• Journal of Environmental Science International
• /
• v.29 no.4
• /
• pp.325-337
• /
• 2020

The purpose of this study was to analyze the soil environment of urban neighborhood parks and to use them as basic data for evaluating the ecological functions of urban parks such as groundwater regeneration, flood control, microclimate regulation, adsorption and purification. The landscape design criteria were generally evaluated as advanced, and further monitoring and studies are needed to evaluate the various ecological functions. It is also necessary to improve the phosphoric acid and nitrogen contents, which tended to be low. In addition, continuous monitoring is needed to assess the proper soil environment according to the biological species, and to evaluate the ecological functions. The results of this study can be used to evaluate the groundwater recharge of urban parks. In particular, when the land of the neighboring park is used for various purposes, the level of access of the user may be increased. Therefore, factors that may adversely affect the user's health, such as heavy metals and organic matters, should be selected and selected as management criteria. In addition, follow-up studies considering fertilization standards suitable for trees and growth of introduced vegetation, etc. are needed urgently to improve the soil environment.

• Environmental Engineering Research
• /
• v.19 no.1
• /
• pp.37-40
• /
• 2014

This research investigates the quality changes during composting of bagasse and pig manure amended with 30% of surfactant-coated charcoal (SC). Two treatments, 30% uncoated charcoal (UC) amendment and no charcoal (NC) amendment, were done as control. Charcoal was coated with 0.37 mM tetradecyltrimethylammonium bromide (TDMA), a cationic surfactant, at the dosage of 10 g/L. At the end of the composting period, the carbon to nitrogen (C/N) ratio of SC amendment was 9.7; whereas, the C/N ratios of UC and NC amendment were 12.6 and 21.4, respectively. Plant nutrients contents of the compost produced from SC amendment were 20.7 mg $NH_4{^+}-N/g$, 42.8 mg $NO_3{^-}-N/g$, and 41.7 mg P/g. High nitrate and phosphate concentrations in SC amendment were due to the adsorption of these anions on the positive charge of TDMA. Desorption of plant nutrients retained in the compost pellets was also investigated. It was predicted that nitrate was fully desorbed from a pellet at 23 days for SC amendment, which was later than UC (14 days) and NC (10 days) amendment. A slow release of nitrate from the compost pellet will reduce the nitrate leaching into the environment. Thus, the adding of SC in the compost pile is one of the alternative methods to improve the quality of compost and plant nutrient retention.

• Environmental Engineering Research
• /
• v.19 no.4
• /
• pp.309-316
• /
• 2014

The water quality improvement of golf course ponds, as representative stagnant stream channels, was evaluated by applying a biological activated carbon (BAC) process composed of four consecutive activated carbon reactors. The study was performed from autumn to winter in order to evaluate the feasibility of the BAC process under low temperature conditions. In the study, water quality of pond A (target pond) and pond B (reference pond) were monitored. Pond water was pumped into the BAC process, and was then returned to the pond after treatment. The optimal conditions were determined to be 2 hr of empty bed contact time (EBCT) at a temperature above $4^{\circ}C$, in which improvements of chemical oxygen demand (COD), total nitrogen (TN) and total phosphorus (TP) of pond A compared to pond B were 3.62%, 3.48% and 1.81%, respectively. On the other hand, as the temperature was below $4^{\circ}C$, some degree of water quality improvement was achieved even when EBCT were 1 or 0.5 hr, suggesting that the BAC process can be successfully applied for the improvement of pond water quality in winter months. The values of biomass concentration and microorganism activity in each condition were highest where 2 hr of EBCT was applied at a temperature above $4^{\circ}C$, but values were similar throughout all treatment conditions, and thus, adsorption is considered to be the dominant factor affecting process efficiency. From the denaturing gel gradient electrophoresis (DGGE) results, no significant differences were observed among the activated carbon reactors, suggesting that the number of reactors in the system could be decreased for a more compact application of the system.

