• Advances in environmental research
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• 제1권3호
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• pp.181-189
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• 2012

Trihalomethanes, produced as a result of chlorination of drinking water, are considered a potential health hazard. The trihalomethane formation potential (THMFP) of a raw water source may indicate the maximum trihalomethanes (THMs) that are likely to be produced when chlorine reacts with natural organic matter (NOM) present in the water. A study was conducted to evaluate the THMFP in seven different drinking water sources in the vicinity of Kalpakkam, a rural township, on the east coast of India. Water from seven stations were analysed for THMFP. THMFP was compared with surrogate parameters such as dissolved organic carbon (DOC), ultraviolet absorbance ($UV_{254}$) and bromide. The data showed that THMFP was high in water from open wells as compared to closed bore wells, possibly due to more photosynthetic activity. Proximity to sea, and consequently the levels of bromide, was an important factor that influenced THM formation. THM surrogate parameters showed good correlation with THMFP.

• 한국분말재료학회지
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• 제22권5호
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• pp.350-355
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• 2015

Perforated polygonal cobalt oxide ($Co_3O_4$) is synthesized using electrospinning and a hydrothermal method followed by the removal of a carbon nanofiber (CNF) template. To investigate their formation mechanism, thermogravimetric analysis, field-emission scanning electron microscopy, transmission electron microscopy, X-ray diffraction, and X-ray photoelectron spectroscopy are examined. To obtain the optimum condition of perforated polygonal $Co_3O_4$, we prepare three different weight ratios of the Co precursor and the CNF template: sample A (Co precursor:CNF template- 10:1), sample B (Co precursor:CNF template-3.2:1), and sample C (Co precursor:CNF template-2:1). Among them, sample A exhibits the perforated polygonal $Co_3O_4$ with a thin carbon layer (5.7-6.2 nm) owing to the removal of CNF template. However, sample B and sample C synthesized perforated round $Co_3O_4$ and destroyed $Co_3O_4$ powders, respectively, due to a decreased amount of Co precursor. The increased amount of the CNF template prevents the formation of polygonal $Co_3O_4$. For sample A, the optimized weight ratio of the Co precursor and CNF template may be related to the successful formation of perforated polygonal $Co_3O_4$. Thus, perforated polygonal $Co_3O_4$ can be applied to electrode materials of energy storage devices such as lithium ion batteries, supercapacitors, and fuel cells.

• The Korean Journal of Ceramics
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• 제2권1호
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• pp.19-24
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• 1996

The phase distribution and interface chemistry by the solid-state reaction between SiC and nickel were studied at temperatures between $550 \;and\; 1250^{\circ}C$ for 0.5-100 h. The reaction with the formation of silicides and carbon was first observed above $650^{\circ}C$. At $750^{\circ}C$, as the reaction proceeded, the initially, formed $Ni_3Si_2$ layer was converted to $Ni_2$Si. The thin nickel film reacted completely with SiC after annealing at $950^{\circ}C$ for 2 h. The thermodynamically stable $Ni_2$Si is the only obsrved silicide in the reaction zone up to $1050^{\circ}C$. The formation of $Ni_2$Si layers with carbon precipitates alternated periodically with the carbon free layers. At temperatures between $950^{\circ}C$ and $1050^{\circ}C$, the typical layer sequences in the reaction zone is determined by quantitative microanalysis to be $SiC/Ni_2$$Si+C/Ni_2$$Si/Ni_2$$Si+C/…Ni_2$Si/Ni(Si)/Ni. The mechanism of the periodic band structure formation with the carbon precipitation behaviour was discussed in terms of reaction kinetics and thermodynamic considerations. The reaction kinetics is proposed to estimate the effective reaction constant from the parabolic growth of the reaction zone.

• 상하수도학회지
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• 제22권6호
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• pp.641-646
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• 2008

In this research, recovery of high quality organics from excess activated sludge and its potential as a external carbon sources for BNR process was studied. By simultaneous treatment of alkali and ozone, TSS concentration was reduced by 32%, and RBDCOD fraction was increased by 76.2%, and major constitute of produced organic were acetic acid and propionic acid. Also, nitrogen and phosphorus were greatly solubilized. However, because acid-hydrolyzable phosphorus(AHP) was major part of solubilized phosphorus, $NH_4{^+}-N$ and $PO_4{^3}-P$ concentration were insufficient for effective formation of crystal like as MAP(Magnesium Ammonium Phosphate) and hydroxyapatite. By placing BPR reactor before alkali-ozone treatment reactor, $PO_4{^3}-P$ concentration in pretreated sludge was increased by 1.8 times, and improved potential of phosphorus recovery by crystallization. In experiment of crystallization, hydroxyapatite formation was more easily applied than MAP. By hydroxyapatite formation, $SCOD/PO_4-P$ ratio was greatly increased from 32.7 at control to 141.9 at $Ca^{2+}/PO{_4}^{3-}-P$ mole ratio of 2.4. The results based on this study indicated that the proposed system configuration has potential to reduce the excess sludge production, to recover phosphorus in usable forms as well as utilize organics as a external carbon source in BNR process.

