聚丙烯腈基碳纤维原丝在纺丝过程中纳米孔变化规律与机理研究

应用小角X射线散射等方法, 系统、定量地测试表征了聚丙烯腈基碳纤维原丝中纳米孔的尺寸、形状、体积分数、单位体积中纳米孔绝对数量以及纤维总孔洞率等形态结构参量, 并对这些参量在水洗、水洗牵伸、热致密化、高压蒸汽牵伸及热稳定化等工艺过程中的变化规律及原因进行了研究. 结果表明, 纺丝过程中牵伸及高温热处理均可使纤维总孔洞率逐步下降. 纳米孔尺寸体积分数V_i测试表明, 对于小于10 nm³的小纳米孔和大于10³ nm³的较大纳米孔, 两者的V_i在纺丝初期水洗牵伸工艺中分别为0.217和0.369, 而在纺丝后期热稳定化处理后发生大幅度改变, 分别为0.948 与0.015. 其原因并不是在高压蒸汽牵伸及热稳定处理中较小纳米孔含量的增加, 而是较大纳米孔含量的大幅度减少. 纳米孔形状研究表明, 纺丝工艺中的多次牵伸处理均使纳米孔的长短轴比加大, 而大于玻璃化温度的热处理均使纳米孔长短轴比收缩, 并且对于较小纳米孔来说这种收缩更为显著.     

R型铁氧体BaFe4-xTi2+xO11的化学组态以及磁性行为的研究

本文通过传统的固相反应法制备了R型六角铁氧体BaFe_4-xTi_2+xO₁₁ (x= 0, 0.25, 0.5, 0.75, 1), 并且对它的原子价态以及磁性行为进行了研究. X 射线光电子能谱(XPS)结果显示了随着掺杂含量的增加, 体系中Fe³⁺离子逐渐减少而Fe²⁺离子逐渐增加. 由于具有非对称结构的阻挫晶格中存在各种关联作用的竞争, 使得BaFe_4-xTi_2+xO₁₁体系表现出了复杂的磁有序行为, 在T₁～250 K和T₂～83 K两处存在磁转变. 对这一系列掺杂样品, 在相变温度T₁之上表现顺磁行为, 而在相变温度T₂前后的磁化强度都表现出低场下随磁场的增加快速增加, 高场下则线性变化且在5×10⁴ Oe时还未达到饱和的行为, 表明这一系列掺杂样品是典型的倾斜反铁磁态(canted antiferromagnetic) 或者亚铁磁态.     

大耕深旋耕刀激光冲击强化残余应力研究

研究了激光冲击强化对回转半径为350mm大耕深旋耕刀残余应力的影响,利用ANSYS对旋耕刀进行理论应力分析,发现应力集中在刀柄外弯角处,同时进行了激光冲击强化模拟,得到理论残余应力引入值。利用X射线衍射法对激光冲击强化前后旋耕刀表面进行了残余应力测试。结果表明,ANSYS模拟激光冲击强化引入的残余应力值与试验实测的结果吻合得较好,相比未经处理的旋耕刀,激光冲击强化后刀具表面残余应力明显增大,最大残余压应力达412.25 MPa,增幅达166%,残余压应力的引入可消除旋耕刀工作的应力集中,提高了刀具使用寿命。研究结果为进一步提高和优化大耕深旋耕刀制造工艺提供了新的参考依据。     

多层CT与DSA对急性冠状动脉综合征患者冠状动脉支架置入术后通畅性及狭窄程度的影响

研究多层CT与DSA对急性冠状动脉综合征患者冠状动脉支架置入术后通畅性及狭窄程度的影响。以我院2017年8月-2018年11月在我院诊断治疗的急性冠脉综合征患者80例作为研究对象,对所有患者进行经皮冠状动脉介入治疗(percutaneous coronary intervention,PCI)手术后,分别进行DSA检查以及64排螺旋CT检查。分析不同检查的冠状动脉狭窄、通畅性之间的差异以及不同检查的一致性。通过对CT检查结果以及DSA检查结果的配对卡方检验,两组患者的检查结果之间的差异不存在统计学意义,两种检查对患者的冠状动脉的狭窄情况诊断一致性较好;两种检查方法对患者的管壁厚度以及管径直径诊断之间的差异不存在统计学意义,两种检验方法对患者的管壁厚度以及管径直径诊断一致性较好。总之,多层CT与DSA对急性冠状动脉综合征患者冠状动脉支架置入术后通畅性及狭窄程度的诊断具有较高的一致性,建议临床推广。     

