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A rapidly emerging research community at the intersection of sport and human-computer interaction (SportsHCI) explores how technology can support physically active humans, such as athletes. At highly competitive levels, coaching staff play a central role in the athlete experience by using data to enhance performance, reduce injuries, and foster team success. However, little is known about the practices and needs of these coaching staff. We conducted five focus groups with 17 collegiate coaching staff across three women’s teams and two men’s teams at an elite U.S. university. Our findings show that coaching staff selectively use data with the goal of balancing performance goals, athlete emotional well-being, and privacy. This paper contributes design recommendations to support coaching staff in operating across the data life cycle through gathering, sharing, deciding, acting, and assessing data as they aim to support team success and foster the well-being of student-athletes. 

Poly(ether ether ketone) (PEEK) was found to form gels in the benign solvent 1,3-diphenylacetone (DPA). Gelation of PEEK in DPA was found to form an interconnected, strut-like morphology composed of polymer axialites. To our knowledge, this is the first report of a strut-like morphology for PEEK aerogels. PEEK/DPA gels were prepared by first dissolving PEEK in DPA at 320 °C. Upon cooling to 50 °C, PEEK crystallizes and forms a gel in DPA. The PEEK/DPA phase diagram indicated that phase separation occurs by solid–liquid phase separation, implying that DPA is a good solvent for PEEK. The Flory–Huggins interaction parameter, calculated as χ12 = 0.093 for the PEEK/DPA system, confirmed that DPA is a good solvent for PEEK. PEEK aerogels were prepared by solvent exchanging DPA to water then freeze-drying. PEEK aerogels were found to have densities between 0.09 and 0.25 g/cm3, porosities between 80 and 93%, and surface areas between 200 and 225 m2/g, depending on the initial gel concentration. Using nitrogen adsorption analyses, PEEK aerogels were found to be mesoporous adsorbents, with mesopore sizes of about 8 nm, which formed between stacks of platelike crystalline lamellae. Scanning electron microscopy and X-ray scattering were utilized to elucidate the hierarchical structure of the PEEK aerogels. Morphological analysis found that the PEEK/DPA gels were composed of a highly nucleated network of PEEK axialites (i.e., aggregates of stacked crystalline lamellae). The highly connected axialite network imparted robust mechanical properties on PEEK aerogels, which were found to densify less upon freeze-drying than globular PEEK aerogel counterparts gelled from dichloroacetic acid (DCA) or 4-chlorphenol (4CP). PEEK aerogels formed from DPA were also found to have a modulus–density scaling that was far more efficient in supporting loads than the poorly connected aerogels formed from PEEK/DCA or PEEK/4CP solutions. The strut-like morphology in these new PEEK aerogels also significantly improved the modulus to a degree that is comparable to high-performance crosslinked aerogels based on polyimide and polyurea of comparable densities. 

Blocky bromination of PEKK yields superior crystallizability, high %X_c,T_g,T_m,T_c, and faster crystallization kinetics compared to random analogs. 

Alternative polymer feedstocks are highly desirable to address environmental, social, and security concerns associated with petrochemical-based materials. Lignocellulosic biomass (LCB) has emerged as one critical feedstock in this regard because it is an abundant and ubiquitous renewable resource. LCB can be deconstructed to generate valuable fuels, chemicals, and small molecules/oligomers that are amenable to modification and polymerization. However, the diversity of LCB complicates the evaluation of biorefinery concepts in areas including process scale-up, production outputs, plant economics, and life-cycle management. We discuss aspects of current LCB biorefinery research with a focus on the major process stages, including feedstock selection, fractionation/deconstruction, and characterization, along with product purification, functionalization, and polymerization to manufacture valuable macromolecular materials. We highlight opportunities to valorize underutilized and complex feedstocks, leverage advanced characterization techniques to predict and manage biorefinery outputs, and increase the fraction of biomass converted into valuable products. 

Fossil fuels are a cheap and abundant feedstock for polymeric materials that have enabled innumerable quality-of-life improvements. Yet, their declining supply and non-renewable nature have driven the pursuit of bio-based alternatives. Lignin represents the largest natural source of aromatic carbon on the planet, and thus, lignin-derived products have emerged as critical elements in the next generation of polymers. The relative abundance, large concentration of functional handles, and thermal stability of lignin make it an attractive target for bio-based polymers. However, the valorization of lignin to high-performance and cost-competitive materials remains a challenge. In this review, developments in the translation of lignin into value-added macromolecular components are discussed. Strategies to incorporate bulk lignin in polymer blends and composites are introduced with a focus on applications. Furthermore, recent advances in the preparation of higher-value thermoplastics, thermosets, and vitrimers from deconstructed lignin products are highlighted from a synthetic perspective. Finally, key hurdles and future opportunities in lignin valorization are explored.