Experimente zum Strömungswiderstand in gekrümmten,rotierenden Kanälen mit quadratischem Querschnitt

Zusammenfassung Bei ausgebildeter Strömung wurde der Druckverlust in rotierenden, gekrümmten Kanalstrecken experimentell ermittelt. Speziell interssierte der Einfluß der Krümmung auf den Reibungswiderstand und im besonderen der der Rotation, die sowohl in Richtung der Durchflußgeschwindigkeit als auch entgegengesetzt dazu erfolgte. Die strömungsspezifischen Parameter wie Reynolds-und Taylor-Zahl erfuhren eine Änderung im Bereich 3·10²<Re<2·10⁵ und 0Ta<10⁵. Das Krümmungsverhältnis variierte zwischen 0,0496a/r _m 0,337. Aufgezeigt wird die Möglichkeit einer universellen Darstellung des Widerstandsbeiwertes für den nicht rotierenden Kanal bei einerseits laminarer und anderseits bei turbulenter Bewegung. Im rotierenden Kanal beobachtet man beträchtliche Druckverlusterhöhungen, deren Größe von der Rotationsrichtung abhängt. Bei großen Taylor-Zahlen wurde eine Unabhängigkeit des Strömungswiderstandes vom Krümmungsverhältnis festgestellt.

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Experimental investigations on the friction resistance in rotating curved channels with square cross-section

Summary For fully developed flow the pressure loss in rotating curved channels was investigated experimentally. The influence of the curvature on the friction coefficient and particularly on the rotation, which was realized in the direction of the through flow as well as in the opposite direction was of special interest. The specific parameters of the flow field, like the Reynolds-number and the Taylor-number were varied within the range of 3·10²<Re<2·10⁵ and 0Ta<10⁵. The curvature ratio were varied within 0,0496a/r _m 0,337. The possibility of an universal presentation of the friction coefficient for the nonrotating channel is shown for laminar and turbulent through flow. In the rotating channel a considerable pressure loss increase can be observed. The magnitude depends on the direction of rotation. In case of great Taylor-numbers the curvature ratio was found to be independent of the friction resistance.

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Bezeichnungen a Kantenlänge - mittlere Geschwindigkeit - l Kanallänge - r _m Krümmungsradius - Volumenstrom - _p Druckdifferenz - Widerstandsbeiwert - =57/Re Widerstandsbeiwert des geraden Kanals - dynamische Viskosität - Dichte - Winkelgeschwindigkeit - Dean-Zahl - Reynolds-Zahl - Taylor-Zahl Mit 6 Abbildungen     

On grammar forms with terminal context

Summary A context-free grammar form G defines a family of context-free grammars {ie397-01}(G). In this paper {ie397-02}(G) is extended to give the family of terminal context grammars {ie397-03}(G), which were introduced by Book [4]. It is shown that the families of languages defined by {ie397-04}(G) and {ie397-05}(G) are equal when G is an -free context-free grammar form. This generalizes the result of Book [4] for context-free grammars and underlines the usefulness of the notion of grammar forms in formal language theory.The work of the second author was carried out partially under a National Research Council of Canada Grant. No. A-7700 and partially under the auspices of the University of Karlsruhe     

On a direct algorithm for the generation of log-normal pseudo-random numbers

The random variable \(\left( {\prod {_{i = 1}^n {{X_i } \mathord{\left/ {\vphantom {{X_i } {X_{i + n} }}} \right. \kern-0em} {X_{i + n} }}} } \right)^{{1 \mathord{\left/ {\vphantom {1 {\sqrt {2n} }}} \right. \kern-0em} {\sqrt {2n} }}}\) is used to generate standard log-normal variables Λ(0, 1), where theX _i are independent uniform variables on [0, 1].     

Polynomoperatoren in C k [a,b]

Some estimations for the relative projection constantP(∏ _n+k ^k ,Csik[a,b]) are given. By constructing an associated polynomial operatorL _n :C ⁰[a,b]→∏ _n ⁰ to a given polynomial operatorH _n+k :C ^k [a,b]→∏ _n+k ^k we get a lower bound for the projection constant. An upper bound forP(∏ _n+k ^k ,C ^k [a,b]) is obtained by the determination of the norms of appropriate polynomial operatorsP _n+k :C ^k [a,b]→∏ _n+k ^k . Further we give a convergence property for the sequence (P _n+k ) _n∈?.     

