上软下硬地层隧道围岩渐进破坏机制分析

软硬结构面的存在阻断了岩体性质的连续性,结构面倾角的位置和角度会造成多种破坏模式。文章对上软下硬地层隧道的破坏过程和破坏模式进行数值模拟研究。结果表明：分界结构面倾角在30°~75°时隧道稳定性较差;围岩变形破坏特征在对称模式下,围岩位移、破坏区和塑性区呈对称分布;在非对称模式下,结构面倾角和围岩的力学参数决定了破坏区的位置和范围,破坏区的位置主要受结构面倾角的影响。

EFFECTS OF BRAZING ATMOSPHERES ON INTERFACIAL MICROSTRUCTURE BETWEEN DIAMOND GRITS AND BRAZING ALLOY

The samples of brazed diamond grits with NiCr brazing alloy are prepared in vacuum and argon gas. The microstructures are analyzed with scanning electron microscope （SEM）, energy dispersive X-ray spectroscopy （EDS） and X-ray diffraction（XRD）. The effects of brazing atmospheres on the as-brazed NiCr brazing alloy composite structures and interracial microstructure are studied between diamond grits and brazing alloy. Results show that： （1） There are different composite structures of as-brazed NiCr brazing alloy under different oxygen partial pressures in vacuum and argon gas. B203 exists on the surface of the brazed samples under argon gas furnace brazing. It indicates that oxygen plays an important role in the resultants of as-brazed NiCr brazing alloy during the brazing process. （2） There are different interfacial microstructures in different brazing atmospheres, but the main reaction product is chromium carbides. The chromium carbides in argon gas furnace brazing grow in a disordered form, but those in vacuum furnace brazing grow radiated. And the scale of grains in argon gas is smaller than those in vacuum.

Energy Dependence of Interface Trap Density——Investigated by Relaxation Spectral Technique

According to the definition of interface traps,a new application of relaxation spectral technique to sub-threshold swing shift and sub-threshold gate voltage shift is proposed to extract interface trap density in 1.9nm MOSFET.And thus the energy distribution of interface trap can be determined.According to the two methods,the energy profile of interface traps agrees with those reported in literature.Compared to other methods,this method is simpler and more convenient.

Orientation and Motion of Water Molecules at Air/Water Interface

Here we report a quantitative study of the orientational structure and motion of water molecule at the air/water interface. Analysis of Sum Frequency Generation （SFG） vibrational peak of the free O-H stretching band at 3700 cm^-1 in four experimental configurations showed that orientational motion of water molecule at air/water interface is libratory within a limited angular range. The free OH bond of the interracial water molecule is tilted around 33°from the interface normal and the orientational distribution or motion width is less than 15°. This picture is significantly different from the previous conclusion that the interracial water molecule orientation varies over a broad range within the ultrafast vibrational relaxation time, the only direct experimental study concluded for ultrafast and broad orient, ational motion of a liquid interface by Wei et al. （Phys. Rev. Lett. 86, 4799, （2001）） using single SFG experimental configuration.

Orientation and Structure of Ionic Liquid Cation at Air/[bmim][BF4] Aqueous Solution Interface

The watermiscible room temperature ionic liquid 1butyl3methylimidazolium tetrafluorob orate （[bmim] [BF4]） is a model system for studying the interactions between ionic liquid and water molecules. In this work the orientational structure of the low concentrated aqueous solution of [bmim] [BF4] at the air/liquid interface was investigated by sum frequency gener ation vibrational spectroscopy. It has been found that at very low concentrations, the butyl chain exhibited a significant gauche defect, indicating a disordered conformation; and the cation ring oriented with a fairly small tilting angle at the surface. When the concentration increased, the cation ring tended to lie flat at the surface, and the gauche defects of the butyl chain decreased due to the intermolecular chainchain interactions and the consequent more ordered interfacial molecular arrangement. Additionally, the antisymmetric stretching mode in the PPP and SPS spectra exhibited a peak shift, showing that there exists more than one kind of orientation or chemical environment for the butyl CH3 group. These results may shed new light on understanding the surface behavior of watermiscible ionic liquids as well as the imidazolium based surfactants.

