• 제목/요약/키워드: $FeSO_4$

검색결과 1,147건 처리시간 0.03초

정색반응(呈色反應)에 의(依)한 싸리속(屬)의 분류학적(分類學的) 연구(硏究) (Taxonomic Study of the Genus Lespedeza by Means for Colour Reactions)

  • 박종열;이창복
    • 한국산림과학회지
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    • 제14권1호
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    • pp.21-31
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    • 1972
  • 화학약품(化學藥品)에 의(依)한 목재(木材)의 정색반응(呈色反應)을 이용(利用)하여 지피조성용(地被造成用), 사료자원, 밀원자원, 공예자원, 및 섬유자원으로서 중요시 되고 있는 우리나라의 싸리 속(屬) 중에서 다음 7 수종(樹種)에 대한 분류상(分類上)의 식별점(識別點)을 조사(調査)하였다. (1) Lespedeza bicolor Turcz 싸리 (2) Lespedeza bicolor var. melanantha(Nak.) T. Lee 쇠싸리 (3) Lespedeza cyrtobotrya Miq. 참싸리 (4) Lespedeza japonica var. intermedia Nakai 풀싸리 (5) Lespedeza maritina Nakai 해변싸리 (6) Lespedeza maximowiczii Schneider 조록싸리 (7) Lespedeza maximowiczii var. tomentella Nakai 털조록싸리 처리 방법(方法)은 시료분말을 직접 염산에 처리하여 나타나는 정색반응을 검토하는 방법과 목재분말(木材粉末)의 methanol 침출액에 각종 시약을 적하한 후 그 정색반응을 관찰하는 두가지 방법을 적응했으며 시약으로는 $K_2Cr_2O_7$, $FeSO_4{\cdot}7H_2O$, $FeCl_3$, $KMnO_4$, $KH_2PO_4$, $NH_4OH$, HCl의 7 가지 시약을 사용하였다. 본 실험을 통하여 구명된 결과를 요약하면 다음 검색표와 같다. 1. 침출액에 $K_2Cr_2O_7$ 적하반응에서 chrome lemon으로 정색했다${\cdots}{\cdots}$2 1. 침출액에 $K_2Cr_2O_7$ 적하반응에서 sun flower yellow색으로 정색했다${\cdots}{\cdots}$털조록싸리 2. $KH_2PO_4$ 용액의 적하반응에서 oyster white, $FeCl_3$ 용액을 적용반응하면 golden yellows로 정색한다${\cdots}{\cdots}$3 2. $KH_2PO_4$ 용액을 적하반응시키면 cream 색을 정색한다${\cdots}{\cdots}$6 3. $NH_4OH$ 용액의 적하반응에서 oyster white, $FeSO_4{\cdot}7H_2O$ 적하반응에서 corn 색을 정색한다${\cdots}{\cdots}$4 3. $NH_4OH$ 용액의 적하반응에서 cream 색을 정색한다 ${\cdots}{\cdots}$5 4. $KMnO_4$ 용액의 적하반응에서 van dyke brown, HCl 주가가열반응에서 sea shall pink 로 정색한다${\cdots}{\cdots}$풀싸리 4. $KMnO_4$ 용액의 적하반응에서 sepia, HCl 주가가열 반응에서 honey 색을 정색한다${\cdots}{\cdots}$해변싸리 5. $FeSO_4{\cdot}7H_2O$ 용액의 적하반응에서 golden rod, 분말(粉末)에 직접 HCl을 첨가하여 andover green 색을 정색한다${\cdots}{\cdots}$쇠싸리 5. $FeSO_4{\cdot}7H_2O$ 용액의 적하반응에서 yellow ochre, 분말에 직접 HCl을 첨가하여 sand warm gray 색을 정색한다 6. $FeCl_3$ 용액의 적하법에서 amber graw 색을 정색한다${\cdots}{\cdots}$참싸리 6. $FeCl_3$ 용액의 적하법에서 leather brown 색을 정색한다$\cdots}{\cdots}$조록싸리.

