Determination of isotherms and initial heat of adsorption of CO2 and N2O in four A zeolites from infrared measurements

Author(s):  
Yves Delaval ◽  
Robert Seloudoux ◽  
Evelyne Cohen de Lara
1984 ◽  
Vol 49 (12) ◽  
pp. 2739-2743 ◽  
Author(s):  
Miloslav Křivánek ◽  
Pavel Jírů

The degree and heat of adsorption of 1-butylamine and ammonia were measured on samples of NaHY zeolites activated at 400-600°C. The adsorption isotherms and calorimetric curves were compared for the two bases, and the amount of Bronsted and Lewis acid centres was determined from the calorimetric curves.


2020 ◽  
Vol 8 ◽  
Author(s):  
Eduardo Pérez-Botella ◽  
Raquel Martínez-Franco ◽  
Nuria González-Camuñas ◽  
Ángel Cantín ◽  
Miguel Palomino ◽  
...  

2005 ◽  
Vol 430 (1) ◽  
pp. 343-353 ◽  
Author(s):  
Cs. Kiss ◽  
U. Klaas ◽  
D. Lemke

1986 ◽  
Vol 133 (10) ◽  
pp. 2165-2168 ◽  
Author(s):  
J. L. Regolini ◽  
J. P. Stoquert ◽  
C. Ganter ◽  
P. Siffert

2019 ◽  
Vol 2 (1) ◽  
Author(s):  
Emilia V. Silletta ◽  
Alexej Jerschow ◽  
Guillaume Madelin ◽  
Leeor Alon

AbstractNon-invasive measurement of absolute temperature is important for proper characterization of various pathologies and for evaluation of thermal dose during interventional procedures. The proton (hydrogen nucleus) magnetic resonance (MR) frequency shift method can be used to map relative temperature changes. However, spatiotemporal variations in the main magnetic field and the lack of local internal frequency reference challenge the determination of absolute temperature. Here, we introduce a multinuclear method for absolute MR thermometry, based on the fact that the hydrogen and sodium nuclei exhibit a unique and distinct characteristic frequency dependence with temperature and with electrolyte concentration. A one-to-one mapping between the precession frequency difference of the two nuclei and absolute temperature is demonstrated. Proof-of-concept experiments were conducted in aqueous solutions with different NaCl concentrations, in agarose gel samples, and in freshly excised ex vivo mouse tissues. One-dimensional chemical shift imaging experiments also demonstrated excellent agreement with infrared measurements.


1983 ◽  
Vol 61 (2) ◽  
pp. 305-308
Author(s):  
M. S. Mathur ◽  
H. C. Card ◽  
K. C. Kao ◽  
S. R. Mejia ◽  
G. C. Tabisz

Hydrogenated amorphous-silicon thin films (a-Si:H) were deposited by microwave plasma chemical-vapour decomposition of SiH4, on thin polyethylene sheets. The high-resolution, far infrared measurements were performed on these films in the 700–50 cm−1 region on a Nicolet far infrared interferometer. The use of polyethylene as the substrate material permitted the determination of the absorption bands at 656.4, 652, 639.4, and 543 cm−1 with a shoulder at 539 cm−1 and a broad feature at 70.8 cm−1. These features provided evidence for SiH, SiH2 (as predicted by Lucovsky et al.), and SiH3 combinations in the film, as well as far more complex systems.


A Beeck-type calorimeter has been used to measure the integral heat of adsorption of oxygen on evaporated films of titanium, chromium, manganese, iron, cobalt, nickel, niobium, molybdenum, rhodium, palladium, tantalum, tungsten, platinum and aluminium. The variation of the heat with the extent of the adsorption has also been determined, except with palladium, platinum and aluminium, for which the amounts of oxygen adsorption were too small to allow this to be done. The heats of adsorption reported are based on a careful determination of the heat capacity of the calorimeter and the overall error is not more than ± 5 kcal/mole. Some investigations of calorimetric behaviour have been made. The surface areas of the films have been measured before and after an adsorption by the B.E.T. method; krypton isotherms at — 196 °C were used for this purpose. From these data, it has been possible to estimate the number of atoms of oxygen adsorbed per surface metal atom. In most cases, this quantity, together with the heat of adsorption, can be related to the oxygen/metal ratios and the heats of formation of certain oxides; this observation is remarkable in view of the limited extent of the adsorption. In the cases of rhodium, palladium and platinum the adsorption stops short of a monolayer and is probably true chemisorption rather than oxide formation. For those metals on which oxide formation occurs, the decrease in heat of adsorption with increasing coverage has been interpreted, in general, in terms of an increase in the oxidation number of surface metal ions by electron transfer within the adsorbed layer. Some theoretical correlations between the heat of adsorption and the atomic and the bulk properties of the species concerned have been examined and found of little value; an empirical relation with the metallic radius is given.


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