Sodium-fluoride pH of South-Western Australian soils as an indicator of P-sorption

Soil Research ◽  
1994 ◽  
Vol 32 (4) ◽  
pp. 755 ◽  
Author(s):  
RJ Gilkes ◽  
JC Hughes
Keyword(s):  
Clay Minerals ◽  
Iron Oxides ◽  
Sorption Capacity ◽  
Sodium Fluoride ◽  
Secondary Importance ◽  
P Sorption ◽  
Soil Constituent ◽  
Western Australian ◽  
Soil Constituents ◽  
Measuring Ph

Phosphate sorption by the surface horizon of 228 acid to neutral Western Australian (W.A.) soils is more closely related (r(2) = 0.76) to the content of oxalate-extractable aluminium than to any other soil constituent. This fraction corresponds to poorly ordered inorganic and organic Al compounds that release considerable amounts of OH- to NaF solution. Thus the abundance of these compounds in soil may be estimated by measurement of the pH of a NaF extract (pH((NaF)) This association enables the rapid and moderately accurate prediction in the field of the P-sorption capacity of soils (r(2) = 0.72) by measuring pH(NaF) With a. simple, portable pH meter. For many W.A. soils, it is probable that well crystalline aluminium and iron oxides, clay minerals and other soil constituents are of secondary importance in determining P-sorption and that most P-sorption is due to poorly ordered and organically complexed forms of Al.

Comparison of seven phosphorus sorption indices

Soil Research ◽  
1996 ◽  
Vol 34 (1) ◽  
pp. 81 ◽  
Author(s):  
MDA Bolland ◽  
RJ Gilkes ◽  
RF Brennan ◽  
DG Allen
Keyword(s):  
Sorption Capacity ◽  
Buffer Capacity ◽  
Sorption Isotherms ◽  
Phosphorus Sorption ◽  
P Sorption ◽  
P Sorption Capacity ◽  
Routine Procedures ◽  
P Addition ◽  
Western Australian ◽  
Extractable Iron

Seven methods of estimating or predicting phosphorus (P) sorption capacity were compared for 47 neutral to acid Western Australian soils. Two methods, the P buffer capacity (PBC) and the Fox and Kamprath procedure, provided reliable indices of P sorption from well defined P sorption isotherms, but they are not quick routine methods because several levels of P addition are required. The other five routine procedures included two versions of the P retention index (PRI), determined by adding one level of P, and three soil properties, oxalate extractable iron (oxalate Fe), oxalate extractable aluminium (oxalate Al), and pH measured in sodium fluoride [pH (F)], that are known to indicate P sorption capacity. All the indices were well related to one another. The oxalate Fe index was the least well related to PBC whereas oxalate Al, one of the PRI indices, and pH (F) were closely related to PBC and could be used as quick, economical procedures to assess the P sorption capacity of soils.

scholarly journals Nano-Sized Minerals from Lower Cretaceous Sandstones in Israel Observed by Transmission Electron Microscopy (TEM)

2021 ◽  
Author(s):  
Nurit Taitel-Goldman ◽  
Vladimir Ezersky
Keyword(s):  
Clay Minerals ◽  
Iron Oxides ◽  
Lower Cretaceous ◽  
Fine Fraction ◽  
Anatase Tio2 ◽  
Rutile Tio2 ◽  
Transmission Electron ◽  
Quartz Arenite ◽  
Dark Violet ◽  
Hematite Fe2o3

Fine fraction in quartz arenite sandstones from Lower Cretaceous Hatira formation in Israel was observed by Transmission electron microscope (TEM). Samples were collected from Hatira and Ramon craters located in southern part of Israel and from Manara cliff from the northern part of Israel. The additional phases cause yellow, red, dark red and dark violet colors of the layered sandstones. The motivation was to identify the minerals of the fine factions that cause the variations in the colors. The minerals observed were clay minerals, mainly kaolinite (Al4Si4O20(OH)8), some illite (K0.65Al2.0[Al0.65Si3.35O10](OH)2) and smectite. Iron oxides were goethite (FeOOH) and hematite (Fe2O3), Titanium-iron oxides observed was ilmenite (FeTiO3), and Titanium-oxides were rutile (TiO2), and anatase (TiO2). Sulphates observed were jarosite (KFe3(SO4)2(OH)6) and alunite (KAl3(SO4)2(OH)6). Some of the hematite was formed by recrystallization of goethite. Ilmenite disintegrated into small iron oxides mainly hematite. Euhedral to sub-hedral rutile (TiO2) and anatase (TiO2) were preserved in clay-minerals. Crystals of alunite and jarosite were observed in sandstones in both craters. They probably crystallized due to some transgression of the Thetis Sea.

