负载型纳米钛酸锶钡对水中Cd~(2+)吸附行为研究

采用络合溶胶-凝胶法制备了钛酸锶钡溶胶,将其浸渍在硅胶G上,经高温煅烧后,制得固载于硅胶G上的纳米钛酸锶钡,以X射线衍射(XRD)、扫描电镜(SEM)和傅里叶变换红外光谱(FTIR)进行了表征.以火焰原子吸收为检测手段,系统地研究了负载型纳米钛酸锶钡对水中CA2+的吸附行为.结果表明,纳米钛酸锶钡能够牢固地负载于硅胶G表面.当介质的pH值为4～7时,该吸附剂对水中的CA2+具有很强的吸附能力,其吸附行为符合Freundlich吸附等温模型和HO准二级动力学方程式,并分别计算了吸附过程的焓变(△H),自由能变(△G)和熵变(AS)等热力学参数,表明该吸附过程是自发的吸热物理过程.被吸附的CA2+可用1 mol·L-1的硝酸完全洗脱回收.将其应用于水中痕量CA2+的吸附,建立了负载型纳米钛酸锶钡吸附富集,火焰原子吸收法测定水中痕量Cd2+的新方法.用于自来水和地表水中镉的测定,结果满意.     

钡-偶氮胂Ⅲ-锌(钴)-邻菲啰啉多元配合物显色反应的研究

在近中性环境中,研究了钡与偶氮胂Ш、锌(钴)、邻菲啰啉形成多元配合物的条件及其配合物组成.显色体系的摩尔吸光系数由二元配合物的2.1×104L·mol-1·cm-1提高到7.4×104L·mol-1·cm-1.用此方法,经过简单的分离后,可作硅钡合金中钡的光度法测定.     

钛酸锶钡纳米管的制备及其红外吸收性能研究

首次采用溶胶凝胶法结合通孔阳极氧化铝模板, 成功制备出了钛酸锶钡纳米管. 该制备工艺简单、易实现而且成本低. 首先制备通孔阳极氧化铝模板和钛酸锶钡溶胶, 然后通过浸渍加上匀胶的方法将钛酸锶钡溶胶引入到通孔阳极氧化铝模板的纳米孔洞中, 最后在650℃下煅烧1 h形成钛酸锶钡纳米管. X射线衍射(XRD)证明, 制得的钛酸锶钡纳米管为立方钙钛矿相, 主要沿(110)晶向生长. 扫描电子显微镜(SEM)显示, 钛酸锶钡纳米管外径、内径和管长分别为75 nm, 50 nm, 16 μm. 傅里叶变换显微红外光谱仪(FTIR)测试结果表明在波数为1350-1650 cm^-1红外波段, 阳极氧化铝/钛酸锶钡纳米管复合结构较钛酸锶钡薄膜有两处明显的吸收峰, 吸收峰位于1470和1550 cm^-1处, 与通孔阳极氧化铝模板相比其吸收峰强度高出一倍, 最后分析了出现这一现象的可能原因.     

电离层中性气体释放的早期试验效应研究

在电离层释放电子吸附类中性气体能够引起电离层电子密度耗空,在释放之后快速形成"电离层洞";同时,由于释放气体的快速膨胀,挤压背景等离子体,在电离层洞的外边缘产生"壳状"电子密度增强结构,电离层洞和电子密度增强结构同时存在是释放早期试验效应的显著特征.本文研究了电离层中性气体释放的早期试验效应,建立了释放早期电子密度的时空演化物理模型,仿真了释放早期电子密度的时空演化过程,同时采用射线追踪方法研究了释放后10 s和120 s不同频率信号在扰动区的传播效应,并反演得到了电离层垂直探测电离图,反演结果与一次火箭喷焰的实际观测结果吻合较好,初步验证了本模型的正确性.     

