Stress relaxation through thermal crack formation in CVD TiCN coatings grown on WC-Co with different Co contents
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Authors
Organisational units
External Organisational units
- Materials Center Leoben Forschungs GmbH
- Institute of Coastal Research
- Ceratizit Austria GmbH
Abstract
TiCN coatings were grown by chemical vapor deposition (CVD) on WC-Co substrates with different Co contents, in order to control thermal stress. The driving force for the development of thermal stress is attributed to the difference between room and deposition temperature (ΔT ≈ −780 °C), and the mismatch of the coefficient of thermal expansion (CTE) between substrate and coating. Co contents of 6, 7.5, 10, 12.5, and 15 wt% were utilized to adjust the CTE of the substrate, and therefore tune the stress in TiCN coatings. Dilatometry of the substrates and high temperature X-ray diffraction of a powdered TiCN coating indicate a decreasing CTE-mismatch for increasing substrate Co contents. In consequence, residual stress in TiCN determined by X-ray diffraction increases up to 662 ± 8 MPa with decreasing Co contents down to 10 wt%. For Co contents below 10 wt%, the residual stress decreases. The formation of thermal crack networks in TiCN, analyzed by scanning electron microscopy, coincides with 10 wt% Co. Stress relaxation in TiCN coatings through the formation of thermal cracks becomes evident. A finite element simulation utilized for the calculation of residual stress distributions reveals shielding effects, which occur with the introduction of thermal cracks. Discrepancies between experimental and simulated thermo-elastic stresses imply the presence of secondary relaxation sources. High temperature residual stresses in TiCN, determined up to 1000 °C (i.e. above deposition temperature), suggest additional thermal crack formation for substrate Co contents of 6 wt%.
Details
Original language | English |
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Article number | 105102 |
Number of pages | 9 |
Journal | International journal of refractory metals & hard materials |
Volume | 86.2020 |
Issue number | January |
Early online date | 16 Oct 2019 |
DOIs | |
Publication status | Published - Jan 2020 |