• 한국작물학회지
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• 제59권2호
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• pp.188-193
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• 2014

Seed viability testing provides valuable information for assessing seed lot germinability. However, most testing methods require destruction of seed prior to test. Because the dissected seeds for viability test cannot be used further evaluation, the nondestructively X-ray photography technique that can be applied for the evaluation of seed quality has been developed. In order to know the validity and accuracy of X-ray photography technique in seed evaluation test that conducted to remove the abnormal seed from a seed lot, we have compared the results from tetrazolium viability test, germination test and X-ray contrast method in cotton. Metallic salts treatment increased the efficiency of X-ray photographic method by enhancing the penetration of X-ray in abnormal or damaged seeds rather than normal seeds that have strong and well-organized tissues in seed. Cotton seeds presoaked for 16 hr in distilled water followed by soaking into metallic salt solution (5% NaI in water) for 60 min were easily classified seeds into dead seed and viable seed based on the radiography images obtained by X-ray radiation. We concluded that soft X-ray photography was reliable to find out the various defective characters due to heat and mechanical damage of seeds.

• 공업화학
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• 제7권5호
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• pp.946-953
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• 1996

동시조사법에 의한 아크릴산의 폴리프로필렌 부직포에 대한 그라프트 반응에서 조사량, 조사선량률, 금속염 및 용매가 그라프트 반응에 미치는 영향을 조사하였다. 같은 조사선량에서는 선량률이 낮을수록 높은 그라프트율을 나타냈다. 한편 조사선량률을 달리하여 일정 시간 동안 그라프트 반응시키면 조사선량률이 높을수록 그라프트율은 높았으며, 첨가한 금속염의 종류에 관계없이 그라프트 속도는 조사선량률의 0.74 차수에 비례하였다. 사용한 금속염 중에서 $FeSO_4{\cdot}7H_2O$가 가장 우수하였으며, 첨가제의 함량이 증가하면 할수록 그라프트율은 감소하였지만 적정농도이하에서는 그라프트용액이 고화되어 그라프트 반응시킬 수 없었다.

• Nuclear Engineering and Technology
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• 제54권2호
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• pp.653-660
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• 2022

The interaction between UN and CdCl₂ in the LiCl-KCl molten eutectic was studied at 1023 K. The chlorination was monitored by sampling and recording the redox potential of the medium. At 1023 K the chlorination of UN with cadmium chloride in the molten LiCl-KCl eutectic proceeds completely and results in the formation of uranium chlorides. The melts of the LiCl-KCl-UCl₃ or LiCl-KCl-UCl₄ compositions can be obtained by the end of experiment depending on the presence of metallic cadmium in the reaction zone. The higher the concentration of the chlorinating agent, the faster the reaction rate. At [CdCl₂]/[UN] = 1.65 (10% excess) the reaction proceeds to completion in about 7.5 h. At [CdCl₂]/[UN] = 7 the complete chlorination takes 2.5-3 h.

• 한국건설순환자원학회논문집
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• 제1권2호
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• pp.136-143
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• 2013

하수시설 및 복개 구조물 등은 용해 시 산성으로 작용하는 황화수소에 크게 노출되어, 황산화균의 작용에 의해 강산성의 황산이온이 생성된다. 이에 따라 콘크리트의 생화학적 부식에 의한 열화가 촉진되며, 콘크리트 손상을 더욱 가속화하여 내구성이 크게 저하될 수 있다. 본 연구에서는 콘크리트에서 황산화균이 유기 생체적으로 사용하는 황화수소를 제거하기 위해, 금속의 살균성을 이용하여 금속 및 금속염 분말을 콘크리트에 혼입한 후, 황산화 억제 성능을 평가하였다. 이를 위해 중성화한 콘크리트 시편의 황산화균에 대한 항균 성능을 비교 평가하였고, 급속 염소이온 침투시험을 통해 금속 및 금속염계 항균제 첨가량에 따른 콘크리트 염화물 침투깊이 및 확산계수를 측정하였다. 또한 야외에서 폭로시킨 콘크리트 시편의 표면 상태의 생화학적 상태를 관측하여, 항균콘크리트의 성능 및 적용성을 확인하였다.

