1. How does oxygen window relate to the use of high O2 mixes for deco, especially if we already know that diffusion of one gas in solution is not affected by the presence of other gases (and therefore enlarging the oxygen window will unlikely promote tissue gas removal)?
2. If pressure gradient is the single parameter dictating the deco efficiency (and DCI risk), why do we use high O2 mixes at depth instead of just ascending to a shallower depth with our backgas to get to the same pressure gradient of non-metabolic gases?
3. Is it possible to have oxygen bubbles formed when one switches from pure O2 to backgas during air breaks?
Thank you for any insights.
2. If pressure gradient is the single parameter dictating the deco efficiency (and DCI risk), why do we use high O2 mixes at depth instead of just ascending to a shallower depth with our backgas to get to the same pressure gradient of non-metabolic gases?
3. Is it possible to have oxygen bubbles formed when one switches from pure O2 to backgas during air breaks?
Thank you for any insights.