中国电机工程学报
中國電機工程學報
중국전궤공정학보
ZHONGGUO DIANJI GONGCHENG XUEBAO
2012年
13期
138-143
,共6页
兰莉%吴建东%纪哲强%王俏华%李酷%肖登明%尹毅
蘭莉%吳建東%紀哲彊%王俏華%李酷%肖登明%尹毅
란리%오건동%기철강%왕초화%리혹%초등명%윤의
低密度聚乙烯%氧化硅%纳米复合介质%击穿强度%威布尔(Weibull)分布
低密度聚乙烯%氧化硅%納米複閤介質%擊穿彊度%威佈爾(Weibull)分佈
저밀도취을희%양화규%납미복합개질%격천강도%위포이(Weibull)분포
low density polyethylene(LDPE)%silica%nanocomposite dielectrics%breakdown strength%Weibull distribution
聚合物纳米复合介质的击穿强度与纳米填充颗粒的质量分数、粒径和表面处理密切相关。以不同表面处理的纳米SiO2颗粒为填料,制备了不同填充质量分数、粒径的纳米SiO2/低密度聚乙烯(low density polyethylene,LDPE)复合介质,测试了其在交流、直流正极性和直流负极性3种不同类型电场下的击穿场强。结果表明:在所研究范围内,填充纳米SiO2颗粒可以提高低密度聚乙烯的击穿场强,并且随着填充质量分数的增加,复合介质的击穿场强有升高的趋势。纳米颗粒填充质量分数相同时,在12~16am粒径下,复合介质的击穿场强有随纳米SiO2粒径的升高而降低的趋势;在7nm小粒径下,可能由于纳米颗粒容易团聚,导致击穿场强较粒径大时要低。另外,纳米SiO2颗粒表面经疏水性处理后,能够有效提高复合介质的击穿场强。
聚閤物納米複閤介質的擊穿彊度與納米填充顆粒的質量分數、粒徑和錶麵處理密切相關。以不同錶麵處理的納米SiO2顆粒為填料,製備瞭不同填充質量分數、粒徑的納米SiO2/低密度聚乙烯(low density polyethylene,LDPE)複閤介質,測試瞭其在交流、直流正極性和直流負極性3種不同類型電場下的擊穿場彊。結果錶明:在所研究範圍內,填充納米SiO2顆粒可以提高低密度聚乙烯的擊穿場彊,併且隨著填充質量分數的增加,複閤介質的擊穿場彊有升高的趨勢。納米顆粒填充質量分數相同時,在12~16am粒徑下,複閤介質的擊穿場彊有隨納米SiO2粒徑的升高而降低的趨勢;在7nm小粒徑下,可能由于納米顆粒容易糰聚,導緻擊穿場彊較粒徑大時要低。另外,納米SiO2顆粒錶麵經疏水性處理後,能夠有效提高複閤介質的擊穿場彊。
취합물납미복합개질적격천강도여납미전충과립적질량분수、립경화표면처리밀절상관。이불동표면처리적납미SiO2과립위전료,제비료불동전충질량분수、립경적납미SiO2/저밀도취을희(low density polyethylene,LDPE)복합개질,측시료기재교류、직류정겁성화직류부겁성3충불동류형전장하적격천장강。결과표명:재소연구범위내,전충납미SiO2과립가이제고저밀도취을희적격천장강,병차수착전충질량분수적증가,복합개질적격천장강유승고적추세。납미과립전충질량분수상동시,재12~16am립경하,복합개질적격천장강유수납미SiO2립경적승고이강저적추세;재7nm소립경하,가능유우납미과립용역단취,도치격천장강교립경대시요저。령외,납미SiO2과립표면경소수성처리후,능구유효제고복합개질적격천장강。
The breakdown strength of polymer nanocomposite is related to the properties of nano-additive, such as doping concentration, particle size and surface treatment. Specimen with different doping concentration, particle size and particle surface treatment were made to test the breakdown strength under AC, positive DC and negative DC voltage, respectively. It is shown that in the context of this study, doping nano-SiO2 can increase the breakdown strength of low density polyethylene(LDPE); and the breakdown strength of nano-SiO2/LDPE composite increases with the increasing of doping concentration. Under the same doping concentration, when particle size is between 12 nm and 16 nm, the breakdown strength of nanocomposite decreases with the increasing of particle size. When particle size is 7 nm, the breakdown strength is smaller than that of the bigger particle size, which is probably caused by the coalescence of 7nm nano-SiO2 particles. Besides, hydrophobic surface treatment of nano-SiO2 particles can enhance the breakdown strength of nanocomposite.