简介:在电的运输性质上评估Ni替换的影响,p类型skutteruditesRyFe3NiSb12(R=Ba,Nd和Yb)系统地从2.5K被调查到800K。由小心地修改三fillers,Ba,Nd和Yb的充满的部分,搬运人集中精确被调整,它按比例改变到数统治的原子价计算的名字的价值。活动性和Seebeck系数的搬运人集中依赖表示在原子价乐队的二乐队贡献,和为热电的性能的优化搬运人集中在之间(5–9)×1020厘米−3。样品的热电导率用稀土元素的元素(Nd和Yb)填满的格子作为与相比显著地更低充满Ba,由于更低的反响的频率并且部分充满。与公司替换相比,Ni替换趋于关上乐队差距,它为RyFe3NiSb12。然而由于状态的密度的改进,当搬运人集中是类似的时,RyFe3NiSb12比RyFe2公司2在更低的温度范围的Sb12。0.73的ZT价值为Yb0.77Fe3在600K的NiSb12。
简介:Thepurposeofthepresentstudywastosynthesizeanewcompositesscaffoldcontainingpoly(γ-benzyl-L-glutamate)modifiedhydroxyapatite/(poly(L-lacticacid))(PBLG-g-HA/PLLA)andtoinvestigatetheirinvitrobehaviouronbonemesenchymalstromalcells(BMSCs).TheresultsdemonstratedthatBMSCproliferationwassignificantlyincreasedonPBLG-g-HA/PLLAscaffoldsafter3and7dayspostseedingwhencomparedtoPLLAandHA/PLLAscaffolds.TheinvitroosteogenicdifferentiationalsofavouredthecompositePBLG-g-HA/PLLAscaffoldswhencomparedtocontrolsbysignificantlyincreasingRunx2,ALPorosteocalcinmRNAexpressionasassessedbyreal-timePCR.TheresultsillustratethepotentialofPBLG-g-HA/PLLAscaffoldsforbonetissueengineeringapplications.AndtheinvivotestingfurtherconfirmsthePBLG-gHA/PLLAscaffolds'potentioalforhealingcriticalbonedefects.
简介:三新奇Ba_5RNiNb_9O_(30)(R=La,Nd和Sm)陶艺在BaO-R_2O_3-NiO-Nb_2O_5系统被准备并且描绘。所有三混合物areparaelectjicphasesadopting。在房间温度的充满的四角形的钨铜(TB)结构。在1MHz,Ba_5RNiNb_9O_(30)陶艺有高电介质在范围193-245.3,在范围0.0059-0.0087的低绝缘的损失,和在范围的绝缘的常数(tau_e)的温度系数的常数-1140-1310X10~(-6)中心点degC。他们绝缘的常数的温度系数显著地Ba_5RNiNb_9O_(30)与那些相比被减少(R=La,Nd,Sm)陶艺。
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简介:Aseriesofcross-linkedhydrogelsforcolon-specificdrugdeliveryweresynthesizedbygraftcopolymerizationofChitosanandacrylicacidusingN,N'-methylene-bis-(acrylamide)asacross-linker.TheirswellingbehaviorindifferentpHbuffersolutionsandcolonicenzymaticdegradabilitywerestudied.TheobtainedresultsshowthatthesehydrogelshavegoodpHsensitivitywhichcanavoiddrugreleaseinstomach,andtheirswellingkineticsinstimulantintestinalenvironmentfollowsecond-orderswellingkineticsequation.Thefactorsinfluencingtheswellingkineticsincludethedegreeofcross-linkingandthecomposition,whichmaycontrolnoreleaseoralittleamountreleaseofdruginsidethehydrogelsinthesmallintestinebytailoringthesefactors.Thegelsaredegradablebycolonicenzymesandthereisacorrelativitybetweenthedegradationofnetworksandtheswellingdegreeofthegels,whichmaytriggerthereleaseofdruginthecolon.Thehydrogelsshowagreatpotentialfortheirapplicationinoralcolon-specificdrugdeliverysystem.
简介:通过自由基共聚的方法制备了聚偏氟乙烯-g-聚(N-异丙基丙烯酰胺)(PVDF—g-PNIPAAm)共聚物,进而采用浸没沉淀相转化法制备了PVDF—g—PNIPAAm共聚膜。采用超声时域反射法研究了不同凝固浴温度下PVDF—g-PNIPAAm的成膜动力学。结合PVDF—g—PNIPAAm的成膜动力学,研究了凝固浴温度对膜结构与性能的影响。结果表明,在不同凝固浴温度下,PVDF—g—PNIPAAm的成膜过程均由液液分相来控制,凝固浴温度为30℃时成膜时间最长,40℃时成膜时间最短;不同凝固浴温度下制备的PVDF—g—PNIPAAm共聚膜保持了PVDF的结晶特性,随着凝固浴温度的升高,结晶度降低。同PVDF—g—PNIPAAm共聚物相比,PNIPAAm在PVDF—g—PNIPAAm膜表面的含量更高,其中,30℃时所成膜表面的PNIPAAm含量最高。不同凝固浴温度下所成的膜均呈指状孔结构,其中,30℃下所成的膜指状孔最大,孔隙率最高。25℃下制备的PVDF—g—PNIPAAm膜具有明显的温度响应性能,其水通量在30℃附近有显著增加。