잉어, Cyprinus carpio를 대상으로 고수온 스트레스 발생 시 코티졸 호르몬 변화 및 누적 사망 률을 조사하였다. 수온 변화에 따른 20℃, 24℃ 및 28℃ 실험군의 코티졸 변화는 수온 변화 후 6시간에 코티졸 함량이 증가하다가 24시간 이후부터 감소하여 20℃ 및 24℃ 실험군은 실험 전 의 코티졸 함량에 가까운 수치로 감소하였다. 48시간의 28℃ 실험군 코티졸 함량은 실험 전의 코티졸 함량보다 높았으나 24시간의 코티졸 함량보다는 유의한 차이를 보이며 감소하였다. 반면, 32℃ 실험군은 수온 변화 후 6시간부터 코티졸 함량이 증가하여 24시간에 코티졸 함량 이 최대치로 증가하였으며 48시간까지 코티졸 함량이 감소하지 않고 유지되는 경향이 나타났 다. 20℃, 24℃ 및 28℃ 실험군은 수온 변화 후 12시간까지 누적 사망률이 증가하다가 그 이 후부터 사망하는 개체가 발생하지 않았으나, 32℃ 실험군은 실험 종료 시(48시간)까지 지속적 으로 누적 사망률이 증가하는 경향이 나타났다. 본 연구로 도출된 결과를 이용하여 호르몬 분 석을 통해 특정지역의 폐사 위험 정도를 확인할 수 있는 방안으로 활용 가능할 것이다.

본 연구는 수산양식분야에서 용수를 살균하기 위해 제품화되어 있는 UV 및 플라즈마 장치를 100 ℓ 수조에 적용하고 처리수를 1 ℓ씩 채수, 농축하여 시료 내 세균 수의 변화를 확인하여 두 가지 처리 방식에 따른 효과를 비교하였다. 각 장치를 6시간 동안 작동시키면서 일반 해 수 내 세균을 MA, TCBS, SS 배지에 배양하여 세균 수 변화를 확인하였고, 살균처리된 해수 내 Edwardsiella piscicida를 인위 접종한 후 처리수 내 E. piscicida 세균 수 변화를 확인한 결과 UV 장치와 플라즈마 장치 간의 세균 저감 효율은 99.5~99.9% 수준으로 거의 유사한 수준으로 확 인되었다. 2가지 장치를 적용하여 100 ℓ의 수량을 동일한 시간 동안 처리하였을 때, 플라즈마 방식의 경우 UV 장치와 비교하여 더 짧은 시간 안에 세균을 사멸하는 것으로 나타났다. 하지 만 본 연구에서는 단기적(6시간)으로만 세균 수 변화를 확인한 것으로, 사료찌꺼기, 배설물, 연 안 오염 등에 따라 수질의 변동이 크고 biofilm과 유기물이 많이 존재하는 실제 양식환경을 고려할 때, 탁도와 유기물의 존재에 따라 한계가 있는 UV 처리 방식보다는 지속적이고 일정 한 효과를 유지할 수 있는 플라즈마 처리 방식이 보다 효율적일 것으로 사료된다.

In this work, we study physical and mechanical properties of oxide films formed on AZ91D magnesium alloy by plasma anodization at different temperatures. It is found that the higher the electrolyte temperature, the lower is the breakdown voltage of oxide layer. This is probably because films formed at higher temperatures are thinner and denser. Moreover, electrolyte temperature plays an important role in the physical properties of the films. As the electrolyte temperature increases from 20 to 50℃, the hardness of the oxide layer increases. Friction test against steel balls indicates that wear scars become narrower for films formed at higher temperatures because the films are harder, as indicated by the Vickers hardness. The thinner and denser nature of the oxide film formed at 50°C is also advantageous for heat transfer when film is used as a heat sink. Laser flash test results show very fast heat transfer for AZ91D with plasma anodized oxide layer formed at higher temperatures.

Molybdenum is a low-resistivity transition metal that can be applied to silicon devices using Si-metal electrode structures and thin film solar cell electrodes. We investigate the deposition of metal Mo thin film by plasma-enhanced atomic layer deposition (PE-ALD). Mo(CO)6 and H2 plasma are used as precursor. H2 plasma is induced between ALD cycles for reduction of Mo(CO)6 and Mo film is deposited on Si substrate at 300℃. Through variation of PE-ALD conditions such as precursor pulse time, plasma pulse time and plasma power, we find that these conditions result in low resistivity. The resistivity is affected by Mo pulse time. We can find the reason through analyzing XPS data according to Mo pulse time. The thickness uniformity is affected by plasma power. The lowest resistivity is 176 μΩ·cm at Mo(CO)6 pulse time 3s. The thickness uniformity of metal Mo thin film deposited by PE-ALD shows a value of less than 3% below the plasma power of 200 W.

