DESIGN, ASSEMBLY AND CHARACTERIZATION OF COMPOSITE ...

More documents

Recommendations

Info

Figure 2.24 Approximate time scale for liquid phase sintering, where densification occurs by a progression of overlapping stages after the liquid forms. 38 2.5.4.1 Solubility Interactions After the formation of liquid phase, there are four possible solubility interactions, as shown in Table 2.5. For classic liquid-phase sintering, the solid is soluble in the liquid, but the reverse solubility of the liquid in the solid is low. This ensures that the liquid is not transient. Table 2.5 Solubility interactions during liquid phase sintering. 38 Liquid solubility in solid Low High 44 Solid solubility in liquid Low High Limited densification & rearrangement Swelling & transient liquid phase Extensive densification Mixed swelling & densification
2.5.4.2 Rearrangement With the formation of a wetting liquid, particles may pack to a higher density rapidly, releasing liquid to fill pores between grains. The solid-liquid surface energy is lower than the solid-vapor surface energy, resulting in reduced system energy. During rearrangement the compact exhibits viscous response to the capillary action. The apparent viscosity of the compact increases due to elimination of porosity; as a consequence, the densification rate decreases continuously. Full density by rearrangement is possible if enough liquid is formed. Rearrangement may be inhibited, if rigid particle contacts formed through compaction or solid-state diffusion are present. 2.5.4.3 Dissolution-Precipitation As densification by rearrangement slows, solubility and diffusivity effects become dominant. The solubility of a grain in its surrounding liquid varies inversely with the grain size: small grains have a higher solubility than large ones. The difference in solubility establishes a concentration gradient in the liquid. Material is transported from the small grains to the large grains by diffusion through the liquid. The net result is a progressive growth of the larger grains at the expense of the smaller grains, giving fewer grains with a larger average size. This allows the growing grains to better fill in space. 2.5.4.4 Final densification In the final stage, liquid-phase sintering is controlled by the slow densification of the rigid solid structure. Processes dominant in this stage have been active earlier, but only become significant late in the cycle. Microstructural coarsening continues and the residual pores enlarge if they contain trapped gas, giving compact swelling. In general, 45
Page 1 and 2:
DESIGN, ASSEMBLY AND CHARACTERIZATI
Page 3 and 4:
ACKNOWLEDGEMENTS First and foremost
Page 5 and 6:
CHAPTER 5 BARIUM TITANATE NICKEL CO
Page 7 and 8:
Table 6.1 Formulations of aqueous c
Page 9 and 10: Figure 2.12 Schematic illustrations
Page 11 and 12: Figure 2.35 Schematic of the SHS pr
Page 13 and 14: Figure 4.9 Sintered nickel lattices
Page 15 and 16: Figure 6.12 Optical image of the cr
Page 17 and 18: 1.1. Motivation CHAPTER 1 INTRODUCT
Page 19 and 20: and characterizing rheological prop
Page 21 and 22: 2.1. Materials System CHAPTER 2 BAC
Page 23 and 24: 2.2. Reentrant Structures and Ceram
Page 25 and 26: devices would provide self-sustaini
Page 27 and 28: a) b) Figure 2.4 Schematic illustra
Page 29 and 30: production of concept models, injec
Page 31 and 32: Fused Deposition Modeling (FDM) was
Page 33 and 34: Laser Engineered Net Shaping (LENS)
Page 35 and 36: Inkjet printing (IP) 27 is based on
Page 37 and 38: Table 2.1 Comparisons of various SF
Page 39 and 40: Figure 2.11 Processing steps involv
Page 41 and 42: 2.4.1 Colloidal Inks The printing i
Page 43 and 44: Robocasting has lacked a well-desig
Page 45 and 46: Table 2.2 Example polymers that dep
Page 47 and 48: 2.6. Sintering In robocasting, sint
Page 49 and 50: Figure 2.15 Sphere and plate model
Page 51 and 52: where
Page 53 and 54: 2.5.3 Solid State Sintering In this
Page 55 and 56: Figure 2.18 Illustration of neck gr
Page 57 and 58: 2.5.3.4 Final Stage During this sta
Page 59: Figure 2.23 Schematic diagram of th
Page 63 and 64: 2.5.4.6 Spreading of Sintering Aid
Page 65 and 66: Driven by reduction of free energy,
Page 67 and 68: 2.5.5 Sintering Atmosphere Sinterin
Page 69 and 70: 2.7. Composite Materials In this re
Page 71 and 72: Figure 2.29 Types of composite mate
Page 73 and 74: Table 2.6 Examples of composite mat
Page 75 and 76: Table 2.7 Examples of FGM applicati
Page 77 and 78: 2.7.3 Processing For the fabricatio
Page 79 and 80: prepared discrete layers of uniform
Page 81 and 82: Powder densification processes gene
Page 83 and 84: The specific volume fraction beyond
Page 85 and 86: a) b) Figure 2.34 a) Volume fractio
Page 87 and 88: When the powders are densified in s
Page 89 and 90: Various FGM coating processes are a
Page 91 and 92: of FGMs, such as partially reactive
Page 93 and 94: leading to a characteristic time τ
Page 95 and 96: 3.1 Introduction CHAPTER 3 AQUEOUS
Page 97 and 98: occurs in a multi-step process: fir
Page 99 and 100: a) b) Figure 3.1 a) SEM image of as
Page 101 and 102: 3.2.3 Preparation of Carbon Black C
Page 103 and 104: 3.2.5 Drying Shrinkage Characteriza
Page 105 and 106: the optimized surfactant concentrat
Page 107 and 108: The storage modulus of a colloidal
Page 109 and 110: For HA ink, yield stress
Page 111 and 112:
In the case of the aqueous carbon b
Page 113 and 114:
PPO units of Pluronic F-127 may ads
Page 115 and 116:
a) b) Figure 3.6 A carbon black lat
Page 117 and 118:
a) b) Figure 3.7 SEM images of a) c
Page 119 and 120:
TGA plot is in agreement with previ
Page 121 and 122:
a) b) Figure 3.9 Thermogravimetric
Page 123 and 124:
3.3.8 Fabrication of Complex Cerami
Page 125 and 126:
c) d) 109
Page 127 and 128:
3.4 Conclusion A fugitive support m
Page 129 and 130:
metal inks have been reported for R
Page 131 and 132:
Midland, MI) 5% by weight stock sol
Page 133 and 134:
4.2.5. Thermal Degradation of Binde
Page 135 and 136:
4.3. Results and Discussion 4.3.1.
Page 137 and 138:
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 and 190:
thickness. Each layer of the struct
Page 191 and 192:
6.2.6. Hardness Test Microindentati
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
Page 241 and 242:
150. Atkinson, A., Growth of Nio an
Page 243 and 244:
APPENDICES A. Mathematical Modeling
Page 245 and 246:
and
Page 247 and 248:
conditions: Equation A.12 is solved
Page 249 and 250:
and with
Page 251 and 252:
a) b) Figure B.1 a) Freeze-dried st
Page 253 and 254:
a) Figure C.1 Cr-Ni lattices of 5Cr
Page 255 and 256:
E. Binary Phase Diagram of ZnO-B2O3
Page 257 and 258:
References A.1. Du, Z., Sarofim, A.
Page 259:
Name: Jian Xu Date of Degree: May,
show all

DESIGN, ASSEMBLY AND CHARACTERIZATION OF COMPOSITE ...

You also want an ePaper? Increase the reach of your titles

Delete template?

Save as template?