简介：

简介：Dispersionofmulti-walledcarbonnanotubesinpoly(p-phenylene)compositeexposedtotoluenewasexperimentallyinvestigated.3mgofmulti-walledcarbonnanotubeswithnominalsizeof20nmwascompoundedwith30mgofpoly(p-phenylene)withthepresenceofterpineolasbindinginitiator.Toinvestigateanoptimalconditionforhomogenizingallconstituents,ultrasonicationwithanoutputpowerof750Wwasemployedwithcompoundingtimeof3,10,20and30min.WithFTIRanalyses,itcouldbeconfirmedthathomogeneouscompositeofmulti-walledcarbonnanotubesandpoly(p-phenylene)couldbeprepared.SEManalyseswerealsoconductedtoexaminethedispersionofmulti-walledcarbonnanotubesinthepolymermatrix.Thenintrinsicelectricalresistanceofthecompositesafterbeingexposedtotoluenewasalsoinvestigated.Itwasfoundthatthecompositefilmpreparedwithultrasonicationfor20mincouldprovidesufficientlysensitiveresponsewithrespecttovariedconcentrationoftoluene.

简介：PureAl2O3-2SiO2powderswerepreparedbysol-gelandcoprecipitationmethods,andtheiralkaliactivationreactivitieswerecompared.Thealkali-activationreactivityofthepowderpreparedbythesol-gelmethodwashigherthanthatofthepowderpreparedbythecoprecipitationmethod.Thepowderswereinvestigatedby27AIand29Simagic-anglespinningnuclearmagneticresonancespectroscopy（MASNMR）tounderstandtherelationshipbetweentheirstructureandalkali-activationreactivity.The27AlMASNMRdatashowedthatthefive-coordinateAIcontentofthepowderpreparedbythesol-gelmethodwashigherthanthatofthepowderpreparedbycoprecipitation.Thehighercontentoffive-coordinateAlcorrespondedtohigheralkali-activationreactivity.The29SiMASNMRdatashowedthatforthepowderpreparedbythesol-gelmethod,siliconwasreplacedbyaluminumatsecondarycoordinationsitesofthecentralSiatomsduringcalcination.However,forthepowderpreparedbysingle-batchcoprecipitation,themainchangewasfromalowdegreeofpolycondensationtoahighdegreeofpolycondensation.