Wastewater COD characterization: biodegradability of physico-chemical fractions

2002 ◽  
Vol 45 (6) ◽  
pp. 89-97 ◽  
Author(s):  
P. Ginestet ◽  
A. Maisonnier ◽  
M. Spérandio
Keyword(s):  
Hydrolysis Rate ◽  
Affinity Constant ◽  
Characterization Methods ◽  
First Order ◽  
Physico Chemical ◽  
Wastewater Samples ◽  
Solids Analysis ◽  
Activated Sludge Processes ◽  
Limited Surface

Physico-chemical and biological characterization methods were applied to wastewater samples originating from 7 French WWTPs. The settleable fraction (S), unsettleable-coagulable fraction (US-C) and unsettleable-uncoagulable fraction (US-UC) were separated. Special emphasis was put on the determination of hydrolysis kinetics associated with coagulable- and settleable-fractions in order to model their behaviour in activated sludge processes, as both these fractions are influenced by the SRT. The “soluble” fraction (i.e. US-UC) was composed of readily biodegradable COD (2 to 27%), readily hydrolysable COD (37 to 90%) and inerts (2 to 47%). The “colloidal” fraction (i.e. US-C) was composed of heterotrophic biomass (9 to 24%) and readily hydrolysable COD (6 to 82%), with the rest being inerts or very slowly biodegradable COD (0 to 70%). The “particulate” fraction (i.e. settleable) was composed of biomass (14 ± 6%), readily hydrolysable COD (21 ± 14%), slowly hydrolysable COD (about 45–50%) and 15 to 20% which can be considered as inert matter (XI). “Readily hydrolysable COD” was correctly modeled by a global first-order reaction. First-order constants (KH) were 9 ± 2 d−1 for raw-wastewater, 12 ± 3 d−1 for primary settled-wastewater and 16 ± 5 d−1 for coagulated-wastewater. “Slowly hydrolysable COD” was correctly modeled by a limited surface reaction. Concerning this fraction, the specific hydrolysis rate (kH) ranged from 0.25 to 1.05 d−1, and the affinity constant (KX) ranged from 0.33 to 0.95 gCOD/gCOD based on settleable solids analysis.

scholarly journals Determination of Ketorolac in the Effluent from a Hospital Treating Plant and Kinetics Study of Its Photolytic Degradation

2017 ◽  
Vol 2017 ◽  
pp. 1-9
Author(s):  
Hector Hugo Ortega Soto ◽  
Jorge Javier Ramírez García ◽  
Paula Gamboa Suárez ◽  
Angie Michelle Dávila Estrada
Keyword(s):  
High Performance ◽  
Solid Phase ◽  
Degradation Kinetics ◽  
Treatment Plant ◽  
Order Model ◽  
Dark Chamber ◽  
First Order ◽  
Photolytic Degradation ◽  
Wastewater Samples

In this work, two specific, sensitive, and rapid analytical methods were developed. One of them was for the determination of ketorolac in a hospital wastewater treatment plant where there is no interference with other organic substances; the other one was for the determination of the degradation kinetics in aqueous medium. Ketorolac was extracted from wastewater samples through solid-phase extraction (SPE) cartridges, then it was identified and quantified by high-performance liquid chromatography (HPLC). Ketorolac was detected in concentrations between 0.1376 and 0.2667 μg/L. Photolytic degradation was performed on aqueous solutions of ketorolac tromethamine reference substance, at a concentration of 50 μg/mL. Samples were in direct contact with ultraviolet light in a dark chamber, equipped with two mercury lamps (254 nm) at a radiation source of 15 W. The results of the photolytic degradation were adjusted to a first-order model, obtaining a half-life of 4.8 hrs.

scholarly journals Sand Dune Characterization for Preparing Metallurgical Grade Silicon

2018 ◽  
Vol 16 (1) ◽  
pp. 1227-1232 ◽  
Author(s):  
S. Anas Boussaa ◽  
A. Kheloufi ◽  
N. Boutarek Zaourar
Keyword(s):  
Optical Observations ◽  
X Ray Diffraction ◽  
Dune Sand ◽  
Metallurgical Grade Silicon ◽  
Characterization Methods ◽  
Physico Chemical ◽  
Photovoltaic Applications ◽  
Different Shapes ◽  
Crystalline Nature

AbstractDune sand, from Biskra, Algeria which is in the Great Algerian huge desert attracts tourists from all over the world. Dune sand composes around 80% of the total area of the desert. To date only a few studies have been conducted on this sand. The purpose of the present study is to shed light on the textural and physico-chemical characteristics of this sand using several characterization methods, and to understand the potential for using for photovoltaic applications. The chemical composition of Biskra sand indicated a high purity quartz with 97.6% silica, and a presence of others oxides. Granular analysis enabled the determination of the size of the sand grains which was found to be fine to medium. On the other hand, a Scanning Electron Microscopy and optical observations were carried out, the micrographs observations indicated the presence of different shapes of sand grain, some rounded whereas others are angular edged or elongated. X-ray diffraction indicates the highly crystalline nature of the Biskra sand.

