• 제목/요약/키워드: chromium ($Cr^{3+}$

검색결과 461건 처리시간 0.027초

알칼리토 금속산화물이 함유된 붕규산염계 유리를 이용한 용액 중 Cr6+ 이온 제거 기구 (Mechanism of Removal of Cr(VI) Ions from Solution by Borosilicate Glasses Containing Alkaline Earth Oxides)

  • 백일희;임형봉;김철영
    • 한국세라믹학회지
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    • 제48권3호
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    • pp.222-227
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    • 2011
  • The hexavalent chromium ions in wastewater are highly toxic chemicals even at low concentrations. It causes serious diseases, such as cancer, skin disease, digestive trouble et. al. In this study, $Cr^{6+}$ ions were removed by using borosilicate glasses. Various glasses system with different compositions were prepared and then reacted in a solution contaning $Cr^{6+}$ ions. After the reaction, the concentration of the $Cr^{6+}$ ions remained in the solution was measured by ICP-OES. The reacted surface of the glasses was also analyzed by using a XRD, SEM, and EDS. When $Na_2O-RO-SiO_2-B_2O_3$ (RO=MgO, CaO, SrO, BaO) glasses were reacted with a solution containing $Cr^{6+}$ ions, the optimum removal efficiency of $Cr^{6+}$ ions was observed in the BaO glass. $Ba^{2+}$ ions leached out of these glasses combine with $Cr^{6+}$ ions in a solution to form $BaCrO_4$ crystals on the glass surface. In this manner, the $Cr^{6+}$ ions can be removed from the solution. It is conceivable that $Ba^{2+}$ ions are reacted with $Cr^{6+}$ ions in a solution immedeately after leaching out of the glasses. The pH of the solution for optimum removal of $Cr^{6+}$ ions were 3.0~5.0.

수생식물을 이용한 중금속 제거에 관한 연구 (Removal of Heavy Metals using Aquatic Plant)

  • 이상호;이인구
    • 한국지반환경공학회 논문집
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    • 제3권4호
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    • pp.5-10
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    • 2002
  • Pistia stratiotes(Water Lettuce)는 고도처리를 위한 폐수로부터 무기오염원 제거에 적용되어질 수 있다. 본 연구는 2차 처리된 폐수로부터 중금속을 제거하기 위하여 시도하였다. 납(Pb)과 크롬(Cr(VI))의 초기 농도를 0.5, 1.0, 1.5mg/L로 각각 다르게 적용되어 졌다. 그 외에 납(Pb)과 크롬(Cr(VI))을 혼합하여 제거효율을 관찰하였다. Pistia stratiotes에 의해 납(Pb)은 41.0~72.0%의 제거효율을 보였고 크롬(Cr(VI))은 25.0~30.0%의 제거효율을 보였다. Pistia stratiotes는 정지된 상태에서 수일 동안 중금속에 노출되어 중금속을 제거할 수 있었다. 그러나, 중금속은 식물에 독성을 일으켜 엽록소합성을 억제하고 생체량이 감소하면서 결국은 식물의 일부가 사멸하는 것이 관찰되었다. Pistia stratiotes에 의한 납(Pb)과 크롬(Cr(VI))의 제거효율은 식물의 성장과 함께 증가하였다.

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Electrochemical Performance and Cr Tolerance in a La1-xBaxCo0.9Fe0.1O3-δ (x = 0.3, 0.4 and 0.5) Cathode for Solid Oxide Fuel Cells

