Structure Of Bacterial Cellulose Research Articles

Effects of Anchovy, Mussel, and Shrimp Powders on the Flame Retardancy of Bacterial Cellulose

ABSTRACT This study aims to fabricate bacterial cellulose with improved flame retardancy by applying anchovy, mussel, and shrimp powders. The elemental analysis confirmed that raw marine powders contained nitrogen and sulfur elements which could play important roles in enhancing the flame retardancy of bacterial cellulose. Thermogravimetric analysis revealed the improved thermal stability of bacterial cellulose following entrapping and crosslinking of the marine powders. The fabricated bacterial celluloses with marine powders had similar levels of flame retardancy as that of bacterial cellulose treated with a commercial flame-retardant, sodium metasilicate nonahydrate, which was confirmed by the vertical flammability test and limiting oxygen index. The char morphology analysis revealed intumescent char on the surface of the samples, confirming the effect of marine powders on the flame retardancy of bacterial cellulose. Moreover, the marine powders were entrapped and crosslinked with bacterial cellulose nanostructures, and the chemical and crystalline structures of bacterial cellulose were retained. This study proposes an efficient method to improve the flame retardancy of bacterial cellulose by introducing marine powders via the combined entrapment and crosslinking method.

Bacterial cellulose materials in sustainable energy devices: A review.

This article provides a comprehensive review of the processing and applications of bacterial cellulose (BC) for energy conversion and storage devices. These emerging technologies enable the transformation of sustainable energy sources into electricity. Once converted, energy storage devices are vital for stable energy supply. To promote green manufacturing practices in this field, bio-based materials are explored as alternative materials for energy devices, addressing the growing demand for sustainable solutions. From a research and development perspective, the materials chosen for energy devices must exhibit exceptional mechanical, electrical, and thermal properties, along with the necessary chemical reactivity to unlock new applications. Furthermore, for successful commercialization and industrialization, these materials must be suitable for large-scale production within practical timeframes. BC fulfills all of these requirements. The review begins with an overview of BC growth, detailing the composition and operating parameters of the culture medium and the design of bioreactors for large-scale production. It then defines and summarizes both in-situ and ex-situ modifications and processing strategies, offering a comprehensive perspective on these techniques. Unique and interesting properties linking BC's structure to its properties are reviewed to demonstrate its potential as a substitute for benchmark materials. The exceptional performance and synergistic effects of BC-derived hybrid materials highlight their potential for state-of-the-art applications in energy devices, and are suitable for the next-generation energy devices. The papers reviewed in this work have gained significant attention and been widely cited over the past 10years for their relevance to various practical applications, allowing readers to have a better understanding in development of BC based materials for energy conversion and conversion devices.

Self-assembled bacterial cellulose-based photo-enzyme coupled system enabled by visible light-driven for efficient dye degradation

To achieve efficient dye degradation, we reported a visible light-driven biomass photo-enzyme coupled system, which was constructed by assembling g-C3N4 during in situ culture and immobilizing laccase via metal–organic framework (MOF). Benefited from the network and porous structure of bacterial cellulose (BC), the g-C3N4 could be stably interspersed, and MOF grew g-C3N4/BC to encapsulate laccase. BC improves the reusability of the system, while combined with MOF encapsulation, avoiding direct contact between photo- and enzyme- catalysts. Importantly, thanks to the existence of electron transfer from photocatalysis to enzyme, the photogenerated electron hole recombination within the photocatalyst reduced, improving catalyzed reaction efficiency. The degradation efficiency of the catalysis system within 10 min for methylene blue and rhodamine B could reach 100 % and 96.1 %, respectively, which could rapidly degrade dye and recycle for more than 10 times. This research can shine new light on the development of advanced wastewater treatment.