钡—偶氮胂Ⅲ—锌（钴）—邻菲罗啉多元配合物显色反应的研究

在近中性环境中，研究了钡与偶氮胂Ⅲ、锌（钴）、邻菲罗啉形成多元配合物的条件及其配合物组成。显色体系的摩尔吸光系数由二元配合物的2.1×10^4L·mol^-1·cm^-1提高到7.4×10^4L·mol^-1·cm^-1。用此方法，经过简单的分离后，可作硅钡合金中钡的光度法测定。     

BaxOy小团簇修饰Ru(0001)表面的结构稳定性和氮分子吸附性质

为了说明钡助剂的存在形式, 本文采用第一性原理方法研究了Ba_xO_y小团簇修饰Ru(0001)表面的结构稳定性和氮分子吸附性质. 基于总能的热力学分析发现, 在实验条件下(500 K, P_H2O/P_H2<10^-3), Ba₂O团簇比BaO₂, BaO, Ba和O等团簇(原子)更加稳定. 这证实含有金属性钡原子的团簇也是氧化钡助剂可能的工作状态. 表面电荷差分密度说明Ba₂O团簇的氧和钡原子与衬底的作用不同. 不过Ba₂O团簇氧和钡原子附近的氮分子吸附行为相似, Ba₂O团簇增强了氮分子和衬底的相互作用. Ba₂O团簇氧和钡原子附近的氮分子吸附能分别为0.78 和0.88 eV, 均大于清洁表面的0.67 eV. 氮分子间距和氮分子的拉伸振动频率都表明Ba₂O团簇在一定程度上活化了吸附氮分子. Ba₂O团簇氧和钡原子附近的N–N键长分别为0.117和0.116 nm, 大于清洁表面的0.114 nm. 氧和钡原子附近氮分子的拉伸振动频率分别为 1888 和1985 cm^-1, 小于清洁表面的2193 cm^-1. 电荷差分密度的计算结果说明, 削弱作用主要来自于Ba₂O团簇中钡离子和氮分子间的静电作用. 两者间的静电作用增加了氮分子π 反键轨道的占据数, 促进了氮分子极化, 从而削弱氮分子键.     

不同释放高度的化学物质的电离层扰动特性

在电离层释放H₂O, CO₂, H₂和SF₆等中性气体能导致释放区域电子损耗, 形成明显的人工电离层洞, 是电离层人工变态的重要而有效的手段之一. 本文在改进电离层化学物质释放三维动力学模型的基础上, 对不同释放量级的H₂O 和SF₆在不同释放高度下产生的电离层洞形态结构及其时空演化规律进行了系统对比研究, 探讨了释放高度对化学物质释放电离层扰动效果、电离层洞形态及其动力学特性等的影响, 并对其成因进行了分析. 关键词： 化学物质释放 电离层扰动 人工电离层洞 三维动力学模型     

铌酸锶钡薄膜的微结构与电光性能的研究

本文叙述了使用溶胶凝胶法在MgO(0 0 1)的衬底上制备铌酸锶钡薄膜的过程 ,膜层厚度可达 5 μm。通过X射线衍射、摇摆曲线、扫描、拉曼散射光谱等方法研究了薄膜的微结构性能 ,实验发现 ,铌酸锶钡薄膜具有了较好的 (0 0 1)方向的优先取向性能 ,并且随着薄膜厚度的增加 ,其晶体取向性也会随之不断改进。熔石英的透明衬底上生长的SBN薄膜具有较大的电致双折射效应 ,其有效电光系数能够高达 6 6 2× 10 -11m/V。     

陕西战国秦墓出土玻璃和汉紫六博棋子分析研究

利用超景深显微镜（OM）、激光拉曼光谱仪(Raman)、X射线荧光光谱仪(XRF)、扫描电子显微镜能谱(SEM-EDS)、色度仪等多种手段,对陕西战国秦墓出土的两种质地、颜色不同的六博棋子进行了综合分析检测。鉴定出蓝色样品为铅钡玻璃,紫色样品为中国紫制品,发现了中国紫在战国时期的新用途。并对比陕西出土的铅钡玻璃制品与两湖、四川地区出土的同时代的铅钡玻璃制品在成分组成上的差异,推测战国时期铅钡玻璃的制作工艺已成熟,可根据器物形制的需求进行不同的成分配比。同时,还发现当时的玻璃制作已有旧料重熔制作新器的现象。在确定中国紫成分的基础上,利用色度计进行色度测试,根据光谱数据,首次为人造硅酸铜钡颜料确定了特征光谱峰,使快速、无损的对人造硅酸铜钡颜料的鉴定识别成为可能。     

