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Nanocellulose is gaining evident interest from researchers and engineers because of its renewability, biocompatibility, biodegradability, high mechanical strength, abundant hydroxyl groups for potential functionality, and extensive raw materials. Versatile sources are accordingly explored like harvested wood, annual plants, and agricultural residues. However, an abundant shrub plant, Amorpha f ruticosa Linn., has not yet been reported for isolating nanocellulose. We accordingly propose a green method with low energy consumption to extract nanocellulose from the vast shrub source via combined grinding and successive homogenization treatments. The derived nanocellulose possesses a fine structure with a diameter of ∼10 nm and an aspect ratio over 1000, high thermal stability with a maximum decomposition temperature of 337 °C, and similar composition with a hydroxyl group and a crystal I structure to that of natural cellulose. The demonstrated nanopaper presents visible light transmittance over 90% and haze below 15%, which further confirms the fine structure of the derived nanocellulose. Such a method could potentially broaden the major shrub plant with green, sustainable, up-scaled, and value-added applications in highend domains like electronics, biomedicine, aerospace, energy, environments, etc.

Solid wood materials and wood-plastic composites as two kinds of lightweight materials are attracting great interest from academia and industry due to their green and recycling nature. However, the relatively lower specific strength limits their wider applications. In particular, solid wood is vulnerable to moisture and decay fungi in nature, resulting in its poor durability for effectively long-term utilization. Inspired from the porous structure of wood, we propose a new design to build a wood-based nanocomposite with higher specific strength and satisfactory durability by in situ generation of organic-inorganic hybrid polymer within wood via a sol-gel method. The derived composite has 50-1200% improvement of impact toughness, 56-192% improvement of tensile strength, and 110-291% improvement of flexural strength over those of typical wood-plastic composites, respectively; and even 34% improvement of specific tensile strength than that of 36A steel; 208% enhancement of hardness; and 156% enhancement of compression strength than those of compared solid wood, respectively; as well as significantly improved dimensional stability and decay resistance over those of untreated natural wood. Such materials could be potentially utilized as lightweight and high-strength materials for applications in construction and automotive industries. This method could be extended to constitute other inorganic nanomaterials for novel organic-inorganic hybrid polymer within wood.

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