Application of response surface methodology for optimization of important parameters in decolorizing treated distillery wastewater using Aspergillus ... Biodeterioration & Biodegradation]
Book Details
PublisherElsevier
ISBN / ASINB000RR9QBU
ISBN-13978B000RR9QB5
AvailabilityAvailable for download now
Sales Rank99,999,999
MarketplaceUnited States 🇺🇸
Description
This digital document is a journal article from International Biodeterioration & Biodegradation, published by Elsevier in 2006. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.
Description:
Distillery wastewater causes many environmental problems and colored substances must be removed from it before discharge into the environment. Decolorization of anaerobically treated distillery wastewater was therefore studied using locally isolated Aspergillus fumigatus. As cultural conditions are very important for the decolorization process, the combined effect of initial maltose concentration, pH and mycelial mass was studied using response surface methodology. A central composite design for the three variables was employed to study the combined effect on decolorization efficiency of distillery wastewater. The optimum initial maltose concentration was found to be 15.13g/l, the optimum pH was 5.57 and the optimum mycelial mass 2.57g/l.
Description:
Distillery wastewater causes many environmental problems and colored substances must be removed from it before discharge into the environment. Decolorization of anaerobically treated distillery wastewater was therefore studied using locally isolated Aspergillus fumigatus. As cultural conditions are very important for the decolorization process, the combined effect of initial maltose concentration, pH and mycelial mass was studied using response surface methodology. A central composite design for the three variables was employed to study the combined effect on decolorization efficiency of distillery wastewater. The optimum initial maltose concentration was found to be 15.13g/l, the optimum pH was 5.57 and the optimum mycelial mass 2.57g/l.