  • Choe, Yeong-Ju;Hwang, Hae-Jin
    • 한국세라믹학회지
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    • 제52권5호
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    • pp.308-314
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    • 2015
  • The electrochemical performance and Cr poisoning behavior of $La_{1-x}Ba_xCo_{0.9}Fe_{0.1}O_{3-{\delta}}$ (LBCF, x = 0.3, 0.4, 0.5) and $La_{0.6}Sr_{0.4}Co_{0.2}Fe_{0.8}O_{3-{\delta}}$ (LSCF) cathodes were investigated for solid oxide fuel cells (SOFCs). The polarization resistance of the LBCF/GDC/LBCF symmetrical cell was found to decrease with increasing Ba content (x value). This phenomenon might be associated with the high oxygen vacancy concentration in the LBCF sample, with x = 0.5. In addition, there was no chromium poisoning in the LBCF cathode. On the other hand, the polarization resistance of the LSCF cathode was found to significantly increase after exposure to gaseous chromium species; it appears that this result stemmed from the formation of $SrCrO_4$ phase. Therefore, it can be expected that LBCF can be a durable potential cathode material for intermediate-temperature solid oxide fuel cells (IT-SOFC).

Effect of Organic Acids on Cr(III) Oxidation by Mn-oxide

  • Chung, Jong-Bae
    • Applied Biological Chemistry
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    • 제41권4호
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    • pp.241-245
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    • 1998
  • Two oxidation states of chromium commonly occur in natural soil/water systems, Cr(III) and Cr(VI). The oxidized form, Cr(VI), exists as the chromate ion and is more mobile and toxic than Cr(III). Therefore oxidation of Cr(III) by various Mn-oxides in natural systems is a very important environmental concern. Organic substances can inhibit the Cr(III) oxidation by binding, Cr(III) strongly and also by dissolving Mn-oxides. Most of Cr(III) oxidation studies were carried out using in vitro systems without organic substances which exist in natural soil/water systems. In this study effect of organic acids - oxalate and pyruvate - on Cr(III) oxidation by $birnessite({\delta}-MnO_2)$ was examined. The two organic acids significantly inhibited Cr(III) oxidation by birnessite. Oxalate showed more significant inhibition than pyruvate. As solution pH was lowered in the range of 3.0 to 5.0, the Cr(III) oxidation was more strongly depressed. Addition of more organic acids reduced the Cr(III) oxidation mare extensively. Different inhibition effects by the organic acids could be due to their ability of reductive dissolution of Mn-oxides and/or Cr(III) binding. Organic acids dissolved Mn-oxide during the Cr(III) oxidation by the oxide, Dissolution by oxalic acid was much greater than that by pyruvate, and the dissolution was more extensive at lower pH. Inhibition of Cr(III) oxidation was parallel to the dissolution of Mn-oxide by organic acids. Although the effect of Cr(III) binding by organic acids on Cr(III) oxidation is not known yet, Mn-oxide dissolution by organic acids could be a main reason for the inhibition of Cr(III) oxidation by Mn-oxide in presence of organic acids. Thus oxidation of Cr(III) to Cr(VI) by various Mn-oxides in natural systems could be much less than the oxidation estimated by in vitro studies with only Cr(III) and Mn-oxides.

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Na2CrO4·4H2O를 흡입한 랫드의 호흡기 조직변화에 관한 연구 (The Changes of the Respiratory Organ after Inhalation of Na2CrO4·4H2O in Rat)

  • 이경열;박일권;박미선;송치원;이미영;김현영;김무강
    • 대한수의학회지
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    • 제43권2호
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    • pp.171-180
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    • 2003
  • Certain hexavalent chromium compounds when administered via inhalation have the potential to induce lung injury in human and experimental animals. In present study, the inhalation effect of hexavalent chromium on morphological change and weight change of rat organ were investigated. Rats were exposed to hexavalent chromium ($Na_2CrO_4{\cdot}4H_2O$) at concentration of $0.36mg/m^3$ (group 1), $1.8mg/m^3$ (group 2), ascorbic acid and $1.8mg/m^3$ (group 3) and filtered air (group 0, control group) for I week, 2 weeks and 3 weeks. The weight of lung and kidney in group 2 and group 3 significantly higher than in control group at same exposure period. The epithilial cells of bronchiole in group 1, 2, 3 were more flatten than group 0. In the lung, the number of macrophage was significantly increased and morphologically changed macrophages were observed in group 1, 2, 3. The morphological change of the lung did not significant between group 2 and group 3, however, in group 1 was milder than in group 2 and group 3. The severity of morphological change were depend on exposure period in the lung. The morphological changes by hexavalent chromium of the liver and kidney were also observed These results suggest that inhalation of hexavalent chromium effects on not only respiratory organ, but also the liver and the kidney via blood stream.

