A lithium-bearing aluminian regular mixed layer montmorillonite-chlorite from Huy, Belgium

Clay Minerals ◽  
1974 ◽  
Vol 10 (3) ◽  
pp. 135-144 ◽  
Author(s):  
G. Brown ◽  
P. Bourguignon ◽  
J. Thorez
Keyword(s):  
Mixed Layer ◽  
Cation Exchange Capacity ◽  
Structural Formula ◽  
Exchange Capacity ◽  
X Ray Diffraction ◽  
X Ray ◽  
Saturated Clay ◽  
Bluish Green ◽  
Image Position ◽  
Green Clay

AbstractA bluish-green clay found in veins cutting across brecciated slates of the Llanvirnian stage at Huy, Belgium, is shown by X-ray diffraction and chemical analysis to be a lithium-bearing, aluminium-rich, regular mixed layer montmorillonite-chlorite with associated pyrophyllite, nacrite and quartz and smaller amounts of calcite and ankerite. The cation exchange capacity of the purified air-dry magnesium saturated clay is 49 mEq/100 g and its structural formula isThe problem of the nomenclature of regular mixed layer montmorillonite-chlorites is discussed.

SEM, XRF, XRD, Nitrogen Adsorption, Fosters Swelling and Capacity Adsorption Characterization of Cloisite 30 B

2012 ◽  
Vol 727-728 ◽  
pp. 1591-1595 ◽  
Author(s):  
Aline Cadigena Lima Patrício ◽  
Marcílio Máximo da Silva ◽  
Anna Karoline Freires de Sousa ◽  
Mariaugusta Ferreira Mota ◽  
Meiry Glaúcia Freire Rodrigues
Keyword(s):  
Quaternary Ammonium ◽  
Cation Exchange Capacity ◽  
Nitrogen Adsorption ◽  
Exchange Capacity ◽  
X Ray Diffraction ◽  
Oil And Grease ◽  
X Ray ◽  
Quaternary Ammonium Cations ◽  
Cloisite 30B

Cationic surfactants, such as quaternary ammonium cations, have been used, in order to ameliorate the oil sorption capacity of inorganics materials, such as clays. Clays modified with quaternary ammonium cations (organoclays) have better performance in sorption, remove oil and grease from water at seven times the rate of activated carbon, as well as they can be used like perforation fluids of oil wells to the oil base, lubricants, among others industries. This work aims characterize the Cloisite 30B using various techniques: X-Ray Diffraction (XRD), Specific Surface Area (BET) and Cation Exchange Capacity. Different organic solvents, namely gasoline, diesel and kerosene were used in order to investigate the clays compatibility after orgophilization.

Physico-Mineralogical Characterization: Bentonitic Clays Recently Found in Olivedos, Paraíba, Brazil

2015 ◽  
Vol 820 ◽  
pp. 56-59
Author(s):  
F.K.A. Sousa ◽  
I.A. Silva ◽  
W.S. Cavalcanti ◽  
Gelmires Araújo Neves ◽  
Heber Carlos Ferreira
Keyword(s):  
Cation Exchange Capacity ◽  
Petroleum Industry ◽  
Specific Area ◽  
Exchange Capacity ◽  
X Ray Diffraction ◽  
Mineralogical Characterization ◽  
X Ray ◽  
Petroleum Wells ◽  
The Town

Used in various branches of the industry, bentonitic clays are considered a valuable mineral, used specially in the petroleum industry for manufacturing of fluids used the drilling of petroleum wells in long depth. Recently, a deposit of this valuable mineral was discovered in the town of Olivedos-PB. There are data that prove that this is a very poor and underdeveloped town. So, this work aims at the physico-mineralogical characterization of clays recently discovered and, this way, verify if they present similar characteristics which allow them to replace the clays from Boa Vista-PB, and if they can be used by the industry, thus bringing social development for that town. The characterization was made by means of the analysis of chemical composition by X-ray fluorescence (EDX), thermogravimetric and thermal differential analyses (TG and DTA), X-ray diffraction (XRD), cation-exchange capacity (CEC) and specific area (SA). The results show that the clays recently discovered in Olivedos-PB are polycationic clays, presenting MgO, CaO and K2O content, and that they are constituted by smectitic clay mineral, by quartz and kaolinite.

