Elastic scattering of Ni+Ni near the Coulomb barrier

Elastic scattering angular distributions have been measured for ⁵⁸Ni+⁶⁴Ni at three energies around the Coulomb barrier employing a new kinematic coincidence technique. The data are compared with the results of coupled-channels calculations including inelastic excitations as well as one-and two-neutron transfer reactions. The agreement is good and the calculations also agree well with the available transfer and fusion reaction data.     

Structure-Activity Relationship in Ambergris-Type Woody Odorants possessing a hydronaphthalene skeleton

A series of methyl hydronaphthyl alcohols, formates, acetates, and ketones were prepared and their odour properties evaluated. Minor structural changes, even opposite to the osmophoric group, were found to have major effects on the odour. ¹³C? NMR shift assignments of the hydronaphthyl derivatives are presented.     

On the Structure of MHD Shock Waves in Diffusive-Dispersive Media

We consider the equations of compressible magnetohydrodynamics including the diffusive effects of fluid viscosity, thermal heat conductivity, electrical resistivity, and, in particular, the dispersive influence of the Hall term. The equations describe the dynamics of a plasma as it arises in astrophysical and technical applications. For a model problem we prove an existence result for shock profiles for all values of the Hall parameter. The same question for the complete six-dimensional system seems to be only solvable for small values of the Hall parameter, that is, viewing the Hall effect as a perturbation. To obtain substantial information on the complete system for all ranges of the dissipation parameters we present a careful numerical study. In particular the study confirms a well-known conjecture on the existence and bifurcation of orbits and illustrates the breaking of symmetry due to the Hall term.     

Investigation on ignition behaviors of pulverized coal particles in a tubular swirl burner

This paper intensively investigated the ignition of turbulent coal flames in a novel fully-mixed tubular swirl burner. The Nikon D300s digital camera was used to capture the statistical ignition behavior of dispersed coal particle streams in different ambiences. Meanwhile, the combustion dynamics of individual coal particles were also recorded by means of high-speed photography. Two low-rank coal samples, Hulunbel lignite and Zhundong coal, were tested in this study. The ignition delay times of coal particles in the swirl burner were compared with those in a flat-flame burner. In contrast to previous work on a laminar flat-flame burner, the current experimental results show that the turbulent ambience significantly enhances the ignition of all coal samples, which is exceptionally pronounced under high temperature and low oxygen conditions. In addition, the sensitivity analysis suggests that both the enhanced heat and mass transfer contribute to the early ignition in turbulence. The effect of elevated mass transfer coefficient turns prominent in low oxygen fraction ambience, wherein the volatile barrier effect is suppressed by the enhanced mixing process. The combined effect of turbulence favors the shifting of ignition modes to the heterogeneous-dominant region. Last but not least, the ceased volatile flame that visualized in turbulent low oxygen ambience further confirms the important role of heterogeneous ignition.     

Experimental and modeling assessment of sulfur release from coal under low and high heating rates

Coal combustion releases elevated amounts of pollutants to the atmosphere including SO_X. During the pyrolysis step, sulfur present in the coal is released to the gas phase as many different chemical species such as H₂S, COS, SO₂, CS₂, thiols and larger tars, also called SO_X precursors, as they form SO_X during combustion. Understanding the sulfur release process is crucial to the development of reliable kinetic models, which support the design of improved reactors for cleaner coal conversion processes. Sulfur release from two bituminous coals, Colombian hard coal (K1) and American high sulfur coal (U2), were studied in the present work. Low heating rate (LHR) experiments were performed in a thermogravimetric analyzer coupled with mass spectrometry (TG-MS), allowing to track the mass loss and the evolution of many volatile species (CO, CO₂, CH₄, SO₂, H₂S, COS, HCl and H₂O). High heating rate (HHR) experiments were performed in an entrained flow reactor (drop-tube reactor – DTR), coupled with MS and nondispersive infrared sensor (NDIR). HHR experiments were complemented with CFD simulation of the multidimentional reacting flow field. A kinetic model of coal pyrolysis is employed to reproduce the experiments allowing a comprehensive assessment of the process. The suitability of this model is confirmed for LHR. The combination of HHR experiments with CFD simulations and kinetic modeling revealed the complexity of sulfur chemistry in coal combustion and allowed to better understand of the individual phenomena resulting in the formation of the different SO_X precursors. LHR and HHR operating conditions lead to different distribution of sulfur species released, highly-dependent on the gas-phase temperature and residence time. Higher retention of total sulfur in char is observed at LHR (63%) when compared to HHR (37–44%), at 1273 K. These data support the development of reliable models with improved predictability.     

