scholarly journals Model reduction by mean-field homogenization in viscoelastic composites. II. Application to rigidly reinforced solids

Author(s):  
Martín I. Idiart ◽  
Noel Lahellec ◽  
Pierre Suquet

The mean-field homogenization scheme proposed by Lahellec & Suquet (2007 Int. J. Solids Struct. 44 , 507–529 ( doi:10.1016/j.ijsolstr.2006.04.038 )) and revisited in a companion paper (Idiart et al . 2020 Proc. R. Soc. A 20200407 ( doi:10.1098/rspa.2020.0407 )) is applied to random mixtures of a viscoelastic solid phase and a rigid phase. Two classes of mixtures with different microstructural arrangements are considered. In the first class the rigid phase is dispersed within the continuous viscoelastic phase in such a way that the elastic moduli of the mixture are given exactly by the Hashin–Shtrikman formalism. In the second class, both phases are intertwined in such a way that the elastic moduli of the mixture are given exactly by the Self-Consistent formalism. Results are reported for specimens subject to various complex deformation programmes. The scheme is found to improve on earlier approximations of common use and even recover exact results under several circumstances. However, it can also generate highly inaccurate predictions as a result of the loss of convexity of the free-energy density. An auspicious procedure to partially circumvent this issue is advanced.

Author(s):  
Noel Lahellec ◽  
Martín I. Idiart ◽  
Pierre Suquet

The mean-field homogenization scheme for viscoelastic composites proposed by Lahellec & Suquet (2013 Int. J. Plasticity 42, 1–13 ( doi:10.1016/j.ijplas.2012.09.005 )) is revisited from the standpoint recently adopted in a companion paper (Idiart MI et al. 2020 Proc. R. Soc. A 20200407 ( doi:10.1098/rspa.2020.0407 )). It is shown that the scheme generates a reduced-order approximation wherein the microscopic kinetics of the composite are described in terms of a finite set of macroscopic forces identified with the phase averages and intraphase covariances of the various microscopic force fields, which can be evaluated by mean-field homogenization techniques. The approximation exhibits a two-potential structure with a convex complementary energy density but a non-convex force potential. The consequential properties of the approximation are exposed and their implications are discussed. The exposition is supplemented by proofs of equivalence between the present scheme and other candidate schemes proposed in the literature for composites with elementary local rheologies of Maxwellian type.


Author(s):  
S. Hardt ◽  
To Baier

A reduced-order model is developed allowing for a fast computation of the temperature field in multichannel microreactors. The model regards the fluid and the solid phase as interpenetrating continua and incorporates heat exchange between the two phases via a heat-transfer coefficient characteristic for the channel geometry under study. The geometry of the channel walls determines the components of the thermal conductivity tensor which govern conductive heat transfer to the envelope of the reactor. The mean-field model is solved numerically for a test case inspired from practical applications. Parallel to that, a detailed model is set up with the purpose to benchmark the results of the mean-field model. This full model incorporates the geometric details of the multichannel reactor and contains consider-ably more degrees of freedom than the mean-field model, resulting in a much larger computational effort. It is found that the temperature fields computed with the two models agree reasonably well. Thus, the mean-field model appears as an efficient tool to evaluate the thermal performance of multichannel microreactors, especially in the context of parameter studies or system optimization.


Author(s):  
Klaus Morawetz

The classical non-ideal gas shows that the two original concepts of the pressure based of the motion and the forces have eventually developed into drift and dissipation contributions. Collisions of realistic particles are nonlocal and non-instant. A collision delay characterizes the effective duration of collisions, and three displacements, describe its effective non-locality. Consequently, the scattering integral of kinetic equation is nonlocal and non-instant. The non-instant and nonlocal corrections to the scattering integral directly result in the virial corrections to the equation of state. The interaction of particles via long-range potential tails is approximated by a mean field which acts as an external field. The effect of the mean field on free particles is covered by the momentum drift. The effect of the mean field on the colliding pairs causes the momentum and the energy gains which enter the scattering integral and lead to an internal mechanism of energy conversion. The entropy production is shown and the nonequilibrium hydrodynamic equations are derived. Two concepts of quasiparticle, the spectral and the variational one, are explored with the help of the virial of forces.


