• Proceedings of the Korea Water Resources Association Conference
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• 2011.05a
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• pp.309-309
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• 2011

지구온난화와 도시기후 변화에 대응하기 위해 자연의 생태적 기능을 복원하고 환경에 대한 오염부하를 저감하여 도시 환경의 건강성과 지속성을 높이기 위해 도심 내 물순환시스템(urban water circulating system)의 구축이 요구된다. 즉, 물순환시스템을 활용하여 도심 내 다양한 수원(생태하천/호수 유지용수, 하수처리수, 우수, 지하수 등)을 네트워크 및 통합 관리하여 도시 내 물순환의 건전성과 수자원의 재이용률을 향상시킬 수 있다. 이를 위해서 연중 발생량이 일정하고 막대한(66.4억톤/년, 2009년 기준) 하수처리수 방류수는 고도처리를 통해 수질이 양호하며 안정적인 대체 수자원으로 고려된다. 또한, 하수처리수의 재이용은 공공수역으로 배출되는 오염부하량의 총량 삭감 및 상수사용량의 절감과 수자원을 효율적으로 이용한다는 면에서 최근 재이용 사례가 증가하고 있는 추세이다. 그러나, 도심 내 친수공간(생태하천/호수)은 저류수량에 비해 유입수량이 적어 체류시간이 비교적 장시간이고, 이로 인해 부영양화가 쉽게 발생해 수질이 악화된다. 따라서, 본 연구에서는 하수처리수 재이용수를 도심 내 친수공간의 유지용수로 활용 시, 수질정화공정(응집 후 여과, 응집 후 여과+한외여과, 응집 후 여과+한외여과+역삼투 공정)이 친수공간 내 조류성장에 미치는 영향을 파악하기 위해, 하수처리수 재이용수 pilot plant의 수질정화공정별 유출수를 활용해 M. aeruginosa를 시험조류로 조류성장(growth kinetics)을 조사하였다. 조류는 $5\times104$ cells/mL의 초기 농도로 접종하여 배양하였으며, 조류성장에 직접적인 제한인자인 용존반응성인의 농도에 따른 성장속도를 Monod와 변형 Monod Kinetics를 이용해 반포화상수(Ks)와 최대 성장속도(${\mu}$max)를 산정하였다. 실험결과, 역삼투 공정을 제외한 다른 수질정화공정은 비록 영양염류가 80~90% 이상 제거되어 수계의 화학적 성상이 변하였으나 조류성장역학의 변화는 통계학적 (p=0.05)으로 유의할만한 수준은 아닌 것으로 판명되었다. 또한, 수리학적 체류시간이 2주 이상이 될 경우, 역삼투 공정을 제외한 수질정화공정 별 유출수에서는 조류의 과다성장으로 인해 부영양화가 발생하는 것으로 판명되었다. 결론적으로 하수처리수 재이용수를 친수용수로 활용시, 조류성장을 방지하기 위하여 용존반응성인의 농도를 중점적으로 관리하는 수질정화공정 및 유지용수 공급방안을 고려해야하는 것으로 판단된다.

• Economic and Environmental Geology
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• v.31 no.3
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• pp.185-199
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• 1998

Hydrogeochemical and environmental isotope studies were undertaken for various kinds of water samples collected in 1995-1996 from the Bugok geothermal area. Physicochemical data indicate the occurrence of three distinct groups of natural water: Group I ($Na-S0_4$ type water with high temperatures up to $77^{\circ}C$, occurring from the central part of the geothermal area), Group II (warm $Na-HCO_{3}-SO_{4}$ type water, occurring from peripheral sites), Group III ($Ca-HCO_3$ type water, occurring as surface waters and/or shallow cold groundwaters). The Group I waters are further divided into two SUbtypes: Subgroup Ia and Subgroup lb. The general order of increasing degrees of hydrogeochemical evolution (due to the degrees of water-rock interaction) is: Group III$\rightarrow$Group II$\rightarrow$Group I. The Group II and III waters show smaller degrees of interaction with rocks (largely calcite and Na-plagioclase), whereas the Group I waters record the stronger interaction with plagioclase, K-feldspar, mica, chlorite and pyrite. The concentration and sulfur isotope composition of dissolved sulfate appear as a key parameter to understand the origin and evolution of geothermal waters. The sulfate was derived not only from oxidation of sedimentary pyrites in surrounding rocks (especially for the Subgroup Ib waters) but also from magmatic hydrothermal pyrites occurring in restricted fracture channels which extend down to a deep geothermal reservoir (typically for the Subgroup Ia waters). It is shown that the applicability of alkaliion geothermometer calculations for these waters is hampered by several processes (especially the mixing with Mg-rich near-surface waters) that modify the chemical composition. However, the multi-component mineral/water equilibria calculation and available fluid inclusion data indicate that geothermal waters of the Bugok area reach temperatures around $125^{\circ}C$ at deep geothermal reservoir (possibly a cooling pluton). Environmental isotope data (oxygen-18, deuterium and tritium) indicate the origin of all groups of waters from diverse meteoric waters. The Subgroup Ia waters are typically lower in O-H isotope values and tritium content, indicating their derivation from distinct meteoric waters. Combined with tritium isotope data, the Subgroup Ia waters likely represent the older (at least 45 years old) meteoric waters circuated down to the deep geothermal reservoir and record the lesser degrees of mixing with near-surface waters. We propose a model for the genesis and evolution of sulfate-rich geothermal waters.

• Korean Journal of Mineralogy and Petrology
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• v.35 no.3
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• pp.313-331
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• 2022

Natural or native abiotic molecular hydrogen (H₂) is a major component in natural gas, however yet its importance in the global energy sector's usage as clean and renewable energy is underestimated. Here we review the occurrence and geological settings of native hydrogen to demonstrate the much widesprease H₂ occurrence in nature by comparison with previous estimations. Three main types of source rocks have been identified: (1) ultramafic rocks; (2) cratons comprising iron (Fe²⁺)-rich rocks; and (3) uranium-rich rocks. The rocks are closely associated with Precambrian crystalline basement and serpentinized ultramafic rocks from ophiolite and peridotite either at mid-ocean ridges or within continental margin(Zgonnik, 2020). Inorganic geological processes producing H₂ in the source rocks include (a) the reduction of water during the oxidation of Fe²⁺ in minerals (e.g., olivine), (b) water splitting due to radioactive decay, (c) degassing of magma at low pressure, and (d) the reaction of water with surface radicals during mechanical breaking (e.g., fault) of silicate rocks. Native hydrogen are found as a free gas (51%), fluid inclusions in various rock types (29%), and dissolved gas in underground water (20%) (Zgonnik, 2020). Although research on H₂ has not yet been carried out in Korea, the potential H₂ reservoirs in the Gyeongsang Basin are highly probable based on geological and geochemical characteristics including occurrence of ultramafic rocks, inter-bedded basaltic layers and iron-copper deposits within thick sedimentary basin and igneous activities at an active continental margin during the Permian-Paleogene. The native hydrogen is expected to be clean and renewable energy source in the near future. Therefore it is clear that the origin and exploration of the native hydrogen, not yet been revealed by an integrated studies of rock-fluid interaction studies, are a field of special interest, regardless of the presence of economic native hydrogen reservoirs in Korea.