scholarly journals CORRELATIONS BETWEEN HOT CALCIUM CHLORIDE-EXTRACTED BORON AND CHEMICAL AND PHYSICAL ATTRIBUTES OF SOME BRAZILIAN SOILS

1999 ◽  
Vol 56 (2) ◽  
pp. 295-300
Author(s):  
Luís Reynaldo Ferracciú Alleoni ◽  
Otávio Antonio de Camargo ◽  
José Maria Aires Silva Valadares
Keyword(s):  
Organic Carbon ◽  
Aluminum Oxide ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Clay Content ◽  
Exchange Capacity ◽  
High Positive Correlation ◽  
Aluminum Oxides ◽  
Physical Attributes

Relationship between soluble boron extracted with a hot CaCl2 0.01 mol L-1 solution and pH; organic carbon; exchangeable cations; cation exchange capacity (CEC); base saturation; total, free and amorphous iron and aluminum oxide contents; clay content; and specific surface area were performed for surface and subsurface samples of five soils. The soils were a Rhodic Hapludox, an Arenic Paleudalf and three Typic Hapludox, all representative soils of the State of São Paulo, Brazil. To quantify the relations between soluble boron and the different soil characteristics, simple linear correlations and multiple regressions, using a stepwise regression program, were performed. Hot-CaCl2 extractable boron (HCB) was significantly correlated with clay content (r = 0.69*), specific surface area (r = 0.68*), CEC (r = 0.63*) and total aluminum oxides (r = 0.70*) in all five soils. In addition, there was a correlation between HCB and organic carbon (r = 0.75*) in the four Oxisols. The correlation coefficient between the product (carbon x clay) and soluble boron contents was also highly significant (r = 0.78**). Multiple regression analysis showed that total aluminum oxide, as well as exchangeable calcium and aluminum, were correlated with HCB, explaining 85% of the variation. The product (carbon x clay) took into account the effect of textural gradient and showed high positive correlation with hot-CaCl2 0.01 mol L-1extractable boron.

Binding of water-extractable organic carbon to clay subsoil: effects of clay subsoil properties

Soil Research ◽  
2015 ◽  
Vol 53 (1) ◽  
pp. 81 ◽  
Author(s):  
Shinhuey Lim ◽  
Trung-Ta Nguyen ◽  
Petra Marschner
Keyword(s):  
Organic Carbon ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Sandy Soils ◽  
Clay Content ◽  
Sodium Absorption ◽  
Oxide Content ◽  
Relative Importance ◽  
Water Extractable

Addition of clay-rich subsoils to sandy soils can increase yield and may increase organic carbon (OC) retention in soils. The ability of clays to bind OC is likely to be influenced by clay properties, but little is known about the relative importance of properties of clay subsoils for binding of OC. A batch sorption experiment was conducted using seven clay subsoils collected from agricultural lands where claying was carried out. Clay subsoils were shaken for 17 h at 4°C with different concentrations of water-extractable OC (WEOC: 0, 2.5, 5.0, 7.5, and 9.0 g kg–1 soil) derived from mature wheat (Triticum aestivum L.) straw at a 1 : 10 soil : extract ratio. Sorption of WEOC was positively correlated with clay content, specific surface area and concentration of iron oxides. Further, WEOC sorption was negatively correlated with total OC content, sodium absorption ratio and cation ratio of soil structural stability. However, the relative importance of these properties for WEOC sorption differed among soils. In conclusion, OC retention in clay-amended sandy soils will be positively related to clay soil properties such as clay and Fe oxide content and specific surface area.

Chemical EOR in Low Permeability Sandstone Reservoirs: Impact of Clay Content on the Transport of Polymer and Surfactant

2021 ◽  
Author(s):  
Imane Guetni ◽  
Claire Marlière ◽  
David Rousseau
Keyword(s):  
Porous Media ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Clay Content ◽  
Low Permeability ◽  
Depth Propagation ◽  
The Impact ◽  
Polymer Retention ◽  
Injection Strategies