2000 ◽  
Vol 61 (17) ◽  
pp. 11521-11528 ◽  
Author(s):  
Sergio A. Cannas ◽  
A. C. N. de Magalhães ◽  
Francisco A. Tamarit

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Yiyong Wei ◽  
Donghang Zhang ◽  
Jin Liu ◽  
Mengchan Ou ◽  
Peng Liang ◽  
...  

Abstract Background Metabolic status can be impacted by general anesthesia and surgery. However, the exact effects of general anesthesia and surgery on systemic metabolome remain unclear, which might contribute to postoperative outcomes. Methods Five hundred patients who underwent abdominal surgery were included. General anesthesia was mainly maintained with sevoflurane. The end-tidal sevoflurane concentration (ETsevo) was adjusted to maintain BIS (Bispectral index) value between 40 and 60. The mean ETsevo from 20 min after endotracheal intubation to 2 h after the beginning of surgery was calculated for each patient. The patients were further divided into low ETsevo group (mean − SD) and high ETsevo group (mean + SD) to investigate the possible metabolic changes relevant to the amount of sevoflurane exposure. Results The mean ETsevo of the 500 patients was 1.60% ± 0.34%. Patients with low ETsevo (n = 55) and high ETsevo (n = 59) were selected for metabolomic analysis (1.06% ± 0.13% vs. 2.17% ± 0.16%, P < 0.001). Sevoflurane and abdominal surgery disturbed the tricarboxylic acid cycle as identified by increased citrate and cis-aconitate levels and impacted glycometabolism as identified by increased sucrose and D-glucose levels in these 114 patients. Glutamate metabolism was also impacted by sevoflurane and abdominal surgery in all the patients. In the patients with high ETsevo, levels of L-glutamine, pyroglutamic acid, sphinganine and L-selenocysteine after sevoflurane anesthesia and abdominal surgery were significantly higher than those of the patients with low ETsevo, suggesting that these metabolic changes might be relevant to the amount of sevoflurane exposure. Conclusions Sevoflurane anesthesia and abdominal surgery can impact principal metabolic pathways in clinical patients including tricarboxylic acid cycle, glycometabolism and glutamate metabolism. This study may provide a resource data for future studies about metabolism relevant to general anaesthesia and surgeries. Trial registration www.chictr.org.cn. identifier: ChiCTR1800014327.


2020 ◽  
Vol 79 (Suppl 1) ◽  
pp. 1961.1-1961
Author(s):  
J. Knitza ◽  
J. Mohn ◽  
C. Bergmann ◽  
E. Kampylafka ◽  
M. Hagen ◽  
...  