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Fe(II)/과황산/전기화학적 산화 공정에 의한 2,4-D의 제거 (Removal of 2,4-D by an Fe(II)/persulfate/Electrochemical Oxidation Process)

  • 현영환;최지연;신원식
    • 한국지하수토양환경학회지:지하수토양환경
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    • 제26권1호
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    • pp.45-53
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    • 2021
  • The removal of 2,4-dichlorophenoxyacetic acid (2,4-D) in aqueous solution by coupled electro-oxidation and Fe(II) activated persulfate oxidation process was investigated. The electrochemical oxidation was performed using carbon sheet electrode and persulfate using Fe(II) ion as an activator. The oxidation efficiency was investigated by varying current density (2 - 10 mA/㎠), electrolyte (Na2SO4) concentration (10 - 100 mM), persulfate concentration (5 - 20 mM), and Fe(II) concentration (10 - 20 mM). The 2,4-D removal efficiency was in the order of Fe(II) activated persulfate-assisted electrochemical oxidation (Fe(II)/PS/ECO, 91%) > persulfate-electrochemical oxidation (PS/ECO, 51%) > electro-oxidation (EO, 36%). The persulfate can be activated by electron transfer in PS/ECO system, however, the addition of Fe(II) as an activator enhanced 2,4-D degradation in the Fe(II)/PS/ECO system. The 2,4-D removal efficiency was not affected by the initial pHs (3 - 9). The presence of anions (Cl- and HCO3-) inhibited the 2,4-D removal in Fe(II)/PS/ECO system due to scavenging of sulfate radical. Scavenger experiment using tert-butyl alcohol (TBA) and methanol (MeOH) confirmed that although both sulfate (SO4•-) and hydroxyl (•OH) radicals existed in Fe(II)/PS/ECO system, hydroxyl radical (SO4•-) was the predominant radical.

물리, 화학적 처리방법에 의한 염색폐수의 색도제거에 관한 연구 (A Study on the Reduction of Color in Dye Wastewaters by Physico-chemical Processes)

  • 이준석;김민호;김영규
    • 한국환경보건학회지
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    • 제19권3호
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    • pp.29-35
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    • 1993
  • This study was performed to obtain optimal conditions for reduction of color in dye wastewaters using coagulation-sedimentation processes with redox reactions. The reduction of color as well as organic matters variation was observed after coagulation-sedimentation processes using FeSO$_4$ $\cdot$ 7H$_2$O and NaOCl. Coagulation-redox reaction was done with the dose of Coagulant and oxidant at various pH values. Redox reaction was done through jar-mixing and aeration. The results of study were as follows: 1. In the coagulation-sedimentation processes using FeSO$_4$ $\cdot$ 7H$_2$O, color reduction was heigher at pH 3. With variance of dosage of FeSO$_4$ $\cdot$ 7H$_2$O, color reduction was higher at 250 mg/l. When coagulation-sedimentation using FeSO$_4$ $\cdot$ 7H$_2$O 250 mg/l was added at pH 3, the reduction of color, COD$_{Mn}$, and COD$_{Cr}$ showed 47.6%, 21.3% and 22.1%, respectively. 2. When NaOCI was added at level of 100 ppm in raw wastewater at pH 3, the reduction of color, COD$_{Mn}$, and COD$_{Cr}$ showed 30.2%, 5.5% and 6.2%, respectively. 3. After coagulation-sedimentation processes by addition of FeSO$_4$ $\cdot$ 7H$_2$O, when NaOCl was added at level of 250 mg/l in supernant, color reduction was 47.8% in aeration and 37.5% in jar-mixing. 4. Color reduction by aeration was higher than that by jar-mixing.

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산소 결함 Magnetite를 이용한 이산화탄소의 분해 (The Decomposition of Carbon-dioxide Using the Oxygen Deficient Magnetite)

  • 김승호;박영구;이승훈
    • 한국환경보건학회지
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    • 제21권2호
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    • pp.68-74
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    • 1995
  • The optimum conditions was synthesized for the formation of Magnetite ($Fe_3O_4$) by air bubbling with the suspensions obtained by mixing Ferrous sulfate ($FeSO_4\cdot 7H_2O$) and Sodium Hydroxide (NaOH) solution in various values equivalent ratio($R=2NaOH/FeSO_4$) were studied. The changes of the structure were measured with XRD, $EM and BET. Equivalent ratio R: 0.65 was synthesized Goethite ($\alpha$-FeOOH), which becomes Maghemite ($\gamma=Fe_2O_3$) by dehydration, reduction and oxidation process. At the equivalent ratio over 1 (R>1), Magnetite ($Fe_3O_4$) was synthesized directly. The oxygen-deficient Magnetite ($Fe_3O_{4-\delta}$), which is obtained by flowing $H_2$ gas(100 ml/min) through the synthesis Magnetite at 350$\circ$C for 4 hr. By using it, was researched the decomposition reaction of $CO_2$. $CO_2$ was decomposed nearly 100% in 45 minutes by the oxygen-deficient Magnetite.

