• 제목/요약/키워드: Nitrite oxidizer

검색결과 16건 처리시간 0.017초

개량된 초임계수 산화법에 의한 염소계 유기물(PCB, 4-DCBz)의 완전분해반응 (Complete Decomposition of Chlorinated-Organic Compounds(PCB, 4-DCBz) with Improved Supercritical Water Oxidation Method)

  • 이상환;박기철;박윤열;양종규;김정성;부안 박
    • 한국환경과학회지
    • /
    • 제14권5호
    • /
    • pp.513-520
    • /
    • 2005
  • For the destruction of toxic chlorinated organic compounds, this study proposes improved supercritical water oxidation method (multistep oxidation) using sodium nitrate as an oxidizer. This method solves the problems involved in the existing supercritical water oxidation method. Multistep oxidation means that $NaNO_3$ is oxidized to $N_2\;via\;NaNO_2$ and NO. Toxic and hard to destroy organic substances like para-dichlorobenzen(4-DCBz), polychlorinate biphenyl(PCB) ware oxidized to non toxic substances in a condition, in which rapid pressure and temperature rise is restrained as much as possible. 4-dichlorobenzene(4-DCBz) and Polychlorinate biphenyl(PCB) in condition$(450^{\circ}C,\;p_w=0.25g/cm^3,\;30min)$ Was discomposed perfectly.

Decomposition of PVC and Ion Exchange Resin in Supercritical Water

  • Kim Jung-Sung;Lee Sang-Hwan;Park Yoon-Yul;Yasuyo Hoshikawa;Hiroshi Tomiyasu
    • 한국환경과학회지
    • /
    • 제14권10호
    • /
    • pp.919-928
    • /
    • 2005
  • This study introduces the development of new supercritical water oxidation(SCW)(multiple step oxidation) to destruct recalcitrant organic substances totally and safely by using sodium nitrate as an oxidant. This method has solved the problems of conventional SCW, such as precipitation of salt due to lowered permittivity, pressure increase following rapid rise of reaction temperature, and corrosion of reactor due to the generation of strong acid. Destruction condition and rate in the supercritical water were examined using Polyvinyl Chloride(PVC) and ion exchange resins as organic substances. The experiment was carried out at $450^{\circ}C$ for 30min, which is relatively lower than the temperature for supercritical water oxidation $(600-650^{\circ}C)$. The decomposition rates of various incombustible organic substances were very high [PVC$(87.5\%)$, Anion exchange resin$(98.6\%)$, Cationexchange resin$(98.0\%)$]. It was observed that hetero atoms existed in organic compounds and chlorine was neutralized by sodium (salt formation). However, relatively large amount of sodium nitrate (4 equivalent) was required to raise the decomposition ratio. For complete oxidation of PCB was intended, the amount of oxidizer was an important parameter.

Decomposition of PVC and Ion exchange resin in supercritical water

  • Lee, Sang-Hwan;Yasuyo, Hosgujawa;Kim, Jung-Sung;Park, Yoon-Yul;Hiroshi, Tomiyasu
    • 한국환경과학회:학술대회논문집
    • /
    • 한국환경과학회 2005년도 봄 학술발표회지 제14권(제1호)
    • /
    • pp.267-271
    • /
    • 2005
  • This experiment was carried out at 450"C, which is relatively lower than the temperature for supercritical water oxidation (600-650$^{\circ}C$). In this experiment, the decomposition rates of various incombustible organic substances were very high. In addition, it was confirmed that hetero atoms existed in organic compounds and chlorine was neutralized by sodium(salt formation).However, to raise the decomposition rate, relatively large amount of sodium nitrate(3-4 times the equivalent weight) was required. When complete oxidation is intended as in the case with PCB, the amount of oxidizer and decomposition cost is important. But when vaporization reduction is required as in the case with nuclear wastes, the amount of radioactive wastes increases instead. But as can be seen in the result of XRD measurement, unreacted sodium nitrate remained unchanged. If oxidation reaction of organic substance simply depends on collision frequency, unreacted sodium nitrate can be recovered and reused, then oxidation equivalent weight would be sufficient. In the gas generated, toxic gas was not found. As the supercritical water medium has high reactivity, it is difficult to generate relatively low energy level SO$_{X}$, and NO$_{X}$.

