entrance face
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2020 ◽  
Vol 992 ◽  
pp. 971-975
Author(s):  
O. Pikoul ◽  
Nikolay V. Sidorov ◽  
Mikhail N. Palatnikov

Interference patterns of single crystals of LiNbO3:Gd, LiNbO3:Er, obtained by laser conoscopy, allow us to estimate the optical homogeneity of the samples under study. The observation of conoscopic patterns of the LiNbO3:Gd single crystal shows that with an increase in the percentage impurity concentration, the anomalous biaxiality in these samples manifests itself to a much greater degree. Anomalous biaxiality for the sample LiNbO3:Er [3.60 wt.%] is present at almost every point of the entrance face, which is manifested in conoscopic patterns in the form of enlightenment and rupture of the “Maltese cross”, which corresponds to the angle 2V~1° between the anomalous axes.



Author(s):  
Sameer Ranjan Sahu ◽  
Dipti Prasad Mishra

Conservation equations of mass, momentum and energy have been solved numerically along with a two-equation-based k-ɛ turbulent model to determine the air entrainment into a mixing pipe. Two different louvered pipe configurations (one with entrance face closed to atmosphere while the other was opened) were used to entrain air into the mixing pipe and by changing various design parameters, the resulting effects were studied. For both the configurations, the opening area and the number of nozzles (assumed exhaust pipe) had significant effect in bringing down the exhaust temperature especially the configuration with its entrance face opened to atmosphere. Temperature as low as 309 K (approx.) was successfully achieved in the analysis. Nozzle protrusion length also proved to be an important parameter among other parameters like nozzle pitch circle diameter, inclination angle and pipe diameter.



Two popular electrochemical methods for the investigation of the permeability of metal membranes to atomic hydrogen are critically discussed. In the potentiostatic (P) method, hydrogen is generated at constant potential at the entrance face; in the galvanostatic (G) method, it is generated at constant current. In both, the concentration at the exit face of the membrane is zero. The boundary condition at the entrance face usually taken to correspond with these experiments is either that the surface concentration is constant (the C case) or that the flux of hydrogen entering the membrane is constant (the F case). It is pointed out that the widespread assumptions that use of the P technique guarantees the C boundary condition, and that use of the G technique guarantees the F condition, are incorrect. The boundary condition actually established depends on the relative rates of the various steps involved in hydrogen evolution at the entrance face and its diffusion through the membrane. Experimental work on ca . 25 μm thick nickel and palladium, which supports this contention, is described. The F boundary condition is readily established by the G experiment on palladium, but the C condition cannot be established by the P experiment. The converse is true for nickel. These differences are explained in terms of the greater solubility and diffusivity of hydrogen in palladium as compared with nickel. An extended potentiostatic experiment, termed the P f experiment, is described. In the P f experiment, all the potentiostatically generated hydrogen enters the membrane. The currents passing at both faces of the membrane are measured during permeation, and also as they decay after the potential of the entrance face is switched to that of the exit face, causing hydrogen to diffuse out of both sides of the membrane. The P f experiment is shown to work well with thin palladium membranes, and to provide crosschecks on the diffusivity of hydrogen. The diffusion coefficient of hydrogen in nickel is sensitive to the thermal history of the metal. Decay transients give some evidence for the existence of hydrogen traps in both nickel and palladium. The potential of the entrance face during G experiments on either metal is not related to the surface concentration of hydrogen by the Nernst equation. It is concluded that a full analysis of the permeation transients obtained by P or G experiments should be made to establish the boundary conditions actually created by the experimental procedure. Some pr­eviously published permeation work is critically examined in the light of this conclusion.



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