You will first need to tell us what change in the response variable (Y, Dried Cell Weight) is of practical value? What is the smallest increment of change that matters to you and what is the target value? Also did you keep track of run order?
Looking at your design, you have 4 treatments at the bottom with vastly different level setting? These are not center points. Curious as to how you came up with these treatment combinations?
First look (again this is a blind look as I don't know if the variation created has any real value):
1. You have an unusually large result for the treatment where the result is 0.706. This large value (special cause like) is likely due to noise in the experiment not due to treatment effects so be cautious in using quantitative analysis. This potential inflates experimental error.
2. I did the analysis without the last 4 treatments and attached the analysis (JMP Journal) using a saturated model. This is a screening of the linear effects of each of the factors and associated interactions (you have started with a rather high resolution design). Typically, you would simplify the model by removing insignificant terms and re-run the analysis to get residuals to assess the adequacy of the model. To do this, first you must determine if these results are of any practical significance.
3. I played with removing terms that met a practical significance of a .05 change in Y (Pareto Plot) and also showed statistical significance (Half normal plot). The results of this analysis are also in the attached journal. The residuals look a bit bimodal and there may be an outlier as well indicating there may be some issues with the model. I saved the residuals and the prediction formula for this analysis.
4. I then added the additional 4 treatments you had in your original data set. The prediction formula did a very poor job of predicting those 4 points (perhaps not unusual since those 4 points were well beyond the design space inference.). Looking at factor B, this factor appears to have a non-linear effect.
I'm sure others may take a different approach...let me know if you have any questions.
"All models are wrong, some are useful" G.E.P. Box