• Journal of the Mineralogical Society of Korea
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• v.3 no.2
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• pp.79-88
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• 1990

고령토의 조직과 산출상태의 관찰결과 산화철 광물을 침전시킨 철의 주요 근원은 모암인 회장암에 함유된 각섬석과 녹니석이다. X선 회절 분석결과 침철석은 녹니석이 버미큘 라이트로 변질되고 각섬석이 용해되기 시작하는 하부 백색 광석에서 우세하며, 적철석은 각섬석, 녹니석 및 버미큘라이트가 심한 용탈작용을 받는 상부 적갈색 광석이나 열 개에서 침철석과 함께 산출된다. 침철석 및 적철석내 Fe에 대한 Al의 치환량은 각각 6~26 mol% 및 5~8mol%이며 이 두 값 사이에는 비례 관계가 있다. 회절선폭의 크기로부터 계산된 침철석과 적철석의 평균 입자크기는 340$\AA$ 이하이며 침철석은 약간의 침상을 보이는 반면 적철석은 탁상이다. 전자현미경 관찰에 의하면 버미큘라이트와 수반되는 침철석은 침상 또는 성상이나 적갈색 광석에서는 그러한 특징이 작다. 적철석은 육각 또는 원형을 보이나 상부 적갈색 광석에서는 보다 불？칙한 모양이다. 적철석과 침철석의 광물학적 특성을 합성실험에서 보고된 결과들과 비교하여 성인적 측면에서 논의되었다. 이 지역에서는 침철석과 적철석의 생성에 적합한 기후조건들이 중첩된 것으로 생각된다.

• Journal of the Mineralogical Society of Korea
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• v.24 no.3
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• pp.195-204
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• 2011

Exsolution intergrowth of ilmenite and hematite was studied by the Rietveld refinement method. According to the analysis on these two structural analog minerals, it was found that octahedron (M2) of Ti in ilmenite is in the least deformation, then that (M1) of Fe in ilmenite is deformed next, and octaheron deformation of Fe in hematite is between M1 and M2. High pressure compression experiment was performed up to 5.8 GPa, where two minerals' XRD peaks merged completely. Ilmenite shows normal compression behavior, whereas hematite shrinks in very small amount. This kind of abnormal behavior might be due to the differential response to the applied pressure corresponding to the different compressibilities of the minerals each other.

• Journal of the Mineralogical Society of Korea
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• v.26 no.3
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• pp.139-150
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• 2013

In order to effectively leach Fe from pyrite, the application of microwave energy and ammonia solution has been conducted. Pyrite transforms into hematite and pyrrhotite when treated with microwave radiation for 60 minutes, and in this time the highest amount of Fe was leached by the ammonia solution. Up to 99% of the Fe was leached when the experimental conditions were: 325-400 mesh particle size for the pyrite and 60 min. was the microwave exposure time. The ammonia leaching conditions were 0.3 M sulfuric acid, 2.0 M ammonium sulfate and 0.1 M hydrogen peroxide concentration. The pyrite, hematite, and pyrrhotite were not detected using XRD analysis from the solid-residues treated by the ammonia solution except for quartz.

• Journal of the Mineralogical Society of Korea
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• v.28 no.3
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• pp.233-244
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• 2015

In order to study the phase transformation of pyrite and to determine the maximum Fe leaching factors, pyrite samples were an electric furnace and microwave oven and then ammonia leaching was carried out. The rim structure of hematite was observed in the sample exposed in an electric furnace, whereas a rim structure consisting of hematite and pyrrhotite were found in the microwave treated sample. Numerous interconnected cracks were only formed in the microwave treated sample due to the arcing effect, and these cracks were not found in the electric furnace treated sample. Under XRD analysis, pyrite and hematite were observed in the electric furnace treated sample, whereas pyrite, hematite and pyrrhotite were found in the microwave treated sample. The results of the pyrite sample leaching experiments showed that the Fe leaching was maximized with the particle size of -325 mesh, sulfuric acid of 2.0 M, ammonium sulfate of 1.0 M, and hydrogen peroxide of 1.0 M. The electric furnace and microwave treated samples were tested under the maximum leaching conditions, the Fe leaching rate was much greater in the microwave treated sample than in the electric furnace treated sample and the maximum Fe leaching time was also faster in the microwave treated sample than in the electric furnace treated sample. Accordingly, it is expected that the microwave heating can enhance (or improve) Fe leaching in industrial minerals as well as pyrite decomposition in gold ores.

