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按照IEC 61000-4-4/GB 17626.4—1998的要求,首先应用PSPICE仿真确定电路中各元件的参数值,然后基于拉普拉斯变换用MATLAB求解二阶电路验证各元件参数。在此基础上研制了一台以开关电源作为高压直流电源、以氢闸流管作为主控开关的脉冲群电源。该电源体积小、重量轻、效率高、成本低廉。试验结果表明,其输出信号符合标准要求,可用于快速瞬变脉冲群抗扰度试验。 相似文献
95.
研究了Pt,Ru,Ni为活性金属的负载型催化剂上甲醇质量分数为5%的水溶液的液相重整反应。在合适的温度、体积空速下,Pt基催化剂表现出较好的反应性能,甲醇转化率可达99%,H2选择性达98%以上,产物中CO体积分数小于0.01%。Ni/Al2O3催化剂可使甲醇转化率最高达到98%以上,H2选择性随转化率升高而下降,但不低于80%。Ru/Al2O3催化剂上甲醇的转化率最高,可达到98%以上,但其H2选择性随着转化率的升高,从68%快速下降至20%,明显与Pt、Ni基催化剂上的反应机理不同。根据反应条件和产物组成变化,进一步探讨甲醇反应路径,当产物中H2与CH4选择性比值高于2/3时,反应路径以重整制氢为主;当比值低于2/3时,反应路径以甲烷化为主。 相似文献
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The electron spin resonance (ESR) spectra of end‐group spin labelled poly(ethylene oxide) (SLPEO) using 2,2,6,6‐tetramethyl‐piperdine‐1‐oxyl nitroxide and its blends with poly(styrene‐co‐4‐vinylphenol) (STVPhs) of different hydroxyl contents were recorded over a wide temperature range. For a blend of SLPEO and pure polystyrene (PS), the ESR spectrum was composed of a single motion component, indicating that PS was immiscible with PEO. For blends composed of SLPEO and different‐hydroxyl‐content STVPhs, two spectral components with different motion rates were observed over a certain temperature range. The difference between the motion rates should be attributed to micro‐heterogeneity in the blends, with the faster rate corresponding to a nitroxide radical motion trapped in the PEO‐rich domain and the slower rate corresponding to a nitroxide radical motion trapped in the STVPh‐rich domain. Variations in the values of a number of the ESR parameters (Ta, Td and T50G) and the apparent activation energy (Ea) with hydroxyl content in the blends indicated that the miscibility of the blends increased with increasing hydrogen‐bonding density due to specific interactions between the hydroxyl groups in STVPh and the ether oxygens in PEO. Copyright © 2004 Society of Chemical Industry 相似文献
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Yu. F. Smirnov 《Measurement Techniques》2007,50(3):293-297
Metrological characteristics of active hydrogen frequency standards are investigated on the basis of internal and external
comparisons. The stability of random changes and drift of hydrogen frequency standards and also the potential capabilities
of time scale preservation with effective consideration of systematic changes in their frequency are demonstrated.
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Translated from Izmeritel’naya Tekhnika, No. 3. pp. 42–45, March, 2007. 相似文献
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Akbar Eslami Simin Nasseri Bahram Yadollahi Alireza Mesdaghinia Foroogh Vaezi Ramin Nabizadeh Shahrokh Nazmara 《Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986)》2008,83(11):1447-1453
BACKGROUND: Over the past several decades methyl tert‐butyl ether (MTBE) as additive to gasoline, intended to either boost ratings of fuel or to reduce air pollution, has been accepted worldwide. Since MTBE has high water solubility, the occurrence of fuel spills or leaks from underground storage tanks or transferring pipeline has led to the contamination of natural waters. In this study the degradation of aqueous MTBE at relatively high concentrations was investigated by a UV‐visible/ZnO/H2O2 photocatalytic process. The effects of important operational parameters such as pH, amount of H2O2, catalyst loading and irradiation time were also investigated. Concentration of MTBE and intermediates such as tert‐butyl formate and tert‐butyl alcohol were measured. RESULTS: Time required for complete degradation increased from 20 to 150 min when the initial concentration was increased from 10 to 500 mg L?1. The first‐order rate constants for degradation of MTBE were estimated to be 0.183–0.022 min?1 as the concentration increased from 10 to 500 mg L?1. Study of the overall mineralization monitored by total organic carbon analysis showed that at an initial concentration of 100 mg L?1 MTBE complete mineralization was obtained after 100 min under UV‐visible/ZnO/H2O2 photocatalysis. CONCLUSION: The data presented in this paper clearly indicated that UV‐visible/ZnO/O2 as an advanced oxidation process provides an efficient treatment alternative for the remediation of MTBE‐contaminated waters. Copyright © 2008 Society of Chemical Industry 相似文献
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