• Title/Summary/Keyword: organic carbon transport

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A Study on Transport Characteristics of Organic and Inorganic Carbons in the Open Estuary of the Tamjin River, Korea (탐진강 열린하구에서 탄소물질의 성상별 이동 특성 연구)

  • Park, Hyung-Geun;Ock, Giyoung
    • Korean Journal of Environmental Biology
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    • v.36 no.4
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    • pp.665-671
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    • 2018
  • This paper represents an investigation into the pattern of carbon transportation and composition on an open estuary in the transition zone between the river and marine environment in Tamjin River where stream water flows into the Gangjin Bay. To conduct the study, seven plots were established along an environmental gradient from river and estuary to the ocean. Surface water samples were collected thrice during the summer rainfalls and non-flooding seasons in 2017. The samples were then measured for the concentrations of dissolved organic carbon ([DOC]), particulate organic carbon ([POC]) and dissolved inorganic carbon ([DIC]). An analysis of the results showed that [POC] did not increase in the river even during the summer rainfall. However, [DOC] increased resulting in a higher [DOC]:[POC] ratios for the non-flooding season compared to summer rainfall events. On the other hand, the marine site of the estuary bay showed the highest [DIC] which was stable relative to those of river sites. The results suggest that in an open estuary zone, river and ocean supplied the open estuary zone with different types of carbon materials; mainly DOC supplied from the river and DIC sourced from the ocean.

pH-Controlled Synthesis of Carbon Xerogels for Coin-Type Organic Supercapacitor Electrodes (pH를 조절하여 제조한 카본제어로젤을 이용한 코인타입 유기계 슈퍼커패시터 전극)

  • Ji Chul Jung;Wonjong Jung
    • Korean Journal of Materials Research
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    • v.33 no.10
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    • pp.430-438
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    • 2023
  • In this study, we synthesized pH-controlled resorcinol-formaldehyde (RF) gels through the polymerization of two starting materials: resorcinol and formaldehyde. The prepared RF gels were dried using an acetone substitution method, and they were subsequently carbonized under nitrogen atmosphere to obtain carbon xerogels (CX_Y) prepared at different pH (Y). The carbon xerogels were utilized as active materials for coin-type organic supercapacitor electrodes to investigate the influence of pH on the electrochemical properties of the carbon xerogels. The carbon xerogels prepared at lower pH (CX_9.5 and CX_10) exhibited sufficient particle growth, with a three-dimensional network of particles during the RF gel formation, resulting in the development of abundant mesopores. Conversely, the carbon xerogels prepared at higher pH (CX_11 and CX_12) retained densely packed structures of small particles, leading to pore collapse and low specific surface areas. Consequently, CX_9.5 and CX_10 showed high specific surface areas, and provided ample adsorption sites for the formation of electric double layers with electrolyte ions. Moreover, the three-dimensional particle network in CX_9.5 and CX_10 significantly enhanced electrical conductivity. The presence of well-developed mesopores in these materials further facilitated the effective transport of electrolyte ions, contributing to their superior performance as organic supercapacitor electrodes. This study confirmed that pH-controlled carbon xerogels are one of the promising active materials for organic supercapacitor electrodes. Furthermore, we concluded that pH during RF gel formation is a crucial factor determining the electrode performance of the carbon xerogels, highlighting the need for precise pH control to obtain high-performance carbon xerogel electrodes.

Transport Characteristic of Heavy Metals in Contaminated Soil (오염된 토양층내의 중금속 이동 특성)

  • 조재범;현재혁;정진홍;김원석
    • Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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    • 1998.11a
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    • pp.236-239
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    • 1998
  • This research was performed to check the transport characteristics of heavy metals in contaminated soil, that is, the influence of humic acid and phosphate on transport characteristics of heavy metals was studied. From the results of column mode experiments about heavy metal behavior, the order time to reach breakthrough and equilibrium was soil + humic acid( 20g ) > soil + humic acid ( 5 g ) > soil without Humic acid addition > soil+humic acid( 50g ). It is because the dissolved organic carbon content increased as the soil organic matter content increased. As the phosphate increased, so did the time to reach breakthrough and equilibrium. The order of time was soil + phosphate( 50 mg ) > soil + phosphate( 20 mg ) > soil . phosphate( 10 mg ) > soil without phosphate addition. It is because the phosphate ion worked as alkalinity donor and the calcium ion co-injected worked as the accelerator of coprecipitation of heavy metals.

