Effect of morphology of mesoporous silica on characterization of protic ionic liquid-based composite membranes

Effects caused by the morphology of mesoporous silica on the characterization of protic ionic liquid-based composite membranes for anhydrous proton exchange membrane applications are investigated. Two types of SBA15 materials with platelet and fiberlike morphologies are synthesized and incorporated into a mixture of polymerizable monomers together with an ionic liquid (IL) [1-butyl-3-methylimidazolium bis(trifluoromethane sulfone)imide (BMIm-TFSI)] to form new conducting membranes using an in situ photo crosslinking process. Incorporation of a defined amount of fiber-shaped SBA 15 and platelet 15 significantly increases the ionic conductivity to between two and three times that of a plain poly(methyl methacrylate) (PMMA)/IL membrane (2.3 mS cm⁻¹) at 160 °C. The protic ionic liquid (PIL) retention ability of the membranes is increased by the capillary forces introduced by the mesoporous silica materials, while ionic conductivity loss after leaching test is retarded. The highest ionic conductivity (5.3 mS cm⁻¹) is obtained by incorporating 5 wt% of P-SBA 15 in the membrane to about six times that of plain PMMA/IL membrane (0.9 mS cm⁻¹) at 160 °C after leaching test.     

Elongational creep experiments - A new method for investigations of morphology development in polymer blends

This work is focused on the changes of phase structure in polystyrene/polyethylene blends with up to 15 wt.% of dispersed phase during elongational experiments in creep. In the first part, features of the experiments at constant stress with a special attention to morphology development in polymer blends are discussed. In the second part of the paper the deformation behavior of the dispersed droplets in dependence on applied stress and total strain is studied. It was found that with increasing the initial particle size the formation of homogeneously deformed long fibrils is preferred during the elongation. A maximum deformability of the droplets was observed, which cannot be increased by applying higher stresses, although the affine deformation of the droplets was not reached.     

Kinetics of Isothermal Crystallization of Hydrogenated Castor Oil-in-Water Emulsions

Kinetics of isothermal crystallization of hydrogenated castor oil in water emulsions exhibiting multiple crystal morphologies have been studied experimentally by DSC and polarized light microscopy. The induction time of nucleation increases with the increase of the isothermal temperature under which crystallization occurred. Crystal growth has been observed by microscopy showing that both crystal morphologies, fibers and rosettes, grow linearly at the initial stage of crystallization and then slow down to reach a plateau value. The Avrami model, which has been widely used in kinetics studies of triacylglycerol systems, was employed to fit experimental results at different isothermal temperatures. It was found that experimental trends could be captured by introducing the volume fraction of each type of morphology into three-dimensional and one-dimensional full Avrami models.     

Structure,morphology, and photoluminescence of porous Si nanowires: effect of different chemical treatments

The structure and light-emitting properties of Si nanowires (SiNWs) fabricated by a single-step metal-assisted chemical etching (MACE) process on highly boron-doped Si were investigated after different chemical treatments. The Si nanowires that result from the etching of a highly doped p-type Si wafer by MACE are fully porous, and as a result, they show intense photoluminescence (PL) at room temperature, the characteristics of which depend on the surface passivation of the Si nanocrystals composing the nanowires. SiNWs with a hydrogen-terminated nanostructured surface resulting from a chemical treatment with a hydrofluoric acid (HF) solution show red PL, the maximum of which is blueshifted when the samples are further chemically oxidized in a piranha solution. This blueshift of PL is attributed to localized states at the Si/SiO₂ interface at the shell of Si nanocrystals composing the porous SiNWs, which induce an important pinning of the electronic bandgap of the Si material and are involved in the recombination mechanism. After a sequence of HF/piranha/HF treatment, the SiNWs are almost fully dissolved in the chemical solution, which is indicative of their fully porous structure, verified also by transmission electron microscopy investigations. It was also found that a continuous porous Si layer is formed underneath the SiNWs during the MACE process, the thickness of which increases with the increase of etching time. This supports the idea that porous Si formation precedes nanowire formation. The origin of this effect is the increased etching rate at sites with high dopant concentration in the highly doped Si material.     

SYNTHESIS,RHEOLOGICAL BEHAVIOR,AND MECHANICAL PROPERTIES OF GRAFT-TYPE ACS RESIN

Graft-type ACS resin and α-methylstyrene (α-Mst)-containing ACS were synthesized by suspension polymerization. The effect of concentration of initiator and polyvinyl alcohol (PVA) on reaction was discussed. The graft efficiency (GE) increased with the increasing concentration of initiator in the first stage, but it began to decrease when the initiator concentration exceeded 3.3–3.5×10^?4mol L^?1. The GE decreased gradually with the increasing concentration of PVA. The rheological behavior, mechanical properties, and morphological structure of resins were studied. The rheological behavior became worse with the increasing content of chlorinated polyethylene and the melt is a pseudo-plastic liquid. The impact strength of graft-type ACS resin increased as the content of chlorinated polyethylene increased. The rheological behavior and impact properties of α-Mst-containing ACS resin got better because of the introduction of α-Mst, and the comprehensive properties was the best at the 5% α-Mst content of ACS resin.     

