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Thesis - faculty.ait.ac.th - Asian Institute of Technology

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change in <strong>th</strong>e predominant species while carbon assimilation metabolism wi<strong>th</strong> different<br />

substrates.<br />

The yield depends upon <strong>th</strong>e oxidation state <strong>of</strong> <strong>th</strong>e carbon sources and nutrient<br />

elements, degree <strong>of</strong> polymerization <strong>of</strong> <strong>th</strong>e substrate, pa<strong>th</strong>way <strong>of</strong> metabolism, grow<strong>th</strong> rate<br />

and o<strong>th</strong>er physical parameters <strong>of</strong> cultivation (Tchobanoglous, et al., 2003). The maximum<br />

yield coefficient <strong>of</strong> <strong>th</strong>e b<strong>ac</strong>terial culture was found to be greater <strong>th</strong>an <strong>th</strong>at <strong>of</strong> <strong>th</strong>e yeast<br />

culture signifies <strong>th</strong>at b<strong>ac</strong>terial grow<strong>th</strong> is more pronounced <strong>th</strong>an <strong>th</strong>at <strong>of</strong> <strong>th</strong>e yeast culture.<br />

This is fur<strong>th</strong>er supported by <strong>th</strong>e evidence <strong>th</strong>at <strong>th</strong>e specific grow<strong>th</strong> rate <strong>of</strong> <strong>th</strong>e b<strong>ac</strong>terial<br />

culture was 0.42 d -1 compared to <strong>th</strong>at <strong>of</strong> 0.27 d -1 <strong>of</strong> <strong>th</strong>e yeast culture.<br />

The grow<strong>th</strong> rate <strong>of</strong> <strong>th</strong>e b<strong>ac</strong>terial culture was almost 1.53 times <strong>th</strong>e yeast culture at a<br />

maximum substrate concentration <strong>of</strong> around 40 mg/L COD. Such an observation is in<br />

<strong>ac</strong>cordance wi<strong>th</strong> <strong>th</strong>e biokinetic studies conducted by Dan (2002) in high saline wastewater,<br />

where <strong>th</strong>e yeast culture showed a lower yield coefficient and specific grow<strong>th</strong> rate in <strong>th</strong>e<br />

yeast system compared to <strong>th</strong>at <strong>of</strong> <strong>th</strong>e b<strong>ac</strong>terial system.<br />

4.2.3 Toxicity Studies<br />

In addition to many organic and inorganic compounds <strong>th</strong>at are present in <strong>th</strong>e landfill<br />

le<strong>ac</strong>hate, <strong>th</strong>e presence <strong>of</strong> toxic substances also persists. These toxic compounds not only<br />

pose harm to <strong>th</strong>e environment when released but also affect <strong>th</strong>e efficiency <strong>of</strong> <strong>th</strong>e biological<br />

treatment system. These metals affect <strong>th</strong>e performance <strong>of</strong> <strong>th</strong>e biore<strong>ac</strong>tors by inhibiting <strong>th</strong>e<br />

b<strong>ac</strong>terial grow<strong>th</strong>. Oxygen consumption in a biological system has been monitored in<br />

several studies to monitor <strong>th</strong>e toxicity <strong>of</strong> <strong>th</strong>e wastewater from several sources (Solyom, et<br />

al., 1976; Solyom, 1977). For an aerobic organism, toxicity test could be measured by<br />

measuring <strong>th</strong>e oxygen uptake rate (OUR) in presence <strong>of</strong> <strong>th</strong>e toxicant, which will signify <strong>th</strong>e<br />

inhibitory effect <strong>of</strong> <strong>th</strong>e toxicant on <strong>th</strong>e microorganism (Chen, et al., 1997).<br />

(1) Ammonia Toxicity<br />

The ammonium concentration in <strong>th</strong>e le<strong>ac</strong>hate is usually found to be very high. As<br />

mentioned by Keenan, et al. (1984), <strong>th</strong>e high concentration <strong>of</strong> ammonia is a challenge for<br />

<strong>th</strong>e biological treatment <strong>of</strong> le<strong>ac</strong>hate as it may brings about toxicity to <strong>th</strong>e organisms. For<br />

better understanding <strong>of</strong> <strong>th</strong>e effect <strong>of</strong> <strong>th</strong>e ammonia concentration on <strong>th</strong>e grow<strong>th</strong> <strong>of</strong> <strong>th</strong>e<br />

organisms used in <strong>th</strong>e present study, toxicity test was done wi<strong>th</strong> ammonium chloride as <strong>th</strong>e<br />

source <strong>of</strong> ammonia. The operational parameters for <strong>th</strong>e toxicity test are described in Table<br />

3.3. The procedure <strong>of</strong> toxicity test is described in section 3.4.1. The ammonium chloride<br />

concentration used in <strong>th</strong>e study were 70, 1000, 1500 and 2000 mg/L. The substrate<br />

concentration used in <strong>th</strong>e study was 7 mg COD/L for <strong>th</strong>e b<strong>ac</strong>terial system and 5.6 mg<br />

COD/L for <strong>th</strong>e yeast system.<br />

An aerobic biological process contains two major classes <strong>of</strong> aerobic microorganisms,<br />

namely nitrifying b<strong>ac</strong>teria and heterotrophic b<strong>ac</strong>teria. The heterotrophs represent <strong>th</strong>e<br />

microorganisms responsible for carbon<strong>ac</strong>eous removal. Nitrifying b<strong>ac</strong>teria (Nitrosomonas<br />

and Nitrob<strong>ac</strong>tor) are responsible for <strong>th</strong>e oxidation <strong>of</strong> ammonia to nitrite and nitrate<br />

nitrogen. The optimum pH is 7.5 to 8.6 for Nitrosomonas and 6.0 to 8.0 for Nitrob<strong>ac</strong>tor.<br />

The range <strong>of</strong> free ammonia concentration affecting to Nitrosomonas had been investigated<br />

by some researcher is around 7 to 150 mg/L and Nitrob<strong>ac</strong>tor is around 0.1 to 1.0 mg/L<br />

(Barnes, 1983; Abeling and Seyfried, 1992). It was observed by Blum and Speece (1992)<br />

75

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