Silylation of a crystalline silicic acid: an MAS NMR and porosity study

2002 ◽  
Vol 12 (10) ◽  
pp. 3010-3015 ◽  
Author(s):  
Peter Heinrich Thiesen ◽  
Klaus Beneke ◽  
Gerhard Lagaly
1979 ◽  
Vol 34 (4) ◽  
pp. 648-649 ◽  
Author(s):  
Klaus Beneke ◽  
Gerhard Lagaly

Abstract Silica-X described in 1964 as a new SiO2 modification is the dehydrated form of the crystalline silicic acid H2Si8O17 · xH2O which is obtained by cation exchange from the potassium silicate K2Si8O17 · xH2O.


2012 ◽  
Vol 368 (1) ◽  
pp. 447-455 ◽  
Author(s):  
Peter J. Swedlund ◽  
Yantao Song ◽  
Zoran D. Zujovic ◽  
Michél K. Nieuwoudt ◽  
Andreas Hermann ◽  
...  

ChemInform ◽  
1987 ◽  
Vol 18 (7) ◽  
Author(s):  
J. M. ROJO ◽  
J. SANZ ◽  
E. RUIZ-HITZKY ◽  
J. M. SERRATOSA

1973 ◽  
Vol 28 (5-6) ◽  
pp. 234-238 ◽  
Author(s):  
Gerhard Lagaly ◽  
Klaus Beneke ◽  
Armin Weiss

A crystalline silicic acid H2Si14O29 · 5H2O has been prepared by topochemical reaction of sodium silicate Na2Si14O29·12H2O with acids. The compound has a layer structure with silicate sheets of about 11.2 Å thickness. The layer structure is clearly established by two dimensional reactions, mainly the formation of intercalation compounds with X-oxides (dimethylsulfoxide, pyridine-N-oxides etc.), acid amides, urea and its derivatives and bases such as hydrazine and pyridine. Typical exemples are 2 (CH3)2SO · H2Si14O29, 2C5H5NO · H2Si14O29, 2, 7 HCONHCH3 · H2Si14O29; 2, 3 HCON (CH3)2 · H2Si14O29; 1, 6 HCONHC2H5 · H2Si14O29; 1, 6 HCON (C2H5)2 · H2Si14O29.


1989 ◽  
Vol 267 (9) ◽  
pp. 844-852 ◽  
Author(s):  
H. -H. Kruse ◽  
K. Beneke ◽  
G. Lagaly

1987 ◽  
Vol 552 (9) ◽  
pp. 236-240 ◽  
Author(s):  
D. Hoebbel ◽  
G. Engelhardt ◽  
A. Samoson ◽  
K. �jsz�szy ◽  
Yu. I. Smolin

Clay Minerals ◽  
1993 ◽  
Vol 28 (1) ◽  
pp. 39-48 ◽  
Author(s):  
J. Döring ◽  
G. Lagaly

AbstractAmines are strongly adsorbed by the crystalline silica H4Si20O42·4H2O and are intercalated into the interlayer spaces. The adsorption of butyl-, hexyl-, octyl-, and decylamine from alcoholic solutions (ethanol, butanol…decanol) is competitive as both types of molecules, amines and alcohols, are adsorbed in the interlamellar space. The adsorption isotherms are presented as composite isotherms showing the specific reduced surface excess of amine, n°(n)/m, as a function of the molar fraction of amine in the equilibrium solution. These isotherms increase to a plateau-like section (n°(n)/m≈1·4 mmol/g) when the interlamellar adsorption is restricted to formation of monolayers of flat-lying molecules (in water, ethanol and butanol). In the presence of longer chain alcohols, the isotherms increase stepwise to a second "plateau" (at n1°(n)/m = 2·2-2·7 mmol/g) which corresponds to paraffin-type bilayers of amine and alcohol molecules. The composition of the adsorption phase is estimated from the specific reduced surface excess of amine on the basis of the interlamellar structure derived from basal spacing measurements.


ChemInform ◽  
1988 ◽  
Vol 19 (9) ◽  
Author(s):  
D. HOEBBEL ◽  
G. ENGELHARDT ◽  
A. SAMOSON ◽  
K. UJSZASZY ◽  
YU. I. SMOLIN

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