• 한국식품영양과학회지
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• 제24권2호
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• pp.299-304
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• 1995

Antioxidative effect of tea extracts from green tea(steamed, roasted), oolong tea and black tea was investigated. Antioxidative activities of the crude catechin fraction were the most effective in oolong tea which contained the highest level of (-)-epigallocatechin gallate(EGCg). The water-soluble fraction obtained from oolong tea exhibited binding with more ferrous than copper ions. It showed a synergistic effect when used with an antioxidant such as BHT(0.5mg) and $\alpha$-tocopherol(2mg). Especially, this synergistic effect was exhibited more with BHT than with $\alpha$-tocopherol. Also steamed green tea, roasted green tea and oolong tea showed remarkable free radical scavenging action. The SC50(the concentration of a water-soluble fraction which is required to scavenge 50% of 100$\mu$M 1, 1-diphenyl-2-picryl hydrazyl radicals) of steamed and roasted green tea, oolong tea and black tea extracts were 11.3$\mu\textrm{g}$/ml, 11.4$\mu\textrm{g}$/ml, 12.7 $\mu\textrm{g}$/ml and 14.9$\mu\textrm{g}$/ml, respectively. It is assumed that the antioxidative activity of tea extracts is due to inhibition of peroxidation free radical scavenging and binding action of ferrous ions by mainly tea polyphenol compounds.

• 한국광물학회지
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• 제6권2호
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• pp.105-115
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• 1993

철을 함유하는 전기적 광물들의 뫼스바우어 및 적외선 흡수 스펙트럼들은, 철 2가와 철 3가 이온들이 Y와 Z팔면체 자리에 들어가는 것을 보여준다. 철 이온들은 대개 2가인데, 대부분 Y자리에 분포되며 부분적으로 Z자리에도 들어간다. 흑갈색 전기석 광물들은 청색/녹색 전기석들 보다 Z자리의 철 2가 성분이 높다. 그러므로, 광학 스펙트럼으로 보면 흑갈색 전기석의 720 nm 피크가 청색/녹색 전기석의 피크보다 더 넓게 나타난다. 실험에 이용된 녹색/청색 전기석 광물들은 모두 철 2가 이온들만 가지고 있다. 전기석들의 적외선 스펙트럼들은 화학 분석결과로 보아 OH 주위의 양이온들의 환경에 따라 민감한 변화를 보인다. 열처리한 시료의 분석결과를 보면, O(1)H와 O(3)H의 적외선 흡수 스펙트럼 특성에는 차이를 보이지 않았다. 철 2가와 OH를 가지는 규산염 광물의 경우, $3565cm^{-1}$ 피크를 특징적으로 가지는데 이들의 탈수온도는 $700{\sim}800^{\circ}C$이다.

• Bulletin of the Korean Chemical Society
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• 제27권4호
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• pp.489-494
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• 2006

Goethite, hematite, magnetite and synthesized iron oxide are used as catalysts for Fenton-type oxidation of phenol. The synthesized iron oxides were characterized by X-ray diffraction (XRD), BET, X-ray photoelectron spectroscopy (XPS), and electron paramagnetic resonance (EPR). The catalytic activity of these materials is classified according to the observed rate of phenol oxidation. The effectiveness of the catalysts followed the sequence: ferrous ion > synthesized iron oxide >> magnetite hematite > goethite. According to these results, the most effective iron oxide catalyst had the structure similar to natural hematite. The surface oxidation state of the catalyst was between magnetite and hematite (+2.5 ~ +3.0). Phenol degraded completely in 40 min at neutral pH (pH = 7). Soluble ferric and ferrous ions were not detected in the filtrate from Fenton reaction solution by AAS. The formation of hydroxyl radicals was confirmed by EPR.

• 한국전기전자재료학회논문지
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• 제11권1호
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• pp.62-66
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• 1998

M$\ddot{o}$ssbauer spectra of ferrimagnetic $Fe_2SE_8$ prepared with $^{57}Fe$ enriched iron have been taken at 298 K and below 78K, and Fe\ulcornerSe\ulcorner has been studied by X-ray diffraction. The crystal structure is found to be a "3c" hexagonal superstructure of the NiAs structure. Three sets of six-line hyperfine patterns were obtained and assigned to three magnetically nonequivalent sites of a superstructure of the crystal. The iron ions at all three sites are found to be in a highly covalent ferrous state. It is shown that the results obtained at the low temperature region are well consistent with Okazaki's "3c" superstructure model.uperstructure model.

