• 한국의류학회지
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• 제18권1호
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• pp.113-120
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• 1994

The Purpose of this study was to improve the moisture related properties of viscose rayon fibers. Viscose rayon filament yarns were partially etherified to make CMC fibers. CMC fibers were converted to the sodium, calcium, and ferric salt forms by an ion exchange method. The property changes of ion exchanged CMC fibers were examined. Cation contents of fibers were varied depending on the degree of substitution of CMC fibers. The strength of Na, Ca, Fe-CMC was higher than H-CMC owing to the plasticization by moisture sorption and the crosslinking by cations. The moisture regain was increased by carboxymethylation and that of Fe-CMC showed the highest value. The degree of swelling determined by the water retention value was observed to be Na-CMC > Ca-CMC > H-CMC > Fe-CMC. The solution retention value was decreased in the order . Ca-CMC > Na-CMC > H-CMC > Fe-CMC.

• 한국세라믹학회지
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• 제30권4호
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• pp.259-264
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• 1993

In this research, the organic tenside R11OSO3- with long alkyl-chain was synthesized, and the intercalationscomplexes fo montmorillonite were formed by the substitution of metallic cation in the montmorilonite by the synthesized organic tenside in following two methods, and the behaviors of the tenside R11OSO3- in the interlamellar space of montmorillonite were studied udner various conditions: 1) In order to protonize the sulfate group of R11OSO3-, the H3O-Montomorillonite, which acts as acid, was synthesized. And then, the organic tenside was intercalated in the interlamellar space of this H3O-Montomorillonite. And thus, the intercalations-complex of R11S-H3O-Montomorillonite was formed. The basal spacing obtained was about 33.84$\AA$. 2) The betaine compound R11OSO3- as a neutral molecule was direct intercalated in the interlamellar space of Na-Montmorillonite under water, and the intercalations-complexes of R11S-H2O-Montmorillonite was synthesized. In this case, the based spacing of bout 23.62$\AA$ was obtained.

• Bulletin of the Korean Chemical Society
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• 제30권7호
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• pp.1588-1592
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• 2009

Lithium cyanoaluminum hydride (LCAH) was prepared by the metal cation exchange reaction of sodium cyanoaluminum hydride with lithium chloride in tetrahydrofuran. The reducing characteristics of LCAH were explored systematically by the reaction with selected organic compounds containing representative functional groups under the standardized conditions (tetrahydrofuran, 0 ${^{\circ}C}$). The reducing ability of LCAH was also compared with of the sodium derivative, sodium cyanoaluminum hydride (SCAH). Generally, the reducing behavior of LCAH resembles that of SCAH closely, but the reactivity of LCAH toward representative organic functional groups appeared to be stronger than that of SCAH. Thus, the regent reduces carbonyl compounds, epoxides, amides, nitriles, disulfides, carboxylic acids and their acyl derivatives to the corresponding alcohols or amines, at a relatively faster rate than that of SCAH. The cyano substitution, a strong election-withdrawing group, diminishes the reducing power of the parent metal aluminum hydrides and hence effects the alteration of their reducing characteristics.

• 공학논문집
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• 제6권2호
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• pp.119-124
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• 2004

본 연구에서는 양이온교환방응에 의해 몬모릴로나이트 층 내의 금속 양이온을 긴 알킬 사슬을 갖는 유기 양이온으로 치환시켜 물성이 전혀 다른 유기 점토화합물인 몬모릴로나이트 층간 화합물을 합성한 후, 이 층간화합물을 증류수, 메탄올, 아세톤, 에테를 및 아세토니트릴 등과 같은 상이한 팽윤액체와 반응시켜 팽윤거동에 대하여 연구하였다. 특히 연구에 사용된 점토로는 한국산과 터키산의 두 가지 상이한 몬모릴로나이트를 선정하여 두 점토의 층간화합물 및 팽윤거동에 대하여 비교.분석하였다.

