The electrical connection between zinc metal and iron in contact with water prevents oxidation of iron until all zinc is dissolved, which is called a zinc sacrificial anode phenomenon. In the case of water pipes, zinc is often attached to the outside of the pipe, but examples of mounting zinc inside the pipe to prevent iron corrosion are not well known. Zinc devices sold for water pipes vary in the amount of zinc installed depending on the diameter of the pipe and the conditions of use, but the life of the product is generally expected to be 10-20 years until all zinc dissolves and disappears. Zinc ions dissolved from zinc to water in the pipe react with the calcium carbonate scale generated inside the pipe to consume zinc ions, and it was confirmed that the needle-shaped aragonite was converted into highly crystalline calcium after observing the scale crystal through an electron microscope. In addition, it is estimated that calcium ions of scale are replaced by zinc ions, gradually losing crystallinity, being deintercalated into the pipe, and oxygen in the water is consumed during the dissolution of zinc ions from zinc metals, turning red rust hematite (Fe2O3) into magnetite (Fe3O4). In addition, zinc ions were expected to move hundreds to thousands of meters depending on the diameter of the pipe in the new pipe, but it was confirmed that the travel distance was shortened in the case of pipes with many corrosion products.

Scale and rust generation in water pipes is a common phenomenon when cast iron water pipes have been used for a long time. A physical water treatment device is known among various means for suppressing rust in a water pipe, and a zinc ionization device for putting zinc metal into a pipe and emitting the zinc cation into water is one of such devices. This research measured the amount of zinc ion generated, which is known to exhibit an effect of inhibiting rust and scale generation in a pipe, and examined the scale and rust inhibition effect of the ionization device installed for ground or building water supply. In the case of distilled water, the concentration of zinc ion increased by circulating water in the ionization device several times, and it was verified to be hundreds of μg/L, and in the case of discharging ground or tap water, it was verified to be tens of μg/L. In addition, a verification pipe was installed to confirm the change inside the pipe before and after installation of the zinc ionization device, and the internal condition of the pipe was observed 3 months to several years after installation. It was confirmed that the corrosion area of the surface of the pipe was no longer increased by installing a corrosion inhibitor, and if the pipe was already filled with corrosion products, the amount of corrosion products gradually decreased every year after installation. The phenomenon of fewer corrosion products could be interpreted as expanding the space in the pipe due to the corrosion product as Fe2O3 adhered to the inner surface of the pipe and turned into a smaller black Fe3O4. In addition, we found that scale such as CaCO3 together in the corrosion by-products gradually decreased with the attachment of the ionization device.

초지 또는 농경지에 살포되는 퇴비와 액비에 의해 발생될 수 있는 악취민원에 대처하기 위하여, 돼지의 분과 뇨에 존재하는 악취물질 농도를 비교 분석하였다. 1.비육돈의 분과 뇨에 함유된 휘발성유기물의 농도 비교페놀, p-크레졸 및 페놀류 농도는 분 보다 뇨에서 높았으며(p<0.05), 분 보다 뇨에 축적된 비율이 페놀은 138배, p-크레졸은 545배 높았다. 인돌 농도는 분 보다 뇨에서 높았으며, 스카톨은 뇨 보다 분에서 높았다(p<0.05). 휘발성유기물은 대부분 뇨로 배설되었으며, 이 중 농도 및 악취강도가 가장 높은 물질인 p-크레졸이 뇨에 많이 함유되어 있다. 돼지 분뇨를 고액분리 하였을 때 퇴비로 이용되는 고체보다 액비로 이용되는 액상물질에서 악취가 훨씬 강할 것으로 예측된다. 2.비육돈의 분과 뇨에 함유된 휘발성지방산의 농도 비교아세트산과 단쇄지방산 농도는 분 보다 뇨에서 높았으며 (p<0.05), 부티르산과 프로피온산은 차이가 없었다(p> 0.05). 이성체지방산 중 I-부티르산의 농도는 뇨 보다 분에서 높았지만(p<0.05), I-발레르산과 이성체지방산은 차이가 없었다(p>0.05). 휘발성지방산 중에서 아세트산과 프로피온산은 분에서 각각 65와 20%, 뇨에서는 각각 93과 4%로 휘발성지방산의 대부분을 차지하였지만 아세트산과 프로피온산을 포함하는 단쇄지방산은 악취강도가 낮다. 반면에 악취강도가 상대적으로 높은 이성체지방산은 분과 뇨 간에 차이가 없기 때문에 휘발성지방산이 악취강도에 미치는 영향은 크지 않을 것으로 판단된다. 이상의 연구결과를 종합하면, 돼지 분뇨의 악취물질 중 악취강도가 높은 p-크레졸은 뇨에 많이 함유되어 있기 때문에 퇴비와 액비 생산과정 중 액상처리 시 악취강도가 매우 높을 것으로 추정된다. 다만, 악취강도는 휘발성지방산의 농도 변화에 따라 차이가 있을 것으로 생각된다.

