In this study, we used activated carbon(AC) as a carbon source, along with zeolite, to prepare spherical carbons using sucrose, starch and phenolic resin(PR) as binder material. The physicochemical characteristics of the three samples(AZ4P, AZ6P and AZ8P) were examined by BET, XRD, SEM, EDX, H2S/NH3 gas adsorption, compressive strength and ignition test techniques. Through comparative analysis of the compressive strength and ignition test results the AZ8P sample was found to have the best hardness and the highest temperature resistance capacity. After activation, the AZ8P sample had the best H2S adsorption capacity, and AZ6P was the most suitable for the adsorption of ammonia.

Biogas from anaerobic digestion of biological wastes is a renewable energy resource. It has been utilized to provideheat and electricity. Raw biogas contains about 55~65% methane, 30~45% carbon dioxide, 0.5% of hydrogen sulfidegas and fraction of water vapor. The presence of CO2 and H2S in biogas affects less caloric value of raw biogas andcorrosion of engine etc.. Reducing CO2 and H2S contents improves a quality of fuel. In this paper, the absorption processusing aqueous monoethanol amine has been investigated as one of the leading technologies to purify the biogas. Liquidabsorbent is circulated through the reactor, contacting the biogas in countercurrent flow. The experimental results of themethane purification in simulated biogas mixture consisted of methane, carbon dioxide and hydrogen sulfide werepresented. It was shown that using aqueous solution used is effective in reacting with CO2 in biogas and it was possibleto achieve the purification of methane from the concentration of 55% up to 98%. This technique proved to be efficientin enriching and purifying of biogas, and has to be used to improve process efficiency.

We investigated the effect of temperature and pressure in breakthrough performance of various sorbents for dechlorination and desulfurization. Based on the results obtained during the desulfurization (Fe2O3, Fe3O4, ZnO) and the dechlorination (Na2CO3, NaHCO3, trona) screening tests, ZnO and trona were selected as preferred optimum sorbents. H2S breakthrough time corresponds to an effective capacity of approximately 11 g H2S/100 g of sorbent. Also, HCl breakthrough time corresponds to an effective capacity of approximately 5 g HCl/100 g of sorbent. ZnO and trona at high temperature of around 550oC display high sorption performance and removal efficiency for synthsis gas from waste gasification. Although there is an issue of CO2 recovery in hot gas cleanup technology for desulfurization, we have obtained an interesting new alternative hot gas cleanup system with heat budget merit.

Simultaneous removal of NH3, H2S and toluene in a contaminated air stream was investigated over 185 days in a biofilter packed with Zeocarbon granule as microbial support. In this study, multi-microorganisms including Nitrosomonas and Nitrobacter for nitrogen removal, Thiobacillus thioparus (ATCC 23645) for H2S removal, and Pseudomonas aeruginosa (ATCC 15692), Pseudomonas putida (ATCC 17484) and Pseudomonas putida (ATCC 23973) for toluene removal were used simultaneously. The empty bed residence time (EBRT) was 40-120 seconds and the feed (inlet) concentrations of NH3, H2S and toluene were 0.02-0.11, 0.05-0.23 and 0.15-0.21 ppmv, respectively. The observed removal efficiency was 85%-99% for NH3, 100% for H2S, and 20-90% for toluene, respectively. The maximum elimination capacities were 9.3, 20.6 and 17 g/m3/hr for NH3, H2S and toluene, respectively. The results of kinetic model analysis showed that there were no particular evidences of interactions or inhibitions among the microorganisms, and that the three biodegradation reactions took place independently within a finite area of biofilm developed on the surface of the Zeocarbon carrier.

This study compared the performance of a bioscrubber, a biofilter, and a combined system of bioscrubber and biofilter employed being operated at the laboratory-scale. for the removal of hydrogen sulfide. The bioscrubber maintained 100% removal of hydrogen sulfide up to inlet load of 56 g-S/m3․hr, while the removal efficiency was decreased with the increase of inlet load. The biofilter showed 100% removal efficiency up to inlet load of 126 g-S/m3․h and the maximum elimination capacity of 126 g S/m3․h for the inlet load of 224 g-S/m3․h. On the other hand, the combined system of bioscrubber and biofilter showed 100% removal for an inlet hydrogen sulfide load of up to 85 g-S/m3․h and the maximum elimination capacity of 153 g-S/m3․h for inlet loads of 224 g-S/m3․h.

A biofiltration system using activated carbon/polyurethane composite as solid support inoculated with Bacillus sp. was developed for treating a gaseous stream containing high concentrations of H2S. The effects of operating condition such as the influent H2S concentration and the empty bed contact time (EBCT) on the removal efficiency of H2S were investigated. The biofilter showed the stable removal efficiencies of over 99 % under the EBCT range from 15 to 60 sec at the 300 ppmv of H2S inlet concentration. When the inlet concentration of H2S was increased, the removal efficiencies decreased, reaching 95 and 74%, at EBCTs of 10 and 7.5 sec, respectively. The maximum elimination capacity in the biofilter packed with activated carbon/polyurethane composite media was 157 g/m3/hr.

Sorbents of calcined limestone and oyster particles having a diameter of about 0.63㎜ were exposed to simulated fuel gases containing 5000ppm H2S for temperatures ranging from 600 to 800℃ in a TGA (Thermalgravimetric analyzer). The reaction between CaO and H2S proceeds via an unreacted shrinking core mechanism. The sulfidation rate is likely to be controlled primarily by countercurrent diffusion through the product layer of calcium sulfde(CaS) formed. The kinetics of the sorption of H2S by CaO is sensitive to the reaction temperature and particle size, and the reaction rate of oyster was faster than the calcined limestone.