Bacterial Cellulose Aerogels Research Articles

Bacterial cellulose/polyethylene glycol composite aerogel with incorporated graphene and metal oxides for VOCs detection

It is important to monitor and detect volatile organic compounds (VOCs) for environmental protection, occupational safety and human health. Portable and compact VOC sensing devices with a fast response are needed for real-time monitoring and simple analysis. Using solvent exchange and freeze-drying techniques, an ultralight 3D bacterial cellulose (BC) aerogel is prepared and modified by polyethylene glycol with the functionalization of graphene and metal oxides to detect VOC gases. Unlike commercially available flat VOC sensors, the 3D structure of our VOC sensor with high permeability of BC composite provides superior sensing characteristics for acetone, formaldehyde and ethanol in a wider range of scenarios. The portable BC composite sensor exhibits remarkable sensitivity and selectivity toward VOCs detection. The BC composite with TiO2 has a response time of about 20 s to 1 ppm acetone and can detect as low as 1.43 ppm at room temperature. In addition, BC composites with ZnO are suitable for detecting formaldehyde in indoor air.

In-situ bioprocessing of bacterial cellulose aerogel with covalent organic frameworks for enhanced uranium extraction

Developing efficient and cost-effective uranium adsorbents remain a significant challenge due to the complex composition of seawater. Herein, this study for the first time utilized an in-situ spray gel-assisted biosynthesis strategy to homogeneously incorporate the covalent organic frameworks (COF) into the three-dimensional pores of bacterial cellulose (BC) hydrogel during the culture of K. sucrofermentans. The BCCOF-SO3NH4 aerogel was fabricated through ammoniating modification of BC/COF (BCCOF-SO3H) hydrogel and freeze-drying processes. The BCCOF-SO3NH4 aerogels are characterized by the in-situ entanglement of COF within the three-dimensional network of BC, resulting in enhanced mechanical strength and groups interactions. The experimental maximum adsorption capacity of BCCOF-SO3NH4 aerogel reached 883.44 mg g−1, demonstrating exceptional uranium adsorption capacity compared with most of the reported adsorbents. The adsorption process follows the pseudo-second-order model and Langmuir isotherm. Throughout seven adsorption–desorption cycles, BCCOF-SO3NH4 maintained a stable adsorption capacity and desorption efficiency. The adsorption mechanism is verified by experiments and DFT calculations, which involves not only the ion exchange between uranyl and NH4+, but also the strong coordination interaction between the active groups (sulfonic acid group, hydroxyl group) and uranium. The in-situ biosynthesis strategy of composites shows a great application prospect in the preparation of high adsorption performance materials.

Supercritical carbon dioxide–activated copper/bacterial cellulose aerogels for the capture of hydrophobic organic liquids

In this study, bacterial cellulose was derived from coconut water via fermentative production of nata de coco, a common food in Southeast Asia. Bacterial cellulose offers distinct advantages over plant cellulose resources, including three-dimensional structure, high porosity, high cellulose purity, and the absence of required polluting treatments, making it an ideal candidate for the facile preparation of various functional aerogel materials. Surface modification of nata de coco-derived cellulose fibers was obtained by incorporating Cu species (approximately 15 wt%) through an aqueous reaction of Cu(CH3COO)2 with N2H4 at room temperature. The Cu-coated bacterial cellulose aerogels were fabricated via supercritical carbon dioxide drying to maintain the natural three-dimensional matrix and subsequently characterized by various techniques confirming high porosity and crystallinity and successful Cu coating onto the cellulose fiber surface. The Cu-containing aerogel showed a significantly improved adsorption uptake for n-hexane (12.6 g g−1) in comparison with pure bacterial cellulose–based aerogel (3.2 g g−1). Furthermore, notable adsorption performances of 13.6–19.9 g g−1 were found for cyclohexane, ethyl acetate, and soybean oil, indicating the high efficiency of the supercritical carbon dioxide–activated bacterial cellulose aerogel containing Cu species in the adsorption of water-insoluble liquids. Notably, applying supercritical carbon dioxide drying afforded the stable aerogel structure for reusing over several cycles with almost unchanged trapping capacity.

Engineering Shewanella oneidensis-Carbon Felt Biohybrid Electrode Decorated with Bacterial Cellulose Aerogel-Electropolymerized Anthraquinone to Boost Energy and Chemicals Production.

