简介:包含磷氮(MSMM-Al-P)的新奇包含的火焰retardant被与聚酰胺66包含准备(PA66-MSMM-Al-P)为聚酰胺6的火焰延迟(PA6)。结构和PA66-MSMM-Al-P的热性质被Fourier变换红外线的光谱学,X光检查光电子光谱学和thermogravimetric分析描绘。包含火焰retardants(MSMMAl-P和PA66-MSMM-Al-P)的PA6易燃被限制的氧索引测试,垂直燃烧测试和锥热量计调查。火焰retardancy和锥calorimetric分析在flame-retardantPA6建议了在PA66和MSMM-Al-P之间的synergistic效果。flame-retardantPA6的热稳定性也被调查。
简介:Anumberofnaphthalenedonorcompoundsthatpossessanadamantanaminebindingmoietyandan(OCH2CH2)n(nn1,2,3,4,6,8)spacerweresynthesized.Thefluorescencequenchingbetweenthesedonorsubstratesandmono-6-O-p-nitrobenzoyl-β-cyclodextrin(pNBCD)andmono-6-O-m-nitrobenzoyl-β-cyclodextrin(mNBCD)wasstudiedindetail.Itwasfoundthatveryefficientfluorescencequenchingcouldoccurinthesesupramolecularsystems.Thisquenchingwasattributedtothephotoinducedelectrontransferinsidethesupramolecularassemblybetweenthenaphthalenedonorsandcyclodextrinacceptors.DetailedStern-VolmerconstantsweremeasuredandtheywerepartitionedintodynamicStern-Volmerquenchingconstantsandstaticbindingconstants.Itwasdemonstratedthatthebindingconstantsbetweenallthenaphthalenecompoundsandcyclodextrinsarethesameastheypossessthesamebindingsite,i.e.,adamantanamine.
简介:Polyamide/acrylonitrile-butadiene-styrenecopolymer(PA/ABS)blendshavedrawnconsiderableattentionfrombothacademiaandindustryfortheirimportantapplicationsinautomotiveandelectronicareas.DuetopoormiscibilityofPAandABS,developinganeffectivecompatibilizationstrategyhasbeenanurgentchallengetoachieveprominentmechanicalproperties.Inthisstudy,wecreateasetofmechanicallyenhancedPA6/ABSblendsusingtwomulti-monomermelt-graftedcompatibilizers,SEBSg-(MAH-co-St)andABS-g-(MAH-co-St).Thedisperseddomainsizeissignificantlydecreasedandmeanwhiletheunique“softshell-encapsulating-hardcore”structuresforminthepresenceofcompatibilizers.Theoptimummechanicalperformancesmanifestanincreaseof36%intensilestrengthandanincreaseof1300%inimpactstrength,comparedwiththeneatPA6/ABSbinaryblend.
简介:研究了YBaCu3O6~7超导催化剂上CO2的加氢制醇反应。考察了温度、压力和空速等条件对催化剂反应性能的影响。反应的主要产物是甲醇、CO和少量甲醚。利用XPS、XRD和AFM等技术对催化剂的结构、铜的存在状态和反应活性位进行表征发现,在反应过程中,YBa2Cu3O6~7由orthombic相转变为tetragonal相。反应活性位可能是Cu(I)物种。反应后催化剂颗粒的分散程度明显提高
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简介:PolysaccharidecoatedPLAnanoparticlesbearingaldehydegroupswerepreparedbydialysisofDMSOsolutionofcholesterolhydrophobic-modifieddextranpolyaldehydeandPLAagainstwater.Theaveragediameterofthenanoparticleswasabout160nm,andthesizedistributionwasnearlyhomogenous.ThenanoparticleswerefunctionalizedsimultaneouslywithCD71andEGFRantibodythroughtheSchiff'sbasereaction,andthenradiolabeledwith~(99m)Tc.Afterperfusedtheradiolabelednanoparticlesintotumor-bearing...
简介:ThecrystalstructureofN-(2,3,4,6-tetra-O-acetyl-β-D-gly-cosyl)-thiocarbamicbenzoylhydrazine(C22H27N3O9S)wasdeterminedbyX-raydiffractonmethod.Thehexopyranosylringadoptsachairconformation.Alltheringsubstituentsareintheequatorialpositions.Theacetoxyl-methylgroupisinsynclinalconformation.TheSatomisinsynperiplanarconformationwhilethebenzoylhydrazinemoietyisanti-periplanar.Thethiocarbamicmoietyisalmostcompanarwiththebenzoylhydrazinegroup.Therearetwointramolecularhydrogenbondsandoneintermolecularhydrogenbondforeachmoleculeinthecrystalstructure.Themoleculesformanetworkstructurethroughintermolecularhydrogenbonds.
简介:Insitucompatibilizationoflowdensitypolyehylene(LDPE)(30%)andnylon-6(70%)blendsthroughone-stepreactiveextrusionusingt-BuOOHasaninitiatorandlowmolec-ularweightinterfacialagentsascompatibilizerswasstudied.Thecompatibilizercontainedalongchainbydrocarbon,doublebondandtwopolarfunctionalgroupswhichwascapableofreactingwithbothLDPEandnylon-6inthepresenceofinitiatortoformacopolymerattheinterfaceofthetwopolymerphases.Theextrudedblendsexhibitedsignificanten-hancementintheircompatibilitybasedonmorphological,thermalanalysisandmechanicalstudies.Theeffectofthehydrocarbonchainlengthandstructureofthefunctionalgroupofthecompatibilizerwasalsoexamined.Itwasfoundthatblendspreparedbyusingthecompatibilizercontaininglongerhydrocarbonchainandamidegrouphadbettermechanicalproperties.