Facile synthesis and electrochemical performance of bacterial cellulose/reduced graphene oxide/NiCo-layered double hydroxide composite film for self-standing supercapacitor electrode

This study employs a cost-efficient method to create a pliable BC/rGO-NiCo-LDH electrode film on a bacterial cellulose base. X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), and scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDX) analyses verified the incorporation of reduced graphene oxide (rGO) and nickel–cobalt layered double hydroxide (NiCo-LDH) into the bacterial cellulose structure. The BC/rGO-NiCo-LDH composite material exhibited high-temperature stability and achieved a specific capacitance of 311 F g−1 at a scan rate of 0.1 mV/s, surpassing that of earlier cellulose electrodes. The electrode film showed exceptional mechanical capabilities, displaying flexibility and load resistance without any structural damage. The film’s flexibility and lightweight properties were improved due to the low density of 0.656 g cm−3, which is a result of the nanoporous structure and intrinsic low density of rGO and cellulose. A retention ratio of 0.40 for storage modulus at a glass transition temperature of around 90°C demonstrated positive mechanical performance. This cost-effective and uncomplicated synthesis approach produced a BC/rGO-NiCo-LDH electrode with potential. The material possessed favourable mechanical and electrochemical characteristics, making it suitable for wearable electronics.

Development of bacterial cellulose with enhanced flame retardancy and flexibility by phosphorylation with phytic acid and xylitol

This study aims to develop bacterial cellulose with enhanced flame retardancy and flexibility. The bacterial cellulose was phosphorylated with phytic acid to improve its flame retardancy. Urea and xylitol were used as plasticizers, and their effects in improving the flexibility of bacterial cellulose were compared and evaluated. The optimal conditions for producing phosphorylated bacterial cellulose were found to be as follows: phytic acid:xylitol molar ratio of 1:10, phytic acid concentration of 10% (o.w.f.), and shaking at 30°C for 30 min at 90 rpm in a shaking water bath. A thermogravimetric analysis revealed that phosphorylated bacterial cellulose exhibited enhanced thermal properties compared with the original bacterial cellulose. Fourier transform infrared spectroscopy and X-ray diffraction confirmed that the chemical and crystalline structures of bacterial cellulose remained unchanged after phosphorylation. Mechanical properties such as the tensile strength, flexibility, and dimensional stability of the as-produced phosphorylated bacterial cellulose improved by using xylitol. In particular, the tensile strength and flexibility of the phosphorylated bacterial cellulose increased 5.7 and 2-fold, respectively, compared with those of the original bacterial cellulose. Therefore, this study demonstrated that the flame retardancy and flexibility of bacterial cellulose can be improved by using eco-friendly materials such as phytic acid and xylitol. The as-produced phosphorylated bacterial cellulose can be proposed as a fabric material with sufficient mechanical properties.

Production and characterization of bacterial cellulose utilizing Iraqi vinegar’s mother pellicles

Bacterial cellulose is an exopolymer prepared of α-1, 4 D glucopyranose units, created by several bacteria belonging to several genera, available in a multitude of implementations because of its greater chemical, mechanical and thermal characteristics combined with good biocompatibility and biodegradability. This present study aimed to produce low-cost, environmentally friendly Bacterial cellulose utilizing Iraqi vinegar’s mother pellicle (BCIVMP) and to study its properties. Bacterial cellulose was purified by using 0.1M NaOH and distilled water to study the properties. The chemical composition, crystallinity, particle size and surface shapes were studied using various devices. Ultraviolet -Visible Spectroscopy (UV Vis spectra) showed the optical transmission of bacterial cellulose. The mean values observed for bacterial cellulose were 273 and 542 nm. The FTIR spectrum confirmed the presence of the following functional groups –C–O and/or –C–C–, –C–O–C and/or –C–C–O and–O–H in the bacterial cellulose. The BCIVMP surface was examined by Scanning electron microscopy (SEM). At low amplification, the BCIVMP showed an extremely spongy construction with different levels of pore size. At higher amplification, both small and large clustered nanocrystals were seen. The average diameter was 17-29 nm. Ehlers-Danlos syndromes (EDS) analysis was performed to confirm the presence of the elements belonging to the functional groups present in the structure of bacterial cellulose. X-ray diffraction (XRD) diffractogram of (BCIVMP) showed the sample's high crystallinity due to the narrow double peak. The crystallinity index of(BCIVMP was found to be 91.5%. The study concluded that bacterial cellulose production from the Iraqi vinegar’s mother pellicles is eco-friendly, recyclable, and inoffensive to humans.

