Mechanisms involved by reactive elements upon high temperature chromia scale growth

被引:32
作者
Chevalier, S
Bonnet, G
Borchardt, G
Colson, JC
Larpin, JP
机构
[1] Univ Bourgogne, UMR 5613 CNRS, Lab Rech React Solides, FR-21078 Dijon, France
[2] Univ Rochelle, Lab Eudes Mat Millieux Agressifs, FR-17042 Nantes 01, France
[3] Tech Univ Clausthal, Inst Allgemeine Met, DE-38678 Clausthal Zellerfeld, Germany
来源
HIGH TEMPERATURE CORROSION AND PROTECTION OF MATERIALS 5, PTS 1 AND 2 | 2001年 / 369-3卷
关键词
chromia growth mechanisms; chromia-former alloys; Nd2O3; Pr2O3; reactive element effects; SM2O3; Y2O3; Yb2O3;
D O I
10.4028/www.scientific.net/MSF.369-372.327
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The influence Of Y2O3, Pr2O3, Nd2O3, Sm2O3 and Yb2O3 coatings on Fe-30Cr alloy oxidation behaviour was investigated at 1000 degreesC in air under atmospheric pressure. Isothermal exposures indicated that the Y2O3 coating was the most protective after 100 hours. Pr2O3. Nd2O3 and Sm2O3 coatings were less effective, but the less beneficial effect was observed when Yb2O3 coating was applied onto the Fe-Cr alloy surface. Two-stage oxidation experiments in O-16(2) and then O-18(2) were performed to get information about the chromia growth phenomena with and without reactive elements. The O-18-tracer distribution was determined by secondary ion mass spectrometry (SIMS) and sputtered neutral mass spectrometry (SNMS). The experiments performed on uncoated samples clearly demonstrated that chromia growth mechanism was controlled by chromium cationic diffusion, whereas on reactive element coated samples the external diffusion of chromium ions was not predominant.
引用
收藏
页码:327 / 336
页数:10
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