• 한국진공학회:학술대회논문집
• /
• 한국진공학회 2013년도 제44회 동계 정기학술대회 초록집
• /
• pp.132-132
• /
• 2013

Colloidal synthesis of nanoparticles with well-controlled size, shape, and composition, together with development of in situ surface science characterization tools, such as ambient pressure X-ray photoelectron spectroscopy (APXPS), has brought new opportunities to unravel the surface structure of working catalysts. Recent studies suggest that surface oxides on transition metal nanoparticles play an important role in determining the catalytic activity of CO oxidation. In this talk, I will outline the recent studies on the influence of surface oxides on Rh, Pt, Ru and Co nanoparticles on the catalytic activity of CO oxidation [1-3]. Transition metal nanoparticle model catalysts were synthesized in the presence of poly(vinyl pyrrolidone) polymer capping agent and deposited onto a flat Si support as two-dimensional arrays using the Langmuir-Blodgett deposition technique. APXPS studies exhibited the reversible formation of surface oxides during oxidizing, reducing, and CO oxidation reaction [4]. General trend is that the smaller nanoparticles exhibit the thicker surface oxides, while the bigger ones have the thin oxide layers. Combined with the nature of surface oxides, this trend leads to the different size dependences of catalytic activity. Such in situ observations of metal nanoparticles are useful in identifying the active state of the catalysts during use and, hence, may allow for rational catalyst designs for practical applications. I will also show that the surface oxide can be engineered by using the simple surface treatment such as UV-ozone techniques, which results in changing the catalytic activity [5]. The results suggest an intriguing way to tune catalytic activity via engineering of the nanoscale surface oxide.

• 공업화학
• /
• 제33권4호
• /
• pp.386-393
• /
• 2022

본 연구에서는 실란 커플링제 옥틸트리메톡시실란(octyltrimethoxysilane, OTMS)을 사용하여 친수성 탄산칼슘(CaCO₃) 나노입자의 표면을 개질하였으며, OTMS에 의한 CaCO₃ 나노입자의 표면 개질은 FT-IR, DSC, XRD XPS 및 TGA 분석을 통하여 확인하였다. 또한 부유 시험과 접촉각 측정을 통하여 OTMS 농도가 CaCO₃ 나노입자의 표면 소수성 변화에 미치는 영향에 관하여 살펴보았다. 부유 시험 결과에 따르면 1 wt% OTMS 농도 조건에서 측정한 active ratio 값이 97.0 ± 0.5%로서, OTMS가 CaCO₃ 나노입자 표면을 매우 효율적으로 소수화 개질하는 실란 커플링제임을 알 수 있었다. 또한 OTMS로 개질된 CaCO₃ 나노입자 1 wt%를 함유하는 수용액에 대한 기포 안정성 측정 결과, OTMS 농도가 1 wt%인 조건에서 가장 안정한 기포가 생성되며, 접촉각은 91.8 ± 0.7°임을 확인하였다. 또한 동일한 1 wt% OTMS 농도 조건에서 에멀젼 입자 크기가 가장 작은 안정한 상태의 에멀젼이 형성됨을 확인하였다. 이러한 결과들은 OTMS로 개질된 CaCO₃ 나노입자가 다양한 산업 응용 분야에서 기포 안정화제 및 에멀젼 유화제로서 적용이 가능함을 의미하는 것이다.

• 설비공학논문집
• /
• 제18권11호
• /
• pp.867-873
• /
• 2006

Vertical falling liquid film is extensively used in heat and mass transfer processes of many applications, such as evaporative coolers, cooling towers, and absorption chillers. In such cases, it is required that the falling film spreads widely in the surface forming thin liquid film to enlarge contact surface. An addition of surface active agent to a falling liquid film or hydrophilic surface treatment affects the fluid physical properties of the film. Surfactant addition not only decreases contact angle between the liquid and solid surface but also changes the surface from hydrophobicity to hydrophilicity. In this study, the effects of contact angle on falling film characteristics over a vertical surface have been investigated experimentally. The contact angle is varied either by an addition of surfactant to the liquid or by hydrophilic surface treatment. It is found that the wetted area is increased and film thickness is decreased by the hydrophilic treatment as compared with those of other surfaces. With this hydrophilic treatment, the falling liquid film spreads out widely in the surface. As surfactant concentration is increased, wetted area is also increased and the film thickness is substantially decreased.

