• 대한기계학회논문집B
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• 제31권6호
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• pp.499-506
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• 2007

This study aims to propose evaluation methods of chemical washing performance and estimate the washing capability by flowing detergent/water solution for application to home appliances such as dishwashers. Standard pollutant is stearic acid. A numerical study is also tried using a SIMPLER code. Preliminary experiments are performed by varying the concentration and temperature of the solution. From the pre-experiments, 10 minute pre-curing time is found to be necessary to remove the stearic acid. Stoichiometric ratio and detergent consumption coefficient of reaction between the detergent and stearic are estimated following a proposed method. Washing experiments of pollutant to compare with the numerical results are performed. The relative errors between the experimental and the numerical results with pre-curing time included are less than 7%. In conclusion, important mechanisms of chemical washing are revealed and methods of predicting washing performance are well established.

• 한국콘텐츠학회논문지
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• 제16권1호
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• pp.52-59
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• 2016

동절기에 타설되는 대부분의 콘크리트 구조물에서 가설 초기단계에서의 양생방법의 선정은 매우 중요한 요소이다. 동절기에는 초기균열과 강도저하를 방지하기 위하여 열선과 조강시멘트를 이용한 발열양생방법을 주로 적용하게 된다. 하지만 그 적용기법의 단순화 및 경험적 판단에의 의존으로 인하여 대부분의 건설현장에서 최적의 양생방법을 선정하지 못하고 있는 실정이다. 이에 따라 본 논문에서는 비정상상태의 열전달 해법을 통하여 가장 적절한 열선의 가열온도, 기간, 열선 배치간격을 선정하는 평가 알고리즘을 개발하였다. 이를 위하여 관리 매개변수에 주안점을 둔 구조해석 시스템을 통한 사용자 중심의 OOP 루틴을 적용하였다. 본 시스템에서는 입력모듈, DB 모듈, DB저장 모듈, 해석모듈 및 결과분석모듈로 구분하였으며, 각 모듈간의 연계는 visual c# 루틴으로 처리하였다. 또한 그래픽 인터페이스와 DB 테이블은 사용자 편의성을 고려하여 개발하였다.

• Restorative Dentistry and Endodontics
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• 제25권1호
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• pp.85-90
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• 2000

For more esthetic treatments the use of composite in molar areas are increasing. But polymerzation shrinkage that cause marginal leakage and cuspal deflection has been the problems of composites. The purpose of this study is to compare the effect of low intensity curing and polishing period on marginal leakage. Cavities were prepared on the buccal or lingual surface of forty five sound extracted human teeth and etching, application of bonding agent and filling of composite was done. Group 1 was light cured at intensity of 600$mW/cm^2$ for 41 seconds and polished. Group 2 was light cured at intensity of 300$mW/cm^2$ for 2 seconds and polished and after polishing it was light cured for 40 seconds at 600$mW/cm^2$. Group 3 was light cured at intensity of 300$mW/cm^2$ for 2 seconds and waited for 5 minutes and after curing at 600$mW/cm^2$ for 40 seconds polishing was done. The specimens were thermocycled at $5^{\circ}C$ and $55^{\circ}C$ for 1000 cycles and immersed in 2% methylene blue solution for 24 hours. Composite-tooth interface was examined under stereobinocular microscope for dye penetration. The results were as follows : 1. Group which were cured at low intensity and polished after curing at high intensity showed less marginal leakage than group which were cured at high intensity for 41 seconds(p<0.05). 2. Marginal leakage between group which were cured at low intensity and polished immediately and group which were cured at high intensity for 41 second were not significantly different. Light curing at low intensity can reduce marginal leakage but polishing immediately after curing at low intensity for short time can affect marginal leakage.

• 한국의류학회지
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• 제29권7호
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• pp.997-1007
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• 2005

