Biopolymer aerogels were among the first aerogels produced, but only in the last decade has research on biopolymer and biopolymer-composite aerogels become popular, motivated by sustainability arguments, their unique and tunable properties, and ease of functionalization. Biopolymer aerogels and open-cell foams have great potential for classical aerogel applications such as thermal insulation, as well as emerging applications in filtration, oil-water separation, CO2 capture, catalysis, and medicine. The biopolymer aerogel field today is driven forward by empirical materials discovery at the laboratory scale, but requires a firmer theoretical basis and pilot studies to close the gap to market. This Review includes a database with over 3800 biopolymer aerogel properties, evaluates the state of the biopolymer aerogel field, and critically discusses the scientific, technological, and commercial barriers to the commercialization of these exciting materials.

Biopolymer Aerogels and Foams: Chemistry, Properties, and Applications.

Lightweight, robust, and thin aerogel films with multifunctionality are highly desirable to meet the technological demands of current society. However, fabrication and application of these multifunctional aerogel films are still significantly underdeveloped. Herein, we demonstrate a multifunctional aerogel film composed of strong aramid nanofibers (ANFs), conductive carbon nanotubes (CNTs), and hydrophobic fluorocarbon (FC) resin. The obtained hybrid aerogel film exhibits large specific surface area (232.8 m2·g-1), high electrical conductivity (230 S·m-1), and excellent hydrophobicity (contact angle of up to 137.0°) with exceptional Joule heating performance and supreme electromagnetic interference (EMI) shielding efficiency. The FC coating renders the hydrophilic ANF/CNT aerogel films hydrophobic, resulting in an excellent self-cleaning performance. The high electrical conductivity enables a low-voltage-driven Joule heating property and an EMI shielding effectiveness (SE) of 54.4 dB in the X-band at a thickness of 568 μm. The specific EMI SE is up to 33528.3 dB·cm2·g-1, which is among the highest values of typical metal-, conducting-polymer-, or carbon-based composites. This multifunctional aerogel film holds great promise for smart garments, electromagnetic wave shielding, and personal thermal management systems.

Multifunctional Aramid Nanofiber/Carbon Nanotube Hybrid Aerogel Films.

Aerogels are a special class of nanostructured materials with very high porosity and tunable physicochemical properties. Although a few types of aerogels have already reached the market in construction materials, textiles and aerospace engineering, the full potential of aerogels is still to be assessed for other technology sectors. Based on current efforts to address the material supply chain by a circular economy approach and longevity as well as quality of life with biotechnological methods, environmental and life science applications are two emerging market opportunities where the use of aerogels needs to be further explored and evaluated in a multidisciplinary approach. In this opinion paper, the relevance of the topic is put into context and the corresponding current research efforts on aerogel technology are outlined. Furthermore, key challenges to be solved in order to create materials by design, reproducible process technology and society-centered solutions specifically for the two abovementioned technology sectors are analyzed. Overall, advances in aerogel technology can yield innovative and integrated solutions for environmental and life sciences which in turn can help improve both the welfare of population and to move towards cleaner and smarter supply chain solutions.

/pdf/an-opinion-paper-on-aerogels-for-biomedical-and-2e6aczc9x6.pdf

An Opinion Paper on Aerogels for Biomedical and Environmental Applications.

Generally produced by solvent sublimation via freeze-drying or critical point drying treatment, nanocellulose-based aerogels have attracted considerable interest in offering the features such as sustainability, available surface reactivity, lightweight, high porosity, and specific surface area. This study presents a novel strategy for the preparation of fluorescent aerogels based on covalent linkage between the natural skeleton of a cellulose nanofibril (CNF) and a fluorescent carbon dot (CD). The maximum CD grafting content on the CNF-based aerogel was 113 mg g-1, providing bright blue fluorescence under ultraviolet radiation with a high fluorescence quantum yield of 26.2%. Besides improved mechanical properties with a 360% increase in compression strength, the covalently bonded CD nanoparticle further serves as a structural stabilizer to endow the characteristic of shape recovery in water for the fabricated fluorescent aerogel. Finally, this aerogel displays high sensitivity and selection on the recognition of NO x and aldehyde species, which is studied for the detection of glutaraldehyde at ultralow concentrations (ppm) in water. Using the innovation of an organic solvent-free route and avoiding the toxic crosslinking reagents or fluorescent sources, the CNF/CD-based fluorescent aerogel developed in this study is a promising functional material for potential optical sensing application.

