• 멤브레인
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• 제12권3호
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• pp.171-181
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• 2002

이온교환막의 전압-전류곡선의 plateau length를 결정하는 변수를 다양한 NaCl 농도와 유속 하에서 연구하였다. 또한, 한계전류밀도 이상의 전류에서 전기투석공정 운전의 타당성을 검토하기 위해 다양한 전류밀도의 전원을 공급하면서 0.1 M NaCl 용액의 탈염실험을 실시하여 이온의 제거효율, 전류효율, 에너지소비량, 물 분해 현상을 측정하였다. NaCl 용액의 농도와 유속이 감소하면서 확산경계층의 두께도 함께 감소하였으며, 본 확산경계층의 두께는 plateau length와도 밀접한 관련이 있는 것으로 나타났다. 탈염실험에서 측정된 이온 제거 효율 및 전류효율은 한계전류밀도 이상에서도 한계전류밀도 이하에서의 탈염실험과 크게 차이 나지 않은 것으로 보아 한계전류밀도 이상에서도 대부분의 전류는 이온교환막 표면의 물분해에 의한 것이 아니라 막을 통한 이온의 이동에 의한 것으로 사료된다. 한계전류밀도 이상에서의 탈염운전에 대한 에너지소비량은 plateau length의 영향으로 한계전류밀도 이하에서의 탈염운전 보다 다소 높지만, 한계전류밀도 이상에서는 전류밀도의 증가에도 에너지소비량이 증가하지 않았다. 이러한 결과들은 물분해 현상이 심각하게 일어나지 않는 한 한계전류밀도 이상에서도 매우 경제적으로 전기투석 공정을 운전찬 수 있다는 것을 제시해 주는 것이다.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2013년도 제45회 하계 정기학술대회 초록집
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• pp.77.1-77.1
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• 2013

Atomic layer deposition (ALD) is known for its self-limiting reaction, which offers atomic-level controllability of the growth of thin films for a wide range of applications. The self-limiting mechanism leads to very useful properties, such as excellent uniformity over a large area and superior conformality on complex structures. These unique features of ALD provide promising opportunities for future electronics. Although the ALD of Al2O3 film (using trimethyl-aluminum and water as a metal precursor and oxygen source, respectively) can be regarded as a representative example of an ideal ALD based on the completely self-limiting reaction, there are many cases deviating from the ideal ALD reaction in recently developed ALD processes. The nonconventional aspects of the ALD reactions may strongly influence the various properties of the functional materials grown by ALD, and the lack of comprehension of these aspects has made ALD difficult to control. In this respect, several dominant factors that complicate ALD reactions, including the types of metal precursors, non-metal precursors (oxygen sources or reducing agents), and substrates, will be discussed in this presentation. Several functional materials for future electronics, such as higher-k dielectrics (TiO2, SrTiO3) for DRAM application, and resistive switching materials (NiO) for RRAM application, will be addressed in this talk. Unwanted supply of oxygen atoms from the substrate or other component oxide to the incoming precursors during the precursor pulse step, and outward diffusion of substrate atoms to the growing film surface even during the steady-state growth influenced the growth, crystal structure, and properties of the various films.

• 한국작물학회지
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• 제33권4호
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• pp.353-359
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• 1988

