본 연구는 경주시 가로변의 침입외래식물을 조사, 분석하여 가로경관 및 조경수관리에 필요한 기초 자료를 제공하는데 목적이 있다. 분류군수는 24과 69속 94종 1변종 등 95분류군으로 요약되었다. 원산지 분석 결과, 아프리카 2분류군, 오스트레일리아 1분류군, 아시아 5분류군, 유라시아 8분류군, 유럽 40분류군, 북아메리카 26분류군, 남아메리카 6분류군, 열대아메리카 7분류군이었다. 귀화도의 경우 1등급 9분류군, 2등급 22분류군, 3등급 28분류군, 4등급 9분류군, 5등급 27분류군이며, 이입시기는 1기와 3기 각 39분류군, 2기 17분류군이었다. 전국확산 예상종은 콩다닥냉이, 울산도깨비바늘, 만수국아재비, 큰김의털 등 13분류군이었다. 생활형 분석 결과, 교목 2분류군, 관목 1분류군, 지표식물 6분류군, 반지중식물 22분류군, 지중식물 5분류군, 일년생 식물 59분류군으로 나타났다. 생태계교란생물은 애기수영, 가시박, 도깨비가지, 돼지풀, 서양금혼초, 가시상추, 미국쑥부쟁이 7분류군이었다.

최근 환경규제가 강화됨에 따라 액화천연가스(Liquefied Natural Gas)를 이용하여 전력을 생산해내는 신규발전설비인 부유식 LNG 발전설비(floating LNG power plant)가 개발되고 있다. 부유식 LNG 발전설비는 운용 시 증발가스가 발생하고 이를 제거하거나 회수할 수 있는 시스템의 설계가 필요하다. 그러나 해양플랜트는 해상요건에 따라 설계가 상이하고, 부유식 LNG 발전설비의 설계 전 시행착오를 줄이기 위해 지속적으로 수정이 가능한 BOG 회수시스템 공정모사 모델이 필요하다. 따라서 본 연구에서는 상용공정시뮬레이션 프로그램을 통해 부유식 LNG 발전설비에 적합한 모델을 모델링하고자 냉매사용 유무에 따라 서로 다른 BOG(Boil-Off Gas) 회수시스템을 모델링하여 BOG의 회수율과 액화점을 비교 및 분석하였으며, 그 결과 질소냉매를 사용한 BOG 회수시스템 모델을 부유식 LNG 발전설비용 BOG 회수시스템 모델로 제안하고자 한다.

본 연구에서는 동맥스핀라벨링을 이용하는 비 조영증강 기법인 4D TRANCE으로 동정맥기형 환자를 진단함에 있어 기존에 사용하고 있는 4D TRAK과 조영증강 3D TOF으로 얻는 진단적 정보의 재현성과 유용성을 알아보고자 하였다. 연구방법 은 동정맥기형 추적검사를 하는 환자 14명을 대상(남자 4명, 여자 10명)으로 하여 뇌혈관 영상을 각각 4D TRANCE, 4D TRAK, 조영증강 3D TOF를 순서로 획득하였다. 영상의학과 전문의 2명이 3 영상의 진단적 평가와 영양동맥(feeding artery, FA)과 배출정맥(draining vein, DV)을 비교 평가하였고, 동일한 부위의 병소(nidus)와 내경동맥에 대한 대조도 잡음비를 비교 분석하였다. 정성평가는 4D TRANCE는 진단적 정확도 3.93(3.89~4.04), FA 3.75(3.55~3.95), DV 1.96(1.77~2.16) 으로 모든 구간에서 4D TRAK과 비교하여 통계적으로 유의하였으나(p＜0.001), 유일하게 DV에서 유의하지 않았다. 정량 분석에서는 4D TRANCE와 3D TOF의 대조도 잡음비에 따른 독립표본 T검정 결과, 조영증강되는 병소에서는 4D TRANCE가 3D TOF에 비해 15.50의 차이로 높았으며, 통계적으로 유의하였다. 본 연구는 동정맥기형 추적검사에 대해 4D TRANCE는 4D TRAK보다 다소 저하된 영상품질을 보여주었으나, 3D TOF와 비교했을 때 혈관 해부학 및 혈류역학 정보를 제공하기 때문에 더 신뢰할 수 있는 정보를 제공하여 임상 영상 평가에 유용하게 사용할 수 있다.

