• Bulletin of the Korean Chemical Society
• /
• 제28권1호
• /
• pp.41-48
• /
• 2007

Large colorless single crystals of sodium zeolite X, stoichiometry |Na80 |[Si112Al80O384]-FAU, with diameters up to 200 μm and Si/Al = 1.41 have been synthesized from gels with the composition of 2.40SiO2 : 2.00NaAlO2 : 7.52NaOH : 454H2O : 5.00TEA. One of these, a colorless octahedron about 200 μm in cross-section has been treated with aqueous 0.1 M KNO3 for the preparation of K+-exchanged zeolite X. The crystal structure of |K80|[Si112Al80O384]-FAU per unit cell, a = 24.838(4) A, dehydrated at 673 K and 1 × 10-6 Torr, has been determined by single-crystal X-ray diffraction techniques in the cubic space group Fd at 294 K. The structure was refined using all intensities to the final error indices (using only the 707 reflections for which Fo > 4σ (Fo)) R1 = 0.075 (based on F) and R2 = 0.236 (based on F2). About 80 K+ ions per unit cell are found at an unusually large number of crystallographically distinct positions, eight. Eleven K+ ions are at the centers of double 6-rings (D6Rs, site I; K-O = 2.492(6) A and O-K-O (octahedral) = 88.45(22)o and 91.55(22)o). Site-I' position (in the sodalite cavities opposite D6Rs) is occupied by five K+ ions per unit cell; these K+ ions are recessed 1.92 A into the sodalite cavities from their 3-oxygen planes (K-O = 2.820(19) A, and O-K-O = 78.6(6)o). Twety-three K+ ions are found at three nonequivalent site II (in the supercage) with occupancies of 5, 9, and 9 ions; these K+ ions are recessed 0.43 A, 0.75 A, and 1.55 A, respectively, into the supercage from the three oxygens to which it is bound (K-O = 2.36(13) A, 2.45(13) A, and 2.710(13) A, O-K-O = 116.5(20)o, 110.1(17)o, and 90.4(6)o, respectively). The remaining sixteen, thirteen, and twelve K+ ions occupy three sites III' near triple 4-rings in the supercage (K-O = 2.64(3) A, 2.94(3) A, 2.73(5) A, 2.96(6) A, 3.06(4) A, and 3.08(3) A).

• Bulletin of the Korean Chemical Society
• /
• 제10권3호
• /
• pp.243-247
• /
• 1989

Two crystal structures of dehydrated $Ag^+\;and\;Ca^{2+}$ exchanged zeolite A, $Ag_2Ca_$5-A, reacting with 0.01 Torr of Cs vapor at $200^{\circ}C$ for 2 hours and 0.1 Torr of Cs vapor at $250^{\circ}C$ for 48 hours, respectively, have been determined by single crystal X-ray diffraction techniques. Their structures were solved and refined in the cubic space group Pm3m at $21(1)^{\circ}C$. The stoichiometry of first crystal was $Ag_2Ca_5$-A (a = 12.294(1)${\AA}$), indicating that Cs vapor did not react with cations in zeolite A and that of second crystal was $Ag_2Cs_{10}$-A (a = 12.166(1)${\AA}$), indicating that all $Ca^{2+}$ ions were reduced by Cs vapor and replaced by $Cs^+$ ions. Full-matrix least-squares refinements of $Ag_2Ca_5-A\;and\;Ag_2Cs_{10}$-A has converged to the final error indices, $R_1\;=\;0.041\;and\;R_2$ = 0.048 with 227 reflections, and $R_1\;=\;0.117\;an\;n\;fdd\;R_2$ = 0.120 with 167 reflections, respectively, for which I > $3{\sigma}$(I). In the structure of $Ag_2Ca_5$-A, both $Ag^+$ ions and $Ca^{2+}$ ions lie on two crystal symmetrically independent threefold axis sites on the 6-rings; $2\;Ag^+$ ions are recessed 0.33 ${\;AA}$ from the (111) planes of three O(3) oxygens and 5 $Ca^{2+}$ ions lie on the nearly center of each 6-oxygen planes. In the structure of $Ag_2Cs_{10}-A,\;Cs^+$ ions lie on the 5 different crystallographic sites. 3 $Cs^+$ ions lie at the centers of the 8-rings at sites of D4h symmetry. 6 $Cs^+$ ions lie on the threefold axes of unit cell: $4\;Cs^+$ ions are found deep in the large cavity and 2 $Cs^+$ ions are found in the sodalite cavity. One $Cs^+$ ion is found in the large cavity near a 4-ring.

