• Journal of Electrochemical Science and Technology
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• 제14권3호
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• pp.262-271
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• 2023

For electrode stability and the electrochemical performance of the Li-ion cell, it is essential that the active ingredients and unique additives in the polymer binder be well dispersed with the solvent-based slurry. The efficient procedure used to create the slurry affects the rheological characteristics of the electrode slurry. When successively adding different steps of Nmethyl-2-pyrrolidone (NMP) solvent to the cathode composition, it is evenly disseminated. The electrochemical performance of the Li-ion cells and the electrodes made with slurry formed by single step and multiple steps of addition of NMP solvent are examined. To preform rheological properties of cathode electrode slurry on Ni-rich Lithium Nickel-Cobalt-Aluminum Oxide (LiNi_0.80Co_0.15Al_0.05) (NCA). Also, we investigate different step addition of electrode formation and mechanical strength characterization like peel strength. According to the EIS study, a multi-step electrode slurry has lower internal resistance than a single-step electrode slurry, which results in better electrical characteristics and efficiency. Further, microstructure of electrodes is obtained electrochemical performance in the 18650 cylindrical cells with targeted capacity of 1.5 Ah. The slurry of electrodes prepared by single step and multiple steps of addition of NMP solvent and its effect on the fabrication of 1.5 Ah cells. A three-step solvent addition on slurry has been found to be a lower internal resistance than a single-step electrode slurry as confirmed by the EIS analysis, yielding improved electrical properties and efficiency.

• 제어로봇시스템학회논문지
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• 제13권10호
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• pp.990-999
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• 2007

We deal with second order NMP(Non-Minimum Phase) systems which are difficult to control with conventional methods because of their inherent characteristics of undershoot. In such systems, reducing the undesirable undershoot phenomenon makes the response time of the systems much longer. Moreover, it is impossible to control the magnitude of undershoot in a direct way and to predict the response time. In this paper, we propose a novel two sliding mode control scheme which is capable of determining the magnitude of undershoot and thus the response time of NMP systems a priori. To do this, we introduce two sliding lines which are in charge of control in turn. One is used to stabilize the system and achieve asymptotic regulation eventually like the conventional sliding mode methods and the other to stably control the magnitude of undershoot from the beginning of control until the state meets the first sliding line. This control scheme will be proved to have an asymptotic regulation property. The computer simulation shows that the proposed control scheme is very effective and suitable for controlling the second order NMP system because it can decide the magnitude of undershoot in a direct and stable way and reduce the response time compared with the conventional ones.

• 한국추진공학회지
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• 제8권1호
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• pp.1-7
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• 2004

과염소산암모늄(AP)의 N-메틸피롤리돈(NMP) 용액으로부터 초미세 크기를 갖는 과염소산암모늄(UFAP) 결정의 결정화 연구를 수행하였고, 침전된 결정들의 특성들을 scanning electron micrograph(SEM)와 X-ray diffraction(XRD) 그리고 thermogravimetric analysis(TGA)를 사용하여 분석하였다. 침전용매로 클로로포름, 염화메틸렌 그리고 톨루엔이 사용되었을 경우, 2$\mu\textrm{m}$ 이하의 크기를 갖는 결정들이 제조되었다. 제조된 UFAP의 결정학적 특성과 열분해 거동은 상용으로 사용되는 AP와 거의 유사하였다.

• 한국막학회:학술대회논문집
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• 한국막학회 1996년도 추계 총회 및 학술발표회
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• pp.43-44
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• 1996

Water-swollen-hydrogel membranes for gas separation were prepared by dipcoating and thermal crosslinking of poly(vinylalcohol) (PVA) - poly(acrylacid) (PAA) blends on asymmetric porous polyetherimide(PEI) supporters. The polyetherimide supporters, prepared by phase inversion of polyetherimide solutions in N-methylpyrrolidone(NMP) (composition of PEI/NMP=25/75), had good heat and chemical resistane. The coating materials with different blending ratios of PVA/PAA(=90/10, 80/20, 70/30) were characterized with differential scanning calorimetry (DSC), infrared spectroscopy(IR) and the water swelling ratios. The permeabilities and the separation factors of carbon dioxide through these membranes were measured by a mass flow meter and gas chromatograph at different temperatures, respectively, under a vacuum mode of downstream.

• 한국염색가공학회지
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• 제15권2호
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• pp.68-75
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• 2003

In this work, ultrafiltration(UF) membranes were prepared using polyethersulfone(PES). The polymer was dissolved in various solvent, such as N, N-dimethyl formamide(DMF), N,-dimethyl acetamide (DMAc), N,N-dimethyl sulfoxide(DMSO) and N-methyl-2- pynolidone(NMP). Each polymer solution was casted on the glass plate, and immersed into non-solvent bath. In this way finely porous UF membranes were prepared by phase inversion method. The cross sectional structure of PES membrane was asymmetric which was consist of sponge-like sublayer, finger-like toplayer, and active skin layer. From the solute rejection experiments, the molecular weight cut off of the prepared membrane in various solvent was evaluated 10,000 for DMF, 30,000 for DMAc, 50,000 for DMSO, and 10,000 for NMP respectively.

