• 대한화학회지
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• 제9권1호
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• pp.16-22
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• 1965

Sodium alginate-$CaSO_4{\cdot}$1/2 $H_2O$의 gel에 미치는 alkali鹽의 遲延효果를 Miyake date와 比較하고, Schwedoff法을 改良한 連續的 測定方法을 써서, 金屬酸化物의 添加에 依한 彈性 gel의 生成速度 및 彈性의 變化를 硏究하였다. 즉 (1) sample의 張力變化를 連續的으로 測定하여, sodium alginate와 $CaSO_4{\cdot}$1/2 $H_2O$ aqueous sol의 gel化 過程을 觀察하였다. (2) 彈性 gel의 生成速度에 미치는 $Na_3PO_4$의 遲延효果는 $Na_2CO_3$보다 크다는 點에서는 Miyake 報告와 一致하였으나, Miyake date처럼 兩者間에 그리 큰 差가 없었다. (3) 金屬酸化物이 彈性 gel生成速度에 미치는 影響에 어떤 規則性은 없었지마는 $SiO_2$와 MgO는 比較的 큰 速度增大효果를 나타내고 ZnO는 比較的 적었다. 그러나 $Al_2O_3$, $Sb_2O_3$와 $TiO_2$는 速度低下효果를 나타냈다. 結果的으로 酸化物의 種類나 그 添加量에 따라 어떤 明確한 規則性을 觀察하지 못하였다. (4) 彈性率과 生成速度에 미치는 효果사이에 比例關係는 없없으나 金屬酸化物을 添加하면 一般的으로 彈性率이 增加하였다. 이들 酸化物 中에서 彈性率增大효果가 가장 큰 것은 MgO였다.

• 한국식품위생안전성학회지
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• 제14권3호
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• pp.227-232
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• 1999

세균오염지표인 대장균군의 균종별 분포를 조사함으로써 세균학적 의미를 조사하고자 본 실험을 실시하였다. 1997년 6-7월에 서울시 보건환경 연구원에 의뢰된 옹달샘 시료와 지하수 시료를 실험에 사용하였고, 옹달샘 유래 대장균군 112주와 지하수 유래 대장균군 24주를 IMViC test와 API 20E kit(BioMeriux)를 사용하여 균 분리 동정한 후 합계 136균주를 대상으로 실험하였다. 대장균군을 분리 동정한 결과 23균종이 분리되었으며, 균종별로는 Esherichia 속균 39주(28.6%), Klebsiella 속균 32주(23.5%), Enterobacter 속균 30주(22.1%), Serratia 속균 19주(14.0%), Citrobacter 속균 6주(4.4%), Kluyvera 속균 4주*3.0%) 그리고 기타 6주 (4.4%)로 나타났다. 분리 균주들의 EMB agar상의 집락 색상은 녹색 금속 광택 50.7%, 분홍색 44.2%, 자주색 5.1%로 나타났고, 형태는 smooth colony 64.7%, mucoid colony 34.6%, rough colony 0.7%로 각각 나타났다. 생화학적 시험결과 lactose broth 에서는 가스를 생성하였으나 KIA에서는 gas를 생성치 않은 균종이 Ent. intermedium, Ser. liquefaciencs, Ser. marcescenes 그리고 Sal. arizoae이었고, H2S를 생성한 대장균군으로는 Kleb. pneumoniae, Kleb. oxytoca, Kleb. ornithinolytica, Ent. sakasakii, Ent. cloacae, Ser. Liquefaciens, Ser. ficaria, Cit. freundii 그리고 Sal. arizoae이었다. 이상의 결과 대장균군 정성시험 양성을 나타내는 대장균군은 대부분이 E. coli, Klebsilla 속균 그리고 Enterobacter 속균이었다. 또한 향후 대장균군 정성시험 시 EMB agar 상에서 녹색 금석성 광택 집락 외에도 분홍색 집락이 주의시되어지며, rough colony는 대장균군 분리에서 제외되는 것이 좋을 것으로 사료된다. 한편, 생화학적 성상 검토 결과 새로운 형태의 대장균군 출현 가능성이 있을 것으로 전망된다.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2010년도 제39회 하계학술대회 초록집
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• pp.88-88
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• 2010

