Probing Nanoscale Morphology of PS/PMMA/CdS &PS/PVC/CdS Polymeric Nanocomposites through Small Angle X-Ray Scattering Analysis

Polymeric nanocomposites of PS/PMMA/CdS and PS/PVC/CdS samples have been synthesized through dispersion solution casting technique. The nanoparrticles of CdS were prepared by simple chemical method using CdCl2 and H2S gas produced from thiourea. The nanoscale morphology of the prepared polymeric nanocomposite samples is probed through small angle X-ray scattering (SAXS). The SAXS study reveals that CdS nanoparticles take place at voids position in the respective plymer blend matrix and exhibit their nano nature with very little tendency to agglomerates.

Stability of the Dividing Distribution Function Method for ParticleSize Distribution Analysis in Small Angle X－Ray Scattering

The Dividing Distribution Function (DDF) method is one of the methods by which the particle size distribution of ultrafine powder can be evaluated from its small angle X-ray scattering data. In this paper, the stability of the solution obtained from DDF method has been investigated through optimizing the coefficient matrix, introducing a damping factor and a least square treatment. All calculations were accomplished with a microcomputer. It was shown that the average deviations of the size distribution obtained are not larger than the assigned random errors to the scattering intensities as long as the corresponding requirements are satisfied.

A new package:MySAS for small angle scattering data analysis

In this paper,A MySAS package,which is verified on Windows XP,can easily convert two-dimensional data in small angle neutron and X-ray scattering analysis,operate individually and execute one particular operation as numerical data reduction or analysis,and graphical visualization.This MySAS package can implement the input and output routines via scanning certain properties,thus recalling completely sets of repetition input and selecting the input files.On starting from the two-dimensional files,the MySAS package can correct the anisotropic or isotropic data for physical interpretation and select the relevant pixels.Over 50 model functions are fitted by the POWELL code using x^2 as the figure of merit function.

Small Angle X-ray Scattering Study of Precipitation Kinetics in Al-Zn-Mg-Cu Alloys

The evolution of microstructure parameters （precipitate size and volume fraction） for two types of Al-Zn-Mg-Cu alloys （7075 and 7055） during aging has been studied by synchrotron-radiation small angle X-ray scattering （SAXS）.The results show that the precipitates are only a few nanorneters for both alloys ageing even at higher temperature of 160℃ for 72 h （4.44 and 5.82 nm, respectively）. The maximum of the precipitate volume fraction increases with in creasing Zn content and is about 0.023-0.028 and 0.052-0.054, respectively. The coarsening of precipitate is consistent with LSW （Lifshitz-Slyozov-Wagner） model even at the initial stage where volume fraction is still varying.The activation energy of coarsening regime has been determined to be about 1.22±0.02 eV and 1.25±0.02 eV for alloys 7075 and 7055, respectively.

Small-angle X-ray scattering investigation of aging behavior of Al-Cu-Mg-Ag alloys using synchrotron radiation

The aging behavior of Al-Cu-Mg-Ag alloys with high Cu/Mg was studied by transmission electron microscopy (TEM) and small-angle X-ray scattering (SAXS) using synchrotron radiation. TEM study reveals that the major strengthening phases of the alloy after aging at 160?C for 10 h are Ω and less θ′. SAXS study shows that the scattering patterns are composed of several concentric circles at the beginning of aging process, which is replaced by the butterfly-wings scattering patterns with the increase of aging time. The butterfly-wings scattering patterns are composed of several branches. The angles between the branches are roughly equal to that between the habit planes of precipitates. The evolution of Guinier radius with aging time indicates the good coarsening resistance of the precipitates. The evolution of integrated intensity is consistent with the classical two-step precipitation process.

Growth Kinetics of Nanocrystals and Nanorods by Employing Small-angle X-ray Scattering (SAXS) and Other Techniques

In this article, we report the results of our detailed investigations of the growth kinetics of zero-dimensional nanocrystals as well as one-dimensional nanorods by the combined use of small angel X-ray scattering （SAXS）, transmission electron microscopy （TEM） along with other physical techniques. The study includes growth kinetics of gold nanocrystals formed by the reduction of HAuCl4 by tetrakis（hydroxymethyl） phosphonium chloride in aqueous solution, of CdSe nanocrystals formed by the reaction of cadmium stearate and selenium under solvothermal conditions, and of ZnO nanorods formed by the reaction of zinc acetate with sodium hydroxide under solvothermal conditions in the absence and presence of capping agents. The growth of gold nanocrystals does not follow the diffusion-limited Ostwald ripening, and instead follows a Sigmoidal rate curve. The heat change associated with the growth determined by isothermal titration calorimetry is about 10 kcal·mol^-1 per I nm increase in the diameter of the nanocrystals. In the case of CdSe nanocrystals also, the growth mechanism deviates from diffusion-limited growth and follows a combined model containing both diffusion and surface reaction terms. Our study of the growth kinetics of uncapped and poly（vinyl pyrollidone） （PVP）-capped ZnO nanorods has yielded interesting insights. We observe small nanocrystals next to the ZnO nanorods after a lapse of time in addition to periodic focusing and defocusing of the width of the length distribution. These observations lend support to the diffusion-limited growth model for the growth of uncapped ZnO nanorods. Accordingly, the time dependence on the length of uncapped nanorods follows the L3 law as required for diffusion-limited Ostwald ripening. The PVP-capped nanorods, however, show a time dependence, which is best described by a combination of diffusion （L^3） and surface reaction （L^2） terms.

