Full-Field Determination of Principal-Stress Directions Using Photoelasticity with Plane-Polarized RGB Lights

In this paper, we propose a new three-wavelength method for automatic measurement of principal-stress directions over an entire model on the basis of four-step phase shift method. This method uses four fringe patterns captured by a color charge-coupled devices (CCD) camera corresponding to four angular position arrangements of polaroids in a dark-field plane polariscope. The principal-stress directions can be determined by a single calculation. The method is applied to a circular disc under compression. The principal-stress direction distributions obtained from the proposed method are compared with those obtained from a conventional method and theory. It can be obviously seen that the proposed method accurately yields the principal-stress directions compared with the conventional method.     

Phase separation of off‐critical polymer blends of poly(styrene‐co‐maleic anhydride) and poly(methyl methacrylate). II. Morphology and mechanical properties

The effects of the phase‐separation temperature and time on the mechanical properties and morphology of poly(methyl methacrylate)/poly(styrene‐co‐maleic anhydride with 10 wt% ethyl acrylate) (SMA) blends were studied. Two compositions (20/80 and 40/60 w/w SMA/PMMAe) were prepared with a miniature twin‐screw extruder. Compared with those of the miscible blends, the Young's modulus values of the blends increased after the phase separation of the 40/60 SMA/PMMAe blend and within the early stage of spinodal decomposition of the 20/80 SMA/PMMAe blend. The mechanical properties, in terms of the tensile strength at break and the elongation, were better for the miscible blends than for the phase‐separation blends. This was believed to be the result of changes in the composition and molecular reorganization. The changes in the phase‐separating domains of both compositions, as observed by transmission electron microscopy, had no significant influence on the tensile moduli. Detailed studies of the morphology revealed a cocontinuous structure, indicating that the blends underwent spinodal decomposition. A morphological comparison of the two compositions illustrated the validity of the level rule. The growth rate of the droplet size was determined by approximation from the light scattering data and by direct measurements with transmission electron microscopy. The discrepancies observed in the droplet size growth rate were attributed to heat variations induced by the different sample thicknesses and heat transfer during the investigation. © 2004 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 42: 886–897, 2004     

On the universality of crossing probabilities in two-dimensional percolation

Six percolation models in two dimensions are studied: percolation by sites and by bonds on square, hexagonal, and triangular lattices. Rectangles of widtha and heightb are superimposed on the lattices and four functions, representing the probabilities of certain crossings from one interval to another on the sides, are measured numerically as functions of the ratioa/b. In the limits set by the sample size and by the conventions and on the range of the ratioa/b measured, the four functions coincide for the six models. We conclude that the values of the four functions can be used as coordinates of the renormalization-group fixed point.     

Growth and characterization of nanostructured anatase phase TiO<Subscript>2</Subscript> thin films prepared by DC reactive unbalanced magnetron sputtering

Titanium dioxide thin films were deposited on three different unheated substrates by unbalanced magnetron sputtering. The effects of the sputtering current and deposition time on the crystallization of TiO₂ thin films were studied. The TiO₂ thin films were deposited at three sputtering current values of 0.50, 0.75, and 1.00 A with different deposition times of 25, 35, and 45 min, respectively. The surface morphology of the films was investigated by atomic force microscopy (AFM). The structure was characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM). The film thickness was determined by field emission scanning electron microscopy (FE-SEM), and the optical property was evaluated with spectroscopic ellipsometry. The results show that polycrystalline anatase films were obtained at a low sputtering current value. The crystallinity of the anatase phase increases as the sputtering current increases. Furthermore, nanostructured anatase phase TiO₂ thin films were obtained for all deposition conditions. The grain size of TiO₂ thin films was in the range 10–30 nm. In addition, the grain size increases as the sputtering current and deposition time increase.     