常见客体分子对笼型水合物晶格常数的影响

Natural gas hydrates are considered as ideal alternative energy resources for the future, and the relevant basic and applied research has become more attractive in recent years. The influence of guest molecules on the hydrate crystal lattice parameters is of great significances to the understanding of hydrate structural characteristics, hydrate formation/decomposition mechanisms, and phase stability behaviors. In this study, we test a series of artificial hydrate samples containing different guest molecules (e.g. methane, ethane, propane, iso-butane, carbon dioxide, tetrahydrofuran, methane + 2, 2-dimethylbutane, and methane + methyl cyclohexane) by a low-temperature powder X-ray diffraction (PXRD). Results show that PXRD effectively elucidates structural characteristics of the natural gas hydrate samples, including crystal lattice parameters and structure types. The relationships between guest molecule sizes and crystal lattice parameters reveal that different guest molecules have different controlling behaviors on the hydrate types and crystal lattice constants. First, a positive correlation between the lattice constants and the van der Waals diameters of homologous hydrocarbon gases was observed in the single-guest-component hydrates. Small hydrocarbon homologous gases, such as methane and ethane, tended to form sI hydrates, whereas relatively larger molecules, such as propane and iso-butane, generated sⅡ hydrates. The hydrate crystal lattice constants increased with increasing guest molecule size. The types of hydrates composed of oxygen-containing guest molecules (such as CO₂ and THF) were also controlled by the van der Waals diameters. However, no positive correlation between the lattice constants and the van der Waals diameters of guest molecules in hydrocarbon hydrates was observed for CO₂ hydrate and THF hydrate, probably due to the special interactions between the guest oxygen atoms and hydrate "cages". Furthermore, the influences of the macromolecules and auxiliary small molecules on the lengths of the different crystal axes of the sH hydrates showed inverse trends. Compared to the methane + 2, 2-dimethylbutane hydrate sample, the length of the a-axis direction of the methane + methyl cyclohexane hydrate sample was slightly smaller, whereas the length of the c-axis direction was slightly longer. The crystal a-axis length of the sH hydrate sample formed with nitrogen molecules was slightly longer, whereas the c-axis was shorter than that of the methane + 2, 2-dimethylbutane hydrate sample at the same temperature.     

Be-composition effect on structure, electronic and optical properties of BexZn1-xO alloys

This paper carries out first principles calculation of the structure,electronic and optical properties of Be x Zn 1 x O alloys based on the density-functional theory for the compositions x = 0.0,0.25,0.5,0.75,1.0.The lattice constants deviations of alloys obey Vegard’s law well.The Be x Zn 1 x O alloys have the direct band gap(Γ-Γ) character,and the bowing coefficients are less than the available theoretical values.Moreover,it investigates in detail the optical properties(dielectric functions,absorption spectrum and refractive index) of these ternary mixed crystals.The obtained results agree well with the available theoretical and experimental values.     

Synthesis and magnetic properties of Fe100-xMox alloy nanowire arrays

The Fe100-xMox(13≤x≤25) alloy nanowire arrays are synthesized by electrodeposition of Fe 2+ and Mo 2+ with different ionic ratios into the anodic aluminum oxide templates.The crystals of Fe100-xMox alloy nanowires gradually change from polycrystalline phase to amorphous phase with the increase of the Mo content and the nanowires are of amorphous structure when the Mo content reaches 25 at%,which are revealed by the X-ray diffraction and the selected area electron diffraction patterns.As the Mo content increases,the magnetic hysteresis loops of Fe100-xMox alloy nanowires in parallel to the nanowire axis are not rectangular and the slopes of magnetic hysteresis loops increase.Those results indicate that the magnetostatic interactions between nanowires and the magnetocrystalline anisotropy both have significant influences on the magnetization reversal process of the nanowire arrays.     

Neutron diffraction study on composite compound Nd2Co7

The crystallographic and the magnetic structures of the composite compound Nd₂Co₇ at 300 K are investigated by a combined refinement of X-ray diffraction data and high-resolution neutron diffraction data. The compound crystallizes into a hexagonal Ce₂Ni₇-type structure and consists of alternately stacking MgZn₂-type NdCo₂ and CaCu₅-type NdCo₅ structural blocks along the c axis. A magnetic structure model with the moments of all atoms aligning along the c axis provides a satisfactory fitting to the neutron diffraction data and coincides with the easy magnetization direction revealed by the X-ray diffraction experiments on magnetically pre-aligned fine particles. The refinement results show that the derived atomic moments of the Co atoms vary in a range of 0.7 μ_B-1.1 μ_B and the atomic moment of Nd in the NdCo₅ slab is close to the theoretical moment of a free trivalent Nd³⁺ ion, whereas the atomic moment of Nd in the NdCo₂ slab is much smaller than the theoretical value for a free Nd³⁺ ion. The remarkable difference in the atomic moment of Nd atoms between different structural slabs at room temperature is explained in terms of the magnetic characteristics of the NdCo₂ and NdCo₅ compounds and the local chemical environments of the Nd atoms in different structural slabs of the Nd₂Co₇ compound.     

Short range order transformation and magnetostriction of Fes3Ga17 ribbons

The relationship between magnetostriction and structure of melt-spun Fes3Ga17 ribbons are investigated by XRD and M5ssbauer spectrum technique （MS）. As the heat-treatment temperature increases from 650℃ to 800℃, the magnetostriction coefficient of Fes3Ga17 ribbon first increases and then decreases. The largest magnetostriction coeiffcient （-578.4 ppm） is achieved in those specimens quenched at 750oc. According to the XRD and MSssbauer spectrum anal- ysis, a small quantity of DO3 phase is precipitated in Fe83Ga17 ribbons when quenched from 650℃ and the DO3 phase is gradually transformed into B2-1ike phase if quenched at higher temperature. However, both DO3 and B2-1ike phases disappear when the temperature increases up to 800℃. From this point of view, B2-1ike phase might be beneficial to the enhancement of magnetostrictive properties of melt-spun ribbons.     

Single-molecule surface-enhanced Raman scattering of R6G in aqueous environment under non-resonance conditions

The single-molecule surface-enhanced Raman scattering(SERS) spectra of Rhodamine 6G(R6G) in an aqueous environment under non-resonance conditions are studied.Series of spectra are recorded in timemapping mode,and intensity fluctuations of SERS signals and spectral diffusion are observed.The correlations between the presence frequency of SERS spectra and number of hot spots as well as the quantity of molecules in scattering volume are examined thoroughly.The results indicate that only molecules located at hot spots produce good signal-to-noise ratio Raman spectra and the origin of fluctuating SERS signals are mainly ascribed to the movement of hot spots.