材料保护
材料保護
재료보호
MATERIALS PROTECTION
2010年
3期
34-37
,共4页
王绍华%王军丽%徐瑞东%章俞之
王紹華%王軍麗%徐瑞東%章俞之
왕소화%왕군려%서서동%장유지
双脉冲%Ni-W-P/CeO2-SiO2%纳米复合材料%电沉积%脉冲时间%沉积速率%显微硬度
雙脈遲%Ni-W-P/CeO2-SiO2%納米複閤材料%電沉積%脈遲時間%沉積速率%顯微硬度
쌍맥충%Ni-W-P/CeO2-SiO2%납미복합재료%전침적%맥충시간%침적속솔%현미경도
dual pulse%Ni-W-P/CeO2-SiO2%nanocomposite%electrodeposition%microhardness%working time%deposition rate
通过Ni,W,P与CeO2,SiO2纳米颗粒的双脉冲电沉积,在普通碳钢表面制备了Ni-W-P/CeO2-SiO2纳米复合材料沉积层.在正、反向脉冲占空比(10%,30%)和正、反向脉冲平均电流密度(15.0,1.5 A/dm2)恒定下,研究了正、反向脉冲时间对纳米复合材料电沉积的影响.采用能谱、硬度测试和扫描电镜等方法,对纳米复合材料沉积层的化学组成、沉积速率、显微硬度和表面形貌进行了表征.结果表明:当正、反向脉冲时间分别控制在300 ms和40 ms时,Ni-W-P基质金属轮廓清晰,晶粒细小而均匀,CeO2和SiO2纳米颗粒在基质金属中均匀弥散分布;沉积层的化学组成(质量分数)为:70.89%Ni,9.89%W,8.59%P,7.35%CeO2,2.81%SiO2;沉积速率为45.1μm/h,显微硬度为706 HV.
通過Ni,W,P與CeO2,SiO2納米顆粒的雙脈遲電沉積,在普通碳鋼錶麵製備瞭Ni-W-P/CeO2-SiO2納米複閤材料沉積層.在正、反嚮脈遲佔空比(10%,30%)和正、反嚮脈遲平均電流密度(15.0,1.5 A/dm2)恆定下,研究瞭正、反嚮脈遲時間對納米複閤材料電沉積的影響.採用能譜、硬度測試和掃描電鏡等方法,對納米複閤材料沉積層的化學組成、沉積速率、顯微硬度和錶麵形貌進行瞭錶徵.結果錶明:噹正、反嚮脈遲時間分彆控製在300 ms和40 ms時,Ni-W-P基質金屬輪廓清晰,晶粒細小而均勻,CeO2和SiO2納米顆粒在基質金屬中均勻瀰散分佈;沉積層的化學組成(質量分數)為:70.89%Ni,9.89%W,8.59%P,7.35%CeO2,2.81%SiO2;沉積速率為45.1μm/h,顯微硬度為706 HV.
통과Ni,W,P여CeO2,SiO2납미과립적쌍맥충전침적,재보통탄강표면제비료Ni-W-P/CeO2-SiO2납미복합재료침적층.재정、반향맥충점공비(10%,30%)화정、반향맥충평균전류밀도(15.0,1.5 A/dm2)항정하,연구료정、반향맥충시간대납미복합재료전침적적영향.채용능보、경도측시화소묘전경등방법,대납미복합재료침적층적화학조성、침적속솔、현미경도화표면형모진행료표정.결과표명:당정、반향맥충시간분별공제재300 ms화40 ms시,Ni-W-P기질금속륜곽청석,정립세소이균균,CeO2화SiO2납미과립재기질금속중균균미산분포;침적층적화학조성(질량분수)위:70.89%Ni,9.89%W,8.59%P,7.35%CeO2,2.81%SiO2;침적속솔위45.1μm/h,현미경도위706 HV.
Ni-W-P/CeO2-SiO2 nanocomposite coatings were prepared on the surface of carbon steel by dual pulse co-deposition of Ni, W, P and particles of nano-CeO2 and nano-SiO2. The influence of positive and negative pulse working time on the electredeposition of the nanocomposite was researched at constant positive and negative pulse duty cycles of 10% and 30 % and constant average pulse current densities of 15.0 A/dm2 and 1.5 A/dm2. The microhardness of the coatings was measured by using a microhardness meter, while the composition, deposi-tion rate and surface morphology of the coatings were analyzed by means of scanning electron microscopy and energy dispersive spectrometry. Results show that when the positive and negative pulse working time is controlled at 300 ms and 40 ms respective-ly, the resulting nanocomposite coating possesses clear outline of Ni-W-P matrix metal crystallite, fine and uniform crystals, as well as uniform distribution of nano-CeO2 and nano-SiO2 parti-cles within the matrix metal. The chemical composition of the coating was determined to be 70. 89% Ni, 9. 89% W, 8.59% P, 7.35% CeO2 and 2.81% SiO2(mass fraction) , and the dep-osition rate and microhardness of the coating were determined to be 45.1 μm/h and 706 HV.