Novel Sustainable Cellulose Acetate Based Biosensor for Glucose Detection

In this study,green zinc oxide(ZnO)/polypyrrole(Ppy)/cellulose acetate(CA)film has been synthesized via solvent casting.This film was used as supporting material for glucose oxidase(GOx)to sensitize a glucose biosensor.ZnO nanoparticles have been prepared via the green route using olive leaves extract as a reductant.ZnO/Ppy nanocomposite has been synthesized by a simple in-situ chemical oxidative polymerization of pyrrole(Py)monomer using ferric chloride(FeCl3)as an oxidizing agent.The produced materials and the composite films were characterized using X-ray diffraction analysis(XRD),scanning electron microscope(SEM),Fourier transform infrared(FTIR)and thermogravimetric analysis(TGA).Glucose oxidase was successfully immobilized on the surface of the prepared film and then ZnO/Ppy/CA/GOx composite was sputtered with platinum electrode for the current determination at different initial concentrations of glucose.Current measurements proved the suitability and the high sensitivity of the constructed biosensor for the detection of glucose levels in different samples.The performance of the prepared biosensor has been assessed by measuring and comparing glucose concentrations up to 800 ppm.The results affirmed the reliability of the developed biosensor towards real samples which suggests the wide-scale application of the proposed biosensor.

Research Progress of Environment Friendly Plasticizers for Cellulose Acetate Processing

Cellulose acetate(CA)is an important cellulose derivative that can undergo thermoplas-tic processing.Plasticizers can form stable hydrogen bonds with CA molecular chains,reducing intermolecular and intramolecular interactions,and play an important role in the melting processing of CA.In recent years,environmentally friendly plasticizers that are natural,non-toxic,odorless,low dissolution,and low migration have received increas-ing attention in plastic processing.This article reviews the research progress of environ-mentally friendly plasticizers such as natural plasticizers,ionic liquid plasticizers,citrate plasticizers,and polyethylene glycol plasticizers in the processing of cellulose acetate,and looks forward to the application prospects of environmentally friendly plasticizers.

Reaction pathways and selectivity in the chemo-catalytic conversion of cellulose and its derivatives to ethylene glycol:A review

Biomass-to-ethylene glycol is an effective means to achieve high-value utilisation of cellulose but is hindered by low conversion efficiency and poor catalyst activity and stability.Glucose and cellobiose are derivatives of cellulose conversion to ethylene glycol,and it is found that studying the reaction process of both can help to understand the reaction mechanism of cellulose.It is desirable to develop a reusable,highly active catalyst to convert cellulose into ethylene glycol.This ideal catalyst might have one or more active sites described the conversion steps above.Here,we discuss the catalyst development of celluloseto-ethylene glycol,including tungsten,tin,lanthanide,and other transition metal catalysts,and special attention is given to the reaction mechanism and kinetics for preparing ethylene glycol from cellulose,and the economic advantages of biomass-to-ethylene glycol are briefly introduced.The insights given in this review will facilitate further development of efficient catalysts,for addressing the global energy crisis and climate change related to the use of fossil fuels.

Sustainable, thermoplastic and hydrophobic coating from natural cellulose and cinnamon to fabricate eco-friendly catering packaging

Non-degradable polymers cause serious environmental pollution problem,such as the widely-used while unrecyclable coatings which significantly affect the overall degradation performance of products.It is imperative and attractive to develop biodegradable functional coatings.Herein,we proposed a novel strategy to successfully prepare biodegradable,thermoplastic and hydrophobic coatings with high transparence and biosafety by weakening the interchain interactions between cellulose chain.The natural cellulose and cinnamic acid were as raw materials.Via reducing the degree of polymerization(DP)of cellulose and regulating the degree of substitution(DS)of cinnamate moiety,the obtained cellulose cinnamate(CC)exhibited not only the thermalflow behavior but also good biodegradability,which solves the conflict between the thermoplasticity and biodegradability in cellulose-based materials.The glass transition temperature(T_(g))and thermalflow temperature(T_(f))of the CC could be adjusted in a range of 150–200℃ and 180–210℃,respectively.The CC with DS<1.2 and DP≤100 degraded more than 60%after an enzyme treatment for 7 days,and degraded more than 80%after a composting treatment for 42 days.Furthermore,CC had no toxicity to human epidermal cells even at a high concentration(0.5 mg mL^(-1)).In addition,CC could be easily fabricated into multifunctional coating with high hydrophobicity,thermal adhesion and high transparence.Therefore,after combining with cellophane and paperboard,CC coating with low DP and DS could be used to prepare fully-biodegradable heat-sealing packaging,art paper,paper cups,paper straws and food packaging boxes.

