• Journal of the Mineralogical Society of Korea
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• v.13 no.2
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• pp.65-72
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• 2000

미생물을 이용한 광물 합성은 현재 초기 연구단계에 있으나 신소재 개발측면에서 다야한 활용성을 보인다. 본 연구의 목적은 철환원 박테리아를 이용한 자철석 합성에 있어 미치는 환경조건들을 알아보는데 있다. 본 연구를 위해 지하 3-km 코아 시료에서 분리한 호열성 철 환원 박테리아인 TOR-39을 이용하였다. TOR-39은 $65^{\circ}C$에서 12시간이내에 비정질 철수화물을 환원시켜 자철석을 형성한다. 25일 동안 배양하여 형성된 자철석은 정육각형 모양으로 입자 크기는 50-100 나노미터이다. TOR-39을 이용한 자철석 합성시 적절한 조건은 pH는 7.9-8.5, Eh는 -200 mV 이하, 배양기간은 3-25일 그리고 온도는 $45-75^{\circ}C$이다. 미생물에 의한 자철석 합성은 나노미터 크기의 광물을 직접 합성하므로, 산업적으로 많은 이용 가치를 가질 것으로 본다.

• Journal of the Mineralogical Society of Korea
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• v.14 no.2
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• pp.111-118
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• 2001

The use of bacteria as a novel biotechnology to facilitate the production of nanoparticles is in its infancy. Cobalt-substituted magnetite nanoparticles were synthesized by a thermophilic iron(III)-reducing bacterium, TOR-39, under anaerobic conditions using amorphous Fe(III) oxyhydroxides plus cobalt ( $Co^{2+}$ and $Co^{3+}$ ) as an electron acceptor and organic carbon as an electron donor. Microbial processes produced copious amounts of nm-sized cobalt substituted magnetites. Chemical analysis and X-ray powder diffraction analysis showed that cobalt was substituted into biologically facilitated magnetites. Microbially facilitated synthesis of the cobalt-substituted magnetites may expand the possible use of the specialized ferromagnetic particles.

• Journal of the Mineralogical Society of Korea
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• v.24 no.1
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• pp.37-42
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• 2011

Magnetic properties at low-temperatures can diagnose the presence of certain magnetic minerals in rocks. At the Verwey transition temperature ($T_v$, ~105~120 K), magnetite transforms from monoclinic to cubic structure as the temperature increases. At the isotropic point ($T_i$, ~135 K), magnetocrystalline anisotropic constant of magnetite passes through zero (from negative to positive) as the temperature decreases so that its optimal remanence acquisition axis changes from [111] to [001]. A sharp remanence drop was observed at $T_v$ during warming of LTSIRM (low-temperature saturation isothermal remanent magnetization). For cooling of RTSIRM (room-temperature saturation isothermal remanent magnetization), the remanence decreased on passing $T_i$ and $T_v$. On warming of RTSIRM, remanence recovery becomes more prominent as the average grain size of magnetite increases. In summary, the SIRM memory decreases with increasing grain size of magnetite. A similar, but rather gradual, remanence transition occurs for natural samples due to contribution of cations other than Fe. As a non-destructive tool, low-temperature magnetic behavior is sensitive to unravel the magnetic remanence carriers in terrestrial rocks or meteorites.

• Economic and Environmental Geology
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• v.45 no.2
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• pp.195-204
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• 2012

Biomineralization has been explored for geochemical cycles and microbial tolerance mechanisms to metal toxicity. Here, we are introducing NanoFermentation which enables economic, environmentally friendly, requiring low input energy, and scalable manufacturing of nano-dimensioned magnetite. We are also focusing on controlling factors of crystallite size which can determine superparamagnetism and ferrimagnetism. Controlling factors are such as microbial species, temperature, incubation time, medium composition, substituted elements and their concentration, precursor type, reaction volume, precursor concentration density and their combinations. Crystallite size distribution of biomagnetite depends on the balance between nuclei generation and crystal growth. Biomineralization will elucidate elemental cycles on earth crust and microbial ecology as well as it will be applied to material sciences and devices via massive production of nanomaterials.