The textile finishing methods utilizing chitosan have been mostly focused on the applications in the improvement of the dyeing of cotton fabrics, or the improvement of hand of the cotton or wool fabrics. On the other hand, it Is difficult to find the application examples in the synthetic fiber fabrics including polyester and nylon fabrics. The aim of this study is to improve the stiffness and the poor wash fastness of the fabrics treated only with chitosan. We tried to improve the softness by employing chitosan and polyurethane mixture solution and to prevent the detachment of the chitosan from the fabric. The treatment was applied to cotton, polyester, and nylon fabrics. The change of the properties of the treated fabrics were investigated. The optimum finishing condition was sought by changing the mixture ratio of the chitosan/PU(polyurethane) solutions. The adjusted ratios of the chitosan/PU solutions were 1 : 0, 1 : 0.25, 1 : 0.5, and 1 : 2 during the mixture solution preparation. Using the KES(Kawabata Evaluation System), the physical and mechanical properties of the finished fabric specimens were analyzed, and hand values of the specimens were calculated through the use of translational formulas. According to the chemical composition of the fibers, chitosan solution or chitosan/PU mixture exhibited wide range of coating effect. Since the chitosan acid solution has high polarity, the bonding force with the cotton fibers is high. By the appropriate addition of PU in the chitosan treatment of cotton, KOSHI and HARI values of the fabric improved. The air permeability of the chitosan/PU treated cotton fabric specimen improved, resulting in the highest value at the mixture of chitosan : PU=1:0.25.

• Advances in concrete construction
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• 제9권3호
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• pp.267-278
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• 2020

This paper reports on the result of an experimental investigation carried out to study the compressive strength and sorptivity properties of blended cement concrete exposed to 5% and 10% MgSO₄ solution using fly ash (FA) and silpozz. Usually in sulphate environment the minimum grade of concrete is M30 and the mix design is done for target mean strength of 39 MPa. Silpozz is manufactured by burning of agro-waste rice husk in designed furnace in between 600° to 700℃ which is one of the main agricultural residues obtained from the outer covering of rice grains during the milling process. There are four mix series taken with control mix. The control mix made 0% replacement of FA and silpozz with Ordinary Portland Cement (OPC). The first mix series made 0% FA and 10-30% replacement of silpozz with OPC. The second mix series made with 10% FA and 10-40% replacement of silpozz with OPC. The third mix series made 20% FA and 10-30% replacement of silpozz with OPC and the fourth mix series made 30% FA and 10-20% silpozz replaced with OPC. The samples (cubes) are prepared and cured in normal water and 5% and 10% MgSO₄ solution for 7, 28 and 90 days. The studied parameters are compressive strength and strength deterioration factor (SDF) for 7, 28 and 90 days. The water absorption and sorptivity tests have been done after 28 days of normal water and magnesium sulphate solution curing. The investigation reflects that the blended cement concrete incorporating FA and silpozz showing better resistance against MgSO₄ solution when compared to normal water curing (NWC) samples.

• 한국산업융합학회 논문집
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• 제26권4_2호
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• pp.591-598
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• 2023

In this study, the corrosion resistance by salt spray was evaluated using A6061-T6 for an electric vehicle battery pack case coated with an organic/inorganic hybrid solution. The lowest curing temperature of 190 ℃ resulted in significant corrosion and pitting. Meanwhile, no corrosion was observed in the coated specimens at 210 ℃ and 230 ℃ except at 210 ℃ - 6 min and 8 min. The surface of the as-received coating specimen observed by FE-SEM exhibited streaks and dents in the rolling direction, but the coating surface was clean. On the 190 ℃ - 6 min coating specimen, which had a lot of corrosion, rolling streaks spread, and dents were caused by corrosion. The 200 ℃ - 12 min coating specimen did not show corrosion, but it showed an etched surface. In the line profile, Si, the main component of the coating solution, was detected the most, and Ti was also detected. In the coating specimens with salt spray, O increased and Si decreased, regardless of corrosion. The peeling rate by adhesion evaluation was 26 - 87% for the 190 ℃ coating specimen, 4 - 83% for the 210 ℃ coating specimen, and 94 - 100% for the 230 ℃ coating specimen. The optimal curing conditions for the coating solution used in this study were 210 ℃ for 10 min.

• 한국세라믹학회지
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• 제29권11호
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• pp.863-869
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• 1992

A SOG(spin glass) solution with excellent wetting to Si wafers was prepared by acid-hydrolysis of Si(OEt)4 and Me2Si(OEt)2. The solution was spin coated on Si wafers, and effects of heat treatment of the film were characterized by TG/DTA, FTIR and Ellipsometry. Silica film was obtained by heat treatment at $600^{\circ}C$ within one hour, but heat treatment at 80$0^{\circ}C$ caused interfacial oxidation of the silicon substrate. Unexpectedly silica films with much better adhesion were obtained by curing at $600^{\circ}C$ for over 30 min. than those obtained by thermal oxidation.

