While about 80% of Jeju soils are classified as Andisols, the soils derived from volcanic ash in Dangsanbong are not Andisols. There is a significant difference of precipitation in localities of Jeju island. The study area is characterized by the lowest amount of annual rainfall in Jeju Island, and by the layered silicates as dominant solid phase in clay fraction. The purpose of this study was to characterize the mineralogy of the non-Andie soils in detail, especially hydroxy-interlayered silicates. Two major soil horizons are recognized in the soil profile developed in the Dangsanbong area, which can be designated as A and C. The soil pH($H_{2}0$), ranges from 6.6 to 7.3 increasing with depth, is higher than that of typical Andisols(pH<6.0). While the pH(NaF), ranges from 9.49 to 9.81, indicates that significant amount of amorphous phases might be present as exchanging complexes. It is estimated to about 1.542.88 wt% by using chemical selective dissolution. The organic content of surface horizon is about 2 wt%. This soil are composed of quartz, feldspar and olivine as major constituents with minor of silicate clays. Quartz is frequently observed in A and distinctly decreases in its amount with depth, while olivine is dominant phase in C and rarely observed in A. In the <0.2$\mu\textrm{m}$ size fraction, smectite and kaolinite/smectite interstratification are dominant with minor of illite. The amounts of smectite decrease with depth, while the amounts of kaolinite/smecite interstratification increase with depth, which indicates the trend of mineral transformation with increasing the degree of weathering. The proportion of kaolinite in kaolinite/smectite interstratification is about 85%, and is not changed significantly through the profile. In the 2-0.2$\mu\textrm{m}$size fraction, vermiculite, smectite, illite and kaolinite are major components with minor of chlorite. Most of chlorite are interstratified with smectite. Chlorite which is not interstratified with smectite occurs only in surface horizon. The proportion of the chlorite in the chlorite/smectite interstratification is 59-70(%) and increases with depth. Hydroxy-interlayered vermiculite(HIV) with hydroxy-Fe/AI in their interlayers occurs in both A and C horizon. The amounts of hydroxy-Fe/AI decrease with depth. Hydroxy-interlayered smectite(HIS) of which interlayers might be composed of hydroxy-Mg/Al occurs only in C horizon. As the results of mineralogical investigation for the soil profile in the study area, clay minerals might be changed and evolved through the following weathering sequences: 1) Smectite Kaolinite, HIS, Vermiculite, 2) Vermiculite HIV Chlorite.
Ha, Sangbeom;Khim, Boo-Keun;Cho, Hyen Goo;Colizza, Ester
Journal of the Mineralogical Society of Korea
/
v.31
no.1
/
pp.1-12
/
2018
A gravity core (RS14-C2) was collected at site RS14-C2 in the continental slope to the east of Pennell-Isellin Bank of the Ross Sea (Antarctica) during PNRA XXIX (Rosslope II Project) Expedition. In order to trace the sediment source, magnetic susceptibility (MS), sand fraction, and clay mineral compositions were analyzed, and AMS $^{14}C$ ages were dated. Core sediments consist mostly of hemipelagic sandy clay or silty clay including ice-rafted debris (IRD). AMS $^{14}C$ age of core-top indicates the modern and Holocene sediments. Based on AMS $^{14}C$ dating, sediment color, MS and sand fraction, core sediments are divided into interglacial and glacial intervals. The interglacial brown sediments are characterized by low MS and sand fraction, whereas the glacial gray sediments are characterized by high MS and sand fraction. Among clay mineral compositions of core sediments, illite is highest (61.8~76.7%), and chlorite (15.7~21.3%), kaolinite (3.6~15.4%), and smectite (0.9~5.1%) are in decreasing order, and these compositions are also divided into the interglacial and glacial/deglacial intervals. During the glacial period, the high content of illite and chlorite indicate sediment supply from the bedrocks of Transantarctic Mountains under the Ross Ice Sheet. In contrast, because of decreasing supply of illite and chlorite by the glacial retreat, smectite and kaolinite contents increased relatively during the interglacial period. During the interglacial period, smectite may be transported additionally by the northeastward flowing surface current from the coast of Victoria Land in the western Ross Sea. Kaolinite may be also supplied to the continental slope by the Antarctic Slope Current from the kaolin-rich metasedimentary rock outcropped on the Edward VII Peninsula.
