scholarly journals Dissipation Behavior of a Mancozeb Residue (Dithiocarbamate Fungicide) in Tomato Under South Moroccan Climatic Condition

Author(s):  
El Habib Ait Addi

<div><p><em>Dissipation behavior of mancozeb, a widely used dithiocarbamte fungicide, applied under field condition on tomato at recommended dose was undertaken under greenhouses and open field during October and March in Souss-Massa area (south of Morocco) climatic condition. Residue levels of mancozeb were determined by using a simple method consisting in a hot acid digestion of the whole sample to evolve carbon disulfide (CS<sub>2</sub>), which is further quantified by spectrophotometry. Degradation rate in both open field and greenhouse followed first order kinetic. Half lives were 1.77 and 1.3 days in open field and in greenhouse were 2.0 and 1.8 days for October and March period respectively. Based on the observation reported, a pre harvested interval of at least three days after pesticide application at recommended dose may be suggested.</em></p></div>

2013 ◽  
Vol 2013 ◽  
pp. 1-7 ◽  
Author(s):  
Li Yu ◽  
Yongkui Huang ◽  
Yun Yang ◽  
Yulin Xu ◽  
Guohong Wang ◽  
...  

H4SiW6Mo6O40/SiO2was sensitized by H2O2solution that significantly improved its catalytic activity under simulated natural light. Degradation of basic fuchsin was used as a probe reaction to explore the influencing factors on the photodegradation reaction. The results showed that the optimal conditions were as follows: initial concentration of basic fuchsin 8 mg/L, pH 2.5, catalyst dosage 4 g/L, and light irradiation time 4 h. Under these conditions, the degradation rate of basic fuchsin is 98%. The reaction of photocatalysis for basic fuchsin can be expressed as the first-order kinetic model. After being used continuously for four times, the catalyst kept the inherent photocatalytic activity for degradation of dyes. The photodegradation of malachite green, methyl orange, methylene blue, and rhodamine B were also tested, and the degradation rate of dyes can reach 90%–98%.


2021 ◽  
Vol 63 (3) ◽  
pp. 35-41
Author(s):  
Dang Giang Chau Nguyen ◽  
◽  
Thi Lan Anh Tran ◽  
Thi Thanh Lam Tran ◽  
Thi My Duyen Ngo ◽  
...  

Pesticide dissipation on foods like vegetables, fruits, and cereals is one of the most concerning aspects in pesticide toxicology as it involves risks to human health and food safety. In light if this, a laboratory-scale study was conducted for two separate systems, green onions (Allium fistulosum) and mustard greens (Brassica juncea),in order to identify the dissipation of fipronil and cypermethrin, two commonly used insecticides, under a tropical climate. After the pesticide application, vegetable samples from these microcosms were collected each day for 7 days to measure fipronil and cypermethrin (n=3) residues. The analytical method was validated and showed repeatability and trueness. The decay equations fit well to first-order kinetics with a correlation coefficient of R2>0.93 and p<0.0005. The calculated half-life values of fipronil were 2.9 d for green onions and 3.2 d for mustard greens while those of cypermethrin were, respectively, 4.5 d and 3.2 d. To meet the maximum residue levels (MRL) of fipronil (0.02 mg/kg) and cypermethrin (0.7 mg/kg) on vegetables, the estimated pre-harvest intervals should be updated to 23 d and 7.5 d, respectively.


2013 ◽  
Vol 709 ◽  
pp. 70-73
Author(s):  
Guo Bin Duan ◽  
Yong Kui Huang ◽  
Li Yu ◽  
Shui Jin Yang

H3PW6Mo6O40/SiO2 was prepared by sol-gel method, and sensitized by H2O2 solution. The photocatalytic degradation of methyl violet by H3PW6Mo6O40/SiO2 under simulated natural light irradiation was investigated. The results demonstrated that at optimal condition (initial concentration of methyl violet is 10 mg/L, and the pH is 2.5, the dosage of catalyst is 0.5% based on feed stocks), the degradation rate of methyl violet is as high as 88.7 % after 2.5h simulated natural light irradiation. The reaction of photocatalysis for methyl violet can be expressed as first-order kinetic model.