Comparing the Continuous Chaotic and Shear Mixing-Induced Morphology Development of Polyblend and its Nanocomposites

Continuous chaotic and shear mixing-induced morphology development of 60/40 w/w polypropylene/polyamide 6 (PP/PA6) blend and its nanocomposite with 5 wt% clay was investigated. PP and PP nanocomposite were mixed with PA6 in a single-screw extruder, respectively. Two screw geometries were used to induce chaotic and shear mixing, respectively. It was demonstrated that for PP/PA6 blend, the PA6 domains were transformed from large particles to short striations and to small droplets finally in shear mixing, whereas morphology of PA6 phase developed from lamellar layers to a partial continuous structure finally in chaotic mixing. For (PP/clay)/PA6 blend nanocomposite, the PA6 domains were deformed gradually from droplets to irregular fibrils in shear mixing and from short layers to thin fibrils in chaotic mixing. The PA6 fibrils formed finally in the latter were much thinner and uniform than those in the former. The dynamic storage moduli of samples prepared in both shear and chaotic mixing with these PA6 fibrils presented a solid-like response at lower frequencies. Moreover, the clay platelets dispersed initially in the PP phase migrated into PA6 phase finally in both shear and chaotic mixing and the exfoliation of clay platelets in PA6 phase was obviously improved in the latter.     

New modelling approach to liquid–solid reaction kinetics: From ideal particles to real particles

Typical features of liquid–solid reactions were reviewed: reaction kinetics, mass transfer effects and particle morphology. It was concluded that classical liquid–solid models based on ideal, non-porous geometries (sphere, infinite cylinder, slab) cannot satisfactorily describe real reactive solid particles with various surface defects, such as cracks, craters and limited porosity. Typically a too low reaction order for the reactive solid is predicted by the classical models. The surface morphology can be revealed by electron microscopy, which gives inspiration to develop new mathematical models for reactive solids.     

The influence of polymer morphology on the performance of molecularly imprinted polymers

This is the first in-depth study examining the effect of morphology on the performance of 2-aminopyridine (2-apy) imprinted polymers. A series of polymers were prepared by varying the amount of crosslinking monomer (EGDMA) whilst the other polymer components remained constant. Physical characterisation was carried out using conventional techniques, such as nitrogen sorption porosimetry and solvent swelling studies. The use of a novel thermal desorption GC-MS technique suggested higher levels of polymer degradation with prolonged exposure to elevated temperatures for those polymers formed with lower amounts of EGDMA. The thermal desorption GC-MS profiles obtained correlated with the physical characteristics of the polymers, where higher levels of polymer bleed was found to occur with larger average pore diameters. Polymer physical characteristics were also found to correlate with the binding parameters (number of binding sites and polymer-template association energy) obtained from the Langmuir-Freundlich Isotherm (L-FI) and affinity distribution spectra (AD). The flexibility of the polymers formed from lower amounts of EGDMA combined the swelling effect of the solvents on the polymers resulted in an increase in affinity, which was both specific and non-specific in nature.     

Influence of Substrate Temperature on Stress and Morphology Characteristics of Co Doped ZnO Films Prepared by Laser-Molecular Beam Epitaxy

Znl_xCoxO （x = 0.05） thin films are deposited on sapphire （0001） substrates by laser-molecular beam epitaxy technique at different substrate temperatures. The structural, stress and morphology evolution features are investigated by means of X-ray diffraction and atomic force microscopy. The surface parameters of roughness exponent α, root mean square （RMS） roughness w and autocorrelation length ~ are calculated and the surface parameters are preliminarily analyzed. The values of ~ vary from 0.7 to 0.9. The RMS roughness w is less than 2.2 nm, and it increases with increasing Ts from 300 to 400 °C, and then decreases when Ts is 500 °C. The autocorrelation length ~ decreases monotonously with the increase in Ts from 300 to 500 °C, which indicates that the increase in Ts restrains the spread of the surface fluctuations until Ts is higher than 400 °C.     

Micro-flowers of poly(p-phenylene pyromelliteimide) crystals

Morphology control of poly(p-phenylene pyromelliteimide) (PPPI) crystals was examined using reaction-induced crystallization of oligomers during solution polymerization of self-polymerizable N-(4′-aminophenyl)-3-carboxyl-4-alkoxycarbonylphthalimide. Micro-flowers of the PPPI needle-like crystals were formed in which the needle-like crystals grew radially from the center part as petals. The molecules aligned regularly along the long axis of the needle-like crystal. The structure of alkoxy group in the monomer and the monomer concentration influenced the size of the needle-like crystals, and their average length and width were changeable from 640 nm to 1.69 μm and from 110 nm to 210 nm, respectively. The average thickness was 20 nm. The obtained micro-flowers possessed high crystallinity and exhibited excellent thermal stability.