Acid Character of Sauconite: Increase in Cation Exchange Capacity on Aging in Water and the Role of Zn2+ and Al3+ Ions

1971 ◽  
Vol 19 (6) ◽  
pp. 391-397 ◽  
Author(s):  
R. P. Mitra
Clay Minerals ◽  
1972 ◽  
Vol 9 (4) ◽  
pp. 425-433
Author(s):  
B. S. Kapoor

AbstractThe cation exchange capacity (C.E.C.) of nontronite was determined by titrating the acid clay, prepared by the action of H-resin on nontronite, in water and some nonaqueous solvents. The base-titratable acidities of the acid nontronite, freshly prepared as well as aged, were found to be greater than the acidities extractable with 1 N NaCl; the difference was attributed to the non-exchangeable pH-dependent component of C.E.C. In the freshly prepared sample, H+ and Fe3+ ions were the only exchangeable cations. Ageing produced basic Fe ions which were exchangeable and whose amount increased at the cost of H− and Fe3+ ions. Whatever the age, the total quantity of these exchangeable cations corresponding to the total isomorphous charge, remained constant. The amount of the pH-dependent acidity also remained unchanged. A likely mechanism to account for the observed pH-dependent component of the C.E.C, of nontronite is suggested.


2007 ◽  
Vol 121-123 ◽  
pp. 1245-1248 ◽  
Author(s):  
Eglantina Benavente ◽  
Yuri Echeverría ◽  
Vladimir Lavayen ◽  
Clivia M. Sotomayor Torres ◽  
G. Gonzáles

The intercalation of [Eu(2,2 bipyridine)2 ]3+ and [Eu(1,10 phenantroline)2]3+ into bentonite results in new nanocomposites which preserve the emission properties of the lanthanide. The exchange of sodium by lanthanide in the bentonite correlates with the host cation exchange capacity as well as with the guest molecular size and the interlaminar volume available in the clay. The intercalated complexes exhibit luminescence indicating an efficient protecting role of the matrix. This in turn points to lanthanide-clay nanocomposite as novel optical materials.


Holzforschung ◽  
2000 ◽  
Vol 54 (6) ◽  
pp. 591-596 ◽  
Author(s):  
G. Staccioli ◽  
A. Meli ◽  
G. Menchi ◽  
U. Matteoli ◽  
G. Ricottini

Summary Fossil samples of Pinus sylvestris found near Siena (Tuscany, Italy) in geological formations 2–3 million years old were chemically examined in order to solve the problem of the contrast between the age of geological formations and their good degree of preservation. Comparison with a living Pinus sylvestris was carried out on standard wood component analyses, cation exchange capacity and residual terpene content. The analyses of wood components were close to those of the reference pine, whilst the cation exchange capacity values showed remarkable changes. The increase of salt carboxyls suggested the hydrolysis of ester carboxyls originally present, whilst the reduction of total carboxyls revealed a partial loss of hemicelluloses. Both changes were attributed to the percolation of salt-bearing water through the wood, thus causing ester hydrolysis, carboxyl salification and hemicellulose solubilisation. Residual terpene analysis showed, for the first time in a terrestrial fossil, tetrahydroabietic acid which forms by disproportion of the abietic acid. The 14C dating assigned the fossil to an age of about 18,000 years and suggested a landslide of Wurmian interglacial age occurred inside the geological formations of 2–3 million years old. Transient terpene compounds, formed in incipient diagenesis, are proposed as tracers for the assessment of particular ranges of fossil age, as previously suggested by the analyses of both a Larix decidua 14,500 years old and a Picea abies 100,000 years


Geophysics ◽  
1973 ◽  
Vol 38 (6) ◽  
pp. 1181-1181
Author(s):  
A. E. Worthington

The purpose of this paper is to make available a practical, rapid, relatively inexpensive, and reasonably accurate method of measuring cation exchange capacity (CEC) of oil‐field rocks. There is no dearth of sound, detailed descriptions of how this information should be used by explorationists to enhance their ability to interpret resistivity and SP logs in shaly sands (see references in Introduction). Waxman and Thomas (1972) have subsequently published additional information on the application to oil‐saturated shaley sands. Smits (1969) has confirmed the role of CEC in shales, a matter not considered in this paper.


2013 ◽  
Vol 12 (3) ◽  
pp. 248-255

A High Cation Exchange Capacity (HCM) montmorillonite clay has been prepared by acetate treatment of Zenith clay. The HCM has been evaluated for metal-uptake from aqueous solutions. The present data show that the cation exchange sites can play a significant role in the adsorption of metals in smectite clays. A theoretical analysis scheme has been developed which shows that permanent-charge sites can become dominant in metal-uptake by clays. In addition, it was shown that the permanent charge can influence the ionic-strength sensitivity of the Point of Zero Charge of the clay.


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