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The mechanical stretching behavior of the poly(styrene-b-ethylene-co-butylene-b-styrene) (SEBS) triblock copolymer (87 wt% polyethylene-co-butylene (PEB), 13 wt% polystyrene (PS)) was investigated under three different stretching modes and through in situ small-angle X-ray scattering (SAXS) analysis. The strain energy density function was investigated based on the stress and stretching ratio (λ) relationship under uniaxial, planar extension, and equi-biaxial stretching modes. As a result, the cross-effect of strain represented by the second invariants of the deformation tensor (I2) was identified, and only the Ogden model found to fit the data. In the cyclic stretching tests, SEBS exhibited smaller hysteresis during cyclic equi-biaxial stretching compared to uniaxial stretching. In other words, the Mullins effect was found to be more obvious for uniaxial stretching than equi-biaxial stretching. The λ and the stretching ratio obtained from the crystal planes by SAXS (λSAXS) were compared to investigate the relationship between the change in the microdomain structure and the macroscopic mechanical properties. Thus, affine deformation was found to occur in the smaller λ region for both uniaxial and equi-biaxial stretching and deviation from affine deformation occurred for uniaxial stretching in the larger λ region. This is because the entangled loops of PEB chains serve as cross-linking points when the films are stretched under equi-biaxial stretching. The mechanical stretching behavior of poly(styrene-b-ethylene-co-butylene-b-styrene) (SEBS) was investigated under three different stretching modes and through in situ SAXS analysis. SEBS exhibited smaller hysteresis during cyclic equi-biaxial stretching than that of uniaxial stretching. SAXS measurement revealed that affine deformation occurred in the smaller stretching ratio (λ) region for both uniaxial and equi-biaxial stretching modes and deviation from affine deformation occurred for uniaxial stretching mode at the larger λ region. This is because entangled loops of poly(ethylene-co-butylene) chains serves as cross-linking points when films are stretched under equi-biaxial stretching mode.

The specific deformation behavior of crystalline polymer films, namely unoriented crystallized isotactic polypropylene (it PP) films, was investigated under a multiaxial stress field.

The strength of silica-based mechanochromic nanocomposites was improved by a novel nanocomposite synthesized by grafting poly(butyl acrylate) (PBA)-b-poly(methyl methacrylate) (PMMA) from silica na...

The deformation behavior of polythiourethane (PTU) elastomers was investigated using in situ small-angle X-ray scattering (SAXS), wide-angle X-ray diffraction (WAXD), and X-ray absorption fine stru...

The local mechanical properties of crystalline polymer were evaluated using synchrotron radiation X-ray diffraction with 10 μm lateral resolution. A nonoriented isotactic polypropylene (iPP) film with isolated spherulites in a crystallized matrix was used as a model sample. In situ wide-angle X-ray diffraction (WAXD) measurement was performed on the iPP film using a microbeam synchrotron radiation X-ray under sinusoidal strain. The lattice spacing of the crystal planes increased and decreased in response to the applied sinusoidal strain. Local dynamic viscoelastic functions (dynamic storage and loss moduli (

It is desirable to establish a method for evaluating mechanical properties, such as modulus and strength, of micrometer and sub-micrometer thick polymer films. Bulge tests, where bulge deformation is imposed on films by the pressure of an inert gas, are suitable for satisfying this demand. However, very few studies on polymer films exist in the literature. In this study, bulge testing equipment for in situ synchrotron radiation wide-angle X-ray diffraction (WAXD) measurements is designed and used to study the relationship between the molecular aggregation structure and the mechanical properties of a crystalline nylon 12 (Ny12) film during bulge testing. Isothermally crystallized and quenched Ny12 films exhibited stress-strain curves similar to those obtained by conventional uniaxial elongation. In situ WAXD measurements during bulge testing revealed that the lattice extension of the crystallites is clearly dependent on crystallinity. Concretely, crystallites in the isothermally crystallized film show higher elastic properties than those in the quenched one. The results of the molecular aggregation structure, including the crystal structure and the amorphous chain surrounding the crystallites, of the films during bulge deformation firstly obtained in this study must be useful for designing toughened polymer films.

The scratch test was conducted for polycarbonate (PC) and poly(methyl methacrylate) (PMMA) with a load-progressive mode. Changes in the molecular aggregation structure of PC and PMMA induced by the scratch test were investigated based on polarized optical microscopic observation and small-angle X-ray scattering (SAXS) measurement. The scratching coefficient of friction (SCOF), the ratio of tangential load to normal load, of PC was much larger than that of PMMA. The width and depth of the damage on the scratch path was increased monotonically with the increase in the normal load. Hardness obtained by nanoindentation and microindentation tests were similar to those with SCOF, indicating that compression resistance mainly governs the scratch properties. The polarized optical microscopic images revealed that molecules were oriented from the edge to the center of the scratch path at a certain acute angle for both PC and PMMA. SAXS measurement revealed that microfibrils were formed along the direction of stress for PC.

The advantages of bulge testing as a method of mechanical property analysis for polymer films was described. Deformation and rupture mechanisms of glassy polymer films during bulge testing were investigated by in situ molecular aggregation structure analyses. Heat-pressed polycarbonate (PC, weight-average molecular weight (Mw) = 38k) and poly(methyl methacrylate) (PMMA, Mw = 70k and 1.2 M (PMMA-70k and PMMA-1.2 M)) films were employed as transparent glassy polymers. Evaluations of molecular aggregation structures during bulge testing were conducted by polarized high-speed camera observation and wide-angle X-ray diffraction (WAXD) measurements. PC and PMMA-1.2 M films showed a yield point in their stress-strain curves, indicating ductility, while PMMA-70k film showed brittleness. WAXD measurements revealed that the distances between the main chains slightly increased with increasing strain. With increasing film strain above the yield point, a craze-like morphology with thinning of the film was seen for the PC film, likely due to the flexible PC molecules. Although it is difficult for PMMA molecules to orient along applied stress, a transition to the thinner state with the formation of wrinkled structures occurred for the PMMA-1.2 M film above the yield point. The transition to the thinner state, which corresponds to a discontinuous decrement of the cross-section area by deformation, might be categorized as two-dimensional crazing and/or shear deformation. PMMA-70k did not show such behavior because of the small number of entanglements. The use of a small amount of films in terms of thickness and size and the capability of observation of the entire film were given as advantages of the bulge test.