EFFECTS OF SOME CHEMICAL TREATMENTS ON K/Ca CATION EXCHANGE SELECTIVITY OF LAYER SILICATES

1972 ◽  
Vol 52 (2) ◽  
pp. 151-161 ◽  
Author(s):  
M. A. ARSHAD ◽  
P. M. HUANG ◽  
R. J. ST. ARNAUD

The effects of chemical treatments commonly employed to remove amorphous materials, on the K/Ca cation exchange selectivity (CES) of montmorillonite, kaolinite, chlorite, vermiculite, biotite, muscovite, and soil clays were studied. The K/Ca CES values for biotite and muscovite decreased appreciably upon peroxidation. Both the Na–dithionite–citrate–bicarbonate and boiling 0.5 N NaOH dissolution treatments resulted in a substantial increase in the K/Ca CES of biotite and muscovite. This was attributable to increases in the wedge-zone sites resulting from partial K-depletion of these minerals. Furthermore, the release of structural cations and their subsequent precipitation on mineral surfaces appears to have resulted in the "preferential occupation" of Ca-adsorbing sites and thus contributed to the lower selectivity of Ca ions. However, these two treatments affected the K/Ca CES of illite slightly. Acid NH4-oxalate extraction reduced the K/Ca CES values for all layer silicates investigated except chlorite for which the reverse was true. Selectivity of Ca and the CEC of illite were substantially increased by this treatment. The data suggested that the naturally occurring amorphous inorganic and organic constituents may have higher selectivity towards Ca relative to K. However, the degree of variation in the K/Ca CES seems to be further controlled by the amount, nature, and composition of amorphous materials and the mechanisms by which they are associated with the crystalline mineral components.

2009 ◽  
Vol 73 (3) ◽  
pp. 928-942 ◽  
Author(s):  
Christophe Tournassat ◽  
Hélène Gailhanou ◽  
Catherine Crouzet ◽  
Gilles Braibant ◽  
Anne Gautier ◽  
...  

2013 ◽  
Vol 5 (4) ◽  
Author(s):  
Nenad Tomašić ◽  
Štefica Kampić ◽  
Iva Cindrić ◽  
Kristina Pikelj ◽  
Mavro Lučić ◽  
...  

AbstractThe adsorption properties in terms of cation exchange capacity and their relation to the soil and sediment constituents (clay minerals, Fe-, Mn-, and Al-oxyhydroxides, organic matter) were investigated in loess, soil-loess transition zone, and soil at four loess-soil sections in North-Western Croatia. Cation exchange capacity of the bulk samples, the samples after oxalate extraction of Fe, Mn and Al, and after removal of organic matter, as well as of the separated clay fraction, was determined using copper ethylenediamine. Cation exchange capacity (pH∼7) of the bulk samples ranges from 5 to 12 cmolc/kg in soil, from 7 to 15 cmolc/kg in the soil-loess transition zone, and from 12 to 20 cmolc/kg in loess. Generally, CEC values increase with depth. Oxalate extraction of Fe, Mn, and Al, and removal of organic matter cause a CEC decrease of 3–38% and 8–55%, respectively, proving a considerable influence of these constituents to the bulk CEC values. In the separated clay fraction (<2 μm) CEC values are up to several times higher relative to those in the bulk samples. The measured CEC values of the bulk samples generally correspond to the clay mineral content identified. Also, a slight increase in muscovite/illite content with depth and the vermiculite occurrence in the loess horizon are concomitant with the CEC increase in deeper horizons, irrespective of the sample pretreatment.


1985 ◽  
Vol 60 (2) ◽  
pp. 264-267 ◽  
Author(s):  
H. Izawa ◽  
S. Kikkawa ◽  
M. Koizumi

1976 ◽  
Vol 48 (3) ◽  
pp. 458-464 ◽  
Author(s):  
Robert. Smits ◽  
Desire L. Massart ◽  
Jean. Juillard ◽  
Jean P. Morel

1988 ◽  
Vol 52 (366) ◽  
pp. 371-375 ◽  
Author(s):  
Sridhar Komarneni ◽  
Stephen Guggenheim

AbstractGanophyllite and [Na+ + Al3+]-substituted tobermorite exhibited similar cation exchange properties and, in particular, selective cesium exchange. [Na+ + Al3+]-substituted tobermorite and ganophyllite showed a selective Cs exchange of 10.77 and 8.71 meq/100 g from 0.02N NaCl and of 11.08 and 9.04 meq/100 g from 0.02N CaCl2, respectively. The [Na+ + Al3+]-substituted tobermorite is structurally similar to ganophyllite: both are roughly analogous to 2:1 layer silicates, both have cross-linking tetrahedra across the interlayer region, and both have exchangeable cations located in zeolite-like sites in the interlayer region. The similarities in cation exchange properties imply that the residual charge configuration of the analogue 2 : 1 layer must be approximately equivalent also.


2013 ◽  
Vol 117 (12) ◽  
pp. 6245-6251 ◽  
Author(s):  
Xinmin Liu ◽  
Hang Li ◽  
Wei Du ◽  
Rui Tian ◽  
Rui Li ◽  
...  

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