• 한국도로학회논문집
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• 제14권3호
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• pp.1-7
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• 2012

본 논문에서는 ASTM C 1260을 이용하여 국내산 골재를 대상으로 알칼리-실리카 반응 판정 결과 반응성으로 판정된 골재를 대상으로 알칼리-실리카 반응 억제효과를 고찰하기 위하여 플라이애시와 질산리튬을 사용한 시멘트 경화체의 ASTM C 1260 적용성을 평가하였다. 알칼리-실리카 반응에 의한 팽창현상이 발생하는 지역에서 CaO 함량이 낮은 플라이애시를 시멘트 중량의 10, 20, 30%를 대체하는 경우 ASTM C 1260으로 알칼리-실리카 반응 억제효과를 확인할 수 있었다. 그러나 질산리튬을 사용할 경우는 ASTM C 1260은 시편을 1N NaOH 수용액에 수침하여 $80^{\circ}C$의 온도로 길이변화를 유도하므로 시편내에 혼입된 질산리튬 성분이 외부로 용출될 수 있기 때문에 알칼리-실리카 반응 억제효과를 도출하지 못하였다. 따라서 질산리듐의 ASR 억제효과를 확인하기 위해서는 다른 시험방법을 고려해야 한다.

• International Journal of Concrete Structures and Materials
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• 제8권4호
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• pp.315-326
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• 2014

This study evaluates the dosages of Class F fly ash, lithium nitrate and their combinations to suppress the excessive expansion caused by alkali-silica reactivity (ASR). In order to serve the proposed objective, the mortar bar specimens were prepared from (1) four dosages of Class F fly ash, such as 15, 20, 25 and 30 % as a partial replacement of Portland cement, (2) up to six dosages of lithium nitrate, such as lithium-to-alkali molar ratios of 0.59, 0.74, 0.89, 1.04, 1.19 and 1.33, and (3) the combination of lithium salt (lithium-to-alkali molar ratio of 0.74) and two dosages of Class F fly ash (15 and 20 % as a partial replacement of Portland cement). Percent contribution to ASR-induced expansion due to the fly ash or lithium content, test duration and their interaction was also evaluated. The results showed that the ASR-induced expansion decreased with an increase in the admixtures in the mortar bar. However, the specimens made with the both Class F fly ash and lithium salt produced more effective mitigation approach when compared to those prepared with fly ash or lithium salt alone. The ASR-induced expansions of fly ash or lithium bearing mortar bars by the proposed models generated a good correlation with those obtained by the experimental procedures.

• 한국에너지공학회:학술대회논문집
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• 한국에너지공학회 1996년도 추계학술발표회 논문집
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• pp.190-192
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• 1996

본 연구는 기존의 Water-Lithium Bromide(H2O/LiBr) 용액에 비해 부식성이 낮은 Water-Lithium bromide-Lithium Nitrate계(H2O/LiBr-LiNO3)용액의 용해도, 증기압, 점도, 표면장력 등의 물리적 성질을 조사하였다. 또한 용해도가 가장 큰 최적의 혼합 몰비를 구하여 증기압 및 점도, 표면장력등의 물성을 구함으로써 흡수식 냉온수기용 홉수제 개발의 기본 자료를 확보하였다. 이러한 연구 결과로부터 다성분 Lithium 염 혼합물계로 이루어진 흡수용액 개발의 기초자료로 이용하고자 한다.

• International Journal of Industrial Entomology and Biomaterials
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• 제34권1호
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• pp.6-10
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• 2017

Dissolution of Antheraea yamamai silkworm cocoon was carried out in various solvent systems with various dissolving conditions including dissolution salts, salt concentration, dissolving temperature, and time. General chaotropic salt for Bombyx mori silk fibroin does not work for A. yamamai silkworm cocoon. Lithium bromide 9.3 M at $100^{\circ}C$ also does not work to dissolve wild silkworm cocoon. However, 9 M of lithium thiocyanate treatment at $100^{\circ}C$ induced 100% dissolution of wild silkworm cocoon. But it could not be dissolved lower than $60^{\circ}C$. Like lithium thiocyanate, less than $60^{\circ}C$ treatment with molten calcium nitrate 4 hydrate could not dissolve wild silkworm cocoon. As the dissolution temperature increased up to $100^{\circ}C$, the solubility of wild one was reached over 90%. SDS-PAGE showed broad tailing stream pattern that means the molecule of wild silk was depolymerized with dissolution temperature and time. From the above results, the best chaotropic salt for A.yamamai silkworm cocoon is calcium nitrate 4 hydrate.

• 자원리싸이클링
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• 제30권6호
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• pp.43-52
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• 2021

본 연구에서는 Taguchi method을 사용하여 폐 배터리 셀 분말(LiNi_xCo_yMn_zO₂, LiCoO₂)으로부터 선택적 리튬 침출을 위한 최적의 질산염화 공정에 대한 연구를 진행했다. 질산염화 공정은 질산 침출 및 배소를 통해 질산리튬을 제외한 질산 화합물을 산화물로 변환하여 선택적 리튬 침출을 하는 공정이다. 따라서 전처리 온도, 질산 농도, 질산 침적 양, 배소 온도에 대하여 Taguchi method를 적용하여 인자가 미치는 영향에 대한 분석을 실시하였다. L₁₆(4⁴)직교 배열표를 사용하여 실험하였으며, 신호 대 잡음비(S/N) 및 분산 분석(ANOVA)을 분석하였다. 그 결과 배소 온도가 가장 크게 영향을 미쳤으며 질산 농도, 전처리 온도, 질산 사용량 순으로 영향을 미쳤다. 각 인자에 대해 세부적인 실험을 진행한 결과 전처리 700℃에서 10시간, 10 M 질산 2 ml/g 침출, 275℃ 배소 10시간이 적절하였다. 그 결과 80% 이상의 리튬을 침출을 확인하였다. 400℃ 이상 배소 시 급격하게 리튬 침출율이 감소원인 분석을 위해 질산리튬과 질산 화합물을 배소 후 D.I water에서 침출하지 잔류물에 대해 XRD 분석을 진행하였다. 분석 결과 질산리튬과 질산망간과 400℃ 이상의 온도에서 리튬 망간 옥사이드의 형성하며 D.I water에서 침출하지 않음을 확인하였다. 질산염화 공정 시 침출된 용액을 고액분리 후 증발농축하여 XRD 분석한 결과 LiNO₃의 회수를 확인하였다.

