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电压稳定剂改善聚乙烯共混材料绝缘性能的研究 被引量:5
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作者 陈向荣 玉林威 +3 位作者 刘海燕 戴超 魏作君 周浩 《西安交通大学学报》 EI CAS CSCD 北大核心 2019年第12期87-96,共10页
为了开发新一代可回收电缆材料,提升其绝缘性能,选取间氨基苯硼酸、2-甲氧基-5-吡啶硼酸和间氨基苯甲酸3种新型电压稳定剂添加入聚乙烯共混物中,分析其对聚乙烯共混物绝缘性能的改善作用及机理。采用溶液法将质量分数为1%的电压稳定剂... 为了开发新一代可回收电缆材料,提升其绝缘性能,选取间氨基苯硼酸、2-甲氧基-5-吡啶硼酸和间氨基苯甲酸3种新型电压稳定剂添加入聚乙烯共混物中,分析其对聚乙烯共混物绝缘性能的改善作用及机理。采用溶液法将质量分数为1%的电压稳定剂添加入含质量分数为10%高密度聚乙烯(HDPE)的低密度聚乙烯(LDPE)共混材料,通过热压法制备试样,利用红外光谱、差式扫描量热法、X射线衍射、电树枝起始实验、直流电导率和空间电荷测量对材料进行物理化学分析和电气性能测试。研究结果表明,聚乙烯共混提升了热稳定性和结晶度,添加电压稳定剂后进一步提升了共混物的结晶度,对共混物的熔融特性无明显影响。添加了电压稳定剂的共混物的电树枝起始电压均明显提高,间氨基苯甲酸共混物的电树枝起始电压比LDPE/HDPE共混物提高了47%。电压稳定剂对共混物的直流电导率作用明显,间氨基苯甲酸能够明显降低共混物的直流电导率。3种电压稳定剂对共混物的空间电荷积累具有明显的抑制作用,且添加了间氨基苯硼酸的共混物具有最少的空间电荷积累。陷阱能级和视在迁移率计算发现,添加了电压稳定剂的共混物中浅陷阱密度增加,视在电荷迁移率增大,有利于抑制材料中空间电荷的积累。实验结果可为新一代环保电缆的开发提供一定参考。 展开更多
关键词 聚乙烯 电压稳定剂 电树枝 空间电荷 电导率
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涡轮转子叶尖泄漏涡涡核稳定性及控制 被引量:7
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作者 魏佐君 段文华 +2 位作者 乔渭阳 刘建 韩品连 《航空动力学报》 EI CAS CSCD 北大核心 2018年第9期2139-2149,共11页
以GE-E3第一级涡轮转子为研究对象,对转子叶尖泄漏涡涡核破碎特征和稳定性机理进行了分析和归纳。研究表明:叶尖泄漏涡涡核破碎的动力是离心不稳定性;发生失稳后,涡核区域迅速膨胀,形成低速的回流区;涡核的稳定性取决于螺旋因子和逆压... 以GE-E3第一级涡轮转子为研究对象,对转子叶尖泄漏涡涡核破碎特征和稳定性机理进行了分析和归纳。研究表明:叶尖泄漏涡涡核破碎的动力是离心不稳定性;发生失稳后,涡核区域迅速膨胀,形成低速的回流区;涡核的稳定性取决于螺旋因子和逆压梯度两个因素。然后,从涡核稳定性的角度开展了叶尖泄漏损失控制的研究,计算表明:叶尖叶型的负荷前移能够减少叶片尾缘附近间隙内的横向压力梯度;吸力面喉部位置以后型线拉直能够减少喉道后的扩压系数;通过这两个措施生成的新叶片能够有效地减弱叶尖泄漏涡,抑制涡核的不稳定性,减少叶尖泄漏流损失。 展开更多
关键词 涡轮 叶尖泄漏涡 涡核稳定性 涡核破碎 稳定性控制 气动损失
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刮削作用对涡轮转子机匣通道涡形成的影响 被引量:2
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作者 魏佐君 乔渭阳 +1 位作者 段文华 刘建 《航空动力学报》 EI CAS CSCD 北大核心 2018年第7期1695-1704,共10页
采用数值方法求解耦合剪切应力输运(SST)湍流模型的雷诺平均Navier-Stokes方程组,研究了不同间隙尺寸下GE-E3高压涡轮第一级转子内刮削作用对机匣通道涡形成和发展的影响。通过与轮毂通道涡结构的对比,发现机匣通道涡层次结构与经典二... 采用数值方法求解耦合剪切应力输运(SST)湍流模型的雷诺平均Navier-Stokes方程组,研究了不同间隙尺寸下GE-E3高压涡轮第一级转子内刮削作用对机匣通道涡形成和发展的影响。通过与轮毂通道涡结构的对比,发现机匣通道涡层次结构与经典二次流理论存在明显的差异,并对该差异形成的原因进行了深入探索。结果表明:叶顶对机匣边界层的刮削作用在机匣通道涡的形成过程中占主导作用,刮削作用使得流向叶片吸力面的来流机匣边界层在交汇点区域从内层向外层卷起,形成层次结构相反的机匣通道涡;叶顶浸入比值是影响转子机匣通道涡形成的重要参数,随着比值的增大,机匣通道涡损失先增大后减小;只有在间隙尺寸较大情况下,叶尖间隙的"抽吸作用"才能抑制机匣通道涡的发展。 展开更多
关键词 涡轮转子 机匣通道涡 刮削作用 二次流 叶尖间隙尺寸
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Tip-leakage flow loss reduction in a two-stage turbine using axisymmetric-casing contouring 被引量:9
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作者 wei zuojun Qiao weiyang +2 位作者 Shi Peijie Chen Pingping Zhao Lei 《Chinese Journal of Aeronautics》 SCIE EI CAS CSCD 2014年第5期1111-1121,共11页
In order to reduce the losses caused by tip-leakage flow, axisymmetric contouring is applied to the casing of a two-stage unshrouded high pressure turbine(HPT) of aero-engine in this paper. This investigation focuses ... In order to reduce the losses caused by tip-leakage flow, axisymmetric contouring is applied to the casing of a two-stage unshrouded high pressure turbine(HPT) of aero-engine in this paper. This investigation focuses on the effects of contoured axisymmetric-casing on the blade tipleakage flow. While the size of tip clearance remains the same as the original design, the rotor casing and the blade tip are obtained with the same contoured arc shape. Numerical calculation results show that a promotion of 0.14% to the overall efficiency is achieved. Detailed analysis indicates that it reduces the entropy generation