Isomeric and ground-state decay of 215 Bi

A new high-spin isomer in ²¹⁵Bi, with a half-life of 36.9(6) s, has been identified at the PSB-ISOLDE on-line mass separator using the pulsed-release technique combined with the element selective RILIS source. A decay scheme of Bi was constructed and complemented with the low-spinstructure observed in Bi decay. The population of a cascade on top of the level in ²¹⁵Poprovides evidence for Gamow-Teller -decay of the high-spin ²¹⁵Bi isomer.Received: 3 March 2003, Revised: 10 June 2003, Published online: 9 October 2003PACS: 23.20.Lv transitions and level energies - 27.80.+w - 29.30.Kv X- and -ray spectroscopyV. Fedoseyev: Present address: ISOLDE, CERN-PPE, CH-1211, Geneva 23, Switzerland.M. Górska: Present address: GSI, Darmstadt, D-64220, Germany.M. Huhta: Present address: Nokia, Tampere, Finland.     

Can the glass transition in bulk polymers be modeled by percolation picture?

Recent observations (Eur. Phys. J. E 9, 135 (2002)) showed that the vitrification process, which sets in during the linear bulk methyl methacrylate (MMA) polymerization carried out below glass transition temperatures, can be modelled by static percolation picture. To generalize this observation for different kind of bulk linear or crosslinked polymers not enough data are present in the literature. To cover partly this deficit we studied the glass transition of MMA and styrene (Sty) crosslinking copolymerization in varying ratios of MMA and Sty. Both the fluorescence intensity I and the lifetime of pyrene (Py) used as a nanosecond in situ fluoroprobe were monitored during the gelation time. Both I and increase dramatically as a result of the reduced mobility of the probes trapped in the glassy regions, appearing near the glass transition point. The average size of the glassy regions just below, and the strength of the infinite network formed upon the connection of the glassy regions above the glass transition point obey power law relations. The data around were interpreted on the basis of the percolation theory and we observed that the corresponding exponents and give static percolation values independent of the polymer composition.Received: 9 July 2004, Published online: 1 October 2004PACS: 64.60.Ak Renormalization-group, fractal, and percolation studies of phase transitions - 64.70.Pf Glass transitions - 82.35.Jk Copolymers, phase transitions, structure     

Miscible displacement of non-Newtonian fluids in a vertical tube

The influence of rheology on the miscible displacement of a viscous fluid by a less viscous, Newtonian one in a vertical tube is studied experimentally as a function of the flow velocity. For Newtonian displaced fluids the transient residual film thickness is nearly of the tube radius at large viscosity ratios between the two fluids in agreement with experimental and numerical results from the literature. For shear-thinning fluids with a zero yield stress (mostly xanthan-water solutions), decreases down to of the radius for the most concentrated solutions. For fluids with a non-zero yield stess, further decreases down to 24-25% of the radius. The orders of magnitude of these values can be obtained through numerical simulations (commercial code) for the various types of fluids. Instabilities of the film at its boundary develop downstream and lead to a reduction of the final thickness of the film at longer times: this reduction is larger for lower viscosity ratios and larger velocities.Received: 15 February 2003, Published online: 8 July 2003PACS: 47.20.Gv Hydrodynamic stability: Viscous instability - 83.60.Wc Rheology: Flow instabilities     

Exact effective force between star-polymers in a $\Theta$-solvent

We re-examine here the computation of the effective force between two star-polymers of respective numbers of branches f₁ and f₂, immersed in a common -solvent. Such a force originates essentially from the repulsive three-body interactions. To achieve this, we take advantage of some established results using renormalization theory for three-dimensional star-polymers, or conformal invariance for two-dimensional ones. We first show that, in dimension d = 3, the force, , decreases with the center-to-center distance r as , with the exact universal amplitude . Second, in dimension d = 2, we find that the force decays more slowly as , with the exact universal amplitude . For high distances compared to the gyration radius, , of a single polymer chain at the -point, an exponential decay of the force is expected.Received: 3 February 2004, Published online: 24 May 2004PACS: 61.25.Hq Macromolecular and polymer solutions; polymer melts; swelling - 05.20.-y Classical statistical mechanics     

The effect of thermal fluctuations on Schulman area elasticity

We study the elastic properties of a two-dimensional fluctuating surface whose area density is allowed to deviate from its optimal (Schulman) value. The behavior of such a surface is determined by an interplay between the area-dependent elastic energy, the curvature elasticity, and the entropy. We identify three different elastic regimes depending on the ratio between the projected (frame) and the saturated areas. We show that thermal fluctuations modify the elastic energy of stretched surfaces ( ), and dominate the elastic energy of compressed surfaces ( ). When the elastic energy is not much affected by the fluctuations; the frame area at which the surface tension vanishes becomes smaller than and the area elasticity modulus increases.Received: 14 July 2002, Published online: 19 August 2003PACS: 87.16.Dg Membranes, bilayers, and vesicles - 68.03.Cd Surface tension and related phenomena - 05.70.Np Interface and surface thermodynamicsP. Pincus: Also at Physics and Materials Departments and Program in Biomolecular Science and Engineering, UCSB.     

