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91.
92.
T. Ericsson A. G. Nord M. M. O. Ahmed A. Gismelseed F. Khangi 《Hyperfine Interactions》1990,57(1-4):2179-2186
Mössbauer spectra of triclinic Fe2P2O7 indicate the existence of two crystallographic metal positions in the structure. In the paramagnetic region the two Mössbauer doublets are closely overlapping. The magnetic transition takes place at ≈ 21 K and the saturated fields are around 12 tesla for the two positions. In monoclinic Fe2P4O12 the two octahedrally coordinated metal positions give quite different quadrupole splittings (1.5 and 3 mm/s at room temperature) and hyperfine field values (42 and 12.5 Tesla at 5 K). The transition temperature is at ≈ 18.5 K. 相似文献
93.
Ahmed Fitouhi 《Constructive Approximation》1989,5(1):241-270
We generalize the theory of the heat polynomials introduced by P. V. Rosenbloom and D. V. Widder for a more general class of singular differential operator on (0, ). The heat polynomials associated with the Bessel operator and studied by D. T. Haimo appear as a particular case in this paper. In the special cases of second derivative and Bessel operators the heat polynomials are in fact polynomials inx andt, however, this property does not hold in general.Communicated by Tom. H. Koornwinder. 相似文献
94.
Mark S. Daskin Ali E. Haghani Mandar Khanal Chryssi Malandraki 《Annals of Operations Research》1989,18(1):113-139
The level of aggregation is critical in discrete location analyses as it affects the level of data collection required, computation times and the usefulness of the analyses. We examine the effects of three alternative nodal aggregation schemes on (i) the model's solution times, (ii) the locational decisions indicated by the maximum covering model, (iii) the coverage provided by the aggregate solutions compared with the optimal solutions, and (iv) the coverage predicted by the aggregate model compared with the coverage that results from using the aggregate model's facility sites and the disaggregate demands. The results suggest that considerable aggregation can be tolerated without incurring large errors in total coverage, but that location errors are introduced at moderate levels of aggregation. The magnitude of these errors is significantly affected by the aggregation scheme employed. 相似文献
95.
The surface modification of tire rubber after treatment with saturated NaOH aqueous solution was investigated by HATR infrared analysis, potentiometric titration, and contact angle measurements. Infrared analysis of the powdered treated rubber showed a decrease in absorption at 1540, 1450, and 1395 cm(-1). This decrease is attributed to the removal of zinc stearate, an additive present in tire formulations that often migrates and diffuses to the surface, resulting in poor adhesion between the rubber and other materials. The potentiometric titration of the suspension of powdered rubber in 0.1 M NaCl showed that more hydrochloric acid was consumed by the untreated rubber, most likely a result of the hyrdrolysis of the zinc stearate to the organic acid. Contact angles of flat tire pieces showed an homogeneity enhancement of the treated rubber surface. The decrease of the zinc stearate on the treated rubber surface explains the improvement in the adhesion of this material to the cement matrix, observed in a previous research. The promising results of this study are a starting point for future research on incorporating rubber particles into cementitious materials as a means of successfully utilizing the vast amounts of tire waste currently in landfills. 相似文献
96.
Th. Kappe E. Ziegler M. Ali A. Chirazi 《Monatshefte für Chemie / Chemical Monthly》1969,100(1):142-145
Zusammenfassung Perimidon (1) reagiert mit monosubstit. Malonsäure-trichlorphenylestern (2) bei 250° zu 9-Hydroxy-5,7-dioxo-4,5-dihydro-7H-pyrido[1,2,3-cd]perimidinen (3), die durch saure Hydrolyse zu 10-Amino-4-hydroxy-benzo[h]carbostyrilen (4) gespalten werden.
Syntheses of heterocycles, CXXII: Reaction of perimidone with reactive malonates
Perimidone (1) reacts with monosubstituted 2.4.6-trichlorophenyl malonates at 250° to 9-hydroxy-5.7-dioxo-4.5-dihydro-7H-pyrido[1.2.3-cd]perimidines (3), which are cleaved by acid yielding 10-amino-4-hydroxy-benzo[h]quinolin-2-ones (4).相似文献
97.
BIOLOGICAL ACTIVITIES OF PHTHALOCYANINES-X. SYNTHESES AND ANALYSES OF SULFONATED PHTHALOCYANINES 总被引:5,自引:0,他引:5
Hasrat Ali Réjean Langlois J. Richard Wagner Nicole Brasseur Benoit Paquette Johan E. VAN Lier 《Photochemistry and photobiology》1988,47(5):713-717
Abstract— Synthetic methods to obtain selectively sulfonated metallo phthalocyanines are compared. Both condensation and direct sulfonation procedures lead to mixtures of mono- to tetrasulfonated products which are resolved by reverse phase liquid chromatography in buffered aqueous-methanol. The proportion of sulfonated derivatives is examined as a function of the starting reagents in the case of the condensation method, and as a function of the temperature and reaction time in the case of the direct sulfonation procedure. The number of sulfonate groups per phthalocyanine molecule is determined by oxidative degradation of the phthalocyanine ring followed by quantitative chromatographic analysis of the sulfophthalamide and phthalamide fragments. 相似文献
98.
Toluene was methylated with methanol and disproportionated using catalysts containing different Pt contents (0.2, 0.4 and 0.6%) supported on H‐ZSM‐5 or H‐mordenite (H‐M) zeolites in a fixed‐bed flow‐reactor operated atmospherically at temperatures of 300–500 °C in a flow of hydrogen. Platinum dispersion in the zeolite supports and acid sites strength distribution were evaluated using hydrogen chemisorption (1:1 stoichiometry) and ammonia temperature programmed desorption (TPD) in a differential scanning calorimeter (DSC). Toluene methylation was much faster on all catalysts than toluene disproportionation (DISP). Both reactions were more accelerated using H‐ZSM‐5 containing catalysts than H‐M containing catalysts. The yield of xylenes, and in particular para‐xylene, was significantly influenced by the yield of trimethylbenzenes (TMBs) in product. The selectivities for para‐, ortho‐ and meta‐xylenes production were found largely dependent on the Pt content in the catalysts, particularly when supported on H‐ZSM5‐zeolite. However, using Pt/H‐M catalysts, these selectivities were not strictly controlled by Pt content in the catalysts. 相似文献
99.
A straightforward and effective procedure for the conversion of benzylic, allylic and aliphatic alcohols to the corresponding iodides using Ph3P/I2 under solvent-free conditions using microwave irradiation is reported. 相似文献
100.
Summary Complexes of CoII, NiII, CuII, PdII, and PtIV with 2,4,5-trihydroxybenzoic acid and its substituted phenylazoderivatives have been prepared, together with some mixed-metal (Co, Cu or Ni, Cu) complexes of itsm-nitro,m-carboxy andm-hydroxyarylazo derivatives. The stereochemistries and the modes of bonding of the complexes were elucidated by spectral and magnetic susceptibility measurements.Abstracted from her Ph.D. thesis. 相似文献