Approche DFA et conception fonctionnelle de produits modulaires : le modèle FARD

International audienceCet article présente notre démarche de conception fonctionnelle de produits modulaires intégrant, dès les phases amont duprocessus de conception, les contraintes liées au métier de l’assemblage, à travers un modèle méthodologique baptiséFARD (Functional And Robust Design method). Le modèle FARD s’inscrit dans une démarche plus globale de conceptionroutinière et hautement productive de systèmes mécaniques, qui s’appuie sur les connaissances et savoir-faire métierproduit-process, et en particulier sur les contraintes liées au métier de l’assemblage, à travers la génération semi-automatique de séquences d’assemblage admissibles dès les phases amont de la conception. Cette démarche s’inscrit dansun contexte économique fortement concurrentiel, où la personnalisation de masse, la conception par plates-formes autourd’architecture produit-process prédéfinies et la conception fonctionnelle et modulaire à base de connaissances métier,représentent des axes stratégiques pour les entreprises qui veulent rester compétitives. Pour ce faire, nous proposons unnouvel algorithme de génération des séquences d’assemblage prenant en compte la structure modulaire d’un produit,calquée sur la décomposition fonctionnelle du besoin client. Suite à un état de l’art et à une description des différentesétapes de notre démarche, un cas d’application est présenté : le module vanne d’un marteau burineur pneumatique

Toward a methodology of structuring the interactions dynamic within the Multi-Domains and Multi-Views design model (Application to the design of modular product families)

Dans le contexte économique actuel, il faut proposer des produits personnalisés dequalité, à faible coût et dans des délais de plus en plus courts. La société MABI a choisi devoir chacune de ces contraintes comme une opportunité de repenser ses produits en misantsur l innovation. Il faut alors optimiser certaines tâches routinières d ingénierie afin dedégager du temps pour la conception des nouveaux produits. Le travail de recherche réalisés inscrit dans le cadre d une thèse en convention CIFRE en partenariat entre la société MABIet le laboratoire IRTES-M3M de l UTBM. MABI conçoit, assemble, commercialise et assurele service après-vente de produits propres dans le domaine de la protection et la rénovationdes bâtiments. Ses besoins d amélioration concernent le processus de développement deproduits qui doivent répondre aux besoins des clients tout en respectant des contraintesd assemblage spécifiques à l entreprise. La finalité industrielle de la thèse consiste à décliner au niveau du domaine du Produit , la méthodologie générique élaborée sur la base de notre travail de recherchescientifique. A ce niveau, notre problématique scientifique consiste à rendre opérationnel etdynamique le modèle Multi-Domaines et Multi-Vues (MD-MV), structuré de manière plutôtstatique , en y apportant des éléments de raisonnement contribuant à créer des interactionsinter-domaines et inter-points de vue. Pour ce qui est du domaine du Produit , il endécoule la méthodologie FARD (Functional And Robust Design) qui vise à concevoir et àgénérer rapidement l ensemble des variantes de produits d une même famille modulaire touten assurant le respect des besoins clients (conception fonctionnelle) et des contraintesd assemblage à travers une aide à la décision pour le choix de la séquence d assemblage,contribuant ainsi à créer une interaction dynamique avec le domaine du Process . Quatrethèmes de recherche sont abordés : la modularité, la conception fonctionnelle, la conceptionpour l assemblage (dès les phases amont du processus de conception) et la simulation(accélérée grâce au paramétrage du maillage). Habituellement, le domaine de la modularitéest souvent associé à celui de la conception fonctionnelle ou encore à celui de la conceptionpour l assemblage, mais rarement les trois ensemble, ce qui constitue la spécificité de nostravaux. Enfin, l aspect paramétrique de la méthodologie FARD, à travers les liens établisentre les quatre thèmes de recherche évoqués précédemment, rend possible la générationrapide des produits d une même famille à partir d un produit générique et ainsi de gagner dutemps de conception, en vue d atteindre nos objectifs de conception routinière HautementProductive . Trois cas d études industriels et académiques illustrent l application et lafaisabilité la méthodologie FARD...In current economic context, enterprises must provide quality custom products at alower cost and a shorter delay. MABI Company chose to consider these constraints as anopportunity to rethink its products through innovation. Then certain routine tasks must beoptimized to free up time in order to have more time to innovate and design new products.This thesis is part of a CIFRE partnership between the MABI Company and the IRTES-M3Mlaboratory at UTBM. MABI designs, assembles, sells and provides after-sales service ofproducts in the field of the protection and the renovation of buildings. MABI needs ofimprovement are in the development process of its products that must meet customer needs,while respecting its assembly constraints.The industrial purpose of the thesis is to decline in the Product domain, the genericmethodology developed on the basis of our scientific research work. At this level, ourscientific problematic is to make operational and dynamic the Multi-Domains and Multi-Viewsdesign model (MD-MV), structured in a "rather static" way, and to enriched these models byadding reasoning procedures. It follows the FARD methodology (Functional And RobustDesign) which aims to design and quickly generate variants of a modular product family whileensuring compliance with customer requirements (functional design) and assemblyconstraints. Four domains are covered: modularity, functional design, design for assembly (atthe early stages of the design process) and simulation (accelerated through theparameterisation of the mesh). Usually the domain of modularity is often associated withfunctional design or with the design for assembly, but rarely the three together, thatconstitutes one of our added values. Finally, the parametric aspect of the FARDmethodology, that is the link between the four domains, allows accelerated the generation ofproducts of the same family from a generic product and thus saving design time to achieveour goal of "High Productive" routine design. Three industrial and academic case studiesillustrate the application and the feasibility of the FARD methodology...BELFORT-UTBM-SEVENANS (900942101) / SudocSudocFranceF

