退火温度对掺杂钼板性能的影响

本文简述了退火温度对掺杂钼板的室温抗拉性能、弯曲塑－脆转变温度及室浊反复弯曲性能影响。试样经１３００℃真空退火－小时后，其室温抗拉强度为５８５ＭＰａ，伸长率为３１％，弯曲塑－脆转转变温度低于－７８℃，室浊进反复弯曲９０度的次２１次；经１８００℃退火后，其室温抗拉强度为４９５ＭＰａ，伸长率为４８％，弯曲塑－脆转变温度为４０℃，室温时反复弯曲９０度的次数为６次。     

掺杂石墨/Cu钎焊接头残余应力的分布特征及中间层的作用

利用有限元方法,模拟分析了掺杂石墨/Cu钎焊接头残余应力的分布特征。分析结果表明,对接头有害的较大残余应力分布在石墨棱角距离焊缝约0.8mm处的狭小区域;降低连接温度、减少连接时间及增加钎焊压力均有利于减小接头残余应力,优化接头的界面应力状态;中间层的加入在一定程度上缓和了接头的残余应力。从缓和效果来看,Cu比Mo作中间层好,而Cu/Mo复合中间层的缓和效果最好,是较理想的中间层材料。     

Yb3+掺杂KLa(WO4)2激光晶体生长与光谱分析

采用提拉法生长出掺镱钨酸镧钾[Yb:KLa(WO4)2,Yb:KLW]晶体,测试了晶体的红外光谱和Raman光谱,对出现的振动模式进行了归属.从X射线衍射分析得到晶胞参数a=b=0.532 nm,c=1.189 nm.通过热重-差热分析得到晶体的熔点为1 119 ℃,在熔点以下没有相变.测试了晶体的吸收光谱和荧光光谱,计算了相应的光谱参数.结果表明:该晶体发射波长为1 021 nm,在931,981 nm附近有较强、较宽的吸收峰,适合用InGaAs半导体激光泵浦.     

Mn2+在Zn2SiO4中的发光

利用Sol-gel法制备掺Mn^2 的Zn2SiO4的前驱体，并将前躯体在弱氧化气氛下在1000℃煅烧2h，得到掺Mn^2 的Zn2SiO4试样。X射线衍射分析确定试样为α-Zn2SiO4晶相。荧光分析测定试样的激发光谱和发射光谱。结果显示Mn^2 掺杂的α-Zn2SiO4可发蓝色和绿色荧光，这一结果显然不同于以前的文献报道。同时，我们讨论了Mn^2 在Zn2SiO4中产生这一新型发光性质的机理。     

不同Li/Nb摩尔比In∶Fe∶LiNbO_3晶体的生长及其光学性能

在Li NbO3(LN)中掺摩尔分数为1%的In和掺质量分数为0.03%的Fe,用提拉法技术生长具有不同n(Li)/n(Nb)[n(Li)/n(Nb)=0.94,1.05,1.20,1.38]的In∶Fe∶LN晶体。测试不同n(Li)/n(Nb)的In∶Fe∶LN晶体的吸收光谱、抗光致散射能力和指数增益系数,并计算晶体的有效载流子浓度。结果表明晶体样品随着n(Li)/n(Nb)增加,吸收光谱的吸收边发生紫移,抗光致散射能力增加,指数增益系数和有效载流子浓度增大。采用n(Li)/n(Nb)=1.38的In∶Fe∶LN晶体作记录介质,n(Li)/n(Nb)=1.05的In∶Fe∶LN晶体作位相共轭镜进行全息关联存储实验。实验表明存储系统具有实时处理,成像质量好,信噪比高和能反复使用等优点。     

Synergistic effects of doped Fe3+ and deposited Au on improving the photocatalytic activity of TiO2

Fe³⁺ doped together with Au deposited TiO₂ (Au/Fe³⁺–TiO₂) was successfully prepared, which shows excellent photocatalytic activity for degradation of methyl orange (MO) under both UV and visible light (λ > 420 nm) illumination. Fe³⁺ has been confirmed by EPR to substitute for Ti⁴⁺ in the TiO₂ lattice, and Au exists as Au⁰ on the surface of the photocatalyst indicated by the results of XRD. Fe³⁺ and Au have synergistic effects on improving the photocatalytic activity of TiO₂. A proposed mechanism concerning the synergistic effects is discussed to explain the improvement of the photocatalytic activities.     