Small Angle X-ray Scattering Study of PS Conformation in Tetrahydrofuran Solvent with Gas Anti-solvent

Small angle X-ray scattering (SAXS) was used to study the effect of dissolved CO2 on the conformation of polystyrene (PS) in PS/tetrahydrofuran(THF) solution at 308.15 K and at pressures up to 3 MPa. The cloud pressure and the expansion curve of the solution were also determined. The dependence of the conformation on pressure was discussed.

Scanning Microfocus Small Angle X-ray Scattering Study of the Avian Eggshell

Synchrotron microfocus small angle X-ray scattering was used to investigate the nanostructure and microscopic variation of eggshells. It uses a microbeam allowing the ability to probe interactions between the organic and inorganic components at nanometer level and is ideal for mapping over small areas to obtain a detailed analysis of structural variations. Thin sections of eggshells were scanned from the shell membrane （inner） to the cuticle （outer） surface. The data collected was used to produce two-dimensional maps showing microscopic changes within the different layers of the eggshell. The structural alterations ap- parently could have implications at the macroscopic level of the resulting eggshell. As the organic matrix is embedded within the eggshell this may contribute to the variations observed in calcite crystal form and texture, Structural information obtained about a biomaterial at different length scales is important in relating the structure to its functional properties. This knowledge and the principles behind the formation of biomaterials could be used in the attempt of bioengineering new systems.

Characteristics of AOT Microemulsion Structure: a Small Angle X-ray Scattering Study

The method of synchrotron radiation small-angle X-ray scattering (SR-SAXS) has been used to obtain structural information on the system of bis (2-ethylhexyl) sulfosuccinate (AOT)/H2O/isooctane. By using the Guinier plot (Ln I (q) versus q(2)) on the data sets in a defined small q range (0.03-0.06 Angstrom (-1)), the gyration radius at different water/surfactant molar ratio, W-0, was obtained. With the increase of W-0, the gyration radius (R-g) increased at the range of 23.2 similar to 52.7 Angstrom.

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 devel- oping 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 lW2A 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.

DETERMINATION OF SIZE DISTRIBUTION OF THE CRYSTALLINE PARTICLE IN AGED METALLIC GLASS BY SMALL ANGLE X-RAY SCATTERING

Ⅰ. INTRODUCTIONAlthough many authors have investigated the structure of annealed metallic glass by means of small angle X-ray scattering (SAXS), there has been no report in which size distribution of the crystalline particle in aged metallic glass is determined. Determining size distribution of the crystalline particle will be beneficial to understanding the nucleation and growth process of the crystalline particle. In this note, size distribution of the crystalline parti-

DETERMINATION OF THE SHAPE AND DIMENSION OF PRECIPITATE FROM AGED Lc4 ALUMINIUM ALLOY BY SMALL ANGLE X-RAY SCATTERING

Small angle X-ray scattering (SAXS) is extensively used for determining the dimension of a particle, but rarely used for determining its shape. The difficulty is that it needs to do extensive calculations. In addition, it can only be carried out for the mono-dispersion system. In re cent years, Reuther et al. succeeded in determining the shape and dimension of the particle of a polymer gel.

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

The nanopore structures in precursors Four carbon-fiber precursors are prepared. They are crucial to the performance of PAN-based carbon fibers 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.

Nano-scale pore distribution characterisation of coal using small angle X-ray scattering

In the process of coal seam fracturing with liquid nitrogen(LN_(2)),the change of coal pore structure has an important influence on the efficiency of coalbed methane(CBM)extraction.The nano-scale pore size distribution(PSD)in coal particles before and after freezing with LN_(2) are experimentally studied in this work.Coal samples are collected from four coal mines,where coal and gas outburst accidents have occurred.Small angle X-ray scattering technology(SAXS)and scanning electron microscopy(SEM)are used to study the pore structure changes of coal samples quantitatively and qualitatively.It is found that the scattering intensity of coal samples increases after freezing.The PSD of all samples significantly changes in the range of 0.8–7 nm,showing new pore spaces in 0.8–4 nm and fewer pores in the 4–7 nm range.Both the pore fractal dimension and the radius of gyration of coal samples increase after freezing and are mainly affected by the changes in pores and the anisotropy of the coal matrix.Crack expansion and pore connections are observed in the surface structure of the coal sample using SEM.This study provides a better understanding of the nano-scale mechanism of coal seam fracturing with LN_(2) for the prevention of coal and gas outbursts.