  • PDF

LITHOAUTOTROPHIC NITROGEN REMOVAL WITH ANAEROBIC GRANULAR SLUDGE AS SEED BIOMASS AND ITS MICROBIAL COMMUNITY

  • Ahn, Young-Ho;Lee, Jin-Woo;Kim, Hee-Chul;Kwon, Soo-Youl
    • Environmental Engineering Research
    • /
    • 제11권4호
    • /
    • pp.173-180
    • /
    • 2006
  • Autotrophic nitrogen removal and its microbial community from a laboratory scale upflow anaerobic sludge bed reactor were characterized with dynamic behavior of nitrogen removal and sequencing result of molecular technique (DNA extraction, PCR and amplification of 16S rDNA), respectively. In the experiment treating inorganic wastewater, the anaerobic granular sludge from a full-scale UASB reactor treating industrial wastewater was inoculated as seed biomass. The operating results revealed that an addition of hydroxylamine would result in lithoautotrophic ammonium oxidation to nitrite/nitrate, and also hydrazine would play an important role for the success of sustainable nitrogen removal process. Total N and ammonium removal of 48% and 92% was observed, corresponding to nitrogen conversion of 0.023 g N/L-d. The reddish brown-colored granular sludge with a diameter of $1{\sim}2\;mm$ was observed at the lower part of sludge bed. The microbial characterization suggests that an anoxic ammonium oxidizer and an anoxic denitrifying autotrophic nitrifier contribute mainly to the nitrogen removal in the reactor. The results revealed the feasibility on development of high performance lithoautotrophic nitrogen removal process with its microbial granulation.

토양처리형 제초제가 질소비료의 무기화작용에 미치는 영향 II 밭 토양 조건 (The Influence of Some Soil-treated Herbicides on the Mineralization of Nitrogen Fertilizers II. In an upland soil)

  • 김무기
    • 한국응용곤충학회지
    • /
    • 제16권3호
    • /
    • pp.149-154
    • /
    • 1977
  • 밭 토양에서 Simazine, Nitrofen, Propanil 및 Butachlor 등의 제초제가 시비한 질소의 변화과정에 미치는 영향을 조사하기 위하여 요소와 약제를 처리한 후 $20\pm1^{\circ}C$에서 배양하면서 암모니아태, 아질산태 및 질산태 질소와 pH의 변화를 검토하였던 바 다음과 같은 결과를 얻었다. 1. 요소분해에 의한 암모니아태 질소의 생성에 있어서 모든 약제가 실용농도 수준에서는 아무런 영향이 없었다. Butachlor는 실용농도의 10배와 50배 수준에서, Nirtofen은 50배 수준에서 일시적인 억제효과가 인정되었으나 시일이 경과하면서 정상으로 회복되었다. Simazine과 Propanil은 전 처리수준에서 영향이 없었다. 2. 질화작용에 있어서도 모든 약제가 실용농도수준에서는 영향이 없었다. 실용농도의 10배와 50배 수준에서 Butachlor와 Nitrofen은 아질산의 산화를 억제하였으며 Propanil은 암모니아의 산화를 크게 억제하였으나 아질산의 산화억제 효과는 없었다. 그러나 이 산화억제 효과는 시일이 경과하면서 정상으로 회복되었다. Simazine은 전 처리수준에서, 질화작용에 대해 영향을 인정할 수 없었다. 3. 약제처리구와 무처리구에서의 pH 변화경향은 양 중 질소의 형태변화를 잘 반영하여 주었으며 약에 의한 직접적인 영향은 찾을 수 없었다.

  • PDF

공정 안정성에 대한 입상 및 고정화 혐기성 암모늄 산화균의 질소제거효율 비교 (Comparison of nitrogen removal efficiency on process stability for granular and immobilized anammox bacteria)

  • 최대희;배효관;정진영;김상현
    • 상하수도학회지
    • /
    • 제28권2호
    • /
    • pp.195-206
    • /
    • 2014
  • Immobilization of anaerobic ammonium oxidizing bacteria has been studied to enhance the biomass retention of the slowly growing bacteria and the process stability. The purpose of this study was to compare the nitrogen removal efficiency of granular and immobilized anammox bacteria with poly vinyl alcohol and alginate. The specific anammox activity of the granular, homoginized and immobilized anammox bacteria were $0.016{\pm}0.0002gN/gVSS/d$, $0.011{\pm}0.001gN/gVSS/d$ and $0.007{\pm}0.0005gN/gVSS/d$, respectively. Although the activity decreased to 43.7 % of the original one due to low pH and $O_2$ exposure during the homogination and the immobilization, it was rapidly recovered within 7 days in the following continuous culture. When synthetic T-N concentrations of 100, 200, 400, 800 mg/L were fed, the immobilized anammox bacteria showed higher nitrogen removal efficiencies at all operational conditions than those of granular anammox bacteria. When the sludge retention time was shorten below 30.7 days and the reject water was fed, the nitrite removal efficiency of the granular anammox bacteria dropped to 8 % of the initial value, while that of the immobilized anammox bacteria was maintained over 95 % of the initial one. The immobilization with poly vinyl alcohol and alginate would be a feasible method to improve the performance and stability of the anammox process.