Phase transformation behavior of nanocrystalline Ni-W-P alloys containing various W and P contents

被引:45
|
作者
Balaraju, J. N. [1 ]
Kalavati [2 ]
Manikandanath, N. T. [1 ]
Grips, V. K. William [1 ]
机构
[1] CSIR Natl Aerosp Labs, Surface Engn Div, Bangalore 560017, Karnataka, India
[2] CSIR Natl Aerosp Labs, Div Mat Sci, Bangalore 560017, Karnataka, India
来源
SURFACE & COATINGS TECHNOLOGY | 2012年 / 206卷 / 10期
关键词
Electroless; Ternary Ni-W-P; XRD DSC; Phase transformation; NICKEL-PHOSPHORUS DEPOSITS; CRYSTALLIZATION KINETICS; ELECTROLESS DEPOSITION; THERMAL-STABILITY;
D O I
10.1016/j.surfcoat.2011.11.024
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
In the present investigation, electroless (EL) ternary Ni-W-P coatings were prepared using hypophosphite based alkaline bath by varying sodium tungstate as tungsten source (5-80 g/L). Maximum amount of W incorporation (8.2 +/- 1 wt.%) was obtained when the bath contained about 20 g/L of tungsten source. At very high concentrations of W source in the bath the deposit contained about 4 wt.% W and 2 wt.% P. All the as-deposited ternary coatings exhibited nodular surface morphology. X-ray diffractograms (XRD) obtained for as-deposited EL NiWP alloys indicated that crystallinity of the coatings increased with decrease in phosphorus content. Calculated grain size for the deposits varied from 1.2 to 12.7 nm when the tungsten source varied from 5 to 80 g/L in the bath. Higher crystallization temperatures were obtained due to W codeposition in NiP matrix. Presence of metastable phases such as Ni5P2 and NiP apart from stable Ni and Ni3P was identified for the heat treated deposits (400 degrees C/1 h) containing lower amount of W and higher amount of P. Whereas other ternary deposits after the heat treatment predominantly revealed face centered cubic (f.c.c.) Ni (111) peak. Activation energy for the crystallization of all the alloys has been carried out by modified Kissinger method. Microhardness measurements were carried out on all the deposits isothermally heat treated at 600 degrees C for 1 h. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:2682 / 2689
页数:8
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