共查询到12条相似文献,搜索用时 46 毫秒
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Self-assembly behaviour of amphiphilic diblock copolymer in selective solvents studied by synchrotron small-angle x-ray scattering 下载免费PDF全文
The aggregation behaviour of styrene-vinyl benzoic acid (PSm-b-PVBAn) amphiphilic diblock copolymers in selective solvents with different m and n was investigated by synchrotron small-angle x-ray scattering (SAXS). We have carried out a detailed analysis of scattering intensity, dimension, shape and microstructure of the diblock copolymers of narrow distribution in water, methanol, ethanol and isopropanol selective solvents, respectively. We have found that the aggregation behaviour of the copolymer depends on the nature of the solvent and the micelle forms fiat disc objects with the ratio of radius ω=0.4. The average radius gyration Rg of the copolymer decreases as solvents change from isopropanol to ethanol and to methanol, and increases with increasing pH in aqueous solution, but decreases with the addition of COCl2 in ethanol solvent. The scattering intensity of diblock copolymer micelle follows I(h) ∝ h^-α in different selective solutions, suggesting that the PSm-b-PVBAn coils have self-similar structure behaviour or a fractal structure in the selective solvents. All of these revealed that the aggregation behaviour of the diblock copolymer changes dramatically with experimental condition in the selective solvent. The increase of mass fractal dimension (Dm) from 2.12 to 2.47 indicates that the copolymer chain changes from a swollen coil to a rather compact disc in the course of changing solvents, decreasing surface fractal dimension (Ds) from 2.98 to 2.58 indicates that the copolymer micelle change from a rather rough surface to a smooth form in the course of increasing pH in aqueous solutions, and increasing Dm and Ds from 2.29 to 2.35 and 2.70 to 2.90, respectively, indicates the shrinkage of copolymer micelle to a rather compact and rough disc form by adding COCl2 in ethanol solvents. 相似文献
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The small-angle x-ray scattering (SAXS) resulting from a non-ideal two-phase system having sharply defined phase boundaries but with micro-fluctuations of electron density within any phase shows a positive deviation from Debye's theory. We have found a simple method suitable for fitting the slit-smeared SAXS data and correcting the positive deviation. The validity of this procedure is tested on porous ZrO_2 xerogel prepared using the sol-gel process. 相似文献
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In-situ study of precipitates in Al–Zn–Mg–Cu alloys using anomalous small-angle x-ray scattering 下载免费PDF全文
In the present work,the precipitate compositions and precipitate amounts of these elements(including the size distribution,volume fraction,and inter-precipitate distance) on the Cu-containing 7000 series aluminum alloys(7150 and 7085 Al alloys),are investigated by anomalous small-angle x-ray scattering(ASAXS) at various energies.The scattering intensity of 7150 alloy with T6 aging treatment decreases as the incident x-ray energy approaches the Zn absorption edge from the lower energy side,while scattering intensity does not show a noticeable energy dependence near the Cu absorption edge.Similar results are observed in the 7085 alloy in an aging process(120℃) by employing in-situ ASAXS measurements,indicating that the precipitate compositions should include Zn element and should not be strongly related to Cu element at the early stage after 10 min.In the aging process,the precipitate particles with an initial average size of ~ 8 ?A increase with aging time at an energy of 9.60 ke V,while the increase with a slower rate is observed at an energy of 9.65 ke V as near the Zn absorption edge. 相似文献
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Investigation of the topological shape of bovine serum albumin in solution by small-angle x-ray scattering at Beijing synchrotron radiation facility 下载免费PDF全文
This paper reports that at a newly constructed small-angle x-ray scattering station of Beijing Synchrotron Radia- tion Facility, the topological shape of ligand-free bovine serum albumin in solution has been investigated. An appropriate scattering curve is obtained and the calculated value of the gyration radius is 31.2~=t=0.25 ~_ (11=0.1 nm) which is co- incident with other ones' results. It finds that the low-resolution structure models obtained by making use of ab initio reconstruction methods are fitting the crystal structure of human serum albumin very well. All of these results perform the potential of the beamline to apply to structural biology studies. The characteristics, the defects, and the improving measures of the station in future are also discussed. 相似文献
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采用x射线小角散射(SAXS)技术研究了由射频等离子体增强化学气相沉积(rf-PECVD)、 热丝化学气相沉积(HWCVD)和等离子体助热丝化学气相沉积(PE-HWCVD)技术制备的微晶硅( μc-Si:H)薄膜的微结构.实验发现,在相同晶态比的情况下,PECVD沉积的μc-Si:H薄膜微 空洞体积比小,结构较致密,HWCVD沉积的μ-Si:H薄膜微空洞体积比大,结构较为疏松,PE -HWCVD沉积的μc-Si:H薄膜,由于等离子体的敲打作用,与HWCVD样品相比,微结构得到明 显改善.采用HWCVD二步法和PE-HWCVD加适量Ar离子分别沉积μc-Si:H薄膜,实验表明,微结 构参数得到了进一步改善.45°倾角的SAXS测量显示,不同方法制备的μc-Si:H薄膜中微空 洞分布都呈各向异性.红外光谱测量也证实了SAXS的结果.
