• 제목/요약/키워드: Degradation Rate

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광촉매 공정에 따른 이부프로펜의 분해 특성 (Degradation Properties of Ibuprofen Using Photocatalytic Process)

  • 채금화;나승민;안윤경;이세반;김지형
    • 한국환경과학회지
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    • 제21권4호
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    • pp.411-419
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    • 2012
  • In this study, Ibuprofen (IBP) degradation by the photo catalytic process was investigated under various parameters, such as UV intensity, optimum dosage of $TiO_2$, alkalinity, temperature and pH of bulk solution. The pseudo-first order degradation rate constants were in the order of $10^{-1}$ to $10^{-4}min^{-1}$ depending on each condition. The Photocatalytic IBP degradation rate increased with an increase in the applied UV power. At high UV intensity a high rate of tri-iodide ($I_3{^-}$) ion formation was also observed. Moreover, in order to avoid the use of an excess catalyst, the optimum dosage of catalyst under the various UV intensities (30 and 40 W/L) was examined and ranged from approximately 0.1 $gL^{-1}$. The photo catalytic IBP degradation rate was changed depending on the alkalinity and temperature and pH in the aqueous solution. This study demonstrated the potential of photo catalytic IBP degradation under different conditions.

Pseudomonas putida F1과 Burkholderia cepacia G4에 의한 BTEX, trichloroethylene 분해 (Degradation of BTEX and Trichloroethylene by Pseudomonas putida F1 and Burkholderia cepacia G4)

  • 이승우;이준명;장덕진
    • KSBB Journal
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    • 제13권5호
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    • pp.561-568
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    • 1998
  • Two cometabolic trichloroethylene (TC) degraders, Pseudomonas putida F1 and Burkholderia (Pseudomonas) cepacia G4, were found to catabolize phenol, benzene, toluene, and ethylbenzene as carbon and energy sources. Resting cells of P. putida F1 and B. cepacia G4 grown in the presence of toluene and phenol, respectively, were able to degrade not only benzene, toluene and ethylenzene but also TCE and p-xylene. However, these two strains grown in the absence of toluene or phenol did not degrade TCE and p-xylene. Therefore, it was tentatively concluded that cometabolic degradation of TC and p-xylene was mediated by toluene dioxygenase (P. putida F1) or toluene-2-monooxygenase (B. cepacia G4). Maximal degradation rates of BTEX and TCE by toluene- and phenol-induced resting cells of P. putida F1 and B. cepacia G4 were appeared to be 4-530 nmol/(min$.$mg cell protein) when a single compound was solely served as a target substrate. In case of double substrates, the benzene degradation rate by P. putida F1 in the presence of toluene was decreased up to one seventh of that for the single substrate. TCE degradation rate was also linearly decreased as toluene concentration increased. On the other hand, toluene degradation rate was enhanced by benzene and TCE. For B. cepacia G4, degradation rates of TCE and toluene increased 4 times in the presence of 50 ${\mu}$M phenol. From these results, it was concluded that a degradation rate of a compound in the presence of another cosubstrate(s) could not be predicted by simply generalizing antagonistic or synergistic interactions between substrates.

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담수토양중(湛水土壤中)에 있어서 살균제(殺菌劑) IBP의 분해속도(分解速度)에 미치는 각종(各種) 토양환경조건(土壤環境條件)의 영향(影響) (Effect of soil environmental conditions on the degradation rate of the fungicide IBP in flooded soils)

  • 문영희
    • Applied Biological Chemistry
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    • 제33권2호
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    • pp.133-137
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    • 1990
  • 담수토양중(湛水土壤中)에 있어서 IBP의 분해(分解)에 미치는 각종(各種) 토양환경조건(土壤環境條件)의 영향(影響)에 대하여 연구검토(硏究檢討)하였다. IBP는 비담수조건(非湛水條件)에서 보다 담수조건(湛水條件)에서 느리게 분해(分解)되었다. 분해속도(分解速度)는 토양종류(土壤種類)에 따라 크게 변화(變化)되었으며, 유기물함양(有機物含量)이 높은 토양(土壤)에서보다 낮은 토양(土壤)에서 빨랐다. IBP는 저온(低溫)에서보다 고온(高溫)의 토양(土壤)에서, 고농도(高濃度)에서보다 저농도(低濃度) 첨가(添加)에서 빨리 분해(分解)되었다. 토양중(土壤中) 분해속도(分解速度)는 볏짚첨가에 의하여 현저히 저하(低下)되었으나, 복합비료(複合肥料)나 타농약(他農藥) fenitrothion과 butachlor의 첨가(添加)에 의하여는 영향(影響)을 받지 않았다. 토양중(土壤中) IBP는 호기적(好氣的) 미생물(微生物)에 의하여 분해(分解)되는 것으로 추정(推定)되었다.

