• 제목/요약/키워드: Degradation rate constant

검색결과 225건 처리시간 0.032초

입체화학을 이용한 생분해성 고분자의 분해속도에 관한 연구 (Study on Degradation Rates of Biodegradable Polymers by Stereochemistry)

  • 박찬영;최용해;이원기
    • 한국환경과학회지
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    • 제18권7호
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    • pp.797-802
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    • 2009
  • To control degradation rate of biodegradable poly(lactide)s (PLA), the stereochemical PLAs with different ratios of d-lactide and l-lactide units were synthesized by the ring open polymerization and the their degradation kinetics were measured by a Langmuir film balance. The alkaline (pH=11) degradation of poly(l-lactide) (l-PLA) monolayer showed the faster rate at a surface pressure of 4 mN/m in the ranges from to 0 to 7 mN/m. However, the enzymatic degradation of l-PLA with Proteinase K did not occur until 4 mN/m. Above a constant surface pressure of 4 mN/m, the degradation rate was increased with a constant surface pressure. These behaviors might be attributed to the difference in the contacted area with degradation medium: alkaline ions need small contact area with l-PLA while enzymes require much bigger one to be activated due to different medium sizes. The stereochmical PLA monolayers showed that the alkaline degradation was increased with their optical impurities while the enzymatic one was inversed. These results could be explained by the decrease of crystallinity with the optical impurity and the inactivity of enzyme to d-LA unit.

Stability of Tetracycline Hydrochloride in Reverse Micelles

  • Kim, Hyun-Joo;Lee, Hwa-Jeong;Sah, Hong-Kee
    • Journal of Pharmaceutical Investigation
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    • 제35권5호
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    • pp.333-336
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    • 2005
  • The objective of this study was to investigate the stability of tetracycline HCl on encapsulation into and inside reverse micelles. To do so, tetracycline HCl was first mixed with cetyltrimethylammonium bromide, water and ethyl formate to make reverse micelles. The degradation kinetics of tetracycline HCl inside the reverse micelles was then assessed by scrutinizing its stability data. Under our experimental conditions, the reverse micelles formed spontaneously in absence of any mixing devices. During the preparation of the reverse micelles, however, considerable portions of tetracycline HCl underwent a chemical reaction (e.g., epimerization). For instance, $51.4{\pm}0.6%$ of an initial concentration of tetracycline HCl was transformed into a degradation product. Once dissolved inside the reverse micelles, the degradation of tetracycline HCl followed an exponential decay pattern. The plot of log{the degradation rate of tetracycline HCl} versus log{tetracycline HCl concentration} made it possible to determine the order of degradation reaction and rate constant. It was proven that the degradation of tetracycline HCl inside the reverse micelles followed a first order kinetics with a rate constant of 0.0027 $hour^{-1}$. Meriting further investigation might be formulation studies to stabilize tetracycline HCl on encapsulation into and inside the reverse micelles.

Degradation Kinetics of Three Veterinary Antibiotics in Composted and Stockpiled Manure

  • Kim, Sung-Chul;Yang, Jae-E.;Ok, Yong-Sik;Jung, Doug-Young;Carlson, Kenneth
    • 한국토양비료학회지
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    • 제45권1호
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    • pp.43-50
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    • 2012
  • Two typical animal waste management practices, composting and stockpiling, were evaluated for their effect on the degradation of three veterinary antibiotics (VAs), chlortetracycline (CTC), tylosin (TYL), and monensin (MNS). The VAs were applied to horse manure plots subject to composting or stockpiling, and core samples were collected over a period of time. Selected buffer solutions were used to extract the VAs and analysis for concentration was conducted with solid phase extraction (SPE) followed by high performance liquid chromatography tandem mass spectrometry (HPLC/MS/MS) technique. The VAs demonstrated rapid dissipation within ten days followed by a gradual decrease in concentration until the end of the experimental period (141 days). All three VAs degraded more rapidly in the composting samples than in the stockpiling samples, particularly between 20 and 60 days of the observation period. Degradation of the three VAs generally followed a first-order kinetic model, and a fitted model with a calculated rate constant was determined for each treatment. TYL in composting showed the fastest degradation, with a calculated rate constant of $0.91day^{-1}$; the slowest degradation was exhibited by MNS in stockpiling, with rate constant of $0.17day^{-1}$. Calculated correlation coefficients ranged from 0.89 to 0.96, indicating a strong correlation between measured concentrations and fitted values in this study. Although concentration of TYL in composting treatment showed below detection limit during the test period, this study suggests that composting can reduce animal waste contaminants prior to field application as fertilizer.