Abstract Application of chemical enhanced oil recovery (C-EOR) processes to low-permeability sandstone reservoirs (in the 10-100 mD range) can be very challenging as strong retention and difficult in-depth propagation of polymer and surfactant can occur. Transport properties of C-EOR chemicals are particularly related to porous media mineralogy (clay content). The present experimental study aimed at identifying base mechanisms and providing general recommendations to design economically viable C-EOR injection strategies in low permeability clayey reservoirs. Polymer and surfactant injection corefloods were conducted using granular packs (quartz and clay mixtures) with similar petrophysical characteristics (permeability 70-130 mD) but having various mineralogical compositions (pure quartz sand, sand with 8 wt-% kaolinite and sand with 8 wt-% smectite). The granular packs were carefully characterized in terms of structure (SEM) and specific surface area (BET). The main observables from the coreflood tests were the resistance and residual resistance factors generated during the chemical injections, the irreversible polymer retention and the surfactant retention in various injection scenarios (polymer alone, surfactant alone, polymer and surfactant). A first, the impact of the clay contents on the retention of polymer and surfactant considered independently was examined. Coreflood results have shown that retention per unit mass of rock strongly increased in presence of both kaolinite and smectite, but not in the same way for both chemicals. For polymer, retention was about twice higher with kaolinite than with smectite, despite the fact that the measured specific surface area of the kaolinite was about 5 times less than that of the smectite. Conversely, for surfactant, retention was much higher with smectite than with kaolinite. Secondly, the impact of the presence of surfactant on the polymer in-depth propagation and retention was investigated in pure quartz and kaolinite-bearing porous media. In both mineralogies, the resistance factor quickly stabilized when polymer was injected alone whereas injection of larger solution volumes was required to reach stabilization when surfactant was present. In pure quartz, polymer retention was shown, surprisingly, to be one order of magnitude higher in presence of surfactant whereas with kaolinite, surfactant did not impact polymer retention. The results can be interpreted by considering adsorption-governed retention. The mechanistic pictures being that (a) large polymer macromolecules are not able to penetrate the porosity of smectite aggregates, whereas surfactant molecules can, and (b) that surfactant and polymer mixed adsorbed layers can be formed on surfaces with limited affinity for polymer. Overall, this study shows that C-EOR can be applied in low permeability reservoirs but that successful injection strategies will strongly depend on mineralogy.

scholarly journals Boron adsorption in soils from the State of São Paulo, Brazil

2000 ◽  
Vol 35 (2) ◽  
pp. 413-421 ◽  
Author(s):  
LUÍS REYNALDO FERRACCIÚ ALLEONI ◽  
OTÁVIO ANTONIO DE CAMARGO
Keyword(s):  
Aluminum Oxide ◽  
Correlation Coefficients ◽  
Clay Content ◽  
Sao Paulo ◽  
The State ◽  
São Paulo ◽  
Aluminum Oxides ◽  
Freundlich Isotherms ◽  
Physical Attributes ◽  
Boron Adsorption

Boron adsorption was studied in five representative soils (Rhodic Hapludox, Arenic Paleudalf and three Typic Hapludox) from the State of São Paulo, Brazil. Adsorption was higher in the clayey Oxisols, followed by the Alfisol and the coarser Oxisols. Calcium carbonate promoted an increase in the amount of adsorbed boron in all soils, with the most pronounced effect in the coarser-textured Oxisols. High correlation coefficients were found between adsorbed boron and clay and amorphous aluminum oxide contents and specific surface area (r = 0.79, 0.76 and 0.73, respectively, p < 0.01). Clay content, free aluminum oxide, and hot CaCl2 (0.01 mol L-1)-extracted boron explained 93% of the variation of adsorbed boron. Langmuir and Freundlich isotherms fitted well to the adsorbed data, and highest values for maximum boron adsorption were found in clayey soils, which were significantly correlated with contents of total, free and amorphous iron and aluminum oxides, as well with the physical attributes. Ninety four percent of the variation in the maximum adsorption could be related to the free iron content.

Mineralogical study of clays from Dobrodo, Serbia, for use in ceramics

Clay Minerals ◽  
2019 ◽  
Vol 54 (4) ◽  
pp. 369-377 ◽  
Author(s):  
Maja Milošević ◽  
Predrag Dabić ◽  
Sabina Kovač ◽  
Lazar Kaluđerović ◽  
Mihovil Logar
Keyword(s):  
Specific Surface ◽  
Cation Exchange ◽  
Surface Area ◽  
Specific Surface Area ◽  
Cation Exchange Capacity ◽  
Mineralogical Composition ◽  
Exchange Capacity ◽  
Mineralogical Characterization ◽  
Mineralogical Study

AbstractThis study focuses on the mineralogical characterization of four raw clay samples from Dobrodo deposit, Serbia. Several analytical methods were applied to determine the chemical and mineralogical composition, morphology and physical properties (colour, plasticity, specific surface area, particle size and cation-exchange capacity) of the clay samples. Kaolinite, smectite and illite are the predominant phases in all of the samples studied that contain between 60.2 and 87.1 wt.% of clay. Quartz, feldspars, paragonite and Ti- and Fe-bearing phases were also identified. The relatively high SiO2/Al2O3 mass ratio indicates abundant quartz. The cation-exchange capacity of the samples varied between low and moderately charged clay minerals (12–52 mmol 100 g–1) with specific surface area values ranging from 94 to 410 m2 g–1. The plasticity index values (11–23%) suggest low to moderate plasticity. Preliminary results show that most of the raw clay from Dobrodo deposit might be suitable for use in ceramic applications.