Interfacial electron transfer between electroactive microorganisms (EAMs) and electrodes underlies a wide range of bio-electrochemical systems with diverse applications. However, the electron transfer rate at the biotic-electrode interface remains low due to high transmembrane and cell-electrode interfacial electron transfer resistance. Herein, a modular engineering strategy is adopted to construct a Shewanella oneidensis-carbon felt biohybrid electrode decorated with bacterial cellulose aerogel-electropolymerized anthraquinone to boost cell-electrode interfacial electron transfer. First, a heterologous riboflavin synthesis and secretion pathway is constructed to increase flavin-mediated transmembrane electron transfer. Second, outer membrane c-Cyts OmcF is screened and optimized via protein engineering strategy to accelerate contacted-based transmembrane electron transfer. Third, a S. oneidensis-carbon felt biohybrid electrode decorated with bacterial cellulose aerogel and electropolymerized anthraquinone is constructed to boost the interfacial electron transfer. As a result, the internal resistance decreased to 42 Ω, 480.8-fold lower than that of the wild-type (WT) S. oneidensis MR-1. The maximum power density reached 4286.6 ± 202.1mWm-2, 72.8-fold higher than that of WT. Lastly, the engineered biohybrid electrode exhibited superior abilities for bioelectricity harvest, Cr6+ reduction, and CO2 reduction. This study showed that enhancing transmembrane and cell-electrode interfacial electron transfer is a promising way to increase the extracellular electron transfer of EAMs.

Effect of Drying Methods on the Thermal and Mechanical Behavior of Bacterial Cellulose Aerogel.

Bacterial cellulose (BC) presents significant promise as a biomaterial, boasting unique qualities such as exceptional cellulose purity, robust mechanical strength, heightened crystalline structure, and biodegradability. Several studies have highlighted specific effects, such as the impact of dehydration/rehydration on BC tensile strength, the influence of polymer treatment methods on mechanical properties, the correlation between microorganism type, drying method, and Young's modulus value, and the relationship between culture medium composition, pH, and crystallinity. Drying methods are crucial to the structure, performance, and application of BC films. Research findings indicate that the method used for drying can influence the mechanical properties of BC films, including parameters such as tensile strength, Young's modulus, and water absorption capacity, as well as the micromorphology, crystallinity, and thermal characteristics of the material. Their versatility makes them potential biomaterials applicable in various fields, including thermal and acoustic insulation, owing to their distinct thermal and mechanical attributes. This review delves into the thermal and mechanical behavior of bacterial cellulose aerogels, which are profoundly impacted by their drying mechanism.

Bacterial cellulose-derived porous carbon aerogel containing FeS as the self-supporting anode for high-efficiency lithium-ion storage

Lithium-ion hybrid capacitors (LIHCs) attract extensive attention because of the urgent demands for high-energy density and high-power density devices. Here, a free-standing FeS@C/carbonized bacterial cellulose aerogel (FeS@C/CBC) -based anode for LIHCs is developed by growth of MIL-88-NH2 on bacterial cellulose (BC) substrate, followed by simultaneous carbonization and sulfidation. The obtained FeS@C/CBC inherits the three-dimensional, highly porous structure, and free-standing properties of CBC. FeS is uniformly distributed in the nitrogen-rich carbon and tightly deposited on the CBC fibers, and such structure favors a fast Li/e− transport. As a result, the free-standing FeS@C/CBC delivers a high reversible capacity of 669 mAh g−1 after 1000 cycles at 1 A g−1. Additionally, when the obtained anode is combined with the KCBC as the cathode, the resulting full cellulose-based cell exhibits an impressive cycling stability with the capacity retention of 77.8 % over 10,000 cycles at 5 A g−1 and a high energy density of 172 Wh kg−1 within the voltage window of 0.01–4.2 V, demonstrating a promising potential for practical applications in the field of LIHCs.

Synthesis strategies, regeneration, cost analysis, challenges and future prospects of bacterial cellulose-based aerogels for water treatment: A review

Clean water is an integral part of industries, agricultural activities and human life, but water contamination by toxic dyes, heavy metals, and oil spills is increasingly serious in the world. Aerogels with unique properties such as highly porous and extremely low density, tunable surface modification, excellent reusability, and thermal stability can contribute to addressing these issues. Thanks to high purity, biocompatibility and biodegradability, bacterial cellulose can be an ideal precursor source to produce aerogels. Here, we review the modification, regeneration, and applications of bacterial cellulose-based aerogels for water treatment. The modification of bacterial cellulose-based aerogels undergoes coating of hydrophobic agents, carbonization, and incorporation with other materials, e.g., ZIF-67, graphene oxide, nanoparticles, polyaniline. We emphasized features of modified aerogels on porosity, hydrophobicity, density, surface chemistry, and regeneration. Although major limits are relevant to the use of toxic coating agents, difficulty in bacterial culture, and production cost, the bacterial cellulose aerogels can obtain high performance for water treatment, particularly, catastrophic oil spills.

