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简介：1-(2-chlorophenyl)ethanol(CPE)isofhealthandenvironmentalconcernduetoitstoxicityanditsuseasaninter-mediateinpharmaceuticalmanufacturing.ThecurrentworkdealswiththecatalyticreductivedechlorinationanddetoxificationofCPEbyPd/Febimetal.CPEwaseffectivelydechlorinatedto1-phenylethanol(PE)accompaniedbytheequivalentreleaseofchloride.TheextentofCPEdechlorinationincreasedwithtemperature,FedosageandPdloading.AdecreaseinsolutionpHincreasedCPEdechlorination,resultingpresumablyfromanincreaseinhydrogenproduction.Underthespecificconditionsof20g/LPd/Fe,0.10%Pd(w/w)andinitialpH5-6,theCPEdechlorinationwascompletedwithin145min.Thedechlorinationfol-lowedapseudo-first-orderkineticswithanactivationenergyof56.7kJ/mol.TheresultsoftoxicitytestingshowedthatCPEwasverytoxictoChlorella,whereasPEshowedlittletoxicity.Thetoxicityofthereactionsolutiondeclinedgraduallyandthepro-motingeffectsonChlorellaintensifiedconsequentlywiththedechlorinationprocess.Thus,thereductivedechlorinationofCPEtoPEbyPd/Fewasadetoxificationprocess.ItmaybeusedtoeffectivelyreducethetoxicologicaleffectsofCPE-contaminatedwastewater,therebyenhancingtheperformanceofsubsequentbiologicalprocessesinwastewatertreatment.

简介：AnewlayeredCu-basedoxychalcogenideBa3Fe2O5Cu2S2hasbeensynthesizedanditsmagneticandelectronicpropertieswererevealed.Ba3Fe2O5Cu2S2isbuiltupbyalternativelystacking[Cu2S2]2-layersandironperovskiteoxide[（FeO2）（BaO）（FeO2）]2-layersalongthecaxisthatareseparatedbybariumionswithFe3+fivefoldcoordinatedbyasquare-pyramidalarrangementofoxygen.Fromthebondvalencearguments,weinferredthatinlayeredCuCh-based（Ch=S,Se,Te）compoundsthe+3cationinperovskiteoxidesheetprefersasquarepyramidalsite,whilethelowervalencecationprefersthesquareplanarsites.Thestudiesonsusceptibility,transport,andopticalreflectivityindicatethatBa3Fe2O5Cu2S2isanantiferromagneticsemiconductorwithaNe′eltemperatureof121Kandanopticalbandgapof1.03eV.Themeasurementofheatcapacityfrom10Ktoroomtemperatureshowsnoanomalyat121K.TheDebyetemperatureisdeterminedtobe113K.TheoreticalcalculationsindicatethattheconductionbandminimumispredominantlycontributedbyO2pand3dstatesofFeionsthatantiferromagneticallyarrangedinFeO2layers.TheFe3dstatesarelocatedatlowerenergyandresultinanarrowbandgapincomparisonwiththatoftheisostructuralSr3Sc2O5Cu2S2.

简介：A60%Fe/Al2O3catalystwaspreparedbytheco-precipitationmethod.ItwasreducedbyH2toproducemetallicFe,whichwasthensulfidedbyCS2toFe0.96SandFe3S4orphosphidedbytriphenylphosphine(PPh3)inliquidphasestoFe2PandFeP.Itwasfoundthattheironsulfides(Fe0.96SandFe3S4)exhibitedthelowactivityforthehydrodesulfurization(HDS)reactions.TheHDSactivitywasalsolowontheFe(metal)/Al2O3andFe2P/Al2O3catalystssincetheywereconvertedintoFe0.96SandFe3S4duringtheHDSreactions.Incontrast,theFeP/Al2O3wasfoundtobestableandactivefortheHDSreactions.Inparticular,FeP/Al2O3possessedsignificantlysmallerFePparticlesthanFeP/C,leadingtothesignificanthigherHDSactivityofFeP/Al2O3thanFeP/C.