Unraveling the Rheology of Nanocellulose Aqueous Suspensions:A Comprehensive Study on Biomass-Derived Nanofibrillated Cellulose

The rheological properties of nanocellulose aqueous suspensions play a critical role in the development of nanocellulose-based bulk materials.High-crystalline,high-aspect ratio,and slender nanofibrillated cellulose(NFC)were extracted from four biomass resources.The cellulose nanofibrils and nanofibril bundles formed inter-connected networks in the NFC aqueous suspensions.The storage moduli of the suspensions with different concentrations were higher than their corresponding loss moduli.As the concentration increased,the storage and loss modulus of NFC dispersion increased.When the shear rate increased to a certain value,there were differences in the changing trend of the rheological behavior of NFC aqueous suspensions derived from different biomass resources and the suspensions with different solid concentrations.NFC dispersion’s storage and loss modulus increased when the temperature rose to nearly 80℃.We hope this study can deepen the understanding of the rheological properties of NFC colloids derived from different biomass resources.

Preparation of Cellulose Acetate Butyrate Porous Micro/Nanofibrous Membranes and Their Properties

Cellulose acetate butyrate(CAB)is a cellulose ester that is commonly used in applications such as coatings and leather brighteners.However,its appearance in a fibrous form is rarely reported.CAB porous micro/nanofibrous membranes with a large number of nanopores on the fiber surface were successfully prepared by electrospinning with dichloromethane(DCM)/acetone(AC)as the mixed solvent.Apparent morphology,porosity,moisture permeability,air permeability,static water contact angles,and thermal conductivity of the fibrous membranes were investigated at different spinning voltages.The results showed that with the increase of the spinning voltage,the average fiber diameter of the CAB porous micro/nanofibrous membranes gradually decreased and the fiber diameter distribution was more uniform.When the spinning voltage reached 40 kV,the porosity reached 91.38%,the moisture permeability was up to 7430 g/(m^(2)·d),the air permeability was up to 36.289 mm/s,the static water contact angle was up to 145.0°,while the thermal conductivity of the fibrous membranes reached 0.030 W/(m·K).The material can be applied as thermal-insulation,waterproof and moisture-permeable membranes.

Microporous Cyclodextrin Film with Funnel-type Channel Polymerized on Electrospun Cellulose Acetate Membrane as Separators for Strong Trapping Polysulfides and Boosting Charging in Lithium-Sulfur Batteries

The“shuttle effect”of polysulfides hampers the commercialization of lithium-sulfur(Li-S)batteries.Here,a thin molecular sieve film was decorated on the surface of an electrospun cellulose acetate(CA)membrane derived from recycled cigarette filters,where the truncated cone structureβ-cyclodextrin(β-CD)was selected as the building block to physically block and chemically trap polysulfides while simultaneously dramatically speeding up ion transport.Furthermore,on theβ-CD free side of the separator facing the cathode,graphite carbon(C)was sputtered as an upper current collector,which barely increases the thickness.These benefits result in an initial discharge performance of 1378.24 mAh g^(−1) and long-term cycling stability of 863.78 mAh g^(−1) after 1000 cycles at 0.2 C for the battery with theβ-CD/CA/C separator,which is more than three times that of the PP separator after 500 cycles.Surprisingly,the funnel-type channel ofβ-CD generates a differential ionic fluid pressure on both sides,speeding up ion transport by up to 69%,and a 65.3%faster charging rate of 9484 mA g^(−1) was achieved.The“funnel effect”of a separator is regarded as a novel and high-efficiency solution for fast charging of Li-S and other lithium secondary batteries.

