• 한국작물학회지
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• 제44권1호
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• pp.49-54
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• 1999

An experiment was carried out using pots to investigate the effects of Chinese milk vetch on the seedling establishment and growth in rice. Four irrigations with five-day intervals and three different levels of vetch straw were investigated. Significantly higher panicle numbers were obtained in vetch-treated pots. Vetch levels were non-treatment as checks, vetch with top removed, root plus shoot 7.5 ton/ha, and root plus shoot 3.0 ton/ha. The time for complete degradation of vetch straws was reduced from 10 days to 5 days as submerged time was delayed, and was affected by the amount of mulched vetch straws. As the mulched vetch amount increased, the time for a complete degradation was extended from 4 days to 12 days. Grain yield and its components were significantly affected by irrigation time and mulched vetch amount. Effectively controlled, lowered reduction damage from the degrading vetch straw, irrigation date and vetch amount were the most important factors for the improving of seedling establishment in direct-sown rice.

• 한국연소학회:학술대회논문집
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• 한국연소학회 2006년도 제33회 KOSCO SYMPOSIUM 논문집
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• pp.299-303
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• 2006

From the analysis of fly ash, which contains unburned carbon, collected from the coal-fired Yong Hung power station, most particles are turned out to be hollow cenosphere and agglomerated soot particles. The sooting potential from six coals used in the plant were investigated with CPD model. The results show that the higher potential presented to Peabody, Arthur, Shenhua coals rather than other coals. It is necessary to measure the coal flow rates at each coal feeding pipe for four burner levels since they affect the extent of mixing of soot with oxidant, in turn, the oxidation rate of soot particles. The unbalance in coal flow rate was found in several coal pipes. We successfully reduced unburned carbon in ash by increasing the excess air and changing the SOFA yaw angle.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2002년도 하계학술대회 논문집 Vol.3 No.2
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• pp.1002-1005
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• 2002

We have synthesized novel stilbenequinone derivatives(ASQ, PSQ) and investigated the properties of their electron drift mobility. Characteristics of the ionization potential Ip and electron affinity Ea of the ASQ were investigated by determining both oxidation and reduction potentials. There were estimated Ip = 7.1 eV and Ea = 3.6 eV. The electron drift mobility of ASQ mixture(R:t-Bu 10wt%) was $1.5{\times}10^{-5}cm^2/V{\cdot}sec$ at $6.15{\times}10^{5}V/cm$ and $1.3{\mu}m$ thickness.

• 한국염색가공학회:학술대회논문집
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• 한국염색가공학회 2000년도 춘계학술대회 논문집
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• pp.150-151
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• 2000

Some chromophores that can undergo a pronouncend colour change when acted upon an extenal agency, such as light, heat, pH, or chemical agents, have many potential applicationa as functional dyes. They may be used as indicators, optical sensors, biochemical probes, optical and thermal recording materials. The results will investigate donor-acceptor chromophores which have the potential for such colour change processes. In particular, cross-conjugated donor-acceptor chormophores, analogous to indigo and squarylium-type chromophores, will be examined for pH sensitizing and for their oxidation-reduction colour change behaviour.

• 한국축산식품학회지
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• 제23권1호
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• pp.86-95
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• 2003

비타민 E에 의한 육색소의 산화 안정성 향상 기작을 정리하였다. 지용성 산화제인 $\alpha$-토코페롤이 수용성 단백질인 옥시마이오글로빈을 보호하는 원리가 밝혀지고 있다. 최근의 연구들에서 $\alpha$-토코페롤이 세포막 지방산화의 2차 산화물들의 방출을 지연시켜 옥시마이오글로빈 산화를 억제시키고 식육의 바람직한 육색을 유지시킨다는 증거가 제시되고 있다. 지방산화물의 한 그룹인 $\alpha$,$\beta$-분포화 알데하이드들은 단백질과 서로 결합하는 역할을 하여 옥시마이오글로빈의 산화를 증진시키는 것으로 밝혀졌다. 만약 $\alpha$-토코페롤이 이런 활동적인 알데하이드들의 발생을 지연시킨다면 이런 지방산화물들이 옥시마이오글로빈의 산화에 미치는 영향도 억제될 것이다. 또한$\alpha$-토코페롤은 메트마이오글로빈의 환원에 작용하여 쇠고기의 육색 안정성 유지에 일정부분 역할을 담당하는 것으로 사료된다.

• 대한화학회지
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• 제46권1호
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• pp.14-18
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• 2002

산화질소 분자(NO)가 전자 한 개를 받아 산화질소 음이온$(NO^-)$으로 환원되는 반응의 정도가 진동에너지에 따라 크게 달라질 수 있음을 제시하였다. NO와 $NO^-$의 포텐샬에너지 표면은 진동에너지가 많아짐에 따라 NO 분자가 전자를 받아 $NO^-$음이온으로 바뀔수 있는 에너지적 측면을 가짐을 보여준다. 또한, 진동 파동함수간의 Franck-Condon 인자를 계산하였다. 진동에너지가 많아지면 NO에서 $NO^-$로 바뀔 경로가 더 많이 증가함을 보인다. 이 결과는 NO 분자에게 적절한 빛을 조사시킴으로 $NO^-$이온으로의 환원반응속도를 조절할 수 있음을 의미한다.

