• Korean Journal of Microbiology
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• v.49 no.4
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• pp.321-327
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• 2013

In the present work, the reactors that harbor bacterial biofilms including ammonia-oxidizing bacteria (AOB) and heterotrophic bacteria were treated with a continuous dose of chlorite ($0.66{\pm}0.01mg/L$) either with or without monochloramine at $1.77{\pm}0.03mg/L$. Both chlorite alone and combined chlorite-monochloramine applications effectively reduced biofilm and bulk AOB levels to near or below the detection limit ($0.6MPN/cm^2$ and 0.2 MPN/ml). The combined chlorite-monochloramine application exhibited greater AOB inactivation than chlorite alone. Unlike AOB, heterotrophic plate count (HPC) was unaffected by chlorite alone. In contrast to chlorite-only application, a combination of chlorite and monochloramine resulted in a significant reduction in HPC levels with log reductions of 3.1 and 3.0 for biofilm and bulk water, respectively. The results demonstrate that the combined chlorite-monochloramine application can provide an effective treatment for the inhibition of AOB and heterotrophic bacteria in a drinking water distribution system.

• Journal of the Mineralogical Society of Korea
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• v.13 no.4
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• pp.196-204
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• 2000

We present characteristics of hydrothermal chlorite and its interstratification with 7-$\AA$ mineral phase that occur in the propylitic alteration zone of the Bobae sericite deposit formed in rhyodacitic tuff. Chlorite is found as disseminated fine-grained aggregate or replacement materials of precursor minerals such as Fe-oxides and amphibole. Based on X-ray diffraction(XRD), all chlorites belong to IIb polytype and the (060) reflections averaging $1.53~1.54\AA$ indicate a trioctahedral structure. Chemical compositions of chlorite show that the Fe/(Fe+Mg) values are mostly in the range of 0.44~0.53, and cation deficiencies in octahedral sites range from 0.06 to 0.37. Under scanning electron microscope(SEM) chlorite occurs as well-crystallized aggregates and is subparallely stacked in interstices or between grain boundaries of associated minerals. transmission electron microscopic(TEM) images reveal that chlorite shows regular layers with $14-\AA$ spacings, locally interstratified with $7-\AA$ or $21-\AA$ periodicities. The $21- \AA$ periodicity corresponds to the sum of the $d_{001}$ values of chlorite and $7-\AA$ phase. The chlorite packet coexisting with 7-$\AA$ layers displays abundant defects such as edge dislocations and layer terminations. Selected-area electron diffraction(SAED) indicates that chlorite and $7-\AA$ phase are randomly interstratified in the mixed-layer areas. We propose a lateral change of layers for the polymorphic transition of $7-\AA$ phase to chlorite.e.

• Journal of the Mineralogical Society of Korea
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• v.12 no.2
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• pp.66-76
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• 1999

Intergrowth texture of biotite and chlorite crystals within an amphibolitic schist of the northwestern Okchon metamorphic belt was investigated using back-scattered electron (BSE) imaging and high-resolution transmission electron microscopy (HRTEM). BSE images show that thin chlorite and biotite packets are mixed along (001) plane to result in intergrowth texture. In addition, rutile particles of submicron size occur exclusively at the boundaries between biotite and chlorite stacks. HRTEM investigation and remnant biotite layers are closely associated with such boundaries, suggestinga possibility that chlorite layers were formed from biotite during retrograde metamorphic reaction. Such intepretation of the origin of intergrowth texture can be further supported biotite is approximately 2 w%, and that of chlorite usually lower than 0.2 wt%. Ti was apparently leached out during the alteratin of biotite to precipitate rutile particles at the such rutile particles could be an important indicator showing that the intergrowth texture of chlorite and biotite is originated by a retrograde metamorphism rather than by incomplete chlorite-to-biotite reaction during prograde metamorphism. Biotite crystals contain intercalated chlorite layers will result in somewhat high Mg and Al, and the use of such inhomogeneous biotite will result in impreciese geothermobarometric calculations.

