• 제목/요약/키워드: acid precipitation

검색결과 729건 처리시간 0.03초

산성광산배수에서 광물의 침전에 따른 미량 원소의 거동 (Behaviors of Trace Elements Caused by the Precipitation of Minerals in Acid Mine Drainage)

  • 윤영진;이지은;방상제;백영두;김영규
    • 한국광물학회지
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    • 제31권3호
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    • pp.173-182
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    • 2018
  • 산성광산배수에서 철광물의 침전 및 상전이 과정은 배수 내의 미량원소의 거동에 많은 영향을 미친다. 그러나 자연에서 일어나는 이러한 과정을 정확하게 추적하기는 쉽지 않아 많은 연구들이 산성광산배수에서 일어나는 광물의 침전 및 상전이에 대하여 실내 실험에 의존하는 경우가 많았다. 본 연구에서는 달성광산에서 채취한 배수를 대상으로 실제 산성광산배수에서 서로 다른 pH 값을 갖는 조건에서 시간이 지남에 따라 일어나는 광물의 침전과 이에 따른 배수 내의 미량 원소 변화를 살펴보았다. 침전된 광물의 양이 많지 않아 동정이 어려운 경우도 있었지만 침전된 광물들의 정보를 종합해 보면 대체적으로 비정질의 광물 먼저 형성된 후 아마도 슈베르트마나이트를 거쳐서 추후에 침철석이 침전된 것으로 사료된다. 그러나 시료 중 pH가 높은 경우(10)에는 계속적으로 비정질 상태로 남아있었다. 시간이 지남에 따라 광물의 침전 및 전이에 의하여 배수의 pH는 계속적으로 낮아지는 경향을 보였다. 모든 원소들이 높은 pH (8, 10)에서 낮은 농도를 보였는데 이는 높은 pH에서의 광물의 침전과 표면전하의 영향으로 판단되며 각 원소의 농도는 시간이 지남에 따라 조금씩 증가하였다. 황의 농도는 슈베르트마나이트에서 침철석으로의 전이의 영향으로 배수 내에서 역시 증가하였다.

소다배소 처리된 탈질 폐촉매로부터 황산침출과 가수분해 침전반응에 의한 TiO2의 회수 (Titanium Dioxide Recovery from Soda-roasted Spent SCR Catalysts through Sulphuric Acid Leaching and Hydrolysis Precipitation)

  • 김승현;친빅하;이재령
    • 자원리싸이클링
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    • 제29권5호
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    • pp.48-54
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    • 2020
  • 소다배소 처리한 탈질폐촉매의 수침출 잔사로부터 TiO2 회수를 위하여 황산침출과 가수분해 반응을 실시하였다. Ti 성분의 황산침출은 70 ℃, 3 시간, 교반속도 500 rpm, 슬러리 농도 100 g/L로 고정하여 실시하였고, 황산농도는 4~8 M로 변화시키며 진행하였다. 침출액으로부터 Ti 성분의 침전회수는 가수분해반응을 이용하였으며, 실험조건은 100 ℃, 반응시간 2 시간으로 고정하였고, Ti 성분의 침전율은 침출액과 증류수의 혼합비와 침전반응 Seed 혼입유무에 따라 비교하였다. Ti의 침출율은 6 M에서 최대 95.2 %까지 도달 후 점차 감소하는 경향을 나타내었고, Si의 침출율은 황산농도 증가에 반비례하여 급격히 감소하여 91.7 %에서 8 M 조건에서는 3.0 %까지 억제되었다. 침출액을 이용한 가수분해는 부성분인 Si의 함량이 가장 낮은 8 M 침출액을 이용하여 진행하였다. 침출액의 혼합비에 의한 Ti의 침전회수율은 반응시간에 비례하였고 혼합비에 반비례하였다. 또한, 침전반응의 가속화를 위해 TiO2(#325~#400 mesh, 0.2 g) seed를 첨가하였을 경우에 모든 혼합조건에서 침전회수율이 상승하였으며, 혼합비(침출액:증류수) 1:9~3:7 구간에서 98.8~99.8 %의 침전율이 달성되었다. 회수된 TiO2의 순도는 침출액 혼합비 1:9~3:7 구간에서 혼합비가 낮을수록 증가하여 최대 99.46 %까지 상승함을 확인하였다.

한반도 배경지역 (안면, 울진, 고산) 상수의 산성도와 화학특성 (Acidity and Chemical Composition of Precipitation at Background Area of the Korean Peninsula (Anmyeon, Uljin, Gosan))

  • 김상백;최병철;오숙영;김산;강공언
    • 한국대기환경학회지
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    • 제22권1호
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    • pp.15-24
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    • 2006
  • Precipitation samples were collected at Anmyeon (1997 - 2004), Uljin, and Gosan (1998 ~ 2004), the background area of the Korean Peninsula. These samples were analyzed for the concentration of 9 major ionic components ($F^{-}$,$Cl^{-}$, $NO_{3}^{-}$, $SO_{4}^{2-}$, $Na^{+}$, $NH_{4}^{+}$, $K^{+}$, $Mg^{2+}$, $Ca^{2+}$) with including a pH and an electric conductivity. Data quality for these samples was verified by ion balance and conductivity balance which are based on GAW manual for precipitation chemistry and the number of valid data at Anmyeon, Uljin, and Gosan is 249, 173, and 188, respectively. During the study period, the precipitation-weighted average pH at Anmyeon, Uljin, and Gosan was found to be 4.81, 4.87 and 4.89, respectively and each annual average pH was showed below pH 5.6 for every site. From the frequency survey on the precipitation acidity, the occurrence rate of acid rain below pH 5.6 is greater than $80\%$ for every site. Particularly, the highest occurrence rate for strong acid rain below pH 4.5 was found at Anmyeon, $32.1\%$, compared with other sites ($10.4\%$ at Uljin, $15.4\%$ at Gosan). That's because acidifying species (nss-$SO_{4}^{2-}$, $NO_{3}^{-}$) are remarkably high concentration at Anmyeon.

