Bacterial Cellulose/Zwitterionic Dual-network Porous Gel Polymer Electrolytes with High Ionic Conductivity

Bacterial cellulose(BC)was innovatively combined with zwitterionic copolymer acrylamide and sulfobetaine methacrylic acid ester[P(AM-co-SBMA)]to build a dual-network porous structure gel polymer electrolytes(GPEs)with high ionic conductivity.The dual network structure BC/P(AM-co-SBMA)gels were formed by a simple one-step polymerization method.The results show that ionic conductivity of BC/P(AM-co-SBMA)GPEs at the room temperature are 3.2×10^(-2) S/cm@1 M H_(2)SO_(4),4.5×10^(-2) S/cm@4 M KOH,and 3.6×10^(-2) S/cm@1 M NaCl,respectively.Using active carbon(AC)as the electrodes,BC/P(AM-co-SBMA)GPEs as both separator and electrolyte matrix,and 4 M KOH as the electrolyte,a symmetric solid supercapacitors(SSC)(AC-GPE-KOH)was assembled and testified.The specific capacitance of AC electrode is 173 F/g and remains 95.0%of the initial value after 5000 cycles and 86.2%after 10,000 cycles.

The use of bacterial cellulose from kombucha to produce curcumin loaded Pickering emulsion with improved stability and antioxidant properties

Curcumin is a bioactive molecule with limited industrial application because of its instability and poor solubility in water.Herein,curcumin-loaded Pickering emulsion was produced using purified bacterial cellulose from fermented kombucha(KBC).The morphology,particle size,stability,rheological properties,and antioxidant activities of the curcumin-loaded Pickering emulsion were investigated.The fluorescence microscope and scanning electron microscopy images showed that the curcumin-loaded Pickering emulsion formed circular droplets with good encapsulation.The curcumin-load Pickering emulsion exhibited better stability under a wide range of temperatures,low p H,sunlight,and UV-365 nm than the free curcumin,indicating that the KBC after high-pressure homogenization improved the stability of the CPE.The encapsulated curcumin retained its antioxidant capacity and exhibited higher functional potential than the free curcumin.The study demonstrated that the KBC could be an excellent material for preparing a Pickering emulsion to improve curcumin stability and antioxidant activity.

A Mini-review for the Application of Bacterial Cellulose-based Composites

Countries are duly focusing more on biomass resources because of the increasing oil crisis.Owing to their excellent properties,such as natural characteristics,good mechanical performance,and outstanding chemical properties,cellulose-based materials are highly valued as promising bioderived nanomaterials,especially bacterial cellulose(BC).The main advantage lies in eliminating the problem of removing lignin and hemicellulose from woody cellulose.Moreover,the use of BC reduces the consumption of wood,the excessive use of which aggravates global warming.Herein,we summarize the applications of BC composites in filter,medical,and conductive materials,and other fields.This review contributes to further expand the applications of this renewable polymer.

Bacterial Cellulose Nanofibers as Reinforcement for Preparation of Bamboo Pulp Based Composite Paper

Bamboo fibers(BFs),with features of renewability and biodegradability,have been widely used in paper-making products.In order to improve the mechanical properties and water absorption behaviors of the BF paper,bacterial cellulose nanofibers(BCNFs)as environmentally friendly nano-fibrillated cellulose(NFC)were combined with BFs.The structures and properties of the BF/BCNF composite paper were characterized by field emission scanning electron microscopy(FE-SEM),X-ray diffraction(XRD),Fourier transforms infrared(FTIR)spectroscopy,mechanical tests,pore size tests,and water absorption tests.The results indicated that the addition of BCNFs could significantly improve the water absorption capacity and mechanical properties.The water absorption ratio of the BF/BCNF composite paper with a BCNF mass fraction of 9%comes to 443%,about 1.33 times that of the pure BF paper.At the same BCNF content,the tensile strength of the BF/BCNF composite paper in dry and wet states was 12.37 MPa and 200.9 kPa,respectively,increasing by 98.24%and 136.91%as compared with that of the BF paper.

