Zur Bestimmung des Stickstoffs in organischen Substanzen

Ohne Zusammenfassung     

Children's Books Reviewed

Maps and Globes Jack Knowlton Hurricane Watch Franklyn M. Branley Sunshine Makes the Seasons Franklyn M. Branley Heart Disease America's No. 1 Killer Dr. Alvin and Virginia B. Silverstein Cuts, Breaks, Bruises and Burns Joanna Cole Auks, Rocks, and the Odd Dinosaur Inside Stories from the Smithsonian Institute by Peggy Thomson The Secret Life of Cosmetics: A Science Experiment Book Vicki Cobb A Children's Zoo Tana Hoban Milk Donald Carrick Wallaby Creek Joyce Powzyk Being a Twin, Having a Twin Maxine Rosenberg     

Parametric methods in integer linear programming

In contrast to methods of parametric linear programming which were developed soon after the invention of the simplex algorithm and are easily included as an extension of that method, techniques for parametric analysis on integer programs are not well known and require considerable effort to append them to an integer programming solution algorithm.The paper reviews some of the theory employed in parametric integer programming, then discusses algorithmic work in this area over the last 15 years when integer programs are solved by different methods. A summary of applications is included and the article concludes that parametric integer programming is a valuable tool of analysis awaiting further popularization.     

On Some Families of Modules for the Current Algebra

Given a finite-dimensional module V for a finite-dimensional, complex semi-simple Lie algebra \(\mathcal {g}\), and a positive integer m, we construct a family of graded modules for the current algebra \(\mathcal {g}[t]\) indexed by simple C \(\mathcal {S}_{m}\)-modules. These modules are free of finite rank for the ring of symmetric polynomials and so can be localized to give finite-dimensional graded \(\mathcal {g}[t]\)-modules. We determine the graded characters of these modules and show that these graded characters admit a curious duality.     

Synthesis of glycerol carbonate from glycerol and urea with gold-based catalysts

The reaction of glycerol with urea to form glycerol carbonate is mostly reported in the patent literature and to date there have been very few fundamental studies of the reaction mechanism. Furthermore, most previous studies have involved homogeneous catalysts whereas the identification of heterogeneous catalysts for this reaction would be highly beneficial. This is a very attractive reaction that utilises two inexpensive and readily available raw materials in a chemical cycle that overall, results in the chemical fixation of CO(2). This reaction also provides a route to up-grade waste glycerol produced in large quantities during the production of biodiesel. Previous reports are largely based on the utilisation of high concentrations of metal sulfates or oxides, which suffer from low intrinsic activity and selectivity. We have identified heterogeneous catalysts based on gallium, zinc, and gold supported on a range of oxides and the zeolite ZSM-5, which facilitate this reaction. The addition of each component to ZSM-5 leads to an increase in the reaction yield towards glycerol carbonate, but supported gold catalysts display the highest activity. For gold-based catalysts, MgO is the support of choice. Catalysts have been characterised by XRD, TEM, STEM and XPS, and the reaction has been studied with time-on-line analysis of products via a combination of FT-IR spectroscopy, HPLC, (13)C NMR and GC-MS analysis to evaluate the reaction pathway. Our proposed mechanism suggests that glycerol carbonate forms via the cyclization of a 2,3-dihydroxypropyl carbamate and that a subsequent reaction of glycerol carbonate with urea yields the carbamate of glycerol carbonate. Stability and reactivity studies indicate that consecutive reactions of glycerol carbonate can limit the selectivity achieved and reaction conditions can be selected to avoid this. The effect of the catalyst in the proposed mechanism is discussed.     

An antimicrobial zinc based molecule for cross linking poly-acrylic acid

A system for incorporating antimicrobial zinc into polymeric materials, in particular hydrogel type polymers has been developed. Zn(Bipy-(MMOES)₂) a zinc carboxylate monomer was designed with the purpose of mimicking commercial cross linking agents such as ethylene glycol diacrylate, as well as containing antimicrobial zinc ions (Zn²⁺), with the intention that it can be used to cross link into any polymeric material, the example here being polyacrylic acid. Two systems were studied: a homopolymer of the Zn(Bipy-(MMOES)₂) and copolymers of Zn(Bipy-(MMOES)₂) with acrylic acid (AA). The AA – Zn(Bipy-(MMOES)₂) produced water swellable polymers which retained antimicrobial activity. The ability of the polymers to release the zinc ions was shown to be pH responsive and the leachate analysed to give a proposed mechanism of action. The Zn(Bipy-(MMOES)₂) monomer and polymers have shown antibacterial activity against both gram positive Methicillin susceptible staphylococcus aureus (MSSA 476) and gram negative Pseudomonas aeruginosa (PA01).     

Low-temperature tunneling and rotational dynamics of the ammonium cations in (NH4)2B12H12

Low-temperature neutron scattering spectra of diammonium dodecahydro-closo-dodecaborate [(NH(4))(2)B(12)H(12)] reveal two NH(4)(+) rotational tunneling peaks (e.g., 18.5 μeV and 37 μeV at 4 K), consistent with the tetrahedral symmetry and environment of the cations. The tunneling peaks persist between 4 K and 40 K. An estimate was made for the tunnel splitting of the first NH(4)(+) librational state from a fit of the observed ground-state tunnel splitting as a function of temperature. At temperatures of 50 K-70 K, classical neutron quasi-elastic scattering appears to dominate the spectra and is attributed to NH(4)(+) cation jump reorientation about the four C(3) axes defined by the N-H bonds. A reorientational activation energy of 8.1 ± 0.6 meV (0.79 ± 0.06 kJ/mol) is determined from the behavior of the quasi-elastic linewidths in this temperature regime. This activation energy is in accord with a change in NH(4)(+) dynamical behavior above 70 K. A low-temperature inelastic neutron scattering feature at 7.8 meV is assigned to a NH(4)(+) librational mode. At increased temperatures, this feature drops in intensity, having shifted entirely to higher energies by 200 K, suggesting the onset of quasi-free NH(4)(+) rotation. This is consistent with neutron-diffraction-based model refinements, which derive very large thermal ellipsoids for the ammonium-ion hydrogen atoms at room temperature in the direction of reorientation.