We synthesized molybdenum thin films deposited by RF magnetron sputtering and physicochemical analysis was performed. The physical and chemical properties of these films were examined with X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The obtained film at the oxygen ratio of 0% showed crystallinity of cubic Mo(110) phase. After the oxygen ratio increased more than 5% in the sputter gas, the molybdenum films were formed as an amorphous phase. The thickness of the Mo thin film was drastically decreased from 1000 nm to ca 70 nm after introduction of oxygen in the sputter gas confirmed by spectroscopic ellipsometer (SE) and scanning electron spectroscopy (SEM). The calculated band gap of the film deduced from SE data increased from 3.17 to 3.63 eV by addition of oxygen in the sputter gas. The roughness of the Mo film was examined with atomic force microscopy (AFM) and it was dramatically decreased by introducing of oxygen during sputtering. XPS results revealed that the ratio of metallic Mo species in the film decreased by the contents of Mo(VI) species increased at the ratio of oxygen increased in the sputter gas and fully oxidized at low content of oxygen in the sputter gas.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2016년도 제50회 동계 정기학술대회 초록집
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• pp.167.1-167.1
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• 2016

The interaction between adsorbed water and hydrogen on metallic surfaces is important for fundamental understanding of heterogeneous catalysis and electrode surface reactions in acidic environment. Here, we explore a long-standing question of whether hydronium ion can exist or not on a Pt surface coadsorbed with atomic hydrogen and water. Studies based on mass spectrometry and infrared spectroscopy show clear evidence that hydrogen atoms are converted into hydrated protons on a Pt(111) surface. The preferential structures of hydrated protons are identified as multiply hydrated $H_5O_2{^+}$ and $H_7O_3{^+}$ species rather than as hydronium ions. The multiply hydrated protons may be regarded as two dimensional zundel ($H_5O_2{^+}$) and Eigen cation ($H_7O_3{^+}$) in water-metal interface. These surface-bound hydrated protons may be key surface intermediates of the electrochemical interconversion between adsorbed hydrogen atoms and solvated protons.

• 대한기계학회논문집A
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• 제30권2호
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• pp.179-186
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• 2006

Dielectrophoresis has received considerable attention for separating nanotubes according to electronic types. Here we examine the effects of surface conductivity of semiconducting single-walled carbon nanotubes (SWNT), induced by ionic surfactants, on the sign of dielectrophoretic force. The crossover frequency of semiconducting SWNT increases rapidly as the conductivity ratio between the particle and medium increases, leading to an incomplete separation of ionic surfactant suspended SWNT at an electric field frequency of 10 MHz. The surface charge of SWNT is neutralized by an equimolar mixture of anionic surfactant sodium dodecyl sulfate (SDS) and cationic surfactant cetyltrimenthylammonium bromide (CTAB), resulting in negative dielectrophoresis of semiconducting species at 10 MHz. A comparative Raman spectroscopy study shows a nearly complete separation of metallic SWNT.

• 한국세라믹학회지
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• 제55권1호
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• pp.1-20
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• 2018

Semiconducting nanomaterials have attracted considerable interest in recent years due to their high sensitivity, selectivity, and fast response time. In addition, for portable applications, they have low power consumption, lightweight, simple in operation, a low maintenance cost. Furthermore, it is easy to manufacture microelectronic sensor structures with metallic oxide sensitive thin layers. The use of semiconducting metal oxides to develop highly sensitive chemiresistive sensing systems remains an important scientific challenge in the field of gas sensing. According to the sensing mechanisms of gas sensors, the overall sensor conductance is determined by surface reactions and the charge transfer processes between the adsorbed species and the sensing material. The primary goal of the present study is to explore the possibility of using semiconducting mixed metal oxide nanostructure as a potential sensor material for selective gases.