• Journal of the Mineralogical Society of Korea
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• v.26 no.4
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• pp.299-312
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• 2013

Magnetite, a major constituent mineral of the Hongcheon carbonatite-phoscorite complex, was produced over three stages in each rock type and decreased in quantity toward the late stage. Electron microprobe analyses for magnetite revealed that Ti and V were detected in traces, but showed increasing tendency from early to late stage. On the contrary, Mg and Mn decreased distinctly, and it is the general differentiation trend of carbonatitic magma. Al also showed decreasing tendency in carbonatite and phoscorite, and Cr was mostly below detection limit except late phoscorite. In early stage, $Fe^{2+}$ was largely replaced by $Mg{2+}$ and $Mn^{2+}$, and $Fe^{3+}$ by $Al^{3+}$ in magnetite, but it has nearly pure composition in late stage. Tendency of increase in V and decrease in Mn toward late stage represents that magma differentiation progressed under the condition of decreasing oxygen fugacity. Low concentrations of Mg, Al, Cr and Ti, as well as the absence of olivine and phlogopite, suggest that the Hongcheon carbonatite-phoscorite complex was generated from depleted magma. Especially, lower concentrations of Mg in magnetite compared to other typical carbonatite-phoscorite complex, and abundant occurrence of Fe-carbonate minerals and quartz in late stage, suggest that magma differentiation of the Hongcheon carbonatite-phoscorite proceeded to the latest stage.

• Journal of the Mineralogical Society of Korea
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• v.21 no.4
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• pp.425-434
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• 2008

Arsenic contamination in soil and groundwater has recently been one of the most serious environmental concerns. This arsenic contamination can be originated from natural or anthropogenic sources. It has been well known that arsenic behavior in geo-environmental is controlled by various oxides or hydroxides, such as those of iron, manganese, and aluminum, and clay minerals. Among those, particularly, iron (oxy)hydroxides are the most effective scavengers for arsenic. For this reason, this study characterized arsenic adsorption of magnetite which is a kind of iron oxide in nature. The physicochemcial features of the magnetite were investigated to evaluate adsorption of arsenite [As(III)] and arsenate [As(V)] onto magnetite. In addition to experiments on adsorption equilibria, kinetic experiments were also conducted. The point of zero charge (PZC) and specific surface area of the laboratory-synthesized magnetite used as an arsenic adsorbent were measured 6.56 and $16.6\;g/m^2$, which values seem to be relatively smaller than those of the other iron (oxy)hydroxides. From the results of equilibria experiments, arsenite was much more adsorbed onto magnetite than arsenate, indicating the affinity of arsenite on magnetite is larger than arsenate. Arsenite and arsenate showed adsorption maxima at pHs 7 and 2, respectively. In particular, adsorption of arsenate decreased with increase in pH as a result of electrical repulsion caused by anionic arsenate and negatively-charged surface of magnetite. These results indicate that the surface charge of magnetite and the chemical speciation of arsenic should be considered as the most crucial factors in controlling arsenic. The results of kinetic experiments show that arsenate was adsorbed more quickly than arsenite and adsorption of arsenic was investigated to be mostly completed within the duration of 4 hours, regardless of chemical speciation of arsenic. When the results of kinetic experiments were fitted to a variety of kinetic models proposed so far, power function and elovich model were evaluated to be the most suitable ones which can simulate adsorption kinetics of two kinds of arsenic species onto magnetite.

• The Journal of the Petrological Society of Korea
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• v.7 no.2
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• pp.98-110
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• 1998

Hongcheon magnetite deposit is embedded, as a lens shape, in biotite banded gneiss belonging to the Gyeonggi metamorphic complex. It gradationally changes to the host quartz-feldspathic banded gneiss in the mineral composition. Magnetite ore bodies are composed of magnetite ores and magnetite banded gneiss which gradationally change each other in the amount of magnetite. They consist mainly of magnetite, quartz, plagioclase and chlorite accompanied with amphibole, biotite, muscovite, monazite, apatite, ankerite, siderite, rhodochrositic dolomite, calcite and rutile. Amphibole is subdivided into hornblende, richterite and magnesio-riebekite in magnetite ores, and magnesio-, ferro- or actinolitic hornblende in magnetite banded gneiss. The variation in chemical composition may be influenced by bulk composition and controlled mainly by glaucophane $Na(M4)Al_3^{VI}=CaMg$ and richterite Na(M4)Na(A)=Ca substitutions. Biotite in magnetite banded gneiss has an annite composition. Chlorite changes in chemical composition from pycnochlorite to diabantite in magnetite ores and belongs to pycnochlorite in magnetite banded gneiss. The mafic minerals and feldspar have been strongly altered by carbonate minerals which are secondarily formed by introduced hydrothermal solution. Fe-bearing carbonate minerals can be subdivided into ankerite, siderite and rhodochrositic dolomite according to the ratio of Fe-Mg-Mn component.