Fluorescent Aerogels Based on Chemical Crosslinking between Nanocellulose and Carbon Dots for Optical Sensor

Four-dimensional printing of shape memory polyurethanes with high strength and recyclability based on Diels-Alder chemistry

Shape memory polymers (SMPs) remember and return to an original shape when triggered by a suitable stimulus, typically a change in temperature. They are pursued as cost-effective, low-density, higher-strain-tolerant alternatives to shape memory alloys. Arguably, porous SMPs may offer the near-ultimate refinement in terms of density reduction. To that end, shape memory polymeric aerogels (SMPAs) may offer a viable approach. The necessary condition for SMPs is rubber-like superelasticity, which is introduced via cross-linking. Cross-linking is also a necessary condition for inducing phase separation during solution-phase polymerization of suitable monomers into 3D nanoparticle networks. Such networks form the skeletal frameworks of polymeric aerogels. Those principles were explored here with rigid trifunctional isocyanurate cross-linking nodes between flexible urethane tethers from four short oligomeric derivatives of ethylene glycol: H(OCH2CH2)nOH (1 ≤ n ≤ 4). Formation of self-supporting 3D particle netwo...

Shape Memory Superelastic Poly(isocyanurate-urethane) Aerogels (PIR-PUR) for Deployable Panels and Biomimetic Applications

Thermodynamic-kinetic relationships are not uncommon, but rigorous correlations are rare. On the basis of the parabolic free-energy profiles of elastic deformation, a generalized Marcus-type thermodynamic-kinetic relationship was identified between the shape recovery rate, Rt( N), and the elastic modulus, E, in poly(isocyanurate-urethane) shape memory aerogels. The latter were prepared with mixtures of diethylene, triethylene, and tetraethylene glycol and an aliphatic triisocyanate. Synthetic conditions were selected using a statistical design of experiments method. Microstructures obtained in each formulation could be put into two groups, one consisting of micron-size particles connected with large necks and a second one classified as bicontinuous. The two types of microstructures could be explained consistently by spinodal decomposition involving early versus late phase separation relative to the gel point. Irrespective of microstructure, all samples showed a shape memory effect with shape fixity and shape recovery ratios close to 100%. Larger variations (0.35-0.71) in the overall figure of merit, the fill factor, were traced to a variability in the shape recovery rates, Rt( N), which in turn were related to the microstructure. Materials with bicontinuous microstructures were stiffer and showed slower recovery rates. Thereby, using the elastic modulus, E, as a proxy for microstructure, the correlation of Rt( N) with E was traced to a relationship between the activation barrier for shape recovery, Δ A#, and the specific energy of deformation, (reorganization energy, λ), which in turn is proportional to the elastic modulus. Data were fitted well ( R2 = 0.92) by the derived equations. The inverse correlation between Rt( N) and the elastic modulus, E, provides a means for qualitative predictability of the shape recovery rates, the fill factors, and the overall quality of the shape memory effect.

Nanostructure-Dependent Marcus-Type Correlation of the Shape Recovery Rate and the Young's Modulus in Shape Memory Polymer Aerogels.

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Shape Memory Superelastic Poly(isocyanurate-urethane) Aerogels (PIR-PUR) for Deployable Panels and Biomimetic Applications

Nanostructure-Dependent Marcus-Type Correlation of the Shape Recovery Rate and the Young's Modulus in Shape Memory Polymer Aerogels.