Comparison of Nanofibrillated Cellulose and Hydroxyethyl Cellulose in Improving the Storage Stability of Waterborne Coatings

Waterborne coatings often delaminate and settle during long-term storage,requiring the addition of thickeners.The effects of nanofibrillated cellulose(NFC)and the commonly used thickener,hydroxyethyl cellulose(HEC),on the storage stability of waterborne coatings were compared in this study.The morphology of NFC was characterized using infrared spectroscopy(FT-IR)and scanning electron microscopy(SEM).The rotational viscosity and rheological properties of the waterborne coatings with NFC and HEC were tested.Stationary settling experiments were also conducted at different temperatures to compare the difference of NFC and HEC on improving the storage stability of the waterborne coatings.The results showed that the waterborne coating with NFC exhibited pseudoplastic fluid characteristics;a small addition of NFC can achieve the same improvement effect on the storage stability of waterborne coatings as HEC.Further,the improvement effect of NFC was not affected by temperature.The waterborne coating with NFC still exhibited good storage stability at high temperatures,which was significantly superior to that of HEC.Therefore,NFC is a feasible agent for improving the prolonged storage stability and warming-induced delamination of waterborne coatings.

Homogeneous modification of carbon nanotubes with cellulose acetate

An efficient strategy that comprised shorten, chain extension, active groups introducing and homogeneous reaction tactics, was adopted to modify multiwalled carbon nanotubes （MWNTs） with cellulose acetate （CA）. Specially, by utilizing 2,4,6-trichloro- 1,3,5-triazine, a reactive intermediate of the MWNTs （MWNT-triazine） was obtained. Suitable solubility of the MWNT-triazine helps make the homogeneous modification become reality. Detailed characterizations further verified that reaction between chloride atoms in the MWNT-triazine and hydroxyl groups in the CA had contributed to the formation of MWNT-CA conjugates. The novel MWNT-CA consists of carbon （76.3%）, oxygen （18.4%） and nitrogen （5.3%）. With a nanotube-attached CA content of 42.8 wt%, the MWNT-CA is readily soluble in DMSO, NMP, DMF and DMAc. Confirmation of the CA-based modification route might lead to studies aiming for specific sorption and isolation.

Preparation and Characterization of a Novel Spherical Cellulose Adsorbent for Reduction Adsorption of Trichloroacetic Acid

A novel spherical cellulose adsorbent has been prepared by homogeneous graft polymerization of N,N＇-methylenebisacrylamide （MBA） onto cellulose in an ionic liquid, 1-N-butyl-3-methylimidazolium chloride （BMIMC1）, which was then partially amine methylated through Mannich reaction to get bifunctionalized materials containing both amide and sulphinate moities. Factors affecting the attachment of functional groups were investigated. The adsorbent was characterized by Elemental Analysis （EA）, Fourier Transform Infrared Spectroscopy （FTIR） and Scanning Electron Microscope （SEM）. Cellulose adsorbent was then tested for its potential applications in the reduction adsorption oftrichloroacetic acid （TCAA） from aqueous solutions.

CHARACTERIZATION OF REGENERATED CELLULOSE MEMBRANES HYDROLYZED FROM CELLULOSE ACETATE

A series of cellulose acetate membranes were prepared by using formamide as additive, and then were hydrolyzed in 4 wt% aqueous NaOH solution for 8 h to obtain regenerated cellulose membranes. The dependence of degree of substitution, structure, porous properties, solubility and thermal stability on hydrolysis time was studied by chemical titration, Fourier transform infrared spectroscopy, scanning electron microscopy, wide-angle X-ray diffraction, and differential scanning calorimetry, respectively. The results indicated that the pore size of the regenerated cellulose membranes was slightly smaller than that of cellulose acetate membrane, while solvent-resistance, crystallinity and thermostability were significantly improved. This work provides a simple way to prepare the porous cellulose membranes, which not only kept the good pore characteristics of cellulose acetate membranes, but also possessed solvent-resistance, high crystallinity and thermostability. Therefore, the application range of cellulose acetate membranes can be expanded.

