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1.
Effect of the subdivision strategy on convergence and efficiency of some global optimization algorithms 总被引:2,自引:0,他引:2
Hoang Tuy 《Journal of Global Optimization》1991,1(1):23-36
We investigate subdivision strategies that can improve the convergence and efficiency of some branch and bound algorithms of global optimization. In particular, a general class of so called weakly exhaustive simplicial subdivision processes is introduced that subsumes all previously known radial exhaustive processes. This result provides the basis for constructing flexible subdivision strategies that can be adapted to take advantage of various problem conditions. 相似文献
2.
Starting from the total Hamiltonian of an excited exciton–biexciton system, nonresonant renormalizations in the electronic spectrum of a coherently driven direct semiconductor are considered. Stringent group-theoretical inclusion of the particle spin in the Hamiltonian allows one to account for the dependence of different renormalization effects on polarizations of the incident laser fields. On the example of circularly polarized driving and probing pulses it is shown that the kind of observed renormalization is defined by the pump-and-probe polarization geometry. Thus, the exciton optical Stark effect must appear in the case of co-circular pump-and-probe, whereas a mixing of the polariton and biexciton spectra is possible only in the case of counter-circular pump-and-probe. The polariton--biexciton dispersion renormalization may manifest itself as synchronous splittings of the exciton--polariton and biexciton spectra under resonant pumping at a frequency of the polariton--biexciton transition, or in their shifts in opposite directions under near-resonant pumping. The mechanisms of both kinds of renormalization effects are analyzed, and the dependence of their characteristics on the pump parameters and microscopic parameters of the exciton–biexciton–photon system is established. An evaluation of the characteristics shows that the effect of polariton–biexciton dispersion renormalization dominates in the spectra of semiconductors with stable biexciton formation. Results of the theoretical study provide an adequate explanation of available experimental data. 相似文献
3.
Hoang The Ban Kei Nishii Yasuo Tsunogae Takeshi Shiono 《Journal of polymer science. Part A, Polymer chemistry》2007,45(13):2765-2773
This article reports a synthetic method for a norbornene–ethylene–styrene (N‐E‐S) terpolymer, which has not been well investigated so far, via incorporation of styrene (S) into vinyl‐type norbornene–ethylene (N‐E) copolymers catalyzed by a substituted ansa‐fluorenylamidodimethyltitanium [Me2Si(3,6‐tBu2Flu)(tBuN)]TiMe2 catalyst ( I ) activated with a [Ph3C][B(C6F5)4]/Al(iBu)3 cocatalyst at room temperature in toluene. The resulting terpolymerization product contained the targeted N‐E‐S terpolymer and the contaminated homopolymers, which were then able to be completely removed by solvent fractionation techniques. While homopolystyrene was easily extracted by fractionation with methylethylketone as a soluble part, homopolyethylene and a trace amount of homopolynorbornene could be perfectly separated by fractionation with chloroform as insoluble parts. The detail characterizations of a chloroform‐soluble polymer with gel permeation chromatography, nuclear magnetic resonance, and differential scanning calorimetry analyses proved that it contained a true N‐E‐S terpolymer with long N‐E sequences incorporated with isolated or short styrene sequences. The homogeneity of the morphology together with a single glass transition temperature that proportionally decreased with the increase of the styrene contents indicated that the N‐E‐S terpolymer obtained in this work is a random polymer with an amorphous structure. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 2765–2773, 2007 相似文献
4.
John R. Peterson Tamara J. Winter Hoang D. Do Robin D. Rogers 《Journal of chemical crystallography》1989,19(1):135-145
Structural and conformational information obtained from the crystal structure and solution1H nmr investigations of the title compound are compared. The 4-aryltetralone, C24H24O10, crystallizes as a chloroform solvate in the monoclinic space group, P21/n, witha=12.519(4),b=17.938(6),c=12.534(9)Å,=111.90(5)°, and Dcalc=1.51 g cm–3 forZ=4. The data for this compound were collected at –150°C. Least-squares refinement of 2796 observed [F
o5(F
o)] reflections led to the final agreement index ofR=0.062. A threefold static disorder was observed for one of the carboxyl groups. The second carboxyl group participates in an intramolecular hydrogen bond and is thus ordered. The1H nmr spectrum revealed the title compound to exist as a keto-enol tautomeric mixture in solution. Vicinal hydrogen coupling constant analysis proved reliable in ascertaining B-ring stereochemistry of 2,3-disubstituted-4-aryltetralones. 相似文献
5.
