Mobility of phosphate from waste water in calcareous sands of Rottnest Island (WA)

Soil Research ◽  
1993 ◽  
Vol 31 (3) ◽  
pp. 235 ◽  
Author(s):  
RG Gerritse

Natural levels of inorganic phosphate in soils of Rottnest Island are quite high: about 300 mg/kg as P (or about 4 t of P per ha per meter depth of soil). In comparison, the production of phosphorus in wastewater from sewage, treated on Rottnest Island, amounts to approximately 2 t per year. The phosphate, occurring in the soil naturally, is mainly in mineral form and not very soluble. Solution concentrations in the soils are less than 0.001 mg/L P-PO4 (at pH values of 8.5-8.9). Conditions in the calcareous soils of Rottnest Island are favourable for precipitation of phosphate as calcium phosphates. Theoretically >>99% of phosphate in wastewater from treated sewage can be stored indefinitely as hydroxy-, fluoro- and chloro-apatites. In practice, however, application of wastewater to these soils will result in a (kinetically defined) finite concentration of phosphate to move through the soil slowly as a sharp front. The effective width of the frontal zone was taken to be equal to the longitudinal hydrodynamic dispersivity. Mobilities, relative to water, of fronts resulting from step increases of phosphate in soils were then calculated with an experimentally obtained, time-dependent, adsorption equation and the average residence time of phosphate in the frontal zone. Calculated mobilities were verified experimentally by leaching phosphate through small columns of soil at different concentrations of phosphate and rates of infiltration. For concentrations in wastewater between 10 and 15 mg/L P-PO4, mobilities of phosphate, relative to water, in soils of Rottnest Island are less than 2% for expected infiltration rates of wastewater between 0.5 and 1 cm/day.

1989 ◽  
Vol 56 (3) ◽  
pp. 335-341 ◽  
Author(s):  
Rafael Berrocal ◽  
Serge Chanton ◽  
Marcel A. Juillerat ◽  
Blaise Favillare ◽  
Jean-Claude Scherz ◽  
...  

SummaryCasein phosphopeptides (GPP) were produced by tryptic hydrolysis of sodium caseinate and further purified by precipitation and chromatography on QAE-Sephadex A-25. Their physico-chemical properties were compared with the properties of an enzymically dephosphorylated equivalent preparation (DPP). Binding of Ca2+ to the peptides was measured using a Ca selective electrode and was found to increase with pH and to show 1/1 stoicheiometry Ca/Porg in CPP at pH 6·5 a.nd 7·6. Klotz plots indicated equivalent binding sites at these two pH values, but some heterogeneity was seen at pH 3·5. In contrast, DPP did not bind significant amounts of Ca2+.CPP effectively inhibited the formation of insoluble calcium phosphates at different Ca/P ratios. The effective CPP concentration was 10 mg/1 and complete stability of calcium phosphate solutions was obtained at about 100 mg/1. This stabilizing effect was dependent on the presence of organic P.


1964 ◽  
Vol 62 (1) ◽  
pp. 93-97 ◽  
Author(s):  
O. Talibudeen ◽  
P. Arambarri

The kinetics of the isotopic exchange of phosphate ions in soils with and without phosphate added in the laboratory were examined in relation to the amount and origin of the CaCO3 they contained. The isotopic exchange index, ‘Pr/Pe’, and the recovery of added phosphate were inversely proportional to carbonate content in soils containing carbonates of similar geological origin; soils from the Lower Lias showed the biggest change in Pr/Pe with carbonate content.In soils from the Cretaceous Chalk, the first-order rate of isotopic exchange of the ‘slow’ phosphate fraction was constant. It increased to a larger but constant value in the soils incubated for 6 months after adding phosphate in the laboratory. This rate constant is therefore specific to the calcium phosphates in a group of soils derived from the same calcareous parent material and with similar phosphate manuring.


1989 ◽  
Vol 69 (2) ◽  
pp. 235-242 ◽  
Author(s):  
W. VAN LIEROP ◽  
N. A. GOUGH

The objective of this study was to evaluate the Kelowna multiple element extractant and some EDTA and DTPA modifications for simultaneous determination of potassium and sodium in acid and calcareous soils. To that end, the relationships between K and Na concentrations extracted with 1 N NH4OAc and the Kelowna multiple element extractant (0.25 N HOAc + 0.015 N NH4F) were assessed. However, relationships between K and Na concentrations removed by the modified Kelowna multiple element extractants containing either EDTA or DTPA (KEDTA & KDTPA with NH4F; and AAEDTA & AADTPA without NH4F) were evaluated by comparing values against those obtained with the Kelowna extractant. Addition of these complexing agents was of interest because of their potential in enabling simultaneous extraction of available Zn. The procedures were evaluated by contrasting K and Na concentrations extracted from 100 Canadian soils — half which had pH values between 4.1 and 6.9 (H2O) and a second group with values between 7 and 9.6 — by means of graphing, regression and correlation techniques. Potassium and sodium concentrations removed by the Kelowna extractant ranged from 25 to 510 μg and from 10 to 1420 μg mL−1 soil, respectively. The Kelowna and its EDTA and DTPA modifications extracted K and Na as effectively from acid as calcareous soils. This conclusion was supported by the similar regression slopes obtained when relating concentrations of K and Na removed from these soil groups by the multiple element extractants against those removed by 1 N NH4OAc (r-values ≥ 0.97**). However, the new multiple element extractants removed an average of about 20% less K than 1 N NH4OAc from these soils, though similar Na levels. The lower K levels removed from the Kelowna extractant, or by one of its modifications, may require that soil test interpretation norms be adjusted to compensate for the lower values when using one of these to determine K-availability. A significant correlation was found between extracted Na levels and 1:2 vol/vol water-extract conductivities (r ≥ 0.83**) suggesting that "higher" Na levels may be soluble instead of exchangeable. Some Na test interpretations are discussed in the text. Key words: EDTA, DTPA


