Models for potassium release kinetics of four Humic Gleysols high in clay by electro-ultrafiltration

2001 ◽  
Vol 81 (5) ◽  
pp. 603-611 ◽  
Author(s):  
N. Ziadi ◽  
R. R. Simard ◽  
T. S. Tran

The rate of K release from the soil solid phase to its solution, especially from its rapidly and slowly exchangeable forms, can affect plant K uptake. The electro-ultrafiltration (EUF) technique was used to kinetically characterize the K release from four soils (Humic Gleysols) from Abitibi-Temiscaming, Quebec, Canada. Potassium was desorbed from soils that received over 166 kg K ha-1 yr-1 from 1994 to 1996. The desorption was carried out for 58 min (4, 4, and every 5 min thereafter for a total of 12 desorptions) at 400 V and 80°C. The amount of K desorbed was between 199 and 342 mg kg-1. Cumulative K desorption was described by the following six equations: power function, simplified Elovich, extended Elovich, parabolic diffusion, zero-order, and first-order. An incremental first-order equation was also tested. The studied soils have large K supplying capacities as suggested by forage K-uptake and total soil K desorption by EUF. In general, all tested equations adequately described the K release by EUF from the four soils. The incremental first-order equation, used for the first time, described well the soil K release data. The k rate constant from this model was significantly related to forage K uptake (R2 = 0.58). Results from this study indicate that the investigated soils have large K reserves and that the incremental first-order equation and most of the cumulative ones are suitable for describing the kinetics of the large K release from these fine-textured Gleysols. Key Words: Potassium, desorption, cumulative model, incremental model

2008 ◽  
Vol 32 (2) ◽  
pp. 533-540 ◽  
Author(s):  
Vladimir Antônio Silva ◽  
Giuliano Marchi ◽  
Luiz Roberto Guimarães Guilherme ◽  
José Maria de Lima ◽  
Francisco Dias Nogueira ◽  
...  

Kinetic studies on soil potassium release can contribute to a better understanding of K availability to plants. This study was conducted to evaluate K release rates from the whole soil, clay, silt, and sand fractions of B-horizon samples of a basalt-derived Oxisol and a sienite-derived Ultisol, both representative soils from coffee regions of Minas Gerais State, Brazil. Potassium was extracted from each fraction after eight different shaking time periods (0-665 h) with either 0.001 mol L-1 citrate or oxalate at a 1:10 solid:solution ratio. First-order, Elovich, zero-order, and parabolic diffusion equations were used to parameterize the time dependence of K release. For the Oxisol, the first-order equation fitted best to the experimental data of K release, with similar rates for all fractions and independent of the presence of citrate or oxalate in the extractant solution. For all studied Ultisol fractions, in which K release rates increased when extractions were performed with citrate solution, the Elovich model described K release kinetics most adequately. The highest potassium release rate of the Ultisol silt fraction was probably due to the transference of "non-exchangeable" K to the extractant solution, whereas in the Oxisol exchangeable potassium represented the main K source in all studied fractions.


Materials ◽  
2019 ◽  
Vol 12 (5) ◽  
pp. 730 ◽  
Author(s):  
Anna Lisik ◽  
Witold Musiał

The aim of this study was to verify the effect of the formulation on the release kinetics of active substances from preparations containing iron ions using in-line conductivity measurements. A simple, fast method was developed and may be applied for detailed evaluation of some kinetics factors obtained from the release data. Four different equations were used: zero-order equation, first-order equation, models: Korsmeyer–Peppas and Hixson–Crowell. Values of the determined half-time release for zero and first-order kinetic models ranged from 11.56 to 89.97 min. In the case of analysis according to these typical models, the values of the square root of the correlation coefficients were included between 0.9916 and 0.9995. The results transformed for the Hixson–Crowell model as constant release Ks, ranged between 0.0160 and 0.0437. The values of the respective calculated squares of the correlation coefficient ranged from 0.9933 to 0.9959. The determined release rate constants according to the Korsmeyer–Peppas model were between 0.0023 and 0.1630. The coefficients ‘n’ of the Korsmeyer–Peppas equation did not exceed 1.2 with the corresponding r2 values 0.9408–0.9960. Obtained results confirmed that the method is applicable for evaluation of selected drug compositions containing iron ions.


2014 ◽  
Vol 22 (2) ◽  
pp. 171-176
Author(s):  
Kan WANG ◽  
Zifang WANG ◽  
Ming GAO ◽  
Yaohua HUANG ◽  
Xiaofei HAN ◽  
...  

1976 ◽  
Vol 29 (2) ◽  
pp. 443 ◽  
Author(s):  
MA Haleem ◽  
MA Hakeem

Kinetic data are reported for the decarboxylation of β-resorcylic acid in resorcinol and catechol for the first time. The reaction is first order. The observation supports the view that the decomposition proceeds through an intermediate complex mechanism. The parameters of the absolute reaction rate equation are calculated.


2012 ◽  
Vol 554-556 ◽  
pp. 1925-1928 ◽  
Author(s):  
Ji Wu Li ◽  
Xiao Hong Zhu ◽  
Jun Ya Pan

The stain of Fusarium sp. HJ01 used in 4-chlorophenol (4-CP) degradation was isolated in our laboratory. The effects of pH, temperature, 4-CP concentration, carbon source on 4-CP degradation rate were studied. It was concluded that Fusarium sp. HJ01 could grow with 4-CP as the sole carbon and energy source. 4-CP concentration of 100mg/L in the pH range of 4~10 and temperature range of 25°C~35°C could be degraded completely. The capacity of 4-CP degradation was effectively enhanced by the addiction of sucrose. The kinetics of 4-CP degradation could well accord with the Haldane model for 4-CP as the sole carbon source and with first order equation for added other sucrose.


