Gezielte Nutzung biologischer Systeme

Directed exploitation of biological systems . During the past few decades, our knowledge of molecular process responsible for genetics has increased dramatically. Discovery of the giant molecule deoxyribonucleic acid – abbreviated as DNA – as the carrier of genetic information heralded in a development which nowadays permits us to effect directed changes in the genetic material of an organism. Thus we can provide easily cultured microorganisms with genes which were previously located in a completely different genetic environment. This helps us to obtain high yields of proteins or other substances which were formerly very difficult to obtain. Higher organisms such as animals and plants can also undergo modification of their genetic equipment. This adds a new dimension to the breeding of such species. Above all, genetic engineering provides new insights into the enormously complex interplay of molecules which go to make up a living cell. The resulting understanding of life processes on a molecular level permits recognition of malfunction and therapy of the ensuring disease by new drugs. In addition to these positive aspects, genetic engineering provides scope for conducting experiments whose ethical implications demand very earnest consideration.     

COMPUTER SIMULATION OF HYDRODEMETALLATION IN FIXED-BED REACTORS

An isothermal model for hydrodemetallation (HDM) of crude oils in catalytic fixed-bed reactors is proposed. This model involves a consecutive reaction mechanism, which is capable of accounting for particle deposit profiles with interior maxima. Consistent with the fact that HDM catalysts are conglomerates formed by precipitation, the porous catalyst itself is modeled as randomly overlapping spheres of equal size. The metal is deposited as growing metal sulfide crystallites on the inner surface of the catalyst. These crystallites originate from a certain number of randomly scattered nuclei and increase in size as the deposition proceeds. The random sphere model for the catalyst and the deposit provides the changes in the catalyst pore structure—local porosity and surface area.

The mass transport within the domain of the particle is due to restricted liquid diffusion, since the diameter of the metal bearing compound (porphyrin) and the intermediate are comparable to the pore size. The diffusion restrictions taken into account are the enhanced drag imposed on a molecule by adjacent pore walls and steric partitioning.

Since the deposition process is much slower than diffusion and reaction, the pseudo-steady-state assumption can be justified. The equations of conservation for mass are solved by orthogonal collocation on finite elements. Based on this solution technique a computer simulation program of HDM is designed that allows two modes of operation: constant temperature and constant conversion. The simulation program “SIMULA” is highly flexible with regard to reaction kinetics, catalyst structure, reactor design, and operating conditions. In comparison to a base case with uniform activity, the effect of intraparticle (radial) and bed (axial) activity profiles on the conversion rate is discussed. For the case investigated, a radial distribution of activity higher at the center of the particle than at the edge can increase catalyst life by 25%, but axial distribution was less successful.     

Untersuchung des einflusses molekularer parameter auf morphologie und eigenschaften von polyethylenen niedriger dichte

Based on the example of PE-LD grades and on model substances obtained by preparative fractionation (fractions in the molecular weight range M?_w = 1.2 ? 390·10⁴ g/mol), comprehensive investigations regarding the problems of structure/properties have been carried out. The correlations of M?_w with 15 physical and application technological perameters have been investigated taking into account the reaction mechanism during the manufacturing of PE-LD in the tubular and agitated autoclave reactor, resulting in the formation of so-called primary structure perameters M?_n, M?_w, molar mass distribution, short chain branching and long chain branching. For the interpretation of the results, among other factors, also the morphological conditions have been taken into consideration, which in connection with the molecular parameters reveal — for specific M?_w-ranges — strong changes and saturation ranges, resp., for the physical and application technological properties.     

Effect of ultrasound on thermoset polyurethane: NMR relaxation and diffusion measurements

Recycling of rubber-based materials is of increasing industrial environmental importance. In order to characterize the effect of ultrasound on polymer networks, nuclear magnetic resonance (NMR) relaxation and pulsed-gradient diffusion measurements were made at 70.5 °C in polyurethane rubber (PUR) and foam after subsequent treatment by intense ultrasound. The proton transverse relaxation decay was analyzed in terms of molecular and segmental mobilities of all motional species, a chemical and physical network as well as diffusing sol. The diffusivity spectrum, measurable in foams, reflected the changing molecular weight distribution of low-molecular weight sol and oligomers. It was observed that the effect of ultrasound was less pronounced in PUR than rubbers like SBR, PDMS and BR owing to its low degree of unsaturation. The investigation on the foams is the first of its kind to be reported.     

On‐the‐fly generation and rendering of infinite cities on the GPU

In this paper, we present a new approach for shape‐grammar‐based generation and rendering of huge cities in real‐time on the graphics processing unit (GPU). Traditional approaches rely on evaluating a shape grammar and storing the geometry produced as a preprocessing step. During rendering, the pregenerated data is then streamed to the GPU. By interweaving generation and rendering, we overcome the problems and limitations of streaming pregenerated data. Using our methods of visibility pruning and adaptive level of detail, we are able to dynamically generate only the geometry needed to render the current view in real‐time directly on the GPU. We also present a robust and efficient way to dynamically update a scene's derivation tree and geometry, enabling us to exploit frame‐to‐frame coherence. Our combined generation and rendering is significantly faster than all previous work. For detailed scenes, we are capable of generating geometry more rapidly than even just copying pregenerated data from main memory, enabling us to render cities with thousands of buildings at up to 100 frames per second, even with the camera moving at supersonic speed.     

A simple method for the objective characterisation of fabric softness. Part 1: Influence of bleaching,dyeing and crosslinking of wool*

A simple method for the characterisation of fabric softness using a conventional tensile tester and a special measurement device has been developed. The method is demonstrated to be especially useful in detecting changes in softness of a given substrate due to different treatments. The results obtained, particularly hysteresis at 75% of the maximum extension, provide a good correlation with subjective ranking for samples that are subjectively distinguishable; they also differentiate well between samples which seem subjectively indistinguishable. Screening tests were carried out, mainly on wool fabrics, to find the effect of different treatments such as oxidative (alkaline and acidic) and reductive (Blankit IN) bleaching, dyeing with acid and a 1:2 metal complex, chrome and (mono and bi)reactive dyes, the effect of the antisetting agent Basolan AS (BASF) and of crosslinking with Irgasol HTW (CGY) on fabric softness.     

The determination of molecular weights of polymers from critical concentrations of ternary systems polymer-polymer-solvent

The dependence of the critical concentration of the ternary system polymer-polymer-solvent on the molecular weight can be expressed by the relation where c_c is the critical concentration, M? the appropriate average of the molecular weight of both polymers; A and c_c∞ are constants for the given system. The possibility of determining the molecular weight of one of the polymers from the value c_c and the molecular weight of the known polymer with the aid of equation (1) is discussed.