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1.
Angew Chem Int Ed Engl ; 57(26): 7580-7608, 2018 06 25.
Artículo en Inglés | MEDLINE | ID: mdl-29316086

RESUMEN

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.


Asunto(s)
Biopolímeros/química , Geles/química , Bases de Datos de Compuestos Químicos
2.
Adv Sci (Weinh) ; 11(24): e2307921, 2024 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-38477181

RESUMEN

Additive manufacturing (AM) is widely recognized as a versatile tool for achieving complex geometries and customized functionalities in designed materials. However, the challenge lies in selecting an appropriate AM method that simultaneously realizes desired microstructures and macroscopic geometrical designs in a single sample. This study presents a direct ink writing method for 3D printing intricate, high-fidelity macroscopic cellulose aerogel forms. The resulting aerogels exhibit tunable anisotropic mechanical and thermal characteristics by incorporating fibers of different length scales into the hydrogel inks. The alignment of nanofibers significantly enhances mechanical strength and thermal resistance, leading to higher thermal conductivities in the longitudinal direction (65 mW m-1 K-1) compared to the transverse direction (24 mW m-1 K-1). Moreover, the rehydration of printed cellulose aerogels for biomedical applications preserves their high surface area (≈300 m2 g-1) while significantly improving mechanical properties in the transverse direction. These printed cellulose aerogels demonstrate excellent cellular viability (>90% for NIH/3T3 fibroblasts) and exhibit robust antibacterial activity through in situ-grown silver nanoparticles.


Asunto(s)
Celulosa , Impresión Tridimensional , Celulosa/química , Ratones , Animales , Células 3T3 NIH , Geles/química , Nanofibras/química , Plata/química , Antibacterianos/farmacología , Antibacterianos/química , Nanopartículas del Metal/química
3.
Carbohydr Polym ; 292: 119675, 2022 Sep 15.
Artículo en Inglés | MEDLINE | ID: mdl-35725170

RESUMEN

Cellulose aerogels are potential alternatives to silica aerogels with advantages in cost, sustainability and mechanical properties. However, the density dependence of thermal conductivity (λ) for cellulose aerogels remains controversial. Cellulose aerogels were produced by gas-phase pH induced gelation of TEMPO-oxidized cellulose nanofibers (CNF) and supercritical drying. Their properties are evaluated by varying the CNF concentration (5-33 mg·cm-3) and by uniaxial compression (9-115 mg·cm-3). The aerogels are transparent with specific surface areas of ~400 m2·g-1, mesopore volumes of ~2 cm3·g-1 and a power-law dependence of the E-modulus (α ~ 1.53, and the highest reported E of ~1 MPa). The dataset confirms that λ displays a traditional U-shaped density dependence with a minimum of 18 mW·m-1·K-1 at 0.065 g·cm-3. For a given density, λ is ~5 mW·m-1·K-1 lower for compressed aerogels due to the alignment of nanofibers, confirmed by small angle X-ray scattering (SAXS).


Asunto(s)
Nanofibras , Celulosa/química , Geles/química , Nanofibras/química , Dispersión del Ángulo Pequeño , Difracción de Rayos X
4.
Adv Sci (Weinh) ; 9(11): e2105819, 2022 04.
Artículo en Inglés | MEDLINE | ID: mdl-35195354

RESUMEN

Inspired by the solar-light-driven oxygen transportation in aquatic plants, a biomimetic sustainable light-driven aerogel pump with a surface layer containing black manganese oxide (MnO2 ) as an optical absorber is developed. The flow intensity of the pumped air is controlled by the pore structure of nanofilbrillated cellulose, urea-modified chitosan, or polymethylsilsesquioxane (PMSQ) aerogels. The MnO2 -induced photothermal conversion drives both the passive gas flow and the catalytic degradation of volatile organic pollutants. All investigated aerogels demonstrate superior pumping compared to benchmarked Knudsen pump systems, but the inorganic PMSQ aerogels provide the highest flexibility in terms of the input power and photothermal degradation activity. Aerogel light-driven multifunctional gas pumps offer a broad future application potential for gas-sensing devices, air-quality mapping, and air quality control systems.


Asunto(s)
Contaminantes Ambientales , Compuestos de Manganeso , Biomimética , Celulosa/química , Óxidos
5.
Carbohydr Polym ; 247: 116680, 2020 Nov 01.
Artículo en Inglés | MEDLINE | ID: mdl-32829808

RESUMEN

The functionality of biopolymer aerogels is inherently linked to its microstructure, which in turn depends on the synthesis protocol. Detailed investigations on the macroscopic size change and nanostructure formation during chitosan aerogel synthesis reveal a new aspect of biopolymer aerogels that increases process flexibility. Formaldehyde-cross-linked chitosan gels retain a significant fraction of their original volume after solvent exchange into methanol (50.3 %), ethanol (47.1 %) or isopropanol (26.7 %), but shrink dramatically during subsequent supercritical CO2 processing (down to 4.9 %, 3.5 % and 3.7 %, respectively). In contrast, chitosan gels shrink more strongly upon exchange into n-heptane (7.2 %), a low affinity solvent, and retain this volume during CO2 processing. Small-angle X-ray scattering confirms that the occurrence of the volumetric changes correlates with mesoporous network formation through physical coagulation in CO2 or n-heptane. The structure formation step can be controlled by solvent-polymer and polymer-drying interactions, which would be a new tool to tailor the aerogel structure.


Asunto(s)
Biopolímeros/química , Dióxido de Carbono/química , Quitosano/química , Hidrogeles/química , Solventes/química , 2-Propanol/química , Adsorción , Biopolímeros/análisis , Desecación/métodos , Etanol/química , Formaldehído/química , Heptanos/química , Metanol/química , Microscopía Electrónica de Rastreo , Nanoestructuras/química , Nitrógeno/química , Tamaño de la Partícula , Porosidad , Dispersión del Ángulo Pequeño , Factores de Tiempo
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