Abstract
Circular economy policies and recycling play a pivotal role in fostering sustainable models for the wood industry capable of reducing the environmental impact of our consumption patterns. The production of Particleboard is a good example of industry that uses high quantities of recycled wood. However, it poses risks since wood often have contaminants that compromise compliance of safety standards. Thus, it is necessary to develop methodologies for rapid analysis of chemical contaminants in wood wastes that allow easy detection of these elements. In this work, the capability of Laser-induced breakdown spectroscopy (LIBS) to detect a set of heavy metals in wood samples was explored. Some advantages of this technique, such as portability, minimal to no sample preparation, and quick analysis are characteristics that make this method one of the most suitable for this purpose of analysis. In the majority of cases, the contamination comes from the pigments used in paints, varnishes, or coatings. Titanium (Ti) e.g. is a common element in white pigments and Chromium (Cr) in red and green pigments. To ensure the presence or absence of Cr and Ti, a set of 3 lines was analysed. The results revealed the presence of these elements and that 30% of the samples seem to be highly contaminated. The LIBS technique proved to be a powerful methodogy for decision-making purposes.

Abstract
The application of surface treatments to cork stoppers is presently a common practice in the wine industry, designed to achieve maximum performance and optimal costumer experience of premium products. Unfortunately, current coating techniques lack efficient process control tools, often resulting in faulty products being detected too late, already in use, compromising performance, product quality and mining consumer confidence. In this work a fully automated system equipped with machine vision and automatic feeding of corks, was coupled with an imaging LIBS setup and used to perform a benchmarking against conventional quality control methods. Results clearly demonstrate the capability of the new LIBS system to effectively evaluate in real time the quality of silicone-based surface coatings in cork stoppers, effectively working as a tool for process control providing a route for effective optimization.

Abstract
Recycling of post-consumer wood waste into wood-based panels may be hindered by the presence of physical and chemical impurities in the waste stream. Therefore greater attention should be given to assessing the quality of wood waste and in particular to heavy metals contamination. One of the elements that poses concern is Chromium (Cr). Cr compounds can be toxic, particularly hexavalent chromium (Cr(VI)), which is a known human carcinogen. Hence, screening for Cr in wood waste plays a pivotal role in enhancing recycling facility operations and mitigating contamination before final product incorporation. In this study, a Laser-Induced Breakdown Spectroscopy (LIBS) methodology was optimized for screening wood waste for Cr and validated by X-ray Fluorescence (XRF) measurements. LIBS spectral complexity and sample matrix effects challenges were addressed through careful selection of Cr lines and tailored data analysis algorithms. The results showed that LIBS imaging successfully provided a straightforward timely output revealing the contaminated wood samples, crucial for quick decision-making in production lines.

Abstract
Spectral imaging is a powerful technology that uses spatially referenced spectral signatures to create informative visual maps of sample surfaces that can reveal more than what conventional RGB-visual images can show. Indeed, different spectroscopy modalities can provide different information about the same sample: for instance, Laser-Induced Breakdown Spectroscopy (LIBS) imaging can detect the presence of specific elements on the surface, while Raman imaging can identify the molecular structures and compositions of the sample, both of which have potential applications in various industrial processes, from quality control to material sorting. In the path from science to technology, the increasing accessibility to such solutions and the strong market pull have opened a window of opportunity for innovative multimodal imaging solutions, where information from distinct sources is set to be combined in order to enhance the capabilities of the single modality system. However, the practical implementation of multimodal spectral imaging is still a challenge, despite its theoretical potential, and as such, it is yet to be achieved. In this work, we will go over multimodal spectral knowledge distillation, a disruptive approach to multimodal spectral imaging techniques that tries to explore the combination of two techniques to capitalize on their individual strengths. In specific, this approach allows us to utilize one technique as an autonomous supervisor for the other, leveraging the higher degree of knowledge and interpretability of one of the techniques to increase the performance and transparency of the other. We present some example scenarios with LIBS and HSI and Raman spectroscopy and LIBS, discussing the impact of this new approach for scientific and technological applications.

Abstract
As lithium-bearing minerals become critical raw materials for the field of energy storage and advanced technologies, the development of tools to accurately identify and differentiate these minerals is becoming essential for efficient resource exploration, mining, and processing. Conventional methods for identifying ore minerals often depend on the subjective observation skills of experts, which can lead to errors, or on expensive and time-consuming techniques such as Inductively Coupled Plasma Mass Spectrometry (ICP-MS) or Optical Emission Spectroscopy (ICPOES). More recently, Raman Spectroscopy (RS) has emerged as a powerful tool for characterizing and identifying minerals due to its ability to provide detailed molecular information. This technique excels in scenarios where minerals have similar elemental content, such as petalite and spodumene, by offering distinct vibrational information that allows for clear differentiation between such minerals. Considering this case study and its particular relevance to the lithium- mining industry, this manuscript reports the development of an unsupervised methodology for lithium-mineral identification based on Raman Imaging. The deployed machine-learning solution provides accurate and interpretable results using the specific bands expected for each mineral. Furthermore, its robustness is tested with additional blind samples, providing insights into the unique spectral signatures and analytical features that enable reliable mineral identification.

Abstract
Sensing at the single cell level can provide insights into its dynamics and heterogeneity, yielding information otherwise unattainable with traditional biological methods where average population behavior is observed. In this context, optical tweezers provide the ability to select, separate, manipulate and identify single cells or other types of microparticles, potentially enabling single cell diagnostics. Forward or backscatter analysis of the light interacting with the trapped cells can provide valuable insights on the cell optical, geometrical and mechanical properties. In particular, the combination of tweezers systems with advanced machine learning algorithms can enable single cell identification capabilities. However, typical processing pipelines require a training stage which often struggles when trying to generalize to new sets of data. In this context, fully automated tweezers system can provide mechanisms to obtain much larger datasets with minimum effort form the users, while eliminating procedural variability. In this work, a pipeline for full automation of optical tweezers systems is discussed. A performance comparison between manually operated and fully automated tweezers systems is presented, clearly showing advantages of the latter. A case study demonstrating the ability of the system to discriminate molecular binding events on microparticles is presented.