• Journal of the Korean Vacuum Society
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• v.19 no.4
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• pp.275-280
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• 2010

The influence of $O_2$-plasma treatment on $H_2$ post-treated BZO (ZnO:B) thin film using MOCVD (Metal-Organic Chemical Vapor Deposition) are investigated. An $O_2$-plasma treatment of the $H_2$ post-treated BZO thin films resulted in XRD peak of (100), (101) and (110). Also, electrical properties resulted in an increase in sheet resistance and work function. The weighted optical transmittance and haze at 300~1,100 nm of BZO thin films with $O_2$-plasma treatment on the $H_2$ post-treatment show approximately 86% and 15%, respectively.

• Journal of Bio-Environment Control
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• v.26 no.3
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• pp.158-166
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• 2017

The object of this study was to improve tomato seedling quality in low temperature(below 7, $10^{\circ}C$ during night time or daily mean air temperature was $18^{\circ}C$) by application of silicate fertilizer. Six different silicate fertilizer concentrations (8, 16, 32, 64, 128, and 256mM) or water as the control were applied to tomato seedlings twice a week for 20 days. Positive effects were observed in the growth parameters of the seedlings treated with 16 and 32mM silicate fertilizer; the most effective concentration of silicate at which seedlings showed the best performance was 16mM. However, a high concentration of silicate (256mM) caused negative effects on the growth. The transpiration rate decreased alongside with the increase of silicate concentration up to 32mM, possibly due to the increased stomatal diffusive resistance. Silicate stimulated the growth and development of tomato seedlings, resulting in increased growth parameters and root morphology. However, no significant differences were observed among treatment numbers of soil-drenching wuth the silicate (6, 10, or 20 times with 16mM) for 20 days, suggesting that silicate treatment with 6 times may be sufficient to induce the silicate effects. The application of 16mM of silicate fertilizer reduced relative ion leakage and chilling injury during low temperature storage. In addition, the seedlings treated with silicate fertilizer recovered faster than those without silicate treatment after low temperature storage.

• Journal of the Korean Vacuum Society
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• v.21 no.6
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• pp.333-341
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• 2012

Indium Tin Oxide (ITO) thin films were prepared by RF magnetron sputtering with different flow rates of $O_2$ gas from 0 to 12 sccm. Electrical and optical properties of these films were characterized and analyzed. ITO deposited on soda lime glass and RF power was 2 kW, frequency was 13.56 MHz, and working pressure was $1.0{\times}10^{-3}$ Torr, Ar gas was fixed at 1,000 sccm. The transmittance was measured at 300~1,100 nm ranges by using Photovoltaic analysis system. Electrical properties were measured by Hall measurement system. ITO thin films surface were measured by Scanning electron microscope. Atomic force microscope surface roughness scan for ITO thin films. ITO thin films secondary electron emission coefficient(${\gamma}$) was measured by ${\gamma}$-Focused ion beam. The resistivity is about $2.4{\times}10^{-4}{\Omega}{\cdot}cm$ and the weighted average transmittance is about 84.93% at 3 sccm oxygen flow rate. Also, we investigated Work-function of ITO thin films by using Auger neutralization mechanism according to secondary electron emission coefficient(${\gamma}$) values. We confirmed secondary electron emission peak at 3 sccm oxygen flow rate.

• Journal of the Korean Electrochemical Society
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• v.26 no.1
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• pp.1-10
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• 2023

The cathode, which is one of the four major components of a lithium secondary battery, is an important component responsible for the energy density of the battery. The mixing process of active material, conductive material, and polymer binder is very essential in the commonly used wet manufacturing process of the cathode. However, in the case of mixing conditions of the cathode, since there is no systematic method, in most cases, differences in performance occur depending on the manufacturer. Therefore, LiMn₂O₄ (LMO) cathodes were prepared using a commonly used THINKY mixer and homogenizer to optimize the mixing method in the cathode slurry preparation step, and their characteristics were compared. Each mixing condition was performed at 2000 RPM and 7 min, and to determine only the difference in the mixing method during the manufacture of the cathode other experiment conditions (mixing time, material input order, etc.) were kept constant. Among the manufactured THINKY mixer LMO (TLMO) and homogenizer LMO (HLMO), HLMO has more uniform particle dispersion than TLMO, and thus shows higher adhesive strength. Also, the result of the electrochemical evaluation reveals that HLMO cathode showed improved performance with a more stable life cycle compared to TLMO. The initial discharge capacity retention rate of HLMO at 69 cycles was 88%, which is about 4.4 times higher than that of TLMO, and in the case of rate capability, HLMO exhibited a better capacity retention even at high C-rates of 10, 15, and 20 C and the capacity recovery at 1 C was higher than that of TLMO. It's postulated that the use of a homogenizer improves the characteristics of the slurry containing the active material, the conductive material, and the polymer binder creating an electrically conductive network formed by uniformly dispersing the conductive material suppressing its strong electrostatic properties thus avoiding aggregation. As a result, surface contact between the active material and the conductive material increases, electrons move more smoothly, changes in lattice volume during charging and discharging are more reversible and contact resistance between the active material and the conductive material is suppressed.