• Journal of the Mineralogical Society of Korea
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• v.13 no.2
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• pp.53-64
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• 2000

Chlorite from the talc deposits in the Chungnam area, Korea, has been studied using electron microprobe analysis and high resolution transmission electron microscopy (HRTEM), Talc orea are hydrothermal alteration products of serpentinite which was originated from ultramafic rocks. Chlorite occurs in close association with talc ores of with the black alteration zone between talc ore bodies and granitic gneiss. It is the most abundant impurity mineral of talc ores. Chlorite in association with talc is characterized by very high but narrow variation in Mg/(Mg+Fe) ratios (0.784~0.951), significant octahedral substitution (-0.200~0.692), wide variation in Al contents (1.085~3.160 / 14 oxygens), and high Cr and Ni contents. It was formed under a very limited but high Mg/(Mg+Fe) condition in close connection with serpentinite. Chlorite in the black alteration zone is characterized by a high Fe content, wide variation in Mg/(Mg+Fe) ratios (0.378~0.852), narrow octahedral substitution (-0.035~0.525), high narrow Al contents (1.468~2.959), and low Cr and Ni contents. It was formed under a low Mg/(Mg+Fe) and relatively Al-rich condition in close connection with county rocks. Two different chemical modes for chlorite suggest two different origins for two different chlorites. Although most of chlorites show typical 14-$\AA$ lattice fringe images under HRTEM, some chlorites show fringe images of 21-$\AA$ (14$\AA$+7$\AA$) spacings within (001) lattice-fringe images of chlorite (14$\AA$). But brown chlorite from the black zone has high Ti and K contents suggesting that mica was the precursor of brown chlorite. Such possibility is also supported by the fact that lattice-fringe images of brown chlorite show 14-$\AA$ chlorite layers in which 10-$\AA$ mica single layer or packets are interlayered. Partial terminations from 3 mica layers to 2 chlorite layers are often observed. It, therefore, is suggested that the chlorite associated with talc ores is a hydrothermal alteration products of serpentinite, whereas the chlorites in the black alteration zone is a hydrothermal alteration product of granitic gnesis under a partial influence of serpentinite.

• Journal of the Mineralogical Society of Korea
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• v.10 no.1
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• pp.60-73
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• 1997

The talc of the Daeheung, Pyeongan, and Cheongdang (Shinyang) talc deposits in the Yesan-Gongju-Cheongyang area is a hydrothermal alteration product of serpentinite originated from ultramafic rocks. The mineral assemblages in alteration zones are: serpentine, serpentine-talc, talc, talc-chlorite, talc-phlogopite-chlorite, and talc-tremolite-chlorite. Chemical distributions in both the Al2O3-FeO-MgO system and the immobile elements suggest that the serpentine-talc and talc rocks are the reaction product of ultramafic rocks and silicic hydrothermal solution without addition of other granitic components, whereas chlorite-, phlogopite-, and tremolite-bearing rocks are the metasomatic alteration product of serpentinite by hydrothermal solution affected by granitic gneiss. Discontinuities in the immobile element ratios of mineral assemblages are due to changes in their mineralogy. The relative contents of Al2O3, TiO2, Zr in the talc-phlogopite-chlorite and talc-tremolite-chlorite rocks increase irregularly with increasing phlogopite, tremolite, and/or chlorite contents in contrast to other ore types. But the relative contents of Cr, Ni, and Co are uniform in all the mineral assemblages. Chemistry of each mineral assemblage formed by steatitization of serpentinite suggests that Cr, Co, Ni, MgO, and Fe2O3 are relatively immobile during the alteration, whereas SiO2, Al2O3, CaO, and K2O are highly increased. The contents of chlorite, phlogopite, and tremolite in each mineral assemblage might be controlled by addition of Al2O3, K2O, and CaO, respectively. The high contents of other elements than immobile elements in the altered rocks as compared with unaltered rocks indicate that a large amount of elements were introduced from hydrothermal solution up to about 8∼41% in total mass showing maximum value in the talc-phlogopite-chlorite rock.

