Ultrasonic wood welding is an ecofriendly method for rapidly joining wooden components in less than 2 s. However, this dynamic process results in low mechanical performance and poor durability under wet conditions. Inspired by natural wood's robust interlocking cellular structure, which leverages lignin fusion to enhance structural integrity, lignin fusion at wood interfaces is optimized, significantly improving lap shear strength and wet durability. These results demonstrate that enhanced lignin fusion at interfaces is crucial for obtaining strong wood joints by positioning lignin as a sustainable energy concentrator, promoting greener manufacturing of sustainable structures into complex shapes. The joints exhibit lap shear strengths and wet durability comparable to those achieved with water-based wood and epoxy adhesives, while also demonstrating conductivity which could be leveraged for multifunctional features such as strain sensing. The approach can be extended to other manufacturing methods, such as hot-pressing and continuous robotic manufacturing, emphasizing its potential for scalability and broad industrial adoption.

Since the inception of fibre-reinforced composite materials, they have been widely acknowledged for their unparalleled weight-to-performance ratio. Nonetheless, concerns are escalating regarding the environmental impact of these materials amidst global warming and pollution. This perspective explores a ground-breaking shift towards harnessing living organisms to produce composite materials. Living composites not only offer sustainable, carbon-capturing alternatives but also afford an unprecedented level of control over shape and anisotropy. Recent advancements in biology, particularly genetic engineering and sequencing, have provided extraordinary control over living organisms. Coupled with ever-evolving additive manufacturing techniques, these breakthroughs enable the construction of engineered living materials from the ground up. Here, we explore the key factors propelling the emergence of engineered living materials for structural applications and delves into the capabilities of living organisms that can be harnessed for creating functional materials, including harvesting energy, forming structures, sensing/adapting, growing and remodelling. Incorporating living organisms can revolutionise manufacturing for renewable and sustainable composite materials, unlocking previously unattainable functionalities.

Ultrasonic welding is a fast and promising joining technique for thermoplastic composite parts. Understanding how changing the part thickness affects the process is crucial to its future upscaling and industrialization. This article presents an initial insight into the effect of the adherend’s thickness on the near-field ultrasonic welding of CF/LMPAEK thermoplastic composites. Different thicknesses of the top and bottom adherend were welded and analyzed using the output data of the welding equipment, temperature measurements, and other visual characterization techniques. Increasing the thickness of both the top and the bottom adherends showed to increase the power consumed during welding. An overshoot in the power needed at the onset of the welding process for increased thickness of the top adherend precluded welding beyond a threshold thickness of 4.72 mm. In the case of the thicker top adherends, there was also melting of the energy director and early fiber squeeze-out within the top adherend as a result of increased bulk heating. Increased bulk heating was hypothesized to be caused by increased hammering, as indicated by the amplitude readings for thicker adherends. Welding with a higher force, which is known to reduce hammering, corroborated this hypothesis as fiber squeeze-out within the top adherend was not observed. It is believed that hammering contributes to heating by causing an oscillatory impact excitation that is close to the natural frequencies of the system, which would result in amplification of the cyclic strain and subsequent increase in the viscoelastic heating in the adherend.