• Journal of the Korea Academia-Industrial cooperation Society
• /
• v.13 no.4
• /
• pp.1915-1922
• /
• 2012

In this study, synthesis of mesoporous silica such as, SBA-15, MCM-41, MCM-48, KIT-6 according to various experimental conditions. The CMK(Carbon Mesoporous Korea) was synthsized by various mesoporous silica. Finally, the mesoporous transition metal structure synthesized using CMK structure. Nitrogen adsorption/ desorption, SEM, low angle X-ray diffraction were carried for analysis of each sample. The optimum synthesis condition of mesoporous transition metal structure derived from characteristic analysis. The SBA-15 is best precursor for synthesis of mesoporous transition metal structure. The surface area of copper mesorporous structure from CMK(SBA-15) is $225m^2/g$, pore diameter is 2.91nm by BET analysis.

• Journal of Korean Society of Environmental Engineers
• /
• v.22 no.12
• /
• pp.2141-2148
• /
• 2000

This study is to investigate changes of pore structure with different burn-off degree of steam activated carbons manufactured from domestic anthracite. The activated carbons were characterized by adsorption of nitrogen at 77 K. Steam activation substantially enhanced the porosity of the activated carbons. Burn-off increased linearly according to increasing activation time, and total pore volume and BET surface area increased with burn-off. Activation at $800^{\circ}C$ increased more micropore volume than that at $950^{\circ}C$. Activated carbons manufactured at high temperature had less microporosity than that at lower temperature, but had more developed macroporosity. The steam activation produced an enlargement of pore below $100{\AA}$ diameter in the activated carbons. Furthermore, the porosity in the $6{\sim}40{\AA}$ pore diameters range increased considerably with the degree of burn-off.

• Environmental Engineering Research
• /
• v.21 no.3
• /
• pp.291-296
• /
• 2016

Application of photocatalytic nanoparticles has been recently gaining an increased attention as air purifying material for sustainable urban development. The present work reports the photocatalytic removal of gaseous phase nitrogen oxides ($NO_x$) using $TiO_2$-coated zeolite to be applied as a filter media for the urban green infrastructure such as raingardens. The $TiO_2$-coated zeolite was synthesized by simple wet chemistry method and tested in a continuous-flow photo-reactor for its removal efficiency of $NO_x$ under different conditions of the weight percentage of $TiO_2$ coated on the zeolite, and gas retention time. The removal efficiency of $NO_x$ in general increased as the weight percentage of $TiO_2$ coated on the zeolite increased up to 15-20%. Greater than 90% of $NO_x$ was removed at a retention time of one minute using the $TiO_2$-coated zeolite ($TiO_2$ weight percentage = 20%). Overall, $TiO_2$-coated zeolite showed greater efficiency of $NO_x$ removal compared to $TiO_2$ powder probably by providing additional reaction sites from the porous structure of zeolite. It was presumed that the degradation of $NO_x$ is attributed to both the physical adsorption and photocatalytic oxidation that could simultaneously occur at the catalyst surface.

• Membrane Journal
• /
• v.14 no.2
• /
• pp.99-107
• /
• 2004

Carbon molecular sieve (CMS) membranes were prepared by pyrolysis of polyimides having carboxylic acid groups and applied to the hydrogen separation. The polymeric membranes having carboxylic acid groups showed different steric properties as compared with polymeric membranes having other side groups ($-CH_3$ and $-CF_3$) because of the hydrogen bond between the carboxylic acid groups. However, the microporous CMS membranes were significantly affected by the decomposable side groups evidenced from the wide angle X-rat diffraction, nitrogen adsorption isotherms, and single gas permeation measurement. Furthermore, the gas separation properties of the CMS membranes were essentially affected by the pyrolysis temperature. As a result, the CMS membranes Prepared by Pyrolysis of polyimide containing carboxylic acid froups at $700^{\circ}C$ showed the $H_2$ permeability of 3,809 Baller [$1{\times}10^{-10}$ H $\textrm{cm}^$(STP)cm/$\textrm{cm}^2$.s.cmHg], $H_2$/$N_2$, selectivity of 46 and $H_2$/$CH_4$ selectivity of 130 while the CMS membranes derived from polyimide showed the H$_2$ permeability of 3,272 Barrer, $H_2$/$N_2$ selectivity of 136 and $H_2$/$CH_4$ selectivity of 177.

