Entropy and specific heat as a measure of fluctuations in multiparticle production in relativistic nuclear collisions

An analysis to disentangle information about the occurrence of dynamical fluctuations in multiparticle production in high energy nucleus-nucleus collisions has been carried out in terms of fractal moments and entropy for the experimental and simulated data using FRITIOF, UrQMD and HIJING generators. Although there is a possibility to thermodynamically interpret the final state of multiparticle production by calculating the values of specific heat, c, using G _q - and F _q -moments. However, both these moments give markedly different values of c. The constancy observed in the values of specific heats calculated from either G _q - or F _q -moments is in accord with the predictions of constant specific heat approximation. Variations of multifractal and factorial moments and various other parameters calculated from these moments predict the presence of non-statistical fluctuations in high energy nuclear collisions.     

Scheme for the teleportation of bipartite entangled state of the two cavity modes

In this paper, we propose a scheme for the teleportation of general two-partite entangled state of zero and one photon state from one bimodal cavity to another. The scheme can be realized by using cavity quantum electrodynamics (QED).     

Living fungal hyphae-templated porous gold microwires using nanoparticles as building blocks

Abstract  

A simple and environmentally benign green method is reported to decorate growing fungal hyphae with high loading of gold nanoparticles, which were initially produced using aqueous tea extract as a sole reducing/stabilizing agent. Inoculation of fungal spores in aqueous suspension of nanoparticles led to the growth of intensely red-coloured fungal hyphae due to the accumulation of gold nanoparticles. Heat treatment of these hybrid materials led to the formation of porous gold microwires. This report is thus an interesting example of using green and sustainable approach to produce nanostructured materials which have potential applications in catalysis, sensing and electronics.     

Cohomology and Support Varieties for Restricted Lie Superalgebras

Let $(\mathfrak{g}, [p]) $ be a restricted Lie superalgebra over an algebraically closed field k of characteristic p?>?2. Let $\mathfrak{u}(\mathfrak{g})$ denote the restricted enveloping algebra of $\mathfrak{g}$ . In this paper we prove that the cohomology ring $\operatorname{H}^\bullet(\mathfrak{u}(\mathfrak{g}), k)$ is finitely generated. This allows one to define support varieties for finite dimensional $\mathfrak{u}(\mathfrak{g})$ -supermodules. We also show that support varieties for finite dimensional $\mathfrak{u}(\mathfrak{g})$ - supermodules satisfy the desirable properties of a support variety theory.     

Tris(2‐aminoethyl)amine‐based ferrocene‐terminated dendrimers as burning rate catalysts for ammonium perchlorate‐based propellant decomposition

Ferrocene‐based derivatives show potential application as burning rate catalysts (BRCs) for solid composite propellants. However, migration problems of simple ferrocene‐based derivatives limit their application as BRCs in solid composite propellants. To overcome the migration problems of ferrocene‐based BRCs and to enhance the burning rate of ammonium perchlorate (AP)‐based propellants, zero‐ to second‐generation tris(2‐aminoethyl)amine‐based ferrocene‐terminated dendrimers (G0, G1 and G2) were synthesized. The structures of G0, G1 and G2 were confirmed using ¹H NMR, Fourier transform infrared and UV–visible spectroscopies. The electrochemical behavior of G0, G1 and G2 was investigated using cyclic voltammetry. It was found that G0, G1 and G2 showed redox behavior due to the presence of ferrocene and this redox behavior was diffusion controlled over the investigated scan range. The burning rate catalytic effect of G0, G1 and G2 on thermal decomposition of AP was investigated using thermogravimetry and differential thermogravimetry. G0, G1 and G2 showed good catalytic effect on the thermal decomposition of AP. Anti‐migration studies showed that migration of G0, G1 and G2 was much slower than that of 2,2‐bis(ethylferrocenyl)propane (catocene) and ferrocene.     

Spectrophotometric Quantitation of Fluoxetine Hydrochloride Using Benzoyl Peroxide and Potassium Iodide

 Fluoxetine hydrochloride reacts with benzoyl peroxide and potassium iodide, after heating for 1 min at 30 °C, to give a blue colour having maximum absorbance at 570 nm. The reaction is selective for fluoxetine with 0.01 mg/mL as visual limit of quantitation and provides a basis for a new spectrophotometric determination. The colour reaction obeys Beer’s law from 0.1 mg/10 mL to 2.0 mg/10 mL of fluoxetine and the relative standard deviation is 0.68%. The qualitative assessment of tolerable amounts of other drugs is also studied. Received September 21, 1998. Revision September 10, 1999.     

