Small angle X-ray scattering of the colloidal crystal

The monodisperse polystyrene spheres are assembled into the colloidal crystal on the glass substrate by vertical deposition method, which is aimed at the so-called photonic crystal applications. The structural information of the bulk colloidal crystal is crucial for understanding the crystal growth mechanism and developing the various applications of colloidal crystal. Small-angle X-ray scattering (SAXS) technique was used to obtain the bulk structure of the colloidal crystal at Beamline 1W2A of BSRF. It is found that the SAXS pattern is sensitive to the relative orientation between the colloidal sample and the incident X-ray direction. The crystal lattice was well distinguished and determined by the SAXS data.     

蠕变镍基单晶高温合金微观结构与界面特征的X射线小角散射研究

利用SAXS技术对蠕变过程中不同尺度范围的微观结构变化分析表明X射线小角散射(SAXS)与中子小角散射(SANS)测量的二维散射图具有明显的差异,由散射强度曲线的变化说明了蠕变过程中二次析出γ'相形貌和不同区域尺寸特征的改变情况.分析结果表明二次析出γ'相存在两类特征尺寸,在蠕变过程中沿[100]或[010]方向的变化趋势类似,均是在第一和第二阶段有所减小,在第三阶段又有所增大,相较而言,特征尺寸较大的γ'相变化也较为显著.二次析出γ'相在蠕变第二阶段元素扩散最严重,相表面最粗糙,在第三阶段两相界面又进一 关键词： 单晶高温合金 二次析出γ'相 X射线小角散射 微观结构     

Small angle neutron scattering and small angle X-ray scattering studies of platinum-loaded carbon foams

The morphology of carbon nanofoam samples comprising platinum nanoparticles dispersed in the matrix was characterized by small angle neutron scattering (SANS) and small angle X-ray scattering (SAXS) techniques. Results show that the structure of pores of carbon matrix exhibits a mass (pore) fractal nature and the average radius of the platinum particles is about 2.5 nm. The fractal dimension as well as the size distribution parameters of platinum particles varies markedly with the platinum content and annealing temperature. Transmission electron micrographs of the samples corroborate the SANS and SAXS results.      

A colloidal crystal double-heterostructure fabricated with the angle controlled inclined deposition method

A self-assembly method, named the angle controlled inclined deposition method, is developed for fabricating well-ordered silica and polystyrene colloidal crystals. A high-quality colloidal crystal with a flat and uniform surface over a large area can be produced rapidly using a minute quantity of suspension and without any additional equipment. By controlling the inclined angle, we can fabricate colloidal crystals with diverse numbers of layers. A colloidal crystal double-heterostructure (composed of three different colloidal photonic crystals) can be rapidly fabricated with this method. Both experimental and simulation results show that the photonic band gap of the double-heterostructure is not a simple superposition of that of the compositional colloidal crystals along the stacking direction.     

Pt/C催化剂中纳米Pt颗粒团聚效应的小角X射线散射

应用小角X射线散射(SAXS)技术,对乙二醇合成法、浸渍还原法和微波加热法制备的Pt/C催化剂粉体内纳米Pt颗粒的团聚效应进行了研究,得到了不同方法制备的Pt颗粒及其团聚体的特征尺寸、体积分布、表面积变化、团聚程度等信息,并利用透射电镜（TEM）对3种样品进行了测试。实验结果表明:微波加热法制备的催化剂中,Pt颗粒较好地分散于C载体上,且Pt颗粒具有尺度小、分布范围窄、总表面积大和团聚体较少等特征;常规浸渍和乙二醇还原两种方法制备的催化剂中Pt颗粒大小分布相似,但乙二醇还原法制备的催化剂总表面积和团聚体尺度更大,数量也更多。     

Cu60Zr30Ti10非晶合金弛豫和晶化过程的小角X射线散射研究

应用小角X射线散射技术研究了Cu₆₀Zr₃₀Ti₁₀非晶合金从300到813 K之间微结构的演化情况.发现在淬火状态下Cu₆₀Zr₃₀Ti₁₀非晶合金中存在直径30 nm左右的富Cu区.非晶的结构弛豫包括573 K之前的低温结构弛豫和573 K到玻璃转变温度的高温结构弛豫，弛豫的结果是产生含有有序原子团簇的富Cu区，这些有序原子团簇的富Cu区是随后晶化过程中晶核产生的基础.Porod曲线分析表明，晶化生成的纳米体心立方CuZr相和基体之间有明锐的界面. 关键词： 小角X射线散射 非晶合金 结构弛豫 晶化     

Influence of colloidal particle transfer on the quality of self-assembling colloidal photonic crystal under confined condition

The relationship between colloidal particle transfer and the quality of colloidal photonic crystal(CPC) is investigated by comparing colloidal particle self-assembling under the vertical channel(VC) and horizontal channel(HC) conditions.Both the theoretical analyses and the experimental measurements indicate that crystal quality depends on the stability of mass transfer.For the VC,colloidal particle transfer takes place in a stable laminar flow,which is conducive to forming high-quality crystal.In contrast,it happens in an unstable turbulent flow for the HC.Crystals with cracks and an uneven surface formed under the HC condition can be seen from the images of a field emission scanning electron microscope(SEM) and a three-dimensional(3D) laser scanning microscope(LSM),respectively.     