• 자원환경지질
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• 제36권1호
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• pp.39-48
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• 2003

본 연구에서는 황철석과 흑운모를 이용한 회분식반응조실험(batch reactor experiment)을 통하여 수용성 Cr(Ⅵ)의 제거 및 반응속도를 살펴보았으며 이에 따른 산화환원 반응기작을 고찰하였다. 황철석 실험군이 흑운모실험 군에 비해 산화환원반응속도가 100배정도 빨랐으며, pH 3의 실험군이 pH 4 실험군에 비해 Cr(III)으로의 환원반응속도가 빠르게 나타났다. 황철석 실험군에서 Cr(Ⅵ) 초기농도치 90%이상이 제거되는데 걸리는 시간은 pH가 4일때 4시간, pH가 3일 때 40분 이내였다. 반면에, 흑운모 실험군의 경우 pH가 3인 조건에서도 Cr(Ⅵ) 초기농도의 90%이상이 제거되는데 400시간 이상이 걸렸다. 모든 조건에서 Cr(III)치 농도는 초기에 증가하는 경향을 보이다가 일정시간이 지나면 안정한 농도로 고정되었다. 산성의 반응용액에서 Cr(Ⅵ)의 환원반응속도는 이 두 광물이 포함하고 있는 2가 철의 해리속도와 관련이 있음을 의미한다. pH 4의 조건인 실험군에서는 용액 내 Cr(Ⅵ)이 Cr(III)으로 환원되고 Fe(II)가 Fe(III)로 산화된 후, (Cr, Fe)(OH)$_3$$_{ (s)}$와 같은 침전물을 생성하여 상대적으로 용액내 Cr(III)과 Fe(III)농도가 낮은 것으로 여겨진다. pH 3의 실험군을 화학양론적 고찰하였으며, 흑운모의 실험에서는 수용성 Fe(II)의 감소된 양과 Cr(Ⅵ)의 환원된 양의 이론적인 몰비가 [3Fe(II) : 1Cr(Ⅵ)]임에도 그 몰 비가 약 1:1로서 1 mole의 Cr(Ⅵ)을 환원시키는데 Fe(II)이 적게 소비되었으며, 이는 광물에서 해리되는 Fe(II)에 의한 Cr(Ⅵ)의 환원뿐만 아니라 흑운모 구조 내 Fe(II)이 용액 내 Fe(III) 이온을 Fe(II) 이온으로 환원시키는 불균질산화환원반응이 발생하고 이 반응으로 생성된 Fe(II) 이온이 다시 Cr(Ⅵ)의 환원반응에 기여하였기 때문이다. 그러나 황철석 실험의 경우, 그 몰비가 약 2.90:1 로서 3에 가까우며, 이는 황철석의 빠른 산화를 통하여 급속한 Fe(II) 이온이 공급됨으로서 Cr(Ⅵ)의 환원반응이 이론적 화학양론의 반응 몰비에 부합한 결과를 보인 것으로 판단된다.

• Bulletin of the Korean Chemical Society
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• 제10권1호
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• pp.27-30
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• 1989

Lithium has been intercalated into $FeMoO_4Cl$, and deintercalated from $LixFeMoO_4Cl$ both electrochemically and chemically. The inserted $Li^+$ ions are stabilized in the distorted octahedral field in interlayer space of $FeMoO_4Cl$. The crystal symmetry is reduced from tetragonal to monoclinic due to the reduction of ferric to ferrous ions in $LixFeMoO_4Cl$ upon lithium intercalation. From the magnetic and structural data, it has been concluded that the high-spin electronic configuration of $Fe^{2+}(d_{xz}^2{d_{y2}^1}{d_1}{2d_z^12}{\cdot}_y2)$, corresponding to $^5E_g$, group term in $D_{4h}$ symmetry, can be stabilized by the elongation of $FeO_4Cl_{2-}$octahedra in a weak ligand field.

• Journal of Microbiology and Biotechnology
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• 제1권2호
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• pp.136-141
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• 1991

Optimum culture conditions for the formation of nitrile hydratase by Brevibacterium sp. CH2 were investigated. Addition of ferric and ferrous ions greatly increased the nitrile hydratase formation. The effects of nitriles, amides, and acids as an inducer on the formation of nitrile hydratase were investigated. Isobutyramide was the best inducer among the tested compounds. When Brevibacterium sp. CH2 was cultivated for 23 h at $30^{\circ}C$ in a optimized medium containing 15 g of glucose, 5 g of bacto peptone, 3 g of yeast extract, 3 g of malt extract, 1 g of $KH_2$$PO_4$, 1 g of $K_2$$HPO_4$, 1 g of NaCl, 0.5 g of isobutyramide, 0.2 g of MgSO$_4$ㆍ7$H_2O$, and 0.02g of $FeSO_4$ㆍ$7H_2$O per liter of distilled water with pH controlled at 7.1, the maximum total activity was 665 units/ml of the culture broth and the specific activity was 70 units/mg of the dry cells. The medium optimization increased the specific activity of Brevibacterium sp. CH2 2.2 times.

