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71.
采用X射线衍射(XRD),程序升温还原(TPR)等表征手段考察了TiO2改性对CuO(或NiO)在γ-Al2O3表面上分散以及还原性能的影响,同时检测了这些改性的催化剂在CO+O2反应中的活性.结果表明:TiO2的改性使得CuO和NiO在γ-Al2O3载体上的分散复杂化,产生了多种状态的氧化铜(氧化镍)物种.当负载量低于其在γ-Al2O3上的分散容量(0.56 mmol Ti4+/100 m2γ-Al2O3)时,TiO2的加入主要是抑制了CuO和NiO在γ-Al2O3载体上的分散;而当负载量远大于其分散容量时,出现了CuO和NiO在晶相TiO2(锐钛矿)上的分散.无论其负载量如何,TiO2的加入促进了CuO的还原.因此,在250℃的CO+O2反应中,改性的催化剂中具有更多的活性位,因而显示出更高的活性;相反,TiO2的改性则抑制了NiO的还原.因此,在350℃的CO+O2反应中,可还原的氧化镍的量明显少于未经改性的催化剂,导致改性催化剂的活性降低. 相似文献
72.
SYNTHESIS AND-CHARACTERIZATION OF THE SOLUBLE, HIGH MOLECULAR WEIGHT AND LADDERLIKE POLYHYDROSILSESQUIOXANE AND ITS COPOLYMERS 总被引:3,自引:0,他引:3
The high molecular ladderlike polyhydrosilsesquioxane (LPHSQ) and its copolymer, ladderlike random copolymethylhydrosilsesquioxane (LR-PMHSQ) and ladderlike block copolymethylsilsesqui-oxane(LB-PMHSQ) have been synthesized by a preaminolysis reaction of the corresponding trichlorosilane with 1 ,4-phenylene diamine(PDA) then by hydrolysis and polycondensation reactions The thermographs of these polymers measured by DSC method indicate that these macromolecular backbones are very rigid as seen from the DSC curves which are almost horizontal from room temperature until 350 ~C without noticeable glass transition. The content of Si—H group in the polymers can be regulated by changing the composition of the two copolymerized monomers. So the ladderlike polymers including its copolymers can be the useful precursors for the functional polymers, especially such as fishbone-like liquid crystalline polymers. 相似文献
73.
A general, rapid and highly efficient method for the synthesis of diaryl ethers under the assistance of microwave irradiation was described. A series of diaryl ethers were prepared by direct coupling of phenols and aryl halides in good to excellent yields in anhydrous DMF or NMP at 150 ℃ within 20 rain. The presence of water was found to have a significant impact on the Ullmann C-O coupling reaction between aryl halides and phenols under microwave irradiation. 相似文献
74.
IntroductionMononuclear ,dinuclearandpolymerictypesofcrys talstructuresforlanthanidecomplexeswithbenzoicacidanditsderivativeshavebeenobtainedbecauseofthevari ationofbridgingformsforcarboxylategroupandcoordina tionabilityofdiammineligands ,suchas 1,10 phena… 相似文献
75.
A free standing film of polyaniline as large as 18 cm×18cm×0.002 cm can be obtained by evaporation of a solution of the chemically synthesized base in NMP. Its structure was examined by the elemental analysis, IR, U.V.-visible spectra, XPS, DSC, SEM and X-ray scattering and its conducting behavior as well as electrochemical properties were studied. Results show that the composition, structure of main chain, physical properties of the free standing film of polyanilme is similar to that of the powder. However, some differences in its electronic structure, conductivity at room temperature and potential of redox couple between the flee standing film and powder are observed, which may be due to cross-linking of the film of polyaniline. 相似文献
76.
