Figure 2 (a), (b) and (c) shows that the XRD results of coated TiCoCr, TiN and TiO2 on 316L SS specimens. The samples were analyzed over a range from 10° to 80°. Figure 2 (a) shows the sharp peaks and proves the formation of Titanium at 35.93, 40.142 and 53.01, Cobalt at 62.925, 75.867 and Chromium at 44.244, 38.386. The crystal plane index was found for Titanium, Cobalt and Chromium such as (101), (110) and (100) and it was evident in JCPDS file number 653362, 897373, 892871, respectively. Owing to their minimum weight percentage proportion, the intensity of diffraction peaks was low for Co and Cr corresponds with titanium. Similarly, Fig. 2 (b) shows the characterization of sharp peaks and proves the formation of TiN located at 36.675, 42.797, 61.857 and 74.445. The crystal plane index was found for TiN such as (111), (200), (220), (311) and it was evident in JCPDS file number 870633. Similar indications were noted in Fig. 2 (c) the XRD graph of TiO2 coated surface on 316L SS. The strong 2 theta peaks at 25.102, 36.485 and 48.912 equal to the miller indices plane (101), (004) and (200) were confirms the presence of Ti and O molecules in the coated surface. Thus the coating on 316L SS is effective, which produce considerable amount of dopants on the substrate. Figure 3 (a), (b) and (c) shows the EDAX spectrum of TiCoCr, TiN and TiO2 coated 316L steel specimens. It is noted that the spectrum for TiCoCr gives the atoms of Co, Cr and Ti with different keV values.
Table 3 shows the micro abrasion properties such as wear volume and specific wear rate of various coating done on stainless steel substrate. The incremental in wear volume of 71% and 261.8% was noted for 1 N and 1.5N loading conditions. This notably higher wear volume and specific wear rate was the reason for adhesion and three body abrasion wear loss mechanism. Thus higher wear loss is evidenced at higher loading condition. Figure 4 shows the SEM worn surface tracks of uncoated 316L SS specimens at different loading conditions.
Table 3
Wear behavior of uncoated 316L SS substrate
Coating time ( min) | Load (N) | Wear volume ×10− 5 m3 | Specific wear rate ×10− 14 mm3/Nm |
Uncoated | 0.5 | 18.54 | 1.027 |
1 | 31.72 | 0.881 |
1.5 | 67.08 | 0.931 |
Table 4 shows the wear volume and specific wear rate of TiN coated 316L SS substrate with different loading conditions and coating time. It is noted that the wear volume of 16.5, 12.8 and 10x10− 5 mm3 was observe for 1.5N load at 30, 60 and 90 min coating time respectively. Table 5 shows the TiO2 coating on 316L SS at 0.5, 1.0 and 1.5N loads and 30, 60 and 90 min coating time. The wear volume and wear rate is significantly higher for TiO2 coating by 30 and 60 min. This increment in the wear volume and specific wear rate is the reason for no strengthening mechanism of TiO2 on steel surface. Moreover, there is no evidence for pitting marks and dimple, which confirms the high wear resistance behavior of material even after the shear force is applied.
Table 6 shows the wear volume and war rate is significantly reduced for TiCoCr coating by 30, 60 and 90 min. On comparing to the uncoated surface the TiCoCr coated steel gives very high wear resistance. A very lowest wear volume of 7.372×10− 5m3 is observed for coating done for 90 min at 0.5N loading condition. Moreover in 90 min coating time all the loading values gives improved abrasion resistance. This is because of higher penetration time of Co and Cr atoms onto the surface of steel. The addition of Cr and Co may produce fine intermetallic on the substrate’s surface, thus giving higher wear resistance. Both the Co and Cr may reinforce into the surfaces of steel and produced high surface rigidity and also giving lesser 3 body abraded particle and wavy structure.