人工电离层洞形态调制及其对短波传播的影响

本文在电离层中性气体点源扩散近似解的基础上,给出了多源释放动力学模型.分析了释放物质、释放高度、释放模式和释放量等因素对人工电离层洞形态调制的影响,并利用电离层短波三维数字射线追踪技术,对不同调制电离层洞的电波传播效应进行了数值模拟和分析. 关键词： 化学物质释放 人工电离层洞 形态调制 电波传播效应     

BaTiO_3纳米粉体的制备及结构的光谱表征

采用钛酸丁脂和八水氢氧化钡为原料的溶胶-凝胶法制备了纳米BaTiO3粉体。经不同温度烧结,并利用X射线衍射和Raman光谱分析进行结构表征。实验表明,经1073K烧结后粉体粒径为26 2nm,颗粒分布均匀,还有少量BaCO3存在。在这个温度下得到的晶粒主要是立方相,并含有少量的四方相。经1273K烧结后,BaTiO3完全是四方相,粉体粒径为80 0nm,此时BaCO3已完全分解。另外探讨了溶胶-凝胶制备纳米BaTiO3粉体的反应机理,解释了BaTiO3物相的形成。     

Nanocrystals formation on Ho doped strontium barium niobate glass

The study of two different methods to obtain strontium barium niobate nanocrystals immersed in a glass matrix has been carried out. Ho₂O₃-doped SrO-BaO-Nb₂O₅-B₂O₃ glasses were fabricated using the melt quenching method. Glass ceramic samples were obtained from the precursor glass by thermal treatment in a furnace and by laser irradiation. These glass ceramic samples are formed by a glassy phase and a crystalline phase of strontium barium niobate nanocrystals. This structure was confirmed by X-ray diffraction and Atomic Force Microscope images. The incorporation of Ho³⁺ ions in the strontium barium niobate nanocrystals were corroborated by optical measurements, which produced an increment in the luminescence intensity compared to the precursor glass.     

The occurence of barium in the corneal surface of the barking deer, Muntiacus Muntjak (Zimmerman) as revealed by energy dispersive x-ray micro-analysis

Energy dispersive X-ray micro-analysis with simultaneous visual display by secondary electron emission mode of scanning electron microscopy reveals the occurrence of barium, in addition to silicon, phosphorus, sulphur, potassium and calcium in the corneal surface of the barking deer, Muntiacus muntjak. The lenticular surface on the other hand shows the presence of aluminium silicon, phosphorus and sulphur but no barium.Quantitative data obtained by using the ZAF-4/FLS programme (Link) shows that the relative percentage of barium is the highest of all the elements detected in the cornea, whereas in the lens-surface, sulphur constitutes the maximum percentage.     

An effective quantum defect theory for the diamagnetic spectrum of a barium Rydberg atom

A theoretical calculation is carried out to investigate the spectrum of a barium Rydberg atom in an external magnetic field. Using an effective approach incorporating quantum defect into the centrifugal term in the Hamiltonian, we reexamine the reported spectrum of the barium Rydberg atom in a magnetic field of 2.89 T [J. Phys. B 28 L537 (1995)]. Our calculation employs B-spline basis expansion and complex coordinate rotation techniques. For single photon absorption from the ground 6s2 to 6snp Rydberg states, the spectrum is not influenced by quantum defects of channels ns and nd. The calculation is in agreement with the experimental observations until the energy reaches E = 60 cm-1 . Beyond this energy, closer to the threshold, the calculated and experimental results do not agree with each other. Possible reasons for their discrepancies are discussed. Our study affirms an energy range where the diamagnetic spectrum of the barium atom can be explained thoroughly using a hydrogen model potential.     

