数字式时差法超声流量计的设计与实现

基于时差法原理,采用数字化方案设计实现了一种超声波流量计.系统以TMS320F28335数字信号控制器(DSC)为核心,扩展ADS807流水线ADC实现高速数据采集,模拟前端实现超声发射、接收信号调理.DSC软件算法通过互相关及拟合算法求解顺逆流传播时间差,希尔伯特变换与小波变换结合确定渡越时间,在此基础上计算流量.经过流量实测证明,设计的超声流量计充分发挥了数字化方案的优势,较好地完成了流量测量工作.     

Dynamic surface control of a piezoelectric fuel injector during rate shaping

Fuel injection rate shaping is a strategy to improve fuel efficiency and reduce harmful emissions in diesel engines. Due to their fast response, piezoelectric fuel injectors are capable of rate shaping operation. This paper describes a model-based closed-loop controller of injection flow rate for a piezoelectric fuel injector. This within-an-engine-cycle control strategy utilizes a dynamic surface control scheme and shows an injection flow rate tracking capability. Practical issues with LabVIEW FPGA control implementation are also addressed. The performance of the controller is verified with simulation and experimental results at different rail pressures and desired injection rates. The experiments show a maximum error of total fuel per one injection event of 2.5%. A stability analysis is also included.     

Preparation and characterization of antibacterial silver-dispersed activated carbon aerogels

Silver-dispersed carbon aerogels (CAs) were obtained by direct immersion of organic aerogels prepared by ambient pressure drying technique in AgNO₃ aqueous solution and then carbonization. The effect of preparation conditions such as the resorcinol/catalyst ratio, the feed AgNO₃ concentration, the ratio of aerogel mass/solution volume, immersion time and carbonization temperature on the bulk density and silver content as well as the BET surface area of the dispersed CAs was studied. The dispersion and structure of silver nanoparticles in obtained materials were investigated by means of scanning electron microscopy, transmission electron microscopy and X-ray diffraction. The Ag-dispersed CAs prepared exhibit strong and long-term antibacterial activity.     

Measurement of residual stresses in injection‐molded polymer parts by time‐resolved fluorescence

Time‐resolved fluorescence properties of 9‐methylanthracene (9MAn) dispersed in film of polyvinylchloride (PVC) containing carbon black were studied under tensile loadings. The fluorescence lifetime of 9MAn decreased from 5.70 to 5.55 ns, whereas the stresses acting on the films increased from 0 to 3 MPa. The change in fluorescence lifetimes of 9MAn during the stress relaxation process showed that the fluorescence lifetimes were correlated with the stresses, not with the strains. The results suggest that 9MAn is a useful probe for monitoring stresses acting on the matrix. With the use of the fluorescence properties of 9MAn, the residual tensile stresses on the skin‐layer of PVC injection‐molded test pieces were estimated. The estimated residual stresses were about ～ 1 MPa. The residual stresses were relaxed to 0 MPa with annealing at 100°C. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 2600–2603, 2002     

Effectiveness test of alginate‐derived polymeric surfactants

A series of alginate‐derived polymeric surfactants (APSs) with a linear alkyl group (C8, C12, C16) was synthesized by oxidation followed by reductive amination of 2,3‐dialdehydic alginate. The products were characterized by measuring IR spectra, NMR spectra, surface tension and critical micelle concentration (cmc). They were also tested for the solubilization of azobenzene and adsorption of heavy metal. In the case of 40% CHO‐C8 APSs, the lowest interfacial tension value (31.5 m Nm^?1) was obtained at the cmc value of 1.35 g dm^?3. The dissolving capacity of 40% CHO‐C8 APS towards azobenzene was 27 times greater than that of alginate. The overall cobalt (Co²⁺) removal efficiency by adsorption using APSs was high compared with that of sodium alginate at pH 3, 5 and 7. Equilibrium aspects of cobalt adsorption onto 10% CHO‐APSs were studied, and the results show that APSs had high equilibrium capacities for cobalt uptake, 115.5 mgg^?1. © 2002 Society of Chemical Industry     

