range of diesel exhaust (200–450°C). This observation is ascribed to copper-promoted redox conduct of Mo(VI) in the oxidation reaction of soot. Kinetics of the reaction was studied non-isothermally, and the kinetic parameters (A, k, ΔE and the reaction order) were calculated. 相似文献