In this study, we investigated to the heat transfer performance of coating nano-structure with various shapes and patterns on the heat transfer surface. As a result of the measurement of the 3D nano shape, it was confirmed that the roughness generally increases when the adhesive is sprayed on the coating surface and finished durability experiment. In the case of TEOS adhesive, the roughness increased by 0.074 ㎛, 0.012 ㎛ and 0.015 ㎛, and the contact angle decreased 12.64°, 1.31°, 9.84° at the coating time of 120 seconds, 180 seconds and 240 seconds, respectively. In the case of PVA adhesive, the roughness increased by 0.069 ㎛, 0.056 ㎛ and 0.03 ㎛, and the contact angle decreased 2.85°, 4.82°, 6.96° at the coating time of 120 seconds, 180 seconds and 240 seconds, respectively. In the case of DGEBF adhesive, the roughness increased by 0.042 ㎛, 0.053 ㎛ and 0 ㎛, and the contact angle decreased 0.81° at the coating time of 120 seconds, increased 4.82°, 6.96° at the coating time of 180 seconds and 240 seconds, respectively. As a result, the durability tends to decrease as more nano-structures are deposited, and 3D nano shapes, contact angles and SEM photographs showed that the performance of the PVA adhesive was superior among the three adhesives.

This study evaluated the concentration(OU/m3) of a complex odor being discharged from tire, feedstuff, bakery, paper, casting and painting manufacturing process, correlation between odor concentration(OU/m3) and the odor sensor was investigated. 4 type(A, B, C, D) gas sensors of metal oxide compounds are used in this study. Each odor sample of manufacturing process is diluted with odorless air and diluted odor samples were prepared for five different concentrations. Correlation results(R) of odor sample of tire, feedstuff, bakery, paper manufacturing process ware 0.86~0.99, and odor sample of casting, painting manufacturing process ware more than 0.93. Thus the odor concentration(OU/m3) evaluation by odor sensor was to determine the possible. In particular odor sensor B and D are likely to be effective for evaluation of odor concentration. However, odor samples before evaluation is needed the calibration process depending on the field odor sample to field apply.

This study was conducted to test whether the transgenic cattle pass the transgene to their progeny through germ cells, and whether the transgene is expressed in the mammary gland of ransgenic cows. Two male ransgenic calves were born from IVF-derived embryos injected with bovine β-casein/human lactoferrin fusion gene and then grew up to be reproducible. Semen was collected from a transgenic bull after 18 mon of age and then frozen. Bovine oocytes matured in vitro were fertilized with spermatozoa of the transgenic bull and cultured in 50㎕ drops of CRlaa medium supplemented with 3 mg/mL BSA. After 48 h of culture, cleaved embryos were determined for the presence of transgenes by DNA polymerase chain reaction (PCR). Proportion of transgene positives among bovine embryos fertilized with sperm of the transgenic bull was 20.9% (28/134). One of transgenic bulls did not produce transgenic sperm. Out of 34 calves produced from recipient heifers inseminated with semen of the other bull, 3 (8.8%) were transgenic animals (2 females and 1 male). Thus, one transgenic bull showed a low transmission frequency below Mendelian levels in both the IVF-derived embryos and his progeny. It was demonstrated by Southern blot that copy numbers of the transgene in the transgenic progeny enhanced about 1.8 times as compared to those of the founder bull The results demonstrate that the transgenic bull carrying human lactoferrin gene could pass his transgene to the progeny through germ cells, although he is a germ-line mosaic.

