激光重熔高速电弧喷涂FeNiCrAl涂层的组织与断裂韧性

采用激光技术对高速电弧喷涂FeNiCrAl涂层进行重熔处理.分析了重熔前后涂层的组织结构、物相成分、显微硬度与断裂韧性.结果表明:重熔后,喷涂层片层状堆叠结构与孔隙得到消除,组织结构变得均匀、致密,涂层与基体由机械结合变为冶金结合.喷涂层物相主要有α-Fe及金属间化合物AlFe₃,AlFe和Al_0.4Fe_0.6,重熔后,生成了新相Fe-Cr,［Fe, Ni］固溶体和碳化物NiC_○x.重熔后涂层的平均显微硬度为7.79GPa,约为基体硬度(2.5GPa)的3倍,约为喷涂层硬度(6.0GPa)的1.3倍.载荷为4.9,9.8N时,喷涂层的压痕尖头出现裂纹,涂层平均断裂韧性为1.20MPa·m^1/2,载荷为2.94~9.8N时,重熔后涂层的压痕尖头均没有观察到裂纹.     

Lattice orientation within stirring-induced crystals of polyethylene

Micro-shish-kebab stirring-induced polyethylene crystals, as defined and described in the preceding paper, are flat, ribbon-shaped fibers. Selected area electron-diffraction techniques were used to determine the orientation of the crystal axes with respect to the external fiber shape. It has been shown that in addition to the crystal-lographic c-axis laying along the fiber direction, the normal to the ribbon plane is parallel to the crystallographic a-axis.     

Stroboscopic microscopy—direct imaging of structure development and phase separation during spin‐coating

Spin‐coated polymer blends possess a rich variety of accessible non‐equilibrium morphologies, formed through a process of phase separation and self‐assembly, the complexities of which remain incompletely understood. The technique of stroboscopic microscopy has now been developed to allow direct observations of microscopic and mesoscopic morphological development during spin‐coating and has afforded unequivocal information regarding morphological development. The technique so far has three modes of operation providing information on topographical, compositional, and crystal development. In this review, we look at the technique's development, its applications and comment on the future potential for this technique. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 17–25     

Limit theorems for the pre-averaged Hayashi–Yoshida estimator with random sampling

We will focus on estimating the integrated covariance of two diffusion processes observed in a nonsynchronous manner. The observation data is contaminated by some noise, which possibly depends on the time and the latent diffusion processes, while the sampling times also possibly depend on the observed processes. In a high-frequency setting, we consider a modified version of the pre-averaged Hayashi–Yoshida estimator, and we show that such a kind of estimator has the consistency and the asymptotic mixed normality, and attains the optimal rate of convergence.     

简单方法制备与表征新颖复合凝胶及表面微结构——由科研成果转化的化学综合实验

材料表面的微结构会赋予材料独特的性能，水凝胶在生物医学领域有广泛的应用前景。采用紫外光刻蚀法创新性地实现了复合凝胶的制备和凝胶表面图案化微结构的构筑一步完成；通过原子力显微镜和光学显微镜的表征，复合凝胶聚N-异丙基丙烯酰胺/聚乙二醇二丙烯酸酯兼具了温敏性能与图案化微结构的新颖性能结构特征。本实验有助于培养学生的创新意识，激发学生的学习兴趣以及未来从事科研的兴趣。     

Analysis of polished polycrystalline diamond using dual beam focused ion beam microscopy

This paper presents a study on polycrystalline diamond (PCD) polished by dynamic friction polishing (DFP) with the aid of advanced dual beam FIB (focused ion beam) microscopy. After disclosing a variety of wear tracks by DFP using electron imaging in combination with the ion channelling effect, a dual beam FIB was successfully employed at wear track sites to specifically create both the large cross-sectional specimen for microanalysis and thin foil for nanoanalysis. The study concluded that the polished PCD subsurface was free from microscale cracking. However, the attached debris layer on the top surface contained metal oxides and non-diamond carbon phase with inhomogeneous distributions of C, Fe, Cr, Ni, Si and O across the layer. An attached layer directly above a diamond grain was composed of essentially amorphous carbon, suggesting that a direct phase transformation from diamond crystalline to amorphous occurred during DFP.     