• Resources Recycling
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• v.31 no.4
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• pp.56-65
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• 2022

Copper is one of the non-ferrous metals used in the electrical/electronic manufacturing industries due to its superior properties particularly the high conductivity and less resistivity. The effluent generated from the surface finishing process of these industries contains higher copper content which gets discharged in to water bodies directly or indirectly. This causes severe environmental pollution and also results in loss of an important valuable metal. To overcome this issue, continuous R & D activities are going on across the globe in adsorption area with the purpose of finding an efficient, low cost and ecofriendly adsorbent. In view of the above, present investigation was made to compare the performance of a plant root (Datura root powder) as a bio-adsorbent to that of the synthetic one (Tulsion T-42) for copper adsorption from such effluent. Experiments were carried out in batch studies to optimize parameters such as adsorbent dose, contact time, pH, feed concentration, etc. Results of the batch experiments indicate that 0.2 g of Datura root powder and 0.1 g of Tulsion T-42 showed 95% copper adsorption from an initial feed/solution of 100 ppm Cu at pH 4 in contact time of 15 and 30 min, respectively. Adsorption data for both the adsorbents were fitted well to the Freundlich isotherm. Experimental results were also validated with the kinetic model, which showed that the adsorption of copper followed pseudo-second order rate expression for the both adsorbents. Overall result demonstrates that the bio-adsorbent tested has a potential applicability for metal recovery from the waste solutions/effluents of metal finishing units. In view of the requirements of commercial viability and minimal environmental damage there from, Datura root powder being an effective material for metal uptake, may prove to be a feasible adsorbent for copper recovery after the necessary scale-up studies.

• Applied Chemistry for Engineering
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• v.9 no.3
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• pp.355-360
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• 1998

Reduction activity of precious metal-loaded HZSM-5 for NO has been studied and was compared to that of Cu-HZSM-5 in the presence of excess oxygen. It was found that among the catalysts used in this study, Ru-HZSM-5 was the most active catalyst for the reduction of NO to $N_2$ in the absence of hydrocarbon reductant. The highest conversion obtained was 45%. No severe inhibition of water vapor to the reduction was observed. It is suggested that the higher catalytic activity of Ru-HZSM-5 may result from the better ability to oxidize NO to $NO_2$ in the presence of excess oxygen. A proposed reaction mechanism for the reduction of NO to $N_2$ in the presence of excess oxygen is that NO is oxidized to $NO_2$ on the surface of Ru-HZSM-5 catalyst and the adsorbed $NO_2$ on the surface is then decomposed to $N_2$. $NO_2$ is supposed to the reaction.

• Journal of Soil and Groundwater Environment
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• v.10 no.5
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• pp.11-17
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• 2005

Characteristics of phenanthrene removal in the Electrokinetic (EK)-Fenton process were investigated in a 2-dimensional test cell in a viewpoint of the effect of gravity and electrosmotic flow (EOF). When the constant voltage of 100 V was applied to this system, the current decreased from 1,000 to 290 mA after 28 days, because soil resistance increased due to the exhaustion of ions in soil by electroosmosis and electromigration. Accumulated EOF in two cathode reservoirs was 10.3 L and the EOF rate was kept constant for 28 days. At the end of operation, the concentration of phenanthrene was observed to be very low near the anode and increased in the cathode region because hydrogen peroxide was supplied from anode to cathode region following the direction of EOP. Additionally, the concentration of phenanthrene decreased at the bottom of the test cell because the electrolyte solution containing hydrogen peroxide was largely transported toward the bottom due to a low capillary action in the soil with high porosity. Average removal efficiency of phenanthrene by EK-Fenton process was 81.4% for 28 days. In-situ EK-Fenton process would overcome the limitations of conventional remediation technologies and effectively remediate the contaminated sites.