The advanced oxidation treatment using persulfate and zero-valent iron (ZVI) has been evaluated as a very effective technology for remediation of soil and groundwater contamination. However, the high rate of the initial reaction of persulfate with ZVI causes over-consumption of an injected persulfate, and the excessively generated active species show a low transfer rate to the target pollutant. In this study, ZVI was modified using selenium with very low reactivity in the water environment with the aim of controlling the persulfate activation rate by controlling the reactivity of ZVI. Selenium-modified ZVI (Se/ZVI) was confirmed to have a selenium coating on the surface through SEM/EDS analysis, and low reductive reactivity to trichlroethylene (TCE) was observed. As a result of inducing the persulfate activation using the synthesized Se/ZVI, the persulfated consumption rate was greatly reduced, and the decomposition rate of the model contaminant, anisole, was also reduced in proportion. However, the final decomposition efficiency was rather increased, which seems to be the result of preventing persulfate over-consumption. This is because the transfer efficiency of the active species (SO4-∙) of persulfate to the target contaminant has been improved. Selenium on the surface of Se/ZVI was not significantly dissolved even under oxidation conditions by persulfate, and most of it was present in the form of Se/ZVI. It was confirmed that the persulfate activation rate could be controlled by controlling the reactivity of ZVI, which could greatly contribute to the improvement of the persulfate oxidation efficiency.

Forests are valuable natural resources for people living around the mountains. In particular, the comfortable feeling or healing is one of the most important benefits obtained from forests. This healing can be possible by many aspects of forests, including the landscape, natural sounds, anions, and pleasant aromas. We focused on the volatile organics from forest causing pleasant aromas, phytoncides. Twenty phytoncides were monitored from February to September in a national tree garden (BaekDoDaeGan SooMokWon). Five sites were monitored two times per month and 20 phytoncides were detected. Borneol showed the highest annual average concentration and the order of concentration was borneol > mycene > sabinene > limonene > α-pinene. The average phytoncide concentration was relatively high in spring and summer season when the trees were physiologically active. Daily monitoring showed that the afternoon hours had higher concentrations of phytoncides than the morning hours, which may be due to the stabilized atmospheric conditions at the sites. Among the five sites, coniferous forests gave higher phytoncide emissions than broadleaf tree forests. The current study showed that forests produce several phytoncides that cause a healing effect and a forest bath may be beneficial to the health of visitors to forests.

Environmental contamination by organic compounds are not only restricted to water, but extends to soil and groundwater as well. However, highly oxidized compounds, such as halogenated organics and nitro-compounds, can be detoxified employing reducing methods. Permeable reactive barrier is one of the representative technologies where zero-valent metals (ZVMs) are employed for groundwater remediation. However, organics contaminates often contaminate the unsaturated zone above the groundwater. Despite the availability of technologies like soil vapor extraction and bioremediation, removing organic compounds from this zone represents several challenges. In this study, the reduction of nitrobenzene to aniline was achieved using zero-valent iron (ZVI) under unsaturated conditions. Results indicated that the water content was an important variable in this reaction. Under dry conditions (water content = 0.2%), the reduction reaction was inhibited; however, when the water content was between 10% and 25% (saturated condition), ZVI can reduce nitrobenzene. Palladized iron (Pd/Fe) can be used to reduce nitrobenzene when the water content is between 2.5% and 10%. The reaction was evaluated over a wide range of temperatures (10 – 40 °C), and the results indicated that increasing the temperature resulted in increased reaction rates under unsaturated conditions.

Organic contaminants can be released into water environments due to chemical accidents and exist as dissolved and non-aqueous phase liquids (NAPL). Fenton oxidation was tested for bisphenol A and nitrobenzene as model organic contaminants in dissolved and NAPL states. Fenton oxidation was successfully applied for both of the dissolved and NAPL states of the two pollutants and the results indicated that a quick treatment was needed to reduce the risk from a chemical accidents instead of carrying out oxidation after the contaminants dissolve in water. A set of Fenton reactions were tested under seawater conditions because chemical accidents often occurs in the ocean. Chloride ions act as radical scavengers and inhibit Fenton oxidation. The reaction rate is inversely proportional to salt contents and the reduced reaction rate can be compensated by increasing the quantity of the oxidizing agents. The current study showes that Fenton oxidation could be applied as a quick treatments for organic contaminant in dissolved and NAPL state organic contaminants released as a result of leaks or chemical accidents.

