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60%氟吗啉·唑嘧菌胺干悬浮剂高效液相色谱分析方法研究 Title:AStudyontheHigh-PerformanceLiquidChromatographicAnalysisMethodfor60%Flumioxazin·ProthioconazoleSuspensions Abstract: Theaimofthisstudywastodevelopahigh-performanceliquidchromatographic(HPLC)analysismethodforthedeterminationof60%flumioxazin·prothioconazolesuspensions.ThemethodinvolvedtheseparationandquantificationoftheactiveingredientsusinganHPLCsystemandappropriatemobilephase.Thedevelopedmethodshowedexcellentlinearity,precision,accuracy,andsensitivity.Thisresearchprovidesaneffectiveanalyticaltoolforqualitycontrolandanalysisof60%flumioxazin·prothioconazolesuspensions. 1.Introduction: Flumioxazinandprothioconazolearewidelyusedinagricultureasherbicidesandfungicides,respectively.Thecombinationofthesetwoactiveingredientsina60%suspensionformulationoffersimprovedcontrolofbothweedsandplantdiseases.Toensurethesafetyandefficacyofthesesuspensions,itisessentialtodevelopananalyticalmethodforaccuratedeterminationoftheactiveingredients.HPLCisacommonlyemployedtechniquefortheanalysisofpesticidesduetoitshighsensitivity,selectivity,andaccuracy. 2.MaterialsandMethods: 2.1Instrumentation: Ahigh-performanceliquidchromatographequippedwithaUV-VISdetectorandanauto-samplerwasusedfortheanalysis.TheseparationwascarriedoutusingaC18reverse-phasecolumn. 2.2PreparationofStandardSolutions: Individualstocksolutionsofflumioxazinandprothioconazolewerepreparedbydissolvingthepurecompoundsinanappropriatesolvent.Thesestocksolutionswerethenusedtoprepareaseriesofstandardsolutionswithknownconcentrations. 2.3SamplePreparation: The60%flumioxazin·prothioconazolesuspensionswerethoroughlymixed,andanaliquotofthesuspensionwastaken.Thesamplewasdilutedwithanappropriatesolvent,andthentheparticleswereremovedbycentrifugation.Theresultingsupernatantwasfilteredthrougha0.22μmmembranefilterandanalyzedbyHPLC. 3.OptimizationofHPLCConditions: TheHPLCconditionswereoptimizedbyadjustingthemobilephasecomposition,columntemperature,andflowrate.Themobilephaseconsistedofamixtureofacetonitrileandwater,

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