Dynamics of propylene glycol and its oligomers confined in clay

The dynamics of propylene glycol (PG) and its oligomers 7-PG and PPG, with (about 70 monomers), confined in a Na-vermiculite clay have been investigated by quasi-elastic neutron scattering and dielectric spectroscopy. The liquids are confined to a single molecular layer between the clay platelets, thus giving a true 2D liquid. The results show that the average relaxation time , deduced from neutron scattering at a momentum transfer Q of about , is in perfect agreement with the dielectric -relaxation time, although neutron scattering does not only probe the main ( -) relaxation, but all motions of hydrogens on the experimental time scale. At room temperature is proportional to Q ², indicating that the relaxations are mainly due to ordinary translational diffusion. The most unexpected finding is that (or the dielectric -relaxation time) is almost unaffected by the 2D confinement, in contrast to the dielectrically active normal mode of PPG which is substantially slower in the confinement. Only the 7-mer has a significantly slower segmental translational diffusion in the clay. The results suggest that the interactions to the clay surfaces are weak and that the present 2D confinement has a very small influence on the time scale of all our observed relaxation processes, except the normal-mode relaxation.Received: 1 January 2003, Published online: 8 October 2003PACS: 61.25.Em Molecular liquids - 68.35.Ja Surface and interface dynamics and vibrations - 61.12.-q Neutron diffraction and scattering     

Monte Carlo simulation of particle aggregation and gelation: II. Pair correlation function and structure factor

Diffusion-limited cluster aggregation and gelation are studied using lattice and off-lattice Monte Carlo simulations. The pair correlation function g(r) and the structure factor S(q) of the particle gels were investigated as a function of the volume fraction ( ) and time. At volume fractions below , the gel structure is fractal on small length scales with . g(r) shows a weak minimum at the correlation length ( ), before reaching the average concentration at large length scales. The cut-off function of g(r) varies during the aggregation process, but at a given , where is the gel time, it is a universal function of . At high volume fractions, the structure is dominated by excluded-volume interactions, while at low volume fractions, it is determined by the connectivity.Received: 27 April 2004, Published online: 26 October 2004PACS: 64.60.Ak Renormalization-group, fractal, and percolation studies of phase transitions - 02.70.Uu Applications of Monte Carlo methods     

Boltzmann-Uehling-Uhlenbech calculation of total reaction cross-section and fragmentation cross-section

, and have been calculated via the BUU model with soft EOS and 0.8 times of . The density distribution without any adjustable parameters which comes from the RMF model has been introduced into the BUU calculation to replace the normally used one-parameter square-type distribution. The calculated results can reproduce the experimental data well for both halo- and stable-nuclei-induced reactions. Here or is calculated as the difference between of halo nucleus and core nucleus, by assuming . It indicates that this assumption works very well at high energy in the BUU calculation. More experimental measurements are necessary to test the validity of this assumption at intermediate energy.Received: 12 June 2003, Revised: 29 September 2003, Published online: 27 April 2004PACS: 24.10.-i Nuclear reaction models and methods - 25.60.Dz Interaction and reaction cross-sections - 25.60.Gc Breakup and momentum distributions - 27.20. + n      

Irreversible adsorption from dilute polymer solutions

We study irreversible polymer adsorption from dilute solutions theoretically. Universal features of the resultant non-equilibrium layers are predicted. Two broad cases are considered, distinguished by the magnitude of the local monomer-surface sticking rate Q: chemisorption (very small Q) and physisorption (large Q). Early stages of layer formation entail single-chain adsorption. While single-chain physisorption times are typically micro- to milli-seconds, for chemisorbing chains of N units we find experimentally accessible times , ranging from seconds to hours. We establish 3 chemisorption universality classes, determined by a critical contact exponent: zipping, accelerated zipping and homogeneous collapse. For dilute solutions, the mechanism is accelerated zipping: zipping propagates outwards from the first attachment, accelerated by occasional formation of large loops which nucleate further zipping. This leads to a transient distribution of loop lengths s up to a maximum size after time t. By times of order the entire chain is adsorbed. The outcome of the single-chain adsorption episode is a monolayer of fully collapsed chains. Having only a few vacant sites to adsorb onto, late-arriving chains form a diffuse outer layer. In a simple picture we find for both chemisorption and physisorption a final loop distribution and density profile whose forms are the same as for equilibrium layers. In contrast to equilibrium layers, however, the statistical properties of a given chain depend on its adsorption time; the outer layer contains many classes of chain, each characterized by a different fraction of adsorbed monomers f. Consistent with strong physisorption experiments, we find the f values follow a distribution .Received: 13 January 2003, Published online: 8 July 2003PACS: 82.35.-x Polymers: properties; reactions; polymerization - 05.40.-a Fluctuation phenomena, random processes, noise, and Brownian motion - 68.08.-p Liquid-solid interfaces     

