The anorthositic rocks and the many other plutons which are of different varieties and age were distributed in the northern extremity of the distributed areas of H-S anorthositic rocks. The purpose of this study was to find plutons which had comagmatic relationships, and to make clear the magmatic process of anorthositic magma. The plutons were classified, and the petrological and the geochemical characteristics of the plutons were compared and researched in this study. And, because, like anorthosite, the rocks which intrude in the deep crust accompany assimilation, an AFC model calculation was performed to make the differentiation process of the anorthositic rocks clear. The plutons in this area were classified into three groups, and the three groups were composed of the Precambrian anorthositic rocks and related rocks, the Jurassic gabbro, and the plutons of undnown age. The anorthositic magma was differentiated from the anorthositic rocks through the tonalite to the alkali-feldspar granite, and it was differentiated under K, Mg, Fe free/lack condition. It was found from the result of AFC model that the anorthositic rocks were differentiated by fractional crystallization, but they were assimilated with wall-rocks, and the assimilation was performed at the rate of r$\leq$0.1. The plutons which intruded the anorthositic rocks subsequently consisted of the gabbro, the megacrystic granite, the fine-grained granite, and the gneissose granite. But they were formed by the repeated intrusion of magma, which may, or may not, be of the same origin. According to the result of the RCF model, these plutons were differentiated by simple fractional crystallization, and they were assimilated relatively less than the anorthositic rocks.

This study introduces a new structural model of 1M 2:1 trioctahedral clay minerals or, more generally, 2:1 trioctahedral phyllosilicates. The structural model requires only the chemical formulae of the clay minerals as an input and uses the regression relation (Radoslovich, 1962) to calculate the a- and b-dimensions of the phyllosilicates with the given chemical formulae. The atomic coordinates of the constituent atoms are geometrically calculated for C2/m space group under the assumption that the interatomic distances are constant. To determine the c-dimension, this study calculates the binding energies of 1M 2:1 trioctahedral phyllosilicates as a function of d(001) and find the minimum energy producing d(001). The structural model generates the cell dimensions, interaxial angles, interatomic distances, octahedral, tetrahedral and interlayer thickness, polyhedron deformation angles and atomic coordinates in the unit cell. The simulated structural parameters of phlogopite and annite are very close to the reported data by Hazen and Burnham (1973), suggesting that the structure simulation using only the chemical formule is successful, and thus, that the structural model of this study overcomes the difficulties in the previous models by other investigators.

Three fully dehydrated fully Rb+-exchanged zeolite A single crystals have been prepared by the reduction of all Na+ ions in dehydrated Na12-A by rubidium vapor at various experimental conditions (220 $\leq$ T $\leq$ 33$0^{\circ}C$, 2 $\leq$ t $\leq$24 hours, and 0.1 $\leq$ PRb $\leq$ 1.1 Torr). Their structures were determined by single-crystal X-ray diffraction methods in the space group {{{{ RHO }}m3m (a=12.245(3) A) at 22(1)$^{\circ}C$. In these structures 12.6(2) to 13.5(2) Rb species are found per unit cell, more than the 12 Rb+ ions needed to balance the anionic charge of the zeolite framework, indication that the sorption of Rb0 has occurred. In each structure, three Rb+ ions per unit cell are located at the centers of 8-rings. Beyond that, the fractional occupancies observed are simply explained by two unit cell arrangments. In one, two Rb+ ions are in the sodalite unit near opposite 6-rings, six are in the large cavity near 6-ring, and one is in the large cavity near a 4-ring. In the other, three Rb species in the sodalite cavity (forming a triangle 3.7 A on an edge) each bond (3.4 A) through a 6-ring to an Rb species in the large cavity to give an (Rb6)4+ cluster of symmetry 3m (C3V). Five additional Rb+ ions fill the remaining large-cavity 6-ring sites.

