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Maxime Rivard

Publications and source records attributed to Maxime Rivard.

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Anomaly Detection in Automated Fibre Placement: Learning with Data Limitations

Conventional defect detection systems in Automated Fibre Placement (AFP) typically rely on end-to-end supervised learning, necessitating a substantial number of labelled defective samples for effective training. However, the scarcity of such labelled data poses a challenge. To overcome this limitation, we present a comprehensive framework for defect detection and localization in Automated Fibre Placement. Our approach combines unsupervised deep learning and classical computer vision algorithms, eliminating the need for labelled data or manufacturing defect samples. It efficiently detects various surface issues while requiring fewer images of composite parts for training. Our framework employs an innovative sample extraction method leveraging AFP's inherent symmetry to expand the dataset. By inputting a depth map of the fibre layup surface, we extract local samples aligned with each composite strip (tow). These samples are processed through an autoencoder, trained on normal samples for precise reconstructions, highlighting anomalies through reconstruction errors. Aggregated values form an anomaly map for insightful visualization. The framework employs blob detection on this map to locate manufacturing defects. The experimental findings reveal that despite training the autoencoder with a limited number of images, our proposed method exhibits satisfactory detection accuracy and accurately identifies defect locations. Our framework demonstrates comparable performance to existing methods, while also offering the advantage of detecting all types of anomalies without relying on an extensive labelled dataset of defects.

cs.CV

Imaging the noncentrosymmetric structural organisation of tissue with Interferometric Second Harmonic Generation microscopy

We report the imaging of tendon, a connective tissue rich in collagen type I proteins, with Interferometric Second Harmonic Generation (I-SHG) microscopy. We observed that the noncentrosymmetric structural organization can be maintained along the fibrillar axis over more than 150 μm, while in the transverse direction it is ~1-15 μm. Those results are explained by modeling tendon as a heterogeneous distribution of noncentrosymmetric nanocylinders (collagen fibrils) oriented along the fibrillar axis. The preservation of the noncentrosymmetric structural organization over multiple tens of microns reveals that tendon is made of domains in which the fraction occupied by fibrils oriented in one direction is larger than in the other.

physics.bio-ph