Aluminium distribution in soils in relation to surface area and cation exchange capacity

Geoderma ◽  
1971 ◽  
Vol 5 (4) ◽  
pp. 255-260 ◽  
Author(s):  
D.T. Pritchard
Materials ◽  
2021 ◽  
Vol 14 (10) ◽  
pp. 2617
Author(s):  
Alicja Szatanik-Kloc ◽  
Justyna Szerement ◽  
Agnieszka Adamczuk ◽  
Grzegorz Józefaciuk

Thousands of tons of zeolitic materials are used yearly as soil conditioners and components of slow-release fertilizers. A positive influence of application of zeolites on plant growth has been frequently observed. Because zeolites have extremely large cation exchange capacity, surface area, porosity and water holding capacity, a paradigm has aroused that increasing plant growth is caused by a long-lasting improvement of soil physicochemical properties by zeolites. In the first year of our field experiment performed on a poor soil with zeolite rates from 1 to 8 t/ha and N fertilization, an increase in spring wheat yield was observed. Any effect on soil cation exchange capacity (CEC), surface area (S), pH-dependent surface charge (Qv), mesoporosity, water holding capacity and plant available water (PAW) was noted. This positive effect of zeolite on plants could be due to extra nutrients supplied by the mineral (primarily potassium—1 ton of the studied zeolite contained around 15 kg of exchangeable potassium). In the second year of the experiment (NPK treatment on previously zeolitized soil), the zeolite presence did not impact plant yield. No long-term effect of the zeolite on plants was observed in the third year after soil zeolitization, when, as in the first year, only N fertilization was applied. That there were no significant changes in the above-mentioned physicochemical properties of the field soil after the addition of zeolite was most likely due to high dilution of the mineral in the soil (8 t/ha zeolite is only ~0.35% of the soil mass in the root zone). To determine how much zeolite is needed to improve soil physicochemical properties, much higher zeolite rates than those applied in the field were studied in the laboratory. The latter studies showed that CEC and S increased proportionally to the zeolite percentage in the soil. The Qv of the zeolite was lower than that of the soil, so a decrease in soil variable charge was observed due to zeolite addition. Surprisingly, a slight increase in PAW, even at the largest zeolite dose (from 9.5% for the control soil to 13% for a mixture of 40 g zeolite and 100 g soil), was observed. It resulted from small alterations of the soil macrostructure: although the input of small zeolite pores was seen in pore size distributions, the larger pores responsible for the storage of PAW were almost not affected by the zeolite addition.


Clay Minerals ◽  
2013 ◽  
Vol 48 (2) ◽  
pp. 343-361 ◽  
Author(s):  
M. Valter ◽  
M. Plötze

AbstractBentonite is a potential material for use in the engineered barrier of radioactive waste repositories because of its low hydraulic permeability, self-sealing capability and retention capacity. It is expected that bentonite would react at the elevated temperatures accompanying the radioactive decay in the nuclear waste. The presented study was started in order to improve understanding of the coupled influence of temperature and (pore) water on the physicochemical and mineralogical properties of bentonite during thermal treatment under near-field relevant conditions. Granular Na-bentonite MX-80 was differently saturated (Sr = 1–0.05) and stored at different temperatures (50–150°C) in a closed system. Upon dismantling after different periods of time (3 to 18 months), mineralogical characteristics, cation exchange capacity and content of leachable cations, as well as physicochemical properties such as surface area and water adsorption were investigated.The results showed a high mineralogical stability. A slight conversion from the sodium to an earth alkali form of the bentonite was observed. However, considerable changes in the physicochemical properties of the bentonite were observed, particularly by treatment above the critical temperature of 120°C. The cation exchange capacity decreased during heating at 150°C by approximately. 10%. The specific surface area dropped by more than 50%. The water uptake capacity under free swelling conditions showed a slight tendency to lower values especially for samples heated for more than 12 months. The water vapour adsorption ability in contrast drops by 25% already within three months at T = 120°C. These changes are mostly related to the variations in the interlayer cation composition and to smectite aggregation processes. The observed alterations are rather subtle. However, temperatures ⩾ 120°C had a remarkable negative influence on different properties of MX-80.


Clay Minerals ◽  
2019 ◽  
Vol 54 (4) ◽  
pp. 369-377 ◽  
Author(s):  
Maja Milošević ◽  
Predrag Dabić ◽  
Sabina Kovač ◽  
Lazar Kaluđerović ◽  
Mihovil Logar

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.


2016 ◽  
Vol 30 (3) ◽  
pp. 369-374 ◽  
Author(s):  
Kamil Skic ◽  
Patrycja Boguta ◽  
Zofia Sokołowska

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.


1966 ◽  
Vol 12 (6) ◽  
pp. 1235-1246 ◽  
Author(s):  
G. Stotzky

The stimulation of bacterial respiration by clay minerals was related to certain physicochemical characteristics of clays. Respiration increased with an increase in the cation exchange capacity and surface area of the particles. The importance of surface area, however, could not be unequivocally established, as some of the methods used to determine this characteristic on certain clay species were questionable. Particle size did not appear to be a critical characteristic. The implications of the cation exchange capacity of clay minerals in the activity, ecology, and population dynamics of microorganisms in nature are discussed.


Author(s):  
Atma Sharma ◽  
Budhaditya Hazra ◽  
Giovanni Spagnoli ◽  
Sreedeep Sekharan

Specific surface area (SSA) and cation exchange capacity (CEC) are two fundamental clay properties. However, the determination of CEC and SSA is challenging due to inherent uncertainties and difficulty in experimental measurement. Popular approach is to employ transformation models for its estimation. However, most of the existing models were developed on limited sample sizes, and quantification of uncertainty associated with the estimate is not possible. Therefore this study proposes a multivariate probabilistic approach for estimation of CEC and SSA. First, a five-dimensional database (278×5) for parameters liquid limit (LL), plasticity index (PI), clay fraction (CF), CEC and SSA (labelled as CLAY/C-S/5/278) is developed. Thereafter, multivariate distribution for the five parameters in the database is constructed using vine copula approach. Implementation of the proposed approach is demonstrated by updating prior/unconditional probability density function (PDFs) of CEC and SSA given single/ multiple clay parameters using Bayes’ rule. The posterior/conditional PDFs of CEC and SSA are also summarized as practitioner friendly analytical expressions. Two geotechnical application examples are also shown. In the proposed approach, CEC and SSA are characterized by their complete joint distribution, and is, therefore, superior to the popular deterministic transformation approach in literature.


1982 ◽  
Vol 62 (2) ◽  
pp. 291-296 ◽  
Author(s):  
L. J. EVANS

Thirty-four samples from the Ap horizons of heavy-textured Orthic Humic Gleysols (Typic Haplaquolls) were sampled in southwestern Ontario. Surface areas of the soils ranged from 79–223 m2/g and multiple regression analysis indicated that the surface area of the clay fractions was 207 m2/g and that of the organic matter 805 m2/g. Approximately 74% of the variability in cation exchange capacity could be attributed to their clay and organic C contents at pH 4 and about 86% at pH 8. A value of 181 meq/100 g was calculated as the cation exchange capacity of organic matter at pH 4 and of 316 meq/100 g at pH 8. Mean cation exchange capacities at pH 4 were 20.3 meq/100 g and 31.6 meq/100 g at pH 8.


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