Conditions for codeposition of Al and Cr on Ni base superalloys by pack cementation process

被引:52
作者
Xiang, ZD [1 ]
Burnell-Gray, JS [1 ]
Datta, PK [1 ]
机构
[1] Northumbria Univ, Sch Engn, Adv Mat Res Inst, Newcastle Upon Tyne NE1 8ST, Tyne & Wear, England
关键词
D O I
10.1179/026708401101517890
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Both theoretical and experimental studies were carried out to identify pack powder compositions and coating conditions suitable for codeposition of Al and Cr by the pack cementation process. It has been demonstrated that for pack powders containing chloride salts as activators and elemental Al and Cr as source materials, codeposition of Al and Cr occurs when the partial pressures P-AlCl and P-CrCl are comparable or when P-AlCl/P-CrCl is close to one. But, only Al or Cr may be deposited when P-AlCl/P-CrCl is much larger or smaller than one. Pack powder compositions suitable for codeposition of Al and Cr depend very much on the type of activators used. For pack powders containing 25 wt-% of source elements of Al and Cr, codeposition of Al and Cr may occur when the Al content is within the range 1.25-1.90 wt-% for the packs activated by 3 wt-%oNH(4)Cl, and 1.85-1.95 wt-% for the pack activated by 4wt-%CrCl(3)6H(2)O. However, codeposition of At and Cr may be not achievable with pack powders activated by NaCl and CrCl3. Elemental Al and Cr may be used as source materials for codeposition purposes instead of Cr-Al master alloys as conventionally recommended. The coatings formed by codeposition at 1100 degreesC showed a complex structure consisting of three or four major distinctive layers depending on the pack powder composition and coating conditions used, suggesting that the coatings were formed by a sequential deposition mechanism. Both Al and Cr were deposited in the initial and interim stages. However, only Cr was deposited in the final stage, producing a Cr rich top surface layer.
引用
收藏
页码:287 / 294
页数:8
相关论文
共 13 条
[1]   PACK CEMENTATION ALUMINIDE COATINGS ON SUPERALLOYS - CODEPOSITION OF CR AND REACTIVE ELEMENTS [J].
BIANCO, R ;
RAPP, RA .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1993, 140 (04) :1181-1190
[2]  
CHOQUET PA, 1989, MAT SCI ENG A-STRUCT, V121, P413
[3]  
Costa W. D., 1994, J ELECTROCHEM SOC, V141, P1464
[4]   CHEMSAGE - A COMPUTER-PROGRAM FOR THE CALCULATION OF COMPLEX CHEMICAL-EQUILIBRIA [J].
ERIKSSON, G ;
HACK, K .
METALLURGICAL TRANSACTIONS B-PROCESS METALLURGY, 1990, 21 (06) :1013-1023
[5]   SIMULTANEOUS CHROMIZING-ALUMINIZING COATING OF LOW-ALLOY STEELS BY A HALIDE-ACTIVATED, PACK-CEMENTATION PROCESS [J].
GEIB, FD ;
RAPP, RA .
OXIDATION OF METALS, 1993, 40 (3-4) :213-228
[6]   CHROMALUMINIZING OF NICKEL AND ITS ALLOYS [J].
GODLEWSKA, E ;
GODLEWSKI, K .
OXIDATION OF METALS, 1984, 22 (3-4) :117-131
[7]   MECHANISMS OF FORMATION OF DIFFUSION ALUMINIDE COATINGS ON NICKEL-BASE SUPERALLOYS [J].
GOWARD, GW ;
BOONE, DH .
OXIDATION OF METALS, 1971, 3 (05) :475-&
[8]   ANALYSES OF THE GASEOUS SPECIES IN HALIDE-ACTIVATED CEMENTATION COATING PACKS [J].
KUNG, SC ;
RAPP, RA .
OXIDATION OF METALS, 1989, 32 (1-2) :89-109
[9]  
MEVREL R, 1986, MAT SCI TECHNOL, V87, P367
[10]  
Walsh P. N., 1973, P 4 INT C CHEM VAP D, P147