简介:Eightnovelcompoundshavebeensynthesizedandtheyaretwoseriesofmixedtri(butyl/cyclohexyl)tincarboxylates:BunCy3-nSnO2CR(n=1,2;R=n-C3H7,C6H5,4-ClC6H4,4-NO2C6H4).InadditiontothestudiesoftheirstructureswithIR,119Snand13CNMR,wetestedtheirfungicidal,insec-ticidalandacaricidalactivities.Thepercentageofinhibitiontotheaforementionedphytopathogenisabout80—100%at50ppminglasshouseand100%forT.Uriticaeat500ppm.Thosefindingsindicatethatthiskindofcompoundshavebothfungicidalandacaricidalactivitiesandmayhaveagoodprospectforapplications.
简介:SnO2preparedwiththesol-geltechniqueatdifferenttemperatureswasusedasananodematerialofthelithium-ionbattery.Weobtainedthequalititaverelationshipbetweentheelectrochemicalperformanceoftinoxideanodematerialandeachofitscarboncomponent,particlesize,structureandsurfacemorphologyindetail.ItwasfoundthatthebestelectrochemicalperformancecanbereachedbycontrollingthephysicalcharacteristicsofSnO2,whichwasaffectedgreatlybythetreatmenttemperature.TheSnO2obtainedat600℃waspure.Whenitwasusedastheanodematerialofthelithium-ionbattery,itdemonstratedahighinitialspecificcapacityof770mA·h/g.
简介:Sn(OH)4waspreparedbytheconventionalsolutionprecipitatemethod,followedbysupercriticalCO2drying.TheresultantSn(OH)4wasdividedintothreealiquotsandcalcinedat400,600and800°C,respectively,thusSnO2nanoparticleswithaveragecrystallitesizesof5,10and25nmwereobtained.Furthermore,threeSnO2thickfilmgassensors(denotedassensorsS-400,S-600andS-800)werefabricatedfromtheaboveSnO2nanoparticles.Theadhesionofsensingmaterialsonthesurfaceofaluminatubeisgood.ComparedtothesensorsS-600andS-800,sensorS-400showedamuchhighersensitivityto1000μL/Lethanol.Ontheotherhand,sensorS-800showedamuchlowerintrinsicresistanceandimprovedselectivitytoethanolthansensorsS-400andS-600.X-Raydiffraction(XRD),transmissionelectronmicroscopy(TEM)andselectiveareaelectrondiffraction(SAED)measurementswereusedtocharacterizetheSnO2nanoparticlescalcinedatdifferenttemperatures.Thedifferencesinthegassensingperformanceofthesesensorswereanalyzedonthebasisofscanningelectronmicroscopy(SEM).
简介:Thesolidaddofthefirstprotonatedzincoborophosphate,(H3O)Zn(H2O)2BP2O8·H2O(1),wassoventothermallysyn-thesizedbythereactionofZn(NO3)2·6H2OandH3BO3withH3PO4inamixedsolvent,andstructurallycharacterizedbysingle-ystalX-raydiffractionanalysis.ItcrystallizesinthehexagonalP6122,a=0.9604(4)nm,c=1.5297(6)nm,V=1.2218(8)nm^3,Dc=2.921g/cm^3,Z=6,F(000)=1080,μ=3.495mm^-1.Thestmchwefeaturesthatthetetrahedra-te-trahedrahdlcesinterconnectedbyoctahedraandstronghydro-gembondinteractionsformathree-dimensionalframework.Theprotonatedwatermoleculesarelocatedatuniquepositions.othercharacterizationsbyIRandthermalanalysisarealsode-scribed.
简介:0.5%Pt-K/γ-Al2O3catalystsforthesynthesisofo-phenylphenol(OPP)fromo-cyclohexenyl-cyclohexanone(dimer)dehydrogenationwerepreparedbymeansofatwosubsequentimpregnationmethod.Theeffectsofcatalystpreparationparameters,suchasKpromoters,calcination,andreductionconditions,wereinvestigated.TheresultsshowedthattheadditionofK2SO4toPt/γ-Al2O3catalystnotablypromotedtheselectivityofOPP,anditsoptimumcontentwasfoundtobe6%inmassfraction.ThehigheractivitywasobtainedwhenPt/γ-Al2O3catalystwascalcinedinnitrogenatmosphereat400―500°Candthenreducedatthesametemperaturefor3hinhydrogenatmosphere.TheconversionofthedimerandtheselectivityofOPPwerealwaysabove99%and90%,respectively,over0.5%Pt-6%K2SO4/γ-Al2O3catalystduringthepilotscaletestof8000h.
