A field-study of leaching and degradation of nine pesticides in a sandy soil

Soil Research ◽  
1995 ◽  
Vol 33 (6) ◽  
pp. 1019 ◽  
Author(s):  
RS Kookana ◽  
HJ Di ◽  
LAG Aylmore
Keyword(s):  
Field Study ◽  
Sandy Soil ◽  
Water Contamination ◽  
High Performance ◽  
Dilute Solution ◽  
Ground Water Contamination ◽  
First Order ◽  
Degradation Rates ◽  
Residue Concentration ◽  
Different Depths

A field study was conducted on a coastal sandy soil (Karrakata sand) of Western Australia from July to December 1990, to measure the leaching and degradation rates of chlorpyriphos, chlorthal dimethyl, fenamiphos, linuron, metalaxyl, metribuzin, prometryne, propyzamide and simazine. Commercial grade products were sprayed in dilute solution form at recommended rates to the surface of held plots. Irrigation was applied daily which together with rainfall gave effective rainfall equivalent to at least 120% of potential evaporation. Pesticide residue concentrations in soil samples taken at 5 cm increments down to 50 cm, at different days after application, were determined by high performance liquid chromatography (HPLC). Mean leaching depths (MLDs) were calculated by weighting the percentage residues remaining at different depths in the soil profile. The MLDs for the 5 month period followed the order: chlorpyriphos and chlorthal dimethyl (<5 cm) < linuron and simazine (6) < propyzamide (8) and prometryne (9) < metribuzin (12) < metalaxyl (18) < fenamiphos and metabolites (28). This generally corresponded inversely with the sorption coefficients (K-oc). The degradation rates (i.e. decreases with time of total residue concentration in the sampled profile) could mostly be described by first-order regressions (R(2) = 0.59-0.95). Calculated half-lives showed the order: metribuzin (27 days), simazine (28) < fenamiphos (43), chlorthal dimethyl (45) < prometryne (58), propyzamide (59) < metalaxyl (70) < chlorpyriphos (81) < fenamiphos plus metabolites (98) < linuron (219). The potential for causing ground water contamination, as indicated by the ratio of half-life to Koc followed the order: chlorthal dimethyl, chlorpyriphos < metribuzin, prometryne < simazine, propyzamide < linuron < metalaxyl < fenamiphos and metabolites.

scholarly journals Study on environmental behaviour of fluopyram in different banana planting soil

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Jia Zhou ◽  
Shuilian Liang ◽  
Yuanyuan Cui ◽  
Yu Rong ◽  
Jia Song ◽  
...  
Keyword(s):  
Sandy Soil ◽  
Alluvial Soil ◽  
Order Kinetic ◽  
Environmental Behaviour ◽  
First Order ◽  
Degradation Rates ◽  
And Migration ◽  
Agricultural Areas ◽  
Banana Leaf ◽  
Order Kinetic Equation

AbstractFluopyram is commonly used to control banana leaf spot, anthracnose, and scab in tropical agricultural areas. To explore its behaviour in tropical agricultural environments, dissipation, adsorption, and leaching behaviours of fluopyram in three typical banana planting soils were studied. Also, its dissipation and migration capabilities in different regions and different soil types were evaluated. The results showed that the dissipation of fluopyram was in accordance with the first-order kinetic equation in the three banana soils, but the degradation rates were quite different. The degradation half-lives in the Hainan latosol, Yunnan sandy soil, and Fujian Plain alluvial soil were 46.21 days, 36.48 days and 57.76 days, respectively. Fluopyram also exhibited high adsorption and low leachability in the three soils. The Fujian Plain alluvial soil had the highest adsorption capacity for fluopyram, while fluopyram had the low leachability in the Yunnan sandy soil.

scholarly journals Degradation of Bisphenol A in an Aqueous Solution by a Photo-Fenton-Like Process Using a UV KrCl Excilamp

2021 ◽  
Vol 18 (3) ◽  
pp. 1152
Author(s):  
Denis Aseev ◽  
Agniya Batoeva ◽  
Marina Sizykh ◽  
Daniil Olennikov ◽  
Galina Matafonova
Keyword(s):  
Bisphenol A ◽  
High Performance ◽  
Aqueous Media ◽  
Chain Mechanism ◽  
Efficient Removal ◽  
Radical Chain ◽  
First Order ◽  
Degradation Rates ◽  
Endocrine Disrupting ◽  
Flow Through