一种基于空间滤波的钢轨表面擦伤检测改进算法

钢轨表面擦伤检测是保障铁路运输安全的重要手段之一。应用图像处理和模式识别技术来处理钢轨数字图像,检测并定位擦伤区域是一种可行且发展迅速的研究手段。课题组在前期工作中提出了一种鲁棒实时的钢轨表面擦伤检测算法,该算法首先对钢轨图像进行灰度对比度增强,在此基础上定位可疑擦伤区域并进行判定。算法对于常规擦伤图像具有较高的检测性能,但对于钢轨图像包含多处擦伤且擦伤区域灰度值差异较大的情况,往往造成漏检。针对原算法的不足,提出了一种基于空间滤波的钢轨表面擦伤检测改进算法,该算法对原算法检测到的擦伤区域进行钢轨灰度图均值填充,并对填充后的图像进行二次检测,在重新生成的灰度对比度图中,原检测图像中灰度值不明显的擦伤区域的灰度对比度值得到增强,从而增加了检出的可能性。经实验结果验证,改进算法具有较高的检测性能:在总的时间耗费没有明显增加的情况下,检测的平均准确率为90.8%,平均漏检率为4.0%,较原算法有较大改善。     

N-烷基苯并三氮唑阳离子表面活性剂的合成及性能

以苯并三氮唑、不同链长的卤代烷烃、硫酸二甲酯为原料合成了几种N-烷基苯并三氮唑阳离子表面活性剂,通过IR1、HNMR对中间产物进行结构表征,并对最终产物进行定性分析。测定了所得产物的表面活性和发泡性能,结果表明,合成的N-丁基、辛基、十二烷基、十六烷基苯并三氮唑阳离子表面活性剂最低表面张力分别为:51.0 mN/m、36.5 mN/m、33.4 mN/m、35.4 mN/m;临界胶束浓度分别为:9.0×10-2mol/L、4.8×10-2mol/L、3.0×10-3mol/L、9.7×10-3mol/L。N-丁基、辛基、十二烷基苯并三氮唑阳离子表面活性剂最低表面张力随烷基链增长而降低,但N-十六烷基苯并三氮唑阳离子表面活性剂的最低表面张力却高于N-十二烷基苯并三氮唑阳离子表面活性剂的最低表面张力。合成的表面活性剂中,N-十二烷基苯并三氮唑阳离子表面活性剂的发泡性能最佳,而所有的泡沫稳定性均较差。     

Silica Nanoboxes as New Nano-structured Materials: Their Secondary Synthesis from Alumina-Rich Zeolites

Novel silica nanoboxes were prepared by controlled dealumination of Na-X and Ca-A type zeolites using ammonium hexafluorosilicate (AHFS). The silica-richer the parent zeolite, the smaller the average pore size produced and the narrower the pore size distribution obtained. This was due to the specific reactivity of the extracting agent with the zeolite framework aluminum atoms. High temperature calcination of the dealuminated X-zeolite (ammonium form) resulted in mesoporous materials exhibiting an ink-bottle shape, a quite high surface area (330 m²/g, no micropores), an average pore diameter of 4.5 nm with a quite narrow pore size distribution (± 1.0 nm) and finally, a pore opening diameter of 3.9 nm. The latter was determined by using the nitrogen sorption isotherms (BET technique) and related pore volume data. The sorption behavior also suggested the interconnecting character of the newly created nanoboxes. The periodicity of these nanoboxes throughout the mesoporous material was clearly shown by X-ray powder diffraction at very small angles. These materials, herein called monomodal nanoboxes because of the absence of micropores in the structure, were also thermally stable. Incorporation of orthosilicate into the obtained silica nanoboxes, in accordance with the recently developed technique for pore size engineering in zeolites, led to materials with smaller pore openings but having almost the same textural properties. Solid superacidic materials were prepared by incorporating a liquid superacid (triflic acid or trifluoromethanesulfonic acid) into the silica nanoboxes using the wet impregnation technique. The maximum triflic acid loading which did not significantly affect the mesoporous framework of the materials was 24 wt%. As a reference, the maximum loading of less acidic sulfuric acid was slightly lower. All this showed the high chemical stability of the silica nanoboxes for supporting very acidic species. Temperature-programmed desorption using a combined DTA/TGA system allowed the identification of the bound phases and some liquid phase of the loaded triflic acid.     

Exploration of mesoporous structure of tunisian raw and acid-leached phosphate ore particles

Rock phosphate fractions were examined for their porous structure by nitrogen adsorption. The pore size distribution and the shape of pores does not seem to depend on the particle size. The specific surface area values present two regions, one above and one below that of the particles with 125 μrn diameter. Particles of a given size were leached with dilute phosphoric acid (1.5 mass% P₂O₅) at 25°C. It was observed that there is a widening of the initial pores during leaching. The particles collected at the initial period of the reaction are pitted and those collected at the final period are disintegrated.