Figures & data
Table 1. Thermophysical properties of the mould and part constituents.
Table 2. Kinetics parameters for THERMEL1 natural rubber.
Figure 3. Example 1, cooling inside the mould – – Temperatures and vulcanization rate computed at different points of the part.
![Figure 3. Example 1, cooling inside the mould – – Temperatures and vulcanization rate computed at different points of the part.](/cms/asset/c34e4bab-b4a7-4dce-ad59-8327e112a6a8/gipe_a_459460_f0003.gif)
Table 3. Discretization of the prescribed temperatures.
Figure 4. Experimental and theoretical temperature values achieved in different points of the moulded part during a moulding cycle.
![Figure 4. Experimental and theoretical temperature values achieved in different points of the moulded part during a moulding cycle.](/cms/asset/a35c74de-b5b8-4d16-837c-2f04bca3e421/gipe_a_459460_f0004.gif)
Figure 5. Comparison between the vulcanization front position obtained experimentally (a) and calculated (b).
![Figure 5. Comparison between the vulcanization front position obtained experimentally (a) and calculated (b).](/cms/asset/5fc431b6-b52f-47cf-bda6-5510d5e17f0a/gipe_a_459460_f0005.gif)
Figure 6. Example 2, 1000 s cooling outside the mould: ,
– temperatures and vulcanization rate computed at different points of the part.
![Figure 6. Example 2, 1000 s cooling outside the mould: , – temperatures and vulcanization rate computed at different points of the part.](/cms/asset/723e6427-d971-48d0-8126-db7b3035d02e/gipe_a_459460_f0006.gif)
Figure 14. Least squares criterion versus iteration numbers – a: Example 1 (Nt = 12); b: effect of the initial cycle; c: Example 1 (Nt = 1).
![Figure 14. Least squares criterion versus iteration numbers – a: Example 1 (Nt = 12); b: effect of the initial cycle; c: Example 1 (Nt = 1).](/cms/asset/585de82a-d39b-4fa4-8525-eec3158076c8/gipe_a_459460_f0014.gif)
Figure 20. Vulcanization rate within the part thickness – a: desired vulcanization rate; b: vulcanization rate obtained with estimated cycle; c: vulcanization rate obtained with initial cycle.
![Figure 20. Vulcanization rate within the part thickness – a: desired vulcanization rate; b: vulcanization rate obtained with estimated cycle; c: vulcanization rate obtained with initial cycle.](/cms/asset/7dc055cc-59e9-4895-815b-fbe53ee6ec4e/gipe_a_459460_f0020.gif)
Figure 22. Chemical reaction progress within the part thickness. Desired vulcanization rate: 0.9 – a: α obtained at the end of heating in the mould with the estimated cycle, b: α obtained at the end of heating in the mould with the initial cycle, c: α obtained at the end of cooling outside the mould with the estimated cycle, d: α obtained at the end of cooling outside the mould with the initial cycle.
![Figure 22. Chemical reaction progress within the part thickness. Desired vulcanization rate: 0.9 – a: α obtained at the end of heating in the mould with the estimated cycle, b: α obtained at the end of heating in the mould with the initial cycle, c: α obtained at the end of cooling outside the mould with the estimated cycle, d: α obtained at the end of cooling outside the mould with the initial cycle.](/cms/asset/c69804be-775c-4467-b716-dc9036508914/gipe_a_459460_f0022.gif)