• 한국입자에어로졸학회지
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• 제9권1호
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• pp.7-21
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• 2013

Twelve-hour size-resolved atmospheric aerosols were measured to determine size distributions of water-soluble organic carbon(WSOC) during daytime and nighttime, and to investigate sources and formation pathways of WSOC in individual particle size classes. Mass, WSOC, ${NO_3}^-$, $K^+$, and $Cl^-$ at day and night showed mostly bimodal size distributions, peaking at the size range of $0.32-0.55{\mu}m$(condensation mode) and $3.1-6.2{\mu}m$(coarse mode), respectively, with a predominant condensation mode and a minor coarse mode. While ${NH_4}^+$ and ${SO_4}^{2-}$ showed unimodal size distributions which peaked between 0.32 and $0.55{\mu}m$. WSOC was enriched into nuclei mode particles(< $0.1{\mu}m$) based on the WSOC-to-mass and WSOC-to-water soluble species ratios. The sources and formation mechanisms of WSOC were inferred in reference to the size distribution characteristics of inorganic species(${SO_4}^{2-}$, ${NO_3}^-$, $K^+$, $Ca^{2+}$, $Na^+$, and $Cl^-$) and carbon monoxide. Nuclei mode WSOC was likely associated with primary combustion sources during daytime and nighttime. Among significant sources contributing to the condensation mode WSOC were homogeneous gas-phase oxidation of VOCs, primary combustion emissions, and fresh(or slightly aged) biomass burning aerosols. The droplet mode WSOC could be attributed to aqueous oxidation of VOCs in clouds, cloud-processed biomass burning aerosols, and small contributions from primary combustion sources. From the correlations between WSOC and soil-related particles, and between WSOC and sea-salt particles, it is suggested that the coarse mode WSOC during daytime is likely to condense on the soil-related particles($K^+$ and $Ca^{2+}$), while the WSOC in the coarse fraction during nighttime is likely associated with the sea-salt particles($Na^+$).

• 한국약용작물학회지
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• 제2권1호
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• pp.44-50
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• 1994

1. 2.4-D 0.5mg/1에서 배발생캘러스 생장과 발생빈도가 가장 양호하였다. 2. 배지 중에서 MS배지가 체세포배 형성과 생육에 좋았으며, 1X MS배지 보다 1/2X MS배지가 배형성에 더 효과적이었다. 3. 탄소원으로는 sucrose가 효과적이었다. 농도는 1%처리가 가장 양호하였으며 농도가 높아짐에 따라 체세포배 형성이 억제되었다. 4. Sucrose 대신 sugar 처리에서도 체세포배 형성이 앙호하였다. 5. 질소원으로는 $KNO_3\;825mg\;/\;l$ 와 $NH_{4}NO_3$ 238mg /l 처리가 배발생에 가장 효과적이었다.

• 한국진공학회:학술대회논문집
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• 한국진공학회 1997년도 제13회 학술발표회 논문개요집
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• pp.36-36
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• 1997

• 분석과학
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• 제6권2호
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• pp.149-156
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• 1993

고온고압하(高溫高壓下)에서의 Ni-C 액상(液相) 중에서 구상흑연입자(球狀黑鉛粒子)의 형성과정을 밝히기 위한 실험적인 관찰을 행하였다. 구상 흑연입자는 다이아몬드 안정역에서 유지하는 동안 안정한 형태로 생성되어 성장하였다. 이 때의 구상 흑연입자는 다결정형태(多結晶形態)가 아닌 연속적으로 성장한 많은 결함을 포함하는 단결정형태(單結晶形態)(fullerene형(型))를 하고 있었다. 표면분석기(表面分析機)(Auger electron spectroscope) 및 고분해능(高分解能) 투과전자현미경(透過電子顯微鏡)을 이용한 분석결과 구상 흑연 입자는 $sp^2$ 및 $sp^3$ 결합을 갖는 탄소원자가 혼재(混在)되어 있는 결정상태임이 밝혀졌다. 다이아몬드 안정역으로부터 흑연 안정역으로 압력이 감소함에 따라 흑연입자의 모양이 구형(球形)에서 평판형(平板形)으로 연속적으로 변해가는 것이 관찰되었다. 다이아몬드 안정역에서 형성되는 구상 흑연입자는 $sp^3$ 결합을 가지는 탄소 원자의 안정적인 존재 때문인 것으로 해석되었다. 많은 결함을 포함하는 큰 크기의 fullerene형(型) 구상 흑연입자가 연속적으로 성장하는 사실은 Kroto가 예측한 대형 fullerene의 성장과정을 실험적으로 뒷받침해 주는 결과라 생각한다.

• 한국주조공학회지
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• 제15권3호
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• pp.272-282
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• 1995

Iron-based metal matrix composites have been recently investigated for the use of inexpensive abrasion resistance material. This paper carried out to investigate the in-situ reaction effects on the microstructural characteristics and the formation mechanism of tungsten carbides in a white cast iron matrix. The specimens of Fe-3.2%C-2.8%Si alloy cast-bonded with tungsten wire were cast in the metal mold and isothermally heat treated at $950^{\circ}C$ up to 48 hours. The typical microstructure of heat treated specimens showed the reaction layer of WC at the interface of tungsten wire and the carbon depletion zone between the WC layer and the matrix. During the formation of WC layer, if the carbon supply is insufficient due to the decarburization of matrix or the isolation of matrix by cast-bonded W wires, the reaction layer develops coarse hexagonal crystalline WC. From the microstructural investigation, it was found that the volume of WC layer and the carbon depletion zone increased linearly with the isothermal heat treating time. This results supported that the formation rate of WC in the white cast iron matrix is controlled by the interfacial reaction with a constant reaction rate.

• 반도체디스플레이기술학회지
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• 제2권1호
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• pp.21-24
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• 2003

Sludged silicon powders that are generated during silicon ingot slicing process have potential usage as silicon source in fabricating silicon carbide powders by adding carbon. A thermodynamic calculation is performed to consider a plausible formation condition for the silicon carbide powders. A thin silicon oxide layer around silicon powder is sufficient to supply equilibrium oxygen partial pressure at the formation temperature($1400^{\circ}C$) of the silicon carbide in the Si-C-O ternary system. Formation of silicon carbide by using the sludged silicon powders is more efficient than by using silicon oxide powders.