Lahcen Daoudi

Elucidating the crystal-chemistry of Jbel Rhassoul stevensite (Morocco) by advanced analytical techniques

Abstract The composition of Rhassoul clay is controversial regarding the nature of the puremineral clay fraction which is claimed to be stevensite rather than saponite. In this study, the raw and mineral fractions were characterized using various techniques including Fourier transform infrared spectroscopy and magic angle spinning nuclear magnetic resonance (MAS NMR). The isolated fine clay mineral fraction contained a larger amount of Al (>1 wt.%) than that reported for other stevensite occurrences. The 27Al MAS NMR technique confirmed that the mineral is stevensite in which the Al is equally split between the tetrahedral and octahedral coordination sites. The 29Si NMR spectrum showed a single unresolved resonance indicating little or no short-range ordering of silicon. The chemical composition of the stevensite from Jbel Rhassoul was determined to be ((Na0.25K0.20)(Mg5.04Al0.37Fe0.20⃞0.21)5.61(Si7.76Al0.24)8O20(OH)4). This formula differs from previous compositions described from this locality and shows it to be an Al-bearing lacustrine clay mineral.

MINERALOGICAL AND PHYSICO-CHEMICAL CHARACTERIZATIONS OF FERRUGINOUS BEIDELLITE-RICH CLAY FROM AGADIR BASIN (MOROCCO)

The mechanism of formation of detrital, beidellite-rich clay occurring in the Agadir basin (Morocco) is well documented, but its detailed characterization is incomplete which limits its application. The aim of the present study was to provide further details of the mineralogical and physico-chemical characteristics of this clay. Bulk raw clay and its Na+-saturated, <2 μm fraction were characterized using chemical, structural, and thermal techniques. Measurements of induced streaming potential (e.g. particle charge) and of specific surface area and porous volume are reported. The raw clay contained carbonate and quartz as associated minerals along with phyllosilicates (<2 μm particle size). X-ray diffraction and scanning electron microscopy analyses showed that the <2 μm fraction was dominated by a dioctahedral smectite. Because dehydroxylation of this mineral occurred at 510°C, and because it re-expanded in ethylene glycol after Li+-saturation followed by heating at 240°C for 24 h, the mineral was shown to be a beidellite rather than montmorillonite. This assertion was further supported by 27Al and 29Si magic-angle spinning nuclear magnetic resonance spectra showing predominantly negative charges in the tetrahedral sheets due to notable Al-for-Si substitutions. The chemical composition of the <2 μm fraction showed an Fe2O3 content which was ~7.52 wt.% greater than those of other beidellite occurrences but not so much that it would be identified as a nontronite. The absence of stretching and bending absorption bands corresponding to characteristic (Fe2OH) units in mid-infrared spectra and their corresponding fundamental overtones or combination bands in near-infrared spectra supported this notion. The structural formula of the beidellite in the present study was determined to be (Si7.51Al0.49)(Al2.99Fe0.68Mg0.33) (Ca0.03Na0.54Mg0.11)O20(OH)4, having dioctahedral ferruginous characteristics with almost 60% of the negative charge found in tetrahedral sheets. The cation exchange capacity determined from the structural formula was ~108 meq/100 g. The specific surface area and total pore volume were ~82.2 m2/g and 0.136 cm3/g, respectively. Interestingly, a detrital rather than a hydrothermal-alteration origin, as reported for other beidellite occurrences, explains its natural abundance and emphasizes the great interest in it.

Occurrences and genesis of palygorskite/sepiolite and associated minerals in the Barzaman formation, United Arab Emirates

Abstract The Barzaman Formation exposed in the United Arab Emirates was deposited as a series of fluvial sediment sequences lying along the western margin of the Hajar Mountains, part of the Oman-UAE ophiolite. This formation consists of a sequence of rocks dominated by variably cemented and altered conglomerates comprising calcareous siltstones and calcareous clays deposited during the Miocene to Pliocene under a humid climate. The conglomerates are composed largely of ultramafic and lesser-mafic clasts. The present study was undertaken in order to understand the occurrence and genesis of palygorskite and sepiolite in relation to the environmental changes including evaporitic and sabkha environments. Sediments were collected from two trenches and a drill hole of ∼22 m depth. Samples were analysed by optical petrograpy, X-ray diffraction and scanning electron microscopy. Pedogenesis occurred at the deeper level in well cemented conglomerate which constitutes the hard crust. Post-depositional erosion started in marine phreatic or vadose zones as shown by the neoformation of serpentine from the weathering of olivine as well as of calcite and dolomite. Neoformation of palygorskite, sepiolite, dolomite and halite occurred under evaporitic conditions on calcareous silty clay facies. Relatively hot, vadose and oxidizing environmental conditions affected the calcareous siltstone facies leading to the genesis of dolomite and palygorskite by direct precipitation from solution rich in Ca, Mg, Al, Fe and Si ions.

Clays and Clay Minerals in Western High Atlas: Characterization, Geological Significance and Industrial Uses

In the area of the western High Atlas, the clay formations are very abundant and much diversified. However, the use of clays in industry is still very restricted and the industrial exploitation remains insufficient. The Triassic detrital formations provide the most developed and representative outcrops of clays of the area; they were exploited formerly for the industry of the terra cotta. In the Jurassic-Cretaceous series, the clay assemblage evolution shows a very important geographical and stratigraphical variation. However, because of their low content in the sediments, clays are mainly exploited in the industry of cements. In the Tertiary series, when fibrous minerals characterize the clay fraction of the Palaeocene-Eocene formations, semectites are the most abundant mineral during the Miopliocene. These clay materials have been used since ancient times for cottage industry. The Quaternary continental formations present a clay fraction dominated by the illite and sometimes by kaolinite or smectite. The industrial exploitation of these clays is the most significant in the area. They are especially used in cottage industry and in the industry of the bricks.