In-Situ Alloying Dynamics and Phase Morphology of Binary Polymer Blends

2014 ◽  
Vol 67 (1) ◽  
pp. 93
Author(s):  
Jing-qing Li ◽  
Gui-qiu Ma ◽  
Xu-bo Yuan ◽  
Jing Sheng

In-situ alloying of polypropylene (PP)/polystyrene (PS) binary polymer blends using anhydrous aluminum chloride as a catalyst was investigated by small angle light scattering. The phase structures, morphology, and compatibilization effect in the obtained alloys during the in-situ alloying process were investigated by Rayleigh scattering. The content of compatible domains between the two phases of PP and PS in the in-situ alloys, i.e. the volume fraction of the interfacial transition layer, and the ‘invariant’ of the alloys were first calculated to describe the in-situ alloying dynamics, which reveals that the resulting in-situ PP/PS alloys are partially compatible. The relationship between the volume fraction of the interfacial transition layer or ‘invariant’ and the in-situ alloying reactive conditions are discussed in detail. The phase structural parameters, including correlation distance and average chord lengths, were calculated to characterize the phase size evolutions of the in-situ alloys, confirming the validity of using the volume fraction of the interfacial transition layer or ‘invariant’ to investigate the in-situ alloying dynamics.






1988 ◽  
Vol 133 ◽  
Author(s):  
M. G. Mendiratta ◽  
D. M. Dimiduk

ABSTRACTIn the Nb-Si system, it is possible to produce in-situ composites consisting of a brittle Nb5Si3 intermetallic matrix and ductile Nb particles. The two phases are thermochemically stable up to ∼ 1500∼C and are amenable to wide microstructural variations including morphology, volume fraction, and the size of the individual microconstituents. This paper presents microstructures and phase transformations in these composites as a function of composition and heat treatments and bend properties from room-temperature to 1400°C.



Author(s):  
H. Kung ◽  
A.J. Griffin ◽  
Y.C. Lu ◽  
K.E. Sickafus ◽  
T.E. Mitchell ◽  
...  

Materials with compositionally modulated structures have gained much attention recently due to potential improvement in electrical, magnetic and mechanical properties. Specifically, Cu-Nb laminate systems have been extensively studied mainly due to the combination of high strength, and superior thermal and electrical conductivity that can be obtained and optimized for the different applications. The effect of layer thickness on the hardness, residual stress and electrical resistivity has been investigated. In general, increases in hardness and electrical resistivity have been observed with decreasing layer thickness. In addition, reduction in structural scale has caused the formation of a metastable structure which exhibits uniquely different properties. In this study, we report the formation of b.c.c. Cu in highly textured Cu/Nb nanolayers. A series of Cu/Nb nanolayered films, with alternating Cu and Nb layers, were prepared by dc magnetron sputtering onto Si {100} wafers. The nominal total thickness of each layered film was 1 μm. The layer thickness was varied between 1 nm and 500 nm with the volume fraction of the two phases kept constant at 50%. The deposition rates and film densities were determined through a combination of profilometry and ion beam analysis techniques. Cross-sectional transmission electron microscopy (XTEM) was used to examine the structure, phase and grain size distribution of the as-sputtered films. A JEOL 3000F high resolution TEM was used to characterize the microstructure.



Author(s):  
H. Q. Ye ◽  
T.S. Xie ◽  
D. Li

The Ti3Al intermetallic compound has long been recognized as potentially useful structural materials. It offers attractive strength to weight and elastic modulus to weight ratios. Recent work has established that the addition of Nb to Ti3Al ductilized this compound. In this work the fundamental problem of this alloy, i.e. order-disorder and antiphase domain structures was investigated at the atomic scale.The Ti3Al+10at%Nb alloys used in this study were treated at 1060°C and then aged at 700°C for 2 hours. The specimens suitable for TEM were prepared by standard jet electrolytic-polishing technique. A JEM-200CX electron microscope with an interpretable resolution of about 0.25 nm was used for HREM.The [100] and [001] projections of the α2 phase were shown in Fig.l.The alloy obtained consist of at least two phases-α2(Ti3Al) and β0 structures. Moreover, a disorder α phase with small volume fraction was also observed. Fig.2 gives [100] and [001] diffraction patterns of the α2 phase. Since lattice parameters of the ordered α2 (a=0.579, c=0.466 nm) and disorder α phase (a0=0.294≈a/2, c0=0.468 nm) are almost the same, their diffraction patterns are difficult to be distinguished when they are overlapped with epitaxial orientation relationships.



2003 ◽  
Vol 780 ◽  
Author(s):  
P. Thomas ◽  
E. Nabighian ◽  
M.C. Bartelt ◽  
C.Y. Fong ◽  
X.D. Zhu

AbstractWe studied adsorption, growth and desorption of Xe on Nb(110) using an in-situ obliqueincidence reflectivity difference (OI-RD) technique and low energy electron diffraction (LEED) from 32 K to 100 K. The results show that Xe grows a (111)-oriented film after a transition layer is formed on Nb(110). The transition layer consists of three layers. The first two layers are disordered with Xe-Xe separation significantly larger than the bulk value. The third monolayer forms a close packed (111) structure on top of the tensile-strained double layer and serves as a template for subsequent homoepitaxy. The adsorption of the first and the second layers are zeroth order with sticking coefficient close to one. Growth of the Xe(111) film on the transition layer proceeds in a step flow mode from 54K to 40K. At 40K, an incomplete layer-by-layer growth is observed while below 35K the growth proceeds in a multilayer mode.



Soft Matter ◽  
2021 ◽  
Author(s):  
D. Zeb Rocklin ◽  
Lilian C Hsiao ◽  
Megan E Szakasits ◽  
Michael J Solomon ◽  
Xiaoming Mao

Rheological measurements of model colloidal gels reveal that large variations in the shear moduli as colloidal volume-fraction changes are not reflected by simple structural parameters such as the coordination number,...



Coatings ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 584
Author(s):  
Rui Dang ◽  
Liqiu Ma ◽  
Shengguo Zhou ◽  
Deng Pan ◽  
Bin Xia

Ultra-high molecular weight polythene (UHMWPE), with outstanding characteristics, is widely applied in modern industry, while it is also severely limited by its inherent shortcomings, which include low hardness, poor wear resistance, and easy wear. Implementation of feasible protection on ultra-high molecular weight polythene to overcome its shortcomings would be of significance. In the present study, amorphous carbon (a-C) film was fabricated on ultra-high molecular weight polythene (UHMWPE) to provide good protection, and the relevant growth mechanism of a-C film was revealed by controlling carbon plasma currents. The results showed the in situ transition layer, in the form of chemical bonds, was formed between the UHMWPE substrate and the a-C film with the introduction of carbon plasma, which provided strong adhesion, and then the a-C film continued epitaxial growth on the in situ transition layer with the treatment of carbon plasma. This in situ growth of a-C film, including the in situ transition layer and the epitaxial growth layer, significantly improved the wetting properties, mechanical properties, and tribological properties of UHMWPE. In particular, good protection by in situ growth a-C film on UHMWPE was achieved during sliding wear.



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