Kinetics and Mechanism of Degradation of Aqueous Promecarb Insecticide Studied by UV Spectrophotometry and HPLC

2017 ◽  
Vol 42 (2) ◽  
pp. 145-153 ◽  
Author(s):  
Hayet Bakhti ◽  
Najib Ben Hamida
Keyword(s):  
Degradation Mechanism ◽  
Aqueous Media ◽  
Reversed Phase ◽  
Activation Entropy ◽  
Uv Spectrophotometry ◽  
Order Kinetic ◽  
First Order ◽  
Mechanism Of Degradation ◽  
Order Kinetic Model

The present paper deals with the degradation mechanism of the insecticide promecarb, or 3-isopropyl-5-methylphenyl- N-methylcarbamate, in aqueous media. The reaction kinetics have been investigated using UV spectrophotometry and reversed phase HPLC. The determination of 3-isopropyl-5-methylphenol as the main product of promecarb hydrolysis gives evidence for the significant reactivity of this insecticide in alkaline solution. The rate constants were determined following a proposed first-order kinetic model. The positive activation entropy obtained Δ S≠ = +66.82 J mol−1 K−1 and the absence of general basic catalysis indicates an E1cB mechanism involving unimolecular collapse of the promecarb via a methylisocyanate intermediate. These results were confirmed by the fact that promecarb fits well into Brønsted and Hammett plots obtained for a series of substituted N-methylcarbamates for which the decomposition in aqueous media was established to follow an E1cB mechanism.

scholarly journals The Determination of Anaerobic Biodegradability Rates Livestock Byproducts Using Double First-Order Kinetic Model

2015 ◽  
Vol 48 (5) ◽  
pp. 542-548
Author(s):  
Kook-Sik Shin ◽  
Young-man Yoon ◽  
Ha-Il Jung ◽  
Byung-Geun Hyun ◽  
Hyun-Joon Cho ◽  
...  
Keyword(s):  
Kinetic Model ◽  
Order Kinetic ◽  
First Order ◽  
Anaerobic Biodegradability ◽  
Order Kinetic Model

Kinetics of bioactive compounds in functional spice Jiangpo during thermal processing

2012 ◽  
Vol 8 (3) ◽  
Author(s):  
Xiaoyan Dai ◽  
Chenhuan Yu ◽  
Qiaofeng Wu
Keyword(s):  
Kinetic Parameters ◽  
Bioactive Compounds ◽  
Thermal Processing ◽  
Order Rate Constant ◽  
Heat Processing ◽  
Order Kinetic ◽  
Time Intervals ◽  
First Order ◽  
Order Kinetic Model ◽  
Kinetics Of

Abstract Jiangpo is an increasingly popular East Asian spice which is made from Mangnolia officinalis bark and ginger juice. Since it induces bioactive compounds decomposition and has influence on final flavor and fragrance, cooking is regarded as the key operation in preparation of Jiangpo. To evaluate the bioactive compounds content changes of Jiangpo during thermal processing, kinetic parameters including reaction order, rate constant, T1/2 and activation energy of bioactive markers namely honokiol, magnolol and curcumin were determined. Cooking was set at temperatures 60, 90 and 120 °C for selected time intervals. Results displayed the thermal kinetic characteristics of the three compounds. Thermal degradation of Honokiol and magnolol both followed first order kinetic model and the loss of curcumin fitted second order. A mathematical model based on the obtained kinetic parameters has also been developed to predict the degradation of honokiol, magnolol and curcumin in non-isothermal state. All the information in this paper could contribute necessary information for optimizing the existing heat processing of Jiangpo.

scholarly journals Municipal Leachate Treatment by Fenton Process: Effect of Some Variable and Kinetics

2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
Mohammad Ahmadian ◽  
Sohyla Reshadat ◽  
Nader Yousefi ◽  
Seyed Hamed Mirhossieni ◽  
Mohammad Reza Zare ◽  
...  
Keyword(s):  
Reaction Time ◽  
Color Removal ◽  
Molar Ratio ◽  
Order Kinetic ◽  
Fenton Process ◽  
Solution Ph ◽  
Leachate Treatment ◽  
First Order ◽  
Order Kinetic Model ◽  
Better Than