두께가 서로 다른 $C_3$ 식물의 잎은 단위엽면적당 광합성 능력에 있어서도 차이가 나는 바 잎의 내부구조와 기체교환 사이의 관계를 바탕으로 그 원인을 구명하였다. 광합성의 2대 제한요인으로 기체확산과 생화학적 과정의 상대적인 중요도를 결정하기 위해 중엽세포의 표면은 기체확산 저항의, 그리고 세포의 체적은 탄소고정 능력의 지표로 가정하였다. 즉 세포의 표면적이 증가하면 이산화탄소의 액상확산 저항이 감소하며 체적이 증대되면 carboxylation, oxygenation, 그리고 dark respiration 반응속도가 증가한다고 간주하였다. 이러한 개념을 함축하는 광합성 모형을 작성하고 이 가설의 검증을 위해 대두 품종 Amsoy잎을 이용한 실험을 수행하였다. 생장조절실내에서 200, 400, 600$\mu$mol photons m$^{-2}$ s$^{-1}$ PAR을 공급하여 서로 다른 두께의 잎을 준비하였으며 제3 및 4본엽에 대해 1,000 $\mu$mol photons m$^{-2}$ s$^{-1}$ PAR 및 28 기온 환경하에서 이산화탄소 흡수속도를 측정한 결과 세포의 체적과 표면적의 영향을 동시에 고려한 광합성 모형이 세포 표면적만을 고려한 경우 보다 실측치에 가까운 예측치를 산출하였다. 이로 미루어 세포의 표면적과 체적은 잎의 두께 및 그에 따른 광합성 능력의 예측에 적절한 변수로 간주된다.

• 대한기계학회논문집
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• 제11권6호
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• pp.991-1000
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• 1987

본 연구에서는 과농-희박 연료장에서 화염들의 상호작용에 관하여 이론적 해 석 및 실험적 검증을 통해 연구하였고, 이 중 특히 두 개의 예혼합화염 사이에 확산화 염이 형성되어 세 개의 화염이 존재하는 영역을 고찰하였다.

• 대한화학회지
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• 제15권6호
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• pp.347-352
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• 1971

The variations of the positive and negative electrode potentials, and of internal pressure were measured during the charge of the sealed type Ni-Cd cell. Both polarization characteristics of a paste type Cd-electrode as a gas diffusion electrode in 30% KOH solution and the effects of active carbon electrode as an oxygen consuming auxiliary electrode of the Ni-Cd cell on the charging characteristics of the cell were studied. Peak voltage at the end of charge of the cell is ascribed to the peak at the negative electrode potential, which is due to the concentration polarization by the lack of $Cd^{++}$ ion and oxygen concentration. And the recovery of the negative electrode potential is resulted from depolarization by the increasing diffusion limiting current density with the increasing oxygen pressure. The active carbon electrode was effective as an oxygen consuming auxiliary electrode. The internal pressure of the cell could be maintained below 200mmHg even at one hour rate charge and overcharge by the use of active carbon electrode as an auxiliary electrode.

• Nuclear Engineering and Technology
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• 제41권7호
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• pp.885-892
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• 2009

This manuscript will discuss a numerical method where the six equations of two-phase flow, the solid heat conduction equations, and the two equations that describe neutron diffusion and precursor concentration are solved together in a tightly coupled, nonlinear fashion for a simplified model of a nuclear reactor core. This approach has two important advantages. The first advantage is a higher level of accuracy. Because the equations are solved together in a single nonlinear system, the solution is more accurate than the traditional "operator split" approach where the two-phase flow equations are solved first, the heat conduction is solved second and the neutron diffusion is solved third, limiting the temporal accuracy to $1^{st}$ order because the nonlinear coupling between the physics is handled explicitly. The second advantage of the method described in this manuscript is that the time step control in the fully implicit system can be based on the timescale of the solution rather than a stability-based time step restriction like the material Courant limit required of operator-split methods. In this work, a pilot code was used which employs this tightly coupled, fully implicit method to simulate a reactor core. Results are presented from a simulated control rod movement which show $2^{nd}$ order accuracy in time. Also described in this paper is a simulated rod ejection demonstrating how the fastest timescale of the problem can change between the state variables of neutronics, conduction and two-phase flow during the course of a transient.