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Determining Factors for the Protectiveness of the Passive Film of FeCrN Stainless Steel Formed in Sulfuric Acid Solutions

  • Ha, Heon-Young;Lee, Tae-Ho
    • Corrosion Science and Technology
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    • 제12권4호
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    • pp.163-170
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    • 2013
  • In NaCl solutions acidified with $H_2SO_4$, Fe20Cr1.1N alloy showed enhanced pitting corrosion resistance than Fe20Cr alloy. An XPS analysis revealed that the passive film of Fe20Cr1.1N alloy contained higher cationfraction of Cr than that of Fe20Cr alloy, and nitrogen was incorporated into the film. In addition, it was found that the passive film of Fe20Cr1.1N alloy was thinner and had higher oxygen vacancy density than that of Fe20Cr alloy. Based on these observations, it was concluded that the chemical composition was the determining factor for the protectiveness of the passive film of Fe20Cr based alloy in dilute $H_2SO_4$ solution.

무기질 염이 Sisomicin 발효 수율의 증가에 미치는 영향 (Effects nit Mineral Salts on the Improvements of Sisomicin field)

  • Shin, Chul-S;Sang H. Han;Lee, Sang H.
    • 한국미생물·생명공학회지
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    • 제17권3호
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    • pp.247-251
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    • 1989
  • 여러가지 염이 sisomicin 발효에 미치는 영향에 대해 살펴본 결과, CoCl$_2$만이 항생물질 생성의 대사반응에 cofactor로서 작용하였으며 16.8 $\mu$M에서 최대항생물질의 수율이 얻어졌다. 한편, 앞의 경우보다 훨씬 높은 염농도에서 ZnSO$_4$, KH$_2$PO$_4$, FeSO$_4$그리고 MgSO$_4$가 각각 발효배지에 첨가되었다. ZnSO$_4$와 KH$_2$PO$_4$는 전혀 효과가 없었으나 FeSO$_4$는 약간 항생물질 수율의 향상을 가져왔다. 그러나 MgSO$_4$의 경우, 매우 높은 염농도에서도 균체생육의 저해가 약간 일어났으며, 최종 항생물질의 수율은 100% 이상 증가되었다. 이러한 결과는 부분적으로 발효 중 균체내에 생성된 항생물질이 균체외로 유출되는 효과가 증진된 것에 기인한다.

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응집조건이 염색폐수의 색도제거에 미치는 영향 (Decolorization of Real Textile Wastewater by Coagulation Conditions)

  • 홍영호
    • 공업화학
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    • 제20권1호
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    • pp.34-39
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    • 2009
  • 본 연구는 염색폐수 처리공정에서 발생하는 슬러지 및 색도제거에 관한 연구로 응집제가 색도제거에 미치는 영향에 대한 상관성을 규명하는데 목적이 있다. 이를 위해 실제공정에서 배출되는 염색폐수를 대상으로 응집조건에 따른 특성을 분석하였다. 응집제로 $FeCl_3$, $FeSO_4$, $Al_2(SO_4)_3$를 사용하였으며, 실험에 사용된 염색폐수의 BOD, COD, pH, 그리고 색도의 평균값은 각각 800 mg/L, 600 mg/L, 9.7, 182 이었다. 실험결과에 의하면 응집제의 농도가 335~2000 mg/L 이고 NaOH의 농도가 500 mg/L인 조건에서 응집제로 $FeCl_3$를 사용하였을 때 색도제거효과가 가장 우수하였다. 색도제거효과는 폐수의 pH와 응집제의 농도에 따라 결정된다고 할 수 있다.

Seasonal color change of the oxyhydrous precipitates in the Taebaek coal mine drainage, south Korea, and implications for mineralogical and geochemical controls