• 한국세라믹학회지
• /
• 제55권1호
• /
• pp.74-79
• /
• 2018

Active clay, bentonite and zeolite were used as porous materials for humidity controlling ceramic boards. The specific area and the pore volume of active clay were higher than those of bentonite and zeolite. It was effective to add white cement as well as a retarding agent to control the setting time of the ceramic paint. As the amount of added porous materials increases, the specific surface area and total pore volume of ceramic paint increase, but the average pore diameter decreases. The addition of porous materials having a high specific area and a large pore volume improves the moisture absorptive and desorptive performance of the ceramic paint. Therefore, in this experiment, the moisture absorptive and desorptive properties were best when active clay was added. Also, as the added amount of porous materials increases, the moisture absorptive and desorptive properties improve. In this experiment, when 70 mass% of active clay was added to ceramic paint, the hygroscopicity was highest at about $80g/m^2$.

• 한국표면공학회지
• /
• 제26권2호
• /
• pp.55-62
• /
• 1993

The effect of interlayer coating thickness of Ni and Ti on corrosion behavior was studied for TiN ion plat-ed steel plate. Interlayer coating was carried out in a single and bi-layer to a various thickness combination prior to final TiN coating. Corrosion behavior was evaluated by anodic polarization test in 1N H2SO4 as well as salt spray test. Ni interlayer coating was effectived in reducing corrosion current density of active region and Ti interlayer coating over Ni coating reduced the anodic corrosion current density by an order of 4 with increasing the thickness of Ti up to$ 3\mu\textrm{m}$. The improvement of corrosion resistance by Ni/Ti interlayer coating was attributed to the effective prevention of penetration of active corrosion agent resulting from the inherent corrosion resistance of Ni and Ti. Putting corrosion behavior was observed from salt spray test result for all specimens and corrosion resistance at salt atmosphere was enhanced with increasing Ni and Ti thickness, Cor-lay TiN coating was spalled out by the generation of corrosion products.

• Applied Biological Chemistry
• /
• 제31권3호
• /
• pp.226-233
• /
• 1988

수도작(水稻作)에 있어 주요한 병해(病害)의 하나인 문고병(紋枯病)을 조기(早期)에 생력적(省力的)으로 방제할 수 있는 신농약제형(新農藥劑型)의 개발가능성을 검토(檢討)하기 위하여 pencycuron과 flutolanil을 유효성분으로 하고 식물성유지(植物性油脂)와 계면활성제(界面活性劑)를 각각 부유제(浮遊劑) 및 확전제(擴展劑)로 사용하여 4%의 수면부유제(水面浮遊劑) 시제품(試製品)을 제조(製造), 그의 이화학성(理化學性)과 생물효과를 조사(調査)한 바 다음과 같은 결과를 얻었다. 시제품(試製品)의 수면확전성(水面擴展性)은 $35cm^2/mg$ 이상으로 우수하였으며 담수중(湛水中) 유효성분의 분포(分布)는 pencycuron 시제품(試製品)이 수표면(水表面)에 존재한 반면 flutolanil은 담수중(湛水中)으로의 확산(擴散)이 용이하였다. 시제품(試製品)은 사용(使用)한 부제(副劑)의 종류(種類)에 관계없이 모두 주성분(主成分)의 경시분해(經時分解)가 완만하여 화학적(化學的)으로 안정(安定)하였다. 실험실하(實驗室下)에서 pencycuron 시제품(試製品)의 균핵발아저지력(菌核發芽沮止力)은 30일 이상 지속하였다. 친유성(親油性) 계면활성제(界面活性劑)를 사용하여 제조한 pencycuron 시제품(試製品)은 수도유묘이앙(水稻幼苗移秧) 1일(日) 전(前)에 유효성분으로 20g/10a을 수면살포(水面撒布)하였을 매 수화제(水和劑)와 동등한 방제효과가 있었다. 약제처리후(藥劑處理後) 5일 이내의 담수범람(湛水汎濫)은 방제효과를 현저히 저하시켰다.