• 한국전기전자재료학회논문지
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• 제11권12호
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• pp.1139-1145
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• 1998

In this paper, to fabricate a superconducting fault current limiter(FCL) of thick film type, $YBa_2Cu_3O_X superconducting thick films were fabricated by surface diffusion process using the screen printing method. Powder mixture of $3BaCuO_2$+2CuO was screen printed on $Y_2BaCuO_5$(d=15mm). And critical current densities of the thick films were observed as the sintering temperature(92$0^{\circ}C$~95$0^{\circ}C$) and holding time(2h~10h). Based on experimental data, the thick films for superconducting FCL were sintered at $940^{\circ}C$ in 2 hours. The superconducting FCL with a current limiting area of 1mm wide and 66mm long was prepared on $Y_2BaCuO_5$ substrate. To measure the characterization of the fabricated FCL, an alternating voltage (60Hz) was applied to the FCL in 77K liquid nitrogen. At an applied voltage of 4V, the FCL was limited from 20A into 0.6A not farther than 0.5ms.

• Environmental Engineering Research
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• 제18권1호
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• pp.45-53
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• 2013

Biocarrier beads with dead biomass, Bacillus drentensis, immobilized in polymer polysulfone were synthesized to remove heavy metals from wastewater. To identify the sorption mechanisms and theoretical nature of underlying processes, a series of batch experiments were carried out to quantify the biosorption of Pb(II) and Cu(II) by the biocarrier beads. The parameters obtained from the thermodynamic analysis revealed that the biosorption of Pb(II) and Cu(II) by biomass immobilized in biocarrier beads was a spontaneous, irreversible, and physically-occurring adsorption phenomenon. Comparing batch experimental data to various adsorption isotherms confirmed that Koble-Corrigan and Langmuir isotherms well represented the biosorption equilibrium and the system likely occurred through monolayer sorption onto a homogeneous surface. The maximum adsorption capacities of the biocarrier beads for Pb(II) and Cu(II) were calculated as 0.3332 and 0.5598 mg/g, respectively. For the entire biosorption process, pseudo-second-order and Ritchie second-order kinetic models were observed to provide better descriptions for the biosorption kinetic data. Application of the intra-particle diffusion model showed that the intraparticle diffusion was not the rate-limiting step for the biosorption phenomena. Overall, the dead biomass immobilized in polysulfone biocarrier beads effectively removed metal ions and could be applied as a biosorbent in wastewater treatment.

• 전력전자학회논문지
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• 제24권6호
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• pp.411-418
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• 2019

Light-triggered thyristors (LTTs) are essential components in high-power applications, such as HVDC transmission and several pulsed-power applications. Generally, LTT fabrication includes a deep diffusion of aluminum as a p-type dopant to form a uniform p-base region, which needs careful concern for contamination and additional facilities in silicon semiconductor manufacturing factories. We fabricated 4-inch 5,000 V LTTs with boron implantation and diffusion process as a p-type dopant. The LTT contains a main cathode region, edge termination designed with a variation of lateral doping, breakover diode, integrated resistor, photosensitive area, and dV/dt protection region. The doping concentration of each region was adjusted with different doses of boron ion implantation. The fabricated LTTs showed good light triggering characteristics for a light pulse of 905 nm and a blocking voltage (V_DRM) of 6,500 V. They drove an average on-state current (I_TAVM) of 2,270 A, peak nonrepetitive surge current (I_TSM) of 61 kA, critical rate of rise of on-state current (di/dt) of 1,010 A/㎲, and limiting load integral (I²T) of 17 MA²s without damage to the device.

• Applied Science and Convergence Technology
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• 제24권4호
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• pp.96-101
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• 2015

Quantitative evaluation of photocatalytic activity of oxide nanoparticles in aqueous solution is quite challenging in that the kinetic reaction rate is determined by a complicated interplay among various limiting factors such as light scattering and absorption, diffusion and adsorption of reactants in condensed liquid phase, photoexcited charge separation and recombination rate, and the exact nature of active sites determined by detailed morphology and crystallinity of nanocrystals. Here, we present our simple experimental results showing that the kinetic regime of a typical photocatalytic degradation experiment over UV-irradiated $TiO_2$ nanoparticles in aqueous solution is in that dominated by the photoactivity of $TiO_2$ and its concentration. This result lays a firm ground of using the measured kinetic reaction rate in evaluating photocatalytic efficiency of oxide nanocrystals under evaluation.