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21.
We present a new approach, requiring the solution of a SemiDefinite Program, for decomposing the Hessian of a nonseparable mixed-integer quadratic problem to permit using perspective cuts to improve its continuous relaxation bound. The new method favorably compares with a previously proposed one requiring a minimum eigenvalue computation. 相似文献
22.
Claudio Ciofi degli Atti 《Acta Physica Hungarica A》2006,27(1):79-86
Semi-exclusive processes and grey track production in DIS off nuclear targets are analyzed as possible tools to investigate the space time evolution of hadronization. 相似文献
23.
The classical (non-quantum) cohomology of the Becchi-Rouet-Stora-Tyutin (BRST) symmetry in phase space is defined and worked out. No group action for the gauge transformations is assumed. The results cover, therefore, the general case of an open algebra and are valid off-shell. Each cohomology class contains all BRST invariant functions with fixed ghost number (an integer) which differ from each other by a BRST variation. If the ghost number is negative there is only the trivial class whose elements are equivalent to zero. If the ghost number is positive or zero there is a bijective correspondence between the BRST classes and those of the exterior derivative along the gauge orbits. These gauge orbits lie in the phase space surface on which the gauge generators are constrained to vanish. The BRST invariant functions of ghost numberp are then related to closedp-forms along the orbits. The addition of a BRST variation corresponds to the addition of an exact form. Some comments about the quantum case are included. The physical meaning of the classes with ghost number greater than zero is not discussed.Chercheur qualifié du Fonds National de la Recherche Scientifique (Belgium) 相似文献
24.
Claudio Albanese Jürg Fröhlich Thomas Spencer 《Communications in Mathematical Physics》1988,119(4):677-699
This is our second paper devoted to the study of some non-linear Schrödinger equations with random potential. We study the non-linear eigenvalue problems corresponding to these equations. We exhibit a countable family of eigenfunctions corresponding to simple eigenvalues densely embedded in the band tails. Contrary to our results in the first paper, the results established in the present paper hold for an arbitrary strength of the non-linear (cubic) term in the non-linear Schrödinger equation. 相似文献
25.
Claudio Albanese 《Journal of statistical physics》1989,55(1-2):297-309
The quantum, antiferromagnetic, spin-1/2 Heisenberg Hamiltonian on thed-dimensional cubic lattice
d
is considered for any dimensiond. First the anisotropic case is considered for small transversal coupling and a convergent expansion is given for a family of eigenprojections which is complete in all finite-volume truncations. Then the general case is considered, for which an upper bound to the ground-state energy is given which is optimal for strong enough anisotropy. This bound is expressed through a functional involving the statistical expectation value at finite temperature of a certain correlation function of an Ising model defined on the lattice
d
itself. 相似文献
26.
Antonio Tiripicchio Marisa Tiripicchio Camellini Mauro Ghedini Giuliano Dolcetti 《Transition Metal Chemistry》1980,5(1):102-105
Summary The structure of [Ir(NO)(phen)(PPh3)2][PF6]2 has been determined from x-ray diffractometer data. The compound crystallizes in space groupPnam with four molecules in a unit cell witha = 19.924(12),b = 14.793(9) andc = 16.348(9) A. Full-matrix least-squares refinement has led to a final R value of 0.061 for the 4796 observed reflections. The structure consists of well-separated ions, and the geometry around the metal is trigonal bipyramidal with nitrosyl and bidentate 1,10-phenanthroline (in spite of the very narrow bite angle of 75.8°) ligands occupying the equatorial positions and the triphenylphosphine ligands the axial positions. The cation has an imposed crystallographicm symmetry. Important bond lengths are as follows: Ir-P, 2.391(3): Ir-N (nitrosyl) 1.700(12): Ir-N (1,10-phenanthroline) 2.103(12) and 2.142(11): N-O, 1.201(18)A. The nitrosyl ligand is linear [Ir-N-O = 179.9(9)°] so that this complex can be formulated as an NO+ complex of iridium(I). 相似文献
27.
