表面技术
錶麵技術
표면기술
Surface Technology
2015年
10期
1-6,15
,共7页
欧阳珂宁%赵景茂%谢雄%付文景
歐暘珂寧%趙景茂%謝雄%付文景
구양가저%조경무%사웅%부문경
镁合金%微弧氧化%电源模式%电泳%Y2 O3%耐蚀性
鎂閤金%微弧氧化%電源模式%電泳%Y2 O3%耐蝕性
미합금%미호양화%전원모식%전영%Y2 O3%내식성
magnesium%micro arc oxidation( MAO)%power mode%electrophoresis%Y2 O3%corrosion resistance
目的:采用含颗粒电解液是目前最常用制备具有更佳性能微弧氧化膜层的方法之一,主要研究微弧氧化过程中颗粒掺杂与电源模式的关系。方法在Y2 O3颗粒质量浓度为0~10 g/L的电解液中,分别以单极脉冲和双极脉冲电源模式制备一系列微弧氧化膜层,并从表面形貌、表面元素组成、截面形貌及耐蚀性能等方面对膜层进行综合评价。结果分散在电解液中的颗粒带有负电荷,在微弧氧化过程中发生电泳现象。在单极脉冲电源模式下,颗粒受正电吸引而发生定向迁移,在试样附近聚集并且吸附至表面,从而参与下一步的微弧氧化膜层形成过程。随着电解液中颗粒浓度的提高,分散在微弧氧化膜层表面的Y2 O3颗粒数量增多,膜层表面的Y元素含量增加,膜层变得致密,耐蚀性能因而提高。在双极脉冲电源作用下,由于电场的交替变化,颗粒难以聚集在试样周围,颗粒的掺杂只能通过随机熔融包覆进行,因而参与到微弧氧化过程中的颗粒数量较少。结论颗粒掺杂受电场力影响,在单极脉冲模式下,颗粒的掺杂浓度对膜层的性能影响明显;在双极脉冲电源模式下,负向电流的引入不利于颗粒掺杂至氧化膜层,颗粒的掺杂浓度对膜层的性能影响不明显。
目的:採用含顆粒電解液是目前最常用製備具有更佳性能微弧氧化膜層的方法之一,主要研究微弧氧化過程中顆粒摻雜與電源模式的關繫。方法在Y2 O3顆粒質量濃度為0~10 g/L的電解液中,分彆以單極脈遲和雙極脈遲電源模式製備一繫列微弧氧化膜層,併從錶麵形貌、錶麵元素組成、截麵形貌及耐蝕性能等方麵對膜層進行綜閤評價。結果分散在電解液中的顆粒帶有負電荷,在微弧氧化過程中髮生電泳現象。在單極脈遲電源模式下,顆粒受正電吸引而髮生定嚮遷移,在試樣附近聚集併且吸附至錶麵,從而參與下一步的微弧氧化膜層形成過程。隨著電解液中顆粒濃度的提高,分散在微弧氧化膜層錶麵的Y2 O3顆粒數量增多,膜層錶麵的Y元素含量增加,膜層變得緻密,耐蝕性能因而提高。在雙極脈遲電源作用下,由于電場的交替變化,顆粒難以聚集在試樣週圍,顆粒的摻雜隻能通過隨機鎔融包覆進行,因而參與到微弧氧化過程中的顆粒數量較少。結論顆粒摻雜受電場力影響,在單極脈遲模式下,顆粒的摻雜濃度對膜層的性能影響明顯;在雙極脈遲電源模式下,負嚮電流的引入不利于顆粒摻雜至氧化膜層,顆粒的摻雜濃度對膜層的性能影響不明顯。
목적:채용함과립전해액시목전최상용제비구유경가성능미호양화막층적방법지일,주요연구미호양화과정중과립참잡여전원모식적관계。방법재Y2 O3과립질량농도위0~10 g/L적전해액중,분별이단겁맥충화쌍겁맥충전원모식제비일계렬미호양화막층,병종표면형모、표면원소조성、절면형모급내식성능등방면대막층진행종합평개。결과분산재전해액중적과립대유부전하,재미호양화과정중발생전영현상。재단겁맥충전원모식하,과립수정전흡인이발생정향천이,재시양부근취집병차흡부지표면,종이삼여하일보적미호양화막층형성과정。수착전해액중과립농도적제고,분산재미호양화막층표면적Y2 O3과립수량증다,막층표면적Y원소함량증가,막층변득치밀,내식성능인이제고。재쌍겁맥충전원작용하,유우전장적교체변화,과립난이취집재시양주위,과립적참잡지능통과수궤용융포복진행,인이삼여도미호양화과정중적과립수량교소。결론과립참잡수전장력영향,재단겁맥충모식하,과립적참잡농도대막층적성능영향명현;재쌍겁맥충전원모식하,부향전류적인입불리우과립참잡지양화막층,과립적참잡농도대막층적성능영향불명현。
ABSTRACT:Objective Particles-containing electrolytes are commonly employed as one of the most important methods to produce better micro arc oxidation coatings. The relationship between the MAO coating property and power mode used was described in this paper. Methods Ceramic coatings were produced by micro arc oxidation in electrolyte containing various particles concentration in unipolar and bipolar power mode, respectively. The properties of coatings were evaluated in respect of surface morphologies, ele-mentary distribution, cross-section morphologies, and corrosion resistance. Results The particles dispersed in electrolyte were nega-tively charged, and particles-doping during MAO process was driven by electrophoresis. Particles were directly migrated to the anode in unipolar power mode, accumulating around the sample and adsorbed to the sample surface to participate in the formation process of the micro arc oxidation coatings. With increasing particles concentration in electrolyte, the amount of Y2 O3 particles and the con-tent of Y element on the surface of the MAO coatings increased, enhancing the density and corrosion resistance of the coatings. However, only a few particles doped in MAO coating as the power mode turned to bipolar due to alternate variations of electric field. The influences of particles concentration on the surface and cross-section morphologies, surface elementary distribution, cor-rosion resistance of MAO coatings were not apparent. Conclusion Particles-doping was affected by electric force. In unipolar power mode, the doping concentration of particles had obvious effect on the performance of the coatings, whereas in the bipolar power mode, introduction of negative current had adverse effect on the doping of particles into the oxidation coatings, and the doping con-centration of particles had no obvious effect on the coating performance.