Odor intensities, odor concentrations and volatile amine compounds were investigated at the two piggeries in Korea and the one in Japan. It was confirmed that the piggery where odor control had been carried out intentionally showed the lower values of sensory measurement than those where the odor control had not been under consideration and also found that the concentrations of volatile amines in the odor-controlled piggery showed lower values rather than the uncontrolled. In this investigation, we conclude that the activities such as circulation of air in pig houses, spraying deodorants and feeding the additive that is effective for reducing malodors from piggery could decrease the odors and the concentrations of volatile amines that are the cause of offensive odors from piggery.

Volatile organic compounds and malodors emitted from painting operations are of primary concern in the automotive industry and pressured to be abated by newly amended VOC rule and offensive odor law in Korea. Over-sprayed paints in painting booths are delivered into water surface by downward stream of clean air and collected in water circulating pools. The circulating water mixed with waste paints generated from paint booths put out floating sludge by addition of chemical killing agent and floating agent and the odors evolved from this procedure has been under the circumstance that it must be validated to match the new rules. The activated sludge method that the circulating water pond would be considered as a huge bioreactor was applied to this over-sprayed sludge tank. and we got some remarkable reductions of sludge, odours, VOCs and dirts on air dusts. Herein, some abbreviated results will be reported.

In this paper, theoretical efficiencies of Korean and Japanese determination methods for dilution factors of odor samples were considered. The Korean official method points out over 5 persons but the Japanese over 6 as assessors, and 6-4 selection and 2 bags comparison methods, being used mainly in Japan as simplified of the official method, describe over 2 persons. The Korean method practices 10-dilution as starting factor in case of low odor concentrations and 300-dilution in high concentrations. In Japan, the determination of low odor concentrations has been carried out from 10-dilution like Korean, but high concentrations start from 100-dilution, being allowed to be changeable of starting dilution. In two official methods, it has been in concord with each other that maximum and minimum threshold values should be excluded, but not calculation methods of average dilution value of each panelist, resulting in indicating that the final result of panelers" assessment of an odor sample in Japan has been about 1.8 times higher than that in Korea. Quantity of consumed bags for determination of dilution factor is expected to be about 1.8 times more in the Japanese than ill the Korean in case of low odor concentrations but almost same in high concentrations. And so in high concentrations, the Korean method is expected to be a bit more economical and effective than the Japanese, but not accurate in low concentrations.

Aliphatic amine compounds have very low detectable threshold value concentrations, and especially trimethyl amine is one of the main odor-active compounds in atmospheric environment. Concentration of a large amount (10~100 L) of air sample was needed to detect trace amounts of amine compounds by GC/FTD. Amine compounds in ambient air were absorbed in sulfuric acid solution by using impingers and sampling pump. Some amount of the absorption solution was injected in bubbling bottle which a concentration tube was connected with, and that amine gas which was isolated from bubbling bottle was trapped in a concentration tube dipped in liquid argon under a constant helium flow. A concentration tube was disjoined from the bubbling bottle and was connected to injection port of gas chromatograph. Amine compounds trapped in a concentration tube was introduced into the packed column by thermal desorption after flow rate of carrier gas and detector signal had been stabilized enough. Sampling volume of ambient air was different from place to place in the range of 10~100 L, and flow rate through impingers was 5 L/min. Atmospheric concentrations of trimethyl amine were below 16.0 ppbv in the boundary of business establishment and below 420.0 ppbv at the gas releasing port of business establishment in the industrial area.