Living anionic polymerization of (E)‐1,3‐pentadiene and (Z)‐1,3‐pentadiene isomers

The anionic polymerization of (E)‐1,3‐pentadiene (EP) and (Z)‐1,3‐pentadiene (ZP) together with mixture of the E/Z isomers are investigated, respectively. The kinetic analysis shows that the activation energy for EP (86.17 kJ/mol) is much higher than that for ZP (59.03 kJ/mol). GPC shows that it is the EP rather than the ZP isomer that undergoes anionic living polymerization affording quantitative products of the polymers with well‐controlled molecular weights and narrow molecular weight distributions (1.05 ≤? ≤ 1.09). In addition, THF as polar additive has proved its validity to reduce the molecular weight distribution of poly(ZP) from 1.38 to as low as 1.19. The microstructure and sequence distributions of polypentadiene are characterized by ¹H NMR and quantitative ¹³C NMR. Finally, the distinctive reaction activity of two isomers can be elucidated by two different mechanisms which involve the presence of four forms of zwitterions for EP and the typical [1,5]‐sigmatropic hydrogen‐shift phenomenon for ZP. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54, 2291–2301     

Characterizing polymer macrostructures by identifying and locating microstructures along their chains with the kerr effect

In this brief report, we demonstrate that Kerr effect measurements, which determine the excess birefringence contributed by polymer solutes in dilute solutions observed under a strong electric field, are highly sensitive to and capable of determining their microstructures, as well as their locations along the macromolecular backbone. Specifically, using atactic triblock copolymers with the same overall composition of styrene (S) and p-bromostyrene (pBrS) units, but with two different block arrangements, that is, pBrS₉₀-b-S₁₂₀-b-pBrS₉₀ (I) and S₆₀-b-pBrS₁₈₀-b-S₆₀ (II), which are indistinguishable by NMR, we detected a dramatic difference in their molar Kerr constants (_mK), in agreement with those previously estimated. Although similar in magnitude, their Kerr constants differ in sign, with _mK(II) positive and _mK(I) negative. In addition, S/pBrS random and gradient copolymers synthesized by reversible addition-fragmentation chain-transfer (RAFT) polymerization exhibit a heretofore unexpected enhanced enchainment of racemic (r) pBrS-pBrS diads. Comparison of their observed and calculated _mKs suggests that the gradient S/pBrS copolymers possess an unanticipated additional gradient in stereosequence that parallels their comonomer gradient, that is, as the concentration of pBrs units decreases from one end of the copolymer chain to the other, so does the content of r diads. This conclusion could only be reached by comparison of observed and calculated Kerr effects, which access the global properties of macromolecules, and not NMR, which is only sensitive to local polymer structural environments, but not to their locations on the copolymer chains. Molar Kerr constants are characteristic of entire polymer chains and are highly sensitive to their constituent microstructures and their distribution along the chain. They may be used to both identify constituent microstructures and locate them along the polymer chain, thereby enabling, for the first time, characterization of their complete macrostructures. © 2013 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys, 2013     

RAFT polymerization of alternating styrene‐pentafluorostyrene copolymers

Reversible addition‐fragmentation chain‐transfer (RAFT) polymerization was used to control the alternating copolymerization of styrene and 2,3,4,5,6‐pentaflurostyrene. The RAFT polymerization yields a high degree of control over the molecular weight of the polymers and does not significantly influence the reactivity ratios of the monomers. The controlled free‐radical polymerization could be initiated using AIBN at elevated temperatures or using a redox couple (benzoyl peroxide/N,N‐dimethylaniline) at room temperature, while maintaining control over molecular weight and dispersity. The influence of temperature and solvent on the molecular weight distribution and reactivity ratios were investigated. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 1555–1559     

Development of liquid-nitrogen-cooling friction stir spot welding for AZ31 magnesium alloy joints

A liquid-nitrogen-cooling friction stir spot welding (C-FSSW) technology was developed for welding AZ31 magnesium alloy sheets. The liquid-nitrogen cooling degraded the deformability of the welded materials such that the width of interfacial cracks increased with increasing cooling time. The grain size of the stirred zone (SZ) and the heat-affected zone (HAZ) of the C-FSSW-welded joints decreased, whereas that of the thermomechanically affected zone (TMAZ) increased with increasing cooling time. The maximum tensile shear load of the C-FSSW-welded joints welded with a cooling time of 5 or 7 s was larger than that of the friction stir spot welding (FSSW)-welded joint, and the tensile shear load decreased with increasing cooling time. The microhardness of the C-FSSW-welded joints was greater than that of the FSSW-welded joint. Moreover, the microhardness of the SZ and the HAZ of the C-FSSW-welded joints increased, whereas that of the TMAZ decreased, with increasing cooling time.