A vibrational study of the activation sequence of C–H and C–C bonds of isobutene and 1-butene on Mo(110) and (4 × 4)-C/Mo(110) surfaces

The thermal decomposition pathways of isobutene and 1-butene on both Mo(110) and 4 × 4-C/Mo(110) surfaces have been studied using high-resolution electron energy loss spectroscopy (HREELS) in order to highlight the substantially different activities of these two surfaces towards the cleavage of C–H and C–C bonds. On clean Mo(110), the CH₂ group of isobutene decomposes upon heating to 150 K, producing either a /-bonded isobutenylidene [(CH₃)₂CCH] species or a 1,1-di-/-bonded isobutenyl [(CH₃)₂CC] species. Upon further heating, extensive C–H bond scission occurs to form hydrocarbon fragments which do not contain CH₃ or CH₂ groups, but appear to have largely intact carbon skeletons. By contrast, isobutene is molecularly adsorbed on the carbide-modified surface at 150 K. Further heating produces isobutylidyne [(CH₃)₂HCC] by 300 K, which subsequently decomposes via C–C bond scission to generate surface methyl groups. The different activation sequence of the C–H and C–C bonds of isobutene on clean and carbide-modified Mo(110) surfaces is also qualitatively confirmed by comparative studies of 1-butene on the two surfaces.     

Messung der Selbstdiffusion im System Polystyrol-Benzol; Temperatur-, Konzentrations- und Molekulargewichtsabhängigkeit

Self-diffusion of benzene and polystyrene in the system benzene-polystyrene is studied by means of spin-echo-technique as function of temperature, concentration and polymer molecular weight. From the dependence of temperature the activation energies are calculated as function of concentration and molecular weight. The concentration dependence is discussed in terms of restricted diffusion and the Fujita Free-Volume-Theory. The computed free volume shows a significant maximum at 50°C. This effect may be attributed to a change in the mobility of the phenyl side groups of polystyrene and is vanishing with decreasing molecular weight. The free-volume-temperature curves are giving references to the glass transition.     

Tomorrow’s ethics and today’s response: An investigation into the ways information systems professionals perceive and address emerging ethical issues

This paper explores the question of how foresight and futures research can identify and address ethical issues in the field of Information Systems (IS). Starting from the premise that such IS are part of socio-technical systems, the interaction between technology and human actors raise ethical concerns. Early recognition of these concerns can address ethical issues and improve the use of the technology for a range of social and organisational goals. This paper discusses research conducted in two futures research projects. Both projects investigated emerging information and communication technologies (ICTs) and ethics. The first project established approaches for identifying future technologies and their related ethical concerns. This led to the identification of 11 emerging ICTs and their associated ethical concerns. The second project took these general ethical concerns and focused on their role in IS. Specifically, how IS professionals view future emerging technologies, their associated ethical concerns, and how they think these concerns could be addressed. The key findings are that IS professionals are primarily interested in the job at hand and less so in the ethical concerns that the job might bring; ethics is a concern that is best left for others to deal with. This paper considers the implications of research on ethics in emerging ICTs and draws general conclusions about the relevance of future technologies research in IS.     

Zur oligomerenbildung bei der thermischen polymerisation von styrol

It is shown that in thermal polymerization of styrene four dimers and six trimers are formed by parallel occurring oligomerization reactions. With increasing temperature the rate of oligomerization increases more rapidly than the rate of polymerization. The relativ yields of the different oligomers depend on temperature, too.     

Struktur und eigenschaften von ABS-polymeren. IX. Quantitative untersuchungen zur morphologie von ABS-polymerisaten

The technological properties of ABS polymers largely depend on the structure of the elastomer phase as well as on the elastomer/thermoplast interface. The morphological structure of such polymers can be determined from electron micrographs of ultramicrotome sections – after selective contrasting of the polybutadiene phase – or of replicas of fracture surfaces after selective chemical degradation. The various ABS polymers are classified by their manufacturing processes and their morphologies and characterized by electron micrographs. The degree and place of grafting are of particular importance. The quantitative determination of the surface- and internal grafting is achieved by combining the determination of the degree of grafting (extraction), the evaluation of the results obtained on particle counting, and a morphometric process. It is demonstrated that the morphometric process can in general be applied for the quantitative determination of the contrastable component in two-phase polymers.     