Concentrations of hydrogen sulfide in ambient air have been measured from January 2014 to June 2016 in a coastal area near the Ulsan National Industrial Complex. The measurement sites were 1 km, 2.6 km, 5.6 km, and 20 km away from a kraft pulp mill, which is located at the most southern edge of the complex. Concentrations above 0.4 ppb were monitored every 5 min and the highest concentration of the day was determined. From a total of 775 measurement days, hydrogen sulfide concentrations > 20 ppb were recorded on 36 and 38 days at the measurement site closest to the mill and the residential area 2.6 km away from the mill, respectively. At the site farthest from the mill, the concentrations were always 20 ppb lower than the malodor regulation for the residential area but sometimes higher than the odor recognition threshold for hydrogen sulfide. Although several emission sources of hydrogen sulfide have been published in the Pollutant Release and Transfer Register of Korea, the kraft pulp mill is considered to be the biggest contributor of atmospheric hydrogen sulfide in the southern coastal area of Ulsan.

In order to prepare the information needed to construct a reduction system for volatile organic compounds (VOCs) exhausted from ship-block paint-booths in a giant shipyard, VOCs in paint-shop airs were analyzed and compared to the components in paint thinners. Aromatic hydrocarbons containing eight and nine carbon atoms are known to be major VOC compounds found in shipyard paint-shops. The total hydrocarbon (THC(C7)) concentrations calibrated using toluene gas, were measured in block paint-shops with two photo-ionization detector (PID) meters, and the resulting THC(C7) data were converted to THC(C1) concentrations according to the Standard Methods for the Measurements of Air Pollution in South Korea. THC(C1) concentrations near the spray site ranged from 10 to 2,000 ppm, but they were less than 400 ppm near the walls of the paint-booth. The measurements of THC concentrations, based on the height of the monitoring sites, were related to the height of the target to which the spray paints were applied. The maximum concentrations occurred at almost the same height as the spray targets. When painted blocks had been dried-by warming with no spraying, the THC concentrations were 80~100 ppm.

In this study, we analyzed the content and compensation factors of 337 cases of national environmental disputes from five recent years (2000~2014). Causes of damage were noise-vibration in 234 cases (69%), sunlight in 48 cases (14%), air pollution in 19 cases (6%), water pollution in 15 cases (4%), odor in 13 cases (4%), and others factors in 8 cases (3%). Sources of damage were construction in 224 cases (66%), structures in 36 cases (11%), vehicle on road in 31 cases (9%), industry in 18 cases (5%), environmental facility in 11 cases (3%), livestock facility in 6 cases (2%), and other sources in 11 cases (3%). From the results of logistic regression analysis, important factors associated with compensation were found to be damage amount, damage distance, zoning districts, source, and administrative disposition.

Regional air quality regulation is a system that allows the Minister of Environment to designate the local area as air quality control region where the concentrations of air pollutants are exceeding the environmental standards, and the local governments that administrate the regulated area have to develop and practise a plan for reducing the air pollutants. From the data observed yearly by the monitoring stations in 8 provincial cities with more than 0.5 million people was judged the compliance with air quality standards in each municipality for the period of 2003 to 2013. As the result of investigation on air pollutants concentrations of each city, it was found that there was no station that exceeds the ambient air quality standards of CO, SO2 and 24-hour NO2. But all municipalities exceeded the standards of 8-hour O3, annual and 24-hour PM10, and therefore 8 municipalities can be designated to be under the local air regulation. For the annual NO2 were the monitoring sites necessary requirements for designation of the air quality regulation region in Cheongju, Cheonan, Daejeon and Gwangju area. Incase of 1-hour O3, some of stations in Pohang, Cheongju, Cheonan and Changwon area were over the designation standards for the air quality control region.