• Corrosion Science and Technology
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• 제9권6호
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• pp.265-269
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• 2010

This paper describes the exfoliation and surface modification of muscovite mica for UV coating formulation. For the exfoliation of the mica, hydrothermal process was used in the presence of lithium nitrate ($LiNO_3$). After the cation exchange with $Li^+$ ions, the surface of the mica was modified with several amphiphilic substances to increase compatibility and storage stability in UV coating formulation. Such a hydrophobic surface modification affected colloidal stability as well as dispersibility of the exfoliated mica in UV coating solution. Anticorrosive property of mica/UV coated steel plates was tested by salt spray test (SST) and compared with sodium montmorillonite ($Na^+$-MMT)/UV coated steel plates.

• Nuclear Engineering and Technology
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• 제9권4호
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• pp.211-222
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• 1977

고준위 방사성 폐액의 고화처리 방법들 중 하나인 Vitrification Process의 연구로서 핵연료 재처리 과정에서 유출되는 가상적인 비활성폐액 중에 함유되어 있는 분열 및 부식 생성물들의 질산화물과 유리화시키기 위해 사용되는 첨가제의 열분해에 관하여 연구 조사되었다. 결정수를 갖고 있는 화합물들의 열분해시점은 75$^{\circ}C$이하였지만, 무수화합물들은 비교적 높은 분포를 보였다. 110$0^{\circ}C$까지 가열하여 얻어진 질량손실율을 이론치와 비교하였을 때, 대부분의 화합물은 릴치하거나 근사하였지만, Sodium, Cesium, Lithium, Ruthenium 등의 질산화물의 질량손실율은 이론치 보다 훨씬 높았다. 여기서 얻어진 결과는 고준위 폐액의 가소처리과정 또는 조사된 화합물들의 혼합에 따른 열분해를 분석하는데도 이용될 수 있을 것이다.

• 한국잠사곤충학회지
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• 제39권1호
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• pp.44-55
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• 1997

This study was carried out to find out the relationship between qualities and contraction phenomenon of silk fibers by treatment of concentrated neutral salts. The contraction effects of silk fibers showed the critical point on the treatment conditions of concentration, temperature and time, among three kinds of neutral salts such as calcium nitrate, calcium chloride and lithium bromide. But, The silk fibers, pretreated with bromide and/or formaldehyde, did not show the contraction upon treating with calcium nitrate. This indicates that tyrosine and serine can be correlated with the contraction reaction because of coupling these amino acids with bromide and formaldehyde. In conclusion, a mechanism for the contraction of silk fiber with highly concentrated calcium nitrate solution is supposed as follows. At the initial stage of ration, the water was penetrated into the amorphous regions and fibers swollen, therefore, the contraction took place mainly in amorphous regions, which have plenty of functional groups with hydroxyl residues. Then, as the calcium nitrate is penetrated into the microfibril, the gydrogen bonds of tyrosine and serine residues and broken and crystalline regions are more and more influenced by increasing concentration of calcium nitrate solution. Microgibrils of crystalline regions become entangled, contracted to linear direction and rearranged to form new stable hydrogen bonds.

• 한국세라믹학회지
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• 제43권9호
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• pp.588-593
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• 2006

Spinel phase $LiMn_2O_4$ is of great interest as cathode materials for lithium-ion batteries. In this study, SHS (Self propagating High-temperature Synthesis) method to synthesize spinel $LiMn_2O_4$ directly from lithium nitrate, manganese oxide, manganese and sodium chloride were investigated. The influence of Li/Mn ratio, the heat-treated condition of product have been explored. The resultant $LiMn_2O_4$ synthesized under the optimum synthesis conditions shows perfect spinel structure, uniform particle size and excellent electrochemical performances.

• 한국전기전자재료학회논문지
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• 제19권8호
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• pp.737-743
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• 2006

[ $Li[Co_{0.50}Li_{0.17}Mn_{0.33}]O_2$ ] powder was prepared using a simple combustion method. specially, ratio of 2:1, 3:2, 1:1, 2:3, 1:2 was adopted as acetate source/nitrate source. The diffraction pattern of $Li[Co_{0.50}Li_{0.17}Mn_{0.33}]O_2$ powder showed that this compound could be classified as hexagonal $a-NaFeO_2$ structure (space group : $R\bar{3}m$). The size of powder was less than $1{\mu}m$. Small particle size of cathode powder would give a good ionic and electronic conductivity to cathode electrode, which made of cathode powder. As the increase of nitrate source-ratio, discharge capacity of $Li[Co_{0.50}Li_{0.17}Mn_{0.33}]O_2$ at high charge-discharge rate was increased. When the ratio of acetate source/nitrate source was 1:2, discharge capacity at 10 C rate (2000 mA/g) was 180 mAh/g. It was $10{\sim}15%$ larger than that of powder, which have 2:1 as acetate source/nitrate ratio.