Alteration of smectites induced by hydrolytic exchange

Clay Minerals ◽  
2005 ◽  
Vol 40 (1) ◽  
pp. 15-24 ◽  
Author(s):  
S. Ramirez ◽  
D. Righi ◽  
S. Petit
Keyword(s):  
Infrared Spectroscopy ◽  
Cation Exchange ◽  
Cation Exchange Capacity ◽  
Relative Increase ◽  
Exchange Capacity ◽  
Capacity Analysis ◽  
Soluble Salts ◽  
X Ray Diffraction ◽  
X Ray ◽  
Mixed Layers

AbstractHydrolytic exchange was performed experimentally on four smectitic clays to evaluate the extent of clay alteration induced by this process and the associated ‘auto-transformation’ of H+ clays. Clay samples were Na-saturated and submitted to 10, 50 and 100 wetting-drying (WD) cycles and characterized after treatment using X-ray diffraction (XRD), infrared spectroscopy (FTIR) and cation exchange capacity analysis. Evidence for hydrolytic exchange was given by increasing amounts of exchangeable Mg2+ and precipitation of Na soluble salts for samples subjected to 100 WD cycles. Results indicated a decrease in the interlayer charge after 10 WD cycles but no further decrease was observed after 50 and 100 WD cycles. For one sample, XRD data indicated a decrease in the proportion of the smectite phase and a relative increase in the concentration of illite-smectite mixed layers also present in the sample. The results suggested that the reaction induces first a decrease in the layer charge and then a partial dissolution of some smectite layers.

scholarly journals Characterisation of Natural and HDTMA-Br Modified Dijah-Monkin Bentonite Clay: FTIR, XRF, XRD and SEM

2021 ◽  
Vol 7 (5) ◽  
pp. 2010-2018
Author(s):  
Olukayode Gideon Oloyede ◽  
◽  
Umar Omeiza Aroke ◽  
Saidat Olanipekun Giwa ◽  
Alexander Asanja Jock ◽  
...  
Keyword(s):  
Cation Exchange Capacity ◽  
Bentonite Clay ◽  
Exchange Capacity ◽  
Basal Spacing ◽  
Hexadecyltrimethylammonium Bromide ◽  
Acid Activation ◽  
X Ray Diffraction ◽  
X Ray ◽  
North East ◽  
Scanning Electron

In this study, Dijah-Monkin bentonite clay was modified with a cationic surfactant hexadecyltrimethylammonium bromide (HDTMA-Br) at the level of twice the cation exchange capacity (CEC). This process results in the development of hydrophobic organoclay with an improved adsorption capacity. The clay obtained from Zing LGA Taraba State, North-East Nigeria, was beneficiated and pulverised to a particle size of 125 µm. The modification was performed without acid activation to prevent damages to the clay’s crystal structure. The organoclay was characterised for chemical composition, functional groups, mineralogical and surface morphology using X-ray fluorescence (XRF), Fourier Transform Infrared (FTIR) spectroscopy, X-ray diffraction (XRD) and scanning electron microscopy (SEM), respectively. The XRD showed an increase in the basal spacing from 15.681Å to 17.758 Å, while the XRF revealed a 5.35% concentration of Br on the modified clay, indicating successful intercalation. The FTIR spectra also revealed the appearance of symmetric and asymmetric stretching bands at 2847.7cm-1 and 2914.8cm-1, respectively, as a consequence of the modification, resulting in more sites for adsorption.

scholarly journals Study On The Performance Of Carbonate-Mineralized Bacteria Combined With Eggshell For Immobilizing Pb and Cd in Water And Soil

