• Applied Chemistry for Engineering
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• v.7 no.4
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• pp.614-622
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• 1996

Efficient removal of nickel from the ferric chloride etching solution has been studied. At first, $Fe^{3+}$ was reduced to $Fe^{2+}$ by the electrolytic iron flake or the waste shadow mask iron plate. And then, $Ni^{2+}$ was removed from the solution by electrolytic iron powder. Under the optimum conditions the reduced rates of nickel were 99 % and 98%, respectively at the initial $Ni^{2+}$ concentrations of 1.0% and 0.1%. Sludge formed during reduction of $Fe^{3+}$ in the solution were analyzed by XRD and SEM.

• Clean Technology
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• v.13 no.4
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• pp.274-280
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• 2007

A liquid-liquid solvent extraction process was developed in this study to recover Fe and Ni from heavily concentrated aqueous ferric chloride solution, in an effort to substitute the conventional iron reduction method. Solvent composition and extraction conditions were first developed from the laboratory experiments, and the pilot system was designed and built for commercialization. Stage numbers for extraction and stripping were determined from pilot plant runs, and other operation data were obtained for mass production.

• Textile Coloration and Finishing
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• v.2 no.1
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• pp.31-36
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• 1990

The electrically conducting cellulose acetate/polypyrrole composite films were synthesized by exposing cellulose acetate film containing oxidizing agent to pyrrole vapour and the formation of polypyrrole is confirmed by IR and electron microscopic studies. The morphologies of polypyrrole in the composites are different depending on the oxidizing agent. Ferric chloride is most effective among several metallic chlorides to synthesize the composites with high electrical conductivity. The conductivity of composite films synthesized with 50 wt.% of ferric chloride reaches upto $10^{-2}S/cm$.

• Resources Recycling
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• v.17 no.6
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• pp.17-23
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• 2008

In order to simulate the leaching solution of copper sulfide ore in $FeCl_3$ solutions, synthetic solutions with composition of $FeCl_3$-$FeCl_2$-$CuCl_2$-CuCl-NaCl-HCl-$H_2O$ were prepared. The concentration of iron and copper chloride was varied from 0.1 to 1 m in synthetic solutions. The effect of composition on the mixed solution pH and potential at $25^{\circ}C$ was measured. When HCl concentration was constant, the increase of CuCl concentration increased solution pH. The increase of other solutes excluding HCl and CuCl decreased solution pH owing to the increase of the activity coefficient of hydrogen ion. A high CuCl concentration favored the redox equilibrium in the direction of Cu(I), while $FeCl_3$ had the opposite effect.

• Journal of the Korean Chemical Society
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• v.54 no.5
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• pp.573-578
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• 2010

In this study, iron(III)-2,4-dihydroxysalophen chloride (Fe(2,4-DHSalophen)Cl), has been synthesized by combination of 2,4-dihydroxysalophen (2,4-DHSalophen) with $FeCl_2$ in a solvent system. This complex combination was characterized using UV-vis and IR spectroscopies. Subsequently, the interaction between native calf thymus deoxyribonucleic acid (ct-DNA) and Fe(2,4-DHSalophen)Cl, was investigated in 10 mM Tris/HCl buffer solution, pH 7.2, using UV-visible absorption and fluorescence spectroscopies, thermal denaturation technique and viscosity measurements. From spectrophotometric titration experiments, the binding constant of Fe(2,4-DHSalophen)Cl with ct-DNA was found to be $(1.6{\pm}0.2){\times}10^3\;M^{-1}$. The fluorescence study represents the quenching effect of Fe(2,4-DHSalophen)Cl on bound ethidium bromide to DNA. The quenching process obeys linear Stern-Volmer equation in extended range of Fe(2,4-DHSalophen)Cl concentration. Thermal denaturation experiments represent the increasing melting temperature of DNA (about $4.3^{\circ}C$) due to binding of Fe(2,4-DHSalophen)Cl. These results are consistent with a binding mode dominated by interactions with the groove of ct-DNA.

• Resources Recycling
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• v.17 no.5
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• pp.37-43
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• 2008

Stripping experiments of iron from the loaded Alamine336 by sulfurous, chloric and sulfuric acid solutions have been performed by varying the concentration of acid and stripping conditions. The stripping percentage of iron decreased with the increase of HCl and $H_{2}SO_4$ concentration, while that increased with the increase of $H_{2}SO_3$ concentration up to 3 M. Stripping temperature had adverse effect on the stripping percentage of iron in the stripping by $H_{2}SO_3$ solution, while the stripping percentage of iron by HCl solution increased with the increase of temperature. Stripping isotherm of iron by 0.1 M HCl and 0.1 M $H_{2}SO_4$ solution indicated that three and four stripping stages could result in a solution containing 0.05 M iron at an O/A ratio of 1/10 from the loaded Alamine336 phase where iron concentration was 0.5 M.