Bisphenol A (BPA), a precursor to important plastics, is regarded as a common aquatic micropollutant with endocrine-disrupting activity. In the present study, we explored the capability of a UV KrCl excilamp (222 nm) to degrade BPA by a photo-Fenton-like process using persulfate under flow-through conditions. The first-order rate constants of degradation were obtained and the mineralization of dissolved organic carbon (DOC) was estimated. The results showed complete BPA degradation and high DOC mineralization (70–97%). A comparative analysis of degradation rates and DOC removal in the examined systems (UV, Fe2+/S2O82−, UV/S2O82− and UV/Fe2+/S2O82−) revealed a significant synergistic effect in the photo-Fenton-like system (UV/Fe2+/S2O82−) without the accumulation of toxic intermediates. This indicated that the BPA was oxidized via the conjugated radical chain mechanism, which was based on the photo-induced and catalytic processes involving HO• and SO4−• radicals. The primary intermediates of BPA degradation in the UV/Fe2+/S2O82− system were identified by HPLC/MS and the oxidation pathway was proposed. The high performance of the photo-Fenton-like process employing a quasi-monochromatic UV radiation of a KrCl excilamp offers promising potential for an efficient removal of such micropollutants from aqueous media.

Two-stage self-seeding method for preparation of single crystals of poly(phenylene sulfide)

1989 ◽  
Vol 47 ◽  
pp. 368-369
Author(s):  
Sengshiu Chung ◽  
Peggy Cebe
Keyword(s):  
Single Crystals ◽  
High Performance ◽  
Dilute Solution ◽  
Two Stage ◽  
Annealing Behavior ◽  
High Performance Polymers ◽  
Seeding Method ◽  
Phenylene Sulfide

We are studying the crystallization and annealing behavior of high performance polymers, like poly(p-pheny1ene sulfide) PPS, and poly-(etheretherketone), PEEK. Our purpose is to determine whether PPS, which is similar in many ways to PEEK, undergoes reorganization during annealing. In an effort to address the issue of reorganization, we are studying solution grown single crystals of PPS as model materials.Observation of solution grown PPS crystals has been reported. Even from dilute solution, embrionic spherulites and aggregates were formed. We observe that these morphologies result when solutions containing uncrystallized polymer are cooled. To obtain samples of uniform single crystals, we have used two-stage self seeding and solution replacement techniques.

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.

Electrochemical Oxidation of Perfluorooctanesulfonate by Magnéli Phase Ti4O7 Electrode in the Presence of Trichloroethylene

2020 ◽  
Vol 1 (4) ◽  
Author(s):  
Peizeng Yang ◽  
Yaye Wang ◽  
Junhe Lu ◽  
Viktor Tishchenko ◽  
Qingguo Huang ◽  
...  
Keyword(s):  
Electrochemical Oxidation ◽  
Current Density ◽  
First Order ◽  
Degradation Rates ◽  
Oxidation Technology ◽  
Magnéli Phase ◽  
Polyfluoroalkyl Substances ◽  
Titanium Suboxide ◽  
Gas Tight ◽  
Magneli Phase

This study examined the degradation of perfluorooctanesulfonate (PFOS) in electrochemical oxidation (EO) processes in the presence of trichloroethylene (TCE). The EO experiment was performed in a gas-tight reactor using Magnéli phase titanium suboxide (Ti4O7) as the anode. The experimental data demonstrated that 75% of PFOS (2 μM) was degraded at 10 mA/cm2 current density in 30 min without TCE present in the solution, while the presence of 76 μM TCE apparently inhibited the degradation of PFOS, reducing its removal down to 53%. Defluorination ratio suggested that PFOS was significantly mineralized upon EO treatment, and it appeared to be not influenced by the presence of TCE. The respective pseudo-first order rate constants (kobs) of PFOS removal were 0.0471 and 0.0254 min-1 in the absence and presence of TCE. The degradation rates of both PFOS and TCE increased with current density rising from 2.5 to 20 mA/cm2. In the presence of TCE, chloride, chlorate, and perchlorate were formed that accounted for 79.7 %, 5.53%, and 1.51% of the total chlorine at 60 min. This work illustrates the promise of the Magnéli phase Ti4O7 electrode based electrochemical oxidation technology for degrading per- and polyfluoroalkyl substances (PFASs) and co-contaminants in groundwaters.

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