• Bulletin of the Korean Chemical Society
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• 제22권12호
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• pp.1323-1327
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• 2001

The catalyst Ni/MgO (Ni : 15 wt%) has been applied to methane reforming reactions, such as steam reforming of methane (SRM), partial oxidation of methane (POM), and oxy-steam reforming of methane (OSRM). It showed high activity and good stability in all the reforming reactions. Especially, it exhibited stable catalytic performance even in stoichiometric SRM (H2O/CH4 = 1). From TPR and H2 pulse chemisorption results, a strong interaction between NiO and MgO results in a high dispersion of Ni crystallite. Pulse reaction results revealed that both CH4 and O2 are activated on the surface of metallic Ni over the catalyst, and then surface carbon species react with adsorbed oxygen to produce CO.

• Journal of Microbiology and Biotechnology
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• 제21권2호
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• pp.115-123
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• 2011

To investigate the effects of pipe materials on biofilm accumulation and water quality, an annular reactor with the sample coupons of four pipe materials (steel, copper, stainless steel, and polyvinyl chloride) was operated under hydraulic conditions similar to a real plumbing system for 15 months. The bacterial concentrations were substantially increased in the steel and copper reactors with progression of corrosion, whereas those in stainless steel (STS) and polyvinyl chloride (PVC) reactors were affected mainly by water temperature. The heterotrophic plate count (HPC) of biofilms was about 100 times higher on steel pipe than other pipes throughout the experiment, with the STS pipe showing the lowest bacterial number at the end of the operation. Analysis of the 16S rDNA sequences of 176 cultivated isolates revealed that 66.5% was Proteobacteria and the others included unclassified bacteria, Actinobacteria, and Bacilli. Regardless of the pipe materials, Sphingomonas was the predominant species in all biofilms. PCR-DGGE analysis showed that steel pipe exhibited the highest bacterial diversity among the metallic pipes, and the DGGE profile of biofilm on PVC showed three additional bands not detected from the profiles of the metallic materials. Environmental scanning electron microscopy showed that corrosion level and biofilm accumulation were the least in the STS coupon. These results suggest that the STS pipe is the best material for plumbing systems in terms of the microbiological aspects of water quality.

• 한국재료학회지
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• 제24권4호
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• pp.194-200
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• 2014

Metallic Cr film coatings of $1.2{\mu}m$ thickness were prepared by DC magnetron sputter deposition method on c-plane sapphire substrates. The thin Cr films were ammoniated during horizontal furnace thermal annealing for 10-240 min in $NH_3$ gas flow conditions between 400 and $900^{\circ}C$. After annealing, changes in the crystal phase and chemical constituents of the films were characterized using X-ray diffraction (XRD) and energy dispersive X-ray photoelectron spectroscopy (XPS) surface analysis. Nitridation of the metallic Cr films begins at $500^{\circ}C$ and with further increases in annealing temperature not only chromium nitrides ($Cr_2N$ and CrN) but also chromium oxide ($Cr_2O_3$) was detected. The oxygen in the films originated from contamination during the film formation. With further increase of temperature above $800^{\circ}C$, the nitrogen species were sufficiently supplied to the film's surface and transformed to the single-phase of CrN. However, the CrN phase was only available in a very small process window owing to the oxygen contamination during the sputter deposition. From the XPS analysis, the atomic concentration of oxygen in the as-deposited film was about 40 at% and decreased to the value of 15 at% with increase in annealing temperature up to $900^{\circ}C$, while the nitrogen concentration was increased to 42 at%.

• Nuclear Engineering and Technology
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• 제56권1호
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• pp.34-41
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• 2024

This work presents experimental data and modelling of the release of Mo from high-burnup spent nuclear fuel (63 MWd/kgU) at two different pH values, 8.4 and 13.2 in air. The release of Mo from SF to the solution is around two orders of magnitude higher at pH = 13.2 than at pH = 8.4. The high Mo release at high pH would indicate that Mo would not be congruently released with uranium and would have an important contribution to the Instant Release Fraction, with a value of 5.3%. Parallel experiments with pure non irradiated Mo(s) and XPS determinations indicated that the faster dissolution at pH = 13.2 could be the consequence of the higher releases from metallic Mo in the fuel through a surface complexation mechanism promoted by the OH^- and the oxidation of the metal to Mo(VI) via the formation of intermediate Mo(IV) and Mo(V) species.