CoN_(x)C active sites-rich three-dimensional porous carbon nanofibers network derived from bacterial cellulose and bimetal-ZIFs as efficient multifunctional electrocatalyst for rechargeable Zn–air batteries

In this work, a CoNxC active sites-rich three-dimensional porous carbon nanofibers network derived from bacterial cellulose and bimetal-ZIFs is prepared via a nucleation growth strategy and a pyrolysis process.The material displays excellent electrocatalytic activity for the oxygen reduction reaction, reaching a high limiting diffusion current density of -7.8 mA cm^(-2), outperforming metal–organic frameworks derived multifunctional electrocatalysts, and oxygen evolution reaction and hydrogen evolution reaction with low overpotentials of 380 and 107 mV, respectively. When the electrochemical properties are further evaluated, the electrocatalyst as an air cathode for Zn-air batteries exhibits a high cycling stability for63 h as well as a maximum power density of 308 mW cm^(-2), which is better than those for most Zn-air batteries reported to date. In addition, a power density of 152 mW cm^(-2) is provided by the solid-state Zn-air batteries, and the cycling stability is outstanding for 24 h. The remarkable electrocatalytic properties are attributed to the synergistic effect of the 3 D porous carbon nanofibers network and abundant inserted CoNxC active sites, which enable the fast transmission of ions and mass and simultaneously provide a large contact area for the electrode/electrolyte.

Layer-by-Layer Assembled Bacterial Cellulose/Graphene Oxide Hydrogels with Extremely Enhanced Mechanical Properties

Uniform dispersion of two-dimensional(2 D) graphene materials in polymer matrices remains challenging. In this work, a novel layer-by-layer assembly strategy was developed to prepare a sophisticated nanostructure with highly dispersed 2 D graphene oxide in a three-dimensional matrix consisting of onedimensional bacterial cellulose(BC) nanofibers. This method is a breakthrough, with respect to the conventional static culture method for BC that involves multiple in situ layer-by-layer assembly steps at the interface between previously grown BC and the culture medium. In the as-prepared BC/GO nanocomposites, the GO nanosheets are mechanically bundled and chemically bonded with BC nanofibers via hydrogen bonding,forming an intriguing nanostructure. The sophisticated nanostructure of the BC/GO leads to greatly enhanced mechanical properties compared to those of bare BC. This strategy is versatile, facile, scalable, and can be promising for the development of high-performance BC-based nanocomposite hydrogels.

Bacterial Cellulose Composite Solid Polymer Electrolyte With High Tensile Strength and Lithium Dendrite Inhibition for Long Life Battery

The development of metallic lithium anode is restrained by lithium dendrite growth during cycling.The solid polymer electrolyte with high mechanical strength and lithium ion conductivity could be applied to inhibit lithium dendrite growth.To prepare the high-performance solid polymer electrolyte,the environment-friendly and cheap bacterial cellulose(BC)is used as filler incorporating with PEO-based electrolyte owing to good mechanical properties and Li salts compatibility.PEO/Li TFSI/BC composite solid polymer electrolytes(CSPE)are prepared easily by aqueous mixing in water.The lithium ion transference number of PEO/Li TFSI/BC CSPE is 0.57,which is higher than PEO/Li TFSI solid polymer electrolyte(SPE)(0.409).The PEO/Li TFSI/BC CSPE exhibits larger tensile strength(4.43 MPa)than PEO/Li TFSI SPE(1.34 MPa).The electrochemical window of composite electrolyte is widened 1.43 V by adding BC.Density functional theory calculations indicate that flex of PEO chains around Li atoms is suppressed,suggesting the enhanced lithium ion conductivity.Frontier molecular orbitals results suggest that an unfavorable intermolecular charge transfer lead to achieve higher potential for BC composite electrolyte.All solid-state Li metal battery with PEO/Li TFSI/BC CSPE delivers longer cycle life for 600 cycles than PEO/Li TFSI SPE battery(50 cycles).Li symmetrical battery using PEO/Li TFSI/BC CSPE could be stable for 1160 h.

Bacterial Cellulose-Silver Antibacterial Composites：Effects of Drying Processes of Bacterial Cellulose

A type of antibacterial bacterial cellulose(BC) film was prepared for potential uses as wound dressing.In order to obtain a high antibacterial effect,some forms of BC films,including the wet and dried ones were utilized as the template to in situ synthesize silver nanoparticles(AgNPs).The effects of drying methods including freeze-drying,heat drying and air drying,on the microstructures and physical properties of BC,as well as the silver contents and the antibacterial performances of the BC/AgNPs composites were investigated.It was found that the AgNPs impregnated on the dried BC films were inclined to achieve a faster silver releasing rate than the wet one,which was suitable for acute traumas treatment.

