Abstract:
The present invention provides a method for evaluating the rebound resilience, hardness, or energy loss of polymer materials, capable of sufficiently evaluating the difference in performance between samples with excellent measurement accuracy. The present invention relates to a method for evaluating the rebound resilience, hardness, or energy loss of a polymer material, including irradiating the polymer material with X-rays or neutrons to perform X-ray scattering measurement or neutron scattering measurement.
Abstract:
Provided is a transparent conductive film including a transparent plastic film substrate and an indium-tin composite oxide transparent conductive film laminated on at least one surface of the transparent plastic film substrate, a value of the normalized integrated intensity of a diffraction peak measured by X-ray diffractometry in the (222) plane due to a crystal of the transparent conductive film being 4 to 25 cps• ∘ /nm.
Abstract:
A sample holder 2 for holding a capillary 40 for X-ray analysis has a first thermal transport member 36 on the base portion 14 on one side of a longitudinal slit 12 and a second thermal transport member 38 on the base portion 16 on the other side. The thermal transport members 36, 38 are compressed between a frame 30 and the base portion 14,16 in the transverse direction to urge the edges of the first and second thermal transport members together, to hold a capillary 40 longitudinally aligned with the longitudinal slit 12.
Abstract:
The inventors discovered that viscosity of a protein solution can be estimated by measuring the apparent particle size or apparent molecular weight by a small angle X-ray scattering (SAXS) method or X-ray solution scattering method, which enables measurement of small amounts of samples, and then correlating those measurement results with viscosity of the protein solution.
Abstract:
The present invention provides a method for evaluating abrasion resistance of a polymeric material, wherein the method provides sufficient evaluation of the difference in performance between samples with excellent measurement accuracy. The method includes irradiating the polymeric material with X-rays or neutrons to perform X-ray scattering measurements or neutron scattering measurements. The abrasion resistance is evaluated based on the number per unit volume of scatterers having a correlation length in the range 0.1 nm to 100 microns.