INFLUENCE OF CLAY MINERALS ON MICROORGANISMS: III. EFFECT OF PARTICLE SIZE, CATION EXCHANGE CAPACITY, AND SURFACE AREA ON BACTERIA

1966 ◽  
Vol 12 (6) ◽  
pp. 1235-1246 ◽  
Author(s):  
G. Stotzky
Keyword(s):  
Particle Size ◽  
Cation Exchange ◽  
Surface Area ◽  
Clay Minerals ◽  
Cation Exchange Capacity ◽  
Physicochemical Characteristics ◽  
Exchange Capacity ◽  
Bacterial Respiration ◽  
Effect Of Particle Size ◽  
Stimulation Of

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.

scholarly journals Effect of Low Zeolite Doses on Plants and Soil Physicochemical Properties

Materials ◽  
2021 ◽  
Vol 14 (10) ◽  
pp. 2617
Author(s):  
Alicja Szatanik-Kloc ◽  
Justyna Szerement ◽  
Agnieszka Adamczuk ◽  
Grzegorz Józefaciuk
Keyword(s):  
Plant Growth ◽  
Physicochemical Properties ◽  
Cation Exchange ◽  
Surface Area ◽  
Cation Exchange Capacity ◽  
N Fertilization ◽  
Exchange Capacity ◽  
First Year ◽  
Soil Physicochemical Properties ◽  
Water Holding

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.

Characteristics of variably saturated granular bentonite after long-term storage at near-field relevant temperatures

Clay Minerals ◽  
2013 ◽  
Vol 48 (2) ◽  
pp. 343-361 ◽  
Author(s):  
M. Valter ◽  
M. Plötze
Keyword(s):  
Physicochemical Properties ◽  
Cation Exchange ◽  
Surface Area ◽  
Cation Exchange Capacity ◽  
Elevated Temperatures ◽  
Near Field ◽  
Exchange Capacity ◽  
Hydraulic Permeability ◽  
Cation Composition ◽  
Retention Capacity

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.

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.

Determination of the Cation Exchange Capacity of Clays by Surface Tension Measurements

Clay Minerals ◽  
1993 ◽  
Vol 28 (3) ◽  
pp. 475-481 ◽  
Author(s):  
G. Burrafato ◽  
F. Miano
Keyword(s):  
Surface Tension ◽  
Cation Exchange ◽  
Clay Minerals ◽  
Cation Exchange Capacity ◽  
Mixing Time ◽  
Aqueous Suspension ◽  
Exchange Capacity ◽  
Drilling Fluids ◽  
Accurate Analysis

AbstractThe cation exchange capacity (CEC) of clay minerals has been determined by titration of aqueous suspension of clays with hexadecylpyridinium chloride, monitored using surface tension measurements. In order to make the method suitable for an accurate analysis of the CEC of the clays in drilling fluids or in soils, some parameters affecting the CEC determination (e.g. the presence of carboxymethylcellulose, mixing time and measurement device) have been investigated.

scholarly journals Influence of clay minerals and exchangeable cations on the formation of humic-like substances (melanoidins) from D-glucose and L-tyrosine

Clay Minerals ◽  
1999 ◽  
Vol 34 (3) ◽  
pp. 487-497 ◽  
Author(s):  
P. Arfaioli ◽  
O. L. Pantani ◽  
M. Bosetto ◽  
G. G. Ristori
Keyword(s):  
Cation Exchange ◽  
Clay Minerals ◽  
Cation Exchange Capacity ◽  
Exchange Capacity ◽  
Exchangeable Cations ◽  
Reaction Conditions ◽  
Polymeric Compounds

AbstractThe ability to produce humic-like polymeric compounds, with D-glucose and L-tyrosine as starting materials, was evaluated in different mineral systems: (1) Ca-, Al- and Cu(II)-saturated montmorillonite; (2) Ca-, Al- and Cu(II)-saturated kaolinite; (3) quartz in the presence of two different amounts of the same cations (according to the cation exchange capacity of the clays); and (4) untreated quartz (as control). All systems proved to be effective in the formation of humic-like compounds, particularly quartz, in the presence of cations. The effectiveness in promoting humification reactions was strictly related to the amounts of added cations. In the reaction conditions considered, the humification appears to be due more to the cations than to the type of clay minerals. The clayey systems synthesized more complex (aromatic) substances than the quartz ones.

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