DESIGN, ASSEMBLY AND CHARACTERIZATION OF COMPOSITE ...

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260 °C. Co-sintering of BT-Ni'(m) green structures is performed with a 2 hour isothermal hold at 1000 °C in the tube furnace (GSL 1600X, MTI Corporation, Richmond, CA), as shown in Figure 6.1. The 2 hour isothermal hold at 600 °C is intended to ensure complete decomposition of LiAC∙2H2O to form Li2O. 167 A 5 °C/min temperature ramp rate is used to heat the furnace to 600 °C and a 2.5 °C/min temperature ramp rate is used from 600 °C to 1000 °C. The slower ramp rate is intended to mitigate possible temperature gradient in the sample structure. Controlled sintering atmosphere involves the use of either dry N2 gas or moist 5%H2/95%N2 gas mixture. The latter will require a subsequent re-oxidation step in dry N2 atmosphere at 800 °C for 24 hours or longer. Figure 6.1 Temperature profile used for liquid phase sintering of BT-Ni composites. 174
6.2.6. Hardness Test Microindentation Vickers test (0.5 kgf load for 5 seconds) is used to measure hardness of LFBT composites. Cylindrical rod specimens are sintered in moist H2/N2 gas at 1000 °C for 2 hours according to Figure 6.1. In preparation for hardness test, these specimens are cross-sectioned using a diamond saw (Labcut 1010, Extec, Enfield, CT), embedded in epoxy resin, and then polished (Labpol 8-12, Extec, Enfield, CT) with diamond pastes at 3 to 0.25 µm particle size (DiaDuo, Struers, Denmark). 6.2.7. Energy Dispersive Spectroscopy (EDS) Characterization EDS is used to examine the element distribution in sintered composite structures. Composite lattice structures resembling MLCCs, similar to those shown in Figure 5.9, are assembled by co-printing the LFBT and low-fire 20BT80Ni/LiAC composite inks. The sintered specimen is embedded in epoxy resin and diced using a diamond saw (Labcut 1010, Extec, Enfield, CT). Afterward, the cross-section of the specimen is polished (Labpol 8-12, Extec, Enfield, CT) with particle size=9, 3, and 0.25 mm diamond pastes (DiaDuo, Struers, Denmark). Energy dispersive spectrometry (FEI Quanta 600 field emission gun ESEM with Evex EDS, Hillsboro, Oregon) is used for the examination. 6.2.8. Piezoelectricity and Dielectric Constant Square LFBT specimens (16×16×4 mm) are printed using a space-filling pattern and sintered (LHT 02/17, Nabertherm GmbH, Lilienthal, Germany) in air at 1000 °C for 2 hours for electric characterization. Top and bottom surfaces of these specimens are polished with particle size=9, 3, and 0.25 mm diamond pastes. Electrodes layers are gold sputter-coated for poling at 7 kV, and piezoelectric coefficient is measured afterwards. 175
Page 1 and 2:
DESIGN, ASSEMBLY AND CHARACTERIZATI
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ACKNOWLEDGEMENTS First and foremost
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CHAPTER 5 BARIUM TITANATE NICKEL CO
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Table 6.1 Formulations of aqueous c
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Figure 2.12 Schematic illustrations
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Figure 2.35 Schematic of the SHS pr
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Figure 4.9 Sintered nickel lattices
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Figure 6.12 Optical image of the cr
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1.1. Motivation CHAPTER 1 INTRODUCT
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and characterizing rheological prop
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2.1. Materials System CHAPTER 2 BAC
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2.2. Reentrant Structures and Ceram
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devices would provide self-sustaini
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a) b) Figure 2.4 Schematic illustra
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production of concept models, injec
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Fused Deposition Modeling (FDM) was
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Laser Engineered Net Shaping (LENS)
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Inkjet printing (IP) 27 is based on
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Table 2.1 Comparisons of various SF
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Figure 2.11 Processing steps involv
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2.4.1 Colloidal Inks The printing i
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Robocasting has lacked a well-desig
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Table 2.2 Example polymers that dep
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2.6. Sintering In robocasting, sint
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Figure 2.15 Sphere and plate model
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where
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2.5.3 Solid State Sintering In this
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Figure 2.18 Illustration of neck gr
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2.5.3.4 Final Stage During this sta
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Figure 2.23 Schematic diagram of th
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2.5.4.2 Rearrangement With the form
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2.5.4.6 Spreading of Sintering Aid
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Driven by reduction of free energy,
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2.5.5 Sintering Atmosphere Sinterin
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2.7. Composite Materials In this re
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Figure 2.29 Types of composite mate
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Table 2.6 Examples of composite mat
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Table 2.7 Examples of FGM applicati
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2.7.3 Processing For the fabricatio
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prepared discrete layers of uniform
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Powder densification processes gene
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The specific volume fraction beyond
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a) b) Figure 2.34 a) Volume fractio
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When the powders are densified in s
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Various FGM coating processes are a
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of FGMs, such as partially reactive
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leading to a characteristic time τ
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3.1 Introduction CHAPTER 3 AQUEOUS
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occurs in a multi-step process: fir
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a) b) Figure 3.1 a) SEM image of as
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3.2.3 Preparation of Carbon Black C
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3.2.5 Drying Shrinkage Characteriza
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the optimized surfactant concentrat
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The storage modulus of a colloidal
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For HA ink, yield stress
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In the case of the aqueous carbon b
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PPO units of Pluronic F-127 may ads
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a) b) Figure 3.6 A carbon black lat
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a) b) Figure 3.7 SEM images of a) c
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TGA plot is in agreement with previ
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a) b) Figure 3.9 Thermogravimetric
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3.3.8 Fabrication of Complex Cerami
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c) d) 109
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3.4 Conclusion A fugitive support m
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metal inks have been reported for R
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Midland, MI) 5% by weight stock sol
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4.2.5. Thermal Degradation of Binde
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4.3. Results and Discussion 4.3.1.
