DESIGN, ASSEMBLY AND CHARACTERIZATION OF COMPOSITE ...

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Figure 3.4 Comparison of oscillatory behavior between φsolids = 0.44 carbon black gels stabilized by Makon 10 and NP 4070 respectively. 3.3.4 Gelation Mechanism The gel behavior of this carbon black gel is the result of a synergy between carbon black particles and all non-ionic polymer molecules. The gelation mechanism of many ceramic inks used in robocasting is assumed to use reversible electrostatic cross- linking between adsorbed polyelectrolyte molecules and oppositely charged polyelectrolyte in solution, e.g. ammonium polyacrylate and poly(ethylenimine). In a sense, these gels may be regarded as particle filled, polymeric hydrogels that have properties between those of high concentration polymeric hydrogels and high concentration colloidal gels of pure ceramic particles based on electrostatic double layers. 94
In the case of the aqueous carbon black gels studied here, no bridging flocculation by polyelectrolyte is possible; and gelation is dependent on hydrogen bonding of the non- ionic polymers, with the reinforcing effect of the carbon black particles. The polymer concentration is significantly higher than in ceramic colloidal gels, partly because of the higher specific surface area of smaller particles. The dissolved polymer Pluronic F-127 has a concentration enough to form a hydrogel without carbon black particles, but it would be a much weaker one. Enough hydrogen bonding sites must be present to allow gel behavior. In the absence of extra polymer free in solution, the solid volume fraction of carbon black dispersion has to be greater than a threshold value Φgel so that the inter-particle separation may fall below twice of the surfactant layer thickness, resulting in compression and inter- penetration of PEO chains of adsorbed NP4070 molecules. 98 After that, gel behaviors replace viscous flow; elasticity increases as the particles network compacts further. It has been shown that terminally anchored PEO tails (MW = 4800) may extend more than 30 nm in good solvent condition 111 . For the NP4070 surfactant with MW = 1600 PEO tails, a value of around 10 nm is reasonable in water. Layer thicknesses for similarly-structured nonylphenol polypropylene oxide-polyethylene oxide surfactants adsorbed on carbon black in highly concentrated dispersions were calculated. 98 which also supports the estimate of 10 nm thickness for the NP4070 surfactant. The average separation distance between carbon black particles is estimated for different φsolids and packing types in Table 3.3. Considering the hierarchy structure of carbon black aggregates, 102 the maximum packing density by weight for the carbon black gel is unlikely to be very high, much volume must be occupied by the internal voids in those aggregates. This calculation 95
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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
Page 59 and 60: Figure 2.23 Schematic diagram of th
Page 61 and 62: 2.5.4.2 Rearrangement With the form
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: For HA ink, yield stress
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
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mixing, BT and Ni phases appear uni
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The combined use of PAA and PAA-90K
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To quantify this difference in sint
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As the BT and Ni particles used in
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The reducing atmosphere used in the
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Figure 5.7 Vickers hardness number
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5.3.6. Fabrication of BT-Ni composi
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modify the sintering kinetics of th
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a) b) Figure 5.10 Co-sintered compo
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5.4. Conclusions Freeform fabricati
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Liquid phase sintering involves usi
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(pH=4.4, 31.5% by weight) (Adva Flo
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concentration of 7 mg/mL in the aqu
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Table 6.1 Formulations of aqueous c
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thickness. Each layer of the struct
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6.2.6. Hardness Test Microindentati
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micrographs for these two powders.
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Second, the added LiAC∙2H2O is am
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Figure 6.3 Oscillatory behavior for
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a) b) Figure 6.4 Sintering strain c
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mass transport in LFBT network. 167
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The above discussion is mainly focu
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Figure 6.8 shows the bowtie-shaped
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Figure 6.10 A NPR composite of para
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etween BT and Ni phases. But Zn ele
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Figure 6.13 Scanning electron micro
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Figure 6.15 shows the mapping of Ti
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Figure 6.17 and Figure 6.18 show el
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Figure 6.19 shows element mapping f
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6.3.7. Piezoelectricity and Dielect
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6.4. Conclusions Aqueous colloidal
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geometric features, including non-s
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3. Development of aqueous colloidal
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7.2. Recommendations In the context
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gelation behavior. κ-carrageenan i
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REFERENCES 1. Larsson 9301647, 1993
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29. Simchi, A.; Petzoldt, F.; Pohl,
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61. Bouvard, D., Acta Metallurgica
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92. Morissette, S. L.; Lewis, J. A.
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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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