简介:Wereportonanunexplainedhighstatisticssignalthatmayindicatetheexistenceofasuperlightscalarboson[1].Thequestionwhetherthereexistsa(scalar)bosonwithamassofabout38MeVdoesnotdependexclusivelyontheexistenceofaresonance-likestructure(Fig.1)intheexperimentaldataofRef.[2],yetitisatpresenttheclearestsignalwehavefoundinmanyexperiments.
简介:FK01isanewstrainofoil-sunflowerwithcytoplasmicmalesterilelineHAasfemaleparentandcytoplasmicmalesterilerestorerline19540asmaleparent.19540isamutantirradiatedbycarbonionwhichseedoilcontentincreases.FK01joined2014Gansuprovinceregionaltestofoil-sunflowerandplantedinsixsites:Jingyuanagriculturaltechniquespreadingcenter,Minqinagriculturaltechniquespreadingcenter,Jingtaiagriculturaltechniquespreadingcenter,Jiuquanagriculturalsciencesresearchinstitute,Tianshuiagriculturalsciencesresearchinstitute,andHuanxianseedcontrolstation.
简介:Highenergyprotonbeamhasthelongpenetrationlengthinsolidmatteranditcouldproducetheradiographsandindicatethetomographyandmaterialpropertiesinsideofthespecimen.Consideringtheexpensivecoststoconstructahighenergyprotonaccelerator,theothercandidateofhighenergyelectronbeambecomesmoreacceptable[1??3].Duetothehighspatialandtemperalresolutionofhighenergyelectronbeam.Itisapowertooltodiagnosetheinnerstructurechangeduringthehighenergydensitymatterproductionandtheinertialconfinementfusionprocess.Inordertostudythedensityresolutionofthehighenergyelectronbeamradiography,astep-targetwasdesignedandproduced.ThestructureandthetargetpicturesareshowninFig.1andtheSitargetswithdifferentslot-widthwereproducedbyusingthemicroetchtechnics.
简介:ThisworkismainlytostudytheeffectofheavyionirradiationonthedamageofsinglelayerMoS2.ThenumberoflayersofMoS2preparedbyCVD(chemicalvapordeposition)methodwasdeterminedbyopticalmicroscopyandRamanspectroscopy.ThemonolayerMoS2preparedbyCVDunderhighenergy209BiionirradiationwasanalyzedbyRamananalysisandAFMobservation.AndtheresultsarecomparedandanalyzedbeforeandafterthebeamirradiationofsinglelayerMoS2preparedbymechanicalstrippingmethod.
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.