Geochemical composition and clay minerals of surface and core sediments around off the Jeju Island were analyzed for identification of sediment origins. The clay mineral distribution is mainly controlled by the sediment source and the dominant circulation pattern. Smectite is highly concentrated (>8%) in the northwest near the South Yellow Sea and in the outer-shelf mud patch. It seems to be due to the high supply of smectite transported from China where fine-grained sediments are discharged from modern and ancient Huanghe River. The relatively high abundance of kaolinite are found in northeastern nearshore area and the southwest near Changjiang estuary. It seems to be supplied from Changjiang River and the southwestern Korea rivers. The sediment accumulation rates measured by $^{210}Pb$ geochronrom mowere 0.20 to 0.54cm/mr or 0.15 to $0.42g/cm^2{\cdot}mr^{-1}$ AOJI, with decreasing rates from the west part to the east part, resulting in the supply of fine-grained suspended sediments from the Changjiang and Huanghe Rivers system. The discrimination diagrams clearly show that the sediments around Jeju Island in the northern East China Sea are ultimately sourced from Chinese rivers, especially from the Huanghe River, whereas the sediment in the northeast part might come from Korean rivers and the Jeju Island.
Mineralogical and chemical examinations were performed on interstratified illite-smectite (I-S) minerals that occur in the mudstones from a petroleum exploration well in the Tertiary marine basin, Japan. X-ray diffraction analysis shows that component layers of illite in the interstratified I-S increase with increasing burial depth while those of smectie decrease. In addition, the randomly (R=0) interstratified illite-smectite is changed into Rp1 ordered I-S at a depth of about 4,000 m, which corresponds to the result of organic analysis and indicates a burial temperature of about $100^{\circ}C$. However, the present geothermal gradient shows that the conversion of the random I-S to R=0 ordered I-S is likely to occur at 3,000 m. This discrepancy may be interpreted by the reverse fault at 2,500 m which resulted in a deeper burial of sediments up to 1,000 m. Chemical analysis also shows the compositional variation in I-S with increasing depth: a decrease in Si and an increases in Al and K, indicating that the substitution of Al for Si in tetrahedral sheets is compensated by the addition of K to interlayers. K may be derived from K-feldspar and micas, which is present in the mudstones.
The clay minerals such as sericite, pyrophyllite, chlorite and smectite abundantly occur in the Bobae pottery stone mine in Pusan. In this study, the processes which are responsible for the formation of these minerals were studied by examing their occurrence and mineralogical properties. The so-called pottery stone of this mine is characterized by the predominance of sericite and quartz. The sericite of the pottery stone is mostly $2M-{1}$ type. And many of quartz particles are smaller than a few micron in diameter. The pottery stone also contained a small amount of pyrophyllite and muscovite. The pottery stone deposit occurs within the Cretaceous rhyodacite and is particularly well developed near the contact with the quartz porphyry which intrudes the rhyodacite. The fact implies that the pottery stone is the product of hydrothermal alteration of the rhyodacite by the intrusion of quartz porphyry. The pottery stone was formed by the alteration that accompanies the dissociation of feldspar and chlorite in parent rocks and subsequent formation of sericte and quartz. Smectite, laumontite and kaolinite occur locally within the altered rocks. These minerals were formed after formation of pottery stone. It is noteworthy that beidellite occurs as a pink-colored clay from the altered rocks in the mine.
