scholarly journals Degradation of Diallyl Phthalate (DAP) by Fenton Oxidation: Mechanistic and Kinetic Studies

2018 ◽  
Vol 9 (1) ◽  
pp. 23
Author(s):  
Sondos Dbira ◽  
Nasr Bensalah ◽  
Moustafa Zagho ◽  
Ahmed Bedoui
Keyword(s):  
High Performance ◽  
Hplc Analysis ◽  
Degradation Mechanism ◽  
Kinetic Studies ◽  
Cost Effective ◽  
Fenton Oxidation ◽  
Fenton’S Reaction ◽  
Toc Removal ◽  
Initial Ph ◽  
Diallyl Phthalate

In this work, the degradation and mineralization of Diallyl Phthalate (DAP) in water by Fenton oxidation was investigated. The effects of different experimental parameters including the initial pH, the hydrogen peroxide (H2O2) dose, the catalyst (Fe2+) dose, the iron source, and the DAP concentration on the rate and the yield of DAP degradation by Fenton oxidation were evaluated. DAP and its intermediates were quantified by high performance liquid chromatography (HPLC) analysis and the measurement of total organic carbon (TOC) during Fenton oxidation. The results obtained confirmed that hydroxyl radicals (HO•) generated from Fenton’s reaction were capable of completely eliminating DAP from water. Fenton oxidation of 100 mg/L DAP aqueous solution at pH = 3.2 required 1000 mg/L H2O2 and 50 mg/L Fe2+. Under these conditions, more than TOC removal exceeded 95% after 300 min Fenton oxidation. The competition kinetics method was used to determine an absolute rate constant of 7.26.109 M−1 s−1 for the reaction between DAP and HO• radicals. HPLC analysis showed that phthalic acid, 1,2-dihydroxybenzene, 1,2,4-trihydroxybenzene, maleic acid, formic acid and oxalic acid were the main intermediates formed during DAP degradation. Accordingly, a simple DAP degradation mechanism by the Fenton reaction was proposed. These promising results proved the potential of Fenton oxidation as a cost-effective method for the decontamination of wastewaters containing phthalates.

scholarly journals Determination of Pesticide Residue in Brinjal Sample Using HPTLC and Developing a Cost-Effective Method Alternative to HPLC

2020 ◽  
Vol 2020 ◽  
pp. 1-12
Author(s):  
Muzammil Hussain ◽  
Kiran Aftab ◽  
Munawar Iqbal ◽  
Shafaqat Ali ◽  
Muhammad Rizwan ◽  
...  
Keyword(s):  
High Performance ◽  
Hplc Analysis ◽  
Organophosphorus Pesticide ◽  
Analytical Techniques ◽  
Cost Effective ◽  
Local Market ◽  
Standard Samples ◽  
Residual Concentration ◽  
Food And Agriculture ◽  
Cost Effective Method

Two analytical techniques HPLC (high performance liquid chromatography) and HPTLC (high performance thin layer chromatography) were validated to reveal the quality and quantity of pesticide residues (organophosphorus, organochlorine, and pyrethroids) in brinjal samples collected from a local market of Faisalabad. The HPTLC methods showed linear behavior for standard samples and residue was in the range of 1–130 ng. The organochlorine (α-endosulfan) contaminates the samples at 4, 5, 9, and 10 weeks, and detected quantity was less than MRL (minimum residue level) of the FAO (Food and Agriculture Organization of United Nations), i.e., 0.5 mg·kg−1. The organophosphorus pesticide (chlorpyriphos, methamidophos, monocrotophos, dichlorvos, carbosulfan, profenophos, and dimethoate) residue contaminated the samples and violated the MRL limit. Pyrethroids (deltamethrin, β-cyhalothrin, and cypermethrin) were present at appreciable levels, in samples of 1, 3, 4, 6, 8, and 9 weeks. The concentration of β-cyhalothrin (0.25 mg·kg−1) and cypermethrin (0.205 mg·kg−1) was significantly higher than that of all detected pesticides. The carbosulfan and deltamethrin contaminated all 10-week samples. The HPLC analysis of samples was carried out to confirm the efficiency of HPTLC as cost-effective method. The concentration of α-endosulfan, chlorpyriphos, dimethoate, monocrotophos, profenophos, deltamethrin, and cypermethrin in brinjal samples through the HPTLC method showed similar residual concentration with HPLC analysis.

scholarly journals Equilibrium and Kinetic Studies of Biosorptive Removal of 2,4,6-Trichlorophenol from Aqueous Solutions Using Untreated Agro-Waste Pine Cone Biomass

