• Title/Summary/Keyword: 염소제거

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Removal of impurity in rare earth solution with Karr Column (Karr column 추출기에 의한 희토류 용액중 불순물(Fe) 제거)

  • Lee, Jin-Young;Eom, Hyoung-Choon;Park, Kae-Sung;Kim, Jun-Soo
    • 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.

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Removing Sapstain of Radiata Pine by Bleaching (표백에 의한 라디에타소나무의 청변 제거)

  • Kim, Gyu-Hyeok;Kim, Hyung-Jun;Ra, Jong-Bum;Kim, Jae-Jin
    • Journal of the Korean Wood Science and Technology
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    • v.31 no.1
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    • pp.46-51
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    • 2003
  • The feasibility of using bleaching treatments for removing fungal stain was evaluated on heavily stained raiadta pine sapwood. Sodium chlorite and sodium hypochlorite appeared to destain fungal discoloration by providing proper treatment conditions (chemical concentration, treatment temperature, and treatment time), while hydrogen peroxide did not remove fungal stain under the bleaching regimes evaluated. The addition of sodium silicate and sodium hydroxide in the hydrogen peroxide solution as a buffer could remove fungal discoloration completely; however, the color of wood surface turned faint green after bleaching, thereby reducing the lightness of bleached samples. The results suggest that hydrogen peroxide bleaching could be a feasible method for removing fungal discoloration of stained radiata pine sapwood, although further research is needed to solve the problem of color change after bleaching. Also, further tests under field conditions are recommended.

Removal of Diclofenac, Ibuprofen and Naproxen using Oxidation Processes (산화공정에서의 Diclofenac, Ibuprofen 및 Naproxen의 제거특성 평가)

  • Son, Hee-Jong;Yoo, Soo-Jeon;Hwang, Young-Do;Roh, Jae-Soon;Yoo, Pyung-Jong
    • Journal of Korean Society of Environmental Engineers
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    • v.31 no.10
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    • pp.831-838
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    • 2009
  • In order to evaluate a removal characteristic of diclofenac, ibuprofen and naproxen by oxidizing agents, $Cl_2,\;O_3$ and $O_3/H_2O_2$ are used as oxidants in this study. In case of that $Cl_2$ is used for oxidizing pharmaceuticals, ibuprofen is not removed entirely at $Cl_2$ dose range of 0.5~5.0 mg/L for 60 minutes, however, removal tendency of diclofenac and naproxen are so obviously at $Cl_2$ dose higher than 0.5 mg/L. In addition, as $Cl_2$ dose and contact time are increased, the removal rate of diclofenac and naproxen is enhanced. When $O_3$ is used as oxidizing agent, ibuprofen is not eliminated at $O_3$ dose range of 0.2~5.0 mg/L. On the contrary, 72~100% of diclofenac and 49~100% of naproxen are removed at $O_3$ dose of 0.2~5.0 mg/L. From experiments using $O_3/H_2O_2$ as an oxidant, we can find that $O_3/H_2O_2$ is much more effective than $O_3$ only for removal of diclofenac and naproxen. Moreover, the efficiency is raised according to increase of $H_2O_2$ dose, however, experiments using $O_3/H_2O_2$ show that oxidation of pharmaceuticals is less effective as $H_2O_2$ to $O_3$ ratio increased to above approximately 1.0. On reaction rate constant and half-life of diclofenac, ibuprofen and naproxen depending on $Cl_2$, $O_3$ and $O_3/H_2O_2$ dose, an oxidation of pharmaceuticals by $Cl_2$ and $O_3$ particularly has a comparatively high reaction rate constant and short half-life comparing $O_3/H_2O_2$. From above results, we can fine that diclofenac and naproxen can be easily eliminated in oxidation processes.