The barium titano-silicate phosphors doped with Eu3+ were synthesized by high temperature solid state reaction. The structures of as-synthesized samples were characterized by powder XRD. The maximum peaks of emission spectra of Ba2TiSi2O8 and Ba2TiSi2O8∶Eu3+ were respectively located at 450 and 618 nm, coming from the transitions of charge-transfer bands of Ti4+-O2- and forced electric-dipole transition 5D0-7F2 of Eu3+. The luminous mechanisms of Ba2TiSi2O8 and Ba2TiSi2O8∶Eu3+ were suggested. The effects of concentration of Eu3+ on the luminous performance of Ba2TiSi2O8∶Eu3+ were also studied and the results showed that the optimum concentration of Eu3+ was 0.12 mol per mole of matrix. 相似文献
77.
利用电动势法得到了牛血清白蛋白(BSA)与十二烷基硫酸钠(SDS)相互作用的结合等温线. 通过四阶导数紫外光谱法和荧光光谱法研究了相互作用过程中芳香族氨基酸残基微环境极性的变化. 通过研究发现, 随着SDS浓度的逐渐增大, SDS在BSA上的平均结合数(v)逐渐增大, 色氨酸(Trp)残基所处微环境的极性在减弱后保持基本不变, 酪氨酸残基所处微环境的极性在明显增强后稍有减弱, 苯丙氨酸残基所处微环境的极性略有增强. 结果表明, 当v由0增大到14时, SDS主要结合在BSA的Trp-213附近并逐渐形成聚集体, 从而诱导BSA由结构域ⅡA 开始逐渐展开. 此后, SDS呈正协同作用的特点与BSA 结合, v急剧增大. 当v约为302 时, SDS在BSA上的结合基本达到饱和, BSA的构象趋于稳定. 相似文献
78.
乙胺嘧啶(商品名:达拉匹林)是一种抗寄生虫药物,改进了合成方法,并设计转化为创新型综合教学实验。从对氯苯乙腈出发,使用丙酸乙酯为酰化试剂,在叔丁醇钾作用下得到烯醇前体。在三甲基氧鎓四氟硼酸盐(Me3O·BF4,Meerwein盐)和碱作用下进行选择性甲基化反应得到烯醇甲醚后,与胍在碱性条件下环化得到最终产物达拉匹林,并通过红外光谱、核磁共振对其结构进行表征。改进后的实验方法具有重现性好、毒性低、操作方便、实验微型化等优点。实验过程中不仅提升了学生的实验技能和科研思维,更提高了学生的创新能力和绿色环保意识。 相似文献
79.
利用电动势法得到了牛血清白蛋白(BSA)与十二烷基硫酸钠(SDS)相互作用的结合等温线. 通过四阶导数紫外光谱法和荧光光谱法研究了相互作用过程中芳香族氨基酸残基微环境极性的变化. 通过研究发现, 随着SDS浓度的逐渐增大, SDS在BSA上的平均结合数(v)逐渐增大, 色氨酸(Trp)残基所处微环境的极性在减弱后保持基本不变, 酪氨酸残基所处微环境的极性在明显增强后稍有减弱, 苯丙氨酸残基所处微环境的极性略有增强. 结果表明, 当v由0增大到14时, SDS主要结合在BSA的Trp-213附近并逐渐形成聚集体, 从而诱导BSA由结构域ⅡA 开始逐渐展开. 此后, SDS呈正协同作用的特点与BSA 结合, v急剧增大. 当v约为302 时, SDS在BSA上的结合基本达到饱和, BSA的构象趋于稳定. 相似文献
80.
Poly{2, 5- bis [ (p- methoxyphenyl ) oxycarbonyl] styrene } was successfully syn-thesized. This new polymer has a structure characteristic of mesogen-jacketed liquidcyrstalline polymers (MJLCPs) and does form a liquid crystal phase above its glass tran-sition. It thus became the starting member of a new series of MJLCPs. The synthesis ofthe polymer as well as the liquid crystalline properties of the polymer and its monomerwas discussed. A brief comparison of the new monomer and polymer with some previouslyreported counterparts was also included. 相似文献