Numerous clay veins along fractures such as fault, joints, cracks and small fissures are found in granitic rocks in the Korean Peninsula. Granitic rocks of three geological stages (Jurassic, Cretaceous and Paleogene) occur in the Korean Peninsula, and are known as the Daebo, Bulguksa and Hoam granites, respectively. Specimens from clay veins composed or mainly mica clay mineral (illite) were dated using the K-Ar method with the hosted granitoids. The respective ages were as follows. Jurassic: granites 143.7 Ma and 160 Ma, clay mineral veins 104 Ma and 107 Ma: Cretaceous: granite 133.2 Ma, clay mineral veins 93.6 Ma, 84.2 Ma and 84.3 Ma: Paleogene: granite 39.7 Ma and 35.4Ma, clay mineral veins 27.1 Ma and 23.9 Ma. The ages of the clay veins in the Korean Peninsula are clearly much younger than those of their hosted granitoids. This contrasts with data for similar clay veins in Cretaceous and Paleogene granitoids in southwest Japan, where the K-Ar ages of mica clay minerals are slightly younger than their host rocks, or are almost the same.
This study reports on the genesis and mineralogical characteristics of the clay minerals in the soils derived from the five major parent rocks of granite, granite-gneiss, limestone, shale, and basalt in Korea. The investigation on the mineralogical aspects of primary and secondary minerals of the rocks and coarse fractions in the soils have been already reported. In this report, the identification of clay minerals in the soil clay fractions was done through the analyses of chemical, X-ray diffraction, and thermal methods. The studies showed clearly that much of the clay minerals was evolved by the weathering of primary minerals and some were further developed by the transformation of secondary minerals. Cation exchange capacity(CEC) of the clay fractions increased with higher amotunts of vermiculite, chlorite, and illite, however, decreased with higher hydroxy octahedral sheet within the interlayer spaces of vermiculite even if dominant clay with vermiculite. Feldspars in the granite and granite-gneiss might be completely transformed to kaolin mineral, Illite, chlolrite, and vermiculite formed by the alteration of micas, amphibole, augite, and primary chlorile seem to be subsequently transformed to the mixed layer minerals such as illite/vermiculite, illite/chlorite, and chlorite/vermiculite. These weathering products may be ultimately transformed into kaolin minerals. The smectite minerals in the clay fractions of the soils developed on the limestone are considerably present and they seem to be formed directly by the precipitation from high Mg solution and/or by the transformation of vermiculite from micas and chlorite in the parent materials. Abundant presence of illite in the soil clays developed on the shale is considered to have inherited from the fine particles and more resistant hydrous muscovite. The weathering sequences of the hydrous muscovite were as follows according to the degree of soil development ; hydrous muscovite ${\rightarrow}$ illite/vermiculite mixed layer(Inceptisols, Daegu series) and hydrous muscovite ${\rightarrow}$ illite/vermiculite mixed layer ${\rightarrow}$ vermiculite ${\rightarrow}$ kaolin mineral(Alfisols, Buyeo series). The plagioclase in the basalt might be mostly weathered to kaolin minerais. The augite in the basalt is likely to be transformed through progressive stage of weathering, augite ${\rightarrow}$ chlorite ${\rightarrow}$ chlorote/vermiculite mixed layer ${\rightarrow}$ vermiculite ${\rightarrow}$ kaolin. Another weathering sequence of augite could be expected, augite ${\rightarrow}$ chlorite ${\rightarrow}$ illite by the presence of illite and illite/vermiculite mixed layer in the clay fractions. Vermiculite and gibbsite were quantified from thermogravimetry(TG) and kaolin minerals, from both TG and differerential thermal analysis (DTA). Vermiculite in Jangseong series from the limestone was the dominant clay mineral of 21.7 percent and had a range in the order of 9.2 percent in Buyeo series to 5.4 percent in Daegu series from the shale. The rest soils ranged from 8.8 to 28.3 percent. Kaolin minerals were the dominant clay mineral of 32.7 percent in Asan series from the granite-gneiss and Gueom series of 32.0 percent from the basalt. The soils from the limestone ranged from 9.4 to 14.9 percent. The rest soils ranged from 8.9 to 28.6 percent. Gibbsite were 3.9 and 2.3 percent for Weoljeong and Chahang series from the granite, respectively. In Asan and Cheongsan series from the giranite-gneiss were 1.4 and 4.5 percent, respectively, and 3.6 percent in Jangpa series from the basalt.