Table 4
Wear behavior of TiN coated 316L SS substrate
Coating time ( min) | Load (N) | Wear volume ×10− 5 m3 | Specific wear rate ×10− 14 mm3/Nm |
30 | 0.5 | 15.9 | 0.883 | |
1 | 16.3 | 0.452 | |
1.5 | 16.5 | 0.229 | |
60 | 0.5 | 9.7 | 0.538 | |
1 | 9.9 | 0.275 | |
1.5 | 12.8 | 0.177 | |
90 | 0.5 | 9.4 | 0.522 | |
1 | 9.5 | 0.263 | |
1.5 | 10 | 0.138 | |
Table 5
Wear behavior of TiO2 coated 316L SS substrate
Coating time ( min) | Load (N) | Wear volume ×10− 5 m3 | Specific wear rate ×10− 14 mm3/Nm |
30 | 0.5 | 21.94 | 1.219 |
1 | 22.79 | 0.633 |
1.5 | 23.38 | 0.324 |
60 | 0.5 | 18.84 | 1.047 |
1 | 20.25 | 0.562 |
1.5 | 20.94 | 0.290 |
90 | 0.5 | 13.51 | 0.750 |
1 | 13.66 | 0.379 |
1.5 | 14.15 | 0.196 |
Table 6
Wear behavior of TiCoCr coated 316L SS substrates with different load and coating time
Coating time ( min) | Load (N) | Wear volume ×10− 5m3 | Specific wear rate ×10− 14 mm3/Nm |
30 | 0.5 | 13.017 | 0.722 |
1 | 13.360 | 0.371 |
1.5 | 13.54 | 0.188 |
60 | 0.5 | 8.212 | 0.456 |
1 | 8.405 | 0.233 |
1.5 | 9.074 | 0.126 |
90 | 0.5 | 7.372 | 0.409 |
1 | 7.524 | 0.208 |
1.5 | 7.600 | 0.105 |
Figure 5 (a), (b) and (c) observed COF of 0.09, 0.053, 0.05 and 0.041 in 0.5 N load, 0.118, 0.082, 0.091 and 0.077 in 1N and 0.311, 0.169, 0.178 and 0.123 in 1.5N were noted for coating time 30 min at different loads. At higher loading condition such as 1.5N the uncoated 316L SS substrate gives higher COF. This is because of higher affinity of uncoated surface to the abrasion ball and lesser sliding velocity. On comparing to all coating time the 90 min coating time gives typically lesser COF, which indicates the higher wear resistance of 90 min coated substrates.
Figure 6 shows the micro hardness values of coated surfaces with respect to the loads. It is noted that the uncoated surfaces have the surface hardness of 210HV at 5N, 191HV at 10N, 179HV at 20N, 175HV at 30N and 172HV at 40N. This nominally lesser hardness is the reason for coarse grain structure in the substrate material. However the doping of reinforcement such as TiN, TiO2 and TiCoCr onto the 316L SS surface the surface hardness is increased. This is because of adding Ti atoms to the surface along with N, Co and Cr. Figure 7 shows the AFM resulting of TiN, TiO2 and TiCoCr coated on the 316L SS substrate at 30, 60 and 90 min respectively. Moreover, the coated grains were coarser and flatter, which increased the plastic deformation rate. The AFM image of TiCoCr coated 316L SS at 30, 60 and 90 min coating time. The thickness of 110nm, 170nm and 260nm were achieved, which is eventually higher than TiN and TiO2 coatings on the substrate.
Figure 8 and 9 shows the graph of surface roughness (Ra) and the adhesion strength of various coating done using 316L SS substrate with different coating time. It is observed that the surface roughness of 30, 60 and 90 min coated surfaces show significant changes in the surface roughness. The coated surfaces at the lesser coating time (30 min), the surface roughness is typically higher and the same decreases with increase of coating time up to 90 min. It is noted that the surface roughness of 0.31, 0.38 and 0.28µm were noted for TiN, TiO2 and TiCoCr coating on 316L SS substrate at the lesser coating time 30 min. However the aged coating time up to 60 and 90 min led lesser surface roughness of 0.25, 0.33, 0.22 and 0.19, 0.26, 0.17µm for TiN, TiO2 and TiCoCr coating at 60 and 90 min respectively. The values showed reduction trend in surface roughness with respect to the coating time. This reduction in the coating roughness is the reason for uniform filling of atom at the aged coating process.
Figure 9 shows the adhesion strength of various coatings on 316L SS substrate with various coating time. It is noted that the 30 min coating time in TiO2, TiN and TiCoCr gives marginal adhesion strength of 26.7, 32.4 and 34.2 MPa. However when the coating time increases the there is a marginal shift in adhesion strength. The coating time 60 min yield improved adhesion strength of 28.8, 35.5 and 36.4MPa, which is equal to 7.86%, 9.56% and 6.43% on compare to the 30 min coating time. This improvement is the reason for effective layer building and high cohesive strength of particle. When the coating time is higher the particle settling and the cohesive force between the TiO2, TiN and TiCoCr increases, which resulted higher adhesion strength when the shear force is applied. It is further noted that the prolonged coating time up to 90 min significantly reduced the adhesion strength. There is a marginal dip in the strength is observed in all coating materials such as TiO2, TiN and TiCoCr respectively. The observed adhesion strength of 28.1, 34.8 and 35.8MPa were noted for 90 min coating time in TiO2, TiN and TiCoCr respectively. This is about 2.43%, 1.97% and 1.64% of decrement on compare with the 60 min coating on the substrate.
It is noted that on comparing TiN, TiO2 and TiCoCr the higher adhesion strength of 36.4MPa was observed for 60 min coated TiCoCr on 316L SS substrate. This higher adhesion strength for TiCoCr is the reason for higher cohesive force of atoms with each other than the 90 min coated substrate. Moreover it is noted that by comparing all the TiCoCr coating gave improved results in 60 min coating time. This is the reason for high cohesion strength of Ti, Co and Cr atoms and their penetration ability. Thus the 60 min coating time yields higher adhesion strength in all coated substrates.