UV/H2O2 고도산화기술을 이용한 수중 잔류의약물질 제거 (Degradation of residual pharmaceuticals in water by UV/H2O2 advanced oxidation process)

  • 박진영;서상원;조익환;전용성;하현섭;황태문
    • 상하수도학회지
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    • 제33권6호
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    • pp.469-480
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    • 2019
  • This study was conducted to evaluate the degradation and mineralization of PPCPs (Pharmaceuticals and Personal Care Products) using a CBD(Collimated Beam Device) of UV/H2O2 advanced oxidation process. The decomposition rate of each substance was regarded as the first reaction rate to the ultraviolet irradiation dose. The decomposition rate constants for PPCPs were determined by the concentration of hydrogen peroxide and ultraviolet irradiation intensity. If the decomposition rate constant is large, the PPCPs concentration decreases rapidly. According to the decomposition rate constant, chlortetracycline and sulfamethoxazole are expected to be sufficiently removed by UV irradiation only without the addition of hydrogen peroxide. In the case of carbamazepine, however, very high UV dose was required in the absence of hydrogen peroxide. Other PPCPs required an appropriate concentration of hydrogen peroxide and ultraviolet irradiation intensity. The UV dose required to remove 90% of each PPCPs using the degradation rate constant can be calculated according to the concentration of hydrogen peroxide in each sample. Using this reaction rate, the optimum UV dose and hydrogen peroxide concentration for achieving the target removal rate can be obtained by the target PPCPs and water properties. It can be a necessary data to establish design and operating conditions such as UV lamp type, quantity and hydrogen peroxide concentration depending on the residence time for the most economical operation.

정전류/정출력 고속충전 방식에 따른 리튬이온전지의 열화 비교 연구 (Effect of Fast Charging Mode on the Degradation of Lithium-Ion Battery: Constant Current vs. Constant Power)

  • 박선호;오은택;박시영;임지훈;최진혁;이용민
    • KEPCO Journal on Electric Power and Energy
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    • 제6권2호
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    • pp.173-179
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    • 2020
  • 전기자동차의 보급이 확대됨에 따라, 소비자의 고속충전에 요구가 높아지고 있으나 관련 연구는 미흡한 실정이다. 본 연구에서는 LiNi0.5Co0.2Mn0.3O2/Graphite 18650 실린더형 리튬이온전지를 이용하여, 정전류와 정출력 충전방식에 따른 전지 열화현상을 비교한다. 정전류모드의 충전속도를 1C, 2C, 3C, 4C로 설정하고, 각 충전속도에서의 에너지를 기반으로 정출력값을 산정하였다. 따라서, 동일 충전 에너지를 기반하여, 두 충전방식에 따른 전지 열화를 분석한 결과, 3C의 높은 율속에서 정출력 충전방식이 전지의 열화를 늦출 수 있음이 전압곡선, 용량유지율, 직류저항값으로 확인되었다. 그러나, 충전속도를 4C 이상 높이면, 충전방식보다 전지간 편차가 열화 거동을 지배하였다.

Efficient Removal of Sulfamethoxazole in Aqueous Solutions Using Ferrate (VI): A Greener Treatment

  • Lalthazuala, Levia;Tiwari, Diwakar;Lee, Seung-Mok;Choi, Suk Soon
    • 공업화학
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    • 제32권3호
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    • pp.340-347
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    • 2021
  • The aim of this research is to assess the use of high purity potassium ferrate (VI) for the efficient removal of sulfamethoxazole (SMX), one of the potential micro-pollutant found in aqueous waste. In addition, various parametric studies have enabled us to deduce the mechanism in the degradation process. The pH and concentration of sulfamethoxazole enable the degradation of pollutants. Moreover, the time-dependent degradation nature of sulfamethoxazole showed that the degradation of ferrate (VI) in presence of sulfamethoxazole followed the pseudo-second order kinetics and the value of rate constant increased with an increase in the SMX concentration. The stoichiometry of SMX and ferrate (VI) was found to be 2 : 1 and the overall rate constant was estimated to be 4559 L2/mmol2/min. On the other hand, the increase in pH from 8.0 to 5.0 had catalyzed the degradation of SMX. Similarly, a significant percentage in mineralization of SMX increased with a decrease in pH and concentration. The presence of co-existing ions and SMS spiked real water samples was extensively analyzed in the removal of SMX using ferrate (VI) to simulate studies on real matrix implication of ferrate (VI) technology.

Photocatalytic Degradation of 2,4,6-Trinitrotoluene in Wastewater Using a Thin-Film TiO2 Reactor

  • Shin, Gi-Bum;Kim, Yeong-Kwan
    • Environmental Engineering Research
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    • 제13권1호
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    • pp.28-32
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    • 2008
  • The photocatalytic treatment of water contaminated with 2,4,6-trinitrotoluene (TNT) was explored in bench-scale experiments in batch mode using a Pyrex tube coated with a thin film of $TiO_2$ located inside a photoreactor. The reactor was aerated by purging it with compressed air before initiating the photocatalytic reaction. The rate of TNT degradation approximated first-order kinetics. The reaction rate constant decreased as the TNT concentration increased from 25 to 100 mg/L, while the first-order kinetics could be modeled using a Langmuir adsorption isotherm. The addition of the organic reductants methanol and EDTA significantly enhanced the rate of TNT degradation, with optimum results in the presence of 20% methanol by volume. EDTA increased the rate of TNT removal by enhancing the role of the reductants.

