ADSORPTION OF PHOSPHORUS BY FOUR SASKATCHEWAN SOILS

1959 ◽  
Vol 39 (1) ◽  
pp. 64-75 ◽  
Author(s):  
D. A. Rennie ◽  
R. B. McKercher

The adsorption of phosphorus by four soils of differing colloid content showed close agreement with the Langmuir isotherm when final phosphorus solution concentrations were less than 20 μg. P/ml. Calculated adsorption maximum for the four soils were 79.1, 87.7, 150.4 and 164.4 μg. P per g. of soil. The average value of the constant k, related to the bounding energy of the soil for phosphorus, was 0.141.The percentage phosphorus saturation of the adsorption maximum was closely correlated with the equilibrium phosphorus concentration in the soil suspension. At an equilibrium concentration of 28.7 μg. P/ml., 100 per cent saturation of the adsorption capacity of the four soils was obtained; the total adsorbed phosphorus on the four soils was not related to the phosphorus concentration of the soil solution but varied considerably depending on the colloid content of the respective soils.Carbonated water extractable phosphorus, and 'surface' phosphorus measured by P32 equilibrium studies, were not related to the equilibrium concentration of phosphorus of the soil solution. It appears that the percentage phosphorus saturation of the adsorption maximum may prove a more reliable measure of the capacity of the soil to supply phosphorus to the soil solution than either of the 'quick' tests used.Organic matter appeared to be equally as important as the inorganic colloids in determining the phosphorus adsorption capacity of the soils. Differences in exchangeable calcium were not closely related to the adsorption maximum.

2020 ◽  
Vol 2020 ◽  
pp. 1-13
Author(s):  
Yue Yin ◽  
Gaoyang Xu ◽  
Linlin Li ◽  
Yuxing Xu ◽  
Yihan Zhang ◽  
...  

A more applicable adsorbent was fabricated using industrial wastes such as red mud, fly ash, and riverbed sediments. The heavy metal inside the raw materials created metal hydroxy on the adsorbent surface that offered elevated adsorption capacity for phosphorus. The required equilibrium time for the adsorption is only 10 min. The theoretical maximum adsorption capacity of the adsorbent was 9.84 mg·g−1 inferred from the Langmuir adsorption isotherm. Higher solution pH favored phosphorus adsorption. Kinetics study showed that the adsorption could be better fitted by the pseudo-second-order kinetic model. The presence of coexisting anions had no significant adverse impact on phosphorus removal. The speciation of the adsorbed phosphorus indicated that the adsorption to iron and aluminum is the dominating adsorption mechanism. Moreover, a dynamic adsorption column experiment showed that, under a hydraulic time of 10 min, more than 80% of the phosphorus in the influent was removed and the surplus phosphorus concentration was close to 0.1 mg L−1. The water quality after adsorption revealed its applicability in real treatment. Consequently, the adsorbent synthesized from industrial wastes is efficient and applicable due to the high efficiency of phosphorus removal and eco-friendly behavior in solutions.


2020 ◽  
Vol 20 (6) ◽  
pp. 2226-2236
Author(s):  
Fazhi Xie ◽  
Kang Song ◽  
Shixiong Geng ◽  
Lu Li

Abstract Phosphate removal from eutrophic lakes has caused wide concern in the world, while an effective process is still lacking. A novel synthetic magnesium carbonate with spherical flower-like structure (MCSF) was prepared. Its performance for phosphorus adsorption from a eutrophic lake by in situ magnesium phosphate formation was tested and characterized. The effect of initial phosphorus concentration, adsorption time, adsorption dose, temperature, ionic strength and pH on phosphorus adsorption by MCSF was investigated. Results showed that higher initial phosphorus concentration and longer adsorbing time could improve the adsorption capacity. The maximum sorption capacity was 143.27 mg/g under initial pH value 7.0. The phosphate adsorption process was fitted with the Langmuir isotherm model and pseudo-second-order model. Thermodynamic parameter values revealed that the sorption process at 298–318 K was spontaneous and endothermic. The X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) characterization of MCSF revealed that electrostatic attraction and chemical conversion were the major contributors for phosphate adsorption. MCSF releases magnesium ions from its surface and rapidly combines with phosphate to form insoluble magnesium phosphate precipitate. The prepared MCSF has the potential to be used for the restoration of eutrophic lakes by removing phosphate with higher adsorption capacity.