• Economic and Environmental Geology
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• v.34 no.1
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• pp.147-156
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• 2001

Titanomagnetites, the primary magnetic mineral in submarine basalts, generally has undergone some degree of low temperature oxidation to cation-deficient titanomaghemites. Synthetic analogues of natural titanomaghemite have been prepared by the removal of iron mechanism employing a low-temperature aqueous oxidation method. Along with the low-temperature oxidation of titanomagnetite, magnetic properties of titanomagnetite change sensitively. The results show that as the degree of oxidation increases, the Curie temperature (Tc) increases from $166^{\circ}C$ to $400^{\circ}C$, saturation magnetization (Ms) at room temperature decreases from 126.30 kAlm (25.26 emu/g) to 16.55 kAlrn (3.31 emu/g) monotonously, and coercive force (Hc) and coercivity of remanence (Hcr) increase from 6.13 kAlm (77 Oe) and 23.24 kAlm (292 Oe) to 38.83 kNm (488 Oe) and 47.03 kAlm (591 Oe), respectively. Low field susceptibility (X) decreases from $2023{\times}10^{-6}SI$ to $84{\times}10^{-6}S1$. Based on the results of this study, it is interpreted that the NRM intensity variations of the oceanic crust of presetnt day to 30 Ma is due to the formation of titanomahemites of various degree of oxidation by the low-temperature aqueous oxidation of titanomagnetite, while the magnetic intensity changes of the oceanic crust older than 30 Ma is presumably caused by the combined effect of the formation of titanomaghemites and subsequent inversion of titanomagnemites. DetaileJ causes of the variations of NRM intensity of the oceanic crust may be revealed by systematic studies of the oceanic-floor basalts in the future.

• Journal of the Mineralogical Society of Korea
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• v.19 no.4 s.50
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• pp.265-275
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• 2006

It is in its infancy to use bacteria as a novel biotechnology for leaching precious and heavy metals from raw materials. The objective of this study was to investigate biogeochemical processes of iron leaching from magnetite reduction by iron-reducing bacteria isolated from intertidal flat sediments, southwestern part of Korea. Microbial leaching experiments were performed using commercial magnetite, Aldrich magnetite, in well-defined mediums with and without bacteria. Water soluble Fe production was determined by ICP analysis of bioleached samples in comparison to uninoculated controls, and the resulting precipitated solids were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). The extent of iron leaching from magnetite in the aerobic conditions (Fe = 107 ppm) was higher than that in the anaerobic environments (Fe = 94 ppm). In the anaerobic conditions, Fe(III) in commercial magnetite was also reduced to Fe(II), but no secondary mineral phases were observed. Amorphous iron oxides formed in the medium under aerobic conditions where there was sufficient supply of oxygen from the atmosphere. SEM observation suggests that the reduction process involves dissolution-precipitation mechanisms as opposed to solid state conversion of magnetite to amorphous iron oxides. The ability of bacteria to leach soluble iron and precipitate amorphous iron oxides from crystalline magnetite could have significant implications for biogeochemical processes in sediments where Fe(III) in magnetite plays an important role in the largest pool of electron acceptor as well as the tool as a novel biotechnology for leaching precious and heavy metals from raw materials.

• Journal of the Korea Institute of Building Construction
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• v.17 no.6
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• pp.483-492
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• 2017

Recently, the coastal area has become the popular place for infrastructure development. To provide a beautiful scenary of costal area to nearby facilities without any hinderance, and also to protect those facilities from the sea water overflow, it is necessary to develop a new type of wave dissipating block, which is a turning wave block. It is noticeable that the top of the turning wave block is flat and thus can provide spaces for various purposes. However, the unit weight of the block decreases due to the presence of pipeline that is installed for turning the direction of the waves. In order to mitigate such problem, a heavyweight concrete needs to be used to increase the resistance against tidal waves. The copper slag and magnetite were used as a source of fine and coarse aggregate, respectively. The 28 day compressive strength of concrete incorporating ordinary and heavyweight aggregate did not show significant differences. It should be noted that the chloride ion penetration resistance was evaluated using NT-BUILD 492 rather than ASTM C 1202 method because concrete incorporating magnetite as a coarse aggregate showed excessive current flow by ASTM C 1202 method. According to the results from NT Build 492 method, which uses the penetration depth of chlorine ions to obtain chloride ion diffusivity, the heavyweight concrete incorporating the copper slag and the magnetite showed the best resistance against the chloride ion penetration. Therefore, it is reasonable to say that heavyweight concrete made with copper slag and magnetite can be used for production of turning wave block.