岩盐用作路基填料的力学性质试验

通过试验,研究了察尔汗岩盐用作路基填料的压实特性、抗压强度以及循环荷载下的变形性状。主要探讨了岩盐试样中细粒含量比例对试样压实特性的影响规律;天然岩盐抗压强度的大小分布,以及岩盐抗压强度与粒径、干密度、含水量的关系;交通循环荷载作用下,岩盐的动应变发展情况等。这些结论对盐湖公路建设具有一定的指导意义。     

拉压性能不同材料厚壁圆筒和厚壁球壳的极限压力分析

本文用广义双剪应力强度理论对拉压性能不同的材料制成的厚壁圆筒和厚壁球壳进行了弹塑性应力分析，得出与拉压比有关的弹性极限内压力、塑性极限内压力、弹塑性区的应力以及弹塑性内压力与弹塑性半径之间的关系式．     

ANISOTROPIC STRENGTH CRITERION BASED ON T CRITERION AND THE TRANSFORMATION STRESS METHOD 1)

岩土材料通常呈现出成层水平分布特点, 即可将其视为横观各向同性材料, 横观各向同性对于岩土材料的变形以及强度值都会产生显著的影响. 基于已提出的t强度准则, t强度准则是基于各向同性单元体中存在有效滑移面来构建的, 并根据该空间有效滑移面上主剪应力与主法向应力的比值达到一定阈值为破坏条件. 在空间中存在有效滑移面与物理沉积面, 基于上述两个面在空间的位置关系, 用两面夹角作为表征横观各向同性对剪切强度影响程度的参量, 并假定当该夹角值越大, 则各向异性对强度贡献程度越大, 对应更大的应力比强度值, 反之, 则对应更小的应力比强度值. 基于上述思路并类比将其推广为正交三维各向异性准则, 基于三维各向异性材料的三维沉积面, 提出了三维特征沉积面的概念, 并基于空间滑移面与三维特征沉积面之间的夹角作为度量各向异性程度的变量, 提出了基于两面角作为参量考虑原生各向异性的应力比强度公式, 并利用该应力比强度公式来修正已提出的t强度准则, 最终建立了考虑各向异性影响的t准则公式. 在上述准则基础上, 考虑将各向异性应力空间转换为各向同性应力空间的思路, 在各向异性t准则基础上, 推导得到了基于各向异性强度t准则的变换应力公式, 利用变换应力公式可以将传统的以p, q为变量的各向同性本构模型转变为可考虑各向异性的三维本构模型. 通过对岩土材料的强度以及真三轴条件下的应力应变关系试验数据预测, 验证了所提的各向异性t准则及其变换应力公式的有效性及适用性.     

Anchoring Mechanism of ZnO Nanoparticles on Graphitic Carbon Nanofiber Surfaces through a Modified Co‐Precipitation Method to Improve Interfacial Contact and Photocatalytic Performance

A facile three‐step co‐precipitation method is developed to synthesize graphitic carbon nanofibers (CNFs) decorated with ZnO nanoparticles (NPs). By interchanging intermediate steps of the reaction processes, two kinds of nanohybrids are fabricated with stark morphological and physicochemical differences. The morphologies differ because of the different chemical environments of the NP/nanocluster formation. The hybrid with larger and non‐uniform ZnO nanocluster size is formed in liquid phase and resulted in considerable interfacial defects that deteriorate the charge‐transfer properties. The hybrid with smaller and uniform ZnO NPs was formed in a dry solid phase and produced near‐defect‐free interfaces, leading to efficient charge transfer for superior photocatalytic performance. The results broaden the understanding of the anchoring/bonding mechanism in ZnO/CNF hybrid formation and may facilitate further development of more effective exfoliation strategies for the preparation of high‐performance composites/hybrids.     

Effect of polyethylene glycol on the crystallization and impact properties of polylactide‐based blends

Polylactide (PLA) was plasticized by polyethylene glycols (PEGs) with five different molecular weights (M_w = 200–20,000 g/mol). The effects of content and molecular weight of PEG on the crystallization and impact properties of PLA were studied by wide‐angle X‐ray diffraction, differential scanning calorimetry, scanning electron microscopy, transmission electron microscopy, and V‐notched impact tests, respectively. The results revealed that PEG‐10,000 could significantly improve the crystallization capacity and impact toughness of PLA. When the PEG‐10,000 content ranged from 0 to 20 wt%, the increases in both V‐notched Izod and Charpy impact strengths of PLA/PEG‐10,000 blends were 206.10% and 137.25%, respectively. Meanwhile, the crystallinity of PLA/PEG‐10,000 blends increased from 3.95% to 43.42%. For 10 wt% PEG content, the crystallization and impact properties of PLA/PEG blends mainly depended upon PEG molecular weight. With increasing the M_w of PEG, the crystallinity and impact strength of PLA/PEG blends first decreased and then increased. The introduction of PEG reduced the intermolecular force and enhanced the mobility of PLA chains, thus improving the crystallization capacity and flexibility of PLA. Copyright © 2015 John Wiley & Sons, Ltd.     

