The samples were added to a set of aqueous solutions of various
cellulase concentrations, namely, 0, 5, 10, 15, and 20 g/L. The pH of
the treatment bath was regulated to 4.5 by using acetic acidesodium acetate buffer solution. Each solution had a liquor ratio of
15:1. Heating was done at 45
C for 3 h.
The samples were added to a set of aqueous solutions of variouscellulase concentrations, namely, 0, 5, 10, 15, and 20 g/L. The pH ofthe treatment bath was regulated to 4.5 by using acetic acidesodium acetate buffer solution. Each solution had a liquor ratio of15:1. Heating was done at 45C for 3 h.
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