Effect of Temperature on Aluminum Coordination in Zeolites H−Y and H−USY and Amorphous Silica−Alumina:  An in Situ Al K Edge XANES Study

2005 ◽  
Vol 109 (19) ◽  
pp. 9280-9283 ◽  
Author(s):  
Anna Omegna ◽  
Roel Prins ◽  
Jeroen A. van Bokhoven
2012 ◽  
Vol 118 ◽  
pp. 374-381 ◽  
Author(s):  
M. Zabeti ◽  
T.S. Nguyen ◽  
L. Lefferts ◽  
H.J. Heeres ◽  
K. Seshan

2012 ◽  
Vol 116 (40) ◽  
pp. 21416-21429 ◽  
Author(s):  
Emiel J.M. Hensen ◽  
Dilip G. Poduval ◽  
Volkan Degirmenci ◽  
D.A J. Michel Ligthart ◽  
Wenbin Chen ◽  
...  

2013 ◽  
Vol 45 (1) ◽  
pp. 89-98 ◽  
Author(s):  
Weihong Dong ◽  
Gengxin Ou ◽  
Xunhong Chen ◽  
Zhaowei Wang

In this study, in situ and on-site permeameter tests were conducted in Clear Creek, Nebraska, USA to evaluate the effect of water temperature on streambed vertical hydraulic conductivity Kv. Fifty-two sediment cores were tested. Five of them were transferred to the laboratory for a series of experiments to evaluate the effect of water temperature on Kv. Compared with in situ tests, 42 out of the 52 tests have higher Kv values for on-site tests. The distribution of water temperature at the approximately 50 cm depth of streambed along the sand bar was investigated in the field. These temperatures had values in the range 14–19 °C with an average of 16 °C and had an increasing trend along the stream flow. On average, Kv values of the streambed sediments in the laboratory tests increase by 1.8% per 1 °C increase in water temperature. The coarser sandy sediments show a greater increase extent of the Kv value per 1 °C increase in water temperature. However, there is no distinct increasing trend of Kv value for sediment containing silt and clay layers.


Author(s):  
Tobias Orlander ◽  
Katrine Alling Andreassen ◽  
Ida Lykke Fabricius

Abstract Development of high-pressure, high-temperature (HPHT) petroleum reservoirs situated at depths exceeding 5 km and in situ temperature of 170 °C increases the demand for theories and supporting experimental data capable of describing temperature effects on rock stiffness. With the intention of experimentally investigating temperature effects on stiffness properties, we investigated three sandstones from the deep North Sea Basin. As the North Sea Basin is presently undergoing substantial subsidence, we assumed that studied reservoir sandstones have never experienced higher temperature than in situ. We measured ultrasonic velocities in a low- and high-stress regime, and used mass density and stress–strain curves to derive, respectively, dynamic and static elastic moduli. We found that in both regimes, the dry sandstones stiffens with increasing testing temperature and assign expansion of minerals as a controlling mechanism. In the low-stress regime with only partial microcrack closure, we propose closure of microcracks as the stiffening mechanism. In the high-stress regime, we propose that thermal expansion of constituting minerals increases stress in grain contacts when the applied stress is high enough for conversion of thermal strain to thermal stress, thus leading to higher stiffness at in situ temperature. We then applied an extension of Biot’s effective stress equation including a non-isothermal term from thermoelastic theory and explain test results by adding boundary conditions to the equations.


2017 ◽  
Vol 60 (19-20) ◽  
pp. 1554-1564 ◽  
Author(s):  
Vicente Sanchez Escribano ◽  
Gabriella Garbarino ◽  
Elisabetta Finocchio ◽  
Guido Busca

1982 ◽  
Vol 36 (4) ◽  
pp. 361-368 ◽  
Author(s):  
Larry F. Wieserman ◽  
David M. Hercules

This study compares the properties of γ-alumina, silica, and titania using ESCA and in situ FT-IR. The FWHM's of the O1s and metal 2p ESCA peaks increased systematically from titania to γ alumina; the O1s/metal 2p ESCA peak area ratios were nearly equal for γ-alumina and silica. For titania, however, the value was half that obtained for γ-alumina. In situ FT-IR showed hydroxyl bands with increasing frequencies from titania to silica. Alumina and titania form carbonate-type structures after exposure to CO at elevated temperatures. Silica exhibited no additional bands after CO treatment that could be assigned to physically adsorbed CO or carbonate-type structures. At 100°C, there is a direct correlation between the specific surface area and the intensity of infrared absorbance of the free-hydroxyl and the hydrogen-bonded hydroxyl bands for silica. The intensities of the infrared bands due to matrix modes were not affected by surface area.


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