Water adsorption isotherms are systematically summarized by using celluloses and polysaccharides as hydrophilic crystal/amorphous materials with functional groups, silicas as hydrophilic porous materials, and inorganic salts, sugar alcohols, and amino acids as hygroscopic deliquescent materials. For hydrophilic fibers such as celluloses and polysaccharides, water was adsorbed on amorphous solids, and water clusters were formed around functional groups. For porous materials such as silicas, capillary condensation occurred in the micropores of silicas. For deliquescent materials such as inorganic salts, sugar alcohols, and amino acids, water adsorption rapidly increased stepwise at a specific threshold relative humidity, accompanied with a structure transformation to a liquid state. In addition, the water activity (Aw) of materials used in packed products was able to be estimated from the water adsorption isotherms of the pure component. This indicated that the deliquescent materials have a great effect on the depression of Aw for the suppression of microbial growth at an extremely high water content. The deliquescent materials could be useful to develop new environmentally and sustainable products and technologies with the mediation of water vapor and/or hydration.
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http://dx.doi.org/10.1021/acsomega.3c06642 | DOI Listing |
Chem Sci
October 2024
State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences Fuzhou 350002 P. R. China
Balancing the critical property requirements is key to surmounting the obstacles in the application of nonlinear optical (NLO) crystals. Tricoordinated units, characterized by nearly the lowest coordination number, are common in inorganic NLO-active oxides; however, crystals solely composed of such units are rare. Herein, by assembling three distinct tricoordinated units (SbO, TeO, and NO) into a single crystal, a pioneering fully tricoordinated NLO material, (SbTeO)(NO), was synthesized a facile volatilization method.
View Article and Find Full Text PDFChempluschem
October 2024
school of Mechanical Engineering, Qinghai University, Xining, 810016, PR China.
In this study, ultrafine linear nanostructured SiC with high wettability and large specific surface area were synthesized via the carbothermal reduction method. These nanowires were impregnated with NaSO ⋅ 10HO, CaCl ⋅ 6HO, MgCl ⋅ 6H2O, and CaMgCl ⋅ 12HO to obtain composite phase change materials (CPCMs), which demonstrated improved phase separation and significantly reduced supercooling. In particular, the supercooling degree of CaCl ⋅ 6HO was minimized to 0.
View Article and Find Full Text PDFJ Phys Chem A
August 2024
The Institute of Chemical Physics, School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing 100081, China.
The deliquescence phase transition of atmospheric aerosols is crucial for radiative forcing and atmospheric chemistry. However, the deliquescence kinetics of micrometer-sized aerosols, especially the formation and evolution of surface solution films, remain poorly understood. In this study, IR spectral characteristics were employed for the first time to quantify the solute concentration evolution in surface solution films.
View Article and Find Full Text PDFRSC Adv
May 2024
School of Geography, Earth and Environmental Sciences, University of Birmingham Edgbaston B15 2TT Birmingham UK
Single particle levitation techniques allow us to probe samples in a contactless way, negating the effect that surfaces could have on processes such as crystallisation and phase transitions. Small-angle X-ray scattering (SAXS) is a common method characterising the nanoscale order in aggregates such as colloidal, crystalline and liquid crystalline systems. Here, we present a laboratory-based small-angle X-ray scattering (SAXS) setup combined with acoustic levitation.
View Article and Find Full Text PDFEur J Pharm Biopharm
August 2024
Department of Chemical and Pharmaceutical Sciences, University of Trieste, P.le Europa 1, 34127 Trieste, Italy. Electronic address:
We report an intriguing example of enantioselectivity in the formation of new multicomponent crystalline solid containing vinpocetine and malic acid. Several experimental data sets confirmed that the multicomponent system presents a clear enantiospecific crystallisation behaviour both in the solid-state and in solution: only the system consisting of vinpocetine and L-malic acid produces a free-flowing solid consisting of a new crystalline form, while the experiments with D-malic acid produced an amorphous and often deliquescent material. The new vinpocetine-L-malic system crystallizes in the monoclinic space group of P2 and in a 1:1 molar ratio, where the two molecules are linked through intermolecular hydrogen bonds in the asymmetric unit.
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