• 한국지하수토양환경학회지:지하수토양환경
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• 제25권1호
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• pp.62-73
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• 2020

PAHs commonly found in industrial sites such as manufactured gas plants (MGP) are potentially toxic, mutagenic and carcinogenic, and thus require immediate remediation. In-situ chemical oxidation (ISCO) is known as a highly efficient technology for soil and groundwater remediation. Among the several types of oxidants utilized in ISCO, persulfate has gained significant attention in recent years. Peroxydisulfate ion (S₂O₈^2-) is a strong oxidant with very high redox potential (E⁰ = 2.01 V). When mixed with Fe²⁺, it is capable of forming the sulfate radical (SO₄^-·) that has an even higher redox potential (E⁰ = 2.6 V). In this study, the influence of various iron activators on the persulfate oxidation of PAHs in contaminated soils was investigated. Several iron sources such as ferrous sulfate (FeSO₄), ferrous sulfide (FeS) and zero-valent iron (Fe(0)) were tested as a persulfate activator. Acenaphthene (ANE), dibenzofuran (DBF) and fluorene (FLE) were selected as model compounds because they were the dominant PAHs found in the field-contaminated soil collected from a MGP site. Oxidation kinetics of these PAHs in an artificially contaminated soil and the PAH-contaminated field soil were investigated. For all soils, Fe(0) was the most effective iron activator. The maximum PAHs removal rate in Fe(0)-mediated reactions was 92.7% for ANE, 83.0% for FLE, and 59.3% for DBF in the artificially contaminated soil, while the removal rate of total PAHs was 72.7% in the field-contaminated soil. To promote the iron activator effect, the effects of hydroxylamine as a reducing agent on reduction of Fe³⁺ to Fe²⁺, and EDTA and pyrophosphate as chelating agents on iron stabilization in persulfate oxidation were also investigated. As hydroxylamine and chelating agents (EDTA, pyrophosphate) dosage increased, the individual PAH removal rate in the artificially contaminated soil and the total PAHs removal rate in the field-contaminated soil increased.

• 전기화학회지
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• 제9권2호
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• pp.95-99
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• 2006

마이크로전극을 사용하여 니켈-수소 전지의 전극 활물질인 수소저장합금$(MmNi_{3.55}Co_{0.75}Mn_{0.4}Al_{0.3})$과 수산화니켈의 단일입자에 대하여 전기화학적 특성을 평가하였다. 즉 마이크로 전극을 활물질 입자 한 개 위에 전기적인 접촉을 이루도록 조정하고 전위 주사(Cyclic Voltammograms) 및 포텐셜 스텝(Potential Step)으로 실험을 실시하였다. 그 결과 수소저장 합금 입자의 경우 -0.9, -0.75, -0.65V 부근에서 3개의 산화 피크 및 -0.98V에서 수소발생 전위, 그리고 수산화니켈 입자의 경우 프로톤 산화 환원 반응(0.45V, 0.32V)과 산소 발생 반응 전위를 보다 명확하게 확인 할 수 있었다. 그리고 수소흡장합금 입자 내에서의 수소 흡장 및 방출 전 과정에 대해 수소 확산계수 $(D_{app})\;(10^{-9}\sim10^{-10}cm^2/s)$가 얻어졌다.

• 한국지하수토양환경학회지:지하수토양환경
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• 제20권6호
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• pp.117-126
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• 2015

Reductive degradation of hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) by nanoscale zero-valent iron (nZVI) was investigated to evaluate the feasibility of using it for in-situ groundwater remediation. Batch experiments were conducted to quantify the kinetics and efficiency of RDX removal by nZVI, and to determine the effects of pH, dissolved oxygen (DO), and ionic strength on this process. Experimental results showed that the reduction of RDX by nZVI followed pseudo-first order kinetics with the observed rate constant (k_obs) in the range of 0.0056-0.0192 min⁻¹. Column tests were conducted to quantify the removal of RDX by nZVI under real groundwater conditions and evaluate the potential efficacy of nZVI for this purpose in real conditions. In column experiment, RDX removal capacity of nZVI was determined to be 82,500 mg/kg nZVI. pH, oxidation-reduction potential (ORP), and DO concentration varied significantly during the column experiments; the occurrence of these changes suggests that monitoring these quantities may be useful in evaluation of the reactivity of nZVI, because the most critical mechanisms for RDX removal are based on the chemical reduction reactions. These results revealed that nZVI can significantly degrade RDX and that use of nZVI could be an effective method for in-situ remediation of RDX-contaminated groundwater.

• Restorative Dentistry and Endodontics
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• 제18권2호
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• pp.431-445
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• 1993

The purpose of this study was to observe corrosion characteristics of six dental amalgams and was to analyse corrosion products electrochemically. After each amalgam alloy and Hg was triturated as the direction of the manufacturer by using mechanical amalgamator, the triturated mass was inserted into the cylinderical metal mold ($12{\times}10mm$) and was condensed with 160kg/$cm^2$ by using the hydrolic press. The specimen was removed from the mold and was stored at room temperature for 1 week, and was polished with amalgam polishing kit. The anodic and cathodic polarization curve was obtained by using cyclic voltammetric method with 3-electrode potentiostat in saline for each amalgam and Ag, Sn, Cu plate specimen at $37{\pm}0.5^{\circ}C$. The potential sweep range was -1.7V~0. 4V(vs SCE) in working electrode and scan rate was 50mV/s and the exposed surface area of each specimen to the electrolytic solution was $0.79cm^2$. The results were as follows. 1. In anodic-cathodic polarization curve of amalgam specimens, two anodic current rising areas and two cathodic current peaks were obtained at the low Cu amalgam(CF, CS) specimen and three anodic current rising areas and three cathodic current peaks were obtained at the high Cu amalgam (TY, DS, HV) specimen. 2. As this compared with the anodic and cathodic current peak potentials of Sn, Cu and Ag specimen, the first cathodic current peak I c was caused by the reduction of divalent tin salt, second cathodic current peak IIIc results from the reduction of quadravalent tin salt, and third cathodic current peak me results from the reduction of copper salt. 3. As reverse potential sweeping was done repeatedly, anodic current was decreased slightly in all amalgam specimens.