Regulating the Function of Nanocomposite Made from Hydroxypropyl Methyl Cellulose with Bacterial Cellulose Nanocrystal

Hydroxypropyl methyl cellulose(HPMC)-based hybrid nanocomposites reinforced with bacterial cellulose nanocrystals(BCNC) were prepared and characterized.The HPMC nanocomposites exhibited good thermal stability,with a thermogravimetric peak temperature of around 346℃.The addition of BCNC did not significantly affect the thermal degradation temperature or improve the transparency of HPMC nanocomposites.However,the addition of BCNC favorably affected the light scattering properties of the nanocomposites and enhanced mechanical properties such as tensile stress and Young's modulus from 65 MPa and 1.5 GPa up to 139 MPa and 3.2 GPa,respectively.The oxygen permeability of the HPMC nanocomposites also increased with increase in the amount of BCNC added.

Study of Nanoskin ECM-Bacterial Cellulose Wound Healing/United Arab Emirates

Natural extracellular matrices (ECMs) perform the tasks necessary for tissue formation, maintenance, regulation and function, providing a powerful means of controlling the biological performance of regenerative materials. In addition, biomedical materials have claimed attention because of the increased interest in tissue engineering materials for wound care and regenerative medicine. Moreover, the nanostructure and morphological similarities with collagen make BC attractive for cell immobilization, cell support and Natural Extracellular Matrix (ECM) Scaffolds. In this work, we present the extracellular matrix (ECM) using the bacterial cellulose (Nanoskin®) which regulates cell behavior by influencing cell proliferation, survival, shape, migration and differentiation. Bacterial cellulose fermentation process is modified before the bacteria are inoculated for mimicking ECM to cells support and built new local material for wound healing. Chemical groups influences and thermal behavior in bacterial cellulose were analyzed using transmission infrared spectroscopy (FTIR) and thermogravimetric analysis (TGA), respectively. Besides, In vivo analysis was evaluated with clinical study at Sharjah Kuwait Hospital.

Difficulties in the Use of Ground Bacterial Cellulose(BC)as Reinforcement of Polylactid Acid(PLA)Using Melt-Mixing and Extrusion Technologies

Bacterial cellulose (BC) was ground to make the material suitable for compounding with polylactid acid (PLA). The content of BC in PLA was changed between 5 and 20 wt%. By increasing the BC content of the composite DSC measurements showed an increase of crystallinity (χ c ). Annealing at 90?C resulted in a further increase of χ c . Analysis of the dynamic mechanical behavior showed a sharp decline of the storage module (G’) above the glass transition temperature (T g ) while such a sharp decline did not occur for annealed samples. This indicates that the stiffness of PLA even above T g can be improved by BC and annealing.

Nanofibrillation of Bacterial Cellulose Using High-Pressure Homogenization and Its Films Characteristics

The microstructure of bacterial cellulose nanofibers(BCNs)film affects its characteristic.One of several means to engineer the microstructure is by changing the BCNs size and fiber distribution through a high-pressure homogenizer(HPH)process.This research aimed to find out the effects of repetition cycles on HPH process towards BCNs film characteristics.To prepare BCNs films,a pellicle from the fermentation of pineapple peels waste with Acetobacter xylinum(A.xylinum)was extracted,followed by crushing the pellicle with a high-speed blender,thereafter,homogenized using HPH at 150 bar pressure with variations of 5,10,15,and 20 cycles.The BCNs films were then formed through the casting process and drying in the oven at 60°C for 8 h followed by structural,morphological,and optical properties investigation using X-ray diffraction(XRD),scanning electron microscopy(SEM)and Fourier transform infrared(FTIR)spectrometer along with BCNs films porosity,tensile and roughness test.The research showed that the effect of HPH cycle on BCNs resulted in the highest film tensile strength by 109.15 MPa with the lowest surface roughness(Ra)of 0.93±0.10μm at 10 cycles.The HPH process is effective in controlling BCNs film porosity level.The HPH cycles influence the crystalline index and crystallite size,slightly.