  • Kim, J. J.;C. O. Choo;Kim, S. J.;K. Tazaki
    • 한국광물학회:학술대회논문집
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    • 한국광물학회.한국암석학회 2001년도 공동학술발표회 논문집
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    • pp.38-39
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    • 2001
  • The seasonal changes in pH, Fe, Al and SO$_4$$\^$2-/ contents of acid drainage released from coal mine dumps play a major role in precipitation of metal hydroxides in the Taebaek coal field area, southeastern Korea. Precipitates in the creeks underwent a cycle of the color change showing white, reddish brown and brownish yellow, which depends on geochemical factors of the creek waters. White precipitates consist of Al-sulfate (basaluminite and hydrobasaluminite) and reddish brown ones are composed of ferrihydrite and brownish yellow ones are of schwertmannite. Goethite coprecipitates with ferrihydrite and schwertmannite. Ferrihydrite formed at higher values than pH 5.3 and schwertmannite precipitated below pH 4.3, and goethite formed at the intermediate pH range between the two minerals. With the pH being increased from acid to intermediate regions, Fe is present both as schwertmannite and goethite. From the present observation, the most favorable pH that basauluminte can precipitate is in the range of pH 4.45-5.95. SEM examination of precipitates at stream bottom shows that they basically consist of agglomerates of spheroid and rod-shape bacteria. Bacteria species are remarkably different among bottom precipitates and, to a less extent, there are slightly different chemical compositions even within the same bacteria. The speciation and calculation of the mineral saturation index were made using MINTEQA2. In waters associated with yellowish brown precipitates mainly composed of schwertmannite, So$_4$ species is mostly free So$_4$$\^$2-/ ion with less AlSo$_4$$\^$+/, CaSo$\sub$(aq)/, and MgSo$\sub$4(aq)/. Ferrous iron is present mostly as free Fe$\^$2+/, and FeSo$\sub$4(aq)/ and ferric iron exists predominantly as Fe(OH)$_2$$\^$+/, with less FeSo$\sub$4(aq)/, Fe(OH)$_2$$\^$-/, FeSo$_4$$\^$-/ and Fe$\^$3+/, respectively Al exists as free Al$\^$3+/, AlOH$_2$$\^$-/, (AlSo$_4$)$\^$+/, and Al(So$_4$)$\^$2-/. Fe is generally saturated with respect to hematite, magnetite, and goethite, with nearly saturation with lepidocrocite. Aluminum and sulfate are supersaturated with respect to predominant alunite and less jubanite, and they approach a saturation state with respect to diaspore, gibbsite, boehmite and gypsum. In the case of waters associated with whitish precipitates mainly composed of basaluminite, Al is present as predominant Al$\^$3+/ and Al(SO$_4$)$\^$+/, with less Al(OH)$\^$2+/, Al(OH)$_2$$\^$+/ and Al(SO$_4$)$\^$2-/. According to calculation for the mineral saturation, aluminum and sulfate are greatly supersaturated with respect to basaluminite and alunite. Diaspore is flirty well supersaturated while jubanite, gibbsite, and boehmite are already supersaturated, and gypsum approaches its saturation state. The observation that the only mineral phase we can easily detect in the whitish precipitate is basaluminite suggests that growth rate of alunite is much slower than that of basaluminite. Neutralization of acid mine drainage due to the dilution caused by the dilution effect due to mixing of unpolluted waters prevails over the buffering effect by the dissolution of carbonate or aluminosilicates. The main factors to affect color change are variations in aqueous geochemistry, which are controlled by dilution effect due to rainfall, water mixng from adjacent creeks, and the extent to which water-rock interaction takes place with seasons. pH, Fe, Al and SO$_4$ contents of the creek water are the most important factors leading to color changes in the precipitates. A geochemical cycle showing color variations in the precipitates provides the potential control on acid mine drainage and can be applied as a reclamation tool in a temperate region with four seasons.

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암모니아 용출용액을 이용한 저 품위 엽납석으로부터 Fe 제거 효율과 용해 동역학 (The Efficiency of Fe Removal for Pyrophyllite by Ammonia Leaching Solution, and Their Dissolution Kinetics)

  • 김봉주;조강희;최낙철;박천영
    • 한국광물학회지
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    • 제27권1호
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    • pp.53-62
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    • 2014
  • 저 품위 엽납석 광석에 포함된 불순물 Fe를 제거하기 위하여 입도크기, 황산농도, 황산암모늄농도, 과산화수소농도 그리고 온도변화에 따른 제거 효율에 대하여 연구하였다. 저 품위 엽납석 광석에서 자형의 입방체 황철석이 포함된 것을 반사현미경으로 관찰할 수 있었으며, X-선 회절분석결과 주 구성광물은 석영과 딕카이트였다. 실험 결과 Fe 용출율이 최대로 나타나는 입도 -325 mesh에서, 황산농도는 2.0 M에서, 황산암모늄 농도는 10.0 g/l, 과산화수소 농도 3.0 M 그리고 최적의 용출 온도는 $70^{\circ}C$에서였다. 용해 동역학 분석에서, Fe 용해는 황철석 표면에서 일어나며 화학적 반응에 통제되는 것으로 그리고 0.066/R, $[H_2SO_4]^{1.156}$, $[(NH_4)_2SO_4]^{0.745}$, $[H_2O_2]^{0.428}$에 비례하는 것으로 나타났다.