Development of silanized bacterial cellulose aerogels for the incorporation of natural oils with healing properties: Copaiba (Copaifera officinalis), bourbon geranium (Pelargonium X ssp.) essential oils and buriti (Mauritia flexuosa) vegetable oil

Bacterial cellulose (BC) represents a promising biomaterial, due to its unique and versatile properties. We report, herein, on purposely-designed structural modifications of BC that enhance its application as a wound dressing material. Chemical modification of the functional groups of BC was performed initially to introduce a hydrophobic/oleophilic character to its surface. Specifically, silanization was carried out in an aqueous medium using methyltrimethoxisilane (MTMS) as the silanizing agent, and aerogels were subsequently prepared by freeze-drying. The BC-MTMS aerogel obtained displayed a highly porous (99 %) and lightweight structure with an oil absorption capacity of up to 52 times its dry weight. The XRD pattern indicated that the characteristic crystallographic planes of the native BC were maintained after the silanization process. Thermal analysis showed that the thermal stability of the BC-MTMS aerogel increased, as compared to the pure BC aerogel (pBC). Moreover, the BC-MTMS aerogel was not cytotoxic to fibroblasts and keratinocytes. In the second step of the study, the incorporation of natural oils into the aerogel's matrix was found to endow antimicrobial and/or healing properties to BC-MTMS. Bourbon geranium (Pelargonium X ssp.) essential oil (GEO) was the only oil that exhibited antimicrobial activity against the tested microorganisms, whereas buriti (Mauritia flexuosa) vegetable oil (BVO) was non-cytotoxic to the cells. This study demonstrates that the characteristics of the BC structure can be modified, while preserving its intrinsic features, offering new possibilities for the development of BC-derived materials for specific applications in the biomedical field.

A Tent-Inspired Portable Solar-Driven Water Purification Device for Wilderness Explorers.

Wilderness adventure favored by many enthusiasts often endanger lives due to lacking freshwater or drinking contaminated water. Therefore, compared to the inefficient methods of filtration, steaming, and direct solar heating, it is of great meaningfulness to develop a solar-driven water purification device with efficiency, lightweight, portability, and multi-water-quality purification by taking full advantage of solar-driven interfacial evaporation. Here, a tent-inspired portable solar-driven water purification device consisting of Janus-structured bacterial cellulose aerogel (JBCA) solar evaporator and tent-type condensation recovery device is reported. For the JBCA solar evaporator, it is prepared from biomass bacterial cellulose (BC) as raw material and hydroxylated carbon nanotubes (HCNT) as photothermal material, and the Janus property is achieved by the assistance of hydrophobic and hydrophilic chemical cross-linking. It exhibits lightweight, unibody, high photothermal conversion, efficient evaporation, and multi-water-quality purification capability for representative seawater, urine, and bacterial river water. For the tent-type condensation recovery device, it is based on the prototype of tent and uses flexible ultra-transparent polyvinyl chloride (PVC) film as raw material. Thanks to the rational prototype and material selection, it displays outstanding portability and lightweight through the folding/unfolding method. Therefore, the designed tent-inspired portable solar-driven water purification device demonstrates great potential application in wilderness exploration.

Preparation of imprinted bacterial cellulose aerogel with intelligent modulation of thermal response stimulation for selective adsorption of Gd(III) from wastewater.

