• 환경영향평가
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• 제19권6호
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• pp.625-631
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• 2010

The objective of this work was to investigate how carbon sink and sequestration of vegetation and soil in the development project area can impact the land use plan, in addition to carbon emission capacity of the development project when we conduct environmental impact assessment. Especially, we did this work for a development project of solar power plant which would be constructed in forest area. Through this work, we found that 1) the amount of carbon sink and sequestration largely decreased due to reduction of the green area, 2) in terms of carbon sink and sequestration, conservation of natural green area is better than construction of newly vegetated area, 3) biochar application into soil can become an alternative for increase of carbon sink, and 4) even though a solar power production does hugely reduce carbon emissions and offset the carbon sink and sequestration capacity from the forest, it is necessary to consider the public value of the forest(reduction of heat island, habitat etc.) in siting for development area.

• 한국산림과학회지
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• 제110권4호
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• pp.554-568
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• 2021

산림은 육상생태계에서 가장 큰 탄소흡수원으로 기후변화 대응에 있어 산림의 대기 중 이산화탄소 농도 저감 역할은 중요하다. 최근 '2050 탄소중립 계획'에 산림의 탄소흡수 기능의 강화가 기본 방향으로 제시되면서 정확한 산림의 탄소흡수량 산정이 강조되고 있다. 산림부문의 탄소흡수량은 Intergovernmental Panel on Climate Change 지침을 따라 산림 내 생물량, 고사목, 임상 유기물층, 토양층, 수확된 목재제품 등 여러 탄소 저장고 내 탄소축적 변화량으로부터 산정한다. 그러나 국내 산림의 경우 하층 식생을 제외한 주요 수종의 임목 재적 증가로부터 추정한 생물량 증가량만을 산림의 탄소흡수량으로 산정하고 있어 실제 산림의 탄소흡수량과 큰 차이가 발생할 수 있다. 이에 본 연구에서는 경기도 광주시 태화산에 위치한 57년생 잣나무 조림지에서 에디 공분산 시스템과 자동화 토양챔버 시스템을 이용한 탄소 플럭스 관측을 통해 산림의 탄소 교환량 및 순 탄소흡수량을 정량화하고, 이를 현재 산림의 탄소흡수량 산정 방법에 따라 법정림 임분수확표 내 연평균 생장량과 국가 고유계수를 이용하여 계산한 잣나무 조림지 임목의 생물량 증가량과 비교하였다. 또한 탄소 플럭스 관측기반의 순 탄소흡수량과 잣나무 조림지의 생물량 증가량 및 임상 유기물층의 탄소저장 변화량 등의 차이로부터 나머지 탄소 저장고에서 연간 탄소저장 변화량을 추정하였다. 그 결과 탄소 플럭스로부터 계산한 잣나무 조림지의 연간 순 탄소흡수량은 5.96 MgC ha^-1으로 생물량 증가로부터 계산한 임목의 연간 탄소흡수량 2.77 MgC ha^-1보다 약 2.2배 많았다. 연간 임상 유기물층의 탄소저장 변화량은 0.75 MgC ha^-1로 추정되어, 연간 하층 식생, 고사목, 토양층 등의 탄소 저장고로 유입되는 탄소의 양이 2.45 MgC ha^-1으로 추정되었다. 본 연구의 결과는 국내 산림이 현재 평가 수준보다 더 큰 탄소흡수원임을 보여주며, 탄소 플럭스 관측과 더불어 하층 식생, 고사목, 토양층 등의 탄소 저장고에서 탄소축적 변화량의 정량화를 통해 더욱 정확한 산림부문 탄소흡수량 산정이 필요함을 시사한다.

• Journal of Forest and Environmental Science
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• 제37권2호
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• pp.116-127
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• 2021

Predicting carbon distribution of soil aggregates is difficult due to complexity in organo-mineral formation. This limits global warming mitigation through soil carbon sequestration. Therefore, knowledge of land use effect on carbon stabilization requires quantification of soil mineral cations. The study was conducted to quantify carbon and base cations on soil mineral fractions in Natural Forest, Plantation Forest and Farm Land. Five 0.09 ha were demarcated alternately along 500 m long transect with an interval of 50 m in Natural Forest (NF), Plantation Forest (PF) and Farm Land (FL). Soil samples were collected with soil cores at 0-15, 15-30 and 30-45 cm depths in each plot. Soil core samples were oven-dried at 105℃ and soil bulk densities were computed. Sample (100 g) of each soil core was separated into >2.0, 2.0-1.0, 1.0-0.5, 0.5-0.05 and <0.05 mm aggregates using dry sieve procedure and proportion determined. Carbon concentration of soil aggregates was determined using Loss-on-ignition method. Mineral fractions of soil depths were obtained using dispersion, sequential extraction and sedimentation methods of composite soil samples and sieved into <0.05 and >0.05 mm fractions. Cation exchange capacity of two mineral fractions was measured using spectrophotometry method. Data collected were analysed using descriptive and ANOVA at α_0.05. Silt and sand particle size decreased while clay increased with increase in soil depth in NF and PF. Subsoil depth contained highest carbon stock in the PF. Carbon concentration increased with decrease in aggregate size in soil depths of NF and FL. Micro- (1-0.5, 0.5-0.05 and <0.05 mm) and macro-aggregates (>2.0 and 2-1.0 mm) were saturated with soil carbon in NF and FL, respectively. Cation exchange capacity of <0.05 mm was higher than >0.05 mm in soil depths of PF and FL. Fine silt (<0.05 mm) determine the cation exchange capacity in soil depths. Land use and mineral size influence the carbon and cation exchange capacity of Gambari Forest Reserve.

