scholarly journals Preliminary Feasibility Study of Benzo(a)Pyrene Oxidative Degradation by Fenton Treatment

2009 ◽  
Vol 2009 ◽  
pp. 1-6 ◽  
Author(s):  
Vera Homem ◽  
Zélia Dias ◽  
Lúcia Santos ◽  
Arminda Alves
Keyword(s):  
Removal Efficiency ◽  
Water Contamination ◽  
Oxidative Degradation ◽  
Degradation Process ◽  
Fenton Reagent ◽  
Laboratory Unit ◽  
Ion Concentrations ◽  
New Methods ◽  
Polycyclic Aromatic ◽  
Aqueous Matrices

Polycyclic aromatic hydrocarbons (PAHs) are considered priority compounds due to their toxic and carcinogenic nature. The concern about water contamination and the consequent human exposure has encouraged the development of new methods for PAHs removal. The purpose of this work was to study the feasibility of a degradation process of benzo(a)pyrene (BaP) in aqueous matrices by oxidation with Fenton reagent. A laboratory unit was designed to optimize the factors which may influence the process: pH (3.5 to 6.0), temperature (30 to70°C),H2O2(20 to 150 mgL-1),Fe2+concentration (2.75 to 5.50 mgL-1), and the initial concentration of the pollutant (10 to 100 μgL-1). The pH did not influence significantly the results in the range studied. An increase in temperature from 30 to70°Cimproved the removal efficiency from 90% to 100%. The same effect was observed for ferrous ion concentrations from 2.75 to 5.50 mgL-1(increase from 78% to 100% removal). TheH2O2concentration played a double role during the process: from 20 to 50 mgL-1an increase in the removal efficiency was achieved, but for higher concentrations (>50 mgL-1) the degradation is lower. This study proved that the degradation of benzo(a)pyrene by Fenton's reagent is a viable process.

scholarly journals Heat Aged Tensile Strength Retention of Poly (p-phenylene terephthalamide) Sewing Thread

2008 ◽  
Vol 3 (4) ◽  
pp. 155892500800300 ◽  
Author(s):  
Walter R. Hall ◽  
Warren F. Knoff
Keyword(s):  
Hydrolytic Degradation ◽  
Oxidative Degradation ◽  
Thermal Exposure ◽  
Strength Loss ◽  
Degradation Process ◽  
Downstream Processing ◽  
Kink Bands ◽  
Sewing Thread ◽  
Continuous Filament ◽  
Strength Retention

The strength retention after exposure to elevated temperature in air of continuous filament and staple spun PPTA sewing thread and the precursor yarns was determined. For both types, the process of converting the greige yarn to thread reduced the amount of strength retained after thermal exposure. The continuous filament products retained more strength than the staple products. The data was fitted to a kinetic rate model in which two strength loss processes occurred. The first process occurred within about the first 5 minutes of thermal exposure and is hypothesized to be hydrolytic degradation. The estimated secondary degradation process activation energy suggests this to be thermo-oxidative degradation. Optical microscopy of filaments indicates a higher level of kink banding and other damage in continuous filament versus staple products and in finished thread versus the precursor yarns. The kink bands and damage are believed to be caused by the staple manufacturing process and the downstream processing of precursor yarn to finished sewing thread. The kink bands and damage are hypothesized to be responsible for the differences in strength retention.

Study of structural and morphological changes during acсelerated oxidative degradation of mixtures of polyoxybutyrate with polycaprolactane

2021 ◽  
Vol 5 ◽  
pp. 60-69
Author(s):  
V. N. Vasilets ◽  
◽  
A. P. Pankina ◽  
E. A. Nemets ◽  
V. Yu. Belov ◽  
...  
Keyword(s):  
Morphological Changes ◽  
Oxidative Degradation ◽  
Initial Mixture ◽  
Polymer Composite Material ◽  
Degree Of Crystallinity ◽  
Fenton Reagent ◽  
Dsc Method ◽  
The Degree Of Crystallinity ◽  
Composite Samples ◽  
Scanning Electron

Structural and morphological changes in the films of poly(oxybirutyrate-co-oxyvalerate) (P(OB-OV)) with poly-e-caprolactone (PCL) were studied by IR spectroscopy, DSC, and scanning electron microscopy during accelerated oxidative degradation under tests in Fenton reagent. It is shown by the DSC method that the phase separation of the P(OB-OV) and PCL components is observed in the initial mixture. The melting of various phases of P(OB-OV) is observed at temperatures of 147 °C and 157 °C, and PCL melts at a temperature of 61 °C. The degree of crystallinity of P(OB-OV) and PCL in the mixture is 67 % and 50 %, respectively. It was found that the degradation of poly(oxybirutyrate-co-oxyvalerate) prevails during incubation of composite samples in Fenton solution for 2 to 12 weeks. By changing the ratio of the components, it is possible to significantly change the rate of oxidative degradation, the molecular weight and the degree of crystallinity of the polymer composite material P(OB-OV):PCL.

