Topotactic route to synthesis of novel hydroxylated phases: I. Trioctahedral Micas

Clay Minerals ◽  
1986 ◽  
Vol 21 (2) ◽  
pp. 125-131 ◽  
Author(s):  
S. Komarneni ◽  
R. Roy

AbstractK-depleted phlogopite mica was used as a topotactic precursor and treated with alkali (Li+, K+, , Rb+, Cs+), alkaline-earth (Mg2+, Ca2+, Sr2+, Ba2+) and trivalent (Al3+) cations under hydrothermal conditions of 200°C and 30 MPa pressure. K-, NH4-, Rb- and Cs-aluminosilicate micas were synthesised at 200°C in one day. The synthesis of Cs-aluminosilicate mica, with potential applications in the management of nuclear wastes, has been achieved for the first time by this approach. Ion exchange by Li+, Na+ and alkaline-earth cations under hydrothermal conditions did not produce anhydrous mica phases but resulted in hydrous phases with one or two layers of water molecules between the clay layers. The formation of hydrous phases may be attributed to the high hydration energy of the above cations compared to K+, , RB+ and Cs+. Ion exchange with Al3+ produced a chlorite-like phase because of the hydrolysis of Al3+ under these hydrothermal conditions. These studies are of relevance in the immobilization of wastes where hazardous ions can be fixed in highly stable insoluble phases like mica or chlorite.

2015 ◽  
Vol 71 (3) ◽  
pp. 222-228 ◽  
Author(s):  
Mohamed Abdellatif Bensegueni ◽  
Aouatef Cherouana ◽  
Slimane Dahaoui

Two alkaline earth–tetrazole compounds, namelycatena-poly[[[triaquamagnesium(II)]-μ-5,5′-(azanediyl)ditetrazolato-κ3N1,N1′:N5] hemi{bis[μ-5,5′-(azanediyl)ditetrazolato-κ3N1,N1′:N2]bis[triaquamagnesium(II)]} monohydrate], {[Mg(C2HN9)(H2O)3][Mg2(C2HN9)2(H2O)6]0.5·H2O}n, (I), and bis[5-(pyrazin-2-yl)tetrazolate] hexaaquamagnesium(II), (C5H3N6)[Mg(H2O)6], (II), have been prepared under hydrothermal conditions. Compound (I) is a mixed dimer–polymer based on magnesium ion centres and can be regarded as the first example of a magnesium–tetrazolate polymer in the crystalline form. The structure shows a complex three-dimensional hydrogen-bonded network that involves magnesium–tetrazolate dimers, solvent water molecules and one-dimensional magnesium–tetrazolate polymeric chains. The intrinsic cohesion in the polymer chains is ensured by N—H...N hydrogen bonds, which formR22(7) rings, thus reinforcing the propagation of the polymer chain along theaaxis. The crystal structure of magnesium tetrazole salt (II) reveals a mixed ribbon of hydrogen-bonded rings, of typesR22(7),R22(9) andR24(10), running along thecaxis, which are linked byR24(16) rings, generating a 4,8-cflunet.


1998 ◽  
Vol 33 (11) ◽  
pp. 1581-1586 ◽  
Author(s):  
Charles H Mahler ◽  
Brian L Cushing ◽  
John N Lalena ◽  
John B Wiley

1996 ◽  
Vol 14 (4) ◽  
pp. 209-216
Author(s):  
O.S. Banakh ◽  
R.I. Baranskyi ◽  
V.J. Rogovyk ◽  
I.M. Zybak

Based on zeolites of types X, Y and M, with and without binding clay, ion-exchange modifications containing alkali and alkaline earth cations (silver and copper) and different quantities of water have been prepared. Data obtained with these zeolites have enabled their retention volumes and selectivities towards low boiling hydrocarbons and oxide gases to be calculated. Sharp changes were observed in these parameters when the chromatography of ethane and other gases was conducted on such zeolites with up to 10% K+, Rb+ and Cs+ cations replaced, i.e. when low replacement of exchangable cations had been effected. The same effect was encountered with CO and olefins when 0.08CuNaY zeolite was employed. An increase in temperature and the introduction of water into the system caused a decrease in the effect. These observations have prove useful in the construction of chromatographic columns and adsorption filters for the extraction and concentration of certain pollutants.


Author(s):  
Abderrahmen Guesmi ◽  
Ahmed Driss

The two title compounds, potassium diaquacobalt(II) borodiphosphate 0.48-hydrate and potassium–calcium(0.172/0.418) diaquacobalt(II) borodiphosphate monohydrate, were synthesized hydrothermally. They are new members of the borophosphate family characterized by∞[BP2O8]3−helices running along [001] and constructed of boron (Wyckoff position 6b, twofold axis) and phosphorus tetrahedra. The [CoBP2O8]−anionic frameworks in the two materials are structurally similar and result from a connection in theabplane between the CoO4(H2O)2coordination octahedra (6bposition) and the helical ribbons. Nevertheless, the two structures differ in the disorder schemes of the K,Ca and H2O species. The alkali cations in the structure of the pure potassium compound are disordered over three independent positions, one of them located on a 6bsite. Its framework is characterized by double occupation of the tunnels by water molecules located on twofold rotation axes (6b) and a fraction of alkali cations; its cell parameters, compared with those for the mixed K,Ca compound, show abnormal changes, presumably due to the disorder. For the K,Ca compound, the K and Ca cations are on twofold axes (6b) and the channels are occupied only by disordered solvent water molecules. This shows that it is possible, due to the flexibility of the helices, to replace the alkali and alkaline earth cations while retaining the crystal framework.


2006 ◽  
Vol 106 (12) ◽  
pp. 2422-2427 ◽  
Author(s):  
Maria Barysz ◽  
Dariusz K??dziera ◽  
Jerzy Leszczyński ◽  
Aleksander Bilewicz

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