• Fibers and Polymers
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• 제3권2호
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• pp.55-59
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• 2002

The thermal reaction of acetoacetanilide in the presence of aniline or phenol yielded carbanilide in quantitative yields. This reaction was applied to the synthesis of polyurea. Bisacetoacetamides were prepared from diamines and diketene in DMF. They were thermally polymerized in the presence of phenol or a diamine (6FDA) to yield polyureas of low molecular weights. The polymers were soluble in DMSO and NMP. $^1{H-NMR}$ analysis showed that they had amino group terminated structures. Poly(urea-imide) was synthesized by the reaction of an oligourea diamine with pyromellitic dianhydride in NMP. The concentration of terminal amino groups was determined by an acid-base titration. The thermal property of poly(urea-imide) was evaluated by thermogravimetric analysis (TGA). Initial decompisition took place at 332-$350^{\circ}C$.

• 한국전자파학회논문지
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• 제8권4호
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• pp.373-381
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• 1997

디지틀 마이크로파 전송시스템은 다중경로 페이딩에 대한 대응책으로서 등화기를 필수적으로 장착하고 있다. 본 논문에서는 페이딩의 형태에 따라 기준탭의 위치를 가변시키는 기준탭 위치 가변방식 동기화를 제안하였다. 제안된 등화기는 기존의 등화기에 비해 우수한 성능을 나타내는데 MP 상황에서는 약 4~5 dB 정도의 성능개선을 얻을 수 있었으며 NMP 상황에서는 2~3 dB 정도의 성능 개선을 얻을 수 있음을 시뮬레이션 결과를 통하여 증명하였다.

• 한국막학회:학술대회논문집
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• 한국막학회 1995년도 추계 총회 및 학술발표회
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• pp.45-46
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• 1995

Generally, two different techniques have been employed for the precipitation of membranes from a polymer casting solution. In the first method, a precipitant is introduced from a vapor phase. In this case the precipitaion rate is very slow and a more or less symmetric structure is formed. In the second method, a precipitant is added to a casting solution by immersing the cast polymer film in a nonsolvent bath. In this case the precipitation rate is very fast and a skinned asymmetric membrane structure is obtained. In this study, we introduced water-vapor to PSf/NMP solution and took photographs of phase separation phenomena of polymer lean phase.

• Elastomers and Composites
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• 제54권4호
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• pp.321-329
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• 2019

A series of poly(hyroxyamide)s (PHAs) was prepared by direct polycondensation reaction of 4,4'-(2,3-pyridinedioxy)dibenzoic acid and/or isophthalic acid with 3,3'-dihydroxybenzidine. The yield percentages of the products were high, and the inherent viscosities of the polymer in DMAc solution at 35℃ were 0.31-0.59 dL/g. All PHA polymers were found to be soluble in polar aprotic solvents such as DMAc, DMSO, NMP, and DMF. On the other hand, LiCl was required to dissolve IPHA-1 in aprotic solvents. Poly(benzoxazole)s (PBOs) were partially soluble in conc-H₂SO₄; IPBO-4, -5, and -6 were partially soluble in NMP only when LiCl was added to the solution, and the solution was heated. The PBO polymers showed a maximum weight loss in the temperature range of 654-680℃, and the char yields at 900℃ under nitrogen atmosphere exceeded 63%.

• Elastomers and Composites
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• 제55권3호
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• pp.205-214
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• 2020

A series of wholly aromatic polyhyroxyamide (PHA) copolymers were prepared by direct polycondensation reaction of isophthalic acid and diacids containing bulky units with 3,3'-dihydroxybenzidine. The inherent viscosities of the PHAs measured at 35℃ in DMAc solution were in the range of 0.31-0.56 dL/g. The solubility study revealed that the PHAs were readily soluble in aprotic solvents such as, dimethylacetamide (DMAc), dimethyl sulfoxide (DMSO), and N-methyl-2-pyrrolidone (NMP) at room temperature and in less polar solvent such as pyridine. However, the polybenzoxazole (PBO) copoymers were quite insoluble in all organic solvents except partially soluble in concentrated sulfuric acid and partially soluble in NMP containing LiCl. The PBO copolymers showed maximum weight loss temperature in the range of 593-632℃ and high char yields in the range of 65.0-71.2% at 900℃ in a nitrogen atmosphere.