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简介：合成了氰根桥联配合物Co[Fe(CN)5NO].5H2O,使用元素分析、热重分析、红外光谱、XRD对配合物进行了表征。红外光谱显示金属离子通过氰根桥联即FeII-CN-NiII传递磁相互作用,是属于桥式氰根配体的CN伸缩振动,而粉末XRD衍射图表明此化合物为面心立方体结构(FCC),空间群为Fm3m(225),晶格常数a=10.2856。通过对该配合物的直流变温磁化率和交流磁化率测定表明金属离子通过氰根传递弱反铁磁作用,根据Curie-Weiss定律,拟合数据获得居里常数C=1.55cm3·K/mol,顺磁居里温度θ=-1.87K。

简介：AnewSnO_2-Fe_2O_3/SWCNTs(single-walledcarbonnanotubes)ternarynanocompositewasfirstsynthesizedbyafacilehydrothermalapproach.SnO_2andFe_2O_3nanoparticles(NPs)werehomogeneouslylocatedonthesurfaceofSWCNTs,asconfirmedbyX-raydiffraction(XRD),transmissionelectronmicroscope(TEM)andenergydispersiveX-rayspectroscopy(EDX).Duetothesynergisticeffectofdifferentcomponents,theassynthesizedSnO_2-Fe_2O_3/SWCNTscompositeasananodematerialforlithium-ionbatteriesexhibitedexcellentelectrochemicalperformancewithahighcapacityof692mAh·g~(-1)whichcouldbemaintainedafter50cyclesat200mA·g~(-1).Evenatahighrateof2000mA·g~(-1),thecapacitywasstillremainedat656mAh·g~(-1).

简介：AnapplicatiopnoftheopticalpyrometerisstudiedformeasuringmonochromaticemissivitiesofcementclinkerwithvariousFe2O3contnet.Theidsaofusing“brightnesstemperature”isintroducedintotheeimssivitymeasurement.Inthismethod,thereisnoneedformeasuringanactualtemperatureofsamplesurfaces,onlywithdeterminingbothbrightnesstemperaturesofasampleandablackbodycantherequiredemissivitybeevaluatedaccordingtoWien'sradiationlaw.Inpractice,thecementclinkerisregardedasagreybody,themonochromaticemissivityisapproximatelyequaltothetotalemissivity,soasingle-colouropticalpyrometerisappliedforthispurpose,Testmeasurementsarecarriedouton10kindsofcementclinkers,Experimentaldataaretreatedbytheleastsquaremethod.Asaresult,theemissivityvariationwithtemperatureatacertainFe2O3contentisquitewellrepresentedbyεn=a+bT.Furthermore,thisworkfirstreportedthattheeimissivitiesofcementclinkerchangeconsierablywithFe2O3contents.Inmultiplecementproductionthisconclusionisveryimportant.

简介：Theremediationofgroundwaterwhichcontainschlorinatedorganiccompounds(COCs)bynanoscalebimetalliccatalystshasreceivedincreasinginterestinrecentyears.Thisreportpresentsthedechlorinationof2,4-dichlorophenol(2,4-DCP)byPd-Febimetallicnanoparticlesinthepresenceofhumicacid(HA)toinvestigatethefeasibilityofusingPd-Fefortheinsituremediationofcontaminatedgroundwater.OurexperimentalresultsindicatedthatHAhadanadverseeffectonthedechlorinationof2,4-DCPbyPd-Fenanoparticles.Therateconstantkvaluesof2,4-DCPdechlorinationwere0.017,0.013,0.009,0.006and0.004min?1forHAconcentrationsof0,5,10,15and20mg/L,respectively.TherelationshipbetweenHAdosageandkvaluescanbedescribedasalinearmodel.