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A Mathematical Model Development for the Nitrification-Denitrification Coupled Process

  • ;;T. Prabhakar Clement
    • Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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    • 2003.04a
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    • pp.430-433
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    • 2003
  • Nitrogen pollution in urban and rural groundwater is a common problem and poses a major threat to drinking water supplies based on groundwater. In this work, the kinetics of nitrification-denitrification coupled reactions are modeled and new reaction modules for the RT3D code describing the fate and transport of nitrogen species, dissolved oxygen, dissolved organic carbon, and biomass are developed and tested. The proposed nitrogen transformations and transport model showed very good match with the results of other public codes.

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A Geochemical Boundary in the East Sea (Sea of Japan): Implications for the Paleoclimatic Record

  • Han, Sang-Joon;Hyun, Sang-Min;Huh, Sik;Chun, Jong-Hwa
    • Ocean and Polar Research
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    • v.24 no.2
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    • pp.167-175
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    • 2002
  • Sediment from six piston cores from the East Sea (Sea of Japan) was analyzed for evidence of paleoceanographic changes and paleoclimatic variation. A distinct geochemical boundary is evident in major element concentrations and organic carbon content of most cores near the 10-ka horizon. This distinctive basal Holocene change is interpreted to be largely the result of changing sediment sources, an interpretation supported by TiO_2/Al_2O_3$ ratios. Organic carbon and carbonate contents also differ significantly between the Holocene and glacial intervals. The C/N ratio of organic matter is greater than 10 during the glacial period, but is less than 10 for the Holocene, suggesting that the influx of terrigenous organic matter was more volumetrically important than marine organic matter during glacial times. The chemical index of weathering (CIW) is higher for the Holocene than the glacial interval, and changes markedly at the basal Holocene geochemical boundary. Silt fractions are higher in the glacial interval, suggesting a strong effect of climate on silt particle transportation: terrigenous aluminosilicates and continental organic carbon transport were higher during glacial times than during the Holocene. Differences in sediment composition between the Holocene and glacial period are interpreted to have been climatically induced.

Characterization of Clastic and Organic Sediments Near Dokdo, Korea (독도 인근 해저퇴적물과 유기 퇴적물 분포 특성)

  • Jun, Chang Pyo;Kim, Chang Hwan;Lee, Seong-Joo
    • Journal of the Mineralogical Society of Korea
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    • v.26 no.2
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    • pp.65-80
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    • 2013
  • Sediment transport mechanism and distribution of organic sediments are elucidated by the study of particle size, mineralogy, organic matters and microfossils of the surface samples collected from seafloor adjacent Dokdo island. Shallow marine sediments are dominated by coarse- grained sediments including gravel and sand, and their sedimentation has mainly been controlled by traction. While the samples collected from oceanic zone are characterized by high contents of fine- grained sediments such as silt and mud in bulk sediments, and the changes of mineral compositions including clay minerals and feldspar, and the fine sediments have been deposited mainly by suspension. The change of organic sedimentary communities is detected between neritic and oceanic zone. Although marine organic matter is predominant in neritic zone, terrestrial organic matter is monopolized according to increasing water depth. This trend is associated with grain size of sediments. The results also suggest that high pollen concentrations in whole organic matters may played an important role in excessive organic carbon in sediment.

Radiocarbon for Studies of Organic Matter Cycling in the Ocean (방사성탄소를 이용한 해양 유기탄소 순환 연구 동향)

  • Hwang, Jeomshik
    • The Sea:JOURNAL OF THE KOREAN SOCIETY OF OCEANOGRAPHY
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    • v.17 no.3
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    • pp.189-201
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    • 2012
  • Radiocarbon is a powerful tool for studies of carbon cycling in the ocean. Development of measurement technology of accelerator mass spectrometry has enabled researchers to measure radiocarbon even in specific compounds. In this paper, a brief introduction on radiocarbon measurement and reporting of radiocarbon data is provided. Researches that used radiocarbon measurements on bulk organic matter, organic compound classes, and specific organic compounds are reviewed. Examples include works to understand the cycling of particulate and dissolved organic matter, biochemical composition of particulate organic matter, post-depositional transport of sedimentary organic matter, selective incorporation of fresh organic matter by benthic organisms, chemoautotrophy by archaea, and sources of halogenated chemical compounds found in marine mammals.