Research on recycling of used rare earth elements has been of great interest. Adsorption is one of the advantageous methods to recover gadolinium with high value. In the process of adsorption and separation of gadolinium from materials, the selectivity of materials for gadolinium can be significantly improved by using ion imprinting technique. However, gadolinium elution process is a traditional pickling process, which may affect the construction of imprinting sites. In this study, bacterial cellulose with three-dimensional spatial structure was used as the base material of aerogel material, and functional materials containing a large number of carboxyl groups were introduced by chemical grafting method. In combination with ion imprinting technology and N-polyacrylamide as intelligent temperature control valve, intelligent imprinting aerogel (PNBC-IIPS) with specific selectivity to gadolinium was prepared. The properties of aerogel materials were analyzed by SEM, FT-IR, and BET characterization. The experimental analysis shows that the desorption of gadolinium can be achieved by controlling the temperature change. The adsorption experiments show that PNBC-IIPS can selectively adsorb gadolinium ions from aqueous solution. The maximum adsorption capacity reached 95.51mgg-1. Compared with unimprinted aerogel, the maximum adsorption capacity of gadolinium ion is significantly increased, which proves that the introduced ion imprinting technique plays a key role in the adsorption process. Cyclic experiments show that the adsorption capacity of PNBC-IIPS can still maintain 88% of the original adsorption capacity after 5 times of adsorption and desorption. In conclusion, PNBC-IIPS is a green adsorbent for selective recovery of gadolinium ions.

Nata de coco as an abundant bacterial cellulose resource to prepare aerogels for the removal of organic dyes in water

A hydrogel-like product of the bacterial fermentation of coconut water is well-known as nata de coco which contains low-cost and high-quality bacterial cellulose. In this work, nata de coco was applied for the facile preparation of lightweight bacterial cellulose aerogels upon grinding and subsequent freeze-drying. The obtained aerogels possessed the three-dimensional network containing bacterial cellulose fibers with high crystallinity and porosity. The experimental results proved the high affinity of the bacterial cellulose network to the cationic dyes with adsorption capacities from 25 to 81 mg/g. By contrast, the aerogel was inefficient with most of the tested anionic dyes except for congo red which afforded a significant adsorption capacity of 145 mg/g. The promising results were obtained without any further chemical modification being applied to the bacterial cellulose aerogels and notably comparable to the previous performances of biomass-based sorbents. This biomaterial showed a great potential in environmentally-friendly treating organic dyes-polluted wastewater.

Immobilization of UiO-66-NH2 into Bacterial Cellulose Aerogels for Efficient Particulate Matter Filtration

Metal–organic frameworks (MOFs) hold great potential for efficient removal of particulate matter (PM) due to their high porosity and tunable surface groups. In this work, sustainable bacterial cellulose (BC) was employed as a substrate for Zr-based MOF (i.e., UiO-66-NH2) deposition. Specifically, the UiO-66-NH2@BC aerogel exhibits a multi-level pore structure with a specific surface area of 103 m2/g. Pristine BC aerogels indicated a removal efficiency of 50.6% for PM2.5, with a pressure drop of 22.8 Pa. While UiO-66-NH2@BC aerogels showed a PM2.5 removal efficiency of 96.9%. The filtration mechanism can be assigned to the following reasons: (i) the interception/impaction of PM with the fibrous and porous aerogel network; and (ii) the presence of polar amine groups that boost electrostatic interactions between PM and MOFs. Moreover, as-prepared filters can be regenerated in a facile way with good reusability and long-term stability.

Bacterial Cellulose Aerogels Derived from Pineapple Peel Waste for the Adsorption of Dyes.

Valorization of pineapple peel waste is an attractive research topic because of the huge quantities of this byproduct generated from pineapple processing industries. In this study, the extract from pineapple waste was collected to produce a hydrogel-like form containing bacterial cellulose fibers with a three-dimensional structure and nanoscale diameter by the Acetobacter xylinum fermentation process. The bacterial cellulose suspension was subsequently activated by freeze-drying, affording lightweight aerogels as potential adsorbents in wastewater treatment, in particular the adsorptive removal of organic dyes. Intensive tests were carried out with the adsorption of methylene blue, a typical cationic dye, to investigate the influence of adsorption conditions (temperature, pH, initial dye concentration, time, and experiment scale) and aerogel-preparation parameters (grinding time and bacterial cellulose concentration). The bacterial cellulose-based aerogels exhibited high adsorption capacity not only for methylene blue but also for other cationic dyes, including malachite green, rhodamine B, and crystal violet (28-49 mg/g). However, its activity was limited for most of the anionic dyes, such as methyl orange, sunset yellow, and quinoline yellow, due to the repulsion of these anionic dyes with the aerogel surface, except for the case of congo red. It is also an anionic dye but has two amine groups providing a strong interaction with the hydroxyl group of the aerogel via hydrogen bonding. Indeed, the aerogel has a substantially large congo red-trapping capacity of 101 mg/g. Notably, the adsorption process exhibited similar performances, upscaling the solution volume to 50 times. The utilization of abundant agricultural waste in the simple aerogel preparation to produce a highly efficient and biodegradable adsorbent is the highlight of this work.