• Korean Journal of Agricultural Science
• /
• v.46 no.4
• /
• pp.907-914
• /
• 2019

Ammonia (NH₃) that reacts with nitric or sulfuric acid in the air is the major culprit contributing to the formation of fine particulate matter (PM_2.5). NH₃ volatilization mainly originates from nitrogen fertilizer and livestock manure applied to arable soil. Cation exchange capacity (CEC) of peat moss (PM) and zeolite (ZL) is high enough to adsorb ammonium (NH₄⁺) in soil. Therefore, they might inhibit volatilization of NH₃. The objective of this study was to compare the effect of PM and ZL on NH₃ volatilization from upland soil. For this, a laboratory experiment was carried out, and NH₃ volatilization from the soil was monitored for 12 days. PM and ZL were added at the rate of 0, 1, 2, and 4% (wt wt^-1) with 354 N g m^-2 of urea. Cumulative NH₃-N volatilization decreased with increasing addition rate of both materials. Mean value of cumulative NH₃-N volatilization across application rate with PM was lower than that with ZL. CEC increased with increasing addition rate of both materials. While the soil pH increased with ZL, it decreased with PM. Increase in CEC resulted in NH₄⁺ adsorption on the negative charge of the external surface of both materials. In addition, decrease in soil pH hinders the conversion of NH₄⁺ to NH₃. Based on the above results, the addition of PM or ZL could be an optimum management to reduce NH₃ volatilization from the soil. However, PM was more effective in decreasing NH₃ volatilization than ZL due to the combined effect of CEC and pH.

• Carbon letters
• /
• v.13 no.2
• /
• pp.109-114
• /
• 2012

A nuclear, biological, chemical (NBC) canister was indigenously developed using active carbon impregnated with ammoniacal salts of copper (II), chromium (VI) and silver (I), and high efficiency particulate aerosol filter media. The NBC canister was evaluated against carbon tetra chloride ($CCl_4$) vapours, which were used as a simulant for persistent chemical warfare agents under dynamic conditions for testing breakthrough times of canisters of gas masks in the National Approval Test of Respirators. The effects of $CCl_4$ concentration, test flow rate, temperature, and relative humidity (RH) on the breakthrough time of the NBC canister against $CCl_4$ vapour were also studied. The impregnated carbon that filled the NBC canister was characterized for surface area and pore volume by $N_2$ adsorption-desorption isotherm at liquid nitrogen temperature. The study clearly indicated that the NBC canister provides adequate protection against $CCl_4$ vapours. The breakthrough time decreased with the increase of the $CCl_4$ concentration and flow rate. The variation in temperature and RH did not significantly affect the breakthrough behaviour of the NBC canister at high vapour concentration of $CCl_4$, whereas the breakthrough time of the NBC canister was reduced by an increase of RH at low $CCl_4$ vapour concentration.

• Carbon letters
• /
• v.28
• /
• pp.47-54
• /
• 2018

High surface carbon aerogels with hierarchical and tunable pore structure were prepared using ionic liquid as carbon precursor via a simple salt templating method. The as-prepared carbon aerogels were characterized by nitrogen sorption measurement and scanning electron microscopy. Through instant visual observation experiments, it was found that salt eutectics not only serve as solvents, porogens, and templates, but also play an important role of foaming agents in the preparation of carbon aerogels. When the pyrolyzing temperature rises from 800 to $1000^{\circ}C$, the higher temperature deepens the carbonization reaction further to form a nanoporous interconnected fractal structure and increase the contribution of super-micropores and small mesopores and improve the specific surface area and pore volume, while having few effects on the macropores. As the mass ratio of ionic liquid to salt eutectics drops from 55% to 15%, that is, the content of salt eutectics increases, the salt eutectics gradually aggregate from ion pairs, to clusters with minimal free energy, and finally to a continuous salt phase, leading to the formation of micropores, uniform mesopores, and macropores, respectively; these processes cause BET specific surface area initially to increase but subsequently to decrease. With the mass ratio of ionic liquids to salts at 35% and carbonization temperature at $900^{\circ}C$, the specific surface area of the resultant carbon aerogels reached $2309m^2g^{-1}$. By controlling the carbonization temperature and mass ratio of the raw materials, the hierarchically porous architecture of carbon aerogels can be tuned; this advantage will promote their use in the fields of electrodes and adsorption.