Antithrombin-mediated Inhibition of Factor Vlla-Tissue Factor Complex by the Synthetic Pentasaccharide Representing the Heparin Binding Site to Antithrombin

1996 ◽  
Vol 76 (01) ◽  
pp. 005-008 ◽  
Author(s):  
Jean Claude Lormeau ◽  
Jean Pascal Herault ◽  
Jean Marc Herbert
Keyword(s):  
Binding Site ◽  
Tissue Factor ◽  
Residual Activity ◽  
Coagulation Factors ◽  
Heparin Binding ◽  
Experimental Conditions ◽  
First Order ◽  
Heparin Binding Site ◽  
Coagulant Activity

SummaryWe examined the effect of the synthetic pentasaccharide representing the minimal binding site of heparin to antithrombin on the antithrombin-mediated inactivation of factor Vila bound to tissue factor. This effect was compared to the effect of unfractionated heparin. Using purified recombinant human coagulation factors and either a clotting or an amidolytic assay for the determination of the residual activity of factor Vila, we showed that the pentasaccharide was an efficient antithrombin-dependent inhibitor of the coagulant activity of tissue factor-factor Vila complex. In our experimental conditions, assuming a mean MW of 14,000 for heparin, the molar pseudo-first order rate constants for ATIII-mediated FVIIa inhibition by ATIII-binding heparin and by the synthetic pentasaccharide were found to be similar with respective values of 104,000 ± 10,500 min-1 and 112,000 ± 12,000 min-1 (mean ± s.e.m., n = 3)

Statistical method of steepest improvement of response

2018 ◽  
Vol 84 (11) ◽  
pp. 74-87
Author(s):  
V. B. Bokov
Keyword(s):  
Statistical Method ◽  
Linear Model ◽  
Response Prediction ◽  
Initial Experiment ◽  
First Order ◽  
Prediction Response ◽  
Conditional Extremum ◽  
Order Polynomial ◽  
Limiting Values

A new statistical method for response steepest improvement is proposed. This method is based on an initial experiment performed on two-level factorial design and first-order statistical linear model with coded numerical factors and response variables. The factors for the runs of response steepest improvement are estimated from the data of initial experiment and determination of the conditional extremum. Confidence intervals are determined for those factors. The first-order polynomial response function fitted to the data of the initial experiment makes it possible to predict the response of the runs for response steepest improvement. The linear model of the response prediction, as well as the results of the estimation of the parameters of the linear model for the initial experiment and factors for the experiments of the steepest improvement of the response, are used when finding prediction response intervals in these experiments. Kknowledge of the prediction response intervals in the runs of steepest improvement of the response makes it possible to detect the results beyond their limits and to find the limiting values of the factors for which further runs of response steepest improvement become ineffective and a new initial experiment must be carried out.

Development and Validation of Derivative Spectroscopic Method for Simultaneous Estimation of Cefadroxil and Probenecid

2014 ◽  
Vol 7 (1) ◽  
pp. 2350-2355
Author(s):  
Pratik S Mehta ◽  
Pratik R. Patel ◽  
Rajesh R Parmar ◽  
M M K Modasiya ◽  
Dushyant A Shah
Keyword(s):  
Spectroscopic Method ◽  
Spectral Interference ◽  
Synthetic Mixture ◽  
Simultaneous Estimation ◽  
Zero Crossing ◽  
First Order ◽  
Derivative Spectroscopy ◽  
Development And Validation ◽  
Crossing Point

A novel, simple, accurate, sensitive, precise and economical derivative spectroscopic method was developed and validated for the determination of cefadroxil and probenecid in synthetic mixture. First order derivative spectroscopy method was adopted to eliminate spectral interference. The method obeys Beer’s Law in concentration ranges of 4-36 μg/ml for cefadroxil and of 5-25 μg/ml of probenecid. The zero crossing point for cefadroxil and probenecid was 260 nm and 237.8 nm respectively in 0.1N HCl. The method was validated in terms of accuracy, precision, linearity, limits of detection, limits of quantitation. This method has been successively applied to synthetic mixture and no interference from the synthetic mixture’s excipients was found.   

