• 한국표면공학회지
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• 제26권6호
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• pp.291-298
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• 1993

In order to substitute for porous nickel anode in Molten Carbonate Fuel Cell(MCFC), porous cermet elec-trode was fabricated with Ni and Ni-P coated ceramic powder. Ni and Ni-P were coated by electroless plat-ing method in the nickel solution containing of hydrazine and sodium hypophosphate as a reducing agent. The plating solution was stirred by air and mechanical agitator. Ultrasonic irradiation was applied to the plating bath to improved the effect of agitation and coating speed. Electorde was formed by pressing method and doc-tor blade method followed by sinterd at$ 800^{\circ}C$ for 6 hours in H2 environment. Anode performance test carried out by potentiodynamic polarization technique in the MCFC operating condition and 154-161mA/$\textrm{cm}^2$ as ob-tained as a anode current density at the+100mV overpotential.

• 분석과학
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• 제33권3호
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• pp.115-124
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• 2020

마킹펜류는 어린이제품법의 안전확인으로 관리되는 학용품 품목으로서, 폼알데하이드 함유량에 대한 안전기준은 20 mg/kg이다. 시중에 유통되는 마킹펜 9 종을 현행 시험법인 백포 필기 후 증류수 추출액을 UV/Vis 흡광광도계로 분석(이하 Nash-UV/Vis 방법)한 결과 폼알데하이드가 검출되지 않았고 수성 잉크와 같이 항시 추출액이 유색을 띠는 경우 거짓 양성 결과를 보였다. 반면, 잉크를 직접 초음파를 이용하여 용해한 증류수 액을 DNPH 유도체화 한 후 HPLC/DAD로 분석(이하 DNPH-HPLC/DAD 방법)한 결과, 최소 3.2 mg/kg ~ 최고 93.2 mg/kg이었고, 3 종 제품이 안전기준 20 mg/kg을 초과하였다. 따라서, 추출과정이 빠르고 용이하도록 잉크를 직접 증류수에 용해한 후 DNPH-HPLC/DAD 분석 방법으로 잉크 내 폼알데하이드 안전기준 20 mg/kg 이하 여부를 판단할 수 있도록 제안하고자 하며, 이 방법은 Nash-UV/Vis 방법의 검출한계 및 색상 물질 추출 시의 거짓 양성 결과의 한계를 극복할 수 있다. 형광펜, 보드마카, 물백묵, 페인트마카의 잉크 매트릭스를 사용하여 20 mg/kg 및 40 mg/kg의 범위에서 스파이킹 방법으로 산출한 DNPH-HPLC/DAD 분석방법의 정확도 및 정밀도는 각각 90.1 ~ 105.4 % 및 0.6 ~ 3.3 %이다.

• 생명과학회지
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• 제21권1호
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• pp.56-61
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• 2011

본 연구는 청나래고사리 성엽 추출물의 항산화물질의 함량과 항산화능을 향상시킬 수 있는 효과적인 추출방법을 개발하기 위하여 시행하였다. 동결건조한 청나래고사리 성엽의 분쇄시료 1 g을 메탄올, 80% 에탄올 및 물 등 3가지 용매와 섞은 후 6시간 동안 상온 침지, $60^{\circ}C$ 가열 및 200 rpm에서 교반하여 추출하거나 42 kHz의 초음파 수조에서 15, 30, 45분 동안 추출하였다. 추출물은 여과한 다음 가용성고형분, 총 폴리페놀 및 총 플라보노이드의 함량을 측정하였으며, 항산화활성은 DPPH와 ABTS radical 소거활성을 $RC_{50}$으로 환산하여 측정하였다. 80% 에탄올을 용매로 하여 30분 동안 초음파추출 하였을 때 가용성고형분(0.317 $g{\cdot}g^{-1}$ db), 총 폴리페놀(70.90 $mg{\cdot}g^{-1}$ db) 및 총 플라보노이드(41.53 $mg{\cdot}g^{-1}$ db)의 추출수율이 가장 우수하였으며, DPPH와 ABTS radical 소거활성 또한 가장 우수하였다(각 $RC_{50}$=0.14 $mg{\cdot}ml^{-1}$와 0.09 $mg{\cdot}ml^{-1}$). 상기의 연구결과에 따라 청나래고사리의 성엽은 천연항산화소재로 활용가능하며, 80% 에탄올을 용매로 15-30분 동안 초음파추출하는 것이 추출물의 항산화효과를 증가시키며 추출에 소요되는 시간을 줄일 수 있는 효과적인 추출방법으로 생각되었다.