关键词:
微晶硅薄膜
微结构
微空洞
x射线小角散射 相似文献
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采用小角X射线散射(SAXS)方法对Ti-Mo合金氢化物的微观缺陷进行了研究.结果表明,氢化物样品中Mo含量为5at%时,所测定的SAXS强度在高散射角区明显低于其他样品的SAXS强度.氢化物中的晶粒及其内部的亚结构是引起SAXS现象的散射体,而这些亚结构是由合金氢化时引入的大量位错所产生.Mo 含量为5at%合金主要为hcp结构而其他合金为bcc结构,但两种合金氢化后都成为fcc结构的氢化物.据此,认为hcp结构与bcc结构Ti-Mo合金在氢化时氢化物结构相同但引入的位错缺陷特征不同.
关键词:
Ti-Mo合金氢化物
小角X射线散射
微观缺陷 相似文献
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Morten Ring Eskildsen 《Frontiers of Physics》2011,6(4):398-409
Here we review recent small-angle scattering studies of the vortex lattice in a range of type-II superconductors carried out by our group. Emphasis is placed on providing examples of the kind of information which can be obtained by such measurements, focusing in particular on studies of the vortex lattice structure and form factor in LuNi2B2C, TmNi2B2C, CeCoIn5 and Ba(Fe0.93Co0.07)2As2. 相似文献
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应用中子小角散射技术研究了水溶液中富勒烯-PVP聚合物的链团结构及其大小以及它们在不 同富勒烯含量下的变化.结果表明:当加入富勒烯后,不论是PVP单体分子链还是大分子链团 ,其相关长度与纯PVP溶液相比均变小,且大分子链团的变化更为明显;在不同富勒烯含量 情况下,高富勒烯含量的富勒烯-PVP分子链团的体积更小.
关键词:
中子小角散射
富勒烯
PVP聚合物 相似文献
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T. Striffler U. Stuhr H. Wipf H. Hahn S. Egelhaaf 《The European Physical Journal B - Condensed Matter and Complex Systems》2000,17(2):245-251
By means of small-angle neutron scattering the microstructure of two nanocrystalline Pd samples (prepared by inert gas condensation)
has been studied at room temperature in a Q-range from [0pt] to [0pt] . An additional subsequent doping of the two samples with H as well as with D (concentrations < 4 at%) caused contrast variations
that provided more detailed structural information. The measured scattering intensity was modeled by a Porod contribution
from large heterogenities (e.g. pores) and a contribution from spherical grains with a log-normal distribution of their radii. To account for the presence
of grain boundaries, the grains were considered to be surrounded by a shell with a reduced Pd density and a thickness half
as large as the thickness of the grain boundaries. For the above model, the data of the H-doped, D-doped and undoped sample
were simultaneously fitted with one single set of adjustable parameters. The fits yielded for the two samples volume-weighted
mean grain radii of 10 nm and 13 nm. The values for the grain boundary thickness lie between 0.2 and 0.8 nm. Almost all of
the H- and D-atoms are, at low hydrogen concentrations, located in the grain boundaries.
Received 1 May 2000 相似文献