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Wyświetlanie 1-3 z 3
Tytuł:
Measurement and Comparison of Reliability Performance of Photovoltaic Power Optimizers for Energy Production
Autorzy:
Catelani, M.
Ciani, L.
Graditi, G.
Adinolfi, G.
Powiązania:
https://bibliotekanauki.pl/articles/220657.pdf
Data publikacji:
2015
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
photovoltaic
DMPPT converter
reliability
MIL-HDBK-217F
Siemens SN29500
Opis:
Photovoltaic (PV) power optimizers are introduced in PV systems to improve their energetic productivity in presence of mismatching phenomena and not uniform operating conditions. Commercially available converters are characterized by different DC-DC topologies. A promising one is the boost topology with its different versions. It is characterized by its circuital simplicity, few devices and high efficiency values - necessary features for a Distributed Maximum Power Point Tracking (DMPPT) converter. PV power optimizer designs represent a challenging task since they operate in continuously changing operating conditions which strongly influence electronic component properties and thus the performance of complete converters. An aspect to carefully analyze in such applications is the thermal factor. In this paper, a necessity to have a suitable temperature monitoring system to avoid dangerous conditions is underlined In addition, another important requirement for a PV power optimizer is its reliability, since it can suggest a useful information on its diagnostic aspects, maintenance and investments. In fact, a reliable device requires less maintenance services, also improving the economic aspect. The evaluation of the electronic system reliability can be carried out using different reliability prediction models. In this paper, reliability indices, such as the Mean Time Between Failure (MTBF) or the Failure Rate of a Diode Rectification (DR) boost, are calculated using the evaluation of the Military Handbook 217F and Siemens SN29500 prediction models. With the reliability prediction results it has been possible to identify the most critical components of a DMPPT converter and a measurement setup has been developed in order to monitor the component stress level on the temperature, power, voltage, current, and energy in the DMPPT design phase avoiding the occurrence of a failure that might decrease the service life of the equipment.
Źródło:
Metrology and Measurement Systems; 2015, 22, 1; 139-152
0860-8229
Pojawia się w:
Metrology and Measurement Systems
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Novel isoforms of transcript of the EDA gene confirm X-linked inheritance of anhidrotic ectodermal dysplasia
Autorzy:
Kobielak, K
Kobielak, A.
Trzeciak, W.H.
Powiązania:
https://bibliotekanauki.pl/articles/2043606.pdf
Data publikacji:
1999
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
dysplasia
inheritance
anhidrotic ectodermal dysplasia
Christ-Siemens-Touraine syndrome
Tabby gene
EDA gene
gene transcript
Źródło:
Journal of Applied Genetics; 1999, 40, 4; 355-364
1234-1983
Pojawia się w:
Journal of Applied Genetics
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Is the recently discovered EDA gene associated with anhidrotic ectodermal dysplasia?
Autorzy:
Kobielak, K
Kobielak, A
Trzeciak, W H
Powiązania:
https://bibliotekanauki.pl/articles/2046683.pdf
Data publikacji:
1997
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
ectodermal-mesodermal interaction
X chromosome
submicroscopic deletion
hyperthermia
Christ-Siemens-Touraine syndrome
hybridization
ectodermal dysplasia
mutation
somatic cell
linkage analysis
embryonic life
transmembrane receptor
Opis:
The evidence from literature strongly suggests that Christ-Siemens-Touraine (CST) syndrome is associated with mutations of the newly discovered EDA gene. The gene is situated on the long arm of the X chromosome (Xq12.2-q13.1) and contains two exons separated by a 200 kbp intron. The 5’-untranslated region and most of the coding sequence are localized in exon 1, while three C-terminal amino acids are encoded by exon 2. The coding sequence was interrupted by translocations in three affected females: t(X;l), t(X;12), t(X;9), and submicroscopic deletions of the EDA gene were found in five males with CST syndrome, and point mutations were discovered in exon 1 in nine other patients. Northern blot analysis and in situ hybridization studies revealed that the EDA gene was expressed in the foetus, and postnatally in a specific type of skin cell and that the expression was limited to cells of ectodermal origin. A predicted protein product of the EDA gene contains 135 to 140 amino acids, organized in three distinct domains and may belong to class II transmembrane receptors.
Źródło:
Journal of Applied Genetics; 1997, 38, 3; 343-357
1234-1983
Pojawia się w:
Journal of Applied Genetics
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-3 z 3

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