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4.3.2. Preparation of Nickel Ink Su
Page 139 and 140: 260 °C for 8 hours, the residual c
Page 141 and 142: Table 4.1 Calculated residual carbo
Page 143 and 144: a) b) Figure 4.6 Sintered Ni struct
Page 145 and 146: temperature 138, 139 lead to 92-95%
Page 147 and 148: Figure 4.8 Scanning electron microg
Page 149 and 150: c) Figure 4.9 Sintered nickel latti
Page 151 and 152: 5.1. Introduction CHAPTER 5 BARIUM
Page 153 and 154: materials within the overall struct
Page 155 and 156: 40:60, 60:40, 80:20 are separately
Page 157 and 158: 5.2.3. Rheological Characterization
Page 159 and 160: 5.2.5. Co-sintering and Re-oxidatio
Page 161 and 162: mixing, BT and Ni phases appear uni
Page 163 and 164: The combined use of PAA and PAA-90K
Page 165 and 166: To quantify this difference in sint
Page 167 and 168: As the BT and Ni particles used in
Page 169 and 170: The reducing atmosphere used in the
Page 171 and 172: Figure 5.7 Vickers hardness number
Page 173 and 174: 5.3.6. Fabrication of BT-Ni composi
Page 175 and 176: modify the sintering kinetics of th
Page 177 and 178: a) b) Figure 5.10 Co-sintered compo
Page 179 and 180: 5.4. Conclusions Freeform fabricati
Page 181 and 182: Liquid phase sintering involves usi
Page 183 and 184: (pH=4.4, 31.5% by weight) (Adva Flo
Page 185 and 186: concentration of 7 mg/mL in the aqu
Page 187 and 188: Table 6.1 Formulations of aqueous c
Page 189: thickness. Each layer of the struct
Page 193 and 194: micrographs for these two powders.
Page 195 and 196: Second, the added LiAC∙2H2O is am
Page 197 and 198: Figure 6.3 Oscillatory behavior for
Page 199 and 200: a) b) Figure 6.4 Sintering strain c
Page 201 and 202: mass transport in LFBT network. 167
Page 203 and 204: The above discussion is mainly focu
Page 205 and 206: Figure 6.8 shows the bowtie-shaped
Page 207 and 208: Figure 6.10 A NPR composite of para
Page 209 and 210: etween BT and Ni phases. But Zn ele
Page 211 and 212: Figure 6.13 Scanning electron micro
Page 213 and 214: Figure 6.15 shows the mapping of Ti
Page 215 and 216: Figure 6.17 and Figure 6.18 show el
Page 217 and 218: Figure 6.19 shows element mapping f
Page 219 and 220: 6.3.7. Piezoelectricity and Dielect
Page 221 and 222: 6.4. Conclusions Aqueous colloidal
Page 223 and 224: geometric features, including non-s
Page 225 and 226: 3. Development of aqueous colloidal
Page 227 and 228: 7.2. Recommendations In the context
Page 229 and 230: gelation behavior. κ-carrageenan i
Page 231 and 232: REFERENCES 1. Larsson 9301647, 1993
Page 233 and 234: 29. Simchi, A.; Petzoldt, F.; Pohl,
Page 235 and 236: 61. Bouvard, D., Acta Metallurgica
Page 237 and 238: 92. Morissette, S. L.; Lewis, J. A.
Page 239 and 240: 120. Boehm, H. P., Some Aspects of
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150. Atkinson, A., Growth of Nio an
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APPENDICES A. Mathematical Modeling
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and
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conditions: Equation A.12 is solved
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and with
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a) b) Figure B.1 a) Freeze-dried st
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a) Figure C.1 Cr-Ni lattices of 5Cr
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E. Binary Phase Diagram of ZnO-B2O3
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References A.1. Du, Z., Sarofim, A.
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Name: Jian Xu Date of Degree: May,
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