土-钢组合铁路桥的动力响应

对长跨钢涵洞铁路桥进行实际动力响应研究。桥为土-钢组合结构,长11m。通过测量不同车速下桥的应变和位移,对桥进行试验,同时,对垂直道床振动以及制动力的影响也进行了测量。研究显示:车速对位移、推力和力矩的影响较大;所测的动态位移与推力比超出相应静态响应的20%,远大于桥设计规范所规定的值;力矩到1/4点时,动荷系数高达1·45,高于关键点的值。鉴于从强迫振动试验中测得了高的阻尼值,与普通桥相比这种桥的类型对共振并不敏感。     

A novel multi−wavelength photoacoustic spectrometer for the measurement of the UV–vis-NIR spectral absorption coefficient of atmospheric aerosols

A multi-wavelength photoacoustic instrument is described, which measures the wavelength dependent optical absorption coefficient (OAC) of soot or soot-containing aerosols in-situ in a range from the ultra-violet to the near-infrared region. The instrument combines a Nd:YAG disc laser (fundamental wavelength 1064 nm, harmonics at 532, 355 and 266 nm) and four photoacoustic detection cells, each purged with the same aerosol sample flow, while being irradiated with one of the four light beams. With the help of a supplementary optical arrangement to illuminate each detection cell with 532 nm light, the system is calibrated against OAC by purging the cells with known concentrations (and hereby known OAC values) of NO₂. This calibration eliminates differences in sensitivity of the detection PA cells and makes the measurement of OAC absolute.The minimum detectable OAC was determined to be 0.2 Mm^?1 at 1064 nm and 35.5 Mm^?1 at 266 nm, corresponding to a minimum detectable black carbon mass concentration of about 0.1–1 μg/m³, depending on the wavelength. Comparison measurements with artificially generated soot aerosols showed good agreement of the device with a reference instrument, based on a long path extinction cell (LOPES).     

Crystalline BaTiO3 synthesis by ultrasound and microwave‐assisted sol–gel process

Highly crystalline BaTiO₃ particles were prepared by sol–gel process. Ultrasound and microwave techniques were used to facilitate the synthesis of BaTiO₃. BaTiO₃ samples were characterized by X‐ray diffraction (XRD), scanning electron microscopy (SEM), particle size analyser, and high temperature differential scanning calorimetry/thermogravimetric analysis (DSC/TGA). The results indicate that both barium and titanium sources and preparation techniques affected BaTiO₃ purity and crystallite size. The smallest particle and crystallite sizes were obtained by using BaCl₂ and (C₄H₉O)₄Ti and the crystallite size of BaTiO₃ was 8 ± 1 nm via MW technique.     

Effects of pectin and guar gum on creaming stability, microstructure and rheology of egg yolk plasma-stabilized emulsions

The influence of pectin and guar gum on the creaming stability, microstructure and rheological properties of 1.0% (w/v) egg yolk plasma (EYP)-stabilized 25.0% (v/v) soybean oil-in-water emulsions was studied at pH 7.0. Addition of pectin/guar gum decreased creaming percentage, and no creaming was detected in the presence of 0.5% (w/v) pectin/guar gum as a result of increasing viscosity. At the end of 10 h, creaming percentage decreased from 61 to 57% with the addition of 0.05% (w/v) guar gum and to 39% with the addition of 0.2% (w/v) guar gum. Microscopic observations represented the droplet aggregation arising from the presence of nonabsorbing biopolymers. At \mathop g^. \mathop \gamma \limits^{.}  = 10 s⁻¹, a tenfold increase in viscosity was observed in the presence of 0.5% (w/v) guar gum compared to the presence of 0.1% guar gum due to the thickening effect of polysaccharide. Increasing gum concentrations enhanced the viscosity and hence the consistency index. All emulsions, except for those containing 0.5% (w/v) guar gum, reflect the near-Newtonian behaviour with flow behaviour index, n, of 0.9–1.0. All emulsions exhibited a liquid-like behaviour at low frequencies (<7.0 Hz) where G″ values were higher than G′. Both G′ and G″ showed a frequency dependency and these two moduli crossed each other at higher frequencies (>7.0 Hz), G′ became greater than G″ and the system behaved like an elastic solid. Addition of pectin at all levels cause no significant change in G′ and G″ values, whereas addition of guar gum, especially at a concentration of 0.5% (w/v), significantly improved these values.     

Synthesis and phosphorescence properties of Mn, La and Ho in MgAl2Si2O8

Mn⁴⁺, La³⁺ and Ho³⁺ doped MgAl₂Si₂O₈-based phosphors were first synthesized by solid state reaction. They were characterized by thermogravimetry (TG), differential thermal analysis (DTA), X-ray powder diffraction (XRD), photoluminescence (PL) and scanning electron microscopy (SEM). The phosphors were obtained at about 1300 °C. They showed broad red and fuchsia-pink emission bands in the range of 610-715 nm and had a different maximum intensity when activated by UV illumination. Such a fuchsia-pink emission can be attributed to the intrinsic d-d transitions of Mn⁴⁺.     

Host-sensitized phosphorescence of Mn4+, Pr3+,4+ and Nd3+ in MgAl2Si2O8

Mn⁴⁺ doped and Pr^3+,4+, Nd³⁺ co-doped MgAl₂Si₂O₈-based phosphors were first of all synthesized about 1300 °C. They were characterized by thermogravimetry (TG), differential thermal analysis (DTA), X-ray powder diffraction (XRD), photoluminescence (PL) and scanning electron microscopy (SEM). The luminescence mechanism of the phosphors, which showed broad red emission bands in the range of 610–715 nm and had a different maximum intensity when activated by UV illumination, was discussed. Such a red emission can be attributed to the intrinsic d–d transitions of Mn⁴⁺.