scholarly journals Exploring Temperature-Related Effects in Catch Crop Net N Mineralization Outside of First-Order Kinetics

Nitrogen ◽  
2021 ◽  
Vol 2 (2) ◽  
pp. 110-127
Author(s):  
Jorge Federico Miranda-Vélez ◽  
Iris Vogeler
Keyword(s):  
Goodness Of Fit ◽  
Variable Temperature ◽  
Net N Mineralization ◽  
Catch Crop ◽  
Plant Type ◽  
Catch Crops ◽  
Mineral N ◽  
First Order ◽  
Residue Decomposition ◽  
First Order Kinetics

Catch crops are an effective method for reducing nitrogen (N) leaching in agriculture, but the mineralization of incorporated catch crop residue N is difficult to predict and model. We conducted a five-month incubation experiment using fresh residue from three catch crops (hairy vetch, fodder radish and ryegrass) with three temperature treatments (2 °C, 15 °C and 2–15 °C variable temperature) and two termination methods (glyphosate and untreated). Mineral N (ammonium and nitrate) in soil was quantified at 0, 1, 2, 4, 8 and 20 weeks of incubation. Ammonium accumulation from residue decomposition showed a lag at low and variable temperature, but subsequent nitrification of the ammonium did not. Mineral N accumulation over time changed from exponential to sigmoidal mode at low and variable temperature. Incubation temperature significantly affected mineralization rates in a first-order kinetics (FOK) model, while plant type and termination method did not. Plant type alone had a significant effect on the final mineralized fraction of added catch crop N. FOK models modified to accommodate an initial lag were fitted to the incubation results and produced better goodness-of-fit statistics than simple FOK. We suggest that initial lags in residue decomposition should be investigated for the benefit of mineralization predictions in cropping models.

scholarly journals Comparison Of Empirical Models For Estimating The Mineralization Potential Of Soil Nitrogen

2017 ◽  
Vol 7 (4) ◽  
pp. 1189-1202
Author(s):  
Zoubeir Bensid
Keyword(s):  
Nitrogen Mineralization ◽  
Goodness Of Fit ◽  
Empirical Models ◽  
The Other ◽  
Kinetics Model ◽  
Strong Positive Correlation ◽  
Mineralization Process ◽  
First Order ◽  
First Order Kinetics ◽  
Significant Difference

Modeling is an attempt to describe a natural event mathematically.  The modeling of N mineralization process has a dual interest, agronomical and ecological.  The objective of this study is to evaluate several mathematical models to describe the nitrogen mineralization process of soil samples. These samples were collected from 34 sites spatially distributed in the semi-arid region of El-Madher (the Aures area, north-east of Algeria). Using an auger, the systematic surveys have been carried out and composite samples of soils were collected in the field, and subjected to physical and chemical analyzes. In order to track the kinetic organic nitrogen mineralization, similar samples were collected and taken into cool boxes have been incubated in laboratory, sieved (2 mm) and stored at 4°C before use and then incubated at 28°C for 56 weeks. To facilate comparison, all results have been statistically analyzed, by nonlinear regression and analysis of variance method. Four empirical models were tested to fitt the value found experimentally. The linear kinetics model Nm=k t Ni, the single first-order kinetics model (MI) Nm = Ni e-kt + No (1 - e-kt), the double first-order and the exponential kinetics model (MII) Nm=Ni e-kt + No (1 - e-kt) + e-ht and the hyperbolic kinetics model (MH) Nm=NoH.t/(Tc+t) Ni were used to simulate the cumulative mineralized N (NH4+-N and NO3- -N) in the laboratory incubation. In order to test the performance and robustness of the different models three goodness of fit (coefficient of determination R2, Root Mean Square RMS and Mean Relative Error RMSE) were used. Moreover, the parameters obtained by the different models determined the predictions of nitrogen mineralization. The best results were obtained using the double first-order and exponential kinetics model. The results showed no significant difference between nitrogen mineralized for 56 weeks and nitrogen predicted by various models. However, the N predicted by the MII appears to be the best compared to other models. Indeed, the overestimation of nitrogen potentially mineralizable (N0) obtained by this model was relatively lower than other models. This has been confirmed by the study of multiple correlations between net mineral nitrogen and nitrogen predicted by each model. Thus, the results obtained showed a strong positive correlation between mineralized nitrogen values and those of nitrogen predicted by the different models. The correlation coefficients values indicate the folowing order MII (r = 0.878)> MI (r = 0.748)> MH (r = 0.709). The MII model has, therefore, highlighted that two pools of organic matter that mineralize simultaneously were detected in soil. One pool is stable and the other one is labile. One pool evolves with first-order kinetics and the other with exponential kinetics.