• 폴리머
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• 제34권6호
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• pp.534-539
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• 2010

라텍스 블렌딩 기법을 이용하여 폴리스티렌(PS)/다중벽 탄소나노튜브(MWCNT) 나노복합재료를 제조하여 나노튜브 길이에 따른 나노복합재료의 유변학적 특성을 고찰하였다. 나노복합재료 제조에 사용된 단분산 PS 입자는 무유화제 유화중합으로 제조하였고, MWCNT는 불순물 제거와 분산성 향상을 위해 표면개질 과정을 거친 후 사용하였다. 최종적인 나노복합재료는 단분산 PS 입자와 개질한 MWCNT를 초음파 교반조에서 분산시킨 후 동결건조 과정을 거쳐 제조하였다. 나노복합재료의 MWCNT 함량과 나노튜브 길이에 따른 유변학적 특성은 소진폭 진동 전단유동을 부과시켜 평가하였다. 본 연구에서 고찰한 PS/MWCNT 나노복합재료는 MWCNT의 함량이 증가할수록, 나노튜브 길이가 길수록 유변물성 향상 효과가 뚜렷하였다. 이는 MWCNT 함량이 증가할수록 나노복합재료의 유변학적 특성이 액체적 특성에서 점차 고체적 특성으로 변화하기 때문이며, 나노튜브 길이가 길수록 네트워크 구조를 달성하는 임계 농도가 작아지기 때문인 것으로 판단된다.

• Korean Chemical Engineering Research
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• 제53권1호
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• pp.83-90
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• 2015

본 연구에서는 multi-walled carbon nanotube (MWCNT) 표면에 자유 라디칼 중합 가능한 methacrylate기를 다량으로 도입하기 위한 연구를 수행하였다. 먼저, MWCNT 표면에 카르복실기(-COOH)를 도입하기 위하여 황산과 질산의 혼산으로 초음파로 처리하면서 2시간 산화시켜 MWCNT-COOH를 합성하였다. 합성된 MWCNT-COOH를 염화티오닐(thionyl chloride)와 반응시켜 MWCNT-COCl을 합성하고, triethylenetetramine (TETA)와 반응시켜 MWCNT-$NH_2$를 합성하였다. 합성된 MWCNT-$NH_2$와 3-(acryloyloxy)-2-hydroxypropyl methacrylate (AHM)의 투입 몰 비를 변화시키면서 Michael 부가 반응으로 MWCNT 표면에 methacrylate기가 도입된 MWCNT-AHM을 합성하였다. MWCNT의 표면 개질정도는 fourier transform infrared (FTIR) spectroscopy, thermogravimetric analysis (TGA)와 원소분석(elemental analysis, EA) 분석을 통해 개질 반응의 진행 정도와 최적 개질 조건을 확인하였다. 그 결과 MWCNT-$NH_2$에 접목되어 있는 TETA에 대하여 AHM의 반응 몰 비를 1:10로 하고 8시간 반응시켰을 때 methacrylate기가 가장 많이 도입되는 조건임을 확인하였다.

• 구강회복응용과학지
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• 제22권3호
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• pp.211-220
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• 2006

Need of porcelain-repair system is largely demanding as dental porcelain restorations are increased in clinical dentistry. This study investigated shear bond strength of commercial porcelain-repair systems on dental porcelain and their reliability. Experimental groups were as follows; Group A Super Bond C&B, Group B Porcelain repair kit, Group C Ceramic repair, and Group D Spectrum system as a control. Porcelain disks were fired and embedded in epoxy resin. Porcelain surface were ground using 220 grit SiC disk, then cleaned in ultrasonic bath. Then porcelain specimens were treated with each repair system. A clear polystyrene cylinder 3.5 mm in internal diameter was filled with composite resin. Then the resin cylinder was polymerized with a visible light curing unit. Thirty one specimens at each group were prepared and stored at $37^{\circ}C$ distilled water for 48 h. Specimens were tested in an Instron testing machine according to ISO TR 11405. Mean shear bond strength and standard deviation of each group was $15.7{\pm}4.1MPa$ (Group A), $12.8{\pm}4.9MPa$ (Group B), $7.2{\pm}3.0MPa$ (Group C) and $9.6{\pm}2.2MPa$ (Group D). ANOVA and Tukey HSD post-hoc test showed that there were significant differences between groups (p<0.05). Data of bond strength were analyzed with two-parameter Weibull distribution. Confidence interval of Weibull modulus (m-parameter) at 95% of Group A (3.5-6.3) and Group D (3.6-6.0) were significantly higher than Group B (2.2-3.7) and Group C (2.0-3.4). There was little correlation between mean shear bond strength and Weibull modulus. Results indicated that acid-etching of porcelain surface increased porcelain-resin shear bonding strength.

