The presence of ammoniacal nitrogen (N-NH3) in leachate is one of the problems normally faced by landfill operators. Slow leaching of wastes producing nitrogen and no significant mechanism for transformation of N-NH3 in the landfills causes a high concentration of ammoniacal nitrogen in leachate over a long period of time. A literature review showed that the removal of ammoniacal nitrogen from leachate was not well documented and to date, there were limited studies in Malaysia on this aspect, especially in adsorption treatment. The main objective of the present study was to investigate the suitability of activated carbon, limestone and a mixture of both materials as a filtering medium, in combination with other treatments capable of attenuating ammoniacal nitrogen which is present in significant quantity (between 429 and 1909 mg L(-1)) in one of the landfill sites in Malaysia. The results of the study show that about 40% of ammoniacal nitrogen with concentration of more than 1000 mg L(-1) could be removed either by activated carbon or a mixture of carbon with limestone at mixture ratio of 5:35. This result shows that limestone is potentially useful as a cost-effective medium to replace activated carbon for ammoniacal nitrogen removal at a considerably lower cost.
Suspended solids, colour and chemical oxygen demand (COD) are among the main pollutants in landfill leachate. Application of physical or biological processes alone is normally not sufficient to remove these constituents, especially for leachate with a lower biochemical oxygen demand (BOD)/ COD ratio. The main objective of this research was to investigate the efficiency of coagulation and flocculation processes for removing suspended solids, colour and COD from leachate produced in a semi-aerobic landfill in Penang, Malaysia. A 12-month characterization study of the leachate indicated that it had a mean annual BOD/COD ratio of 0.15 and was partially stabilized, with little further biological degradation likely to occur. Particle size analysis of the raw leachate indicated that its 50th percentile (d50) was 11.68 microm. Three types of coagulants were examined in bench scale jar test studies: aluminium sulphate (alum), ferric chloride (FeCl3) and ferrous sulphate (FeSO4). The effects of agitation speed, settling time, pH, coagulant dosages and temperature were examined. At 300 rpm of rapid mixing, 50 rpm of slow mixing, and 60 min settling time, higher removals of suspended solids (over 95%), colour (90%) and COD (43%) were achieved at pH 4 and 12. FeCl3 was found to be superior to other coagulants tested. At pH 4 and 12, fair removal of suspended solids was observed at a reasonably low coagulant dose, i.e., 600 mg L(-1); hHowever, about 2500 mg L(-1) of coagulant was required to achieve good removals at pH 6. Better removals were achieved at higher temperature. The d50 of sludge after coagulation at pH 4 with a 2500 mg L(-1) FeCl3 dose was 60.16 microm, which indicated that the particles had been removed effectively from the leachate. The results indicate that coagulation and flocculation processes can be used effectively in integrated semi-aerobic leachate treatment systems, especially for removing suspended solids, colour and COD.
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