Development and Pharmacokinetics Study of Antifungal Peptide Nanoliposomes by Liquid Chromatography-tandem Mass Spectrometry

2019 ◽  
Vol 15 (4) ◽  
pp. 312-318
Author(s):  
Shuoye Yang
Keyword(s):  
Mass Spectrometry ◽  
Biological Properties ◽  
Pharmacokinetic Property ◽  
Antifungal Peptide ◽  
Simple Liquid ◽  
Physico Chemical ◽  
Liquid Chromatography Tandem Mass ◽  
Pegylated Lipids

Background: The therapeutic ability and application of antifungal peptide (APs) are limited by their physico-chemical and biological properties, the nano-liposomal encapsulation would improve the in vivo circulation and stability. </P><P> Objective: To develop a long-circulating liposomal delivery systems encapsulated APs-CGA-N12 with PEGylated lipids and cholesterol, and investigated through in vivo pharmacokinetics. Methods: The liposomes were prepared and characterized, a rapid and simple liquid chromatographytandem mass spectrometry (LC-MS/MS) assay was developed for the determination of antifungal peptide in vivo, the pharmacokinetic characteristics of APs liposomes were evaluated in rats. Results: Liposomes had a large, unilamellar structure, particle size and Zeta potential ranged from 160 to 185 nm and -0.55 to 1.1 mV, respectively. The results indicated that the plasma concentration of peptides in reference solutions rapidly declined after intravenous administration, whereas the liposomeencapsulated ones showed slower elimination. The AUC(0-∞) was increased by 3.0-fold in liposomes in comparison with standard solution (20 mg·kg-1), the half-life (T1/2) was 1.6- and 1.5-fold higher compared to the reference groups of 20 and 40 mg·kg-1, respectively. Conclusion: Therefore, it could be concluded that liposomal encapsulation effectively improved the bioavailability and pharmacokinetic property of antifungal peptides.

In-vitro Kinetic Hydrolysis Study of Metronidazole Derivatives with Carvacrol and Eugenol Using Validated RP-HPLC Method

2020 ◽  
Vol 16 ◽  
Author(s):  
M. Alarjah
Keyword(s):  
Half Life ◽  
Hplc Method ◽  
Hydrolysis Rate ◽  
First Order ◽  
First Order Kinetics ◽  
Rp Hplc ◽  
Pharmacokinetic Properties ◽  
Pseudo First Order ◽  
Kinetic Hydrolysis

Background: Prodrugs principle is widely used to improve the pharmacological and pharmacokinetic properties of some active drugs. Much effort was made to develop metronidazole prodrugs to enhance antibacterial activity and or to improve pharmacokinetic properties of the molecule or to lower the adverse effects of metronidazole. Objective: In this work, the pharmacokinetic properties of some of monoterpenes and eugenol pro metronidazole molecules that were developed earlier were evaluated in-vitro. The kinetic hydrolysis rate constants and half-life time estimation of the new metronidazole derivatives were calculated using the validated RP-HPLC method. Method: Chromatographic analysis was done using Zorbbax Eclipse eXtra Dense Bonding (XDB)-C18 column of dimensions (250 mm, 4.6 mm, 5 μm), at ambient column temperature. The mobile phase was a mixture of sodium dihydrogen phosphate buffer of pH 4.5 and methanol in gradient elution, at 1ml/min flow rate. The method was fully validated according to the International Council for Harmonization (ICH) guidelines. The hydrolysis process carried out in an acidic buffer pH 1.2 and in an alkaline buffer pH 7.4 in a thermostatic bath at 37ºC. Results: The results followed pseudo-first-order kinetics. All metronidazole prodrugs were stable in the acidic pH, while they were hydrolysed in the alkaline buffer within a few hours (6-8 hr). The rate constant and half-life values were calculated, and their values were found to be 0.082- 0.117 hr-1 and 5.9- 8.5 hr., respectively. Conclusion: The developed method was accurate, sensitive, and selective for the prodrugs. For most of the prodrugs, the hydrolysis followed pseudo-first-order kinetics; the method might be utilised to conduct an in-vivo study for the metronidazole derivatives with monoterpenes and eugenol.

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