• Journal of the Mineralogical Society of Korea
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• v.18 no.3 s.45
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• pp.195-204
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• 2005

Interlayered structures of talc and chlorite in the talc deposits of the Yugu area are studied using transmission electron microscope. Packets of chlorite-like layer in talcs or packets of talc-like layer in chlorites are commonly observed. Randomly interlayered features of talc and chlorite are locally observed in some specimens. Reactions observed in the present study include the addition or removal of a brucite-like layer in the interlayer region of the talc or chlorite resulting in the , transformation between a talc and a chlorite layers and breakdown or formation of a talc-like layer resulting in transformation between two talc layer and one chlorite layer. Both reactions are accompanied by a significant change in volume. In addition to these mechanisms, there are two volume conserving mechanisms; the combination of both mechanisms and mutual transformation in a complex manner. Reactions from 2 chlorite layers to 3 talc layers, from 2 chlorite layers + 1 talc layers to 1 chlorite layers + 3 talc layers, and from 3 chlorite layers to 5 talc layers are observed among the complex type mechanisms.

• Journal of the Mineralogical Society of Korea
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• v.8 no.1
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• pp.1-12
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• 1995

옥천 변성대 남서부 지역에서 산출되는 변성 니질암에서는 muscovite, biotite 및 chlorite를 주로하는 phyllosilicate가 서로 intergrowth 또는 interlayer를 이루는 것이 편광현미경 관찰, EPMA 분석, Back Scattered Electron (BSE) image 관찰 및 Transmission Electron Micro-scope(TEM) 관찰을 통하여 확인되었다. 이들 광물들은 편광현미경 관찰에서 흔히 각각의 입자를 식별할 수 없을 정도의 미세 규모로 서로 intergrow 되어 있으며BSE image에서는 0.1$\mu\textrm{m}$ 이하의 아주 작은 크기에서부터 10.0$\mu\textrm{m}$ 정도 크기까지 다양한 규모의 intergrow를 형성하고 있음이 관찰되었다. TEM scale에서는 개별 layer 크기(약 10$\AA$)에서부터 수십 개 layer 크기의 interlayering을 보여준다. 이와 같은 intergrowth 또는 interlayering의 결과로 EPMA 분석에서 종종 보기에는 규진(homogeneous)한 입자라 하더라도 두 개 이상의 광물 성분이 섞여 있는 분석값을 나타내며 이러한 nonstoichiometry는 BSE image에서 interlayer(또는 intergrow) 된 것으로 관찰되는 부분에서 더욱 두드러진다.Chlorite zone에서는 chlorite와 muscovite의 interlayering (C/M)이 주로 발견되며 biotite zone과 garnet zone에서는 chlorite와 biotite의 interlayer (C/B)가 주로 관찰된다. 이는 chlorite zone에서는 속성작용에서 보편적으로 나타나는 C/M으로부터 chlorite가 분리되는 광물반응이 일어나는데 반해서 biotite zone과 garnet zone에서는 chlorite로부터 C/B를 거쳐 biotite를 생성하는 광물반응이 일어나는 것을 의미한다. 이와 같은 현상은 변성작용에서 phollosilicate의 광물반응의 엄밀한 의미에서는 평형(equilibrium) 상태에서 균질한 광물을 생성하기보다는 비평형(disequilibrium) 반응으로 일어난다는 것을 의미한다.

