Near-Infrared Spectroscopic Monitoring of the Water Adsorption/Desorption Process in Modern and Archaeological Wood

2008 ◽  
Vol 62 (8) ◽  
pp. 860-865 ◽  
Author(s):  
Tetsuya Inagaki ◽  
Hitoshi Yonenobu ◽  
Satoru Tsuchikawa
2012 ◽  
Vol 33 (5) ◽  
pp. 791-796 ◽  
Author(s):  
Rohit P. Rao ◽  
Michael J. Danduran ◽  
Rohit S. Loomba ◽  
Jennifer E. Dixon ◽  
George M. Hoffman

Seikei-Kakou ◽  
2021 ◽  
Vol 33 (5) ◽  
pp. 176-181
Author(s):  
Shunsuke Hosoe ◽  
Yuta Hikima ◽  
Masahiro Ohshima ◽  
Masahiro Watari ◽  
Akihiro Naito

2012 ◽  
Vol 326-328 ◽  
pp. 690-695
Author(s):  
C.R. Ruivo ◽  
J.J. Costa ◽  
A.R. Figueiredo

In this paper, the performance of a channel element of a hygroscopic matrix is evaluated by detailed numerical modeling. The adopted physical model takes into account the gas-side and solid-side resistances to heat and mass transfer, as well as the simultaneous heat and mass transfer occurring simultaneously with the water adsorption/desorption process in the desiccant porous channel wall domain. The desiccant medium is silica gel RD, the equilibrium being characterized by sorption isotherms. Appropriate convective transfer coefficients are taken into account for the calculation of the heat and mass transfer phenomena between the airflow and the channel wall. The response of the channel element to a step change in the airflow states is simulated, the results enabling the investigation of some differences between the adsorption and desorption processes.


2020 ◽  
Vol 2 (1) ◽  
pp. 15
Author(s):  
Gianfranco Carotenuto

Powdered zeolites are used as a desiccant in the preservation of many types of vegetable foods (e.g., cereal grain, corn, etc.). Natural clinoptilolite is a very abundant, inexpensive, nontoxic, regenerable, and environmentally friendly zeolite with good desiccant properties. Here, water adsorption/desorption properties of natural clinoptilolite have been investigated by a novel technique based on a.c. electrical measurements. In particular, owing to the presence of extra-framework cations, zeolites are ionic conductors. The presence of water in cationic sites significantly modifies cation mobility, because strong electrostatic interactions act between cations and nucleophilic areas in 3D-frameworks, and non-hydrated cations have a near zero mobility, while hydrated cations have enough mobility at room temperature. The type of law controlling the adsorption/desorption process has been established by monitoring the real-time behavior of relative current intensity moving in the sample surface biased by a sinusoidal voltage signal of 20Vpp (5 kHz) and exposed to a constant moisture atmosphere (75%) at 25 °C. An intergranular diffusion control was active at the beginning of hydration because of the lamellar texture, then Lagergren irreversible pseudo-first-order kinetics took place. To confirm the adsorption mechanism and possibility of regenerating the clinoptilolite desiccant, dehydration by silica gel was electrically monitored and an exponential kinetic law found.


1992 ◽  
Vol 67 (4 Spec No) ◽  
pp. 407-411 ◽  
Author(s):  
Y A Wickramasinghe ◽  
L N Livera ◽  
S A Spencer ◽  
P Rolfe ◽  
M S Thorniley

Author(s):  
Gianfranco Carotenuto

Zeolites are ionic conductors and the cation electrical mobility in zeolites depends on their hydration state; consequently, the water adsorption/desorption process can be simply investigated by measuring the temporal evolution of current intensity in samples exposed to an environment with constant humidity or dry air, respectively. According to this kinetic analysis, a mechanism has been formulated for the water adsorption process able to justify the Lagergren pseudo-first-order kinetics observed for adsorption and the first-order kinetics observed for desorption. In this mechanism water molecules are first attract by the electric field of the cations and then they move at cation-framework interface to maximize the hydrogen bond interactions.


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