• The Korean Journal of Ceramics
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• 제6권1호
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• pp.47-52
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• 2000

Lanthanides such as La, Gd and Ce have recognized as elements of high level radioactive wastes immobilized by forming solid solution with $CaTiO_3$. For easy forming solid solution between $CaTiO_3$and lanthanides, the combustion synthesis process was applied and the powder characteristics and sinterability were investigated. The proper selection of the type and the composition of fuels are important to get the crystalline solid solution of $CaTiO_3$and lanthanides. When glycine or the mixtures of urea and citric acid with stoichiometric composition was used as a fuel, the solid solution of $CaTiO_3$with $La_2O_3$or $Gd_2O_3$or $CeO_2$was produced very well by the combustion process. The combustion synthesized powder seemed to have a good sinterability with the linear shrinkage of more than 25% up to $1500^{\circ}C$, while that of the solid state reacted powder was less than 10% at the same condition.

• 한국재료학회지
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• 제33권10호
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• pp.385-392
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• 2023

A solution combustion process for the synthesis of hollandite (BaAl₂Ti₆O₁₆) powders is described. SYNROC (synthetic rock) consists of four main titanate phases: perovskite, zirconolite, hollandite and rutile. Hollandite is one of the crystalline host matrices used for the disposal of high-level radioactive wastes because it immobilizes Sr and Lns elements by forming solid solutions. The solution combustion synthesis, which is a self-sustaining oxi-reduction reaction between a nitrate and organic fuel, generates an exothermic reaction and that heat converts the precursors into their corresponding oxide products in air. The process has high energy efficiency, fast heating rates, short reaction times, and high compositional homogeneity. To confirm the combustion synthesis reaction, FT-IR analysis was conducted using glycine with a carboxyl group and an amine as fuel to observe its bonding with metal element in the nitrate. TG-DTA, X-ray diffraction analysis, SEM and EDS were performed to confirm the formed phases and morphology. Powders with an uncontrolled shape were obtained through a general oxide-route process, confirming hollandite powders with micro-sized soft agglomerates consisting of nano-sized primary particles can be prepared using these methods.

• 한국재료학회지
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• 제11권9호
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• pp.797-801
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• 2001

In this study, the solution combustion method was employed to synthesize stoichiometric mullite, and hence the attrition process was employed to prepare ultrafine mullite particles with nano size. The thermal decomposition behavior and partial pressure of equilibrium species of both oxidizer and fuel were considered during solution combustion process. The synthesized product was mullite phase with 40 nm crystalline size, and the alumina contents of the product by TEM/EDS quantity analysis was 3.12$\pm$04 mole. The result showed that the synthesized mullite was almost close to the it's stoichiometric composition. For attrition process, the dispersion behavior of the mullite suspension was controlled and was comminuted with the condition of 800 rpm for 4 hours using 0.3 mm zirconia ball media. As a result of comminution, the mean particle size was 80 nm.

• 한국분말재료학회지
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• 제8권1호
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• pp.13-19
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• 2001

Ni and NiO particles were made by a combustion synthesis process. The characteristics of synthesized powders were investigated with various kinds and amounts of fuels such as urea, citric acid and glycine. Ni phase particles without NiO phase were obtained through combustion synthesis process in air atmosphere with-out further calcinations process, when the content of glycine was 2.44 times of the stoichiometric ratio in the precursor solution. Primary particle sizes of synthesized Ni and NiO particles were about 20∼30 nm.

• 한국연소학회지
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• 제13권1호
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• pp.17-22
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• 2008

A partly implicit/quasi-explicit method is introduced for the solution of detailed chemical kinetics with stiff source terms based on the standard fourth-order Runge-Kutta scheme. Present method solves implicitly only the stiff reaction rate equations, whereas the others explicitly. The stiff equations are selected based on the survey of the chemical Jaconian matrix and its Eigenvalues. As an application of the present method constant pressure combustion was analyzed by a detailed mechanism of hydrogen-air combustion with NOx chemistry. The sensitivity analysis reveals that only the 4 species in NOx chemistry has strong stiffness and should be solved implicitly among the 13 species. The implicit solution of the 4 species successfully predicts the entire process with same accuracy and efficiency at half the price.

• 한국세라믹학회지
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• 제35권10호
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• pp.1078-1084
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• 1998

금속 질산염과 urea를 사용하여 연소합성법에 의해 LaCrO3 분말을 제조하고, 용액의 pH를 HNO3와 NH4OH로 조절한 후, 용매의 가열방법에 따른 연소 생성물인 LaCrO3의 형상을 고찰하였다. 연소생성물의 수율은 용액의 pH에 의해 크게 좌우되었다. 용액의 pH가 0.7~4 사이에서는 90% 이상의 수율이 얻어졌으나, 5 이상 또는 0.5 이하의 pH에서는 수율이 크게 감소하였다. 한편, 연소생성물의 형상은 용액의 pH에 무관하였고 용액의 가열방법에 좌우되었다. 용액을 저항가열법으로 가열하여 연소반응시킨 경우의 분말은 미세한 일차입자들이 2차원적으로 연결된 응집체를 형성하고 있었으나, 마이크로파를 인가하여 가열한 경우에는 용액의 pH에 관계없이 미세한 LaCrO3 분말이 얻어졌다. BET 분석 결과, 마이크로파 가열에 의해 얻어진 입자의 비표면적은 25~32m2/g으로 저항가열법으로 가열한 경우의 10-14m2/g에 비해 더 큰 값을 보였다. 이러한 결과는 마이크로파에 의한 연소반응물의 균일한 가열이 연소생성물의 2차원적인 강항 응집체 형성을 억제할 수 있음을 보여 주었다.