From Infinite Chains according to 1∞[Zr(S2O7)4/2] in Zr(S2O7)2 to the unprecedented [Zr(S2O7)4]4– Anion in Ag4[Zr(S2O7)4]

The reaction of ZrCl₄ with oleum (65 % SO₃) in the presence of Ag₂SO₄ at 250 °C yielded colorless single crystals of Zr(S₂O₇)₂ [orthorhombic, Pccn, Z = 4, a = 709.08(6) pm, b = 1442.2(2) pm, c = 942.23(9) pm, V = 963.5(2) × 10⁶ pm³]. Zr(S₂O₇)₂ shows Zr⁴⁺ ions in an eightfold distorted square antiprismatic coordination of oxygen atoms belonging to four chelating disulfate units. Each S₂O₇^2– ion is connected to a further Zr⁴⁺ ion leading to chains according to ¹_∞[Zr(S₂O₇)_4/2]. The same reaction at a temperature of 150 °C resulted in the formation of Ag₄[Zr(S₂O₇)₄] [monoclinic, C2/c, Z = 4, a = 1829.35(9) pm, b = 704.37(3) pm, c = 1999.1(1) pm, β = 117.844(2)°, V = 2277.6(2) × 10⁶ pm³]. Ag₄[Zr(S₂O₇)₄] exhibits the unprecedented [Zr(S₂O₇)₄]^4– anion, in which the central Zr⁴⁺ cation is coordinated by four chelating disulfate units. Thus, in Ag₄[Zr(S₂O₇)₄] the ¹_∞[[Zr(S₂O₇)_4/2] chains observed in Zr(S₂O₇)₂ are formally cut into pieces by the implementation of Ag⁺ ions.     

Activation of Molecular Hydrogen by Bis(η5,η1‐pentafulvene)‐titanium Complexes – Efficient Formation of Titanium(III)hydrides

The synthesis and crystal structures of two dinuclear titanocene hydride complexes are reported. Both complexes, namely bis(η⁵‐(di‐para‐tolylmethyl)cyclopentadienyl)titanium hydride dimer, [(η⁵‐C₂₀H₁₉)₂Ti(μ‐H)]₂ ( 2a ), and bis(η⁵‐2‐adamantylcyclopentadienyl)‐titanium hydride dimer, [(η⁵‐C₁₅H₁₉)₂Ti(μ‐H)]₂ ( 2b ), are formed via activation of molecular hydrogen by the corresponding bis(η⁵,η¹‐pentafulvene)titanium complexes 1a and 1b at ambient temperatures and pressures in high yields. The hydride complexes 2a and 2b exhibit planar [Ti₂H₂] cores and, as a result of the heterolytic cleavage of molecular hydrogen, substituted Cp Ligands were formed during the reaction.     

Comparison of CCD,CMOS and intensified cameras

The properties of digital cameras are often important to obtain accurate results with image based measurement techniques. Unfortunately, a detailed comparison of the sensor specifications and performance is not accessible as this information is normally not provided by the manufacturers and no generally accepted comparison standard exists. Therefore, a detailed quantitative comparison was performed to evaluate and assess the characteristics of state-of-the-art CCD, CMOS and intensified CMOS sensors. These results may be of assistance when selecting the appropriate sensor for a desired application.