In this study, we investigate the effect of Al/N source ratios and growth rates on the growth and structural properties of AlN films on c-plane sapphires by plasma-assisted molecular beam epitaxy. Both growth rates and Al/N ratios affect crystal qualities of AlN films. The full width at half maximum (FWHM) values of (1015) X-ray rocking curves (XRCs) change from 0.22 to 0.31° with changing of the Al/N ratios, but the curves of (0002) XRCs change from 0.04 to 0.45° with changing of the Al/N ratios. This means that structural deformation due to dislocations is slightly affected by the Al/N ratio in the (1015) XRCs but affected strongly for the (0002) XRCs. From the viewpoint of growth rate, the AlN films with high growth rate (HGR) show better crystal quality than the low growth rate (LGR) films overall, as shown by the FWHM values of the (0002) and (1015) XRCs. Based on cross-sectional transmission electron microscope observation, the HGR sample with an Al/N ratio of 3.1 shows more edge dislocations than there are screw and mixed dislocations in the LGR sample with Al/N ratio of 3.5.

Oxide coatings are formed on die-cast AZ91D Mg alloy through an environmentally friendly plasma electrolytic oxidation(PEO) process using an electrolytic solution of NaAlO2, KOH, and KF. The effects of PEO condition with different duty cycles (10 %, 20 %, and 40 %) and frequencies(500 Hz, 1,000 Hz, and 2,000 Hz) on the crystal phase, composition, microstructure, and micro-hardness properties of the oxide coatings are investigated. The oxide coatings on die-cast AZ91D Mg alloy mainly consist of MgO and MgAl2O4 phases. The proportion of each crystalline phase depends on various electrical parameters, such as duty cycle and frequency. The surfaces of oxide coatings exhibit as craters of pancake-shaped oxide melting and solidification particles. The pore size and surface roughness of the oxide coating increase considerably with increase in the number of duty cycles, while the densification and thickness of oxide coatings increase progressively. Differences in the growth mechanism may be attributed to differences in oxide growth during PEO treatment that occur because the applied operating voltage is insufficient to reach breakdown voltage at higher frequencies. PEO treatment also results in the oxide coating having strong adhesion properties on the Mg alloy. The micro-hardness at the cross-section of oxide coatings is much higher not only compared to that on the surface but also compared to that of the conventional anodizing oxide coatings. The oxide coatings are found to improve the micro-hardness with the increase in the number of duty cycles, which suggests that various electrical parameters, such as duty cycle and frequency, are among the key factors controlling the structural and physical properties of the oxide coating.

Benzo[α]pyrene (BaP), a carcinogenic polycyclic aromatic hydrocarbon, is ubiquitous in nature. It is generally found in heat-treated foods like roasted sesame seeds. BaP degradation has attracted attention due to the recalcitrant nature of BaP. In this study, corona discharge plasma jet (CDPJ) was used to degrade BaP on glass slides and in food materials. The plasma discharges were generated using air as working gas under atmospheric pressure conditions and at different currents (1.00, 1.25, and 1.50 A). Optimal BaP degradation was observed upon using CDPJ generated at 1.50 A current and at 15 mm sample-to-electrode distance (STED). Under these conditions, initial BaP concentration on slides was reduced maximally by 87.09% in 30 min. The degradation kinetics were well-fitted by Weibull tail model compared with others. In food commodities (roasted sesame and perilla seeds), the average levels of BaP degradation ranged between 32.96-45.90% following CDPJ treatment for 30 min.

Sodium dodecylbenzen sulfonate (DBS) and linear alkylbenzene sulfonate (LAS) are widely used in dishwashing products. Residual levels of these surfactants are commonly found on the surfaces of dishware following dishwashing. Residual surfactants and detergents can act as potential toxicants and may pose health risks. This study explored the applicability of dielectric barrier discharge plasma (DBDP) for the degradation of residual surfactants in order to minimize their harmful effects. The plasma was generated using 10 kV pulsed DC power supply at different input currents (2.0-3.0 A) and at various inter-electrode gaps (2.0-3.0 mm). Under simulatory treatment conditions, diluted surfactants (DBS and LAS) and DBS-containing dishwashing detergents dispersed on slide glasses were exposed to DBDP for predetermined periods of time. Results indicated that, under optimal treatment conditions of 3.0 A current and 2.0 mm inter-electrode gap, tested surfactants and surfactants in detergents were degraded in the range of 60- 70% following the plasma treatment for 120 min. Modeling of degradation kinetics indicated that Weibull distribution was the best-fit model, and decimal degradation times (δ) were calculated. Pure surfactants were degraded at relatively higher level than surfactants in detergents. Among these anionic surfactants, DBS was more rapidly degraded than LAS by plasma treatment.