Associative polymer/particle dispersion phase diagrams III: Pigments

2006 ◽  
Vol 3 (3) ◽  
pp. 165-171 ◽  
Author(s):  
Edward Kostansek
Materials ◽  
2020 ◽  
Vol 13 (1) ◽  
pp. 225 ◽  
Author(s):  
Sara Dalle Vacche ◽  
Dragan Damjanovic ◽  
Véronique Michaud ◽  
Yves Leterrier

Composites in which particles of ferroelectric ceramic phase are randomly dispersed in a polymeric matrix are of interest because of flexibility, conformability, and ease of processing. However, their piezoelectric properties are rather low, unless very high volume fractions of ceramics are used. This brings agglomeration and porosity issues due to the large mismatch between the surface energies of the ceramics and of the polymer. Particle surface modification is a common approach for better dispersion; however, it may bring other effects on the properties of the composites, which are usually concealed by the huge improvement in performance due to the more homogenous microstructure. In this work, we compared poly(vinylidene fluoride–trifluoroethylene)/barium titanate composites containing 15 vol.% and 60 vol.% of pristine ceramic particles or particles modified with an aminosilane or a fluorosilane. Similar morphology, with good particle dispersion and low porosity, was achieved for all composites, owing to an efficient dispersion method. The materials were poled with two different poling procedures, and the piezoelectric coefficient d33, the relative permittivity, and the poling degree of barium titanate were followed in time. We highlighted that, although similar d33 were obtained with all types of particles, the nature of the particles surface and the poling procedure were associated with different charge trapping and influenced the evolution of d33 with time.


1993 ◽  
Vol 304 ◽  
Author(s):  
Connie S. Heck ◽  
J. E. Roberts

AbstractThe adsorption behavior of model associative polymers in aqueous titanium dioxide (TiO2) and polystyrene latex (PS) particle dispersions has been studied using liquid-state Nuclear Magnetic Resonance (NMR) and a modified serum replacement technique (SRT). The structure of the associative polymer is a linear, water soluble, A-B-A block copolymer with a polyethylene oxide backbone and hydroxyl (H) or hexadecyl (C16H33) endgroups.Absolute intensity NMR measurements allow the determination of the adsorbed polymer configuration at the solid-solution interface and adsorption isotherms for comparison to the SRT results. Both the SRT and NMR results demonstrate that the adsorption/desorption of the C16 and H polymers is strongly affected by the substrate. For the polymer/PS particle systems, there is good agreement in complete surface saturation values for the SRT and NMR methods. In the polymer/TiO2 systems, the H polymer plateau as determined by NMR differs slightly from that determined by SRT. For the C16/TiO2 system the interpretation is less straightforward. Either the NMR saturation value is at least double that of the SRT value or the C16 and H polymers have very similar isotherms by NMR. This would suggest that on TiO2 the effect of the hydrophobe is minimal. For all the polymers the polymer/particle interaction on PS is strong and desorption is difficult while on TiO2 it is weak and completely reversible. A pancake-to-brush conformation change on the PS surface is evident for the C16 polymers and probably for the H polymer as well. The H polymer seems to form a multi-layered structure on PS from the NMR and laser light scattering results. The contribution of the hydrophobe and the effect of increasing the backbone molecular weight are clearly illustrated.


1992 ◽  
Vol 287 ◽  
Author(s):  
He-Zhuo Miao ◽  
Long-Hao Qi ◽  
De-Jin Ma ◽  
Zuo-Zhao Jiang

ABSTRACTSi3N4 ceramics are excellent metal cutting materials. The cutting behavior can be improved by hard particle dispersion phase hardening and heat treatment so as to reduce glass phase in the grain boundaries. Compared with cemented carbide tools, the cutting life of the composite Si3N4 cutting tool is about 10-100 times longer, and the optimum cutting speed is about 3-10 times faster. It performs well in cutting hardened tools, nickel based alloys, and other hard materials and can sustain shock loads in operations such as milling, planing and other types of interrupted cutting. Applications in various fields show that machining efficiency can be increased by 3-10 times resulting in savings of time, electricity, and machining of 30-70% or even more.


Soft Matter ◽  
2016 ◽  
Vol 12 (3) ◽  
pp. 658-663 ◽  
Author(s):  
Fei Xie ◽  
Clifford E. Woodward ◽  
Jan Forsman

We construct a polymer + particle dispersion model which displays a non-monotonic response to temperature changes, in agreement with recent experimental findings.


2018 ◽  
Vol 916 ◽  
pp. 184-189
Author(s):  
Mohammed A. Hefni ◽  
Ferri P. Hassani ◽  
Mehrdad F. Kermani

This study is part of large and ongoing investigation into the potential use of calcium carbonate nanoparticles (NCaCO3) to improve the mechanical and physical properties of mine backfill. The investigation was conducted in two phases. In phase I, gold tailings were used to prepare backfill sample using Portland cement (PC) as the binding agent under various NCaCO3 and superplasticizer (SP) dosages. In phase II, fine silica sand was used to minimize the reactive nature of tailings, which can adversely affect uniaxial compressive strength (UCS). Samples in this phase were prepared under various NCaCO3 dosages using slag:PC weight ratios of 80:20 as the binding agent. Select samples from phase II were subjected to Mercury Intrusion Porosimetry (MIP) to compare microstructural properties before and after addition of NCaCO3. Phase I results showed that the UCS of samples containing NCaCO3 was low, even when SP was used to improve particle dispersion. Phase II samples exhibited up to 9.5% higher UCS after 28 days of curing at a NCaCO3 dosage of 6% by weight of binder. MIP results showed that samples containing NCaCO3 were less porous than the corresponding controlled silica sand backfill samples, which in turn influenced the UCS results.


Author(s):  
E. R. Kimmel ◽  
H. L. Anthony ◽  
W. Scheithauer

The strengthening effect at high temperature produced by a dispersed oxide phase in a metal matrix is seemingly dependent on at least two major contributors: oxide particle size and spatial distribution, and stability of the worked microstructure. These two are strongly interrelated. The stability of the microstructure is produced by polygonization of the worked structure forming low angle cell boundaries which become anchored by the dispersed oxide particles. The effect of the particles on strength is therefore twofold, in that they stabilize the worked microstructure and also hinder dislocation motion during loading.


Author(s):  
A. Zangvil ◽  
L.J. Gauckler ◽  
G. Schneider ◽  
M. Rühle

The use of high temperature special ceramics which are usually complex materials based on oxides, nitrides, carbides and borides of silicon and aluminum, is critically dependent on their thermomechanical and other physical properties. The investigations of the phase diagrams, crystal structures and microstructural features are essential for better understanding of the macro-properties. Phase diagrams and crystal structures have been studied mainly by X-ray diffraction (XRD). Transmission electron microscopy (TEM) has contributed to this field to a very limited extent; it has been used more extensively in the study of microstructure, phase transformations and lattice defects. Often only TEM can give solutions to numerous problems in the above fields, since the various phases exist in extremely fine grains and subgrain structures; single crystals of appreciable size are often not available. Examples with some of our experimental results from two multicomponent systems are presented here. The standard ion thinning technique was used for the preparation of thin foil samples, which were then investigated with JEOL 200A and Siemens ELMISKOP 102 (for the lattice resolution work) electron microscopes.


Sign in / Sign up

Export Citation Format

Share Document