다종 중금속으로 오염된 사질토에 대한 EK Flushing 기술 적용

  • 김병일;한상재;이군택;김수삼
    • 한국지하수토양환경학회:학술대회논문집
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    • 한국지하수토양환경학회 2003년도 추계학술발표회
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    • pp.310-313
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    • 2003
  • The precipitation of heavy metals within the region of pH jump is inevitable in the conventional electrokinetic remediation technology. This study prevents the interest species from precipitating through the injection of flushing solutions in which HCl, acetic acid, citric acid, EDTA and SDS dissolved. The cumulative flow resulted from electroosmosis appear in order of Citric acid

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침전법과 흡착법을 이용한 중금속 처리 (Treatment of Heavy Metal Wastewater by Pricipitation and Adsorption)

  • 심순보;이요상
    • 한국수자원학회:학술대회논문집
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    • 한국수자원학회 1992년도 수공학연구발표회논문집
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    • pp.325-328
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    • 1992
  • The purpose of this research is to develop the technique of heavy metal removal from wastewater. The research is divided into two parts, one part uses complex precipitation and the other uses adsorption. In the first part of the study, humic acid is used as the complex agent, humic acid is a polyelectrolyte with a high complexation affinity. Lead, copper, zinc and cadmium were studied for their complex precipitation efficiencies. In the batch studies, humic acid was effective in removing 100% of the lead and 48.2% of the copper respectively from wastewater without anytreatment. The efficiency of cadmium and zinc, however, was very low. In the second part of the study, wastewater is introduced at the top of a silicagel adsorption column and then bottom effluent concentration is analyzed. The results of the analysis are used to draw a breakthrough curve.

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Effect of Trichloroacetic Acid on the Solubility of Caseinomacropeptide

  • Shin, Sung-Chul;Jang, Hae-Dong
    • Preventive Nutrition and Food Science
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    • 제7권1호
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    • pp.43-47
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    • 2002
  • Crude caseinomacropeptide (CMP) was prepared from Na-caseinate using a commercial renneting enzyme. Most of the crude CMP was released from the Na-caseinate by hydrolyzing with the enzyme for 40 min. The hydrolysis of the k-casein with carbohydrate was slower than that of the k-casein without carbohydrate, as shown by the analyses of the sialic acid content and the tricine-SDS-polyacrylamide gel electrophoresis. The yield of crude CMP from Na-caseinate was 3.7%. Cation exchange chromatography showed that the crude CMP consisted of 40.5% CMP and 59.5% caseinogylcomacropetide (CGP). The effect of the TCA concentration on the solubility of CMP and CGP was determined by using crude CMP. The amounts of crude CMP and sialic acid decreased in the proportion to the increase of trichloroacetic acid (TCA) concentration from 2 to 12%, suggesting that the CGP containing carbohydrate, as well as the CMP having no carbohydrate, was precipitated in a range of 4 to 12%, depending on the TCA concentration. This result supports the hypothesis that the different non-glycosylated and glycosylated forms of CMP have different sensitivities to TCA precipitation.

Precipitation Stripping법에 의한 고순도 Oxalate 분말의 제조 (Preparation of High-purity Zinc Oxalate Powder by the Precipitation Stripping Method)

  • 이재천;이강인;유효신
    • 한국세라믹학회지
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    • 제29권12호
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    • pp.963-969
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    • 1992
  • This paper describes the feasibility for a direct production of zinc oxalate powders from zinc-loaded D2EHPA solutions combining the purification and the precipitation in one operation unit. This process has the potential as an alternative to conventional method for the synthesis of zinc oxide precursor particles from the hydrometal-lurgical processes. Zinc was extracted into D2EHPA in kerosene and then zinc-loaded D2EHPA solution was emulsified with oxalic acid-HCl solution to precipitate zinc oxalate powder, which was readily calcined to zinc oxide. The precipitation kinetics and yield were sensitive to experimental conditions. The morphology, size and size distribution of the zinc oxalate powders varied with zinc/oxalate ion riatio, temperature, and the presence of SPAN 60, which affected nucleation, growth, and the emulsion characteristics.

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Development of Diffusion - Precipitation Method to Determine AVS Concentrations in Freshwater Sediments

  • Song, Ki-Hoon
    • 환경생물
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    • 제23권4호
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    • pp.374-378
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    • 2005
  • A diffusion - precipitation method was developed to determine acid volatile sulfide (AVS) concentrations in freshwater sediments. This method uses silver nitrate as a sulfide trap solution and the concentration of trapped sulfide is determined gravimetrically. The proposed diffusion - precipitation method is more rapid and less expensive than previously developed purge- and - trap methods. Spiked sodium sulfide recoveries using this method $(97\~120\%)$ were similar with a previously developed diffusion - absorption method $(93.8\~115\%)$ and about $20\%$ greater than a previously developed purge-and-trap method $(74.6\~105\%)$. Detection limit of this method $(0.1\;{\mu}mole\;S\;g^{-l})$ was comparable with that of diffusion-absorption method $(0.06\;{\mu}mole\;S\;g^{-l})$ and purge-and-trap method $(0.05\~0.5\;{\mu}mole\;S\;g^{-l})$.