• 폴리머
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• 제25권5호
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• pp.691-698
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• 2001

에폭시 (diglycidyl ether of bisphenol A: DGEBA), 경화제 (dicyandiamide; DICY), 촉매 (benzyl dimethyl amine : BDMA), 그리고 유기치환된 실리케이트 (organically modified mica type silicate: OMTS)를 용융법 및 용액법을 이용해 나노복합체를 제조하였고, $170^{\circ}C$에서 시간에 따라 경화 반응을 진행하면서 X선 회절분석기 (XRD)와 소각 X선 산란장치 (SAXS)를 이용하여 구조 변화를 관찰하였다. 용융법으로 제조된 치료의 경우 박리된 구조를 관찰할 수 없었으나 용액법에 의해 제조된 경우 박리된 구조를 관찰할 수 있었다. 이는 OMTS 층 내ㆍ외부의 경화 속도차이 때문인 것으로 생각된다. 박리된 에폭시 나노복합체의 OMTS 첨가량에 따른 기계적 물성을 동적기계적 분석기 (DMA)를 이용해 측정한 결과 OMTS의 첨가량이 증가할수록 모둘러스는 증가하였으나 유리전이온도는 큰 차이가 없었다. OMTS 첨가량에 따른 열적 성질을 열중량분석기(TGA)와 한계산소지수 (LOI)를 이용해 측정한 결과 OMTS양이 증가할수록 OMTS 판의 차단효과로 인해 열분해 시작 온도와 LOI 값이 증가하였다.

• 폴리머
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• 제35권1호
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• pp.47-51
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• 2011

본 연구는 에폭시의 난연 특성을 향상시키기 위하여 친환경, 저가, 고종횡비(high aspect ratio)를 갖는 무기계 난연첨가재인 일라이트를 사용하였고, 친수성 일라이트의 소수성 에폭시 내 분산 문제점을 개선하기 위하여 불소화 반응을 이용하여 인의 소수화 개질을 실시하였다. 일라이트의 불소화 개질에 의하여 경화 전 에폭시 용액 내에서 일라이트의 분산성 및 경화 후 형성된 복합체 내에서의 일라이트 분산성도 향상되었다. 이러한 분산성의 향상은 일라이트 불소화 개질로 인하여 소수화된 일라이트의 에폭시 용액에 대한 친화성 향상과 복합체 형성 시 에폭시 고분자의 일라이트 층간 삽입 혹은 에폭시에 의한 일라이트의 박리현상 등에 의하여 나타난 현상으로 판단된다. 따라서, 한계 산소 지수(limited oxygen index, LOI)는 일라이트의 불소화 영향으로 에폭시만의 값에 비해 약 24% 정도 증가한 것으로 보아 불소화 일라이트/에폭시 복합제의 제조로 에폭시의 난연 특성을 향상시킬 수 있음을 알 수 있었다.

• Restorative Dentistry and Endodontics
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• 제25권3호
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• pp.482-486
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• 2000

The purpose of the present study was first, to evaluate the relationship between composite surface conversion and surface discoloration, second, to know if there was difference in surface discoloration between celluloid-strip-finished composite surface and polished surface. In addition, the discoloration of composite surface was also evaluated with visual inspection or digital camera with high resolution monitor, Z100, Tetric Ceram, Spectrum, and Aelitfil were used. The composite surfaces were celluloid-strip finished (group 1), polished (group 2), celluloid-strip finished under nitrogen gas purging (group 3) or only light cured without finishing or polishing under nitrogen gas purging (group 4). The microhardness of each samples were also measured in each group. The samples of each group were also divided into 4 subgroup whether they were immediately placed in disclosing solution (0.2% Elythrosin, pH 7.0) (subgroup1), 1 day after light curing(subgroup 2), 3day after light curing(subgroup 3) or 7 day after light curing(subgroup 4). The computer controlled spectrophotometer was used to determine CIELAB coordinates ($L^*$, $a^*$, $b^*$). The amounts of color difference were compared. The results were as follows; 1. There was no difference in discoloration between celluloid strip finished composite surface and polished surface. 2. The samples discolored more when they were placed in disclosing solution immediately after polymerization than other groups. 3. When the samples were light cured under nitrogen gas purging and without polishing process, they discolored more than other groups even though they showed higher micro hardness. 4. With visual inspection or digital camera, only a limited information was available in detecting composite surface discoloration.