简介：合成了一维绳梯链状双金属化合物[Ni(en)2]3[Fe(CN)6]2·2H2O,并对其变温穆斯堡尔谱进行了研究,结果表明该分子磁体中铁的电子态为低自旋Fe3+,而大的四极分裂值(QS)表明此化合物的[Fe(CN)6]3-单元对称结构发生了形变,低温时出现的磁弛豫谱,给出了在该温度点附近出现铁磁耦合相互作用的信息。

简介：AfacilehydrothermalmethodwasdevelopedforthepreparationofFe2O3@CnanocompositesusingFeCl3·6H2Oasironsourceandglucoseascarbonsourceunderalkalinecondition.Themorphologyandstructureoftheas-preparedproductwereidentifiedbytransmissionelectronmicroscopy(TEM),highresolutiontransmissionelectronmicroscopy(HRTEM),field-emissionscanningelectronmicroscopy(FESEM),X-raydiffraction(XRD),Ramanspectroscopy,FourierTransforminfraredspectroscopy(FTIR),andthermogravimetricanalysis(TGA).Theas-prepareα-Fe2O3@Cnanocompositeswereemployedforsupercapacitorelectrodematerial.Thesynergisticcombinationofcarbonelectricaldouble-layercapacitanceandα-Fe2O3pseudo-capacitanceestablishedsuchnanocompositesasversatileplatformforhighperformancesupercapacitors.Thesynthesismethoddevelopedhereisexpectedtoobtainothermetaloxide/carboncomposite.

简介：Cu-Fecompositeoxideswerepreparedbyco-precipitationmethodandtestedforhigheralcoholsynthesisfromsyngas.TheselectivitytoC2+OHandC6+OHinalcoholdistributionwasveryhighwhilethemethaneproductfractioninhydrocarbondistributionwasratherlow,demonstratingapromisingpotentialinhigheralcoholssynthesisfromsyngas.ThedistributionofalcoholsandhydrocarbonsapproximatelyobeyedAnderson-Schulz-Florydistributionwithsimilarchaingrowthprobability,indicatingalcoholsandhydrocarbonsderivedfromthesameintermediates.TheeffectsofCu/Femolarratio,reactiontemperatureandgashourlyspacevelocity(GHSV)oncatalyticperformancewerestudiedindetail.ThesamplewithaCu/Femolarratioof10/1exhibitedthebestcatalyticperformance.Higherreactiontemperatureacceleratedwater-gas-shiftreactionandledtolowertotalalcoholsselectivity.GHSVshowedgreateffectoncatalyticperformanceandhigherGHSVincreasedthetotalalcoholselectivity,indicatingthereexistedvisibledehydrationreactionofalcoholintohydrocarbon.

简介：Wemeasurethecurrent–voltage(I–V)characteristicsforthesinglecrystalofTl0.4K0.41Fe1.71Se2withthesuperconductingtransitiontemperature(TC)around30.5K,undera10Tmagneticfieldappliedperpendicularandparalleltotheabplane.WefindthattheshapesoftheI–Visothermsareverydifferentfromthedescriptionbythevortex-glass(VG)model.CombiningtheoreticalcalculationsandanalysisoftheρH⊥ab–TandρHab–Tdata,wegiveanexplicitdiscussionoverthesuitabilityoftheVGmodelfortheA0.8Fe2Se2superconductors,andpointoutthepossibilityofthematerialactingasaconvenientplatformforre-examinationandfurtherstudyofthecomplexvortexbehaviorsinthelayeredsuperconductors.

简介：与黄金和氧化铁nanoparticles并且与silibinin装载的PEGylated-PLGA随机的nanofibrous膜被electrospinning免职准备。nanofibrous膜能遥远地被控制并且由一盏激光灯或磁场激活在需求上释放生物代理人。nanosystems用扫描电子显微镜学被描绘，红外线的光谱学，原子磁性的回声光谱学，和thermogravimetric分析的Fourier变换。装载效率和药内容百分比的药被紫外力的光吸收光谱学决定。nanofibrous膜由相对低紧张的激光照耀或由一个磁场刺激了为至少60h显示出持续silibinin版本，没有爆炸效果。建议便宜electrospinning过程能够集合，经由一个一步舞过程，有外部地为控制的药交货要激活的金属性的nanoparticles的刺激应答的装载药的nanosystem。

