yes. if i mix one buffer (TES), which has a pKa listed of 7.4 and another buffer (MOPS), which has pKa of 7.2, and put them into solution, what is the resulting pKa of that buffering solution. If one would dose titate a TES buffered solution, you would see one curve and you could take the midpoint of the steep slope and it would align to ~7.4...or the pKa value. The same would hold true for MOPS, which would be ~7.2. If I mixthe two buffers, you would see the plot moves to a point between the TES-only and MOPS-only buffers. The resulting pKa of the mixed buffer solution is between that of the single buffer solutions. This is a way to fine-tune or adjust the pKa or optimal buffering capacity of a buffer solution. I was simply wondering if one could calculate this new pKa value of the mixed-buffer solution, rather than doing the tedious dose-titrations. Is ist as easy as simply averaging the reported pKa values?