2012 ◽  
Vol 9 (4) ◽  
pp. 1968-1975 ◽  
Author(s):  
S. M. Tabatabaei ◽  
A. Mehrizad ◽  
P. Gharbani

In this paper, efficiency of nano-ZnO particles on catalytic ozonation of 4-nitrochlorobenzene (4NCB) using semi-batch reactor has been studied at various pHs. During the catalytic ozonation, TOC and concentration of nitrate ions was monitored. Results indicate that degradation of 4NCB was improved by combination of nano-ZnO with ozone. The effect of ZnO particle size and pH are also examined. According to the results, concentration of 4NCB decreased with increasing of particle size from nanosized to microsized and pH from 3.0 to 9.0. Based on the results, it suggests radical hydroxyl does not affect on the degradation of 4NCB in catalytic ozonation, but the surface of catalyst plays main role. Kinetic studies showed degradation of 4NCB followed pseudo-first-order kinetic and maximum degradation rate was observed at pH=3.


2002 ◽  
Vol 46 (11-12) ◽  
pp. 127-132 ◽  
Author(s):  
M. Ike ◽  
M. Asano ◽  
F.D. Belkada ◽  
S. Tsunoi ◽  
M. Tanaka ◽  
...  

The degradation kinetics of biotransformation products of nonylphenol polyethoxylates (NPEOs), nonylphenol (NP), nonylphenol monoethoxylate (NP1EO) and nonylphenoxy carboxylic acid (NP1EC), by ozonation and UV/TiO2 (ultraviolet photocatalytic degradation in the presence of titanium dioxide suspension as a catalyst) were investigated using lab-scale reactors. The degradation rate of NP by UV/TiO2 was the highest among the tested NPEOs metabolites, while NP1EC showed the lowest degradation rate. In contrast, ozonation was especially effective for the breakdown of NP1EC. NP could be also degraded efficiently by ozonation, however, it was much less effective for NP1EO decomposition. Degradation of NP by both chemical oxidation processes followed first-order kinetics. The degradation curves of NP1EO and NP1EC could be approximately described by first-order kinetics also, although the degradation of NP1EC by ozonation seemed to follow a second-order kinetic.


TAPPI Journal ◽  
2018 ◽  
Vol 17 (03) ◽  
pp. 167-178 ◽  
Author(s):  
Xin Tong ◽  
Jiao Li ◽  
Jun Ma ◽  
Xiaoquan Chen ◽  
Wenhao Shen

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.


2014 ◽  
Vol 28 (2) ◽  
pp. 231-237 ◽  
Author(s):  
Lech W. Szajdak ◽  
Jerzy Lipiec ◽  
Anna Siczek ◽  
Artur Nosalewicz ◽  
Urszula Majewska

Abstract The aim of this study was to verify first-order kinetic reaction rate model performance in predicting of leaching of atrazine and inorganic compounds (K+1, Fe+3, Mg+2, Mn+2, NH4 +, NO3 - and PO4 -3) from tilled and orchard silty loam soils. This model provided an excellent fit to the experimental concentration changes of the compounds vs. time data during leaching. Calculated values of the first-order reaction rate constants for the changes of all chemicals were from 3.8 to 19.0 times higher in orchard than in tilled soil. Higher first-order reaction constants for orchard than tilled soil correspond with both higher total porosity and contribution of biological pores in the former. The first order reaction constants for the leaching of chemical compounds enables prediction of the actual compound concentration and the interactions between compound and soil as affected by management system. The study demonstrates the effectiveness of simultaneous chemical and physical analyses as a tool for the understanding of leaching in variously managed soils.