Photo-catalytic degradation of gaseous pollutants in paper mills of southern China

TAPPI Journal ◽  
2018 ◽  
Vol 17 (03) ◽  
pp. 167-178 ◽  
Author(s):  
Xin Tong ◽  
Jiao Li ◽  
Jun Ma ◽  
Xiaoquan Chen ◽  
Wenhao Shen
Keyword(s):  
Degradation Rate ◽  
Southern China ◽  
Catalytic Degradation ◽  
Pulp And Paper ◽  
Gaseous Pollutants ◽  
Pulp And Paper Mills ◽  
Paper Mills ◽  
Initial Concentration ◽  
First Order ◽  
First Order Kinetics

Studies were undertaken to evaluate gaseous pollutants in workplace air within pulp and paper mills and to consider the effectiveness of photo-catalytic treatment of this air. Ambient air at 30 sampling sites in five pulp and paper mills of southern China were sampled and analyzed. The results revealed that formaldehyde and various benzene-based molecules were the main gaseous pollutants at these five mills. A photo-catalytic reactor system with titanium dioxide (TiO2) was developed and evaluated for degradation of formaldehyde, benzene and their mixtures. The experimental results demonstrated that both formaldehyde and benzene in their pure forms could be completely photo-catalytic degraded, though the degradation of benzene was much more difficult than that for formaldehyde. Study of the photo-catalytic degradation kinetics revealed that the degradation rate of formaldehyde increased with initial concentration fitting a first-order kinetics reaction. In contrast, the degradation rate of benzene had no relationship with initial concentration and degradation did not conform to first-order kinetics. The photo-catalytic degradation of formaldehyde-benzene mixtures indicated that formaldehyde behaved differently than when treated in its pure form. The degradation time was two times longer and the kinetics did not reflect a first-order reaction. The degradation of benzene was similar in both pure form and when mixed with formaldehyde.

Kinetic of oxidation of methyl orange by vanadium(V) under conditions VO2+ and decavanadates coexist: Catalysis by Triton X-100 micellar medium

2019 ◽  
Author(s):  
Chem Int
Keyword(s):  
Methyl Orange ◽  
Solution Ph ◽  
Vanadium Concentration ◽  
Limiting Behavior ◽  
First Order ◽  
First Order Kinetics ◽  
Ph Range ◽  
Kinetic Pattern ◽  
Triton X ◽  
Kinetics Of

The kinetics of oxidation of methyl orange by vanadium(V) {V(V)} has been investigated in the pH range 2.3-3.79. In this pH range V(V) exists both in the form of decavanadates and VO2+. The kinetic results are distinctly different from the results obtained for the same reaction in highly acidic solution (pH < 1) where V(V) exists only in the form of VO2+. The reaction obeys first order kinetics with respect to methyl orange but the rate has very little dependence on total vanadium concentration. The reaction is accelerated by H+ ion but the dependence of rate on [H+] is less than that corresponding to first order dependence. The equilibrium between decavanadates and VO2+ explains the different kinetic pattern observed in this pH range. The reaction is markedly accelerated by Triton X-100 micelles. The rate-[surfactant] profile shows a limiting behavior indicative of a unimolecular pathway in the micellar pseudophase.

