• Title/Summary/Keyword: 초음파분해

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Sonochemical Destruction of Aliphatic Aldehydes in an Aqueous Solution (수용액중 초음파조사에 의한 Aldehyde류의 초음파분해)

  • Yoo, Young-Eok;Howang, Kyu-Tak;Maeda, Yasuaki
    • Journal of Environmental Health Sciences
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    • v.23 no.4
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    • pp.39-44
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    • 1997
  • Propionaldehyde, n-Butyraldehyde, n-Valeraldehyde 수용액에 주파수 200 kHz, 출력 6.0 W/cm$^2$의 초음파조사후 그 분해반응에 관해 고찰했다. Aldehyde류는 초음파 조사에 의해 빠르게 분해되었고, 분해형태는 유사1차 반응을 나타내었다. 이들의 분해 속도는 Propionaldehyde

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Application of Ultrasound for the Decomposition of Musty-Odorous Compounds in Water (수용액 중 Musty-Odorous Compound류의 분해에 따른 초음파의 응용)

  • 유영억;영전양웅;전전태소
    • Journal of environmental and Sanitary engineering
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    • v.13 no.1
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    • pp.1-8
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    • 1998
  • Musty-odorous compound (Geosmin, 2-Methylisobrneol) 수용액 중에 초음파 (200kHz, $6.0W/cm^{2}$)를 조사시켜 조사시간에 따른 농도 및 취기의 변화를 고찰했다. 초음파 조사에 의해 이 물질들은 빠르게 분해되었고 분해 형태는 농도에 대한 유사1차 반응을 나타내었다. 공기 포화 분위기에서 이들의 초기 분해속도는 각각 2.5 $10^{-3}{\;}Msec^{-1}$(2-MIB), 3.2 $10^{-3}{\;}Msec^{-1}$ (Geosmin)로 나타났다. 초음파 조사 시 포화가스 (Envelope gas)의 영향은 아르곤(Ar) 산소($O_{2}$) 공기(Air) 질소($N_{2}$) 순서로 순수한 아르곤(Ar) 분위기에서 musty-odorous compound 류의 분해가 가장 빠르게 진행되었고 그 분해생성물로 CO, $CO_{2}$ 그리고 HCOOH, $CH_{3}COOH$ 등의 저급 유기산류가 검출되었다. 또한 이들의 분해반응은 물의 초음파분해에 따라 생성된 hydroxylradical에 의한 radical반응, cavitation bubble내에서의 고온고압에 의한 열분해 및 직접연소반응으로 진행됨을 알 수 있었다.

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Effect of Ultrasound on the Decomposition of Sodium Dodecylbenzene Sulfonate in Aqueous Solution (Sodium Dodecylbenzene Sulfonate 수용액의 분해반응에서 초음파 효과)

  • Yim, Bong-Been
    • Journal of the Korean Chemical Society
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    • v.48 no.6
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    • pp.561-567
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    • 2004
  • The influence of ultrasound frequency, dissolved gases, and initial concentration on the decomposition of sodium dodecylbenzene sulfonate(DBS) aqueous solution was investigated using ultrasound generator with 200 W ultrasound power. The decomposition rates at three frequencies(50, 200, and 600 kHz) examined under argon atmosphere were highest at 200 kHz. The highest observed decomposition rate at 200 kHz occurred in the presence of oxygen followed by air and argon, helium, and nitrogen. The effect of initial concentration of DBS on the ultrasonic decomposition was decreased with increasing initial concentration and would depend upon the formation of micelle in aqueous solution. It appears that the ultrasound frequency, dissolved gases, and initial concentration play an important role on the sonolysis of DBS. Sonolysis of DBS mainly take place at the interfacial region of cavitation bubbles by both OH radical attack and pyrolysis to alkyl chain, aromatic ring, and headgroup.

Comparison of the Sonodegradation of Naphthalene and Phenol by the Change of Frequencies and Addition of Oxidants or Catalysts (주파수 변화 및 보조제 첨가에 따른 나프탈렌 및 페놀의 초음파 분해효율 비교)

  • Park, Jong-Sung;Her, Nam-Guk
    • Journal of Korean Society of Environmental Engineers
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    • v.32 no.7
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    • pp.706-713
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    • 2010
  • The research seeks to find the optimal conditions for sonodegradation of naphthalene and phenol as exemplary organic pollutants to be subjected to ultrasound in varying frequencies (28 kHz, 580 kHz, and 1,000 kHz) and in the presence of different kinds of additive (T$TiO_2$, $H_2O_2$, $FeSO_4$, Zeolite, and Cu). In cases of both naphthalene and phenol, 580 kHz of ultrasound has proven to be the most effective among others at sonodegradation. Based on the observation that OH radicals are also produced in maximum under exposure of 580 kHz of ultrasound, we concluded that this frequency of ultrasound creates hospitable condition for the combined process of degradation by pyrolysis and oxidization. $FeSO_4's$ degradation rate and k1 value have increased by approximately 1.8 times compared with the results of the solutions without any additives. This seems to be the result of ultrasound reaction which, accompanied by Fenton's reaction, increased the oxidative degradation and the production of OH radicals. However, application of ultrasound and Fenton's reaction is limited to the batch type conditions, as its use in continuous system can cause loss of iron or decay of the cistern, thereby creating additional pollutants. When the additive is replaced with $TiO_2$, on the contrary, the rate of sonodegradation has increased up to 20% compared to when there was no additive. We therefore conclude that $TiO_2$ could prove to be an effective additive for ultrasound degradation in continuous treatment system.