Ecological modeling for toxic substances - I . Numerical simulation of transport and fate of Nonylphenol in Tokyo Bay- (유해화학물질의 생태계 모델링 - I. 동경만 Nonylphenol의 환경동태 해석 -)

  • Kim Dong-Myung;Shiraishi Hiroaki
    • Journal of Environmental Science International
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    • v.14 no.9
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    • pp.827-835
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    • 2005
  • A three-dimensional ecological model (EMT -3D) was applied to Nonylphenol in Tokyo Bay. EMT -3D was calibrated with data obtained in the study area. The simulated results of dissolved Nonylphenol were in good agreement with the observed values, with a correlation coefficient(R) of 0.7707 and a coefficient of determination (R2) of 0.5940. The results of sensitivity analysis showed that biodegradation rate and bioconcentration factor are most important factors for dissolved Nonylphenol and Nonylphenol in phytoplankton, respectively. In the case of Nonylphenol in particulate organic carbon, biodegradation rate and partition coefficient were important factors. Therefore, the parameters must be carefully considered in the modeling. The mass balance results showed that standing stocks of Nonylphenol in water, in particulate organic carbon and in phytoplankton are $8.60\times 10^5\;g,\;2.19\times 10^2\;g\;and\;3.78\times 10^0\;g$ respectively. With respect to the flux of dissolved Nonylphenol, biodegradation in the water column, effluent to the open sea and partition to particulate organic carbon were $6.02\times10^3\;g/day,\;6.02\times10^2\;g/day\;and\;1.02\times10^1\;g/day$, respectively.

Removal of Natural Organic Matter (NOM) by Carbon Nanotubes Modified PVDF Membrane (탄소나노튜브(CNT)-PVDF 막을 이용한 자연용존유기물 제거)

  • Cho, Hyun-Hee;Cha, Min-Whan;Park, Jae-Woo
    • Journal of Korean Society on Water Environment
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    • v.28 no.1
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    • pp.148-156
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    • 2012
  • In this research, the application of carbon nanotubes (CNTs) modified PVDF (polyvinylidene fluoride) membrane was tested as a simply and beginning attempt to overcome membrane fouling because CNTs importantly affect the transport of natural organic matter (NOM). Suwannee River fulvic acid (SRFA) as the representative of NOM was selected and its sorption results with single-walled CNT (SWCNT), multi-walled CNT (MWCNT), and oxidized MWCNT (O-MWCNT) were obtained through the batch experiment. SRFA sorption isotherms had a strong nonlinearity and its sorption capacity followed the order O-MWCNT < MWCNT < SWCNT. The adsorbed mass of SRFA on each CNT decreased as a function of pH due to their charge repulsion. For the CNT-PVDF membrane filtration experiments, the suspended CNT solution (10 mg/40 mL) was incorporated into $0.45{\mu}m$-PVDF membrane and 5 mg/L of SRFA solution was monitored using UV detector connected with high pressure pump after passing through CNT-PVDF membrane. The SRFA removal efficiency by MWCNT-PVDF membrane was the strongest among other modified membranes. This suggests that the CNT modified microfiltration (MF) membrane might effectively and selectively apply to treat the contaminated water including organic compounds in the presence of NOM.

A New Approach on Adsorption and Transport of Cesium in Organic Matter-rich Soil and Groundwater Environments Changed by Wildfires (산불로 인해 변화하는 토양지하수 환경에서의 세슘 흡착 및 거동에 대한 새로운 고찰)

  • Bae, Hyojin;Choung, Sungwook;Jeong, Jina
    • Journal of Korean Society on Water Environment
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    • v.38 no.1
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    • pp.10-18
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    • 2022
  • This study was conducted to investigate the effect of soil and groundwater environment changed by wildfire on cesium adsorption and transport. Soil samples (A, B) used in the study were collected from Gangwon-do, where wildfires frequently occur, and the adsorption and transport of cesium in the samples were evaluated through batch and column experiments. As a result of the batch adsorption experiments with various concentrations of cesium (CW ≈ 10~105 ㎍/L), the adsorption distribution coefficient (Kd) of cesium was higher in sample A for all observed concentrations. It means that the adsorption capacity of sample A was higher to that of sample B, which was also confirmed through the parameters of adsorption isotherm models (Freundlich and Langmuir model) applied to the experimental results. The fixed bed column experiments simulated the actual soil and groundwater environment, and they showed that cesium was retarded approximately 43 and 27 times than a nonreactive tracer in sample A and B, respectively. In particular, a significant retardation occurred in the sample A. Although sample A contains little clays, total organic carbon (TOC) contents were 3 times greater than sample B. These results imply that particulate organic matter caused by wildfire might influence the adsorption and transport of cesium in the organic matter-rich soil and groundwater environment.