• Bulletin of the Korean Chemical Society
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• 제10권6호
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• pp.500-503
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• 1989

Synthetic studies have been carried out for the addition or substitution of phosphorus nucleophiles to the cation $[(exo-6-R-{\eta}^ {5_-}2-MeO-C_6H_5)Mn(CO)_2NO]PF_6,$ 2. $PPh_3$ reacts with 2 to yield the CO displaced product and $MePPh_2$ attacks the dienyl ring of 2 to yield the phosphonium adduct or the metal to give the CO displaced depending upon the reaction temperatures. Nucleophilic addition of HPPh2 to the dienyl ring of 2 gives a neutral substituted product. $P(OMe)_3$ reacts with 2 to yield a mixture of ring adduct and CO displaced product at room temperature. $At - 20^{\circ}C,\;P(OMe)_3$ attacks the dienyl ring of 2 to give a posphonium adduct, which underwent Arbuzov reaction. This reaction affords a new route to the phosphonate complexes.

• 대한화학회지
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• 제48권2호
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• pp.129-136
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• 2004

타이테늄과 [타이테늄 + 나트륨 (칼륨)]으로 치환된 11${\AA}$의 토버모라이트 고체가 180 $^{\circ}C$의 수열반응 조건하에서 합성되었고, 이 화합물은 Fe$^{2+},\;Zn^{2+},\;Cd^{2+},\;Pb^{2+}$과 같은 중금속 양이온에 대해서 양이온 교환 성질을 보였다. 이 고체에 흡착된 중금속 양이온은 Fe$^{2+}>Zn^{2+}>Cd^{2+}>Pb^{2+}$의 순서로 그 양이 감소하였고, 10% [타이테늄 + 칼륨]으로 치환된 토버모라이트가 최대값을 보였다. 총 양이온 교환능은 10% [타이테늄 + 칼륨]으로 치환된 토버모라이트와 타이테늄으로만 치환된 토버모라이트에 대해서 각각 71에서 89 meq/100 g와 50에서 56 meq/100 g로 측정되었다. 이 결과는 10% [타이테늄 + 칼륨]치환이 비치환 토버모라이이트 보다 2.4배 이상의 양이온 교환능이 있음을 보여준다. 이는 교환체의 활성자리 수의 증가에 의한 것이다. 합성된 토버모라이트의 격자구조로의 타이테늄과 [타이테늄 + 나트륨 (칼륨)]의 포함은 각각 Ti$^{4+}\;{\Leftrightarrow}\;2Ca^{2+}$와 Ti$^{4+}+2Na^+(K^+)\;{\Leftrightarrow}\;3Ca^{2+}$의 치환에 의한 것이다. 합성과정 중 고체의 결정 격자로의 타이테늄과 [타이테늄 + 나트륨 (칼륨)]의 포함에 관한 메커니즘과 이들 고체에 의한 중금속 양이온 흡수가 연구되었다.

• Bulletin of the Korean Chemical Society
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• 제30권11호
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• pp.2559-2562
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• 2009

The lattice vibration and crystal structure of alkaline earth metal-substituted $RuSr_{1.9}A_{0.1}GdCu_{2}O_{8}$ (A = Ca, Sr, and Ba) have been investigated with micro-Raman spectroscopy. The present $RuSr_{1.9}A_{0.1}GdCu_{2}O_{8}$ materials show not only several weak Raman peaks corresponding to the vibrations of $O_{Cu}$ and $O_{Ru}$ but also strong characteristic phonon lines related to $O_{Sr}$ vibration mode. A comparison between the frequency of $O_{Sr}$ vibration and the bond distances of (Ru$O_{Sr}$) and (Cu‒$O_{Sr}$) in the present ruthenocuprates reveals that the vibration energy of $O_{Sr}$ is mainly dependent on the bond distance of (Ru‒$O_{Sr}$). The peak splitting of the $O_{Sr}$ phonon lines was observed for the unsubstituted $RuSr_{1.9}A_{0.1}GdCu_{2}O_{8}$, suggesting the existence of two different (Ru‒$O_{Sr}$) bond distances. Such a peak splitting caused by the appearance of low-energy shoulder reflects the presence of internal charge transfer pathway from the $RuO_2$ plane to the superconductive $CuO_2$ one. After the substitution of Sr with Ca or Ba, the low-energy shoulder peak of $O_{Sr}$ vibration becomes suppressed, underscoring the depression of internal charge transfer between the $RuO_2$ and $CuO_2$ planes. The weakened role of $RuO_2$ layer as charge reservoir in the $RuSr_{1.9}A_{0.1}GdCu_{2}O_{8}$8 (A = Ca, Ba) would be responsible for the depression of $T_c$ upon the Ca/Ba substitution.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2001년도 하계학술대회 논문집
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• pp.455-458
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• 2001

