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Hidemasa Teraoka

Publications and source records attributed to Hidemasa Teraoka.

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Cooperative effects of membrane confinement and gelation on PEG crystallization pathway

Lipid-coated microscale hydrogels provide confined, hydrated environments in which polymer phase behavior can differ markedly from that in bulk. Here, we investigate the crystallization pathway of poly(ethylene glycol) (PEG) encapsulated in lipid-coated agarose microgels. Surprisingly, polarized-light microscopy reveals birefringence in the microgels under conditions where PEG remains non-crystalline in the corresponding bulk solution. The birefringence disappears upon heating and spontaneously reappears after further cooling or upon local mechanical stimulation. Infrared microspectroscopy demonstrates that the birefringent microgels contain crystalline PEG, whereas non-birefringent microgels contain PEG in an amorphous-like state, indicating the existence of a metastable precursor prior to crystallization. Furthermore, cooling below the phase-separation temperature produces PEG-rich domains preferentially near the membrane, suggesting that membrane wetting governs the spatial distribution of PEG before crystallization. Together, these results indicate that membrane confinement and agarose gelation cooperatively alter the local hydration environment of PEG, thereby stabilizing an amorphous-like precursor and redirecting the subsequent crystallization pathway. Our findings identify the coupling of membrane wetting and gelation as a key factor governing PEG crystallization in confined soft materials.

cond-mat.soft

Impurity contribution to ultraviolet absorption of saturated fatty acids

Saturated fatty acids are abundant organic compounds in oceans and sea sprays. Their photochemical reactions induced by solar radiation have recently been discovered as an abiotic source of volatile organic compounds, which serve as precursors of secondary organic aerosols. However, photoabsorption of wavelengths longer than 250 nm in liquid saturated fatty acids remains unexplained, despite being first reported in 1931. Here we demonstrate that the previously reported absorption of wavelengths longer than 250 nm by liquid nonanoic acid [CH3(CH2)7COOH)] originates from traces of impurities (0.1% at most) intrinsically contained in nonanoic acid reagents. Absorption cross sections of nonanoic acid newly obtained here indicate that the upper limit of its photolysis rate is three-to-five orders of magnitude smaller than those for atmospherically relevant carbonyl compounds.

cond-mat.mtrl-sci