Improving the impact property and heat‐resistance of PLA/PC blends through coupling molecular chains at the interface

The influences of both the molecular structure and the melt viscosity differences between Poly(lactic acid) (PLA) and polycarbonate (PC) on the interpenetration of molecular chains at the interface were investigated by comparing the dynamic mechanical properties and morphologies of the as‐prepared PLA/PC solution‐casting blends with those of their corresponding annealed (180°C, 8 h) samples or PLA/PC melt blends. Additionally, two chain extenders containing epoxy groups (ADR and TGDDM) were used to improve the interfacial strength. Subsequently, the interpenetration of PLA and PC molecular chains at the interface was also surveyed. Finally, the effects of the morphology formed by after adding ADR or TGDDM on the impact property, and heat resistance were discussed. The results showed that there was no interpenetration of molecular chains at the interface in PLA/PC melt blends because of the serious hindrance of the molecular structure and the melt viscosity differences. Although the interfacial strength achieved significant increase after adding ADR or TGDDM, the increase of the interfacial strength should be caused by the connection of ADR or TGDDM molecules with PLA and PC molecules at the interface through chemical bonds rather than the entanglements of PLA and PC molecular chains because of no interpenetration of PLA and PC molecular chains at the interface. Thus, the morphology formed after adding ADR or TGDDM is still the type of complete phase separation, which may be the most suitable morphology for achieving high impact and heat resistance PLA/PC blends because these two properties strongly depend on the crystallinity of PLA phase. Copyright © 2015 John Wiley & Sons, Ltd.     

Thermodynamic studies on protonation constant of adenosine and guanosine at different temperatures and ionic strengths

Stepwise protonation constants of two purine nucleosides (adenosine and guanosine) were determined at different temperatures (293.15 to 308.15) and various ionic strengths (0.101 to 3.503 mol · kg⁻¹ NaClO₄) using a combination of potentiometric and spectrophotometric method. The thermodynamic parameters (i.e. enthalpy change, ΔH, and entropy change, ΔS) of the protonations were calculated at different temperatures using van’t Hoff and virial equations. The dependence of the protonation constant on ionic strength is modeled by a Debye–Hückel type equation and discussed. Finally, the protonation constants of the nucleosides and the enthalpy change of protonations were determined at zero ionic strength.     

Dynamic polarizability of two‐electron ions under Debye screening

The effect of plasma screening on the dynamic dipole polarizability (DPP) of two‐electron ions Be²⁺, B³⁺, and C⁴⁺ has been investigated using highly correlated exponential wave functions within the framework of pseudostate summation technique and Debye screening concept. Plasma‐screening effect on the oscillator strengths (OS) of the ultraviolet and visible series has also been investigated for the systems Li⁺, Be²⁺, B³⁺, C⁴⁺. The DPP are reported as functions of screening parameters. The OS for S‐P transitions are also reported for various screening parameters. The OS and dynamic polarizability show interesting behavior with increasing screening strength and nuclear charge. © 2015 Wiley Periodicals, Inc.     

Dependency of dynamic interlaminar shear strength of composites on test technique used

Studies are presented on dependency of dynamic interlaminar shear (ILS) strength on the experimental technique used for a typical plain weave E-glass/epoxy composite. Dynamic ILS strength was determined based on two experimental techniques, namely torsional split Hopkinson bar (TSHB) apparatus using thin walled tubular specimens and compressive split Hopkinson pressure bar (SHPB) apparatus using single lap specimens. The results obtained from these techniques are compared. In general, it is observed that dynamic ILS strength for composites obtained by TSHB testing using thin walled tubular specimens is lower than the dynamic ILS strength obtained using single lap specimens in compressive SHPB. The issues involved in TSHB testing of thin walled tubular specimens made of composites are discussed and the reasons for reduced dynamic ILS strength using thin walled tubular specimens are highlighted. Finite element analysis (FEA) of thin walled tubular specimens made of composite and resin subjected to quasi-static torsional loading is presented. Using FEA results, the reasons for lower ILS strength of composite thin walled tubular specimens are substantiated.     

Interfacial bonding mechanism and bonding strength of AlTiCrN coating by cathodic arc ion plating

AlTiCrN coating was prepared on the surface of YT14 tungsten carbide cutting tools by cathodic arc ion plating with Ti, Al and Cr as targets. The surface morphologies, interface energy spectrum, phase and elements' binding energy of the coatings were observed with SEM, EDS, XRD and XPS, respectively, and bonding strength of the coating interface was measured with scratch tester. The results show that the phases of AlTiCrN coating are mainly composed of AlN, CrN and TiN, the crystal plane of (111) has a strong preferred orientation. The concentrations of Al, Ti, Cr, N in the coating are higher than those in the substrate, showing the gradient diffusion distribution at the bonding interface, while C atoms of the substrate have diffused into the lattices of TiN, AlN and CrN to form an obvious interdiffusion layer, and the average bonding strength of coating interface is 57.65 N. Copyright © 2014 John Wiley & Sons, Ltd.