Claudio Arato E. Kendall Pye Gordon Gjennestad 《Applied biochemistry and biotechnology》2005,123(1-3):871-882
Processes that produce only ethanol from lignocellulosics display poor economics. This is generally overcome by constructing
large facilities having satisfactory economies of scale, thus making financing onerous and hindering the development of suitable
technologies. Lignol Innovations has developed a biorefining technology that employs an ethanol-based organosolv step to separate
lignin, hemicellulose components, and extractives from the cellulosic fraction of woody biomass. The resultant cellulosic
fraction is highly susceptible to enzymatic hydrolysis, generating very high yields of glucose (>90% in 12–24h) with typical
enzyme loadings of 10–20 FPU (filter paper units)/g. This glucose is readily converted to ethanol, or possibly other sugar
platform chemicals, either by sequential or simultaneous saccharification and fermentation. The liquor from the organosolv
step is processed by well-established unit operations to recover lignin, furfural, xylose, acetic acid, and a lipophylic extractives
fraction. The process ethanol is recovered and recycled back to the process. The resulting recycled process water is of a
very high quality, low BOD5, and suitable for overall system process closure. Significant benefits can be attained in greenhouse gas (GHG) emission reductions,
as per the Kyoto Protocol. Revenues from the multiple products, particularly the lignin, ethanol and xylose fractions, ensure
excellent economics for the process even in plants as small as 100 mtpd (metric tonnes per day) dry woody biomass input—a
scale suitable for processing wood residues produced by a single large sawmill. 相似文献
28.
G. Giraudi Claudio Baggiani Antonella Cosmaro Emilio Santià Adriano Vanni 《Analytical and bioanalytical chemistry》1998,360(2):235-240
A very selective polyclonal antiserum against 1,1,1-trichloro-2,2-bis-(4-chlorophenyl)-ethane (p,p′-DDT) was obtained by a careful choice of the haptenic structure (2,2-bis(4-chlorophenyl)-ethanol hemisuccinate). This hapten was conjugated to BSA to prepare the immunogen. The effects of different types of solid phases on the equilibrium reaction between the hapten on solid phase and the polyclonal antiserum were evaluated to obtain a fine tuning of the antiserum performances in terms of specificity for p,p′-DDT and sensitivity to low levels of this pesticide. The calibration curves obtained show that it is possible to set up a sensitive assay for p,p′-DDT, employing a p,p′-dichlorodiphenylacetic acid-based solid phase, with a detection limit of 0.12 ng/mL and a working range of about 0.21–40 ng/mL. Selectivity towards several p,p′-DDT-related substances was good (o,p-DDT 17%, p,p′-DDD 1.2% o,p-DDD 6.3%, p,p′-DDE 6.7%). 相似文献
29.
Francesco Ghetti Giuliano Colombetti Francesco Lenci Enzo Campani Erseo Polacco Maurizio Quaglia 《Photochemistry and photobiology》1985,42(1):29-33
Abstract— The spectroscopic characterization of the photoreceptor pigment is one of the main questions in the study of the photosensory transduction chains in photomotile microorganisms. One of the possible techniques that can be used is in vivo microspectrofluorometry. By means of a tunable dye-laser microspectrofiuorometer developed by us, we have investigated some of the spectroscopic properties of the photoreceptor pigment of the green flagellate Euglena gracilis. The in vivo fluorescence excitation spectrum has been determined and the fluorescence quantum yield has been measured. The results show that flavins are indeed present in the paraflagellar body of E. gracilis and that their fluorescence quantum yield is much lower than that of a free flavin. An estimate of the order of magnitude of the rate constants for primary molecular reactions is tentatively given. 相似文献
30.
Pau Bernadó Renato Barbieri Esteve Padrós Claudio Luchinat Miquel Pons 《Journal of the American Chemical Society》2002,124(3):374-375
Addition of Tb3+ to purple membrane (PM) suspensions changes the orientation of the menbrane normal from parallel to perpendicular with respect to the magnetic field. Residual dipolar couplings measured in protein L in the presence of PM are scaled by a factor of -1/2. NMR line broadening and cross-correlation effects induced by the addition of PM are partially reversed by Tb3+ but not by Tm3+ that has no effect on the orientation of PM. This is interpreted as the result of anisotropically restricted motion of protein L in the transiently PM-bound form. 相似文献