• 한국버섯학회지
• /
• 제22권1호
• /
• pp.22-26
• /
• 2024

본 실험은 송이버섯의 인공재배에 있어 기주식물에 대한 의존성을 줄이기 위한 일환으로 송이 균환의 토양 미생물을 활용하여 진행되었다. 이를 위해 송이 자실체가 발달하는 9월을 대상으로 송이 자생지 내 균환으로부터 토양 내 균주들을 분리하였으며, 1점의 세균과 2점의 진균을 대상으로 대조구 대비 생장한 송이 균사체의 크기 퍼센트를 이용한 생장 촉진 결과를 확인하였다. 또한 확보된 균주들에 대한 동정을 위해 NCBI blast 과정과 phylogenetic tree 제작 과정을 거쳤다. 다만 본 실험에서 확보한 미생물과 동일한 동정명의 균을 이용한 동일 조건의 실험 결과와 비교하였을 때, 본 실험에서 확보한 미생물에 의한 송이 균사에 대한 생장촉진 정도가 다소 낮게 나타남을 확인하였다. 그러나 실제 자연계에서 송이와 같은 외근균성 버섯과 작용하는 미생물의 사례가 매우 다양하기 때문에 송이에 대해 균사 생장을 촉진시키는 미생물 데이터베이스 축적에 있어 그 의의가 있다고 볼 수 있다. 또한 축적된 미생물 데이터베이스를 토대로 송이 균사의 생장촉진 나아가 송이 자실체의 발달촉진에 공통적으로 작용하는 미생물 유래 분비물질 고찰에 있어서도 본 실험의 결과가 기여하는 바가 크다고 볼 수 있다. 이에 더해 미생물 군집 내 촉진균 우점도 및 송이 발생지와 미발생지 사이에 있는 미생물 우점도 차이에 대한 추가적인 분석을 통해 향후 송이 발생에 활용할 수 있는 생태모방에 활용할 가능성 또한 존재한다. 추후 지속적인 연구를 통해 균환 유래 토양 미생물에 의한 송이 작용에 대한 실험이 계속 진행되어야 할 필요가 있다.

• Bulletin of the Korean Chemical Society
• /
• 제32권4호
• /
• pp.1253-1257
• /
• 2011

The surface structures, adsorption conditions, and thermal desorption behaviors of cyclopentanethiol (CPT) self-assembled monolayers (SAMs) on Au(111) were investigated by scanning tunneling microscopy (STM), X-ray photoelectron spectroscopy (XPS), and thermal desorption spectroscopy (TDS). STM imaging revealed that although the adsorption of CPT on Au(111) at room temperature generates disordered SAMs, CPT molecules at $50^{\circ}C$ formed well-ordered SAMs with a $(2{\surd}3{\times}{\surd}5)R41^{\circ}$ packing structure. XPS measurements showed that CPT SAMs at room temperature were formed via chemical reactions between the sulfur atoms and gold surfaces. TDS measurements showed two dominant TD peaks for the decomposed fragments ($C_5H_9^+$, m/e = 69) generated via C-S bond cleavage and the parent molecular species ($C_5H_9SH^+$, m/e = 102) derived from a recombination of the chemisorbed thiolates and hydrogen atoms near 440 K. Interestingly, dimerization of sulfur atoms in n-alkanethiol SAMs usually occurs during thermal desorption and the same reaction did not happen for CPT SAMs, which may be due to the steric hindrance of cyclic rings of the CPT molecules. In this study, we demonstrated that the alicyclic ring of organic thiols strongly affected the surface structure and thermal desorption behavior of SAMs, thus providing a good method for controlling chemical and physical properties of organic thiol SAMs.