• 한국산학기술학회논문지
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• 제13권11호
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• pp.5595-5600
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• 2012

본 논문은 poly(lactic acid)의 내열성을 향상시키기 위한 결정화 핵제의 검토 및 연구에 대한 것이다. 네 종류의 미세분말 핵제인 금속염 2,2'-methylene bis(4,6-di-tert-butylphenol) salt를 결정화 핵제로 사용하였다. 폴리머 컴파운드의 열적 및 기계적 특성은 DSC, HDT, UTM을 통해 측정하였다. 이 연구의 결과로서, 컴파운드 한 폴리머 샘플들의 내열특성은 핵제의 함량 증가와 미세분말 일수록 선형적으로 증가 하였다. 그 중에서MPZ2의 함량이 2 wt%일때 가장 높은 내열특성을 나타내었으며, PL98Z2 컴파운드의 열변형 온도는 $116^{\circ}C$를 나타내었다 (ASTM D 648, 0.455MPa).

• 한국세라믹학회지
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• 제30권4호
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• pp.325-331
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• 1993

Aqueous solutions of metallic salts, ZrO(NO3)2.2H2O and Y(NO3)3.5H2O were used as raw materials to synthesize crystalline submicron spherical powders of Zr0.94Y0.06O1.97 with tetragonal crystal phase. Each aqueous solution was mixed on the magnetic stirrer to homogenize for 12 hours. The concentration of the mixed solutionwas changed from 0.01mol/$\ell$ to 0.1mol/$\ell$ calculated as the concentration of Zr0.94Y0.06O1.97. Ultrafine droplets of starting mixed solution were sprayed by the ultrasonic vibrator and carried into the furnace kept at 55$0^{\circ}C$, $650^{\circ}C$, 75$0^{\circ}C$ and 85$0^{\circ}C$ using carrier gas of air (10$\ell$/min) and pyrolysed to form Y-TZP fine powders. The results of this exeriment were as follows. 1) Synthesized powders were nonagglomerated and spherical type. 2) Particle size distribution was narrow between 0.1${\mu}{\textrm}{m}$ and 1${\mu}{\textrm}{m}$. 3) Forming reaction Y-TZP was finished above synthetic temperature 75$0^{\circ}C$. 4) As the synthetic temperature rised from 55$0^{\circ}C$ to 85$0^{\circ}C$, the mean particle size decreased from 0.35${\mu}{\textrm}{m}$ to 0.22${\mu}{\textrm}{m}$ in the concentration of starting solution with 0.02mol/$\ell$. 5) At 75$0^{\circ}C$ of synthetic temperature, the concentration changes of starting solution from 0.01mol/$\ell$ to 0.1mol/$\ell$ increased the mean particle size from 0.24${\mu}{\textrm}{m}$ to 0.38${\mu}{\textrm}{m}$. 6) Chemical compositions of each synthesized particle were homogeneous nearly.

• Applied Biological Chemistry
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• 제23권4호
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• pp.211-217
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• 1980

강력(强力)한 inulin 분해력(分解力)을 가진 Streptomyces chibaensis균주(菌株)를 이용하여, 효소생산(酵素生産)에 효과적인 배양조건 및 배지조성을 검토(檢討)하여 다음과 같은 결과를 얻었다. 1. 효소생산배지(酵素生産培地)의 최적 초기 pH는 7.5였으며, 이 조건하에서 $30^{\circ}C$에서 84시간 배양했을 때 가장 높은 효소역가를 나타냈다. 2. Inulase를 다량생산(多量生産)하기 위한 배지의 탄소원(炭素源)으로서는 다른 탄소원(炭素源)에 비하여 inulin이 가장 효과적이었다. 3. 무기질소원(無機質素源)으로는 $(NH_4)_2HPO_4$가 inulase생산(生産)에 가장 효과적(效果的)이었고, 유기질소원(有機窒素源)으로는 corn steep liquor가 효과적(效果的)이었다. 4. 무기염(無機鹽)으로 KCI 0.01%, $MgSO_4$ 0.05%, 그리고 $FeSO_4$ 0.0001% 첨가하였을 때 가장 효과가 컸다. 5. 탄소원(炭素源)(inulin) 1%와 질소원(窒素源)(corn steep liquor) 2%의 비율(比率)로 혼합(混合)하여 만든 배지(培地)에서 가장 효소생산(酵素生産)이 높았다.

