Deep drawing of square pieces with variable tribological conditions on the flange

The research results of blank holding force (BHF) influence on the process of plastic forming are presented in this paper. BHF is the normal force and very important factor of friction on the flange. BHF control enables friction control and in that way significant influence on the forming process. Geometry of the work piece is prismatic with square cross section. Material is standard deep drawing thin sheet (0.8 mm thickness). BHF has constant intensity, on one side (based on common recommendations and performed optimization) and, on other side, regime of decreased intensity with constant specific contact pressure. Coefficient of friction is dictated by application of: dry surfaces, oil for deep drawing and polyethylene foil with oil. The following properties are monitored: main surface strains distributions and their relationship to forming limit diagram, thickness strain distribution, change of final deep drawing depth and change of forming forces. If there is final drawing depth (without any defects) as main criteria for successful forming process this research clearly shows significant possibilities of BHF influence on improvement of square pieces deep drawing process results.Publishe

Uticaj sile držanja i stanja površina na duboko izvlačenje „tailored blanks”

During the deep drawing of tailored blanks, tribological conditions make an influence on a forming process in a very complex way. The blank holding force and contact surfaces state of tools and materials are important parameters, which the final parameters of a deep drawing process depend on. In the paper the results of experimental analysis of deep drawing of tailored blanks and basic blanks they were made of, were shown. The influences of the different blank holding forces and different tribologic conditions were investigated, using the main deformations distributions and the deep drawing force change during the process.Publishe

Distributed/virtual manufacturing system cell: an experimental installation

The main objectives of the “Distributed/Virtual Manufacturing System (D/V MS) Cell” project are: (1) The development of Tele-services technologies and organisation for the production planning and control functions; (2) The development of permanent high performance laboratory facilities that enable development and demonstration of D/V MS design and control, i.e., global distribution of production planning and control functions; (3) The development of an abstract environment, i.e., a virtual environment for design and real time control of manufacturing systems, or one of its elements, independent of the physical implementations. The D/V MS Cell satisfies the defined hierarchical distributed control model The Hardware System of the D/V MS Cell is composed by: (1) Machine tool cell: CNC milling machine, external sensors and actuators, interface computer with communications links, (2) Machine cell: Two machine simulators, PLC, sensors and actuators, computer based local controller, (3) Robot cell: Robot SCORBOT ER-VII, artificial vision system, conveyor system, computer based local controller, (4) Control centre: Video projector, computer based remote controller, computer based real time video and audio system. The Software System of the D/V MS Cell is composed by: (1) Applications for Human-Computer Interface (HMI): Interfaces for machine tool and robot programming and control, interface for production planning and control, (2) Computer-Machine Interface, via RS-232C, (3) Computer-Computer Interface, for communications via Internet. The hardware structure of the (D/V MS) Cell is already implemented and interfaces for machine tool programming and control are developed (software system). The operation of the complete system is planned for the year 1999

Episomal Viral cDNAs Identify a Reservoir That Fuels Viral Rebound after Treatment Interruption and That Contributes to Treatment Failure

Viral reservoirs that persist in HIV-1 infected individuals on antiretroviral therapy (ART) are the major obstacle to viral eradication. The identification and definition of viral reservoirs in patients on ART is needed in order to understand viral persistence and achieve the goal of viral eradication. We examined whether analysis of episomal HIV-1 genomes provided the means to characterize virus that persists during ART and whether it could reveal the virus that contributes to treatment failure in patients on ART. For six individuals in which virus replication was highly suppressed for at least 20 months, proviral and episomal genomes present just prior to rebound were phylogenetically compared to RNA genomes of rebounding virus after therapy interruption. Episomal envelope sequences, but not proviral envelope sequences, were highly similar to sequences in rebounding virus. Since episomes are products of recent infections, the phylogenetic relationships support the conclusion that viral rebound originated from a cryptic viral reservoir. To evaluate whether the reservoir revealed by episomal sequence analysis was of clinical relevance, we examined whether episomal sequences define a viral population that contributes to virologic failure in individuals receiving the CCR5 antagonist, Vicriviroc. Episomal envelope sequences at or near baseline predicted treatment failure due to the presence of X4 or D/M (dual/mixed) viral variants. In patients that did not harbor X4 or D/M viruses, the basis for Vicriviroc treatment failure was indeterminate. Although these samples were obtained from viremic patients, the assay would be applicable to a large percentage of aviremic patients, based on previous studies. Summarily, the results support the use of episomal HIV-1 as an additional or alternative approach to traditional assays to characterize virus that is maintained during long-term, suppressive ART