2021 ◽  
Author(s):  
Ting Wei ◽  
Noman Yashir ◽  
Fengqiu An ◽  
Syed Asad Imtiaz ◽  
Xian Li ◽  
...  
Keyword(s):  
Cation Exchange Capacity ◽  
Exchange Capacity ◽  
Contaminated Water ◽  
Carbonate Precipitation ◽  
Bacterial Isolates ◽  
X Ray Diffraction ◽  
X Ray ◽  
Soil Enzymatic Activity ◽  
Microbially Induced Carbonate Precipitation ◽  
Eggshell Waste

Abstract Microbially induced carbonate precipitation (MICP) is an advanced bioremediation approach to remediate heavy metals (HMs) contaminated water and soil. In this study, metal tolerant urease-producing bacterial isolates, namely UR1, UR16, UR20 and UR21, were selected based on their urease activity. The efficiency of these isolates in water for Pb and Cd immobilization was explored. Our results revealed that UR21 had the highest removal rates of Pb (81.9%) and Cd (65.0%) in solution within 72 h through MICP. The scanning electron microscopy-energy dispersive x-ray and x-ray diffraction analysis confirmed the structure and the existence of PbCO3 and CdCO3 crystals in the precipitates. In addition, the strain UR21, in combination with urea/eggshell waste (EGS) or both, was further employed to investigate the effect of MICP on soil enzymatic activity, chemical fractions and bioavailability of Pb and Cd. The outcomes indicated that the applied treatments reduced the proportion of soluble-exchangeable Pb and Cd, resulted an increment in carbonated bound Pb and Cd in the soil. The DTPA extractable Pb and Cd was reduced by 29.2% and 25.2% with the treatment of UR21 + urea + EGS as compared to the control. Besides, the application of UR21 and EGS significantly increased the soil pH, cation exchange capacity, and enzyme activities. Our findings may provide a novel perceptive for an eco-friendly and sustainable approach to remediate heavy metal contaminated environment through a combination of metal-resistant ureolytic bacterial strain and EGS.

Inhibition of Ribonuclease Activity by Bentonite

1973 ◽  
Vol 51 (11) ◽  
pp. 1558-1565 ◽  
Author(s):  
G. G. Jacoli ◽  
W. P. Ronald ◽  
L. Lavkulich
Keyword(s):  
Cation Exchange Capacity ◽  
Protein Molecule ◽  
Exchange Capacity ◽  
Ribonuclease Activity ◽  
X Ray Diffraction ◽  
Tertiary Structures ◽  
Similar Treatment ◽  
X Ray ◽  
Denatured Protein ◽  
Clay Matrix

The inhibition of ribonuclease activity by bentonite and the adsorption of the protein molecule within the clay matrix were assessed by enzyme and X-ray diffraction analysis, respectively.Pretreatment of bentonite with EDTA, potassium, barium, and barium–EDTA caused varying expansion of the d(001) spacing of the clay. The d(001) variation was sensitive to pH.Inhibition of the enzyme activity generally followed the pattern of expansion of the d(001) spacing of the clay, but failed when the interlayers of bentonite expanded beyond their maximum capability.Vermiculite, which is a clay having a higher cation exchange capacity than bentonite, did not expand from the normal state after similar treatment nor did it inhibit ribonuclease activity.When the secondary and tertiary structures of the protein molecule were disrupted, the denatured protein still entered the interlayers of bentonite, but caused a greater expansion of the d(001) spacing than the native ribonuclease.

scholarly journals Composition variation of illite-vermiculitesmectite mixed-layer minerals in a bentonite bed from Charente (France)

Clay Minerals ◽  
2004 ◽  
Vol 39 (3) ◽  
pp. 317-332 ◽  
Author(s):  
A. Meunier ◽  
B. Lanson ◽  
B. Velde
Keyword(s):  
Cation Exchange Capacity ◽  
Exchange Capacity ◽  
X Ray Diffraction ◽  
X Ray ◽  
Hydration Behaviour ◽  
Composition Variation ◽  
Ash Layer ◽  
Diffraction Patterns ◽  
Aquitaine Basin ◽  
Low Charge