In this study, the applicability of reduction-oxidation-linked treatment was evaluated for nitrobenzene and a by-product by analyzing the reaction kinetics. Nitrobenzene showed very low reactivity to persulfate that was activated using various methods. Nitrobenzene effectively reacted through the reduction process using Zero-Valent Iron (ZVI). However, aniline, a toxic substance, was produced as a by-product. Reduction-oxidation-linked treatment is a method that can allow the oxidative degradation of aniline after reducing nitrobenzene to aniline. The experimental results show improved reactivity and complete decomposition of the by-product. Improved reactivity and decomposition of the by-product were observed even under conditions in which the reduction-oxidation reaction was induced simultaneously. No activator was injected for persulfate activation in the process of reducing oxidant linkage, and the activation reaction was induced by ferrous iron eluted from the ZVI. This indicates that this method can be implemented relatively simply.

Oxidative degradation of phenol, three monochlorophenols (2-chlorophenol, 2-CP; 3-chlorophenol, 3-CP; 4-chlorophenol, 4-CP), four dichlorophenols (2,3-dichlorophenol, 2,3-DCP; 2,4-dichlorophenol, 2,4-DCP; 2,5-dichlorophenol, 2,5-DCP; 2,6-dichlorophenol, 2,6-DCP), and two trichlorophenols (2,4,5-trichlorophenol, 2,4,5-TCP; 2,4,6-trichlorophenol, 2,4,6-TCP) was conducted with heat activated persulfate. As the number of chlorinations increased, the reaction rate also increased. The reaction rate was relatively well fitted to the zero-order kinetic model, rather than the pseudo-first order kinetic model for the reactions at 60℃, which can be explained by insufficient activation of the persulfate at 60℃, and the oxidation reaction of 2,4,6-TCP at 70℃ was relatively well fitted to the pseudo-first order kinetic model. The oxidation reaction rate generally increased with increase of persulfate concentration in the solution. 2,6-dichloro-2,5-cyclohexadiene-1,4-dione was found as a degradation product in a GC/MS analysis. This compound is a non-aromatic compound, and one chlorine was removed. This result is similar to the result of previous studies. The current study proved that heat activated persulfate activation could be an alternative remediation technology for phenol and chlorophenols in soil and groundwater.

Arsenic is among the heavy metals commonly found in aqueous environments. Iron oxide is known as an efficient adsorbent for the arsenic. A new synthetic method was applied to provide iron oxide giving a large specific surface area. The mixing method affects the formation of iron oxide. Ultrasonic waves assisted the formation of very fine iron oxide in an organic phase. The synthesized iron oxide is amorphous type with a high surface area of more than 181.3 m2/g. Sorption capacity of the synthesized adsorbent was relatively very high for arsenic and varied depending on the oxidation state of arsenic: a higher capacity was obtained with As(V). Lower solution pH provided a higher sorption capacity for As(V). The competitive effect of co-exist anions such as chloride, nitrate, and sulfate was minimal in sorption capacity of the iron oxide for arsenic.

During the past few decades, significant increase in the consumption of coffee has led to rapid increase in the production of coffee waste in South Korea. Spent coffee waste is often treated as a general waste and is directly disposed without the necessary treatment. Spent Coffee Grounds (SCGs) can release several organic contaminants, including caffeine. In this study, leaching tests were conducted for SCGs and oxidative degradation of caffeine were also conducted. The tested SCGs contained approximately 4.4 mg caffeine per gram of coffee waste. Results from the leaching tests show that approximately 90% of the caffeine can be extracted at each step during sequential extraction. Advanced oxidation methods for the degradation of caffeine, such as UV/H2O2, photo-Fenton reaction, and UV/O3, were tested. UV radiation has a limited effect on the degradation of caffeine. In particular, UV-A and UV-B radiations present in sunlight cause marginal degradation, thereby indicating that natural degradation of caffeine is minimal. However, O3 can cause rapid degradation of caffeine, and the values of pseudo-first order rate constants were found to be ranging from 0.817min-1 to 1.506 min-1 when the ozone generation rate was 37.1 g/m3. Additionally, the degradation rate of caffeine is dependent on the wavelength of irradiation.