1994 ◽  
Vol 61 (3) ◽  
pp. 355-363 ◽  
Author(s):  
Georges Daufin ◽  
Jean-Pierre Labbe ◽  
Auguste Quemerais ◽  
Françoise Michel ◽  
Uzi Merin

SummaryWhey clarification can be achieved by using a lipid aggregation step followed by microfiltration. The results from using an M5 Carbosep membrane to ultrafilter defatted sweet whey at pH values in the range 8·0–1·5 furnished understanding of the fouling process so that fouling may be minimized. The conventional method of aggregation, allowing the pH to decrease naturally, has been compared with a modified aggregation process in which the pH was maintained constant. These two methods differed significantly in their influence on the subsequent ultrafiltration (UF), with respect to the UF hydraulic characteristics, i.e. reversible, irreversible and overall fouling resistance. Optimal UF performance was obtained at a pH equal to or slightly higher than the aggregation pH (7·5) owing to the limited fouling contribution of proteins and calcium phosphates. The modified process permitted UF at fluxes in the range 50–115 1 h-1 m-2, with moderate transraembrane pressure, even with a protein content two to five times higher than that of regular whey.


1978 ◽  
Vol 26 (1) ◽  
pp. 93 ◽  
Author(s):  
CA Anderson ◽  
PY Ladiges

In the Otways district, Vic., Eucalyptus obliqua exhibits a wide edaphic tolerance and evidence is presented for the existence of ecotypes in this region. A comparison of three populations from acidic loam, neutral sand and alkaline sand showed significant differences in yield response when grown under glasshouse conditions. A tall open- forest population, naturally occurring on fertile acidic loams (pH 4.6-5.2), showed a marked reduction in yield, was severely chlorotic and developed red and necrotic patches on leaves when grown on calcareous sands of pH 6.5 and 8.0. Open-forest and low open-forest populations native to the sands of pH 6.5 and 8.0 respectively also developed some chlorosis, but maintained greater yields, particularly on the soil of pH 6.5. Chlorosis in all populations was correlated with decreased levels of chlorophylls a and b, and carotenoids; on soil of pH 8.0, all populations showed increases in calcium, potassium, magnesium, sodium, phosphorus and the phosphorus/iron ratio in leaf tissue. Populations showed differing contents of iron in seedlings (but with no particular trends), and the low open-forest population developed a significantly low phosphorus/iron ratio when grown on Leached calcareous soil of pH 6.5.


2008 ◽  
Vol 47-50 ◽  
pp. 1307-1310 ◽  
Author(s):  
Ya Qin Huang ◽  
Lu Jun Sun ◽  
Ai Hua He ◽  
Qin Qin Wang ◽  
Charles C. Han

The effect of pH value at different initial Ca/P molar ratio on the composition and crystal phase of the calcium phosphates synthesized through chemical precipitation method was studied in detail. After calcining at 900°C, the products were characterized by XRD and chemical analysis. The results showed that the composition and crystal phase of the resultant powders can be controlled by pH value at different initial Ca/P molar ratio. When Ca/P molar ratio was 1.667, pure HA was obtained at pH values of both 12.0 and 11.0. When initial Ca/P molar ratio was 1.500, pure β-TCP was obtained at pH value from 11.0 to 9.0. CPP was obtained at pH value from 6.0 to 4.0 when initial Ca/P molar ratio was 1.000.


2015 ◽  
Vol 71 (6) ◽  
pp. 892-897 ◽  
Author(s):  
Raffaele Taddeo ◽  
Raghida Lepistö

The release of nitrogen (N) and phosphorus (P) from agro-industrial sources is a major environmental concern. Furthermore, the scarcity of mineable P and the growing demand for food worldwide necessitate that we find an alternative P source. This study applied struvite precipitation for N-P recovery to slurries with high levels of organics and ammonia to achieve environmental protection from excessive nutrients diffusion and to generate a sustainable P source. Batch tests were carried out on raw and co-digested swine slurries to study the feasibility of struvite precipitation and the effect of several parameters, including pH, reaction time, competing ions (Ca2+, K+), total solids (TS), and alkalinity. The batch assays with raw swine slurries showed high N-P removals (up to 80%), while the anaerobic liquor returned lower recovery efficiency due to the high solids and alkali content. Struvite crystallization was detected at pH values as low as 6, and the characteristics of the recovered struvite matched those of the theoretical. Slight co-precipitation of calcium–phosphates occurred and was dependent on the Ca2+/Mg2+ ratio rather than on varying pH values. Struvite precipitation was shown to be feasible in complex matrices as agro-industrial effluents, characterized by high NH4+, alkalinity, solids and organic content, and interfering ions such as Ca2+ and K+.


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