Development of Biofunctionalized Cellulose Acetate Nanoscaffolds for Heart Valve Tissue Engineering

Currently-used mechanical and biological heart valve prostheses have a satisfactory short-term performance, but may exhibit several major drawbacks on the long-term. Mechanical prostheses, based on carbon, metallic and polymeric components, require permanent anticoagulation treatment, and their usage often leads to adverse reactions, e.g. thromboembolic complications and endocarditis. In recent years, there is a need for a heart valve prosthesis that can grow, repair and remodel. The concept of tissue engineering offers good prospects into the development of such a device. An ideal scaffold should mimic the structural and purposeful profile of materials found in the natural extracellular matrix (ECM) architecture. The goal of this study was to develop cellulose acetate scaffolds (CA) for valve tissue regeneration. After their thorough physicochemical and biological characterization, a biofunctionalization process was made to increase the cell proliferation. Especially, the surface of scaffolds was amplified with functional molecules, such as RGD peptides (Arg-Gly-Asp) and YIGSRG laminins (Tyrosine-Isoleucine-Glycine-Serine-Arginine-Glycine) which immobilized through biotin-streptavidin bond, the strongest non-covalent bond in nature. Last step was to successfully coat an aortic metallic valve with CA biofunctionallized nanoscaffolds and cultivate cells in order to create an anatomical structure comparable to the native valve. Promising results have been obtained with CA-based nanoscaffolds. We found that cells grown successfully on the biofunctionalized valve surface thereby scaffolds that resemble the native tissues, elaborated with bioactive factors such as RGD peptides and laminins not only make the valve’s surface biocompatible but also they could promote endothyliazation of cardiac valves causing an anti-coagulant effect

Interfacial Properties of Ethyl Cellulose/Cellulose Acetate Blends by HPLC

The high performance liquid chromatography method (HPLC) with ethyl cellulose/cellulose acetate (EC/CA) blends and EC as column packing material, and small molecular weight compound as probe molecules was employed to measure the retention volume (VR) and equilibrium distribution coefficient (K) of both inorganic and organic solutes. The interfacial separation properties of EC/CA blends were characterized by the HPLC data. The effects of the blends on the interfacial adsorption properties, hydrophilicity, affinity, polar and non-polar parameters of EC membrane materials were studied subsequently. The research results indicate that the interfacial adsorption properties and hydrophilicity of EC have been improved by solution blending with CA. The alloys are superior to EC in the separation efficiency for non-dissociable polar organic solute. The EC/CA alloy (80:20, ω) is suitable for desalting and desaccharifying.

THERMAL BEHAVIOR OF THERMOTROPIC HYDROXYETHYL CELLULOSE ACETATE/POLYETHYLENE BLENDS

The thermal behavior of thermotropic hydroxyethyl cellulose acetate (HECA)/polyethylene (PE) blends has been studied by DSC. It is found that the blends of HECA and PE are immiscible but the crystallization of PE is affected by HECA chains in the blends with more than 50% HECA, which results in the subordinate crystallization of PE and the formation of imperfect structures in the PE crystals. The imperfection of PE crystals in the blends can be eliminated after annealing at 393K.

Evaluation of Several Procedures for Immobilizing Cholesterol Oxidase Based on Cellulose Acetate Membrane

Immobilized cholesterol oxidase (COD) membrane with higher catalytic activity is important for biosensor. In this paper, several procedures for immobilizing COD based on cellulose acetate (CA) membrane are studied. Reasons causing different catalytic activities are also discussed.

Application and Characterization of Cellulose Acetate Membrane Produced from Herbaceous Plant: Solidago Canadensis L.

