I'm sorry for the multitude of questions. It is extremely hard to provide specific advice when the engineering or science is not adequately described, which I completely understand is beyond the scope of this forum. Most of the equations I ask, don't need to be answered here, but are for your own thought processes. On one hand you are running a DSD which, by definition, is a screening design meant to identify active factors/interactions for further investigation. These typically use bold level settings to exaggerate factor effects. Your reactor issue sounds challenging because you can't exaggerate the volume effect (Or can you?) Since the DSD experiment looks at the relative effect of the design factors, and their levels are exaggerated, it can be challenging to compare the relative effect of a factor with a much narrower level setting. In this context, the comparison may be biased.
I will continue the beatings until the morale improves...
These reactors seem like micro-reactors. Are these for production or development? Is the reaction ego or end thermic? How is the temperature managed? How is it the volume of the reactor impacts the performance measures of the material being made in the reactor? How much space is need for the reaction? Does the reaction happen in the reactor at all places in the reactor simultaneously? Have you assessed/measured within reactor variation? Why would you have to spend the money to fix the supplier's issue of variation in reactor? Is it possible to have different processing factors and levels for each reactor?
"manufacturing variation of this reactor is +/- 0.1mL". what is +/-, is this the total distribution or 1 standard deviation? What I don't understand is, for each reactor, the "volume" is not changing, correct? It is only that you have additional reactors that there is a potential effect of the volume, correct? So in your first experiment (the DSD), you did these treatments in one reactor, correct?
Are you concerned the effects of the factors in your initial DSD experiment will change if the reactor volume changes? (this is, BTW an interaction of reactor and design factors)
As I see it, here are some options for you:
1. Run the second replicate of the first DSD with the second reactor (make sure all of the levels set in the first replicate are "identical". There is no need for center points as the reactor is not a continuous variable. Model the design factor effects, reactor and 2nd order design factor by reactor effects.
2. Record a measure of the actual reactor volume for each treatment of the first DSD, run a replicate of the DSD with the second reactor and record the actual value of the volume. Treat the volume as a covariate in your analysis.
3. Treat the reactor as a whole plot factor and the DSD as a sub-plot of a split-plot design.
4. Take the results of your first DSD and sample those "preferred settings" over multiple reactors where within reactor is within subgroup and between reactor is between subgroup.
"So currently we just ignore the confounding."
My advice is never to ignore the confounding, but identify it. If the confounding is specifically identified, strategies to un-confound are more readily found.
"All models are wrong, some are useful" G.E.P. Box