• 청정기술
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• 제30권3호
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• pp.239-247
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• 2024

The removal of volatile organic compounds (VOCs) from spent polypropylene (PP) sourced from the bumpers and interiors of used cars was carried out by using high-temperature supercritical carbon dioxide (scCO₂) extraction. The recycled polymers from the bumpers and interiors contained other additives beside PP such as polyethylene (PE), talc, and carbon black, which modified the properties of PP. The crystallinity of the recycled bumper and interior PP was significantly lower than that of the virgin PP pellet. The decomposition temperatures of the recycled bumper and interior PP was slightly higher than that of the virgin PP pellet, while the melting and crystallization points were slightly lower. The effect of process conditions on VOC removal was studied by varying the time (2 ~ 720 min), pressure (6.4 ~ 14 MPa), and temperature (298 ~ 473 K). Since VOC removal at 2 min produced satisfying results, times below 2 min (10 ~ 120 s) were also studied. The main goal of scCO₂ extraction was to reduce the xylene content, as the xylene content of the recycled bumpers was higher than the allowable limit. A temperature above 373 K was needed to remove the xylene from the waste PP samples. The optimum condition for VOC removal from bumper waste was determined to be 433 K, 8 MPa, and 60 s. The car interior waste had VOC content within the allowable limit, so no further treatment was needed.

• 상하수도학회지
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• 제12권1호
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• pp.88-95
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• 1998

The Electron/Hole Pair is generated when the Activation Energy produces by Ultraviolet Ray illumination to the Semiconductor. And $OH^-$ ion produces by Water Photo-Cleavage reacts with Positive Hole. As a result, OH Radical acting as strong oxidant is generated and then Photocatalytic Oxidation Reaction occurs. The Photocatalytic Oxidation can oxidize the chlorophenol to Chloride and Carbon Dioxide easier, safer and shorter than conventional Water Treatment Process With the same degree of chlorination, the $Cl^-$ ion at para (C4) position is most easily replaced by the OH radical. And then, the blocking effect of $OH^-$ ion between the $Cl^-$ ions and $Cl^-$ ions at symmetrical location is easily replaced by the OH radical. For mono-, di-, tri-chlorophenols, there is no obvious difference in decomposition rate, decomposition efficiency and completeness of the decomposition reaction except for 2,3-dichloropheno, 2,4,5-, 2,3,4-trichlorophenol. The decomposition efficiency is higher than 75% and completeness of the decomposition reaction is higher than 70%. Therefore, continuous flow photocatalytic reactor is promising process to remove the chlorinated aromatic compounds which is more toxic than non-chlorinated aromatic compound.

• 폴리머
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• 제34권6호
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• pp.507-510
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• 2010

이산화탄소와 에폭사이드를 크롬계 전이 금속촉매를 이용하여 교대 공중합하여 poly(cyclohexane carbonate) diol(PCCD)을 분자량 별로 제조하였다. 이산화탄소를 기반으로 한 폴리카보네이트(PCCD)의 응용분야 탐색을 위하여 수분산 폴리우레탄(PUD) 제조를 위한 전구체로 적용하여 보았다. 상업화되어 사용중인 폴리카보네이트 디올과 신규 PCCD로 제조한 PUD의 내스크래치 특성과 열적 특성을 비교 분석하였다. PCCD를 사용하여 제조된 PUD 필름의 내스 크래치성과 열분해온도는 PCD를 사용한 경우보다 떨어지지만, 유리전이온도는 증가하는 것을 알 수 있었다. 이것은 PCCD의 강직한 사이클로 헥산 구조에 기인한 것으로 생각된다.

• 한국산학기술학회논문지
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• 제13권1호
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• pp.431-438
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• 2012

아민 수용액을 이용한 이산화탄소 포집기술은 현재 가장 넓게 연구되는 분야이다. 전체 공정은 선택적 이산화탄소 흡수를 위한 흡수탑과 흡수제를 재생하고 고순도 이산화탄소를 얻기 위한 재생탑으로 이루어져있다. 공정 성능에 영향을 미치는 복잡한 설계 변수들이 존재하기 때문에 상업적으로 신뢰할만한 공정을 설계하기 위해서는 모델링을 통한 공정 해석과 최적화가 필요하다. 본 연구에서는 공정의 수렴문제를 고려하여 분해방법을 사용하였고, 아민계 흡수제를 이용하는 이산화탄소 포집 공정의 변수들에 대한 민감도 분석을 수행하였다. 현실적인 설계 결과를 얻기 위해 비평형 모델을 사용하였고 95% 이상의 순도로 90%의 이산화탄소를 회수할 수 있는 최적화된 공정을 설계할 수 있었다.

