Premium
Stability enhancement of anaerobic digestion through membrane gas extraction under organic shock loads
Author(s) -
Voolapalli Ravi K.,
Stuckey David C.
Publication year - 1998
Publication title -
journal of chemical technology and biotechnology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.64
H-Index - 117
eISSN - 1097-4660
pISSN - 0268-2575
DOI - 10.1002/(sici)1097-4660(1998100)73:2<153::aid-jctb939>3.0.co;2-1
Subject(s) - chemical oxygen demand , membrane , extraction (chemistry) , anaerobic digestion , chemistry , membrane reactor , anaerobic exercise , chemical engineering , degradation (telecommunications) , hydrogen peroxide , chromatography , oxygen , hydrogen , environmental engineering , methane , wastewater , biochemistry , organic chemistry , environmental science , biology , physiology , telecommunications , computer science , engineering
A novel submerged silicone membrane extraction technique for removing the dissolved gases, CO 2 and H 2 , was explored as a method for enhancing the stability of anaerobic digesters under shock loads. The effectiveness of this strategy was demonstrated during a five‐fold step increase in the feed concentration from 4 kg m −3 to 20 kg m −3 Chemical Oxygen Demand (COD) to two anaerobic chemostats, a control and a membrane reactor, operating under steady state. Data revealed that membrane extraction of CO 2 enabled neutral pH values to be maintained during the shock, in contrast to the control; and this appeared to enhance acetate degradation. In addition, while liquid phase hydrogen removal was only partially successful due to a biofilm building up on the membrane, it also appeared to enhance the rate of volatile fatty acid degradation, and hence improved reactor stability. Floc sizes were monitored during the course of the shock load experiment and found to decrease from 46 μm to 30 μm over 35 days in the control, but from 37 μm to <5 μm in the membrane reactor. This decrease in floc size was postulated to be due to the growth of a relatively pure methanogenic biofilm on the membrane. © 1998 Society of Chemical Industry