An occurrence of polymorphic halloysite in granite saprolite of the Bayerischer Wald, Germany

Clay Minerals ◽  
1978 ◽  
Vol 13 (1) ◽  
pp. 67-77 ◽  
Author(s):  
B.-M. Wilke ◽  
U. Schwertmann ◽  
E. Murad
Keyword(s):  
Trace Elements ◽  
Clay Minerals ◽  
Iron Oxides ◽  
Aqueous Phase ◽  
Mixed Layer ◽  
Thin Plates ◽  
Low Crystallinity

AbstractXRD, DTA and IR patterns showed clay veins filling fissures in a granite of the Bayerischer Wald (eastern Bavaria) to consist mainly of hydrated halloysite of low crystallinity with traces of gibbsite, 2:1 (mixed layer) clay minerals and iron oxides. The halloysite forms thin plates which exhibit varying degrees and types of enrolment, resulting in platy, tubular and spheroidal crystals within the same sample. Concentrations of the trace elements Rb, Sr, Ba, Zr, Y, Ce, Pb, Zn and Cu indicate halloysite formation to have taken place via an aqueous phase under the influence of vadose waters circulating in fissures.

Thermal study of some manganese oxide minerals

1950 ◽  
Vol 29 (210) ◽  
pp. 239-251 ◽  
Author(s):  
J. Laurence Kulp ◽  
Jose N. Perfetti
Keyword(s):  
Thermal Analysis ◽  
Differential Thermal Analysis ◽  
Manganese Oxide ◽  
Clay Minerals ◽  
Iron Oxides ◽  
Theoretical Background ◽  
Thermal Study ◽  
The Past ◽  
Considerable Success ◽  
Oxide Minerals

In the past decade, differential thermal analysis has developed into a very useful mineralogical technique. The theoretical background for this method has been treated by Speil, Berkelhamer, Pask, and Da vies (1945) and has been modified by Kerr and Kulp (1948, 1949). The application of the method to the clay minerals has been carried out with considerable success by a number of workers in Europe and America. In particular, Grim and co-workers (1942, 1947, 1948) have produced a number of significant papers dealing with the thermal analysis of clays. The method has been extended to other mineral groups such as the carbonates (Faust, 1949; Beck, 1946; Kerr and Kulp, 1947; Cuthbert and Rowland, 1947; Kulp, Kent, and Kerr, 1950), phosphates (Manly, 1950), sulphates (Kulp and Adler, 1950), quartz (Faust, 1948), and the hydrous iron oxides (Kulp and Trites, 1950).

Phosphorus Extraction with Soil Test Methods Affected by Soil P Sorption Capacity

2020 ◽  
Vol 20 (4) ◽  
pp. 1882-1890 ◽  
Author(s):  
Gilmar Luiz Mumbach ◽  
Luciano Colpo Gatiboni ◽  
Daniel João Dall’Orsoletta ◽  
Djalma Eugênio Schmitt ◽  
Patrícia Pretto Pessotto ◽  
...  
Keyword(s):  
Sorption Capacity ◽  
Test Methods ◽  
Soil Test ◽  
Soil P ◽  
P Sorption ◽  
P Sorption Capacity ◽  
Phosphorus Extraction

Pathways and Mechanisms for Removal of Dissolved Organic Carbon from Leaf Leachate in Streams

1981 ◽  
Vol 38 (1) ◽  
pp. 68-76 ◽  
Author(s):  
Clifford N. Dahm
Keyword(s):  
Organic Carbon ◽  
Dissolved Organic Carbon ◽  
Clay Minerals ◽  
Iron Oxides ◽  
Amorphous Solid ◽  
Microbial Utilization ◽  
Physical Chemical ◽  
Fine Particulate ◽  
Solid Phases ◽  
Aluminum And Iron Oxides

