Corneliussengilliam7152

A series of 22-membered unclosed cryptands end-capped with intra-annular methyl (1), phenyl (2), p-tert-butylphenyl (3), and p-nitrophenyl (4) amide substituents (lariat arm) were synthesized to elucidate the effect of steric and electronic factors on their anion recognition behavior. The 1H NMR titrations in DMSO-d6 with 0.5% water reveal enhanced selectivity for H2PO4- vs Cl- and PhCO2-. The para-attachment of the electron-withdrawing nitro group (-NO2 vs -H and -t-Bu) was found to increase anion-binding affinity, whereas the steric bulkiness of lariat arm (methyl vs aryl) has a marginal effect. DFT calculations reveal that binding of H2PO4- is associated with minimal conformational change in the lariat arm moiety and involve four hydrogen bond acceptor and one donor sites of host.Ag/Al2O3 catalysts containing different precipitable silver compounds (AgCl, Ag2SO4, and Ag3PO4) were synthesized and investigated for NOx reduction in H2-assisted C3H6-selective catalytic reduction (SCR). The samples were systematically characterized by N2 adsorption, X-ray diffraction (XRD), UV-Vis, X-ray photoelectron spectroscopy (XPS), and high-resolution transmission electron microscopy (HR-TEM). N2 adsorption revealed that the introduction of anions (Cl-, SO42-, and PO43-) did not significantly affect the surface and structural properties of the Al2O3 support. However, XRD patterns and HR-TEM images indicated that the addition of Cl- anions caused the agglomeration of silver species to form large AgCl particles on the AgCl/Al2O3 catalysts. In contrast, the silver species dispersed well on Ag2SO4/Al2O3 and Ag3PO4/Al2O3 catalysts. In situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) revealed that partial oxidation of C3H6 on Ag2SO4/Al2O3 produced large amounts of reactive enolic species, while it tended to yield inert formate on AgCl/Al2O3. As a result, Ag2SO4/Al2O3 catalysts, especially 3% Ag2SO4/Al2O3, exhibited superior water and sulfur tolerance in H2-assisted C3H6-SCR.Herein, single-domain κ-Ga2O3 thin films were grown on FZ-grown ε-GaFeO3 substrates via a step-flow growth mode. The ε-GaFeO3 possessing the same crystal structure and similar lattice parameters as those of the orthorhombic κ-Ga2O3 facilitated the growth of κ-Ga2O3 thin films, as observed by the X-ray diffraction (XRD) analysis. Furthermore, the surface morphologies of the κ-Ga2O3 thin films exhibited a step-terrace and atomically flat structure. XRD φ-scan and transmission electron microscopy with selected area electron diffraction revealed that there is no occurrence of in-plane rotational domains in the κ-Ga2O3 thin films on ε-GaFeO3 substrates and that the κ-Ga2O3 thin film comprised a single domain. TEM analysis revealed that there were no clear dislocations in the observation area. selleck inhibitor Moreover, high-resolution TEM observation showed that the atomic arrangements of the film and the substrate were continuous without the presence of an intermediate layer along the growth direction and were well-aligned in the in-plane direction.This study details the preparation and application of supramolecular host-guest inclusion complexes entrapping biomineralized microspheres for long-term storage and their pH-responsive behavior. The microspheres were assembled using a CaCO3 synthesis process coupled with cyclodextrin-tetrahydrocurcumin (CD-THC) inclusion complexes, forming fine-textured and mechanically stable hybrid materials. The products were successfully characterized using field-emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray spectroscopy (EDS), Fourier transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD), and particle size analysis (PSA). Various parameters such as the Brunauer-Emmett-Teller (BET) surface area, single point total pore volume, and pore size via adsorption/desorption analysis were also determined. The obtained THC-entrapped hybrid microspheres contained as high as 20 wt % THC loading and were very stable, preserving 90% of the initial concentration over four weeks of storage at different temperatures, largely limiting THC leaching and indicating high stability in a physiological environment. In addition, the pH-responsive release of THC from the hybrid microspheres was observed, showing potential use for application to weakly acidic skin surfaces. To our knowledge, this is the first demonstration of antiaging cosmetic formulation technology using biomineralization based on the co-synthesis of CaCO3 and CD-THC complexes.This work presents the results of thermogravimetric analysis of decantoil. The microstructure of the extracted petroleum coke during the thermolysis of decantoil in an inert nitrogen atmosphere at 1000 °C was studied by scanning electron microscopy and interpreted as acicular. The model free kinetic approach based on Friedman's isoconversion method was used to calculate the kinetic characteristics of decantoil thermolysis-activation energy and pre-exponential factor. The individual hydrocarbon composition of decantoil was determined by gas chromatography mass spectrometry, which was used to determine the activation energy of evaporation of its fractions. The total energy spent on the chemical reactions of cracking and thermopolycondensation was determined when the degree of decantoil conversion was changed from 0.1 to 0.9.The development of eco-friendly fiber-reinforced composite resins is an important objective from an environmental perspective, and nanofibrillated bacterial cellulose (NFBC), with extremely long high-aspect-ratio fibers, is a filler material with high potential for use in such composite