Functional design method for improving safety and ergonomics of mechanical products

In order to help companies to improve their competetiveness, it is important to develop new design methodologies. In this framework, a Functional And Robust Design (FARD) methodology dedicated to routine design of “highly productive” modular product ranges is proposed including principles of functional analysis, Design For Assembly (DFA), and techniques of modelling and simulation for ergonomics consideration. This paper focuses on the application of this original method applied to mechanical vibration and ergonomics problems of a scraper. Including biomechanical aspect in the design methodology, it is possible to identify the impact of a vibration tool on its users using numerical models of the tool coupled to a finite element model of the human hand. This method can proactively warn very early, in the design process, the risks of causing musculoskeletal disorders and facilitate an optimization of the mechanical tool. This study is a first step in a context of human-centered design

Understand the Potential Role of Aureobasidium pullulans, a Resident Microorganism From Grapevine, to Prevent the Infection Caused by Diplodia seriata

Grapevine trunk diseases (GTDs) are one of the major concern amongst grapevine diseases, responsible for the decline of vineyards and for several economical losses. Since grapevine is naturally colonized by resident microorganisms such as Aureobasidium pullulans, the present challenge is to understand their biocontrol potential and how such microorganisms can be successfully integrated in the control of GTDs. In this context, the first priority consists to exploit the plant-beneficial-phytopathogen interactions in plant model systems, to identify the most prevalent equilibrium limiting expression of GTDs. In the current study, we deep characterized the interaction of a resident and abundant microorganism from grapevine – Aureobasidium pullulans strain Fito_F278 – against D. seriata F98.1, a Botryosphaeria dieback agent, and with plant (cv Chardonnay). Results revealed that A. pullulans strain Fito_F278 was able to reduce significantly the mycelium growth of D. seriata F98.1 at 33.41 ± 0.55%, under in vitro conditions, though this reduction is possibly dependent on a direct interaction between strain Fito_F278 and pathogen. Furthermore, strain Fito_F278 was able to promote an induction of some plant defense responses in cutting plants, 1 week after the D. seriata F98.1 infection. Results evidenced that strain Fito_F278 colonized efficiently grapevine at both epiphyte and endophyte level, could persist on plant roots for long-periods (up to 2 months after its inoculation) and grow at different pH and high salinity conditions. Moreover, a significant decrease of the microbial load from soil and rhizosphere was observed in plants treated with the strain Fito_F278, suggesting its competitivity potential in a microbial ecosystem. Altogether, the present study gives the first insights about the interaction of A. pullulans strain Fito_F278, a resident microorganism, with grapevine, its potential role against a Botryosphaeria dieback agent, and highlights its importance to toward more resilient grapevine

Physical losses could partially explain modest carotenoid retention in dried food products from biofortified cassava

Gari, a fermented and dried semolina made from cassava, is one of the most common foods in West Africa. Recently introduced biofortified yellow cassava containing provitamin A carotenoids could help tackle vitamin A deficiency prevalent in those areas. However there are concerns because of the low retention of carotenoids during gari processing compared to other processes (e.g. boiling). The aim of the study was to assess the levels of true retention in trans–β-carotene during gari processing and investigate the causes of low retention. Influence of processing step, processor (3 commercial processors) and variety (TMS 01/ 1371; 01/1368 and 01/1412) were assessed. It was shown that low true retention (46% on average) during gari processing may be explained by not only chemical losses (i.e. due to roasting temperature) but also by physical losses (i.e. due to leaching of carotenoids in discarded liquids): true retention in the liquid lost from grating negatively correlated with true retention retained in the mash (R = -0.914). Moreover, true retention followed the same pattern as lost water at the different processing steps (i.e. for the commercial processors). Variety had a significant influence on true retention, carotenoid content, and trans-cis isomerisation but the processor type had little effect. It is the first time that the importance of physical carotenoid losses was demonstrated during processing of biofortified crops

Um ano de escola n'A Minha Praia – sensibilização para a problemática do lixo marinho utilizando a ciência-cidadã como ferramenta