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순환회분식 광촉매시스템의 영향인자 연구: 광촉매 주입량, 용존산소, 체류시간,전자포획 첨가금속 (Factors influencing a Photocatalytic System in Circulating Batch Mode: Photocatalyst Dosage, DO, Retention Time and Metal Impurities)

  • 김일규
    • 상하수도학회지
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    • 제27권1호
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    • pp.49-58
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    • 2013
  • A selected halogenated organic contaminant, monochlorophenol was successfully degraded by photocatalytic reaction in a circulating batch system. The photocatalytic degradation in most cases follows first-order kinetics. The photocatalytic reaction rate increased in the $TiO_2$ dosage range of 0.1 g/L to 0.4 g/L, then decreased with further increase of the dosage. Also the degradation rate increased over the range of the retention time from 0.49 min. to 0.94 min., then decreased with further increase of the retention time in the circulating batch reactor. The photocatalytic activity was enhanced by addition of metal impurities, platinum(Pt) and palladium(Pd) onto the photocatalysts. The photocatalytic degradation rate increased with the increase of Pt and Pd in the content range of 0 to 2wt %, then decreased with further increase of the metal contents. Therefore the metal loading to $TiO_2$ influence the degradation rate of a halogenated organic compound by acting as electron traps, consequently reducing the electron/positive hole pair recombination rate.

Influence of Temperature and pH on the Stability of Dimethoxy Biphenyl Monocarboxylate${\cdot}$HCl Solutions

  • Choi, Woo-Chang;Kim, Dae-Duk;Shin, Young-Hee;Lee, Chi-Ho
    • Archives of Pharmacal Research
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    • 제24권2호
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    • pp.159-163
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    • 2001
  • The accelerated stability of dimethoxy biphenyl monocarboxylate.HCl (DDB-S) was investigated in 6 mg/mL water solution in the pH ranging 2-10 and the temperature of $45-85^{\circ}C$. The observed rate of degradation followed first-order kinetics. The energy of activation for DDB-S degradation was calculated to be 14.1 and 16.5 $Kcal/mole$ at pH 5 and in distilled watery respectively. The degradation rate constant ($K_{25^{\circ}C}$) obtained by trending line analysis of Arrhenius plots for DDB-S was $5.3{\times}10^{-6}h^{-1}$. The times to degrade 10% ($t_{10}$) and 50% $t_{500}$) at $K_{25^{\circ}C}$ were 829 and 5,416 days, respectively. DDB-S exhibited the fastest degradation at pH 10 and the slowest rate at pH 5. In addition, at $K_{65^{\circ}C}$, degradation rate constants of DDB-S were 0.066, 0.059, 5.460, 32.171, and $1.4{\times}10^{-6}h^{-1}$ at pH 2, 5, 8, 10 and in distilled water, respectively. These observations indicated that the rate-pH profile of DDB-S showed general acid-base catalysis reaction in the range of pH 2-10.

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세팔로스포린계 유도체 CKD-604 물성연구 : 수용액중에서의 안정화 및 가용화 (Physicochemical Characteristics of Cephalosporin Derivative, CKD-604 : Stabilization and Solubilization in Aqueous Media)

  • 권수연;신희종;김종국
    • Journal of Pharmaceutical Investigation
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    • 제29권3호
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    • pp.205-210
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    • 1999
  • To formulate the parenteral delivery of a new cephalosporin derivative, 7-${\beta}$-[(2)-2-(2-arninothiazol-4-yl)-2methoxyiminoacetamido]- 3- [(2,3-cyclopenteno-4-carbamoyl-l-pyridinium)methyl]- 3-cephem-4-carboxylate sulfate( CKD604), the stability and solubility of CKD-604 in various aqueous media were investigated. The degradation kinetics of CKD-604 in aqueous solutions (ionic strength 0.1, pH 1-8) were studied at $37^{\circ}C$. The observed degradation rates followed pseudo first order kinetics. The pH-rate profile exhibited a minimum degradation rate at pH 5. The Arrhenius activation energy was 14.2 kcal/mol in pH 5 buffer solution. Excellent agreement between the cephalosporins' theoretical pH-rate profile and the experimental data indicated that the degradation pathway of CKD-604 could be predicted according to the general pathway of cephalosporins. The solubility of CKD-604 was 8.16 mg/ml at $25^{\circ}C$. To enhance the solubility and adjust the suitable pH, CKD-604 was solubilized by using sodium ascorbate, ascorbic acid and urea. The compositions were obtained to satisfy optimum pH and concentration, and the total amount of additives was several times of the active ingredient, CKD-604.

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A Novel Oxidation Model with Photolysis for Degradation of Trichlorobenzenes (TCBs)

  • Kim, Jae-Hyoun
    • Environmental Analysis Health and Toxicology
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    • 제12권3_4호
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    • pp.1-13
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    • 1997
  • First- and second-order kinetic oxidation rates of trichlorobenzenes (TCBs) were obtained and compared by a chemical activation system (CAS) which mimics mixed functional oxidase activity. The system consists of EDTA, ferrous sulfate, ascorbic acid, and $H_2O_2$ in potassium phosphdte buffer (monobasic at pH 7.4). The rate of transformation in CAS was enhanced in the presence and absence of catalase in the sequence 1, 2, 3-TCB < 1, 2, 4-TCB < 1, 3, 5-TCB. In general, the rates of degradation were greater in the test media with catalase. The effect of photolysis on the degradation of the TCBs with the CAS were examined. Sensitized photolysis with nitrite, Fenton's reagent, TiO$_2$ and triethylamine (TEA) studied in concert with the CAS demonstrated significant enhancement of the degradation rate of TCBs. Disappearance rates of TCBs in CAS with prior photolysis or prior photosensitization were at least 10-fold higher than the sum of the rate for each single experiment. This study proves that the combination of the CAS and photolysis can be used as a suitable technique for enhancing degradation of TCBs in aqueous systems.