In this work,the viability of Solidago Canadensis L. for cellulose acetate membrane production was tested. The cellulose was extracted from Solidago Canadensis L. stem by organic solvents,and the cellulose diacetate was obtained by acetylization of cellulose. The properties of the intermediate products of cellulose pulp and cellulose diacetate were characterized by FT-IR and XRD. Compared with commercial cellulose diacetate,the properties of cellulose diacetate were similar to those of the commercial cellulose diacetate. The cellulose acetate membrane with desirable pure water flux and rejection rate was obtained from cellulose diacetate by solution casting. The membrane showed favorable hydrophilic property so that it had good anti-pollution performance. The maximum pure water flux of the membrane was 27. 21 m L /( cm2· h) and the maximum rejection rate was 80. 39%. The results demonstrated that the membrane obtained from herbaceous plant: Solidago Canadensis L. had good performance of ultrafiltration.

Surface Modifications of Cellulose Acetate Film for the Application of Face Shield

During the COVID-19 pandemic, personal protective equipment (PPE) has become crucial to protect humans from the transmission of the virus. The face shield is a simple and effective PPE to prevent the viral and bacterial contact. Since COVID-19 is known to be spread via respiratory droplets, the face shield has become increasingly important PPE. However, the common materials used in face shields are synthetic, environmentally unfriendly polymers, which cause an accumulation of plastic waste once disposed. Cellulose acetate (CA) can be used as an alternative for face shield films due to its ability to decompose safely in the environment;however, pristine CA cannot serve as an effective face shield due to its low hydrophobicity. In this research, the somewhat hydrophilic character of CA with a water contact angle of 55° is experimented on: hexamethyldisilazane (HMDS) is utilized to improve the hydrophobicity of CA up to a water contact angle of 77°. After the oxidization of the surface of CA via oxygen plasma, implementing HMDS shows a significant increase in hydrophobicity of the film.

LYOTROPIC AND THERMOTROPIC LIQUID CRYSTALL INE TRIALKYL CELLULOSES OBTAINED DIRECTLY FROM CELLULOSE ACETATE IN DIMETHYL SULFOXIDE

Highly substituted n-atkyl celluloses with sidechains 3 to 10 carbon atoms long have been prepared from cellulose acetate, sodium hydroxide and n-alkyl bromides with dimethyl sulfoxide as solvent. Synthetic conditions of n-alkyl celluloses were studied with respect to reaction temperature, time and yield. The molecular structure of the n-alkyl celluloses, which were obtained as white powders or as sticky, soft and birefringent solids at room temperature, was investigated by IR and NMR spectra and elemental analysis. The highly substituted n-alkyl celluloses all exhibited both therotropic and lyotropic liquid crystalline cholesteric phases in some non-polar solvents. The metting behavior and solubility of the n-alkyl celluloses were examined.

Synthesis and Characterization of a New Cellulose Acetate-Propionate Gel: Crosslinking Density Determination

Crosslinking is one of the most commonly reactions used to improve the physical properties of cellulose derivatives. Cellulose Acetate Propionate (CAP) is a commercial ester obtained as a cellulose derivative and it can be used as basis for the synthesis of crosslinked chains as described in this work. Typical used crosslinkers are di-functional compounds, such as dianhydrides or diisocyanate. The formation of polymeric 3D structures as described in this work occurs typically by the reaction of the linear chains bearing free OH groups with crosslinking agents such as dianhydrides. These reactions are used to make a very absorbent material, typically a gel. The syntheses were performed in homogeneous medium with acetate propionate in a very dry atmosphere by employing PMDA (Pyromellitic Dianhydride) and BTDA (3,3’, 4,4’ Benzophenone Tetracarboxylated Dianhydride) as crosslinking agents in a reflux system. TGA analysis has shown the different thermal stability of the gels when compared with CAP. Typical TGA curves have demonstrated the lower stability of the crosslinked chains when compared to CAP as consequence of esther linkages formed in the gels structures. The Mc, which is the value for the molar mass between crosslinkings points in 3D structure, was determined according to Flory-Rehner theory. This important parameter has demonstrated greater reactivity of PMDA in comparison with the BTDA in the reactions conditions’ employed in this work.

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.