• 한국결정성장학회지
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• 제31권1호
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• pp.16-23
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• 2021

리튬이차전지 제조 공정 중 발생한 폐액으로부터 회수된 탄산리튬의 경우, 이차전지 양극재의 원료인 코발트, 니켈 및 망간의 중금속이 함유되어 있다. 본 연구에서는 탄산리튬의 재결정화를 통하여 순도 98.28 %의 저급 탄산리튬 분말에 함유된 중금속을 제거하고 탄산리튬의 순도를 높이고자 하였다. 먼저 염산 수용액을 이용하여 탄산리튬의 침출 효율을 살펴보았으며, pH 5 조건으로 침출 후 탄산나트륨의 당량 및 농도의 탄산리튬 재결정에 대한 영향을 확인하였다. 리튬의 함량 기준 대비 탄산나트륨 1 당량에서 1.5로 증가할수록, 농도 1.4 M에서 2.8 M로 증가할수록 회수율은 향상되었으며, 탄산나트륨의 투입 조건이 달라짐에 따라 결정 형상이 달라지는 것을 SEM 분석을 통해 확인할 수 있었다. 재결정된 탄산리튬 분말은 수세하여 순도 99.9 % 이상의 고순도 탄산리튬을 회수할 수 있었다.

• 환경위생공학
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• 제15권1호
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• pp.95-101
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• 2000

This study was investigated to the reaction of alumina sintering with alkaline. The soluble $NaAlO_2$ was made after the commercial ${\alpha}-Al_2O_3$ was calcinated with NaOH. The reaction of alumina was carried out to be based on the effects of calcination temperature, time, and the mixing ratio of ${\alpha}-Al_2O_3/NaOH$. The alumina was calcined over $500^{\circ}C$ with NaOH powder after it was sieved with 170/270 mesh. The calcined alumina with NaOH powder was dissolved into $25^{\circ}C$ distilled water and filtrated, and HCI was added to adapt pH 6.5~7.5. The residue was separated with vacuum pump for filtration after it was adapted to proper pH, and aluminum compound was precipitated with $Al(OH)_3$. The investigation was carried out with the variables; the calcination temperature($500-900^{\circ}C$), the calcination time (30~90 min), and the concentration of HCI when leaching(0.5~3.0N) respectively. In this investigation, the main product of ${\alpha}-Al_2O_3$ and NaOH was $NaAlO_2$ and the maximum conversion ratio was 91.4% under the optimum conditions as followed ; the ratio of NaOH/${\alpha}-Al_2O_3$ was 1.5 and the calcination conditions were $800^{\circ}C$ and 90 min.

• 한국전기전자재료학회논문지
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• 제26권3호
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• pp.221-226
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• 2013

The water soluble quantum dots (QDs) are synthesized by the phase transfer and silica coating reaction. The photoluminescence intensity of silica-coated QDs are mainly affected by the amount of phase transfer agent, SDS (sodium dodecyl sulfate), and the maximum value is obtained at the cmc (critical micell concentration) concentration of SDS in the phase transfer reaction. Based on fluorescence spectra and field emission transmission electron microscope (FETEM), the energy transfer rate by forster resonance energy transfer (FRET) is increasing with the thickness of the silica shell coated on CdSe/ZnS QDs.

• Advances in environmental research
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• 제7권3호
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• pp.225-237
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• 2018

The sorption of metal ions with low-cost adsorbents plays an important role in sustainable development. In the present study, the efficacy of sugarcane bagasse, rain tree fruits (samaneasaman), banana stem and their mixtures, used as bio-sorbents, in the removal of Cu(II) and Pb(II) ions from aqueous solution is evaluated. Batch studies are conducted, and residual ions were measured using Inductively Coupled Plasma (ICP)-atomic spectrometer. Effect of pH, initial metal ion concentration, reaction time and adsorbent dosage are studied. The Pb(II) removal efficiency was observed to be 97.88%, 98.60% and 91.74% for rain tree fruits, banana stem and a mixture of adsorbents respectively. The highest Cu(II) ion removal was observed for sugarcane bagasse sorbent with an efficiency of 82.10% with a pH of 4.5 and a reaction time of 90 min. Finally, desorption studies were carried out to study the leaching potential of adsorbent, and it was found that the adsorbent is stable in water than the other leaching agents such as HCl, ammonium acetate, Sodium EDTA. Hence, these adsorbents can be effectively used for the removal of these heavy metals.