Um ano de escola n’A Minha Praia – sensibilização para a problemática do lixo marinho utilizando a ciência-cidadã como ferramenta O Algarve reúne um conjunto de características que o tornam particularmente vulnerável à presença de lixo marinho e aos seus efeitos nefastos: uma orla costeira longa (aprox. 200km), um destino turístico muito popular, uma população residente concentrada no litoral e uma fração significativa da sociedade cuja subsistência depende de atividades económicas ligadas ao mar (pesca, marisqueio, extração de sal, passeios turísticos, etc.). Foi tendo em conta a magnitude e as consequências da propagação do lixo marinho na região que o Centro Ciência Viva de Tavira coordenou o projeto A Minha Praia, um dos vencedores da primeira edição do Orçamento Participativo Portugal (OPP) em 2017, e cuja execução foi garantida pela colaboração entre os três Centros Ciência Viva (CCVs) no Algarve, com o envolvimento de várias entidades regionais e nacionais. Este projeto permitiu que cerca de 933 alunos provenientes de 17 escolas fossem sensibilizados para a conservação do meio marinho, para hábitos de consumo sustentáveis e para o civismo ambiental, em simultâneo com ações de ciência-cidadã, nas quais periodicamente monitorizavam a presença de lixo marinho em seis praias da costa sul do Algarve. Ainda dentro da função didática do projeto, demonstramos a valorização do plástico (que é o maior componente do lixo marinho), aproveitando-o, reciclando-o e transformando-o em novos objetos que prolongam a sua utilidade.Esta apresentação foi dinamizada no âmbito do projecto OPP-A Minha (OPP220/437), financiado pela Ciência Viva - Agência Nacional para a Cultura Científica e Tecnológica e pela FCT - Fundação para a Ciência e Tecnologia.info:eu-repo/semantics/publishedVersio

Preferential Entry of Botulinum Neurotoxin A Hc Domain through Intestinal Crypt Cells and Targeting to Cholinergic Neurons of the Mouse Intestine

Botulism, characterized by flaccid paralysis, commonly results from botulinum neurotoxin (BoNT) absorption across the epithelial barrier from the digestive tract and then dissemination through the blood circulation to target autonomic and motor nerve terminals. The trafficking pathway of BoNT/A passage through the intestinal barrier is not yet fully understood. We report that intralumenal administration of purified BoNT/A into mouse ileum segment impaired spontaneous muscle contractions and abolished the smooth muscle contractions evoked by electric field stimulation. Entry of BoNT/A into the mouse upper small intestine was monitored with fluorescent HcA (half C-terminal domain of heavy chain) which interacts with cell surface receptor(s). We show that HcA preferentially recognizes a subset of neuroendocrine intestinal crypt cells, which probably represent the entry site of the toxin through the intestinal barrier, then targets specific neurons in the submucosa and later (90–120 min) in the musculosa. HcA mainly binds to certain cholinergic neurons of both submucosal and myenteric plexuses, but also recognizes, although to a lower extent, other neuronal cells including glutamatergic and serotoninergic neurons in the submucosa. Intestinal cholinergic neuron targeting by HcA could account for the inhibition of intestinal peristaltism and secretion observed in botulism, but the consequences of the targeting to non-cholinergic neurons remains to be determined

The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

Abstract: Breast cancer is a common disease partially caused by genetic risk factors. Germline pathogenic variants in DNA repair genes BRCA1, BRCA2, PALB2, ATM, and CHEK2 are associated with breast cancer risk. FANCM, which encodes for a DNA translocase, has been proposed as a breast cancer predisposition gene, with greater effects for the ER-negative and triple-negative breast cancer (TNBC) subtypes. We tested the three recurrent protein-truncating variants FANCM:p.Arg658*, p.Gln1701*, and p.Arg1931* for association with breast cancer risk in 67,112 cases, 53,766 controls, and 26,662 carriers of pathogenic variants of BRCA1 or BRCA2. These three variants were also studied functionally by measuring survival and chromosome fragility in FANCM−/− patient-derived immortalized fibroblasts treated with diepoxybutane or olaparib. We observed that FANCM:p.Arg658* was associated with increased risk of ER-negative disease and TNBC (OR = 2.44, P = 0.034 and OR = 3.79; P = 0.009, respectively). In a country-restricted analysis, we confirmed the associations detected for FANCM:p.Arg658* and found that also FANCM:p.Arg1931* was associated with ER-negative breast cancer risk (OR = 1.96; P = 0.006). The functional results indicated that all three variants were deleterious affecting cell survival and chromosome stability with FANCM:p.Arg658* causing more severe phenotypes. In conclusion, we confirmed that the two rare FANCM deleterious variants p.Arg658* and p.Arg1931* are risk factors for ER-negative and TNBC subtypes. Overall our data suggest that the effect of truncating variants on breast cancer risk may depend on their position in the gene. Cell sensitivity to olaparib exposure, identifies a possible therapeutic option to treat FANCM-associated tumors