Spinel $LiMn_{2-y}$$M_{y}$ $O_4$powder was prepared solid-state method by calcining the mixture of LiOH - $H_2O$, Mn $O_2$, ZnO and MgO at 80$0^{\circ}C$ for 36h. To investigate the effect of substitution with Mg, Zn cation, charge-discharge experiments and initial impedance spectroscopy performed. The structure of $LiMn_{2-y}$$M_{y}$ $O_4$crystallites was analyzed from powder X-ray diffraction data as a cubic spinel, space group Fd3m. all cathode material showed spinel phase based on cubic phase in X-ray diffraction. Ununiform which calculated by (111) face and (222) face was constant in spite of the change of y value, except PUf\ulcorner LiM $n_2$ $O_4$. The discharge capacities of the cathode for the cation subbstitUtes $LiMn_{2-y}$$M_{y}$ $O_4$/Li cell at the 1st cycle and at the 40th cycle were about 120~124 and 108~112mAh/g except LiM $n_{1.9}$Z $n_{0.1}$ $O_4$/Li cell, respectively. This cell capacity is retained by 93% after 40th cycle. AC impedance of $LiMn_{2-y}$$M_{y}$ $O_4$/Li cells revealed the similar resistance of about 65~110$\Omega$ before cycling. before cycling.g.g.

• Journal of Magnetics
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• 제20권1호
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• pp.26-30
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• 2015

The crystallographic and magnetic properties of gallium-substituted cobalt ferrite ($CoGa_xFe_{2-x}O_4$) were investigated. The new material was synthesized using conventional ceramic methods, with gallium substituted for ferrite in the range of x = 0.0 to 1.0, in steps of 0.2. X-ray diffraction and M$\ddot{o}$ssbauer spectroscopy were used to confirm the presence of crystallized particles in the $CoGa_xFe_{2-x}O_4$ ferrite powders. All of the samples exhibited a single phase with a spinel structure, and the lattice parameters decreased as the gallium content increased. The particle size of the samples also decreased as gallium increased. For $x{\leq}0.4$, the M$\ddot{o}$ssbauer spectra of $CoGa_xFe_{2-x}O_4$ could be fitted with two Zeeman sextets, which are the typical spinel ferrite spectra of $Fe^{3+}$ with A- and B-sites. However, for $x{\geq}0.6$, the M$\ddot{o}$ssbauer spectra could be fitted with two Zeeman sextets and one doublet. The variation in the M$\ddot{o}$ssbauer parameters and the absorption area ratio indicated a cation distribution of $(Co_{0.2-0.2x}Ga_xFe_{0.8-0.6x})[Co_{0.8+0.2x}Fe_{1.2-0.4x}]O_4$, and the magnetic behavior of the samples suggested that the increase in gallium content led to a decrease in the saturation magnetization and in the coercivity.

• 한국세라믹학회지
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• 제34권2호
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• pp.139-144
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• 1997

결정학적으로 T' 구조인 Nd2-xCexCuO4-$\delta$ 회토류 구리산화물 초전도체는 지금까지 매우 복잡한 미세구조를 지닌 것으로써 잘 알려져 있다. 이 구리산화물 초전도체가 초전도 특성을 띠려면, Nd3+ 이온이 Ce4+ 이온에 의해 소량 치환되고 동시에 산소환원이 필요하다. 본 연구에서는 투과전자현미경의 수렴성 전자회절(CBED)패턴을 이용하여 Nd2-xCexCuO4-$\delta$ 의 Ce 미량 첨가와 미량의 산소환원에 따른 결정구조의 전이 발생 여부에 관하여 고찰하였다. 세 가지의 서로 다른 시편 Nd2CuO3,Nd1.85Ce0.15CuO4 와Nd1.85Ce0.15CuO3.965을 고상소결에 의하여 만들어 이들 각각 시편에 대한 CBED패턴을 주사투과전자현미경(STEM)으로 관찰하였다. 그리고 실험에 의하여 얻은 이들 HOLZ선들과 컴퓨터 계산에 의해 그려진 이론적인 HOLZ선들과 비교하는 방법에 의하여 Nd1.85Ce0.15CuO4의 격자상수를 구하였다.