Comparative Study of Antibacterial Activity of Bacterial Cellulose/AgNPs Composites Prepared by Different Methods

Bacterial cellulose(BC) is a type of nanoscale cellulose produced by microorganisms.In this work,BC films were utilized as a template to in situ synthesize silver nanoparticles(AgNPs) by a variety of simple chemical strategies,including chemical reduction with NaBH4 or vitamin C,hydrothermal treatment and UV radiation.A comparative study of the formation of AgNPs such as the silver particle size and silver content,as well as the antibacterial activity of the BC-AgNPs nanocomposites by different preparation methods and reaction conditions was investigated.A beneficial support was provided for future applications of AgNPs contained BC composites with antibacterial properties.

Characterization of Bacterial Cellulose From Oil Palm Shoot Juices and Coconut Juice/Poly(ethylene glycol) Biocomposite

A new biocomposite was preformed between bacterial cellulose(BC)pellicle and polyethylene glycol(PEG)at different concentrations(0%,5,10%,15%and 20%)and different molecular weight(600,1000 and 2000).The structure and mechanical properties of BC/PEG biocomposite were investigated.The results indicated that the properties of the BC were improved by the addition of PEG.The morphology of the BC and BC/PEG blend was examined by a scanning electron microscope(SEM).These showed that PEG was coated with a large pore size fibril on the BC and the BC/PEG was dense with an even and smooth surface.All the Fourier transform infrared spectroscopy(FT-IR)thermograms of BC/PEG showed the same functional groups as typical BC and PEG.The DSC result showed that the thermal stability improved which might be associated with a weak interaction between BC and PEG,and may be useful for applications.

Bacterial Cellulose for Several Medicine Areas: Future Insights

Bacterial cellulose (BC)-Nanoskin® has become established as a new biomaterial and can be used in several medicine areas, especially for medical devices mainly in dental and orthopedics applications. In addition, biomaterials have rise because of the increased interest in tissue engineering and regeneratine medicine materials for wound care and skin cancer treatment. The BC process production can be changed by different fermentation process. It has particular properties that make it an ideal candidate as a medical material: high mechanical properties, biocompatibility to the host tissue, and production in various shapes and sizes. This review describes a behavior investigation of this biomaterial in human medicine with bacterial cellulose, skin cancer, covid-19 and 3-D print for medical area.

Analysis of Bacterial Cellulose/Ionic Liquid MWCNTs via Cyclic Voltammetry

Cyclic voltammetry based on an electrochemical technique is one of the current methods that measure the developments of the electrochemical properties in biomaterial samples under conditions. Biomaterial structure was changed by conductive material while these materials caused a connective network in whole of them and was able to transfer electrons inside of biomaterials. These changes in physical and chemical properties are investigated by analysis tools such as cyclic voltammetry (CV), X-radiation (XRF) and Ultraviolet-visible spectroscopy (UV-Vis). Bacterial cellulose is biodegradable, biosynthesis of A. xylinum which is a three-dimensional nano-network structure with a distinct tunnel and pore structure. In this study, the composite process produced electrically conducting bacterial cellulose pellicles containing well-dispersed and embedded multi-walled carbon nanotubes (MWCNTs) Ionic liquids (ILs), as observed in cyclic voltammetry (CV). For this purpose, we used a special tool, called OriginLab which is an industry-leading scientific graphing and data analysis software. The cyclic voltammetry graph presents the behavior of this composite which consists of a relationship between CNT dispersion, conductivity rate and changes in bacterial cellulose structure. The electrical conductivity of the cellulose/MWCNT composite was found different with respect to CNT dispersion. It was found that the incorporation process was a useful method not only for dispersing MWCNTs-ILs in an ultrafine fibrous network structure, but also for enhancing the electrical conductivity of the polymeric membranes.

Preparation and Properties of pH-Responsive Intelligent Medical Dressing Based on Bacterial Cellulose/Polyacrylic Acid

Bacterial cellulose/polyacrylic acid (BC/PAA) pH-responsive hydrogels were prepared by free-radical polymerization (in situ) using BC as the raw material and AA as the monomer. The hydrogels were loaded with curcumin (Cur) to prepare pH-responsive intelligent medical dressings. The preparation process of the hydrogels was optimized by a single factor and response surface experiment using their swelling degree as an index. The structures of BC/PAA pH-responsive hydrogels were characterized by scanning electron microscope (SEM), Fourier Transform Infrared spectrometer (FTIR), X-ray diffraction (XRD), and tensile tester, and the swelling properties, mechanical properties, bacteriostatic properties, and drug release behavior were investigated. The results showed that the BC/PAA pH-responsive hydrogel has a three-dimensional network structure with the swelling rate up to 1600 g/g, compressive strength of up to 8 KPa, and good mechanical properties, and the drug release behavior was in line with the logistic dynamics model, and it has good inhibitory effects on common pathogens of wound infection: E. coli, S. aureus, and P. aeruginosa.

