The sensitivity of radiative transfer calculations to the changes in the HITRAN database from 1982 to 2004

Over the last quarter century, improvements in the determination of the spectroscopic characteristics of the infrared-active trace species have enhanced our ability to retrieve quantitative distributions of temperatures, clouds, and abundances for various trace species within the Earth's atmosphere. These improvements have also allowed for refinements in the estimates of climatic effects attributed to changes in the Earth's atmospheric composition. Modeling efforts, however, have frequently experienced significant delays in assimilating improved spectroscopic information. Such is the case for highly parameterized models, where considerable effort is typically required to incorporate any revisions. Thus, a line-by-line radiative transfer model has been used to investigate the magnitude of the effects resulting from modifications to the spectroscopic information. Calculations from this line-by-line model have demonstrated that recent modifications to the HITRAN (High Resolution Transmission) line parameters, the continuum formulation, and the CO₂ line-mixing formulation can significantly affect the interpretation of the high spectral resolution radiance and brightness temperature retrievals. For certain moderate-resolution satellite remote sensing channels, modifications to these spectroscopic parameters and formulations have shown the capacity to induce changes in the calculated radiances equivalent to brightness temperature differences of 1-2 K. Model calculations have further shown that modifications of the spectroscopic characteristics tend to have a modest effect on the determination of spectrally integrated radiances, fluxes, and radiative forcing estimates, with the largest differences being of order 1 W m⁻² for the total thermal infrared fluxes, and of order 2-3% of the calculated radiative forcing at the tropopause attributed to the combined doubling of CO₂, N₂O, and CH₄. The results from this investigation are intended to function as a guide to differentiate between cases where older parameterizations provide acceptable results, within specified accuracy bounds, and cases where upgrades to the latest spectroscopic database are necessary.     

Fluctuations of order parameters in the highT c superconductors

Recently we have proposed a phenomenological approach in terms of two coexisting macroscopic order parameters corresponding to the superconducting and insulating states and have discussed the electrodynamical responses of the superconducting ceramics. In this paper we discuss the fluctuations of the order parameters both in static and dynamical situations in the mean field approach and obtain results for the electrical conductivity which possesses anomalies as in granular materials.     

Determination of Band Structure Parameters and the Quasi‐Particle Gap of CdSe Quantum Dots by Cyclic Voltammetry

Band structure parameters such as the conduction band edge, the valence band edge and the quasi‐particle gap of diffusing CdSe quantum dots (Q‐dots) of various sizes were determined using cyclic voltammetry. These parameters are strongly dependent on the size of the Q‐dots. The results obtained from voltammetric measurements are compared to spectroscopic and theoretical data. The fit obtained to the reported calculations based on the semi‐empirical pseudopotential method (SEPM)—especially in the strong size‐confinement region, is the best reported so far, according to our knowledge. For the smallest CdSe Q‐dots, the difference between the quasi‐particle gap and the optical band gap gives the electron–hole Coulombic interaction energy (J_e1,h1). Interband states seen in the photoluminescence spectra were verified with cyclic voltammetry measurements.     

Formal and analytic linearizability of families of conformal map germs (ℂ, 0) → (ℂ, 0)

We consider a nondegenerate one-parameter family of germs of conformal maps of (?, 0) into (?, 0). We prove that such a family is analytically linearizable whenever it is formally linearizable. In this case, the linearizing coordinate change analytically depends on the parameter.     

Magnetic Properties of Monocrystal 57Fe/V Multilayers Investigated by CEMS,Nuclear Resonance Reflectivity in the Time Domain and Polarized Neutron Scattering

Hyperfine Interactions - We have performed a depth selective investigation of monocrystalline samples with composition [57Fe(10 ML)/V(5 ML)]20 and [57Fe(7 ML)/V(10 ML)]29 by means of synchrotron...     

