• 대한수학회논문집
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• 제34권4호
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• pp.1175-1199
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• 2019

We construct a general bi-basic inverse series relation which provides extension to several q-polynomials including the Askey-Wilson polynomials and the q-Racah polynomials. We introduce a general class of polynomials suggested by this general inverse pair which would unify certain polynomials such as the q-extended Jacobi polynomials and q-Konhauser polynomials. We then emphasize on applications of the general inverse pair and obtain the generating function relations, summation formulas involving the associated polynomials and derive the p-deformation of some of the q-analogues of Riordan's classes of inverse series relations. We also illustrate the companion matrix corresponding to the general class of polynomials; this is followed by a chart showing the reducibility of the extended p-deformed Askey-Wilson polynomials as well as the extended p-deformed q-Racah polynomials.

• Bulletin of the Korean Chemical Society
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• 제18권2호
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• pp.185-189
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• 1997

The effect of pH and sodium dodecyl sulfate (SDS) micelle on the quenching of Ru(bpy)32+ luminescence by N-alkyl-4,4'-bipyridinium ions (RBPY+: R=methyl, octyl, dodecyl, benzyl) were investigated. In the absence of SDS, the quenching rate at pH 2 is similar to that of the corresponding methylalkyl viologens and much greater than that in pH 8 solution due to greater reducibility of the protonated form of RBPY+ (HRBPY2+). The quenching rate at pH 2 is strongly enhanced by the presence of SDS, while that at basic pH is greatly retarded. These observations are explained by deep embedment of RBPY+ into the hydrophobic hydrocarbon region of the micelle, whereas Ru(bpy)32+ and HRBPY2+ locate in the Stern layer of the micelle.

• Bulletin of the Korean Chemical Society
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• 제9권5호
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• pp.283-288
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• 1988

The titled properties on reduction of the perovskite $LaBO_3$ (B = Fe, Co, Ni) have been investigated by means of temperature-programmed reduction, isothermal reduction and X-ray diffraction methods. Nominal composition of $LaFeO_{3.18},\;LaCoO_{3.00}\;and\;LaNiO_{2.92}$ are determined. Reduction reaction of these mixed oxides differed according to B-site transition metal and thermal stability on reduction decreased as following order: $LaFeO_{3.18}$ > $LaCoO_{3.00}$ > $LaNiO_{2.92}$. From the results of isothermal reaction, kinetics on reduction of the perovskite has been discussed in detail.

• 공업화학
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• 제4권4호
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• pp.823-829
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• 1993

Linseed oil fatty acid(LOFA), phthalic anhydride(PAA) 및 trimellitic anhydride(TMA), trimethylol propane(TMP)을 사용하여 기본적인 유장(oil length) 50%의 중유성 알키드를 합성하고 trimethylol propane triacrylate (TMPTA)를 그라프트 공중합시켜 수용성 TMPTA 변성 알키드수지를 제조하였다. 알키드수지의 산가는 TMA함량으로 제어하였으며, 수용화에는 N,N-Dimethylethanol amino(DMEA)를 중화제로 사용하였다. TMA함량에 따른 산가별 내수성 및 수용화의 최적조건을 산출한 후, TMPTA의 첨가량 변화에 의한 분자량, 유리전이온도, 수용화 후의 점성도, 그라프트율을 측정하였으며, 멜라민 수지를 사용하여 가교시킨 막의 경화온도별 겔분율변화를 조사하였다. TMA첨가량 5.3~7.0%, 산가 40~50의 범위에서 알키드 수지의 내수성과 수용화가 가장 좋은 균형을 나타냈으며, 변성 알키드수지의 경우 TMPTA의 양이 증가할수록 분자량, 수용액의 점성도, 겔분율은 증가하였으나, 유리전이온도(Tg)는 감소하였다. 고형분 함량에 따른 점성도 변화는 고형분 40%일 때보다 50%일 때가 점성도가 낮게 나타났으며 중화도에 따른 수용액의 점성도 변화는 중화도가 높을수록 점성도는 낮아지나 중화도 100~110 사이에서는 거의 변화가 없음을 알 수 있었다. TMPTA의 그라프트율은 TMPTA의 첨가량이 4wt%인 때가 가장 높게 나타남이 확인되었다.

• 청정기술
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• 제21권4호
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• pp.248-256
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• 2015

MnO₂를 KMnO₄와 MnCl₂･4H₂O을 이용해 자연침전을 유도한 후, 수열방법으로 120-200 ℃, 0.5-5시간 범위에서 제조하여 300 ℃에서 열처리 후 CO 산화반응을 수행하였다. 촉매활성 원인의 규명과 물리화학적 특성을 분석하기 위해 X 선 회절 분석, 질소 흡착, 주사전자현미경, 수소 또는 일산화탄소 승온환원 분석(H₂- 또는 CO-TPR)을 실시하였다. 합성조건에 따라 순수한 α-MnO₂ 혹은 α/β-혼합상을 가진 MnO₂가 각각 합성되었다. 촉매활성과 안정성은 순수한 α-MnO₂ 상에서 α/β-혼합상을 가진 MnO₂보다 우수하게 관찰되었다. 특히, 150 ℃에서 1시간 수열 합성된 촉매는 가장 큰 비표면적인 214 m² g^-1을 가졌으며 H₂, CO-TPR 분석에서 가장 우수한 환원성과 격자산소 종의 활성을 보였으며 일산화탄소의 승온 및 등온 산화반응에서 가장 우수한 촉매활성을 나타내었다. 이것은 촉매의 물리화학적 특성에 기인한 것으로 촉매의 결정구조, 비표면적, 환원성 및 격자산소 종의 활성은 촉매활성과 깊은 상관관계가 존재함을 확인하였다.

