Yilmazkerr4255

8-fold increase compared to bulk Bi2WO6. Furthermore, the photoelectrochemical measurements unveil that the significantly higher charge migration and charge carrier dynamic counts for the elevated photocatalytic performance. After careful examination of experimental results, it was proved that the Ti doping mediated crystal defects, and engendered oxygen vacancies are critically important for controlling the photocatalytic performance of Bi2WO6.

To correctly predict the aggregation number and size of wormlike micelles from ionic surfactants, the molecular-thermodynamic theory has to calculate the free energy per molecule in the micelle with accuracy better than 0.01 kT, which is a serious challenge. The problem could be solved if the effects of mutual confinement of micelle counterion atmospheres, as well as the effects of counterion binding, surface curvature and ionic interactions in the electric double layer (EDL), are accurately described.

The electric field is calculated using an appropriate cell model, which takes into account the aforementioned effects. Expressions for the activity coefficients have been used, which vary across the EDL and describe the electrostatic, hard sphere, and specific interactions between the ions. New approach for fast numerical calculation of the electrostatic free energy is developed.

The numerical results demonstrate the variation of quantities characterizing the EDL of cylindrical and spherical micelles withved synergistic effects.

Particle accumulation at liquid-liquid or liquid-gas interfaces can significantly alter capillary behavior and give rise to unusual interfacial phenomena including the asymmetric macroscopic mechanical response of the interface.

This study explores the accumulation of cetyltrimethylammonium bromide-modified nanoparticles at fluid interfaces and the subsequent mechanical response of nanoparticle-coated droplets during contraction and expansion. Droplet tests involve the simultaneous recording of the droplet shape and the capillary pressure. Complementary single-pore experiments examine the response of particle-coated interfaces as they traverse a pore constriction.

Interfaces promote order. The time-dependent nanoparticle accumulation at the interface is diffusion-controlled. The nanoparticle coated droplets can sustain negative capillary pressure before they buckle. Buckling patterns strongly depend on the boundary conditions non-slip boundary conditions lead to crumples while slip boundary conditions rn a nanofluid bath" withstands a significantly higher capillary pressure difference than a "nanofluid droplet in an oil bath". A first-order equilibrium analysis of interaction forces explains the asymmetric response. Single-constriction experiments show that the formation of particle-coated interfaces has a pronounced effect on fluid displacement in porous media.Hierarchical porous hollow carbon nanospheres (HCNSs) were fabricated directly from raw biomass via a one-step method, in which HCNSs were obtained by thermal treatment of raw biomass in the presence of polytetrafluoroethylene (PTFE). The HCNSs possess coupling merits of uniformly distributed hollow spherical architectures, and high specific surface area, abundant accessible/open micropores and reasonable mesopores, the HCNS-based electrodes deliver high electrochemical capacitance. The formation mechanisms of pores and hollow core-shell structures were explored thoroughly, it is found that the key to the formation of hollow core-shell structure is the onset-pyrolysis temperature difference between raw biomass and PTFE. Moreover, the content of silica had significant effects on the textures of HCNSs, and HCNS with the largest SSA of 1984 m2/g was obtained. Accordingly, a possible mechanism of HCNSs formation was proposed here, where PTFE acted as the pore creation and nucleation agents and raw biomasses were the primary carbon precursors.

Pickering emulsions can be produced using raw particles obtained from uncracked vegetal food byproducts as sole stabilizers. The complexity brought by these non-purified ingredients will be their strength since insoluble particles and soluble compounds shall display good complementary properties, at the interface and the continuous phase.

Emulsions were monitored over a one-month storage as regards to oil droplet diameter as main indicator of stability. Then, two main studies were carried out 1) on the whole powders (water binding capacity, dry matter and insoluble content, size and morphology); 2) on the soluble content (size, charge, pH, Brix degree, surface tension measurements).