경남 울산군 농소면의 울산사문석광산에서 세피오라이트(sepiolite)가 발견되었다. 그래서 이 세피오라이트시료에 대해 X-선회절분석, 열분석, 적외선분광분석, 투과전자현미경관찰 및 화학분석을 행하여 그 결과를 기술하였다. 본 세피오라이트는 사문암과 염기성암체와의 접촉부에 발달된 열극충진상 세맥에서 산출된다. 이 세맥내에서 많은 암편들이 포함되어 있는데, 그 기질부분은 회백색을 띠며 연질이고 부드러운 가죽같은 느낌을 준다. 이 기질부분이 거의 순수한 세피오라이트로 구성되어 있다. X-선회절분석의 결과로부터 이 광물시료가 결정도가 높은 {{{{ alpha }}-세피오라이트에 해당된다는 것이 밝혀졌다. 이 세피오라이트의 화학성분은 Mg를 많이 함유하는 일반적인 세피오라이트와 유사하였다. 산상 및 광물학적 특성으로 볼 때 이 세피오라이트는 열수용액에서 직접 침전하여 형성된 것으로 사료된다.

In the southern limb of the Hambaek geosyncline belt, large-scaled skarn deposits are developed in the Cambro-Ordovician sedimentary rocks of the Chosun Supergroup. They are the Sangdong tungsten deposit, Geodo iron-copper deposit, Yeonhwa I and II lead-zinc deposits, and Ulchin zinc-lead deposit, all of which are associated with various skarn minerals. Though different occurrences and paragenesis are found in different deposits, most skarn deposits always have skarns of garnet (andradite-grossular series) and clinopyroxene(heden-bergite-diopside series). Andradite and hedenbergite are Fe-dominant members, but show different oxidation states, that is, Fe3+ for andradite and Fe2+ for hedenbergite. According to iron chemistry and log([Fe/Al]gd/[Fe/Mg]cpx) derived from equilibrium reactions, the diopside-andradite and hedenbergite-grossular pairs suggest the oxidized state (dian type) and reduced state (hegro type), respectively. Among skarn deposits developed in the Hambaek geosynline, it can be classified that the Geodo and Yeonhwa I skarns are of dian type, while the Sangdong, Yeonhwa II, and Ulchin deposits are of hegro type. This classification is not applicable to all kinds of skarn deposits, but may be applicable to such deposits as are more controlled by oxygen fugacity than composition of skarn fluid.

Two illite polytypes, 2M1 and 1Md, have been identified from the sericite deposits of the Bobae mine, Kimhae, Kyungsangnam-do. Each polytype has characteristic grain size, chemical composition, and occurrence. 2M1 illite occurs predominantly in the sericitic alteration zone, while 1Md illite occurs predominantly in the propylitic alteration zone, implying that the former was formed in the higher temperature than the latter. Illites can be subdivided into two types based on their crystal sizes;(1) the $\mu\textrm{m}$-sized illite which is below 0.01mm(100$\mu\textrm{m}$) in size and consists of 2M1 and 1Md type, (2) the mm-sized illite which is above 0.01mm in size and consists only of 2M1 type. Especially illite below 1$\mu\textrm{m}$ is premominantly of 1Md type. Therefore, it seems likely that illite crystal size is to some extent related to the polytype. XRD data show that there is no interstratified layer in illites regardless of the crystal size and polytype. Activity of muscovite component of the $\mu\textrm{m}$-sized illite is 0.843 while that of the mm-sized illite is 0.790. However, the latter is more similar to muscovite in crystal structure than the former is. The mm-sized illite has less Al and more Kthan the $\mu\textrm{m}$-sized illite. In both illites, Si contents show a positive relation to octahedral Mg. Fluid inclusion study and mineral association show that the formation temperature of illite is $270-330^{\circ}C$. The major chemical processes leading to the formation of sericitic deposit as well as the alteration zones are the leaching of SiO2 from the country rock and the addition of Al2O3 and K2O into the sericitic ores.

Minerals of system Ag-Sb have been found in iead-zinc (-silver) ores from the Dongjeom and the Taebaeg ore deposits, which were formed at later stage of the Yeonhwa 1 mine mineralization. The Ag-Sb minerals are intergrown intimately with galena, pyrargyrite and alabandite. Their chemical compositions as determined by electron microprobe analyser show that they are chracterized by relatively high content of S, up to 5.89 atomic percent. Also the composition of the minerals may be separated into two: Ag3.89 Sb1.00-Ag7.19 Sb1.00 and Ag2.96 Sb1.00-Ag4.00 Sb1.00.