Charge Storage Performance of Polyetherimide Ultem®1000-Influence of Secondary Antioxidants and Purification

被引:13
作者
Erhard, Dominik P. [1 ,2 ]
Giesa, Reiner [1 ,2 ]
Altstaedt, Volker [3 ]
Schmidt, Hans-Werner [1 ,2 ]
机构
[1] Univ Bayreuth, Bayreuth Inst Macromol Res, BIMF, D-95440 Bayreuth, Germany
[2] Univ Bayreuth, Bayreuth Ctr Colloids & Interfaces BZKG, D-95440 Bayreuth, Germany
[3] Univ Bayreuth, Polymer Engn & Bayreuth Inst Macromol Res BIMF, D-95440 Bayreuth, Germany
关键词
antioxidants; corona charging; electrets; degradation; high-performance polymers; ISOTACTIC POLYPROPYLENE; MOLECULAR-MECHANISM; ELECTRET PROPERTIES; H2O DIFFUSION; WATER; NUCLEATION; POLYIMIDES; ADDITIVES; DYNAMICS;
D O I
10.1002/app.30823
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The performance of a polymeric electret material depends on many parameters, and besides chemical structure, charging conditions, and application temperature, other factors, such as grade, manufacturer, processing history, and additive package, are critical. Commercial polyetherimide (PEI) Ultem (R) 1000 films exhibited satisfying electret properties as revealed by an isothermal potential decay (ITPD) to 75% of the initial surface charge after 24 h at 90 degrees C. It was found that after purification by reprecipitation this value drops to 34% and that the same PEI synthesized by two different methods revealed to be a very poor electret with charge retention of almost zero. Assuming that an additive in the commercial material might be responsible for this behavior, we identified an organophosphonite which is commonly used as antioxidant in high-temperature polymers. We incorporated this additive by melt compounding into purified PEI and found a dramatic increase in charge retention to 79% of the initial charge at an additive load level of 0.5 wt %. By immersing Ultem (R) 1000 films in water, the electret behavior was further improved and almost 100% charge retention was achieved. (C) 2009 Wiley Periodicals, Inc. J Appl Polym Sci 115:1247-1255, 2010
引用
收藏
页码:1247 / 1255
页数:9
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