• Proceedings of the Korean Institute of Resources Recycling Conference
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• 2006.05a
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• pp.105-109
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• 2006

본 연구는 Karr column을 이용하여 희토류 염화물 수용액상에서 비희토성분인 철의 분리에 대한 기초 연구로서, 아민계 추출제인 Alamine336을 이용하여 염화물 수용액상에서 유기상의 농도, 염소이온 농도, 염산 농도에 따른 철 성분의 분리특성을 파악 하였다. Batch 실험결과 추출제 농도가 증가함에 따라 철성분 제거율이 급격히 상승하였으며, 염산 및 염소이온 농도의 경우도 유사한 결과를 나타내었다. Batch 실험을통해 확인된 불순물(Fe)을 추출하기위한 최적 조건은 염산농도 2M, 추출제 농도 0.1M, 상비 1, 추출시간 30분으로서, 이때 희토류 염화물 수용액상의 철 성분 함량은 0.7ppm 이하로서 제거율은 99.9%였다. 또한 최적의 batch 실험조건에서 반응시간(=체류시간)을 변화시키며 실험한 결과, 반응시간 60분의 조건에서 batch 실험과 유사한 결과를 얻을 수 있었다.

• Journal of Biosystems Engineering
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• v.28 no.2
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• pp.143-150
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• 2003

전분 완충재의 물리적, 기계적 특성을 개선하기 위한 노력들이 많이 이루어지고 있지만 기존의 플라스틱 완충재와 비교하면 더 많은 노력이 요구되어진다. 그래서 본 연구에서는 전분 완충재의 물리적 기계적 특성에 대한 유연제(plasticizers)와 첨가제(additives)의 영향을 규명하였다. 전분과 합성수지 그리고 여러 유연제 또는 첨가제를 혼합한 뒤 Brabender사의 일축 압출기를 이용하여 여러 축속도(60~120 rpm)에서 압출 가공한 후 물리적, 기계적 특성을 조사하였다. 전분 완충재의 밀도(bulk density)와 압축성(bulk compressibility)은 혼합물에서 물의 비율이 증가함에 따라 증가하였지만, 복원성(bulk resiliency)은 조금 감소하였다. 측정되어진 전분 완충재의 특성은 변형전분(hydroxypropylated starch)의 사용으로 향상되었다. 또한, glycerol, glycerol monostearate 그리고 alkylglucosides의 첨가도 전분 완충재의 밀도와 압축성을 증가시켰다. 염화철(II) 0.5%을 포함한 전분 완충재는 첨가제를 포함하지 않은 전분 완충재에 비하여 밀도 42%와 압축성 58%가 각각 감소한 반면, 복원성은 13%포인트 증가하였다. 변형전분과 염화철(II)이 첨가된 전분 완충재는 기존의 플라스틱 완충재에 비하여 밀도와 압축성은 떨어지지만, 대체 사용되어질 수 있는 것으로 판단되었다.

• Resources Recycling
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• v.32 no.3
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• pp.9-17
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• 2023

Efforts are currently underway to develop a method for efficiently recovering lithium from the cathode material of waste lithium iron phosphate batteries (LFP). The successful application of lithium battery recycling can address the regional ubiquity and price volatility of lithium resources, while also mitigating the environmental impact associated with both waste battery material and lithium production processes. The isomorphic substitution leaching process was used to recover lithium from spent lithium iron phosphate batteries. Lithium was leached by the isomorphic substitution of Fe²⁺ in LFP using a relatively inexpensive ferric chloride etching solution as a leaching agent. In the study, the leaching rate of lithium was compared using the ferric chloride etching solution at various multiples of the LFP molar ratio: 0.7, 1.0, 1.3, and 1.6 times. The highest lithium leaching rate was shown at about 98% when using 1.3 times the LFP molar ratio. Subsequently, to eliminate Fe, the leachate was treated with NaOH. The Fe-free solution was then used to synthesize lithium carbonate, and the harvested powder was characterized and validated. The surface shape and crystal phase were analyzed using SEM and XRD analysis, and impurities and purity were confirmed using ICP analysis.

• Applied Chemistry for Engineering
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• v.35 no.3
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• pp.255-259
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• 2024

In this study, an aqueous-based redox flow battery (RFB) was constructed using tungstosilic acid (TSA), which is a kind of polyoxometalate, as the negative electrode active material and iron chloride (FeCl3) as the positive electrode active material in a sulfuric acid (H₂SO₄) supporting electrolyte. As a result of the cell's performance, it exhibited capacity fading and low energy efficiency. To address these issues, malic acid (MA), an organic additive, was introduced to the positive electrode active material and then tested for electrochemical properties and single cell performance. The malic acid in the iron chloride aqueous solution is working as a chelate agent, and two carboxyl groups are effectively coordinated with iron ions. It was found that MA reduced the electrolyte resistance of the positive electrode active material, leading to chemical stabilization and an increase in capacity and energy efficiency.