Journal of the Korean Society of Clothing and Textiles
/
v.38
no.5
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pp.665-674
/
2014
An analysis of the components of clay mineral before and after coloration (XRF) showed that the elements involved in coloration are Fe, Cr, and Ni. Fe accounts for 65% of coloring components on dyed fabric; in addition, Cr and Ni also affect coloring. The optimal coloration condition was to repeat the process of immersing the cotton fabric in $80^{\circ}C$ slurry of 8g of clay mineral to 1g cotton for 60 minutes, dry it for 24 hours and rinse three times. Especially, as the repetition of coloration increased, the $(K/S)_{440}$ value of sample A increased from 1.0 to 2.5, and sample B increased from 1.0 to 1.6. The effect of the repeated process on coloration was significant; consequently, the rinsing and drying process were important to decrease the coloration level. It also showed excellent results in regard to color fastness to washing, light, rubbing, perspiration, and antibiotic effect.
The composition of primary minerals of sand fractions and secondary minerals of clay fractions were investigated on the polder soils developed from alluvio-marine deposits near to Sapgyo-lake, constructed a sea dike across river estuary located in the west coast. The effects of a topographical sequence on the physico-chemical properties and mineralogical characteristics were evaluated using XRD, DTA, and TG with the chemical composition of $H^+$ saturated clays. Soils located on the seashore side were more silt fraction, higher pH and exchangeable cations than the others. The dominant minerals of soil parent materials are in the order of quartz, feldspars, micas, chlorite and amphibole. According to the greater distance from the lake, the amount of 1:1 minerals increased, but 2:1 minerals decreased. The dominant clay minerals of polder soils are kaolinite, vermiculite and illite. Hydroxy interlayer minerals are abundant in the clay fractions derived from the soil parent materials which have relatively low soil pH.
As the groundwater flows along the fractures of crystalline rocks, it will be in contact with the fracture walls mostly coated by secondary minerals which are quite different form those of host rocks. The presence of fracture-filling minerals in crystalline rocks is important on the view point of radioactive waste disposal because of their great surface reactivity. The Surichi drill hole of 200 m in depth in the Yugu area composed mainly of Precambrian gneiss was selected to study the formation process of clay minerals on the fracture wall of gneiss, and their relation with present groundwater. The water-rock interaction in fractures resulted in the formation of gibbsite and clay minerals. They are formed by two different processes : (1) Incongruent dissolution of feldspar by groundwater diffused from a fracture path into rock matrix produced smectite and illite in situ, (2) on the wall of fracture, gibbsite, kaolinite, smectite and illite are formed by precipitation of dissolved species in groundwater. They show the paragenetic sequence such as gibbsite${\leftrightarrow}$kaolinite${\leftrightarrow}$smectite or illite. The paragenetic sequence of fracture-filling minerals was controlled by increase of pH of groundwater, decrease of fracture permeability by precipitation of fillings, and immobility of alkali or alkaline earths in groundwater. The groundwater from the Surichi borehole is a $Na-HCO_{3}$ type with pH range of 8.6-9.2. The sodium and bicarbonate in groundwater would be supplied by the dissolution of albite and calcite, respectively. The saturation index of groundwater and surface water calculated by WATEQ4F indicates that gibbsite and kaolinite are under precipitation to equilibrium state, and that smectite and illite are under equilibrium to redissolution environment. The stability relation of clay minerals in the $Na_{2}O-Al_{2}O_{3}-SiO_{2}-H_{2}O$ system shows that kaolinite is stable for all waters.
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