Surface assembly of cobalt species for simultaneous acceleration of interfacial charge separation and catalytic reactions on Cd_(0.9)Zn_(0.1)S photocatalyst

Although photocatalytic water splitting has excellent potential for converting solar energy into chemical energy,the challenging charge separation process and sluggish surface catalytic reactions significantly limit progress in solar energy conversion using semiconductor photocatalysts.Herein,we demonstrate a feasible strategy involving the surface assembly of cobalt oxide species(CoO_(x))on a visible-light-responsive Cd_(0.9)Zn_(0.1)S(CZS)photocatalyst to fabricate a hierarchical CZS@CoO_(x) heterostructure.The unique hierarchical structure effectively accelerates the directional transfer of photogenerated charges,reducing charge recombination through the smooth interfacial heterojunction between CZS and CoO_(x),as evidenced by photoluminescence(PL)spectroscopy and various electrochemical characterizations.The surface cobalt species on the CZS material also act as efficient cocatalysts for photocatalytic hydrogen production,with activity even higher than that of noble metals.The well-defined CZS@CoO_(x) heterostructure not only enhances the interfacial separation of photoinduced charges,but also improves surface catalytic reactions.This leads to superior photocatalytic performances,with an apparent quantum efficiency of 20%at 420 nm for visible-light-driven hydrogen generation,which is one of the highest quantum efficiencies measured among noble-metal-free photocatalysts.Our work presents a potential pathway for controlling complex charge separation and catalytic reaction processes in photocatalysis,guiding the practical development of artificial photocatalysts for successful transformation of solar to chemical energy.

Orientation Angle of Molecules at Hexadecane-Water Interface Studied with Total Internal Reflection Second Harmonic Generation

The orientation angle is an important parameter that reflects the structure of molecules at interfaces. In order to obtain this parameter, second order nonlinear spectroscopic techniques including second harmonic generation （SHG） and sum frequency generation-vibrational spec- troscopy （SFG-VS） have been successfully applied through analysis of the nonlinear signal from various polarizations. In some SHG and SFG-VS experiments, total internal reflection （TIR） configuration has been adopted to get enhanced signals. However, the reports on the detailed procedure of the polarization analysis and the calculation of the orientation angle of interracial molecules under TIR configuration are still very few. In this paper, we mea- sured the orientation angles of two molecules at the hexadecane-water interface under TIR and Non-TIR experimental configurations. The results measured from polarization analysis in TIR configuration consist with those obtained from Non-TIR configuration. This work demonstrates the feasibility and accuracy of polarization analysis in the determination of the orientation angle of molecules at the interfaces under TIR-SHG configuration.

Open Architecture of Single-processor Real-time Robot Control System Based on Windows NT

This paper introduces the architecture and implementation of an industrial robot control system based on Windows NT. This robot control system, which is based on a single-processor structure, can run on general industrial computers. Owing to using Windows NT's real-time extension RTX, the control system can achieve good realtime performance and friendly user interface in one general-purpose operating system. A three layer hierarchical architecture of control software is proposed to make the system more scalable and flexible. Furthermore a communication and configuration system is implemented to enable modules to communicate with each other, which make the control system scalable and flexible.

Advanced experimental methods toward understanding biophysicochemical interactions of interfacial biomolecules by using sum frequency generation vibrational spectroscopy

Sum frequency generation vibrational spectroscopy(SFG-VS)has been demonstrated to be a powerful technique to study the interfacial structures and interactions of biomolecules at the molecular level.Yet most previous studies mainly collected the SFG spectra in the frequency range of 1500–4000 cm-1,which is not always sufficient to describe the detailed interactions at surface and interface.Thorough knowledge of the complex biophysicochemical interactions between biomolecules and surface requires new ideas and advanced experimental methods for collecting SFG vibrational spectra.We introduced some advanced methods recently exploited by our group and others,including(1)detection of vibration modes in the fingerprint region;(2)combination of chiral and achiral polarization measurements;(3)SFG coupled with surface plasmon polaritons(SPPs);(4)imaging and microscopy approaches;and(5)ultrafast time-resolved SFG measurements.The technique that we integrated with these advanced methods may help to give a detailed and high-spatial-resolution 3D picture of interfacial biomolecules.