山本 拓司

Bicellar mixtures containing diacetylene molecules, such as diynoic acids, can be used as parent materials for functional membranes. A bicellar mixture consisting of a diynoic acid-10,12-tricosadiynoic acid (TCDA)-, a phospholipid-1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC)-, and a detergent-3-[(3-cholamidopropyl) dimethylammonio]-2-hydroxypropanesulfonate (CHAPSO)-was evaluated for its morphology and packing of TCDA molecules in its bicellar mixture. A TCDA/DMPC vesicle was prepared at different molar ratios, TCDA/DMPC = 2/8, 5/5, and 8/2; a TCDA/DMPC/CHAPSO bicellar mixture was prepared by mixing a CHAPSO solution with a TCDA/DMPC vesicle solution as a detergent at different composition ratios, x TCDA/DMPC = [TCDA/DMPC]/([TCDA/DMPC]+[CHAPSO]), of 1.0, 0.70, 0.50, and 0.30. A DMPC molecule formed a bilayer membrane structure and was used to suppress its precipitation. The packing density of the TCDA/DMPC/CHAPSO bicellar mixtures was increased by mixing a CHAPSO molecule in x TCDA/DMPC = 1.0 to 0.70 or 0.50. A TEM image of a TCDA/DMPC/CHAPSO bicellar mixture showed many discoidal assemblies at x TCDA/DMPC = 0.5 of TCDA/DMPC = 5/5. Polymerization of the TCDA molecules in the bicellar mixture by UV light suggested an ordered arrangement of TCDA. Polymerization at x TCDA/DMPC = 0.70 and 0.50 correlated with improved packing density.

Continuous crystallization via indirect cooling of potassium aluminum sulfate dodecahydrate (KAl(SO4)(2)center dot 12H(2)O) was carried out using a draft tube-type crystallizer with a circulation flow path. The crystallizer was equipped with a newly designed system to monitor the degree of supersaturation in the circulation channel. The average degree of supercooling and growth rate were measured. The crystal growth rates calculated by the population balance model and the supersaturation monitor were different but close. The average supersaturation calculated from the supercooling degree and the solubility data in the literature was 0.19 g per 100 g H2O. This system is also expected to be applied to industrial crystallization where impurities are present.

To understand the inclusion of mother liquor in crystals at different sizes, the continuous crystallization of potassium sulfate was investigated. A bench-scale crystallizer of the draft-tube type was employed for both batch cooling and continuous crystallizations. A standard solution of potassium sulfate was employed as the saturated solution at 323 K. The batch cooling crystallization was first performed at 283 K at a rate of 5 K/h, after which the continuous crystallization was performed at 283 K at two different residence times. The crystal size distribution (CSD) of potassium sulfate crystals and the inclusion ratio of mother liquor in the crystals at different sizes were measured. The average size of the crystals was approximately 400-500 mu m, and the inclusion ratio was less than 1% for all sizes; however, the small and large crystals contained a considerable amount of mother liquor, and the specific crystals that exhibited the lowest inclusion ratios were investigated. Moreover, an impurity distribution model for the suspension crystals was proposed based on coreaggregation and shell-growth processes.

A new method for determining the liquidus and solidus pressures of mixtures of C18's unsaturated fatty acids at constant temperatures was proposed, and three binary isothermal SLE data under high-pressure were systematically measured in this study. The liquidus and solidus temperatures of oleic acid, linoleic acid and alpha-linolenic acid commonly rise above their normal melting temperatures when pressure is increased. This new high-pressure experimental system can closely track pressure in real time during pressure swinging changes, making it simple to measure liquidus and solidus pressures using this dynamic measurement method due to fast responsiveness of pressure. In this study, the liquidus pressures of pure oleic acid, linoleic acid, alpha-linolenic acid and three binary mixtures consisted of oleic acid, linoleic acid alpha-linolenic acid at constant temperature were determined. The isothermal SLE were first correlated based on a simple thermodynamic model. (C) 2021 Elsevier Ltd.

Bicelles are extensively used as the parent assemblies of functional membrane materials. This study characterizes membrane fluidity in fatty acid/detergent bicelles containing carboxyl boron-dipyrromethene (BODIPY C12) and pyrromethene as fluorescent probe molecules. The anisotropy value of BODIPY C12 and pyrromethene in the phospholipid vesicles depended on the phase state of the vesicles. The anisotropy of the fluorescent probe molecules in bicelles of oleic acid/3-[(3-cholamidopropyl) dimethylammonio]-2-hydroxypropane sulfonate (OA/CHAPSO) was then evaluated. The OA/CHAPSO bicelles were prepared by mixing CHAPSO detergent solution with OA vesicles at different molar ratios, XOA (= [OA]/([OA]+[CHAPSO])). The anisotropies of the probes in the OA/CHAPSO bicelles increased with decreasing XOA. BODIPY C12 in the range 0.30 ≤ XOA ≤ 0.70 exhibited a distinctly larger anisotropy than pyrromethene. This result agreed with the increase in packing density associated with the adsorption of CHAPSO molecules on the OA bilayer membrane in the OA/CHAPSO bicelle, revealing that the anisotropy of BODIPY C12 molecule enables membrane-fluidity evaluation in OA/CHAPSO bicelles.