We consider the question of whether the simple random walk (SRW) on an infinite tree is transient or recurrent. For random-trees (all vertices of distancen from the root of the tree have degreedn, where {dn} are independent random variables), we prove that the SRW is a.s. transient if lim infnnE(log(dn-1))>1 and a.s. recurrent if lim supnn E(log(dn-1))<1. For random trees in which the degrees of the vertices are independently 2 or 3, with distribution depending on the distance from the root, a partial classification of type is obtained.Research supported in part by NSF DMS 8710027. 相似文献
Ligand exchange method is introduced as an alternative to Job’s and mole ratio methods for studying the stoichiometry of relatively weak metal complexes in solutions. The method involves adding varying amounts of a ligand (L) to an excess constant amount of a colored complex (MX) with appropriate stability and molar absorptivity. The absorbance of each solution is measured at the λmax of the initial complex, MX, and plotted against the concentration of the studied ligand, L. If the newly formed complex ML does not absorb at the λmax of the initial complex, then attenuation of the absorbance of the initial complex on adding varying quantities of the investigational ligand gives an inverse calibration line that intersects with the calibration curve of initial complex at a given point. If a line parallel to the ordinate is drawn from this point to the x-axis, the ratio of the two parts of the x-axis to the left and to the right (α/β) gives the metal to ligand molar ratio in the complex formed, ML. The new method has been applied to the study of the composition of iron (III) complexes with three bisphosphonate drugs: alendronate, etidronate, and ibandronate. The mole ratio was found to be 1:1 with the three investigated bisphosphonates and results were further confirmed by Job’s and mole ratio methods. The ligand exchange method is simpler, quicker, easier to perform and more accurate than Job’s and mole ratio methods for studying weak and relatively weak complexes.
Passively Q-switched thulium doped fiber laser (TDFL) has been successfully demonstrated using gold nanoparticles (GNPs), which were embedded into polyvinyl alcohol as saturable absorber (SA). The stable self-starting Q-switched laser was generated to operate at 1 891 nm when a tiny piece of the prepared film was slot in between two fiber ferrules and incorporated into the laser cavity. The repetition rate can be adjusted from 48.54 kHz to 49.64 kHz while the pulse width decreased from 3.52 μs to 2.38 μs with the increase of 1 550 nm pump power from 840 mW to 930 mW. The corresponding pump power output power linearly increased from 3.62 mW to 6.3 mW with a slope efficiency of 2.53%. The maximum peak power and pulse energy were recorded at about 39 mW and 0.12 µJ, respectively at pump power of 930 mW. The Q-switching operation was caused by the surface plasmon resonance absorption of GNPs. 相似文献
A copper, zinc and aluminium mixed oxides sample having the nominal composition 0.25 CuO/0.03 ZnO/Al2O3 was prepared by impregnating Al(OH)3 with copper and zinc nitrate solutions, drying at 100 °C then heating in air at 600 °C. The obtained solid was exposed to different doses of -rays (20–160 Mrad). The surface characteristics namelySBETVP andr of different treated adsorbents were determined from N2 adsorption isothems measured at –196 °C. The catalytic activity of various irradiated solids was determined by following up the kinetics of CO-oxidation by O2 at 150–200 °C. The results showed that the doses up to 80 Mrad resulted in no significant change in theSBET but increased slightly theVP (20%) of the treated adsorbents. The irradiation at 160 Mrad caused an increase of 20% in theSBET of the irradiated solid sample. The catalytic activity increased progressively by increasing the dose, a dose of 160 Mrad brought about an increase of 140% in the catalyst's activity. The apparent activation energy of the catalytic reaction decreased monotonically by increasing the absorbed dose of -rays which was attributed to a parallel induced decrease in the value of pre-exponential term of the Arrhenius equation. The observed increase in the catalytic activity due to -irradiation has been interpreted as a result of increasing the concentration of catalytically-active sites contributing in chemisorption and catalysis of CO-oxidation via a possible fragmentation of CuO crystallites. 相似文献
Nucleophilic attack by N2 of N1N2-diarylformamides 1a-c on C-2 of chloranil (2) and subsequently by N1 on C-1 of 2 initiates the formation of benzimidazolinones 8a-c. In contrast, when 1b-e is reacted with 2,3-dichloro-1,4-naphthoquinone (9) , both chlorine atoms are successively substituted by the two nitrogen atoms and 2-(arylamino)-3-(N-formylarylamino)-1,4-naphthoquinones 13b-e result, which (probably via their cyclic tautomers 12b-e ) may be cyclodehydrogenated to form N1,N3-diarylnaphtho[2,3-d] imidazoline-2,4,9-triones (as 14b,c ). On the other hand, N1,N2diarylacetamidines 15a-d attack 2 and 9 at C-2 with N2 but subsequently exert nucleophilic character at the acetamidine α-carbon attacking C-1 of 2 and 9 , respectively, thus forming 1-aryl-2-(arylimino)-3a-hydroxy-2,3,3a,6-tetrahydro-1N-indol-6-ones 18a-d and 3-aryl-2-(arylimino)-9b-hydroxy-2,3,5,9b-tetrahydro-1-H-benz[e]indol-5-ones 19b,c , respectively. The latter may be thermally dehydrated to the fully conjugated 2,5-dihydro-3H-benz[e]indol-5-ones 20b,c. Unambiguous structural assignments for 18b and 20c are made on the basis of X-ray crystal structure analyses. 相似文献
The aim of this work is to characterize the active constituents present in the ethyl acetate fraction of Senna tora, L. Roxb. seeds. Due to the fact that the main biological activity of S. tora, L seeds is attributed to its phenolic compounds which are mainly isolated from Ethyl acetate fraction, to avoid repetition of work and to save time, it was deemed necessary to confirm the identity of these phenolic compounds. This was done by GC-MS and LC-MS analysis of the ethyl acetate fraction where the structures of the isolated compounds were established on the basis of molecular ion peak and their fragmentation pattern. They were identified as Chrysophanol, Chrysarobin, 10-hydroxy-5-methoxy-2-methyl-1, 4-anthracenedione, Rubrofusarin, Parietin, Griseoxanthone-B, Isotorachrysone, and Cumbiasin B.
4-Phenyl-2,3-dioxobutyro-1,4-lactone ( 1 ) gave with phenylhydrazine and ils p-Cl, p-Br, p-I and p-NO2 derivatives, bishydrazones which were eyclized to 1-aryl-3-(α-hydroxybenzyl)-4,5-dione-4-arylhydrazones. With o-phenylene diamine, compound 1 gave either a Schiff base or a substituted quinoxaline, depending upon the ratio of the reactants. 相似文献
In this article we consider a class of first order nonlinear integro-differential equations with delay. We propose new approach for investigating local and global existence of the solutions of its Cauchy problem. This approach gives new results. 相似文献