简介：WhileFe-basedoxygencarriers(OC)areregardedtobepromisingforchemicalloopingcombustion(CLC),thedecreaseofCO2selectivityduringdeepreductionprocessandthesevereagglomerationofFe2O3oftenoccuraftermultipleredoxcyclesduetothelowoxygenmobility.Herein,Fe-substitutedBahexaaluminates(BaFexAl12–xO19,denotedasBFxA-H,x=1and2)preparedbyamodifiedtwo-stepmethodexhibitednotonlyhigheramountofconvertedoxygen(Ot)andCH4conversion(77%and81%vs.17%and75%)thanthosepreparedbythetraditionalco-precipitationmethod(BFxA-C,x=1and2)butalsohighCO2selectivityabove92%duringthenearlywholereductionfromFe3+toFe2+.Furthermore,theBFxA-Hexhibitedtheexcellentrecyclabilityduring50cycles.ThebetterperformancewasascribedtothemarkedlyenhancedoxygenmobilitywhichresultedfromdominantoccupancyofFecationsinAl(5)sites(Fe5:71%and70%vs.49%and41%)inmirrorplanesofhexaaluminateleadingtolargeramountoflatticeoxygencoordinatedwithFe5(O–Fe5)(0.45and0.85mmol/gvs.0.31and0.50mmol/g).TheimprovementofoxygenmobilityalsofavoredthepreservationofchemicalstateofFecationsinhexaaluminatestructureinthere-oxidationstep,resultingintheexcellentrecyclabilityofBFxA-H.

简介：Chemicalloopingdryreforming（CLDR）isaninnovativetechnologyforCO2utilizationusingthechemicalloopingprinciple.TheCLDRprocessconsistsofthreestages,i.e.CH4reduction,CO2reforming,andairoxidation.Spinelnickelferrite（NiFe2O4）waspreparedanditsmulti-cycleperformanceasanoxygencarrierforCLDRwasexperimentallyinvestigated.X-raydiffraction（XRD）andLaserRamanspectroscopyshowedthatapurespinelcrystallinephase（NiFe2O4）wasobtainedbyaparallelflowco-precipitatingmethod.NiFe2O4wasreducedintoFe-Nialloyandwustite（FexO）duringtheCH4reductionprocess.SubsequentoxidationofthereducedoxygencarrierwasperformedwithCO2asanoxidanttoformanintermediatestate:amixtureofspinelNi1-xFe2+xO4,Fe2+yO4andmetallicNi.AndCOwasgeneratedinparallelduringthisstage.Approximate185mLofCOwasgeneratedfor1gspinelNiFe2O4inasinglecycle.TheintermediateoxygencarrierwasfullyoxidizedintheairoxidationstagetoformamixtureofNi1+xFe2-xO4andFe2O3.Althoughtheoriginalstateofoxygencarrier（NiFe2O4）wasnotfullyregeneratedandagglomerationwasobserved,agoodrecyclabilitywasshownin10successiveredoxcycles.更多还原

简介：Toeffectivelysolvetheagglomerationproblemsinthesolidstatereactionprocess,pre-addingglucoseisadoptedtothesynthesisofLiFePO4/CenergymaterialsusingFe–Pwasteslag.Theaverageparticle&grainsizeofLiFePO4/Cdecreases,andtheimpuritiesinLiFePO4/Ccompositesreducetoagreatextent.Itmakesgreatsensetothemassindustrialproduction.Theoptimumsynthesisconditionsdeterminedinthisworkarebasedontheorthogonalexperiments.Thesamplessynthesizedinascaleof500gexhibithighpurity,excellentelectrochemicalperformance,highreactionactivity,goodreversibility,andlowpolarizationlevel.Thedischargecapacitiesare145,134,117,and102mAh/gatthecurrentdensitiesof0.1C,0.2C,0.5Cand1C,respectively.ThisworkputsforwardapracticalsuggestionformassproducingenvironmentalbenignandlowcostLiFePO4/Cascathodematerialsoflithiumionbatteries.

简介：对CALYPSO预测方法的原理和核心技术进行了详细的介绍,并应用该方法分别研究了单质锂晶体和硼原子团簇结构的有关粒子空间分布构造问题,从而对CALYPSO方法有了更深入的了解和认识。

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