Cellulose Nanomaterials as a Future, Sustainable and Renewable Material

Cellulose nanomaterials (CNs) are renewable, bio-derived materials that can address not only technological challenges but also social impacts. This ability results from their unique properties, for example, high mechanical strength, high degree of crystallinity, biodegradable, tunable shape, size, and functional surface chemistry. This minireview provides chemical and physical features of cellulose nanomaterials and recent developments as an adsorbent and an antimicrobial material generated from bio-renewable sources.

A room-temperature self-healing elastomer with ultra-high strength and toughness fabricated via optimized hierarchical hydrogen-bonding interactions

The preparation of room-temperature self-healing polymeric materials with good healing efficiency and high mechanical strength is challenging. Two processes are essential to realise the room-temperature self-healing of materials: (a) a...

Super-Assembly of Freestanding Graphene Oxide-Aramid Fiber Membrane with T-Mode Subnanochannels for Sensitive Ion Transport

Biomimetic nacre-like membranes composed of two-dimensional lamellar sheets and one-dimensional nanofibers exhibit high mechanical strength and excellent stability. Thus, they show substantial application in the field of membrane science and...

Development of Pectin-Based Aerogels with Several Excellent Properties for the Adsorption of Pb2+

Traditional aerogels lack specific functional groups for the adsorption of Pb2+, which results in a low adsorption capacity and limits the application scope. Novel porous pectin-based aerogels (PPEAs) were prepared by incorporating polyethylenimine (PEI) using ethylene glycol diglycidyl ether (EGDE) as a cross-linker for the removal of Pb2+ from water. The cross-linking mechanism, morphology, mechanical strength, thermal stability, adsorption properties, and mechanism of the aerogels were investigated. The aerogels possessed several desirable features, such as a large maximum Pb2+ adsorption capacity (373.7 mg/g, tested at pH 5.0), ultralight (as low as 63.4 mg/cm3), high mechanical strength (stress above 0.24 MPa at 50% strain), and easy recyclability. Meanwhile, the equilibrium adsorption data was well described by the Langmuir–Freundlich (Sips) model and the kinetic adsorption process was well fitted using the pseudo-second-order model. The donor groups, such as -NH2, and oxygen-containing functional groups were responsible for the Pb2+ adsorption, which was confirmed by the FTIR and XPS analysis. The excellent characteristics mean that PPEAs are highly effective adsorbents in the remediation of lead-containing wastewater.

Microstructural and Optical Properties of MgAl2O4 Spinel: Effects of Mechanical Activation, Y2O3 and Graphene Additions

Magnesium aluminate and other alumina-based spinels attract attention due to their high hardness, high mechanical strength, and low dielectric constant. MgAl2O4 was produced by a solid-state reaction between MgO and α-Al2O3 powders. Mechanical activation for 30 min in a planetary ball mill was used to increase the reactivity of powders. Yttrium oxide and graphene were added to prevent abnormal grain growth during sintering. Samples were sintered by hot pressing under vacuum at 1450 °C. Phase composition and microstructure of sintered specimens were characterized by X-ray powder diffraction and scanning electron microscopy. Rietveld analysis revealed 100% pure spinel phase in all sintered specimens, and a decrease in crystallite size with the addition of yttria or graphene. Density measurements indicated that the mechanically activated specimen reached 99.6% relative density. Furthermore, the highest solar absorbance and highest spectral selectivity as a function of temperature were detected for the mechanically activated specimen with graphene addition. Mechanical activation is an efficient method to improve densification of MgAl2O4 prepared from mixed oxide powders, while additives improve microstructure and optical properties.

A Fast-Response Electroactive Actuator Based on TEMPO-Oxidized Cellulose Nanofibers

Cellulose-based electroactive actuators are promising candidates for biomimetic robots and biomedical applications due to their lightweight, high mechanical strength, and natural abundance. However, cellulose-based electroactive actuators exhibit lower actuation performance than traditional conductive polymer actuators. This work reports a fast-response cellulose-based electroactive actuator based on 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) oxidized nanocellulose (TOCNF) film with layered structure fabricated by evaporation, and gold electrodes prepared by ion sputtering. The residual ions during the TEMPO oxidation process and the layered structure due to self-assembly accelerate the ion migration efficiency in actuators. The proposed actuator can reach a tip displacement of 32.1 mm at a voltage of 10 V and deflect 60° in 5 s. After applying a reverse 10 V voltage, the actuator can also be quickly deflected (42.5 mm). In addition, the actuator also shows high electrical actuation performance at low voltage (5 V). The excellent electroactive performance of as-prepared TOCNF/Au enables the feasibility to be applied to actuators.