Search results for "Detection limit"

showing 10 items of 810 documents

Micellar modified spectrophotometric determination of nitrobenzenes based upon reduction with tin(II), diazotisation and coupling with the Bratton–Ma…

1997

Abstract Nitrobenzenes, such as the antibiotic chloramphenicol, the vasodilator nicardipine, and the herbicides dinitramin, dinobuton, fenitrothion, methylparathion, oxyfluorfen, parathion, pendimethalin, quintozene, and trifluralin, were determined by using a spectrophotometric method in the visible region (540 nm). The method was based on the reduction of the nitrobenzenes to arylamines with tin(II) chloride, diazotisation of the arylamines and coupling of the diazonium ions with the Bratton–Marshall reagent. The two latter reactions were performed in a micellar medium of sodium dodecyl sulphate. The linear calibration range was 2×10 −6 to 7×10 −5 M ( r >0.999), with limits of detection i…

Detection limitChromatographySodiumTrifluralinchemistry.chemical_elementChlorideAnalytical ChemistryNitrobenzenechemistry.chemical_compoundParathionchemistryReagentmedicineTinmedicine.drugTalanta
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Determination of pesticides in soil samples by solid phase extraction disks

1993

A systematic study comparing the methodology and analytical results obtained in an investigation of seven pesticide residues (Molinate, Atrazine, Carbofuran, Pirimicarb, Prometryn, Malathion and Tetrachlorvinphos) in soil samples is reported. Solid-phase extraction (SPE) using glass columns and 47 mm disks of octyl and octadecyl-bonded silica was used in the pesticide analysis. The best extraction efficiency and clearest extracts are obtained with C8 disks. The analyses were carried out by capillary gas chromatography with nitrogen and phosphorus detection. Recovery experiments were performed at ppb levels in spiked soil samples. The average recoveries of the compounds were 53–77%. Detectio…

Detection limitChromatographySoil testPesticide residueOrganic ChemistryClinical BiochemistryExtraction (chemistry)BiochemistryAnalytical Chemistrychemistry.chemical_compoundchemistryEnvironmental chemistrySolid phase extractionGas chromatographyAtrazineCarbofuranChromatographia
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Implementing the contamination prevention programs in the pesticide industry by infrared spectroscopy.

2014

Abstract An infrared spectroscopy based methodology has been successfully developed to implement contamination prevention programs in the pesticide industry. Sensitivity of the IR procedure, traditionally considered the Achilles Hell of the technique, has been improved by using a transmission cell with an open upper side, an internal volume of 35 µL and an optical pathlength of 0.5 mm, providing detection limits of 32 mg L−1 for folpet and 48 mg L−1 for cymoxanil. The manufacturing of folpet and cymoxanil was employed as an example and the IR methodology was validated for the implementation of contamination prevention programs in the pesticide industry. The swab test and rinsate method were…

Detection limitChromatographySpectrophotometry InfraredChemistryChlorpyrifos-methylAnalytical chemistryInfrared spectroscopyContaminationPesticideOptical pathlengthGas Chromatography-Mass SpectrometryAnalytical ChemistryLimit of DetectionChemical IndustryEnvironmental PollutantsPesticidesTalanta
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Amphetamine and methamphetamine determination in urine by reversed-phase high-performance liquid chromatography with sodium 1,2-napthoquinone 4-sulfo…

1995

A rapid method is described for the identification and determination of amphetamine and methamphetamine in human urine samples by liquid chromatography with UV-Vis detection. The samples were transferred onto a C18 solid-phase extraction column and chromatographed on a Hypersil ODS RP C18, 5 microns (250 x 4 mm I.D.) with an acetonitrile-water elution gradient containing propylamine. Under these conditions, the amines are eluted with a short retention time. The procedure has been applied to the determination of amphetamine and methamphetamine in the range 0.3-4.0 micrograms/ml in spiked urine samples. The detection limits at 280 nm were 4 and 2 ng/ml for amphetamine and methamphetamine, res…

Detection limitChromatographySpectrophotometry InfraredElutionChemistryExtraction (chemistry)Reproducibility of ResultsPropylamineGeneral ChemistryMethamphetamineHigh-performance liquid chromatographyMethamphetamineAmphetaminechemistry.chemical_compoundmedicineHumansIndicators and ReagentsSolid phase extractionQuantitative analysis (chemistry)Chromatography High Pressure LiquidNaphthoquinonesmedicine.drugJournal of Chromatography B: Biomedical Sciences and Applications
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Determination of caffeine in tea samples by Fourier transform infrared spectrometry

2002

A sustainable and environmentally friendly procedure has been developed for the FTIR determination of caffeine in tea leaf samples. The method is based on the extraction with ammonia and CHCl3 and direct determination of caffeine on the chloroform extracts using peak height absorbance measurements at 1658.5 cm(-1) and external calibration. The method provides a sensitivity of 0.2142 absorbance units mg(-1) mL and a limit of detection of 1 mg L(-1), corresponding to 0.002% m/m caffeine in tea leaves. As compared with a reference procedure, based on UV absorbance measurement at 276 nm after low pressure column chromatography, the developed procedure reduces the consume of CHCl3 by a factor of…