resins. In this study, we investigated chemical modification of the surfaces of NFBC fibers by coupling with (3-aminopropyl)trimethoxysilane and fabricated nanocomposite materials using the prepared surface-modified NFBC. The product prepared by the one-pot reaction of (3-aminopropyl)trimethoxysilane with NFBC microfibrils dispersed in aqueous acid retained the same nanofibril structure as the intact NFBC. The degree of molar substitution and the silicon states on the surface of the product depended on the NFBC/(3-aminopropyl)trimethoxysilane ratio. The thermal analysis revealed that the thermal degradation temperature of the products increases with an increase of degree of molar substitution. Highly transparent (78-89% at 600 nm) poly(methyl methacrylate)-based nanocomposites were prepared by solvent casting; the nanocomposite containing 1.0 wt % (3-aminopropyl)trimethoxysilylated NFBC was only 8% less transparent than neat poly(methyl methacrylate) at 600 nm. In addition, the tensile strength of the nanocomposite was more than twice that of neat poly(methyl methacrylate) when 1 wt % of the surface-modified NFBC was added. The surface-modified NFBC is expected to be a reinforcing nanofiber material that imparts excellent physical properties to fiber-reinforced resins.Raman spectroscopy can be used as a tool to study virus entry and pathogen-driven manipulation of the host efficiently. To date, Epstein-Barr virus (EBV) entry and altered biochemistry of the glial cell upon infection are elusive. In this study, we detected biomolecular changes in human glial cells, namely, HMC-3 (microglia) and U-87 MG (astrocytes), at two variable cellular locations (nucleus and periphery) by Raman spectroscopy post-EBV infection at different time points. Two possible phenomena, one attributed to the response of the cell to viral attachment and invasion and the other involved in duplication of the virus followed by egress from the host cell, are investigated. These changes corresponded to unique Raman spectra associated with specific biomolecules in the infected and the uninfected cells. The Raman signals from the nucleus and periphery of the cell also varied, indicating differential biochemistry and signaling processes involved in infection progression at these locations. Molecules such as cholesterol, glucose, hyaluronan, phenylalanine, phosphoinositide, etc. are associated with the alterations in the cellular biochemical homeostasis. These molecules are mainly responsible for cellular processes such as lipid transport, cell proliferation, differentiation, and apoptosis in the cells. Raman signatures of these molecules at distinct time points of infection indicated their periodic involvement, depending on the stage of virus infection. Therefore, it is possible to discern the details of variability in EBV infection progression in glial cells at the biomolecular level using time-dependent in vitro Raman scattering.Previous studies on glass-transition temperature (Tg) prediction mainly focus on developing diverse methods with higher regression accuracy, but very little attention has been paid to the dataset. Generally, a large range of Tg values of a specified polymer could be found in the literature but which one should be selected into a dataset merely depends on the implicit preference rather than a recognized and clear criterion. In this paper, limiting glass-transition temperature (Tg(∞)), a constant value obtained at the infinite number-average molecular weight Mn, was validated to be an adequate bridge index in the Tg prediction models. Furthermore, a new dataset containing 198 polymers was established to predict Tg(∞) using the improved group contribution method and it showed a good correlation (R2 = 0.9925, adjusted R2 = 0.9894). The method could also generate Tg-Mn curves by introducing the Tg(∞) function and provide more information to polymer scientists and engineers for material selection, product design, and synthesis.Supercritical carbon dioxide (scCO2) has gained considerable attention in the process industry due to its favorable economic, environmental, and technical characteristics. Polymer processing is one of the key industrial applications where scCO2 plays an important role. In order to be able to efficiently design the polymer processing equipment, understanding the phase behavior and partition of solutes between scCO2 and polymers is necessary. This paper investigates the partitioning of acetone - a conventional polar cosolvent - between scCO2 and polystyrene - a glassy polymer. We highlight the importance of taking into account the polar interactions between acetone molecules and their role in the polymer phase behavior. The system is modeled under a wide range of temperatures and pressures (278.15-518.2 K and 1.0-20.0 MPa) using the polar version of the perturbed chain statistical associating fluid theory (polar PC-SAFT) equation of state. The results show that at relatively low pressure, the system exhibits a vapor-liquid-liquid (VLL) three-phase region bounded by two two-phase regions (VL and LL). At high pressure, VLL and VL regions disappear and only the LL region remains. The temperature effect is more interesting, showing a transition of upper critical solution temperature behavior to lower critical solution temperature behavior at 10 MPa and 398.15 K. It is found that neglecting the polar term can lead to significant changes in the description of the polymeric-system phase behavior especially at lower temperatures. No such differences are observed at higher temperatures (above 500 K) where the effect of polar interaction is considerably weaker.