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Yoshifumi Amamoto

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2 published item(s)

preprint2026arXiv

Integrating Bayesian Spectral Deconvolution and Expert Scientific Reasoning for Robust Peak Estimation

Spectral deconvolution is essential for extracting peak structures that encode material properties and chemical structures, but conventional automated methods often fail when spectra contain high-intensity noise or unknown background components. In practice, scientists rarely interpret spectra in isolation. Instead, they identify physically meaningful peaks by relating spectral structures to auxiliary information such as physical-property values, chemical structures, and trends across related measurements. Here, we propose a Bayesian framework that integrates spectral deconvolution with a model of expert scientific reasoning. In this work, expert scientific reasoning refers to the practice of evaluating candidate spectral structures by their consistency with independently measured physical-property values, rather than to manual expert intervention during inference. We formalize this reasoning as a physical-property regression layer, implemented using Gaussian process regression, and couple it with Bayesian spectral deconvolution. By averaging the physical-property likelihood over posterior predictive spectra inferred from Bayesian spectral deconvolution, the proposed method selects spectral models according to the consistency between inferred spectral structures and physical-property information. We validate the framework using synthetic spectra with high-intensity noise or unknown backgrounds and infrared spectra of poly(lactic acid). The method recovers physically meaningful peak structures that conventional Bayesian spectral deconvolution misses or misidentifies from spectra alone, including weak peaks in poly(lactic acid) IR spectra related to measured degradation rates. These results demonstrate that integrating expert scientific reasoning with Bayesian spectral deconvolution enables robust peak estimation under conditions where spectrum-only inference is unreliable.

preprint2021arXiv

Different Response of Molecular Aggregation Structure of Styrenic Triblock Copolymer under Cyclic Uniaxial and Biaxial Stretching Modes

Mechanical stretching behavior of poly(styrene-b-ethylene-co-butylene-b-styrene) (SEBS) triblock copolymer (87 wt% polyethylene-co-butylene (PEB) block, 13 wt% polystyrene (PS) block) was investigated by three different stretching and in situ small angle X ray scattering (SAXS) measurements. Strain energy density function was investigated based on the stress stretching ratio (λ) relationship under uniaxial, planar extension, and equi-biaxial stretching modes. As the result, cross effect of strain represented by second invariants of the deformation tensor (I2) existed and only Ogden model can be used to fit the data. In the cyclic stretch testing, SEBS exhibited smaller hysteresis during cyclic equi biaxial stretching mode than for uniaxial stretching one. λ and stretching ratio obtained from crystal planes by SAXS (λSAXS) were compared to investigate relationship between microdomain structure change and macroscopic mechanical property. SAXS measurement revealed that affine deformation occurred in the smaller 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 PEB loop chains could work as cross-linking points when films are stretched by equi-biaxial stretching mode.