• 제목/요약/키워드: Ferric ferrocyanide

검색결과 6건 처리시간 0.024초

수열 합성법에 의해 페릭페로시아나이드가 코팅된 마이카 티나니아 진주광택안료의 합성 및 특성 (Synthesis and Characteristic of Ferric Ferrocyanide Coated Titania/Mica Pearlescent Pigments by Hydrothermal Synthesis Method)

  • 이관식;이동규
    • 한국응용과학기술학회지
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    • 제28권3호
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    • pp.335-344
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    • 2011
  • The pearlesent pigment has received attention in a diversity of fields like cosmetics, inks, paints and so on. Ferric Ferrocyanide, one of the nano sized pearlescent pigment, is a kind of surface modification pigment that covers a metal oxidized substance or a coloring agent with uniform thickness. Characteristics of pearlescent pigment are various interference color, intense gloss effect and a three-dimensional effect. We synthesised the pearlesent pigment that ferric ferrocyanide can be deposited on the titania/mica surface by hydrothermal synthesis method. The process parameters are concentration of precursor, controlling pH and reaction temperature. The optimun conditions is that amount of iron(III) chloride hexahydrate is 3.1 wt% and amount of potassim ferrocynide trihydrate is 3.6 wt% in the started pH 4.5 at $70^{\circ}C$. The coating rate and coating efficiency of ferric ferrocyanide was about 1.47 % and 96.7 %, respectively. The synthesised pearlesent pigment was characterized by SEM, XRD, FT-IR and EDS.

Entropy, enthalpy, and gibbs free energy variations of 133Cs via CO2-activated carbon filter and ferric ferrocyanide hybrid composites

  • Lee, Joon Hyuk;Suh, Dong Hack
    • Nuclear Engineering and Technology
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    • 제53권11호
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    • pp.3711-3716
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    • 2021
  • The addition of ferric ferrocyanide (Prussian blue; PB) to adsorbents could enhance the adsorption performance of 133Cs. Toward this goal, we present a heterogeneously integrated carbonaceous material platform consisting of PB in direct contact with CO2-activated carbon filters (PB-CACF). The resulted sample retains 24.39% more PB than vice versa probed by the ultraviolet-visible spectrometer. We leverage this effect to capture 133Cs in the aqueous environment via the increase in ionic strength and micropores. We note that the amount of PB was likely to be the key factor for 133Cs adsorption compared with specific surface characteristics. The revealed adsorption capacity of PB-CACF was 21.69% higher than the bare support. The adsorption characteristics were feasible and spontaneous. Positive values of 𝜟Ho and 𝜟So show the endothermic nature and increased randomness. Based on the concept of capturing hazardous materials via hazardous materials, our work will be of interest within the relevant academia for collecting radionuclides in a sufficient manner.

훼로시안化 칼리움에 依한 鐵의 微量適定法 (Volumetric Determination of a small amount of Iron with Potassium Ferrocyanide)

  • 원종훈
    • 대한화학회지
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    • 제5권1호
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    • pp.42-47
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    • 1961
  • A titration of a small amount of iron with standard potassium ferrocyanide using potassium thiocyanate as indicator has been studied. A sample solution containing $0.1{\sim}1.0$ mg. $Fe^{3+}$ in 60 ml. is pipeted into 100 ml. Erlenmyer flask and the pH of the solution is adjusted to $1.5{\sim}3.0$ with 0.1 N or 1 N $HNO_3$ and $NH_4OH.$ To this solution one ml. of 1 M KCNS solution as indicator is added. The solution colored by iron thiocyanate complex is titrated with 1/200 M or 1/400 M standard solution of potassium ferrocyanide from a 5 ml. micro-buret. Near the end point, when the color of sample changes from deep red to green, about 20 ml. of ether is added and shake the flask vigorously. The red color is extracted to the ether layer. To settle the ether layer a few drops of ethanol is added and then standard solution is added dropwise and shake vigorously. The end point is reached when the color of the ether layer disappears owing to the quantitative formation of $Fe_4[Fe(CN)_6]_3.$ In this titration, 0.lmg. of $Fe^{3+}$ can be determined within 1.0% of titration error, provided the following optimum conditions, i.e., pH $1.5{\sim}3.0$, final concentration of KCNS indicator; $0.01{\sim}0.02M$, at room temperature. The titration found to be interfered by the presence of slightly soluble salts, stable complex forming ions and the ions which would be reduced by ferrocyanide or oxidized by ferric ion.

