木质素磺酸钙改良黄土的结构性机理

木质素磺酸钙(CL)改良黄土作用存在强度峰值,且各掺量达到峰值所需养护时间不同,表现出明显的掺量和龄期效应.在土工试验、微观试验和前人成果基础上,研究掺量和养护龄期对于CL改良土结构特征的影响,探讨其作用机理.研究表明,CL通过胶结、填充和团粒化作用,将素土的“颗粒,镶嵌+架空,接触”结构转变为“团粒,镶嵌,胶结+接触”结构,并降低颗粒的双电层厚度和表面溶液张力,从而提高工程性能.过量掺量的CL因强黏结性和引气作用,导致CL改良土向“团粒+片状,镶嵌+架空,胶结”结构转变,颗粒咬合摩擦降低,并产生大量气泡起到润滑作用,工程性能降低.

Hydrothermal synthesis, characterization and optical properties of La_2Sn_2O_7:Eu^(3+) micro-octahedra

Pyrochlore structure La2Sn2O7：Eu3＋ microcrystals with uniform octahedron shape were successfully synthesized via a hydrothermal route at 180 °C for 36 h. The crystal structure, particle size, morphologies, and optical properties of the as-synthesized products were investigated by XRD, TEM, SEM, EDS, FT-IR, Raman spectroscopy and PL. The effects of pH of precursor solution, precursor concentration, reaction temperature, and time were investigated. The results reveal that pH of the precursor solution not only plays an important role in determining the phase of the as-synthesized products, but also has a significant influence on the morphologies of the samples. High-quality and uniform octahedrons with an average size of about 700 nm could be easily obtained at the pH value of 12. The possible formation mechanism of octahedral-like La2Sn2O7：Eu3＋ microcrystals was briefly proposed. The photoluminescence spectra show that La2Sn2O7：Eu3＋ micro-octahedra display stronger emission in the range of 582-592 nm compared with the samples with other shapes.

DFT Study on Molecular Structures and ROS Scavenging Mechanisms of Novel Antioxidants from Lespedeza Virgata

The molecular structure and radical scavenging activity of three novel antioxidants from Lespedeza Virgata, lespedezavirgatol, lespedezavirgatal, and lespedezacoumestan, have been studied using density functional theory with the B3LYP and BhandHLYP methods. The optimized geometries of neutral, radical cation, radical and anion forms were obtained at the B3LYP/6-31G（d） level, in which it was found that all the most stable conformations contain intramolecular hydrogen bonds. The same results were obtained from the MP2 method. The homolytic O-H bond dissociation enthalpy and the adiabatic ionization potential of neutral and anion forms for the three new antioxidants and adiabatic electron affinity and H-atom affinity for hydroxyl radical, superoxide anion radical, and hydrogen peroxide radical were determined both in gas phase and in aqueous solution using IEF-PCM and CPCM model with UAHF or Bondi cavity. The antioxidant activities and reactive oxygen species scavenging mechanisms were then discussed, and the results obtained from different methods are consistent. Furthermore, the antioxidant activities are consistent with the experimental findings of the compounds under investigation.

Ethylene Polymerization with Palygorskite Supported Nickel-Diimine Catalyst

A nickel-diimine catalyst [N, N'-bis(2,6-diisopropylphenyl)-1,4-diaza-2,3-dimethyl-1, 3-butadiene nickel dibromide, DMN] was supported on palygorskite clay for ethylene slurry polymerization. The effect of supporting methods on the catalyst impregnation was studied and compared. Pretreatment of the support with methylalumi-noxane (MAO) followed by DMN impregnation gave higher catalyst loading and catalytic activity than the direct impregnation of DMN. Catalyst activity as high as 5.42×105g PE·molNi-1·h-1 was achieved at ethylene pressure of 6.87×105 Pa and polymerization temperature of 20℃. In particular, the morphological change of the support during MAO treatment was characterized and analyzed. It was found that nano-fiber clusters formed during the support pretreatment, which increased the surface area of the support and favored the impregnation of the catalyst. The investigation of polymerization behavior of supported catalyst revealed that the polymerization rate could be kept at a relatively high level for a long time, different from the homogeneous catalyst. By analyzing the SEM photographs of the polymer produced by the supported catalyst, the morphological evolution of polymer particles was preliminarily studied.