• Economic and Environmental Geology
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• v.26 no.3
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• pp.289-309
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• 1993

Milyang pyrophyllite deposit which was formed by hydrothermal alteration occurs in Late Cretaceous andesitic tuff in the Milyang area, Gyeongsangnamdo. The wall rock alteration and genesis of the Milyang pyrophyllite deposit were studied. The ore minerals are composed dominantly of pyrophyllite accompanied by small amounts of quartz, kaolinite, pyrite, dumortierite and diaspore. The alteration halo of this deposit can be divided into three zones on the basis of mineral assemblage; pyrophyllite, sericite and chlorite zone. The common mineral assemblages of each alteration zone are as follows: (1) pyrophyllite zone; pyrophyllite-quartz-kaolinite-pyrite-dumortierite-diaspore, (2) sericite zone; sericite-quartz-pyrite-kaolinite, and (3) chlorite zone; chlorite-plagioclase-quartz. Major element chemistry shows that characteristic depletion in MgO, CaO, and $Na_2O$ and relative increase in FeO from less altered chlorite zone to extensively altered pyrophyllite zone corresponding to variation in mineral assemblages. The paragenesis of ore minerals, oxygen isotope data, chlorite and illite geothermometry suggest that ore deposit was formed at about $250{\sim}330^{\circ}C$. Both hydrogen and silica activities are high in pyrophyllite zone. Potassium activity increases in sericite zone while hydrogen activity becomes low in chlorite zone. The pyrophyllite zone was formed relatively higher temperature than those of sericite and chlorite zones. The ore fluid was considered to be magmatic water in origin derived from the residual granitic magma which interacted with meteoric water.

• Economic and Environmental Geology
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• v.30 no.2
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• pp.163-174
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• 1997

Precambrian metapelites and metapsammites of the Jinan-Osu area (so-called Seologri and Yongamsan Formation) consist of black slate, phyllite, mica schist, quartzite and rarely calc schist. They are intruded by Sunkagsan granite gneiss, Foliated granodiorite, Amphibolite, Sunchang foliated granite and Namwon granite. Mylonite texture, crenulation cleavage and minor shear zone are common. The meta-sedimentary rocks include various rock-fragments xenoliths in size (up to 3 cm) and rock-type. They have various porphyroblastic spots in size (up to 1 cm) and their mineral composition is different. The xenoliths are schists, granite and quartzite, which are rectangular or lens form and recrystallized muscovite, chlorite and quartz. Spots are andalusite and biotite aggregates extensively replaced by chlorite. The metamorphic terrain is divided into three zones of progressive metamorphism on the basis of mineral assemblage. They are chlorite zone, chloite-biotite zone and andalusite-biotite zone ascending order, from west to east approximately. Isograd reactions are phengitic muscovite + chlorite = less phengitic muscovite + biotite + quartz + $H_2O$ and muscovite + chlorite + quartz = andalusite + biotite + $H_2O$ between the chlorite zone and chlorite-biotite zone, and between the chloritebiotite zone and andalusite-biotite zone, respectively. Sample B6 (exposed near the Obong-ri) includes staurolites and greenish biotites, that is different in mineral assemblage and chemical composition from the meta-sedimentary rocks. Sample A12 (exposed near the Shinam-ri) has greenish white spots (up to 1 cm in diameter) mainly composed of Kfeldspar, quartz and sillimanite replaced by muscovite.

• Journal of the Korean Chemical Society
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• v.44 no.6
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• pp.556-562
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• 2000

The determination of chlorite ion by flow injection analysis(FIA) with iodometric UV detection were investigated. Under rather acidic condition, chlorite ion react with iodide ion to form iodine and itself is reduced to chloride ion. The chlorite ion was determined indirectly by measuring absorbance of yellow colored iodine at 370 nm. The lengths of the mixing coil and the reaction coil, the pH of the acid stream, the concentration of the iodide ion, the injection loop volume, temperature, and flowrate were optimized as parameters for selectively determining a sort of inorganic disinfection by-product, chlorite ion by using FIA-UV detection setup. Masking agents for removing oxidants or interferences from the prepared water were tested. Independent calibration curve presented linear range of 0.002-0.2 mg/L for chlorite ion with a correlation coefficient of 0.999 or better. The limit of detection(LOD) was 0.18 ${\mu}g/L$ for chlorite ion.