Applications of heat-diffusion equation for surface wrapping: hole detection and normal orientation

This paper presents a method for detecting holes during the surface wrapping process which cause surface leaks into the volume parts that shall not be meshed. The method solves a heat-diffusion equation on the background octree mesh, which is generated based on user-defined parameters, and its resolution corresponds to the resolution of the wrapper surface mesh. The heat problem is posed with the constant heat source in the volume, and the holes are detected as regions of high temperature gradients. The method detects both holes with open-boundary edges and semantic holes due to some missing parts. The sensitivity of the method is controlled via user-adjustable parameter which represents the ratio between the volume that shall not be meshed and the area of the hole. In addition, it is demonstrated that the method can be used to correct the orientation of normals in the surface mesh by utilising the property that high temperature is always found inside the volume. The potential of the method is presented on complex engineering examples.     

Imaging and probing catalytic surface reactions on the nanoscale: Field Ion Microscopy and atom-probe studies of O2–H2/Rh and NO–H2/Pt

We present dynamic studies of surface reactions using video-Field Ion Microscopy (FIM) along with Pulsed Field Desorption Mass Spectrometry (PFDMS). Catalytic water formation is followed using rhodium and platinum 3D field emitter crystals for the oxidation of hydrogen with either oxygen (Rh) or NO (Pt). Strongly non-linear dynamics are observed with nanoscale spacial resolution. For both reactions quasi-oscillatory behaviour exists under certain conditions of temperatures and partial pressures. An influence of the probing electric field is observed and possibly essential in establishing oscillatory behaviour. Local chemical probing of selected surface areas with up to 400 atomic surface sites proves catalytic water formation to take place. Since water ions (H₂O⁺/H₃O⁺) cause image formation of the O₂–H₂ reaction on Rh, respective videos provide space-time resolved information on the catalytically active sites. Atom-probe data also reveal that the surface of the Rh sample reversibly switches from a metallic to an oxidized state during oscillations. As to the NO–H₂ reaction on Pt, fast ignition phenomena are observed to precede wave fronts. After catalytic water formation, NO molecules diffuse into emptied areas and cause high image brightness. Depending on the size of the Pt crystal, the reaction may ignite in planes or kinked ledges along the <100> zone lines. Thus FIM provides clear experimental evidence that kinks are more reactive than steps in the catalytic NO + H₂ reaction. Pt surface oxidation occurs and has probably been underestimated in previous FIM studies.     

Photodegradation of ethylene–propylene copolymer and ethylene–propylene–ethylidenenorbornene terpolymer

Significant progress has been made in recent years regarding the photooxidation of olefin copolymers, but questions still remain. This paper reviews the progress and probes the photooxidative chemistry of ethylene–propylene (EP) and ethylene/propylene/diene monomer (EPDM) copolymers. Both stabilized and unstabilized polymer plaques were irradiated in a xenon are and the surface chemistry followed using infra-red spectroscopy. Model compounds were used to help elucidate the chemistry caused by unique structural features present in the copolymers. Volatile products evolved during photooxidation were determined giving valuable insight into the degradation chemistry.     

Sodium molybdate—a possible alternate additive for sodium dichromate in the electrolytic production of sodium chlorate

Sodium dichromate is commonly used in sodium chlorate production to maintain high current efficiency; however, it is also a well documented carcinogen. To reduce the environmental impact, identification of a suitable alternative with similar buffering characteristics to dichromate and without adverse effect on the electrolytic performance of sodium chlorate production is important; sodium molybdate is a good candidate. Molybdate ion and its conjugated acid work as a buffer pair at pH 5–6, a lower and slightly narrower pH window than the typical buffer region of dichromate. Nonetheless, the molybdate buffer works effectively during the electrolytic process by maintaining pH at 5.9. Although the use of molybdate buffer will lower the overpotential of hydrogen evolution reaction (HER) by 100 mV, the average off-gas oxygen content is noticeably compromised at 3.6–4.6%, measured using a pilot cell operated at 3 kA m⁻²and 80 °C during a 3-day trial. The resulting current efficiency of 91 92% is significantly lower than when dichromate is employed as the process additive (> 96%). Mixtures of different dichromate and molybdate ratio were also investigated in terms of the resulting cathode surface potential.     