Biodegradation rates of aromatic contaminants in biofilm reactors

1995 ◽  
Vol 31 (1) ◽  
pp. 117-128 ◽  
Author(s):  
Jean-Pierre Arcangeli ◽  
Erik Arvin
Keyword(s):  
Aromatic Hydrocarbons ◽  
Competitive Inhibition ◽  
Removal Rate ◽  
First Order ◽  
Biofilm Reactors ◽  
First Order Kinetics ◽  
Reducing Conditions ◽  
Low Concentrations ◽  
Degradation Rates ◽  
Order Surface

This study has shown that microorganisms can adapt to degrade mixtures of aromatic pollutants at relatively high rates in the μg/l concentration range. The biodegradation rates of the following compounds were investigated in biofilm systems: aromatic hydrocarbons, phenol, methylphenols, chlorophenols, nitrophenol, chlorobenzenes and aromatic nitrogen-, sulphur- or oxygen-containing heterocyclic compounds (NSO-compounds). Furthermore, a comparison with degradation rates observed for easily degradable organics is also presented. At concentrations below 20-100 μg/l the degradation of the aromatic compounds was typically controlled by first order kinetics. The first-order surface removal rate constants were surprisingly similar, ranging from 2 to 4 m/d. It appears that NSO-compounds inhibit the degradation of aromatic hydrocarbons, even at very low concentrations of NSO-compounds. Under nitrate-reducing conditions, toluene was easily biodegraded. The xylenes and ethylbenzene were degraded cometabolically if toluene was used as a primary carbon source; their removal was influenced by competitive inhibition with toluene. These interaction phenomena are discussed in this paper and a kinetic model taking into account cometabolism and competitive inhibition is proposed.

In-vitro Kinetic Hydrolysis Study of Metronidazole Derivatives with Carvacrol and Eugenol Using Validated RP-HPLC Method

2020 ◽  
Vol 16 ◽  
Author(s):  
M. Alarjah
Keyword(s):  
Half Life ◽  
Hplc Method ◽  
Hydrolysis Rate ◽  
First Order ◽  
First Order Kinetics ◽  
Rp Hplc ◽  
Pharmacokinetic Properties ◽  
Pseudo First Order ◽  
Kinetic Hydrolysis

Background: Prodrugs principle is widely used to improve the pharmacological and pharmacokinetic properties of some active drugs. Much effort was made to develop metronidazole prodrugs to enhance antibacterial activity and or to improve pharmacokinetic properties of the molecule or to lower the adverse effects of metronidazole. Objective: In this work, the pharmacokinetic properties of some of monoterpenes and eugenol pro metronidazole molecules that were developed earlier were evaluated in-vitro. The kinetic hydrolysis rate constants and half-life time estimation of the new metronidazole derivatives were calculated using the validated RP-HPLC method. Method: Chromatographic analysis was done using Zorbbax Eclipse eXtra Dense Bonding (XDB)-C18 column of dimensions (250 mm, 4.6 mm, 5 μm), at ambient column temperature. The mobile phase was a mixture of sodium dihydrogen phosphate buffer of pH 4.5 and methanol in gradient elution, at 1ml/min flow rate. The method was fully validated according to the International Council for Harmonization (ICH) guidelines. The hydrolysis process carried out in an acidic buffer pH 1.2 and in an alkaline buffer pH 7.4 in a thermostatic bath at 37ºC. Results: The results followed pseudo-first-order kinetics. All metronidazole prodrugs were stable in the acidic pH, while they were hydrolysed in the alkaline buffer within a few hours (6-8 hr). The rate constant and half-life values were calculated, and their values were found to be 0.082- 0.117 hr-1 and 5.9- 8.5 hr., respectively. Conclusion: The developed method was accurate, sensitive, and selective for the prodrugs. For most of the prodrugs, the hydrolysis followed pseudo-first-order kinetics; the method might be utilised to conduct an in-vivo study for the metronidazole derivatives with monoterpenes and eugenol.