Due to complex composition of leachate, the comprehensive leachate treatment methods have been not demonstrated. Moreover, the improper management of leachate can lead to many environmental problems. The aim of this study was application of Fenton process for decreasing the major pollutants of landfill leachate on Kermanshah city. The leachate was collected from Kermanshah landfill site and treated by Fenton process. The effect of various parameters including solution pH, Fe2+and H2O2dosage, Fe2+/H2O2molar ratio, and reaction time was investigated. The result showed that with increasing Fe2+and H2O2dosage, Fe2+/H2O2molar ratio, and reaction time, the COD, TOC, TSS, and color removal increased. The maximum COD, TOC, TSS, and color removal were obtained at low pH (pH: 3). The kinetic data were analyzed in term of zero-order, first-order, and second-order expressions. First-order kinetic model described the removal of COD, TOC, TSS, and color from leachate better than two other kinetic models. In spite of extremely difficulty of leachate treatment, the previous results seem rather encouraging on the application of Fenton’s oxidation.

Performance of poly-o-phenylenediamine and its carbon dot composite electrode in the removal of Cu2+ from its aqueous solution

2021 ◽  
pp. 2151037
Author(s):  
Yu Meng ◽  
Qing Zhong ◽  
Arzugul Muslim
Keyword(s):  
Aqueous Solution ◽  
Electrochemical Reduction ◽  
Composite Electrode ◽  
Reduction Process ◽  
Order Kinetic ◽  
Carbon Dot ◽  
First Order ◽  
Oxidation Reduction ◽  
Order Kinetic Model ◽  
Optimal Ph

Because −NH2 and −NH− in poly-[Formula: see text]-phenylenediamine (P[Formula: see text]PD) can interact strongly with the empty orbitals of Cu to show unique electrochemical activity, P[Formula: see text]PD is suitable for the removal of Cu[Formula: see text] by electrochemical oxidation–reduction process. In this study, with P[Formula: see text]PD and its carbon dot composite (CDs/P[Formula: see text]PD) as working electrodes, the electrochemical reduction and removal of Cu[Formula: see text] in the aqueous solution were carried out with the potentiostatic method. According to effects of voltage, pH of the solution, initial concentration of Cu[Formula: see text], and electrochemical reduction time on the Cu[Formula: see text] removal, the Cu[Formula: see text] removal ratios of P[Formula: see text]PD and CDs/P[Formula: see text]PD were up to 64.69% and 73.34%, respectively, at −0.2 V and the optimal pH. Additionally, results showed that these processes were in line with the quasi-first order kinetic model. Both P[Formula: see text]PD and CDs/P[Formula: see text]PD showed good reproducibility in six cycles. After five times of repeated usage, the regeneration efficiencies of P[Formula: see text]PD and CDs/P[Formula: see text]PD dropped to 77.04% and 79.36%, respectively.

scholarly journals Optimization of process parameters for heavy metals biosorption onto mustard waste biomass

2016 ◽  
Vol 14 (1) ◽  
pp. 175-187 ◽  
Author(s):  
Lăcrămioara (Negrilă) Nemeş ◽  
Laura Bulgariu
Keyword(s):  
Heavy Metals ◽  
Aqueous Media ◽  
Order Kinetic ◽  
Waste Biomass ◽  
Solution Ph ◽  
Biosorption Process ◽  
Optimization Of Process Parameters ◽  
Removal Of Heavy Metals ◽  
Equilibrium Data ◽  
Order Kinetic Model

AbstractMustard waste biomass was tested as a biosorbent for the removal of Pb(II), Zn(II) and Cd(II) from aqueous solution. This strategy may be a sustainable option for the utilization of such wastes. The influence of the most important operating parameters of the biosorption process was analyzed in batch experiments, and optimal conditions were found to include initial solution pH 5.5, 5.0 g biosorbent/L, 2 hours of contact time and high temperature. Kinetics analyses show that the maximum of biosorption was quickly reached and could be described by a pseudo-second order kinetic model. The equilibrium data were well fitted by the Langmuir model, and the highest values of maximum biosorption capacity were obtained with Pb(II), followed by Zn(II) and Cd(II). The thermodynamic parameters of the biosorption process (ΔG, ΔH and ΔS) were also evaluated from isotherms. The results of this study suggest that mustard waste biomass can be used for the removal of heavy metals from aqueous media.

scholarly journals Enhanced photocatalytic activity of wool-ball-like TiO2 microspheres on carbon fabric and FTO substrates

2018 ◽  
Vol 38 ◽  
pp. 02014
Author(s):  
Yu Zhang ◽  
Jian Gu ◽  
Mengqi Zhang
Keyword(s):  
Hydrothermal Method ◽  
Order Kinetic ◽  
Carbon Fabric ◽  
Facile Hydrothermal Method ◽  
Sem Images ◽  
First Order ◽  
Good Crystallinity ◽  
Degradation Rate Constant ◽  
Order Kinetic Model ◽  
Pseudo First Order