• 한국표면공학회지
• /
• 제21권4호
• /
• pp.149-159
• /
• 1988

Electrodeposition of chromium from low concentration chromjum (III) sulfate complexess in aqueous using sodium formate-glycine mixtures as a complexing agent was studied. In the bath formation, it is found that the optimum again temperature and time for equilibration of the electrolytes are nrcessary for 24 hrs at 45$^{\circ}C$and the optimum elecrical charge for low current electrolysis which might be produced Cr(II) ions in the electrolytes is necessary for minum 2Ah/$\ell$. The optmun concentration off standard electrolyte for main composition is 0.05M chromium(III) sulfate, 0.2M sodium formate-0.2M glycine, and I mMNaSCN as a catalysea, respectivwly. The standard electrolyte is shows good covering, good throwing power, and 6% of current efficiency (Cr(III)basis). The oppearance of electrodeposits shows att active bright chromium. The SEM morphology of the chromjum coating is observed as smooth surfaces and dispersed micro prcro pores. X-ray diffraction analysis shows a bcc structure which the perferred orintation of the chromium electrodeposits is strongin(200)plane.

• 한국생물공학회:학술대회논문집
• /
• 한국생물공학회 2003년도 생물공학의 동향(XII)
• /
• pp.40-44
• /
• 2003

Soil-borne infectious disease including Pythium aphanidermatum and Rhizoctonia solani causes severe damage to plants, such as cucumber. This soil-borne infectious disease was not controlled effectively by chemical pesticide. Since these diseases spread through the soil, chemical agents are usually ineffective. Instead, biological control, including antagonistic microbe can be used as a preferred control method. An efficient method was developed to select an antagonistic strain to be used as a biological control agent strain. In this new method, surface tension reduction potential of an isolate was included in the ‘decision factor’ in addition to the other factors, such as growth rate, and pathogen inhibition rate. Considering these 3 decision factors by a statistical method, an isolate from soil was selected and was identified as Bacillus sp. GB16. In the pot test, this strain showed the best performance among the isolated strains. The lowest disease incidence rate and fastest seed growth was observed when Bacillus sp. GB16 was used. Therefore this strain was considered as plant growth promoting rhizobacteria (PGPR). The action of surface tension reducing component was deduced as the enhancement of wetting, spreading, and residing of antagonistic strain in the rhizosphere. This result showed that new selection method was significantly effective in selecting the best antagonistic strain for biological control of soil-borne infectious plant pathogen. The antifungal substances against P. aphanidermatum and R. solani were partially purified from the culture filtrates of Bacillus sp. GB16. In this study, lipopeptide possessing antifungal activity was isolated from Bacillus sp. GB16 cultures by various purification procedures and was identified as a surfactin-like lipopeptide based on the Fourier transform infrared spectroscopy (FT-IR), nuclear magnetic resonance (NMR), high performance liquid chromatography mass spectroscopy (HPLC-MS), and quadrupole time-of-flight (Q-TOF) ESI-MS/MS data. The lipopeptide, named GB16-BS, completely inhibited the growth of Pythium aphanidermatum, Rhizoctonia solani, Penicillium sp., and Botrytis cineria at concentrations of 10 and 50 mg/L, respectively. A novel method to prevent the foaming and to provide oxygen was developed. During the production of surface active agent, such as lipopeptide (surfactin), large amount of foam was produced by aeration. This resulted in the carryover of cells to the outside of the fermentor, which leads to the significant loss of cells. Instead of using cell-toxic antifoaming agents, low amount of hydrogen peroxide was added. Catalase produced by cells converted hydrogen peroxide into oxygen and water. Also addition of corn oil as an oxygen vector as well as antifoaming agent was attempted. In addition, Ca-stearate, a metal soap, was added to enhance the antifoam activity of com oil. These methods could prevent the foaming significantly and maintained high dissolved oxygen in spite of lower aeration and agitation. Using these methods, high cell density, could be achieved with increased lipopeptide productivity. In conclusion to produce an effective biological control agent for soil-borne infectious disease, following strategies were attempted i) effective screening of antagonist by including surface tension as an important decision factor ii) identification of antifungal compound produced from the isolated strain iii) novel oxygenation by $H_2O_2-catalase$ with vegetable oil for antifungal lipopeptide production.