Beyer RL Hoang HN Appleton TG Fairlie DP 《Journal of the American Chemical Society》2004,126(46):15096-15105
Short peptides corresponding to two to four alpha-helical turns of proteins are not thermodynamically stable helices in water. Unstructured octapeptide Ac-His1-Ala2-Ala3-His4-His5-Glu6-Leu7-His8-NH(2) (1) reacts with two [Pd((15)NH(2)(CH(2))(2)(15)NH(2))(NO(3))(2)] in water to form a kinetically stable intermediate, [[Pden](2)[(1,4)(5,8)-peptide]](2), in which two 19-membered metallocyclic rings stabilize two peptide turns. Slow subsequent folding to a thermodynamically more stable two-turn alpha-helix drives the equilibrium to [[Pden](2)[(1,5)(4,8)-peptide]] (3), featuring two 22-membered rings. This transformation from unstructured peptide via turns to an alpha-helix suggests that metal clips might be useful probes for investigating peptide folding. 相似文献
6.
Advances in Data Analysis and Classification - Online social network is a major media for many types of information communication. Although the primary purpose of social networks is to connect... 相似文献
7.
T. F. Hoang 《Zeitschrift fur Physik C Particles and Fields》1994,63(2):269-273
The similarity of rapidity distributions of hadrons frompp and $\bar p$ p withe + e ?→π±+... implies a scaling forE cm, reflecting the quark-quark interaction of particle production by $\bar p$ /p+p. This scaling relates the meson multiplicity fromh+p→m $\bar m$ +... to the Fermi-Landau law $n_{ch} = a\sqrt {E_{cm} } $ fore + e ? collisions, without free-parameters, threshold energy being taken into account including the mass of quarks constituent of the projectile and the target, the coefficient behaves like bremsstrahlung a~1/m 2. 相似文献
8.
T. F. Hoang 《Zeitschrift fur Physik C Particles and Fields》1993,59(2):303-306
The limiting temperatureT 0 of secondaries from \(pp/\bar pp\) collisions is estimated on the basis of the Lorentz contraction factor, to be compared with the critical temperatureT c determined by the specific heat. It is found, in terms of the critical exponent law,T 0≈T c ≈215 MeV for π? andK 0. 相似文献
9.
Conclusions Both the extent of C2H4 hydropolymerization, initiated by 0.01% CO, on Co zeolites at a temperature below 100°C, and the initiating effect increase symbatically with increase in the ratio of SiO2/Al2O3 in the zeolite in the investigated limits (from 2 to 10).Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 4, pp. 894–896, April, 1974. 相似文献
10.
Nishi K. Bhardwaj Viet Hoang Vinh Dang Kien L. Nguyen 《Colloids and surfaces. A, Physicochemical and engineering aspects》2006,290(1-3):222-228
A wide range of kraft pulps from radiata pine produced by low-temperature kraft pulping in flow-through reactors was assessed for carboxyl and hexenuronic acid (HexA) contents using the conductometric titrations and UV spectrophotometer, respectively. The Kappa number of pulps varied from 20.8 to 84.7 when using a cooking liquor of 1 M effective alkali as Na2O, 25% sulfidity, and cooking time of 100–250 min. The experimental results showed that the carboxyl groups (including HexA) and HexA groups dissolved and their residual values in the pulp samples correlate linearly with Kappa number and pulp yield. The dissolving rate of all carboxyl groups is much faster than the loss of HexA. The HexA/lignin ratio decreased non-linearly with Kappa number. 相似文献