The wool-ball-like TiO2 microspheres on carbon fabric (TiO2-CF) and FTO substrates (TiO2-FTO) have been synthesized by a facile hydrothermal method in alkali environment, using commercial TiO2 (P25) as precursors. The XRD results indicate that the as-prepared TiO2 have good crystallinity. And the SEM images show that the wool-ball-like TiO2 microspheres with a diameter of 2-3 μm are composed of TiO2 nanowires, which have a diameter of ~50 nm. The photocatalytic behavior of the wool-ball-like TiO2 microspheres, TiO2-CF and TiO2-FTO under ultraviolet light was investigated by a pseudo first-order kinetic model, using methyl orange (MO) as pollutant. The wool-ball-like TiO2 microspheres obtained a degradation rate constant (Kap) of 6.91×10-3 min-1 . The Kap values of TiO2-FTO and TiO2-CF reach 13.97×10-3 min-1 and 11.80×10-3 min-1, which are 2.0 and 1.7 times higher than that of pristine wool-ball-like TiO2 microspheres due to the “sum effect” between TiO2 and substrates. This study offers a facile hydrothermal method to prepare wool-ball-like TiO2 microspheres on CF and FTO substrates, which will improve the recyclability of phtocatalysts and can be extended to other fields.

APPLICATION OF CVD DIAMOND FILMS FOR UV THERMOLUMINESCENCE DOSIMETER

2002 ◽  
Vol 16 (06n07) ◽  
pp. 1003-1007 ◽  
Author(s):  
J. AHN ◽  
B. GAN ◽  
Q. ZHANG ◽  
S. F. YOON ◽  
V. LIGATCHEV ◽  
...  
Keyword(s):  
Activation Energy ◽  
Glow Curve ◽  
Diamond Films ◽  
Frequency Factor ◽  
Cvd Diamond ◽  
Order Kinetic ◽  
First Order ◽  
Order Kinetic Model ◽  
Ionizing Radiations ◽  
Trap Activation

This study presents the investigation of CVD diamond for the application of an UV TL dosimeter. A 9-μm-thick film used in this study presents a TL glow curve with a well-defined first-order kinetic peak (at about 273 K), which norm ally presents in the glow curve from ionizing radiations, is not observed. By fitting the glow curve to a first-order kinetic model, the trap activation energy E t = 0.95 eV and frequency factor s = 5.6 x 106 s -1 have been resolved.

scholarly journals Waste to Carbon: Influence of Structural Modification on VOC Emission Kinetics from Stored Carbonized Refuse-Derived Fuel

2019 ◽  
Vol 11 (3) ◽  
pp. 935 ◽  
Author(s):  
Andrzej Białowiec ◽  
Monika Micuda ◽  
Antoni Szumny ◽  
Jacek Łyczko ◽  
Jacek Koziel
Keyword(s):  
Structural Modification ◽  
Solid Phase ◽  
Gas Chromatography Mass Spectrometry ◽  
Order Kinetic ◽  
Voc Emissions ◽  
Voc Emission ◽  
First Order ◽  
Refuse Derived Fuel ◽  
Volatile Organic ◽  
Order Kinetic Model

The torrefaction of municipal solid waste is one of the solutions related to the Waste to Carbon concept, where high-quality fuel—carbonized refuse-derived fuel (CRDF)—is produced. An identified potential problem is the emission of volatile organic compounds (VOCs) during CRDF storage. Kinetic emission parameters have not yet been determined. It was also shown that CRDF can be pelletized for energy densification and reduced volume during storage and transportation. Thus, our working hypothesis was that structural modification (via pelletization) might mitigate VOC emissions and influence emission kinetics during CRDF storage. Two scenarios of CRDF structural modification on VOC emission kinetics were tested, (i) pelletization and (ii) pelletization with 10% binder addition and compared to ground (loose) CRDF (control). VOC emissions from simulated sealed CRDF storage were measured with headspace solid-phase microextraction and gas chromatography–mass spectrometry. It was found that total VOC emissions from stored CRDF follow the first-order kinetic model for both ground and pelletized material, while individual VOC emissions may deviate from this model. Pelletization significantly decreased (63%~86%) the maximum total VOC emission potential from stored CDRF. Research on improved sustainable CRDF storage is warranted. This could involve VOC emission mechanisms and environmental-risk management.

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