2016 ◽  
Vol 5 (1) ◽  
pp. 31 ◽  
Author(s):  
Jingqiu Piao ◽  
Changyuan Tang ◽  
Toma Matsumaru ◽  
Zhiwei Han ◽  
Hiroki Sakaguchi ◽  
...  

<p>The distribution and adsorption characteristics of phosphorus were investigated in a typical headwater wetland in Ichikawa City, Chiba Prefecture, Japan. Total dissolved phosphorus (TDP) was the main phosphorus fraction in the waters, ranging from limit of quantification (0.002 mg/L) to 0.059 mg/L in spring water, from limit of quantification to 0.128 mg/L in groundwater and from 0.012 to 0.048 mg/L in river water. TDP in 33% water samples were higher than the environmental quality standard for eutrophication (0.020 mg/L). Next, phosphorus adsorption experiment was conducted to study phosphorus distribution in the aquifer where the equilibrium phosphorus concentration (C<sub>EPC</sub>) is the key to access the phosphorus in the waters. In addition, the amount of TDP releasing from the wetland through river was 20.9 g/day.</p>


2021 ◽  
Vol 11 (14) ◽  
pp. 6346
Author(s):  
Laura Patiño-Saldivar ◽  
José A. Hernández ◽  
Alba Ardila ◽  
Mercedes Salazar-Hernández ◽  
Alfonso Talavera ◽  
...  

Bioremediation is a pollutant removal method that has had a great boom due to the diversity of agroindustrial waste that can be used for this purpose, and that has shown having great efficiency and profitability in the adsorption of heavy metals, such as Pb, Cu, and Co. Based on the above, the present work carried out kinetic and equilibrium studies of bioadsorption of Cr (III) using orange peel (OP) as adsorbent, previously treated with methanol, water, and a water–methanol mixture at different pH (0.91, 1.78 and 2.72), and at 30 °C, finding that the adsorption capacity at equilibrium increases with increasing pH, having a maximum of 55 mg g−1 at pH 2.72—under these conditions, lower adsorption energy was used to remove Cr (III). In addition, it was determined that there are no external mass transfer limitations. An isoelectric point analysis indicated that the adsorption is not carried out by electrostatic forces and a FTIR study of the functional groups of OP showed a decrease in the main functional groups (pectin, cellulose, and lignin, among others), which is directly related to the adsorption capacity of the bioadsorbent.


2016 ◽  
Vol 75 (1) ◽  
pp. 106-114 ◽  
Author(s):  
Lucas Meili ◽  
Társila Santos da Silva ◽  
Daniely Carlos Henrique ◽  
João Inácio Soletti ◽  
Sandra Helena Vieira de Carvalho ◽  
...  

In this work, the potential of ouricuri (Syagrus coronata) fiber as a novel biosorbent to remove methylene blue (MB) from aqueous solutions was investigated. The fiber was prepared and characterized according to the fundamental features for adsorption. A 23 experimental design was used to evaluate the effects of adsorbent dosage (M), fiber diameter (D) and agitation (A) on the adsorption capacity. In the more adequate conditions, kinetic and equilibrium studies were performed. The experimental design results showed that M = 10 g L−1), D = 0.595 mm and A = 200 rpm were the more adequate conditions for MB adsorption. Based on the kinetic study, it was found that the adsorption process was fast, being the equilibrium was attained at about 5 min, with 90% of color removal. The isotherm was properly represented by the Sips model, and the maximum adsorption capacity was 31.7 mg g−1. In brief, it was demonstrated that ouricuri fiber is an alternative biosorbent to remove MB from aqueous media, taking into account the process efficiency and economic viewpoint.


2019 ◽  
Vol 65 (9) ◽  
pp. 1262-1272 ◽  
Author(s):  
Luciano Colpo Gatiboni ◽  
Djalma Eugênio Schmitt ◽  
Paulo Cezar Cassol ◽  
Jucinei José Comin ◽  
Joice Crescêncio Heidemann ◽  
...  

Water ◽  
2018 ◽  
Vol 10 (7) ◽  
pp. 957 ◽  
Author(s):  
Muhammad Usman ◽  
Ioannis Katsoyiannis ◽  
Manassis Mitrakas ◽  
Anastasios Zouboulis ◽  
Mathias Ernst