도금업 근로자의 혈청과 공기중 크롬 및 니켈 농도 (Chromium and nickel concentrations in air and in serum of workers in chromium and nickel electroplating plants)

  • 최호춘;김해정;정호근
    • 한국산업보건학회지
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    • 제1권2호
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    • pp.117-127
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    • 1991
  • The exposure level of chromium and nickel for chrome and nickel plating workers were evaluated. Chromium and nickel concentrations in serum from 82 exposed workers and 66 controls, who were not exposed occupationally to metals, were analyzed by flameless atomic absorption spectrophotometry. The results were as follows : 1. The recovery percent of chromium and nickel concentrations in personal air samples were 95-108.2%, 88.0-107.7%, precisions (C.V., %) were 2.7-3.1%, 2.1-4.4%. respectively. 2. The recovery percent of chromium and nickel concentrations in serum were 93.6-106.4%, 91.3-107.9% and precisions (C.V. %) were 1.1-7.6%, 2.4-5.4% respectively. 3. The exposure level of chromium and nickel concentrations in the place of preparation process were $2.0{\pm}2.00{\mu}g/m^3$, chromplating were $35.7{\pm}53.07{\mu}g/m^3$, $2.8{\pm}3.42{\mu}g/m^3$, nickelplating were $4.6.0{\pm}5.8{\mu}g/m^3$, $18.62{\pm}4.41{\mu}g/m^3$, and covering were $2.9{\pm}2.02{\mu}g/m^3$, $1.1{\pm}0.47{\mu}g/m^3$ respectively. There were significant difference of concentrations for chromium and nickel in workplaces by groups statistically. 4. Chromium concentrations in serum of exposed group and control were $0.68{\pm}0.399{\mu}g/l$, $1.41{\pm}0.748{\mu}g/l$, respectively. There were significant difference of concentrations for chromium and nickel in serum by groups statistically. 5. Chromium and nickel concentrations in serum of exposed group were not significant by workplaces.

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Potassium hexathiocyanatochromate (III)의 제조에 관한 실험 (Preparation of potassium hexathiocyanatochromate)

  • 최종인
    • 약학회지
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    • 제13권1호
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    • pp.38-42
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    • 1969
  • Chloropentammine chromium(III) chloride를 출발물질로 하여 여러가지의 thiocyanatoammine계 착화합물을 합성하는 실험에 있어서 그 수득량이 예상보다 매우 적고 그 염의 모액이 농적자색이라는 점으로 보아 그 모액중에 어떠한 다른 착화합물이 다량 형성되어 있으리라고 추측하여 그 분리를 시도하였다든바 미려한 적자색의 결정을 얻었다. 그리고 분석에 의하여 이 물질이 potassium hexathiocyanatochromate(III) 임을 증명하였다. Cr$^{+++}$ 의 thiocyanate 착화합물형성에 관하여는 Niel Bjerrm$^{(8)}$에 의한 보고문이 있고 또 이들의 제법으로서는 Roesler$^{(9)}$들에 의하여 Potassium chromium alum에서부터 이 물질을 만드는 방법만이 보고되어 있을뿐이다. 따라서 Chloropentammine chromium(III) chloride에서 부터 이 물질을 만드는 이 새로운 방법이 이러한 화합물들의 제법으로서 앞으로 이용될 수 있는것으로 사료한다. 제조 방법: Chloropentammine chromium(III) chloride 3g을 KSCN 24g, 빙초산 24ml및 물 48ml의 혼합수용액에 현탁시킨 혼합물을 처음에는 잘 교반하면서 가온하고 다음 완전히 용해될때까지 끊인다. 냉각시킨 다음 생성된 증황색의 침반 Thiocyanatopentammine chromium(III) thiocyanate를 여과하고 여액 65ml에 KSCN 50g을 추가하여 완전용해시킨다. 이 용액을 방냉시키면 적자색의 미려한 결정이 석출되므로 이 결정을 여과하여 ethanol로 세척하고 진공 desiccator중에서 건조시켰다. 수득량 1.2~1.3g.