Characteristics of Decomposition for Refractory Organic Compounds in Aqueous Solution by Sonolysis and Electrolysis (초음파와 전기분해를 이용한 수중의 난분해성 유기물질의 분해 특성)

  • Jeong, Jae-Baek;Lee, Seong-Ho;Bae, Jun-Ung
    • Journal of the Korean Chemical Society
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    • v.50 no.6
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    • pp.454-463
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    • 2006
  • refractory organic compounds in aqueous solution are not readily removed by the existing conventional wastewater treatment process. In recent years, the sonolysis and electrochemical oxidation process had been shown to be promising for wastewater treatment due to the effectiveness and easiness in operation. This study was performed to investigate the characteristics of sonolytic and electrolytic decomposition as the basic data for development of the wastewater treatment process. Trichloroethylene(TCE) and 2,4- dichlorophenol(2,4-DCP) were used as the samples, and their destruction efficiency were measured with various operating parameters, such as initial solution concentration, initial solution pH, reaction temperature, sonic power and current density. Also, the decomposition mechanism conformed indirectly with the effect of NaHCO3 as a radical scavenger on the decomposition reaction. Thermal decompositon reaction is predominant for TCE but thermal and radical decompositon reactions were dominant for 2,4-DCP. Results showed that the destruction efficiencies of all samples were above 65% within 120 minutes by sonolysis and electrolysis at the same time, and were increased with increasing initial concentration, sonic power and current density. Destruction efficiency of TCE was high in the acidic solution, but 2,4-DCP showed high destruction efficiency in basic solution.

A Study on the Disintegration of Sewage Sludge using Batch Ultrasonic Pretreatment (회분식 초음파 전처리를 이용한 하수슬러지의 분해에 관한 연구)

  • Ko, Hyun-Woong;Jung, Byung-Gil;Jung, Yon-Hwa;Kim, Hyeung-Seok;Jang, Seong-Ho;Sung, Nak-Chang
    • Journal of the Korea Organic Resources Recycling Association
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    • v.12 no.4
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    • pp.121-129
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    • 2004
  • Anaerobic digestion is the most common process for sewage sludge stabilization and has benefits of VS reduction and biogas production. Many pretreatment methods have been studied to improve hydrolysis rate because the rate of sewage sludge degradation is slow in anaerobic digestion. This study mainly focused upon the effects on disintegration of sewage sludge by ultrasonic pretreatment according to the variation of acoustic density and duration of sonication time. In this study, acoustic density has been changed as follows : 33W/L, 70W/L, 88W/L, 139W/L in case of 40 kHz with the test time changes of 10min, 20min, 25min, 30min and 40min. In the comparison of $SCOD_{Cr}/TCOD_{Cr}$ variation for excess sludge and mixed sludge disintegration, the rates of $SCOD_{Cr}/TCOD_{Cr}$ have been increased in the condition of denser acoustic density and longer sonication time with acoustic frequency of 40kHz. The pH of the excess sewage sludge and mixed sewage sludge has been decreased in the condition of denser acoustic density and longer sonication time with acoustic frequency of 40kHz.

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A Study on the Characteristics of Sonication Combined with UV in the Degradation of Phenol (초음파와 UV에 의한 페놀 분해 특성에 관한 연구)

  • Kim, Seong-Keun;Son, Hyun-Seok;Im, Jong-Kwon;Khim, Jee-Hyeong;Zoh, Kyung-Duk
    • Journal of Korean Society of Environmental Engineers
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    • v.32 no.7
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    • pp.649-655
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    • 2010
  • This study investigated the degradation of phenol using sonication and/or UV-C. The effects of frequency, temperature, pH in solution, argon purging, with UV intensity were estimated in sonication-only, UV-only, and the combined reaction of sonication with UV. The optimum condition for degrading phenol in the sonication-only reaction was 35 kHz, $5^{\circ}C$, and pH 4. As this condition approximately 30% degradation of phenol was achieved within 360 min. However, phenol in the UV-only at $19.3\;mw/cm^2$ under the same condition was completely degraded within 60 min. In the combined system of sonication with UV, the degradation of phenol was well fitted to first-order rate model, and phenol was completely degraded within 360 min and 45 min at UV intensity of $7.6\;mW/cm^2$($17.3{\times}10^{-3}\;min^{-1}$) and $19.3\;mW/cm^2$($138.1{\times}10^{-3}\;min^{-1}$), respectively. Adding methanol, as a radical scavenger, in the phenol degradation in the sonication reaction indicates that OH radical is a major factor in the degradation of phenol. The order of degradation efficiencies of phenol was in the order of as follows; combined reaction of sonication with UV > UV-only > sonication-only.