• 한국축산시설환경학회지
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• 제11권2호
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• pp.97-102
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• 2005

Anaerobic decomposition is one of the most common processes in nature and has been extensively used in waste and wastewater treatment for several centuries. New applications and system modifications continue to be adapted making the process either more effective, less expensive, or suited to the particular waste in question and the operation to which it is to be applied. Animal manure is a highly biodegradable organic material and will naturally undergo anaerobic fermentation, resulting in release of noxious odors, such as in manure storage pits. Depending on the presence or absence of oxygen in the manure, biological treatment process may be either aerobic or anaerobic. Under anaerobic conditions, bacteria carry on fermentative metabolisms to break down the complex organic substances into simpler organic acids and then convert them to ultimately formed methane and carbon dioxide. Anaerobic biological systems for animal manure treatment include anaerobic lagoons and anaerobic digesters. Methane and carbon dioxide are the principal end products of controlled anaerobic digestion. These two gases are collectively called biogas. The biogas contains $60\~70\%$ methane and can be used directly as a fuel for heating or electrical power generation. Trace amounts of ammonia and hydrogen sulfide ($100\~300\;ppm$) are always present in the biogas stream. Anaerobic lagoons have found widespread application in the treatment of animal manure because of their low initial costs, ease of operation and convenience of loading by gravity flow from the animal buildings. The main disadvantage is the release of odors from the open surfaces of the lagoons, especially during the spring warm-up or if the lagoons are overloaded. However, if the lagoons are covered and gases are collected, the odor problems can be solved and the methane collected can be used as a fuel. Anaerobic digesters are air-tight, enclosed vessels and are used to digest manure in a well-controlled environment, thus resulting in higher digestion rates and smaller space requirements than anaerobic lagoons. Anaerobic digesters are usually heated and mixed to maximize treatment efficiency and biogas production. The objective of this work was to review a current anaerobic biological treatment of animal manure for effective new technologies in the future.

• 한국가스학회지
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• 제2권2호
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• pp.40-47
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• 1998

이산화탄소를 분해할 목적으로 황산철과 수산화나트륨을 이용하여 $Fe_3O_4$를 합성하였다. 합성조건은 황산철과 수산화나트륨의 혼합당량비를 0.50${\~}$l.50까지로 반응온도는 $40^{\circ}C$, 반응시간은 20시간으로 하였다. 또한 혼합당량비를 1.00으로 고정하고, 여기에 $NiCl_2,\;RhCl_3$를 mole$\%$로 첨가하여 합성하였다. 이 합성된 $Fe_3O_4$의 구조변화에 미치는 Ni과 Rh의 영향을 XRD, SEM으로 비교 검토하였다.

• 한국농공학회지
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• 제42권
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• pp.61-67
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• 2000

Composting of hog manure amended with sawdust trials lasted three weeks and used pilot-scale in bin composting system. Results showed that the rise temperature and carbon dioxide evolution in compost during the composting decomposition process were affected by the aeration method, pH, C/N, moisture content, bulk density and particle size distribution. No significant differences existed in biophysical properties of the composit produced from the continuous and intermittent aeration method. The intermittent aeration was very successful in compost odor control and required less time to reach stability than the continuous aeration.