Removal of dissolved organic carbon (DOC) from water resulting from adsorption and microbial uptake was examined to determine the importance of biotic and abiotic pathways. Physical–chemical adsorption to components of the stream sediment or water and biotic assimilation associated with the microbial population was determined in recirculating chambers utilizing leachate from alder (Alnus rubra). Adsorptive mechanisms were further separated into interactions involving (1) specific clay minerals, (2) amorphous solid phases of hydrous aluminum and iron oxides, and (3) fine particulate organic matter. Physical–chemical adsorptive mechanisms for alder leachate removal exhibited rapid kinetic equilibration between the DOC and solid phases, but only a specific fraction of the DOC, likely containing certain chemical functional groups, was adsorbed. The amorphous aluminum and iron oxides possessed a much higher potential capacity than the clay minerals or fine particulate organics for DOC adsorption. Microbial uptake of DOC from the alder leachate was kinetically slower than adsorptive uptake. However, microbial activity was overall much more effective in the removal and degradation of the total DOC pool leached from alder leaves. Over a 48-h period, 97% of added 14C labeled leachate was removed from solution by adsorption (~ 20%) and microbial utilization (~ 77%). The rate of microbial uptake was 45 μg C/g sediment C∙h−1 or 14 mg C∙m−2∙h−1.

Phosphorus sorption and chemical characteristics of lightweight aggregates (LWA)-potential filter media in treatment wetlands

1997 ◽  
Vol 35 (5) ◽  
pp. 103-108 ◽  
Author(s):  
T. Zhu ◽  
P. D. Jenssen ◽  
T. Mæhlum ◽  
T. Krogstad
Keyword(s):  
Sorption Capacity ◽  
Metal Content ◽  
Exchange Capacity ◽  
Chemical Characteristics ◽  
Phosphorus Sorption ◽  
Filter Media ◽  
Total Metal Content ◽  
P Sorption ◽  
P Sorption Capacity ◽  
Total Metal

Five light-weight aggregates (LWAs), suitable for filter media in subsurface flow constructed wetlands, were tested for potential removal of phosphorus (P). P-sorption variation is dependent on the chemical characteristics of the LWA. All LWAs exhibited high pH and high total metal content; however, P-sorption capacity varied by two orders of magnitude. Of the LWAs' chemical characteristics (total metal content, cation exchange capacity, and oxalate soluble Fe and Al), total metal content has the closest relationship with the P-sorption capacity. Among the four major metal ions (Mg, Ca, Fe and Al), Ca has the strongest correlation with the P-sorption capacity.

Phosphorus auditing cannot account for all of the phosphorus applied to different pasture soils

Soil Research ◽  
2004 ◽  
Vol 42 (1) ◽  
pp. 89 ◽  
Author(s):  
L. L. Burkitt ◽  
C. J. P. Gourley ◽  
P. W. G. Sale
Keyword(s):  
Soil Properties ◽  
Sorption Capacity ◽  
Vertical Movement ◽  
Single Application ◽  
Macropore Flow ◽  
P Sorption ◽  
P Sorption Capacity ◽  
Sampling Zone ◽  
P Movement ◽  
Total P

Five field sites established in the high rainfall zone of southern Victoria were used to examine the downwards vertical movement of phosphorus (P) fertiliser on soils which ranged in P sorption capacity. Fertiliser was applied either as a single application of 280 kg P/ha at the beginning of the experiment (April 1998), or as 35�kg�P/ha reapplied every 6 months (totalling 210 kg P/ha by the end of the third year). Soil cores were sampled in June 2001 to a depth of 40 cm, and soil at depths of 0–5, 5–10, 10–20, 20–30, and 30–40 cm was analysed for a range of soil properties and total P concentration.Total P concentration changed very little down the profile, indicating that there was minimal vertical movement of P fertiliser below the 10 cm layer of 5 pasture soils following the single application of 280 kg P/ha or 35 kg P/ha reapplied every 6 months. Soils with low to moderate surface P sorption capacity showed a trend for higher total P concentrations at depth. However, quantitative relationships between vertical P movement and soil properties at depth were poor. A P audit resulted in variable recovery of the applied P (45–128%) in the surface 40 cm at each of the 5 sites. Consistently low P recoveries were achieved at one site, where the surface soil had a high P sorption capacity. Some applied P may have bypassed the high P sorbing surface layers at this site through macropore flow and moved beyond the 40 cm sampling zone, or have been lost to surface runoff. These results question the usefulness of P audit or mass-balance methods for accounting for P movement in a pasture-based system, as spatial heterogeneity of soil properties, both horizontally and vertically, was high in the current study.

Measuring the specific caesium sorption capacity of soils, sediments and clay minerals

2007 ◽  
Vol 22 (1) ◽  
pp. 219-229 ◽  
Author(s):  
A. de Koning ◽  
A.V. Konoplev ◽  
R.N.J. Comans
Keyword(s):  
Clay Minerals ◽  
Sorption Capacity
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