All byproducts stabilized-emulsions were stable during storage. They display various oil droplet sizes with sugar beet<apple<oat. Direct observation of the oil-water interfaces showed adsorption of the solid particles, and some voids corresponding to soluble elements from the byproducts' powders. The latter displayed s stabilize clean-label emulsions.We used the Surface Forces Apparatus to elucidate the interaction mechanism between grafted 5 heptad-long peptides engineered to spontaneously form a heterodimeric coiled-coil complex. AZD5069 The results demonstrated that when intimate contact between peptides is reached, binding occurs first via weakly interacting but more mobile distal heptads, suggesting an induced-fit association process. Precise control of the distance between peptide-coated surfaces allowed to quantitatively monitor the evolution of their biding energy. The binding energy of the coiled-coil complex increased in a stepwise fashion rather than monotonically with the overlapping distance, each step corresponding to the interaction between a quantized number of heptads. Surface forces data were corroborated to surface plasmon resonance measurements and molecular dynamics simulations and allowed the calculation of the energetic contribution of each heptad within the coiled-coil complex.Studies on photocatalytic activity of monophasic and biphasic TiO2 have been well explored. However, detailed studies on the photocatalytic activity of triphasic titania, as opposed to monophasic or biphasic TiO2 are scarce. Here we report a comparative structure-sensitive photocatalytic study of triphasic versus anatase TiO2, both have been synthesized under near-identical conditions through a customized sol-gel approach. The composition of the phases is tuned just by varying the thermal pre-treatment conditions of TiO2 gel that has been subsequently subjected to calcination at 300 °C. Interestingly, when the pre-treatment temperature of the gel is systematically increased from 50 to 250 °C, a transition from anatase to triphasic (anatase, rutile, and brookite) and then again to anatase has been observed. The synthesized TiO2 phase compositions have been thoroughly characterized for their structural, optical, electrical, surface and morphological properties. Among the different phase compositions, triphasic titania having a significant proportion of rutile has been found to exhibit the highest photocatalytic activity, as probed using model organic pollutants, Methylene Blue (MB) and 4-Chlorophenol (4-CP). In addition to the earlier known factors such as effective heterojunction, and favorable position of the valence band (VB), an important contribution to the high photocatalytic activity of triphasic TiO2 has been experimentally found to stem from the additional electron density in VB that is attributed to the lattice contraction of anatase phase owing to the coexistence of other two phases. The study provides fundamental insights into the energetics that impact the photocatalytic activity of triphasic versus anatase TiO2.Compared with the transition metal induced homogeneous catalytic system, the heterogeneous catalytic system based on transition metal-doped metal organic frameworks (MOFs) were stable for the efficient utilization of transition metal and avoiding the metal leaching. The aim of this work is to synthesize Co-doped MIL-53(Al) by one-step solvent thermal method and use it to activate peroxymonosulfate (PMS) to remove tetracycline (TC) in water. The successful synthesis of Co-MIL-53(Al) samples was demonstrated by XDR, SEM and FTIR characterizations. The 25% Co-MIL-53(Al)/PMS system showed the optimal TC removal effect compared to the PMS alone and MIL-53(Al)/PMS system. The catalytic performances of Co-MIL-53(Al)/PMS system in conditions of different pH, co-existing substances and water bodies were investigated. Quenching experiment and electron paramagnetic resonance (EPR) showed that the degradation mechanism by Co-MIL-53(Al) activation PMS was mainly attributed to sulfate radical (SO4•-) and singlet oxygen (1O2) non-radical. The degradation intermediates of TC were also identified and the possible degradation pathways were proposed. Co-MIL-53(Al) showed good activity after four cycles. These findings demonstrated that Co-MIL-53(Al) can be a promising heterogeneous catalyst for activating PMS to degrade TC.Biomimetic nanomaterials have attracted tremendous research interest in the past decade. We recently developed biomimetic core-shell nanoparticles - silica nanocapsules, using a designer dual-functional peptide SurSi under room temperature, neutral pH and without use of any toxic reagents or chemicals. The SurSi peptide is designed capable of not only stabilizing nanoemulsions because of its excellent surface activity, but also inducing the formation of silica through biosilicification at an oil-water interface. However, it remains challenging to precisely control the peptide-induced nucleation and biosilicification specifically at the oil-water interface, thus forming oil-core silica-shell nanocapsules with uniform size and monodispersity. In this study, the fundamental mechanism of silica formation through a peptide catalyzed biosilicification was systematically investigated, so that the formation of oil-core silica-shell nanocapsules can be precisely controlled. The SurSi peptide induced hydrolysis and nucleation of biomineralized silica particles were monitored to study the biosilicification kinetics. Effects of pH, SurSi peptide concentration and pre-hydrolysis of silica precursors were also studied to optimize the formation of biomimetic silica nanocapsules. The fundamental understanding achieved through these systematic studies provides valuable insights for making core-shell nanoparticles via controlling nucleation and reaction at interfaces.Shaping metal-organic frameworks (MOFs) powders into formed bodies plays a crucial role in opening up the excellent properties of MOFs to a broad range of applications. Gallate-based MOFs, termed as M-gallate (M = Co, Mg, Ni), have shown excellent performance for adsorption separation of C2 hydrocarbons. However, the industrial applications of MOF powders will inevitably confront problems of high pressure drop, pipe blockage, and dust pollution. Herein, we use hydroxypropyl cellulose (HPC) as a binder to produce gallate-based MOFs pellets. The crystal structure of the well-shaped materials after molding remained intact, and the surface area of the materials hardly decreases after shaping. Adsorption isotherms of C2 hydrocarbons including ethylene, ethane and acetylene on the activated powders and pellets of M-gallate were recorded and compared with the outperformers. The shaped pellets were also examined by breakthrough experiments on the fixed-bed separation of C2H2/C2H4 (199, v/v) and C2H4/C2H6 (5050, v/v) gas mixtures.