• 한국추진공학회지
• /
• 제14권5호
• /
• pp.57-64
• /
• 2010

75톤급 터보펌프용 추진제 혼합 방지 실의 누설 성능 및 내구 성능을 평가하기 위한 수류환경 성능 시험을 수행하였다. 추진제 혼합 방지 실 시제품은 연료펌프 부와 산화제펌프 부 각각 누적 시험 시간 2,100초 동안 수류환경에서 내구 성능 시험이 이루어 졌다. 1단의 카본 플로팅 링 실로 구성된 연료펌프 부는 성능 시험 동안 평균 실 차압 9.4 bar에서 평균 누설 유량 13.7 gram/sec의 결과를 얻었다. 반면, 2단의 카본 플로팅 링 실로 구성된 산화제펌프 부는 성능 시험 동안 평균 실 차압 9.5 bar에서 평균 누설 유량 7.3 gram/sec의 결과를 얻었다. 내구 성능 시험 후, 추진제 혼합 방지 실은 양호한 상태를 보였다. 향후 액체 질소를 시험 매질로 하는 극저온 환경에서 추진제 혼합 방지 실 누설 성능 시험이 수행될 예정이다.

• Journal of the Korean Wood Science and Technology
• /
• 제35권6호
• /
• pp.57-64
• /
• 2007

연륜연대측정법을 사용하여 전통약장 2점에 대해 제작연대를 밝혀 편년을 정립하고 시대 변천에 따른 약장의 형태적 차이점을 논하고자 하였다. 연륜연대측정법은 목재 내의 연륜을 측정하여 1년의 오차도 없는 정확한 절대연도를 부여함으로써 제작연대를 알아내는 것이다. 경기도산으로 달려진 경기도박물관소장 약장 1점과 덕성여대박물관소장 약장 1점에 대한 연륜분석 결과, 마지막 연륜의 연도가 1884년과 1874년으로 각각 측정되었다. 시기는 거의 같게 나타났으나 형태, 구조, 목재 재질 등의 상이함이 컸다. 이는 시대적인 차이가 아니라 제작자와 사용자의 취향, 안목, 재력 등이 제작에 반영된 결과로 보인다. 한편, 경기도 약장으로 분류된 것이지만 연륜패턴 일치도 분석결과 목재의 산지는 강원도 설악산과 강릉지역으로 나타나 경기 지방의 가구제작에 강원도 목재가 사용되었음을 알 수 있었다.

• 한국진공학회:학술대회논문집
• /
• 한국진공학회 2012년도 제42회 동계 정기 학술대회 초록집
• /
• pp.158-158
• /
• 2012

A new kind of organic-inorganic hybrid polymer, poly(tetraphenyl)silole siloxane (PSS), was invented and synthesized for realization of its unique charge trap properties. The organic portions consisting of (tetraphenyl)silole rings are responsible for electron trapping owing to their low-lying LUMO, while the Si-O-Si inorganic linkages of high HOMO-LUMO gap provide the intrachain energy barrier for controlling electron transport. Such an alternation of the organic and inorganic moieties in a polymer may give an interesting quantum well electronic structure in a molecule. The PSS thin film was fabricated by spin-coating of the PSS solution in THF organic solvent onto Si-wafer substrates and curing. The electron trapping of the PSS thin films was confirmed by the capacitance-voltage (C-V) measurements performed within the metal-insulator-semiconductor (MIS) device structure. And the quantum well electronic structure of the PSS thin film, which was thought to be the origin of the electron trapping, was investigated by a combination of theoretical and experimental methods: density functional theory (DFT) calculations in Gaussian03 package and spectroscopic techniques such as near edge X-ray absorption fine structure spectroscopy (NEXAFS) and photoemission spectroscopy (PES). The electron trapping properties of the PSS thin film of quantum well structure are closely related to intra- and inter-polymer chain electron transports. Among them, the intra-chain electron transport was theoretically studied using the Atomistix Toolkit (ATK) software based on the non-equilibrium Green's function (NEGF) method in conjunction with the DFT.