• 한국해양공학회:학술대회논문집
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• 한국해양공학회 2006년 창립20주년기념 정기학술대회 및 국제워크샵
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• pp.265-268
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• 2006

The preliminary design of a deep-sea injection system for carbon dioxide ocean sequestration is performed. Common functional requirements for a deep-sea injection system of mid-depth type and lake type are determined, Liquid transport system, liquid storage system and liquid injection system are conceptually determined for the functional requirements. For liquid injection system, the control of flow rate and temperature of liquid $CO_2$ in the injection pipe is needed in the view of internal flow. The function of depressing VIV(Vortex Induced Vibration) is also required in the view of dynamic stability of the injection pipe. A case study is performed for $CO_2$ sequestration capacity of 10 million tons per year. In this study, the total number of injection ships, the flow rate of liquid $CO_2$ and the configuration of a injection pipe are designed. The static structural analysis of the injection pipe is also performed. Finally the preliminary design of a deep-sea injection system is proposed.

• Ocean and Polar Research
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• 제27권4호
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• pp.451-461
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• 2005

The $CO_2$ storage in geologic and oceanic reservoirs is considered to be one of the carbon management strategies for responding to global climate change. Ocean carbon sequestration is purposeful storage acceleration into the ocean of large amounts of carbon that would accumulate in the atmosphere and naturally enter the ocean over a longer timespan. Some technologies for $CO_2$ ocean sequestrations have been developed as a nation project. However, $CO_2$ ocean sequestrations are attractive because they have the advantage of vast capacity sequestration far away from industrial areas, and offer easier monitoring whereas less economic advantage has been indicated as one of the key barriers compared with $CO_2$ geosphere sequestration, which is produced as a byproduct. In this paper, a conceptual design for $CO_2$ ocean sequestration is introduced, and the preliminary examination is described. As a result, the $CO_2$ price, US$ 24/t shows far away from the economics. The causes come from the expensive $CO_2$ recovery cost and the low $CO_2$ price. The expensive $CO_2$ recovery cost is because too much electricity and water are consumed. In order to look for an economic balance point for $CO_2$ ocean sequestration, NPV=0, it is increases the $CO_2$ price. Finally 60.4$ per ton is found to be the balance price.

• 설비공학논문집
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• 제15권9호
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• pp.718-726
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• 2003

Carbon dioxide ocean disposal is one of the promising options to reduce carbon dioxide concentration in the atmosphere because the ocean has vast capacity for carbon dioxide sequestration. However, the dissolution rate of liquid carbon dioxide in seawater must be known in advance in order to estimate the amount of carbon dioxide sequestration in the ocean. Therefore, in the present study, calculations of the solubility, the surface concentration and the dissolution behavior of carbon dioxide when liquid carbon dioxide is released at 1,000m and 1,500m in depth are peformed. The results show that the droplet is completely dissolved below 500 m in depth if the carbon dioxide droplet is released both at 1,000m in depth with the initial droplet diameter of 0.011m or less and at 1,500m in depth with the diameter of 0.016 or less. Also, the surface concentration of carbon dioxide droplet with the hydrate film is about 50% of carbon dioxide solubility at 1,500 m in depth and about 60% of carbon dioxide solubility at 1,000 m in depth.

• 태양에너지
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• 제20권2호
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• pp.75-84
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• 2000

Global wanning induced by greenhouse gases such as carbon dioxide is a serious problem for mankind. Carbon dioxide ocean disposal is one of the promising options to reduce carbon dioxide concentration in the atmosphere because the ocean has vast capacity for carbon dioxide sequestration. However, the dissolution rate of liquid carbon dioxide in seawater must be known in advance in order to estimate the amount of carbon dioxide sequestration in the ocean. Therefore, the solubility, the surface concentration, the droplet size and other factors of liquid carbon dioxide at various depths are calculated. The results show that liquid carbon dioxide changes to carbon dioxide bubble around 500 m in depth, and the droplet is completely dissolved below 500 m in depth if carbon dioxide droplet is released both at 1000 m in depth with the initial droplet diameter of 0.011 m or less and at 1500 m in depth with the diameter of 0.015 m or less. In addition, the hydrate film acts as a resistant layer for the dissolution of liquid carbon dioxide. The surface concentration of carbon dioxide droplet with the hydrate film is about 50% at 1500 m in depth and about 60% at 1000 m in depth of the carbon dioxide solubility. Also, the ambient carbon dioxide concentration in the plume is an another crucial parameter for complete dissolution at the intermediate ocean depth, and the injection of liquid carbon dioxide from a moving ship is more effective than that from a fixed pipeline.