Background:Symptom checkers (SC) promise to reduce diagnostic delay, misdiagnosis and effectively guide patients through healthcare systems. They are increasingly used, however little evidence exists about their real-life effectiveness.Objectives:The aim of this study was to evaluate the diagnostic accuracy, usage time, usability and perceived usefulness of two promising SC, ADA (www.ada.com) and Rheport (www.rheport.de). Furthermore, symptom duration and previous symptom checking was recorded.Methods:Cross-sectional interim clinical data from the first of three recruiting centers from the prospective, real-world, multicenter bETTeR-study (DKRS DRKS00017642) was used. Patients newly presenting to a secondary rheumatology outpatient clinic between September and December 2019 completed the ADA and Rheport SC. The time and answers were recorded and compared to the patient’s actual diagnosis. ADA provides up to 5 disease suggestions, Rheport calculates a risk score for rheumatic musculoskeletal diseases (RMDs) (≥1=RMD). For both SC the sensitivity, specificity was calculated regarding RMDs. Furthermore, patients completed a survey evaluating the SC usability using the system usability scale (SUS), perceived usefulness, previous symptom checking and symptom duration.Results:Of the 129 consecutive patients approached, 97 agreed to participate. 38% (37/97) of the presenting patients presented with an RMD (Figure 1). Mean symptom duration was 146 weeks and a mean number of 10 physician contacts occurred previously, to evaluate current symptoms. 56% (54/96) had previously checked their symptoms on the internet using search engines, spending a mean of 6 hours. Rheport showed a sensitivity of 49% (18/37) and specificity of 58% (35/60) concerning RMDs. ADA’s top 1 and top 5 disease suggestions concerning RMD showed a sensitivity of 43% (16/37) and 54% (20/37) and a specificity of 58% (35/60) and 52% (31/60), respectively. ADA listed the correct diagnosis of the patients with RMDs first or within the first 5 disease suggestions in 19% (7/37) and 30% (11/37), respectively. The average perceived usefulness for checking symptoms using ADA, internet search engines and Rheport was 3.0, 3.5 and 3.1 on a visual analog scale from 1-5 (5=very useful). 61% (59/96) and 64% (61/96) would recommend using ADA and Rheport, respectively. The mean SUS score of ADA and Rheport was 72/100 and 73/100. The mean usage time for ADA and Rheport was 8 and 9 minutes, respectively.Conclusion:This is the first prospective, real-world, multicenter study evaluating the diagnostic accuracy and other features of two currently used SC in rheumatology. These interim results suggest that diagnostic accuracy is limited, however SC are well accepted among patients and in some cases, correct diagnosis can be provided out of the pocket within few minutes, saving valuable time.Figure:Acknowledgments:This study was supported by an unrestricted research grant from Novartis.Disclosure of Interests:Johannes Knitza Grant/research support from: Research Grant: Novartis, Jacob Mohn: None declared, Christina Bergmann: None declared, Eleni Kampylafka Speakers bureau: Novartis, BMS, Janssen, Melanie Hagen: None declared, Daniela Bohr: None declared, Elizabeth Araujo Speakers bureau: Novartis, Lilly, Abbott, Matthias Englbrecht Grant/research support from: Roche Pharma, Chugai Pharma Europe, Consultant of: AbbVie, Roche Pharma, RheumaDatenRhePort GbR, Speakers bureau: AbbVie, Celgene, Chugai Pharma Europe, Lilly, Mundipharma, Novartis, Pfizer, Roche Pharma, UCB, David Simon Grant/research support from: Else Kröner-Memorial Scholarship, Novartis, Consultant of: Novartis, Lilly, Arnd Kleyer Consultant of: Lilly, Gilead, Novartis,Abbvie, Speakers bureau: Novartis, Lilly, Timo Meinderink: None declared, Wolfgang Vorbrüggen: None declared, Cay-Benedict von der Decken: None declared, Stefan Kleinert Shareholder of: Morphosys, Grant/research support from: Novartis, Consultant of: Novartis, Speakers bureau: Abbvie, Novartis, Celgene, Roche, Chugai, Janssen, Andreas Ramming Grant/research support from: Pfizer, Novartis, Consultant of: Boehringer Ingelheim, Novartis, Gilead, Pfizer, Speakers bureau: Boehringer Ingelheim, Roche, Janssen, Jörg Distler Grant/research support from: Boehringer Ingelheim, Consultant of: Boehringer Ingelheim, Paid instructor for: Boehringer Ingelheim, Speakers bureau: Boehringer Ingelheim, Peter Bartz-Bazzanella: None declared, Georg Schett Speakers bureau: AbbVie, BMS, Celgene, Janssen, Eli Lilly, Novartis, Roche and UCB, Axel Hueber Grant/research support from: Novartis, Lilly, Pfizer, Consultant of: Abbvie, BMS, Celgene, Gilead, GSK, Lilly, Novartis, Speakers bureau: GSK, Lilly, Novartis, Martin Welcker Grant/research support from: Abbvie, Novartis, UCB, Hexal, BMS, Lilly, Roche, Celgene, Sanofi, Consultant of: Abbvie, Actelion, Aescu, Amgen, Celgene, Hexal, Janssen, Medac, Novartis, Pfizer, Sanofi, UCB, Speakers bureau: Abbvie, Aescu, Amgen, Biogen, Berlin Chemie, Celgene, GSK, Hexal, Mylan, Novartis, Pfizer, UCB


2019 ◽  
Vol 46 (3) ◽  
pp. 54-55
Author(s):  
Thirupathaiah Vasantam ◽  
Arpan Mukhopadhyay ◽  
Ravi R. Mazumdar

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