Ion-conducting Membranes Based on Bacterial Cellulose Nanofibers Modified by Poly(sodium acrylate-co-2-acrylamido-2-methylpropanesulfonic acid)

Green method for preparation of ion-conducting membranes(ICM) based on bacterial cellulose nanofibers(CNF) modified by a copolymer of sodium acrylate and 2-acrylamido-2-methylpropanesulfonic acid was elaborated. FTIR and NMR data confirmed grafting of polyacrylate onto cellulose surface. Formation of porous structure of the ICM was controlled by SEM and AFM. The maximal ionic conductivity of the membranes reaches 1.5 and 3.1 mS·cm^(-1)(60 ℃ and 98% relative humidity) when they are saturated with water or H_2SO_4(1 mol·L^(-1)) electrolyte,respectively. Prepared ICM was tested as a separator in a symmetrical supercapacitor with electrodes based on polyaniline hydrogel. The assembled cell demonstrate ability to operate at high current density up to 100 A·g^(-1) maintaining specific capacitance 165 F·g^(-1). Maximal specific capacitance of 289 F·g^(-1) was achieved at current density 1 A·g^(-1). Retaining of 90% of initial capacitance after 10000 of charge-discharge cycles proves high electrochemical stability of prepared ICM.

Glycerol solutions of highly concentrated biomineral counter-ions towards water-responsive mineralization: Demonstration on bacterial cellulose and its application in hard tissue repair

Mineralization has found widespread use in the fabrication of composite biomaterials for hard tissue regeneration.The current mineralization processes are mainly carried out in neutral aqueous solutions of biomineral counter-ions(a pair of cation and anion that form the corresponding minerals at certain conditions),which are stable only at very low concentrations.This typically results in inefficient mineralization and weak control over biomineral formation.Here,we find that,in the organic solvent glycerol,a variety of biomineral counter-ions(e.g.,Ca/PO_(4),Ca/CO_(3),Ca/SO_(4),Mg/PO_(4),or Fe/OH)corresponding to distinct biominerals at significantly high concentrations(up to hundreds-fold greater than those of simulated body fluid(SBF))are able to form translucent and stable solutions(mineralizing solution of highly concentrated counter-ions(MSCIs)),and mineralization can be triggered upon them with external solvents(e.g.,water or ethanol).Furthermore,with pristine bacterial cellulose(BC)membrane as a model,we demonstrate an effective and controllable mineralization performance of MSCIs on organic substrates.This approach not only forms the homogeneous biominerals on the BC fibers and in the interspaces,but also provides regulations over mineralization rate,mineral content,phase,and dopants.The resulting mineralized BC membranes(MBCs)exhibit high cytocompatibility and favor the proliferation of rat bone marrow mesenchymal stem cells(rBMSC).Following this,we prepare a mineralized bone suture(MBS)from MBC for non-weight bearing bone fixation,which then is tested on a rabbit median sternotomy model.It shows firm fixation of the rabbit sternum without causing discernible toxicity or inflammatory response.This study,by extending the mineralization to the organic solution system of highly concentrated counter-ions,develops a promising strategy to design and build targeted mineral-based composites.

In situ biosynthesis of bacterial cellulose hydrogel spheroids with tunable dimensions

Bacterial cellulose(BC)hydrogel spheroid plays a significant role in diverse fields due to its spatial 3D structure and properties.In the present work,a series of BC spheroids with controllable size and shape was obtained via an in situ biosynthesis.Crucial factors for fabricating BC spheroid in-cluding inoculum concentration of 1.35×10^(3)CFU/mL,shaking speeds at 100 r/min,and 48-96 h incubation time during the biosynthetic process,were comprehensively established.An operable mechanism model for tuning the size of BC spheroids from 0.4 to 5.0 mm was proposed with a fresh feeding medium strategy of dynamic culture.The resulting BC spheroids exhibit an inter-active 3D network of nanofibers,a crystallinity index of 72.3%,a specific surface area of 91.2 m^(2)/g,and good cytocompatibility.This study reinforces the understanding of BC spheroid forma-tion and explores new horizons for the design of BC spheroids-derived functional matrix materials for medical care.