Acid-Base Properties of Zirconium, Cerium and Lanthanum Oxides by Calorimetric and Catalytic Investigation

The combined use of calorimetric and catalytic methods for the investigation of the acid-base properties of oxide systems is discussed with reference to the authors' work on pure and doped zirconia samples, ceria-zirconia and ceria-lanthana solid solutions. Adsorption microcalorimetry of ammonia and carbon dioxide had been used to characterize the samples, whose chemical and thermal history was taken into account. The catalytic behavior of these samples in the conversion of 4-methylpentan-2-ol, route to 4-methylpent-1-ene (starting product for the manufacture of polymers of superior technological properties), had also been studied. On the basis of the calorimetric data, a rationale for interpreting the data for the transformation of 4-methylpentan-2-ol is formulated, which takes into account the role of the concentration and strength of the sites in governing the competition among the various mechanisms for dehydration and dehydrogenation.     

Gold nanoparticles on ceria: importance of O vacancies in the activation of gold

Synchrotron-based techniques (high-resolution photoemission, in-situ X-ray absorption spectroscopy, and time-resolved X-ray diffraction) have been used to study the destruction of SO₂ and the water-gas shift (WGS, CO + H₂O → H₂ + CO₂) reaction on a series of gold/ceria systems. The adsorption and chemistry of SO₂ was investigated on Au/CeO₂(111) and AuO _x /CeO₂ surfaces. The heat of adsorption of the molecule on Au nanoparticles supported on stoichiometric CeO₂(111) was 4–7 kcal/mol larger than on Au(111). However, there was negligible dissociation of SO₂ on the Au/CeO₂(111) surfaces. The full decomposition of SO₂ was observed only after introducing O vacancies in the ceria support. AuO _x /CeO₂ surfaces were found to be much less chemically active than Au/CeO₂(111) or Au/CeO_2−x (111) surfaces. In a separate set of experiments, in-situ time-resolved X-ray diffraction and X-ray absorption spectroscopy were used to monitor the behavior of nanostructured {Au + AuO _x }–CeO₂ catalysts under the WGS reaction. At temperatures above 250 °C, a complete AuO _x → Au transformation was observed with high catalytic activity. Photoemission results for the oxidation and reduction of Au nanoparticles supported on rough ceria films or a CeO₂(111) single crystal corroborate that cationic Au^δ+ species cannot be the key sites responsible for the WGS activity at high temperatures. The active sites in {Au + AuO _x }/ceria catalysts should involve pure gold nanoparticles in contact with O vacancies of the oxide.     

Redox properties of CeO2 and Pt-Rh/CeO2 studied by TAP method

Redox properties of CeO₂ and Pt-Rh/CeO₂ were studied by temporal analysis of products (TAP) method using alternative pulses of CO and O₂. A portion of pulsed CO was oxidized to CO₂ and a portion of CO was adsorbed on the surface. Pulsing ¹⁸O₂ onto the catalyst which has surface species derived from CO, evolved CO₂ contained no ¹⁸O suggesting that the surface species will be carbonate ions.     

Synergistic Catalysis of Carbon Dioxide Hydrogenation into Methanol by Yttria-Doped Ceria/γ-Alumina-Supported Copper Oxide Catalysts: Effect of Support and Dopant

Methanol synthesis from carbon dioxide hydrogenation was studied over ceria/-alumina- and yttria-doped ceria (YDC)/-alumina-supported copper oxide catalysts to seek insight into the catalysis at metal–support interfaces. It was found that, in comparison with Cu/-Al₂O₃, the Cu/CeO₂/-Al₂O₃ and Cu/YDC/-Al₂O₃ catalysts exhibited substantial enhancement in activity and selectivity toward methanol formation. The extent of enhancement was augmented by increased ceria loading on -alumina and with increased yttria doping into ceria. The enhancement is inferred to result from the synergistic effect between copper oxide and surface oxygen vacancies of ceria.