• 공업화학
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• 제31권1호
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• pp.57-60
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• 2020

An acetaldehyde, a representative food waste odor, was decomposed using a hybrid system comprised of a non-thermal plasma and catalyst at an ambient temperature under high humidity. A five wt.% Mn was impregnated on two differently structured microporous zeolites, namely Beta and ZSM-5, with a different molar ratio of SiO₂/Al₂O₃. Under high humidity conditions, the acetaldehyde degradation was higher in zeolites with the high ratio of SiO₂/Al₂O₃. Among studied catalysts, a five wt.% Mn/Beta (SiO₂/Al₂O₃ = 300) showed the highest acetaldehyde removal activity owing to its high hydrophobicity and reducibility. During long term stability test using the same catalyst for 110 hours, the acetaldehyde removal activity was relatively well-maintained.

• 자연과학논문집
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• 제15권1호
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• pp.35-46
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• 2005

$LaFeO_3$ 복합산화물과 부분 치환한 $LaFeO_3$ 복합산화물을 citrate와 Cyanide 공침법으로 합성하여 공기중에서 $850^{\circ}C$로 24시간동안 열처리해 제조방법에 의한 영향을 비교하였다. XRD와 IR의 결과에 의하여면, 합성된 산화물은 Orthorhombic의 Perovskite구조를 나타냈으나 B자리에 0.5mol의 Cu가 치환된 복합산화물은 단일상을 얻지 못하였다. 또한, 이들 산화물의 환원반응은 치환하지 않은 $LaFeO_3.17$ 복합산홤루은 2단계 반응인 반면에 치환한 복합산화물은 3단계 반응으로 Dopant에 의한 새로운 환원단계가 존재함을 알았다.

• Bulletin of the Korean Chemical Society
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• 제24권1호
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• pp.86-90
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• 2003

Reverse-Water-Gas-Shift reaction (RWGSR) was carried out over the ZnO, $Al_2O_3,\;and\;ZnO/Al_2O_3$ catalysts at the temperature range from 400 to 700 ℃. The ZnO showed good specific reaction activity but this catalyst was deactivated. All the catalysts except the $ZnO/Al_2O_3$ catalyst (850 ℃) showed low stability for the RWGSR and was deactivated at the reaction temperature of 600 ℃. The $ZnO/Al_2O_3$ catalyst calcined at 850 ℃ was stable during 210 hrs under the reaction conditions of 600 ℃ and 150,000 GHSV, showing CO selectivity of 100% even at the pressure of 5 atm. The high stability of the $ZnO/Al_2O_3$ catalyst (850 ℃) was attributed to the prevention of ZnO reduction by the formation of $ZnAl_2O_4$ spinel structure. The spinel structure of $ZnAl_2O_4$ phase in the $ZnO/Al_2O_3$ catalyst calcined at 850 ℃ was confirmed by XRD and electron diffraction.

• Bulletin of the Korean Chemical Society
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• 제21권12호
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• pp.1239-1244
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• 2000

A study of K addition to the catalyst of CoMo/ ${\gamma}-Al_2O_3$ was studied. The catalyst with 10 at% of K to Mo atoms in 3C10M, the catalyst added 3 wt% CoO to 10 wt% $MoO_3/{\gamma}-Al_2O_3$, showed the highest activity for water gas shift reaction. The addition of K retarded the reducibility of cobalt-molybdenum catalysts. It gave, however, good dispersion and large BET surface area to the catalysts which were attributed to the disappearance of polymolybdate clustyer such as $Mo_7O_{24}^{6-}$ and the formation of small Mo$O_4^{2-}$ cluster. It was confirmed by the analyses of pore size distribution, activation energy, Raman spectroscopy, and electron diffraction. The activation energies and the frequency factors of the catalysts 3C10M and 5KC10M (the catalyst added 5 at% K for Mo to the catalyst 3C10M) were 43.1 and 47.8 kJ/mole, and 4,297 and 13,505 $sec^{-1}$, respectively. These values were also well correlated with our suggestion. These phenomena were attributed to the direct interaction between K and CoMo oxides irrelevant to the support.

• 한국재료학회지
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• 제29권7호
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• pp.432-436
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• 2019

Zinc oxide(ZnO) micro/nanocrystals are grown via thermal evaporation of ZnO powder mixed with Mn powder, which is used as a reducing agent. The ZnO/Mn powder mixture produces ZnO micro/nanocrystals with diverse morphologies such as rods, wires, belts, and spherical shapes. Rod-shaped ZnO micro/nanocrystals, which have an average diameter of 360 nm and an average length of about $12{\mu}m$, are fabricated at a temperature as low as $800^{\circ}C$ due to the reducibility of Mn. Wire-and belt-like ZnO micro/nanocrystals with length of $3{\mu}m$ are formed at $900^{\circ}C$ and $1,000^{\circ}C$. When the growth temperature is $1,100^{\circ}C$, spherical shaped ZnO crystals having a diameter of 150 nm are synthesized. X-ray diffraction patterns reveal that ZnO had hexagonal wurtzite crystal structure. A strong ultraviolet emission peak and a weak visible emission band are observed in the cathodoluminescence spectra of the rod- and wire-shaped ZnO crystals, while visible emission is detected for the spherical shaped ZnO crystals.