简介:Theenantiomersofthirty-nineO-ethylO-phenylN-isopropylphosphoroamidothioateshavebeenseparatedbyhighperformanceliquidchromatographyonaPirklemodelchiralstationaryphaseusingtenmobilephase.Chromatographicdataarepresentedfortheseparationoftheseorganicphosphorusenantiomersonthechiralphase.Theinfluencesofmolecularstructuresandcompositionsofmobilephaseshavebeendescribed.
简介:采用2步水热法合成了LaPO4∶Eu3+-Fe3O4复合材料.在LaPO4∶Eu3+-Fe3O4复合材料中,LaPO4∶Eu3+为单斜晶相,呈纳米棒状,纳米棒的直径和长度分别为20-100nm和0.2-1μm;Fe3O4为正交晶相、呈20-30nm的颗粒状,Fe3O4粒子紧紧附着在LaPO4∶Eu3+纳米棒的表面;样品的磁性和发光性质研究表明所合成的LaPO4∶Eu3+—Fe3O4复合材料既具有发光性质又具有磁性.
简介:Fivechiralstationaryphases(CSPs)wereusedtoseparatetheenantiomersofaseriesofO,O-diethyl(p-methyl-benzenesulfonamindo)-aryl(alkyl)-methylphosphonates.Achiralrecognitionmechanismwaspresentedtoexplaintheresolutionofthesecompounds.ResultsshowthatCSPwithstrongπ-acceptor3,5-dinitrobenzoylgroupandhighsterichindrancehasthebestresolutionabilityinchiralseparationofO,O-diethyi(p-methyl-benzenesulfonamindo)-aryl(alkyl)-methylphosphonates.WhenaCSPhasjustastrongπ-acceptor3,5-dinitrobenzoylorhighsterichindranceitdoesnothavegoodchiralresolutionability.ThechiralrecognitionismoredifficultwhentheCSPhasmorethanoneasymmetriccenter.
简介:AquantummechanicalcalculationwasperformedtostudytheTranslation-Vibration(T-V)energytransferofacolinearOH+O/OD+Osystem,forwhichDelvescoordinatesandR-matrixpropagatationmethodswereappliedtoaMulius-Blintpotentialenergysurface.ThecalculatedresultoftheT-Venergytransferprobabilityshowsstrongoscillationphenomenaandthecollisiondelaytimeofthetitlesystemwasinthe10-15—10-12stimescale.Thekineticisotopeeffectwasdiscussedinthisworktoo.
简介:FurfuralinaqueoussolutionwastreatedbyUV/O3method.Theresultsshowthattheremovalrateoffurfuralisseverelyenhancedandthesynergismphenomenonappearswhenultravioletandozonearepresenttogether.TheinfluencesofexperimentalparameterssuchaspH,theintensityoflightandthenegative-positiveionsonfurfuraldegradationwereinvestigated.Theresultsindicatethatfurfural(300mg/L)isalmostcompletelydegradedafter3hundertheoptimumconditions.TheintermediateinthefurfuraldegradationwascharacterizedbyGC-MSandIRspectrumandthedegradationmechanismoffurfuralbyUV/O3technologywasproposed.
简介:利用室温液相还原、晶种生长的方法,成功的制备了大小形貌均一、性能稳定且具有磁性的Fe3O4@Cu2O复合纳米粒子,并且对制备的Fe3O4@Cu2O纳米粒子进行了光催化性能的研究.在以紫外光为光源的照射下,合成的Fe3O4@Cu2O纳米粒子对有机染料甲基蓝溶液起到很好的降解作用.更重要的是,在外加磁场的作用下,Fe3O4@Cu2O纳米粒子容易回收,具有良好的可循环利用性能.
简介:Thecrystalandmolecularstructuresof[(C3H7O)2PS2]2(CCDCNo.217201)weredeterminedbymeansofX-raycrystallography.ItcrystallizedinatriclinicsystemwithspacegroupP1^-andlatticeparametersa=0.82794(3)nm,b=0.84764(2)nm,c=0.85034(3)nm,α=97.78(3)°β=110.77(3)°,γ=94.95(3)°,V=0.54701(9)nm^3,Z=1.Inthismolecule,thetwodiisopropyldithiophosphategroups,[(C3H7O)2PS2]2,whichareparalleltoeachother,arelinkedbyanS--Sbondandthereexistinversioncentersinthemolecule,Inthestructure,theP=Sbondsinthetwodithiophosphateunitsaretrans-orientedtoeachother.
简介:TheBiginelli-typecompounds4,5,8a-triarylhexahydropyrimido[4,5-d]pyrimidine-2,7(1H,3H)-dionesweresynthesizedbyaone-potthree-componentreactionusingsulfatedtinoxideasareusablecatalyst.Thismethodhastheadvantagesofhighyields,shortreactiontime,simplestartingmaterialsandreusabilityofcatalystforseveraltimes.