Synthesis and properties of carbamate‐ and amine‐containing poly(phenylacetylenes)

The 3‐ and 4‐aminophenylacetylenes protected by t‐butoxycarbonyl (t‐Boc) and 9‐fluorenylmethoxycarbonyl (Fmoc) groups ( 3a – 6a ) were synthesized and polymerized using [(nbd)RhCl]₂ ( 1 ) and [(nbd)Rh⁺‐η⁶‐PhB^?Ph₃] ( 2 ) catalysts. The t‐Boc‐containing polymers [poly( 3a ) and poly( 4a )] were obtained in high yield (82–91%). Among the Fmoc‐protected monomers, the para‐derivative polymerized well [poly( 6a ); yield = 85–94%], whereas its meta‐substituted analogue did not afford high molecular weight polymer in good yield [poly( 5a ); yield = 10–15%]. The use of KN(SiMe₃)₂ as a cocatalyst in conjunction with 1 led to a dramatic increase in the molecular weight of the polymers. The acid‐ and base‐catalyzed removal of the t‐Boc and the Fmoc groups, respectively, generated primary amine‐containing polymers [poly( 3b )–poly( 6b )] which cannot be obtained directly by the polymerization of the corresponding monomers. The solubility characteristics of the polymers bearing protected amino groups were quite different from those of the unprotected ones, the former being soluble in polar solvents, whereas the latter displayed poor solubility even in polar protic or highly polar aprotic solvents. The attempts to accomplish the free‐standing membrane fabrication by solution casting were successful only for poly( 3a ), and an augmentation in the gas permeability and CO₂/N₂ permselectivity was discerned in comparison with the unsubstituted poly(phenylacetylene) and poly(m‐t‐butyldimethylsiloxyphenylacetylene). © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 1853–1863, 2009     

Momentum space distribution of electrons in an atom using hydrogenic wave functions

A formulation is developed to derive exact analytic expressions for electron-electron correlation and density of electrons in momentum space using hydrogenic wave functions. It is shown that for large atoms the expression for density of electrons has a simple form.     

On‐line Liquid‐liquid Extraction Coupled to a Reversed Micellar‐mediated Chemiluminescence Detection System: Application to the Determination of Amino/Nitroaromatic Compounds

A simple and fast flow method for the trace level determination of p‐toluidine, 2‐methyl‐5‐nitroaniline, and 2,4‐dinitroaniline in aqueous samples is reported. These amino/nitroaromatics are related to trinitrotoluene (TNT) and appear during the degradation process of the explosive. The chemical principles of ion‐pair formation and liquid‐liquid extraction are applied: In aqueous acidic medium, the protonated analyte [HA]⁺ makes an ion‐pair with the tetrachloroaurate(III) ion, followed by on‐line ion‐pair extraction into the dichloromethane carrier used. After membrane separation, the CH₂Cl₂ containing the ion‐pair, [HA]⁺[AuCl₄]⁻, is mixed with the reversed micellar luminescent reagent of luminol (in 0.3 M Na₂CO₃) prepared from cetyl‐trimethylammonium chloride in CH₂Cl₂‐cyclohexane and the [AuCl₄⁻‐luminol chemiluminescence (CL) output is recorded. The detection limits (S/N> 3) are: p‐toluidine, 1.0 × 10⁻⁴M; 2‐methyl‐5‐nitroaniline, 1.0 × 10⁻⁷ M; 2,4‐dinitroaniline, 1.0 × 10⁻⁷ M, while the calibration curves are linear between 1.0 × 10⁻⁴ — 1.0 × 10⁻² M for all the compounds. Although spectral studies indicated the formation and extraction of a very small amount of the ion‐pair species, the reversed micellar‐mediated CL detection system provides an alternative procedure for the determination of degradation products of the explosive TNT in environmental aqueous samples.     

Quark distribution in light nuclei

The distribution of quarks in light nuclei is given using the quark cluster wave function. An analytic expression for the nucleus⁴He is obtained. The distribution so obtained is compared with the one obtained using a different theoretical formulation called mapping.