• 천문학회지
• /
• 제40권1호
• /
• pp.1-7
• /
• 2007

About 10 percent of quasars are known to exhibit deep broad absorption troughs blueward of prominent permitted emission lines, which are usually attributed to the existence of outflows slightly above he accretion disk around the supermassive black hole. Typical widths up to 0.2c of these absorption roughs indicate the velocity scales in which special relativistic effects may not be negligible. Under he assumption of the ubiquity of the broad absorption line region in quasars, the broad emission line flux will exhibit Thomson scattered components from these fast outflows. In this paper, we provide our Monte Carlo calculation of linear polarization of singly Thomson scattered line radiation with the careful considerations of special relativistic effects. The scattering region is approximated by a collection of rings that are moving outward with speeds ${\upsilon}=c{\beta}<0.2c$ near the equatorial plane, and the scattered line photons are collected according to its direction and wavelength in the observer's rest frame. We find that the significantly extended red tail appears in the scattered radiation. We also find that the linear degree of polarization of singly Thomson scattered line radiation is wavelength-dependent and hat there are significant differences in the linear degree of polarization from that computed from classical physics in the far red tail. We propose that the semi-forbidden broad emission line C III]1909 may be significantly contributed from Thomson scattering because this line has small resonance scattering optical depth in the broad absorption line region, which leads to distinct and significant polarized flux in this broad emission line.

• Journal of the Korean Wood Science and Technology
• /
• 제21권2호
• /
• pp.73-80
• /
• 1993

Pinus koraiensis is one of the most important reforestation species which had widely been planted around the country. Therefore, there are great research needs on the fundamental properties of wood to extend the frequency of uses and adequate availabilities. Research results on the characteristics of anatomical wood properties and changes are summarized as follows: 1. At a horizontal direction of tree trunk, the tracheid length at outer wood gradually becomes shorter as it reaches to pith. The tracheid length having between 32 and 42 annual rings showed over 2.5 times longer than that of pith, and also its length increases from the bottom to the top of the stem. 2. The tracheid diameters in latewood showed a little fluctuations, and the shortest near to the pith in earlywood. The tracheid diameters in earlywood are more than 2 times those of latewood, and the differences between the mature and juvenile wood in earlywood are less than 10${\mu}m$. 3. The tracheid wall thickness in early wood showed a little fluctuations. On the contrary, tracheid wall thickness in latewood rapidly increases from the pith to the bark. The tracheid wall of mature wood showed 10 to 20% thicker than that of juvenile wood. 4. The fibril angle at the secondary walls of tracheid within an annual ring showed higher degree in earlywood than that of latewood. The highest tracheid fibril angle was observed at around the pith of both earlywood and latewood. Then, fibril angle slowly decreased toward outer wood, and was stabilized after 15 years. 5. Structural boundaries between mature and juvenile wood from Pinus koraiensis are divided by 13 to 19 annual ring and distance of 5 to 8cm from the pith.

• Bulletin of the Korean Chemical Society
• /
• 제5권4호
• /
• pp.135-140
• /
• 1984

The reduction of vacuum-dehydrated $Na_xAg_{12-x}-A, 0 {\le} x {\le} 9.2$, and its reoxidation by O$_2$, have been studied by X-ray powder diffraction. Also, the structure of $Na_6Na_6-A$ treated with hydrogen at room temperature has been studied by single crystal methods in the cubic space group Pm3m at $24{\circ}C (a = 12.221(2) {\AA})$. The diffraction pattern of dehydrated Ag$_{12}$-A reduced by H$_2$ contains only the (111) and (200) reflections of silver metal, indicationg that the zeolite structure has been lost, but the zeolite's diffraction pattern and structural integrity can be fully restored by oxidation with O$_2$ at 100 or 200${\circ}C$. In contrast, the structures of $Na_xAg_{12-x}-A$, x = 4.5 and 9.2, were not destroyed by treatment with hydrogen. Dehydrated Na$_6Ag_6$-A treated with 50 Torr of hydrogen gas at 24${\circ}C$ for 30 minutes has $6\; Na^+\;and\;1.27\;Ag^+$ ions at 6-ring sites. These $Ag^+ ions are associated with 2.54 Ag${\circ}$ atoms to form 1.27 $Ag_3^+$ clusters per unit cell. Also found were 0.7 $Ag_3^{2+}$ clusters per unit cell near the 8-rings. The structure was refined to the final error indices R$_1$ = 0.134 and R$_2$ (weighted) = 0.147, using 168 independent reflections for which $I_0 >3{\sigma}(I_0)$.