Detection limitChromatographyTeaChemistryExtraction (chemistry)Infrared spectroscopyBiochemistryAnalytical ChemistryPlant LeavesAbsorbancechemistry.chemical_compoundColumn chromatographyCaffeineSpectroscopy Fourier Transform InfraredFourier transform infrared spectroscopyDiethyl etherCaffeineAnalytical and Bioanalytical Chemistry
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Ultra-high performance liquid chromatography-quadrupole time-of-flight mass spectrometry to identify contaminants in water: an insight on environment…

2013

Ultra-high pressure liquid chromatography-quadrupole time-of-flight mass spectrometry (UHPLC-QqTOF-MS) acquiring full scan MS data for quantification, and automatic data dependent information product ion spectra (IDA-MS/MS) without any predefinition of the ions by the user was checked for identifying organic contaminants in water samples. The use of a database with more than 2000 compounds achieved high confidence results for a wide number of contaminants based upon retention time, accurate mass, isotopic pattern and MS/MS library searching. More than 20 contaminants, mostly pharmaceuticals, but also mycotoxins and polyphenols were unambiguously identified. Furthermore, the combination of s…

Detection limitChromatographyTime FactorsChemistryOrganic ChemistryAnalytical chemistryWaterGeneral MedicineContaminationMass spectrometryBiochemistryLibrary searchingAnalytical ChemistryTriple quadrupole mass spectrometerMolecular WeightRiversTandem Mass SpectrometryPrincipal component analysisQuadrupole time of flightUltra high performancePesticidesChromatography High Pressure LiquidWater Pollutants ChemicalJournal of chromatography. A
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Analysis of T-2 toxin by HPLC and GC in samples of corn and oats

1984

HPLC is the only physico-chemical method for the analysis of trichothecenes for which no derivatization is necessary. Hence a combination of different methods can be performed. For exclusion of any faulty interpretation of data and in order to decrease the detection limit HPLC should be followed by GC.

Detection limitChromatographyToxinClinical BiochemistryTrichotheceneGeneral Medicinemedicine.disease_causeHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundchemistrymedicineGeneral Materials ScienceGas chromatographyDerivatizationMycotoxinFresenius' Zeitschrift für analytische Chemie
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Determination of UV-filters in sunscreens by HPLC.

2001

Simultaneous determination of six internationally authorised organic UV-filters in sunscreen formulations was performed by HPLC with UV spectrophotometric detection. The filters determined were: sulisobenzone, oxybenzone, octyl dimethyl PABA, octyl methoxycinnamate, octyl salicylate and homosalate. A C18 stationary phase and a mobile phase of ethanol water acetic acid (70 : 29.5 : 0.5) were used with a flow rate of 0.5 mL/min. UV measurements were carried out at 313 nm. The time required for the analysis was 25 min and the limits of detection were between 0.2 and 2 mg/L, except for sulisobenzone, which gave a limit of detection of 20 mg/L. The procedure proposed provides an accurate, fast a…

Detection limitChromatographyUltraviolet RaysOctyl methoxycinnamateReversed-phase chromatographySulisobenzoneBiochemistryHigh-performance liquid chromatographyHomosalatechemistry.chemical_compoundchemistrymedicineOctyl salicylateIndicators and ReagentsOxybenzoneSunscreening AgentsChromatography High Pressure Liquidmedicine.drugFresenius' journal of analytical chemistry
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A rapid HPLC assay for zearalenone in laboratory cultures ofFusarium graminearum

1993

A high pressure liquid chromatographic (HPLC) method to determine zearalenone in corn contaminated withFusarium graminearum is described. After extraction with methanol-water and solvent partition, samples were cleaned up by applying the extract to a disposable silica cartridge and by eluting the toxin with a mixture of hexane/dry ethyl ether (5/5). Separation was achieved by a reverse phase μBondapak C18 column followed by fluorescence detection using an excitation wavelength at 274 nm and an emission wavelength at 440 nm. Detection limit was about 5 ng. Recoveries ranging from 85.37 to 100.97%, in standard solutions range 30–0.5 µg/ml, were found.

Detection limitChromatographyVeterinary (miscellaneous)Extraction (chemistry)EtherStandard solutionApplied Microbiology and BiotechnologyMicrobiologyHigh-performance liquid chromatographySolventHexanechemistry.chemical_compoundchemistryAgronomy and Crop ScienceZearalenoneMycopathologia
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New Reusable Solid Biosensor with Covalent Immobilization of the Horseradish Peroxidase Enzyme: In Situ Liberation Studies of Hydrogen Peroxide by Po…

2019

Herein, we reported a chemiluminescent biosensor based on the covalent immobilization of the horseradish peroxidase (HRP) enzyme on a polydimethylsiloxane (PDMS) support to quantify in situ hydrogen peroxide (H2O2). The chemiluminescent reaction based on the use of luminol as an oxidizable substrate, with HRP as the catalyst, has been used in order to quantify H2O2 as the oxidizing agent. The performance of the proposed biosensor has been demonstrated to determine H2O2 liberated by cells in a culture medium and for evaluating the delivery of H2O2 from denture cleaner tablets, as examples of application. For both analyses, the results indicated that the biosensor is cost-effective, sensitive…

Detection limitChromatographybiologyGeneral Chemical EngineeringSubstrate (chemistry)General ChemistryHorseradish peroxidaseArticleLuminollaw.inventionchemistry.chemical_compoundChemistrychemistrylawOxidizing agentbiology.proteinHydrogen peroxideBiosensorQD1-999ChemiluminescenceACS omega
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