Hello everyone. I have a question about vibration testing approach.
In vibration testing of a specimen, we are conducting X, Y and Z tests consecutively. As far as I know, it would be ideal to conduct all three simultaneously because that's what the specimen (a satellite component) would experience during launch. But we cannot do that because we don't have three-axis (or even two-axis) shakers.
We recently did such a test for a component. We did sinuzoidal test run first and a random test run afterwards for each axis, with low level random runs in between all for diagnosis purposes. We did this for X, rinsed, and repeated for Y and then for Z. All was fine and our component performed well after the test campaign.
Then we conducted system level tests on our satellite and found that the component experienced a load spectrum that exceeded the one we applied in our component tests. We decided to do a seperate test campaign that will apply only the exceeding spectrum (the frequency range that exceeds the spectrum and the G^2/Hz loads that is applied). This spectrum has lower loads on most of it, but has very high loads in a tight range. This was designed so that we would keep the total Grms low so that we wouldn't put much fatigue on the equipment.
But recently I learned that we have to use a seperate specimen this time, because the previous one is not available. Thus, the previous fatigued specimen won't be used but a new one.
My question is; in light of the information I gave above, do you think testing can be done on seperate specimens for different axes (or runs) and be considered complete? Or should all test runs be conducted on the same specimen? I mean, if I do X axis tests first and Y axis tests second, and if I started a crack on X tests, it will probably propagate in the Y tests. I won't see this effect if I do X and Y on two different specimens. But then again, I wasn't supposed to do them consecutively either? And in my more specialized case; should I apply the full spectrum + the elevated spectrum on the new specimen just to be on the safe side (means more runs and consuming more time), or would the "different specimen for different runs" approach be technically correct?
Tell me if you need any more information. And thanks in advance for all the advice! :)
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