• 한국세라믹학회지
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• 제39권1호
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• pp.74-78
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• 2002

본 연구에서는 전구체 용액의 산화환원 발열반응을 이용하여 다성분계 산화물을 제조할 수 있는 용액연소합성법을 이용하여 페로브스카이트 구조 PZT 세라믹스를 합성하고자 하였다. 산화제/환원제 전구체 혼합물의 열분석(DTA/TG) 결과 산화제와 환원제의 열분해 거동의 차이로 인해 214$^{\circ}C$와 35$0^{\circ}C$에서 발열 피크가 나타났다. PZT세라믹스 합성을 위한 승온 과정에서는 37$0^{\circ}C$에서 연소반응이 일어났으나, 페로브스카이트로의 상전이는 일어나지 않았다. 용액연소과정 중 산화제와 연료의 열분해 거동을 고려하여 $600^{\circ}C$에서 제조한 생성물은 결정크기가 50nm인 정방정의 단일상으로 이루어진 PZT세라믹스이었다. 격자상수를 측정한 결과 a는 3.997$\pm$0.001 $\AA$이었으며, c는 4.147$\pm$0.001 $\AA$으로 나타났다.

• 한국세라믹학회지
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• 제35권5호
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• pp.451-457
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• 1998

$Li_2$$ZrO_3$ powder which is one of the candidates of breeding materials for the fusion reactor was syn-thesized by a precipitation-combustion process. Although precipitates from the reaction between zirconium nitrate and citric acid were existed in a precursor solution. $Li_2$$ZrO_3$ could easily be obtained by using the mixed fuel of urea and citric acid in stoichiometric composition. The phases of as-synthesized powder con-sisted of $Li_2$$ZrO_3$ and small amounts of $Li_6$$Zr_2O_3$ and $Li_2$$ZrO_3$ The latter phases disappeared after the cal-cination at $1100^{\circ}C$ for 2 h. The primary particle size and the specific surface area of as-synthesized powders were smaller than 20nm and 10-14 $M^2$/g, respectively. The primary particle size of the precipitation-combustion synthesized powders was affected by the size of precipitates present in a precursor solution.

• 한국세라믹학회지
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• 제33권4호
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• pp.411-417
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• 1996

Ultrafine NiO/YSZ (Yttria Stabilized Zirconia) powders were made by using a glycine nitrate process which is used as anode material for solid oxide fuel cells. The specific surface areas of synthesized NiO/YSZ powders were examined with controlling pH of a precursor solution and the content of glycine. The binding of glycine with metal nitrates occurring in the precursor solution was analyzed by using FTIR. The characteristics of synthesized powders were examined with X-ray diffraction(XRD) Brunauer Emmett Teller with N2 absorption. scanning electron microscopy (SEM). and transmission electron microscopy (TEM). Ultrafine NiO/YSZ powders of 15-18 m2/g were obtained through GNP when the content of glycine was controlled to 1 or 2 times the stoichiometric ratio in the precursor solutions. Strongly acid precursor solution increased the specific surface area of the synthesized powders. This is suggested to be the increased binding of metal nitrates and glycine under a strong acid solution of pH=0.5 that lets glycine consist of mainly the amine group of {{{{ { NH}`_{3 } ^{+ } }}. After sintering and reducing treatment of NiO/YSZ powders synthesized by GNP the Ni/YSZ pellet showed ideal microstructure where very fine Ni particles of 3-5 ${\mu}{\textrm}{m}$ were distributed uniformly and fine pore around Ni metal particles was formed. leading to anincrease of the triple phase boundary among gas Ni and YSZ.

• Korean Chemical Engineering Research
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• 제52권2호
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• pp.256-260
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• 2014

건축물 내부의 장식을 위해 사용되는 MDF합판은 화염의 착화를 지연시키기 위해 방염처리하도록 규정하고 있어 일반적으로 방염도료나 방염액 또는 방염필름 등을 적용하여 착화를 지연시키는데 이 때 적용하는 시료에 따라 방염성능과 연소 시 발생되는 가스의 유독성의 차이가 발생할 수 있어 본 연구에서는 MDF에 적용된 방염시료들의 방염성능 및 연소특성에 대해 비교분석하였으며 그 결과 방염성능에 부합하는 제품이 확인되었으나 방염처리방법에 따라 방염성능의 차이가 존재함을 확인할 수 있었으며 연소과정에서 발생되어지는 여러 종류의 유독가스의 영향도 함께 고려해야 할 요소임을 확인할 수 있었다.