• 전기화학회지
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• 제26권4호
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• pp.71-79
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• 2023

본 연구에서는 세공충진막 제조를 위해 활용되는 다공성 지지체의 친수화 처리를 위해서 음이온성, 양이온성, 비이온성 계면활성제를 사용하였으며, 계면활성제 종류, 농도 및 함침 시간에 따른 친수화 정도를 확인하였다. 또한 친수화 처리한 지지체를 이용하여 세공충진형 음이온교환막을 제조하고 이온전도도를 비교하여 최적의 친수화 조건을 선정하였다. 본 연구에서 사용한 이온성 계면활성제의 경우에는 함침 적용 농도가 3.0 wt% 이상일 때 함침 초기부터 다른 농도(0.05, 0.5 및 1.0 wt%)에 비해 급격하게 친수화가 진행되는 것을 관찰할 수 있었다. 그에 비해 분자량이 상대적으로 큰 비이온성 계면활성제의 경우는 친수화 진행이 원활하지 않은 것을 관찰할 수 있었다. 친수화 정도와 음이온교환막의 이온전도도와의 상관성이 나타나지 않았는데, 이러한 이유는 다공성 지지체의 친수화 공정 시 과도한 친수화 과정은 다공성 지지체의 소수 표면에 계면활성제가 과도하게 흡착하게 되어 기공률 감소가 커지게 되고 이를 통해 이온을 교환할 수 있는 고분자 전해질의 함량이 낮아지게 됨으로써 막의 전기적 저항을 크게 증가시키는 결과를 초래하게 되는 것으로 나타났다.

• 한국환경생태학회지
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• 제32권4호
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• pp.413-424
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• 2018

본 연구에서는 경주 남산을 대상으로 지형구조 및 해발고도가 음이온 발생량에 미치는 영향을 분석하였다. 분석결과, 기온은 능선부($9.82^{\circ}C$) > 계곡부($8.44^{\circ}C$), 상대습도는 계곡부(59.01%) > 능선부(58.64%), 풍속은 능선부(0.63m/s) > 계곡부(0.37m/s), 일사량은 능선부($34.40W/m^2$) > 계곡부($14.69W/m^2$)로 나타났다. 음이온의 경우 계곡부($636.81ea/cm^3$) > 능선부($580.04ea/cm^3$)로 계곡부가 더 높은 음이온 발생량을 보였다. 해발고도와의 상관성 분석 결과, 계곡부에서는 기온, 상대습도, 일사량, 음이온 발생량과의 상관성이 검증되었으며, 상대습도, 일사량, 음이온 발생량과는 정의 상관관계, 기온과 부의 상관관계가 나타났다. 능선부에서는 기온, 상대습도, 풍속, 일사량, 음이온 발생량과의 상관성이 검증되었으며, 상대습도, 일사량, 음이온 발생량과는 정의 상관관계, 기온, 풍속과는 부의 상관관계가 나타났다. 회귀분석 결과, 기온의 경우 계곡부는 y= -0.006x+9.663 (x=해발고도, y=기온), 능선부의 경우 y= -0.009x+11.595(x=해발고도, y=기온)의 예측식을 얻었다. 상대습도의 경우 계곡부는 y= 0.027x+53.561 (x=해발고도, y=상대습도), 능선부의 경우 y= 0.008x+56.646 (x=해발고도, y=상대습도)의 예측식을 얻었다. 음이온 발생량의 경우 계곡부는 y= 0.577x+521.508 (x=해발고도, y=음이온 발생량), 능선부의 경우 y= 0.605x+549.068 (x=해발고도, y=음이온 발생량)의 예측식을 얻었다.

• 세라미스트
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• 제21권4호
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• pp.312-330
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• 2018

Energy storage/conversion has become crucial not only to meet the present energy demand but also more importantly to sustain the modern society. Particularly, electrical energy storage is critical not only to support electronic, vehicular and load-levelling applications but also to efficiently commercialize renewable energy resources such as solar and wind. While Li-ion batteries are being intensely researched for electric vehicle applications, there is a pressing need to seek for new battery chemistries aimed at stationary storage systems. In this aspect, Zn-ion batteries offer a viable option to be utilized for high energy and power density applications since every intercalated Zn-ion yields a concurrent charge transfer of two electrons and thereby high theoretical capacities can be realized. Furthermore, the simplicity of fabrication under open-air conditions combined with the abundant and less toxic zinc element makes aqueous Zn-ion batteries one of the most economical, safe and green energy storage technologies with prospective use for stationary grid storage applications. Also, Zn-ion batteries are very safe for next-generation technologies based on flexible, roll-up, wearable implantable devices the portable electronics market. Following this advantages, a wide range of approaches and materials, namely, cathodes, anodes and electrolytes have been investigated for Zn-ion batteries applications to date. Herein, we review the progresses and major advancements related to aqueous. Zn-ion batteries, facilitating energy storage/conversion via $Zn^{2+}$ (de)intercalation mechanism.

• Journal of Information Display
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• 제4권3호
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• pp.12-16
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• 2003

In connection with the ion exchange strengthening on soda-lime-silicate, substrate glass for display use was investigated. In the processing, the temperature was varied during the ion exchange in order to make stress profile and to determine optimum condition. In the present work, we found that the maximum value of strength was 617.8 MPa after an ion exchange process at 470 $^{\circ}C$ for 1h, and then, at 450 $^{\circ}C$ for 24h. Also, the effect of residual stress placed on the near surface was measured by analyzing the number of crack branches and brittleness. This approach allowed us the residual stress profile to be engineered to improve mechanical reliability.