오존 접촉 반응기의 용존 오존 농도 및 페놀 분해에 미치는 운전변수의 영향 (Effects of Operating Parameters on Dissolved Ozone and Phenol Degradation in Ozone Contact Reactor)

  • 정재우;박정욱;이춘식
    • 대한환경공학회지
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    • 제32권3호
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    • pp.241-247
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    • 2010
  • 오존 접촉 반응기에서 용존 오존 농도 및 페놀 제거에 미치는 운전변수의 영향에 대해 실험실 규모 실험을 수행하였다. 반응기로 가스상 오존이 공급되고 일정한 시간이 경과한 후에 용존 오존 농도는 포화 농도에 도달하였으며 포화 농도의 크기는 운전 변수에 의해 영향을 받는 것으로 나타났다. 수용액내의 오존은 높은 pH 조건에서 불안정하므로 용존 오존 농도는 용액의 초기 pH값이 증가함에 따라 감소하였다. 일정한 유량의 기체가 반응기로 공급되는 조건에서 가스상 오존 농도의 크기는 용존 오존의 포화농도에 중요한 영향을 미치며 일정한 농도의 가스상 오존이 공급될 때 가스 유량은 용존 오존이 포화되는 속도에 영향을 주는 것으로 관찰되었다. 페놀 제거에 미치는 운전변수의 영향은 각 운전변수가 용존 오존 농도에 미치는 영향과 밀접하게 관련되어 있는 것으로 나타났다. 용존 오존은 높은 pH 조건에서 빠르게 분해되어 페놀과의 반응성이 높은 자유라디칼을 생성시키므로 pH가 증가함에 따라 페놀 제거가 향상되었다. 동일한 pH 조건에서 가스상 오존 농도 및 가스 공급량의 증가는 용존 오존을 증가시킴으로써 페놀 분해를 증진시키는 것으로 나타났다. 메탄올의 주입은 OH 라디칼을 소비시켜 페놀 분해를 방해하는 것으로 관찰되었다.

Effects of Soil Types on the Biodegradation of Crude Oil by Nocardia sp. H17-1

  • Yoon, Byung-Dae;Baek, Kyung-Hwa;Kim, Hee-Sik;Moon, Seong-Hoon;Lee, In-Sook;Oh, Hee-Mock
    • Journal of Microbiology and Biotechnology
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    • 제14권5호
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    • pp.901-905
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    • 2004
  • The degradation and mineralization of crude oil were investigated over 50-days in three soils, loamy sand, sand, and combusted loamy, which were artificially contaminated with crude oil (50 g $kg^{-1}$) and inoculated with Nocardia sp. H17-1. The degradation efficiency of total petroleum hydrocarbon (TPH) in sand was the highest at 76% among the three soils. The TPH degradation rate constants $(k_{TPH})$ in loamy sand, sand, and combusted loamy sand were 0.027 $d^{-1}$, 0.063 $d^{-1}$, and 0.016 $d^{-1}$, respectively. In contrast, the total amount of $CO_2$ evolved was the highest at 146.1 mmol in loamy sand. The $CO_2$ evolution rate constants (k_{CO2})$ in loamy sand, sand, and combusted loamy sand were 0.057 $d^{-1}$, 0.066 $d^{-1}$, and 0.037 $d^{-1}$, respectively. Therefore, it seems that the degradation of crude oil in soils can be proportional to the soil pore space and that mineralization can be accelerated with the increase of organic substance.

UV/TiO2 광촉매반응에 의한 페놀의 분해 특성 (Characteristics of Phenol Degradation by using UV/TiO2 Photocatalysis)

  • 신인수;최봉종;이승목
    • 한국물환경학회지
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    • 제20권5호
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    • pp.488-493
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    • 2004
  • The effects were examined from several conditions of $TiO_2$ photocatalysis reaction to phenols degradation by changing it's reacting conditions such as phenol concentration, pH, $TiO_2$ concentration, $H_2O_2$ concentration, flow rate, and intensity of ultraviolet rays. Phenol degradation was more efficient in low concentration of phenol, neutral pH. Phenol degradation appeared to increase as concentration of $TiO_2$ photocatalyst, that of $H_2O_2$ and intensity of ultraviolet rays increased. As $TiO_2$ dosage increased, initial rate constant k linearly increased. When $H_2O_2$ was injected more than optimum, phenol removal rate didn't increase in proportional to the change of $H_2O_2$ concentration as OH radicals was being consumed. When flow rate is less than $4.75m^3/m^2$ day, phenol removal efficiency appeared to decrease as ultraviolet rays transmission rate becomes low by $TiO_2$ suspension coated in photo reaction column. Meanwhile, initial rate constant according to light intensity change in less than $25mW/cm^2$ appeared to be in proportion to light intensity ($mW/cm^2$) Removal efficiency decreased about 12% after 180 minutes of reaction time while showed stable removal efficiency of 100% after 300 minutes when using regenerated $TiO_2$.