AbstractMineralogical and chemical variations were studied in the upper half of a 1 m thick discontinuous bentonite bed interlaminated in the Lower Cenomanian sedimentary formations of the northern Aquitaine basin (France). X-ray diffraction patterns obtained from the <2 mm fraction in the Ca and K-saturated states were decomposed and compared to those calculated from decomposition parameters. They revealed the presence of two highly expandable illite-expandable (I-Exp) mixedlayer minerals (MLMs). The relative proportions of the two MLMs evolve steadily with depth leading to the decrease of the cation exchange capacity and of the (Na + Ca) content towards the centre of the bentonite bed. However, the system is essentially isochemical and Mg, Al, Si, K and Fe are roughly constant in the bulk samples. It is thought that the mineralogical zonation results from the initial stages of the smectite formation in an ash layer.In the Ca-saturated state, the expandable component of these MLMs was for the most part homogeneous with the presence of 2 sheets of ethylene glycol molecules in the interlayer. However, the heterogeneous hydration behaviour of these expandable layers was enhanced by the K-saturation test. From this test, the presence of three layer types with contrasting layer charge was evidenced from their contrasting swelling abilities. The C12-alkylammonium saturation test applied to samples in which the octahedral charge had previously been neutralized (Hofmann-Klemen treatment) showed that the tetrahedral charge is located on specific layers. These layers are responsible for the heterogeneous hydration behaviour. Low-charge smectite layers are mostly octahedrally substituted, whereas for intermediate- and high-charge layers this montmorillonitic charge is complemented by additional tetrahedral substitutions (0.30 and 0.35–0.40 charge per O10(OH)2, respectively).

Adsorption Removal of Ni(II) from Aqueous Solution by Raw and Acid-Activated Kaolinite

2013 ◽  
Vol 781-784 ◽  
pp. 2269-2272 ◽  
Author(s):  
Shi Yong Wei ◽  
Xu Hong Deng
Keyword(s):  
Cation Exchange Capacity ◽  
Negative Charge ◽  
Physical Adsorption ◽  
Exchange Capacity ◽  
Langmuir Model ◽  
Batch Adsorption ◽  
X Ray Diffraction ◽  
X Ray ◽  
Adsorption Removal ◽  
Adsorption Data

X-ray diffraction (XRD), scanning electron microscopy (SEM), nitrogen physical adsorption, potentiometric titrations and batch adsorption experiments were employed to characterize the crystal structure, micromorphologies and surface properties of raw kaolinite (RKao) and acid-activated kaolinite (AAKao). Compared to RKao, the particle size of AAKao became smaller, but the specific surface area (SSA), cation exchange capacity (CEC) and surface negative charge at pH 5.5 increased. The adsorption capacity (qmax) for Ni (II) of RKao and AAKao was 3.25 mg/g and 5.09 mg/g, respectively. The adsorption data for Ni (II) by RKao and AAKao could be fitted by Langmuir model (R2 =0.991 and 0.989, respectively).

The crystal structure of a pyridine-vermiculite complex

Clay Minerals ◽  
1967 ◽  
Vol 7 (2) ◽  
pp. 145-153 ◽  
Author(s):  
K. Susa ◽  
H. Steinfink ◽  
W. F. Bradley
Keyword(s):  
Cation Exchange Capacity ◽  
Three Dimensional ◽  
Exchange Capacity ◽  
Water Molecules ◽  
Hydrogen Ions ◽  
X Ray Diffraction ◽  
Difference Electron Density ◽  
Cell Water ◽  
X Ray ◽  
Density Maps

AbstractA pyridine-vermiculite complex has been investigated by three dimensional X-ray diffraction techniques. The preparation of the complex was carried out at a pH ∼ 4 using a solution of pyridinium hydrochloride. Exsolved magnesium from the octahedral positions satisfied approximately one-half of the cation exchange capacity. The rest of the exchange capacity is satisfied by hydrogen ions and pyridinium ions which are statistically distributed over crystallographic sites so that less than three electrons per Å3 are present at any given point. Three dimensional difference electron density maps did not locate the carbon atoms except to indicate that the organic molecule occupies positions in the true and in the two pseudo mirror planes in the unit cell. Water molecules were present in the interlayer in octahedral arrangement around the cation as in the natural mineral.

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