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CrN 소결체의 고온 안정성 (High Temperature Stability of Sintered Bulk CrN)

  • 최정호;이동복
    • 한국표면공학회지
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    • 제40권1호
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    • pp.39-43
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    • 2007
  • The pure CrN powders oxidized to $Cr_2O_3$ noticeably above $850^{\circ}C$ in air. When these powders were sintered into bulk samples at $1500^{\circ}C$ under 40 atm of $N_2$ pressure, the CrN phase partly changed into the $Cr_2N$ phase, owing to the partial loss of nitrogen from CrN. When the bulk sample was heated at $1000-1200^{\circ}C$ for 100 hr under vacuum, the CrN phase also progressively changed into $Cr_2N$. At the same time, a relatively thin $Cr_2O_3$ layer formed on the bulk sample due to the reaction of chromium with residual oxygen in vacuum.

Cr 및 N2 함량에 따른 Ti-Cr-N 박막의 부식특성 변화 (Effect of Chromium and Nitrogen content on the corrosion properties of Ti-Cr-N films)

  • 차병철;허성보;박민재;정우창
    • 한국표면공학회:학술대회논문집
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    • 한국표면공학회 2014년도 추계학술대회 논문집
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    • pp.302-303
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    • 2014
  • 유도결합플라즈마 보조 D.C.마그네트론 스퍼터링법을 이용하여 STS316L 위에 Ti-Cr-N 박막의 증착하였으며 크롬과 질소의 함량에 따른 부식특성 변화를 관찰하였다. Ti-Cr-N 박막을 증착시켰을 때는 미처리 STS316L에 비해 더 우수한 부식특성을 보였으며 크롬타겟의 인가전원이 100W 일 때와 질소비가 0.3일 때 가장 우수한 내부식 특성을 나타내었다.

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산소가 혼입된 Cr 박막의 질화처리에 따른 구조적 특성 (Structural Properties of Ammoniated Thin Cr Films with Oxygen Incorporated During Deposition)

  • 김준;변창섭;김선태
    • 한국재료학회지
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    • 제24권4호
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    • pp.194-200
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    • 2014
  • Metallic Cr film coatings of $1.2{\mu}m$ thickness were prepared by DC magnetron sputter deposition method on c-plane sapphire substrates. The thin Cr films were ammoniated during horizontal furnace thermal annealing for 10-240 min in $NH_3$ gas flow conditions between 400 and $900^{\circ}C$. After annealing, changes in the crystal phase and chemical constituents of the films were characterized using X-ray diffraction (XRD) and energy dispersive X-ray photoelectron spectroscopy (XPS) surface analysis. Nitridation of the metallic Cr films begins at $500^{\circ}C$ and with further increases in annealing temperature not only chromium nitrides ($Cr_2N$ and CrN) but also chromium oxide ($Cr_2O_3$) was detected. The oxygen in the films originated from contamination during the film formation. With further increase of temperature above $800^{\circ}C$, the nitrogen species were sufficiently supplied to the film's surface and transformed to the single-phase of CrN. However, the CrN phase was only available in a very small process window owing to the oxygen contamination during the sputter deposition. From the XPS analysis, the atomic concentration of oxygen in the as-deposited film was about 40 at% and decreased to the value of 15 at% with increase in annealing temperature up to $900^{\circ}C$, while the nitrogen concentration was increased to 42 at%.