scholarly journals Stability of tetracycline residues in honey

2012 ◽  
Vol 77 (7) ◽  
pp. 879-886 ◽  
Author(s):  
Cara Cristina ◽  
Dumitrel Gabriela-Alina ◽  
Glevitzky Mirel ◽  
Perju Delia
Keyword(s):  
Life Time ◽  
Order Kinetic ◽  
First Order ◽  
Reaction Rate Constants ◽  
Veterinary Medicines ◽  
West Region ◽  
Tetracycline Degradation ◽  
Order Kinetic Model ◽  
Tetracycline Residues ◽  
Kinetics Of

The problem of availability of veterinary medicines to treat honeybees is discussed extensively worldwide. An uncontrolled administration of antibiotics may lead to contamination of beehive products and contributes to the problem of food safety. In this study, the kinetics of tetracycline (TC) degradation in honey was studied for samples provided by four sideline beekeepers located in the west region of Romania. The samples of honey were stored in the dark at room temperature for 30 days and subsamples were analyzed every 3 days by Elisa method. The results of the study revealed that the level of tetracycline decreases in time for all honey samples. The tetracycline degradation follows a first-order kinetic model with reaction rate constants between 1.2?10-3 - 2?10-3 days-1. The half-life time of tetracycline in monofloral honeys: acacia and lime was 251 and 232 days respectively. Tetracycline degradation in polyfloral honey was accelerated since ?1/2 of TC was 151 days.

Kinetics of Reductive Dechlorination of DDT in Soil with Zero-Valent Iron

2011 ◽  
Vol 295-297 ◽  
pp. 1236-1239
Author(s):  
Yin Hai Lang ◽  
Min Jie Wang ◽  
Nan Nan Wang
Keyword(s):  
Kinetic Model ◽  
Reductive Dechlorination ◽  
Reaction Rate ◽  
Zero Valent Iron ◽  
Order Kinetic ◽  
First Order ◽  
Reaction Rate Constants ◽  
Order Kinetic Model ◽  
Pseudo First Order ◽  
Kinetics Of

In this study, reductive dechlorination of DDT compounds by zero-valent iron in Jiangxi red soil was investigated. DDT compounds were effectively dechlorinated by zero-valent iron. The pseudo-first-order kinetic model for 2,4¢-DDT and 4,4¢-DDT reduction with zero-valent iron was proposed. The reaction rate constants for 2,4¢-DDT and 4,4¢-DDT were 1.19´10-2(min-1) and 1.44´10-2(min-1), respectively. The dechlorination of 2,4¢-DDT and 4,4¢-DDT were mainly affected by the specific surface area of iron. The data from the variable-pH experiments (between 3.6 and 8.8) suggested that pH does not play a role in the rate-determination step.

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.

Kinetic Study of the Adsorption of Dye onto Cotton in SDS-CTAB Reverse Micelles

2015 ◽  
Vol 723 ◽  
pp. 591-595
Author(s):  
Zu Lan Liu ◽  
Lan Qian Li ◽  
Yi Ping Liu ◽  
Ming Lu
Keyword(s):  
Kinetic Study ◽  
Adsorption Kinetics ◽  
Reverse Micelles ◽  
Adsorption Kinetic ◽  
Order Kinetic ◽  
First Order ◽  
Reactive Blue 19 ◽  
Order Kinetic Model ◽  
Pseudo First Order ◽  
Kinetics Of

Adsorption kinetic study of C.I. reactive blue 19 onto cotton was carried out in SDS-CTAB reverse micelles. The data of adsorption kinetics were examined using pseudo first-and second-order kinetic models. It was found that the adsorption kinetics of dye on cotton with diffusion controlling follows the pseudo first-order kinetic model.

scholarly journals The kinetics of chromium(VI) adsorption from water on some natural materials

2002 ◽  
pp. 101-108 ◽  
Author(s):  
Marina Sciban ◽  
Mile Klasnja
Keyword(s):  
Analytical Data ◽  
Kraft Lignin ◽  
Order Kinetic ◽  
Freundlich Model ◽  
First Order ◽  
Wood Sawdust ◽  
Chromium Vi ◽  
Order Kinetic Model ◽  
Kinetics Of ◽  
Best Fit

This paper is concerned with the kinetics of chromium(VI) adsorption by wood sawdust, pulp, and Kraft lignin. In our previous works we determined adsorption efficiency of these adsorbents. In this paper we focused our attention on the influence of contact time on chromium(VI) adsorption from water by the same adsorbents. The analytical data were approached from the following kinetic models: First-order kinetic model, Parabolic diffusion model, Elovich model, and Modified Freundlich model. Elovich model was shown to be the best fit for the description of chromium(VI) adsorption. It was found that adsorption was the fastest on pulp and slowest on Kraft lignin.

scholarly journals Fractional kinetics of photocatalytic degradation

2018 ◽  
Vol 08 (05) ◽  
pp. 1850034 ◽  
Author(s):  
C. L. Wang
Keyword(s):  
Kinetic Model ◽  
Photocatalytic Degradation ◽  
Degradation Process ◽  
Order Kinetic ◽  
Material Parameters ◽  
First Order ◽  
Fractional Kinetics ◽  
Order Kinetic Model ◽  
Kinetics Of ◽  
Degradation Time