Features of formation and structure of bacterial cellulose-carbon nanotube composites

This paper examines the features of formation and structure of bacterial cellulose (BC) composites with carbon nanotubes (CNTs). We aim to study the influence of initial components on structure and crystallinity of BC composites. We use optical microscopy and scanning electron microscopy in order to investigate the surface morphology of BC composite films and X-ray diffraction analysis to determine the crystallographic structure of prepared samples. It is shown that CNT agglomerates in BC composite interact only with the surface layers of BC. CNTs and their bundles up to 50 nm in diameter are able to effectively penetrate into the BC network.

Homogeneous silver nanoparticle loaded polydopamine/polyethyleneimine-coated bacterial cellulose nanofibers for wound dressing

Utilizing mussel-inspired chemistry is an advanced strategy for surface modification, because dopamine (DA) can form a material-independent adhesive coating and further functionalization can be achieved, including the production of silver nanoparticles (AgNPs). Nevertheless, DA easily aggregates in the nanofiber network structure of bacterial cellulose (BC), which not only blocks the pores in the BC structure but also leads to the formation of large silver particles and the burst release of highly cytotoxic silver ions. Herein, a homogeneous AgNP-loaded polydopamine (PDA)/polyethyleneimine (PEI) coated BC was constructed via a Michael reaction between PDA and PEI. Under the action of PEI, the PDA/PEI coating was uniformly attached to the BC fiber surface with a thickness of approximately 4 nm, and homogeneous AgNPs were produced on the uniform PDA/PEI/BC (PPBC) fiber surface. The sustained release of silver ions was better from AgNPs@PPBC than from AgNPs@PDA/BC. The obtained AgNPs@PPBC exhibited excellent antibacterial activities and cytocompatibility. The results of the in vivo assay indicated that the AgNPs@PPBC dressing could inhibit S. aureus infection and inflammation, promote hair follicle growth, enhance collagen deposition, and accelerate wound healing within 12 days compared with BC. These results illustrate that the homogeneous AgNPs@PPBC dressing has great potential for treating infected wounds.

Preparation and Properties of Nano Platinum/Carbon Nanotubes/Bacterial Cellulose Conductive Hydrogel Electrode Films

Using the natural nanomesh structure of bacterial cellulose (BC), the good conductivity of multi-walled carbon nanotubes (MWCNTs) and the good electrocatalytic activity of nano platinum (PtNPs), a three-way porous conductive hydrogel of PtNPs and BC was designed. The infiltrating and doping of MWCNTs on BC thin films was realized by ultrasonic assisted electrophoretic deposition process, which ensured the dual characteristics of ionic and electronic conduction of electrode films. The adsorption capacity of BC for chloroplatinic acid and the strong reductivity of sodium borohydride were also used to realize the high-load PtNPs recombination on MWCNTs/BC porous layered conductive hydrogel electrode films. By testing the electrochemical performance of PtNPs/MWCNTs/BC conductive hydrogel electrode film and characterization of microstructure, the electrode film not only has high electroactive area, low surface charge transfer resistance and good diffusion permeability and other electrochemical characteristics, but also shows high catalytic activity for glucose in PBS solution. The most important finding is that the electrode film can selectively catalyze glucose in oxygen-rich PBS solution. The porous layered structure of PtNPs/MWCNTs/BC electrode membrane and the high load dispersion of PtNPs are the reasons for the selective catalytic ability of PtNPs/MWCNTs/BC conductive hydrogel electrode membrane, which can be used for the implanted surface glucose fuel cell.

Flexible fibrous structure of bacterial cellulose by synergic role carboxymethyl cellulose and glycerol for LiB polymer electrolyte