Characterization of a Green-Emitting Copper-Doped Barium Aluminate Phosphor

A novel green-emitting phosphor copper-doped barium aluminate was synthesized by the conventional ceramic method. The crystallographic phase and microstructure identification were performed by powder X-ray diffraction and scanning electron microscopy. The X-ray diffraction pattern of the sample confirms the formation of the phosphor, and the scanning electron microscope image was recorded to observe the surface morphology. Differential thermal analysis results show that the initiatory decomposition temperature of barium carbonate starts at about 728°C. Cathodoluminescence studies have been undertaken to ensure the successful incorporation of copper ions in the barium aluminate host lattice. Under the excitation of the electron beam, the phosphor can efficiently display a broad green emission centered at 490 nm, corresponding to the transition from the conduction band edge to the excited state of copper in the barium aluminate host. However, there are no data available on copper luminescence in barium aluminate. New results on 3d activators of copper emission in the barium aluminate host are reported in this article, thus extending the list of copper-activated phosphors. These results strongly indicate that the copper-activated barium aluminate is a potential material used as a new high-brightness green phosphor for ultraviolet light-emitting diode and display devices.     

The structural and magnetic properties of barium ferrite powders prepared by the solben gel method

In this paper, M-type hexagonal barium ferrite powders are synthesized using the sol-gel method. A dried precursor heated in air is analyzed in the temperature range from 50 to 1200 ℃ using thermo-gravimetric analysis and differential scanning calorimetry. The effects of the additives and the cacinating temperature on the magnetic properties are investigated, and the results show that single-phase barium ferrite powders can be formed. After heat-treating at 950 ℃ for 4h with 3 wt% additive, the coercivity and saturation magnetization are found to be 440 Oe and 57.9 emu/g, respectively.     

An effective quantum defect theory for the diamagnetic spectrum of barium Rydberg atom

A theoretical calculation is carried out for the spectrum of barium Rydberg atom in an external magnetic field. Using an effective approach incorporating quantum defect into the centrifugal term in the Hamiltonian, we reexamine the reported spectrum of barium Rydberg atom at a magnetic field of 2.89 T [J. Phys. B 28 L537 (1995)]. Our calculation employs B-spline basis expansion and complex coordinate rotation techniques. For single photon absorption from the ground 6s² to 6snp Rydberg states, the spectrum is not influenced by quantum defects of channels ns and nd. The calculation is in agreement with the experimental observation until the energy reaches E=-60 cm^-1. Up beyond in energy, closer to the threshold, the calculated and experimental results do not agree with each other, possible reasons for their discrepancies are discussed. Our study affirms an energy range where the diamagnetic spectrum of barium atom can be explained thoroughly using a hydrogen model potential.     

Texture and self-biased property of an oriented M-type barium ferrite thick film by tape casting

In this paper,the oriented M-type barium ferrite(BaM) thick films with different thicknesses are prepared by tape casting.It is found that the crystallographic alignment degree(f),the pore and the squareness ratio(Mr/Ms) are not affected by the thickness of the film.XRD and SEM results show that the thick film has hexagonal morphology with a crystal texture of c-axis grains perpendicular to film plane.The hysteresis curve indicates that the BaM thick film exhibits a self-biased property with a remanent magnetization of 3.30 T,a squareness ratio(Mr/Ms) of 0.81,and a coercivity of 0.40 T.The results show that the BaM thick film has potential for use in self-biasing microwave devices,and also proves that the tape casting technique is capable of fabricating high-quality barium ferrite films,thus providing a unique opportunity to realize the large area production of thick film.     

Study of the microstructural transformations of borate glass and barium metaborate crystals induced by femtosecond laser

This paper describes the microstructural transformations of borate glass and barium metaborate crystals induced by femtosecond laser. Such structural transformations were verified by Raman spectroscopy. The borate glass is transformed into low temperature (LT) phase of barium metaborate (BaB_2O_4) crystals after being irradiated for 10 min by a femtosecond laser. In addition, after 20 min of irradiation, high temperature (HT) phase of BaB_2O_4 crystals is also produced. Further studies demonstrate that LT phase BaB_2O_4 crystals are formed in the HT phase BaB_2O_4 crystals after femtosecond laser irradiation for 10 s.     

Changing emission of divalent samarium doped into barium octoborate as a function of firing time

Barium octoborate has been synthesized by air firing of co-precipitated borates with additional boric acid. During the firing process, samarium ions doped into the matrix are reduced to the divalent state. Two different divalent samarium emission spectra have been observed from the material as a function of the firing history, even though the structure, as identified by powder X-ray diffraction remained consistent. A minor barium pentaborate impurity, in conjunction with significant thermal variability in the strength of the divalent samarium emission generated by the different sites in the two borate materials, appears to give rise to this phenomenon.