Effect of Ultrasonic Irradiation on Ozone Nanobubble Process for Phenol Degradation (페놀 분해를 위한 오존 나노기포 공정에서 초음파 조사의 영향)

  • Lee, Sangbin;Park, Jae-Woo
    • Journal of the Korean GEO-environmental Society
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    • v.23 no.3
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    • pp.23-29
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    • 2022
  • In this study, we investigated the ozone nanobubble process in which nanobubble and ultrasonic cavitation were applied simultaneously to improve the dissolution and self-decomposition of ozone. To confirm the organic decomposition efficiency of the process, a 200 mm × 200 mm × 300 mm scale reactor was designed and phenol decomposition experiments were conducted. The use of nanobubble was 2.07 times higher than the conventional ozone aeration in the 60 minutes reaction and effectively improved the dissolution efficiency of ozone. Ultrasonic irradiation increased phenol degradation by 36% with nanobubbles, and dissolved ozone concentration was lowered due to the promotion of ozone self-decomposition. The higher the ultrasonic power was, the higher the phenol degradation efficiency. The decomposition efficiency of phenol was the highest at 132 kHz. The ozone nanobubble process showed better decomposition efficiency at high pH like conventional ozone processes but achieved 100% decomposition of phenol after 60 minutes reaction even at neutral conditions. The effect by pH was less than that of the conventional ozone process because of self-decomposition promotion. To confirm the change in bubble properties by ultrasonic irradiation, a Zetasizer was used to measure the bubbles' size and zeta potential analysis. Ultrasonic irradiation reduced the average size of the bubbles by 11% and strengthened the negative charge of the bubble surface, positively affecting the gas transfer of the ozone nanobubble and the efficiency of the radical production.

Sonolysis of Trichloroethylene in the Multi Ultrasound Irradiation Reactor (다중 초음파 조사 반응조에서의 TCE의 초음파 분해)

  • Lee, Min-Ju;Oh, Je-Ill
    • Journal of Korean Society of Environmental Engineers
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    • v.31 no.10
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    • pp.873-882
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    • 2009
  • Sonolysis of TCE (Trichloroethylene) was performed in 584 kHz rectangular reactor. At first, the effect of acoustic power and aqueous temperature which are both important factors to operate ultrasound system on sonolysis of TCE were examined under one side irradiation condition. First degradation rate constants of TCE and chloride yields were increased with increasing acoustic power from 100 to 300 W. And increasing the aqeuous temperature resulted in the increase of first degradation rate constants of TCE and the decrease of chloride yield. Sonolysis of TCE was performed under multi ultrasound irradiation conditions that total acoustic power of 300 W was distributed according to the number of irradiation sides. First degradation rate constants of TCE followed the order 4 sides > 3 sides > 1 side > 2 sides (parallel) > 2 sides (orthogonal). When comparing the experimental results under parallel and orthogonal irradiation conditions of 2 sides with 300 and 450 W, first degradation rate constants of TCE were similar, while production rate constants of hydrogen peroxide were more higher at parallel conditions compared to orthogonal conditions.

Sonolysis of Trichloroethylene in a Continuous Flow Reactor with the Multi Ultrasound Irradiation (연속식 다중 초음파 반응조에서 TCE의 초음파 분해)

  • Lee, Min-Ju;Oh, Je-Ill
    • Journal of Korean Society of Environmental Engineers
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    • v.31 no.6
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    • pp.419-427
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    • 2009
  • To test applicability for continuous flow treatment of ultrasound technology, sonolysis of TCE aqueous solution using 584 kHz multi irradiation reactor was performed under batch and continuous flow conditions. Under batch condition (3 and 4 sides irradiation, 600 W), first order degradation rate constant of TCE was higher under 4 sides than 3 sides irradiation conditions, while the generation of $H_2O_2$ and chloride was similar under both irradiation conditions. Under continuous flow condition with 4 sides irradiation, removal efficiencies of TCE in steady-state were decreased from 83 to 48% with increasing flow rate from 67 to 300 mL/min at 600 W, and were increased from 14 to 75% with increasing acoustic power from 100 to 600 W at 100 mL/min. Removal efficiency of TCE in groundwater was decreased 10% compared to in distilled water at 100 mL/min and 600 W.