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Journal of Materials Science | 1998

Evolution of the formation of barium titanate in the citrate process: the effect of the pH and the molar ratio of barium ion and citric acid

Jenq-Dar Tsay; Tsang-Tse Fang; T. A. Gubiotti; Jackie Y. Ying

In this investigation, several experiments were conducted to study the effects of the molar ratio of barium ion and citric acid and the pH value on the formation of BaTiO3 by the citrate process. It was found that the molar ratio of barium ion and citric acid and the pH value could affect the chelation of carboxylate groups and Ba/Ti ions at temperatures below 450 °C but they seemed not to influence the formation of BaTiO3. The development of an oxycarbonate intermediate during the thermal decomposition of (Ba,Ti) gel was confirmed, which was suggested to possess a structure of BaTiO3, whereby CO−23 was located inside the layer structure.


Journal of Materials Science | 1995

The effect of the molar ratio of cations and citric acid on the synthesis of barium ferrite using a citrate process

Wen-Jiung Lee; Tsang-Tse Fang

A model is presented to evaluate the concentration of species in a citric solution for preparing barium ferrite powder. The evaluated concentration of species provides valuable information and help in selecting the optimal condition for preparation of the barium ferrite powder using the citrate process. The influence of the molar ratio of cations and citric acid on the formation of barium ferrite is studied. The formation temperature of barium ferrite decreases as the ratio increases. When the molar ratio of cations and citric acid is 13∶20, the barium ferrite can completely form at 700 °C.


Materials Chemistry and Physics | 1998

Effects of milling and particle size distribution on the sintering behavior and the evolution of the microstructure in sintering powder compacts

Fuh-Shan Shiau; Tsang-Tse Fang; Tsung-Hsing Leu

Abstract In this investigation, it was observed that the contamination arising from the milling medium has a great influence on the sintering behavior. The densification rate of the powder milled with ZrO2 balls is largely inhibited, and the activation energy of ZrO2-doped alumina is significantly enhanced. The possible reasons for the enhancement of the activation energy were discussed. The effects of particle size distribution of powder compacts on the microstructural evolution of alumina during sintering were proposed and discussed.


Journal of Materials Science | 1995

Forming processes of strontium barium niobate ceramics

Tsang-Tse Fang; Nan-Ti Wu

In forming strontium barium niobate (SBN) ceramics, two methods (pressure filtration and slip casting) were employed to investigate the consolidation behaviour. The zeta potentials were measured to understand the interparticle forces of SBN powders. It was found that the zeta potentials of SBN powders were negative above pH 2.2. Several experiments have been conducted to investigate the effect of pH on the rheological behaviour of SBN slurries with 20 vol% solids loading. The rheological behaviour of the slurries SBN with 20 vol% solids loading at pH 11.5 is shear thinning. It is suggested that the increase of the flow rate of the fluid might have the advantages to enhance the packing density and prevent fine particles from clogging in pressure filtration and slip casting. Two different moulds i.e. plaster and alumina have been used to investigate the effect of pore morphology of the moulds on the cake microstructures. A uniform microstructure of cast cake was formed for using an alumina mould and significant contamination was observed in using a plaster mould.


Journal of Materials Science | 1990

The role of dopants on the formation and defect structures of the M-type of calcium ferrite

Tsang-Tse Fang; K. T. Lee

The formation mechanisms of M-type calcium ferrite were further assessed by doping Y2O3, BaCO3 and SrCO3. It was found that the ionic radius, rather than the valence is the predominant factor in the formation of the magnetoplumbite phase of calcium ferrite. The CaO/sd2Fe2O3 phase which played a precursor role in the formation of the M-type calcium ferrite was further verified. The defect structures based on the substitution of Ca2+ by La3+, the charge compensation by Fe2+, and release of oxygen were supported by DTA-TGA and conductivity data. The conductivity was assumed to, occur through a hopping mechanism as it increased with increasing temperature. The estimated values of the activation energy based on the small-polaron conduction were 0.35 to 0.40 eV in the high temperature region and 0.027 to 0.054 eV in the low temperature region. Moreover, the preexponential factor in the conductivity equation is an exponential function of the fraction of the M phase in the specimen.


Journal of the American Ceramic Society | 2005

Mechanism for developing the boundary barrier layers of CaCu3Ti4O12

Tsang-Tse Fang; Hsu-Kai Shiau


Journal of the American Ceramic Society | 2007

Evidence of Cu Deficiency: A Key Point for the Understanding of the Mystery of the Giant Dielectric Constant in CaCu3Ti4O12

Tsang-Tse Fang; Li-Then Mei


Journal of the American Ceramic Society | 2004

Effects of Molar Ratio of Citric Acid to Cations and of pH Value on the Formation and Thermal-Decomposition Behavior of Barium Titanium Citrate

Jenq-Dar Tsay; Tsang-Tse Fang


Journal of the American Ceramic Society | 2008

Effect of Copper-Rich Secondary Phase at the Grain Boundaries on the Varistor Properties of CaCu3Ti4O12 Ceramics

Li-Then Mei; Hsing I. Hsiang; Tsang-Tse Fang


Journal of the American Ceramic Society | 2005

Densification and Microstructural Development of the Reaction Sintering of Strontium Barium Niobate

Wen-Jiung Lee; Tsang-Tse Fang

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Jenq-Dar Tsay

National Cheng Kung University

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Fuh-Shan Shiau

National Cheng Kung University

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Jung-Cheng Lin

National Cheng Kung University

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Wen-Jiung Lee

National Cheng Kung University

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Han-Yang Chung

National Cheng Kung University

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Li-Then Mei

National Cheng Kung University

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Ma-Shine Wu

National Cheng Kung University

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Tsung-Hsing Leu

National Cheng Kung University

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Chao-Wei Yang

National Cheng Kung University

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Chih-Hao Lee

National Tsing Hua University

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