Unexpectedly high young's moduli recorded for iPP/HDPE blends

Young's moduli of a series of quenched isotactic polypropylene/high‐density polyethylene blends were measured. The moduli of many of the blends exceeded the upper bound, calculated from the parallel model with the moduli of the two quenched homopolymers as those of the two components. In fact, both components crystallized at higher temperatures in the blends than they did on their own. It is argued that the higher crystallization temperatures of the components lead to higher component moduli and that this can explain the observation that the measured moduli of the blends apparently exceeded the upper bound. The implications of this work are discussed in light of other studies concerning the measurement and calculation of blend moduli. © 2001 John Wiley & Sons, Inc. J Polym Sci B Part B: Polym Phys 39: 1404–1414, 2001     

The relationship between microstructure and mode of fracture in polyhydroxybutyrate

Polyhydroxybutyrate (PHB) is a bacterially produced thermoplastic. Melt-cast PHB sheets are usually quite brittle. We show that this brittleness is due to cracks within the spherulites. These cracks, which may be either radial or circumferential within the spherulites, depending on the crystallization temperature, form under conditions of no externally applied stress. When the material is strained the cracks grow and join together, leading to brittle failure. It is possible to produce ductile PHB sheets in two ways: first, the cracks may be “healed” by a cold rolling process; second, special crystallization conditions can be used to produce ductile sheets consisting entirely of crack-free spherulites. The relevance of this work to the ductility of crystalline thermoplastic in general is discussed.     

Development of the large increment method for elastic perfectly plastic analysis of plane frame structures under monotonic loading

The displacement-based finite element method dominates current practice for material nonlinear analysis of structures. However, there are several characteristics that may limit the effectiveness of this approach. In particular, for elastoplastic analysis, the displacement method relies upon a step-by-step incremental approach stemming from flow theory and also requires significant mesh refinement to resolve behavior in plastic zones. This leads to computational inefficiencies that, in turn, encourage the reconsideration of force-based approaches for elastoplastic problems.One of these force algorithms that has been recently developed is the large increment method. The main advantage of the flexibility-based large increment method (LIM) over the displacement method is that it separates the global equilibrium and compatibility equations from the local constitutive relations. Consequently, LIM can reach the solution in one large increment or in a few large steps, thus, avoiding the development of cumulative errors. This paper discusses the extension of the large increment methodology for the nonlinear analysis of plane frame structures controlled by an elastic, perfectly plastic material model. The discussion focuses on the power of LIM to handle these nonlinear problems, especially when plastic hinges form in the frame and ultimately as the structure approaches the collapse stage. Illustrative planar frame examples are presented and the results are compared with those obtained from a standard displacement method.     

On symmetrized stochastic convexity and the inequalities of Hermite–Hadamard type

Aequationes mathematicae - In this paper the concept of symmetrized convex stochastic processes is introduced. Some characterizations involving Hermite–Hadamard type inequalities and a...     

Sol-gel preparation and properties of interpenetrating, encapsulating and blend silica-based urea-formaldehyde hybrid composite materials

Four different silica-based urea-formaldehyde (UF/SiO₂) composite materials were prepared by various sol-gel synthetic procedures to yield an interpenetrating (IPN-UF/SiO₂), a micro-size UF resin encapsulated inside silica shell (Encap-UF/SiO₂), a micro-size silica encapsulated inside UF shell (Encap-SiO₂/UF), and a blend mixture (Blend-UF/SiO₂) hybrid systems. The thermal properties of the obtained organic-inorganic hybrid composite materials were examined by thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). The structure and morphology of the obtained systems were investigated by infrared spectroscopy (FT-IR), powder X-ray diffraction (XRD) and scanning electron microscopy (SEM) techniques. Their surface porosity and acidity were evaluated from the nitrogen adsorption isotherm and the pH of the corresponding 10% aqueous suspension, respectively. All the results provided evidence for the formation of different hybrid systems with different surface, structural and morphological characteristics.     

On the temperature dependence of the fundamental absorption edge in CuInSe2

The temperature dependence behaviour of the energy gap of Cu-III-VI₂ chalcopyrite compound semiconductors is explained by a model which, besides the thermal expansion contribution, takes into account the effect of the electron-phonon interaction by considering the influence of all twenty four vibrational acoustic and optical modes. The results are in good agreement with the experimental data reported for CuInSe₂.     

Sulphur and oxygen isotopic characters of dissolved sulphate in groundwater from the Pleistocene aquifer in the southern Jordan Valley (Jericho area,Palestine)

Sulphate and chloride concentrations in the shallow Pleistocene aquifer systems in the lower Jordan valley area indicate a general trend of increasing salinity eastward and southward. This study was conducted in one of the important sub-basins feeding the Pleo–Pleistocene aquifer in the Jericho area in the southern part of the valley using S and O isotopes of dissolved sulphate. The results show that sulphate has mainly two contributions to the groundwater. One is the surface seepage, which is present as a salty leachate form with the positive δ³⁴S_sulphate values of primary gypsum in Lisan and Samara formations, and the second is the upwelling saline water which was in contact with a deep secondary gypsum, aragonites and salty rocks and rose up under heavy abstraction with depleted ³⁴S in sulphate and relatively high sulphate and chloride content. The latest was clearly shown in the Arab Project wells to the east that is undergoing a continuous heavy abstraction. The isotopic signatures of S and O in these wells to the east show that this depleted ³⁴S and highly concentrated sulphate might also indicate a dissolved sulphate originating from pyrite oxidation that results from the interaction with a pyrite-rich aquifer, which can well up with salty water under heavy abstraction and is oxidised in the upper aerobic shallow aquifer.     

Catalytic Asymmetric Synthesis of Cyclohexanes by Hydrogen Borrowing Annulations

Hydrogen borrowing catalysis serves as a powerful alternative to enolate alkylation, enabling the direct coupling of ketones with unactivated alcohols. However, to date, methods that enable control over the absolute stereochemical outcome of such a process have remained elusive. Here we report a catalytic asymmetric method for the synthesis of enantioenriched cyclohexanes from 1,5‐diols via hydrogen borrowing catalysis. This reaction is mediated by the addition of a chiral iridium(I) complex, which is able to impart high levels of enantioselectivity upon the process. A series of enantioenriched cyclohexanes have been prepared and the mode of enantioinduction has been probed by a combination of experimental and DFT studies.     

Long-Range Lateral Correlation between Self-Assembled Domains of Fluorocarbon-Hydrocarbon Tetrablocks by Quantitative GISAXS

The structure and lateral correlation of fluorocarbon-hydrocarbon tetrablock di(F10Hm) domains at the air/water interface have been determined by quantitative analysis of grazing incidence small-angle X-ray scattering (GISAXS) data. The measured GISAXS signals can be well represented by the full calculation of the form and structure factors. The form factor suggests that di(F10Hm) domains take a hemiellipsoid shape. Both major and minor axes of the hemiellipsoids monotonically increased in response to the elongation of the hydrocarbon blocks, which can be explained by the concominant increase in van der Waals interaction. The structure factor calculated from the GISAXS signals suggests that the domains take an orthorhombic lattice. Remarkably, the lateral correlation can reach over a distance that is more than 14 times longer than the distance to the nearest neighbors. Our data suggest that quantitative GISAXS enables the optimal design of mesoscopic self-assemblies at the air/water interface by fine-tuning of the structures of molecular building blocks.