In this paper, photocatalytic degradation processes of different materials are fitted to the first-order kinetic model, second-order kinetic model and fractional first-order kinetic model. Deterministic coefficients are calculated for the evaluation of the validity of these models. The fitting results show clearly that the degradation process can fit the fractional first-order kinetic model in a very good manner. In this way, two material parameters can be well defined. One is the degradation time, which can be used to describe the photocatalytic degradation process quantitatively. Another is the order of the derivative, which could be related to the material’s microstructure.

scholarly journals Biogas and Methane Potential of Pre-Thermally Disintegrated Bio-Waste

Energies ◽  
2019 ◽  
Vol 12 (20) ◽  
pp. 3880
Author(s):  
Sylwia Myszograj
Keyword(s):  
Process Parameters ◽  
Alternative Energy ◽  
Biogas Production ◽  
Gompertz Model ◽  
Order Kinetic ◽  
Methane Fermentation ◽  
First Order ◽  
Order Kinetic Model ◽  
Methane Potential ◽  
Kinetics Of

One of the environmental solutions employed in order to achieve circular economy goals is methane fermentation—a technology that is beneficial both for the stabilization and reduction of organic waste and for alternative energy generation. The article presents the results of research aimed at determining the biogas and methane potential of bio-waste which has been pre-thermally disintegrated, and determining the influence of variable process parameters of disintegration on the kinetics of fermentation. A first-order kinetic model was used to describe the fermentation as well as two mathematical models: logistic and Gompertz. It has been found that process parameters such as time (0.5, 1 and 2 h) and temperature (between 55 to 175 °C) have a significant effect on the solubilization efficiency of the bio-waste. The methane fermentation of thermally disintegrated bio-waste showed that the highest biogas potential is characterized by samples treated, respectively, for 0.5 h at 155 °C and for 2 h at 175 °C. The best match for the experimental data of biogas production from disintegrated substrates was demonstrated for the Gompertz model.

Significance of the Effect of Mineral Alteration on Nuclide Migration

1993 ◽  
Vol 333 ◽  
Author(s):  
Takashi Murakami ◽  
Toshihiko Ohnuki ◽  
Hiroshi Isobe ◽  
Tsutomu Sato ◽  
Nobuyuki Yanase ◽  
...  
Keyword(s):  
Uranium Concentration ◽  
Order Kinetic ◽  
First Order ◽  
Geologic Time ◽  
Iron Minerals ◽  
Uranyl Phosphate ◽  
Order Kinetic Model ◽  
Uranium Migration ◽  
Mineral Alteration ◽  
Kinetics Of

ABSTRACTIn order to clarify the effect of mineral alteration on nuclide migration, we examined the processes, mechanisms, and kinetics of chlorite weathering, and the uranium concentrations in minerals and rocks at Koongarra, Australia. The observed concentrations of uranium in rocks were compared to those calculated. The sequence of chlorite weathering may be simply expressed as a chlorite → vermiculite → kaolinite conversion. These minerals occur as a function of depth, which corresponds well to uranium concentrations on the meter scale. Iron minerals, closely related to the uranium redistribution, are released during the weathering. The first-order kinetic model of the weathering process suggests that the weathering rate is not constant but time-dependent. The uranium concentrations are qualitatively proportional to the extent of the weathering; the weathered part having higher uranium concentration. Uranium mainly occurs with iron minerals, and sub micron sized saléeite, a uranyl phosphate, is one of the most probable uranyl phases associated with the iron minerals. The uranium fixation mechanisms are probably saléeite microcrystal coprecipitation and sorption to the iron minerals. Our model, which describes uranium concentrations in rocks as a function of time, shows that the transition zone (a vermiculite dominant area) plays an important role in the uranium migration. We have established that weathering of chlorite has affected the redistribution of uranium for more than one million years. The present study demonstrates the significance of mineral alteration when we estimate nuclide migration for geologic time.

scholarly journals Decolorization Kinetics of Acid Azo Dye and Basic Thiazine Dye in Aqueous Solution by UV/H2O2 and UV/Fenton: Effects of Operational Parameters

2017 ◽  
Vol 17 (1) ◽  
pp. 85-94
Author(s):  
Ayda Baffoun ◽  
Amel El Ghali ◽  
Imen Hachani
Keyword(s):  
Order Kinetic ◽  
Operational Parameters ◽  
Operational Conditions ◽  
First Order ◽  
Aqueous Effluents ◽  
Initial Ph ◽  
Order Kinetic Model ◽  
Thiazine Dye ◽  
Kinetics Of ◽  
Decolorization Kinetics

AbstractThe photochemical decolorization of two dyes, namely Acid Yellow 54 and Basic Blue 9, was studied using the UV/H2O2and UV/Fenton processes. The effects of the amount of H2O2and FeSO4as well as the initial pH solution on decolorization kinetics of both the dyes were investigated. The pseudo-first order kinetic model was applied to predict the decolorization of the selected dyes at the different operational conditions and results showed that this model fitted very well with the experimental data. The obtained results also showed the efficiency of UV/Fenton process to quickly degrade aqueous effluents polluted by Acid Yellow 54 and Basic Blue 9 compared to the UV/H2O2process.

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