8 resultados para Ge4
Resumo:
Single crystals of Bi2V1-xGexO5.5-x/2 (x = 0.2, 0.4, and 0.6) were grown by slow cooling of melts. Bismuth vanadate transforms from an orthorhombic to a tetragonal structure and subsequently to an orthorhombic system when the Ge4+ concentration was varied from x = 0.2 to x = 0.6. All of these compositions crystallized in polar space groups (Aba2, F4mm, and Fmm2 for x = 0.2, 0.4, and 0.6, respectively). The structures were fully determined by single crystal X-ray diffraction studies, (C) 1999 Elsevier Science Ltd.
Resumo:
Recently, much research has been focused on finding new thermoelectric materials. Cu-based quaternary chalcogenides that belong to A(2)BCD(4) (A = Cu; B = Zn, Cd; C = Sn, Ge; D = S, Se, Te) are wide band gap materials and one of the potential thermoelectric materials due to their complex crystal structures. In this study, In-doped quaternary compounds Cu2ZnGe1-xInxSe4 (x = 0, 0.025, 0.05, 0.075, 0.1) were prepared by a solid state synthesis method. Powder x-ray diffraction patterns of all the samples showed a tetragonal crystal structure (space group I-42m) of the main phase with a trace amount of impurity phases, which was further confirmed by Rietveld analysis. The elemental composition of all the samples showed a slight deviation from the nominal composition with the presence of secondary phases. All the transport properties were measured in the temperature range 373-673 K. The electrical resistivity of all the samples initially decreased up to similar to 470 K and then increased with increase in temperature upto 673 K, indicating the transition from semiconducting to metallic behavior. Positive Seebeck coefficients for all the samples revealed that holes are the majority carriers in the entire temperature range. The substitution of In3+ on Ge4+ introduces holes and results in the decrease of resistivity as well as the Seebeck coefficient, thereby leading to the optimization of the power factor. The lattice thermal conductivity of all the samples decreased with increasing temperature, indicating the presence of phonon-phonon scattering. As a result, the thermoelectric figure of merit (zT) of the doped sample showed an increase as compared to the undoped compound.
Resumo:
32 p.
Resumo:
AuPtPdC 4 1 0 1 .5mol LHClAuPtPd 91 .2 %1 0 0 .0 %95 .7%Ge4+ Cr6 + Ti4+ ,ICP MSAuPtPd 0 .2 70 .4 0 0 .1 9g Ln =8 ,AuRSD 1 9.2 % ;PtRSD 2 8.1 % ;PdRSD 1 5 .6%
Resumo:
25~100, C0 = 5 g/gpH, (Ge4+). : (1)(pH0 = 2.96), ; , , ; 30.9615.67 kJmol-1. (2)(pH0 = 2.96)(pH0 = 12.08); 40 = 6.38). (3). .
Resumo:
Laboratory-based research studies and full-scale evaluations of the behaviour of ground improved with granular columns are ample regarding bearing capacity, but limited in respect to the settlement response. This paper presents a laboratory model study that considers the settlement performance of isolated pad footings bearing on reinforced sand deposits under the influence of a fluctuating groundwater table. This is a particularly onerous condition for loose sand deposits in coastal areas which may undergo significant collapse settlement over time. Loose and dense experimental sand beds were constructed and the performance of rigid footings under a maintained load and bearing on sand incorporating different column configurations were monitored under cycling of the water table over a period of 28 days, with one filling/empting cycle every 18 h. It was found that settlement, while greatly reduced compared with unreinforced footings, was ongoing and typically occurred at a much greater rate for loose sand than dense sand. Also, settlement rates were slightly higher for fully penetrating than partially penetrating columns and also for footings reinforced by a column group rather than a single column. This was attributed to the migration of sand grains into the larger column voids.
Resumo:
The topic of my thesis was focused on the synthesis of heteroatomic Rh clusters stabilized by carbonyl ligands. I studied the reactivity of [Rh7(CO)16]3- with different Sb3+ and Ge4+ salts, and tried to synthesize new species by changing the reaction conditions. Indeed, in order to obtain new Rh-Sb and Rh-Ge clusters, I employed different stoichiometric ratios, solvents and atmospheres (N2 or CO). As far as the Rh-Sb system is concerned, I successfully synthesized three new compounds through two different reactions, namely [Rh20Sb3(CO)36][NEt4]3, [Rh21Sb2(CO)38][NEt4]5 and [Rh12Sb(CO)24][NEt4]3. At the same time, I investigated the Rh-Ge system and succeeded in the isolation of the new cluster [Rh14Ge2(CO)30][NEt4]2, along with [Rh12SbGePh2(CO)26][NEt4]2, by treating [Rh7(CO)16]3- with both Ge4+ and Sb3+ salts. Each compound has been characterized by IR spectroscopy, ESI-MS spectrometry and single crystal X-ray diffractometry. Finally, I conduced chemical reactivity tests on some of the obtained compounds.