scholarly journals Effect of char layer on transient thermal oxidative degradation of polyethylene

2007 ◽  
Vol 11 (2) ◽  
pp. 23-36 ◽  
Author(s):  
Javad Esfahani ◽  
Ali Abdolabadi
Keyword(s):  
Heat Transfer ◽  
Heat Source ◽  
Solid Phase ◽  
Early Stage ◽  
Radiation Heat Transfer ◽  
Oxidative Degradation ◽  
Degradation Process ◽  
Thermal Oxidative Degradation ◽  
Char Layer ◽  
Effect Of Oxygen

A transient one dimensional model has been presented to simulate degradation and gasification of polyethylene, in early stage of fire growth. In the present model effect of oxygen on degradation and rate of polymer gasification while the sample is subjected to an external radiative heat source is numerically investigated. This model includes different mechanism, which affect the degradation process, such as in depth thermal oxidative decomposition, in depth absorption of radiation, heat transfer, volatiles advection in solid phase and convective heat transfer on surface. Also effects of radiative parameters, due to formation of char layer such as surface reflectivity and absorptivity on thermal degradation of polyethylene are investigated. The results for 40 kW/m2 heat source are reported and yielded realistic results, comparing to the published experimental data. The results show that an increase in oxygen concentration leads to considerable increase in gasification rate and also leads to sharp increase of surface temperature. .

scholarly journals Determination and Remediation of Selected Polycyclic Aromatic Hydrocarbons in Petroleum Contaminated Water

2020 ◽  
Vol 24 (3) ◽  
pp. 459-465
Author(s):  
O.O. Ijaola ◽  
A.Y. Sangodoyin
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Removal Efficiency ◽  
Aromatic Hydrocarbons ◽  
Activated Carbons ◽  
Experimental Result ◽  
Contaminated Water ◽  
Total Efficiency ◽  
Spectroscopic Techniques ◽  
Bambusa Vulgaris ◽  
Polycyclic Aromatic

Determination and remediation of pollutants such as polycyclic aromatic hydrocarbons (PAHs) have not being fully regulated in Nigeria; hence  contamination of surface water by such pollutant is a major concern. This study was designed to determine the level of selected PAHs in petroleum contaminated water using spectroscopic techniques and the efficacy of activated carbons made from Bambusa vulgaris and Oxytenanthera  vabyssinaca. Bambusa vulgaris and Oxytenanthera abyssinaca were carbonized at 350OC and activated with Phosphoric acid (CBV350OC H3PO4) and Potassium chloride (COA 350OC KCl) as dehydrating agent respectively. The adsorbents were then used to remediate PAHs in petroleum contaminated water. Liquid-Liquid extraction procedures were used for extracting selected PAHs from sampled solutions. The batch experiment was performed to study the adsorption capacity of adsorbents at 5hrs contact time. Analysis of PAHs concentration for each sampling day was determined by GC-MS. Total PAHs in simulated wastewater did not show a clear trend, contrary to the expectation that there should be a progressive increase with time due to photolysis or photodecomposition of compounds or PAHs. COA 350OC KCl showed a range of 6.2-19.3% removal efficiency of each selected PAH with a total percentage efficiency of 27.7-70.8 for all days. For CBV350OC H3PO4 removal efficiency ranged from 10.26-19.30% for each selected PAH and a total efficiency of 50.8-100% for all selected PAHs for the 4 days intervals. The experimental result showed that adsorbent made from Bambusa vulgaris and Oxytenanthera abyssinaca and activated with H3PO4 and KCl as dehydrating agentrespectively can efficiently adsorb the selected PAHs in contaminated water. The study also revealed that PAHs in contaminated water increases with time due to photodecomposition, thus necessitating their treatment on time.

scholarly journals Isolation and Structure Determination of Echinochrome A Oxidative Degradation Products