Interaction of methyltin(IV) compounds with carboxylate ligands. Part 2: formation thermodynamic parameters,predictive relationships and sequestering ability

Thermodynamic data of mono‐, di‐ and tri‐methyltin(IV)‐carboxylate complexes (acetate, malonate, succinate, oxydiacetate, diethylenetrioxydiacetate, malate, citrate, 1,2,3‐tricarballylate, 1,2,3,4‐butanetetracarboxylate, 1,2,3,4,5,6‐benzenehexacarboxylate) in aqueous solution are reported at t = 25 °C and I = 0 mol l⁻¹. Thermodynamic parameters obtained were analysed to formulate empirical predictive relationships as a function of different parameters, such as the number of carboxylate groups of the ligand and the charge of the alkyltin(IV) cation. Sequestration diagrams of citrate and 1,2,3‐tricarballylate towards alkyltin(IV) cations at different pH values are also reported and discussed. Copyright © 2007 John Wiley & Sons, Ltd.     

Synthesis and characterization of synthetic polymer colloids colloidally stabilized by cationized starch oligomers

A method is developed for anchoring enzymatically degraded cationized starch as electrosteric stabilizers onto synthetic latices, using cerium(IV) to create free‐radical grafting sites on the starch. Direct anchoring of debranched starch onto a poly(methyl methacrylate) seed latex yields a latex stabilized by well‐defined oligosaccharides. Using α‐amylase to randomly cleave starch to form (1→4)‐α‐glucans, and a comonomer, N‐isopropyl acrylamide (NIPAM), whose corresponding polymer exhibits a lower critical solution temperature (LCST), creates a means to synthesize block (or graft) oligomers of oligosaccharide and synthetic polymer, which are water soluble at room temperature. Above 30 °C, they become amphiphilic and form self‐emulsifying nanoparticles (sometimes termed “frozen micelles”) from which a synthetic latex is grown after addition of methyl methacrylate, the collapsed NIPAM‐containing entities functioning as a type of in situ seed. This synthesis of stable synthetic latex particles is shown to have a high grafting efficiency. The starch fragments were characterized by ¹H solution‐state NMR before grafting, and ¹³C solid‐state cross‐polarization magic‐angle spinning (CP‐MAS) NMR was used to characterize the starch oligomers actually grafted on the final latex. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 1836–1852, 2009     

一类二阶非线性微分方程多点共振边值问题的可解性

讨论了一类二阶非线性微分方程多点共振边值问题,通过运用Mawhin连续定理,我们在一个较简单的条件下得到了问题的解的存在性结果.     

Kinetics and thermodynamics of thermal decomposition of synthetic AlPO<Subscript>4</Subscript>·2H<Subscript>2</Subscript>O

Cumene hydroperoxide (CHP) and its derivatives have caused many serious explosions and fires in Taiwan as a consequence of thermal instability, chemical contamination, and even mechanical shock. It has been employed in polymerization for producing phenol and dicumyl peroxide (DCPO). Differential scanning calorimetry (DSC) was used to analyze the thermal hazard of CHP in the presence of sodium hydroxide (NaOH), sulfuric acid (H₂SO₄), and sodium bisulfite (Na₂SO₃). Thermokinetic parameters for decomposition, such as exothermic onset temperature (T ₀ ), maximum temperature (T _max ), and enthalpy (ΔH), were obtained from the thermal curves. Isothermal microcalorimetry (thermal activity monitor, TAM) was employed to investigate the thermal hazards during CHP storage and CHP mixed with NaOH, H₂SO₄, and Na₂SO₃ under isothermal conditions in a reactor or container. Tests by TAM indicated that from 70 to 90 °C an autocatalytic reaction was apparent in the thermal curves. According to the results from the TAM test, high performance liquid chromatography (HPLC) was, in turn, adopted to analyze the result of concentration versus time. By the Arrhenius equation, the activation energy (E _a ) and rate constant (k) were calculated. Depending on the process conditions, NaOH was one of the incompatible chemicals or catalysts for CHP. When CHP is mixed with NaOH, the T ₀ is induced earlier and the reactions become more complex than for pure CHP, and the E _a is lower than for pure CHP.