Influence of energy bandwidth of pink beam on small angle X-ray scattering

Background Compared with the traditional monochromatic synchrotron radiation beam,a pink beam is a quasimonochromatic beam which can be obtained by screening a harmonic of the undulator.The energy bandwidth(E/E)of a pink beam is about 10−2.Despite the intensity gain from the quasi-monochromatic beam,the decrease in the energy resolution will lead the collected data to be smeared.Purpose To study the influence of the energy bandwidth on the small angle X-ray scattering(SAXS)by experiments and verify the feasibility of SAXS with a pink beam.Method Firstly,the influence of different energy bandwidths on SAXS has been studied by simulation and experiment.Then,TEM tests have been performed and compared with the experimental results.Result It has been shown that the scattering curves deviate slightly from the traditional monochromatic ones.This deviation does not influence the data processing for the maximum deviation of the results is just less than 2%.In return,the gain in the intensity(one to two orders of magnitude)makes the pink beam very important for the time-resolved SAXS.Further,the results of TEM and SAXS have shown an excellent agreement.Conclusion Thiswork proves that the pink beam could be used for SAXS directly without a desmearing procedure.Benefiting from the increase in the beam intensity,the exposure time can be greatly shortened,thus enhancing the utilization efficiency of the synchrotron radiation.

Monodisperse hollow silica spheres： An in-depth scattering analysis

Herein, we fabricate hollow silica nanoparticles with exceptionally narrow size distributions that inherently possess two distinct length scales-tens of nanometers with regards to the shell thickness, and hundreds of nanometers in regards to the total diameter. We characterize these structures using dynamic and static light scattering （DLS and SLS）, small angle X-ray scattering （SAXS）, and transmission electron microscopy （TEM）, and we demonstrate quantitative agreement among all methods. The ratio between the radius of gyration （SLS） and hydrodynamic radius （DLS） in these particles equals almost unity, corresponding to ideal capsule behavior. We are able to resolve up to 20 diffraction orders of the hollow sphere form factor in SAXS, indicating a narrow size distribution. Data from light and X-ray scattering can be combined to a master curve covering a q-range of four orders of magnitude assessing all hierarchical length scales of the form factor. The measured SLS intensity profiles noticeably change when the scattering contrast between the interior and exterior is altered, whereas the SAXS intensity profiles do not show any significant change. Tight control of the aforementioned length scales in one simple and robust colloidal building block renders these particles suitable as future calibration standards.

新型Ni-Cr-Co基高温合金长期时效后的相分析

采用物理化学相分析技术研究了一种新型Ni Cr Co基高温合金长期时效后的析出相γ′(+η),M23C6,MC和M6C(+μ)的相组成,分析了时效温度和时效时间对析出相含量的影响,并用X射线小角散射(SAXS)分析了γ′(+η)相在不同粒度间隔的质量分布。

小角光散射在线系统研究多相聚合物双螺杆挤出过程中的相尺寸——非相容PE/PA1010体系

利用可视化双螺杆挤出机———光散射在线采集与分析系统对不相容聚合物体系聚乙烯 尼龙 10 10(PE PA10 10 )双螺杆挤出过程进行了在线分析 .相尺寸由Debye理论中的相关距离ac,平均弦长L ,以及分散相平均直径D描述 ,给出了几种参数表征适用的范围 .由在线光散射计算出的平均弦长Lscatt、分散相平均粒径Dscatt与电镜照片计算出的平均弦长LSEM 、分散相平均粒径DSEM 作了比较 ,两者比较符合 .结果表明 ,分散相颗粒尺寸沿螺杆挤出方向逐渐变小 ;随着低组分含量 (PA10 10≤ 5 0 % )的增加 ,分散相颗粒尺寸变大 ,在组成比为 70 30和 6 0 4

纳米粒子粒径评估及测试方法的比较

本文介绍了透射电镜综合分析—分散法测定纳米粒子粒径的方法,并将此法与X射线小角散射法及透射电镜暗场法测粒径进行了实验与分析的比较。认为采用X射线小角散射法与透射电镜综合分析—分散法相结合测定评估纳米粒子粒径可以以较快的速度得到准确的结果、综合的信息。

中子小角散射谱仪Q分辨率计算和对形状因子影响分析

介绍了中子小角散射谱仪分辨率函数及其相关的Q标准差计算方法,分析了Q标准差有关谱仪的几何布局、中子的波长弥散对其的影响。介绍了一维Q分辨高斯函数计算方法。结合两个具体谱仪布局和一个理想实心球体的形状因子曲线,卷积得到了不同谱仪布局下形状因子的弥散曲线,对精确分析中子小角散射数据,应结合使用谱仪分辨率函数。