• 한국가금학회지
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• 제16권1호
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• pp.17-22
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• 1989

난백의 열광수성을 순화시키기 위하여 각종금속염(Fe$^{2＋}$, Fe$^{3+}$ , $Al^{3+}$ , Cu$^{2＋}$)을 첨가하고 가훈처리($60^{\circ}C$, 5분간) 전후 난백의 기능성을 검토하였으며 알루미늄염(Al$^{3+}$ )이 첨가된 난백의 pH에 대한효과도 검토하였다. 금속염의 첨가에 의해 가열처리 전후 난백의 탁도는 대체로 증가하였으나 알루미늄염의부가시 탁도의 변화가 가장 작았다. 난백의 기포력은 금속염의 첨가에 의해 전반적으로 증가하였으며 Fe$^{3+}$ 의 첨가효과가 가장 컸다. 특히 가열처리 후 난백의 기포력은Fe$^{3+}$ , Al/ sup 3＋/ 및 Cu$^{2＋}$의 첨가에 의해 크게 증가되었다. 기포안정성의 경우 열처리 전에는 Fe$^{3+}$ , Al/ sup 3＋/의 첨가효과가 있었으나 열처리 후에는 Fe$^{3+}$ 와 Al/ sup 3＋/의 첨가가 효과적이었다. 한편 알루미늄염을 첨가한 난백을 pH 7 -10의 범위에서 가열처리한 결과 pH 7-8.5 범위에서는 탁도 및 기포성의 변화가 크지 않았고 pH 9이상에서는 탁도와 기포성은 낮아졌으나 기포안정성은 향상되었다. 난백액에 Salmonella typhimurium을 $10^{6}$ cells/$m\ell$수준으로 접종 후 $60^{\circ}C$, 5분간의 가열처리 결과 pH에 상관없이 모두 사멸되었다.

• Asian-Australasian Journal of Animal Sciences
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• 제31권6호
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• pp.905-913
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• 2018

Objective: To evaluate the effects of L-lysine (Lys)/L-arginine (Arg) on lipid and protein oxidation of emulsion sausage during storage and its possible mechanism. Methods: Four samples were prepared based on the presence or absence of additional sodium isoascorbate, Lys, or Arg: sample A (control), sample B (0.05 g of sodium isoascorbate), sample C (0.4 g of Lys), and sample D (0.4 g of Arg). Peroxide value (POV), thiobarbituric reactive substances (TBARS), protein carbonyls and thiols were measured. 2,2-Diphenyl-1-picrylhydrazyl (DPPH) and hydroxyl radical-scavenging, ferrous ion-chelating ability were also measured. Results: Compared with the control, the sample treated with sodium isoascorbate, Lys or Arg had significantly lower POV during the initial 20 days, TBARS during the initial 15 days. Protein carbonyls were significantly lower compared Sample B, C, and D with A during the later storage (10 to 25 days); basically, protein thiols became lower during storage when the samples were treated with sodium isoascorbate, Lys, or Arg. Both Lys and Arg had weak reducing power but strong ferrous ion-chelating activity and DPPH radical- and hydroxyl radical-scavenging activity. Conclusion: Both Lys and Arg effectively inhibited the oxidation of lipids and proteins in emulsion sausage by scavenging free radicals and chelating ferrous ions. The results obtained may be favorable for the prevention of lipid and protein oxidation during processing and storage of meat products.

• Membrane and Water Treatment
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• 제11권3호
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• pp.207-215
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• 2020

Vivianite (Fe₃²⁺(PO₄)2·8H₂O) and green rust ([Fe₄²⁺Fe₂³⁺(OH)^-₁₂][SO₄^2-·2H₂O]^2-), ferrous containing minerals, could remove aqueous U(VI) in 5 min. and the efficiencies of green rust were roughly 2 times higher than that of vivianite. The zeta potential measurement results implies that the better performance of green rust might be attributed to the favorable surface charge toward uranyl phosphate species. The removal behaviors of the minerals were well fitted by pseudo-second order kinetic model (R² > 0.990) indicating the dominant removal process was chemical adsorption. Effects of Ca²⁺ and CO₃^2- at pH 7 were examined in terms of removal kinetic and capacity. The kinetic constants of aqueous U(VI) were 8 and 13 times lower (0.492 × 10^-3 g/(mg·min); 0.305 × 10^-3 g/(mg·min)) compared to the value in the absence of the ions. The thermodynamic equilibrium calculation showed that the stable uranyl species (uranyl tri-carbonate) were newly formed at the condition. Surface investigation on the reacted mineral with uranyl phosphates species were carried out by XPS. Ferrous iron and U(VI) on the green rust surface were completely oxidized and reduced into Fe(III) and U(IV) after 7 d. It suggests that the ferrous minerals can retard U(VI) migration in phosphate-rich groundwater through the adsorption and subsequent reduction processes.