Vibrational spectroscopy of porous Vycor glass: surface hydroxyl perturbations upon adsorption of hydrogen

1990 ◽  
Vol 94 (6) ◽  
pp. 2505-2511 ◽  
Author(s):  
T. E. Huber ◽  
C. A. Huber
1974 ◽  
Vol 47 (1) ◽  
pp. 4-8 ◽  
Author(s):  
Keiichiro Hatano ◽  
Norio Shimamoto ◽  
Takashi Katsu ◽  
Yuzaburo Fujita

1974 ◽  
Vol 5 (37) ◽  
Author(s):  
KEIICHIRO HATANO ◽  
NORIO SHIMAMOTO ◽  
TAKASHI KATSU ◽  
YUZABURO FUJITA

1989 ◽  
Vol 168 ◽  
Author(s):  
D. Sunil ◽  
J. Sokolov ◽  
M. H. Rafailovich ◽  
E. Mendoza ◽  
E. Wolkow ◽  
...  

It has recently been demonstrated that highly resolved images can be produced by photochemical deposition of metal oxides in porous Vycor glass. This process has potential applications to the development of integrated optics in glass since it enables one to deposit in the same material refractive index patterns of optically and electro-magnetically active adsorbates. In order to learn in more detail about the interaction of the metal oxides with the glass, we impregnated porous Vycor glass (PVC) with tin or iron oxides and analyzed the samples with electron microscopy, x-ray microprobe analysis, and small angle x-ray scattering (SAXS). The results indicate that even though both oxides produce images of comparable resolution (approx 1μ), the interaction with the glass surface and particulate distribution is different for the two oxides. In particular, the Sn oxide appears to chemically modify the glass surface and prevents its consolidation.


1974 ◽  
Vol 61 (10) ◽  
pp. 4307-4311 ◽  
Author(s):  
Yuzaburo Fujita ◽  
Takashi Katsu ◽  
Mitsuo Sato ◽  
Kazumasa Takahashi

2019 ◽  
Vol 123 (11) ◽  
pp. 6464-6476
Author(s):  
Robert L. Neuweiler ◽  
Edward G. Look ◽  
Luat T. Vuong ◽  
Harry D. Gafney

1990 ◽  
Vol 80 (5-6) ◽  
pp. 315-323 ◽  
Author(s):  
T. E. Huber ◽  
C. A. Huber

1961 ◽  
Vol 39 (1) ◽  
pp. 42-60 ◽  
Author(s):  
L. H. Little ◽  
H. E. Klauser ◽  
C. H. Amberg

The adsorption and reactions of the four butenes on porous Vycor glass at room temperature have been studied by infrared spectroscopy. Initial adsorption was rapid and was found to perturb the surface hydroxyl groups of the glass. In the case of the n-butenes rapid isomerization took place at room temperature. In addition to this the adsorbate spectra showed the occurrence of a slower reaction which led to an increase in saturated C—H groupings. C8 and higher compounds were shown to have formed; on outgassing at room temperature small amounts of cracking products were collected. The polymerization of isobutene was particularly rapid. Experiments at low coverage (θ ∼ 0.001–0.002) gave identical initial spectra for the n-butenes. These were discussed in terms of possible models for butene adsorption. A reduction in the alumina and zirconia content of the glass by acid leaching resulted in decreased rates of isomerization and polymerization, suggesting that one or both of these oxides are at least partially responsible for the activity of the glass. A pure silica aerogel was almost completely inactive. Quantitative measurements of the spectra of several monoolefins in solution were made for comparison with the surface species, in particular with respect to their molar intensities of absorption.


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