In this work, we report a flexible nanofibrous cellulose nanocomposite with great potential for lithium-ion battery (LiB) polymer electrolyte. Flexible and fibrous material is synthesized using a simple and easy technique by synergistically combining carboxymethyl cellulose (CMC) and glycerol (Gly). Flexible porous cellulose forms a three-dimensional network for the mobility of Li ions in the polymer electrolyte of LIB systems. We investigated the effect ionic liquid of flexible fibrous cellulose (BC-CMC-Gly) on the electrochemical properties. The surface interaction between Li ions and the porous network is a key parameter demonstrated by the Li-ion emission line at 610.37 nm using laser inductance breakdown spectroscopy (LiBS). The ionic conductivity of BC-CMC-Gly characterized by EIS measurement is about 1.1 × 10−3 S cm−1. According to linear sweep voltammetry (LSV), BC-CMC-Gly, with a potential window of 4.3 V, shows a more expansive window voltage than pure BC (2.75 V) and BC-CMC (3.3 V). This indicates that the electrochemical stability is good, as wide as the range of voltages that the electrode reactions define. The specific capacity of BC-CMC-Gly containing IL is very high, about 27.6 mAh g−1 compared to BC (7.4 mAh g−1) and BC-CMC (11,5 mAh g−1). All these findings clearly show that forming plasticized structures synergistically with CMC trapped in the BC structure results in the largest Li-ion adsorption capacity and electrochemical performance improvement. Thermal stability up to 200 °C and electrolyte uptake of approx. 189% are the beneficial properties of BC-CMC-Gly fibrous cellulose for LiB electrolyte polymer.

Acetic acid bacteria in agro-wastes: from cheese whey and olive mill wastewater to cellulose

In this study, cheese whey and olive mill wastewater were investigated as potential feedstocks for producing bacterial cellulose by using acetic acid bacteria strains. Organic acids and phenolic compounds composition were assayed by high-pressure liquid chromatography. Fourier-transform infrared spectroscopy, scanning electron microscopy, and X-ray diffraction were used to investigate modifications in bacterial cellulose chemical and morphological structure. Cheese whey was the most efficient feedstock in terms of bacterial cellulose yield (0.300g of bacterial cellulose/gram of carbon source consumed). Bacterial cellulose produced in olive mill wastewater presented a more well-defined network compared to pellicles produced in cheese whey, resulting in a smaller fiber diameter in most cases. The analysis of bacterial cellulose chemical structure highlighted the presence of different chemical bonds likely to be caused by the adsorption of olive mill wastewater and cheese whey components. The crystallinity ranged from 45.72 to 80.82%. The acetic acid bacteria strains used in this study were characterized by 16S rRNA gene sequencing, allowing to assign them to Komagataeibacter xylinus and Komagataeibacter rhaeticus species. This study proves the suitability to perform sustainable bioprocesses for producing bacterial cellulose, combining the valorisation of agro-wastes with microbial conversions carried out by acetic acid bacteria. The high versatility in terms of yield, morphology, and fiber diameters obtained in cheese whey and olive mill wastewater contribute to set up fundamental criteria for developing customized bioprocesses depending on the final use of the bacterial cellulose. KEY POINTS: • Cheese whey and olive mill wastewater can be used for bacterial cellulose production. • Bacterial cellulose structure is dependent on the culture medium. • Komagataeibacter strains support the agro-waste conversion in bacterial cellulose.

Sulfur-doped carbonized bacterial cellulose as a flexible binder-free 3D anode for improved sodium ion storage.

Carbon-based materials have received wide attention as electrodes for energy storage and conversion owing to their rapid mass transfer processes, outstanding electronic conductivities, and high stabilities. Here, sulfur-doped carbonized bacterial cellulose (S-CBC) was prepared as a high-performance anode for sodium-ion batteries (SIBs) by simultaneous carbonization and sulfidation using the bacterial cellulose membrane produced by microbial fermentation as the precursor. Doping sublimed sulfur powder into CBC results in a greater degree of disorder and defects, buffering the volume expansion during the cycle. Significantly, the three-dimensional (3D) network structure of bacterial cellulose endows S-CBC with flexible self-support. As an anode for sodium ion batteries, S-CBC exhibits a high specific capacity of 302.9 mA h g-1 at 100 mA g-1 after 50 cycles and 177.6 mA h g-1 at 2 A g-1 after 1000 cycles. Compared with the CBC electrode, the S-CBC electrode also exhibits enhanced rate performance in sodium storage. Moreover, theoretical simulations reveal that Na+ has good adsorption stability and a faster diffusion rate in S-CBC. The doping of the S element introduces defects that enlarge the interlayer distance, and the synergies of adsorption and bonding are the main reasons for its high performance. These results indicate the potential application prospects of S-CBC as a flexible binder-free electrode for high-performance SIBs.