Processes ◽  
2019 ◽  
Vol 7 (10) ◽  
pp. 757 ◽  
Author(s):  
Siva Kumar ◽  
Asif ◽  
Poulose ◽  
Suguna ◽  
Al-Hazza
Keyword(s):  
Low Cost ◽  
Agricultural Waste ◽  
Kinetic Studies ◽  
Cost Effective ◽  
Biosorption Capacity ◽  
Pine Cone ◽  
Cost Effective Treatment ◽  
Initial Ph ◽  
Equilibrium Data ◽  
Biomass Dosage

The present work discusses the adsorptive removal of a phenolic pollutant, i.e., 2,4,6-trichlorophenol (TCP), using low cost untreated agricultural waste pine cone powder (PCP). The present biosorbent was thoroughly characterized with the help of FTIR, SEM, XRD, and CHN analysis. The presence of amine (-NH2), hydroxyl (-OH) and carbonyl (C=O) functional groups was detected by the FTIR analysis. The important biosorption factors like agitation time, biomass dosage, initial adsorbate concentration, and the initial pH were examined by batch studies. The biosorption kinetic process was fast, reaching equilibrium in 75 min. The experimental kinetic data revealed an excellent agreement with the pseudo second order (PSO) model. On the other hand, the Langmuir isotherm model best described the equilibrium data with the maximum biosorption capacity (qmax) of 243.90 mg/g. These values are better than the adsorption capacities of most agro-based untreated adsorbents previously reported in the literature. Owing to fast removal rates and high biosorption capacity, PCP can be used for cost-effective treatment of TCP from aqueous streams.

scholarly journals Flavonoid Quantification in Onion by Spectrophotometric and High Performance Liquid Chromatography Analysis

HortScience ◽  
2002 ◽  
Vol 37 (4) ◽  
pp. 682-685 ◽  
Author(s):  
Kevin A. Lombard ◽  
Emmanuel Geoffriau ◽  
Ellen Peffley
Keyword(s):  
High Performance Liquid Chromatography ◽  
Liquid Chromatography ◽  
High Performance ◽  
Hplc Analysis ◽  
Correlation Coefficients ◽  
Cost Effective ◽  
Chromatography Analysis ◽  
Cost Effective Method ◽  
Performance Liquid Chromatography Analysis

Direct spectrophotometric determination of quercetin content in onions (Allium cepa L.) was investigated as a possible alternative to high-performance liquid chromatography (HPLC) analysis. Quercetin content in five onion varieties was monitored at 362 nm and quantified using simple spectrophotometric and HPLC methods. HPLC revealed that 3,4'-Qdg and 4'-Qmg comprised up to 93% of total flavonol content detected in the studied varieties. These major quercetin conjugates combined (3,4'-Qdg + 4'-Qmg) and total flavonol conjugates quantified by HPLC correlated closely with spectrophotometer values. Correlation coefficients were 0.96 (P < 0.0001) for 3,4'-Qdg + 4'-Qmg and 0.97 (P < 0.0001) for total flavonol conjugates in onion. Simple spectrophotometric procedure proved to be a valid, efficient, and cost-effective method for the quantification of total quercetin in onion. Chemical names used: quercetin-3,4'-O-diglucoside (3,4'-Qdg); quercetin-4'-O-glucoside (4'-Qmg).

scholarly journals Treatment of Bisphenol-A Using Sonication-assisted Photo-Fenton Hybrid Process

2019 ◽  
Vol 33 (1) ◽  
pp. 43-57 ◽  
Author(s):  
Meral Dükkancı
Keyword(s):  
Bisphenol A ◽  
Ph Value ◽  
Fenton Oxidation ◽  
Toxicity Tests ◽  
Catalyst Loading ◽  
Endocrine Disrupting Compound ◽  
Toc Removal ◽  
Endocrine Disrupting ◽  
Initial Ph ◽  
Solution Volume

Sonication-assisted photo-Fenton oxidation of an endocrine disrupting compound, bisphenol-A (BPA), was studied under visible-light irradiation in the presence of a LaFeO3 perovskite catalyst. The effects of the parameters: initial BPA concentration ([BPA]0), H2O2 concentration ([H2O2]0), catalyst loading, initial pH of the BPA solution, and reaction temperature were studied on the sonication-assisted photo-Fenton oxidation of an aqueous BPA solution. The optimum conditions for the oxidation were determined to be: [BPA]0 = 10 ppm, [H2O2]0 = 4.8 mM, catalyst loading = 0.75 g L–1, pH = 2.6, temperature = 313 K. During all runs, sonication power of 40 W, visible lights power of 150 W+150 W, BPA solution volume (0.5 L), and stirring speed of 500 rpm were kept constant. Under these conditions, degradation of 56.3 %, COD removal of 50.9 %, and TOC removal of 15.6 % were achieved after 6 h of reaction. The small amount of iron that leached into the solution indicated high stability of the catalyst. The sonication-assisted photo-Fenton oxidation of BPA was described by the second order kinetics with an activation energy of 15.34 kJ mol–1. Toxicity tests were also performed and the results revealed that the intermediates formed in the sonication-assisted photo-Fenton oxidation of BPA were less toxic compared to the parent BPA molecule at a neutral pH value. However, the same interpretation was not valid at the acidic pH of 2.6.