• 대한지하수환경학회지
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• 제4권4호
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• pp.212-222
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• 1997

국내 화강암질암내 지하수와의 대수층 지질 및 온도에 따른 지구화학적 특징 차이를 살펴보기 위하여 변성퇴적암류내 지하수와 온천수를 택하였다. 변성퇴적암류를 대수층으로 하는 지하수 내의 $Na^+$ 함량은 화강암질암에 비하여 통계적으로 낮다. 또한 화강암질암의 지하수와는 달리 변성퇴적암류의 지하수는 심부에서도 방해석의 거동에 의해 지하수의 화학조성이 조절됨으로써 $Ca^{2+]$-${HCO_3}^-$ 유형에 속한다. 이는 변성퇴적암류의 대수층 암석에 사장석의 함유량이 극히 적은 것에 기인한다. 요인분석 결과, 변성퇴적암류의100~300 m 심도의 지하수는 1) 방해석 및 Mg-탄산염암의 용해, 2) 백운모의 용해에 의하여 kaolinite가 illite로 전환되는 반응, 3) 지표에서 유입된 형태로 존재하는 $Na^+$ 등의 세 가지 요인으로 압축된다. 화강암질암과 변성퇴적암류에 대하여 도출된 판별함수는 약 81.8%의 판별력을 보였으며 이 판별식에 사장석이 주구성광물로 존재하는 화산암질 지하수를 적용한 결과 모두 화강암질암 그룹에 속하였다. 한편 온천수는 상대적으로 심도가 낮음에도 불구하고 화강암질암의 심부지하수와 유사한 화학적 특징을 보임으로써 고온으로 인해 주변 광물과의 반응이 활성화되었음을 나타낸다.

• 폴리머
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• 제31권5호
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• pp.374-378
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• 2007

Acrylamide(AM), diacetone acrylamide(DAAM) 및 acrylic acid(AAc)를 사용하여 수용성 삼원공중합체를 제조하고, 4-azidoaniline을 반응하여 azido기를 고분자 곁사슬에 도입한 일성분계 포토레지스트를 제조하였다. AM을 주성분으로 하고 DAAM을 공단량체로 사용한 공중합체를 합성하구 광가교제로 4,4'-diazidostilbene 2,2'-disulfuric acid sodium salt(DAS)를 혼합한 이성분계 포토레지스트를 제조하여 두 종류 포토레지스트의 감광특성을 비교하였다. 포토레지스트의 azido기 1 mol에 대한 감광특성은 고분자 곁사슬에 azido기를 가진 일성분계의 경우가 bis-azido기를 가진 이성분계보다 약 4배정도 우수한 감광성을 나타내었다. 직경 $110{\mu}m$ 크기의 원형패턴을 낮은 광세기에서 일성분계 포토레지스트를 사용하여 얻었으며, 노광부와 비노광부 계면에 잔존물이 없이 원형 패턴이 형성되어 블랙 매트릭스용 negative 포토레지스트로 활용이 기대된다.

• Korean Chemical Engineering Research
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• 제61권2호
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• pp.265-272
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• 2023