The impact of alternating and rotating regimes on the heating characteristics of magnetic bacterial cellulose structure

The hyperthermia efficiency itself and the heating effect are determined not only by the material properties but also by the technical-application factors. For this reason, we subjected our experimental materials to experiments in an alternating magnetic field (AMF) as well as in a rotating magnetic field (RMF). According to the known numerical models as well as the results of comparative experiments, the RMF used is expected to be more efficient in heat generation than the AMF. Such tendency can be changed in the systems of higher density. This affects the particles' freedom of movement during field application, and thus there is a block of rotation. To research this, bacterial cellulose (BC) was magnetized in contact with magnetic fluid. By magnetic modification of BC, another range of potential applications is opened up including hyperthermia. Obtained specific absorption rates (SAR) at 3 different frequencies point to the possibility of effective tuning of the heating effect in conditions of alternating magnetic fields. Preliminary temperature evolution data of magnetized cellulose samples in both RMF and AMF indicate an increase in heating rate with applied field intensity proportional to H2 up to 4.3 kA∙m−1. In this AMF value, an inflection point is observed when data are plotted as d2T/dt2. In the case of RMF such tendency is not observed which permits a better temperature evolution prediction even in higher applied fields.

Pre-treatment effect on the structure of bacterial cellulose from Nata de Coco (Acetobacter xylinum)

This paper presents a structural analysis of various methods to produce bacterial cellulose (BC) from Nata de Coco (Acetobacter xyllinum). BC sheet, BC chem and BC mech powder were successfully prepared using oven drying, chemical and mechanical treatment. The X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, and field emission scanning electron microscopy (FESEM) were used to analyze the structure of prepared BC. The structure of bacterial cellulose was compared with the structure of commercial microcrystalline cellulose (MCC) and cotton fabric. The XRD results showed that the BC sheet sample had the highest degree of crystallinity (81.76%) compared to cotton cellulose (75.73%). The crystallite size of cotton was larger than the BC sheet, with the value of 6.83 ηm and 4.55 ηm, respectively. The peaks in the FTIR spectra of all BC were comparable to the commercial MCC and cotton fabrics. FESEM images showed that the prepared BC sheet, BC mech, and BC chem had an almost similar structure like commercial MCC and cotton fabric. It was concluded that simple preparation of BC could be implemented and used for further BC preparation as reinforcement in polymer composites, especially in food packaging.

Regulating the structure of bacterial cellulose by altering the expression of bcsD using CRISPR/dCas9

Gluconacetobacter xylinus is a primary strain producing bacterial cellulose (BC). In G. xylinus, BcsD is a subunit of cellulose synthase and is participated in the assembly process of BC. A series of G. xylinus with different expression levels of the bcsD gene were obtained by using the CRISPR/dCas9 technique. Analysis of the structural characteristics of BC showed that the crystallinity and porosity of BC changed with the expression of bcsD. The porosity varied from 59.95%-84.05%, and the crystallinity varied from 74.26%-93.75%, while the yield of BC did not decrease significantly upon changing the expression levels of bcsD. The results showed that the porosity of bacterial cellulose significantly increased, while the crystallinity was positively correlated with the expression of bcsD, when the expression level of bcsD was below 55.34%. By altering the expression level of the bcsD gene, obtaining BC with different structures but stable yield through a one-step fermentation of G. xylinus was achieved.

An Overview Regarding Microbial Aspects of Production and Applications of Bacterial Cellulose.

Cellulose is the most widely used biopolymer, accounting for about 1.5 trillion tons of annual production on Earth. Bacterial cellulose (BC) is a form produced by different species of bacteria, representing a purified form of cellulose. The structure of bacterial cellulose consists of glucose monomers that give it excellent properties for different medical applications (unique nanostructure, high water holding capacity, high degree of polymerization, high mechanical strength, and high crystallinity). These properties differ depending on the cellulose-producing bacteria. The most discussed topic is related to the use of bacterial cellulose as a versatile biopolymer for wound dressing applications. The aim of this review is to present the microbial aspects of BC production and potential applications in development of value-added products, especially for biomedical applications.

