Modelling legacy telecommunications switching systems for interaction analysis

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Hybrid solutions to the feature interaction problem

In this paper we assume a competitive marketplace where the features are developed by different enterprises, which cannot or will not exchange information. We present a classification of feature interaction in this setting and introduce an on-line technique which serves as a basis for the two novel <i>hybrid</i> approaches presented. The approaches are hybrid as they are neither strictly off-line nor on-line, but combine aspects of both. The two approaches address different kinds of feature interactions, and thus are complimentary. Together they provide a complete solution by addressing interaction detection and resolution. We illustrate the techniques within the communication networks domain

Thelma Rag

Bold title with stylized texthttps://scholarsjunction.msstate.edu/cht-sheet-music/14003/thumbnail.jp

Linear chain ferromagnetic charge transfer compounds

Journal ArticleCharge transfer complexes possessing a ... DADA ... structure with both the donor, D, and acceptor, A, being S = 1/2 radicals may exhibit cooperative magnetic phenomena. The complex [Fe(C5Me5)2]+ [TCNQ]-. exhibits metamagnetic behavior. The similarly structured [TCNE]-. and [C4(CN)6]-. complexes are ferromagnets, whereas the [DDQ]-. salt is a paramagnet. The high temperature magnetic susceptibility obeys the Curie-Weiss expression with 0 = + 30, + 30, and + 3 for the [TCNE]-., [C4(CN)6]-., and [TCNQ]-. salts, respectively. The ferromagnetic [TCNE]-. salt exhibits zero field Zeeman split 57Fe Mossbauer spectra with an internal field of 425.6 kOe at 4.23 K. After reviewing the current papers discussing ferromagnetism in molecular (organic) compounds, a qualitative model consistent with the necessary bulk spin alignment required for a ferromagnet is presented

The Caretaker: Bearing Witness in Public Art an Examination of the Role of Contemporary Artists Addressing the Effects of Environmental Injustice within Michigan Communities

This paper examines public art and the role of contemporary artists in context of their relational experience in communities effected by environmental injustice. As a Michigan resident or as an out-of-state guest invited into an urban neighborhood, each of the twelve artists in this study participates within community through a unique cultural lens. Informed by historical and sociopolitical complexities, the public art bears witness for artists that care about the effects of a city’s water crisis, harm resulting from breached oil pipelines, generational loss of Indigenous traditions, and the inability to breathe unconditionally within certain neighborhood Zip Codes. Engaging in public art in the emerging role of ‘caretaker,’ the artist addresses evolving social narratives in such a way that the aesthetic form through its visual dialogue, becomes a catalyst for change. Current discourse on public art and environmental injustice regards a broad range of social contexts whereby the art performs a certain aesthetic or practical function relevant to location, however, the figure of the artist is rarely discussed. This paper focuses on the figure of the artist. In posing the question, How does public art bear witness for the artist in the role of caretaker?, I argue that the artwork reveals the role of caretaker through the artist’s 1) aesthetic practice, 2) gentleness in form, and 3) particular elucidation that personifies ‘caretaker’ as assessed through aspects of Witness, Testimony, Shelter, and Call, whereby the four categories become markers within the art for attributing the artist’s relational experience within community. The public art fosters consideration for the viewer to gain new insight through aesthetic form that bears witness for the artist as caretaker and to reflect on one’s own role in an environmentally just community.https://digitalmaine.com/academic/1045/thumbnail.jp

Influence of external driving on decays in the geometry of the LiCN isomerization

The framework of transition state theory relies on the determination of a geometric structure identifying reactivity. It replaces the laborious exercise of following many trajectories for a long time to provide chemical reaction rates and pathways. In this paper, recent advances in constructing this geometry even in time-dependent systems are applied to the LiCN $\rightleftharpoons$ LiNC isomerization reaction, driven by an external field. We obtain decay rates of the reactant population close to the transition state by exploiting local properties of the dynamics of trajectories in and close to it. We find that the external driving has a large influence on these decay rates when compared to the non-driven isomerization reaction. This, in turn, provides renewed evidence for the possibility of controlling chemical reactions, like this one, through external time-dependent fields.Comment: Main article has 11 pages, 6 figures. Supplemental material has 4 pages, 1 figur

Magnetic Properties of Linear Chain Systems: Metamagnetism of Single Crystal Co(pyridine)\u3csub\u3e2\u3c/sub\u3eCl\u3csub\u3e2\u3c/sub\u3e

The metamagnetic behavior of the low temperature properties of single crystal Co(pyridine)2Cl2 is discussed. At 1.25 K oriented single crystals exhibit a two‐step metamagnetic transition at applied fields ∼0.8 and 1.6 kG along the b‐axis, a single transition at ∼0.7 kG for applied fields along the a∗ axis, and a single transition at ∼4.2 kG for an applied field along the c axis. Just above the transition fields a moment of 2μB/Co atom is measured for B0 parallel to the a∗ axis or b axis, and 0.4μB/Co atom is measured for the B0 parallel to the c axis. A large field dependent moment is observed at high fields. Many features of this compound closely mirror the behavior of CoCl2⋅2H2O. However, the Co(pyridine)2Cl2 has a much smaller interchain exchange, so that many features can be examined at lower fields. The basic features are consistent with a six‐sublattice model for the ordered antiferromagnetic system. Measurements of magnetic moment versus temperature show that Co(pyridine)2Cl2 does not obey a Curie–Weiss law even at relatively high temperatures

Part Variation Modeling to Avoid Scrap Parts in Multi-stage Production Systems

Manufacturing systems for today's products are complex systems requiring a variety of different processes in order to be able to manufacture all necessary part features. This also applies to the production of rotating components, which have experienced increasing demand at the latest due to the growth in mobility. As in almost every manufacturing process, quality-reducing defects can occur due to deviations for example tool wear, which cannot always be avoided. Those, that have accumulated from previous process steps can cause the occurrence of superimposed defects. This leads to complex relationships between quality defects in the end product and the numerous parameters of the manufacturing processes. To remain competitive, production must be optimized in order to identify defects as early as possible, as well as their dependencies and variation patterns. The paper presents an approach to identify and model part variations within multi-stage production systems. Subsequently, based on a detected deviation, a downstream compensation strategy can be proposed at an early stage of the manufacturing process, which uses the capability of the overall system to fundamentally eliminate rejects

Mean first-passage times for solvated LiCN isomerization at intermediate to high temperatures

The following article appeared in The Journal of Chemical Physics 156 (2022): 034103 and may be found at https://aip.scitation.org/doi/full/10.1063/5.0065090The behavior of a particle in a solvent has been framed using stochastic dynamics since the early theory of Kramers. A particle in a chemical reaction reacts slower in a diluted solvent because of the lack of energy transfer via collisions. The flux-over-population reaction rate constant rises with increasing density before falling again for very dense solvents. This Kramers turnover is observed in this paper at intermediate and high temperatures in the backward reaction of the LiNC ⇌ LiCN isomerization via Langevin dynamics and mean first-passage times (MFPTs). It is in good agreement with the Pollak-Grabert-Hänggi (PGH) reaction rates at lower temperatures. Furthermore, we find a square root behavior of the reaction rate at high temperatures and have made direct comparisons of the methods in the intermediate- and high-temperature regimes, all suggesting increased ranges in accuracy of both the PGH and MFPT approache