• Carbon letters
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• 제10권2호
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• pp.114-122
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• 2009

Crushed, depitted peach stones were impregnated activated with 50% $H_3PO_4$ followed by pyrolysis at $500^{\circ}C$. Two activated carbons were produced, one under its own evolved gases during pyrolysis, and the second conducted with air flow throughout the carbonization stage. Physicochemical properties were investigated by several procedures; carbon yield, ash content, elemental chemical analysis, TG/DTG and FTIR spectra. Porosity characteristics were determined by the conventional $N_2$ adsorption at 77 K, and data analyzed to get the major texture parameters of surface area and pore volume. Highly developed activated carbons were obtained, essentially microporous, with slight effect of air on the porous structure. Oxygen was observed to be markedly incorporated in the carbon matrix during the air treatment process. Cation exchange capacity towards Cu (II) and Cd (II) was tested in batch single ion experimental mode, which proved to be slow and a function of carbon dose, time and initial ion concentration. Copper was up taken more favorably than cadmium, under same conditions, and adsorption of both cations was remarkably enhanced as a consequence of the air treatment procedure. Sequestration of the metal ions was explained on basis of the combined effect of the oxygen functional groups and the phosphorous-containing compounds; both contributing to the total surface acidity character.

• 한국도로학회논문집
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• 제17권2호
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• pp.99-105
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• 2015

PURPOSES: In this study, alkali-activated blast-furnace slag (AABFS) was investigated to determine its capacity to absorb carbon dioxide and to demonstrate the feasibility of its use as an alternative to ordinary Portland cement (OPC). In addition, this study was performed to evaluate the influence of the alkali-activator concentration on the absorption capacity and physicochemical characteristics. METHODS: To determine the characteristics of the AABFS as a function of the activator concentration, blast-furnace slag was activated by using calcium hydroxide at mass ratios ranging from 6 to 24%. The AABFS pastes were used to evaluate the carbon dioxide absorption capacity and rate, while the OPC paste was tested under the same conditions for comparison. The changes in the surface morphology and chemical composition before and after the carbon dioxide absorption were analyzed by using SEM and XRF. RESULTS: At an activator concentration of 24%, the AABFS absorbed approximately 42g of carbon dioxide per mass of paste. Meanwhile, the amount of carbon dioxide absorbed onto the OPC was minimal at the same activator concentration, indicating that the AABFS actively absorbed carbon dioxide as a result of the carbonation reaction on its surface. However, the carbon dioxide absorption capacity and rate decreased as the activator concentration increased, because a high concentration of the activator promoted a hydration reaction and formed a dense internal structure, which was confirmed by SEM analysis. The results of the XRF analyses showed that the CaO ratio increased after the carbon dioxide absorption. CONCLUSIONS : The experimental results confirmed that the AABFS was capable of absorbing large amounts of carbon dioxide, suggesting that it can be used as a dry absorbent for carbon capture and sequestration and as a feasible alternative to OPC. In the formation of AABFS, the activator concentration affected the hydration reaction and changed the surface and internal structure, resulting in changes to the carbon dioxide absorption capacity and rate. Accordingly, the activator ratio should be carefully selected to enhance not only the carbon capture capacity but also the physicochemical characteristics of the geopolymer.

• Environmental Engineering Research
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• 제18권3호
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• pp.151-156
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• 2013

Several soil properties were studied from three young created mitigation wetlands (<10 years old), which were hydrologically comparable in the Piedmont region of Virginia. The properties included soil organic matter (SOM), soil organic carbon (SOC), pH, gravimetric soil moisture, and bulk density ($D_b$). No significant differences were found in the soil properties between the wetlands, except SOM and SOC. SOM and SOC indicated a slight increase with wetland age; the increase was more evident with SOC. Only about a half of SOC variability found in the wetlands was explained by SOM ($R^2$ = 0.499, p < 0.05). The majority of the ratios of SOM to SOC for these silt-loam soils ranged from 2.0 to 3.5, which was higher than the 1.724 Van Bemmelen factor, commonly applied for the conversion of SOM into SOC in estimating the carbon storage or accumulation capacity of wetlands. The results may caution the use of the conversion factor, which may lead to an overestimation of carbon sequestration potentials of newly created wetlands. SOC, but not SOM, was also correlated to $D_b$, which indicates soil compaction typical of most created wetlands that might limit vegetation growth and biomass production, eventually affecting carbon accumulation in the created wetlands.