목질계 바이오매스는 조성분간의 결합이 치밀하고 높은 함량의 리그닌을 포함하여 전처리 공정이 필수적이다. 전처리 용매 중 테트라하이드로퓨란(THF)은 유기용매로 재사용이 가능하다는 장점이 있다. THF는 가격이 저렴하고 다양한 반응 조건에서 선택적으로 리그닌을 제거하고 물 혹은 이온성 액체와 공용매로 사용된다. 수산화 나트륨(Sodium hydroxide)은 바이오매스 내 ether결합을 파괴하여 리그닌을 우선적으로 용해시키며 셀룰로오스와 헤미셀룰로오스의 표면적을 확장시키는 역할을 한다. 본 연구에서는 NaOH/THF 공용매 전처리 공정을 적용하여 효과적 리그닌을 제거를 위한 전처리 특성을 파악하고 후속 공정인 산촉매 전환 공정을 통해 최적의 레불린산 전환 수율을 얻었다. 전처리 공정은 NaOH/THF 공용매 비율을 16가지 부피 비율로 수행되었으며 반응조건은 180℃에서 60분으로 고정하였다. 최적의 공용매 조건은 NaOH(5 wt%)/THF 공용매 90:10(v/v%)이였으며 76.8% 글루칸을 수득과 함께 90.1%의 리그닌을 제거하였다. 전처리 후속 공정인 산촉매 전환 공정은 반응시간 30~90분, 반응온도 160~200 ℃로 수행하였을 때, 산촉매 전환 공정의 최적 조건은 180 ℃에서 반응시간 60분이었며, 이 때의 레불린산 전환수율은 84.7%이다.

• 한국세라믹학회지
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• 제47권5호
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• pp.381-386
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• 2010

Some basic properties of inorganic coatings hardened by the room temperature reaction with alkalies were examined. The coating paste was prepared from the powders in the system $Al_2O_3-SiO_2$-CaO using blast furnace slag, fly ash and amorphous ceramic fiber after mixing with a solution of sodium hydroxide and water glass. The mineralogical and morphological examinations were performed for the coatings prepared at room temperature and after heating to $1200^{\circ}C$ respectively. The binding force of the coating hardened at room temperature was caused by the formation of fairly dense matrix mainly composed of oyelite-containing amorphous phase formed by the reaction between blast furnace slag and alkali solution. At the temperature, fly ash and ceramic fiber was not reacted but imbedded in the binding phase, giving the fluidity to the paste and reinforcing the coating respectively. During heating up to $1200^{\circ}C$, instead of a break in the coating, anorthite and gehlenite was crystallized out by the reaction among the binding phase and unreacted components in ternary system. The crystallization of these minerals revealed to be a reason that the coating maintains dense morphology after heating. The maintenance of binding force after heat treatment is seemed to be also caused by the formation of welldispersed fiber-like mineral phase which is originated from the shape of the amorphous ceramic fiber used as a raw materials.

• ETRI Journal
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• 제26권3호
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• pp.252-256
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• 2004

We formed silver nanocrystallites by the thermal decomposition of a $Ag^{+1}$-oleate complex, which was prepared by a reaction with $AgNO_{3}$ and sodium oleate in a water solution. The resulting monodispersed silver nanocrystallites were produced by controlling the temperature (290$^{\circ}$C). Transmission electron microscopic (TEM) images of the particles showed a 2-dimensional assembly of the particles with a diameter of $9.5{\pm}0.7nm$, demonstrating the uniformity of these nanocrystallites. An energy-dispersive X-ray (EDX) spectrum and X-ray diffraction (XRD) peaks of the nanocrystallites showed the highly crystalline nature of the silver structure. We analyzed the decomposition of the $Ag^{+1}$-oleate complex using a Thermo Gravimetric Analyzer (TGA) and observed the crystallization process using XRD.

• 한국의류학회지
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• 제10권2호
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• pp.79-84
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• 1986

Methacrylic acid was graft polymerized with benzoyl peroxide in itiator onto the commercial PET film. Graft polymerization was carried out in emulsion, which consisted of BPO (1), chlorobenzene(8) as swelling agent, tween 80(1) and sodium lauryl sulfate(1) as emulsifier and water(1,000). Original PET film has poor reactivities and, so the film preswdled with benzyl alcohol($150^{\circ}C$, 1hr) was also examined. The graft yield of PET film was increased with reaction temperature and monomer concentration. The graft yield of preswelled PET film was higher than that of no-treated PET film. Moisture regain was linearly increased with graft yield. DSC thermodiagram showed the Tm of grafted PET film was same as that of original PET film. Grafted PET film was dyed with methylene blue solution. The photograph of the cross section showed that grafting was occured not at the center but near surfaces.