• 한국세라믹학회지
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• 제37권5호
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• pp.511-515
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• 2000

The effect of Ba2+ ion dissolution with different pH and amount of PAA on microstructural changes of green and sintered bodies and its electrical properties was studied in aqueous nano-size BaTiO3 slurry system. The dissolution of Ba2+ was least at strong base, pH 10.8 and by addition of amount of 0.15 wt% PAA. The green body with the lowest of dissolution of Ba2+ at pH 10.8 and 0.15 wt% PAA had minimum values of average pore size, 40nm and shown high increase of sintered density. The compact sintered at 125$0^{\circ}C$ for 2 hr with highest Ba2+ dissolution had low density and dielectric constant due to abnormal grian growth. However, the sintered body with the lowest Ba2+ dissolution had high sintered density and then shown high dielectric constant.

• 분석과학
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• 제17권6호
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• pp.476-480
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• 2004

A simple, rapid, reproducible and selective UV-Visible spectrophotometric method has been developed for determination of germanium in a week acid medium (pH = 3.0) in the presence of mandelic acid (MA) and malachite green (MG). A single extraction in chlorobenzene was used for the analysis. The germanium-MA ion association complex exhibits an absorption maximum at ${\lambda}_{max}=618nm$ with MG as counter ion and has an apparent molar absorptivtity of $1.313{\times}10^5L\;mol^{-1}\;cm^{-1}$. The values obtained by this UV-Visible spectrophotometric method are in good agreement with the values from inductively coupled plasma-mass spectrometer analysis.

• Journal of Electrochemical Science and Technology
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• 제6권3호
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• pp.75-80
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• 2015

We introduce a new synthesis method to prepare small TiO₂ nanoparticles with a narrow particle size distribution, which is achieved by electron beam (E-beam) irradiation. The effects of E-beam irradiation on the synthesis of TiO₂ nanoparticles and the electrochemical performance of TiO₂ nanoparticles as alternative anode materials for Li-ion batteries are investigated. The TiO₂ nanoparticles induced by E-beam irradiation present better cycling performance and rate capability than the TiO₂ nanoparticles synthesized by normal hydrolysis reaction. The better electrochemical performance is attributed to small particle size and narrow particle size distribution, resulting in the large surface area that provides innumerable reaction sites and short diffusion length for Li⁺ through TiO₂ nanoparticles.

• Bulletin of the Korean Chemical Society
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• 제28권2호
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• pp.183-187
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• 2007

A simple and sensitive extractive spectrophotometric method has been described for the determination of buprenorphine either in raw material or in pharmaceutical formulations. The developed method is based on the formation of a colored ion-pair complex (1 : 1 drug/dye) of buprenorphine and bromocresol green (BCG) in buffer pH 3 and extracting in chloroform. The extracted complex shows absorbance maxima at 415 nm. Beer's law is obeyed in the concentration range of 1.32-100.81 μ g mL-1. The proposed method has been applied successfully for the determination of drug in commercial sublingual tablets and injectable dosage form. No significant interference was observed from the excipients commonly used as pharmaceutical aids with the assay procedure.

• 한국전기전자재료학회논문지
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• 제18권12호
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• pp.1101-1105
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• 2005

We have investigated the optical properties of Erbium (Er)-implanted GaN by photoluminescence (PL). Various doses of Er ion were implanted on GaN epilayers by ion implantation. Visible green emission lines due to inner 4f shell transitions for $Er^{3+}$ were observed from the PL spectrum of Er-implanted GaN. The emission spectrum consists of two narrow green lines at 537 and 558 nm. The green emission lines are identified as $Er^{3+}$ transitions from the $^{5}H_{11/2}$ and $^{4}S_{3/2}$ levels to the $^{4}I_{15/2}$ ground state. The stronger peaks in the case with the dose of $5{\times}10^{14}cm^{-2}$, together with the relatively higher intensity of the $Er^{3+}$ luminescence in the lower doped sample. It implies that some damage remains in the case with the dose of $1{\times}10^{16}cm^{-2}$. The peak positions of emission lines due to inner 4f shell transitions for $Er^{3+}$ do not change with increasing temperature. It indicates that $Er^{3+}$ related emission depends very little on the ambient temperature.

• Journal of Electrochemical Science and Technology
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• 제2권3호
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• pp.157-162
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• 2011

We report a simple route for synthesizing multi-dimensional structured silicon anode materials from commercially available bulk silicon powders via metal-assisted chemical etching process. In the first step, silver catalyst was deposited onto the surface of bulk silicon via a galvanic displacement reaction. Next, the silver-decorated silicon particles were chemically etched in a mixture of hydrofluoric acid and hydrogen peroxide to make multi-dimensional silicon consisting of one-dimensional silicon nanowires and micro-scale silicon cores. As-synthesized silicon particles were coated with a carbon via thermal decomposition of acetylene gas. The carbon-coated multi-dimensional silicon anodes exhibited excellent electrochemical properties, including a high specific capacity (1800 mAh/g), a stable cycling retention (cycling retention of 89% after 20 cycles), and a high rate capability (71% at 3 C rate, compared to 0.1 C rate). This process is a simple and mass-productive (yield of 40-50%), thus opens up an effective route to make a high-performance silicon anode materials for lithiumion batteries.