Mechanical properties and fracture mechanism of as-cast MnFeCoCuNix high-entropy alloys

MnFeCoCuNix high-entropy alloys(HEAs)with different Ni contents were fabricated by vacuum induction melting.XRD and SEM−EDS were used to analyze the phase constitution and structure,and the tensile properties of the samples were determined using a universal tensile tester.The results show that the HEAs consist of a dual-phase structure,in which FCC1 phase is rich in Fe and Co,while the FCC2 phase has high contents of Cu and Mn.As Ni content increases,the segregation of Cu decreases,accompanied by the decrease of FCC2 phase.Moreover,the tensile strength of the HEAs increases first and then decreases,and the elongation increases slightly.This is attributed to the combined effect of interface strengthening and solid solution strengthening.The in-situ stretched MnFeCoCuNi0.5 alloy shows obvious neck shrinkage during the tensile fracture process.In the initial deformation stage,the slip lines show different morphologies in the dual-phase structure.However,in the later stage,the surface slip lines become longer and denser due to the redistribution of atoms and the re-separation of the dissolved phase.

Microstructure and mechanical properties of strontium-modified ADC12 alloy processed by heat treatment

The effects of heat treatment and strontium （SO addition on the microstructure and mechanical properties of ADC12 alloys were investigated, and two-stage solution treatment was introduced. The results indicated that the addition of Sr obviously refined the microstructure of ADC12 alloys. When 0.05 wt% Sr was added into the alloy, the eutectic Si phase was fully modified into fine fibrous structure; a-A1 and fl-A15FeSi phases were best refined; and the eutectic AlzCu phase was modified into block-like AlzCu phase that continuously distributed at the grain boundary. The ultimate tensile strength （UTS） （270.63 MPa） and elongation （3.19%） were increased by 51.2% and 73.4% respectively compared with unmodified alloys. After the two-stage solution treatment （500 ~C, 6 h＋520 ~C, 4 h）, for 0.05 wt% Sr modified ADC12 alloys, the Si phases transformed into fine particle structure and AlzCu phases were fully dissolved. The peak hardness value of the alloys processed by the two-stage solution treatment was increased by 8.3% and 6.8% respectively compared to solution treatment at 500 ~C and 520 ~C. After the aging treatment （175 ~C, 7 h）, the hardness and UTS were increased by 38.73% and 13.96% respectively when compared with the unmodified alloy.

Effect of nickel-plated graphite on microstructure and properties of matrix for Fe-based diamond tools

Nickel-plated graphite particles and unmodified graphite particles with different contents were added to the Fe-based diamond composites.The basic properties of those specimens were measured,including relative density,hardness,bending strength,abrasion ratio and holding force coefficient.And also,SEM,XRD and EDS were used to carry out microstructure characterization,phase analysis and element distribution of these specimens.The results show that nickel plating effectively improves the surface wettability of graphite particles.And it is determined that an element diffusion zone is formed on the transition interface between the nickel-plated graphite and the matrix materials,effectively enhancing the interfacial bonding strength.Also,the pores and cracks in the matrix generated by adding the graphite particles are reduced after nickel plating.Thus,the loss of basic properties of the specimens is restrained.But it is found the higher the graphite content is,the weaker the positive effect of nickel plating is.In addition,it is revealed that nickel plating plays a conducive part in the formation of graphite lubricants on the working surface,and nickel-plated graphites can slow down the thermal corrosion of the diamond particles inside the high-temperature sintered specimens.