rate caused by the complex vortex structure in the rotor tip region, especially in the tip-leakage vortex. The low velocity region in the leading edge(LE) part of the tip gap is enlarged and the pressure side/tip junction separation bubble extends much further away from the leading edge in the clearance. So the blocking effect of pressure side/tip junction separation bubble on clearance flow prevents more flow on the tip pressure side from leaking to the suction side, which results in weaker leakage vortex and less associated losses. 展开更多
关键词 泄漏流动 轴对称 涡轮机 轮廓 损失 壳体 叶尖 端部间隙
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Effects of preparation methods of support on the properties of nickel catalyst for hydrogenation of m-dinitrobenzene
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作者 LIU Yingxin wei zuojun +1 位作者 CHEN Jixiang ZHANG Jiyan 《Frontiers of Chemical Science and Engineering》 SCIE EI CSCD 2007年第3期287-291,共5页
Using tetraethyl orthosilicate(TEOS)as the pre-cursor of silica,the silica aerogel and xerogel,which were used as supports of nickel-based catalysts for liquid hydroge-nation of m-dinitrobenzene to m-phenylenediamine,... Using tetraethyl orthosilicate(TEOS)as the pre-cursor of silica,the silica aerogel and xerogel,which were used as supports of nickel-based catalysts for liquid hydroge-nation of m-dinitrobenzene to m-phenylenediamine,were prepared by the sol-gel method combined with supercritical drying(SCD)and conventional drying,respectively.Then,a series of nickel-based catalyst samples supported on these supports were prepared by the incipient wetness impregna-tion method with an aqueous solution of nickel nitrate as well as lanthanum nitrate as impregnation liquids.Based on the characterization results of nitrogen adsorption-desorption(BET),X-ray diffraction(XRD),temperature programmed reduction(TPR),temperature-programmed desorption of hydrogen(H2-TPD),and catalytic activity evaluation,the physico-chemical properties and catalytic performances of the catalysts were investigated.The results show that the nickel crystallites on the binary nickel catalyst using silica aerogel as support are of smaller particle size.However,com-pared with the sample supported on silica xerogel,the nickel catalyst supported on the silica aerogel exhibits lower activity and selectivity for the hydrogenation of m-dinitrobenzene because it has a lesser amount of active sites and weaker absorption ability to reactants caused by sintering of the nickel crystallites.The addition of promoter La2O3 could increase the activity and selectivity of the catalysts.Among all the nickel-based catalyst samples prepared,the La2O3 promoted ternary nickel-based catalyst supported on silica xerogel exhibits the highest activity and selectivity for the hydrogenation of m-dinitrobenzene to m-phenylenediamine,which could be attributed to its highest active surface area and appropriate absorption strength to reactants.Over this prom-ising catalyst,the conversion of m-dinitrobenzene and the yield of m-phenylenediamine could reach 97.0%and 93.1%,respectively,under proper reaction conditions of hydrogen pressure 2.6 MPa,temperature 373 K,and reaction time 1 h. 展开更多
关键词 sol-gel method supercritical drying nickel-based catalyst lanthanum oxide HYDROGENATION m-dinitrobenzene M-PHENYLENEDIAMINE
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