scholarly journals Electrochemical Oxidation of Perfluorooctanoic Acid (PFOA) from Aqueous Solution using Non-Active Ti/SnO2-Sb2O5/PbO2 Anodes

2021 ◽  
pp. 48-67
Author(s):  
S. Singh
Keyword(s):  
Aqueous Solution ◽  
Electrochemical Oxidation ◽  
Degradation Mechanism ◽  
Specific Energy Consumption ◽  
Perfluorooctanoic Acid ◽  
Carbon Chain ◽  
Fluoride Ions ◽  
Toc Removal ◽  
Initial Ph ◽  
Gas Chromatograph Mass Spectrometry

In this study, electrochemical oxidation of perfluorooctanoic acid (PFOA, C7H15CO2H) from aqueous solution was examined in terms of PFOA and total organic carbon (TOC) removal by using Ti/SnO2-Sb2O5/PbO2non-active electrodes. The effects of operating parameters: initial pH (pHo), current density (j), and electrolyte concentration (m) at different time intervals were examined. Specific energy consumption (SEC) was used to determine the process proficiency. The C-C bond between C7F15 was first cleaved and thendegraded into fluoride ions (F−) and short carbon-chain per-fluorinated carboxylic acids (PFCAs) ((∼C2−C7) such as perfluoroethanoic acid (PFEA: C2F5CO2H), perfluoropropanoic acid (PFPA: C3F7CO2H), perfluorobutanoic acid (PFBA: C4F9CO2H), perfluoropentanoic acid (PFPeA: C5F11CO2H), perfluorohexanoic acid (PFHxA: C6F13CO2H), perfluoheptanoic acid (PFHpA: C7F14CO2H). These intermediates by-products were determined using the gas chromatograph-mass spectrometry (GC/MS) analysis. The rate of PFOA decomposition was followed the pseudo-first-order kinetics. About 82%TOC and 94% PFOA removals were formed at the optimal condition of pHo = 3.58, j=168.34 Am-2, and m = 250 mgL-1 at 120 min of electrolysis with SEC = 593 kWh/kg TOC. A plausible degradation mechanism was also proposed at the optimal treatment condition.

scholarly journals Stability Evaluation of Extemporaneously Compounded Vancomycin Ophthalmic Drops: Effect of Solvents and Storage Conditions

Pharmaceutics ◽  
2021 ◽  
Vol 13 (2) ◽  
pp. 289
Author(s):  
Christopher Ross ◽  
Basir Syed ◽  
Joanna Pak ◽  
Vishal Jhanji ◽  
Jason Yamaki ◽  
...  
Keyword(s):  
Normal Saline ◽  
High Performance ◽  
Hplc Analysis ◽  
Room Temperature ◽  
Storage Temperature ◽  
Storage Conditions ◽  
Drug Of Choice ◽  
Initial Ph ◽  
The Stability ◽  
Saline Solutions

Vancomycin is the drug of choice for methicillin-resistant Staphylococcus aureus keratitis and other ocular infections. Vancomycin ophthalmic drops are not commercially available and require compounding. The present study was designed to investigate the stability of vancomycin ophthalmic drops in normal saline, phosphate-buffered saline (PBS), and balanced salt solution (BSS) while stored at room temperature or under refrigeration. Vancomycin ophthalmic drops (50 mg/mL) were aseptically prepared from commercially available intravenous powder using PBS, BSS, and saline. Solutions were stored at room temperature and in a refrigerator for 28 days. The vancomycin stability was tested by a microbiology assay and high-performance liquid chromatography HPLC analysis immediately after formulation and at days 7, 14, and 28 after storage at room temperature or under refrigeration. The pH, turbidity was also tested. Vancomycin formulations in PBS, BSS and normal saline had initial pH of 5; 5.5; 3 respectively. The formulation in PBS developed turbidity and a slight decrease in pH upon storage. Microbiological assay did not show any change in zone of inhibition with any of the formulation upon storage either at room temperature or under refrigeration. HPLC analysis did not detect any decrease in vancomycin concentration or the accumulation of degraded products in any of the formulations upon storage either at room temperature or under refrigeration. Vancomycin ophthalmic drops prepared using PBS, BSS, and normal saline were stable up to the tested time point of 28 days, irrespective of their storage temperature.