Effect of Sugarcane Bagasse Soda-AQ Pulp Bleaching Properties by Type of Chelate Compounds and Simultaneous Process of (DQ) Stage (이산화염소 표백단계와 킬레이트 처리단계 동시 진행 시 킬레이트 종류가 사탕수수 Soda-AQ 펄프 표백에 미치는 영향)

  • Lee, Jai-Sung;Shin, Soo-Jeong
    • Journal of the Korean Wood Science and Technology
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    • v.44 no.1
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    • pp.147-155
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    • 2016
  • Pulp made from sugarcane bagasse (SCB) was bleached in element chlorine free (ECF) sequence. The peroxide bleaching process for the final bleaching process has been introduced in order to reduce the use of chlorine dioxide. Prior to peroxide bleaching, different chelating chemicals were applied. When 4.5% of the total chlorine dioxide was used, bleached SCB pulp using additional DTPA chelate stage (DEDQP) resulted in 87.0% of the ISO brightness. However, bleached pulp using simultaneous stage of DTPA chelate and chlorine dioxide (DE(DQ)P) was reached at 83.9% of the ISO brightness. The viscosity of DEDQP bleached pulp was 25.6 cPs, and the one of DE(DQ)P bleached pulp was 21.9 cPs. Decreasing of chelate effect by chlorine dioxide led to a decrease in the final brightness and a lower viscosity. But simultaneous stage of EDTA chelate and chlorine dioxide (DE(DQ)P) led to higher final brightness (87.0% ISO) and higher viscosity (25.8 cPs) than those of the $DEDQ_{EDTA}P$ bleached pulp (86.4% ISO, 25.2 cPs).

The Treatment of Heavy Metal-cyanide Complexes Wastewater by Zn$^{+2}$/Fe$^{+2}$ Ion and Coprecipitation in Practical Plant (II) (아연백법 및 공침공정을 이용한 복합 중금속-시안착염 폐수의 현장처리(II))

  • Lee, Jong-Cheul;Lee, Young-Man;Kang, Ik-Joong
    • Journal of Korean Society of Environmental Engineers
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    • v.30 no.5
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    • pp.524-533
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    • 2008
  • Industrial wastewater generated in the electroplating and metal finishing industries typically contain toxic free and complex metal cyanide with various heavy metals. Alkaline chlorination, the normal treatment method destroys only free cyanide, not complex metal cyanide. A novel treatment method has been developed which destroys both free and complex metal cyanide as compared with Practical Plant(I). Prior to the removal of complex metal cyanide by Fe/Zn coprecipitation and removal of others(Cu, Ni), Chromium is reduced from the hexavalent to the trivalent form by Sodium bisulfite(NaHSO$_3$), followed by alkaline-chlorination for the cyanide destruction. The maximum removal efficiency of chromium by reduction was found to be 99.92% under pH 2.0, ORP 250 mV for 0.5 hours. The removal efficiency of complex metal cyanide was max. 98.24%(residual CN: 4.50 mg/L) in pH 9.5, 240 rpm with 3.0 $\times$ 10$^{-4}$ mol of FeSO$_4$/ZnCl$_2$ for 0.5 hours. The removal efficiency of Cu, Ni using both hydroxide and sulfide precipitation was found to be max. 99.9% as Cu in 3.0 mol of Na$_2$S and 93.86% as Ni in 4.0 mol of Na$_2$S under pH 9.0$\sim$10.0, 240 rpm for 0.5 hours. The concentration of residual CN by alkaline-chlorination was 0.21 mg/L(removal efficiencies: 95.33%) under the following conditions; 1st Oxidation : pH 10.0, ORP 350 mV, reaction time 0.5 hours, 2nd Oxidation : pH 8.0, ORP 650 mV, reaction time 0.5 hours. It is important to note that the removal of free and complex metal cyanide from the electroplating wastewater should be employed by chromium reduction, Fe/Zn coprecipitation and, sulfide precipitation, followed by alkaline-chlorination for the Korean permissible limit of wastewater discharge, where the better results could be found as compared to the preceding paper as indicated in practical treatment(I).

