Recent reports on the organic structure-directing agent (OSDA)-free synthesis of some zeolites with the aid of seed crystals have opened a new way to the robust and environmentally friendly production of industrially valuable zeolites. However, the details on the crystallization behavior as well as the role of the seeds have not been fully clarified yet. In this study, the crystallization process of zeolite beta in the OSDA-free, seed-embedded Na+−aluminosilicate gel system, which never yields beta in the absence of the seeds, is investigated in detail. The XRD and TEM studies of the solid aluminosilicate products in the course of the hydrothermal treatment suggest that the crystallization of zeolite beta proceeds on the outer surface of amorphous aluminosilicates. The Raman spectroscopy, solid-state 27Al and 23Na MAS NMR and high-energy XRD analyses of seeded and nonseeded amorphous materials just before crystallization reveal that the beta seeds induce no major changes in their structures, implying that the nucleation of beta does not occur directly from the amorphous phase. The intermediate addition of the seeds after prehydrothermal treatment of a nonseeded gel enhances the crystallization rate and results in the increased number of beta crystals with smaller size. It is elucidated that, during the hydrothermal treatment, the beta seeds embedded in the gel provide crystal growth surface after they are exposed and/or released to the liquid phase by partial dissolution of the amorphous aluminosilicates. These findings provide a promising approach to the designed syntheses of valuable zeolites in the completely OSDA-free system.
The stratum corneum (SC), the outermost layer of the epidermis, acts as a barrier against the external environment. It is hydrated by endogenous humectants to avoid desiccation. However, the molecular mechanisms of SC hydration remain unclear. We report that skin-specific retroviral-like aspartic protease (SASPase) deficiency in hairless mice resulted in dry skin and a thicker and less hydrated SC with an accumulation of aberrantly processed profilaggrin, a marked decrease of filaggrin, but no alteration in free amino acid composition, compared with control hairless mice. We demonstrated that recombinant SASPase directly cleaved a linker peptide of recombinant profilaggrin. Furthermore, missense mutations were detected in 5 of 196 atopic dermatitis (AD) patients and 2 of 28 normal individuals. Among these, the V243A mutation induced complete absence of protease activity in vitro, while the V187I mutation induced a marked decrease in its activity. These findings indicate that SASPase activity is indispensable for processing profilaggrin and maintaining the texture and hydration of the SC. This provides a novel approach for elucidating the complex pathophysiology of atopic dry skin.
We found that AlPO-5 crystals can be synthesized at relatively low temperature (120 °C) by hydrothermal reaction. The critical requirement was the adjustment of the gel composition to control the crystallization rates of aluminophosphate phases. The obtained products showed almost the same pore characteristics compared with the reference products synthesized at high temperature.
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