(Digital Presentation) Electrocatalytic and Conductive Vanadium Oxide on Carbonized Bacterial Cellulose Aerogel for the Sulfur Cathode in Li-S Batteries

Li-S chemistry is regarded as promising next-generation battery technology. However, its complex redox process and long-chain lithium polysulfides shuttling are hindering the development of practical Li-S battery technology. To address these problems, many transition-metal-oxide-based catalysts have been investigated to chemically bind soluble lithium polysulfides and accelerate their redox kinetics. However, the intrinsic poor electrical conductivities of these oxides restrict their catalytic performance, consequently limiting the sulfur utilization and the rate performance of Li-S batteries. Herein, we report a freestanding electrocatalytic sulfur host consisting of hydrogen-treated VO2 nanoparticles (H-VO2) anchored on nitrogen-doped carbonized bacterial cellulose aerogels (N-CBC). The hydrogen treatment enables the formation and stabilization of the rutile VO2(R) phase with metallic conductivity at room temperature, significantly enhancing its catalytic capability compared to the as-synthesized insulative VO2(M) phase. We characterized the electrocatalytic performance of this unique H-VO2@N-CBC structure using several methods and found that the activation energy between S8 and polysulfides and the one between polysulfides and Li2S are largely reduced by 28.2 and 43.3 kJ/mol, respectively. Accordingly, the Li-S battery performance is greatly improved, with a high initial specific capacity of 1347 mAh g−1 at 0.1 C and remarkable cycling stability with a capacity of 758 mAh g-1 after 300 cycles at 1 C. This work provides an effective strategy for designing and fabricating conductive oxide catalysts to promote the electrochemical performance of Li-S batteries.

Bacterial cellulose derived carbon nanofiber aerogel assembled with redox active hydrogel and alpha-MoO3 nanoplate for high-performance supercapacitors

Dual-asymmetric supercapacitors (DASCs) with high capacitive performance were developed in this work through carefully design and configuration of all the capacitor components. Free-standing carbon aerogel was directly utilized as the positive electrode, which was fabricated by pyrolyzing bacterial cellulose (BC) aerogel. Its porous structure afforded it excellent interface with the redox active electrolyte. Redox active hydrogel electrolyte based on mixed-valence iron ions (PVA/H2SO4/Fe3+/2+) was prepared with a freezing-thawing method and combined with the carbon aerogel to form the positive compartment of the capacitors. Meanwhile, α-MoO3 nanoplates were fabricated by hydrothermal method and used for the fabrication of negative electrodes, which were assembled with conventional PVA/H2SO4 hydrogel electrolyte to form the negative compartment. The as-assembled DASCs showed a specific capacitance of 560.8 F g−1 at 1 A g−1 and energy density of 131.6 Wh kg−1, indicating its remarkable capacitive performance. Moreover, the optimized DASC displayed a remarkable long-term cycling stability. This work on the design and assembly of the battery-like supercapacitor with carbon aerogel electrodes combined with their corresponding hydrogel electrolytes afforded a new configuration to fabricate the devices with high performance.

Bacterial cellulose biomass aerogels for oil-water separation and thermal insulation

The use of environment-friendly biomass for the preparation of functional materials has attracted increasing attention. In this study, bacterial cellulose (BC) was prepared from fruit waste via kombucha fermentation without involving any secondary enzymatic hydrolysis treatments. A three-dimensional network of bacterial cellulose aerogels (BCAs) with ultralow density (5.693 mg/cm3), high porosity (98–99%), and low thermal conductivity (23.4 mW/(m·K)) were obtained using two directional freeze-drying techniques. Here, the proposed freezing method can not only control the concentration of BC but make access to fibres reassembly by extremely low temperature freezing (−196 °C), which can further form a multi-stage pore structure. To increase their compressive resistance and optimise their ability to adsorb organic solvents and oils, the aerogels were subjected to chemical vapour deposition using methyltrimethoxysilane. The modified biomass aerogel exhibits a compression resilience exceeding 90% and achieves a hydrophobic angle of approximately 146.4°. This cost-effective, environmentally friendly, and highly efficient BCAs can be employed to treat oil spills and industrial waste.

