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ABSTRACT
This study was aimed at producing an alternative energy source(bioethanol)from sulphuric acid
and alkaline hydrogen peroxide treated sugarcane bagasse and rice stalkemploying simultaneous
saccharification and fermentation process using co-cultures of isolated and characterized strains
of Aspergillus niger and Saccharomyces cerevisiae. The proximate composition of the substrates
was determine. The composition of sugarcane bagasse and rice stalk treated with sulphuric acid
were determined to be (6.30% ash), (3.05% protein), (84.15% carbohydrates) and (4.75 ash),
(5.25 protein), (80.55 carbohydrates) respectively, while that of sugarcane bagasse and rice stalk
treated with alkaline peroxide were (7.95% ash), (1.75% protein), (83.20% carbohydrates) and
(5.10% ash), (7.00% protein), (77.65% carbohydrates) respectively.The characterization scheme
used were cultural, morphological and microscopic for A.nigerand cultural, microscopic and
physiological for S. cerevisiae. Garden Soil(GS02) isolateof A. nigerthat possess 6.2mm and
17.1mmdiameter of zone of starch and cellulose hydrolysis respectively and palm wine (PW02)
isolateof S. cerevisiaethat tolerates up to 15% ethanol where selected for the production. At
optimal fermentation conditions of 35ºC temperature, 5.0 pH, 4% substrate concentration,
300rpm agitation rate and 4 days fermentation period, a maximum of 6.20g/100ml and 5.06
g/100ml of ethanol were obtained from sulphuric acid-treated sugarcane bagasse and rice stalk
respectively.After determining the quantity of the ethanol produced using specific gravity
method, qualitative analysis using FTIR-Spectrophotometrywhich showed the absorbance peaks
of the ethanol functional groups of all the ethanol samples produced and the functional groups
had their absorption peaks within their normal ranges of 3100-3600cm-1, 2800-3000cm-1 and
1600-1675cm-1 for hydroxyl functional group, saturated and unsaturated parts of the compound
respectively.
vi
In conclusion, 84.15% was the highest carbohydrate content observed, the isolates GS02 and
PW02 were isolated, identified and employed for bioethanol production. The maximum quantity
of ethanol obtained was 6.20g/100ml from sulphuric acid treated sugarcane bagasse and the
absorption peaks of the functional groups were within their normal ranges.
CHAPTER ONE
1.0 INTRODUCTION
1.1 Background to the Study
Increase in world‘s energy demand and the progressive depletion of oil reserves motivate the
search for alternative energy resources, especially for those derived from renewable materials
such as biomass (Saxenaet al., 2009). Global concern about climate change and the consequent
need to diminish greenhouse gas emissions have encouraged the use of bioethanol as a gasoline
replacement or additive (Balatet al., 2008). This is because cellulosic ethanol and ethanol
produced from other biomass resources have the potential to cut greenhouse gas emissions by
86% (Wang et al., 2007).
The current estimated sugarcane production of Nigeria as at 2008 was put over 1.4m tones. This
figure represents the combined production of both industrial and domestic consumption.
Sugarcane for domestic consumption is produced more than that produced for industrial use.
Thus, chewing cane accounts for between 55 – 65% of the total cane production, the bulk of
whichis consumed raw for the sweetness of it‘s juice but some of it is processed into a variety of
products such as sugar, molasses, bagasse, sweets and left-over leaves/stalks (Busar and Misari,
2007). Although there are vast potential for the commercial production of this crop, its
processing industry did not come into existence in Nigeria until the early 1960s (Abdullahi,
2000).
Aspergillus nigercan be used in the industry in so many ways such as production of citric and
gluconic acids (Ojumu, 2003).It can also be used in biotechnology industry for production of
magnetic isotope-containing variants of biological molecules (Kansoet al., 1999).Furthermore,
Solomon et al.,(1999) reported that A. nigercan be cultured for extraction of enzyme glucose
1
oxidase which can be used in design of glucose biosensors due to its high affinity for beta-D
glucose.
Saccharomyces cerevisiaeis a species of yeast whose cells are round to ovoid, 5–10 μm in
diameter. It reproduces by a process known as budding. It is perhaps the most useful yeast,
having been instrumental in baking, and brewing since ancient times. It is believed to have been
originally isolated from the skin of grapes (one can see the yeast as a component of the thin
white film on the skin to winemaking of some dark-colour fruits such as plums; it exists among
the waxes of the cuticle). It is one of the most intensively studied eukaryoticmodel organism in
molecular and cell biology, just like Escherichia coli. It is the microorganism behind the most
common types of fermentation (Feldmannet al.,2010).
Li
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