Background monitoring and long-range transport of atmospheric CFC-11 and CFC-12 at Kosan, Korea

The background concentrations of atmospheric CFC-11 and CFC-12were monitored to assess their impact on stratospheric ozone depletion and global warming from September 1995 to March 1999 at Kosan, Korea, located at eastern margin of the Asian Continent. The concentrations of atmospheric CFC-11 at Kosan have decreased slightly, at a rate of –2.5 pptv yr^-1, over the period in response to the Montreal Protocol. The CFC-12 mixing ratio at Kosan continues to increase in the atmosphere at a rate of 5.7 pptv yr^-1 despite international regulations, because of its extreme atmosphere persistence. Recent trends ofthese two chlorofluorocarbons at Kosan, Korea were concordant with those of the northern hemispheric background monitored unitat Mauna Loa, Hawaii. The maximum seasonal mean mixing ratios of CFC-11 and CFC-12 at Kosan, Korea, were 270±4 pptv inthe spring and 538±9 pptv in the winter, and the corresponding seasonal minima were 267±7 and 529±12 pptv. This occurred in the summer and was due to southeasterlywinds from the northwestern Pacific Ocean. By performing a three-day isentropic backward trajectory analysis, it was shownthat air masses at Kosan, and with the exception of summer, mainly originated from central and northern China. In particular, the mixing ratios of these two contaminant speciesare closely related with their air mass trajectories.     

Study on Size Distribution of Total Aerosol and Water-Soluble Ions During an Asian Dust Storm Event at Jeju Island, Korea

Soil dust particles transported from loess regions of the Asian continent, called Asian dust, highly influences the air quality of north-eastern Asia and the northern Pacific Ocean. In order to investigate the effects of these dust storms on the chemical composition of atmospheric aerosol particles with different size, measurements of size distributions of total aerosol and major ion species were carried out on Jeju Island, Korea during April 2001. Juju Island was chosen for the study because the levels of emissions of anthropogenic air pollutants are very low. A 5-stage cascade impactor was used to sample size-fractionated aerosol particles. Samples were analyzed for major water-soluble ions using Dionex DX-120 ion chromatograph. The average mass concentration of total aerosol was found to be 24.4 and 108.3 microg m(-3) for non-Asian dust and Asian dust periods, respectively. The total aerosol size distribution, measured during the non-Asian dust period, was bimodal, whereas the coarse particles dominated the size distribution of total aerosol during the Asian dust period. It was found that SO4(2-), NH4+ and K+ were mainly distributed in fine particles, while Cl-, NO3-, Na+, Mg2+ and Ca2+ were in coarse particles. Although SO4(2-) was mainly distributed in fine particles, during the Asian dust period, the concentrations in coarse particles were significantly increased. This indicates heterogeneous oxidation of SO2 on wet surfaces of basic soil dust particles. The NH4+ was found to exist as (NH4)2SO4 in fine particles, with a molar ratio of NH4+ to SO4(2-) of 2.37 and 1.52 for non-Asian dust and Asian dust periods, respectively. Taking into account the proximity of the sampling site to the sea, and the observed chloride depletion, coarse mode nitrate, during the non-Asian dust period, is assumed to originate from the reaction of nitric acid with sodium chloride on the surfaces of sea-salt particles although the chloride depletion was not shown to be large enough to prove this assumption. During the Asian dust period, however, chloride depletion was much smaller, indicating coarse nitrate particles were mainly produced by the reaction of nitric acid with surfaces of basic soil particles. Most chloride and sodium components were shown to originate from sea-salt particles. Asian dust aerosols, arriving at Jeju Island, contained considerable amounts of sea-salt particles as they passed over the Yellow Sea. Ca2+ was shown to be the most abundant species in Asian dust particles.     

Comparison of seven indicator PCBs and three coplanar PCBs in beef, pork, and chicken fat

The risk assessment of polychlorinated biphenyls (PCBs) is difficult since complex congeners were used in many industrial applications for a long period of time and the residue monitoring in foods of animal origin and the environment were not established in comparable systems. The relationships of determined concentrations in indicator PCB congeners (mono- and di-ortho PCBs) and coplanar PCB congeners (non-ortho PCBs) in livestock products are presented in this study. The concentrations of seven indicator PCBs were compared with three coplanar PCBs in beef, pork, and chicken fat. Distributions of concentration for the indicator PCBs in three different animal species were similar except for that of PCB-118 (2,3',4,4',5-pentachlorobiphenyl) in pork fat. The congeners with the highest concentration were PCB-138 (2,2',3,4,4',5'-hexachlorobiphenyl) in beef and pork fat and PCB-28 (2,4,4'-trichlorobiphenyl) in chicken fat. The bioaccumulation and metabolism of PCBs in animal species represent different congener profiles in livestock products. The percentage of the total concentration of three coplanar PCBs was about 2% of the total concentration of the seven indicator PCBs. Relatively high concentration of mono-ortho and di-ortho PCBs in fat samples of livestock products may be calculated with the concentration of coplanar PCBs that can be usually determined on a sequential procedure with dioxin analysis. Therefore, the relationship of the amounts between seven indicator PCBs and three coplanar PCBs may be useful to derive the composition and level of contaminants in beef, pork, and chicken.     