• Journal of the Korean earth science society
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• v.29 no.7
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• pp.523-530
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• 2008

The phase changes and variations of elemental contents in hematite medicinal mineral were investigated by a traditional processing operation including heating and quenching in vinegar. Hematite was processed at $650^{\circ}C$ and $900^{\circ}C$ through at least 5 processing cycles. Metal extraction tests in water were carried out with the processed hematite. Heating and quenching in vinegar could not change the phase of hematite. The effect of this traditional method was not clear because there were no variational trends between extracted elements and the number of processing cycles at $650^{\circ}C$ and $900^{\circ}C$. However, the traditional processing operation of heating and quenching in vinegar was very effective to change the hematite mineral towards soft and easily crushing medicinal material.

• Journal of the Mineralogical Society of Korea
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• v.26 no.1
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• pp.19-25
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• 2013

Recent progress in Martian exploration identified hematite as the major candidate for the strong magnetic anomalies observed in Martian lithosphere. In the present study, grain-size dependence of thermoremanent magnetization and low-temperature stability of room-temperature saturation isothermal remanent magnetization (RTSIRM) were monitored using synthetic hematites. For hematite, the antiferromagnetic spin configuration is re-arranged from being perpendicular to the c-axis to be parallel to the c-axis below the Morin transition ($=T_M$). A large fraction of RTSIRM is demagnetized at $T_M$ (= 260 K) during zero-field cooling from 300 K to 10 K. About 37% of the initial RTSIRM is recovered on warming from 10 K to 300 K. Shallow Martian subsurface at 1~2 km depth would experience low-temperature cooling-warming of $T_M$ because average Martian surficial temperature is about 220 K. However in most Martian lithosphere whose temperatures are higher than 260 K, the very stable magnetic memory of hematite could be a contributor to Martian magnetic anomalies.

• Economic and Environmental Geology
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• v.36 no.6
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• pp.537-543
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• 2003

As pyrite is commonly associated with arsenopyrite, the use of pyrite including arsenopyrite for medicine requires close attention on arsenic toxicity. The toxicity was reduced by traditional processing operations include heating and quenching in vinegar. To verify the scientific effects of this process, pyrite containing many crystals of arsenopyrite was processed at temperatures from 45$0^{\circ}C$ to 85$0^{\circ}C$ and through as many as 5 processing cycles. Arsenopyrite completely disappeared when processed only once at $650^{\circ}C$ while it remained even after 5 processing cycles at 45$0^{\circ}C$. Arsenic was most abundant in medicinal mineral samples processed at 45$0^{\circ}C$ and sharply decreased when processed at $650^{\circ}C$ or 85$0^{\circ}C$ And arsenic extraction test in water was carried out from the processed pyrite medicine on the assumption that pyrite medicines with the lowest As metal content would be most desirable. Arsenic were most abundant in water extracted from medicinal mineral samples processed at 45$0^{\circ}C$ and sharply decreased when processed at $650^{\circ}C$ or 85$0^{\circ}C$. But the extracted As concentrations in water exceeded drinking water standards even when processed at 85$0^{\circ}C$. Increasing temperature promoted elimination of arsenopyrite and reduction of As in medicinal minerals and the extraction solutions. But the effects of processing cycles at the same processing temperature were not clear. Heating temperature is more important than number of processing cycles for the removal of arsenic, and it is necessary to heat pyrite to over $650^{\circ}C$ to remove it.