Bench-scale continuous hydrogenation of Australian coals — study of iron catalysts and recycle solvent composition

The inter-relations between iron catalysts, recycle solvent composition and product yield and composition have been investigated in bench-scale (1–2 kg h^?1) continuous hydrogenation of Australian coals at process severity of 21–22 MPa at 400–430°C. Products and recycle solvent are recovered in batch distillation (atmospheric and vacuum) and the distillate solvent is returned to slurry feed without further treatment. Successive samples of recycle solvent are analysed by g.c.-m.s., i.r. and titrimetry. The effect of adding iron catalysts in the form of red mud - sulphur mixtures or compounds after a short period of continuous operation without catalyst is demonstrated. Distillate yields from black coals increase from 24–34 wt% daf under non-catalytic conditions to 35–53 wt% daf by adding iron catalysts. The composition of the almost equilibrated recycle solvent also changes and a new equilibrium is approached after the iron catalyst is added. The effect of solvent composition on distillate yield can not be determined from these data. The ratio of hydroaromatic components to hydroaromatic plus aromatic components in the solvent increases from ≈0.2 at non-catalytic equilibrium to ≈0.5–0.6 at catalysed equilibrium after adding iron. Other compositional parameters in the recycle solvent do not show any clear responses to the addition of iron. Equilibrium solvent composition under constant operating conditions is attained at ≈10 passes at 1 kg ^h?1 throughput with total system holdup of ≈20 kg. Paraffins for the Queensland subbituminous coal equilibrated at 18–24% in the solvent, phenolics at 16–21%, basic nitrogen at ≈0.4% (as N), and the balance a mixture of aromatics and hydroaromatics. The total aromatics neglecting phenolics in the equilibrium recycle solvent consists of ≈40–50% each of two-and three-ring and 5–10% four-ring members.     

Designing a supply network artifact for data,process, and people integration

E-procurement and supplier-relationship management systems have helped to substantially advance process execution in supply management. However, current supply network systems still face challenges of high data integration efforts, as well as the decoupling of structured data and processes from the growing amount of digitalized unstructured interactions of supply management professionals. Inspired by the room for improvement posed by this challenges, our research proposes a design for a supply network artifact in supplier qualification that addresses these problems by enabling holistic integration of data, processes, and people. The artifact is developed following an action design research approach. Building on a set of meta-requirements derived from literature and practice explorations, we conceptualize two design principles and derive corresponding design decisions that have been implemented in an software artifact. Finally, we formulate testable hypotheses and evaluate the artifact and its design in the context of supplier qualification. Our results show that the proposed design reduces mental effort of supply management professionals and significantly increases efficiency when performing typical supply network tasks such as supplier qualification.     

Computing presentations for subgroups of polycyclic groups and of context-free groups

Algorithms for solving uniform decision problems for algebraic structures crucially depend on the chosen finite presentations for the structures under consideration. Rewriting techniques have been used very successfully to solve uniform decision problems, when the presentations considered involve finite, noetherian, and ()-confluent rewriting systems. Whenever the class of algebraic structures considered is closed under the operation of taking finitely generated substructures, then the algorithms for solving the uniform decision problems can be applied to the substructures as well. However, since these algorithms depend on the form of the presentations, this involves the task of constructing a presentation of a certain form for a substructure given a presentation of this form for the structure itself and a finite set of generating elements for the substructure.This problem, which has received a lot of attention in algebra, is here investigated from an algorithmic point of view. The structures considered are the following two classes of groups, which have been studied extensively before: the polycyclic groups and the context-free groups.Finitely generated context-free groups can be presented by finite, monadic, and -confluent string-rewriting systems. Due to their nice algorithmic properties these systems provide a way to effectively solve many decision problems for context-free groups. Since finitely generated subgroups of context-free groups are again contextfree, they can be presented in the same way. Here we describe a process that, from a finite, monadic, and -confluent string-rewriting system presenting a context-free groupG and a finite subsetU ofG, determines a presentation of this form for the subgroup U ofG that is generated byU. For finitely presented polycyclic groups we obtain an analogous result, when we use finite confluent PCP2-presentations to describe these groups.This work was performed while this author was visiting at the Fachbereich Informatik, Universität Kaiserslautern, during his sabbatical 1991/92     

Picosecond thermal pulses in thin gold films

In this paper it has been shown that, with the advent of lasers with a very short pulse duration, the effect of thermal wave propagation becomes important. To consider this effect, hyperbolic heat conduction in thin gold films was studied. It was shown that for heat fluxes of the order 10⁸ W·cm^–2, a thermal wave is generated in thin gold films. The consideration of the hyperbolicity of heat transfer enables one to describe the temperature profile with one value of fluence.     

Ultraviolet photodetectors and readout based on a-IGZO semiconductor technology

In this work, real-time ultraviolet photodetectors are realized through metal–semiconductor–metal (MSM) structures. Amorphous indium gallium zinc oxide (a-IGZO) is used as semiconductor material and gold as metal electrodes. The readout of an individual sensor is implemented by a transimpedance amplifier (TIA) consisting of an all-enhancement a-IGZO thin-film transistor (TFT) operational amplifier and a switched capacitor (SC) as feedback resistance. The photosensor and the transimpedance amplifier are both manufactured on glass substrates. The measured photosensor possesses a high responsivity R , a low response time t _{R E S} , and a good noise equivalent power value NEP .