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The measurement of real and apparent power derating of three-phase transformers is important for transformers feeding nonlinear loads. This paper presents a new digital data-acquisition method for measuring derating and reactive power demand of three-phase transformers under full or partial load conditions. The accuracy requirements of the instruments employed (potential, current transformers, shunts, voltage dividers, optocouplers volt- and current meters) are addressed. Application examples demonstrate the usefulness of this new digital data-acquisition method. 相似文献
75.
针对钻井井控作业特点及传统钻井井控仿真系统的不足之处,提出利用多智能体(Agent)技术,建立一种新型的基于Agent的智能化分布式井控仿真模型。利用Agent的自主性、协作性和反应性,使井控设备的操作在任意状况下都能够及时准确地反映各种井控规律及井控现象。对钻井井控仿真多Agent系统模型、各Agent的内部结构、Agent的知识表示方法及Agent间通信方式进行了详细阐述。给出了基于Agent的正常钻井井控仿真训练实例,较好地解决了传统井控仿真系统中灵活性和并发性较差的问题,增强了井控仿真系统的综合训练能力。 相似文献
76.
基于VHDL实现单精度浮点数的加/减法运算 总被引:1,自引:0,他引:1
研究了单精度浮点数加/减法的结构及其设计方法,并在Aldec公司的Active—HDL软件环境下,采用VHDL语言进行设计,并进行了仿真验证,计算精度可以达到10^-7。 相似文献
77.
The long‐term thermal‐oxidative aging behavior of polyamide 6 (PA6) was studied by comparison with the stabilized sample in this work. The variation of mechanical properties of the pure and the stabilized samples of PA6 with aging time at 110°C, 130°C, and 150°C were investigated, respectively. The aging mechanism of PA6 under heat and oxygen was studied in terms of the reduced viscosity, crystallization behavior, dynamic mechanical behavior, and chemical composition through the methods of polarized light microscopy (PLM), differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA), X‐ray photoelectron energy spectrum (XPS), and so on. The results indicated that at the initial stage of aging, the molecular crosslinking reaction of PA6 dominated resulting in the increase of the mechanical strength, reduced viscosity, and the glass transition temperature of the sample. And the molecular degradation dominated in the subsequent aging process resulting in the decrease of the melting temperature, the increase of the crystallinity, and the formation of the oxides and peroxides products. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 相似文献
78.
Sodium sulfonate‐terminated dendritic poly(ester‐amine) (SPEA) was synthesized by sulfonation of acrylic double bond‐terminated dendritic poly(ester‐amine) (APEA) with sodium hydrogen sulfite (NaHSO3) in mixture of diglycol and 2‐butanone under normal pressure. The structure of SPEA was characterized by IR, 1H‐NMR, and elemental analysis. SPEA was water‐soluble. 1.0–40.0% (mass) SPEA aqueous solutions appeared as dilatant fluid. When pH value varied from 1.5 to 12.0, the viscosity of 1–5% (mass) SPEA aqueous solutions changed very small, and the electric conductivity almost kept stable within pH 3.0–10.0. The relationship between the viscosity and the concentration of SPEA water solutions was similar to that of NaCl water solutions. The surface tension of SPEA water solutions was lower than that of polyethylene glycol 2000 water solutions with the same concentration. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 相似文献
79.
Biphenol monoacrylate (AL) was combined with a traditional hindered phenolic‐based binary antioxidant system to form a ternary stabilization system for the purpose of further improving the thermal–oxidative stability of polyamide 6 (PA6). The thermal stabilization effect of the antioxidant AL on PA6 was studied in terms of the reduced viscosity, the chemical structure, the yellow index, and the mechanical properties. The results showed that the antioxidant AL, with the proper chemical structure, could improve the thermal stability of PA6 effectively through a unique bifunctional stabilizing mechanism. The interaction of the molecules of PA6 with the antioxidant AL was investigated. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 相似文献
80.
Associations (dimer or aggregate) of anthracene (An) fluorophores tend to interrupt the monomer emission and reduce the quantum yield (ΦPL); therefore, poly(methyl methacrylate) (PMMA) chain was used in this study to chemically link to anthracene and to block the mutual associations among the anthracene fluorophores. With this aim, the target polymers were prepared by anionic polymerizations with 9,10‐dibromoanthracene/s‐butyllithium as initiating system to proceed polymerizations of methyl methacrylate (MMA) directly or in the presence of 1,1‐diphenylethylene (DPE). Use of DPE before addition of MMA produces stable initiating anionic species and avoids potential side reactions during polymerization; however, it also introduces four β‐phenylene rings around the central anthracene ring, which interfere with the corresponding emission pattern and reduce the ΦPL (32%) value due to potential interactions between phenylene rings and anthracene. On the contrast, polymerization without participation of DPE results in polymer with central anthracene ring directly connected to two PMMA chains, which gives clean vibronic emission pattern with limited association emissions and enhanced ΦPL (52%) value. Physical blending of anthracene by PMMA is less efficient to restrain the associations and results in a film of lower ΦPL (20%). © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 相似文献