A Spectroscopic Ellipsometry Study of TiO2 Thin Films Prepared by dc Reactive Magnetron Sputtering： Annealing Temperature Effect

TiO2 thin films are obtained by dc reactive magnetron sputtering. A target of titanium （99.995%） and a mixture of argon and oxygen gases are used to deposit TiO2 films on to silicon wafers （100）. The crystalline structure of deposited and annealed film are deduced by variable-angle spectroscopic ellipsometry （VASE） and supported by x-ray diffractometry. The optical properties of the films are examined by VASE. Measurements of ellipsometry are performed in the spectral range O. 72-3.55 e V at incident angle 75^o. Several SE models, categorized by physical and optical models, are proposed based on the ＇simpler better＇ rule and curve-fits, which are generated and compared to the experimental data using the regression analysis. It has been found that the triple-layer physical model together with the Cody-Lorentz dispersion model offer the most convincing result. The as-deposited films are found to be inhomogeneous and amorphous, whereas the annealed films present the phase transition to anatase and rutile structures. The refractive index of TiO2 thin films increases with annealing temperature. A more detailed analysis further reveals that thickness of the top sub-layer increases, whereas the region of the bottom amorphous sub-layer shrinks when the films are annealed at 300℃.     

The crystallinity and miscibility of syndiotactic polystyrene blends after mixing with low molar mass liquid crystal or commercial lubricant

The quantities of the crystallinity of syndiotactic polystyrene (SPS) blended with another polymer in the group of poly(α-methyl styrene), poly(n-butyl methacrylate) or poly(cyclohexyl acrylate) with or without the additives were measured by X-ray diffraction and calculated by Ruland’s method. The SPS was synthesized by using metallocene catalyst and modified-methylaluminoxane as cocatalyst. The additive of low molar mass liquid crystal chemical (cyclohexyl-biphenyl-cyclohexane (CBC33)) or lubricant (glycerol monostearate (GMS)) was individually added to the blends of SPS in order to investigate the effects on the crystallinity of the blended SPS. From the experimental results, it was found that the percent crystallinities of the blends decreased with decreasing the percent of SPS in the blend because of the dilution of SPS. The depression of the percent crystallinity was in the order of PaMS > PCHA > PBMA according to the compatibility with SPS. The addition of GMS or CBC33 slightly decreased the percent crystallinity of the pure SPS. The addition of GMS impeded the depression of the SPS crystallinity in the blends, because their percent depression from pure SPS is similar (at around 25%) regardless to the components of the blends. The blends with added CBC33 have the similar depression of crystallinity as the pure blends because of the low concentration of CBC33 and the good compatibility of CBC33 with the SPS.     

Phase separation of off‐critical polymer blends of poly(styrene‐co‐maleic anhydride) and poly(methyl methacrylate). I. Kinetics of spinodal decomposition

The kinetics of phase separation via the spinodal decomposition of poly(styrene‐co‐maleic anhydride)/poly(methyl methacrylate) from a delay time period to late stages were investigated with a light scattering technique. The standard procedure for identifying four stages of spinodal decomposition, based on the characteristics of concentration fluctuations, was clearly introduced with the light scattering method. The spinodal limits were divided into four stages: the delay time, the early stage, the intermediate stage, and the late stage. The validity of the linearized theory was reviewed because it was used as an indicator of the limit of the early stage of spinodal decomposition, which divided the delay time period from the early stage and the early stage from the intermediate stage. The linearized theory fit the experimental results very well after the delay time. The scaled structure function of the melt‐mixed blend was analyzed. The universality of the scale structure function, F(x) = S(q,t)q_m³(t) (where S is the structure function, x is equal to q/q_m, q is the scattering wave vector, q_m is the maximum wave vector, and t is the time in seconds), indicated the late stage of phase separation and divided the late stage from the intermediate stage. The simple normalized scaling function profile for the cluster region proposed by Furukawa described the experimental data very well, whereas the profile for deep quenching, which was recently suggested, showed some discrepancies. As a result of the phase separation, the processing of this blend may be able to be developed to provide the most suitable morphology. © 2004 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 42: 871–885, 2004     

ESR Spectrometer as a Possible Tool for Rapid Analysis of Cane Sugar Purity

A method for quantitative/qualitative determination of cane sugar purity by ESR is devised. Relined sugar, plantation white sugar, soft brown sugar and raw sugar are used as samples in this work. The sucrose radical is produced by pulverization of sugar and it increases as the particle size decreases. Based on pulverization-induced sucrose radical, ESR study demonstrates the effects of sugar purity on characteristic of ESR spectrum. The relationship between the sucrose contents and peak area under the ESR spectrum is manifested. It is found that the peak area or sucrose radical concentration increases linearly with the increase of sucrose content. Using the linear regression method, the sucrose amount can be revealed. This approach is a promising fast and accurate method for sugar purity analysis.