Trains have been a major means of transport in Korea during these past decades. However, train facilities such as stations and repair shops are contaminated with organic and inorganic substances. There is a high probability of train facility contamination with polyaromatic hydrocarbons (PAHs). This study evaluated the PAH and heavy metal contamination of soil near railroads in the Kyungpook area. A total of 18 soil samples were collected from the railroads and analyzed for 16 PAHs and 6 heavy metal species. The contamination level of the top soil was found to be slightly higher than that of the subsoil for contamination with PAHs. The ratio of carcinogenic PAH concentration to the total PAH concentration was relatively high, with a maximum of 0.9. The toxicity equivalent (TEQ) of the PAHs were 500.6 ng/kg in the topsoil and 355.5 ng/kg in the subsoil. The ratio of low molecular PAHs (LPAHs) to high molecular PAHs (LPAHs) ranged from 6.7 to 29.5; this shows that contamination is primarily due to combustion of fuel rather than due to petroleum. The ratio of phenanthrene to anthracene and the ratio of fluoranthene to pyrene also show that contamination occurred due to combustion for transportation. The heavy metal contamination level was lower than the Korean standard, but higher than the background concentration; this indicates that the soil was affected by the operation of the railways.

Oxidative degradation of chlorinated ethenes was carried out using heat-activated persulfate. The activation rate of persulfate was dependent on the temperature and the activation reaction rate could be explained based on the Arrhenius equation. The activation energy of persulfate was 19.3 kcal/mol under the assumption that the reaction between the sulfate radical and tricholoroethene (TCE) is very fast. Activation could be achieved at a moderate temperature, so that the adverse effects due to high temperature in the soil environment were mitigated. The reaction rate of TCE was directly proportional to the concentration of persulfate, indicating that the remediation rate can be controlled by the concentration of the injected persulfate. The solution was acidized after the oxidation, and this was dependent on the oxidation temperature. The consumption rate of persulfate was high in the presence of the target organic, but the self-decomposition rate became very low as the target was completely removed.

In this study, the reductive dechlorination of triclosan using zero-valent iron (ZVI, Fe0) and modified zero-valent iron (i.e., acid-washed iron (Aw/Fe) and palladium-coated iron (Pd/Fe)) was experimentally investigated, and the reduction characteristics were evaluated by analyzing the reaction kinetics. Triclosan could be reductively decomposed using zero-valent iron. The degradation rates of triclosan were about 50% and 67% when Fe0 and Aw/Fe were used as reductants, respectively, after 8 h of reaction. For the Pd/Fe system, the degradation rate was about 57% after 1 h of reaction. Thus, Pd/Fe exhibited remarkable performance in the reductive degradation of triclosan. Several dechlorinated intermediates were predicted by GC-MS spectrum, and 2-phenoxyphenol was detected as the by-product of the decomposition reaction of triclosan, indicating that reductive dechlorination occurred continuously. As the reaction proceeded, the pH of the solution increased steadily; the pH increase for the Pd/Fe system was smaller than that for the Fe0 and Aw/Fe system. Further, zero-order, first-order, and second-order kinetic models were used to analyze the reaction kinetics. The first-order kinetic model was found to be the best with good correlation for the Fe0 and Aw/Fe system. However, for the Pd/Fe system, the experimental data were evaluated to be well fitted to the second-order kinetic model. The reaction rate constants (k) were in the order of Pd/Fe > Aw/Fe > Fe0, with the rate constant of Pd/Fe being much higher than that of the other two reductants.