Construction of oxygen vacancy-rich ZnO@carbon nanofiber aerogels as a free-standing anode for superior lithium storage

The development of next-generation high-capacity freestanding materials as electrodes in lithium-ion batteries (LIBs) has significant potential. Here, oxygen vacancy-rich ZnO (Ov-ZnO) deposited on carbonized bacterial cellulose (CBC) aerogels is developed via in-situ uniformly growing ZIF-8-NH2 particles on CBC aerogels, followed by the hydrazine reduction and pyrolysis. The CBC serves as a free-standing skeleton to disperse and support ZIF-8-NH2 derived ZnO while the introduction of oxygen vacancies can effectively promote the internal ion/electron transfer. As a result, the obtained free-standing aerogels (Ov-ZnO@CBC) displays a reversible capacity of 710 mAh g−1 at 1 A g−1 after 1000 cycles, which is superior to ZnO@CBC without hydrazine reduction treatment. Furthermore, the assembled Li free-standing full cell using the Ov-ZnO@CBC composite as the anode and BC@LiFePO4 (BC@LFP) as the cathode exhibits an outstanding cycling performance of 150 mAh g−1 after 100 cycles at 0.1 A g−1, displaying satisfactory lithium-ion storage capability. It is noteworthy that both Ov-ZnO@CBC and BC@LFP are obtained in the form of a free-standing aerogel. This work offers a strategy to prepare high-capacity and long-cycle self-supporting aerogel-based electrodes for flexible LIBs.

Bacterial cellulose aerogel enriched in nanofibers obtained from Kombucha SCOBY byproduct

Symbiotic Culture of Bacteria and Yeast (SCOBY) pellicle is a by-product of Kombucha tea fermentation that can be a cheap and fast-growing source of cellulose. SCOBY develops a 3D cellulose membrane on the surface of Kombucha tea and since its microstructure can be chemically modified, it has promising applications in the development of biocomposites. This study presents a simple procedure to transform Kombucha SCOBY membranes into cellulose nanofiber aerogels. The protocol consisted in an alkaline purification followed by an acidic hydrolysis and lyophilization. The obtained nanofibers presented thickness than ranged principally between 50 and 110 nm, good crystallinity (90%) and thermal stability (343 ºC). The simplicity of this nanofiber aerogel protocol may contribute to the development of nano-scale materials giving higher value to this by-product that generally is composted. Furthers studies should be addressed to test this nanocellulose fibers combined with other polymers for the development of eco-friendly composites.

Highly efficient construction of sustainable bacterial cellulose aerogels with boosting PM filter efficiency by tuning functional group

Air pollution has become a major public health concern, attracting considerable attention from researchers working on environmentally friendly and sustainable materials. In this work, bacterial cellulose (BC) derived aerogels were fabricated by the directional ice-templated method and used as filters to remove PM particles. We modified the surface functional groups of BC aerogel with reactive silane precursors, and investigated the interfacial and structural properties of those aerogels. The results show that BC-derived aerogels have excellent compressive elasticity, and their directional growth orientation inside the structure significantly reduced pressure drop. Moreover, the BC-derived filters exhibit an exceptional quantitative removal effect on fine particulate matter, which, in the presence of high concentrations of fine particulate matter, they can achieve a high-efficiency removal standard of 95 %. Meanwhile, the BC-derived aerogels showed superior biodegradation performance in the soil burial test. These results paved the way for BC-derived aerogels development as a great sustainable alternative to treat air pollution.

Preparation of high elastic bacterial cellulose aerogel through thermochemical vapor deposition catalyzed by solid acid for oil-water separation

Oil pollution has caused more and more serious damages to the environment, especially to water. Oil and water separation technologies based on high-performance absorbing materials have attracted extensive attentions. Herein, elasticity-enhanced bacterial cellulose (BC) aerogel is synthesized for oil/water separation through thermochemical vapor deposition (CVD) catalyzed by 1, 2, 3, 4-butanetetracarboxylic acid (BTCA). BTCA has two functions, namely, esterification with BC and catalyzing CVD. The prepared aerogel could be recovered soon after being compressed and the elastic recovery was >90 % at set maximum deformation of 80 %. And, it also exhibits vigorous fatigue resistance with an elastic deformation of >80 % after 50 cycles. The high elastic and hydrophobic aerogel is very suitable for absorbing and desorbing oils by simple mechanical squeezing. The adsorption capacity for n-hexane and dichloroethane maintain 87 % and 81 % after 50 cycles, respectively, which implies robust reusability. Importantly, the CVD could also be catalyzed by other solid acids such as citric acid and vitamin C. This design and fabrication method offers a novel avenue for the preparation of hydrophobic bacterial cellulose aerogel with high elasticity.