Calculation of the persistence length of a flexible polymer chain with short-range self-repulsion

For a self-repelling polymer chain consisting of n segments we calculate the persistence length , defined as the projection of the end-to-end vector on the direction of the j-th segment. This quantity shows some pronounced variation along the chain. Using the renormalization group and -expansion we establish the scaling form and calculate the scaling function to order . Asymptotically, the simple result emerges for dimension d = 3. Also away from the excluded-volume limit is found to behave very similar to the swelling factor of a chain of length . We carry through simulations which are found to be in good accord with our analytical results. For d = 2 both our and previous simulations as well as theoretical arguments suggest the existence of logarithmic anomalies.Received: 17 November 2003, Published online: 30 March 2004PACS: 61.25.Hq Macromolecular and polymer solutions; polymer melts; swelling - 05.10.Cc Renormalization group methods     

Dynamics of living polymers

We study theoretically the dynamics of living polymers which can add and subtract monomer units at their live chain ends. The classic example is ionic living polymerization. In equilibrium, a delicate balance is maintained in which each initiated chain has a very small negative average growth rate (velocity) just sufficient to negate the effect of growth rate fluctuations. This leads to an exponential molecular weight distribution (MWD) with mean . After a small perturbation of relative amplitude , e.g. a small temperature jump, this balance is destroyed: the velocity acquires a boost greatly exceeding its tiny equilibrium value. For the response has 3 stages: (1) Coherent chain growth or shrinkage, leaving a highly non-linear hole or peak in the MWD at small chain lengths. During this episode, lasting time , the MWDs first moment and monomer concentration m relax very close to equilibrium. (2) Hole-filling (or peak decay) after . The absence or surfeit of small chains is erased. (3) Global MWD shape relaxation after . By this time second and higher MWD moments have relaxed. During episodes (2) and (3) the fast variables ( ) are enslaved to the slowly varying number of free initiators (chains of zero length). Thus fast variables are quasi-statically fine-tuned to equilibrium. The outstanding feature of these dynamics is their ultrasensitivity: despite the perturbations linearity, the response is non-linear until the late episode (3). For very small perturbations, , response remains non-linear but with a less dramatic peak or hole during episode (1). Our predictions are in agreement with viscosity measurements on the most widely studied system, -methylstyrene.Received: 23 September 2003PACS: 82.35.-x Polymers: properties; reactions; polymerization - 05.40.-a Fluctuation phenomena, random processes, noise, and Brownian Motion - 87.15.Rn Biomolecules: structure and physical properties; Reactions and kinetics; polymerization     

Strange particle production at RHIC in the dual parton model

We compute the mid-rapidity densities of pions, kaons, baryons and antibaryons in Au-Au collisions at GeV in the dual parton model supplemented with final state interaction (comovers interaction). The ratios ( ) increase between peripheral ( ) and central ( collisions by a factor 2.4 (2.0) for the , 4.8 (4.1) for the and 16.5 (13.5) for the . The ratio increases by a factor 1.3 in the same centrality range. A comparison with the available data is presented.Received: 28 April 2003, Published online: 11 July 2003     

The $\eta_{c}(2980)$ formation in two-photon collisions at LEP energies

production in interactions has been detected via its decays into ,K ⁺ K ^- K ⁺ K ^- and in the data taken with the DELPHI detector at LEP1 and LEP2 energies. The two-photon radiative width averaged over all observed decay channels is = 13.9 2.0 (stat.) 1.4(syst.) 2.7 (BR) keV. No direct decay channel has been observed. An upper limit < 5.5 keV at 95% confidence level has been evaluated for this decay mode.Received: 3 July 2003, Published online: 7 November 2003     

Enhancement of the orientational order parameter of nematic liquid crystals in thin cells