Einleitung und Abbruch der künstlichen Ernährung beim einwilligungsunfähigen Patienten

Definition of the problem: In Austria the legal discussion on initiating and withdrawing artificial nutrition in incompetent patients has just begun. Arguments and conclusion: Legal regulations are lacking, but there appears to be agreement on accepting advance directives under specific criteria. This would mean that a presumed will and documented refusal of treatment and nutrition has to be respected by physicians. However, there is no consensus with regard to the “supposed will” of an incompetent patient to refuse treatment and nutrition. At present, surrogate decision making with regard to refusing life-sustaining treatment or nutrition is only accepted according to a declared and documented directive of the patient himself. When the patient’s will has to be “surmised” the protection of life has priority. In Austria this concept is based on the national constitution and its duty to protect life.     

Engineered Sleeping Beauty Transposon as Efficient System to Optimize Chimp Adenoviral Production

Sleeping Beauty (SB) is the first DNA transposon employed for efficient transposition in vertebrate cells, opening new applications for genetic engineering and gene therapies. A transposon-based gene delivery system holds the favourable features of non-viral vectors and an attractive safety profile. Here, we employed SB to engineer HEK293 cells for optimizing the production of a chimpanzee Adenovector (chAd) belonging to the Human Mastadenovirus C species. To date, chAd vectors are employed in several clinical settings for infectious diseases, last but not least COVID-19. A robust, efficient and quick viral vector production could advance the clinical application of chAd vectors. To this aim, we firstly swapped the hAd5 E1 with chAd-C E1 gene by using the CRISPR/Cas9 system. We demonstrated that in the absence of human Ad5 E1, chimp Ad-C E1 gene did not support HEK293 survival. To improve chAd-C vector production, we engineered HEK293 cells to stably express the chAd-C precursor terminal protein (ch.pTP), which plays a crucial role in chimpanzee Adenoviral DNA replication. The results indicate that exogenous ch.pTP expression significantly ameliorate the packaging and amplification of recombinant chAd-C vectors thus, the engineered HEK293ch.pTP cells could represent a superior packaging cell line for the production of these vectors.     

Software specification using graph grammars

The following paper demonstrates that programmed sequential graph grammars can be used in a systematic proceeding to specify the changes of high level intermediate data structures arising in a programming support environment, in which all tools work in an incremental and syntax-driven mode. In this paper we lay stress upon the way to get the specification rather than on the result of this process. Therefore, we give here some approach to “specification engineering” using graph grammars. This approach is influenced by the syntactical definition of the underlying language for Programming in the Small, the module concept etc. to be supported on one side but also by the idea of the user interface.     

Inhibitors of Mitochondrial Human Carbonic Anhydrases VA and VB as a Therapeutic Strategy against Paclitaxel-Induced Neuropathic Pain in Mice

Neuropathy development is a major dose-limiting side effect of anticancer treatments that significantly reduces patient’s quality of life. The inadequate pharmacological approaches for neuropathic pain management warrant the identification of novel therapeutic targets. Mitochondrial dysfunctions that lead to reactive oxygen species (ROS) increase, cytosolic Ca²⁺ imbalance, and lactate acidosis are implicated in neuropathic pain pathogenesis. It has been observed that in these deregulations, a pivotal role is played by the mitochondrial carbonic anhydrases (CA) VA and VB isoforms. Hence, preclinical studies should be conducted to assess the efficacy of two novel selenides bearing benzenesulfonamide moieties, named 5b and 5d, and able to inhibit CA VA and VB against paclitaxel-induced neurotoxicity in mice. Acute treatment with 5b and 5d (30–100 mg/kg, per os – p.o.) determined a dose-dependent and long-lasting anti-hyperalgesic effect in the Cold plate test. Further, repeated daily treatment for 15 days with 100 mg/kg of both compounds (starting the first day of paclitaxel injection) significantly prevented neuropathic pain development without the onset of tolerance to the anti-hyperalgesic effect. In both experiments, acetazolamide (AAZ, 100 mg/kg, p.o.) used as the reference drug was partially active. Moreover, ex vivo analysis demonstrated the efficacy of 5b and 5d repeated treatments in reducing the maladaptive plasticity that occurs to glia cells in the lumbar portion of the spinal cord and in improving mitochondrial functions in the brain and spinal cord that were strongly impaired by paclitaxel-repeated treatment. In this regard, 5b and 5d ameliorated the metabolic activity, as observed by the increase in citrate synthase activity, and preserved an optimal mitochondrial membrane potential (ΔΨ) value, which appeared depolarized in brains from paclitaxel-treated animals. In conclusion, 5b and 5d have therapeutic and protective effects against paclitaxel-induced neuropathy without tolerance development. Moreover, 5b and 5d reduced glial cell activation and mitochondrial dysfunction in the central nervous system, being a promising candidate for the management of neuropathic pain and neurotoxicity evoked by chemotherapeutic drugs.