• Journal of the Korean Electrochemical Society
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• v.18 no.2
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• pp.58-67
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• 2015

The effects of electrolyte additives, lithium bis(oxalate)borate (LiBOB), fluoroethylene carbonate (FEC), vinylene carbonate (VC), 2-(triphenylphosphoranylidene) succinic anhydride (TPSA), on high-temperature storage properties of $Li(Ni_{1/3}Co_{1/3}Mn_{1/3})O_2$/graphite are investigated with coin-type full cells. The 1 wt.% LiBOB-containing electrolyte showed the highest capacity retention after high temperature ($60^{\circ}C$) storage for 20 days, 86.7%, which is about 5% higher than the reference electrolyte, 1.15M lithium hexafluorophosphate ($LiPF_6$) in ethylene carbonate/ethyl methyl carbonate (EC/EMC, 3/7 by volume). This enhancement is closely related to the formation of semi-carbonate compounds originated from $BOB^-$ anions, thereby resulting in lower SEI thickness and interfacial resistance after storage. In addition, the 1 wt.% LiBOB-containing electrolyte also exhibited better cycle performance at 25 and $60^{\circ}C$ than the reference electrolyte, which indicates that LiBOB is an effective additive for high-temperature performance of $Li(Ni_{1/3}Co_{1/3}Mn_{1/3})O_2$/graphite chemistry.

• Korean Journal of Soil Science and Fertilizer
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• v.31
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• pp.36-44
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• 1998

