Corrosion of high alloy steels and Fe-Cr-alloys beneath deposits from waste incinerator plants

被引:23
作者
Spiegel, M [1 ]
Schroer, G [1 ]
Grabke, HJ [1 ]
机构
[1] Max Planck Inst Eisenforsch GmbH, D-40237 Dusseldorf, Germany
来源
HIGH TEMPERATURE CORROSION AND PROTECTION OF MATERIALS 4, PTS 1 AND 2 | 1997年 / 251-2卷
关键词
waste incineration atmospheres; deposits; hot corrosion; sulfate melts; basic fluxing; acidic fluxing; heavy metal compounds; active oxidation;
D O I
10.4028/www.scientific.net/MSF.251-254.527
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 corrosion of high alloy steels in N-2-O-2-HCl-SO2 and of Fe-Cr-alloys in N-2-O-2-HCl was investigated in exposures beneath different kinds of deposits from waste incineration plants at 600 degrees C. In both kinds of deposits the formation of a ph and Zn containing sulfate melt was observed. The main corrosion process of high alloy steels is 'hot corrosion' by a sulfate melt. In N-2-O-2 basic fluxing of the oxide scales occurs by formation of PbCrO4 on Cr2O3 forming alloys and zinc-rich spinel on FeCr2O4 forming materials. In N-2-O-2-SO2 acidic fluxing was observed, whereas Cr2O3-scales are resistent. In N-2-O-2-HCl severe corrosion. occurs due to the formation of a sulfate-chloride eutectic by reaction of HCl with sulfates in the deposits to (K,Na)Cl. The (K,Na)CI reacts with the oxide scales to form Cl-2, which initiates 'active oxidation' by metal-chloride formation at the metal\scale interface. Addition of SO2 leads to retardation of the corrosion process, because the sulfates are stabilized by SO2 and acidic fluxing was observed. The Fe-Cr alloys show active oxidation due to the formation of ZnCl2 and PbCl2 in the deposits and also basic fluxing by ZnO.
引用
收藏
页码:527 / 534
页数:8
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