• Economic and Environmental Geology
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• v.53 no.4
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• pp.347-362
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• 2020

Iron (hydro)oxides in aqueous environments are primarily formed due to mining activities, and they are known to be typical colloidal particles disturbing surrounding environments. Among them, hematites are widespread in surface environments, and their behavior is controlled by diverse factors in aqueous environments. This study was conducted to elucidate the effect of environmental factors, such as ionic composition and strength, pH, and natural organic matter (NOM) on the behavior of colloidal hematite particles. In particular, two analytical methods, such as dynamic light scattering (DLS) and single-particle ICP-MS (spICP-MS), were compared to quantify and characterize the behavior of colloidal hematites. According to the variation of ionic composition and strength, the aggregation/dispersion characteristics of the hematite particles were affected as a result of the change in the thickness of the diffuse double layer as well as the total force of electrostatic repulsion and van der Walls attraction. Besides, the more dispersed the particles were, the farther away the aqueous pH was from their point of zero charge (PZC). The results indicate that the electrostatic and steric (structural) stabilization of the particles was enhanced by the functional groups of the natural organic matter, such as carboxyl and phenolic, as the NOM coated the surface of colloidal hematite particles in aqueous environments. Furthermore, such coating effects seemed to increase with decreasing molar mass of NOM. On the contrary, these stabilization (dispersion) effects of NOM were much more diminished by divalent cations such as Ca²⁺ than monovalent ones (Na⁺), and it could be attributed to the fact that the former acted as bridges much more strongly between the NOM-coated hematite particles than the latter because of the relatively larger ionic potential of the former. Consequently, it was quantitatively confirmed that the behavior of colloidal hematites in aqueous environments was significantly affected by diverse factors, such as ionic composition and strength, pH, and NOM. Among them, the NOM seemed to be the primary and dominant one controlling the behavior of hematite colloids. Meanwhile, the results of the comparative study on DLS and spICPMS suggest that the analyses combining both methods are likely to improve the effectiveness on the quantitative characterization of colloidal behavior in aqueous environments because they showed different strengths: the main advantage of the DLS method is the speed and ease of the operation, while the outstanding merit of the spICP-MS are to consider the shape of particles and the type of aggregation.

• Economic and Environmental Geology
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• v.31 no.4
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• pp.291-296
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• 1998

Pedogenic hematite is a well known agent for sink of pollutants and nutrients and for aggregation of particles in soils. Changes in physical and chemical properties of two sandy loam soils (Anahuac and Crowley soils) from the Southern Coastal Plain, the United States of America, were tested after adding finely ground crystalline hematite prepared for drilling fluid weighting material. There was an increase in hydraulic conductivity (HC) of the soils with addition of up to 3% by weight of hematite but a decrease in HC with addition of more hematite. The aggregate stability (AS) of the soils was not affected by adding hematite. Anahuac soil with higher content of organic matter and lower sodium adsorption ratio (SAR) had higher values of HC and AS than Crowley soil. Adding hematite also resulted in a slight increase in zinc (Zn) adsorption by the soils, but had no influence on the adsorption of phosphate.

• Journal of the Mineralogical Society of Korea
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• v.24 no.2
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• pp.63-71
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• 2011

The mineral phases precipitated in the swamp built for the treatment of the mine drainage of the Dalsung Mine were investigated to reveal the mineralogical changes from schwertmannite to goethite and related behavior of heavy metals. Our XRD results show that most schwertmannite were transformed to goethite except the small portions of the samples in the uppermost part. No significant morphological changes were observed in the samples during mineral transformation by SEM, indicating that this transformation process occurred not from dissolution-precipitation process, but in solid state. Among heavy metals sorbed or coprecipitated in the mineral phases, Pb and Cu concentrations were relatively higher compared with their concentrations in the mine drainage. The relative concentrations of other heavy metals show similar values. The heavy metal concentration in the minerals do not show noticeable differences from uppermost schwertmannite to lower goethite samples, indicating the transformation process without any leaching or additional sorption of heavy metals in the solid state.