• Journal of Ecology and Environment
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• 제41권12호
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• pp.336-344
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• 2017

Background: Because of climate change, interest in the development of carbon pools has increased. In agricultural ecosystems, which can be more intensively managed than forests, measures to control carbon dioxide ($CO_2$) emission and absorption levels can be applied relatively easily. However, crop residues may be released into the atmosphere by decomposition or combustion. If we can develop scientific management techniques that enable these residues to be stocked on farmland, then it would be possible to convert farmlands from carbon emission sources to carbon pools. We analyzed and investigated soil respiration (Rs) rate characteristics according to input of carbonized residue of red peppers (Capsicum annuum L.), a widely grown crop in Korea, as a technique for increasing farmland carbon stock. Results: Rs rate in the carbonized biomass (CB) section was $226.7mg\;CO_2\;m^{-2}h^{-1}$, which was 18.1% lower than the $276.9mg\;CO_2\;m^{-2}h^{-1}$ from the red pepper residue biomass (RB) section. The Rs rate of the control was $184.1mg\;CO_2\;m^{-2}h^{-1}$. In the following year, Rs in the CB section was $204.0mg\;CO_2\;m{-2}h^{-1}$, which was 38.2% lower than the $330.1mg\;CO_2\;m^{-2}h^{-1}$ from the RB section; the control emitted $198.6mg\;CO_2\;m^{-2}h^{-1}$. Correlation between Rs and soil temperature ((Ts) at a depth of 5 cm) was $R^2=0.51$ in the RB section, which was higher than the other experimental sections. A comparison of annual decomposition rates between RB and CB showed a large difference, 41.4 and 9.7%, respectively. The results showed that carbonization of red pepper residues reduced the rates of decomposition and Rs. Conclusions: The present study confirmed that the Rs rate can be reduced by carbonization of residue biomass and putting it in the soil and that the Rs rate and Ts (5 cm) were positively correlated. Based on the results, it was determined that approximately $1.2t\;C\;ha^{-1}$ were sequestered in the soil in the first year and $3.0t\;C\;ha^{-1}$ were stored the following year. Therefore, approximately $1.5t\;C\;ha^{-1}year^{-1}$ are expected to be stocked in the soil, making it possible to develop farmlands into carbon pools.

• 한국수소및신에너지학회논문집
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• 제34권3호
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• pp.256-266
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• 2023

Hydrogen production can be classified based on the energy source, primary reactor type, and whether or not it emits carbon dioxide. Utilizing color representation proves to be an effective means of expressing these distinctive characteristics. Among the various clean hydrogen production techniques, there has been a growing interest in turquoise hydrogen production, which involves the decomposition of methane or other fossil fuels. This method offers advantages in terms of large-scale production and cost reduction through the sale of solid-carbon byproduct. In this study, an extensive literature review was conducted to select and analyze several promising candidates for turquoise hydrogen production processes. The efficiency and economics of these processes were evaluated using stream data reported in the literature sources. The findings indicate that the levelized cost of hydrogen production (LCOH) is significantly influenced by the sales of byproducts, specifically the solid-carbon and carbon monoxide byproducts.

• 한국화재소방학회논문지
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• 제15권1호
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• pp.16-22
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• 2001

석유화학플랜트에서 다량 부산되는 가연성 고체인 PP(Polypropylene) 및 LLDPE(Linear low density polyethylene)의 열적특성과 압력용기를 이용하여 산화제와의 혼촉위험성을 조사하였다. 시차주사열량계 및 열중량 분석기를 이용하여 온도에 따른 발열개시온도 및 중량감소를 조사하였고, PP 및 LLDPE의 혼촉위험성을 살펴보고자 소방법상 제1류 위험물로 분류되고 있는 몇 가지 대표적인 산화성 고체와 혼합하여 무게비에 따른 압력용기 내에서의 혼촉위험성을 조사하였다. 또한 가스농도 측정기를 이용하여 PP 및 LLDPE에 대한 연소생성물의 농도를 측정하였다. DSC분석 결과 열분해에 따른 발열 피크가 PP의 경우 220~$250^{\circ}c$ 부근에서 나타나고 있으며, TGA분석결과 PP 및 LLDPE의 분해온도는 각각 200~$350^{\circ}c$, 300~$500^{\circ}c$ 범위이다. 압력용기 시험에 의한 산화제와 PP 및 LLDPE 분진의 혼촉위험성은 오리피스 직경이 감소할수록, 산화제와의 혼촉 무게비가 증가할수록 그리고 시료의 분해온도와 산화제의 분해온도가 비슷한 경우 흔촉위험성이 크게 나타났다. 또한 시료의 연소가스 분석결과 PP의 경우 LLDPE보다 상당히 많은 양의 일 산화탄소가 발생하는 반면 LLDPE가 PP보다 더 많은 양의 이산화탄소 가스를 발생하였다.