Characterization of the nanopore structures of PAN-based carbon fiber precursors by small angle X-ray scattering

The nanopore structures in precursors are crucial to the performance of PAN-based carbon fibers. Four carbon-fiber precursors are prepared. They are bath-fed filaments (A), water-washing filaments (B), hot-stretching filaments (C) and drying-densification filaments (D). Synchrotron radiation small angle X-ray scattering is used to probe and compare the nanopore structures of the four fibers. The nanopore size, discrete volume distribution, nanopore orientation degree along the fiber axis and the porosity are obtained. The results demonstrate that the nanopores are mainly formed in the water-washing stage. During the processes of the subsequent production technologies, the slenderness ratio of nanopores and their orientation degree along the fiber axis increase further and simultaneously, the porosity decreases. These results are helpful for improving the performance of the final carbon fibers.     

小角X射线散射表征非晶合金纳米尺度结构非均匀

表征纳米尺度结构非均匀对于理解非晶合金的变形、弛豫等动力学行为至关重要.受时空尺度限制,非晶合金纳米尺度结构非均匀的实验表征具有很大的挑战性.本文针对一种典型的锆基非晶合金,开展了同步辐射小角X射线散射原位拉伸实验.通过对散射曲线的定量分析,揭示了非晶合金在纳米尺度的非均匀结构图像.首先,Porod散射曲线呈现正偏离行为,表明非晶合金属于非理想两相散射体系,两相界面弥散且任一相内都存在电子密度涨落.基于散射曲线的Guinier定律分析,进一步揭示非晶合金中散射体形状远偏离球形,其特征尺度主要分布在0.8—1.6 nm之间,且在弹性变形阶段几乎不变.最后,通过Debye相关函数分析,发现这些纳米尺度散射体仅在1 nm之内存在强关联,符合非晶合金短程有序、长程无序的结构特征.研究结果表明非晶合金中存在具有复杂空间分布的纳米尺度非均匀结构.     

一种胶体光子晶体修饰的光纤

设计了一种胶体光子晶体修饰的光纤. 采用恒温快速蒸发法直接在经切割刀处理后的光纤端面生长胶体晶体,再与另一根切割后的光纤在毛细玻璃管中完成对接,制备成胶体光子晶体修饰的光纤. 用扫描电子显微镜和光谱分析仪对样品的形貌、结构以及光学特性进行分析. 实验结果表明,粒径为640 nm、体积分数约为0.5%的SiO₂胶体微球溶液在60 ℃的情况下沉积,大约12 h后可得到质量较高的胶体光子晶体. 在SEM下,观察到端面的胶体晶体为面心立方(fcc)结构. 透射光谱证明,该结构在(111)面上     

用小角X射线散射研究纳米粒子的粒度分布

采用小角X射线散射中的对数高斯分布函数的方法，确定了纳米粒子的粒度分布。通过理论分析、计算，对氧化锌纳粒子进行实验测试。结果表明，氧化锌纳米粒子的平均半径尺寸为3．34nm，分布的标准偏差为1．35。     

Small angle neutron scattering study of temperature-independent formulation of mixed micellar structures

SANS measurements have been performed on mixed systems of ionic surfactant sodium dodecyl sulphate (SDS) and nonionic surfactant polyoxyethylene 10 lauryl ether (C12E10). The total concentration of the mixed system was kept fixed (10 wt%) and the ionic to nonionic surfactant ratio varied in the range 0 to 1. The temperature effect on the structures of mixed micelles has been studied for temperatures between 30 and 75°C. Micelles of pure ionic and nonionic surfactants show opposite trends when the temperature is increased. Sizes of pure ionic micelles decrease and those of nonionic micelles increase with increase in temperature. We show a formulation balancing these two effects which is temperature-independent and consists of about 25% of ionic surfactants in the mixed system. Contrast variation SANS measurements by contrast matching one of the surfactant components to the solvent suggest homogeneous single mixed micelles of the two components in the mixed systems.      

Small angle neutron scattering study of mixed micelles of oppositely charged surfactants

Structures of mixed micelles of oppositely charged surfactants dodecyltrimethylammonium bromide (DTAB) and sodium dodecyl sulphate (SDS) have been studied using small angle neutron scattering. The concentration of one of the components was kept fixed (0.3 M) and that of another varied in the range 0 to 0.1 M. The aggregation number and micellar size increase and fractional charge decreases dramatically with the addition of small amount of oppositely charged surfactant. The effect of addition of SDS on DTAB is significantly different from that of the addition of DTAB on SDS. The contrast variation SANS experiments using deuterated surfactant suggests the homogeneous mixing of two components in mixed micellar system.      