• Restorative Dentistry and Endodontics
• /
• 제20권2호
• /
• pp.699-720
• /
• 1995

본 연구는 양이온 계면활성효과를 가져 소독제로 사용되고 있는 benzalkonium chloride 수용액을 상아질 표면에 대한 습윤용 처리제로 적용시킬 경우 상아질접착제의 접착성능에 미치는 영향을 관찰하기 위해 시행되었다. 소의 하악전치 80개를 8개군으로 분류하여 순면의 상아질을 노출시켜서 산처리한 후 물로 습윤 상태를 유지시킨 대조군과 0.1%, 0.5% 및 1% 농도의 benzalkonium chloride 수용액으로 습윤시킨 실험군으로 나누어 NTG-GMA/BPDM계 상아질접착제인 All-bond 2와 DSDM 계 상아질접착제인 Aelitebond를 각각 접착시킨 후 접착시험을 시행하였다. 상아질 표면을 10% 인산수용액으로 처리한 후 습윤과정을 거친 시편을 각 접착시스템의 primer와 bonding resin을 도포하고 Aelitefil 복합레진으로 접 착시 킨후 항온조에서 24시간 방치한 뒤 인장접착강도를 측정하고, 상아질표면 및 파단면의 양상을 주사전자 현미경으로 관찰하였으며 FT-IR을 사용하여 전처리 전후의 상아질 표면을 분석하여 다음의 결과를 얻었다. 1. NTG-GMA/BPDM 계 상아질접착제 (All-bond 2)로 접착시킨 경우 물로 습윤시킨 대조군에 비해 0.1 % benzalkonium chloride 수용액으로 습윤시킨 군에서 유의하게 높은 인장접착강도를 보였으나(p<0.05), 0.5% 및 1.0 % benzalkonium chloride 수용액으로 습윤시킨 군에서는 유의한 차이가 나타나지 않았다. 2. DSDM계 상아질접착제 (Aelitebond) 로 접착시킨 경우 물로 습윤시킨 대조군과 0.1 %, 0.5% 및 1.0 % benzalkonium chloride 수용액으로 습융시킨 군 간의 인장접착강도의 유의한 차이는 없었다(p>0.05). 3. Benzalkonium chloride 수용액의 적용과 관계 없이 전체적으로 NTG-GMA/ BPDM계 상아질접착제로 접착시킨 경우가 DSDM계 상아질접착제로 접착시킨 경우보다 인장접착강도가 높았으며, 파단양상의 관찰결과에서도 NTG-GMA /BPDM계 상아질접착제를 사용한 경우는 응집성 및 혼합성 파단양상이, DSDM 계 상아질접착제를 사용한 경우는 부착성 파단양상이 우세하였다. 4. 주사전자 현미경적 관찰상에서 benzalkonium chloride 수용액 적용 유무에 따른 각 상아질 표면의 primer 도포양상의 뚜렷한 차이는 관찰되지 않았으나, 상아질 표면에 대한 benzalkonium chloride 수용액 적용 전후의 FT-IR 분석결과 에서는 0.1 % benzalkonium chloride 수용액으로 습윤 처리 시킨 군이 대조군에 비해 NTG-GMA/ BPDM 및 DSDM primer의 도포효과를 다소 향상시킨 소견이었다.

• 대한전자공학회:학술대회논문집
• /
• 대한전자공학회 2001년도 The 6th International Symposium of East Asian Resources Recycling Technology
• /
• pp.240-244
• /
• 2001

Recycling process involving mechanical, thermal, hydrometallurgical, and sol-gel step has been applied to recover cobalt and lithium from spent lithium ion batteries and to synthesize LiCoO$_2$from leach liquor as cathodic active materials. Electrode materials containing lithium and cobalt could be concentrated with 2-step thermal and mechanical treatment. Leaching behaviors of the lithium and cobalt in nitric acid media was investigated in terms of reaction variables. Hydrogen peroxide in 1 M HNO$_3$solution turned out to be an effective reducing agent by enhancing the leaching efficiency. O f many possible processes to produce LiCoO$_2$, the amorphous citrate precursor process (ACP) has been applied to synthesize powders with a large specific surface area and an exact stoichiometry. After leaching used LiCoO$_2$with nitric acid, the molar ratio of Li/Co in the leach liquor was adjusted at 1.1 by adding a fresh LiNO$_3$solution. Then, 1 M citric acid solution at a 100% stoichiometry was also added to prepare a gelatinous precursor. When the precursor was calcined at 95$0^{\circ}C$ for 24 hr, purely crystalline LiCoO$_2$was successfully obtained. The particle size and specific surface area of the resulting crystalline powders were 20 пm and 30 $\textrm{cm}^2$/g, respectively The LiCoO$_2$powder was proved to have good characteristics as cathode active materials in charge/discharge capacity and cyclic performance.