• 한국표면공학회지
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• 제50권5호
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• pp.352-359
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• 2017

The growth of nanocrystalline diamond films on a p-type poly silicon substrate was studied using microwave plasma chemical vapor deposition method. A 6 mm thick poly silicon plate was mirror polished and scratched in an ultrasonic bath containing slurries made of 30 cc ethanol and 1 gram of diamond powders having different sizes between 5 and 200 nm. Upon diamond deposition, the specimen scratched in a slurry with the smallest size of diamond powder exhibited the highest diamond particle density and, in turn, fastest diamond film growth rate. Diamond deposition was carried out applying different DC bias voltages (0, -50, -100, -150, -200 V) to the substrate. In the early stage of diamond deposition up to 2 h, the effect of voltage bias was not prominent probably because the diamond nucleation was retarded by ion bombardment onto the substrate. After 4 h of deposition, the film growth rate increased with the modest bias of -100 V and -150 V. With a bigger bias condition(-200 V), the growth rate decreased possibly due to the excessive ion bombardment on the substrate. The film grown under -150V bias exhibited the lowest contact angle and the highest surface roughness, which implied the most hydrophilic surface among the prepared samples. The film growth rate increased with the apparent activation energy of 21.04 kJ/mol as the deposition temperature increased in the range of $300{\sim}600^{\circ}C$.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2005년도 하계학술대회 논문집 Vol.6
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• pp.371-372
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• 2005

Supercapacitors are promising devices for delivering high power density. Digital communications, electric vehicles and other devices that require electrical energy at high power levels in relatively short pulses have prompted considerable research on supercapacitors. In recent years, solid electrolytes have been investigated for supercapacitors. Solid electrolytes are advantageous over liquid electrolytes in respect of easy handling and reliability without electrolyte leakage. In this preliminary study, an electrochemical supercapacitor in all solid configuration has been fabricated using CNF-DAAQ and poly-vinylidenefluoride(PVdF). A new type of Supercapacitor was constructed by using carbon nanofibers(CNFs) and DAAQ(l,5-diaminoanthraquinone) monomer. DAAQ was deposited on the carbon nanofibers by chemical polymerization with $(NH_4)_2S_2O_8$ as oxidant in the 0.1M $H_2SO_4$. Dried SPEEK powder was mixed with N-methyl pyrrolidone to make 10 wt.% solution in an ultrasonic bath, the slurry was cast over a glass substrate heated to $70^{\circ}C$ for solvent evaporation. And then we used solid electrolyte of SPEEK. The unit cell consist of DAAQ-CNF/electrolyte/Pt. From the analysis, it is clear that surface of carbon nanofibers was quite uniformly coated with DAAQ. The performance characteristics of the supercapacitors have been evaluated using Cyclic Voltammetry.

• 한국표면공학회지
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• 제47권5호
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• pp.263-268
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• 2014

Nanocrystalline diamond(NCD) coated SiC balls were applied in a ball-on-disk tribometer. After seeding in an ultrasonic bath containing nanometer diamond powders, $2.2{\mu}m$ thick NCD films were deposited on sintered 3 mm diameter SiC balls at $600^{\circ}C$ in a 2.45 GHz microwave plasma CVD system. Bare $ZrO_2$ and SiC balls were prepared for comparison as test balls. Tribology tests were performed in air with pairs of three different balls and mirror polished steel(SKH51) disk. The wear tracks on balls and disks were examined by optical microscope and alpha step profiler. Under the load of 3 N, the friction coefficients of steel against $ZrO_2$, SiC and NCD-coated balls were between 0.4 and 0.8. After a few thousands sliding laps, the friction coefficient of NCD-coated balls dropped from 0.45 to below 0.1 and maintained thereafter. Under a higher load of 10 N or 20 N with a long sliding distance of 2 km, $ZrO_2$ and SiC balls exhibited the similar friction coefficients as above. The friction coefficient of NCD-coated balls was less than 0.1 from the beginning and increased to above 0.1 steadily or with some fluctuations as sliding distance increased. NCD coating layers were found worn out after long duration and/or high load sliding test, which resulted in the friction coefficient higher than 0.1.

• 한국산업보건학회지
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• 제32권2호
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• pp.102-110
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• 2022

Objectives: The purpose of this study is to analyze the content of N,N-dimethylformamide(DMF) in polyurethane coated gloves(PU-gloves) and to assess the dermal exposure generated by wearing them. Methods: We analyzed the concentrations of DMF in 12 gloves by EN16778 standard. The samples cut into pieces of about 10 by 10 mm and extracted with methanol in flask in an ultrasonic bath at 70℃. An aliquot of the extract is analyzed with GC-MS. The dose of dermal exposure was calculated by ECETOC TRA consumer 3.1 and compared with derived no effect level(DNEL) for systemic effects due to long term exposure by workers. The extracted amount of DMF by saline solution was compared with that by EN16778 standard. Results: The mean concentration of DMF in PU-gloves was 1,377 mg/kg(range 13~3,948 mg/kg). The concentration of DMF showed significantly differences by packing type, manufacturer, and price(p<0.05). The dose of dermal exposure was 0.0007~0.572 mg/kg body weight/day when the DMF content was 10~4,000 mg/kg. The DMF extracted by saline solution was around 11% for 8 hours. Conclusions: The risk of dermal exposure due to the residual DMF in the PU-gloves was not signifiant. But, the limit of 1,000 mg/kg in PU-gloves can be recommended for international standard and trading systems.