Decomposition of 4,4'-(Diazoamino)-bis(5-methoxy-2-methylbenezenesulfonic Acid) in Solutions ofFD&C Red No. 40

1984 ◽  
Vol 67 (4) ◽  
pp. 844-845
Author(s):  
Naomi Richfield-Fratz
Keyword(s):  
Liquid Chromatography ◽  
Aqueous Solutions ◽  
Borate Buffer ◽  
Sodium Borate ◽  
First Order ◽  
First Order Kinetics ◽  
Color Additive ◽  
Sodium Borate Buffer

Abstract 4,4'-(Diazoamino)-bis(5-methoxy-2-methylbenzenesuIfonic acid), when present as a reaction by-product in FD&C Red No. 40, is shown to decompose rapidly in aqueous solutions of the color additive. The decomposition is halted by the addition of sodium borate buffer. Quantitationly liquid chromatography shows that decomposition is nonlinear with time and follows approximate first order kinetics.

scholarly journals Comparative Study of Chemical Stability of Two H1Antihistaminic Drugs, Terfenadine and ItsIn VivoMetabolite Fexofenadine, Using LC-UV Methods

2019 ◽  
Vol 2019 ◽  
pp. 1-10
Author(s):  
Anna Gumieniczek ◽  
Anna Berecka-Rycerz ◽  
Rafał Pietraś ◽  
Izabela Kozak ◽  
Karolina Lejwoda ◽  
...  
Keyword(s):  
Comparative Study ◽  
Chemical Stability ◽  
First Order ◽  
First Order Kinetics ◽  
Kinetics Of Degradation ◽  
Effects Of Temperature ◽  
High Doses ◽  
Antihistaminic Drugs ◽  
Kinetics Of

A comparative study of chemical stability of terfenadine (TER) and itsin vivometabolite fexofenadine (FEX) was performed. Both TER and FEX were subjected to high temperature at different pH and UV/VIS light at different pH and then quantitatively analyzed using new validated LC-UV methods. These methods were used to monitor the degradation processes and to determine the kinetics of degradation for both the compounds. As far as the effects of temperature and pH were concerned, FEX occurred more sensitive to degradation than TER. As far as the effects of UV/VIS light and pH were concerned, the both drugs were similarly sensitive to high doses of light. Using all stress conditions, the processes of degradation of TER and FEX followed the first-order kinetics. The results obtained for these two antihistaminic drugs could be helpful in developing their new derivatives with higher activity and stability at the same time.

The conversion of ethylene to ethylidyne on Pt(111): non-first order kinetics and ensemble effects

1994 ◽  
Vol 301 (1-3) ◽  
pp. 177-196 ◽  
Author(s):  
W. Erley ◽  
Y. Li ◽  
D.P. Land ◽  
John C. Hemminger
Keyword(s):  
First Order ◽  
First Order Kinetics ◽  
Ensemble Effects

scholarly journals Bleaching of chlorophylls by UV irradiation in vitro: The effects on chlorophyll organization in acetone and n-hexane

2008 ◽  
Vol 73 (3) ◽  
pp. 271-282 ◽  
Author(s):  
Jelena Zvezdanovic ◽  
Dejan Markovic
Keyword(s):  
Uv Irradiation ◽  
Photosynthetic Pigments ◽  
Energy Input ◽  
First Order ◽  
First Order Kinetics ◽  
Uv Photons ◽  
The Stability ◽  
Major Factors

The stability of chlorophylls toward UV irradiation was studied by Vis spectrophotometry in extracts containing mixtures of photosynthetic pigments in acetone and n-hexane. The chlorophylls underwent destruction (bleaching) obeying first-order kinetics. The bleaching was governed by three major factors: the energy input of the UV photons, the concentration of the chlorophylls and the polarity of the solvent, implying different molecular organizations of the chlorophylls in the two solvents.

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