Episomal Viral cDNAs Identify a Reservoir That Fuels Viral Rebound after Treatment Interruption and That Contributes to Treatment Failure

Viral reservoirs that persist in HIV-1 infected individuals on antiretroviral therapy (ART) are the major obstacle to viral eradication. The identification and definition of viral reservoirs in patients on ART is needed in order to understand viral persistence and achieve the goal of viral eradication. We examined whether analysis of episomal HIV-1 genomes provided the means to characterize virus that persists during ART and whether it could reveal the virus that contributes to treatment failure in patients on ART. For six individuals in which virus replication was highly suppressed for at least 20 months, proviral and episomal genomes present just prior to rebound were phylogenetically compared to RNA genomes of rebounding virus after therapy interruption. Episomal envelope sequences, but not proviral envelope sequences, were highly similar to sequences in rebounding virus. Since episomes are products of recent infections, the phylogenetic relationships support the conclusion that viral rebound originated from a cryptic viral reservoir. To evaluate whether the reservoir revealed by episomal sequence analysis was of clinical relevance, we examined whether episomal sequences define a viral population that contributes to virologic failure in individuals receiving the CCR5 antagonist, Vicriviroc. Episomal envelope sequences at or near baseline predicted treatment failure due to the presence of X4 or D/M (dual/mixed) viral variants. In patients that did not harbor X4 or D/M viruses, the basis for Vicriviroc treatment failure was indeterminate. Although these samples were obtained from viremic patients, the assay would be applicable to a large percentage of aviremic patients, based on previous studies. Summarily, the results support the use of episomal HIV-1 as an additional or alternative approach to traditional assays to characterize virus that is maintained during long-term, suppressive ART

Interacting new agegraphic viscous dark energy with varying GG

We consider the new agegraphic model of dark energy with a varying gravitational constant, $G$, in a non-flat universe. We obtain the equation of state and the deceleration parameters for both interacting and noninteracting new agegraphic dark energy. We also present the equation of motion determining the evolution behavior of the dark energy density with a time variable gravitational constant. Finally, we generalize our study to the case of viscous new agegraphic dark energy in the presence of an interaction term between both dark components.Comment: 12 pages, accepted for publication in IJTP (2010

Categorizing Different Approaches to the Cosmological Constant Problem

We have found that proposals addressing the old cosmological constant problem come in various categories. The aim of this paper is to identify as many different, credible mechanisms as possible and to provide them with a code for future reference. We find that they all can be classified into five different schemes of which we indicate the advantages and drawbacks. Besides, we add a new approach based on a symmetry principle mapping real to imaginary spacetime.Comment: updated version, accepted for publicatio

Uncovering the nutritional landscape of food

Recent progresses in data-driven analysis methods, including network-based approaches, are revolutionizing many classical disciplines. These techniques can also be applied to food and nutrition, which must be studied to design healthy diets. Using nutritional information from over 1,000 raw foods, we systematically evaluated the nutrient composition of each food in regards to satisfying daily nutritional requirements. The nutrient balance of a food was quantified herein as nutritional fitness, using the food's frequency of occurrence in nutritionally adequate food combinations. Nutritional fitness offers prioritization of recommendable foods within a global network of foods, in which foods are connected based on the similarities of their nutrient compositions. We identified a number of key nutrients, such as choline and alpha-linolenic acid, whose levels in foods can critically affect the foods' nutritional fitness. Analogously, pairs of nutrients can have the same effect. In fact, two nutrients can impact the nutritional fitness synergistically, although the individual nutrients alone may not. This result, involving the tendency among nutrients to show correlations in their abundances across foods, implies a hidden layer of complexity when exploring for foods whose balance of nutrients within pairs holistically helps meet nutritional requirements. Interestingly, foods with high nutritional fitness successfully maintain this nutrient balance. This effect expands our scope to a diverse repertoire of nutrient-nutrient correlations, integrated under a common network framework that yields unexpected yet coherent associations between nutrients. Our nutrient-profiling approach combined with a network-based analysis provides a more unbiased, global view of the relationships between foods and nutrients, and can be extended towards nutritional policies, food marketing, and personalized nutrition.Comment: Supplementary material is available at the journal websit