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화장품 제조에 쓰이는 Pigments 가 수분산 제형에 미치는 영향에 대한 연구 (A Study on the Effect of Pigments used in Cosmetic Manufacturing on the Form of Water Dispersible Formulations)

  • 김현지;오지원;곽병문;이미기;빈범호
    • 대한화장품학회지
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    • 제47권1호
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    • pp.41-48
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    • 2021
  • 수분산 제형은 사용 시 가루 날림이 없고, 끈적이지 않으며 가벼운 사용감을 주면서 밀착력이 높은 특징이 있어 색조 화장품에 많이 이용된다. 하지만 색조 화장품에 사용되는 수분산 제형에서 안료가 미치는 영향에 관한 연구는 거의 검토되지 않았다. 이에 본 연구에서는 색조 화장품 제조에 주로 쓰이는 무기색소, 유기색소, 진주광택안료 등의 안료를 각각 분산시켜 만든 수분산 제형에서 안료가 제형에 미치는 영향에 대하여 외관의 변화, pH의 변화, 광안정성을 측정하고 분석하는 연구를 진행하였다. Carmine 또는 ferric ferrocyanide가 코팅된 이산화티탄 마이카 계 색소는 저점도 수분산 제형에서 수상에 색이 우러나오며, 광안정성이 좋지 않아 사용에 적합하지 않았다. 유기 색소는 수분산 제형에서 1%의 함량으로 광안정성은 양호했으나 수상에 색이 우러나오고, 파우더끼리 뭉쳐서 잘 분산되지 않으므로 사용에 적합하지 않았다. 진주광택안료, 무기 색소, 산화철이 코팅된 이산화티탄 마이카 계 색소는 수분산 제형에서 외관 및 광안정성이 우수하여 사용에 적합하였다. 또한 각각의 안료를 분산시킨 모든 시료의 pH는 모두 3.0 - 9.0 범위 안에 들어 화장품 법에 적합한 것으로 보인다. 이는 색조 화장품 중 수분산 제형에서 안료의 거동을 예상하고 안정한 색소를 선택 및 사용하여 안정한 수분산 제형의 색조 화장품을 제조하는데 도움을 줄 것으로 기대된다.

구연산 발효에 관한 연구 (제 2 보) 국산 포도당을 기질로하고 Asp. niger에 의한 발효 (Studies on the Citric Acid Fermentation (Part 2) The Citric Acid Fermentation by Asp. niger, as the Substrate of Local Commercial Glucose)

  • 이상선;박무영
    • 한국미생물·생명공학회지
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    • 제6권4호
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    • pp.167-171
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    • 1978
  • 전보에 개발된 배지에 국산 포도당을 이용한 발효결과, 구연산 생성은 37∼43g/ι이었다. 제품X의 경우는 제품Y에 비해 구연산 생성이 우수하여 43g/ι가 생성되었다. 국산 포도당을 Ambelite-IR -120으로 처리하고, peptone도 potassium ferrocyan-ide로 처리하여 금속이온을 제거한 뒤에, 10mg/ι의 철 이온을 첨가하였을 때 구연산 생성은 53gm/ι에 달하였다. 또한 원래 Sakaguchi 배지에 비해 3배나 많이 구연산이 생성되었다. 분리 동정된 Asp. niger를 다른 문헌과 비교하였을 때 큰 손색이 없었으며, 앞으로의 생리연구 및 mutation 연구가 필요하겠다.

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도금폐수내 유리시안과 착염시안 및 중금속의 처리특성 (I) (Treatment Characteristics of Plating Wastewater Containing Freecyanide, Cyanide Complexes and Heavy Metals (I))

  • 정연훈;이수구
    • 한국물환경학회지
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    • 제25권6호
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    • pp.979-983
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    • 2009
  • The mean pH of wastewater discharged from the plating process is 2, so a less amount of alkali is required to raise pH 2 to 5. In addition, if sodium sulfite is used to raise pH 5 to 9 in the secondary treatment, caustic soda or slaked lime is not necessary or only a small amount is necessary because sodium sulfite is alkali. Thus, it is considered desirable to use only $FeSO_4{\cdot}7H_2O$ in the primary treatment. At that time, the free cyanide removal rate was highest as around 99.3%, and among heavy metals, Ni showed the highest removal rate as around 92%, but zinc and chrome showed a low removal rate. In addition, the optimal amount of $FeSO_4{\cdot}7H_2O$ was 0.3g/L, at which the cyanide removal rate was highest. Besides, the free cyanide removal rate was highest when pH value was 5. Of cyanide removed in the primary treatment, the largest part was removed through the precipitation of ferric ferrocyanide: $[Fe_4(Fe(CN)_6]_3$, and the rest was precipitated and removed through the production of $Cu_2[Fe(CN)_6]$, $Ni_2[Fe(CN)_6]$, CuCN, etc. Furthermore, it appeared more effective in removing residual cyanide in wastewater to mix $Na_2SO_3$ and $Na_2S_2O_5$ at an optimal ratio and put the mixture than to put them separately, and the optimal weight ratio of $Na_2SO_3$ to $Na_2S_2O_5$ was 1:2, at which the oxidative decomposition of residual cyanide was the most active. However, further research is required on the simultaneous removal of heavy metals such as chrome and zinc.