복합 플라즈마 방전에 의한 폐수 중 페놀의 제거

  • 우인성;김윤선;황명환;이건구;류부형
    • Proceedings of the Korean Institute of Industrial Safety Conference
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    • 2002.11a
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    • pp.131-135
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    • 2002
  • 오존은 공업적으로 상ㆍ하수처리, 펄프표백, 반도체절연막 형성, 레지스트막 제거 등 수많은 분야에 이용되고 있으며, 강력한 산화력을 갖고 있으면서 자연분해 해서 산소로 돌아가 잔류독성을 남기지 않기 때문에 환경문제의 근본적인 해결에 도움이 되는 물질로서 큰 주목을 받고 있다. 그러나 생산비용이 극히 높기 때문에 오존 이용이 바람직한 경우라 할지라도 입수가 용이하고 비교적 염가인 염소를 대용하는 일이 많다.(중략)

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A Study on the TCE/PCE Removal Using Biofiltration and the Microbial Communities Variation Using DGGE Method (생물 여과를 이용한 TCE/PCE제거 및 DGGE법을 이용한 관련미생물 군집변화에 관한 연구)

  • Kim, Eung-In;Park, Ok-Hyun;Jung, In-Gyung
    • Journal of Korean Society of Environmental Engineers
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    • v.30 no.11
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    • pp.1161-1169
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    • 2008
  • The removals of TCE and PCE vapor with or without a supply of toluene as a primary substrate were compared in a biofiltration process, and the variations of microbial communities associated with the removal were also investigated. As a result of investigations on the removals of TCE/PCE in a biofilter B within which TCE/PCE-acclimated sludge was attached on the surface of media without a supply of primary substrate, and those in another biofilter A where toluene-acclimated sludge was attached with a supply of toluene as a primary substrate, followings were found: (i) parts of microbes responsible to the decomposition of toluene vapor participate in the removal of chlorinated VOCs such as TCE and PCE, and (ii) effective biological removals of TCE and PCE vapor do not necessarily need cometabolism. Sequencing of 16S rDNA obtained from the band profile of DGGE (Denaturating Gradient Gel Electrophoresis), it was confirmed that: (i) uncultured alpha proteobacterium, uncultured Desulfitobacterium, uncultured Rhodobacteraceae bacterium, Cupriavidus necator, and Pseudomonas putida were found to be toluene-decomposing microbes, (ii) alpha proteobacterium HTCC396 is a TCE-removing microbe, (iii) Desulfitobacterium sp. is a PCE-decomposing microbe, and (iv) particularly, uncultured Desulfitobacterium sp. is probably a microbe decomposable not only toluene but also various chlorinated VOC vapor including TCE and PCE.

Studies on the Simultaneous Analysis of Organochlorine Pesticide Residues by Gas-Liquid Chromatography (I). Solvent Extraction and Cleanup of Pesticides (기체-액체 크로마토그래피에 의한 잔류 유기염소제 농약들의 동시 분석에 관한 연구 (제1보). 농약의 용매추출 및 불순물 제거)

  • Taek-Jae Kim;Song-Ja Park;Young-Sang Kim
    • Journal of the Korean Chemical Society
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    • v.29 no.5
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    • pp.496-502
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    • 1985
  • The solvent extraction and cleanup processes for the simultaneous gas-liquid cliromatographic determination of 16 kinds of organochlorine pesticide residues were investigated. The pesticides were extracted out from-various crops with the aqueous acetone solution acidified (pH < 1.5) by adding conc. $H_3PO_4$. Most of the pesticides were partitioned from the solution with petroleum ether. Evaporated the extracting solvent, the residues were dissolved in ethylether-petroleum ether (6 : 94) eluent and eluted through the Florisil column activated at 650$^{\circ}$C for 2.5hrs. The extraction efficiency was over 94% and impurities were effectively removed by the column chromatography.

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