Molecules ◽  
2020 ◽  
Vol 25 (20) ◽  
pp. 4778
Author(s):  
Natalia P. Mishchenko ◽  
Elena A. Vasileva ◽  
Andrey V. Gerasimenko ◽  
Valeriya P. Grigorchuk ◽  
Pavel S. Dmitrenok ◽  
...  
Keyword(s):  
Mass Spectrometry ◽  
Degradation Products ◽  
Lethal Dose ◽  
Oxidative Degradation ◽  
Degradation Process ◽  
Oxidation Products ◽  
Chemical Mechanism ◽  
Ionization Mass ◽  
Echinochrome A ◽  
Esi Ms

Echinochrome A (Ech A, 1) is one of the main pigments of several sea urchin species and is registered in the Russian pharmacopeia as an active drug substance (Histochrome®), used in the fields of cardiology and ophthalmology. In this study, Ech A degradation products formed during oxidation by O2 in air-equilibrated aqueous solutions were identified, isolated, and structurally characterized. An HPLC method coupled with diode-array detection (DAD) and mass spectrometry (MS) was developed and validated to monitor the Ech A degradation process and identify the appearing compounds. Five primary oxidation products were detected and their structures were proposed on the basis of high-resolution electrospray ionization mass spectrometry (HR-ESI-MS) as 7-ethyl-2,2,3,3,5,7,8-heptahydroxy-2,3-dihydro-1,4-naphthoquinone (2), 6-ethyl-5,7,8-trihydroxy-1,2,3,4-tetrahydronaphthalene-1,2,3,4-tetraone (3), 2,3-epoxy-7-ethyl-2,3-dihydro-2,3,5,6,8-pentahydroxy-1,4-naphthoquinone (4), 2,3,4,5,7-pentahydroxy-6-ethylinden-1-one (5), and 2,2,4,5,7-pentahydroxy-6-ethylindane-1,3-dione (6). Three novel oxidation products were isolated, and NMR and HR-ESI-MS methods were used to establish their structures as 4-ethyl-3,5,6-trihydroxy-2-oxalobenzoic acid (7), 4-ethyl-2-formyl-3,5,6-trihydroxybenzoic acid (8), and 4-ethyl-2,3,5-trihydroxybenzoic acid (9). The known compound 3-ethyl-2,5-dihydroxy-1,4-benzoquinone (10) was isolated along with products 7–9. Compound 7 turned out to be unstable; its anhydro derivative 11 was obtained in two crystal forms, the structure of which was elucidated using X-ray crystallography as 7-ethyl-5,6-dihydroxy-2,3-dioxo-2,3-dihydrobenzofuran-4-carboxylic acid and named echinolactone. The chemical mechanism of Ech A oxidative degradation is proposed. The in silico toxicity of Ech A and its degradation products 2 and 7–10 were predicted using the ProTox-II webserver. The predicted median lethal dose (LD50) value for product 2 was 221 mg/kg, and, for products 7–10, it appeared to be much lower (≥2000 mg/kg). For Ech A, the predicted toxicity and mutagenicity differed from our experimental data.

Modeling and Optimization of Photocatalytic Degradation of Methylene Blue Using Lanthanum Vanadate

2020 ◽  
Vol 1008 ◽  
pp. 97-103
Author(s):  
Mahmoud Samy ◽  
Mona G. Ibrahim ◽  
Mohamed Gar Alalm ◽  
Manabu Fujii
Keyword(s):  
Methylene Blue ◽  
Photocatalytic Degradation ◽  
Removal Efficiency ◽  
Textile Industry ◽  
Degradation Process ◽  
Optimum Conditions ◽  
Photo Degradation ◽  
Operational Conditions ◽  
Degradation Rates ◽  
Effects Of Ph

Methylene blue (MB) is one of the commonly used dyes in the textile industry and can be used as a model pollutant for the textile industry wastewater. In this work, the photocatalytic degradation of MB by synthesized nanoparticles of lanthanum vanadate (LaVO4) was assessed. The effects of pH, initial MB concentration and catalyst dose on the removal performance of MB were investigated and measuring the optimum values of these operational conditions was performed using response surface methodology (RSM). Catalyst dose of 0.43 g/L, initial MB concentration of 5.0 mg/L, and pH of 6.86 were found to be the optimum conditions in reaction time of 60 min. A mathematical model was formed to relate the removal efficiency of MB to the aforementioned operating parameters. The removal efficiency of MB was 91% without any scavengers at a catalyst dose of 0.3 g/L, pH of 7 and initial MB concentration of 10 mg/L. The trapping experiments confirmed the participation of different reactive species in the photo-degradation process. The degradation rates of MB were 91%, 86%, 81%, 77.70% and 72% in five successive runs using LaVO4.

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