Author(s):  
D. de la Lama-Calvente ◽  
M. J. Fernández-Rodríguez ◽  
J. Llanos ◽  
J. M. Mancilla-Leytón ◽  
R. Borja

AbstractThe biomass valorisation of the invasive brown alga Rugulopteryx okamurae (Dictyotales, Phaeophyceae) is key to curbing the expansion of this invasive macroalga which is generating tonnes of biomass on southern Spain beaches. As a feasible alternative for the biomass management, anaerobic co-digestion is proposed in this study. Although the anaerobic digestion of macroalgae barely produced 177 mL of CH4 g−1 VS, the co-digestion with a C-rich substrate, such as the olive mill solid waste (OMSW, the main waste derived from the two-phase olive oil manufacturing process), improved the anaerobic digestion process. The mixture improved not only the methane yield, but also its biodegradability. The highest biodegradability was found in the mixture 1 R. okamurae—1 OMSW, which improved the biodegradability of the macroalgae by 12.9% and 38.1% for the OMSW. The highest methane yield was observed for the mixture 1 R. okamurae—3 OMSW, improving the methane production of macroalgae alone by 157% and the OMSW methane production by 8.6%. Two mathematical models were used to fit the experimental data of methane production time with the aim of assessing the processes and obtaining the kinetic constants of the anaerobic co-digestion of different combination of R. okamurae and OMSW and both substrates independently. First-order kinetic and the transference function models allowed for appropriately fitting the experimental results of methane production with digestion time. The specific rate constant, k (first-order model) for the mixture 1 R. okamurae- 1.5 OMSW, was 5.1 and 1.3 times higher than that obtained for the mono-digestion of single OMSW and the macroalga, respectively. In the same way, the transference function model revealed that the maximum methane production rate (Rmax) was also found for the mixture 1 R. okamurae—1.5 OMSW (30.4 mL CH4 g−1 VS day−1), which was 1.6 and 2.2 times higher than the corresponding to the mono-digestions of the single OMSW and sole R. okamurae (18.9 and 13.6 mL CH4 g−1 VS day−1), respectively.


1976 ◽  
Vol 56 (2) ◽  
pp. 71-78 ◽  
Author(s):  
D. R. CAMERON ◽  
C. G. KOWALENKO

A small subsystem model was developed to simulate the major nitrogen flow pathways in an unsaturated soil treated with ammonium sulphate. A nonlinear Freundlich equilibrium model and a Langmuir kinetic model were used to describe mathematically the adsorption–desorption of soluble NH4+ to the exchangeable and clay-fixed phases, respectively. Time dependent, microbial mediated first-order kinetic models were used to quantify the ammonification and nitrification processes. The subsystem model was then used as a research tool to derive ammonification and nitrification rate coefficients for a preceding incubation experiment conducted using different soil moisture contents and temperatures. The model yields reasonably good fits to the observed data. A subsequent regression analysis relating the coefficients to temperature and moisture pointed out the importance of the temperature–water content interaction term in quantifying microbial mediated processes.


2007 ◽  
Vol 73 (8) ◽  
pp. 2468-2478 ◽  
Author(s):  
Bernadette Klotz ◽  
D. Leo Pyle ◽  
Bernard M. Mackey

ABSTRACT A new primary model based on a thermodynamically consistent first-order kinetic approach was constructed to describe non-log-linear inactivation kinetics of pressure-treated bacteria. The model assumes a first-order process in which the specific inactivation rate changes inversely with the square root of time. The model gave reasonable fits to experimental data over six to seven orders of magnitude. It was also tested on 138 published data sets and provided good fits in about 70% of cases in which the shape of the curve followed the typical convex upward form. In the remainder of published examples, curves contained additional shoulder regions or extended tail regions. Curves with shoulders could be accommodated by including an additional time delay parameter and curves with tails shoulders could be accommodated by omitting points in the tail beyond the point at which survival levels remained more or less constant. The model parameters varied regularly with pressure, which may reflect a genuine mechanistic basis for the model. This property also allowed the calculation of (a) parameters analogous to the decimal reduction time D and z, the temperature increase needed to change the D value by a factor of 10, in thermal processing, and hence the processing conditions needed to attain a desired level of inactivation; and (b) the apparent thermodynamic volumes of activation associated with the lethal events. The hypothesis that inactivation rates changed as a function of the square root of time would be consistent with a diffusion-limited process.


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