Corrosion resistances of metallic materials in environments containing chloride ions:A review

Corrosion,more specifically,pitting corrosion happening extremely in marine environments,leads to lifespan of materials drastically decreasing in service,which causes enormous economic loss and even environmental disaster and casualties.In the past decade,increasing efforts have been made to study the corrosion behaviors of materials in chloride-containing aqueous environments.Herein,this work provides an overview of recent progress in understanding the degradation mechanism and improving the corrosion resistance and corrosion-wear resistance of materials from bulk metal to surface treatment involving organic coating,metal and its alloy or compound coating.The particular emphasis is given to the periodic layered structures(PLSs),whose anti-corrosion properties outperformed others to some extent,wherever in terms of bulk metal or surface treatment,regardless of aggressive environment(corrosion or corrosion-wear conditions).Numerical simulation based on kinds of models at different scales is introduced to deeply understand the process of corrosion and/or corrosion-wear in chloride-containing aqueous environment.Combined experimental result with numerical simulation,the micro-galvanic corrosion dominated degradation mechanism of PLSs is critically analyzed.Types of setups to realize corrosion-wear in laboratory are also summarized.At last,future research and development are prospected,offering to develop a basic application of PLSs designed by corrosion protection methodology in the near future.

Wave propagation control in periodic track structure through local resonance mechanism

Excessive vibration and noise radiation of the track structure can be caused by the operation of high speed trains.Though the track structure is characterized by obvious periodic properties and band gaps,the bandwidth is narrow and the elastic wave attenuation capability within the band gap is weak.In order to effectively control the vibration and noise of track structure,the local resonance mechanism is introduced to broaden the band gap and realize wave propagation control.The locally resonant units are attached periodically on the rail,forming a new locally resonant phononic crystal structure.Then the tuning of the elastic wave band gaps of track structure is discussed,and the formation mechanism of the band gap is explicated.The research results show that a new wide and adjustable locally resonant band gap is formed after the resonant units are introduced.The phenomenon of coupling and transition can be observed between the new locally resonant band gap and the original band gap of the periodic track structure with the band gap width reaching the maximum at the coupling position.The broader band gap can be applied for vibration and noise reduction in high speed railway track structure.

On the instability of offshore foundations: theory and mechanism

As the offshore engineering moving from shallow to deep waters, the foundation types for fixed and floating platforms have been gradually evolving to minimize engineering costs and structural risks in the harsh offshore environments. Particular focus of this paper is on the foundation instability and its failure mechanisms as well as the relevant theory advances for the prevailing foundation types in both shallow and deep water depths. Piles, spudcans, gravity bases, suction caissons, and plate anchors are detailed in this paper. The failure phenomena and mechanisms for each type of foundations are identified and summarized, respectively. The theoretical approaches along with sophisticated empirical solutions for the bearing capacity problems are then presented. The major challenges are from flow-structure-soil coupling processes, rigorous constitutive modeling of cyclic behaviors of marine sediments, and the spatial variability of soil properties for large-spreading structures. Further researches are suggested to reveal the instability mechanisms for underpinning the evolution of offshore foundations.

Construction of smart inorganic nanoparticle-based ultrasound contrast agents and their biomedical applications

Ultrasound(US) imaging in combination with US contrast agents(UCAs) is a powerful tool in the modern biomedical field because of its high spatial resolution, easy access to patients and minimum invasiveness.The microbubble-based UCAs have been widely used in clinical diagnosis; however, they are only limited to the blood pool imaging and not applicable to the tissue-penetrated imaging due to their large particle size and structural instability. Inorganic nanoparticles(NPs), such as silica,gold and Fe x O y, featured with both satisfactory echogenic properties and structural stability have the potential to be used as a new generation of UCAs. In this review, we present the most recent progresses in the tailored construction of inorganic UCAs and their biomedical applications in the US imaging-involved fields. Firstly, the typical inorganic NPs with different structures including solid, hollow and multiple-layer forms will be comprehensively introduced in terms of their structure design,physicochemical property, US imaging mechanism and diverse applications; secondly, the recent progress in exploring the gas-generating inorganic NP system for US imaging purpose will be reviewed, and these intelligent UCAs are multifunctional for simultaneous US imaging and disease therapy; thirdly, several nanocomposite platforms newly constructed by combining inorganic UCAs with other functional components will be presented anddiscussed. These multifunctional NPs are capable of further enhancing the imaging resolution by providing more comprehensive anatomical information simultaneously.Last but not the least, the design criteria for developing promising UCAs to satisfy both clinical demands and optimized US imaging capability will be discussed and summarized in this review.