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신안풍력발전소 풍력터빈의 성능저하 분석 (Analysis on Wind Turbine Degradation of the Shinan Wind Power Plant)

  • 김현구
    • 한국태양에너지학회 논문집
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    • 제33권4호
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    • pp.46-50
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    • 2013
  • This paper investigated wind turbine degradation quantitatively by analyzing the short-term operation records of the Shinan Wind Power Plant. Instead of a capacity factor which is needed to be normalized its variability due to monthly wind speed change, this study suggests an analysis method by taking the difference between the theoretical power output calculated from the nacelle wind speed and actual power output as the quantitative index of performance degradation. For three-year SCADA data analysis of the Shinan Wind Power Plant, it was confirmed that power output degradation rate of 0.54% per year. This value is within the average reduction rate 0.4%/year~0.9%/year of normalized capacity factor of the onshore wind power plants in U.K. and Denmark; however, lower than the rate 2%/year of Canadian wind power plants.

Kinetics of Thermal Degradation of Polypropylene/Nanoclay/Wood Flour Nanocomposites

  • Mohan, D. Jagan;Lee, Sun-Young;Kang, In-Aeh;Doh, Geum-Hyun;Park, Byung-Dae;Wu, Qinglin
    • 한국응용과학기술학회지
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    • 제24권3호
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    • pp.278-286
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    • 2007
  • As a part of enhancing the performance of wood-plastic composites (WPC), polypropylene (PP)/ nanoclay (NC)/ wood flour (WF) nanocomposites were prepared using melt blending and injection molding process to evaluate their thermal stability. Thermogravimetric analysis (TGA) was employed to investigate thermal degradation kinetics of the nanocomposites both dynamic and isothermal conditions. Dynamic scans of the TGA showed an increased thermal stability of the nanocomposites at moderate wood flour concentrations (up to 20 phr, percentage based on hundred percent resin) while it decreased with the addition of 30 phr wood flour. The activation energy $(E_a)$ of thermal degradation of nanocomposites increased when nanoclay was added and the concentration of wood flour increased. Different equations were used to evaluate isothermal degradation kinetics using the rate of thermal degradation of the composites, expressed as weight loss (%) from their isothermal TGA curves. Degradation occurred at faster rate in the initial stages of about 60 min., and then proceeded in a gradual manner. However, nanocomposites with wood flour of 30 phr heated at $300^{\circ}C$ showed a drastic difference in their degradation behavior, and reached almost a complete decomposition after 40 min. of the isothermal heating. The degree of decomposition was greater at higher temperatures, and the residual weight of isothermal degradation of nanocomposites greatly varied from about 10 to 90%, depending on isothermal temperatures. The isothermal degradation of nanocomposites also increased their thermal stability with the addition of 1 phr nanoclay and of wood flour up to 20 phr. But, the degradation of PP100/NC1/MAPP3/WF30 nanocomposites with 30 phr wood flour occurs at a faster rate compared to those of the others, indicating a decrease in their thermal stability.

자동차 엔진룸용 전장품 유무연 솔더 접합부의 열화특성 (Degradation Characteristics of Eutectic and Pb-free Solder Joint of Electronics mounted for Automotive Engine)

  • 김아영;홍원식
    • Journal of Welding and Joining
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    • 제32권3호
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    • pp.74-80
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    • 2014
  • Due to environmental regulations (RoHS, WEEE and ELV) of the European Union, electronics and automotive electronics have to eliminate toxic substance from their devices and system. Especially, reliability issue of lead-free solder joint is increasing in car electronics due to ELV (End-of-Life Vehicle) banning from 2016. We have prepared engine control unit (ECU) modules soldered with Sn-40Pb and Sn-3.0Ag-0.5Cu (SAC305) solders, respectively. Degradation characteristics of solder joint strength were compared with various conditions of automobile environment such as cabin and engine room. Thermal cycle test (TC, $-40^{\circ}C$ ~ ($85^{\circ}C$ and $125^{\circ}C$), 1500 cycles) were conducted with automotive company standard. To compare shear strength degradation rate with eutectic and Pb-free solder alloy, we measured shear strength of chip components and its size from cabin and engine ECU modules. Based on the TC test results, finally, we have known the difference of degradation level with solder alloys and use environmental conditions. Solder joints degradation rate of engine room ECU is superior to cabin ECU due to large CTE (coefficient of thermal expansion) mismatch in field condition. Degradation rate of engine room ECU is 50~60% larger than cabin room electronics.