Distribution characteristics of nonylphenols in the artificial Lake Shihwa, and surrounding creeks in Korea

Nonylphenols were determined from the water, suspended particle, and sediment samples taken from the Lake Shihwa in Korea and its surrounding creeks flowing through municipal and industrial areas, and into the lake. The nonylphenols were detected at the concentration ranges of 0.0-41.3 microg/l, 0.0-116.6 and 0.3-31.7 mg/kg in water, suspended particle and sediment samples respectively. The contamination levels of nonylphenols were increased along the down stream. Considerably high levels of nonylphenols were found at the industrial area compared to the municipal area. No remarkable differences were found between the isomer patterns of nonylphenols for the sample matrices of each sampling site, i.e. water, suspended solids and sediment. Strong correlations between water and sediment with 10(5.2) of the mean partition coefficient (Koc ) were observed. These indicate that most of nonylphenols came from industrial wastewater at high level. It is thought that the water quality of the Lake Shihwa is affected greatly by industrial environments surrounding.     

Partitioning of naphthalene to gemini surfactant-treated alumina

Partitioning of naphthalene to anionic surfactants adsorbed on alumina in the aqueous phase was studied for immobilization of the contaminant in the subsurface. Three anionic surfactants with different molecular structures were used: a conventional (sodium dodecylbenzene sulfonate, SDDBS), a gemini (dialkylated disulfonated diphenyl oxide with alkyl chain length of 12, DADS-C12), and a dianionic (monoalkylated disulfonated diphenyl oxide with alkyl chain length of 12, MADS-C12). Sorption of the surfactants onto alumina was studied in a series of batch experiments and the effectiveness of the adsorbed surfactants onto aluminum oxide as a sorptive phase for naphthalene was compared.     

Binding of dialkylated disulfonated diphenyl oxide surfactant onto alumina in the aqueous phase

Adsorption of a gemini surfactant that has two monomers and a spacer in a molecule (dialkylated disulfonated diphenyl oxide with alkyl chain lengths of twelve, DADS-C12) onto positively-charged aluminum oxide in water was studied and compared with a single-monomer anionic surfactant (sodium dodecylbenzene sulfonate, SDDBS). More mass of the gemini surfactant was adsorbed than the conventional single-monomer SDDBS. Fewer moles of the first were bound to the substrate than the second indicating that larger molecular structure of the gemini surfactant does not hinder the sorption. Both surfactants followed similar sorption mechanisms, however, stronger hydrophobic interactions were shown in the bilayer formation of the adsorbed gemini surfactant.     

Observations of Dust-Storms in China, Mongolia and Associated Dust Falls in Korea in Spring 2003

A joint monitoring of dust-storms that occurred in East Asia from March until May 2003 has been carried. Our discussions include dust-storm observations in the source areas of China and Mongolia, and measurements with satellites and ground monitors in central Korea. Differences were found in the definition and measurement of dust-storms. Over the source area of Mongolia there were 6 dusty days in March, 18 days in April, and 10 dusty days in May. In Inner Mongolia of northern China there were 4 dust-storms with 14 dusty days observed over the three months. In central Korea, a sink area, there were 4 cases of weak dust-storm and 17 dusty days in the spring of 2003. The highest PM10 value was 607 μgm⁻³ and PM 2.3 was 149 μgm⁻³, respectively. These observations identify the growing need for further universal observation practices and dust-storm reporting in future. Observations indicated that snow covered the central part of the Gobi Desert, near the boundary of China and Mongolia, from December until mid-March. This is in contrast to other years when the Gobi was relatively wet, producing unfavourable conditions for the formation of intense dust-storms. In addition, the very strong winds associated with intense cyclones and anticyclones were not apparent and the systems shifted northward during the spring. As a result, the frequency and intensity of observed dust-storms in 2003 in this region were very low. This confirms that there is variability in the frequency of dust-storm formation due to the current process of desertification and climate change.     

Structural Change of the Manufacturing Sector in Korea: Measurement of Real Energy Intensity and CO2 Emissions

In terms of energy use, it is wellknown that energy intensity in the manufacturingsector is higher than any other sector. In Korea, theenergy intensity of the manufacturing sector hasdeteriorated since the late 1980s. This phenomenonis quite unique compared with the trend of energyintensity in other countries. In this study, weclosely examine the structural composition of Korea'smanufacturing sector from 1981 to 1996, its energyintensity, and its implications for carbon dioxide(CO₂) emissions by introducing the measurement ofreal energy intensity.The conventional index of energy intensity is notappropriate for aggregate industries. Since theaggregation of industries in the manufacturing sectorincludes structural change, it would be better toseparate the effect of structural change. Hence, inthis study, we apply a decomposition methodology forenergy intensity based on the `Divisia Index'. Ateach industry level, energy intensity is a mixedmeasurement of pure energy efficiency improvement andfuel substitution. We also calculate real energyintensity at each industry level. Based on ouranalysis, we derive carbon dioxide (CO₂) intensity and analyze the factors that affect CO₂ emission in this sector.During 1988–1993, the energy intensity of themanufacturing sector in Korea deteriorated. Industrial structural change,the real energy intensity in this sector became evenworse during this period. The primary reason for thisphenomenon was that the share of energy intensiveindustries, such as steel, cement, and petro-chemicalindustries increased. Second, during the sameperiod, liquefied natural gas (LNG) rapidlypenetrated this sector, so that theCO₂ intensity improved. We find thatharmonization of economic development strategies andenvironmental consideration is crucial for sustainabledevelopment. Based on our study, we derived somepolicy implications. Integration of industrialpolicies and energy efficiency improving programs isquite important, as well as the acceleration of fuelsubstitution to less carbon (C) intensive ones. Integration of local and global environmental policiesplays an important role for mitigatingCO₂ emissions.