우리 나라에서 토양의 점토광물에 관한 최초의 연구는 1958년 김제지방의 답 토양에 관한 연구로 (Dewan, 1958)시작되었다. 1960년대 시작하여 1970년대 까지는 주로 토양점토광물의 동정이 이루어 졌다. 점토광물의 동정(同定)에 사용된 잔적토(殘積土)(Residual Soil)로는 화강암(花崗岩), 화강편마암(花崗片麻岩), 현무암(玄武岩), 석회암(石灰岩), 혈암(頁岩), 제(第)3기층(紀層), 홍적층(洪積層) 유래 토양과 토양종류별(土壤種類別)로는 과부식회색토(寡腐植灰色土), 염류토(鹽類土), 충적토(沖積土), 적황색토(赤黃色土), 화산회토(火山灰土), 퇴적토(堆積土), 갈색토(褐色土), 암쇄토(岩碎土), 저위생산답(低位生産畓)이였으며, 토양점토광물(土壤粘土鑛物)과 작물수량성(作物收量性) 관계에 관한 연구가 실시되었다. 1980년대에 들어와서는 토양중의 1차광물과 점토광물의 풍화에 대한 안정도와 1차광물의 동정이 행해졌으며, 이밖에 Kaolinite 입자의 전하에 관한 연구등 점토광물의 흡착과 활성 연구, 점토광물의 토양개량재로서의 흡착과 화학적 특성 변화 연구와 점토광물의 토양개량 시용효과에 관한 연구가 행해졌다. 1990년대에 들어와서는 토양 중의 1차광물과 점토광물의 정량에 대한 자료가 축척되었고, 토양의 풍화에 대한 안정성과 생성기작, Zeolite와 새로운 광물이 합성되었다. 또한 합성광물을 이용한 농업과 산업광물로의 응용성 환경 산업에서의 적용가능성에 대한 평가가 시도되었다. 토양의 점토광물의 조성에 관한 연구는 토양 모재를 중심으로 이루어졌는데, 화강암(花崗岩)에서는 Halloysite, 화강편마암(花崗片麻岩)에서는 Kaolinite, Metahalloysite, Illite, 산성암(酸性岩)에서는 Kaolinite, Venrmiculite와 Chlorite의 중간광물, 현무암(玄武岩)에서는 Illite, Kaolinite, Vermiculite, 석회암(石灰岩)에서는 Vermiculite-Chlorite 중간광물, Kaolinite와 Illite, 혈암(頁岩)에서는 Kaolinite, Halloysite, Illite 외 Vermiculite-Chlorite, 화산회토(火山灰土)에서는 Allophane이 주광물이었다. Soil Taxonomy와 토양광물과의 관계에서, 답 토양에서는 Entisols의 주점토광물은 2:1형과 1:1형 광물이지만 Inceptisols와 Alfisols에서는 Halloysite가 대부분이다. 밭 토양의 경우는 Alfisols의 주점토광물은 Vermiculite, Illite, Kaolinite이었고, Ultisols에서는 Vermiculite-Chlorite 중간광물이었다. 산림토양에서는 Inceptisols중에서 Andept는 Allophane, Alfisols에서는 2:1 광물이지만, Ultisols에서는 Halloysite이다. 모재별 조암 광물의 풍화와 점토광물의 생성과정에서 화강암(花崗岩)과 화강편마암(花崗片麻岩)의 장석류(長石類)는 kaoline광물로, 이 밖의 운모광물(雲母鑛物), 녹니석(綠泥石), 각섬석(角閃石), 휘석(輝石)으로부터 생성된 illite, chlorite, vermiculite는 풍화중간에 혼층단계(混層段階)를 거쳐서 kaoline 광물로 풍화된다. 석회암(石灰岩) 토양의 smectite가 Mg농도가 높은 토양용액으로부터 침전되어 생성되었거나 운모 또는 chlorite에서 유래된 vermiculite의 변성작용에 의해 생성되고, 혈암(頁岩)토양의 점토에 illite가 주로 풍화에 저항성이 큰 미립자의 함수백운모(含水白雲母)로부터 유래되며, 현무암(玄武岩) 중의 장석류(長石類)는 kaoline광물로, 휘석(輝石)은 chlorite${\rightarrow}$illite의 풍화과정을 거친다. Zeolite, 함불석 Bentonite, Bentonite 등 우량점토 광물이 분포과 광물조성, 이화학적 특성이 조사되었고, 토양의 물리적, 화학적 성질의 개선을 필요로 하는 토양의 개량을 위해서 Bentonite, Zeolite, Vermiculite 등의 토양 개량재(改良材)로서의 기초연구와 이들 개량재 시용효과에 관한 연구 등이 주로 논토양에서 수행되었다. 점토광물과 수량관계를 보면 Montmorillonite를 주점토광물로 함유된 답 토양의 수도수량이 1:1 광물을 주점토광물로 함유하고 있는 토양에서의 수도수량 보다 높았다. 토양광물에 관한 기초연구(基礎硏究)로서 양이온교환능과 포화이온의 영향, 입자의 전기화학적 성질, 흡탈착 성질, 표면적과 등전점, 해성점토에 대한 압밀점토(壓密粘土)의 변형율(變形率)의 추정 등이 주로 연구되었다. 부가가치가 낮거나 폐기되는 광물을 이용하여 토양개량재 혹은 흡착제를 형성하는 연구가 알카리 처리에 의한 Zeolite 합성에 집중되었다.

• Applied Chemistry for Engineering
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• v.9 no.2
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• pp.193-199
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• 1998

The mixtures of ultra-high molecular weight polythylene (UHMWPE), high density polyethylene (HDPE), process oil (mineral oil) and potassium hexatitanate whisker were melted and mixed at $150^{\circ}C$ for 30min, and prepared by compression molding to the specimen of separator of about $200{\mu}m$ thickness at the same temperature and 5000 psi. Thereafter the pores were formed by extracting process oil with organic solvents. In this study, the range of PR (the ratio polymer to process oil) was varied from 0.1 to 0.5 because the specimen turned into rubbery phase at which PR was below 0.1 whereas it changed into gel phase at which PR was above 0.5. When the specimen was treated with nonpolar organic solvents, process oil was extracted nearly 98%. Tensile strength was $31kg/cm^2$ at PR = 0.426, and resistance of specimen was $37m{\Omega}/cm^2$ at PR = 0.186, and $53m{\Omega}/cm^2$ at PR = 0.426. The $N_2$ adsorption-desorption isotherm showed a hysteresis representing regions of capillary condensation, and the surface area at PR = 0.186 was relatively large as $130cm^2/g$. Potassium hexatitanate whisker was randomly dispersed in between PE layers. It might be that the whisker is intercalated through the PE thin layers oriented by compression.