PS_(3000)-b-PAA_(5000)球形胶束温度效应的原位小角X射线散射技术研究

应用小角X射线散射技术(SAXS)对两亲嵌段共聚物聚苯乙烯聚丙烯酸(PS-b-PAA)胶束形貌的温度影响进行了原位表征.SAXS结果表明:随着水含量的增加,粒子尺寸相应增加;对于水含量10%的PS_(3000)-b-PAA_(5000)胶束溶液,发现了明显的SAXS双峰现象;双峰的位置不随着温度的变化而改变,但是peak 1和peak 2的相对强度随着温度发生了减弱和增强的交错变化;相邻的SAXS双峰说明在PS_(3000)-b-PAA_(5000)胶束溶液中最初形成的粒子尺寸并不是均匀的,主要分为尺寸极其相近的两种球形粒子;随着温度的升高,粒径大小不同的两种粒子存在着一种消融和生长的过程,并且保持着一个相同的归一化动态平衡速率.     

通讯波段禁带胶体光子晶体的制备及实验参数研究

采用直径为700nm的二氧化硅微球,通过垂直沉积法在玻璃基片上制备了位于光通讯波段的禁带胶体光子晶体。研究了不同蒸发温度、湿度条件、干燥过程对样品晶体质量的影响。用扫描电子显微镜(SEM)对其形貌进行了观测。实验结果表明,在温度为65℃,相对湿度为70%,缓慢干燥条件下制备出的样品具有较好的晶体质量,晶体在大范围内保持了面心立方(FCC)单晶结构,其(111)面平行于生长基片。     

Al-Zn-Mg-Cu-Li合金时效过程微结构演化的小角x射线散射研究

应用小角x射线散射技术分析了Al-Zn-Mg-Cu-Li合金在130，150和160℃温度时效24 h析出粒子的微结构参数的变化情况. 粒子的半径随着时效温度的增高而增加，它的比内表面积和体积百分数随着时效温度的增高而减小. 对Porod曲线q³J(q)-q²的分析表明,析出粒子与基体之间有明显的界面. 关键词： 小角x射线散射 Al-Zn-Mg-Cu-Li合金 时效 析出粒子     

大鼠骨质疏松模型的小角x射线散射研究

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Small angle neutron scattering studies on protein denaturation induced by different methods

Small angle neutron scattering (SANS) has been used to study conformational changes in protein bovine serum albumin (BSA) as induced by varying temperature and in the presence of protein denaturating agents urea and surfactant. BSA has prolate ellipsoidal shape and is found to be stable up to 60°C above which it denaturates and subsequently leads to aggregation. The protein solution exhibits a fractal structure at temperatures above 64°C, with fractal dimension increasing with temperature. BSA protein is found to unfold in the presence of urea at concentrations greater than 4 M and acquires a random coil Gaussian chain conformation. The conformation of the unfolded protein in the presence of surfactant has been determined directly using contrast variation SANS measurements by contrast matching surfactant molecules. The protein acquires a random coil Gaussian conformation on unfolding with its radius of gyration increasing with increase in surfactant concentration      

Al-Zn-Mg-Cu合金时效过程的小角度x射线散射研究

通过同步辐射小角度x射线散射方法（SAXS），研究了三种Al_Zn_ Mg_Cu合金沉淀析出过程显微结构参数（析出相尺寸和体积分数），随时效温度和时效时间 的演化，同时分析了Zn含量对合金沉淀析出过程的影响.结果表明，三种合金（A，B，C） 在实验条件下析出相均属于纳米尺度，析出相的最大体积分数随Zn含量的增加而增加，最大体积分数分别为0.023—0.028，0.052—0.054和0.04.在一定时效温度下，体积分数随时效时间的变化规律，符合析出相的形核、核长大和粗化动力学过程.  关键词： 小角度x射线散射 Al_Zn_Mg_Cu合金 时效 析出相尺寸 析出相体积分数     

基于光纤的三维可调胶体光子晶体

用改进的垂直沉积法在光纤端面制备了高质量的SiO₂胶体光子晶体,经过烧结、固化构成胶体光子晶体-光纤结构. 用扫描电子显微镜确定了样品为面心立方密排结构,其密排面平行于光纤基底表面. 利用全光纤传感网络测试了该胶体光子晶体,反射峰中心位于845 nm处,与Bragg理论计算值符合很好. 将该样品浸入不同折射率的液体中,反射光谱的峰值位置随着液体折射率的改变而发生偏移,近似呈线性关系,实现了峰位可调. 对于不同浓度引起的液体折射率的变化,基于光纤的胶体光子晶体结构也能够很好地分辨出来. 关键词： 可调胶体光子晶体 2微球')" href="#">SiO₂微球 Bragg反射 光纤