The small sized powdered ferric oxy-hydroxide, termed Dust Ferric Hydroxide (DFH), was applied in batch adsorption experiments to remove arsenic species from water. The DFH was characterized in terms of zero point charge, zeta potential, surface charge density, particle size and moisture content. Batch adsorption isotherm experiments indicated that the Freundlich model described the isothermal adsorption behavior of arsenic species notably well. The results indicated that the adsorption capacity of DFH in deionized ultrapure water, applying a residual equilibrium concentration of 10 µg/L at the equilibrium pH value of 7.9 ± 0.1, with a contact time of 96 h (i.e., Q10), was 6.9 and 3.5 µg/mg for As(V) and As(III), respectively, whereas the measured adsorption capacity of the conventionally used Granular Ferric Hydroxide (GFH), under similar conditions, was found to be 2.1 and 1.4 µg/mg for As(V) and As(III), respectively. Furthermore, the adsorption of arsenic species onto DFH in a Hamburg tap water matrix, as well as in an NSF challenge water matrix, was found to be significantly lower. The lowest recorded adsorption capacity at the same equilibrium concentration was 3.2 µg As(V)/mg and 1.1 µg As(III)/mg for the NSF water. Batch adsorption kinetics experiments were also conducted to study the impact of a water matrix on the behavior of removal kinetics for As(V) and As(III) species by DFH, and the respective data were best fitted to the second order kinetic model. The outcomes of this study confirm that the small sized iron oxide-based material, being a by-product of the production process of GFH adsorbent, has significant potential to be used for the adsorptive removal of arsenic species from water, especially when this material can be combined with the subsequent application of low-pressure membrane filtration/separation in a hybrid water treatment process.


2015 ◽  
Vol 7 (3) ◽  
pp. 167-175 ◽  
Author(s):  
M. Seafatullah ◽  
M. A Hoque ◽  
M. S. Islam ◽  
M. M. Islam ◽  
M. N. Islam

One of the approaches for phosphorus fertilizer management is controlling the soil phosphorus adsorption behavior. To examine the effect on phosphorus adsorption behavior, three amended soil samples were prepared by mixing 10% (w/w in dry basis) cow dung, biogas slurry and vermicompost with soil. Phosphorus adsorption behavior was examined by using Langmuir, and Temkin adsorption isotherms. Initially, biogas slurry and vermicompost increased the maximum phosphorus adsorption capacity (MPAC) of soil from 461 µg g-1 (control) to 558.0357 and 586.17 µg g-1 respectively, and then decreased steadily and reached 429.92 and 398.41 µg g-1 respectively in five weeks.  Whereas in case of cow dung, MPAC was initially decreased, then reached maximum in 17 days and ultimately decreased. Thus application of cow dung along with phosphate fertilizer seems to increase the loss of the fertilizer through runoff and leaching. Conversely, biogas slurry and vermicompost prevent phosphorus loss by regulating phosphorus release through initial enhancement followed by gradual decrease in phosphorus adsorption capacity of soil. Both biogas slurry and vermicompost can be considered as good soil amendments as they have the ability to control the release of phosphorus fertilizer as per the need of the plants.


2018 ◽  
Vol 6 (4) ◽  
pp. T819-T833 ◽  
Author(s):  
Yang Gu ◽  
Wenlong Ding ◽  
Min Yin ◽  
Ruyue Wang ◽  
Baocheng Jiao ◽  
...  

The marine shale in South China has great gas exploration potential, and exploration in the Sichuan Basin has been successful, but the degree of exploration remains low in the Guizhou Province. We used organic geochemical analyses (total organic carbon content and kerogen type), scanning electron microscopy (SEM), field emission SEM, nuclear magnetic resonance (NMR), X-ray diffraction analysis, and low-temperature [Formula: see text] and [Formula: see text] adsorption experimental methods to study the micropore types and pore structures and their effects on the methane adsorption capacity of organic-rich shales found in the Fenggang block in northern Guizhou Province. The results indicate that the microscopic surface porosity of the lower Cambrian Niutitang Formation ranges from 2.88% to 5.34%, with an average value of 3.86%. Based on nitrogen adsorption methods, the range of the average pore size distribution is 4.6–9.491 nm, with an average value of 6.68 nm. All of the samples exhibit significant unimodal distributions. The main pore size is less than 10 nm, and these pores account for most of the mesopore volume, which is generally consistent with the NMR results. The methane adsorption capacity of the shale samples gradually increases in the range of 0–8 MPa at 30°C and reaches a maximum at approximately 10 MPa. Positive correlations were found between the gas content and specific surface area, total pore volume, and micropore volume. These strong correlations indicate that the Niutitang Shale has a high specific surface area, a high pore volume, and narrow-diameter pores, demonstrating that it has a high gas adsorption capacity. The results of this study provide valuable information regarding the adsorption characteristics of marine shales and the factors that affect those characteristics.


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