Enzymatic hydrolysis of bacterial cellulose in the presence of a non‐catalytic cerato‐platanin protein

AbstractIn this work, the effect of an expansin‐like cerato‐platanin (CP) protein as a pre‐treatment for the enzymatic hydrolysis of bacterial cellulose (BC) is investigated. To this scope, cellulases from Trichoderma reesei are used as hydrolyzing agent using different enzyme/BC formulations. Turbidity experiments reveal that for the higher enzyme concentrations (formulations 0.5:1 and 1:1) the enzymatic hydrolysis of BC show similar hydrolysis kinetics and is not dependent of the CP. However, at higher BC concentrations (formulations 0.25:1 and 0.33:1), the hydrolysis of BC is hindered by the non‐catalytic protein, as confirmed by the lower content of cellobiose and glucose in the presence of CP. Light scattering experiments show that the addition of CP led to an increase of the BC particle size from (445–630 nm) to (890–1.26 μm) for the formulation 1:1, which is also corroborated by atomic force microscopy and transmission electron microscopy analyses. These results suggest that CP did not positively affect the hydrolysis of BC, in contrast to what was previously observed for plant‐derived cellulose. This work for the first time investigates the anomalous behavior of cerato platanin family members with regard to its loosening activity on the structure of bacterial cellulose.

The influence of alkaline treatment on the mechanical and structural properties of bacterial cellulose

The unique mechanical properties of hydrated bacterial cellulose make it suitable for biomedical applications. This study evaluates the effect of concentrated sodium hydroxide treatment on the structural and mechanical properties of bacterial cellulose hydrogels using rheological, tensile, and compression tests combined with mathematical modelling. Bacterial cellulose hydrogels show a concentration-dependent and irreversible reduction in shear moduli, compression, and tensile strength after alkaline treatment. Applying a poroelastic biphasic model to through-thickness compressive stress-relaxation tests showed the alkaline treatment to induce no significant change in axial compression, an effect was observed in the radial direction, potentially due to the escape of water from within the hydrogel. Scanning electron microscopy showed a more porous structure of bacterial cellulose. These results show how concentration-dependent alkaline treatment induces selective weakening of intramolecular interactions between cellulose fibres, allowing the opportunity to precisely tune the mechanical properties for specific biomedical application, e.g., faster-degradable materials.

Synthesis and characterization of bacterial cellulose by Acetobacter xylinum using liquid tapioca waste

Abstract In this research, liquid tapioca waste was used to produce bacterial cellulose by Acetobacter xylinum. Liquid tapioca waste was heated at 70–80 °C and then mixed with sugar as a nitrogen source and urea as a nitrogen source. Furthermore, Acetobacter xylinum was added and incubated for ten days. The bacterial celluloses resulted were characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD) and Scanning electron microscopy (SEM). FTIR exhibited that bacterial cellulose structure was confirmed. XRD analysis showed the crystalline of the resulted bacterial cellulose. Also, SEM confirmed the 3D network structure of bacterial cellulose. The results showed that liquid tapioca waste could be used as a medium for bacterial cellulose production.

Ultra-Strong, Ultra-Tough, Transparent, and Sustainable Nanocomposite Films for Plastic Substitute

Summary Plastics play a critical role in daily life but possess a considerably increasing negative impact on the environment and human health. Fabrication of biodegradable and eco-friendly alternatives with competitive properties for plastic substitute is urgently needed. Here, inspired by the hierarchical structure of nacre, we firstly developed a high-performance nacre-inspired composite with high transmittance (83.4% at 550 nm) and high haze (88.8% at 550 nm) via an aerosol-assisted biosynthesis process combined with the hot-press technique. The nacre-inspired composite film combines higher strength (482 MPa) and toughness (17.71 MJ m−3) than most other nacre-inspired films, and can be folded into various shapes without visible failure after unfolding. Moreover, compared with most commercial plastic films, it exhibits a lower thermal expansion coefficient (∼3 ppm K−1) and higher maximum service temperature besides better mechanical properties, which makes it a promising alternative to plastics in many technical fields.