scholarly journals Determination of soil specific surface area by water vapor adsorption: II Dependence of soil specific surface area on clay and organic carbon content

1987 ◽  
Vol 59 (2) ◽  
pp. 67-72
Author(s):  
Raina Niskanen ◽  
Väinö Mäntylahti
Keyword(s):  
Water Vapor ◽  
Organic Carbon ◽  
Specific Surface ◽  
Carbon Content ◽  
Surface Area ◽  
Specific Surface Area ◽  
Mineral Soil ◽  
Water Vapor Adsorption ◽  
Organic Carbon Content ◽  
Vapor Adsorption

The specific surface area of 60 mineral soil samples estimated by water vapor adsorption at 20 % relative humidity ranged from 12.1 ± 3.6 to 225.1 ±18.4 m2/g. Clay (range 1—72 %) and organic carbon content (0.7—14.6 %) together explained 84 % of the variation in the surface area. The regression equation predicting the specific surface area of soil was surface area (m2/g) =2.69+ 1.23clay-% +8.69org.C-%.

scholarly journals Analysis of the sorption properties of different soils using water vapour adsorption and potentiometric titration methods

2016 ◽  
Vol 30 (3) ◽  
pp. 369-374 ◽  
Author(s):  
Kamil Skic ◽  
Patrycja Boguta ◽  
Zofia Sokołowska
Keyword(s):  
Specific Surface ◽  
Cation Exchange ◽  
Surface Charge ◽  
Surface Area ◽  
Water Vapour ◽  
Potentiometric Titration ◽  
Specific Surface Area ◽  
Cation Exchange Capacity ◽  
Exchange Capacity ◽  
Sorption Properties

Abstract Parameters of specific surface area as well as surface charge were used to determine and compare sorption properties of soils with different physicochemical characteristics. The gravimetric method was used to obtain water vapour isotherms and then specific surface areas, whereas surface charge was estimated from potentiometric titration curves. The specific surface area varied from 12.55 to 132.69 m2 g−1 for Haplic Cambisol and Mollic Gleysol soil, respectively, and generally decreased with pH (R=0.835; α = 0.05) and when bulk density (R=−0.736; α = 0.05) as well as ash content (R=−0.751; α = 0.05) increased. In the case of surface charge, the values ranged from 63.00 to 844.67 μmol g−1 Haplic Fluvisol and Mollic Gleysol, respecively. Organic matter gave significant contributions to the specific surface area and cation exchange capacity due to the large surface area and numerous surface functional groups, containing adsorption sites for water vapour molecules and for ions. The values of cation exchange capacity and specific surface area correlated linearly at the level of R=0.985; α = 0.05.

scholarly journals The relationship between the liquid limit of clayey soils, external specific surface area and the composition of exchangeable cations / Zależność granicy płynności od zewnętrznej powierzchni właściwej i składu kationów w naturalnym kompleksie wymiennym

2012 ◽  
Vol 17 (1) ◽  
pp. 83-88 ◽  
Author(s):  
Andrzej Olchawa ◽  
Aleksandra Gorączko
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
External Surface ◽  
Exchange Capacity ◽  
Liquid Limit ◽  
Sodium Cation ◽  
Exchangeable Cations ◽  
Clayey Soils ◽  
External Surface Area

Abstract The liquid limit - wL, the external surface area - Se, the concentration of exchangeable cations - Zi and the cation exchange capacity - CEC of seventeen clayey soils were determined. Finding the correlation between the liquid limit, external specific surface area and exchangeable cation concentration was the aim of this study. Experimental study performed using soils of the external surface area within the range of 4.1 to 118.5 m2·g-1. The relative content of sodium cation (i.e. Na+/CEC) varying between 0.03 and 1.0. Obtained results point to statistically significant relationship between these three properties. The greatest predictive power of linear regression was found for soils of external specific surface area larger than 60 m2·g-1. For the soils of comparable external surface area, the liquid limit increase with increasing the ratio of the content of sodium cation to the cation exchange capacity - Na+/CEC. For the soils of comparable composition of exchangeable cations the liquid limit increase with increasing the external surface area. These relationships indicates that interparticle forces have a prominent role in determining liquid limit of clayey soils.

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