Self-diffusion of low-generation PAMAM dendrimers with hydroxyl surface groups in solutions: a general regularity

An experimental study of the self-diffusion and nuclear magnetic relaxation of poly(amidoamine) dendrimers with hydroxyl surface groups (PAMAM-OH) dissolved in methanol over a wide range of concentration (?) is reported. It is shown that experimental concentration dependences of PAMAM-OH self-diffusion coefficients (D) can be reduced to the so-called generalized ? dependence. Over macromolecular concentration range studied, the generalized concentration dependence of PAMAM-OH D coincides with analogous curve obtained for poly(allylcarbosilane) dendrimers of high generations. This result confirms the existence of common regularities of the dendritic macromolecule self-diffusion, and their independence of the individual physicochemical and structural properties of dendrimer, solvent, and features of their interactions in the given systems. The concentration dependence of the PAMAM-OH diffusion also exhibits a clear signature of an inflexible molecule.     

Mullite Coatings on SiC and C/C–Si–SiC Substrates Characterized by Infrared Spectroscopy

Mullite (3Al₂O₃·2SiO₂) coatings on SiC substrates and SiC precoated carbon/carbon composite (C/C-Si-SiC) substrates were produced by pulsed laser deposition (PLD) using pressed mullite powder targets. The layers can be characterized efficiently by IR reflection spectroscopy in the spectral range between 650 and 5000 cm⁻¹. The deposited coatings turn into mullite upon oxidation in air at temperatures between 1400° and 1600°C. Fabry-Perot interferences indicate a high quality and homogeneity of the mullite coating/SiC substrate interface. Amorphous SiO₂ gradually forms during prolonged heating or at higher temperatures.     

Das Verhalten organischer Pigmente in Polymeren

The importance of colouring matter is of prime importance in the plastics industry. The individual behaviour of organic pigments in the various polymer materials necessitates, however, on the part of the plastics manufacturer a precise knowledge of ?which pigment for which plastic”?. For example, a well known Thioindigo pigment behaves very differently in various polymer materials : In polystyrene, depending on the concentration used, it is monomolecularly dissolved, in associated solution or present as undissolved particles. In PVC, however, the good migration fastness is indicative of the insolubility of the pigment in this medium and so it is not surprising that PVC is the ideal plastic medium for this pigment. The behaviour of organic pigments in polymers is largely a function of molecular structure, e. g. intermolecular H-bonds can cause a decrease in solubility of a pigment in a polymer material, which in turn results in improved migration fastness. This is demonstrated by the improved migration fastness of variously substituted β-hydroxy naphthoic acid arylamide derivatives. Many phenomena exist however, which as yet can only be explained on the basis of the crystal structure of the pigment particles, i. e. the presence of aggregates or agglomerates. Such a phenomenon is, for example, the dispersibility of pigments in polymers. Here pigment surface, wettability by polymer and intermolecular forces are all of importance. In general, the dispersibility is better the smaller the specific surface area, as is shown for a typical quinacridone pigment. The influence of the rate of wetting on dispersibility is demonstrated using polyethylene wax. A further effect, which demonstrates the intermolecular forces between pigment and polymer, is the way in which certain pigments influence the rate of crystallization of partly crystalline polymers. This itself is connected with the shape and size of the pigment particles embedded in the polymer material. Such effects are demonstrated by measurements on various polyethylene objects. The pigment in this case was a naphthalene tetra carbonic acid derivative in both cis and trans form with widely varying specific surface areas.