2012 ◽  
Vol 58 (No. 10) ◽  
pp. 471-476 ◽  
Author(s):  
H.R. Motaghian ◽  
A.R. Hosseinpur

The greenhouse experiment was performed to determine Cu release characteristics in the bulk and the rhizosphere of some calcareous soils using rhizobox. The kinetics of Cu release in the bulk and the rhizosphere soils were determined by successive extraction with diethylenetriaminepentaacetic acid-triethanolamine (DTPA-TEA) and 10 mmol/L citric acid in a period of 1 to 504 h at 25 ± 1°C. The results of kinetics study showed that Cu extracted using DTPA-TEA in the rhizosphere soils was significantly (P < 0.01) lower than the bulk soils, while Cu extracted using citric acid in the rhizosphere soils was significantly (P < 0.01) higher than the bulk soils. The mean of released Cu after 504 h using DTPA-TEA were 8.59 and 7.46 mg/kg in the bulk and the rhizosphere soils, respectively. The mean release of Cu after 504 h using citric acid was 14.73 and 16.05 mg/kg in the bulk and the rhizosphere soils, respectively. Release kinetics of Cu in two extractants conformed fairly well to parabolic diffusion, power function, and first order equations. The results of correlation analysis illustrated that a significant correlation between Cu desorption after 504 h with citric acid and Cu concentration in wheat was found (r = 0.96 and r = 0.90 in the rhizosphere and the bulk soils, respectively, P < 0.01). Therefore, application of 10 mmol/L citric acid extractant would be recommended in the future study on the kinetics of release of Cu in calcareous soils.  


2012 ◽  
Vol 58 (No. 7) ◽  
pp. 328-333 ◽  
Author(s):  
A.R. Hosseinpur ◽  
H.R. Motaghian ◽  
M.H. Salehi

The rate of potassium (K) release from soils is a dynamic process, and it is important to the evaluation of soil K availability to plant. The objectives of this study were to determine K release characteristics and the correlation of these parameters with bean plant indices in surface soils of 15 calcareous soils. The kinetics of K release was determined by successive extraction with 0.01 mol/L CaCl<sub>2</sub> in a period of 2&ndash;2017 h at 25 &plusmn; 1&deg;C. The results showed that the cumulative K&rlm; release ranged from 111 to 411 mg/kg. A plot of cumulative amount of K released showed a discontinuity in slope at 168 h. Thus, two equations were applied to segments of the total reaction time (2 to 168 and 168 to 2017 h). The amounts of K released during 2&ndash;168 and 168&ndash;2017 h ranged from 55 to 299 and 44 to 119 mg/kg, respectively. Release kinetics of K conformed fairly well to parabolic diffusion, simplified Elovich and power function models in two segments. Potassium released after 2&ndash;168 and 168&ndash;2017 h and K release rate constants were significantly correlated (P &lt; 0.05) with bean plant indices, while correlation between K extracted by using 1 mol/L NH<sub>4</sub>OAc (ammonium acetate) and plant indices was not significant. The results of this research showed that information obtained from K release studies in laboratory and kinetics equation parameters can help to estimate the K supplying power of soils. &nbsp;


2013 ◽  
Vol 803 ◽  
pp. 157-160
Author(s):  
Zhen Zhen Kong ◽  
Dong Mei Jia ◽  
Su Wen Cui

The composite weakly basic resin (D301Fe) was prepared and examined using scanning electron microscopy and Fourier transform infrared spectroscopy. The adsorption kinetics of glyphosate from aqueous solution onto composite weakly basic resin (D301Fe) were investigated under different conditions. The experimental data was analyzed using various adsorption kinetic models like pseudo-first order, the pseudo-second order, the Elovich and the parabolic diffusion models to determine the best-fit equation for the adsorption of glyphosate onto D301Fe. The results show that the pseudo-second order equation fitted the experimental data well and its adsorption was chemisorption-controlled.


2012 ◽  
Vol 599 ◽  
pp. 91-95 ◽  
Author(s):  
Jin Mei ◽  
Ji Wei Hu ◽  
Xian Fei Huang ◽  
Li Ya Fu ◽  
Jin Luo ◽  
...  

Release kinetics of phosphorus in 17 sediments samples collected from Baihua Lake were determined, and the relationship between the phosphorus release kinetic parameters and the sediment composition was also investigated. The results showed that both the Elovich equation and power function equation were valid models for describing the phosphorus release data in the 17 sediments. Within the beginning 12 h, the rate of phosphorus release was high, and then decreased. Our correlation analysis demonstrates that there were no significant correlations between the maximum capacity of phosphorus release (Qmax) and the content of total nitrogen (TN), organic matter (OM), calcium-bound phosphorus (Ca-P), and organic phosphorus (OP). But the correlation between Qmax and iron/aluminum-bound phosphorus (Fe/Al-P) content was positive (R2 = 0.6064, P < 0.01), suggesting that Fe/Al-P might be the main contributor to the released phosphorus in the sediments.


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