The Scattering Amplitude for the Schrödinger Equation with a Long-Range Potential

We consider the Schr?dinger operator with a long-range potential V(x) in the space . Our goal is to study spectral properties of the corresponding scattering matrix and a diagonal singularity of its kernel (the scattering amplitude). It turns out that in contrast to the short-range case the Dirac-function singularity of at the diagonal disappears and the spectrum of the scattering matrix covers the whole unit circle. For an asymptotically homogeneous function V(x) of order we show that typically , where the module w and the phase ψ are asymptotically homogeneous functions, as , of orders and , respectively. Leading terms of asymptotics of w and ψ at are calculated. In the case ρ=1 our results generalize (in the limit ) the well-known formula of Gordon and Mott. As a by-product of our considerations we show that the long-range scattering fits into the theory of smooth perturbations. This gives an elementary proof of existence and completeness of wave operators in the theory of long-range scattering. In this paper we concentrate on the case ρ>1/2 when the theory of pseudo-differential operators can be extensively used. Received: 29 January 1997 / Accepted: 6 May 1997     

Differential–algebraic equations in multibody system modeling

Numerical methods for the efficient integration of both stiff and nonstiff equations of motion of multibody systems having the form of differential-algebraic equations (DAE) of index 3 are discussed. Linear multi-step ABM and BDF methods are considered for the non-iterational integration of nonstiff DAE. The Park method is proposed for integration of stiff equations. This revised version was published online in June 2006 with corrections to the Cover Date.     

Weierstrass Points and Regular Maps

It was shown by G. A. Jones and the first author in [8] that underlying any map on a compact orientable surface S there is a natural complex structure making S into a Riemann surface. In this paper we consider regular maps and enquire about the Weierstrass points on the underlying Riemann surface. We are particularly interested to know when these are geometric, i.e. whether they lie at vertices, face-centres or edge-centres of the map.     

Distribution of melamine in polyester–melamine surface coatings cured under nonisothermal conditions

The influence of experimental cure parameters on the diffusion of reactive species in polyester–melamine thermoset coatings during curing has been investigated with X‐ray photoelectron spectroscopy and attenuated total reflectance Fourier transform infrared. The diffusion of melamine plays a vital role in the curing process and, therefore, in the ultimate properties of coatings. At a low (<20%) hexamethoxymethylmelamine (HMMM) crosslinker concentration, the matrix composition is uniform, but at high HMMM concentrations, excess HMMM rapidly segregates to the air–coating interface. The rate of migration is governed by the difference in the surface free energies of polyester and HMMM and the concentration gradient of HMMM between the bulk and the surface. An increased rate of energy absorption also increases the rate of migration of HMMM to the surface. A physical model has been proposed to explain this surface segregation phenomenon in terms of cocondensation and self‐condensation reactions. It suggests that an appropriate amount of melamine can be segregated on the surface and allowed to self‐condense to form a desired thickness of a melamine topcoat through the control of the binder composition and cure conditions. This technique can be implemented to apply a melamine topcoat during cure. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 83–91, 2004     

Feasibility Exploration of Laser‐based Techniques for Characterization of a Flashing Jet

Two‐phase flows hold an interest in many areas of science and engineering. In the safety field, one such topic is the accidental release of flammable and toxic pressure‐liquefied gases. In case of such a release, a flashing vapor explosion takes place resulting in a very dense two‐phase cloud. If the released substance is flammable, this cloud can be combustible and can lead to deflagration or detonation. For understanding the source processes of flashing and risk assessment, data related to cloud characteristics (i.e. droplet size, velocity etc.) is needed especially in the near region of the release. Due to the non‐equilibrium nature of the near field regions accurate data measurement is not possible with intrusive techniques. Therefore, laser‐based optical techniques (like Particle Image Velocimetry (PIV), Particle Tracking Velocimetry and Sizing (PTVS), Phase Doppler Anemometry (PDA) etc.) present the only possibility to obtain information for particle diameter and velocity evolution in this harsh environment.     

Unexpected end‐groups of poly(acrylic acid) prepared by RAFT polymerization

Low‐molecular‐weight poly(acrylic acid) (PAA) was synthesized by reversible addition fragmentation chain transfer polymerization with a trithiocarbonate as chain‐transfer agent (CTA). With a combination of NMR spectroscopy and matrix‐assisted laser desorption/ionization time‐of‐flight mass spectrometry, the PAA end‐groups of the polymer were analyzed before and after neutralization by sodium hydroxide. The polymer prior to neutralization is made up of the expected trithiocarbonate chain‐ends and of the H‐terminated chains issued from a reaction of transfer to solvent. After neutralization, the trithiocarbonates are transformed into thiols, disulfides, thiolactones, and additional H‐terminated chains. By quantifying the different end‐groups, it was possible to demonstrate that fragmentation is the rate limiting step in the transfer reaction. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 5439–5462, 2004     

Characterization of high-order harmonic radiation on femtosecond and attosecond time scales

We characterize the temporal structure of high-order harmonic radiation on both the femtosecond and attosecond time scales. The harmonic emission is characterized by mixed-color two-photon ionization with an infrared femtosecond laser using a Mach–Zehnder interferometer where both pump and probe arms travel completely separate paths. In a first experiment, we measure the duration and chirp of individual harmonics. In a second experiment, we resolve, for the first time with this type of setup, the attosecond beating of several harmonics generated under conditions similar to the first experiment. We suggest that the results of both measurements can be combined to determine the full attosecond time structure of the harmonic emission. PACS 32.80.Rm; 42.65.Ky     

UV curing of a novel resin derived from poly(ethylene terephthalate)

The synthesis and characterization of photopolymerizable unsaturated polyester resins based on PET waste are described. The resins came from a depolymerization process based on the glycolysis of PET by diethylene glycol (DEG). Different molecular weights of glycolysates were synthesized. Then, the latter was functionalized by a methyl hemiester of maleic acid to obtain unsatured α,ω‐bismaleate PET oligomers. In the presence of an electron donor monomer, such as triethylene glycol divinyl ether, these electron acceptor oligomers were copolymerized by way of charge‐transfer complexes under UV irradiation. The reaction was monitored in situ by real‐time IR spectroscopy to study the kinetics of photopolymerization. This one was studied in relation with the physical and chemical characteristics of oligoesters and the composition of mixtures containing divinyl ethers. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 1324–1335, 2007     

Fast switching anisotropic networks obtained by in situ photopolymerization of liquid crystal molecules

Lightly cross-linked anisotropic networks with uniaxial and π/2 twisted orientations were produced by photopolymerization of monotropic mixtures containing liquid crystal mono and diacrylates. In this way the polymer backbone was immobilized and became decoupled from the motion of the mesogenic side groups. The networks showed very good reversibility and even after becoming isotropic, upon cooling, the initial orientation was recovered. In the same way, in the presence of electric fields the mesogenic groups could be reoriented in the direction of the electric field, reverting back to the initial orientation on removal of the field at a rate comparable with those observed in the monomeric state. Combining viscoelastic measurements with the dielectric behaviour of the monomeric liquid crystal and the anisotropic network, a comparison between the internal and bulk rotational viscosities was also made.