• Bulletin of the Korean Chemical Society
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• 제21권9호
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• pp.867-874
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• 2000

Two new azobenzene crown ether calix[4]arenes, 10 and 11, were synthesized by two pathways. In the first pathway,two ethoxy nitrobenzene groups were attached to t-butylcalix[4]arenes in a 1,3 position. Subsequent reduction ofthe nitrobenzene group s by metallic zinc in an alkaline solution afforded 10 and 11 in8% and 12%,respectively. In the second pathway,an azobenzene containing two glycolic units was prepared prior connect-ing to t-butylcalix[4]arenes. The yields from the second approach (5%, 8% for 10 and 11, respectively) were lower than those from the former approach. Single crystals of 10 suitable for X-ray crystallography was ob-tained by recrystallization in methanol.Both the X-ray structure and the 1H-NMR spectrum of 10 indicated that the stereoisomer of the azobenzene moiety was trans and the calixarene platform was in cone conformation. 1H NMR spectroscopy suggested that 10 underwent an observable cis-trans isomerization in CDCl3 under room light and upon UV irradiation with cis:trans ratios of 33:67 and 36:64,respectively. Compound 6 which was the precursor of 11showed fluxional behavior and was found to have mixed conformations ofcone and partial cone with a ratio of 47:53 at -30 $^{\circ}C.$ 1H NMR spectrum of 11 suggested that 11 was initially isolated as cis azobenzene with calix[4]arene in cone conformation and underwent conformational interconversion through calix[4]arene annulas in a similar fashion to 6 upon exposing to light. The complexation studies of 10 with picrate salts of Na+ and K+ using 1H NMR spectroscopysuggested that Na+ preferred to bind the cis form of 10 while K+ preferred to bind the trans form. The stereoisomer of the azobenzene unit in 11 changed partially from cis to trans upon complexing with K+.

• 대한금속재료학회지
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• 제46권10호
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• pp.646-651
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• 2008

The electrolytic reduction of spent oxide fuel involves the liberation of oxygen in a molten LiCl electrolyte, which results in a chemically aggressive environment that is too corrosive for typical structural materials. It is essential to choose the optimum material for the process equipment handling molten salt. IN713LC is one of the candidate materials proposed for application in electrolytic reduction process. In this study, yttria-stabilized zirconia (YSZ) top coat was applied to a surface of IN713LC with an aluminized metallic bond coat by an optimized plasma spray process, and were investigated the corrosion behavior at $675^{\circ}C$ for 216 hours in the molten salt $LiCl-Li_2O$ under an oxidizing atmosphere. The as-coated and tested specimens were examined by OM, SEM/EDS and XRD, respectively. The bare superalloy reveals obvious weight loss, and the corrosion layer formed on the surface of the bare superalloy was spalled due to the rapid scale growth and thermal stress. The top coatings showed a much better hot-corrosion resistance in the presence of $LiCl-Li_2O$ molten salt when compared to those of the uncoated superalloy and the aluminized bond coatings. These coatings have been found to be beneficial for increasing to the hot-corrosion resistance of the structural materials for handling high temperature lithium molten salts.

• 방사성폐기물학회지
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• 제21권1호
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• pp.55-64
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• 2023

There is a gap in our understanding of the behavior of fused and molten fuel salts containing unavoidable contamination, such as those due to fabrication, handling, or storage. Therefore, this work used calorimetry to investigate the change in liquidus temperature of PuCl₃, having an unknown purity and that had been in storage for several decades. Further research was performed by additions of NaCl, making several compositions within the binary system, and summarizing the resulting changes, if any, to the phase diagram. The melting temperature of the PuCl₃ was determined to be 746.5℃, approximately 20℃ lower than literature reported values, most likely due to an excess of Pu metal in the PuCl₃ either due to the presence of metallic plutonium remaining from incomplete chlorination or due to the solubility of Pu in PuCl₃. From the melting temperature, it was determined that the PuCl₃ contained between 5.9 to 6.2mol% Pu metal. Analysis of the NaCl-PuCl₃ samples showed that using the Pu rich PuCl₃ resulted in significant changes to the NaCl-PuCl₃ phase diagram. Most notably an unreported phase transition occurring at approximately 406℃ and a new eutectic composition of 52.7mol% NaCl-38.7mol% PuCl₃-2.5mol% Pu which melted at 449.3℃. Additionally, an increase in the liquidus temperatures was seen for NaCl rich compositions while lower liquidus temperatures were seen for PuCl₃ rich compositions. It can therefore be concluded that changes will occur in the NaCl-PuCl₃ binary system when using PuCl₃ with excess Pu metal. However, melting temperature analysis can provide valuable insight into the composition of the PuCl₃ and therefore the NaCl-PuCl₃ system.