We report measurements of birefringence of several nematic liquid crystals having transverse as well as longitudinal dipole moments in thin (1.4 to ) and thick (7 to cells. Rubbed polyimide-coated glass plates are used to get planar alignment of the nematic director in these cells. We find significant enhancement (6 to ) of ( , where S is the orientational order parameter) in thin cells in all compounds with aromatic cores even at temperatures far ( C) below the nematic-isotropic transition point. The enhancement is larger in compounds having several phenyl rings and lower if the number of phenyl rings is reduced. In a compound that does not have an aromatic core no significant enhancement is observed, implying that the strength of the surface potential depends on the aromaticity of the cores. Assuming a perfect orientational order at the surface, calculations based on the Landau-de Gennes theory show that the thickness averaged enhancement of S is sharply reduced as the temperature is lowered in the nematic phase. The measured order parameter S is further enhanced in thin cells because of the stiffening of the elastic constant which reduces the thermal fluctuations of the nematic director. The combined effect is however too small at low temperatures to account for the experimental data.Received: 22 February 2004, Published online: 24 May 2004PACS: 61.30.-v Liquid crystals - 61.30.Pq Microconfined liquid crystals: droplets, cylinders, randomly confined liquid crystals, polymer dispersed liquid crystals, and porous systems - 61.30.Hn Surface phenomena: alignment, anchoring, anchoring transitions, surface-induced layering, surface-induced ordering, wetting, prewetting transitions, and wetting transitionsSurajit Dhara: Present address: Department of Physics, Birla Institute of Technology and Science, Pilani 333 031, India.     

Measurement of isolated prompt photon production in photon-photon collisions at $\sqrt{s_{\rm ee}} = 183$-209 GeV

For the first time at LEP the production of prompt photons is studied in the collisions of quasi-real photons using the OPAL data taken at centre-of-mass energies between 183 GeV and 209 GeV. The total inclusive production cross-section for isolated prompt photons in the kinematic range of transverse momentum GeV and pseudorapidity is determined to be . Differential cross-sections are compared to the predictions of a next-to-leading-order (NLO) calculation.Received: 6 May 2003, Published online: 4 November 2003     

Search for anomalous weak dipole moments of the $\tau$ lepton

The anomalous weak dipole moments of the lepton are measured in a data sample collected by ALEPH from 1990 to 1995 corresponding to an integrated luminosity of 155 pb^-1. Tau leptons produced in the reaction at energies close to the mass are studied using their semileptonic decays to , , or . The real and imaginary components of both the anomalous weak magnetic dipole moment and the CP-violating anomalous weak electric dipole moment, , , and , are measured simultaneously by means of a likelihood fit built from the full differential cross section. No evidence of new physics is found. The following bounds are obtained (95% CL): , , , and .Received: 25 September 2002, Published online: 29 August 2003     

Decay properties of isomeric states in radium isotopes close to N = 126

Isomeric states in ^210-215Ra have been populated by the decay of the compound nuclei ^216,220Ra produced in irradiations of ^204,208Pb with ¹²C at MeV. Published values for -ray energies and half-lives were confirmed for Ra. Our data for Ra agree with the -energies and the half-life measured at the RITU separator, University of Jyväskylä (Finland). Its decay pattern is complex. Two series of -rays of keV and keV were observed. A half-life of s was measured. The isomeric state is attributed to an 8 ⁺ state at E ^* = 2053.8keV. A previously unknown isomeric state was assigned to Ra. It has a half-life of ( ) and it decays by emission of -rays with energies of 396.1keV and 802.0keV. It is attributed to a 13/2 ⁺ state at E ^* = 1198.1 keV.PACS: 23.60. + e decay - 27.90. + b      

Helicity dependence of the \gamma p\rightarrow N \pi channels and multipole analysis in the \Delta region

A high-quality double-polarization data set for the helicity dependence of the total and differential cross-sections for both channels in the region has been obtained in the framework of the GDH experiment. The experiment, performed at the Mainz microtron MAMI, used a 4 detection system, a circularly polarized photon beam, and a longitudinally polarized frozen-spin target. These data are included in the database to perform a multipole analysis to determine the properties of the -resonance. For the resonant (1232) multipoles we find a very good agreement with previous analyses, while the nonresonant ones show significant deviations.Received: 11 July 2003, Revised: 16 January 2004, Published online: 17 August 2004PACS: 13.60.Le Meson production - 14.20.Gk Baryon resonances with S = 0 - 25.20.Lj Photoproduction reactions     

Power correctionsto the space-like transition form factor {{F_{\eta^{\prime}g^{*}g^{*}}(Q^2,\omega )}}

Employing the standard hard-scattering approach (HSA) in conjunction with the running coupling (RC) method, the latter joined with the infrared renormalon calculus, we compute power-suppressed corrections to the massless -meson-virtual-gluon transition form factor (FF) . Contributions to the form factor from the quark and gluon components of the meson are taken into account. Analytic expressions for the FFs and are also presented, as well as Borel transforms and resummed expressions. It is shown that except for , the Borel transform contains an infinite number of infrared renormalon poles. It is demonstrated that in the explored range of the total gluon virtuality , power corrections found with the RC method considerably enhance the FF relative to results obtained only in the context of the standard HSA with a frozen coupling.Received: 19 May 2003, Revised: 24 October 2003, Published online: 8 December 2003Permanent address: S.S. Agaev: High Energy Physics Lab., Baku State University, Z. Khalilov St. 23, 370148 Baku, Azerbaijan