Synthesis and properties of polyethersulphone–polydimethyisiloxane block copolymers

High molecular weight alternating block copolymers of polyethesulphone (PES) and polydimethylsiloxane (PDMS) were prepared by the condensation of dimethylamino-terminated PDMS oligomers and hydroxy-terminated PES oligomers in 1,2-dichlorobenzene. Microphase separation of the block copolymers at exceptionally short block lengths was observed by differential scanning calorimetry (DSC) and transmission electron microscopy (TEM). The Si? O? C intersegment linkage in these materials appeared to display poor hydrolytic stability which is contrary to results obtained for other block copolymers.     

Nonlinear stability of incoherence and collective synchronization in a population of coupled oscillators

A mean-field model of nonlinearly coupled oscillators with randomly distributed frequencies and subject to independent external white noises is analyzed in the thermodynamic limit. When the frequency distribution isbimodal, new results include subcritical spontaneous stationary synchronization of the oscillators, supercritical time-periodic synchronization, bistability, and hysteretic phenomena. Bifurcating synchronized states are asymptotically constructed near bifurcation values of the coupling strength, and theirnonlinear stability properties ascertained.     

The vertex-cover polynomial of a graph

In this paper we define the vertex-cover polynomial Ψ(G,τ) for a graph G. The coefficient of τ^r in this polynomial is the number of vertex covers V′ of G with |V′|=r. We develop a method to calculate Ψ(G,τ). Motivated by a problem in biological systematics, we also consider the mappings f from {1, 2,…,m} into the vertex set V(G) of a graph G, subject to f⁻¹(x)f⁻¹(y)≠ for every edge xy in G. Let F(G,m) be the number of such mappings f. We show that F(G,m) can be determined from Ψ(G,τ).     

The Kosterlitz-Thouless model in Perovskite superconductors

Il Nuovo Cimento D - The applicability of the Kosterlitz-Thouless theory to HTSC is examined. The model initially presented in its general lines for bidimensional systems is then applied to...     

Mechanisms of ion-beam-enhanced diffusion in amorphous silicon

We have investigated ion-beam-enhanced diffusion of Au in undoped and B doped amorphous Si. The diffusion coefficients depend linearly on ion flux and exibit an Arrhenius-like temperature dependence with an activation energy of 0.37 eV in the temperature range 200–350° C. Moreover the diffusivity is enhanced by a factor of 5 by B-doping at a concentration of 1×10²⁰ atoms/cm³. A similar enhancement is observed in thermal diffusion of Au which has an activation energy of 1.5 eV. On the basis of these results a model for the ion-beam-enhanced diffusion of Au is proposed where the high density of defects present in amorphous Si act as traps for the fast moving interstitial Au atoms. The effectiveness of this trapping process can be changed by the high concentration of mobile defects generated by the beam and also by a change in the charge state of the traps induced by the presence of B.     

Biomagnetic measurements utilising a superparamagnetic marker: a feasibility study

Summary A preliminary study is here reported on a new potential marker for biomagnetic measurements. The marker consists of superparamagnetic polymer microspheres which were detected in the presence of external steady magnetic fields by means of an r.f.-SQUID magnetometer. The particles were prepared in samples differing in the concentration value and immersed in a homogeneous magnetic field of variable intensity. A simple model was taken into account for the distribution of the microspheres in the samples, so that the theoretical values were compared to the marker field values measured by the biomagnetic sensor. The overall sensitivity of the experimental apparatus and the minimum concentration value of the marker were then estimated.     

Glass-forming liquids,anomalous liquids,and polyamorphism in liquids and biopolymers

Summary Glass formation in nature and materials science is reviewed and the recent recognition of polymorphism within the glassy state, polyamorphism, is discussed. The process by which the glassy state originates during the continuous cooling or viscous slowdown process, is examined and the three canonical characteristics of relaxing liquids are correlated through the fragility. The conversion of strong liquids to fragile liquids by pressure-induced coordination number increases is discussed, and then it is shown that for the same type of system it is possible to have the same conversion accomplished via a first-order transition within the liquid state. The systems in which this can happen are of the same type which exhibit polyamorphism, and the whole phenomenology can be accounted for by a recent simple modification of the van der Waals model for tetrahedrally bonded liquids. The concept of complex amorphous systems which can lose a significant number of degrees of freedom through weak first-order transitions is then used to discuss the relation between native and denatured hydrated proteins, since the latter have much in common with plasticized chain polymer systems. Finally, we close the circle by taking a short-time-scale phenomenon given much attention by protein physicists,viz., the onset of an anomaly in the Debye-Waller factor with increasing temperature, and showing that for a wide variety of liquids, including computer-simulated strong and fragile ionic liquids, this phenomenon is closely correlated with the experimental glass transition temperature. This implies that the latter owes its origin to the onset of strong anharmonicity in certain components of the vibrational density of states (evidently related to the boson peak) which then permits the system to gain access to its configurational degrees of freedom. The more anharmonic these vibrational components, the closer to the Kauzmann temperature will commence the exploration of configuration space and, for a given configurational microstate degeneracy, the more fragile the liquid will be. Paper presented at the I International Conference on Scaling Concepts and Complex Fluids, Copanello, Italy, July 4–8, 1994.     

Microwve inducdd catalytic decomposition of some alberta oil sands and bitumens

The processing of oil sands materials and upgrading of bitumens present a variety of problems for conventional technologies. This article describes a preliminary study of the concept of using microwave induced catalytic techniques to decompose the complex and viscous hydrocarbon compounds contained in these materials to allow efficient extraction of volatile and economically useful organic products such as C₂ and C₃ hydrocarbons. Addition of water to the tar sand material prior to reaction facilitated separation from the sand component as well as promoting the formation of economically very useful, liquid, oxygenated hydrocarbon products.