Identification and Characterization of Surface Hydroxyl Groups by Infrared Spectroscopy

2014 ◽  
pp. 99-318 ◽  
Author(s):  
Konstantin Hadjiivanov
1970 ◽  
Vol 48 (15) ◽  
pp. 2454-2456 ◽  
Author(s):  
B. A. Morrow ◽  
A. Devi

Infrared spectroscopy has been used to show that the surface hydroxyl groups on highly dehydrated silica will exchange with 18O-labeled water. The degree of exchange depends on the sample temperature and is a maximum at about 400 °C, where approximately 65% of the silanol groups contain 18O. The use of the 18O exchange technique for assigning surface-adsorbate stretching modes is illustrated by considering the infrared spectra of BF3 chemisorbed on silica.


1986 ◽  
Vol 1 (1) ◽  
pp. 114-119
Author(s):  
M. Bretz ◽  
A. G. Shastri ◽  
J. Schwank

A promising method for the preparation of sizeable quantities of structurally well-defined, highpurity MgO powder is reported. The morphology and surface uniformity of the powder is comparable to that of MgO smokes but with narrow size distribution of particles. Sample characterization of these oxide powders is accomplished by combining structural TEM/STEM examination with krypton gas adsorption isotherms. The latter technique is sensitive to the presence of surface hydroxyl groups and of surface roughness on an atomic scale. Highresolution TEM indicates a perfect cubic morphology, intra-crystallite orientation, and dendritic sintering of cubes. In the STEM mode sharp convergent beam electron diffraction patterns are obtained, and in thick specimen regions Kikuchi lines appear, indicating the absence of crystal defects. After prolonged outgassing to remove surface hydroxyl groups, a krypton adsorption isotherm contains a near vertical submonolayer riser and second layer step along with partial wetting features near saturation. These near-ideal dendritic ceramic powders, therefore, provide a research bridge between single crystal surface studies and large-scale powder technology.


2012 ◽  
Vol 512-515 ◽  
pp. 2443-2447 ◽  
Author(s):  
Li Ying Guo

Multiplayer core-shell TiO2/PSt/PVP hybrid microspheres were successfully synthesized by the copolymerization of vinylpyrrolidone in the solution of ethyl acetate with TiO2/PSt core-shell hybrid microspheres which were formed through the encapsulation of KH570-g-TiO2 sol particles with styrene, while the active KH570-g-TiO2 sol particles were prepared by the hydrolysis condensation of KH-570 with tetrabutyl titanate. Characterization technologies of FT-IR and TGA were applied to investigate the structure and the thermal stability of the product. The results showed that the hydroxyl groups from the hydrolysis of KH-570 condensed with the surface hydroxyl groups of TiO2, as well as PSt and PVP were grafted successively onto the surface of KH570-g-TiO2 sol particles. The thermal decomposition temperature of TiO2/PSt/PVP was higher than TiO2/PSt, which also indicated that the obtained product was the final objective product.


Langmuir ◽  
1990 ◽  
Vol 6 (8) ◽  
pp. 1389-1395 ◽  
Author(s):  
A. Burneau ◽  
O. Barres ◽  
A. Vidal ◽  
H. Balard ◽  
G. Ligner ◽  
...  

1986 ◽  
Vol 51 (7) ◽  
pp. 1430-1438 ◽  
Author(s):  
Alena Reissová ◽  
Zdeněk Bastl ◽  
Martin Čapka

The title complexes have been obtained by functionalization of silica with cyclopentadienylsilanes of the type Rx(CH3)3 - xSi(CH2)nC5H5 (x = 1-3, n = 0, 1, 3), trimethylsilylation of free surface hydroxyl groups, transformation of the bonded cyclopentadienyl group to the cyclopentadienyl anion, followed by coordination of (h5-cyclopentadienyl)trichlorotitanium. The effects of single steps of the above immobilization on texture of the support, the number of free hydroxyl groups, the coverage of the surface by cyclopentadienyl groups and the degree of their utilization in anchoring the titanium complex have been investigated. ESCA study has shown that the above anchoring leads to formation of the silica-supported bis(h5-cyclopentadienyl)dichlorotitanium(IV) complex.


Sign in / Sign up

Export Citation Format

Share Document