Mineral/microfibrillated cellulose composite materials: High performance products, applications, and product forms

TAPPI Journal ◽  
2018 ◽  
Vol 17 (09) ◽  
pp. 507-515 ◽  
Author(s):  
David Skuse ◽  
Mark Windebank ◽  
Tafadzwa Motsi ◽  
Guillaume Tellier
Keyword(s):  
Composite Materials ◽  
High Performance ◽  
Aqueous Suspension ◽  
Production Capacity ◽  
Cost Savings ◽  
Cost Effective ◽  
New Materials ◽  
Wet Strength ◽  
Product Forms ◽  
Cellulose Composite

When pulp and minerals are co-processed in aqueous suspension, the mineral acts as a grinding aid, facilitating the cost-effective production of fibrils. Furthermore, this processing allows the utilization of robust industrial milling equipment. There are 40000 dry metric tons of mineral/microfbrillated (MFC) cellulose composite production capacity in operation across three continents. These mineral/MFC products have been cleared by the FDA for use as a dry and wet strength agent in coated and uncoated food contact paper and paperboard applications. We have previously reported that use of these mineral/MFC composite materials in fiber-based applications allows generally improved wet and dry mechanical properties with concomitant opportunities for cost savings, property improvements, or grade developments and that the materials can be prepared using a range of fibers and minerals. Here, we: (1) report the development of new products that offer improved performance, (2) compare the performance of these new materials with that of a range of other nanocellulosic material types, (3) illustrate the performance of these new materials in reinforcement (paper and board) and viscosification applications, and (4) discuss product form requirements for different applications.

Parallel Computing for Tire Simulations

2011 ◽  
Vol 39 (3) ◽  
pp. 193-209 ◽  
Author(s):  
H. Surendranath ◽  
M. Dunbar
Keyword(s):  
High Performance ◽  
Effective Means ◽  
Cost Effective ◽  
Turnaround Time ◽  
Careful Consideration ◽  
Rolling Contact ◽  
Element Analysis ◽  
Parallel Solvers ◽  
Design Changes ◽  
Highly Nonlinear

Abstract Over the last few decades, finite element analysis has become an integral part of the overall tire design process. Engineers need to perform a number of different simulations to evaluate new designs and study the effect of proposed design changes. However, tires pose formidable simulation challenges due to the presence of highly nonlinear rubber compounds, embedded reinforcements, complex tread geometries, rolling contact, and large deformations. Accurate simulation requires careful consideration of these factors, resulting in the extensive turnaround time, often times prolonging the design cycle. Therefore, it is extremely critical to explore means to reduce the turnaround time while producing reliable results. Compute clusters have recently become a cost effective means to perform high performance computing (HPC). Distributed memory parallel solvers designed to take advantage of compute clusters have become increasingly popular. In this paper, we examine the use of HPC for various tire simulations and demonstrate how it can significantly reduce simulation turnaround time. Abaqus/Standard is used for routine tire simulations like footprint and steady state rolling. Abaqus/Explicit is used for transient rolling and hydroplaning simulations. The run times and scaling data corresponding to models of various sizes and complexity are presented.

The Dtermination of Paracetamol by HPLC Validation of the Method and Application on Serum Samples

2018 ◽  
Vol 69 (3) ◽  
pp. 627-631 ◽  
Author(s):  
Viorica Ohriac (Popa) ◽  
Diana Cimpoesu ◽  
Adrian Florin Spac ◽  
Paul Nedelea ◽  
Voichita Lazureanu ◽  
...  
Keyword(s):  
Mobile Phase ◽  
High Performance ◽  
Hplc Analysis ◽  
Emotional Experience ◽  
Optimum Conditions ◽  
Serum Samples ◽  
Liquid Chromatograph ◽  
Mobile Phase Flow Rate ◽  
Quantification Limit

Pain is defined as a disagreeable sensory and emotional experience related to a tissue or potential lesion. Paracetamol (Acetaminophen) is the most used non-morphine analgesic. For the determination of paracetamol we developed and validated the high performance liquid chromatography (HPLC) analysis using a Dionex Ultimate 3000 liquid chromatograph equipped with a multidimensional detector. After determining the optimum conditions of analysis (80/20 water / acetonitrile mobile phase, flow rate 1.0 mL / min, detection wavelength 245 nm) we validated the method following the following parameters: linearity of response function, linearity of results, limit (LD = 0.66 mg / mL) and quantification limit (LQ = 2.00 mg / mL), and precision. The method of determining paracetamol by HPLC was applied to 30 samples of serum collected from patients who had pain and were treated with paracetamol.

Sign in / Sign up

Export Citation Format

Share Document