Right now i am planing to perform a hydrolysis on seaweed. The problem I have is that I am inexperienced and have never done it before. So first I am planning to take 5 grams of the seaweed and put it into 0.4 N HCL 100 ml after that place it into the autoclave at 121 degrees C for 20 minutes. My question is I am not sure after the 20 minutes, should I discard the supernatant or discard the solid. I believe that I should discard the liquid part and then use the solid material in the second step which is enzyme hydrolysis using cellulase and after this enzyme hydrolysis process should i keep the liquid part and discard the solid. I am sorry if this is asking you too much but I am really hoping if you guys can help me. The goal of my experiment is to perform and acid and enzymatic hydrolysis on seaweed. I will then use the hydrolysate for bioethanol production.