In this study, the detection limits of lower fatty acids in air were investigated by using Dynamic SPME(Solid Phase Micro-Extraction), i.e. improved Head Space - SPME method(HS-SPME). This Dynamic SPME, called SPDE(Solid Phase Dynamic Extraction), is the analytical method for volatile compounds in air with the extraction by using a stainless steel needle of which inner surface is coated with adsorption material and following the gas chromatographic analysis by inserting the needle into a injection port of GC and subsequently, desorption of the volatile compounds into a gas- chromatographic column. Extraction was carried out by passing the sample air through the needle with a suction pump which has been used for a detection tube. The result of measurement for the 6 lower fatty acids showed that the detection limits ranged from 0.10 ppm to 0.44 ppm and the linear correlation coefficients were over 0.99. Relative standard deviations obtained from 5 analytical repetition of a ca. 1.6 ppm standard mixture were in the range of 1.87%∼2.47%. This method has been shown to be a adequate for the measuring C2∼C5 fatty acids in air in the concentrations of over several hundreds ppb.

Odor sources of a chemical plant in Ulsan were surveyed and temperatures, humidities and flow rates of each exhaust gas were measured. The air samples collected from each source were transferred to the laboratory for sensory test and their odor concentrations were investigated. The odor emission rate of each source was estimated from the recorded results and assigned the sources expected to be needed for the odor prevention policy using the simple prediction equation of the affection by malodor to the nearest residential area. From the total odor emission rate of the examined plant and the relation table for expectable affection area, it was concluded that total odor emission of this plant might be decreased for the prevention of residential complaint.

The volatile organic compounds(VOCs) emitted from raw garlic and Kimchee were analyzed with thermal desorption or purge & trap/gas chromatography/mass selective detection method. Very offensive compounds such as methyl allyl sulfide, dimethyl sulfide, dimethyl disulfide, diallyl sulfide, methyl allyl disulfide, diallyl disulfide and dimethyl trisulfide were detected, and among them, dimethyl disulfide and dimethyl trisulfide were confirmed to be generated during the precocity of Kimchee or emitted from the stuff of Kimchee other than the garlic. Malodorous compounds emitted from the garlic or Kimchee were detected in the breath of a Korean and the refregirator keeping Kimchee. It was confirmed that the disufides emitted from the garlic or Kimchee were major components of offensive odor in the alveolar air and the refregirator. It was clarified that heat process is very effective to reduce odorous VOCs in garlic or Kimchee.

SPME device was applied to determine the THM in an aqueous solution. The 6 kinds of THM was quantitatively detemined by using GC-ECD which has the sample extracted on the SPME fiber from an aqueous solution for 10 min. The THM components were well separated from CHCl_3 to the last CHBr_3 within 13 mans at the condition. 6 kinds of the volatile halogenated organic compounds: CHCl_3, CHBrCl_2, CHBr_2Cl, CHCl_3, C_2Cl_4, and CHBr_3, showed well defined calibration graph with good linearity from a few ppb level up to several tens of ppb concentration. CHBr_2Cl and C_2Cl_4, were detected from a few samples among the 10 of river samples. CHCl_3, however, was detected in 4 sea water samples with the highest of 10 ppb among the polluted 6 positions. Trace level of CHBr_2Cl and few ppb level of CHBr_3 were also detected at the other two sample stations. Most of the 13 rain water samples collected from 6 sampling stations were contained ppb level of CHCl_3, and also CHBr_2Cl, and C_2Cl_4 were only detected at trace level at a few rain samples among them. We could recognize the fact that our air and water environment has already been contaminated by certain volatile halogenated organic compounds through this study.

Volatile organic compounds in the ambient air were gathered irregularly by normal temperature concentrating method at Odea-ri and Oceon-ri Ulsan-gun in the neighbourhood of Ulsan Petrochemical Industrial Complex and analyzed with gas chromatograph. Several hydrocarbons in common atmospheric air or emitted fugitively from the chemical plants were identified and quantified by comparison with the retention times of standard compounds. The results from several field surveys in 1992 show that the concentrations of styrene at residential area of Odea-ri and Ocheon--ri were less than 0.4 ppm, but once a while greater within the chemical plants area. When it smelled unpleasantly in these area, the concentration of hydrocarbons were also high. It was concluded that the close and long-term investigation about other odorous components but hydrocarbons will be necessary to ascertain the cause of unpleasant odor of these area.